'Lester (signe de)'
(id=16869749 ; fe=Lester (signe de) ; type=1 ; niveau=200 ;
luminosité=25 ;
somme entrante=851 creation date=2021-07-25 touchdate=2025-11-22 00:02:52.000) ≈ 6118 relations sortantes
- Lester (signe de) --
r_associated #0: 60 / 1 ->
signe
n1=Lester (signe de) | n2=signe | rel=r_associated | relid=0 | w=60
- Lester (signe de) --
r_associated #0: 56 / 0.933 ->
Lester
n1=Lester (signe de) | n2=Lester | rel=r_associated | relid=0 | w=56
- Lester (signe de) --
r_associated #0: 33 / 0.55 ->
létal
n1=Lester (signe de) | n2=létal | rel=r_associated | relid=0 | w=33
- Lester (signe de) --
r_associated #0: 29 / 0.483 ->
médecine
n1=Lester (signe de) | n2=médecine | rel=r_associated | relid=0 | w=29
- Lester (signe de) --
r_associated #0: 29 / 0.483 ->
mort
n1=Lester (signe de) | n2=mort | rel=r_associated | relid=0 | w=29
- Lester (signe de) --
r_associated #0: 27 / 0.45 ->
signe de Lester
n1=Lester (signe de) | n2=signe de Lester | rel=r_associated | relid=0 | w=27
- Lester (signe de) --
r_associated #0: 26 / 0.433 ->
onycho-ostéodysplasie
n1=Lester (signe de) | n2=onycho-ostéodysplasie | rel=r_associated | relid=0 | w=26
- Lester (signe de) --
r_associated #0: 25 / 0.417 ->
pathologie
n1=Lester (signe de) | n2=pathologie | rel=r_associated | relid=0 | w=25
- Lester (signe de) --
r_associated #0: 21 / 0.35 ->
en:Lester's sign
n1=Lester (signe de) | n2=en:Lester's sign | rel=r_associated | relid=0 | w=21
- Lester (signe de) --
r_associated #0: 15 / 0.25 ->
létalité
n1=Lester (signe de) | n2=létalité | rel=r_associated | relid=0 | w=15
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
absolu
n1=Lester (signe de) | n2=absolu | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
ce qui provoque la mort
n1=Lester (signe de) | n2=ce qui provoque la mort | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
champignons
n1=Lester (signe de) | n2=champignons | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
charge génétique
n1=Lester (signe de) | n2=charge génétique | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
complet
n1=Lester (signe de) | n2=complet | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
donne
n1=Lester (signe de) | n2=donne | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
en:deadliness
n1=Lester (signe de) | n2=en:deadliness | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
en:deadly
n1=Lester (signe de) | n2=en:deadly | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
en:lethal
n1=Lester (signe de) | n2=en:lethal | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
en:lethality
n1=Lester (signe de) | n2=en:lethality | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
entraîner la mort
n1=Lester (signe de) | n2=entraîner la mort | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
euthanasique
n1=Lester (signe de) | n2=euthanasique | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
faire mourir
n1=Lester (signe de) | n2=faire mourir | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
fatal
n1=Lester (signe de) | n2=fatal | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
fatal
(létal)
n1=Lester (signe de) | n2=fatal (létal) | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
fatale
n1=Lester (signe de) | n2=fatale | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
fatalité
n1=Lester (signe de) | n2=fatalité | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
léthalité
n1=Lester (signe de) | n2=léthalité | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
lugubre
n1=Lester (signe de) | n2=lugubre | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortalité
n1=Lester (signe de) | n2=mortalité | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortel
n1=Lester (signe de) | n2=mortel | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortel
(Adj)
n1=Lester (signe de) | n2=mortel (Adj) | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortel
(Nom)
n1=Lester (signe de) | n2=mortel (Nom) | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortel
(létal)
n1=Lester (signe de) | n2=mortel (létal) | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mortifère
n1=Lester (signe de) | n2=mortifère | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
mycologie
n1=Lester (signe de) | n2=mycologie | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
risque de mortalité
n1=Lester (signe de) | n2=risque de mortalité | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
signe de
n1=Lester (signe de) | n2=signe de | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 10 / 0.167 ->
taux de létalité
n1=Lester (signe de) | n2=taux de létalité | rel=r_associated | relid=0 | w=10
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
animal venimeux
n1=Lester (signe de) | n2=animal venimeux | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
destructeur
n1=Lester (signe de) | n2=destructeur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:'dry' amd seen in most patients, however an exudative 'wet' appearance was observed in the oldest patient from 1 family (examined at age 74)
n1=Lester (signe de) | n2=en:'dry' amd seen in most patients, however an exudative 'wet' appearance was observed in the oldest patient from 1 family (examined at age 74) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:'second wind' phenomenon
n1=Lester (signe de) | n2=en:'second wind' phenomenon | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:'shoulder' pattern of temperature-dependent potassium flux (in some patients)
n1=Lester (signe de) | n2=en:'shoulder' pattern of temperature-dependent potassium flux (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:'variant 2' has isolated methylmalonicaciduria and decreased adocbl
n1=Lester (signe de) | n2=en:'variant 2' has isolated methylmalonicaciduria and decreased adocbl | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:'variant' form of x-linked cgd retains residual cytochrome b(-245)
n1=Lester (signe de) | n2=en:'variant' form of x-linked cgd retains residual cytochrome b(-245) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(1) classic severe (onset of symptoms 4 to 7 days of age)
n1=Lester (signe de) | n2=en:(1) classic severe (onset of symptoms 4 to 7 days of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(1) infantile nephropathic (219800)
n1=Lester (signe de) | n2=en:(1) infantile nephropathic (219800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(2) intermittent
n1=Lester (signe de) | n2=en:(2) intermittent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(2) juvenile or adolescent nephropathic (219900)
n1=Lester (signe de) | n2=en:(2) juvenile or adolescent nephropathic (219900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(3) adult nonnephropathic (219750)
n1=Lester (signe de) | n2=en:(3) adult nonnephropathic (219750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(3) intermediate
n1=Lester (signe de) | n2=en:(3) intermediate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(4) thiamine-responsive form
n1=Lester (signe de) | n2=en:(4) thiamine-responsive form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:(5) dihydrolipoyl dehydrogenase (e3)-deficient
n1=Lester (signe de) | n2=en:(5) dihydrolipoyl dehydrogenase (e3)-deficient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:1 in 17,000 in china
n1=Lester (signe de) | n2=en:1 in 17,000 in china | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:1 in 19,000 in japan
n1=Lester (signe de) | n2=en:1 in 19,000 in japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:1 in 50,000 in korea
n1=Lester (signe de) | n2=en:1 in 50,000 in korea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:1 patient reported (last curated may 2012)
n1=Lester (signe de) | n2=en:1 patient reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:1.02 kb genomic deletion in 85% of batten disease alleles worldwide
n1=Lester (signe de) | n2=en:1.02 kb genomic deletion in 85% of batten disease alleles worldwide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:10-15% with primarily defects of cellular immunity, not manifesting until >2yrs of age
n1=Lester (signe de) | n2=en:10-15% with primarily defects of cellular immunity, not manifesting until >2yrs of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:10% due to paternal deletion
n1=Lester (signe de) | n2=en:10% due to paternal deletion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:12% due to epimutation
n1=Lester (signe de) | n2=en:12% due to epimutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:13% of cases secondary to familial translocation (often maternally derived)
n1=Lester (signe de) | n2=en:13% of cases secondary to familial translocation (often maternally derived) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:14 patients in 8 recessive kindreds reported (as of february 2012)
n1=Lester (signe de) | n2=en:14 patients in 8 recessive kindreds reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:14% of patients survive with polyhydramnios
n1=Lester (signe de) | n2=en:14% of patients survive with polyhydramnios | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:15 patients from 5 kindreds reported (as of february 2012)
n1=Lester (signe de) | n2=en:15 patients from 5 kindreds reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:15% cases are familial
n1=Lester (signe de) | n2=en:15% cases are familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:2 patients described
n1=Lester (signe de) | n2=en:2 patients described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:2-3% due to imprinting defects
n1=Lester (signe de) | n2=en:2-3% due to imprinting defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:2-locus model fits simultaneous autosomal recessive gene and mitochondrial gene mutation
n1=Lester (signe de) | n2=en:2-locus model fits simultaneous autosomal recessive gene and mitochondrial gene mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:2:1 female preponderance
n1=Lester (signe de) | n2=en:2:1 female preponderance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:2% due to paternal uniparental disomy of 15q11.2-q13
n1=Lester (signe de) | n2=en:2% due to paternal uniparental disomy of 15q11.2-q13 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:20-40% patients are asymptomatic
n1=Lester (signe de) | n2=en:20-40% patients are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:20% die before age one (usually secondary to renal or laryngeal defects)
n1=Lester (signe de) | n2=en:20% die before age one (usually secondary to renal or laryngeal defects) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:21 patients from 17 kindreds reported (as of february 2012)
n1=Lester (signe de) | n2=en:21 patients from 17 kindreds reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:21% of hereditary wilms tumor are bilateral
n1=Lester (signe de) | n2=en:21% of hereditary wilms tumor are bilateral | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:22q11.2 deletion can present with a variety of phenotypes including velocardiofacial syndrome (192430)
n1=Lester (signe de) | n2=en:22q11.2 deletion can present with a variety of phenotypes including velocardiofacial syndrome (192430) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:23 patients from 2 kindreds reported (as of february 2012)
n1=Lester (signe de) | n2=en:23 patients from 2 kindreds reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:25% due to mutations in ube3a (601623)
n1=Lester (signe de) | n2=en:25% due to mutations in ube3a (601623) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:3 reported cases, 1 pedigree of affected sibs, neither parent affected
n1=Lester (signe de) | n2=en:3 reported cases, 1 pedigree of affected sibs, neither parent affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:35% of cases involve ileum only (ileitis), 45% of cases involve ileum and colon (ileocolitis), 20% of cases involve colon alone - rectum spared (granulomatous colitis)
n1=Lester (signe de) | n2=en:35% of cases involve ileum only (ileitis), 45% of cases involve ileum and colon (ileocolitis), 20% of cases involve colon alone - rectum spared (granulomatous colitis) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:35% of patients have facial dysmorphism
n1=Lester (signe de) | n2=en:35% of patients have facial dysmorphism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:40 patients in 16 dominant kindreds reported (as of february 2012)
n1=Lester (signe de) | n2=en:40 patients in 16 dominant kindreds reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:40% patients have associated abnormalities
n1=Lester (signe de) | n2=en:40% patients have associated abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:46,xx carriers are unaffected
n1=Lester (signe de) | n2=en:46,xx carriers are unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:46,xy carriers are unaffected
n1=Lester (signe de) | n2=en:46,xy carriers are unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:5-10% of all wilms tumor are bilateral
n1=Lester (signe de) | n2=en:5-10% of all wilms tumor are bilateral | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:5-10% of patients have a first degree relative with ibd (crohn or ulcerative colitis)
n1=Lester (signe de) | n2=en:5-10% of patients have a first degree relative with ibd (crohn or ulcerative colitis) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:5-10% of patients have a first degree relative with ibd (ulcerative colitis or crohn disease)
n1=Lester (signe de) | n2=en:5-10% of patients have a first degree relative with ibd (ulcerative colitis or crohn disease) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:50% of cases are de novo
n1=Lester (signe de) | n2=en:50% of cases are de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:50% of cases represent new mutations associated with advanced paternal age
n1=Lester (signe de) | n2=en:50% of cases represent new mutations associated with advanced paternal age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:50% of females have learning disability or mild mental retardation
n1=Lester (signe de) | n2=en:50% of females have learning disability or mild mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:608292) are at increased risk of developing monoclonal gammopathy of undetermined significance (mgus) or multiple myeloma
n1=Lester (signe de) | n2=en:608292) are at increased risk of developing monoclonal gammopathy of undetermined significance (mgus) or multiple myeloma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:7 unrelated patients have been reported
n1=Lester (signe de) | n2=en:7 unrelated patients have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:70% due to de novo maternal deletion of 15q11.2-q13
n1=Lester (signe de) | n2=en:70% due to de novo maternal deletion of 15q11.2-q13 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:75% of affected individuals are female
n1=Lester (signe de) | n2=en:75% of affected individuals are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:78% due to chromosome 14 maternal uniparental disomy
n1=Lester (signe de) | n2=en:78% due to chromosome 14 maternal uniparental disomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:80% cases new mutations
n1=Lester (signe de) | n2=en:80% cases new mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:85-90% with manifestations in first months of life
n1=Lester (signe de) | n2=en:85-90% with manifestations in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:87% patients are female
n1=Lester (signe de) | n2=en:87% patients are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:94% develop hypertension at 18 years of age or less
n1=Lester (signe de) | n2=en:94% develop hypertension at 18 years of age or less | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:95% of cases are sporadic
n1=Lester (signe de) | n2=en:95% of cases are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:98% of finnish cases due to one mutation
n1=Lester (signe de) | n2=en:98% of finnish cases due to one mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:99+% of the mutations are fgfr3, g380r (134934.0001)
n1=Lester (signe de) | n2=en:99+% of the mutations are fgfr3, g380r (134934.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a heterozygous mutation resulting in haploinsufficiency has been reported in 1 patient
n1=Lester (signe de) | n2=en:a heterozygous mutation resulting in haploinsufficiency has been reported in 1 patient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a milder form has also been reported
n1=Lester (signe de) | n2=en:a milder form has also been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a minority of patients have onset after age 30 years
n1=Lester (signe de) | n2=en:a minority of patients have onset after age 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a mutation in the cxorf5 gene has been reported in 1 affected family
n1=Lester (signe de) | n2=en:a mutation in the cxorf5 gene has been reported in 1 affected family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a mutation in the lbr gene has been identified in 1 patient (as of july 2010)
n1=Lester (signe de) | n2=en:a mutation in the lbr gene has been identified in 1 patient (as of july 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a nonspecific marker of somatic mosaicism
n1=Lester (signe de) | n2=en:a nonspecific marker of somatic mosaicism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a pair of monozygotic twins have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:a pair of monozygotic twins have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a second family had mild intellectual disability
n1=Lester (signe de) | n2=en:a second family had mild intellectual disability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a second patient died at age 3 years
n1=Lester (signe de) | n2=en:a second patient died at age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a severe infantile variant has been rarely reported
n1=Lester (signe de) | n2=en:a severe infantile variant has been rarely reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subgroup of patients with sponastrime dysplasia have severe mental retardation
n1=Lester (signe de) | n2=en:a subgroup of patients with sponastrime dysplasia have severe mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients are responsive to vitamin b12 therapy
n1=Lester (signe de) | n2=en:a subset of patients are responsive to vitamin b12 therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients have a 'visual variant'
n1=Lester (signe de) | n2=en:a subset of patients have a 'visual variant' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients have additional features, including mental retardation and hypogonadism associated with larger deletions at xp22.3
n1=Lester (signe de) | n2=en:a subset of patients have additional features, including mental retardation and hypogonadism associated with larger deletions at xp22.3 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients have heterozygous mutations consistent with a dominant-negative effect
n1=Lester (signe de) | n2=en:a subset of patients have heterozygous mutations consistent with a dominant-negative effect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients have heterozygous mutations, which may predispose to disease development
n1=Lester (signe de) | n2=en:a subset of patients have heterozygous mutations, which may predispose to disease development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients improve with thiamine
n1=Lester (signe de) | n2=en:a subset of patients improve with thiamine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a subset of patients may have congenital abnormalities of the ocular anterior segment
n1=Lester (signe de) | n2=en:a subset of patients may have congenital abnormalities of the ocular anterior segment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:a wnt3 mutation has been identified in 1 affected family
n1=Lester (signe de) | n2=en:a wnt3 mutation has been identified in 1 affected family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:abnormal morphogenesis of first and second branchial arches
n1=Lester (signe de) | n2=en:abnormal morphogenesis of first and second branchial arches | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:abnormal sensitivity to therapeutic radiation
n1=Lester (signe de) | n2=en:abnormal sensitivity to therapeutic radiation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:abnormal transferrin pattern tends to improve with age
n1=Lester (signe de) | n2=en:abnormal transferrin pattern tends to improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 1 to 5% of patients who undergo renal transplantation develop anti-glomerular basement membrane nephritis
n1=Lester (signe de) | n2=en:about 1 to 5% of patients who undergo renal transplantation develop anti-glomerular basement membrane nephritis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 10% of patients develop exercise-induced renal failure and nephrolithiasis
n1=Lester (signe de) | n2=en:about 10% of patients develop exercise-induced renal failure and nephrolithiasis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 10% of patients have a severe early onset in the first months of life
n1=Lester (signe de) | n2=en:about 10% of patients have a severe early onset in the first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 15% of female carriers develop renal insufficiency in the second or third decade
n1=Lester (signe de) | n2=en:about 15% of female carriers develop renal insufficiency in the second or third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 20% of female mutation carriers may show mild muscle weakness
n1=Lester (signe de) | n2=en:about 20% of female mutation carriers may show mild muscle weakness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 25% of cases due to new mutations
n1=Lester (signe de) | n2=en:about 25% of cases due to new mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 5% of patients have a history of febrile seizures
n1=Lester (signe de) | n2=en:about 5% of patients have a history of febrile seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 50% of mutation carriers are asymptomatic
n1=Lester (signe de) | n2=en:about 50% of mutation carriers are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 50% of patients become wheelchair-bound at an average age of 37 years
n1=Lester (signe de) | n2=en:about 50% of patients become wheelchair-bound at an average age of 37 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 50% of patients have intellectual disability and/or hydrocephalus
n1=Lester (signe de) | n2=en:about 50% of patients have intellectual disability and/or hydrocephalus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about 8% of female mutation carriers develop dilated cardiomyopathy
n1=Lester (signe de) | n2=en:about 8% of female mutation carriers develop dilated cardiomyopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about a dozen patients have been reported (as of march 2012)
n1=Lester (signe de) | n2=en:about a dozen patients have been reported (as of march 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about half of individuals are asymptomatic and identified by newborn screening programs
n1=Lester (signe de) | n2=en:about half of individuals are asymptomatic and identified by newborn screening programs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about half of patients become wheelchair bound after long duration
n1=Lester (signe de) | n2=en:about half of patients become wheelchair bound after long duration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about half of patients report vestibular symptoms
n1=Lester (signe de) | n2=en:about half of patients report vestibular symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:about half of patients with gjb2/gjb6 deafness report vestibular symptoms
n1=Lester (signe de) | n2=en:about half of patients with gjb2/gjb6 deafness report vestibular symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:absence of both inner and outer dynein arms of cilia
n1=Lester (signe de) | n2=en:absence of both inner and outer dynein arms of cilia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:absence of premature birth, low birthweight, and exposure to oxygen
n1=Lester (signe de) | n2=en:absence of premature birth, low birthweight, and exposure to oxygen | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:absence seizures show onset between 3.5 and 4 years
n1=Lester (signe de) | n2=en:absence seizures show onset between 3.5 and 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:absence seizures usually remit by puberty
n1=Lester (signe de) | n2=en:absence seizures usually remit by puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acanthosis nigricans fades during adolescence and reappears in pregnancy
n1=Lester (signe de) | n2=en:acanthosis nigricans fades during adolescence and reappears in pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accidental injury to the self (mouth, digits) has been referred by some as 'self-mutilation'
n1=Lester (signe de) | n2=en:accidental injury to the self (mouth, digits) has been referred by some as 'self-mutilation' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for <2% of patients with alzheimer's disease
n1=Lester (signe de) | n2=en:accounts for <2% of patients with alzheimer's disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for 1-2% of lymphomas in adults
n1=Lester (signe de) | n2=en:accounts for 1-2% of lymphomas in adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for 30-50% of lymphomas in children
n1=Lester (signe de) | n2=en:accounts for 30-50% of lymphomas in children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for 5 to 7% of all cases of congenital adrenal hyperplasia
n1=Lester (signe de) | n2=en:accounts for 5 to 7% of all cases of congenital adrenal hyperplasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for 5-15% of childhood epilepsies
n1=Lester (signe de) | n2=en:accounts for 5-15% of childhood epilepsies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for 70% of all usher syndrome patients
n1=Lester (signe de) | n2=en:accounts for 70% of all usher syndrome patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:accounts for approximately 5% of the epilepsies
n1=Lester (signe de) | n2=en:accounts for approximately 5% of the epilepsies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acetazolamide is often effective
n1=Lester (signe de) | n2=en:acetazolamide is often effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acetazolamide may benefit attacks of vertigo
n1=Lester (signe de) | n2=en:acetazolamide may benefit attacks of vertigo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired autoimmune disorder
n1=Lester (signe de) | n2=en:acquired autoimmune disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired disorder
n1=Lester (signe de) | n2=en:acquired disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired form - presence of inhibiting autoantibody (igg) to vwf-cleaving protease
n1=Lester (signe de) | n2=en:acquired form - presence of inhibiting autoantibody (igg) to vwf-cleaving protease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired protein c deficiency seen in liver disease, dic, and following surgery
n1=Lester (signe de) | n2=en:acquired protein c deficiency seen in liver disease, dic, and following surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired protein s deficiency seen in pregnancy, oral contraceptive use, warfarin use, liver disease, dic, and diabetes
n1=Lester (signe de) | n2=en:acquired protein s deficiency seen in pregnancy, oral contraceptive use, warfarin use, liver disease, dic, and diabetes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acquired sporadic disorder
n1=Lester (signe de) | n2=en:acquired sporadic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acral form of skin peeling limited to hands and feet (609796)
n1=Lester (signe de) | n2=en:acral form of skin peeling limited to hands and feet (609796) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acral hemorrhagic variant
n1=Lester (signe de) | n2=en:acral hemorrhagic variant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acute attacks lasting 24-48 hours
n1=Lester (signe de) | n2=en:acute attacks lasting 24-48 hours | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acute attacks rarely occur before puberty
n1=Lester (signe de) | n2=en:acute attacks rarely occur before puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acute encephalopathic episodes may occur
n1=Lester (signe de) | n2=en:acute encephalopathic episodes may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acute episodes decrease with age and disappear
n1=Lester (signe de) | n2=en:acute episodes decrease with age and disappear | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:acute neurologic deterioration after viral illness has been reported
n1=Lester (signe de) | n2=en:acute neurologic deterioration after viral illness has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adams-stokes syndrome
n1=Lester (signe de) | n2=en:adams-stokes syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:additional developmental abnormalities may be seen in some patients
n1=Lester (signe de) | n2=en:additional developmental abnormalities may be seen in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:additional features are variably present
n1=Lester (signe de) | n2=en:additional features are variably present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adolescent or adult onset associated with neuropsychiatric symptoms
n1=Lester (signe de) | n2=en:adolescent or adult onset associated with neuropsychiatric symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adrenal insufficiency usually develops later (first decade)
n1=Lester (signe de) | n2=en:adrenal insufficiency usually develops later (first decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult form is asymptomatic
n1=Lester (signe de) | n2=en:adult form is asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult form onset has after 20 years
n1=Lester (signe de) | n2=en:adult form onset has after 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult is an acronym for acro-dermato-ungual-lacrimal-tooth
n1=Lester (signe de) | n2=en:adult is an acronym for acro-dermato-ungual-lacrimal-tooth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset
n1=Lester (signe de) | n2=en:adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset - 100-1,000 repeats
n1=Lester (signe de) | n2=en:adult onset - 100-1,000 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (18 to 60 years)
n1=Lester (signe de) | n2=en:adult onset (18 to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (20 to 40 years)
n1=Lester (signe de) | n2=en:adult onset (20 to 40 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (20 to 50 years)
n1=Lester (signe de) | n2=en:adult onset (20 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (25-45 years)
n1=Lester (signe de) | n2=en:adult onset (25-45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (27 to 48 years)
n1=Lester (signe de) | n2=en:adult onset (27 to 48 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (37 to 57 years)
n1=Lester (signe de) | n2=en:adult onset (37 to 57 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (40 to 60 years old)
n1=Lester (signe de) | n2=en:adult onset (40 to 60 years old) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (45 to 76 years)
n1=Lester (signe de) | n2=en:adult onset (45 to 76 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (after age 35 years)
n1=Lester (signe de) | n2=en:adult onset (after age 35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (before 50 years)
n1=Lester (signe de) | n2=en:adult onset (before 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean 27 years)
n1=Lester (signe de) | n2=en:adult onset (mean 27 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean 30 years, range 10-65 years)
n1=Lester (signe de) | n2=en:adult onset (mean 30 years, range 10-65 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean 30 years, range 5-60 years)
n1=Lester (signe de) | n2=en:adult onset (mean 30 years, range 5-60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean 60 years)
n1=Lester (signe de) | n2=en:adult onset (mean 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean age 37 years)
n1=Lester (signe de) | n2=en:adult onset (mean age 37 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mean of 30 years)
n1=Lester (signe de) | n2=en:adult onset (mean of 30 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (mid-forties)
n1=Lester (signe de) | n2=en:adult onset (mid-forties) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 12 to 59 years)
n1=Lester (signe de) | n2=en:adult onset (range 12 to 59 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 14 to 70 years)
n1=Lester (signe de) | n2=en:adult onset (range 14 to 70 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 15 to 53 years)
n1=Lester (signe de) | n2=en:adult onset (range 15 to 53 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 19 to 48 years)
n1=Lester (signe de) | n2=en:adult onset (range 19 to 48 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 28 to 55 years)
n1=Lester (signe de) | n2=en:adult onset (range 28 to 55 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 30 to 50 years)
n1=Lester (signe de) | n2=en:adult onset (range 30 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 34 to 66 years)
n1=Lester (signe de) | n2=en:adult onset (range 34 to 66 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 40 to 60 years)
n1=Lester (signe de) | n2=en:adult onset (range 40 to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (range 45 to 70 years)
n1=Lester (signe de) | n2=en:adult onset (range 45 to 70 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (second to sixth decade)
n1=Lester (signe de) | n2=en:adult onset (second to sixth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (sixth decade)
n1=Lester (signe de) | n2=en:adult onset (sixth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (third decade)
n1=Lester (signe de) | n2=en:adult onset (third decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (thirties to forties)
n1=Lester (signe de) | n2=en:adult onset (thirties to forties) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset (wide range of age)
n1=Lester (signe de) | n2=en:adult onset (wide range of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset after puberty
n1=Lester (signe de) | n2=en:adult onset after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset form usually presents with psychiatric manifestations
n1=Lester (signe de) | n2=en:adult onset form usually presents with psychiatric manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset from second to seventh decade
n1=Lester (signe de) | n2=en:adult onset from second to seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset has been rarely reported
n1=Lester (signe de) | n2=en:adult onset has been rarely reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset has been reported
n1=Lester (signe de) | n2=en:adult onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset has been reported (age 50 years)
n1=Lester (signe de) | n2=en:adult onset has been reported (age 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset may also occur
n1=Lester (signe de) | n2=en:adult onset may also occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset may occur
n1=Lester (signe de) | n2=en:adult onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset of gait abnormalities
n1=Lester (signe de) | n2=en:adult onset of gait abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset of muscle symptoms
n1=Lester (signe de) | n2=en:adult onset of muscle symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset of neurologic symptoms (range 30 to 46 years)
n1=Lester (signe de) | n2=en:adult onset of neurologic symptoms (range 30 to 46 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset of neurologic symptoms has been reported in 1 family
n1=Lester (signe de) | n2=en:adult onset of neurologic symptoms has been reported in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset of symptoms has been reported
n1=Lester (signe de) | n2=en:adult onset of symptoms has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset rarely reported
n1=Lester (signe de) | n2=en:adult onset rarely reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult onset, usually 30's to 40's, but up to early 60's
n1=Lester (signe de) | n2=en:adult onset, usually 30's to 40's, but up to early 60's | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult patients have heterogeneous symptoms including some with relapsing-remitting symptoms similar to multiple sclerosis
n1=Lester (signe de) | n2=en:adult patients have heterogeneous symptoms including some with relapsing-remitting symptoms similar to multiple sclerosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult-onset (range early twenties to forties)
n1=Lester (signe de) | n2=en:adult-onset (range early twenties to forties) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult-onset in third to fourth decade
n1=Lester (signe de) | n2=en:adult-onset in third to fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adult-onset is referred to as small fiber neuropathy
n1=Lester (signe de) | n2=en:adult-onset is referred to as small fiber neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adults may be asymptomatic
n1=Lester (signe de) | n2=en:adults may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:adults may lose ability to walk
n1=Lester (signe de) | n2=en:adults may lose ability to walk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected boys in 3 unrelated families have been reported, consistent with x-linked recessive inheritance (last curated september, 2015)
n1=Lester (signe de) | n2=en:affected boys in 3 unrelated families have been reported, consistent with x-linked recessive inheritance (last curated september, 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected females are infertile
n1=Lester (signe de) | n2=en:affected females are infertile | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected females have apparently normal puberty but later develop secondary amenorrhea with anovulatory cycles
n1=Lester (signe de) | n2=en:affected females have apparently normal puberty but later develop secondary amenorrhea with anovulatory cycles | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected females have been reported
n1=Lester (signe de) | n2=en:affected females have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected females may have increased spontaneous abortions
n1=Lester (signe de) | n2=en:affected females may have increased spontaneous abortions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected females report aggravation of symptoms during menstrual periods and pregnancy, with alleviation after menopause
n1=Lester (signe de) | n2=en:affected females report aggravation of symptoms during menstrual periods and pregnancy, with alleviation after menopause | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected fetuses frequently undergo spontaneous abortion
n1=Lester (signe de) | n2=en:affected fetuses frequently undergo spontaneous abortion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected girls have de novo heterozygous mutations consistent with x-linked dominant inheritance
n1=Lester (signe de) | n2=en:affected girls have de novo heterozygous mutations consistent with x-linked dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals are born with normal-appearing skin and develop scaling a few days after birth
n1=Lester (signe de) | n2=en:affected individuals are born with normal-appearing skin and develop scaling a few days after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals are highly prone to burn-related injuries
n1=Lester (signe de) | n2=en:affected individuals are highly prone to burn-related injuries | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals are negative for dermatographism
n1=Lester (signe de) | n2=en:affected individuals are negative for dermatographism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals can pull hair from any part of the body, including eyelashes and eyebrows
n1=Lester (signe de) | n2=en:affected individuals can pull hair from any part of the body, including eyelashes and eyebrows | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals die soon after birth due to respiratory failure
n1=Lester (signe de) | n2=en:affected individuals die soon after birth due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals have a relatively mild ichthyosis phenotype
n1=Lester (signe de) | n2=en:affected individuals have a relatively mild ichthyosis phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals have amnesia for events
n1=Lester (signe de) | n2=en:affected individuals have amnesia for events | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals in 1 family also exhibited severe asymmetric lower limb anomalies, which were believed to be due to mutation in another gene
n1=Lester (signe de) | n2=en:affected individuals in 1 family also exhibited severe asymmetric lower limb anomalies, which were believed to be due to mutation in another gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals may have biallelic or heterozygous mutations
n1=Lester (signe de) | n2=en:affected individuals may have biallelic or heterozygous mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals may have learning or behavioral problems during the period when seizures occur
n1=Lester (signe de) | n2=en:affected individuals may have learning or behavioral problems during the period when seizures occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals may have more than 1 cardiac structural defect, or none at all
n1=Lester (signe de) | n2=en:affected individuals may have more than 1 cardiac structural defect, or none at all | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals remain ambulatory
n1=Lester (signe de) | n2=en:affected individuals remain ambulatory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected individuals remain ambulatory in old age
n1=Lester (signe de) | n2=en:affected individuals remain ambulatory in old age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected infants appear normal
n1=Lester (signe de) | n2=en:affected infants appear normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected infants appear normal at birth
n1=Lester (signe de) | n2=en:affected infants appear normal at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected infants die in neonatal period
n1=Lester (signe de) | n2=en:affected infants die in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected infants often die in utero or in the postnatal period
n1=Lester (signe de) | n2=en:affected infants often die in utero or in the postnatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males are all result of new mutation
n1=Lester (signe de) | n2=en:affected males are all result of new mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males are infertile, whereas affected females have recurrent pregnancy loss
n1=Lester (signe de) | n2=en:affected males are infertile, whereas affected females have recurrent pregnancy loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males are somatic mosaic for mutations
n1=Lester (signe de) | n2=en:affected males are somatic mosaic for mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males have normal pubertal development and are fertile
n1=Lester (signe de) | n2=en:affected males have normal pubertal development and are fertile | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males have onset of poor vision before the age of 2 years
n1=Lester (signe de) | n2=en:affected males have onset of poor vision before the age of 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males have serotonin-related disorders such as migraine headaches and diabetes
n1=Lester (signe de) | n2=en:affected males have serotonin-related disorders such as migraine headaches and diabetes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males show onset of hematuria in first year of life
n1=Lester (signe de) | n2=en:affected males show onset of hematuria in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected males who survive are secondary to new mutations
n1=Lester (signe de) | n2=en:affected males who survive are secondary to new mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected patients have various combinations of the main clinical features
n1=Lester (signe de) | n2=en:affected patients have various combinations of the main clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affected, mild - 50-150 repeats
n1=Lester (signe de) | n2=en:affected, mild - 50-150 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affects 1 in 250,000 to 1 million people worldwide
n1=Lester (signe de) | n2=en:affects 1 in 250,000 to 1 million people worldwide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affects 1 to 3% of the population
n1=Lester (signe de) | n2=en:affects 1 to 3% of the population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affects between 1 in 200 to 1 in 400 individuals of northern european descent
n1=Lester (signe de) | n2=en:affects between 1 in 200 to 1 in 400 individuals of northern european descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affects up to 10% of the population
n1=Lester (signe de) | n2=en:affects up to 10% of the population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:affects up to 10% of women in their reproductive years
n1=Lester (signe de) | n2=en:affects up to 10% of women in their reproductive years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at death:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:age at death:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 2-4 months
n1=Lester (signe de) | n2=en:age at diagnosis 2-4 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 24 +/- 18 years for dominant disease
n1=Lester (signe de) | n2=en:age at diagnosis 24 +/- 18 years for dominant disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 26 +/- 14 years for recessive disease
n1=Lester (signe de) | n2=en:age at diagnosis 26 +/- 14 years for recessive disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 28 +/- 18 years
n1=Lester (signe de) | n2=en:age at diagnosis 28 +/- 18 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 36 +/- 20 years
n1=Lester (signe de) | n2=en:age at diagnosis 36 +/- 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis 9 +/- 6 years
n1=Lester (signe de) | n2=en:age at diagnosis 9 +/- 6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at diagnosis of cataract may range up to 40 years
n1=Lester (signe de) | n2=en:age at diagnosis of cataract may range up to 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at first pregnancy:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:age at first pregnancy:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at menarche:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:age at menarche:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at menopause:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:age at menopause:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset 14 to 44 years
n1=Lester (signe de) | n2=en:age at onset 14 to 44 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset 15 to 25 years
n1=Lester (signe de) | n2=en:age at onset 15 to 25 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset 15 to 33 years
n1=Lester (signe de) | n2=en:age at onset 15 to 33 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset 3 to 23 years
n1=Lester (signe de) | n2=en:age at onset 3 to 23 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset 8 to 55 years (mean 40 years)
n1=Lester (signe de) | n2=en:age at onset 8 to 55 years (mean 40 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset can range from infancy to childhood
n1=Lester (signe de) | n2=en:age at onset can range from infancy to childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset from 3 to 51 years (mean 19.2 years)
n1=Lester (signe de) | n2=en:age at onset from 3 to 51 years (mean 19.2 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset in females ranges from childhood to the fourth decade
n1=Lester (signe de) | n2=en:age at onset in females ranges from childhood to the fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset in males ranges from 3 to 7 years
n1=Lester (signe de) | n2=en:age at onset in males ranges from 3 to 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset most often in childhood (first decade)
n1=Lester (signe de) | n2=en:age at onset most often in childhood (first decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from 16 years to 65 years
n1=Lester (signe de) | n2=en:age at onset ranges from 16 years to 65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from 50 to 70 years
n1=Lester (signe de) | n2=en:age at onset ranges from 50 to 70 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from childhood to adulthood
n1=Lester (signe de) | n2=en:age at onset ranges from childhood to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from early childhood to after age 50 years
n1=Lester (signe de) | n2=en:age at onset ranges from early childhood to after age 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from first to sixth decade
n1=Lester (signe de) | n2=en:age at onset ranges from first to sixth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age at onset ranges from neonatal to adulthood
n1=Lester (signe de) | n2=en:age at onset ranges from neonatal to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset - birth to 15 months
n1=Lester (signe de) | n2=en:age of onset - birth to 15 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 1 to 2 years
n1=Lester (signe de) | n2=en:age of onset 1 to 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 17 to 68 years (mean 39)
n1=Lester (signe de) | n2=en:age of onset 17 to 68 years (mean 39) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 2-8 months
n1=Lester (signe de) | n2=en:age of onset 2-8 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 20-65 years
n1=Lester (signe de) | n2=en:age of onset 20-65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 23-59 years
n1=Lester (signe de) | n2=en:age of onset 23-59 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 25-45 years of age (one patient presented with hearing loss at age 4)
n1=Lester (signe de) | n2=en:age of onset 25-45 years of age (one patient presented with hearing loss at age 4) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 28 to 70 years
n1=Lester (signe de) | n2=en:age of onset 28 to 70 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 30 to 60 years
n1=Lester (signe de) | n2=en:age of onset 30 to 60 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 36 to 55 years (mean 47)
n1=Lester (signe de) | n2=en:age of onset 36 to 55 years (mean 47) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 43-64 years
n1=Lester (signe de) | n2=en:age of onset 43-64 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 5 to 19 years
n1=Lester (signe de) | n2=en:age of onset 5 to 19 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 5 to 22 years (mean 6.9)
n1=Lester (signe de) | n2=en:age of onset 5 to 22 years (mean 6.9) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 5 to 40 years
n1=Lester (signe de) | n2=en:age of onset 5 to 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset 6-12 years
n1=Lester (signe de) | n2=en:age of onset 6-12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset between 20 to 30 years
n1=Lester (signe de) | n2=en:age of onset between 20 to 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset between 5 and 10 years of age
n1=Lester (signe de) | n2=en:age of onset between 5 and 10 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset between 6 and 45 years of age
n1=Lester (signe de) | n2=en:age of onset between 6 and 45 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset between 6 to 10 years of age
n1=Lester (signe de) | n2=en:age of onset between 6 to 10 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset from 10 to 40 years
n1=Lester (signe de) | n2=en:age of onset from 10 to 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset from 18 to 45 years
n1=Lester (signe de) | n2=en:age of onset from 18 to 45 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset from third to sixth decade of life
n1=Lester (signe de) | n2=en:age of onset from third to sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset of distal lower limb weakness 8-16 years
n1=Lester (signe de) | n2=en:age of onset of distal lower limb weakness 8-16 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset of upper limb involvement 10-43 years
n1=Lester (signe de) | n2=en:age of onset of upper limb involvement 10-43 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset ranges from 1 to 47 years
n1=Lester (signe de) | n2=en:age of onset ranges from 1 to 47 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset ranges from infancy to young adulthood (6 months-19 years)
n1=Lester (signe de) | n2=en:age of onset ranges from infancy to young adulthood (6 months-19 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset ranges from neonate to adulthood
n1=Lester (signe de) | n2=en:age of onset ranges from neonate to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset third decade
n1=Lester (signe de) | n2=en:age of onset third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset usually 1 week to 2 years
n1=Lester (signe de) | n2=en:age of onset usually 1 week to 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset varies (7 to 28 years of age)
n1=Lester (signe de) | n2=en:age of onset varies (7 to 28 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset varies between 18 years and 53 years
n1=Lester (signe de) | n2=en:age of onset varies between 18 years and 53 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset varies from 5-32 years of age
n1=Lester (signe de) | n2=en:age of onset varies from 5-32 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset varies ranging from 3 weeks to 22 years
n1=Lester (signe de) | n2=en:age of onset varies ranging from 3 weeks to 22 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset within the first years of life
n1=Lester (signe de) | n2=en:age of onset within the first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset, 6-20 years
n1=Lester (signe de) | n2=en:age of onset, 6-20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age of onset/diagnosis 12-35 years
n1=Lester (signe de) | n2=en:age of onset/diagnosis 12-35 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age on onset - adolescence
n1=Lester (signe de) | n2=en:age on onset - adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age-dependent penetrance
n1=Lester (signe de) | n2=en:age-dependent penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age-related clinical course
n1=Lester (signe de) | n2=en:age-related clinical course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:age:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age:time:pt:^egg donor:qn
n1=Lester (signe de) | n2=en:age:time:pt:^egg donor:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age:time:pt:^patient:qn:calculated
n1=Lester (signe de) | n2=en:age:time:pt:^patient:qn:calculated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age:time:pt:^patient:qn:estimated
n1=Lester (signe de) | n2=en:age:time:pt:^patient:qn:estimated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:age:time:pt:^patient:qn:reported
n1=Lester (signe de) | n2=en:age:time:pt:^patient:qn:reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:aggravated by physical activity
n1=Lester (signe de) | n2=en:aggravated by physical activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:aggressive malignancies
n1=Lester (signe de) | n2=en:aggressive malignancies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alcohol may alleviate symptoms
n1=Lester (signe de) | n2=en:alcohol may alleviate symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all affected individuals have been stillborn or died in the neonatal period
n1=Lester (signe de) | n2=en:all affected individuals have been stillborn or died in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases are de novo
n1=Lester (signe de) | n2=en:all cases are de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases due to de novo mutation (last curated february 2014)
n1=Lester (signe de) | n2=en:all cases due to de novo mutation (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases from a remote village, sabinas, in northern mexico
n1=Lester (signe de) | n2=en:all cases from a remote village, sabinas, in northern mexico | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases have been sporadic
n1=Lester (signe de) | n2=en:all cases have been sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases have been stillborn or immediate neonatal death
n1=Lester (signe de) | n2=en:all cases have been stillborn or immediate neonatal death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases occur in a jewish religious isolate originally from cochin, india
n1=Lester (signe de) | n2=en:all cases occur in a jewish religious isolate originally from cochin, india | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases occur in old order amish, lancaster county, pennsylvania
n1=Lester (signe de) | n2=en:all cases occur in old order amish, lancaster county, pennsylvania | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases presumed de novo mutation
n1=Lester (signe de) | n2=en:all cases presumed de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all cases sporadic (18 males, 7 females)
n1=Lester (signe de) | n2=en:all cases sporadic (18 males, 7 females) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all de novo mutations
n1=Lester (signe de) | n2=en:all de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all features are unilateral
n1=Lester (signe de) | n2=en:all features are unilateral | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all hearing impaired females who had been pregnant reported acute hearing loss and tinnitus immediately after parturition
n1=Lester (signe de) | n2=en:all hearing impaired females who had been pregnant reported acute hearing loss and tinnitus immediately after parturition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all known cases are caused by a finnish founder mutation in the cln8 gene (607837.0001)
n1=Lester (signe de) | n2=en:all known cases are caused by a finnish founder mutation in the cln8 gene (607837.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all patients have duplication of at least the crebbp gene (600140)
n1=Lester (signe de) | n2=en:all patients have duplication of at least the crebbp gene (600140) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all patients have severe hearing loss 10 to 15 years after onset
n1=Lester (signe de) | n2=en:all patients have severe hearing loss 10 to 15 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported cases have de novo mutations (last curated october 2014)
n1=Lester (signe de) | n2=en:all reported cases have de novo mutations (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported cases have occurred de novo
n1=Lester (signe de) | n2=en:all reported cases have occurred de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported cases have occurred sporadically
n1=Lester (signe de) | n2=en:all reported cases have occurred sporadically | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported cases have resulted from de novo mutations
n1=Lester (signe de) | n2=en:all reported cases have resulted from de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported cases result from de novo mutation (last curated july 2014)
n1=Lester (signe de) | n2=en:all reported cases result from de novo mutation (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported mutations have occurred de novo
n1=Lester (signe de) | n2=en:all reported mutations have occurred de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:all reported patients are female
n1=Lester (signe de) | n2=en:all reported patients are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic corneal dystrophy groenow type (121900), thiel-behnke type (602082), lattice type i (122200), avellino type (607541), reis-bucklers type (608470) and epithelial basement membrane (121820)
n1=Lester (signe de) | n2=en:allelic corneal dystrophy groenow type (121900), thiel-behnke type (602082), lattice type i (122200), avellino type (607541), reis-bucklers type (608470) and epithelial basement membrane (121820) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder is brugada syndrome (601144)
n1=Lester (signe de) | n2=en:allelic disorder is brugada syndrome (601144) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder is long qt syndrome-3 (lqt3, 603830)
n1=Lester (signe de) | n2=en:allelic disorder is long qt syndrome-3 (lqt3, 603830) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to a form of dilated cardiomyopathy (cmd1g, 604145)
n1=Lester (signe de) | n2=en:allelic disorder to a form of dilated cardiomyopathy (cmd1g, 604145) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to adult polyglucosan body disease (263570)
n1=Lester (signe de) | n2=en:allelic disorder to adult polyglucosan body disease (263570) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to androgen insensitivity syndrome (ais, 300068)
n1=Lester (signe de) | n2=en:allelic disorder to androgen insensitivity syndrome (ais, 300068) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to ankyloblepharon-ectodermal defects, cleft lip/palate syndrome (aec, 106260)
n1=Lester (signe de) | n2=en:allelic disorder to ankyloblepharon-ectodermal defects, cleft lip/palate syndrome (aec, 106260) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal dominant form (129490)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal dominant form (129490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal dominant nonsyndromic sensorineural deafness (dfna11, 601317) and usher syndrome type ib (276900)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal dominant nonsyndromic sensorineural deafness (dfna11, 601317) and usher syndrome type ib (276900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal dominant optic atrophy and cataract (165300)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal dominant optic atrophy and cataract (165300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal dominant spg13 (605280)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal dominant spg13 (605280) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal recessive charcot-marie-tooth disease type 4c (601596)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal recessive charcot-marie-tooth disease type 4c (601596) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal recessive deafness 21 (dfnb21, 603629)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal recessive deafness 21 (dfnb21, 603629) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal recessive form (224900)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal recessive form (224900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to autosomal recessive hearing loss (dfnb2, 600060) and usher syndrome type ib (276900)
n1=Lester (signe de) | n2=en:allelic disorder to autosomal recessive hearing loss (dfnb2, 600060) and usher syndrome type ib (276900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to benign hereditary chorea (118700), which is less severe
n1=Lester (signe de) | n2=en:allelic disorder to benign hereditary chorea (118700), which is less severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to benign recurrent intrahepatic cholestasis (bric1, 243300)
n1=Lester (signe de) | n2=en:allelic disorder to benign recurrent intrahepatic cholestasis (bric1, 243300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to brachydactyly type b (113000)
n1=Lester (signe de) | n2=en:allelic disorder to brachydactyly type b (113000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to branchiootic syndrome (bos1, 602588) and otofaciocervical syndrome (166780)
n1=Lester (signe de) | n2=en:allelic disorder to branchiootic syndrome (bos1, 602588) and otofaciocervical syndrome (166780) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to branchiootorenal syndrome (bor, 113650) and otofaciocervical syndrome (166780)
n1=Lester (signe de) | n2=en:allelic disorder to branchiootorenal syndrome (bor, 113650) and otofaciocervical syndrome (166780) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to charcot-marie-tooth disease 2f (cmt2f, 606595)
n1=Lester (signe de) | n2=en:allelic disorder to charcot-marie-tooth disease 2f (cmt2f, 606595) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to charcot-marie-tooth disease type 1a (118220)
n1=Lester (signe de) | n2=en:allelic disorder to charcot-marie-tooth disease type 1a (118220) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to charcot-marie-tooth disease type 2a2 (cmt2a2, 609260)
n1=Lester (signe de) | n2=en:allelic disorder to charcot-marie-tooth disease type 2a2 (cmt2a2, 609260) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to charcot-marie-tooth disease type 2d (cmt2d, 601472), but distinguished by less severe distal sensory involvement
n1=Lester (signe de) | n2=en:allelic disorder to charcot-marie-tooth disease type 2d (cmt2d, 601472), but distinguished by less severe distal sensory involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to child syndrome (308050)
n1=Lester (signe de) | n2=en:allelic disorder to child syndrome (308050) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress (610978), which is a more severe disorder
n1=Lester (signe de) | n2=en:allelic disorder to choreoathetosis, congenital hypothyroidism, and neonatal respiratory distress (610978), which is a more severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to cln8 (600143)
n1=Lester (signe de) | n2=en:allelic disorder to cln8 (600143) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to cmt4a (214400)
n1=Lester (signe de) | n2=en:allelic disorder to cmt4a (214400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to corticosterone methyloxidase type i deficiency (203400)
n1=Lester (signe de) | n2=en:allelic disorder to corticosterone methyloxidase type i deficiency (203400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to corticosterone methyloxidase type ii deficiency (610600)
n1=Lester (signe de) | n2=en:allelic disorder to corticosterone methyloxidase type ii deficiency (610600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to dilated cardiomyopathy 1n (cmd1n, 607487)
n1=Lester (signe de) | n2=en:allelic disorder to dilated cardiomyopathy 1n (cmd1n, 607487) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to distal spinal muscular atrophy type v (dsmav, 600794), but distinguished by more severe distal sensory involvement
n1=Lester (signe de) | n2=en:allelic disorder to distal spinal muscular atrophy type v (dsmav, 600794), but distinguished by more severe distal sensory involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to distal spinal muscular atrophy, type v (dsmav, 600794), but distinguished by the presence of spasticity
n1=Lester (signe de) | n2=en:allelic disorder to distal spinal muscular atrophy, type v (dsmav, 600794), but distinguished by the presence of spasticity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to dominant epidermolysis bullosa (ddeb, 131750)
n1=Lester (signe de) | n2=en:allelic disorder to dominant epidermolysis bullosa (ddeb, 131750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to duane-radial ray syndrome (drrs, 607323)
n1=Lester (signe de) | n2=en:allelic disorder to duane-radial ray syndrome (drrs, 607323) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to dunnigan-type familial partial lipodystrophy (151660)
n1=Lester (signe de) | n2=en:allelic disorder to dunnigan-type familial partial lipodystrophy (151660) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to early-onset sarcoidosis (609464)
n1=Lester (signe de) | n2=en:allelic disorder to early-onset sarcoidosis (609464) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to ebs dowling-meara (131760), ebs koebner (131900), and ebs weber-cockayne (131800)
n1=Lester (signe de) | n2=en:allelic disorder to ebs dowling-meara (131760), ebs koebner (131900), and ebs weber-cockayne (131800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (eec3, 604292)
n1=Lester (signe de) | n2=en:allelic disorder to ectrodactyly, ectodermal dysplasia, and cleft lip/palate syndrome 3 (eec3, 604292) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to episodic ataxia-2 (ea2, 108500) and spinocerebellar ataxia-6 (sca6, 183086)
n1=Lester (signe de) | n2=en:allelic disorder to episodic ataxia-2 (ea2, 108500) and spinocerebellar ataxia-6 (sca6, 183086) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to familial cylindromatosis (132700) and brooke-spielger syndrome (bss, 605041)
n1=Lester (signe de) | n2=en:allelic disorder to familial cylindromatosis (132700) and brooke-spielger syndrome (bss, 605041) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to familial hypertrophic cardiomyopathy (cmh, 192600) and laing distal myopathy (160500)
n1=Lester (signe de) | n2=en:allelic disorder to familial hypertrophic cardiomyopathy (cmh, 192600) and laing distal myopathy (160500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to generalized epilepsy with seizures-plus (gefs+, 604233)
n1=Lester (signe de) | n2=en:allelic disorder to generalized epilepsy with seizures-plus (gefs+, 604233) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to glut1 deficiency syndrome 1 (606777)
n1=Lester (signe de) | n2=en:allelic disorder to glut1 deficiency syndrome 1 (606777) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to hyperkalemic periodic paralysis (hypp, 170500)
n1=Lester (signe de) | n2=en:allelic disorder to hyperkalemic periodic paralysis (hypp, 170500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to hyperkalemic periodic paralysis (hypp, 608390)
n1=Lester (signe de) | n2=en:allelic disorder to hyperkalemic periodic paralysis (hypp, 608390) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to hypokalemic periodic paralysis (hokpp, 170400)
n1=Lester (signe de) | n2=en:allelic disorder to hypokalemic periodic paralysis (hokpp, 170400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to ifap syndrome (308205)
n1=Lester (signe de) | n2=en:allelic disorder to ifap syndrome (308205) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to infantile neuroaxonal dystrophy (256600)
n1=Lester (signe de) | n2=en:allelic disorder to infantile neuroaxonal dystrophy (256600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to infantile-onset ascending spastic paralysis (iahsp, 607225)
n1=Lester (signe de) | n2=en:allelic disorder to infantile-onset ascending spastic paralysis (iahsp, 607225) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to intrahepatic cholestasis of pregnancy (icp, 147480)
n1=Lester (signe de) | n2=en:allelic disorder to intrahepatic cholestasis of pregnancy (icp, 147480) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to juvenile amyotrophic lateral sclerosis 2 (als2, 205100)
n1=Lester (signe de) | n2=en:allelic disorder to juvenile amyotrophic lateral sclerosis 2 (als2, 205100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to juvenile nephronophthisis-1 (256100)
n1=Lester (signe de) | n2=en:allelic disorder to juvenile nephronophthisis-1 (256100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to juvenile primary lateral sclerosis (plsj, 606353)
n1=Lester (signe de) | n2=en:allelic disorder to juvenile primary lateral sclerosis (plsj, 606353) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to juvenile-onset amyotrophic lateral sclerosis (als2, 205100)
n1=Lester (signe de) | n2=en:allelic disorder to juvenile-onset amyotrophic lateral sclerosis (als2, 205100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to limb girdle muscular dystrophy type 1c (lgmd1c, 607801)
n1=Lester (signe de) | n2=en:allelic disorder to limb girdle muscular dystrophy type 1c (lgmd1c, 607801) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to limb-girdle muscular dystrophy type 2b (lgmd2b, 253601)
n1=Lester (signe de) | n2=en:allelic disorder to limb-girdle muscular dystrophy type 2b (lgmd2b, 253601) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to limb-mammary syndrome (lms, 603543)
n1=Lester (signe de) | n2=en:allelic disorder to limb-mammary syndrome (lms, 603543) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to long qt syndrome-1 (lqt1, 192500)
n1=Lester (signe de) | n2=en:allelic disorder to long qt syndrome-1 (lqt1, 192500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to margarita island type of ectodermal dysplasia (225060)
n1=Lester (signe de) | n2=en:allelic disorder to margarita island type of ectodermal dysplasia (225060) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to miyoshi muscular dystrophy 3 (mmd3, 613319)
n1=Lester (signe de) | n2=en:allelic disorder to miyoshi muscular dystrophy 3 (mmd3, 613319) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to miyoshi myopathy (254130) and distal myopathy with anterior tibial onset (606768)
n1=Lester (signe de) | n2=en:allelic disorder to miyoshi myopathy (254130) and distal myopathy with anterior tibial onset (606768) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to multiple familial trichoepithelioma 1 (mft1, 601606) and brooke-spiegler syndrome (bss, 605041)
n1=Lester (signe de) | n2=en:allelic disorder to multiple familial trichoepithelioma 1 (mft1, 601606) and brooke-spiegler syndrome (bss, 605041) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to multiple familial trichoepithelioma 1 (mft1, 601606) and familial cylindromatosis (fc, 132700)
n1=Lester (signe de) | n2=en:allelic disorder to multiple familial trichoepithelioma 1 (mft1, 601606) and familial cylindromatosis (fc, 132700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to neurodegeneration with brain iron accumulation 2b (nbia2b, 610217)
n1=Lester (signe de) | n2=en:allelic disorder to neurodegeneration with brain iron accumulation 2b (nbia2b, 610217) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to nf1
n1=Lester (signe de) | n2=en:allelic disorder to nf1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to nieman-pick disease type b (607616)
n1=Lester (signe de) | n2=en:allelic disorder to nieman-pick disease type b (607616) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to niemann-pick disease type a (257200)
n1=Lester (signe de) | n2=en:allelic disorder to niemann-pick disease type a (257200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to northern epilepsy (610003)
n1=Lester (signe de) | n2=en:allelic disorder to northern epilepsy (610003) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to opitz-kaveggia syndrome (305450)
n1=Lester (signe de) | n2=en:allelic disorder to opitz-kaveggia syndrome (305450) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to orofaciodigital syndrome 1 (ofd1, 311200)
n1=Lester (signe de) | n2=en:allelic disorder to orofaciodigital syndrome 1 (ofd1, 311200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to osmed (215150) allelic disorder to weissenbacher-zweymuller syndrome (277610)
n1=Lester (signe de) | n2=en:allelic disorder to osmed (215150) allelic disorder to weissenbacher-zweymuller syndrome (277610) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to osteoporosis-pseudoglioma syndrome (oppg, 259770)
n1=Lester (signe de) | n2=en:allelic disorder to osteoporosis-pseudoglioma syndrome (oppg, 259770) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to paramyotonia congenita (168300)
n1=Lester (signe de) | n2=en:allelic disorder to paramyotonia congenita (168300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to parkinson disease-1 (park1, 168601)
n1=Lester (signe de) | n2=en:allelic disorder to parkinson disease-1 (park1, 168601) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to potassium-aggravated myotonia (608390)
n1=Lester (signe de) | n2=en:allelic disorder to potassium-aggravated myotonia (608390) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to primary erythermalgia (133020)
n1=Lester (signe de) | n2=en:allelic disorder to primary erythermalgia (133020) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to progressive familial intrahepatic cholestasis-1 (pfic1, 211600)
n1=Lester (signe de) | n2=en:allelic disorder to progressive familial intrahepatic cholestasis-1 (pfic1, 211600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to progressive familial intrahepatic cholestasis-2 (pfic2, 601847)
n1=Lester (signe de) | n2=en:allelic disorder to progressive familial intrahepatic cholestasis-2 (pfic2, 601847) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to rapp-hodgkin syndrome (rhs, 129400)
n1=Lester (signe de) | n2=en:allelic disorder to rapp-hodgkin syndrome (rhs, 129400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to rett syndrome (312750)
n1=Lester (signe de) | n2=en:allelic disorder to rett syndrome (312750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to rigid spine muscular dystrophy (rsmd1, 602771)
n1=Lester (signe de) | n2=en:allelic disorder to rigid spine muscular dystrophy (rsmd1, 602771) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to rippling muscle disease (rmd, 606072)
n1=Lester (signe de) | n2=en:allelic disorder to rippling muscle disease (rmd, 606072) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to schindler disease (609241)
n1=Lester (signe de) | n2=en:allelic disorder to schindler disease (609241) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to silver syndrome (270685), but distinguished by lack of spasticity
n1=Lester (signe de) | n2=en:allelic disorder to silver syndrome (270685), but distinguished by lack of spasticity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to spastic paraplegia-3 (spg3, 182600)
n1=Lester (signe de) | n2=en:allelic disorder to spastic paraplegia-3 (spg3, 182600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to spinal muscular atrophy type i (253300)
n1=Lester (signe de) | n2=en:allelic disorder to spinal muscular atrophy type i (253300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to split-hand/foot malformation 4 (shfm4, 605289)
n1=Lester (signe de) | n2=en:allelic disorder to split-hand/foot malformation 4 (shfm4, 605289) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to stickler syndrome 3 (184840)
n1=Lester (signe de) | n2=en:allelic disorder to stickler syndrome 3 (184840) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to t cell-negative, b cell-negative, nk cell- negative scid (601457), which is more severe
n1=Lester (signe de) | n2=en:allelic disorder to t cell-negative, b cell-negative, nk cell- negative scid (601457), which is more severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to the ivic syndrome (147750)
n1=Lester (signe de) | n2=en:allelic disorder to the ivic syndrome (147750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to the zlotogora-ogur syndrome (225000)
n1=Lester (signe de) | n2=en:allelic disorder to the zlotogora-ogur syndrome (225000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to type iv glycogen storage disease (232500)
n1=Lester (signe de) | n2=en:allelic disorder to type iv glycogen storage disease (232500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to usher syndrome type 1f (602083)
n1=Lester (signe de) | n2=en:allelic disorder to usher syndrome type 1f (602083) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorder to van der woude syndrome (vws, 119300) and popliteal pterygium syndrome (pps, 119500)
n1=Lester (signe de) | n2=en:allelic disorder to van der woude syndrome (vws, 119300) and popliteal pterygium syndrome (pps, 119500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with clinical overlap include dss and cmt1b (118200)
n1=Lester (signe de) | n2=en:allelic disorders with clinical overlap include dss and cmt1b (118200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include autosomal dominant emery-dreifuss muscular dystrophy (181350), dilated cardiomyopathy type 1a (115200), and congenital muscular dystrophy (613205).
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include autosomal dominant emery-dreifuss muscular dystrophy (181350), dilated cardiomyopathy type 1a (115200), and congenital muscular dystrophy (613205). | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include charcot-marie-tooth disease type 1 (cmt1b, 118200 and cmt1a, 118220) and dejerine-sottas syndrome (dss, 145900)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include charcot-marie-tooth disease type 1 (cmt1b, 118200 and cmt1a, 118220) and dejerine-sottas syndrome (dss, 145900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include cmt1a (118220), hereditary neuropathy with liability to pressure palsies (hnpp, 162500), and dejerine-sottas syndrome (dss, 145900)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include cmt1a (118220), hereditary neuropathy with liability to pressure palsies (hnpp, 162500), and dejerine-sottas syndrome (dss, 145900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include congenital hypomyelinating neuropathy (chn, 605253) and dejerine-sottas syndrome (dss, 145900)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include congenital hypomyelinating neuropathy (chn, 605253) and dejerine-sottas syndrome (dss, 145900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include dejerine-sottas syndrome (dss, 145900), hereditary neuropathy with liability to pressure palsies (hnpp, 162500), and cmt with deafness (118300)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include dejerine-sottas syndrome (dss, 145900), hereditary neuropathy with liability to pressure palsies (hnpp, 162500), and cmt with deafness (118300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include dss, congenital hypomyelination (chn, 605253), and some forms of axonal cmt2 (see 607677)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include dss, congenital hypomyelination (chn, 605253), and some forms of axonal cmt2 (see 607677) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include hereditary lymphedema type ii (153200), lymphedema and ptosis (153000), and the lymphedema-distichiasis syndrome (153400)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include hereditary lymphedema type ii (153200), lymphedema and ptosis (153000), and the lymphedema-distichiasis syndrome (153400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic disorders with overlapping phenotypes include hereditary lymphedema type ii (153200), lymphedema and ptosis (153000), and yellow nail and lymphedema syndrome (153300)
n1=Lester (signe de) | n2=en:allelic disorders with overlapping phenotypes include hereditary lymphedema type ii (153200), lymphedema and ptosis (153000), and yellow nail and lymphedema syndrome (153300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to acrocapitofemoral dysplasia (607778)
n1=Lester (signe de) | n2=en:allelic to acrocapitofemoral dysplasia (607778) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to acrokeratosis verruciformis (101900)
n1=Lester (signe de) | n2=en:allelic to acrokeratosis verruciformis (101900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to acromesomelic dysplasia, hunter-thompson type (201250), brachydactyly, type c (113100), and fibular hypoplasia nd complex brachydactyly (228900)
n1=Lester (signe de) | n2=en:allelic to acromesomelic dysplasia, hunter-thompson type (201250), brachydactyly, type c (113100), and fibular hypoplasia nd complex brachydactyly (228900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to adult syndrome (103285), shfm4 (605289), hay-wells syndrome (106260), and limb-mammary syndrome (603543)
n1=Lester (signe de) | n2=en:allelic to adult syndrome (103285), shfm4 (605289), hay-wells syndrome (106260), and limb-mammary syndrome (603543) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to adult syndrome (103285), split hand/foot malformation 4 (605289), rapp-hodgkin syndrome (129400), hay-wells syndrome (106260), and limb-mammary syndrome (603543)
n1=Lester (signe de) | n2=en:allelic to adult syndrome (103285), split hand/foot malformation 4 (605289), rapp-hodgkin syndrome (129400), hay-wells syndrome (106260), and limb-mammary syndrome (603543) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to aicardi-goutieres syndrome (225750)
n1=Lester (signe de) | n2=en:allelic to aicardi-goutieres syndrome (225750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to anterior segment mesenchymal dysgenesis (107250)
n1=Lester (signe de) | n2=en:allelic to anterior segment mesenchymal dysgenesis (107250) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to atelosteogenesis, type ii (256050), achondrogenesis, type ib (600972), and multiple epiphyseal dysplasia, type 4 (226900)
n1=Lester (signe de) | n2=en:allelic to atelosteogenesis, type ii (256050), achondrogenesis, type ib (600972), and multiple epiphyseal dysplasia, type 4 (226900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to autosomal recessive pxe (264800)
n1=Lester (signe de) | n2=en:allelic to autosomal recessive pxe (264800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to bannayan-riley-ruvalcaba syndrome (153480), which has an earlier age at onset
n1=Lester (signe de) | n2=en:allelic to bannayan-riley-ruvalcaba syndrome (153480), which has an earlier age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to bardet-biedl syndrome 6 (209900)
n1=Lester (signe de) | n2=en:allelic to bardet-biedl syndrome 6 (209900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to birt-hogg-dube syndrome (135150)
n1=Lester (signe de) | n2=en:allelic to birt-hogg-dube syndrome (135150) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to brachydactyly, type a1 (112500)
n1=Lester (signe de) | n2=en:allelic to brachydactyly, type a1 (112500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to brachydactyly, type a2 (112600)
n1=Lester (signe de) | n2=en:allelic to brachydactyly, type a2 (112600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to cartilage-hair hypoplasia (250250)
n1=Lester (signe de) | n2=en:allelic to cartilage-hair hypoplasia (250250) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to cowden disease (158350), which has a later age at onset
n1=Lester (signe de) | n2=en:allelic to cowden disease (158350), which has a later age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to craniometaphyseal dysplasia (123000)
n1=Lester (signe de) | n2=en:allelic to craniometaphyseal dysplasia (123000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to deafness, autosomal recessive 12 (601386)
n1=Lester (signe de) | n2=en:allelic to deafness, autosomal recessive 12 (601386) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to deafness, autosomal recessive 23 (609533)
n1=Lester (signe de) | n2=en:allelic to deafness, autosomal recessive 23 (609533) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to deafness, neurosensory, autosomal recessive 18 (602092)
n1=Lester (signe de) | n2=en:allelic to deafness, neurosensory, autosomal recessive 18 (602092) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to dentin dysplasia, type 2 (125420)
n1=Lester (signe de) | n2=en:allelic to dentin dysplasia, type 2 (125420) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to dentinogenesis imperfecta 1 (125490)
n1=Lester (signe de) | n2=en:allelic to dentinogenesis imperfecta 1 (125490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to diastrophic dysplasia (222600), achondrogenesis, type 1b (600972), and multiple epiphyseal dysplasia, type 4 (226900)
n1=Lester (signe de) | n2=en:allelic to diastrophic dysplasia (222600), achondrogenesis, type 1b (600972), and multiple epiphyseal dysplasia, type 4 (226900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to diastrophic dysplasia (222600), atelosteogenesis, type ii (256050), and achondrogenesis, type ib (600972)
n1=Lester (signe de) | n2=en:allelic to diastrophic dysplasia (222600), atelosteogenesis, type ii (256050), and achondrogenesis, type ib (600972) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to dyggve-melchior-clausen disease (223800)
n1=Lester (signe de) | n2=en:allelic to dyggve-melchior-clausen disease (223800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to early-onset familial alzheimer disease (ad1, 104300)
n1=Lester (signe de) | n2=en:allelic to early-onset familial alzheimer disease (ad1, 104300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to eec3 (604292), shfm4 (605289), adult syndrome (103285), limb-mammary syndrome (603543), and rapp-hodgkin syndrome (129400)
n1=Lester (signe de) | n2=en:allelic to eec3 (604292), shfm4 (605289), adult syndrome (103285), limb-mammary syndrome (603543), and rapp-hodgkin syndrome (129400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to eec3 (604292), shfm4 (605289), rapp-hodgkin syndrome (129400), hay-wells syndrome (106260), and adult syndrome (103285)
n1=Lester (signe de) | n2=en:allelic to eec3 (604292), shfm4 (605289), rapp-hodgkin syndrome (129400), hay-wells syndrome (106260), and adult syndrome (103285) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to ellis-van creveld syndrome (225500)
n1=Lester (signe de) | n2=en:allelic to ellis-van creveld syndrome (225500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to enhanced s-cone syndrome (268100)
n1=Lester (signe de) | n2=en:allelic to enhanced s-cone syndrome (268100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to fechtner syndrome (153640), may-hegglin anomaly (155100), sebastian syndrome (605249), and epstein syndrome (153650)
n1=Lester (signe de) | n2=en:allelic to fechtner syndrome (153640), may-hegglin anomaly (155100), sebastian syndrome (605249), and epstein syndrome (153650) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly (fuhrmann syndrome, 228930)
n1=Lester (signe de) | n2=en:allelic to fibular aplasia or hypoplasia, femoral bowing, and poly-, syn-, and oligodactyly (fuhrmann syndrome, 228930) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to giant platelet syndrome (231200) and bernard-soulier syndrome, benign, autosomal dominant (153670)
n1=Lester (signe de) | n2=en:allelic to giant platelet syndrome (231200) and bernard-soulier syndrome, benign, autosomal dominant (153670) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to grebe syndrome (200700), brachydactyly type c (113100), and acromesomelic dysplasia, hunter-thompson type (201250)
n1=Lester (signe de) | n2=en:allelic to grebe syndrome (200700), brachydactyly type c (113100), and acromesomelic dysplasia, hunter-thompson type (201250) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to grebe syndrome (200700), brachydactyly, type c (113100), fibular hypoplasia and complex brachydactyly (228900)
n1=Lester (signe de) | n2=en:allelic to grebe syndrome (200700), brachydactyly, type c (113100), fibular hypoplasia and complex brachydactyly (228900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to grebe syndrome (200700), du pan syndrome (228900), and acromesomelic dysplasia, hunter thompson type (201250)
n1=Lester (signe de) | n2=en:allelic to grebe syndrome (200700), du pan syndrome (228900), and acromesomelic dysplasia, hunter thompson type (201250) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to groenouw type 1 corneal dystrophy (121900), thiel-behnke corneal dystrophy (602082), lattice type 1 corneal dystrophy (122200), lattice type iiia corneal dystrophy (608471), and reis-bucklers type corneal dystrophy (608470)
n1=Lester (signe de) | n2=en:allelic to groenouw type 1 corneal dystrophy (121900), thiel-behnke corneal dystrophy (602082), lattice type 1 corneal dystrophy (122200), lattice type iiia corneal dystrophy (608471), and reis-bucklers type corneal dystrophy (608470) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hand osteoarthritis (607850)
n1=Lester (signe de) | n2=en:allelic to hand osteoarthritis (607850) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hawkinsinuria (140350)
n1=Lester (signe de) | n2=en:allelic to hawkinsinuria (140350) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hereditary multiple leiomyoma of skin (see 150800) and hereditary leiomyomatosis and renal cell cancer (150800)
n1=Lester (signe de) | n2=en:allelic to hereditary multiple leiomyoma of skin (see 150800) and hereditary leiomyomatosis and renal cell cancer (150800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hydropic and prenatally lethal chondrodystrophy (215140)
n1=Lester (signe de) | n2=en:allelic to hydropic and prenatally lethal chondrodystrophy (215140) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hyperimmunoglobulinemia d syndrome (hids, 260920)
n1=Lester (signe de) | n2=en:allelic to hyperimmunoglobulinemia d syndrome (hids, 260920) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to hypoparathyroidism-retardation-dysmorphism syndrome (241410)
n1=Lester (signe de) | n2=en:allelic to hypoparathyroidism-retardation-dysmorphism syndrome (241410) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to infantile sialic acid storage disorder (269920)
n1=Lester (signe de) | n2=en:allelic to infantile sialic acid storage disorder (269920) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to joubert syndrome 5 (610188) and leber congenital amaurosis type x (610142)
n1=Lester (signe de) | n2=en:allelic to joubert syndrome 5 (610188) and leber congenital amaurosis type x (610142) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to kenny-caffey syndrome type 1 (244460)
n1=Lester (signe de) | n2=en:allelic to kenny-caffey syndrome type 1 (244460) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to kid syndrome (148210), dfna3 (601544), dfnb1 (220290), vohwinkel syndrome (124500), keratoderma, palmoplantar with deafness (148350)
n1=Lester (signe de) | n2=en:allelic to kid syndrome (148210), dfna3 (601544), dfnb1 (220290), vohwinkel syndrome (124500), keratoderma, palmoplantar with deafness (148350) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to leopard syndrome (151100)
n1=Lester (signe de) | n2=en:allelic to leopard syndrome (151100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to leprechaunism (246200) and insulin-resistant diabetes mellitus with acanthosis nigricans (147670)
n1=Lester (signe de) | n2=en:allelic to leprechaunism (246200) and insulin-resistant diabetes mellitus with acanthosis nigricans (147670) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to marshall syndrome (154780)
n1=Lester (signe de) | n2=en:allelic to marshall syndrome (154780) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to may-hegglin anomaly (155100), fechtner syndrome (153640), epstein syndrome (153650) and deafness, autosomal dominant 17 (603622)
n1=Lester (signe de) | n2=en:allelic to may-hegglin anomaly (155100), fechtner syndrome (153640), epstein syndrome (153650) and deafness, autosomal dominant 17 (603622) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to may-heglin anomaly (155100), sebastian syndrome (605249), epstein syndrome (153650), and deafness, autosomal dominant 17 (603622)
n1=Lester (signe de) | n2=en:allelic to may-heglin anomaly (155100), sebastian syndrome (605249), epstein syndrome (153650), and deafness, autosomal dominant 17 (603622) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to metaphyseal dysplasia without hypotrichosis (250460)
n1=Lester (signe de) | n2=en:allelic to metaphyseal dysplasia without hypotrichosis (250460) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to mevalonic aciduria (610377)
n1=Lester (signe de) | n2=en:allelic to mevalonic aciduria (610377) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to mucolipidosis ii (252500)
n1=Lester (signe de) | n2=en:allelic to mucolipidosis ii (252500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to mucopolysaccharidosis ivb
n1=Lester (signe de) | n2=en:allelic to mucopolysaccharidosis ivb | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to multiple epiphyseal dysplasia, type 5 (607078) and hand osteoarthritis (607850)
n1=Lester (signe de) | n2=en:allelic to multiple epiphyseal dysplasia, type 5 (607078) and hand osteoarthritis (607850) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to multiple pterygium syndrome, lethal type (253290)
n1=Lester (signe de) | n2=en:allelic to multiple pterygium syndrome, lethal type (253290) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to multiple synostoses syndrome 1 (186500), tarsal-carpal coalition syndrome (186570), and stapes ankylosis syndrome without symphalangism (184460)
n1=Lester (signe de) | n2=en:allelic to multiple synostoses syndrome 1 (186500), tarsal-carpal coalition syndrome (186570), and stapes ankylosis syndrome without symphalangism (184460) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to myosin storage myopathy (608358)
n1=Lester (signe de) | n2=en:allelic to myosin storage myopathy (608358) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to naxos disease (601214)
n1=Lester (signe de) | n2=en:allelic to naxos disease (601214) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to nephronophthisis 4 (606966)
n1=Lester (signe de) | n2=en:allelic to nephronophthisis 4 (606966) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to neurofibromatosis-1 (nf1, 162200)
n1=Lester (signe de) | n2=en:allelic to neurofibromatosis-1 (nf1, 162200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to noonan syndrome (163950)
n1=Lester (signe de) | n2=en:allelic to noonan syndrome (163950) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to osmed (215150) and weissenbacher-zweymuller syndrome (277610)
n1=Lester (signe de) | n2=en:allelic to osmed (215150) and weissenbacher-zweymuller syndrome (277610) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to osteoporosis-pseudoglioma syndrome (259770), van buchem type 2 (607636), autosomal dominant osteosclerosis (144750), type i osteopetrosis (607634)
n1=Lester (signe de) | n2=en:allelic to osteoporosis-pseudoglioma syndrome (259770), van buchem type 2 (607636), autosomal dominant osteosclerosis (144750), type i osteopetrosis (607634) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to osteoporosis-pseudoglioma syndrome (259770), van buchem type 2 (607636), high bone mass (601884), autosomal dominant endosteal hyperostosis (144750)
n1=Lester (signe de) | n2=en:allelic to osteoporosis-pseudoglioma syndrome (259770), van buchem type 2 (607636), high bone mass (601884), autosomal dominant endosteal hyperostosis (144750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to pachyonychia congenita jackson-lawler type (167210)
n1=Lester (signe de) | n2=en:allelic to pachyonychia congenita jackson-lawler type (167210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to papillon-lefevre syndrome (245000) and haim-munk syndrome (245010)
n1=Lester (signe de) | n2=en:allelic to papillon-lefevre syndrome (245000) and haim-munk syndrome (245010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to papillon-lefevre syndrome (245000) and juvenile periodontitis (170650)
n1=Lester (signe de) | n2=en:allelic to papillon-lefevre syndrome (245000) and juvenile periodontitis (170650) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to pendred syndrome, deafness with goiter (274600)
n1=Lester (signe de) | n2=en:allelic to pendred syndrome, deafness with goiter (274600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to proximal symphalangism (185800), multiple synostoses syndrome (186500), and stapes ankylosis syndrome without symphalangism (184460)
n1=Lester (signe de) | n2=en:allelic to proximal symphalangism (185800), multiple synostoses syndrome (186500), and stapes ankylosis syndrome without symphalangism (184460) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to proximal symphalangism (185800), multiple synostoses syndrome (186500), and tarsal-carpal coalition syndrome (186570)
n1=Lester (signe de) | n2=en:allelic to proximal symphalangism (185800), multiple synostoses syndrome (186500), and tarsal-carpal coalition syndrome (186570) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to proximal symphalangism (185800), multiple synostoses syndrome 1 (186500), tarsal-carpal coalition syndrome (186570), and stapes ankylosis syndrome without symphalangism (184460)
n1=Lester (signe de) | n2=en:allelic to proximal symphalangism (185800), multiple synostoses syndrome 1 (186500), tarsal-carpal coalition syndrome (186570), and stapes ankylosis syndrome without symphalangism (184460) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to proximal symphalangism (185800), stapes ankylosis syndrome without symphalangism (184460), and tarsal-carpal coalition syndrome (186570)
n1=Lester (signe de) | n2=en:allelic to proximal symphalangism (185800), stapes ankylosis syndrome without symphalangism (184460), and tarsal-carpal coalition syndrome (186570) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to pseudoachondroplasia (177170)
n1=Lester (signe de) | n2=en:allelic to pseudoachondroplasia (177170) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to retinitis punctata albescens (136880), fundus albipunctatus (136880), autosomal recessive retinitis pigmentosa (268000), newfoundland rod-cone dystrophy (607476)
n1=Lester (signe de) | n2=en:allelic to retinitis punctata albescens (136880), fundus albipunctatus (136880), autosomal recessive retinitis pigmentosa (268000), newfoundland rod-cone dystrophy (607476) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to rett syndrome (312750)
n1=Lester (signe de) | n2=en:allelic to rett syndrome (312750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to roberts syndrome (268300)
n1=Lester (signe de) | n2=en:allelic to roberts syndrome (268300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to robinow syndrome, autosomal recessive (268310)
n1=Lester (signe de) | n2=en:allelic to robinow syndrome, autosomal recessive (268310) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to senior-loken syndrome 1 (266900) and joubert syndrome 4 (609583)
n1=Lester (signe de) | n2=en:allelic to senior-loken syndrome 1 (266900) and joubert syndrome 4 (609583) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to senior-loken syndrome 4 (606996)
n1=Lester (signe de) | n2=en:allelic to senior-loken syndrome 4 (606996) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to senior-loken syndrome 6 (610189) and leber congenital amaurosis type x (610142)
n1=Lester (signe de) | n2=en:allelic to senior-loken syndrome 6 (610189) and leber congenital amaurosis type x (610142) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to several forms of autosomal recessive cmt (see 214400)
n1=Lester (signe de) | n2=en:allelic to several forms of autosomal recessive cmt (see 214400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to sialuria, finnish type (604369)
n1=Lester (signe de) | n2=en:allelic to sialuria, finnish type (604369) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to spondyloepimetaphyseal dysplasia, matn-3 related (608728)
n1=Lester (signe de) | n2=en:allelic to spondyloepimetaphyseal dysplasia, matn-3 related (608728) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to stickler syndrome, type 3 (184840) and osmed (215150)
n1=Lester (signe de) | n2=en:allelic to stickler syndrome, type 3 (184840) and osmed (215150) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to stickler syndrome, type 3 (184840) and weissenbacher-zweymuller syndrome (277610)
n1=Lester (signe de) | n2=en:allelic to stickler syndrome, type 3 (184840) and weissenbacher-zweymuller syndrome (277610) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to the less severe harp syndrome (607236), which is distinguished by the presence of hypobetalipoproteinemia and acanthocytosis
n1=Lester (signe de) | n2=en:allelic to the less severe harp syndrome (607236), which is distinguished by the presence of hypobetalipoproteinemia and acanthocytosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to the more severe pantothenate kinase-associated neurodegeneration (nbia1, 234200)
n1=Lester (signe de) | n2=en:allelic to the more severe pantothenate kinase-associated neurodegeneration (nbia1, 234200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to trichorhinophalangeal syndrome, type iii (trps3, 190351)
n1=Lester (signe de) | n2=en:allelic to trichorhinophalangeal syndrome, type iii (trps3, 190351) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to trp1 (190350)
n1=Lester (signe de) | n2=en:allelic to trp1 (190350) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to type i osteopetrosis (607634), osteoporosis-pseudoglioma (259770), high bone mass (601884), autosomal dominant endosteal hyperostosis (144750)
n1=Lester (signe de) | n2=en:allelic to type i osteopetrosis (607634), osteoporosis-pseudoglioma (259770), high bone mass (601884), autosomal dominant endosteal hyperostosis (144750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to type i osteopetrosis (607634), osteoporosis-pseudoglioma (259770), type ii van buchem disease (607636), and high bone mass (601884)
n1=Lester (signe de) | n2=en:allelic to type i osteopetrosis (607634), osteoporosis-pseudoglioma (259770), type ii van buchem disease (607636), and high bone mass (601884) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to tyrosinemia, type iii (276720)
n1=Lester (signe de) | n2=en:allelic to tyrosinemia, type iii (276720) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to ulnar and fibula, absence of, with severe limb deficiency (al-awadi/raas-rothschild/schinzel phocomelia syndrome 276820)
n1=Lester (signe de) | n2=en:allelic to ulnar and fibula, absence of, with severe limb deficiency (al-awadi/raas-rothschild/schinzel phocomelia syndrome 276820) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to usher syndrome, type id (601067)
n1=Lester (signe de) | n2=en:allelic to usher syndrome, type id (601067) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to waardenburg syndrome, type iia (193510)
n1=Lester (signe de) | n2=en:allelic to waardenburg syndrome, type iia (193510) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to wiskott-aldrich syndrome (301000) and severe congenital x-linked neutropenia (300299)
n1=Lester (signe de) | n2=en:allelic to wiskott-aldrich syndrome (301000) and severe congenital x-linked neutropenia (300299) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic to wiskott-aldrich syndrome (301000) and x-linked thrombocytopenia (313900)
n1=Lester (signe de) | n2=en:allelic to wiskott-aldrich syndrome (301000) and x-linked thrombocytopenia (313900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic with cone-rod dystrophy 10 (610283)
n1=Lester (signe de) | n2=en:allelic with cone-rod dystrophy 10 (610283) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic with dentinogenesis imperfecta 1 (125490) and dentin dysplasia, type ii (125420)
n1=Lester (signe de) | n2=en:allelic with dentinogenesis imperfecta 1 (125490) and dentin dysplasia, type ii (125420) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic with retinitis pigmentosa 35 (610282)
n1=Lester (signe de) | n2=en:allelic with retinitis pigmentosa 35 (610282) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:allelic with smith-mccort dysplasia (607326)
n1=Lester (signe de) | n2=en:allelic with smith-mccort dysplasia (607326) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:almost all patients require total parenteral nutrition
n1=Lester (signe de) | n2=en:almost all patients require total parenteral nutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alopecia may spontaneously regress, become chronic, or spread diffusely
n1=Lester (signe de) | n2=en:alopecia may spontaneously regress, become chronic, or spread diffusely | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alopecia usually occurs around puberty
n1=Lester (signe de) | n2=en:alopecia usually occurs around puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alpha thalassemia-mental retardation syndrome
n1=Lester (signe de) | n2=en:alpha thalassemia-mental retardation syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alpha-l-iduronidase activity is <1% for all forms of mps1
n1=Lester (signe de) | n2=en:alpha-l-iduronidase activity is <1% for all forms of mps1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:also called 'heterozygous osmed' and 'autosomal dominant osmed'
n1=Lester (signe de) | n2=en:also called 'heterozygous osmed' and 'autosomal dominant osmed' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:alternating hemiplegia of childhood (104290) is an allelic disorder with an overlapping phenotype
n1=Lester (signe de) | n2=en:alternating hemiplegia of childhood (104290) is an allelic disorder with an overlapping phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ambulation is preserved
n1=Lester (signe de) | n2=en:ambulation is preserved | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ambulation is usually maintained during adulthood
n1=Lester (signe de) | n2=en:ambulation is usually maintained during adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ambulation usually not achieved
n1=Lester (signe de) | n2=en:ambulation usually not achieved | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:amelioration with age
n1=Lester (signe de) | n2=en:amelioration with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:an autosomal recessive form has been reported (269720)
n1=Lester (signe de) | n2=en:an autosomal recessive form has been reported (269720) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia does not respond to alpha-interferon treatment
n1=Lester (signe de) | n2=en:anemia does not respond to alpha-interferon treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia is not responsive to pyridoxine supplementation
n1=Lester (signe de) | n2=en:anemia is not responsive to pyridoxine supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia is responsive to corticosteroid treatment
n1=Lester (signe de) | n2=en:anemia is responsive to corticosteroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia is transfusion-dependent
n1=Lester (signe de) | n2=en:anemia is transfusion-dependent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia may be responsive to iron chelation treatment
n1=Lester (signe de) | n2=en:anemia may be responsive to iron chelation treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia may show favorable response to alpha-interferon treatment
n1=Lester (signe de) | n2=en:anemia may show favorable response to alpha-interferon treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia may show onset in infancy
n1=Lester (signe de) | n2=en:anemia may show onset in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia, diabetes, and deafness often show onset at different ages
n1=Lester (signe de) | n2=en:anemia, diabetes, and deafness often show onset at different ages | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anemia, hypothyroidism, aminoaciduria, and lactic acidosis all occurred in 1 patient
n1=Lester (signe de) | n2=en:anemia, hypothyroidism, aminoaciduria, and lactic acidosis all occurred in 1 patient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anesthesia complications include difficult intubation secondary to microstomia and risk of malignant hyperthermia
n1=Lester (signe de) | n2=en:anesthesia complications include difficult intubation secondary to microstomia and risk of malignant hyperthermia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:antenatal onset
n1=Lester (signe de) | n2=en:antenatal onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:antibodies can develop after pregnancy or transfusion
n1=Lester (signe de) | n2=en:antibodies can develop after pregnancy or transfusion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anticonvulsants are effective (phenobarbital, valproic acid, benzodiazepines)
n1=Lester (signe de) | n2=en:anticonvulsants are effective (phenobarbital, valproic acid, benzodiazepines) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:anticonvulsants are effective one family of thai origin has been reported (last curated march 2013)
n1=Lester (signe de) | n2=en:anticonvulsants are effective one family of thai origin has been reported (last curated march 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:aortic dissection may occur in second decade of life
n1=Lester (signe de) | n2=en:aortic dissection may occur in second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:apparent at birth
n1=Lester (signe de) | n2=en:apparent at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:apparent in newborn at birth
n1=Lester (signe de) | n2=en:apparent in newborn at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:appear normal at birth
n1=Lester (signe de) | n2=en:appear normal at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 10% of als cases are familial
n1=Lester (signe de) | n2=en:approximately 10% of als cases are familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 12 patients have been reported (as of march 2010)
n1=Lester (signe de) | n2=en:approximately 12 patients have been reported (as of march 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 25% have a severe course and die of respiratory failure
n1=Lester (signe de) | n2=en:approximately 25% have a severe course and die of respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 35% of patients die during the first 2 years of life
n1=Lester (signe de) | n2=en:approximately 35% of patients die during the first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 40% of cases are inherited or new germline mutations
n1=Lester (signe de) | n2=en:approximately 40% of cases are inherited or new germline mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 40% of patients die within newborn period
n1=Lester (signe de) | n2=en:approximately 40% of patients die within newborn period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 45% of sma1 patients also are missing both homologs of neuronal apoptosis inhibitory protein (naip, 600355), which may play a role in modifying disease severity
n1=Lester (signe de) | n2=en:approximately 45% of sma1 patients also are missing both homologs of neuronal apoptosis inhibitory protein (naip, 600355), which may play a role in modifying disease severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 50% of cases are acute, severe neonatal illness often with rapid death and 50% are chronic episodic with asymptomatic intervals
n1=Lester (signe de) | n2=en:approximately 50% of cases are acute, severe neonatal illness often with rapid death and 50% are chronic episodic with asymptomatic intervals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 50% of patients have situs inversus
n1=Lester (signe de) | n2=en:approximately 50% of patients have situs inversus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 50db loss in adulthood
n1=Lester (signe de) | n2=en:approximately 50db loss in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 60% of brrs patients have pten mutations
n1=Lester (signe de) | n2=en:approximately 60% of brrs patients have pten mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 60% of cases are due to somatic mutations and are unilateral
n1=Lester (signe de) | n2=en:approximately 60% of cases are due to somatic mutations and are unilateral | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 70-80% of cases are de novo and sporadic
n1=Lester (signe de) | n2=en:approximately 70-80% of cases are de novo and sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 80% of cs patients have pten mutations
n1=Lester (signe de) | n2=en:approximately 80% of cs patients have pten mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately 85% of type ii patients are homozygous for a missense mutation m136t (102600.0003)
n1=Lester (signe de) | n2=en:approximately 85% of type ii patients are homozygous for a missense mutation m136t (102600.0003) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately half of cases are due to de novo deletions
n1=Lester (signe de) | n2=en:approximately half of cases are due to de novo deletions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately half of cases are due to unbalanced rearrangements, which may be familial
n1=Lester (signe de) | n2=en:approximately half of cases are due to unbalanced rearrangements, which may be familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately half of patients need ambulatory support after the fifth decade
n1=Lester (signe de) | n2=en:approximately half of patients need ambulatory support after the fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately half of the mutations are de novo
n1=Lester (signe de) | n2=en:approximately half of the mutations are de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately one-third of patients become seizure-free with age
n1=Lester (signe de) | n2=en:approximately one-third of patients become seizure-free with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:approximately one-third of patients eventually lose outer hair cell function and have profound sensorineural deafness (after 10 to 20 years)
n1=Lester (signe de) | n2=en:approximately one-third of patients eventually lose outer hair cell function and have profound sensorineural deafness (after 10 to 20 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:aquired delta-spd seen in myeloproliferative disorders, myelodysplasia, and acute leukemia
n1=Lester (signe de) | n2=en:aquired delta-spd seen in myeloproliferative disorders, myelodysplasia, and acute leukemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:arrhythmias detected prenatally (in some patients)
n1=Lester (signe de) | n2=en:arrhythmias detected prenatally (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:arteriovenous malformations can occur throughout the body
n1=Lester (signe de) | n2=en:arteriovenous malformations can occur throughout the body | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:arthralgia
n1=Lester (signe de) | n2=en:arthralgia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:as of 2009, one family has been reported
n1=Lester (signe de) | n2=en:as of 2009, one family has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:assisted ambulation or wheelchair-dependent
n1=Lester (signe de) | n2=en:assisted ambulation or wheelchair-dependent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated specifically with the gba d409h mutation (606463.0006)
n1=Lester (signe de) | n2=en:associated specifically with the gba d409h mutation (606463.0006) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with a balanced translocation t(12,22)(p11.2,q13.3)
n1=Lester (signe de) | n2=en:associated with a balanced translocation t(12,22)(p11.2,q13.3) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with a disease-specific sequence change, referred to as 'dsc3,' within an open-reading frame (orf) of a 'multiple transcript system' known as dyt3
n1=Lester (signe de) | n2=en:associated with a disease-specific sequence change, referred to as 'dsc3,' within an open-reading frame (orf) of a 'multiple transcript system' known as dyt3 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with advanced paternal age
n1=Lester (signe de) | n2=en:associated with advanced paternal age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with deletion at chromosome 2q37
n1=Lester (signe de) | n2=en:associated with deletion at chromosome 2q37 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with fragile x syndrome (300624)
n1=Lester (signe de) | n2=en:associated with fragile x syndrome (300624) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with fragile x syndrome (309550)
n1=Lester (signe de) | n2=en:associated with fragile x syndrome (309550) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with hemodialysis
n1=Lester (signe de) | n2=en:associated with hemodialysis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with hla-dqa1*01, hla-dqb1*05, and hla-dqa1*01/dqb1*05 high association with hla-drb1*0102 (relative risk 167.1)
n1=Lester (signe de) | n2=en:associated with hla-dqa1*01, hla-dqb1*05, and hla-dqa1*01/dqb1*05 high association with hla-drb1*0102 (relative risk 167.1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with idiopathic generalized epilepsy (ige, 600669)
n1=Lester (signe de) | n2=en:associated with idiopathic generalized epilepsy (ige, 600669) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with imprinting and epigenetic defects in the g-protein, alpha-stimulating 1 gene (gnas1, 139320)
n1=Lester (signe de) | n2=en:associated with imprinting and epigenetic defects in the g-protein, alpha-stimulating 1 gene (gnas1, 139320) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with increased frequency of autoimmune diseases
n1=Lester (signe de) | n2=en:associated with increased frequency of autoimmune diseases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with increased paternal age
n1=Lester (signe de) | n2=en:associated with increased paternal age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with increasing age
n1=Lester (signe de) | n2=en:associated with increasing age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with iron deficiency anemia
n1=Lester (signe de) | n2=en:associated with iron deficiency anemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with malignant hyperthermia (mhs, 145600)
n1=Lester (signe de) | n2=en:associated with malignant hyperthermia (mhs, 145600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with myoclonic epilepsy
n1=Lester (signe de) | n2=en:associated with myoclonic epilepsy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with several congenital malformation syndromes (wagr 194072, beckwith-wiedemann syndrome 130650, abnormal urogenital development syndromes)
n1=Lester (signe de) | n2=en:associated with several congenital malformation syndromes (wagr 194072, beckwith-wiedemann syndrome 130650, abnormal urogenital development syndromes) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with several loci on chromosomes 11p15 (wt2, 194071), 16 (wt3, 194090), 17 (wt4, 601363), and 7 (wt5, 601583).
n1=Lester (signe de) | n2=en:associated with several loci on chromosomes 11p15 (wt2, 194071), 16 (wt3, 194090), 17 (wt4, 601363), and 7 (wt5, 601583). | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with smoking
n1=Lester (signe de) | n2=en:associated with smoking | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with susceptibility loci on chromosome 11p11 (clls1, 609630), 13q14 (clls2, 109543), 9q34.1 (clls3, 612557), 6p25.3 (clls4, 612558), and 11q24.1 (clls5, 612559)
n1=Lester (signe de) | n2=en:associated with susceptibility loci on chromosome 11p11 (clls1, 609630), 13q14 (clls2, 109543), 9q34.1 (clls3, 612557), 6p25.3 (clls4, 612558), and 11q24.1 (clls5, 612559) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with the tau (157140) h1 haplotype
n1=Lester (signe de) | n2=en:associated with the tau (157140) h1 haplotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with trauma and impaired wound repair (alcoholism, diabetes, substance abuse, liver disease)
n1=Lester (signe de) | n2=en:associated with trauma and impaired wound repair (alcoholism, diabetes, substance abuse, liver disease) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with tuberous sclerosis (191100)
n1=Lester (signe de) | n2=en:associated with tuberous sclerosis (191100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:associated with untreated phenylketonuria (261600)
n1=Lester (signe de) | n2=en:associated with untreated phenylketonuria (261600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:association between hla class ii alleles and presence of autoantibodies
n1=Lester (signe de) | n2=en:association between hla class ii alleles and presence of autoantibodies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:association of cardiac events with exercise
n1=Lester (signe de) | n2=en:association of cardiac events with exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:association with autoimmune diseases
n1=Lester (signe de) | n2=en:association with autoimmune diseases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:association with the hla-drb1*1501-dqb1*0602 haplotype has been repeatedly demonstrated in high-risk (northern european) populations.
n1=Lester (signe de) | n2=en:association with the hla-drb1*1501-dqb1*0602 haplotype has been repeatedly demonstrated in high-risk (northern european) populations. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymmetric muscle involvement
n1=Lester (signe de) | n2=en:asymmetric muscle involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic carriers of a pericentric chromosome 8 inversion, inv(8), have a 6.2% risk of having an affected child with an unbalanced recombinant chromosome 8, rec(8).
n1=Lester (signe de) | n2=en:asymptomatic carriers of a pericentric chromosome 8 inversion, inv(8), have a 6.2% risk of having an affected child with an unbalanced recombinant chromosome 8, rec(8). | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic heterozygotes susceptible to lead toxicity
n1=Lester (signe de) | n2=en:asymptomatic heterozygotes susceptible to lead toxicity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic if papillary zone is spared
n1=Lester (signe de) | n2=en:asymptomatic if papillary zone is spared | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic patients may show changes on sd-oct
n1=Lester (signe de) | n2=en:asymptomatic patients may show changes on sd-oct | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic skin lesions begin on neck in third decade of life
n1=Lester (signe de) | n2=en:asymptomatic skin lesions begin on neck in third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:asymptomatic younger patients show characteristic basal ganglia calcifications
n1=Lester (signe de) | n2=en:asymptomatic younger patients show characteristic basal ganglia calcifications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:at birth, there is generalized red scaly skin
n1=Lester (signe de) | n2=en:at birth, there is generalized red scaly skin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ataxia becomes evident at the end of the first year of life
n1=Lester (signe de) | n2=en:ataxia becomes evident at the end of the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ataxia is nonprogressive
n1=Lester (signe de) | n2=en:ataxia is nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ataxia is slowly progressive
n1=Lester (signe de) | n2=en:ataxia is slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attack frequency may occur several times per week to once per year
n1=Lester (signe de) | n2=en:attack frequency may occur several times per week to once per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks are not responsive to acetazolamide
n1=Lester (signe de) | n2=en:attacks are not responsive to acetazolamide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks may present during or after sleep
n1=Lester (signe de) | n2=en:attacks may present during or after sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks more common in women
n1=Lester (signe de) | n2=en:attacks more common in women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks often drug-induced
n1=Lester (signe de) | n2=en:attacks often drug-induced | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks precipitated by drugs (e.g. barbiturates, sulfonamides), alcohol, infection, starvation, and hormonal changes
n1=Lester (signe de) | n2=en:attacks precipitated by drugs (e.g. barbiturates, sulfonamides), alcohol, infection, starvation, and hormonal changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks precipitated by drugs, alcohol, and endocrine factors (hcp)
n1=Lester (signe de) | n2=en:attacks precipitated by drugs, alcohol, and endocrine factors (hcp) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks precipitated by hypokalemia, administration of glucose or insulin, heavy carbohydrate consumption, stress, fatigue, rest after exercise
n1=Lester (signe de) | n2=en:attacks precipitated by hypokalemia, administration of glucose or insulin, heavy carbohydrate consumption, stress, fatigue, rest after exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks rarely occur before puberty (hcp)
n1=Lester (signe de) | n2=en:attacks rarely occur before puberty (hcp) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks tend to decrease with age
n1=Lester (signe de) | n2=en:attacks tend to decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks triggered by catabolic stress, such as fever or illness
n1=Lester (signe de) | n2=en:attacks triggered by catabolic stress, such as fever or illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:attacks typically last for minutes
n1=Lester (signe de) | n2=en:attacks typically last for minutes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:atypical affected males, 'cardiac variants' 301500.0005 exist
n1=Lester (signe de) | n2=en:atypical affected males, 'cardiac variants' 301500.0005 exist | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:atypical hemolytic-uremic syndrome shows onset in first 12 months
n1=Lester (signe de) | n2=en:atypical hemolytic-uremic syndrome shows onset in first 12 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:atypical: onset in second decade, slow progression, maintenance of independent ambulation up to 40 years later
n1=Lester (signe de) | n2=en:atypical: onset in second decade, slow progression, maintenance of independent ambulation up to 40 years later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:aura may occur
n1=Lester (signe de) | n2=en:aura may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autoimmune features are variable
n1=Lester (signe de) | n2=en:autoimmune features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autoimmune manifestations are present in some patients
n1=Lester (signe de) | n2=en:autoimmune manifestations are present in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autonomic dysfunction usually precedes obvious neurologic deterioration
n1=Lester (signe de) | n2=en:autonomic dysfunction usually precedes obvious neurologic deterioration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autonomic symptoms occur with headaches
n1=Lester (signe de) | n2=en:autonomic symptoms occur with headaches | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant and autosomal recessive forms
n1=Lester (signe de) | n2=en:autosomal dominant and autosomal recessive forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant dopa-responsive dystonia (dyt5, 128230) is an allelic disorder with overlapping features
n1=Lester (signe de) | n2=en:autosomal dominant dopa-responsive dystonia (dyt5, 128230) is an allelic disorder with overlapping features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant inheritance has been rarely reported (187800)
n1=Lester (signe de) | n2=en:autosomal dominant inheritance has been rarely reported (187800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant inheritance has been reported
n1=Lester (signe de) | n2=en:autosomal dominant inheritance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant inheritance has been reported in a single family
n1=Lester (signe de) | n2=en:autosomal dominant inheritance has been reported in a single family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant omodysplasia has also been described (164745)
n1=Lester (signe de) | n2=en:autosomal dominant omodysplasia has also been described (164745) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant transmission has been rarely reported
n1=Lester (signe de) | n2=en:autosomal dominant transmission has been rarely reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant with complete penetrance
n1=Lester (signe de) | n2=en:autosomal dominant with complete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal dominant with incomplete penetrance
n1=Lester (signe de) | n2=en:autosomal dominant with incomplete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive and dominant pedigrees described
n1=Lester (signe de) | n2=en:autosomal recessive and dominant pedigrees described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cases have been reported
n1=Lester (signe de) | n2=en:autosomal recessive cases have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cases tend to have a more severe phenotype
n1=Lester (signe de) | n2=en:autosomal recessive cases tend to have a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cytochrome b-negative cgd (233690)
n1=Lester (signe de) | n2=en:autosomal recessive cytochrome b-negative cgd (233690) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cytochrome b-positive cgd, type i
n1=Lester (signe de) | n2=en:autosomal recessive cytochrome b-positive cgd, type i | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cytochrome b-positive cgd, type i (233700)
n1=Lester (signe de) | n2=en:autosomal recessive cytochrome b-positive cgd, type i (233700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cytochrome b-positive cgd, type ii
n1=Lester (signe de) | n2=en:autosomal recessive cytochrome b-positive cgd, type ii | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive cytochrome b-positive cgd, type ii (233710)
n1=Lester (signe de) | n2=en:autosomal recessive cytochrome b-positive cgd, type ii (233710) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive disorder tends to be more severe
n1=Lester (signe de) | n2=en:autosomal recessive disorder tends to be more severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive form (240220)
n1=Lester (signe de) | n2=en:autosomal recessive form (240220) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive form (277720) has also been described
n1=Lester (signe de) | n2=en:autosomal recessive form (277720) has also been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance (245600) has also been suggested
n1=Lester (signe de) | n2=en:autosomal recessive inheritance (245600) has also been suggested | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance can occur
n1=Lester (signe de) | n2=en:autosomal recessive inheritance can occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has also been reported
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has also been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been described in 2 families
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been described in 2 families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been reported
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been reported (see 601253.0010)
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been reported (see 601253.0010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been reported in 1 case
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been reported in 1 case | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been reported in 1 family
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been reported in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been reported in 1 family (as of april 2011)
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been reported in 1 family (as of april 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance has been suggested
n1=Lester (signe de) | n2=en:autosomal recessive inheritance has been suggested | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance in one family (see 603342.0010)
n1=Lester (signe de) | n2=en:autosomal recessive inheritance in one family (see 603342.0010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance with decreased penetrance (50%) is associated with a susceptibility locus on chromosome 10q26
n1=Lester (signe de) | n2=en:autosomal recessive inheritance with decreased penetrance (50%) is associated with a susceptibility locus on chromosome 10q26 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance with earlier onset has been reported in 3 patients
n1=Lester (signe de) | n2=en:autosomal recessive inheritance with earlier onset has been reported in 3 patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive inheritance with earlier onset has been suggested
n1=Lester (signe de) | n2=en:autosomal recessive inheritance with earlier onset has been suggested | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:autosomal recessive omodysplasia has also been described (258315)
n1=Lester (signe de) | n2=en:autosomal recessive omodysplasia has also been described (258315) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at death is 37 years
n1=Lester (signe de) | n2=en:average age at death is 37 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at diagnosis 17.8 years (range 2-35 years)
n1=Lester (signe de) | n2=en:average age at diagnosis 17.8 years (range 2-35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 16.6 years
n1=Lester (signe de) | n2=en:average age at onset 16.6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 18 years (range 15 to 25 years)
n1=Lester (signe de) | n2=en:average age at onset 18 years (range 15 to 25 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 18.6 years
n1=Lester (signe de) | n2=en:average age at onset 18.6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 19 years (range 5 to 38)
n1=Lester (signe de) | n2=en:average age at onset 19 years (range 5 to 38) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 31 years (range 7 to 54)
n1=Lester (signe de) | n2=en:average age at onset 31 years (range 7 to 54) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 38 years
n1=Lester (signe de) | n2=en:average age at onset 38 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset 66 years although earlier onset may occur
n1=Lester (signe de) | n2=en:average age at onset 66 years although earlier onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset between 40 and 50 years
n1=Lester (signe de) | n2=en:average age at onset between 40 and 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age at onset is 24 years (range 4 to 58 years)
n1=Lester (signe de) | n2=en:average age at onset is 24 years (range 4 to 58 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age of onset 13 years
n1=Lester (signe de) | n2=en:average age of onset 13 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age of onset 15 years (range 4 to 40)
n1=Lester (signe de) | n2=en:average age of onset 15 years (range 4 to 40) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age of onset 57 years
n1=Lester (signe de) | n2=en:average age of onset 57 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average age of onset 6 months (range birth - 2 years)
n1=Lester (signe de) | n2=en:average age of onset 6 months (range birth - 2 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average disease duration of 7 years
n1=Lester (signe de) | n2=en:average disease duration of 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average duration of illness 8 years
n1=Lester (signe de) | n2=en:average duration of illness 8 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average onset 6 months (range 3-9)
n1=Lester (signe de) | n2=en:average onset 6 months (range 3-9) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average onset 6-10 months (range 3-24)
n1=Lester (signe de) | n2=en:average onset 6-10 months (range 3-24) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:average onset of seizures 6 months (range 3-12)
n1=Lester (signe de) | n2=en:average onset of seizures 6 months (range 3-12) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:axial skeleton most commonly affected
n1=Lester (signe de) | n2=en:axial skeleton most commonly affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:basal cell neoplasms develop after second decade
n1=Lester (signe de) | n2=en:basal cell neoplasms develop after second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:basal metabolic rate index:arbitrary concentration:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:basal metabolic rate index:arbitrary concentration:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 4-generation chinese family
n1=Lester (signe de) | n2=en:based on 1 4-generation chinese family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 5-generation family (last curated january 2015)
n1=Lester (signe de) | n2=en:based on 1 5-generation family (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 family (last curated september 2012)
n1=Lester (signe de) | n2=en:based on 1 family (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 large swiss german kindred (last curated august 2015)
n1=Lester (signe de) | n2=en:based on 1 large swiss german kindred (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 patient with compound heterozygous mutation in ttc21b (last curated february 2014)
n1=Lester (signe de) | n2=en:based on 1 patient with compound heterozygous mutation in ttc21b (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 report of monozygotic twins (last curated may 2014)
n1=Lester (signe de) | n2=en:based on 1 report of monozygotic twins (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 reported family (last curated december 2013)
n1=Lester (signe de) | n2=en:based on 1 reported family (last curated december 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 reported family with oca6
n1=Lester (signe de) | n2=en:based on 1 reported family with oca6 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 reported patient (last curated november 2013)
n1=Lester (signe de) | n2=en:based on 1 reported patient (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 1 uruguayan family (last curated april 2014)
n1=Lester (signe de) | n2=en:based on 1 uruguayan family (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 13 patients in one family (last curated november 2012)
n1=Lester (signe de) | n2=en:based on 13 patients in one family (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 cousins in a consanguineous family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on 2 cousins in a consanguineous family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 families described with no mutations in the vitamin d receptor gene (vdr, 601769)
n1=Lester (signe de) | n2=en:based on 2 families described with no mutations in the vitamin d receptor gene (vdr, 601769) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 men from 2 unrelated consanguineous iranian families
n1=Lester (signe de) | n2=en:based on 2 men from 2 unrelated consanguineous iranian families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 patients with p4hb mutations (last curated april 2015)
n1=Lester (signe de) | n2=en:based on 2 patients with p4hb mutations (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 reported patients (last curated january 2013)
n1=Lester (signe de) | n2=en:based on 2 reported patients (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 reported patients, 1 male and 1 female (last curated august 2013)
n1=Lester (signe de) | n2=en:based on 2 reported patients, 1 male and 1 female (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 reports of 3 patients (last curated september 2012)
n1=Lester (signe de) | n2=en:based on 2 reports of 3 patients (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 siblings in 1 family (last curated september 2012)
n1=Lester (signe de) | n2=en:based on 2 siblings in 1 family (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 siblings in a consanguineous family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on 2 siblings in a consanguineous family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 2 unrelated chinese families (last curated july 2014).
n1=Lester (signe de) | n2=en:based on 2 unrelated chinese families (last curated july 2014). | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 3 patients from 2 families (last curated january 2015)
n1=Lester (signe de) | n2=en:based on 3 patients from 2 families (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 4 patients in one family
n1=Lester (signe de) | n2=en:based on 4 patients in one family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on 4 reported patients (last curated april 2013) repeated first-trimester abortions in mothers of 2 probands
n1=Lester (signe de) | n2=en:based on 4 reported patients (last curated april 2013) repeated first-trimester abortions in mothers of 2 probands | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a family from an endogamous jewish community of mosul, iraq (last curated august 2015)
n1=Lester (signe de) | n2=en:based on a family from an endogamous jewish community of mosul, iraq (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a report of 2 affected male cousins (last curated june 2015)
n1=Lester (signe de) | n2=en:based on a report of 2 affected male cousins (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a report of 2 monozygotic twin girls (last curated october 2015)
n1=Lester (signe de) | n2=en:based on a report of 2 monozygotic twin girls (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a report of 2 unrelated saudi patients (last curated september 2015)
n1=Lester (signe de) | n2=en:based on a report of 2 unrelated saudi patients (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a report of 4 patients from 2 consanguineous families (last curated august 2015)
n1=Lester (signe de) | n2=en:based on a report of 4 patients from 2 consanguineous families (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on a report of one dutch family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on a report of one dutch family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on description of 1 family (last curated april 2006)
n1=Lester (signe de) | n2=en:based on description of 1 family (last curated april 2006) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on detailed clinical description of 1 family
n1=Lester (signe de) | n2=en:based on detailed clinical description of 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on four patients in a four generation family
n1=Lester (signe de) | n2=en:based on four patients in a four generation family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one 4-generation german family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one 4-generation german family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one 4-generation italian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one 4-generation italian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one consanguineous palestinian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one consanguineous palestinian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one finnish family
n1=Lester (signe de) | n2=en:based on one finnish family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one italian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one italian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one jordanian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one jordanian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one large consanguineous tunisian family with limited clinical information (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one large consanguineous tunisian family with limited clinical information (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one large dutch family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one large dutch family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one large north american family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one large north american family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one pakistani family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one pakistani family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one patient (last curated february 2015)
n1=Lester (signe de) | n2=en:based on one patient (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one report of 3 consanguineous pakistani families (last curated august 2015)
n1=Lester (signe de) | n2=en:based on one report of 3 consanguineous pakistani families (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one report of 3 sibs and 1 unrelated patient of pakistani origin (last curated december 2015)
n1=Lester (signe de) | n2=en:based on one report of 3 sibs and 1 unrelated patient of pakistani origin (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one report of 4 unrelated sporadic patients
n1=Lester (signe de) | n2=en:based on one report of 4 unrelated sporadic patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one report of a 4-generation family with 4 affected males and 6 affected females
n1=Lester (signe de) | n2=en:based on one report of a 4-generation family with 4 affected males and 6 affected females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one report of brother and sister
n1=Lester (signe de) | n2=en:based on one report of brother and sister | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on one sib pair each in their seventies
n1=Lester (signe de) | n2=en:based on one sib pair each in their seventies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 3-generation family (last curated november 2014)
n1=Lester (signe de) | n2=en:based on report of 1 3-generation family (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 consanguineous kurdish family with 4 affected sisters (last curated october 2014)
n1=Lester (signe de) | n2=en:based on report of 1 consanguineous kurdish family with 4 affected sisters (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 consanguineous pakistani family (last curated may 2015)
n1=Lester (signe de) | n2=en:based on report of 1 consanguineous pakistani family (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 consanguineous turkish family (last curated june 2014)
n1=Lester (signe de) | n2=en:based on report of 1 consanguineous turkish family (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family (last curated december 2012)
n1=Lester (signe de) | n2=en:based on report of 1 family (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family (last curated december 2015)
n1=Lester (signe de) | n2=en:based on report of 1 family (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family (last curated february 2015)
n1=Lester (signe de) | n2=en:based on report of 1 family (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family (last curated january 2014)
n1=Lester (signe de) | n2=en:based on report of 1 family (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family (last curated october 2014)
n1=Lester (signe de) | n2=en:based on report of 1 family (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family of german ancestry (last curated december 2014)
n1=Lester (signe de) | n2=en:based on report of 1 family of german ancestry (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 family with 7 affected members
n1=Lester (signe de) | n2=en:based on report of 1 family with 7 affected members | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 japanese family (last curated november 2013)
n1=Lester (signe de) | n2=en:based on report of 1 japanese family (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 large 6-generation family (last curated july 2015)
n1=Lester (signe de) | n2=en:based on report of 1 large 6-generation family (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 large dutch pedigree (last curated july 2015)
n1=Lester (signe de) | n2=en:based on report of 1 large dutch pedigree (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 saudi arabian family (last curated february 2015)
n1=Lester (signe de) | n2=en:based on report of 1 saudi arabian family (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 1 swiss german kindred and 1 tunisian kindred (last curated august 2015)
n1=Lester (signe de) | n2=en:based on report of 1 swiss german kindred and 1 tunisian kindred (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 affected brothers in 1 family (last curated october 2015)
n1=Lester (signe de) | n2=en:based on report of 2 affected brothers in 1 family (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 affected sisters (last curated march 2016)
n1=Lester (signe de) | n2=en:based on report of 2 affected sisters (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 consanguineous arab families (last curated november 2014)
n1=Lester (signe de) | n2=en:based on report of 2 consanguineous arab families (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 consanguineous pakistani families (last curated march 2016)
n1=Lester (signe de) | n2=en:based on report of 2 consanguineous pakistani families (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 families (last curated january 2014)
n1=Lester (signe de) | n2=en:based on report of 2 families (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 individuals (last curated november 2013)
n1=Lester (signe de) | n2=en:based on report of 2 individuals (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 individuals in 1 consanguineous family (last curated may 2014)
n1=Lester (signe de) | n2=en:based on report of 2 individuals in 1 consanguineous family (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 patients with dhtkd1 mutation (last curated november 2014)
n1=Lester (signe de) | n2=en:based on report of 2 patients with dhtkd1 mutation (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 probands (last curated october 2014)
n1=Lester (signe de) | n2=en:based on report of 2 probands (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 siblings and 1 patient (last curated december 2014)
n1=Lester (signe de) | n2=en:based on report of 2 siblings and 1 patient (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 sibs in 2008
n1=Lester (signe de) | n2=en:based on report of 2 sibs in 2008 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 sisters (last curated october 2012)
n1=Lester (signe de) | n2=en:based on report of 2 sisters (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 turkish sisters (last curated july 2015)
n1=Lester (signe de) | n2=en:based on report of 2 turkish sisters (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 unrelated girls (last curated august 2015)
n1=Lester (signe de) | n2=en:based on report of 2 unrelated girls (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 unrelated japanese girls (last curated october 2015)
n1=Lester (signe de) | n2=en:based on report of 2 unrelated japanese girls (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 unrelated patients
n1=Lester (signe de) | n2=en:based on report of 2 unrelated patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 unrelated patients (last curated february 2016)
n1=Lester (signe de) | n2=en:based on report of 2 unrelated patients (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 2 unrelated patients (last curated may 2015)
n1=Lester (signe de) | n2=en:based on report of 2 unrelated patients (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 3 patients from 2 families (last curated march 2016)
n1=Lester (signe de) | n2=en:based on report of 3 patients from 2 families (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 3 unrelated children (last curated january 2016)
n1=Lester (signe de) | n2=en:based on report of 3 unrelated children (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 3 unrelated patients (last curated january 2016)
n1=Lester (signe de) | n2=en:based on report of 3 unrelated patients (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 4 patients from 1 family (last curated july 2015)
n1=Lester (signe de) | n2=en:based on report of 4 patients from 1 family (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 4 unrelated patients (last curated january 2016)
n1=Lester (signe de) | n2=en:based on report of 4 unrelated patients (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of 5 brothers of arab-moslem descent (last curated february 2015)
n1=Lester (signe de) | n2=en:based on report of 5 brothers of arab-moslem descent (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of a chinese father and son (last curated may 2015)
n1=Lester (signe de) | n2=en:based on report of a chinese father and son (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of a hispanic mother and son (last curated february 2016)
n1=Lester (signe de) | n2=en:based on report of a hispanic mother and son (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of one 5-generation family (last curated december 2015)
n1=Lester (signe de) | n2=en:based on report of one 5-generation family (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of one consanguineous kuwaiti family (last curated december 2014)
n1=Lester (signe de) | n2=en:based on report of one consanguineous kuwaiti family (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of one indian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on report of one indian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on report of one polish roma patient (last curated november 2014)
n1=Lester (signe de) | n2=en:based on report of one polish roma patient (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on reports of a consanguineous jordanian family and a tunisian family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on reports of a consanguineous jordanian family and a tunisian family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on reports of one consanguineous saudi family and one consanguineous turkish family (last curated december 2014)
n1=Lester (signe de) | n2=en:based on reports of one consanguineous saudi family and one consanguineous turkish family (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on reports of one family and one patient (last curated december 2015)
n1=Lester (signe de) | n2=en:based on reports of one family and one patient (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on review of 53 individuals aged 1.2-21.25 years and 11 affected adults (last curated february 2016)
n1=Lester (signe de) | n2=en:based on review of 53 individuals aged 1.2-21.25 years and 11 affected adults (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on the report of 1 consanguineous arab family (last curated january 2014)
n1=Lester (signe de) | n2=en:based on the report of 1 consanguineous arab family (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on the report of 1 japanese family (last curated july 2014)
n1=Lester (signe de) | n2=en:based on the report of 1 japanese family (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on the report of one consanguineous pakistani family (last curated august 2015)
n1=Lester (signe de) | n2=en:based on the report of one consanguineous pakistani family (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:based on the report of one lebanese family (last curated october 2014)
n1=Lester (signe de) | n2=en:based on the report of one lebanese family (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:because fetal chrng (100730) exhibits phenotypic rescue
n1=Lester (signe de) | n2=en:because fetal chrng (100730) exhibits phenotypic rescue | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:because of overlap with bardet-biedl syndrome (209900), patients should be followed by ophthalmology for development of cone-rod dystrophy until at least 10 years of age
n1=Lester (signe de) | n2=en:because of overlap with bardet-biedl syndrome (209900), patients should be followed by ophthalmology for development of cone-rod dystrophy until at least 10 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:begins as focal dystonia, later becomes segmental or generalized
n1=Lester (signe de) | n2=en:begins as focal dystonia, later becomes segmental or generalized | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:begins in feet and legs (peroneal distribution)
n1=Lester (signe de) | n2=en:begins in feet and legs (peroneal distribution) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:begins in hands or feet, later generalized
n1=Lester (signe de) | n2=en:begins in hands or feet, later generalized | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:behavioral problems including stubbornness and rage
n1=Lester (signe de) | n2=en:behavioral problems including stubbornness and rage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:benign condition
n1=Lester (signe de) | n2=en:benign condition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:benign neonatal familial convulsions (see 601764, 121200, 121201, and 269720)
n1=Lester (signe de) | n2=en:benign neonatal familial convulsions (see 601764, 121200, 121201, and 269720) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:benign trait
n1=Lester (signe de) | n2=en:benign trait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:benign, asymptomatic defect
n1=Lester (signe de) | n2=en:benign, asymptomatic defect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bethlem myopathy (158810) is an allelic disorder with a milder phenotype and autosomal dominant inheritance
n1=Lester (signe de) | n2=en:bethlem myopathy (158810) is an allelic disorder with a milder phenotype and autosomal dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:between 2 and 7% of children will develop afebrile seizure disorders later in life
n1=Lester (signe de) | n2=en:between 2 and 7% of children will develop afebrile seizure disorders later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bilateral involvement in 10% of cases
n1=Lester (signe de) | n2=en:bilateral involvement in 10% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bimodal age of onset
n1=Lester (signe de) | n2=en:bimodal age of onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bimodal onset in early childhood (median 5 years) and young adulthood (21 to 30 years)
n1=Lester (signe de) | n2=en:bimodal onset in early childhood (median 5 years) and young adulthood (21 to 30 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:birth date:time stamp -- date and time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:birth date:time stamp -- date and time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:birth incidence approximately 5.1 per million live births
n1=Lester (signe de) | n2=en:birth incidence approximately 5.1 per million live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:birth rate of 7.6 per 1,000,000
n1=Lester (signe de) | n2=en:birth rate of 7.6 per 1,000,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bleeding after trauma or surgery
n1=Lester (signe de) | n2=en:bleeding after trauma or surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bleeding episodes occur early in life and may disappear with age
n1=Lester (signe de) | n2=en:bleeding episodes occur early in life and may disappear with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bleeding is usually delayed-onset after challenge
n1=Lester (signe de) | n2=en:bleeding is usually delayed-onset after challenge | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blindness episodes are not associated with fhm episodes
n1=Lester (signe de) | n2=en:blindness episodes are not associated with fhm episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blistering and erosions tend to occur on extensor surfaces or over bony prominences
n1=Lester (signe de) | n2=en:blistering and erosions tend to occur on extensor surfaces or over bony prominences | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blistering becomes confined to the palms and soles with age
n1=Lester (signe de) | n2=en:blistering becomes confined to the palms and soles with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blistering frequency may decrease with age
n1=Lester (signe de) | n2=en:blistering frequency may decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blistering may worsen during the summer
n1=Lester (signe de) | n2=en:blistering may worsen during the summer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blistering tends to improve with age
n1=Lester (signe de) | n2=en:blistering tends to improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blisters are precipitated by minor skin trauma
n1=Lester (signe de) | n2=en:blisters are precipitated by minor skin trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blood glucose monitor with integrated lancing/blood sample
n1=Lester (signe de) | n2=en:blood glucose monitor with integrated lancing/blood sample | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:blood glucose monitor with integrated voice synthesizer
n1=Lester (signe de) | n2=en:blood glucose monitor with integrated voice synthesizer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:body habitus becomes apparent in childhood
n1=Lester (signe de) | n2=en:body habitus becomes apparent in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bone abnormalities improve with age
n1=Lester (signe de) | n2=en:bone abnormalities improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bone anomalies may be seen on prenatal ultrasound (in some patients)
n1=Lester (signe de) | n2=en:bone anomalies may be seen on prenatal ultrasound (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bone changes tend to develop after first decade
n1=Lester (signe de) | n2=en:bone changes tend to develop after first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bone fragility is not apparent at birth, but becomes evident within several months of life
n1=Lester (signe de) | n2=en:bone fragility is not apparent at birth, but becomes evident within several months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both autosomal dominant and autosomal recessive inheritance has been described
n1=Lester (signe de) | n2=en:both autosomal dominant and autosomal recessive inheritance has been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both autosomal dominant and autosomal recessive inheritance have been reported
n1=Lester (signe de) | n2=en:both autosomal dominant and autosomal recessive inheritance have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both autosomal dominant and recessive inheritance can occur
n1=Lester (signe de) | n2=en:both autosomal dominant and recessive inheritance can occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both contiguous gene syndromes show similar features such as cystinuria, growth impairment, and hypotonia
n1=Lester (signe de) | n2=en:both contiguous gene syndromes show similar features such as cystinuria, growth impairment, and hypotonia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both demyelinating and axonal features
n1=Lester (signe de) | n2=en:both demyelinating and axonal features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both germline (familial) and somatic (sporadic) mutation in kit (164920) and pdgfra (173490) have been found
n1=Lester (signe de) | n2=en:both germline (familial) and somatic (sporadic) mutation in kit (164920) and pdgfra (173490) have been found | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both heterozygous and homozygous mutations have been reported
n1=Lester (signe de) | n2=en:both heterozygous and homozygous mutations have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both heterozygous and homozygous pax3 mutations have been found
n1=Lester (signe de) | n2=en:both heterozygous and homozygous pax3 mutations have been found | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both homozygous and heterozygous edn3 mutations have been found
n1=Lester (signe de) | n2=en:both homozygous and heterozygous edn3 mutations have been found | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both homozygous and heterozygous ednrb mutations have been found
n1=Lester (signe de) | n2=en:both homozygous and heterozygous ednrb mutations have been found | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both homozygous and heterozygous mutations in lrsam1 have been reported
n1=Lester (signe de) | n2=en:both homozygous and heterozygous mutations in lrsam1 have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both mutations occurred de novo
n1=Lester (signe de) | n2=en:both mutations occurred de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both recessive and dominant inheritance have been reported
n1=Lester (signe de) | n2=en:both recessive and dominant inheritance have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:both reported cases survived beyond infancy
n1=Lester (signe de) | n2=en:both reported cases survived beyond infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:boys are more often affected than girls (3:2)
n1=Lester (signe de) | n2=en:boys are more often affected than girls (3:2) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:brain anomalies variable
n1=Lester (signe de) | n2=en:brain anomalies variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:brain mri abnormalities show improvement with time
n1=Lester (signe de) | n2=en:brain mri abnormalities show improvement with time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:brainstem, cerebellum, anterior inner rim of the corpus callosum, posterior limb of the internal capsule and the external capsule, and anterior inner rim of the corpus callosum may show disease involvement on mri
n1=Lester (signe de) | n2=en:brainstem, cerebellum, anterior inner rim of the corpus callosum, posterior limb of the internal capsule and the external capsule, and anterior inner rim of the corpus callosum may show disease involvement on mri | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:brainstem, cerebellum, internal and external capsule, inner rim of the corpus callosum may show disease involvement on mri
n1=Lester (signe de) | n2=en:brainstem, cerebellum, internal and external capsule, inner rim of the corpus callosum may show disease involvement on mri | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:breech position
n1=Lester (signe de) | n2=en:breech position | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:breech presentation
n1=Lester (signe de) | n2=en:breech presentation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:broad range in severity of presentation in sibships
n1=Lester (signe de) | n2=en:broad range in severity of presentation in sibships | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:broad spectrum of optic nerve head anomalies, with significant inter-eye differences in some patients
n1=Lester (signe de) | n2=en:broad spectrum of optic nerve head anomalies, with significant inter-eye differences in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:broad-based gait
n1=Lester (signe de) | n2=en:broad-based gait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:bullae are located randomly in familial cases and apical in sporadic cases
n1=Lester (signe de) | n2=en:bullae are located randomly in familial cases and apical in sporadic cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:by age 50 years, affected family members have a 50mm hg increase in mean arterial blood pressure compared to unaffected relatives
n1=Lester (signe de) | n2=en:by age 50 years, affected family members have a 50mm hg increase in mean arterial blood pressure compared to unaffected relatives | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:c10orf2 mutations account for approximately 35% of all peo cases
n1=Lester (signe de) | n2=en:c10orf2 mutations account for approximately 35% of all peo cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:c3hex (cis-3-hexen-1-ol) is commonly associated with sensory characteristics such as 'green' and 'grassy'
n1=Lester (signe de) | n2=en:c3hex (cis-3-hexen-1-ol) is commonly associated with sensory characteristics such as 'green' and 'grassy' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can also be caused by contiguous gene deletion on chromosome 22q11.2
n1=Lester (signe de) | n2=en:can also be caused by contiguous gene deletion on chromosome 22q11.2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be asymptomatic
n1=Lester (signe de) | n2=en:can be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be categorized into 3 groups
n1=Lester (signe de) | n2=en:can be categorized into 3 groups | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be caused by mutations in nuclear-encoded or mitochondrial-encoded genes
n1=Lester (signe de) | n2=en:can be caused by mutations in nuclear-encoded or mitochondrial-encoded genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be effectively treated with n-carbamylglutamate
n1=Lester (signe de) | n2=en:can be effectively treated with n-carbamylglutamate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be slowly or rapidly progressive
n1=Lester (signe de) | n2=en:can be slowly or rapidly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be treated by bone marrow transplantation
n1=Lester (signe de) | n2=en:can be treated by bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can be treated with physiologic levels of 1,25-dihydroxyvitamin d3 or 1-alpha-hydroxyvitamin d3
n1=Lester (signe de) | n2=en:can be treated with physiologic levels of 1,25-dihydroxyvitamin d3 or 1-alpha-hydroxyvitamin d3 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:can resemble autosomal dominant inheritance with incomplete penetrance because the disorder often results from inheritance of a null fech allele in trans with a low-expression fech mutation (612386.0015) that is prevalent in some populations
n1=Lester (signe de) | n2=en:can resemble autosomal dominant inheritance with incomplete penetrance because the disorder often results from inheritance of a null fech allele in trans with a low-expression fech mutation (612386.0015) that is prevalent in some populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cancer onset usually in mid-adulthood
n1=Lester (signe de) | n2=en:cancer onset usually in mid-adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:candidiasis is restricted to nails of hands and feet
n1=Lester (signe de) | n2=en:candidiasis is restricted to nails of hands and feet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:candidiasis is usually the first symptom
n1=Lester (signe de) | n2=en:candidiasis is usually the first symptom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:capillary malformation are apparent at birth
n1=Lester (signe de) | n2=en:capillary malformation are apparent at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carcinomas tend to develop in mid or late adulthood
n1=Lester (signe de) | n2=en:carcinomas tend to develop in mid or late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac and pulmonary dysfunction normalize in the first year of life
n1=Lester (signe de) | n2=en:cardiac and pulmonary dysfunction normalize in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac arrest and sudden death may occur, even in early childhood
n1=Lester (signe de) | n2=en:cardiac arrest and sudden death may occur, even in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac examination is usually unremarkable
n1=Lester (signe de) | n2=en:cardiac examination is usually unremarkable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac failure at birth
n1=Lester (signe de) | n2=en:cardiac failure at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac features are observed in ~3% of cases
n1=Lester (signe de) | n2=en:cardiac features are observed in ~3% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac involvement occurs between 5 and 12 years
n1=Lester (signe de) | n2=en:cardiac involvement occurs between 5 and 12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiac manifestations are often fatal
n1=Lester (signe de) | n2=en:cardiac manifestations are often fatal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiomyopathy is not a feature
n1=Lester (signe de) | n2=en:cardiomyopathy is not a feature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cardiomyopathy may develop later in the disease
n1=Lester (signe de) | n2=en:cardiomyopathy may develop later in the disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carnitine supplementation can prevent further episodes and declines in cardiac function
n1=Lester (signe de) | n2=en:carnitine supplementation can prevent further episodes and declines in cardiac function | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier female phenotype ranges from normal bone density with no fractures to early-onset osteoporosis and fractures
n1=Lester (signe de) | n2=en:carrier female phenotype ranges from normal bone density with no fractures to early-onset osteoporosis and fractures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females are less affected (short stature with rhizomelic shortening of limbs, mild body asymmetry, and mild mental retardation)
n1=Lester (signe de) | n2=en:carrier females are less affected (short stature with rhizomelic shortening of limbs, mild body asymmetry, and mild mental retardation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females are normal
n1=Lester (signe de) | n2=en:carrier females are normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females are unaffected
n1=Lester (signe de) | n2=en:carrier females are unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females exhibit less severe phenotype attributed to random inactivation of the x chromosome
n1=Lester (signe de) | n2=en:carrier females exhibit less severe phenotype attributed to random inactivation of the x chromosome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females have arthralgias in middle age
n1=Lester (signe de) | n2=en:carrier females have arthralgias in middle age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females have normal funduscopic examinations and normal waveforms on electroretinography.
n1=Lester (signe de) | n2=en:carrier females have normal funduscopic examinations and normal waveforms on electroretinography. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may develop intrahepatic cholestasis of pregnancy (icp, 147480)
n1=Lester (signe de) | n2=en:carrier females may develop intrahepatic cholestasis of pregnancy (icp, 147480) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may have mild features
n1=Lester (signe de) | n2=en:carrier females may have mild features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may have mild intellectual disability
n1=Lester (signe de) | n2=en:carrier females may have mild intellectual disability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may present with postpartum hyperammonemia
n1=Lester (signe de) | n2=en:carrier females may present with postpartum hyperammonemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may show mild features, such as mild contractures, club feet, and intellectual disability
n1=Lester (signe de) | n2=en:carrier females may show mild features, such as mild contractures, club feet, and intellectual disability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may show mild mental retardation or learning disabilities
n1=Lester (signe de) | n2=en:carrier females may show mild mental retardation or learning disabilities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females may show neuropsychologic impairment
n1=Lester (signe de) | n2=en:carrier females may show neuropsychologic impairment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females show no clinical phenotype
n1=Lester (signe de) | n2=en:carrier females show no clinical phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier females show no phenotypic abnormalities, but may have learning difficulties
n1=Lester (signe de) | n2=en:carrier females show no phenotypic abnormalities, but may have learning difficulties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier frequency 1:1,000 in french-canadians in quebec
n1=Lester (signe de) | n2=en:carrier frequency 1:1,000 in french-canadians in quebec | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier frequency 1:200,000 in france
n1=Lester (signe de) | n2=en:carrier frequency 1:200,000 in france | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier frequency 1:700 in bukhara jewish populations
n1=Lester (signe de) | n2=en:carrier frequency 1:700 in bukhara jewish populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier frequency in finland 1/40
n1=Lester (signe de) | n2=en:carrier frequency in finland 1/40 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier frequency in finland is 1 in 230
n1=Lester (signe de) | n2=en:carrier frequency in finland is 1 in 230 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier males are fertile
n1=Lester (signe de) | n2=en:carrier males are fertile | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier males are unaffected except for psychiatric/behavioral abnormalities
n1=Lester (signe de) | n2=en:carrier males are unaffected except for psychiatric/behavioral abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier mothers have urine biochemistry profiles identical to those of their sons
n1=Lester (signe de) | n2=en:carrier mothers have urine biochemistry profiles identical to those of their sons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier rate of 1 in 11 among old order amish
n1=Lester (signe de) | n2=en:carrier rate of 1 in 11 among old order amish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:carrier rate of 1 in 39 in the saguenay-lac-saint-jean region of quebec
n1=Lester (signe de) | n2=en:carrier rate of 1 in 39 in the saguenay-lac-saint-jean region of quebec | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cases reported in the old order amish and one japanese family (last curated april 2014)
n1=Lester (signe de) | n2=en:cases reported in the old order amish and one japanese family (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cases reported include de novo deletions, interstitial deletions, and translocations involving only the terminal band of the reciprocal chromosome
n1=Lester (signe de) | n2=en:cases reported include de novo deletions, interstitial deletions, and translocations involving only the terminal band of the reciprocal chromosome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataract evident at birth
n1=Lester (signe de) | n2=en:cataract evident at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataracts are progressive but may vary between eyes of an individual
n1=Lester (signe de) | n2=en:cataracts are progressive but may vary between eyes of an individual | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataracts develop by second decade of life
n1=Lester (signe de) | n2=en:cataracts develop by second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataracts may be subclinical in some patients
n1=Lester (signe de) | n2=en:cataracts may be subclinical in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataracts present at birth or develop in infancy
n1=Lester (signe de) | n2=en:cataracts present at birth or develop in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cataracts variably present at birth
n1=Lester (signe de) | n2=en:cataracts variably present at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:catshl is an acronym for camptodactyly, tall stature, scoliosis, and hearing loss
n1=Lester (signe de) | n2=en:catshl is an acronym for camptodactyly, tall stature, scoliosis, and hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cause of death usually due to respiratory failure before adulthood
n1=Lester (signe de) | n2=en:cause of death usually due to respiratory failure before adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by 55-200 expanded trinucleotide repeats in the fmr1 gene (309550) referred to as a 'premutation'
n1=Lester (signe de) | n2=en:caused by 55-200 expanded trinucleotide repeats in the fmr1 gene (309550) referred to as a 'premutation' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by a de novo heterozygous gene deletion syndrome at chromosome 15q24
n1=Lester (signe de) | n2=en:caused by a de novo heterozygous gene deletion syndrome at chromosome 15q24 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by a defect in bile acid transport
n1=Lester (signe de) | n2=en:caused by a defect in bile acid transport | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by constitutive activation of the avpr2 receptor
n1=Lester (signe de) | n2=en:caused by constitutive activation of the avpr2 receptor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by heterozygous germline mutation and second-hit somatic mutation
n1=Lester (signe de) | n2=en:caused by heterozygous germline mutation and second-hit somatic mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by inactivating mutations in the parathyroid hormone receptor 1 gene, in contrast to jansen type metaphyseal chondrodysplasia, 156400
n1=Lester (signe de) | n2=en:caused by inactivating mutations in the parathyroid hormone receptor 1 gene, in contrast to jansen type metaphyseal chondrodysplasia, 156400 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by inborn error in bile acid synthesis
n1=Lester (signe de) | n2=en:caused by inborn error in bile acid synthesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by inheritance of the mutation on the maternal allele (imprinting)
n1=Lester (signe de) | n2=en:caused by inheritance of the mutation on the maternal allele (imprinting) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by inheritance of the mutation on the paternal allele (imprinting)
n1=Lester (signe de) | n2=en:caused by inheritance of the mutation on the paternal allele (imprinting) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by paternally-inherited inactivating gnas1 mutations
n1=Lester (signe de) | n2=en:caused by paternally-inherited inactivating gnas1 mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:caused by somatic mutations
n1=Lester (signe de) | n2=en:caused by somatic mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cayler cardiofacial syndrome was classically described as hypoplasia of the depressor anguli oris muscle and congenital heart defects
n1=Lester (signe de) | n2=en:cayler cardiofacial syndrome was classically described as hypoplasia of the depressor anguli oris muscle and congenital heart defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cdags is an acronym - craniosynostosis and clavicular hypoplasia, delayed closure of fontanel, anal anomalies, genitourinary malformations, and skin eruption
n1=Lester (signe de) | n2=en:cdags is an acronym - craniosynostosis and clavicular hypoplasia, delayed closure of fontanel, anal anomalies, genitourinary malformations, and skin eruption | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cells of origin are part of the diffuse neuroendocrine system (dnes)
n1=Lester (signe de) | n2=en:cells of origin are part of the diffuse neuroendocrine system (dnes) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:central apneic episodes may be fatal
n1=Lester (signe de) | n2=en:central apneic episodes may be fatal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:central hypoventilation occurs late in the disease and is often fatal
n1=Lester (signe de) | n2=en:central hypoventilation occurs late in the disease and is often fatal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:centromeric instability of chromosomes 1, 9 and 16 with increased somatic recombination and formation of multibranched configurations
n1=Lester (signe de) | n2=en:centromeric instability of chromosomes 1, 9 and 16 with increased somatic recombination and formation of multibranched configurations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cerebellar ataxia shows onset in young adulthood
n1=Lester (signe de) | n2=en:cerebellar ataxia shows onset in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chands is an acronym for curly hair, ankyloblepharon filiform, nail dysplasia
n1=Lester (signe de) | n2=en:chands is an acronym for curly hair, ankyloblepharon filiform, nail dysplasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:changes more marked in hands than feet
n1=Lester (signe de) | n2=en:changes more marked in hands than feet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:characteristic face and body by age 2 years
n1=Lester (signe de) | n2=en:characteristic face and body by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:characteristic facial features become more apparent with age
n1=Lester (signe de) | n2=en:characteristic facial features become more apparent with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:characterized by calf weakness at onset
n1=Lester (signe de) | n2=en:characterized by calf weakness at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:charcot-marie-tooth disease type 2l (cmt2l, 608673) is an allelic disorder with an overlapping phenotype
n1=Lester (signe de) | n2=en:charcot-marie-tooth disease type 2l (cmt2l, 608673) is an allelic disorder with an overlapping phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:charge acronym (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness, extremity abnormalities)
n1=Lester (signe de) | n2=en:charge acronym (coloboma, heart defect, atresia choanae, retarded growth and development, genital hypoplasia, ear anomalies/deafness, extremity abnormalities) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cheerful disposition
n1=Lester (signe de) | n2=en:cheerful disposition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chelation therapy can result in clinical improvement
n1=Lester (signe de) | n2=en:chelation therapy can result in clinical improvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:child is an acronym for congenital hemidysplasia with ichthyosiform erythroderma and limb defects
n1=Lester (signe de) | n2=en:child is an acronym for congenital hemidysplasia with ichthyosiform erythroderma and limb defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:child often can sit unsupported but never ambulates
n1=Lester (signe de) | n2=en:child often can sit unsupported but never ambulates | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood absence epilepsy (eca1 600131, eca2 607681, eca3 607682)
n1=Lester (signe de) | n2=en:childhood absence epilepsy (eca1 600131, eca2 607681, eca3 607682) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset
n1=Lester (signe de) | n2=en:childhood onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset (average 4 to 6 years)
n1=Lester (signe de) | n2=en:childhood onset (average 4 to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset (range birth to 12 years)
n1=Lester (signe de) | n2=en:childhood onset (range birth to 12 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset has been reported
n1=Lester (signe de) | n2=en:childhood onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset has been reported in 1 family
n1=Lester (signe de) | n2=en:childhood onset has been reported in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset may occur
n1=Lester (signe de) | n2=en:childhood onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood onset rarely occurs
n1=Lester (signe de) | n2=en:childhood onset rarely occurs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood or adolescent onset (usually less than 25 years)
n1=Lester (signe de) | n2=en:childhood or adolescent onset (usually less than 25 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood or adolescent onset, protracted, with myopathy and neuropathy
n1=Lester (signe de) | n2=en:childhood or adolescent onset, protracted, with myopathy and neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:childhood or young adult onset
n1=Lester (signe de) | n2=en:childhood or young adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:children rarely develop the disorder
n1=Lester (signe de) | n2=en:children rarely develop the disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chime is an acronym - ocular colobomas, heart defect, ichthyosiform dermatosis, mental retardation, ear anomalies
n1=Lester (signe de) | n2=en:chime is an acronym - ocular colobomas, heart defect, ichthyosiform dermatosis, mental retardation, ear anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chimeric cyp11b1/cyp11b2 gene is an anti-lepore-like fusion product
n1=Lester (signe de) | n2=en:chimeric cyp11b1/cyp11b2 gene is an anti-lepore-like fusion product | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cholinesterase inhibitors may be beneficial
n1=Lester (signe de) | n2=en:cholinesterase inhibitors may be beneficial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chromosomal hypersensitivity to ionizing radiation and alkylating agents
n1=Lester (signe de) | n2=en:chromosomal hypersensitivity to ionizing radiation and alkylating agents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chromosome rearrangements have been reported
n1=Lester (signe de) | n2=en:chromosome rearrangements have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chronic course with exacerbations and remissions
n1=Lester (signe de) | n2=en:chronic course with exacerbations and remissions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chronic disease
n1=Lester (signe de) | n2=en:chronic disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:chronic, relapsing condition
n1=Lester (signe de) | n2=en:chronic, relapsing condition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:citation:bib:pt:reference lab test:nar
n1=Lester (signe de) | n2=en:citation:bib:pt:reference lab test:nar | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic hepatic form begins in first months of life with hepatic failure and death by age 5 years
n1=Lester (signe de) | n2=en:classic hepatic form begins in first months of life with hepatic failure and death by age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic lesch-nyhan, < 1.5% hypoxanthine phosphoribosyltransferase (hprt) activity
n1=Lester (signe de) | n2=en:classic lesch-nyhan, < 1.5% hypoxanthine phosphoribosyltransferase (hprt) activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic severe form shows onset at 2 to 3 months of age
n1=Lester (signe de) | n2=en:classic severe form shows onset at 2 to 3 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic triad consists of nail dystrophy, skin hyperpigmentation, and mucosal leukoplakia
n1=Lester (signe de) | n2=en:classic triad consists of nail dystrophy, skin hyperpigmentation, and mucosal leukoplakia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic triad is megaloblastic anemia, diabetes, and deafness, but some patients may not have this triad
n1=Lester (signe de) | n2=en:classic triad is megaloblastic anemia, diabetes, and deafness, but some patients may not have this triad | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classic: onset in first decade, rapid progression, loss of independent ambulation within 15 years
n1=Lester (signe de) | n2=en:classic: onset in first decade, rapid progression, loss of independent ambulation within 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:classical form (type i), less severe with survival into adulthood
n1=Lester (signe de) | n2=en:classical form (type i), less severe with survival into adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical and biochemical abnormalities disappear with age
n1=Lester (signe de) | n2=en:clinical and biochemical abnormalities disappear with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical and biochemical abnormalities improve with age
n1=Lester (signe de) | n2=en:clinical and biochemical abnormalities improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical and biochemical symptoms improved with oral administration of creatine monohydrate
n1=Lester (signe de) | n2=en:clinical and biochemical symptoms improved with oral administration of creatine monohydrate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical and pathologic features of both demyelinating and axonal cmt
n1=Lester (signe de) | n2=en:clinical and pathologic features of both demyelinating and axonal cmt | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical details not provided beyond a statement that the phenotype is 'identical to that of lccs3' (611369)
n1=Lester (signe de) | n2=en:clinical details not provided beyond a statement that the phenotype is 'identical to that of lccs3' (611369) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical features based on 1 reported family (last curated august 2013)
n1=Lester (signe de) | n2=en:clinical features based on 1 reported family (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical features in females include mild mental retardation (80%), short stature (50%), prominent forehead, and coarse facies
n1=Lester (signe de) | n2=en:clinical features in females include mild mental retardation (80%), short stature (50%), prominent forehead, and coarse facies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical features may vary
n1=Lester (signe de) | n2=en:clinical features may vary | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical features other than liver findings may vary
n1=Lester (signe de) | n2=en:clinical features other than liver findings may vary | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical features present only if mutation inherited on paternal allele
n1=Lester (signe de) | n2=en:clinical features present only if mutation inherited on paternal allele | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical improvement after 2 to 3 weeks of supportive care
n1=Lester (signe de) | n2=en:clinical improvement after 2 to 3 weeks of supportive care | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical manifestation of some forms of bardet-biedl syndrome requires recessive mutation in 1 of the 6 loci plus an additional mutation in a second locus, or triallelic inheritance
n1=Lester (signe de) | n2=en:clinical manifestation of some forms of bardet-biedl syndrome requires recessive mutation in 1 of the 6 loci plus an additional mutation in a second locus, or triallelic inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical manifestation ranges from mild, transient hypertension to hellp syndrome (hemolysis, elevated liver enzymes, and low platelets)
n1=Lester (signe de) | n2=en:clinical manifestation ranges from mild, transient hypertension to hellp syndrome (hemolysis, elevated liver enzymes, and low platelets) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical manifestations only occur if vel-negative individuals have anti-vel antibodies and are transfused with vel-positive blood
n1=Lester (signe de) | n2=en:clinical manifestations only occur if vel-negative individuals have anti-vel antibodies and are transfused with vel-positive blood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical onset within first 2 years of life
n1=Lester (signe de) | n2=en:clinical onset within first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with charcot-marie-tooth disease type 2c (606071)
n1=Lester (signe de) | n2=en:clinical overlap with charcot-marie-tooth disease type 2c (606071) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with congenital hypomyelinating neuropathy (chn, 605253)
n1=Lester (signe de) | n2=en:clinical overlap with congenital hypomyelinating neuropathy (chn, 605253) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with dejerine-sottas syndrome (dss, 145900)
n1=Lester (signe de) | n2=en:clinical overlap with dejerine-sottas syndrome (dss, 145900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with demyelinating charcot-marie-tooth disease type 1 (see cmt1b, 118200), but much more severe phenotype
n1=Lester (signe de) | n2=en:clinical overlap with demyelinating charcot-marie-tooth disease type 1 (see cmt1b, 118200), but much more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with distal hereditary motor neuropathy type vii (dhmn vii, 158580)
n1=Lester (signe de) | n2=en:clinical overlap with distal hereditary motor neuropathy type vii (dhmn vii, 158580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical overlap with thanatophoric dysplasia i (187600) and severe achondroplasia (100800)
n1=Lester (signe de) | n2=en:clinical overlap with thanatophoric dysplasia i (187600) and severe achondroplasia (100800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical presentation varies
n1=Lester (signe de) | n2=en:clinical presentation varies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical presentation varies from asymptomatic to fulminant course
n1=Lester (signe de) | n2=en:clinical presentation varies from asymptomatic to fulminant course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical severity varies
n1=Lester (signe de) | n2=en:clinical severity varies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood
n1=Lester (signe de) | n2=en:clinical spectrum in males ranges from lethal neonatal onset to milder forms with first recognized episode in late childhood or even in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical triad - dysmorphic features, cardiac arrhythmia, and potassium-sensitive periodic paralysis
n1=Lester (signe de) | n2=en:clinical triad - dysmorphic features, cardiac arrhythmia, and potassium-sensitive periodic paralysis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical variability
n1=Lester (signe de) | n2=en:clinical variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical variability seen in waardenburg syndrome type 1
n1=Lester (signe de) | n2=en:clinical variability seen in waardenburg syndrome type 1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical variability, both pure and complicated forms
n1=Lester (signe de) | n2=en:clinical variability, both pure and complicated forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinical variation
n1=Lester (signe de) | n2=en:clinical variation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically 'silent' nystagmus evident on eye movement recording in carrier females
n1=Lester (signe de) | n2=en:clinically 'silent' nystagmus evident on eye movement recording in carrier females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically classified into classic, atypical, and intermediate phenotypes
n1=Lester (signe de) | n2=en:clinically classified into classic, atypical, and intermediate phenotypes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically mimics congenital torch infections (see 251290)
n1=Lester (signe de) | n2=en:clinically mimics congenital torch infections (see 251290) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically resembles essential tremor, but not responsive to beta-adrenergic blockers
n1=Lester (signe de) | n2=en:clinically resembles essential tremor, but not responsive to beta-adrenergic blockers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically resembles spinal muscular atrophy-1 (sma1, 253300)
n1=Lester (signe de) | n2=en:clinically resembles spinal muscular atrophy-1 (sma1, 253300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clinically unaffected heterozygotes may show changes on electroretinography
n1=Lester (signe de) | n2=en:clinically unaffected heterozygotes may show changes on electroretinography | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clonazepam and diazepam may be effective in preventing or lessening severity
n1=Lester (signe de) | n2=en:clonazepam and diazepam may be effective in preventing or lessening severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clonidine can alleviate hyperhidrosis
n1=Lester (signe de) | n2=en:clonidine can alleviate hyperhidrosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clove - congenital lipomatous overgrowth, vascular malformations, and epidermal nevi
n1=Lester (signe de) | n2=en:clove - congenital lipomatous overgrowth, vascular malformations, and epidermal nevi | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:clubfoot is bilateral in most patients
n1=Lester (signe de) | n2=en:clubfoot is bilateral in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:coagulation specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:coagulation specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:codas is an acronym for cerebral ocular dental auricular skeletal syndrome
n1=Lester (signe de) | n2=en:codas is an acronym for cerebral ocular dental auricular skeletal syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:codominant inheritance has been suggested
n1=Lester (signe de) | n2=en:codominant inheritance has been suggested | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:colchicine treatment is not effective
n1=Lester (signe de) | n2=en:colchicine treatment is not effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cold temeratures exacerbate symptoms
n1=Lester (signe de) | n2=en:cold temeratures exacerbate symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cold-induced sweating develops late in the first decade
n1=Lester (signe de) | n2=en:cold-induced sweating develops late in the first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:coloboma is associated with larger microdeletion (490kb) of 11q13
n1=Lester (signe de) | n2=en:coloboma is associated with larger microdeletion (490kb) of 11q13 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:color vision defects may not be part of the phenotype
n1=Lester (signe de) | n2=en:color vision defects may not be part of the phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:colorectal cancer develops by fourth decade in untreated patients
n1=Lester (signe de) | n2=en:colorectal cancer develops by fourth decade in untreated patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:common (up to 7% of the population)
n1=Lester (signe de) | n2=en:common (up to 7% of the population) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:common in afrikaan population, south africa
n1=Lester (signe de) | n2=en:common in afrikaan population, south africa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:common in japan and other asian populations
n1=Lester (signe de) | n2=en:common in japan and other asian populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:common in populations of finnish descent (incidence of 1:20 000, carrier frequency of 1 in 70)
n1=Lester (signe de) | n2=en:common in populations of finnish descent (incidence of 1:20 000, carrier frequency of 1 in 70) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:common in south african whites
n1=Lester (signe de) | n2=en:common in south african whites | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:communication board, non-electronic augmentative or alternative communication device
n1=Lester (signe de) | n2=en:communication board, non-electronic augmentative or alternative communication device | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complement deficiency (e.g. c2 and c4 null alleles) are susceptible to developing sle
n1=Lester (signe de) | n2=en:complement deficiency (e.g. c2 and c4 null alleles) are susceptible to developing sle | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complementation group b (represented by single atypical patient)
n1=Lester (signe de) | n2=en:complementation group b (represented by single atypical patient) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complementation group c (variant mliii, 252605)
n1=Lester (signe de) | n2=en:complementation group c (variant mliii, 252605) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complementation groups - complementation group a (classic mliii, 252600)
n1=Lester (signe de) | n2=en:complementation groups - complementation group a (classic mliii, 252600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete absence of melanin synthesis
n1=Lester (signe de) | n2=en:complete absence of melanin synthesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete manifestation in males
n1=Lester (signe de) | n2=en:complete manifestation in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete penetrance
n1=Lester (signe de) | n2=en:complete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete penetrance but extreme variability of phenotypic expression
n1=Lester (signe de) | n2=en:complete penetrance but extreme variability of phenotypic expression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete penetrance with variable expressivity
n1=Lester (signe de) | n2=en:complete penetrance with variable expressivity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete recovery during intervals
n1=Lester (signe de) | n2=en:complete recovery during intervals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complete recovery upon treatment of hyperthyroidism
n1=Lester (signe de) | n2=en:complete recovery upon treatment of hyperthyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:complicated and pure forms
n1=Lester (signe de) | n2=en:complicated and pure forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:compound heterozygosity common
n1=Lester (signe de) | n2=en:compound heterozygosity common | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:comprises several subtypes, including
n1=Lester (signe de) | n2=en:comprises several subtypes, including | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:condition is experienced by patients as harmless and is often discovered incidentally
n1=Lester (signe de) | n2=en:condition is experienced by patients as harmless and is often discovered incidentally | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:conduction defect is progressive
n1=Lester (signe de) | n2=en:conduction defect is progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cone-shaped epiphyses appear in early childhood and disappear with premature fusion of growth plate before puberty
n1=Lester (signe de) | n2=en:cone-shaped epiphyses appear in early childhood and disappear with premature fusion of growth plate before puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cone-shaped epiphyses usually not present before age 2 years
n1=Lester (signe de) | n2=en:cone-shaped epiphyses usually not present before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital - over 2,000 repeats
n1=Lester (signe de) | n2=en:congenital - over 2,000 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital abnormality
n1=Lester (signe de) | n2=en:congenital abnormality | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital cataracts, sometimes requiring extraction in childhood due to impairment of vision
n1=Lester (signe de) | n2=en:congenital cataracts, sometimes requiring extraction in childhood due to impairment of vision | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital disorders
n1=Lester (signe de) | n2=en:congenital disorders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital hypotonia from 8 to 12 months, then progressive spasticity resulting in contractures and spastic quadriplegia
n1=Lester (signe de) | n2=en:congenital hypotonia from 8 to 12 months, then progressive spasticity resulting in contractures and spastic quadriplegia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital linear skin defects may disappear within a few months of life
n1=Lester (signe de) | n2=en:congenital linear skin defects may disappear within a few months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital onset
n1=Lester (signe de) | n2=en:congenital onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital onset leading to cochlear implants between 7-10 years of age in ashkenazi jewish families
n1=Lester (signe de) | n2=en:congenital onset leading to cochlear implants between 7-10 years of age in ashkenazi jewish families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital onset or onset before 2 years (prelingual)
n1=Lester (signe de) | n2=en:congenital onset or onset before 2 years (prelingual) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital or early onset hearing loss
n1=Lester (signe de) | n2=en:congenital or early onset hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:congenital reduction in visual acuity is nonprogressive
n1=Lester (signe de) | n2=en:congenital reduction in visual acuity is nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:connatal form (type ii), most severe with death in first decade
n1=Lester (signe de) | n2=en:connatal form (type ii), most severe with death in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered a benign disorder
n1=Lester (signe de) | n2=en:considered a benign disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered a myeloproliferative disorder
n1=Lester (signe de) | n2=en:considered a myeloproliferative disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered a normal variant
n1=Lester (signe de) | n2=en:considered a normal variant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered part of a spectrum of leber hereditary optic atrophy (lhon, 535000)
n1=Lester (signe de) | n2=en:considered part of a spectrum of leber hereditary optic atrophy (lhon, 535000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered to be a manifestation of the caudal regression syndrome
n1=Lester (signe de) | n2=en:considered to be a manifestation of the caudal regression syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered to be a severe form of gaucher disease type ii (230900)
n1=Lester (signe de) | n2=en:considered to be a severe form of gaucher disease type ii (230900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered to be a variant of gaucher disease type iii (231000)
n1=Lester (signe de) | n2=en:considered to be a variant of gaucher disease type iii (231000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:considered to be part of the spectrum of joubert syndrome (213300) and meckel syndrome (249000)
n1=Lester (signe de) | n2=en:considered to be part of the spectrum of joubert syndrome (213300) and meckel syndrome (249000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene deletion of 17q21.3 involves a region which harbors a 900kb inversion polymorphism
n1=Lester (signe de) | n2=en:contiguous gene deletion of 17q21.3 involves a region which harbors a 900kb inversion polymorphism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene deletion syndrome
n1=Lester (signe de) | n2=en:contiguous gene deletion syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene deletion syndrome (in most patients)
n1=Lester (signe de) | n2=en:contiguous gene deletion syndrome (in most patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene deletion syndrome at chromosome 6p
n1=Lester (signe de) | n2=en:contiguous gene deletion syndrome at chromosome 6p | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene deletion syndrome of 5q31
n1=Lester (signe de) | n2=en:contiguous gene deletion syndrome of 5q31 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene duplication syndrome
n1=Lester (signe de) | n2=en:contiguous gene duplication syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene syndrome
n1=Lester (signe de) | n2=en:contiguous gene syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contiguous gene syndrome caused by deletion, duplication, or rearrangement of chromosome 7q21.3 involving the dss1 (601285), dlx5 (600028), and dlx6 (600030) genes and possible regulatory elements in the region
n1=Lester (signe de) | n2=en:contiguous gene syndrome caused by deletion, duplication, or rearrangement of chromosome 7q21.3 involving the dss1 (601285), dlx5 (600028), and dlx6 (600030) genes and possible regulatory elements in the region | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:continuing ovulation and implantation after initiation of another pregnancy
n1=Lester (signe de) | n2=en:continuing ovulation and implantation after initiation of another pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contractures at birth or difficulties in the neonatal period resolve
n1=Lester (signe de) | n2=en:contractures at birth or difficulties in the neonatal period resolve | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contractures most severe by midadolescence
n1=Lester (signe de) | n2=en:contractures most severe by midadolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:contractures other than plantar are less common and less severe
n1=Lester (signe de) | n2=en:contractures other than plantar are less common and less severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:corneal diameter decreases with decreasing axial length
n1=Lester (signe de) | n2=en:corneal diameter decreases with decreasing axial length | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:corneal steepening is proportional to the degree of axial foreshortening
n1=Lester (signe de) | n2=en:corneal steepening is proportional to the degree of axial foreshortening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:coronary artery disease or myocardial infarction in fifth or sixth decade of life
n1=Lester (signe de) | n2=en:coronary artery disease or myocardial infarction in fifth or sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:corrected by bone marrow transplantation
n1=Lester (signe de) | n2=en:corrected by bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:course characterized by repeated relapses precipitated by excessive protein intake, intercurrent infection, or constipation
n1=Lester (signe de) | n2=en:course characterized by repeated relapses precipitated by excessive protein intake, intercurrent infection, or constipation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:crash is an acronym for corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus which encompasses all l1cam diseases
n1=Lester (signe de) | n2=en:crash is an acronym for corpus callosum hypoplasia, retardation, adducted thumbs, spastic paraplegia, and hydrocephalus which encompasses all l1cam diseases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:crisis precipitated by high altitude exposure
n1=Lester (signe de) | n2=en:crisis precipitated by high altitude exposure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:currarino triad includes - hemisacrum, presacral mass (anterior meningocele, enteric cyst, and/or presacral teratoma) and anorectal anomalies
n1=Lester (signe de) | n2=en:currarino triad includes - hemisacrum, presacral mass (anterior meningocele, enteric cyst, and/or presacral teratoma) and anorectal anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cutaneous leiomyomas increase in number over time
n1=Lester (signe de) | n2=en:cutaneous leiomyomas increase in number over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cutaneous symptoms induced by cold exposure or cooling
n1=Lester (signe de) | n2=en:cutaneous symptoms induced by cold exposure or cooling | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cutaneous telangiectases often not evident until 20-30 years of age incidence 1 in 5,000-8,000
n1=Lester (signe de) | n2=en:cutaneous telangiectases often not evident until 20-30 years of age incidence 1 in 5,000-8,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cyclic vomiting syndrome plus (cvs+) is characterized by additional neuromuscular and/or visceral organ manifestations (as indicated above)
n1=Lester (signe de) | n2=en:cyclic vomiting syndrome plus (cvs+) is characterized by additional neuromuscular and/or visceral organ manifestations (as indicated above) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cyp2d6 enzyme is located in the endoplasmic reticulum of the liver
n1=Lester (signe de) | n2=en:cyp2d6 enzyme is located in the endoplasmic reticulum of the liver | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:cyp2d6 represents about 1% of total liver cytochrome p450 content
n1=Lester (signe de) | n2=en:cyp2d6 represents about 1% of total liver cytochrome p450 content | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:d-hus is usually familial
n1=Lester (signe de) | n2=en:d-hus is usually familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:d+hus (typical hus) is usually sporadic, limited to 1 event, and has a good prognosis
n1=Lester (signe de) | n2=en:d+hus (typical hus) is usually sporadic, limited to 1 event, and has a good prognosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date of analysis:tmstp:pt:xxx:qn
n1=Lester (signe de) | n2=en:date of analysis:tmstp:pt:xxx:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date of autopsy:date:pt:^patient:qn
n1=Lester (signe de) | n2=en:date of autopsy:date:pt:^patient:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date of observation:time stamp -- date and time:point in time:to be specified in another part of the message:quantitative
n1=Lester (signe de) | n2=en:date of observation:time stamp -- date and time:point in time:to be specified in another part of the message:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date reference lab test received:time stamp -- date and time:time reported elsewhere:reference lab test:quantitative
n1=Lester (signe de) | n2=en:date reference lab test received:time stamp -- date and time:time reported elsewhere:reference lab test:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date reference lab test sent:time stamp -- date and time:time reported elsewhere:reference lab test:quantitative
n1=Lester (signe de) | n2=en:date reference lab test sent:time stamp -- date and time:time reported elsewhere:reference lab test:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:date ultrasound:date:pt:^patient:qn
n1=Lester (signe de) | n2=en:date ultrasound:date:pt:^patient:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo deletions in 8% of patients (preferentially paternally derived)
n1=Lester (signe de) | n2=en:de novo deletions in 8% of patients (preferentially paternally derived) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation
n1=Lester (signe de) | n2=en:de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation (in some patients)
n1=Lester (signe de) | n2=en:de novo mutation (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation identified in some patients
n1=Lester (signe de) | n2=en:de novo mutation identified in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation in heterozygotes
n1=Lester (signe de) | n2=en:de novo mutation in heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation in most patients
n1=Lester (signe de) | n2=en:de novo mutation in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation in some cases
n1=Lester (signe de) | n2=en:de novo mutation in some cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutation resulting in haploinsufficiency of eftud2 (603892)
n1=Lester (signe de) | n2=en:de novo mutation resulting in haploinsufficiency of eftud2 (603892) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:de novo mutations occur almost exclusively on the paternally derived x chromosome
n1=Lester (signe de) | n2=en:de novo mutations occur almost exclusively on the paternally derived x chromosome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deafness is presenting symptom
n1=Lester (signe de) | n2=en:deafness is presenting symptom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deafness tends to occur before other neurologic signs, except in patients with very early onset
n1=Lester (signe de) | n2=en:deafness tends to occur before other neurologic signs, except in patients with very early onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death about 20 years after symptom onset
n1=Lester (signe de) | n2=en:death about 20 years after symptom onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death at 10 to 15 years
n1=Lester (signe de) | n2=en:death at 10 to 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death at 13 to 30 years
n1=Lester (signe de) | n2=en:death at 13 to 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death at 20 to 40 years
n1=Lester (signe de) | n2=en:death at 20 to 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death at birth or within first 2 years of life (severe form)
n1=Lester (signe de) | n2=en:death at birth or within first 2 years of life (severe form) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death before age 15 in iia
n1=Lester (signe de) | n2=en:death before age 15 in iia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death before age 3 years
n1=Lester (signe de) | n2=en:death before age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death before age 40
n1=Lester (signe de) | n2=en:death before age 40 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death between 2 years of age and young adulthood
n1=Lester (signe de) | n2=en:death between 2 years of age and young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death by age 15 months
n1=Lester (signe de) | n2=en:death by age 15 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death by age 2 years
n1=Lester (signe de) | n2=en:death by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death by age 3 years
n1=Lester (signe de) | n2=en:death by age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death by age 5 (infantile form)
n1=Lester (signe de) | n2=en:death by age 5 (infantile form) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death by age 6-7 years
n1=Lester (signe de) | n2=en:death by age 6-7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death can occur in infancy
n1=Lester (signe de) | n2=en:death can occur in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death due to rapidly progressive pulmonary fibrosis in infancy
n1=Lester (signe de) | n2=en:death due to rapidly progressive pulmonary fibrosis in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death due to respiratory failure or infection
n1=Lester (signe de) | n2=en:death due to respiratory failure or infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death due to respiratory insufficiency within minutes to hours after birth
n1=Lester (signe de) | n2=en:death due to respiratory insufficiency within minutes to hours after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death frequent in severe infantile form
n1=Lester (signe de) | n2=en:death frequent in severe infantile form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death from pneumonia
n1=Lester (signe de) | n2=en:death from pneumonia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death from stroke if untreated
n1=Lester (signe de) | n2=en:death from stroke if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood
n1=Lester (signe de) | n2=en:death in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood is frequent due to respiratory failure
n1=Lester (signe de) | n2=en:death in childhood is frequent due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood may occur
n1=Lester (signe de) | n2=en:death in childhood may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood may occur due to end-stage renal disease
n1=Lester (signe de) | n2=en:death in childhood may occur due to end-stage renal disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood may occur due to infection
n1=Lester (signe de) | n2=en:death in childhood may occur due to infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood occurs without bone marrow transplantation
n1=Lester (signe de) | n2=en:death in childhood occurs without bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood often results from respiratory insufficiency
n1=Lester (signe de) | n2=en:death in childhood often results from respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in childhood secondary to malabsorption
n1=Lester (signe de) | n2=en:death in childhood secondary to malabsorption | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in early childhood
n1=Lester (signe de) | n2=en:death in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in early childhood has been reported in some presumed homozygotes
n1=Lester (signe de) | n2=en:death in early childhood has been reported in some presumed homozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in early childhood may occur
n1=Lester (signe de) | n2=en:death in early childhood may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in early infancy
n1=Lester (signe de) | n2=en:death in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in early infancy (in some patients)
n1=Lester (signe de) | n2=en:death in early infancy (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in first days of life (family b)
n1=Lester (signe de) | n2=en:death in first days of life (family b) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in first days or months of life
n1=Lester (signe de) | n2=en:death in first days or months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in first months of life
n1=Lester (signe de) | n2=en:death in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in first weeks of life
n1=Lester (signe de) | n2=en:death in first weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in first-second decade of life secondary to cardio-respiratory compromise
n1=Lester (signe de) | n2=en:death in first-second decade of life secondary to cardio-respiratory compromise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in fourth to fifth decade
n1=Lester (signe de) | n2=en:death in fourth to fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy
n1=Lester (signe de) | n2=en:death in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy (1 patient)
n1=Lester (signe de) | n2=en:death in infancy (1 patient) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy (patient b)
n1=Lester (signe de) | n2=en:death in infancy (patient b) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy common for patients with the classic neonatal form
n1=Lester (signe de) | n2=en:death in infancy common for patients with the classic neonatal form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy due to hyperthermia or apnea
n1=Lester (signe de) | n2=en:death in infancy due to hyperthermia or apnea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy in 2 patients
n1=Lester (signe de) | n2=en:death in infancy in 2 patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy in majority of patients
n1=Lester (signe de) | n2=en:death in infancy in majority of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy or early childhood
n1=Lester (signe de) | n2=en:death in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy secondary to kernicterus
n1=Lester (signe de) | n2=en:death in infancy secondary to kernicterus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy secondary to pulmonary insufficiency
n1=Lester (signe de) | n2=en:death in infancy secondary to pulmonary insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy secondary to respiratory insufficiency/pneumonia
n1=Lester (signe de) | n2=en:death in infancy secondary to respiratory insufficiency/pneumonia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy without bone marrow transplantation
n1=Lester (signe de) | n2=en:death in infancy without bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in infancy, usually from sepsis, dehydration, or acidosis
n1=Lester (signe de) | n2=en:death in infancy, usually from sepsis, dehydration, or acidosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in majority of infants soon after birth
n1=Lester (signe de) | n2=en:death in majority of infants soon after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in neonatal period
n1=Lester (signe de) | n2=en:death in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in perinatal period
n1=Lester (signe de) | n2=en:death in perinatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in teens secondary to cardiac failure
n1=Lester (signe de) | n2=en:death in teens secondary to cardiac failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in the fifth or sixth decade
n1=Lester (signe de) | n2=en:death in the fifth or sixth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in the first decade, usually from liver failure
n1=Lester (signe de) | n2=en:death in the first decade, usually from liver failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in the first months or years of life
n1=Lester (signe de) | n2=en:death in the first months or years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in the first years of life
n1=Lester (signe de) | n2=en:death in the first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in the mid-twenties
n1=Lester (signe de) | n2=en:death in the mid-twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in third or fourth decades, usually due to respiratory infection
n1=Lester (signe de) | n2=en:death in third or fourth decades, usually due to respiratory infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in untreated children
n1=Lester (signe de) | n2=en:death in untreated children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero
n1=Lester (signe de) | n2=en:death in utero | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero (30%)
n1=Lester (signe de) | n2=en:death in utero (30%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero or as neonate
n1=Lester (signe de) | n2=en:death in utero or as neonate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero or early infancy
n1=Lester (signe de) | n2=en:death in utero or early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero or in early infancy is common
n1=Lester (signe de) | n2=en:death in utero or in early infancy is common | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death in utero or in the perinatal period
n1=Lester (signe de) | n2=en:death in utero or in the perinatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death may occur in childhood due to respiratory failure
n1=Lester (signe de) | n2=en:death may occur in childhood due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death may occur in early infancy
n1=Lester (signe de) | n2=en:death may occur in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death may occur in infancy
n1=Lester (signe de) | n2=en:death may occur in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death may occur in late childhood
n1=Lester (signe de) | n2=en:death may occur in late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death may occur in the first decade
n1=Lester (signe de) | n2=en:death may occur in the first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death occurs 10 to 20 years after onset
n1=Lester (signe de) | n2=en:death occurs 10 to 20 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death occurs 5 to 10 years after onset
n1=Lester (signe de) | n2=en:death occurs 5 to 10 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death occurs before 12 months of age due to cardiorespiratory arrest
n1=Lester (signe de) | n2=en:death occurs before 12 months of age due to cardiorespiratory arrest | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death occurs early in neonatal period due to respiratory failure
n1=Lester (signe de) | n2=en:death occurs early in neonatal period due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death occurs in second or third decade
n1=Lester (signe de) | n2=en:death occurs in second or third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often before age 2
n1=Lester (signe de) | n2=en:death often before age 2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often by age 2 years
n1=Lester (signe de) | n2=en:death often by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in childhood
n1=Lester (signe de) | n2=en:death often in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in early childhood
n1=Lester (signe de) | n2=en:death often in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in early infancy
n1=Lester (signe de) | n2=en:death often in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in first months of life
n1=Lester (signe de) | n2=en:death often in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in infancy
n1=Lester (signe de) | n2=en:death often in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often in the teenage years
n1=Lester (signe de) | n2=en:death often in the teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often occurs during metabolic/acidotic crisis
n1=Lester (signe de) | n2=en:death often occurs during metabolic/acidotic crisis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often occurs in childhood
n1=Lester (signe de) | n2=en:death often occurs in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often occurs in the first decade
n1=Lester (signe de) | n2=en:death often occurs in the first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often secondary to infectious disease
n1=Lester (signe de) | n2=en:death often secondary to infectious disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death often secondary to pneumonia or congestive heart failure
n1=Lester (signe de) | n2=en:death often secondary to pneumonia or congestive heart failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death secondary to renal failure, cardiac or cerebrovascular disease
n1=Lester (signe de) | n2=en:death secondary to renal failure, cardiac or cerebrovascular disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death secondary to respiratory infection or failure
n1=Lester (signe de) | n2=en:death secondary to respiratory infection or failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death secondary to respiratory infection or failure before age 2 years
n1=Lester (signe de) | n2=en:death secondary to respiratory infection or failure before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death secondary to respiratory insufficiency
n1=Lester (signe de) | n2=en:death secondary to respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually by 1 year of age
n1=Lester (signe de) | n2=en:death usually by 1 year of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually by age 10 years
n1=Lester (signe de) | n2=en:death usually by age 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually by age 3 years
n1=Lester (signe de) | n2=en:death usually by age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually due to renal failure by average age 3
n1=Lester (signe de) | n2=en:death usually due to renal failure by average age 3 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually due to respiratory failure
n1=Lester (signe de) | n2=en:death usually due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in childhood
n1=Lester (signe de) | n2=en:death usually in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in early childhood
n1=Lester (signe de) | n2=en:death usually in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in first year of life
n1=Lester (signe de) | n2=en:death usually in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in infancy
n1=Lester (signe de) | n2=en:death usually in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in infancy due to respiratory failure
n1=Lester (signe de) | n2=en:death usually in infancy due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in infancy or early childhood
n1=Lester (signe de) | n2=en:death usually in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in newborn period or infancy
n1=Lester (signe de) | n2=en:death usually in newborn period or infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in sixth decade
n1=Lester (signe de) | n2=en:death usually in sixth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in teenage years
n1=Lester (signe de) | n2=en:death usually in teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in the first 2 years of life
n1=Lester (signe de) | n2=en:death usually in the first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually in the perinatal period
n1=Lester (signe de) | n2=en:death usually in the perinatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs before 5th decade
n1=Lester (signe de) | n2=en:death usually occurs before 5th decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs by 12 months of life
n1=Lester (signe de) | n2=en:death usually occurs by 12 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs by age 2 years
n1=Lester (signe de) | n2=en:death usually occurs by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs in childhood
n1=Lester (signe de) | n2=en:death usually occurs in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs in early infancy
n1=Lester (signe de) | n2=en:death usually occurs in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs in first decade of life
n1=Lester (signe de) | n2=en:death usually occurs in first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs in infancy or childhood if untreated
n1=Lester (signe de) | n2=en:death usually occurs in infancy or childhood if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually occurs in the first weeks to months of life
n1=Lester (signe de) | n2=en:death usually occurs in the first weeks to months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually within first 2 years of life
n1=Lester (signe de) | n2=en:death usually within first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually within first weeks of life
n1=Lester (signe de) | n2=en:death usually within first weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death usually within first year of life
n1=Lester (signe de) | n2=en:death usually within first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within 12 months
n1=Lester (signe de) | n2=en:death within 12 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within 3 months of life
n1=Lester (signe de) | n2=en:death within 3 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within 6 years after onset
n1=Lester (signe de) | n2=en:death within 6 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within first decade
n1=Lester (signe de) | n2=en:death within first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within first months or years of life
n1=Lester (signe de) | n2=en:death within first months or years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within first year of life
n1=Lester (signe de) | n2=en:death within first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within first year of life in 25%
n1=Lester (signe de) | n2=en:death within first year of life in 25% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:death within several months if untreated
n1=Lester (signe de) | n2=en:death within several months if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decrease in frequency and severity of episodes in young adulthood
n1=Lester (signe de) | n2=en:decrease in frequency and severity of episodes in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decrease in seizure frequency in middle age
n1=Lester (signe de) | n2=en:decrease in seizure frequency in middle age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decreased bilirubin concentration with phenobarbital administration
n1=Lester (signe de) | n2=en:decreased bilirubin concentration with phenobarbital administration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decreased fertility
n1=Lester (signe de) | n2=en:decreased fertility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decreased life expectancy
n1=Lester (signe de) | n2=en:decreased life expectancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:decreased penetrance
n1=Lester (signe de) | n2=en:decreased penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:defect in tetrahydrobiopterin (bh4) synthesis
n1=Lester (signe de) | n2=en:defect in tetrahydrobiopterin (bh4) synthesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:defect in urocanic acid conversion to formiminoglutamic acid (figlu)
n1=Lester (signe de) | n2=en:defect in urocanic acid conversion to formiminoglutamic acid (figlu) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:definite diagnosis if 3/4 criteria present (epistaxis, telangiectasia, visceral lesion, or family history)
n1=Lester (signe de) | n2=en:definite diagnosis if 3/4 criteria present (epistaxis, telangiectasia, visceral lesion, or family history) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:delayed psychomotor development apparent in infancy
n1=Lester (signe de) | n2=en:delayed psychomotor development apparent in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:delayed separation of umbilical cord
n1=Lester (signe de) | n2=en:delayed separation of umbilical cord | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deleted region contains 4 genes that are not imprinted, tubgcp2 (608147), nipa1 (608145), nipa2 (608146), and cyfip1 (606322)
n1=Lester (signe de) | n2=en:deleted region contains 4 genes that are not imprinted, tubgcp2 (608147), nipa1 (608145), nipa2 (608146), and cyfip1 (606322) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deletion sizes range from 287kb to 4.4mb
n1=Lester (signe de) | n2=en:deletion sizes range from 287kb to 4.4mb | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deletions in naip gene (600355) found in 18% of sma2 patients
n1=Lester (signe de) | n2=en:deletions in naip gene (600355) found in 18% of sma2 patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deletions in naip gene (600355) found in 18% of smaii patients
n1=Lester (signe de) | n2=en:deletions in naip gene (600355) found in 18% of smaii patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deletions occur de novo
n1=Lester (signe de) | n2=en:deletions occur de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:delta-f508 present in 70% of alleles
n1=Lester (signe de) | n2=en:delta-f508 present in 70% of alleles | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:deposits may recur in graft after corneal transplantation
n1=Lester (signe de) | n2=en:deposits may recur in graft after corneal transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dermatitis resolves in offspring after zinc supplementation and/or weaning
n1=Lester (signe de) | n2=en:dermatitis resolves in offspring after zinc supplementation and/or weaning | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in 3 unrelated infants (last curated january 2013)
n1=Lester (signe de) | n2=en:described in 3 unrelated infants (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in 6 japanese families
n1=Lester (signe de) | n2=en:described in 6 japanese families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in families from galicia, spain
n1=Lester (signe de) | n2=en:described in families from galicia, spain | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in families from western japan
n1=Lester (signe de) | n2=en:described in families from western japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in individuals of jewish bukharian descent
n1=Lester (signe de) | n2=en:described in individuals of jewish bukharian descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in individuals of roma gypsy origin (founder mutation)
n1=Lester (signe de) | n2=en:described in individuals of roma gypsy origin (founder mutation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in one 5-generation pakistani family (last curated april 2013)
n1=Lester (signe de) | n2=en:described in one 5-generation pakistani family (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described in single afrikaner family
n1=Lester (signe de) | n2=en:described in single afrikaner family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:described predominantly in families from the philippines
n1=Lester (signe de) | n2=en:described predominantly in families from the philippines | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:despite voluminous steatorrhea, patients' growth and overall state of health is good
n1=Lester (signe de) | n2=en:despite voluminous steatorrhea, patients' growth and overall state of health is good | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:detailed clinical information provided for 2 klk-mutation-positive families (last curated march 2015)
n1=Lester (signe de) | n2=en:detailed clinical information provided for 2 klk-mutation-positive families (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:detected in 1/50,000 in neonatal screening programs
n1=Lester (signe de) | n2=en:detected in 1/50,000 in neonatal screening programs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:development of afebrile seizures later in childhood
n1=Lester (signe de) | n2=en:development of afebrile seizures later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diabetes and anemia respond to high doses of thiamine supplementation
n1=Lester (signe de) | n2=en:diabetes and anemia respond to high doses of thiamine supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diabetes diagnosed in second or third decade of life
n1=Lester (signe de) | n2=en:diabetes diagnosed in second or third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diabetes mellitus develops in adolescence
n1=Lester (signe de) | n2=en:diabetes mellitus develops in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diabetes mellitus diagnosed between third and fifth decades of life
n1=Lester (signe de) | n2=en:diabetes mellitus diagnosed between third and fifth decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diabetes status:prid:pt:^patient:nom
n1=Lester (signe de) | n2=en:diabetes status:prid:pt:^patient:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosed in second or third decade of life
n1=Lester (signe de) | n2=en:diagnosed in second or third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis in early childhood
n1=Lester (signe de) | n2=en:diagnosis in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis in seventh decade of life
n1=Lester (signe de) | n2=en:diagnosis in seventh decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis in the second decade of life
n1=Lester (signe de) | n2=en:diagnosis in the second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis made if 3/7 defects are present
n1=Lester (signe de) | n2=en:diagnosis made if 3/7 defects are present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis made when at least 2/3 features present (optic nerve hypoplasia, hypopituitarism with pituitary hypoplasia, midline forebrain defects)
n1=Lester (signe de) | n2=en:diagnosis made when at least 2/3 features present (optic nerve hypoplasia, hypopituitarism with pituitary hypoplasia, midline forebrain defects) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis occurs between 23 and 33 weeks' gestation
n1=Lester (signe de) | n2=en:diagnosis occurs between 23 and 33 weeks' gestation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis rarely made before the fourth decade of life
n1=Lester (signe de) | n2=en:diagnosis rarely made before the fourth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis requires 3 major features (a positive family history is also considered a major feature) and at least 3 minor features
n1=Lester (signe de) | n2=en:diagnosis requires 3 major features (a positive family history is also considered a major feature) and at least 3 minor features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis typically between age 10-20 years
n1=Lester (signe de) | n2=en:diagnosis typically between age 10-20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diagnosis within the first 3 months of life
n1=Lester (signe de) | n2=en:diagnosis within the first 3 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diarrhea persists even with vigorous nursing
n1=Lester (signe de) | n2=en:diarrhea persists even with vigorous nursing | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diarrhea worsens in parallel with increases in severity of skin disease
n1=Lester (signe de) | n2=en:diarrhea worsens in parallel with increases in severity of skin disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diarrhea-associated (d+hus), occurs in children younger than 3 years, associated with verotoxin-producing e. coli (90% of patients) (typical hus)
n1=Lester (signe de) | n2=en:diarrhea-associated (d+hus), occurs in children younger than 3 years, associated with verotoxin-producing e. coli (90% of patients) (typical hus) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diarrhea-negative subtype (d-hus), or atypical hus, is more severe and often relapses
n1=Lester (signe de) | n2=en:diarrhea-negative subtype (d-hus), or atypical hus, is more severe and often relapses | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:die at birth or shortly after birth
n1=Lester (signe de) | n2=en:die at birth or shortly after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:difficulty walking
n1=Lester (signe de) | n2=en:difficulty walking | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:digenic form caused by heterozygous mutations in both nek1 (604588) and dyn2ch1 (603297)
n1=Lester (signe de) | n2=en:digenic form caused by heterozygous mutations in both nek1 (604588) and dyn2ch1 (603297) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:digenic form caused by heterozygous mutations in the gpr98 (602851.0010) and pdzd7 (612971.0002) genes
n1=Lester (signe de) | n2=en:digenic form caused by heterozygous mutations in the gpr98 (602851.0010) and pdzd7 (612971.0002) genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:digenic form type id/f caused by digenic mutation in the cdh23 (605516) and pcdh15 genes
n1=Lester (signe de) | n2=en:digenic form type id/f caused by digenic mutation in the cdh23 (605516) and pcdh15 genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:digenic form type id/f caused by digenic mutation in the cdh23 and pcdh15 (605514) genes
n1=Lester (signe de) | n2=en:digenic form type id/f caused by digenic mutation in the cdh23 and pcdh15 (605514) genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dip is a pathologic diagnosis that may represent other disease entities
n1=Lester (signe de) | n2=en:dip is a pathologic diagnosis that may represent other disease entities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disability by end of first decade
n1=Lester (signe de) | n2=en:disability by end of first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:discordant phenotype among monozygotic twins has been reported
n1=Lester (signe de) | n2=en:discordant phenotype among monozygotic twins has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease complicated by recurrent sepsis in some patients
n1=Lester (signe de) | n2=en:disease complicated by recurrent sepsis in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease course depends on age at onset
n1=Lester (signe de) | n2=en:disease course depends on age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease exacerbation during summer due to heat
n1=Lester (signe de) | n2=en:disease exacerbation during summer due to heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease is life-threatening if untreated
n1=Lester (signe de) | n2=en:disease is life-threatening if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease is nonprogressive in most patients
n1=Lester (signe de) | n2=en:disease is nonprogressive in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease shows slow progression
n1=Lester (signe de) | n2=en:disease shows slow progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease steadily progressive
n1=Lester (signe de) | n2=en:disease steadily progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease usually progresses in a cephalocaudal direction
n1=Lester (signe de) | n2=en:disease usually progresses in a cephalocaudal direction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disease-free intervals can last weeks to years during which there is no clinical or biochemical evidence of cholestasis
n1=Lester (signe de) | n2=en:disease-free intervals can last weeks to years during which there is no clinical or biochemical evidence of cholestasis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disorder becomes apparent around age 2 years when patients begin to walk
n1=Lester (signe de) | n2=en:disorder becomes apparent around age 2 years when patients begin to walk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disorder is static for first 2 decades and then shows progression of movement disorders and further cognitive decline
n1=Lester (signe de) | n2=en:disorder is static for first 2 decades and then shows progression of movement disorders and further cognitive decline | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disorder may progress to involve a larger body area
n1=Lester (signe de) | n2=en:disorder may progress to involve a larger body area | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disorder usually remains stable over time
n1=Lester (signe de) | n2=en:disorder usually remains stable over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disorders with overlapping phenotypes can be caused by mutation in the keratin-14 gene (148066)
n1=Lester (signe de) | n2=en:disorders with overlapping phenotypes can be caused by mutation in the keratin-14 gene (148066) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:disproportionately short limbs often noted at birth
n1=Lester (signe de) | n2=en:disproportionately short limbs often noted at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from acquired limb-girdle myasthenia (159400) and congenital limb-girdle myasthenia (254300)
n1=Lester (signe de) | n2=en:distinct disorder from acquired limb-girdle myasthenia (159400) and congenital limb-girdle myasthenia (254300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from autosomal dominant hyper ige syndrome (147060)
n1=Lester (signe de) | n2=en:distinct disorder from autosomal dominant hyper ige syndrome (147060) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from familial erythrocytosis (ecyt1, 133100)
n1=Lester (signe de) | n2=en:distinct disorder from familial erythrocytosis (ecyt1, 133100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from familial limb-girdle myasthenia (254200)
n1=Lester (signe de) | n2=en:distinct disorder from familial limb-girdle myasthenia (254200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from galactosemia (230400)
n1=Lester (signe de) | n2=en:distinct disorder from galactosemia (230400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from hereditary neuropathy with liability to pressure palsies (hnpp, 162500)
n1=Lester (signe de) | n2=en:distinct disorder from hereditary neuropathy with liability to pressure palsies (hnpp, 162500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from marinesco-sjogren syndrome (mss, 248800)
n1=Lester (signe de) | n2=en:distinct disorder from marinesco-sjogren syndrome (mss, 248800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from myasthenia gravis (mg, 254200)
n1=Lester (signe de) | n2=en:distinct disorder from myasthenia gravis (mg, 254200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from parkinson disease (168600)
n1=Lester (signe de) | n2=en:distinct disorder from parkinson disease (168600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from reduced zinc in breast milk (608118)
n1=Lester (signe de) | n2=en:distinct disorder from reduced zinc in breast milk (608118) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct disorder from transient neonatal hyperthyroidism due to maternal graves disease (see 275000)
n1=Lester (signe de) | n2=en:distinct disorder from transient neonatal hyperthyroidism due to maternal graves disease (see 275000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct from pili annulati (180600)
n1=Lester (signe de) | n2=en:distinct from pili annulati (180600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinct from pseudopili annulati (613241)
n1=Lester (signe de) | n2=en:distinct from pseudopili annulati (613241) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinctive and stereotyped sequence of events
n1=Lester (signe de) | n2=en:distinctive and stereotyped sequence of events | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distinguished from nbia1 by the presence of hypobetalipoproteinemia and acanthocytosis
n1=Lester (signe de) | n2=en:distinguished from nbia1 by the presence of hypobetalipoproteinemia and acanthocytosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distribution of involvement is variable and may include craniofacial, thoracic, abdominal, and extremity structures
n1=Lester (signe de) | n2=en:distribution of involvement is variable and may include craniofacial, thoracic, abdominal, and extremity structures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:distribution of lesions may be generalized, palmoplantar, or acral
n1=Lester (signe de) | n2=en:distribution of lesions may be generalized, palmoplantar, or acral | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diurnal fluctuation
n1=Lester (signe de) | n2=en:diurnal fluctuation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diurnal fluctuation of neurologic symptoms
n1=Lester (signe de) | n2=en:diurnal fluctuation of neurologic symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diurnal fluctuation of symptoms
n1=Lester (signe de) | n2=en:diurnal fluctuation of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:diurnal fluctuation, more apparent in earlier years, later subsides
n1=Lester (signe de) | n2=en:diurnal fluctuation, more apparent in earlier years, later subsides | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:divided into isolated cases (75-80%), familial (10-15%), and syndromal (1-5%)
n1=Lester (signe de) | n2=en:divided into isolated cases (75-80%), familial (10-15%), and syndromal (1-5%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:does not lead to hepatic failure
n1=Lester (signe de) | n2=en:does not lead to hepatic failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:does not result in renal failure
n1=Lester (signe de) | n2=en:does not result in renal failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:door is acronym for deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures
n1=Lester (signe de) | n2=en:door is acronym for deafness, onychodystrophy, osteodystrophy, mental retardation, and seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dopa-responsive rigidity
n1=Lester (signe de) | n2=en:dopa-responsive rigidity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dopa-unresponsive
n1=Lester (signe de) | n2=en:dopa-unresponsive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dramatic improvement with proper treatment
n1=Lester (signe de) | n2=en:dramatic improvement with proper treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dramatic late catch-up growth occurs in adolescence
n1=Lester (signe de) | n2=en:dramatic late catch-up growth occurs in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:drug-induced dyskinesias occur in a subset of patients
n1=Lester (signe de) | n2=en:drug-induced dyskinesias occur in a subset of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dryness and impaired vision in older adults
n1=Lester (signe de) | n2=en:dryness and impaired vision in older adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:duane anomaly is not always present
n1=Lester (signe de) | n2=en:duane anomaly is not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:due to lack of epidermal ridging, patients lack fingerprints
n1=Lester (signe de) | n2=en:due to lack of epidermal ridging, patients lack fingerprints | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:duplication of lmnb1 is sufficient for the disorder, although patients may also have larger duplications
n1=Lester (signe de) | n2=en:duplication of lmnb1 is sufficient for the disorder, although patients may also have larger duplications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dwarfism not detectable at birth
n1=Lester (signe de) | n2=en:dwarfism not detectable at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysarthria, dysphonia, or cough precede onset of ataxia
n1=Lester (signe de) | n2=en:dysarthria, dysphonia, or cough precede onset of ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dyskinesia may be precipitated by alcohol, stress, or fatigue
n1=Lester (signe de) | n2=en:dyskinesia may be precipitated by alcohol, stress, or fatigue | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dyskinesia may occur in homozygotes (1 reported case)
n1=Lester (signe de) | n2=en:dyskinesia may occur in homozygotes (1 reported case) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dyskinesias occur in a subset of patients later than seizures (6 to 12 months)
n1=Lester (signe de) | n2=en:dyskinesias occur in a subset of patients later than seizures (6 to 12 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic facial features are subtle
n1=Lester (signe de) | n2=en:dysmorphic facial features are subtle | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic facial features are variable
n1=Lester (signe de) | n2=en:dysmorphic facial features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic facial features may not be present
n1=Lester (signe de) | n2=en:dysmorphic facial features may not be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic facial features reported in 1 family
n1=Lester (signe de) | n2=en:dysmorphic facial features reported in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic features are mild or variable
n1=Lester (signe de) | n2=en:dysmorphic features are mild or variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic features are variable
n1=Lester (signe de) | n2=en:dysmorphic features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic features may be subtle
n1=Lester (signe de) | n2=en:dysmorphic features may be subtle | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dysmorphic features were only reported in 1 patient
n1=Lester (signe de) | n2=en:dysmorphic features were only reported in 1 patient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dystonia and seizures may persist after resolution of episodes
n1=Lester (signe de) | n2=en:dystonia and seizures may persist after resolution of episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dystonia is usually focal or segmental
n1=Lester (signe de) | n2=en:dystonia is usually focal or segmental | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:dystonia occurs later
n1=Lester (signe de) | n2=en:dystonia occurs later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset associated with faster progression and shorter life span
n1=Lester (signe de) | n2=en:earlier onset associated with faster progression and shorter life span | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset associated with increased severity
n1=Lester (signe de) | n2=en:earlier onset associated with increased severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset is associated with a more severe disorder
n1=Lester (signe de) | n2=en:earlier onset is associated with a more severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset is associated with more aggressive disease course
n1=Lester (signe de) | n2=en:earlier onset is associated with more aggressive disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset is associated with more rapid progression
n1=Lester (signe de) | n2=en:earlier onset is associated with more rapid progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset is rare
n1=Lester (signe de) | n2=en:earlier onset is rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earlier onset may occur
n1=Lester (signe de) | n2=en:earlier onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earliest age of onset 12 years of age
n1=Lester (signe de) | n2=en:earliest age of onset 12 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:earliest symptom onset in sixth decade of life
n1=Lester (signe de) | n2=en:earliest symptom onset in sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early adult onset has been reported
n1=Lester (signe de) | n2=en:early adult onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early age of onset
n1=Lester (signe de) | n2=en:early age of onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early age of onset (approximately 45 years)
n1=Lester (signe de) | n2=en:early age of onset (approximately 45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early age of onset (mean age at diagnosis, 36 years) most patients have intraocular pressures within the normal range (21 mmhg or less)
n1=Lester (signe de) | n2=en:early age of onset (mean age at diagnosis, 36 years) most patients have intraocular pressures within the normal range (21 mmhg or less) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early age of onset, usually less than 3 years
n1=Lester (signe de) | n2=en:early age of onset, usually less than 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early childhood lethality may occur
n1=Lester (signe de) | n2=en:early childhood lethality may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early childhood onset (before age 5 years)
n1=Lester (signe de) | n2=en:early childhood onset (before age 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death
n1=Lester (signe de) | n2=en:early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death (in some patients)
n1=Lester (signe de) | n2=en:early death (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death (mean age 13 months)
n1=Lester (signe de) | n2=en:early death (mean age 13 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death (usually by 3 years of age)
n1=Lester (signe de) | n2=en:early death (usually by 3 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death due to infection
n1=Lester (signe de) | n2=en:early death due to infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death due to sepsis
n1=Lester (signe de) | n2=en:early death due to sepsis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death from infection may occur
n1=Lester (signe de) | n2=en:early death from infection may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death from respiratory failure may occur
n1=Lester (signe de) | n2=en:early death from respiratory failure may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death in early adulthood often associated with diverticulitis and intestinal perforation
n1=Lester (signe de) | n2=en:early death in early adulthood often associated with diverticulitis and intestinal perforation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death in males
n1=Lester (signe de) | n2=en:early death in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death in patients with cloverleaf skull
n1=Lester (signe de) | n2=en:early death in patients with cloverleaf skull | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death in some patients due to cardiorespiratory involvement
n1=Lester (signe de) | n2=en:early death in some patients due to cardiorespiratory involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death in the first few weeks of life
n1=Lester (signe de) | n2=en:early death in the first few weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death may occur
n1=Lester (signe de) | n2=en:early death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death may occur due to infection
n1=Lester (signe de) | n2=en:early death may occur due to infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death may occur from cardiogenic shock preceded by arrhythmia
n1=Lester (signe de) | n2=en:early death may occur from cardiogenic shock preceded by arrhythmia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death may occur without bone marrow transplant
n1=Lester (signe de) | n2=en:early death may occur without bone marrow transplant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death occurs in affected infants (days to months after disease onset)
n1=Lester (signe de) | n2=en:early death occurs in affected infants (days to months after disease onset) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death often due to respiratory complications
n1=Lester (signe de) | n2=en:early death often due to respiratory complications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death often occurs from cardiac failure or infection
n1=Lester (signe de) | n2=en:early death often occurs from cardiac failure or infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death without bone marrow transplantation
n1=Lester (signe de) | n2=en:early death without bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death without kidney transplant
n1=Lester (signe de) | n2=en:early death without kidney transplant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early death, usually before age 2 years
n1=Lester (signe de) | n2=en:early death, usually before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early diagnosis and proper treatment with folate replacement therapy can avoid neurologic sequelae
n1=Lester (signe de) | n2=en:early diagnosis and proper treatment with folate replacement therapy can avoid neurologic sequelae | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early diagnosis and treatment prevent many complications
n1=Lester (signe de) | n2=en:early diagnosis and treatment prevent many complications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early exhaustion on exertion
n1=Lester (signe de) | n2=en:early exhaustion on exertion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early lethality
n1=Lester (signe de) | n2=en:early lethality | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early lethality in most cases
n1=Lester (signe de) | n2=en:early lethality in most cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset (1 month to 4 years)
n1=Lester (signe de) | n2=en:early onset (1 month to 4 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset (9-48 years, but reported up to 68 years)
n1=Lester (signe de) | n2=en:early onset (9-48 years, but reported up to 68 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset (average 1 year)
n1=Lester (signe de) | n2=en:early onset (average 1 year) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset has rarely been reported
n1=Lester (signe de) | n2=en:early onset has rarely been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset in some patients
n1=Lester (signe de) | n2=en:early onset in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset of peripheral neuropathy (mean 2.1 years, range 1 to 10 years)
n1=Lester (signe de) | n2=en:early onset of peripheral neuropathy (mean 2.1 years, range 1 to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset of symptoms
n1=Lester (signe de) | n2=en:early onset of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset patients are indistinguishable from those with carbamoyl phosphate synthetase i (cps1) deficiency (237300)
n1=Lester (signe de) | n2=en:early onset patients are indistinguishable from those with carbamoyl phosphate synthetase i (cps1) deficiency (237300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early onset, between 35-60 years
n1=Lester (signe de) | n2=en:early onset, between 35-60 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early treatment can reduce neurologic symptoms
n1=Lester (signe de) | n2=en:early treatment can reduce neurologic symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early-onset
n1=Lester (signe de) | n2=en:early-onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early-onset associated with more severe course and early death
n1=Lester (signe de) | n2=en:early-onset associated with more severe course and early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:early-onset severe renal disease
n1=Lester (signe de) | n2=en:early-onset severe renal disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:echocardiogram and ophthalmologic examination normal
n1=Lester (signe de) | n2=en:echocardiogram and ophthalmologic examination normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:eight patients from 2 unrelated families have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:eight patients from 2 unrelated families have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:eight unrelated patients have been reported (as of september 2011)
n1=Lester (signe de) | n2=en:eight unrelated patients have been reported (as of september 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:electrolyte imbalances can mimic renal bartter syndrome (601678)
n1=Lester (signe de) | n2=en:electrolyte imbalances can mimic renal bartter syndrome (601678) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:electromyography may be normal in infancy, but shows myopathic pattern in adolescence and adulthood
n1=Lester (signe de) | n2=en:electromyography may be normal in infancy, but shows myopathic pattern in adolescence and adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:electroretinogram reduction as early as 4 years of age
n1=Lester (signe de) | n2=en:electroretinogram reduction as early as 4 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:elevated afp can be seen in other disorders
n1=Lester (signe de) | n2=en:elevated afp can be seen in other disorders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:elevated body temperatures to 42 degrees celsius
n1=Lester (signe de) | n2=en:elevated body temperatures to 42 degrees celsius | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:empiric risk for a sib of an affected child between 2 and 5%
n1=Lester (signe de) | n2=en:empiric risk for a sib of an affected child between 2 and 5% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:encephalopathic episodes associated with increased serum and csf lactate
n1=Lester (signe de) | n2=en:encephalopathic episodes associated with increased serum and csf lactate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:end-stage renal disease (ckd stage 5) requiring kidney transplantation is commonly reported
n1=Lester (signe de) | n2=en:end-stage renal disease (ckd stage 5) requiring kidney transplantation is commonly reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:end-stage renal failure in first decade
n1=Lester (signe de) | n2=en:end-stage renal failure in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:end-stage renal failure in first or second decade
n1=Lester (signe de) | n2=en:end-stage renal failure in first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:end-stage renal failure may occur
n1=Lester (signe de) | n2=en:end-stage renal failure may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:endocrine abnormalities confined to kidney
n1=Lester (signe de) | n2=en:endocrine abnormalities confined to kidney | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:endocrine and neurologic defects may become apparent later in life
n1=Lester (signe de) | n2=en:endocrine and neurologic defects may become apparent later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:endocrine defects evolve over time
n1=Lester (signe de) | n2=en:endocrine defects evolve over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:endocrinologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:endocrinologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:enterocolitis tends to remit with age
n1=Lester (signe de) | n2=en:enterocolitis tends to remit with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:environmental triggers - cold and wet exposure
n1=Lester (signe de) | n2=en:environmental triggers - cold and wet exposure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:environmental triggers include (koebner's phenomenon), sunburn, hiv infection, beta-hemolytic streptococcal infection, certain medications, stress, and alcohol
n1=Lester (signe de) | n2=en:environmental triggers include (koebner's phenomenon), sunburn, hiv infection, beta-hemolytic streptococcal infection, certain medications, stress, and alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:enzyme replacement therapy will help visceral manifestations but cannot cross blood-brain barrier, so will not help neurodegeneration
n1=Lester (signe de) | n2=en:enzyme replacement therapy will help visceral manifestations but cannot cross blood-brain barrier, so will not help neurodegeneration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:epilepsy with grand mal seizures on awakening (egma, 607628)
n1=Lester (signe de) | n2=en:epilepsy with grand mal seizures on awakening (egma, 607628) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:epiphyseal stippling is gone by 8 months of age
n1=Lester (signe de) | n2=en:epiphyseal stippling is gone by 8 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episode frequency is monthly to yearly, and decreases with age
n1=Lester (signe de) | n2=en:episode frequency is monthly to yearly, and decreases with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episode, syncopal
n1=Lester (signe de) | n2=en:episode, syncopal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes are followed by exhaustion and sleep
n1=Lester (signe de) | n2=en:episodes are followed by exhaustion and sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes are triggered by cold exposure
n1=Lester (signe de) | n2=en:episodes are triggered by cold exposure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes are triggered by fatigue, illness, or strenuous exercise
n1=Lester (signe de) | n2=en:episodes are triggered by fatigue, illness, or strenuous exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes are triggered by hunger, fatigue, cold, stress
n1=Lester (signe de) | n2=en:episodes are triggered by hunger, fatigue, cold, stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes are triggered by infection, immunization, surgery, strenuous exercise, cold, pregnancy
n1=Lester (signe de) | n2=en:episodes are triggered by infection, immunization, surgery, strenuous exercise, cold, pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes brought on by fasting or infection
n1=Lester (signe de) | n2=en:episodes brought on by fasting or infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes last 1 to 2 days
n1=Lester (signe de) | n2=en:episodes last 1 to 2 days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes last 2 days to 1 week
n1=Lester (signe de) | n2=en:episodes last 2 days to 1 week | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes last about 1.5 hours
n1=Lester (signe de) | n2=en:episodes last about 1.5 hours | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes last from several hours to days
n1=Lester (signe de) | n2=en:episodes last from several hours to days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes may be precipitated by fear, unexpected noises, emotional responses, movement
n1=Lester (signe de) | n2=en:episodes may be precipitated by fear, unexpected noises, emotional responses, movement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes may be triggered by exercise, emotional stress, head trauma, angiography, lack of sleep, heat
n1=Lester (signe de) | n2=en:episodes may be triggered by exercise, emotional stress, head trauma, angiography, lack of sleep, heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes not triggered by alcohol, caffeine, or stress
n1=Lester (signe de) | n2=en:episodes not triggered by alcohol, caffeine, or stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes occur 30 minutes to 3 hours after exposure to cold
n1=Lester (signe de) | n2=en:episodes occur 30 minutes to 3 hours after exposure to cold | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes of fatigue or weakness (in some patients)
n1=Lester (signe de) | n2=en:episodes of fatigue or weakness (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes tend to decrease with age
n1=Lester (signe de) | n2=en:episodes tend to decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes triggered by fasting, illness, fever
n1=Lester (signe de) | n2=en:episodes triggered by fasting, illness, fever | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes typically last 2 to 5 minutes and occur daily or several times per month
n1=Lester (signe de) | n2=en:episodes typically last 2 to 5 minutes and occur daily or several times per month | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodes usually last 1 to 2 days
n1=Lester (signe de) | n2=en:episodes usually last 1 to 2 days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodic
n1=Lester (signe de) | n2=en:episodic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodic decompensation is usually triggered by illness
n1=Lester (signe de) | n2=en:episodic decompensation is usually triggered by illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:episodic metabolic decompensation usually associated with illness
n1=Lester (signe de) | n2=en:episodic metabolic decompensation usually associated with illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:erythema accompanied by stinging or burning sensation in some cases
n1=Lester (signe de) | n2=en:erythema accompanied by stinging or burning sensation in some cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:erythema often triggered by sudden temperature change or emotional stress
n1=Lester (signe de) | n2=en:erythema often triggered by sudden temperature change or emotional stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated carrier frequency 1/100
n1=Lester (signe de) | n2=en:estimated carrier frequency 1/100 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated carrier frequency in charlevoix-saguenay region is 1/22
n1=Lester (signe de) | n2=en:estimated carrier frequency in charlevoix-saguenay region is 1/22 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated carrier frequency of 10-25% in yarmouth county, nova scotia
n1=Lester (signe de) | n2=en:estimated carrier frequency of 10-25% in yarmouth county, nova scotia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated frequence 1/3000 to 1/5000
n1=Lester (signe de) | n2=en:estimated frequence 1/3000 to 1/5000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated frequency 1.6 cases/10,000 live births
n1=Lester (signe de) | n2=en:estimated frequency 1.6 cases/10,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated frequency 1/2000-1/4000 individuals
n1=Lester (signe de) | n2=en:estimated frequency 1/2000-1/4000 individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated frequency of 1 in 40,000 live births
n1=Lester (signe de) | n2=en:estimated frequency of 1 in 40,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated gene carrier frequency of 1 in 5,000
n1=Lester (signe de) | n2=en:estimated gene carrier frequency of 1 in 5,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated incidence 1/20,000 - 1/40,000
n1=Lester (signe de) | n2=en:estimated incidence 1/20,000 - 1/40,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated incidence of 1 in 17,000
n1=Lester (signe de) | n2=en:estimated incidence of 1 in 17,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated incidence of 1-2 in 10,000
n1=Lester (signe de) | n2=en:estimated incidence of 1-2 in 10,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated mutation carrier rate of 1 in 350
n1=Lester (signe de) | n2=en:estimated mutation carrier rate of 1 in 350 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated population frequency of 1 in 13,000-20,000
n1=Lester (signe de) | n2=en:estimated population frequency of 1 in 13,000-20,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated prevalence of 1 in 16,000
n1=Lester (signe de) | n2=en:estimated prevalence of 1 in 16,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:estimated prevalence of 1.6 in 1,000,000 individuals in the u.k.
n1=Lester (signe de) | n2=en:estimated prevalence of 1.6 in 1,000,000 individuals in the u.k. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:evidence of incomplete penetrance in one family
n1=Lester (signe de) | n2=en:evidence of incomplete penetrance in one family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:evidence of prenatal fractures
n1=Lester (signe de) | n2=en:evidence of prenatal fractures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:evidence of systemic iron overload seen in 1 family
n1=Lester (signe de) | n2=en:evidence of systemic iron overload seen in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbated by stress
n1=Lester (signe de) | n2=en:exacerbated by stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbation at puberty
n1=Lester (signe de) | n2=en:exacerbation at puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbation during febrile episodes
n1=Lester (signe de) | n2=en:exacerbation during febrile episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbation following stress, decreased food intake, or alcohol use
n1=Lester (signe de) | n2=en:exacerbation following stress, decreased food intake, or alcohol use | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbation of symptoms during or after pregnancy
n1=Lester (signe de) | n2=en:exacerbation of symptoms during or after pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbation or regression during viral infection
n1=Lester (signe de) | n2=en:exacerbation or regression during viral infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exacerbations during infection
n1=Lester (signe de) | n2=en:exacerbations during infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:excessive postsurgical blood loss
n1=Lester (signe de) | n2=en:excessive postsurgical blood loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:excessive posttraumatic blood loss
n1=Lester (signe de) | n2=en:excessive posttraumatic blood loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:excessive skin picking of sores
n1=Lester (signe de) | n2=en:excessive skin picking of sores | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exercise intolerance often evident in childhood
n1=Lester (signe de) | n2=en:exercise intolerance often evident in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:existence as a distinct entity is not confirmed
n1=Lester (signe de) | n2=en:existence as a distinct entity is not confirmed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:exon 7 of smn1 is absent in 95.6% of sma1 patients
n1=Lester (signe de) | n2=en:exon 7 of smn1 is absent in 95.6% of sma1 patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:expression more severe in females than males, except for mosaic males
n1=Lester (signe de) | n2=en:expression more severe in females than males, except for mosaic males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extracutaneous manifestations are variable
n1=Lester (signe de) | n2=en:extracutaneous manifestations are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extrapyramidal signs show a favorable response to levodopa
n1=Lester (signe de) | n2=en:extrapyramidal signs show a favorable response to levodopa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extreme clinical heterogeneity
n1=Lester (signe de) | n2=en:extreme clinical heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extreme phenotypic variability
n1=Lester (signe de) | n2=en:extreme phenotypic variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extreme sensitivity to chemotherapy
n1=Lester (signe de) | n2=en:extreme sensitivity to chemotherapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extreme variability in severity of features
n1=Lester (signe de) | n2=en:extreme variability in severity of features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:extremely variable phenotype
n1=Lester (signe de) | n2=en:extremely variable phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:eye and vestibular findings were found in some members of one family
n1=Lester (signe de) | n2=en:eye and vestibular findings were found in some members of one family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:eye involvement begins at birth, neurologic involvement begins later
n1=Lester (signe de) | n2=en:eye involvement begins at birth, neurologic involvement begins later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:f syndrome (102510) has many overlapping features
n1=Lester (signe de) | n2=en:f syndrome (102510) has many overlapping features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:facial appearance becomes more apparent with age
n1=Lester (signe de) | n2=en:facial appearance becomes more apparent with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:facial dysmorphic features are mild
n1=Lester (signe de) | n2=en:facial dysmorphic features are mild | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:facial dysmorphic features may not be present and may become less apparent in adulthood
n1=Lester (signe de) | n2=en:facial dysmorphic features may not be present and may become less apparent in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:facial dysmorphism is age-related and alters substantially over time
n1=Lester (signe de) | n2=en:facial dysmorphism is age-related and alters substantially over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:facial palsy often transient in infancy
n1=Lester (signe de) | n2=en:facial palsy often transient in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial (10%) and isolated cases
n1=Lester (signe de) | n2=en:familial (10%) and isolated cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial cases are rare and show incomplete penetrance
n1=Lester (signe de) | n2=en:familial cases are rare and show incomplete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial cases may have affected 46,xx family members who exhibit premature ovarian failure (see pof7, 612964)
n1=Lester (signe de) | n2=en:familial cases may have affected 46,xx family members who exhibit premature ovarian failure (see pof7, 612964) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial cases may have affected 46,xy family members who exhibit sex reversal (see srxy3, 612965)
n1=Lester (signe de) | n2=en:familial cases may have affected 46,xy family members who exhibit sex reversal (see srxy3, 612965) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial form
n1=Lester (signe de) | n2=en:familial form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial form - constitutional deficiency of vwf-cleaving protease
n1=Lester (signe de) | n2=en:familial form - constitutional deficiency of vwf-cleaving protease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial hemiplegic migraine-2 (fhm2, 602481) is an allelic disorder with an overlapping phenotype
n1=Lester (signe de) | n2=en:familial hemiplegic migraine-2 (fhm2, 602481) is an allelic disorder with an overlapping phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:familial occurrence is rare
n1=Lester (signe de) | n2=en:familial occurrence is rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:families a and b had a more severe phenotype resulting in death in early childhood
n1=Lester (signe de) | n2=en:families a and b had a more severe phenotype resulting in death in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:family a had a severe multisystem disorder resulting in death before age 2 years
n1=Lester (signe de) | n2=en:family a had a severe multisystem disorder resulting in death before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:family a has 2 sibs born of consanguineous turkish parents with a milder phenotype with onset in childhood
n1=Lester (signe de) | n2=en:family a has 2 sibs born of consanguineous turkish parents with a milder phenotype with onset in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:family b had a milder phenotype
n1=Lester (signe de) | n2=en:family b had a milder phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:family c had a milder phenotype with survival into adulthood
n1=Lester (signe de) | n2=en:family c had a milder phenotype with survival into adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:family history of sudden death, as early as fourth decade of life
n1=Lester (signe de) | n2=en:family history of sudden death, as early as fourth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fasting status:prthr:pt:^patient:ord:reported
n1=Lester (signe de) | n2=en:fasting status:prthr:pt:^patient:ord:reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fat pads become less prominent with time
n1=Lester (signe de) | n2=en:fat pads become less prominent with time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal before age 2 years
n1=Lester (signe de) | n2=en:fatal before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal if renal transplant is not performed
n1=Lester (signe de) | n2=en:fatal if renal transplant is not performed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal in first few months of life in most cases
n1=Lester (signe de) | n2=en:fatal in first few months of life in most cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal in the neonatal period (in some patients)
n1=Lester (signe de) | n2=en:fatal in the neonatal period (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal multiorgan failure due to severe inflammatory response in some patients
n1=Lester (signe de) | n2=en:fatal multiorgan failure due to severe inflammatory response in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal outcome if untreated
n1=Lester (signe de) | n2=en:fatal outcome if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal without bone marrow transplantation
n1=Lester (signe de) | n2=en:fatal without bone marrow transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal without hematopoietic stem cell transplantation
n1=Lester (signe de) | n2=en:fatal without hematopoietic stem cell transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatal without lung transplant
n1=Lester (signe de) | n2=en:fatal without lung transplant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fatigue
n1=Lester (signe de) | n2=en:fatigue | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable initial response to l-dopa
n1=Lester (signe de) | n2=en:favorable initial response to l-dopa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable management with the fibrinolysis inhibitors (e.g., epsilon-aminocaproic acid and tranexamic acid)
n1=Lester (signe de) | n2=en:favorable management with the fibrinolysis inhibitors (e.g., epsilon-aminocaproic acid and tranexamic acid) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response of episodic attacks to acetazolamide
n1=Lester (signe de) | n2=en:favorable response of episodic attacks to acetazolamide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response of seizures to a ketogenic diet
n1=Lester (signe de) | n2=en:favorable response of seizures to a ketogenic diet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to 3,4-diaminopyridine
n1=Lester (signe de) | n2=en:favorable response to 3,4-diaminopyridine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to a ketogenic diet
n1=Lester (signe de) | n2=en:favorable response to a ketogenic diet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to acetylcholinesterase inhibitors
n1=Lester (signe de) | n2=en:favorable response to acetylcholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to alcohol
n1=Lester (signe de) | n2=en:favorable response to alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to alcohol in about 50%
n1=Lester (signe de) | n2=en:favorable response to alcohol in about 50% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to antibodies against tnf-alpha (tnfa, 191160)
n1=Lester (signe de) | n2=en:favorable response to antibodies against tnf-alpha (tnfa, 191160) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to anticholinesterase medication
n1=Lester (signe de) | n2=en:favorable response to anticholinesterase medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to anticonvulsants
n1=Lester (signe de) | n2=en:favorable response to anticonvulsants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to antiepileptic medication
n1=Lester (signe de) | n2=en:favorable response to antiepileptic medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to bh4
n1=Lester (signe de) | n2=en:favorable response to bh4 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to bh4 therapy
n1=Lester (signe de) | n2=en:favorable response to bh4 therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to cholinesterase inhibitors
n1=Lester (signe de) | n2=en:favorable response to cholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to clonazepam
n1=Lester (signe de) | n2=en:favorable response to clonazepam | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to corticosteroid treatment (1 family)
n1=Lester (signe de) | n2=en:favorable response to corticosteroid treatment (1 family) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to ephedrine treatment
n1=Lester (signe de) | n2=en:favorable response to ephedrine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to flunarizine
n1=Lester (signe de) | n2=en:favorable response to flunarizine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to high-dose steroids
n1=Lester (signe de) | n2=en:favorable response to high-dose steroids | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to hydroxychloroquine treatment
n1=Lester (signe de) | n2=en:favorable response to hydroxychloroquine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to immunotherapy
n1=Lester (signe de) | n2=en:favorable response to immunotherapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to intermittent, low-dose steroid therapy
n1=Lester (signe de) | n2=en:favorable response to intermittent, low-dose steroid therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to l-dopa
n1=Lester (signe de) | n2=en:favorable response to l-dopa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to l-dopa treatment
n1=Lester (signe de) | n2=en:favorable response to l-dopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to l-dopa without side effects
n1=Lester (signe de) | n2=en:favorable response to l-dopa without side effects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to lenalidomide treatment
n1=Lester (signe de) | n2=en:favorable response to lenalidomide treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to oral bile acid therapy
n1=Lester (signe de) | n2=en:favorable response to oral bile acid therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to oral creatine treatment
n1=Lester (signe de) | n2=en:favorable response to oral creatine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to rituxan (in some patients)
n1=Lester (signe de) | n2=en:favorable response to rituxan (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to sodium chloride treatment
n1=Lester (signe de) | n2=en:favorable response to sodium chloride treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to spironolactone
n1=Lester (signe de) | n2=en:favorable response to spironolactone | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to treatment with cholinesterase inhibitors or amifampridine
n1=Lester (signe de) | n2=en:favorable response to treatment with cholinesterase inhibitors or amifampridine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to treatment with coenzyme q10
n1=Lester (signe de) | n2=en:favorable response to treatment with coenzyme q10 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to treatment with minocycline or azithromycin
n1=Lester (signe de) | n2=en:favorable response to treatment with minocycline or azithromycin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to treatment with riboflavin
n1=Lester (signe de) | n2=en:favorable response to treatment with riboflavin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favorable response to ursodeoxycholic acid treatment
n1=Lester (signe de) | n2=en:favorable response to ursodeoxycholic acid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:favoring of fat and protein
n1=Lester (signe de) | n2=en:favoring of fat and protein | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features are highly variable
n1=Lester (signe de) | n2=en:features are highly variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features are variable
n1=Lester (signe de) | n2=en:features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features based on one australian/uk family with tmem98 mutation (last curated august 2014)
n1=Lester (signe de) | n2=en:features based on one australian/uk family with tmem98 mutation (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features in addition to mental retardation are variable
n1=Lester (signe de) | n2=en:features in addition to mental retardation are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features in typical patient include mental retardation, microcephaly, short stature, and lean body build
n1=Lester (signe de) | n2=en:features in typical patient include mental retardation, microcephaly, short stature, and lean body build | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features intermediate between demyelinating cmt and axonal cmt
n1=Lester (signe de) | n2=en:features intermediate between demyelinating cmt and axonal cmt | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features may be bilateral (15/24) or left side (9/24)
n1=Lester (signe de) | n2=en:features may be bilateral (15/24) or left side (9/24) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features occur episodically
n1=Lester (signe de) | n2=en:features occur episodically | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features of aho may rarely be observed, including brachydactyly, short metacarpals, and obesity (see 103580)
n1=Lester (signe de) | n2=en:features of aho may rarely be observed, including brachydactyly, short metacarpals, and obesity (see 103580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features of pseudoxanthoma elasticum seen in later childhood in some surviving patients
n1=Lester (signe de) | n2=en:features of pseudoxanthoma elasticum seen in later childhood in some surviving patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:features usually appear during adulthood
n1=Lester (signe de) | n2=en:features usually appear during adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:febrile attacks disappear in adulthood in some patients
n1=Lester (signe de) | n2=en:febrile attacks disappear in adulthood in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:febrile crises decrease with age, with ataxia becoming the predominant symptom (in some patients)
n1=Lester (signe de) | n2=en:febrile crises decrease with age, with ataxia becoming the predominant symptom (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:febrile seizures remit by age 5 or 6
n1=Lester (signe de) | n2=en:febrile seizures remit by age 5 or 6 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:febrile seizures show onset between 6 months and 3 years
n1=Lester (signe de) | n2=en:febrile seizures show onset between 6 months and 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:feeding difficulties in infancy
n1=Lester (signe de) | n2=en:feeding difficulties in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:feeding difficulties, including aspiration, ameliorate with age
n1=Lester (signe de) | n2=en:feeding difficulties, including aspiration, ameliorate with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:feet are unaffected
n1=Lester (signe de) | n2=en:feet are unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:feet are unaffected in some patients
n1=Lester (signe de) | n2=en:feet are unaffected in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers are unaffected or show neuropsychiatric features
n1=Lester (signe de) | n2=en:female carriers are unaffected or show neuropsychiatric features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers exhibit short stature
n1=Lester (signe de) | n2=en:female carriers exhibit short stature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers experience significant clinical manifestations
n1=Lester (signe de) | n2=en:female carriers experience significant clinical manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may be affected
n1=Lester (signe de) | n2=en:female carriers may be affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may be less severely affected
n1=Lester (signe de) | n2=en:female carriers may be less severely affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may be mildly affected
n1=Lester (signe de) | n2=en:female carriers may be mildly affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may develop mild hearing loss as adults
n1=Lester (signe de) | n2=en:female carriers may develop mild hearing loss as adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have asymptomatic hypercalciuria or hypophosphatemia only
n1=Lester (signe de) | n2=en:female carriers may have asymptomatic hypercalciuria or hypophosphatemia only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have asymptomatic proteinuria or hypercalciuria
n1=Lester (signe de) | n2=en:female carriers may have asymptomatic proteinuria or hypercalciuria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have asymptomatic proteinuria, hypercalciuria, or hypophosphatemia only
n1=Lester (signe de) | n2=en:female carriers may have asymptomatic proteinuria, hypercalciuria, or hypophosphatemia only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have cardiac defects
n1=Lester (signe de) | n2=en:female carriers may have cardiac defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have hearing loss and/or subclinical peripheral neuropathy
n1=Lester (signe de) | n2=en:female carriers may have hearing loss and/or subclinical peripheral neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have mild hearing impairment
n1=Lester (signe de) | n2=en:female carriers may have mild hearing impairment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have mild hearing impairment and/or mild signs of choroideremia
n1=Lester (signe de) | n2=en:female carriers may have mild hearing impairment and/or mild signs of choroideremia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have mild mental retardation
n1=Lester (signe de) | n2=en:female carriers may have mild mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have short stature and premature ovarian failure
n1=Lester (signe de) | n2=en:female carriers may have short stature and premature ovarian failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may have subtle manifestations
n1=Lester (signe de) | n2=en:female carriers may have subtle manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may show intermittent hematuria
n1=Lester (signe de) | n2=en:female carriers may show intermittent hematuria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may show mild learning disabilities
n1=Lester (signe de) | n2=en:female carriers may show mild learning disabilities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female carriers may show some manifestations, such as hearing impairment
n1=Lester (signe de) | n2=en:female carriers may show some manifestations, such as hearing impairment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female mutation carriers are less severely affected than male mutation carriers
n1=Lester (signe de) | n2=en:female mutation carriers are less severely affected than male mutation carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female mutation carriers have earlier age at onset compared to male mutation carriers
n1=Lester (signe de) | n2=en:female mutation carriers have earlier age at onset compared to male mutation carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female mutations carriers have a milder phenotype, with myalgia, calf hypertrophy, or isolated increased serum creatine kinase
n1=Lester (signe de) | n2=en:female mutations carriers have a milder phenotype, with myalgia, calf hypertrophy, or isolated increased serum creatine kinase | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female predominance (4:1)
n1=Lester (signe de) | n2=en:female predominance (4:1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female preponderance
n1=Lester (signe de) | n2=en:female preponderance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female to male ratio 5:1
n1=Lester (signe de) | n2=en:female to male ratio 5:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female to male ratio 8-13:1
n1=Lester (signe de) | n2=en:female to male ratio 8-13:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female to male ratio ranges from 2:1 to 4:1
n1=Lester (signe de) | n2=en:female to male ratio ranges from 2:1 to 4:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:female to male ratio, 1:1
n1=Lester (signe de) | n2=en:female to male ratio, 1:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females are more often affected
n1=Lester (signe de) | n2=en:females are more often affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females are most often affected, but rare male cases have been reported
n1=Lester (signe de) | n2=en:females are most often affected, but rare male cases have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females carriers have more variable age at onset and severity
n1=Lester (signe de) | n2=en:females carriers have more variable age at onset and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females demonstrate lyonization with corresponding phenotypic variation
n1=Lester (signe de) | n2=en:females demonstrate lyonization with corresponding phenotypic variation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females have milder manifestations than males
n1=Lester (signe de) | n2=en:females have milder manifestations than males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females may be unaffected or mildly affected
n1=Lester (signe de) | n2=en:females may be unaffected or mildly affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females more severely affected than males
n1=Lester (signe de) | n2=en:females more severely affected than males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females often show milder phenotype with later onset of cardiac symptoms
n1=Lester (signe de) | n2=en:females often show milder phenotype with later onset of cardiac symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:females tend to have earlier onset
n1=Lester (signe de) | n2=en:females tend to have earlier onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fetal death
n1=Lester (signe de) | n2=en:fetal death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fetal death may occur
n1=Lester (signe de) | n2=en:fetal death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fetal death usually occurs
n1=Lester (signe de) | n2=en:fetal death usually occurs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fever of unknown origin
n1=Lester (signe de) | n2=en:fever of unknown origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fever, muscle cramping, and poor feeding remit by age 2 years
n1=Lester (signe de) | n2=en:fever, muscle cramping, and poor feeding remit by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:few familial (parent offspring) cases reported
n1=Lester (signe de) | n2=en:few familial (parent offspring) cases reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:few patients with mild to moderate mental retardation
n1=Lester (signe de) | n2=en:few patients with mild to moderate mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fifty percent of cases are sporadic
n1=Lester (signe de) | n2=en:fifty percent of cases are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fifty percent of cases secondary to new mutations
n1=Lester (signe de) | n2=en:fifty percent of cases secondary to new mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fifty-percent of individuals responsive to pyridoxine (vitamin b6)
n1=Lester (signe de) | n2=en:fifty-percent of individuals responsive to pyridoxine (vitamin b6) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:figure associated with report or note:-:point in time:^patient:-
n1=Lester (signe de) | n2=en:figure associated with report or note:-:point in time:^patient:- | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:findings in muscle biopsy may be variable
n1=Lester (signe de) | n2=en:findings in muscle biopsy may be variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first described in acadian population of louisiana
n1=Lester (signe de) | n2=en:first described in acadian population of louisiana | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first described in gypsy group from bulgaria
n1=Lester (signe de) | n2=en:first described in gypsy group from bulgaria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first described in the geographically isolated saguenay-lac-saint-jean region of quebec, canada
n1=Lester (signe de) | n2=en:first described in the geographically isolated saguenay-lac-saint-jean region of quebec, canada | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first fracture in early childhood
n1=Lester (signe de) | n2=en:first fracture in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first identified in individuals of cypriot origin
n1=Lester (signe de) | n2=en:first identified in individuals of cypriot origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:first name:pn:pt:^guardian or legally authorized representative:nom
n1=Lester (signe de) | n2=en:first name:pn:pt:^guardian or legally authorized representative:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fish can be used to detect deletions of 4p16.3, the critical region for the phenotype
n1=Lester (signe de) | n2=en:fish can be used to detect deletions of 4p16.3, the critical region for the phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fishy body odor
n1=Lester (signe de) | n2=en:fishy body odor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five affected individuals in one consanguineous pakistani with itpr2 mutation has been described (last curated april 2015)
n1=Lester (signe de) | n2=en:five affected individuals in one consanguineous pakistani with itpr2 mutation has been described (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five children from 2 unrelated consanguineous palestinian families have been reported (last curated january 2016)
n1=Lester (signe de) | n2=en:five children from 2 unrelated consanguineous palestinian families have been reported (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five clinical variants of msud unassociated with genotype
n1=Lester (signe de) | n2=en:five clinical variants of msud unassociated with genotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five patients from 3 unrelated families have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:five patients from 3 unrelated families have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five patients have been reported (as of 8/2011)
n1=Lester (signe de) | n2=en:five patients have been reported (as of 8/2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five patients have been reported (as of april 2011)
n1=Lester (signe de) | n2=en:five patients have been reported (as of april 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five patients have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:five patients have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five patients reported (as of march 2009)
n1=Lester (signe de) | n2=en:five patients reported (as of march 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five reported patients, all boys (as of july 2009)
n1=Lester (signe de) | n2=en:five reported patients, all boys (as of july 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five unrelated cases have been reported (as of march 2012)
n1=Lester (signe de) | n2=en:five unrelated cases have been reported (as of march 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five unrelated patients have been reported (as of december 2009)
n1=Lester (signe de) | n2=en:five unrelated patients have been reported (as of december 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five unrelated patients have been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:five unrelated patients have been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five unrelated patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:five unrelated patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:five unrelated patients have been reported (nov. 2009)
n1=Lester (signe de) | n2=en:five unrelated patients have been reported (nov. 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:flares triggered by viral infection, overexertion, stress
n1=Lester (signe de) | n2=en:flares triggered by viral infection, overexertion, stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:flow cytometry specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:flow cytometry specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:flunarizine treatment may be beneficial
n1=Lester (signe de) | n2=en:flunarizine treatment may be beneficial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fluoxetine therapy may be effective
n1=Lester (signe de) | n2=en:fluoxetine therapy may be effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:focal or segmental onset in cranial-cervical area or upper limbs
n1=Lester (signe de) | n2=en:focal or segmental onset in cranial-cervical area or upper limbs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:following fever in infancy, muscular weakness and poor growth
n1=Lester (signe de) | n2=en:following fever in infancy, muscular weakness and poor growth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:food intolerance
n1=Lester (signe de) | n2=en:food intolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:food related behavioral problems include excessive appetite and obsession with eating
n1=Lester (signe de) | n2=en:food related behavioral problems include excessive appetite and obsession with eating | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:foot deformities are present in infancy or childhood
n1=Lester (signe de) | n2=en:foot deformities are present in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:foot dragging may appear in childhood
n1=Lester (signe de) | n2=en:foot dragging may appear in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:for a similar phenotype with genital anomalies and disordered steroidogenesis see por deficiency (201750)
n1=Lester (signe de) | n2=en:for a similar phenotype with genital anomalies and disordered steroidogenesis see por deficiency (201750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:for autosomal dominant forms of axonal neuropathy, see cmt2a (118210)
n1=Lester (signe de) | n2=en:for autosomal dominant forms of axonal neuropathy, see cmt2a (118210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:for autosomal recessive forms, see cmt2b1 605588 and cmt2b2 605589
n1=Lester (signe de) | n2=en:for autosomal recessive forms, see cmt2b1 605588 and cmt2b2 605589 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:for similar autosomal dominant form, see 162350
n1=Lester (signe de) | n2=en:for similar autosomal dominant form, see 162350 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:for similar autosomal recessive form, see cln4 (204300)
n1=Lester (signe de) | n2=en:for similar autosomal recessive form, see cln4 (204300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:forty percent of patients die in the first year
n1=Lester (signe de) | n2=en:forty percent of patients die in the first year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:found predominantly in the amish population
n1=Lester (signe de) | n2=en:found predominantly in the amish population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:founder effect in irish traveler population
n1=Lester (signe de) | n2=en:founder effect in irish traveler population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:founder effect in turkish families
n1=Lester (signe de) | n2=en:founder effect in turkish families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four cases have been reported, all female
n1=Lester (signe de) | n2=en:four cases have been reported, all female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four clinical forms of krabbe disease
n1=Lester (signe de) | n2=en:four clinical forms of krabbe disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four clinical stages - stage i, early onset stagnation (onset 6 months-1.5 year)
n1=Lester (signe de) | n2=en:four clinical stages - stage i, early onset stagnation (onset 6 months-1.5 year) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four clinically indistinguishable biochemically distinct forms
n1=Lester (signe de) | n2=en:four clinically indistinguishable biochemically distinct forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four clinically indistinguishable biochemically distinct forms (see 252900, 252920, 252930)
n1=Lester (signe de) | n2=en:four clinically indistinguishable biochemically distinct forms (see 252900, 252920, 252930) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four clinically indistinguishable biochemically distinct forms (see, e.g., type iiia, 252900)
n1=Lester (signe de) | n2=en:four clinically indistinguishable biochemically distinct forms (see, e.g., type iiia, 252900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four families have been reported (last curated june 2011)
n1=Lester (signe de) | n2=en:four families have been reported (last curated june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four families have been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:four families have been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four individual patients and 1 saudi family have been reported (as of february 2012)
n1=Lester (signe de) | n2=en:four individual patients and 1 saudi family have been reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four major groups: early infantile, late infantile, juvenile, adult
n1=Lester (signe de) | n2=en:four major groups: early infantile, late infantile, juvenile, adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 2 unrelated families have been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:four patients from 2 unrelated families have been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 families have been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:four patients from 3 families have been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 unrelated families have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:four patients from 3 unrelated families have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients from 3 unrelated families have been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:four patients from 3 unrelated families have been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients have been reported
n1=Lester (signe de) | n2=en:four patients have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients have been reported (as of december 2009)
n1=Lester (signe de) | n2=en:four patients have been reported (as of december 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients have been reported (as of july 2011)
n1=Lester (signe de) | n2=en:four patients have been reported (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients have been reported (last curated june 2013)
n1=Lester (signe de) | n2=en:four patients have been reported (last curated june 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients have been reported from pakistan (as of march 2011)
n1=Lester (signe de) | n2=en:four patients have been reported from pakistan (as of march 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients of canadian cree origin and 1 patient of turkish origin have been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:four patients of canadian cree origin and 1 patient of turkish origin have been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four patients reported (last curated april 2013)
n1=Lester (signe de) | n2=en:four patients reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four separate types - (1) severe perinatal ('lethal') form, (2) severe infantile form, (3) childhood form, and (4) adult form
n1=Lester (signe de) | n2=en:four separate types - (1) severe perinatal ('lethal') form, (2) severe infantile form, (3) childhood form, and (4) adult form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four sibs from the old order mennonite community has been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:four sibs from the old order mennonite community has been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four types of cgd with basically identical clinical phenotypes
n1=Lester (signe de) | n2=en:four types of cgd with basically identical clinical phenotypes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four types of opll - segmental (39%), continuous (27%), mixed (29%), other (5%)
n1=Lester (signe de) | n2=en:four types of opll - segmental (39%), continuous (27%), mixed (29%), other (5%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated boys have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:four unrelated boys have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated families have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:four unrelated families have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated families have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:four unrelated families have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated families have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:four unrelated families have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated families of caucasian european descent have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:four unrelated families of caucasian european descent have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated infants with the disorder and decreased expression of csf2rb in cells have been reported
n1=Lester (signe de) | n2=en:four unrelated infants with the disorder and decreased expression of csf2rb in cells have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:four unrelated patients have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients reported (last curated august 2015)
n1=Lester (signe de) | n2=en:four unrelated patients reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:four unrelated patients with zswim6 mutations have been described (last curated september 2014)
n1=Lester (signe de) | n2=en:four unrelated patients with zswim6 mutations have been described (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fracture frequency constant through childhood, decreases after puberty
n1=Lester (signe de) | n2=en:fracture frequency constant through childhood, decreases after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fracture frequency decreased post puberty
n1=Lester (signe de) | n2=en:fracture frequency decreased post puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fracture frequency increases after menopause and in men ages 60-80
n1=Lester (signe de) | n2=en:fracture frequency increases after menopause and in men ages 60-80 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fractures and dental caries and premature secondary tooth loss occur in adulthood
n1=Lester (signe de) | n2=en:fractures and dental caries and premature secondary tooth loss occur in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fractures can occur in utero, during labor and delivery, or in newborn period
n1=Lester (signe de) | n2=en:fractures can occur in utero, during labor and delivery, or in newborn period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fractures decrease after puberty but increase after menopause
n1=Lester (signe de) | n2=en:fractures decrease after puberty but increase after menopause | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fractures occur in first few months, then decrease in frequency and then occur with ambulation
n1=Lester (signe de) | n2=en:fractures occur in first few months, then decrease in frequency and then occur with ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:fractures often heal without deformity
n1=Lester (signe de) | n2=en:fractures often heal without deformity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency 1/100,000 - 1/130,000 live births
n1=Lester (signe de) | n2=en:frequency 1/100,000 - 1/130,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency and severity of seizures tends to decrease with age
n1=Lester (signe de) | n2=en:frequency and severity of seizures tends to decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency and severity of symptoms do not worsen with age
n1=Lester (signe de) | n2=en:frequency and severity of symptoms do not worsen with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency between 1 in 58,000 to 1 in 1,000,000
n1=Lester (signe de) | n2=en:frequency between 1 in 58,000 to 1 in 1,000,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency increases with advancing age
n1=Lester (signe de) | n2=en:frequency increases with advancing age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency of attack, monthly - bimonthly
n1=Lester (signe de) | n2=en:frequency of attack, monthly - bimonthly | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency of attacks may decrease with age or during pregnancy
n1=Lester (signe de) | n2=en:frequency of attacks may decrease with age or during pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency of episodes ranges from several per week to several per year
n1=Lester (signe de) | n2=en:frequency of episodes ranges from several per week to several per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequency of infections decreases after 3 years of age
n1=Lester (signe de) | n2=en:frequency of infections decreases after 3 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequent falls
n1=Lester (signe de) | n2=en:frequent falls | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequent neonatal sudden death
n1=Lester (signe de) | n2=en:frequent neonatal sudden death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequent new mutations (~60%) and/or gonadal mosaicism in tsc2
n1=Lester (signe de) | n2=en:frequent new mutations (~60%) and/or gonadal mosaicism in tsc2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequent new mutations (~86%) and/or gonadal mosaicism in tsc1
n1=Lester (signe de) | n2=en:frequent new mutations (~86%) and/or gonadal mosaicism in tsc1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequently death in infancy
n1=Lester (signe de) | n2=en:frequently death in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequently fatal within the first year of life
n1=Lester (signe de) | n2=en:frequently fatal within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frequently occurs in navajo children, especially in western reservations
n1=Lester (signe de) | n2=en:frequently occurs in navajo children, especially in western reservations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:frontometaphyseal dysplasia (fmd, 305620) is an allelic disorder
n1=Lester (signe de) | n2=en:frontometaphyseal dysplasia (fmd, 305620) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:full mutations with expanded trinucleotide repeats greater than 200 result in fragile x mental retardation syndrome (300624)
n1=Lester (signe de) | n2=en:full mutations with expanded trinucleotide repeats greater than 200 result in fragile x mental retardation syndrome (300624) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:full recovery after attacks
n1=Lester (signe de) | n2=en:full recovery after attacks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:funduscopy before 2 years of age is unremarkable
n1=Lester (signe de) | n2=en:funduscopy before 2 years of age is unremarkable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gait abnormality
n1=Lester (signe de) | n2=en:gait abnormality | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gait difficulties and beginning of cognitive decline in first decade
n1=Lester (signe de) | n2=en:gait difficulties and beginning of cognitive decline in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gapo is acronym for growth retardation, alopecia, pseudoanodontia, optic atrophy
n1=Lester (signe de) | n2=en:gapo is acronym for growth retardation, alopecia, pseudoanodontia, optic atrophy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gastric suction pump, home model, portable or stationary, electric
n1=Lester (signe de) | n2=en:gastric suction pump, home model, portable or stationary, electric | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gastrointestinal anomalies are not always present
n1=Lester (signe de) | n2=en:gastrointestinal anomalies are not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gei (gene-environment interaction) - association of cardiac events with drug administration
n1=Lester (signe de) | n2=en:gei (gene-environment interaction) - association of cardiac events with drug administration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gender-specific phenotype (homozygous men are fertile)
n1=Lester (signe de) | n2=en:gender-specific phenotype (homozygous men are fertile) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gene frequency in northwest puerto rico 1 in 18
n1=Lester (signe de) | n2=en:gene frequency in northwest puerto rico 1 in 18 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generalized dystonia in some cases
n1=Lester (signe de) | n2=en:generalized dystonia in some cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generalized fatigue
n1=Lester (signe de) | n2=en:generalized fatigue | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generally benign disorder
n1=Lester (signe de) | n2=en:generally benign disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generally considered to be a benign disorder
n1=Lester (signe de) | n2=en:generally considered to be a benign disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generally mild phenotype
n1=Lester (signe de) | n2=en:generally mild phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:generally static disease course
n1=Lester (signe de) | n2=en:generally static disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genes involved in duplication include atg2b (616226), gskip (616605), tcl1a (186960), bdkrb1 (600337), bdkrb2 (113503), and ak7 (615364)
n1=Lester (signe de) | n2=en:genes involved in duplication include atg2b (616226), gskip (616605), tcl1a (186960), bdkrb1 (600337), bdkrb2 (113503), and ak7 (615364) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic anticipation
n1=Lester (signe de) | n2=en:genetic anticipation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic anticipation associated with progressive telomere shortening
n1=Lester (signe de) | n2=en:genetic anticipation associated with progressive telomere shortening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic anticipation has been observed
n1=Lester (signe de) | n2=en:genetic anticipation has been observed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic anticipation occurs
n1=Lester (signe de) | n2=en:genetic anticipation occurs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity
n1=Lester (signe de) | n2=en:genetic heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (autosomal recessive form 224900 and autosomal dominant form 129490)
n1=Lester (signe de) | n2=en:genetic heterogeneity (autosomal recessive form 224900 and autosomal dominant form 129490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (bor2, 610896)
n1=Lester (signe de) | n2=en:genetic heterogeneity (bor2, 610896) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (ccm2 603284, ccm3 603285)
n1=Lester (signe de) | n2=en:genetic heterogeneity (ccm2 603284, ccm3 603285) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (may be caused by mutation in nuclear-encoded or mitochondrial-encoded genes)
n1=Lester (signe de) | n2=en:genetic heterogeneity (may be caused by mutation in nuclear-encoded or mitochondrial-encoded genes) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 116800 for summary)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 116800 for summary) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 125800)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 125800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 145410)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 145410) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 157640)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 157640) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 159900)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 159900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 161400)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 161400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 161800)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 161800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 166600)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 166600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 191100)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 191100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 192600)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 192600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 209850)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 209850) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 213300)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 213300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 214300)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 214300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 259700)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 259700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 266900 for summary)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 266900 for summary) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 304800)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 304800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 601680)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 601680) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 604559)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 604559) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 605407)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 605407) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 606215)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 606215) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 607634)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 607634) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 608638)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 608638) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 609192)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 609192) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 610168)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 610168) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see 613254)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see 613254) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see antenatal bartter syndrome type 1, 601678)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see antenatal bartter syndrome type 1, 601678) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see antenatal bartter syndrome type 2, 241200)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see antenatal bartter syndrome type 2, 241200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see bafme2, 607876)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see bafme2, 607876) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see bfic2, 605751)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see bfic2, 605751) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see bscl1, 608594)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see bscl1, 608594) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see bscl2, 269700)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see bscl2, 269700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cftd1, 255310)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cftd1, 255310) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cms1a1, 605809)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cms1a1, 605809) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt1a 118220, cmt1c 601098, cmt1d 607678, cmt1f 607734)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt1a 118220, cmt1c 601098, cmt1d 607678, cmt1f 607734) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt1b 118200)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt1b 118200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt2a 118210)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt2a 118210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt2a2 609260, cmt2b 600882, cmt2c 606071, cmt2d 601472, cmt2e 607684, cmt2f 606595, cmt2i 607677)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt2a2 609260, cmt2b 600882, cmt2c 606071, cmt2d 601472, cmt2e 607684, cmt2f 606595, cmt2i 607677) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt2b2, 605589)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt2b2, 605589) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt4a 214400)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt4a 214400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt4b1, 601382)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt4b1, 601382) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmt4b2, 604563)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmt4b2, 604563) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cmtdia 606483)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cmtdia 606483) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see cnc2, 605244)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see cnc2, 605244) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see coxpd1, 609060)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see coxpd1, 609060) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see ebn2 121201, ebn3 608217)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see ebn2 121201, ebn3 608217) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see eca1, 600131 and eca3, 607682)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see eca1, 600131 and eca3, 607682) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see edm1 132400, edm2 600204, edm3 600969, edm4 226900)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see edm1 132400, edm2 600204, edm3 600969, edm4 226900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see edm1 132400, edm2 600204, edm4 226900, edm5 607078)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see edm1 132400, edm2 600204, edm4 226900, edm5 607078) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see edm1 132400, edm3 600969, edm4 226900, edm5 607078)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see edm1 132400, edm3 600969, edm4 226900, edm5 607078) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see edm2 600204, edm3 600969, edm4 226900, edm5 607078)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see edm2 600204, edm3 600969, edm4 226900, edm5 607078) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see enfl1, 600513)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see enfl1, 600513) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see etl2, 608096)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see etl2, 608096) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see feb1 121210)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see feb1 121210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see fhm1 141500 and mgr6 607516)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see fhm1 141500 and mgr6 607516) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see gefs+, 604233)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see gefs+, 604233) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see hcfp1, 601471)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see hcfp1, 601471) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see hcfp2, 604185)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see hcfp2, 604185) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see hhf1 256450)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see hhf1 256450) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see hht1, 187300)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see hht1, 187300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see jbts1 213300, jbts2 608091, jbts3 608629)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see jbts1 213300, jbts2 608091, jbts3 608629) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see lgmd1a 159000 for overview)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see lgmd1a 159000 for overview) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see lqt1 192500)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see lqt1 192500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see mada, 248370)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see mada, 248370) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see madb, 608612)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see madb, 608612) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see mcc1 deficiency 210200)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see mcc1 deficiency 210200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see mcc2 deficiency 210210)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see mcc2 deficiency 210210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see npc1, 257220)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see npc1, 257220) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see npc2, 607625)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see npc2, 607625) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see ofc1, 119530)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see ofc1, 119530) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see peoa2 609283, peoa3 609286, and peoa4 610131)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see peoa2 609283, peoa3 609286, and peoa4 610131) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see pfic1, 211600)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see pfic1, 211600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see pfm1, 168500)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see pfm1, 168500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see ppr2, 609572 and ppr3, 609573)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see ppr2, 609572 and ppr3, 609573) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see psnp1 601104)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see psnp1 601104) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see psnp2 609454)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see psnp2 609454) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see rieg2, 601499)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see rieg2, 601499) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see rls2, 608831)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see rls2, 608831) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see rmd, 606072)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see rmd, 606072) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see rmd1, 600332)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see rmd1, 600332) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see sca1, 164000)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see sca1, 164000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see spondyloarthropathy, susceptibility to, 2 183840)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see spondyloarthropathy, susceptibility to, 2 183840) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., 600795, 105550)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., 600795, 105550) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., 608631, 300494, 300497)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., 608631, 300494, 300497) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., 609378, 608636, 608049, 300425, 300495, 300496)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., 609378, 608636, 608049, 300425, 300495, 300496) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., atfb1, 608583)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., atfb1, 608583) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., atfb3, 607554)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., atfb3, 607554) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., cmtdib 606482, cmtdid 607791)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., cmtdib 606482, cmtdid 607791) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., cockayne syndrome type b, 133540)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., cockayne syndrome type b, 133540) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., nys1 310700, nys2 164100, nys4 193003)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., nys1 310700, nys2 164100, nys4 193003) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (see, e.g., sli1 606711 and sli3 607134)
n1=Lester (signe de) | n2=en:genetic heterogeneity (see, e.g., sli1 606711 and sli3 607134) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (sli2 606712, sli3 607134)
n1=Lester (signe de) | n2=en:genetic heterogeneity (sli2 606712, sli3 607134) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity (x-linked form 305100)
n1=Lester (signe de) | n2=en:genetic heterogeneity (x-linked form 305100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity for phenotypically similar disorders with specific language impairment (sli1 606711, sli2 606712, sli3 607134)
n1=Lester (signe de) | n2=en:genetic heterogeneity for phenotypically similar disorders with specific language impairment (sli1 606711, sli2 606712, sli3 607134) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity of axonal cmt (see cmt2a 118210)
n1=Lester (signe de) | n2=en:genetic heterogeneity of axonal cmt (see cmt2a 118210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity of waardenburg syndrome type 2
n1=Lester (signe de) | n2=en:genetic heterogeneity of waardenburg syndrome type 2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, probably determined by major and minor genes, environmental factors, and developmental threshold
n1=Lester (signe de) | n2=en:genetic heterogeneity, probably determined by major and minor genes, environmental factors, and developmental threshold | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see (203300)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see (203300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see ags2 (610181), ags3 (610329), and ags4 (610333)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see ags2 (610181), ags3 (610329), and ags4 (610333) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see also pfic2 (601847), pfic3 (602347)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see also pfic2 (601847), pfic3 (602347) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see apmr1 (203650)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see apmr1 (203650) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see aprm2 (610422)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see aprm2 (610422) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see autosomal recessive inheritance of the disorder (271930)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see autosomal recessive inheritance of the disorder (271930) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see bos2 (120502) and bos3 (608389)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see bos2 (120502) and bos3 (608389) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see cild1 (244400)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see cild1 (244400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see edm1 (132400), edm2 (600204), edm3 (600969), and edm5 (607078)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see edm1 (132400), edm2 (600204), edm3 (600969), and edm5 (607078) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see ekd1 (128200)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see ekd1 (128200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see evr1 (133780)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see evr1 (133780) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see evr2 (305390), evr3 (605750), and evr4 (601813)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see evr2 (305390), evr3 (605750), and evr4 (601813) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see fhm1 141500
n1=Lester (signe de) | n2=en:genetic heterogeneity, see fhm1 141500 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see fhm1, (141500) and mgr1, (157300)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see fhm1, (141500) and mgr1, (157300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see lgmd2a (253600)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see lgmd2a (253600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see mgr1 (157300)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see mgr1 (157300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see mitochondrial inheritance of the disorder (500003)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see mitochondrial inheritance of the disorder (500003) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see ppnad1 (610489)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see ppnad1 (610489) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see ppnad2 (610475)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see ppnad2 (610475) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see sca1 (164400)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see sca1 (164400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see spg3a (182600)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see spg3a (182600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see spg5a (270800)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see spg5a (270800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see spg5a (270800) for overview of recessive spgs
n1=Lester (signe de) | n2=en:genetic heterogeneity, see spg5a (270800) for overview of recessive spgs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, see, e.g., mgr2 (300125), mgr3 (607498), mgr4 (607501), mgr5 (607508), mgr6 (607516)
n1=Lester (signe de) | n2=en:genetic heterogeneity, see, e.g., mgr2 (300125), mgr3 (607498), mgr4 (607501), mgr5 (607508), mgr6 (607516) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genetic heterogeneity, some patients not linked to fgfr3
n1=Lester (signe de) | n2=en:genetic heterogeneity, some patients not linked to fgfr3 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:geneticist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:geneticist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:genomic duplications occur de novo
n1=Lester (signe de) | n2=en:genomic duplications occur de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:germline and somatic mutations contribute to this disorder
n1=Lester (signe de) | n2=en:germline and somatic mutations contribute to this disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:germline or somatic mutations may cause the disorder
n1=Lester (signe de) | n2=en:germline or somatic mutations may cause the disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gestational age:time:pt:^fetus:qn:amniocentesis
n1=Lester (signe de) | n2=en:gestational age:time:pt:^fetus:qn:amniocentesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gliomas may occur in association with other hereditary tumor syndromes (see 276300, 155755, 162200, 101000, 191100)
n1=Lester (signe de) | n2=en:gliomas may occur in association with other hereditary tumor syndromes (see 276300, 155755, 162200, 101000, 191100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:global developmental delay
n1=Lester (signe de) | n2=en:global developmental delay | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:glucocorticoid deficiency occurs in mid-childhood
n1=Lester (signe de) | n2=en:glucocorticoid deficiency occurs in mid-childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gms is goniodysgenesis, mental deficiency, and short stature
n1=Lester (signe de) | n2=en:gms is goniodysgenesis, mental deficiency, and short stature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gonadal and somatic mosaicism reported in parent
n1=Lester (signe de) | n2=en:gonadal and somatic mosaicism reported in parent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gonadal mosaicism may occur
n1=Lester (signe de) | n2=en:gonadal mosaicism may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gonadal mosaicism reported
n1=Lester (signe de) | n2=en:gonadal mosaicism reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to clonazepam
n1=Lester (signe de) | n2=en:good response to clonazepam | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to fibrinolytic inhibitors
n1=Lester (signe de) | n2=en:good response to fibrinolytic inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to gaba-enhancing medications
n1=Lester (signe de) | n2=en:good response to gaba-enhancing medications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to immunotherapy (intravenous igg or plasmapheresis)
n1=Lester (signe de) | n2=en:good response to immunotherapy (intravenous igg or plasmapheresis) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to l-dopa initially
n1=Lester (signe de) | n2=en:good response to l-dopa initially | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to levodopa treatment
n1=Lester (signe de) | n2=en:good response to levodopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to medication
n1=Lester (signe de) | n2=en:good response to medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to phosphate treatment
n1=Lester (signe de) | n2=en:good response to phosphate treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to steroid treatment
n1=Lester (signe de) | n2=en:good response to steroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to vitamin b12 therapy 'variant 1' has isolated homocystinuria and decreased mecbl
n1=Lester (signe de) | n2=en:good response to vitamin b12 therapy 'variant 1' has isolated homocystinuria and decreased mecbl | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good response to vitamin d treatment
n1=Lester (signe de) | n2=en:good response to vitamin d treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:good seizure control with medication
n1=Lester (signe de) | n2=en:good seizure control with medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gradual progression
n1=Lester (signe de) | n2=en:gradual progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gradual progression of hearing loss
n1=Lester (signe de) | n2=en:gradual progression of hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gradual spontaneous improvement in the first year of life
n1=Lester (signe de) | n2=en:gradual spontaneous improvement in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:great variation in extent of hypertrophy in mutation-positive individuals
n1=Lester (signe de) | n2=en:great variation in extent of hypertrophy in mutation-positive individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:greater expression in females
n1=Lester (signe de) | n2=en:greater expression in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:green color resolves if cholestasis is treated
n1=Lester (signe de) | n2=en:green color resolves if cholestasis is treated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:green jaundice occurs only in the context of liver failure or obstructive cholestasis
n1=Lester (signe de) | n2=en:green jaundice occurs only in the context of liver failure or obstructive cholestasis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:griscelli syndrome type 3 (609227) for a similar disorder without neurologic or immunologic abnormalities
n1=Lester (signe de) | n2=en:griscelli syndrome type 3 (609227) for a similar disorder without neurologic or immunologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:group a patients die in the first years of life
n1=Lester (signe de) | n2=en:group a patients die in the first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:group a, found in north american indians, has lactic acidosis and psychomotor retardation
n1=Lester (signe de) | n2=en:group a, found in north american indians, has lactic acidosis and psychomotor retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:group b patients die by 3 months of age
n1=Lester (signe de) | n2=en:group b patients die by 3 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:group b, found in france and united kingdom, severe phenotype
n1=Lester (signe de) | n2=en:group b, found in france and united kingdom, severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:group c is relatively benign
n1=Lester (signe de) | n2=en:group c is relatively benign | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:growth retardation onset in utero
n1=Lester (signe de) | n2=en:growth retardation onset in utero | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:gypsy groups demonstrate a founder effect (1267delg, 100725.0012)
n1=Lester (signe de) | n2=en:gypsy groups demonstrate a founder effect (1267delg, 100725.0012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair is soft, short, and sparse initially, but develops into woolly hair in early childhood
n1=Lester (signe de) | n2=en:hair is soft, short, and sparse initially, but develops into woolly hair in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair loss begins in first years of life
n1=Lester (signe de) | n2=en:hair loss begins in first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair may normalize at puberty
n1=Lester (signe de) | n2=en:hair may normalize at puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair phenotype present at birth and involves entire scalp region
n1=Lester (signe de) | n2=en:hair phenotype present at birth and involves entire scalp region | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair regrowth may occur later in life
n1=Lester (signe de) | n2=en:hair regrowth may occur later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair tends to straighten by 2nd-3rd decade
n1=Lester (signe de) | n2=en:hair tends to straighten by 2nd-3rd decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hair, nails, and teeth are normal
n1=Lester (signe de) | n2=en:hair, nails, and teeth are normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hairy elbows become apparent in infancy and regress during adolescence
n1=Lester (signe de) | n2=en:hairy elbows become apparent in infancy and regress during adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:half (50%) of affected patients have a recurrent episode with worse outcome
n1=Lester (signe de) | n2=en:half (50%) of affected patients have a recurrent episode with worse outcome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:half of cases show retarded head circumference equal to height retardation
n1=Lester (signe de) | n2=en:half of cases show retarded head circumference equal to height retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hand and foot lesions can severely limit dexterity (due to flexion contractures) and mobility (due to painful fissures)
n1=Lester (signe de) | n2=en:hand and foot lesions can severely limit dexterity (due to flexion contractures) and mobility (due to painful fissures) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hand involvement improves with age
n1=Lester (signe de) | n2=en:hand involvement improves with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hands clenched at birth but loosen in infancy
n1=Lester (signe de) | n2=en:hands clenched at birth but loosen in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:haploinsufficiency of grn (138945)
n1=Lester (signe de) | n2=en:haploinsufficiency of grn (138945) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:haploinsufficiency of rps14 (130620)
n1=Lester (signe de) | n2=en:haploinsufficiency of rps14 (130620) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:has also been called 'distal hereditary motor neuronopathy' (dhmn) and 'distal spinal muscular atrophy' (dsma)
n1=Lester (signe de) | n2=en:has also been called 'distal hereditary motor neuronopathy' (dhmn) and 'distal spinal muscular atrophy' (dsma) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:has been described in patients of caucasus jewish origin
n1=Lester (signe de) | n2=en:has been described in patients of caucasus jewish origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:headache duration 4-72 hours
n1=Lester (signe de) | n2=en:headache duration 4-72 hours | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:headaches last hours to days
n1=Lester (signe de) | n2=en:headaches last hours to days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:health data repository:id:pt:repository:nom
n1=Lester (signe de) | n2=en:health data repository:id:pt:repository:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:health insurance plan benefits comment:finding:point in time:^patient:narrative
n1=Lester (signe de) | n2=en:health insurance plan benefits comment:finding:point in time:^patient:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing impairment may improve with age
n1=Lester (signe de) | n2=en:hearing impairment may improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss affects all frequencies
n1=Lester (signe de) | n2=en:hearing loss affects all frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss and hoarseness occur later
n1=Lester (signe de) | n2=en:hearing loss and hoarseness occur later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss and ocular findings are variable
n1=Lester (signe de) | n2=en:hearing loss and ocular findings are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is congenital and nonprogressive
n1=Lester (signe de) | n2=en:hearing loss is congenital and nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is nonprogressive
n1=Lester (signe de) | n2=en:hearing loss is nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is pre- or perilingual in onset
n1=Lester (signe de) | n2=en:hearing loss is pre- or perilingual in onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is progressive and initially affects high-frequencies
n1=Lester (signe de) | n2=en:hearing loss is progressive and initially affects high-frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is usually severe by age 20 years
n1=Lester (signe de) | n2=en:hearing loss is usually severe by age 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss is variable
n1=Lester (signe de) | n2=en:hearing loss is variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss ma be fluctuating or progressive
n1=Lester (signe de) | n2=en:hearing loss ma be fluctuating or progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss may be congenital or rapidly progressive leading to severe hearing loss by age 3 years
n1=Lester (signe de) | n2=en:hearing loss may be congenital or rapidly progressive leading to severe hearing loss by age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss may be stable or progressive
n1=Lester (signe de) | n2=en:hearing loss may be stable or progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss may vary in severity and range between ears
n1=Lester (signe de) | n2=en:hearing loss may vary in severity and range between ears | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss occurs in late childhood
n1=Lester (signe de) | n2=en:hearing loss occurs in late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss occurs later if at all
n1=Lester (signe de) | n2=en:hearing loss occurs later if at all | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss progresses to profound deafness
n1=Lester (signe de) | n2=en:hearing loss progresses to profound deafness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss typically begins between 3 and 4 years of age
n1=Lester (signe de) | n2=en:hearing loss typically begins between 3 and 4 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss was diagnosed between 3 months to 1 year of age
n1=Lester (signe de) | n2=en:hearing loss was diagnosed between 3 months to 1 year of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hearing loss was progressive in some patients
n1=Lester (signe de) | n2=en:hearing loss was progressive in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hematuria may become apparent after respiratory infections (synpharyngitic)
n1=Lester (signe de) | n2=en:hematuria may become apparent after respiratory infections (synpharyngitic) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hemolysis may be exercise-induced
n1=Lester (signe de) | n2=en:hemolysis may be exercise-induced | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hepatic failure develops in first months of life
n1=Lester (signe de) | n2=en:hepatic failure develops in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hepatoerythropoietic porphyria (hep, 176100.0005) is a severe infantile form due to homozygous pct
n1=Lester (signe de) | n2=en:hepatoerythropoietic porphyria (hep, 176100.0005) is a severe infantile form due to homozygous pct | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hepatomegaly improves with age and disappears around puberty
n1=Lester (signe de) | n2=en:hepatomegaly improves with age and disappears around puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hernia occurs in 22% of adults
n1=Lester (signe de) | n2=en:hernia occurs in 22% of adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterogeneous disorder
n1=Lester (signe de) | n2=en:heterogeneous disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygote individuals are average stature and can have mild skeletal abnormalities including brachydactyly, delayed bone age, metatarsus adductus, and finger flexion contractures
n1=Lester (signe de) | n2=en:heterozygote individuals are average stature and can have mild skeletal abnormalities including brachydactyly, delayed bone age, metatarsus adductus, and finger flexion contractures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygote may have elevated serum phosphate and elevated serum 1,25-dihydroxycholecalciferol
n1=Lester (signe de) | n2=en:heterozygote may have elevated serum phosphate and elevated serum 1,25-dihydroxycholecalciferol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes - 39% severe phenotype, 28% clinically symptomatic, 28% x-ray changes only, 4% non-penetrant
n1=Lester (signe de) | n2=en:heterozygotes - 39% severe phenotype, 28% clinically symptomatic, 28% x-ray changes only, 4% non-penetrant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes are not affected
n1=Lester (signe de) | n2=en:heterozygotes are not affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes are usually asymptomatic
n1=Lester (signe de) | n2=en:heterozygotes are usually asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes at risk of developing acute, symptomatic methemoglobinemia after exposure to exogenous, methemoglobin-inducing agents
n1=Lester (signe de) | n2=en:heterozygotes at risk of developing acute, symptomatic methemoglobinemia after exposure to exogenous, methemoglobin-inducing agents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes demonstrate a milder phenotype, consistent with a semidominant inheritance pattern
n1=Lester (signe de) | n2=en:heterozygotes demonstrate a milder phenotype, consistent with a semidominant inheritance pattern | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes exhibit blue sclerae and soft velvety skin
n1=Lester (signe de) | n2=en:heterozygotes exhibit blue sclerae and soft velvety skin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes exhibit subclinical metabolic and immunologic abnormalities
n1=Lester (signe de) | n2=en:heterozygotes exhibit subclinical metabolic and immunologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes have half-normal levels of apob-containing lipoproteins
n1=Lester (signe de) | n2=en:heterozygotes have half-normal levels of apob-containing lipoproteins | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes have mild, transient hypothyroidism in infancy
n1=Lester (signe de) | n2=en:heterozygotes have mild, transient hypothyroidism in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes have milder metabolic defect with increased serum 1,25(oh)2d3 and hypercalciuria, but no bone disease or rickets
n1=Lester (signe de) | n2=en:heterozygotes have milder metabolic defect with increased serum 1,25(oh)2d3 and hypercalciuria, but no bone disease or rickets | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes have plasma levels of triglycerides and/or hdl cholesterol that are intermediate between homozygotes and unaffected individuals
n1=Lester (signe de) | n2=en:heterozygotes have plasma levels of triglycerides and/or hdl cholesterol that are intermediate between homozygotes and unaffected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes may also exhibit small joint hypermobility or conductive hearing loss
n1=Lester (signe de) | n2=en:heterozygotes may also exhibit small joint hypermobility or conductive hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes may also show increased susceptibility to toxic effects of thiopurine treatment
n1=Lester (signe de) | n2=en:heterozygotes may also show increased susceptibility to toxic effects of thiopurine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes may be at increased risk for infection or atypical hemolytic uremic syndrome (235400)
n1=Lester (signe de) | n2=en:heterozygotes may be at increased risk for infection or atypical hemolytic uremic syndrome (235400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygotes may exhibit syndromic manifestations
n1=Lester (signe de) | n2=en:heterozygotes may exhibit syndromic manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous carriers exhibit palmoplantar hyperkeratosis (see 148700)
n1=Lester (signe de) | n2=en:heterozygous carriers exhibit palmoplantar hyperkeratosis (see 148700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous carriers have an increased risk of metabolic dysfunction
n1=Lester (signe de) | n2=en:heterozygous carriers have an increased risk of metabolic dysfunction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous carriers have blue sclerae, small joint hypermobility, and mild thinning of cornea
n1=Lester (signe de) | n2=en:heterozygous carriers have blue sclerae, small joint hypermobility, and mild thinning of cornea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous carriers have decreased blood pressure compared to the general population
n1=Lester (signe de) | n2=en:heterozygous carriers have decreased blood pressure compared to the general population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous deletion of the terminal band 22q13.3 including shank3 (606230)
n1=Lester (signe de) | n2=en:heterozygous deletion of the terminal band 22q13.3 including shank3 (606230) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous female carriers may manifest symptoms
n1=Lester (signe de) | n2=en:heterozygous female carriers may manifest symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females have milder thyroid phenotype and no neurologic abnormalities
n1=Lester (signe de) | n2=en:heterozygous females have milder thyroid phenotype and no neurologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females may exhibit variable degrees of enzyme deficiency
n1=Lester (signe de) | n2=en:heterozygous females may exhibit variable degrees of enzyme deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females may have gout and/or sensorineural deafness
n1=Lester (signe de) | n2=en:heterozygous females may have gout and/or sensorineural deafness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females may have situs inversus or other midline defects
n1=Lester (signe de) | n2=en:heterozygous females may have situs inversus or other midline defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females more mildly affected than hemizygous males
n1=Lester (signe de) | n2=en:heterozygous females more mildly affected than hemizygous males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous females show variable expressivity (mild to severe manifestations) including hypodontia, conical teeth, reduction in scalp/body hair, and difficulty nursing
n1=Lester (signe de) | n2=en:heterozygous females show variable expressivity (mild to severe manifestations) including hypodontia, conical teeth, reduction in scalp/body hair, and difficulty nursing | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutation carriers may have late-onset cardiac arrhythmias
n1=Lester (signe de) | n2=en:heterozygous mutation carriers may have late-onset cardiac arrhythmias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutation carriers may have late-onset of mild symptoms
n1=Lester (signe de) | n2=en:heterozygous mutation carriers may have late-onset of mild symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutation carriers may show mild symptoms
n1=Lester (signe de) | n2=en:heterozygous mutation carriers may show mild symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutation carriers show toxicity to 5-fluorouracil (5fu)
n1=Lester (signe de) | n2=en:heterozygous mutation carriers show toxicity to 5-fluorouracil (5fu) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutation present in 5-7% of the japanese population
n1=Lester (signe de) | n2=en:heterozygous mutation present in 5-7% of the japanese population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous mutations reported, see 606609.0006 and 606609.0007
n1=Lester (signe de) | n2=en:heterozygous mutations reported, see 606609.0006 and 606609.0007 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous parents are phenotypically normal but their cells show premature chromatid separation trait (pcs, 176430)
n1=Lester (signe de) | n2=en:heterozygous parents are phenotypically normal but their cells show premature chromatid separation trait (pcs, 176430) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous titin mutation causes the less-severe tardive tibial muscular dystrophy (600334)
n1=Lester (signe de) | n2=en:heterozygous titin mutation causes the less-severe tardive tibial muscular dystrophy (600334) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:heterozygous, homozygous, and compound heterozygous coq2 mutations have been identified
n1=Lester (signe de) | n2=en:heterozygous, homozygous, and compound heterozygous coq2 mutations have been identified | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hhs is a more severe variant, often resulting in death in childhood
n1=Lester (signe de) | n2=en:hhs is a more severe variant, often resulting in death in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hid (hystrix-like ichthyosis with deafness, 602540) is identical to kid at the molecular level
n1=Lester (signe de) | n2=en:hid (hystrix-like ichthyosis with deafness, 602540) is identical to kid at the molecular level | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high disease prevalence among french-canadians
n1=Lester (signe de) | n2=en:high disease prevalence among french-canadians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high early mortality rate if untreated
n1=Lester (signe de) | n2=en:high early mortality rate if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequencies affected before low frequencies
n1=Lester (signe de) | n2=en:high frequencies affected before low frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency among french-canadians
n1=Lester (signe de) | n2=en:high frequency among french-canadians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency among individuals of ashkenazi jewish descent (1 in 3,300)
n1=Lester (signe de) | n2=en:high frequency among individuals of ashkenazi jewish descent (1 in 3,300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency hearing loss progresses to include all frequencies
n1=Lester (signe de) | n2=en:high frequency hearing loss progresses to include all frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in equatorial africa
n1=Lester (signe de) | n2=en:high frequency in equatorial africa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in finnish population
n1=Lester (signe de) | n2=en:high frequency in finnish population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in hutterite population
n1=Lester (signe de) | n2=en:high frequency in hutterite population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in japan (2 in 20,000, 0.1%)
n1=Lester (signe de) | n2=en:high frequency in japan (2 in 20,000, 0.1%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in northeastern brazil
n1=Lester (signe de) | n2=en:high frequency in northeastern brazil | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in southern india (7% of all epilepsies)
n1=Lester (signe de) | n2=en:high frequency in southern india (7% of all epilepsies) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in the french-canadian population
n1=Lester (signe de) | n2=en:high frequency in the french-canadian population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency in tibetan individuals
n1=Lester (signe de) | n2=en:high frequency in tibetan individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency of absence seizures (several per day)
n1=Lester (signe de) | n2=en:high frequency of absence seizures (several per day) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency of de novo mutations
n1=Lester (signe de) | n2=en:high frequency of de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency of levodopa-induced dyskinesias
n1=Lester (signe de) | n2=en:high frequency of levodopa-induced dyskinesias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high frequency seizures
n1=Lester (signe de) | n2=en:high frequency seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence among ashkenazi jews
n1=Lester (signe de) | n2=en:high incidence among ashkenazi jews | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence among old order amish
n1=Lester (signe de) | n2=en:high incidence among old order amish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence in iraqis and sephardic jewish individuals
n1=Lester (signe de) | n2=en:high incidence in iraqis and sephardic jewish individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence in saguenay-lac st. jean region of the province of quebec, canada and northern europe
n1=Lester (signe de) | n2=en:high incidence in saguenay-lac st. jean region of the province of quebec, canada and northern europe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence in sweden and finland
n1=Lester (signe de) | n2=en:high incidence in sweden and finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence of diabetes mellitus noted in opll patients
n1=Lester (signe de) | n2=en:high incidence of diabetes mellitus noted in opll patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high incidence of e. coli sepsis in untreated neonates
n1=Lester (signe de) | n2=en:high incidence of e. coli sepsis in untreated neonates | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high infant mortality due to malnutrition as well as complications of parenteral nutrition
n1=Lester (signe de) | n2=en:high infant mortality due to malnutrition as well as complications of parenteral nutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high intrafamilial and interfamilial variability
n1=Lester (signe de) | n2=en:high intrafamilial and interfamilial variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high mortality in infancy and early childhood (in some patients)
n1=Lester (signe de) | n2=en:high mortality in infancy and early childhood (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high occurrence of de novo mutations
n1=Lester (signe de) | n2=en:high occurrence of de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high pain threshold
n1=Lester (signe de) | n2=en:high pain threshold | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence among individuals of middle eastern or african descent
n1=Lester (signe de) | n2=en:high prevalence among individuals of middle eastern or african descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence among individuals of portuguese descent
n1=Lester (signe de) | n2=en:high prevalence among individuals of portuguese descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence in charlevoix-saguenay region of northeastern quebec
n1=Lester (signe de) | n2=en:high prevalence in charlevoix-saguenay region of northeastern quebec | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence in holguin province of cuba
n1=Lester (signe de) | n2=en:high prevalence in holguin province of cuba | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence in japan
n1=Lester (signe de) | n2=en:high prevalence in japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high prevalence in the east asian population
n1=Lester (signe de) | n2=en:high prevalence in the east asian population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high recurrence rate
n1=Lester (signe de) | n2=en:high recurrence rate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high risk of death in infancy due to cardiac failure
n1=Lester (signe de) | n2=en:high risk of death in infancy due to cardiac failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:high risk of recurrence after surgery
n1=Lester (signe de) | n2=en:high risk of recurrence after surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highest incidence in men of european descent
n1=Lester (signe de) | n2=en:highest incidence in men of european descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly penetrant, but low morbidity
n1=Lester (signe de) | n2=en:highly penetrant, but low morbidity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable age at onset
n1=Lester (signe de) | n2=en:highly variable age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable age at onset (range 9 to 69 years)
n1=Lester (signe de) | n2=en:highly variable age at onset (range 9 to 69 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable age at onset (range childhood to late adult)
n1=Lester (signe de) | n2=en:highly variable age at onset (range childhood to late adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable clinical and immunologic phenotype
n1=Lester (signe de) | n2=en:highly variable clinical and immunologic phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable clinical phenotype
n1=Lester (signe de) | n2=en:highly variable clinical phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable degree of bone fragility, even among patients carrying the same mutation
n1=Lester (signe de) | n2=en:highly variable degree of bone fragility, even among patients carrying the same mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable dysmorphic features
n1=Lester (signe de) | n2=en:highly variable dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable expression
n1=Lester (signe de) | n2=en:highly variable expression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable expressivity within families
n1=Lester (signe de) | n2=en:highly variable expressivity within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable frequency and duration of episodes
n1=Lester (signe de) | n2=en:highly variable frequency and duration of episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable frequency and severity of attacks
n1=Lester (signe de) | n2=en:highly variable frequency and severity of attacks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable intrafamilial expression
n1=Lester (signe de) | n2=en:highly variable intrafamilial expression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable intrafamilial severity
n1=Lester (signe de) | n2=en:highly variable intrafamilial severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable organ involvement and severity
n1=Lester (signe de) | n2=en:highly variable organ involvement and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable pathologic phenotype
n1=Lester (signe de) | n2=en:highly variable pathologic phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype and age of onset
n1=Lester (signe de) | n2=en:highly variable phenotype and age of onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype and severity
n1=Lester (signe de) | n2=en:highly variable phenotype and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype and severity, even within families
n1=Lester (signe de) | n2=en:highly variable phenotype and severity, even within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype in females
n1=Lester (signe de) | n2=en:highly variable phenotype in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype including fluctuating phenotype ('fluctuans') or severe phenotype ('permanens')
n1=Lester (signe de) | n2=en:highly variable phenotype including fluctuating phenotype ('fluctuans') or severe phenotype ('permanens') | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype that includes several subtypes (see, e.g., 607485, 601104)
n1=Lester (signe de) | n2=en:highly variable phenotype that includes several subtypes (see, e.g., 607485, 601104) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype with regard to pigmentation
n1=Lester (signe de) | n2=en:highly variable phenotype with regard to pigmentation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype with respect to facial dysmorphism and neurologic features
n1=Lester (signe de) | n2=en:highly variable phenotype with respect to facial dysmorphism and neurologic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype, even within families
n1=Lester (signe de) | n2=en:highly variable phenotype, even within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype, ranging from asymptomatic to death by age 3 years
n1=Lester (signe de) | n2=en:highly variable phenotype, ranging from asymptomatic to death by age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype, ranging from asymptomatic to severe
n1=Lester (signe de) | n2=en:highly variable phenotype, ranging from asymptomatic to severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype, ranging from neonatal encephalopathy to mild mental retardation with autistic features
n1=Lester (signe de) | n2=en:highly variable phenotype, ranging from neonatal encephalopathy to mild mental retardation with autistic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable phenotype, some adults may be asymptomatic
n1=Lester (signe de) | n2=en:highly variable phenotype, some adults may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable severity
n1=Lester (signe de) | n2=en:highly variable severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable severity and features
n1=Lester (signe de) | n2=en:highly variable severity and features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable severity of muscle weakness
n1=Lester (signe de) | n2=en:highly variable severity of muscle weakness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:highly variable severity, ranging from death in utero to survival to adulthood with normal intelligence
n1=Lester (signe de) | n2=en:highly variable severity, ranging from death in utero to survival to adulthood with normal intelligence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hip girdle involvement precedes and is usually greater than shoulder girdle involvement
n1=Lester (signe de) | n2=en:hip girdle involvement precedes and is usually greater than shoulder girdle involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hip joint replacement often necessary
n1=Lester (signe de) | n2=en:hip joint replacement often necessary | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hip replacement in early adulthood
n1=Lester (signe de) | n2=en:hip replacement in early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:histologic features overlap with henoch-schonlein purpura (hspn)
n1=Lester (signe de) | n2=en:histologic features overlap with henoch-schonlein purpura (hspn) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hla class ii alleles specify ketosis-prone diabetes (kpd) subgroup
n1=Lester (signe de) | n2=en:hla class ii alleles specify ketosis-prone diabetes (kpd) subgroup | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homo sapiens do not have a functional l-gulonolactone oxidase gene
n1=Lester (signe de) | n2=en:homo sapiens do not have a functional l-gulonolactone oxidase gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygosity for mutation in impg2 was reported in 1 patient with 'mild maculopathy'
n1=Lester (signe de) | n2=en:homozygosity for mutation in impg2 was reported in 1 patient with 'mild maculopathy' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygosity or compound heterozygosity for lamb2 mutations conferring complete loss of function (e.g., truncating mutations) appear to be associated with pierson syndrome
n1=Lester (signe de) | n2=en:homozygosity or compound heterozygosity for lamb2 mutations conferring complete loss of function (e.g., truncating mutations) appear to be associated with pierson syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygotes have earlier onset and a more severe disorder
n1=Lester (signe de) | n2=en:homozygotes have earlier onset and a more severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygotes have more severe disease with earlier onset of thrombosis
n1=Lester (signe de) | n2=en:homozygotes have more severe disease with earlier onset of thrombosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygous 9-snp haplotype in the promoter and coding region of malic enzyme 2 (me2, 154270.0001) increases risk for ige (odds ratio 6.1 with 95% confidence interval 2.9-12.7)
n1=Lester (signe de) | n2=en:homozygous 9-snp haplotype in the promoter and coding region of malic enzyme 2 (me2, 154270.0001) increases risk for ige (odds ratio 6.1 with 95% confidence interval 2.9-12.7) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygous mutation of kcne1 causes jervell and lange-nielsen syndrome (176261.0001)
n1=Lester (signe de) | n2=en:homozygous mutation of kcne1 causes jervell and lange-nielsen syndrome (176261.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygous mutation reported in 1 family, in which heterozygous parents had normal vision and ocular examination
n1=Lester (signe de) | n2=en:homozygous mutation reported in 1 family, in which heterozygous parents had normal vision and ocular examination | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:homozygous patients have earlier-onset and more severe disease
n1=Lester (signe de) | n2=en:homozygous patients have earlier-onset and more severe disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:however, neonatal seizures, severe mental retardation, distinct dysmorphic features, and mitochondrial dysfunction are unique to 2p21 deletion syndrome (2p21del)
n1=Lester (signe de) | n2=en:however, neonatal seizures, severe mental retardation, distinct dysmorphic features, and mitochondrial dysfunction are unique to 2p21 deletion syndrome (2p21del) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hundreds to thousands of patches of pale normal skin appear during childhood and increase in number and size over time
n1=Lester (signe de) | n2=en:hundreds to thousands of patches of pale normal skin appear during childhood and increase in number and size over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hydrops fetalis is associated with death in utero (90%) or within 2 days of birth
n1=Lester (signe de) | n2=en:hydrops fetalis is associated with death in utero (90%) or within 2 days of birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypercalciuria and/or nephrolithiasis occurs in heterozygotes
n1=Lester (signe de) | n2=en:hypercalciuria and/or nephrolithiasis occurs in heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperkeratosis often present at birth but may appear later
n1=Lester (signe de) | n2=en:hyperkeratosis often present at birth but may appear later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperkeratosis triggered by chronic mechanical irritation
n1=Lester (signe de) | n2=en:hyperkeratosis triggered by chronic mechanical irritation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperlipidemia may be partially responsive to fat-restricted diet
n1=Lester (signe de) | n2=en:hyperlipidemia may be partially responsive to fat-restricted diet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperphagia and weight gain as well as immunologic abnormalities and hypogonadism can be reversed by exogenously administered recombinant leptin
n1=Lester (signe de) | n2=en:hyperphagia and weight gain as well as immunologic abnormalities and hypogonadism can be reversed by exogenously administered recombinant leptin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperpigmented patches increased in size and number with age
n1=Lester (signe de) | n2=en:hyperpigmented patches increased in size and number with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperpigmented skin macules appear after age 3 years and increase in frequency with age
n1=Lester (signe de) | n2=en:hyperpigmented skin macules appear after age 3 years and increase in frequency with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypersensitivity to ionizing radiation
n1=Lester (signe de) | n2=en:hypersensitivity to ionizing radiation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypertension is presenting sign
n1=Lester (signe de) | n2=en:hypertension is presenting sign | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyperthermia in early childhood
n1=Lester (signe de) | n2=en:hyperthermia in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypochondrogenesis represents clinical variability within the achondrogenesis-hypochondrogenesis spectrum
n1=Lester (signe de) | n2=en:hypochondrogenesis represents clinical variability within the achondrogenesis-hypochondrogenesis spectrum | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypogonadism reported in a large swedish kindred
n1=Lester (signe de) | n2=en:hypogonadism reported in a large swedish kindred | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hyponatremia usually associated with gastroenteritis
n1=Lester (signe de) | n2=en:hyponatremia usually associated with gastroenteritis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypothyroidism is less severe in individuals with high dietary iodine intake
n1=Lester (signe de) | n2=en:hypothyroidism is less severe in individuals with high dietary iodine intake | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypotonia may respond to treatment with pyridostigmine
n1=Lester (signe de) | n2=en:hypotonia may respond to treatment with pyridostigmine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:hypoventilation occurs in the absence of primary neuromuscular, lung, or cardiac disease, or an identifiable brainstem lesion
n1=Lester (signe de) | n2=en:hypoventilation occurs in the absence of primary neuromuscular, lung, or cardiac disease, or an identifiable brainstem lesion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:icelandic families
n1=Lester (signe de) | n2=en:icelandic families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:icterus can be increased by oral contraceptives, pregnancy, or intercurrent illness
n1=Lester (signe de) | n2=en:icterus can be increased by oral contraceptives, pregnancy, or intercurrent illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:if onset of diabetes is before age 25, the diagnosis is consistent with maturity-onset diabetes of the young type 5 (mody5)
n1=Lester (signe de) | n2=en:if onset of diabetes is before age 25, the diagnosis is consistent with maturity-onset diabetes of the young type 5 (mody5) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:immunodeficiency is progressive
n1=Lester (signe de) | n2=en:immunodeficiency is progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:immunologic defects are variable
n1=Lester (signe de) | n2=en:immunologic defects are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:immunologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:immunologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:immunosuppressive therapy may be beneficial
n1=Lester (signe de) | n2=en:immunosuppressive therapy may be beneficial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:impaired healing
n1=Lester (signe de) | n2=en:impaired healing | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:imprinting at 11p15.5
n1=Lester (signe de) | n2=en:imprinting at 11p15.5 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:improvement of abnormal muscle biopsy and cox deficiency
n1=Lester (signe de) | n2=en:improvement of abnormal muscle biopsy and cox deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:improvement of epimetaphyseal changes with age
n1=Lester (signe de) | n2=en:improvement of epimetaphyseal changes with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:improvement with age
n1=Lester (signe de) | n2=en:improvement with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in 1 family, heterozygous mutations were associated with hypobetalipoproteinemia and acanthocytes without neurologic abnormalities
n1=Lester (signe de) | n2=en:in 1 family, heterozygous mutations were associated with hypobetalipoproteinemia and acanthocytes without neurologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in adults, may be considered part of a spectrum with hemolytic-uremic syndrome (hus, 235400)
n1=Lester (signe de) | n2=en:in adults, may be considered part of a spectrum with hemolytic-uremic syndrome (hus, 235400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in contrast to other forms of progeria, these patients do not have atherosclerosis, cardiac ischemia, or metabolic abnormalities
n1=Lester (signe de) | n2=en:in contrast to other forms of progeria, these patients do not have atherosclerosis, cardiac ischemia, or metabolic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in families with homozygous or compound heterozygous mutations, heterozygous carriers show minimal evidence of eye disease
n1=Lester (signe de) | n2=en:in families with homozygous or compound heterozygous mutations, heterozygous carriers show minimal evidence of eye disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in general, men have more severe disease than women
n1=Lester (signe de) | n2=en:in general, men have more severe disease than women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns
n1=Lester (signe de) | n2=en:in inbred old order mennonite population of lancaster county, msud prevalence is 1/176 newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in most cases capillary lesions are multifocal at birth and may increase in number with age
n1=Lester (signe de) | n2=en:in most cases capillary lesions are multifocal at birth and may increase in number with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in severe attacks, hemiplegia or coma may last days to weeks
n1=Lester (signe de) | n2=en:in severe attacks, hemiplegia or coma may last days to weeks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in some patients, qtc interval is prolonged only during exercise testing
n1=Lester (signe de) | n2=en:in some patients, qtc interval is prolonged only during exercise testing | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:in the absence of hydrops, death occurs within 3 months
n1=Lester (signe de) | n2=en:in the absence of hydrops, death occurs within 3 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:inborn error of the pyrimidine degradation pathway
n1=Lester (signe de) | n2=en:inborn error of the pyrimidine degradation pathway | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence - 1 in 25,000-100,000
n1=Lester (signe de) | n2=en:incidence - 1 in 25,000-100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence - 1/16,000 live births
n1=Lester (signe de) | n2=en:incidence - 1/16,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 15,000-28,000 births
n1=Lester (signe de) | n2=en:incidence 1 in 15,000-28,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 20,000
n1=Lester (signe de) | n2=en:incidence 1 in 20,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 30,000 male births
n1=Lester (signe de) | n2=en:incidence 1 in 30,000 male births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 300,000 in japan
n1=Lester (signe de) | n2=en:incidence 1 in 300,000 in japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 50,000-100,000 in western europe
n1=Lester (signe de) | n2=en:incidence 1 in 50,000-100,000 in western europe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 6,000 to 1 in 8,000 live births
n1=Lester (signe de) | n2=en:incidence 1 in 6,000 to 1 in 8,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1 in 8,000 live births
n1=Lester (signe de) | n2=en:incidence 1 in 8,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1-1.5/1,000 live births
n1=Lester (signe de) | n2=en:incidence 1-1.5/1,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1/1,200-1/15,000 live births
n1=Lester (signe de) | n2=en:incidence 1/1,200-1/15,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1/100,000 - 1/200,000 live births
n1=Lester (signe de) | n2=en:incidence 1/100,000 - 1/200,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 1/20,000-1/64,000 male births
n1=Lester (signe de) | n2=en:incidence 1/20,000-1/64,000 male births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 2-5% of north american children
n1=Lester (signe de) | n2=en:incidence 2-5% of north american children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 5-50 per million (children) and 10-40 per million (adults)
n1=Lester (signe de) | n2=en:incidence 5-50 per million (children) and 10-40 per million (adults) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 7-15% in pacific island populations
n1=Lester (signe de) | n2=en:incidence 7-15% in pacific island populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence 8/1,000 newborns
n1=Lester (signe de) | n2=en:incidence 8/1,000 newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence approximately 2-3/10,000 newborns
n1=Lester (signe de) | n2=en:incidence approximately 2-3/10,000 newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence in finland is 1 in 76,000 births
n1=Lester (signe de) | n2=en:incidence in finland is 1 in 76,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence in japan is 1 in 57,000
n1=Lester (signe de) | n2=en:incidence in japan is 1 in 57,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence in the finnish population of 0.2-1.3 cases per million per year
n1=Lester (signe de) | n2=en:incidence in the finnish population of 0.2-1.3 cases per million per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence in united states of 1 in 55,000
n1=Lester (signe de) | n2=en:incidence in united states of 1 in 55,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence is estimated to be between 1 in 2,000 and 1 in 7,000 live births
n1=Lester (signe de) | n2=en:incidence is estimated to be between 1 in 2,000 and 1 in 7,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence is less than 1 in 70,000 births
n1=Lester (signe de) | n2=en:incidence is less than 1 in 70,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 0.51 per million in france
n1=Lester (signe de) | n2=en:incidence of 0.51 per million in france | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 1,000,000
n1=Lester (signe de) | n2=en:incidence of 1 in 1,000,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 1.5 million births
n1=Lester (signe de) | n2=en:incidence of 1 in 1.5 million births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 10,000 live births
n1=Lester (signe de) | n2=en:incidence of 1 in 10,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 10,000 to 1 in 20,000
n1=Lester (signe de) | n2=en:incidence of 1 in 10,000 to 1 in 20,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 100 in some local nordic areas
n1=Lester (signe de) | n2=en:incidence of 1 in 100 in some local nordic areas | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 100,000
n1=Lester (signe de) | n2=en:incidence of 1 in 100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 100,000 births
n1=Lester (signe de) | n2=en:incidence of 1 in 100,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 100,000 births in caucasians
n1=Lester (signe de) | n2=en:incidence of 1 in 100,000 births in caucasians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 100,000 to 125,000 at birth
n1=Lester (signe de) | n2=en:incidence of 1 in 100,000 to 125,000 at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 120,000 live births
n1=Lester (signe de) | n2=en:incidence of 1 in 120,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 150,000 live births in the general population
n1=Lester (signe de) | n2=en:incidence of 1 in 150,000 live births in the general population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 2,000 in saguenay-lac-saint-jean region
n1=Lester (signe de) | n2=en:incidence of 1 in 2,000 in saguenay-lac-saint-jean region | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 20,000 live births
n1=Lester (signe de) | n2=en:incidence of 1 in 20,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 25,000 livebirths
n1=Lester (signe de) | n2=en:incidence of 1 in 25,000 livebirths | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 25,000 to 1 in 50,000 newborns
n1=Lester (signe de) | n2=en:incidence of 1 in 25,000 to 1 in 50,000 newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 250,000 births
n1=Lester (signe de) | n2=en:incidence of 1 in 250,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 276,000 in the netherlands
n1=Lester (signe de) | n2=en:incidence of 1 in 276,000 in the netherlands | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 3,500 boys
n1=Lester (signe de) | n2=en:incidence of 1 in 3,500 boys | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 3,900 births among jewish persons
n1=Lester (signe de) | n2=en:incidence of 1 in 3,900 births among jewish persons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 300,000
n1=Lester (signe de) | n2=en:incidence of 1 in 300,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 320,000 births among non-jewish persons
n1=Lester (signe de) | n2=en:incidence of 1 in 320,000 births among non-jewish persons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 39,000
n1=Lester (signe de) | n2=en:incidence of 1 in 39,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 40,000 infants worldwide
n1=Lester (signe de) | n2=en:incidence of 1 in 40,000 infants worldwide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 480 among old order amish
n1=Lester (signe de) | n2=en:incidence of 1 in 480 among old order amish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 5,000 to 1 in 10,000
n1=Lester (signe de) | n2=en:incidence of 1 in 5,000 to 1 in 10,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 5,000 to 1 in 7,000 in moroccan jewish individuals
n1=Lester (signe de) | n2=en:incidence of 1 in 5,000 to 1 in 7,000 in moroccan jewish individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 5,000-8,000
n1=Lester (signe de) | n2=en:incidence of 1 in 5,000-8,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 50,000 to 1 in 100,000
n1=Lester (signe de) | n2=en:incidence of 1 in 50,000 to 1 in 100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 500,000 live births
n1=Lester (signe de) | n2=en:incidence of 1 in 500,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 57,000
n1=Lester (signe de) | n2=en:incidence of 1 in 57,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 in 6,000 males
n1=Lester (signe de) | n2=en:incidence of 1 in 6,000 males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1 per 10,000 births in japan
n1=Lester (signe de) | n2=en:incidence of 1 per 10,000 births in japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1/100,000 in italy and finland
n1=Lester (signe de) | n2=en:incidence of 1/100,000 in italy and finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1/50,000 births
n1=Lester (signe de) | n2=en:incidence of 1/50,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 1% in yarmouth county, nova scotia
n1=Lester (signe de) | n2=en:incidence of 1% in yarmouth county, nova scotia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 12.2 per 100,000 in finland
n1=Lester (signe de) | n2=en:incidence of 12.2 per 100,000 in finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of 4 per million per year
n1=Lester (signe de) | n2=en:incidence of 4 per million per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of all forms of cjd is 0.5 to 1.5 per million per year
n1=Lester (signe de) | n2=en:incidence of all forms of cjd is 0.5 to 1.5 per million per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of mh in anesthetized adults is 1 in 50,000-100,000
n1=Lester (signe de) | n2=en:incidence of mh in anesthetized adults is 1 in 50,000-100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence of mh in anesthetized children is 1 in 15,000
n1=Lester (signe de) | n2=en:incidence of mh in anesthetized children is 1 in 15,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence ranges from 1 in 238,095 to 1 in 300,000 births
n1=Lester (signe de) | n2=en:incidence ranges from 1 in 238,095 to 1 in 300,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence ranges from 1 in 40,000 to 1 in 350,000 births
n1=Lester (signe de) | n2=en:incidence ranges from 1 in 40,000 to 1 in 350,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence ranges from 1 in 8,500 to 1 in 12,000 births
n1=Lester (signe de) | n2=en:incidence ranges from 1 in 8,500 to 1 in 12,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence worldwide of 1 in 30,000 to 50,000
n1=Lester (signe de) | n2=en:incidence worldwide of 1 in 30,000 to 50,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence, 1 in 500 heterozygotes, 1 in 1,000,000 homozygotes
n1=Lester (signe de) | n2=en:incidence, 1 in 500 heterozygotes, 1 in 1,000,000 homozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incidence, 1 in 650-1000 live births
n1=Lester (signe de) | n2=en:incidence, 1 in 650-1000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete age-dependent penetrance
n1=Lester (signe de) | n2=en:incomplete age-dependent penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetance of some features
n1=Lester (signe de) | n2=en:incomplete penetance of some features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance
n1=Lester (signe de) | n2=en:incomplete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance - approximately 50% males and 10% females with a pathogenic mtdna mutation develop the optic neuropathy
n1=Lester (signe de) | n2=en:incomplete penetrance - approximately 50% males and 10% females with a pathogenic mtdna mutation develop the optic neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance (50%)
n1=Lester (signe de) | n2=en:incomplete penetrance (50%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance (about 80%)
n1=Lester (signe de) | n2=en:incomplete penetrance (about 80%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance (as low as 30% in some cases)
n1=Lester (signe de) | n2=en:incomplete penetrance (as low as 30% in some cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance (range 13% to 77% by 50 years of age)
n1=Lester (signe de) | n2=en:incomplete penetrance (range 13% to 77% by 50 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance in carrier females
n1=Lester (signe de) | n2=en:incomplete penetrance in carrier females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance in females
n1=Lester (signe de) | n2=en:incomplete penetrance in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance in some families
n1=Lester (signe de) | n2=en:incomplete penetrance in some families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance of optic atrophy
n1=Lester (signe de) | n2=en:incomplete penetrance of optic atrophy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance of the 3 main clinical signs, myopathy, dementia, and paget disease
n1=Lester (signe de) | n2=en:incomplete penetrance of the 3 main clinical signs, myopathy, dementia, and paget disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance of the cardiac phenotype
n1=Lester (signe de) | n2=en:incomplete penetrance of the cardiac phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance with 45 to 51 repeats
n1=Lester (signe de) | n2=en:incomplete penetrance with 45 to 51 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete penetrance, some individuals have only emg changes without other clinical signs
n1=Lester (signe de) | n2=en:incomplete penetrance, some individuals have only emg changes without other clinical signs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete, age-associated penetrance
n1=Lester (signe de) | n2=en:incomplete, age-associated penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incomplete, but high, penetrance
n1=Lester (signe de) | n2=en:incomplete, but high, penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:incompletely penetrant phenotype in heterozygotes
n1=Lester (signe de) | n2=en:incompletely penetrant phenotype in heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased abortuses of homozygous or compound heterozygous fetuses
n1=Lester (signe de) | n2=en:increased abortuses of homozygous or compound heterozygous fetuses | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased aneuploidy in offspring
n1=Lester (signe de) | n2=en:increased aneuploidy in offspring | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased bleeding after surgery
n1=Lester (signe de) | n2=en:increased bleeding after surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency among french-canadians from the charlevoix-saguenay-lac saint jean area of quebec (carrier rate 1 in 26)
n1=Lester (signe de) | n2=en:increased frequency among french-canadians from the charlevoix-saguenay-lac saint jean area of quebec (carrier rate 1 in 26) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency among individuals of ashkenazi jewish descent
n1=Lester (signe de) | n2=en:increased frequency among individuals of ashkenazi jewish descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency among individuals of east asian descent
n1=Lester (signe de) | n2=en:increased frequency among individuals of east asian descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency among japanese and chinese
n1=Lester (signe de) | n2=en:increased frequency among japanese and chinese | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency among jewish iranian individuals from isfahan
n1=Lester (signe de) | n2=en:increased frequency among jewish iranian individuals from isfahan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in ashkenazi jewish population
n1=Lester (signe de) | n2=en:increased frequency in ashkenazi jewish population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in ashkenazi jewish population (1/100 are carriers)
n1=Lester (signe de) | n2=en:increased frequency in ashkenazi jewish population (1/100 are carriers) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in ashkenazi jewish population and in finland
n1=Lester (signe de) | n2=en:increased frequency in ashkenazi jewish population and in finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in ashkenazi jews (carrier frequency 1 in 14)
n1=Lester (signe de) | n2=en:increased frequency in ashkenazi jews (carrier frequency 1 in 14) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in eastern pennsylvania amish
n1=Lester (signe de) | n2=en:increased frequency in eastern pennsylvania amish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in finland
n1=Lester (signe de) | n2=en:increased frequency in finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in finland (incidence 1:60,000 finnish newborns)
n1=Lester (signe de) | n2=en:increased frequency in finland (incidence 1:60,000 finnish newborns) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in finland (prevalence of 1 in 20,000)
n1=Lester (signe de) | n2=en:increased frequency in finland (prevalence of 1 in 20,000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in individuals of asian descent
n1=Lester (signe de) | n2=en:increased frequency in individuals of asian descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in individuals originating from western scotland
n1=Lester (signe de) | n2=en:increased frequency in individuals originating from western scotland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in iraqi jews, selected arab populations, french gypsies, and natives of southern india
n1=Lester (signe de) | n2=en:increased frequency in iraqi jews, selected arab populations, french gypsies, and natives of southern india | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in persian jews (1:1,300)
n1=Lester (signe de) | n2=en:increased frequency in persian jews (1:1,300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the charlevoix and saguenat-lac-st-jean regions of quebec, canada (1 in 2,117 live births, carrier rate 1 in 23)
n1=Lester (signe de) | n2=en:increased frequency in the charlevoix and saguenat-lac-st-jean regions of quebec, canada (1 in 2,117 live births, carrier rate 1 in 23) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the dariusleut hutterites (canada)
n1=Lester (signe de) | n2=en:increased frequency in the dariusleut hutterites (canada) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the faroe islands (carrier 1 in 25)
n1=Lester (signe de) | n2=en:increased frequency in the faroe islands (carrier 1 in 25) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the finnish population
n1=Lester (signe de) | n2=en:increased frequency in the finnish population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the ngobe-bugle tribe in the boca del toro province, on the northwestern caribbean coast of panama
n1=Lester (signe de) | n2=en:increased frequency in the ngobe-bugle tribe in the boca del toro province, on the northwestern caribbean coast of panama | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in the state of bahia, brazil
n1=Lester (signe de) | n2=en:increased frequency in the state of bahia, brazil | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased frequency in vastebotten county in northern sweden and gelenau in southeastern germany
n1=Lester (signe de) | n2=en:increased frequency in vastebotten county in northern sweden and gelenau in southeastern germany | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased incidence in asian countries (e.g., 1.46 per 10,000 live births in taiwan)
n1=Lester (signe de) | n2=en:increased incidence in asian countries (e.g., 1.46 per 10,000 live births in taiwan) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased male to female ratio (7.5:1)
n1=Lester (signe de) | n2=en:increased male to female ratio (7.5:1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased male-to-female ratio (3-4 to 1)
n1=Lester (signe de) | n2=en:increased male-to-female ratio (3-4 to 1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased morbidity/mortality in affected males
n1=Lester (signe de) | n2=en:increased morbidity/mortality in affected males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased paternal age
n1=Lester (signe de) | n2=en:increased paternal age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased penetrance of phenotype when there is maternal transmission of the mutant allele
n1=Lester (signe de) | n2=en:increased penetrance of phenotype when there is maternal transmission of the mutant allele | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence among smokers
n1=Lester (signe de) | n2=en:increased prevalence among smokers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence among the finnish
n1=Lester (signe de) | n2=en:increased prevalence among the finnish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence among women
n1=Lester (signe de) | n2=en:increased prevalence among women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence in individuals of jewish-iraqi origin
n1=Lester (signe de) | n2=en:increased prevalence in individuals of jewish-iraqi origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence in individuals of turkish descent
n1=Lester (signe de) | n2=en:increased prevalence in individuals of turkish descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence in northern finland (7.3/100,000)
n1=Lester (signe de) | n2=en:increased prevalence in northern finland (7.3/100,000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence in persons of ashkenazi jewish descent
n1=Lester (signe de) | n2=en:increased prevalence in persons of ashkenazi jewish descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased prevalence in the french-canadian population
n1=Lester (signe de) | n2=en:increased prevalence in the french-canadian population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased rate of miscarriage in affected individuals
n1=Lester (signe de) | n2=en:increased rate of miscarriage in affected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased recurrence risk with parental translocation
n1=Lester (signe de) | n2=en:increased recurrence risk with parental translocation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of bilateral breast cancer
n1=Lester (signe de) | n2=en:increased risk of bilateral breast cancer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of developing early-onset aggressive cancers
n1=Lester (signe de) | n2=en:increased risk of developing early-onset aggressive cancers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of developing multiple primary cancers
n1=Lester (signe de) | n2=en:increased risk of developing multiple primary cancers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of early death
n1=Lester (signe de) | n2=en:increased risk of early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of miscarriage
n1=Lester (signe de) | n2=en:increased risk of miscarriage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of myeloproliferative disorders in those with somatic mutations
n1=Lester (signe de) | n2=en:increased risk of myeloproliferative disorders in those with somatic mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of post-splenectomy thrombotic complications
n1=Lester (signe de) | n2=en:increased risk of post-splenectomy thrombotic complications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased risk of post-splenectomy thrombotic complications (in some patients)
n1=Lester (signe de) | n2=en:increased risk of post-splenectomy thrombotic complications (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased sensitivity to heat
n1=Lester (signe de) | n2=en:increased sensitivity to heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased sensitivity to valproic acid toxicity
n1=Lester (signe de) | n2=en:increased sensitivity to valproic acid toxicity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased spontaneous abortions in carrier mothers
n1=Lester (signe de) | n2=en:increased spontaneous abortions in carrier mothers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to bacterial and opportunistic infections, such as pneumocystis carinii
n1=Lester (signe de) | n2=en:increased susceptibility to bacterial and opportunistic infections, such as pneumocystis carinii | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to infections
n1=Lester (signe de) | n2=en:increased susceptibility to infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to malignant hyperthermia
n1=Lester (signe de) | n2=en:increased susceptibility to malignant hyperthermia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to multiple carcinomas
n1=Lester (signe de) | n2=en:increased susceptibility to multiple carcinomas | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to neisseria infections
n1=Lester (signe de) | n2=en:increased susceptibility to neisseria infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased susceptibility to toxic effects of treatment with 6-mercaptopurine (6mp), 6-thioguanine (6tg), and azathioprine (aza)
n1=Lester (signe de) | n2=en:increased susceptibility to toxic effects of treatment with 6-mercaptopurine (6mp), 6-thioguanine (6tg), and azathioprine (aza) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increased tendency to chromosomal nondisjunction
n1=Lester (signe de) | n2=en:increased tendency to chromosomal nondisjunction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:increasing hypertension with increasing age
n1=Lester (signe de) | n2=en:increasing hypertension with increasing age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:independent ambulation is maintained
n1=Lester (signe de) | n2=en:independent ambulation is maintained | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:individuals develop ability to stand and walk
n1=Lester (signe de) | n2=en:individuals develop ability to stand and walk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:individuals do not develop erythrocytosis under hypoxic conditions
n1=Lester (signe de) | n2=en:individuals do not develop erythrocytosis under hypoxic conditions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:individuals may accumulate more pigment in hair and eyes with age
n1=Lester (signe de) | n2=en:individuals may accumulate more pigment in hair and eyes with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:individuals with the pcs trait are phenotypically normal
n1=Lester (signe de) | n2=en:individuals with the pcs trait are phenotypically normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infant death may occur secondary to sepsis
n1=Lester (signe de) | n2=en:infant death may occur secondary to sepsis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile form (gene deletion 'complex' with glycerol kinase deficiency and/or duchenne muscular dystrophy and/or congenital adrenal hypoplasia)
n1=Lester (signe de) | n2=en:infantile form (gene deletion 'complex' with glycerol kinase deficiency and/or duchenne muscular dystrophy and/or congenital adrenal hypoplasia) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile form accounts for 90% of cases
n1=Lester (signe de) | n2=en:infantile form accounts for 90% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile form has onset within first 6 months of life
n1=Lester (signe de) | n2=en:infantile form has onset within first 6 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile form usually leads to death by age 2 years
n1=Lester (signe de) | n2=en:infantile form usually leads to death by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile onset
n1=Lester (signe de) | n2=en:infantile onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile onset (in 1 patient)
n1=Lester (signe de) | n2=en:infantile onset (in 1 patient) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile onset with hepatic involvement
n1=Lester (signe de) | n2=en:infantile onset with hepatic involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infantile, late-infantile, juvenile, and adult onset have been reported
n1=Lester (signe de) | n2=en:infantile, late-infantile, juvenile, and adult onset have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants are stillborn or die before age 1
n1=Lester (signe de) | n2=en:infants are stillborn or die before age 1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants are stillborn or die shortly after birth
n1=Lester (signe de) | n2=en:infants are stillborn or die shortly after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants may die from apnea or aspiration
n1=Lester (signe de) | n2=en:infants may die from apnea or aspiration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants may have acute life-threatening crises
n1=Lester (signe de) | n2=en:infants may have acute life-threatening crises | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants occasionally mistaken as having down syndrome
n1=Lester (signe de) | n2=en:infants occasionally mistaken as having down syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infants show normal size and appearance
n1=Lester (signe de) | n2=en:infants show normal size and appearance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infections may precipitate ketotic episodes
n1=Lester (signe de) | n2=en:infections may precipitate ketotic episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:infertility
n1=Lester (signe de) | n2=en:infertility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:inflammatory arthritis may develop in 30% of patients
n1=Lester (signe de) | n2=en:inflammatory arthritis may develop in 30% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:inflammatory bowel disease may develop in childhood or adolescence
n1=Lester (signe de) | n2=en:inflammatory bowel disease may develop in childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:inheritance may be x-linked dominant
n1=Lester (signe de) | n2=en:inheritance may be x-linked dominant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:inheritance pattern is unclear
n1=Lester (signe de) | n2=en:inheritance pattern is unclear | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initial cases reclassified as having schwartz-jampel syndrome (sjs1, 255800)
n1=Lester (signe de) | n2=en:initial cases reclassified as having schwartz-jampel syndrome (sjs1, 255800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initial development may appear normal
n1=Lester (signe de) | n2=en:initial development may appear normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initial hearing loss is mild progressing to severe or profound by the seventh decade
n1=Lester (signe de) | n2=en:initial hearing loss is mild progressing to severe or profound by the seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initial recovery, but residual neurologic impairment occurs after repeated encephalopathic episodes
n1=Lester (signe de) | n2=en:initial recovery, but residual neurologic impairment occurs after repeated encephalopathic episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initially normal for first 6-18 months which is then followed by withdrawal and regression
n1=Lester (signe de) | n2=en:initially normal for first 6-18 months which is then followed by withdrawal and regression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:initially normal rod responses may become significantly reduced at older age
n1=Lester (signe de) | n2=en:initially normal rod responses may become significantly reduced at older age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:insidious onset
n1=Lester (signe de) | n2=en:insidious onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:insulin dependent diabetes mellitus:prthr:pt:^patient:ord
n1=Lester (signe de) | n2=en:insulin dependent diabetes mellitus:prthr:pt:^patient:ord | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intellectual disability is variable
n1=Lester (signe de) | n2=en:intellectual disability is variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intellectual regression and loss of speech precede the onset of motor retardation by more than 10 years
n1=Lester (signe de) | n2=en:intellectual regression and loss of speech precede the onset of motor retardation by more than 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intelligence is normal
n1=Lester (signe de) | n2=en:intelligence is normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:interfamilial and intrafamilial clinical heterogeneity
n1=Lester (signe de) | n2=en:interfamilial and intrafamilial clinical heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:interfamilial and intrafamilial variability in severity of symptoms
n1=Lester (signe de) | n2=en:interfamilial and intrafamilial variability in severity of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intermediate expression in females
n1=Lester (signe de) | n2=en:intermediate expression in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intermediate levels of factor x in mildly symptomatic heterozygotes
n1=Lester (signe de) | n2=en:intermediate levels of factor x in mildly symptomatic heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intermediate: onset in first decade with slow progression or onset in second decade with rapid progression
n1=Lester (signe de) | n2=en:intermediate: onset in first decade with slow progression or onset in second decade with rapid progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intermittent exacerbations
n1=Lester (signe de) | n2=en:intermittent exacerbations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intermittent pyrexia
n1=Lester (signe de) | n2=en:intermittent pyrexia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:internal organ rupture may occur
n1=Lester (signe de) | n2=en:internal organ rupture may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intolerant of heat
n1=Lester (signe de) | n2=en:intolerant of heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intracellular accumulation of material can occur in neuronal and nonneuronal cells
n1=Lester (signe de) | n2=en:intracellular accumulation of material can occur in neuronal and nonneuronal cells | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intracellular accumulation of material may not always be apparent
n1=Lester (signe de) | n2=en:intracellular accumulation of material may not always be apparent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial phenotypic variability ranging from transient or permanent neonatal diabetes (610582) to mody (616329) to impaired fasting glucose or impaired glucose tolerance
n1=Lester (signe de) | n2=en:intrafamilial phenotypic variability ranging from transient or permanent neonatal diabetes (610582) to mody (616329) to impaired fasting glucose or impaired glucose tolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial phenotypic variability, ranging from bilateral to unilateral foot involvement to no split-foot malformation
n1=Lester (signe de) | n2=en:intrafamilial phenotypic variability, ranging from bilateral to unilateral foot involvement to no split-foot malformation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial phenotypic variation may occur
n1=Lester (signe de) | n2=en:intrafamilial phenotypic variation may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability
n1=Lester (signe de) | n2=en:intrafamilial variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in degree of hypotrichosis
n1=Lester (signe de) | n2=en:intrafamilial variability in degree of hypotrichosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in degree of nail involvement
n1=Lester (signe de) | n2=en:intrafamilial variability in degree of nail involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in nail changes
n1=Lester (signe de) | n2=en:intrafamilial variability in nail changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in number of missing teeth
n1=Lester (signe de) | n2=en:intrafamilial variability in number of missing teeth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in severity
n1=Lester (signe de) | n2=en:intrafamilial variability in severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variability in severity of hypothyroidism
n1=Lester (signe de) | n2=en:intrafamilial variability in severity of hypothyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrafamilial variation
n1=Lester (signe de) | n2=en:intrafamilial variation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:intrathecal pressure:pressure:point in time:intrathecal space:quantitative
n1=Lester (signe de) | n2=en:intrathecal pressure:pressure:point in time:intrathecal space:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:involuntary and nonvolitional phenomenon
n1=Lester (signe de) | n2=en:involuntary and nonvolitional phenomenon | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:isolated cases
n1=Lester (signe de) | n2=en:isolated cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:isolated finding
n1=Lester (signe de) | n2=en:isolated finding | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:isolated pulmonary a-v fistulas are typically associated with hereditary hemorrhagic telangiectasia (187300)
n1=Lester (signe de) | n2=en:isolated pulmonary a-v fistulas are typically associated with hereditary hemorrhagic telangiectasia (187300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:itch, pain, and body malodor often
n1=Lester (signe de) | n2=en:itch, pain, and body malodor often | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:jbts shows autosomal dominant inheritance
n1=Lester (signe de) | n2=en:jbts shows autosomal dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:joint dislocations become less frequent with age
n1=Lester (signe de) | n2=en:joint dislocations become less frequent with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:joint laxity decreases with age
n1=Lester (signe de) | n2=en:joint laxity decreases with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:joint replacement often necessary
n1=Lester (signe de) | n2=en:joint replacement often necessary | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:joint symptoms begin in third or fourth decade
n1=Lester (signe de) | n2=en:joint symptoms begin in third or fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile absence epilepsy (jae, 607631)
n1=Lester (signe de) | n2=en:juvenile absence epilepsy (jae, 607631) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile and adult forms are isolated glycerol kinase deficiency
n1=Lester (signe de) | n2=en:juvenile and adult forms are isolated glycerol kinase deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile form has onset between 4 and 19 years
n1=Lester (signe de) | n2=en:juvenile form has onset between 4 and 19 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile myoclonic epilepsy (jme, 606904)
n1=Lester (signe de) | n2=en:juvenile myoclonic epilepsy (jme, 606904) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile onset 4 years to puberty
n1=Lester (signe de) | n2=en:juvenile onset 4 years to puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile patients have slower clinical course with preserved intellect, bulbar signs, ataxia, and spasticity
n1=Lester (signe de) | n2=en:juvenile patients have slower clinical course with preserved intellect, bulbar signs, ataxia, and spasticity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile rigid early-onset form more often paternally inherited
n1=Lester (signe de) | n2=en:juvenile rigid early-onset form more often paternally inherited | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:juvenile-onset (before 15 years of age)
n1=Lester (signe de) | n2=en:juvenile-onset (before 15 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:keratitis-ichthyosis-deafness syndrome
n1=Lester (signe de) | n2=en:keratitis-ichthyosis-deafness syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:keratoconus, which was observed in 1 family, might be secondary to eye rubbing due to lca
n1=Lester (signe de) | n2=en:keratoconus, which was observed in 1 family, might be secondary to eye rubbing due to lca | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ketogenic diet may be effective
n1=Lester (signe de) | n2=en:ketogenic diet may be effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:kid syndrome and hid syndrome are identical at the molecular level
n1=Lester (signe de) | n2=en:kid syndrome and hid syndrome are identical at the molecular level | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:klippel-feil anomaly may be a part of other syndromes, including murcs (601076) and sprengel deformity (184400)
n1=Lester (signe de) | n2=en:klippel-feil anomaly may be a part of other syndromes, including murcs (601076) and sprengel deformity (184400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:known as the 'french variety' of usher syndrome since the majority of families are from poitou-charentes, france
n1=Lester (signe de) | n2=en:known as the 'french variety' of usher syndrome since the majority of families are from poitou-charentes, france | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:l-dopa-induced dyskinesias
n1=Lester (signe de) | n2=en:l-dopa-induced dyskinesias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:laboratory comment:txt:pt:report:nar
n1=Lester (signe de) | n2=en:laboratory comment:txt:pt:report:nar | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:laboratory director name:pn:pt:provider:nom
n1=Lester (signe de) | n2=en:laboratory director name:pn:pt:provider:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:laboratory findings are variable
n1=Lester (signe de) | n2=en:laboratory findings are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lack of treatment results in early death
n1=Lester (signe de) | n2=en:lack of treatment results in early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:laryngeal edema can result in asphyxiation
n1=Lester (signe de) | n2=en:laryngeal edema can result in asphyxiation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:last name:pn:pt:^guardian or legally authorized representative:nom
n1=Lester (signe de) | n2=en:last name:pn:pt:^guardian or legally authorized representative:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late adult onset (after age 55 years)
n1=Lester (signe de) | n2=en:late adult onset (after age 55 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late infantile form has onset between 19 months and 4 years
n1=Lester (signe de) | n2=en:late infantile form has onset between 19 months and 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late infantile onset 6-24 months
n1=Lester (signe de) | n2=en:late infantile onset 6-24 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late onset combined immunodeficiency with allelic variant 102700.0020
n1=Lester (signe de) | n2=en:late onset combined immunodeficiency with allelic variant 102700.0020 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset
n1=Lester (signe de) | n2=en:late-adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset (age 50 or later)
n1=Lester (signe de) | n2=en:late-adult onset (age 50 or later) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset (fifth to sixth decade)
n1=Lester (signe de) | n2=en:late-adult onset (fifth to sixth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset (range 50 to 80 years)
n1=Lester (signe de) | n2=en:late-adult onset (range 50 to 80 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset (usually after age 50 years)
n1=Lester (signe de) | n2=en:late-adult onset (usually after age 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-adult onset has been reported
n1=Lester (signe de) | n2=en:late-adult onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:late-onset, slowly progressing form of retinitis pigmentosa
n1=Lester (signe de) | n2=en:late-onset, slowly progressing form of retinitis pigmentosa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later childhood onset has been reported
n1=Lester (signe de) | n2=en:later childhood onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset (late childhood to young adult) has been reported
n1=Lester (signe de) | n2=en:later onset (late childhood to young adult) has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset associated with milder severity has been reported
n1=Lester (signe de) | n2=en:later onset associated with milder severity has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset can also occur (up to age 17 years)
n1=Lester (signe de) | n2=en:later onset can also occur (up to age 17 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset has been rarely reported (up to age 68 years)
n1=Lester (signe de) | n2=en:later onset has been rarely reported (up to age 68 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset has been reported
n1=Lester (signe de) | n2=en:later onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset has been reported (third or fourth decades)
n1=Lester (signe de) | n2=en:later onset has been reported (third or fourth decades) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset in adolescence has rarely been reported
n1=Lester (signe de) | n2=en:later onset in adolescence has rarely been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset in females
n1=Lester (signe de) | n2=en:later onset in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset is associated with slower progression and lesser severity
n1=Lester (signe de) | n2=en:later onset is associated with slower progression and lesser severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset may occur
n1=Lester (signe de) | n2=en:later onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset may occur (1 to 11 years)
n1=Lester (signe de) | n2=en:later onset may occur (1 to 11 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset of hearing loss in some patients
n1=Lester (signe de) | n2=en:later onset of hearing loss in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset of neurologic features
n1=Lester (signe de) | n2=en:later onset of neurologic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset of ophthalmoparesis
n1=Lester (signe de) | n2=en:later onset of ophthalmoparesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset of optic atrophy (mean 19 years, range 5 to 50 years)
n1=Lester (signe de) | n2=en:later onset of optic atrophy (mean 19 years, range 5 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:later onset with a milder phenotype may also occur
n1=Lester (signe de) | n2=en:later onset with a milder phenotype may also occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:leakage of fluid ('gusher') if the stapes is disturbed
n1=Lester (signe de) | n2=en:leakage of fluid ('gusher') if the stapes is disturbed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:left side involvement associated with serious cardiac defect
n1=Lester (signe de) | n2=en:left side involvement associated with serious cardiac defect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:left side involvement more frequent than right side involvement
n1=Lester (signe de) | n2=en:left side involvement more frequent than right side involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:left sided involvement occurs more frequently
n1=Lester (signe de) | n2=en:left sided involvement occurs more frequently | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:leg pain during childhood
n1=Lester (signe de) | n2=en:leg pain during childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:leigh syndrome, x-linked
n1=Lester (signe de) | n2=en:leigh syndrome, x-linked | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:length of attack, 3 to 7 days
n1=Lester (signe de) | n2=en:length of attack, 3 to 7 days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:length of calorie fast:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:length of calorie fast:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:length of time post dose:time:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:length of time post dose:time:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:leopard is an acronym: lentigines, ekg abnormalities, ocular hypertelorism, obstructive cardiomyopathy, pulmonic stenosis, abnormalities of genitalia, retardation of growth, and deafness
n1=Lester (signe de) | n2=en:leopard is an acronym: lentigines, ekg abnormalities, ocular hypertelorism, obstructive cardiomyopathy, pulmonic stenosis, abnormalities of genitalia, retardation of growth, and deafness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions apparent at birth
n1=Lester (signe de) | n2=en:lesions apparent at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions appear in infancy or early childhood
n1=Lester (signe de) | n2=en:lesions appear in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions are present at birth or become apparent in infancy
n1=Lester (signe de) | n2=en:lesions are present at birth or become apparent in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions continue to grow until epiphyseal plate closure
n1=Lester (signe de) | n2=en:lesions continue to grow until epiphyseal plate closure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions grow and spread with age
n1=Lester (signe de) | n2=en:lesions grow and spread with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions increase in size and number with age
n1=Lester (signe de) | n2=en:lesions increase in size and number with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions may become more prominent with sun exposure
n1=Lester (signe de) | n2=en:lesions may become more prominent with sun exposure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions occur mainly on the pinnae of the ears or on the face
n1=Lester (signe de) | n2=en:lesions occur mainly on the pinnae of the ears or on the face | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lesions provoked by friction, sun exposure, heat, and injury
n1=Lester (signe de) | n2=en:lesions provoked by friction, sun exposure, heat, and injury | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:less severe phenotype in females
n1=Lester (signe de) | n2=en:less severe phenotype in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:less than 20% have onset at 18 years of age or less (dominant and recessive)
n1=Lester (signe de) | n2=en:less than 20% have onset at 18 years of age or less (dominant and recessive) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:less than 50% penetrance in some families
n1=Lester (signe de) | n2=en:less than 50% penetrance in some families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in 40% of patients
n1=Lester (signe de) | n2=en:lethal in 40% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in first weeks of life
n1=Lester (signe de) | n2=en:lethal in first weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in males
n1=Lester (signe de) | n2=en:lethal in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in the neonatal period
n1=Lester (signe de) | n2=en:lethal in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in utero or in the perinatal period
n1=Lester (signe de) | n2=en:lethal in utero or in the perinatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lethal in utero or perinatal lethal
n1=Lester (signe de) | n2=en:lethal in utero or perinatal lethal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:levodopa-induced dyskinesias
n1=Lester (signe de) | n2=en:levodopa-induced dyskinesias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:levodopa-responsive
n1=Lester (signe de) | n2=en:levodopa-responsive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:life-threatening in infancy due to sepsis
n1=Lester (signe de) | n2=en:life-threatening in infancy due to sepsis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:life-threatening infections
n1=Lester (signe de) | n2=en:life-threatening infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifelong occurrence
n1=Lester (signe de) | n2=en:lifelong occurrence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifetime risk of breast cancer in male mutation carriers in 6%
n1=Lester (signe de) | n2=en:lifetime risk of breast cancer in male mutation carriers in 6% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifetime risk of breast cancer in mutation carriers is 60 to 85%
n1=Lester (signe de) | n2=en:lifetime risk of breast cancer in mutation carriers is 60 to 85% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifetime risk of breast cancer in mutation carriers is 80 to 90%
n1=Lester (signe de) | n2=en:lifetime risk of breast cancer in mutation carriers is 80 to 90% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifetime risk of ovarian cancer in mutation carriers is 10 to 20%
n1=Lester (signe de) | n2=en:lifetime risk of ovarian cancer in mutation carriers is 10 to 20% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lifetime risk of ovarian cancer in mutation carriers is 40 to 50%
n1=Lester (signe de) | n2=en:lifetime risk of ovarian cancer in mutation carriers is 40 to 50% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:likely allelic to sc phocomelia syndrome (269000)
n1=Lester (signe de) | n2=en:likely allelic to sc phocomelia syndrome (269000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limb malformations are variable
n1=Lester (signe de) | n2=en:limb malformations are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limb reduction defects typically involve the distal phalanges or entire digit, with rare involvement of more proximal limb structures
n1=Lester (signe de) | n2=en:limb reduction defects typically involve the distal phalanges or entire digit, with rare involvement of more proximal limb structures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limb-girdle muscular dystrophy 1a (lgmd1a, 159000) is an allelic disorder with overlapping clinical features
n1=Lester (signe de) | n2=en:limb-girdle muscular dystrophy 1a (lgmd1a, 159000) is an allelic disorder with overlapping clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limb-girdle muscular dystrophy 1b (lgmd1b, 159001) is an allelic disorder with an overlapping phenotype
n1=Lester (signe de) | n2=en:limb-girdle muscular dystrophy 1b (lgmd1b, 159001) is an allelic disorder with an overlapping phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limb-girdle muscular dystrophy type 2l (lgmd2l, 611307) is an allelic disorder
n1=Lester (signe de) | n2=en:limb-girdle muscular dystrophy type 2l (lgmd2l, 611307) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limited clinical information due to surgical removal of lens in affected individuals
n1=Lester (signe de) | n2=en:limited clinical information due to surgical removal of lens in affected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limited clinical information provided
n1=Lester (signe de) | n2=en:limited clinical information provided | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limited clinical information provided for patients with bbs12 mutations (last curated october 2014)
n1=Lester (signe de) | n2=en:limited clinical information provided for patients with bbs12 mutations (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limited clinical information provided for patients with mks1 mutations (last curated october 2014)
n1=Lester (signe de) | n2=en:limited clinical information provided for patients with mks1 mutations (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:limited clinical information provided on patients with bbs7 mutations
n1=Lester (signe de) | n2=en:limited clinical information provided on patients with bbs7 mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:linked to 10q24 trisomy
n1=Lester (signe de) | n2=en:linked to 10q24 trisomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lipodystrophic appearance may be mild or not present
n1=Lester (signe de) | n2=en:lipodystrophic appearance may be mild or not present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:live born infants die within few hours of birth
n1=Lester (signe de) | n2=en:live born infants die within few hours of birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liveborn often die within first week of life
n1=Lester (signe de) | n2=en:liveborn often die within first week of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver disease may be the most predominant finding
n1=Lester (signe de) | n2=en:liver disease may be the most predominant finding | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver enzymes decrease with age
n1=Lester (signe de) | n2=en:liver enzymes decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver failure episodes associated with fever
n1=Lester (signe de) | n2=en:liver failure episodes associated with fever | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver failure episodes cease in later childhood
n1=Lester (signe de) | n2=en:liver failure episodes cease in later childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver functions return to normal after 3 to 4 months
n1=Lester (signe de) | n2=en:liver functions return to normal after 3 to 4 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver involvement can range from mild to severe
n1=Lester (signe de) | n2=en:liver involvement can range from mild to severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver size returns to normal after 3 months to 3 years
n1=Lester (signe de) | n2=en:liver size returns to normal after 3 months to 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:liver symptoms improve with age and disappear after puberty
n1=Lester (signe de) | n2=en:liver symptoms improve with age and disappear after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lmd is the homozygous form of the less severe leri-weill dyschondrosteosis (127300)
n1=Lester (signe de) | n2=en:lmd is the homozygous form of the less severe leri-weill dyschondrosteosis (127300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:long duration
n1=Lester (signe de) | n2=en:long duration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:long headache duration (greater than 12 hours)
n1=Lester (signe de) | n2=en:long headache duration (greater than 12 hours) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:longer disease duration than creutzfeldt-jakob disease
n1=Lester (signe de) | n2=en:longer disease duration than creutzfeldt-jakob disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss initially affects mid and high frequencies
n1=Lester (signe de) | n2=en:loss initially affects mid and high frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of ambulation
n1=Lester (signe de) | n2=en:loss of ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of ambulation within 10 years of onset
n1=Lester (signe de) | n2=en:loss of ambulation within 10 years of onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of independent ambulation (in 2 of 3 patients)
n1=Lester (signe de) | n2=en:loss of independent ambulation (in 2 of 3 patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of independent ambulation due to muscle weakness in adulthood
n1=Lester (signe de) | n2=en:loss of independent ambulation due to muscle weakness in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of independent ambulation in the second decade
n1=Lester (signe de) | n2=en:loss of independent ambulation in the second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of independent walking by teenage years (in some)
n1=Lester (signe de) | n2=en:loss of independent walking by teenage years (in some) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:loss of tumor suppressor gene
n1=Lester (signe de) | n2=en:loss of tumor suppressor gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:low physical performance
n1=Lester (signe de) | n2=en:low physical performance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lower limb involvement occurs before upper limb involvement
n1=Lester (signe de) | n2=en:lower limb involvement occurs before upper limb involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lower limb involvement precedes upper limb involvement
n1=Lester (signe de) | n2=en:lower limb involvement precedes upper limb involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lower limb weakness is presenting feature
n1=Lester (signe de) | n2=en:lower limb weakness is presenting feature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lower limbs more severely affected
n1=Lester (signe de) | n2=en:lower limbs more severely affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:luton and torrance type differentiated based on histologic findings in cartilage
n1=Lester (signe de) | n2=en:luton and torrance type differentiated based on histologic findings in cartilage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lymphedema occurs in childhood
n1=Lester (signe de) | n2=en:lymphedema occurs in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lymphedema resolves by age 3 years
n1=Lester (signe de) | n2=en:lymphedema resolves by age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lymphedema that presents at puberty is called meige disease (153200)
n1=Lester (signe de) | n2=en:lymphedema that presents at puberty is called meige disease (153200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:lysosomal storage vacuoles in trachea, liver, cartilage, and heart
n1=Lester (signe de) | n2=en:lysosomal storage vacuoles in trachea, liver, cartilage, and heart | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:macular degeneration only occurs in some patients at very late age (over 70)
n1=Lester (signe de) | n2=en:macular degeneration only occurs in some patients at very late age (over 70) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:madelung deformity more frequent and more severe in females
n1=Lester (signe de) | n2=en:madelung deformity more frequent and more severe in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:main aspects of phenotype attributed to defects in gtf2ird1 (604318) and gtf2i (601679)
n1=Lester (signe de) | n2=en:main aspects of phenotype attributed to defects in gtf2ird1 (604318) and gtf2i (601679) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:major cause of death is heart failure
n1=Lester (signe de) | n2=en:major cause of death is heart failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:major fetal plasma protein produced by yolk sac and liver
n1=Lester (signe de) | n2=en:major fetal plasma protein produced by yolk sac and liver | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:major fluid shifts may occur in severe cases
n1=Lester (signe de) | n2=en:major fluid shifts may occur in severe cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority are isolated cases
n1=Lester (signe de) | n2=en:majority are isolated cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority are sporadic cases, affected sibs have been described
n1=Lester (signe de) | n2=en:majority are sporadic cases, affected sibs have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority are stillborn or die in early neonatal period
n1=Lester (signe de) | n2=en:majority are stillborn or die in early neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority cases are sporadic
n1=Lester (signe de) | n2=en:majority cases are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority die in neonatal period secondary to respiratory insufficiency
n1=Lester (signe de) | n2=en:majority die in neonatal period secondary to respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of affected individuals are female (85%)
n1=Lester (signe de) | n2=en:majority of affected individuals are female (85%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases (95%) are sporadic
n1=Lester (signe de) | n2=en:majority of cases (95%) are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases are due to de novo mutation
n1=Lester (signe de) | n2=en:majority of cases are due to de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases are male
n1=Lester (signe de) | n2=en:majority of cases are male | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases are secondary to de novo mutation
n1=Lester (signe de) | n2=en:majority of cases are secondary to de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases are sporadic, often in tall, thin men
n1=Lester (signe de) | n2=en:majority of cases are sporadic, often in tall, thin men | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases are sporadic, some autosomal dominant families have been described
n1=Lester (signe de) | n2=en:majority of cases are sporadic, some autosomal dominant families have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases diagnosed at age 10-15 years
n1=Lester (signe de) | n2=en:majority of cases diagnosed at age 10-15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases from middle eastern countries
n1=Lester (signe de) | n2=en:majority of cases from middle eastern countries | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases have been sporadic
n1=Lester (signe de) | n2=en:majority of cases have been sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases have bilateral involvement
n1=Lester (signe de) | n2=en:majority of cases have bilateral involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases in japan
n1=Lester (signe de) | n2=en:majority of cases in japan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases in manitoba indians, northeastern manitoba, canada
n1=Lester (signe de) | n2=en:majority of cases in manitoba indians, northeastern manitoba, canada | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases in the afrikaner population of south africa
n1=Lester (signe de) | n2=en:majority of cases in the afrikaner population of south africa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases occur in brazilian population
n1=Lester (signe de) | n2=en:majority of cases occur in brazilian population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of cases sporadic
n1=Lester (signe de) | n2=en:majority of cases sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of children die before age 2
n1=Lester (signe de) | n2=en:majority of children die before age 2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of children die between 6 months and 5 yrs
n1=Lester (signe de) | n2=en:majority of children die between 6 months and 5 yrs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of eec cases appear to be secondary to tp63 (603273) mutations
n1=Lester (signe de) | n2=en:majority of eec cases appear to be secondary to tp63 (603273) mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of female carriers have skewed x-inactivation (inactivation of chromosome containing the phf6 (300414) mutation)
n1=Lester (signe de) | n2=en:majority of female carriers have skewed x-inactivation (inactivation of chromosome containing the phf6 (300414) mutation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of individuals are healthy
n1=Lester (signe de) | n2=en:majority of individuals are healthy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients are ambulatory
n1=Lester (signe de) | n2=en:majority of patients are ambulatory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients are pyridoxine-responsive
n1=Lester (signe de) | n2=en:majority of patients are pyridoxine-responsive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients are stillborn or die before 5 months of age
n1=Lester (signe de) | n2=en:majority of patients are stillborn or die before 5 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients develop symptoms within the first few weeks of life
n1=Lester (signe de) | n2=en:majority of patients develop symptoms within the first few weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients die in neonatal period secondary to respiratory insufficiency
n1=Lester (signe de) | n2=en:majority of patients die in neonatal period secondary to respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients from italy and southwestern united states
n1=Lester (signe de) | n2=en:majority of patients from italy and southwestern united states | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of patients have normal intelligence
n1=Lester (signe de) | n2=en:majority of patients have normal intelligence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of por deficiency patients have an abs-like phenotype
n1=Lester (signe de) | n2=en:majority of por deficiency patients have an abs-like phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of wilms tumors are sporadic
n1=Lester (signe de) | n2=en:majority of wilms tumors are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:majority of wws patients die within the first year of life
n1=Lester (signe de) | n2=en:majority of wws patients die within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male infertility
n1=Lester (signe de) | n2=en:male infertility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male patients have more severe disease than female patients
n1=Lester (signe de) | n2=en:male patients have more severe disease than female patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male predominance
n1=Lester (signe de) | n2=en:male predominance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male predominance of 3:1 to 5:1
n1=Lester (signe de) | n2=en:male predominance of 3:1 to 5:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male to female ratio 21:8
n1=Lester (signe de) | n2=en:male to female ratio 21:8 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male to female ratio 4:1
n1=Lester (signe de) | n2=en:male to female ratio 4:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male to female ratio 7:1
n1=Lester (signe de) | n2=en:male to female ratio 7:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male to female ratio is greater than 3:1
n1=Lester (signe de) | n2=en:male to female ratio is greater than 3:1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male-limited trait
n1=Lester (signe de) | n2=en:male-limited trait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male-to-female ratio 3 to 1
n1=Lester (signe de) | n2=en:male-to-female ratio 3 to 1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male-to-female ratio of 3:2 in childhood cases
n1=Lester (signe de) | n2=en:male-to-female ratio of 3:2 in childhood cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:male-to-female ratio, 1.8 to 1
n1=Lester (signe de) | n2=en:male-to-female ratio, 1.8 to 1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males are more commonly affected than females
n1=Lester (signe de) | n2=en:males are more commonly affected than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males are more severely affected
n1=Lester (signe de) | n2=en:males are more severely affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males are more severely affected than females
n1=Lester (signe de) | n2=en:males are more severely affected than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males are most severely affected, but females can also be affected
n1=Lester (signe de) | n2=en:males are most severely affected, but females can also be affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males born to affected females are stillborn with exophthalmos, omphalocele, thin calvaria, curved long bones, and hypoplastic/absence thumbs and halluces
n1=Lester (signe de) | n2=en:males born to affected females are stillborn with exophthalmos, omphalocele, thin calvaria, curved long bones, and hypoplastic/absence thumbs and halluces | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males carry mutations in the somatic mosaic state
n1=Lester (signe de) | n2=en:males carry mutations in the somatic mosaic state | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males died in neonatal period
n1=Lester (signe de) | n2=en:males died in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males may be more affected than females
n1=Lester (signe de) | n2=en:males may be more affected than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males more affected than females (2 to 2.5:1)
n1=Lester (signe de) | n2=en:males more affected than females (2 to 2.5:1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males more frequently have severe lesions
n1=Lester (signe de) | n2=en:males more frequently have severe lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males mores severely affected than females
n1=Lester (signe de) | n2=en:males mores severely affected than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:males tend to have earlier onset than females
n1=Lester (signe de) | n2=en:males tend to have earlier onset than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:malnutrition can be severe, requiring total parenteral nutrition
n1=Lester (signe de) | n2=en:malnutrition can be severe, requiring total parenteral nutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:management of homocystinuria includes low methionine, cystine supplemented diet for pyridoxine nonresponders and pyridoxine supplementation for pyridoxine responders
n1=Lester (signe de) | n2=en:management of homocystinuria includes low methionine, cystine supplemented diet for pyridoxine nonresponders and pyridoxine supplementation for pyridoxine responders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:manifestations continue to appear until 5th decade
n1=Lester (signe de) | n2=en:manifestations continue to appear until 5th decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:manifestations of cushing syndrome may be mild
n1=Lester (signe de) | n2=en:manifestations of cushing syndrome may be mild | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:manifestations present in second decade of life
n1=Lester (signe de) | n2=en:manifestations present in second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:manifests in infancy (including neonatal lethal) or childhood
n1=Lester (signe de) | n2=en:manifests in infancy (including neonatal lethal) or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many adults with typical form remain ambulatory
n1=Lester (signe de) | n2=en:many adults with typical form remain ambulatory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many become wheelchair bound
n1=Lester (signe de) | n2=en:many become wheelchair bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases are asymptomatic
n1=Lester (signe de) | n2=en:many cases are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases are sporadic, but somatic and germline mosaicism has been reported
n1=Lester (signe de) | n2=en:many cases are sporadic, but somatic and germline mosaicism has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases due to de novo mutation
n1=Lester (signe de) | n2=en:many cases due to de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases due to de novo mutation or chromosome aberration
n1=Lester (signe de) | n2=en:many cases due to de novo mutation or chromosome aberration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases have submicroscopic subtelomeric deletions of chromosome 9q leading to haploinsufficiency of ehmt1 (607001)
n1=Lester (signe de) | n2=en:many cases have submicroscopic subtelomeric deletions of chromosome 9q leading to haploinsufficiency of ehmt1 (607001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many cases result from de novo mutations
n1=Lester (signe de) | n2=en:many cases result from de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many features are present only in an untreated patient
n1=Lester (signe de) | n2=en:many features are present only in an untreated patient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients are asymptomatic
n1=Lester (signe de) | n2=en:many patients are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients become wheelchair-bound
n1=Lester (signe de) | n2=en:many patients become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients become wheelchair-bound by second or third decade
n1=Lester (signe de) | n2=en:many patients become wheelchair-bound by second or third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients become wheelchair-bound later in life
n1=Lester (signe de) | n2=en:many patients become wheelchair-bound later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients die by 1-3 years of age
n1=Lester (signe de) | n2=en:many patients die by 1-3 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients lose independent mobility after 25 years
n1=Lester (signe de) | n2=en:many patients lose independent mobility after 25 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients recover normally
n1=Lester (signe de) | n2=en:many patients recover normally | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many patients require cardiac pacemakers
n1=Lester (signe de) | n2=en:many patients require cardiac pacemakers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many studies have reported that the phenotype of tuberous sclerosis-1 (tsc1) is less severe than that of tuberous sclerosis-2 (i.e., higher iq, less macules, fewer seizures)
n1=Lester (signe de) | n2=en:many studies have reported that the phenotype of tuberous sclerosis-1 (tsc1) is less severe than that of tuberous sclerosis-2 (i.e., higher iq, less macules, fewer seizures) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:many studies have reported that the phenotype of tuberous sclerosis-2 (tsc2) is more severe than that of tuberous sclerosis-1 (e.g., lower iq, more seizures, more macules, cust-like cortical tubers)
n1=Lester (signe de) | n2=en:many studies have reported that the phenotype of tuberous sclerosis-2 (tsc2) is more severe than that of tuberous sclerosis-1 (e.g., lower iq, more seizures, more macules, cust-like cortical tubers) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked clinical heterogeneity
n1=Lester (signe de) | n2=en:marked clinical heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked clinical variability within families
n1=Lester (signe de) | n2=en:marked clinical variability within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked favorable response to l-dopa treatment
n1=Lester (signe de) | n2=en:marked favorable response to l-dopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked heterogeneity
n1=Lester (signe de) | n2=en:marked heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked inter- and intrafamilial variability, ranging from prenatal onset with severe symptoms to asymptomatic affected individuals
n1=Lester (signe de) | n2=en:marked inter- and intrafamilial variability, ranging from prenatal onset with severe symptoms to asymptomatic affected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked intrafamilial and interfamilial variability
n1=Lester (signe de) | n2=en:marked intrafamilial and interfamilial variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked intrafamilial variability of clinical features
n1=Lester (signe de) | n2=en:marked intrafamilial variability of clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked phenotypic variability
n1=Lester (signe de) | n2=en:marked phenotypic variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked phenotypic variability, even within an individual
n1=Lester (signe de) | n2=en:marked phenotypic variability, even within an individual | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked variability in severity of the skin lesions
n1=Lester (signe de) | n2=en:marked variability in severity of the skin lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked variability in the deletion size
n1=Lester (signe de) | n2=en:marked variability in the deletion size | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marked variation in severity - severe early onset disease (neonatal period) and milder juvenile disease (onset 8-13 years)
n1=Lester (signe de) | n2=en:marked variation in severity - severe early onset disease (neonatal period) and milder juvenile disease (onset 8-13 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:marshall syndrome is allelic to stickler syndrome, type 2 (604841)
n1=Lester (signe de) | n2=en:marshall syndrome is allelic to stickler syndrome, type 2 (604841) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:masa is an acronym - mental retardation, adducted thumbs, shuffling gait, and aphasia
n1=Lester (signe de) | n2=en:masa is an acronym - mental retardation, adducted thumbs, shuffling gait, and aphasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:massive aortic aneurysm can cause airway compression in affected infants
n1=Lester (signe de) | n2=en:massive aortic aneurysm can cause airway compression in affected infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal anticipation bias
n1=Lester (signe de) | n2=en:maternal anticipation bias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal breast milk is protective
n1=Lester (signe de) | n2=en:maternal breast milk is protective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal imprinting
n1=Lester (signe de) | n2=en:maternal imprinting | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal imprinting of sgce results in reduced penetrance of the disorder when the mutation is inherited from the mother
n1=Lester (signe de) | n2=en:maternal imprinting of sgce results in reduced penetrance of the disorder when the mutation is inherited from the mother | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal oligohydramnios
n1=Lester (signe de) | n2=en:maternal oligohydramnios | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:maternal uniparental disomy (upd)7 reported in some cases
n1=Lester (signe de) | n2=en:maternal uniparental disomy (upd)7 reported in some cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be associated with other anomalies (e.g. okihiro syndrome (607323), wildervanck syndrome (314600))
n1=Lester (signe de) | n2=en:may be associated with other anomalies (e.g. okihiro syndrome (607323), wildervanck syndrome (314600)) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be associated with polymorphisms in some surfactant genes, including sftpa1 (178630), sftpb (178640), and sftpc (178620)
n1=Lester (signe de) | n2=en:may be associated with polymorphisms in some surfactant genes, including sftpa1 (178630), sftpb (178640), and sftpc (178620) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be asymptomatic
n1=Lester (signe de) | n2=en:may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be benign condition
n1=Lester (signe de) | n2=en:may be benign condition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be due to imprinting defect
n1=Lester (signe de) | n2=en:may be due to imprinting defect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be exacerbated by febrile illness
n1=Lester (signe de) | n2=en:may be exacerbated by febrile illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be extreme phenotype of generalized epilepsy with febrile seizures plus (gefs+, 604233)
n1=Lester (signe de) | n2=en:may be extreme phenotype of generalized epilepsy with febrile seizures plus (gefs+, 604233) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be fatal
n1=Lester (signe de) | n2=en:may be fatal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be fatal in infancy
n1=Lester (signe de) | n2=en:may be fatal in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be induced by fever or hot bath
n1=Lester (signe de) | n2=en:may be induced by fever or hot bath | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be lethal if untreated
n1=Lester (signe de) | n2=en:may be lethal if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be lethal in infancy
n1=Lester (signe de) | n2=en:may be lethal in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be lethal in infancy if untreated
n1=Lester (signe de) | n2=en:may be lethal in infancy if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be lethal in the neonatal period
n1=Lester (signe de) | n2=en:may be lethal in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be misdiagnosed as nightmares, night terrors, parasomnias, or psychiatric disorders
n1=Lester (signe de) | n2=en:may be misdiagnosed as nightmares, night terrors, parasomnias, or psychiatric disorders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be precipitated by minor illness (e.g., viral infection, fever)
n1=Lester (signe de) | n2=en:may be precipitated by minor illness (e.g., viral infection, fever) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be present in asymptomatic adults
n1=Lester (signe de) | n2=en:may be present in asymptomatic adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be progressive
n1=Lester (signe de) | n2=en:may be progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be same disorder as autosomal recessive optic atrophy 3 (258501)
n1=Lester (signe de) | n2=en:may be same disorder as autosomal recessive optic atrophy 3 (258501) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be same entity as elejalde syndrome (256710)
n1=Lester (signe de) | n2=en:may be same entity as elejalde syndrome (256710) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be same entity as griscelli syndrome type i (214450) caused by mutation in the myosin va gene (160777)
n1=Lester (signe de) | n2=en:may be same entity as griscelli syndrome type i (214450) caused by mutation in the myosin va gene (160777) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be seen in combination with duchenne muscular dystrophy (dmd, 310200) and/or glycerol kinase deficiency (307030) as part of a contiguous gene deletion syndrome
n1=Lester (signe de) | n2=en:may be seen in combination with duchenne muscular dystrophy (dmd, 310200) and/or glycerol kinase deficiency (307030) as part of a contiguous gene deletion syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be seen with other forms of cancer in a family
n1=Lester (signe de) | n2=en:may be seen with other forms of cancer in a family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be triggered by increased practice
n1=Lester (signe de) | n2=en:may be triggered by increased practice | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be triggered by medications, including antineoplastic agents, immunotherapeutic agents, and antiplatelet agents
n1=Lester (signe de) | n2=en:may be triggered by medications, including antineoplastic agents, immunotherapeutic agents, and antiplatelet agents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be triggered by minor head trauma
n1=Lester (signe de) | n2=en:may be triggered by minor head trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may be x-linked
n1=Lester (signe de) | n2=en:may be x-linked | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may coexist with autoimmune vitiligo or thyroiditis
n1=Lester (signe de) | n2=en:may coexist with autoimmune vitiligo or thyroiditis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may fade with age
n1=Lester (signe de) | n2=en:may fade with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may have less severe phenotype than rsts patients with crebbp mutations
n1=Lester (signe de) | n2=en:may have less severe phenotype than rsts patients with crebbp mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may have seasonal variance in severity
n1=Lester (signe de) | n2=en:may have seasonal variance in severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may manifest as 'ataxic' phenotype without parkinsonian features
n1=Lester (signe de) | n2=en:may manifest as 'ataxic' phenotype without parkinsonian features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may manifest as late-onset 'parkinsonian' phenotype without severe ataxic features
n1=Lester (signe de) | n2=en:may manifest as late-onset 'parkinsonian' phenotype without severe ataxic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may not be clinically manifest until middle life
n1=Lester (signe de) | n2=en:may not be clinically manifest until middle life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may occur cormorbidly with poland syndrome (173800)
n1=Lester (signe de) | n2=en:may occur cormorbidly with poland syndrome (173800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may occur in adults (also in pregnancy)
n1=Lester (signe de) | n2=en:may occur in adults (also in pregnancy) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may or may not be responsive to pyridoxine (vitamin b6) treatment
n1=Lester (signe de) | n2=en:may or may not be responsive to pyridoxine (vitamin b6) treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may present in infancy with episodes of severe metabolic decompensation
n1=Lester (signe de) | n2=en:may present in infancy with episodes of severe metabolic decompensation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may progress to other body regions after many years
n1=Lester (signe de) | n2=en:may progress to other body regions after many years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may progress to upper limbs
n1=Lester (signe de) | n2=en:may progress to upper limbs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may regress
n1=Lester (signe de) | n2=en:may regress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may regress in adulthood
n1=Lester (signe de) | n2=en:may regress in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may respond to cholinesterase inhibitors
n1=Lester (signe de) | n2=en:may respond to cholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may respond to cholinesterase inhibitors of amifampridine
n1=Lester (signe de) | n2=en:may respond to cholinesterase inhibitors of amifampridine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may result in death in neonatal period or early childhood
n1=Lester (signe de) | n2=en:may result in death in neonatal period or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may result in early death
n1=Lester (signe de) | n2=en:may result in early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may result in early death from severe diarrhea
n1=Lester (signe de) | n2=en:may result in early death from severe diarrhea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may result in sudden death
n1=Lester (signe de) | n2=en:may result in sudden death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:may show good response to levodopa
n1=Lester (signe de) | n2=en:may show good response to levodopa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at diagnosis 16 years (range 6 to 22)
n1=Lester (signe de) | n2=en:mean age at diagnosis 16 years (range 6 to 22) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at diagnosis 8.8 years (range 0.2-23 years)
n1=Lester (signe de) | n2=en:mean age at diagnosis 8.8 years (range 0.2-23 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at diagnosis is 38 years(range 11-63 years)
n1=Lester (signe de) | n2=en:mean age at diagnosis is 38 years(range 11-63 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 10.6 years
n1=Lester (signe de) | n2=en:mean age at onset 10.6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 11.4 years (range 4 to 35)
n1=Lester (signe de) | n2=en:mean age at onset 11.4 years (range 4 to 35) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 12.5 years (range 2 to 15 years)
n1=Lester (signe de) | n2=en:mean age at onset 12.5 years (range 2 to 15 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 15.2 years
n1=Lester (signe de) | n2=en:mean age at onset 15.2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 16.5 years (range 9 to 35 years)
n1=Lester (signe de) | n2=en:mean age at onset 16.5 years (range 9 to 35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 22 years (range 7 to 50 years)
n1=Lester (signe de) | n2=en:mean age at onset 22 years (range 7 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 23.9 years (range 10 to 55 years)
n1=Lester (signe de) | n2=en:mean age at onset 23.9 years (range 10 to 55 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 24 years (range 14 to 33 years)
n1=Lester (signe de) | n2=en:mean age at onset 24 years (range 14 to 33 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 27 years (range 9 to 42)
n1=Lester (signe de) | n2=en:mean age at onset 27 years (range 9 to 42) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 28 years
n1=Lester (signe de) | n2=en:mean age at onset 28 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 30.7 years (range 6 to 60 years)
n1=Lester (signe de) | n2=en:mean age at onset 30.7 years (range 6 to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 32 years
n1=Lester (signe de) | n2=en:mean age at onset 32 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 33 years (range 20-60)
n1=Lester (signe de) | n2=en:mean age at onset 33 years (range 20-60) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 35 years (range 20-60)
n1=Lester (signe de) | n2=en:mean age at onset 35 years (range 20-60) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 41 years (range 18 to 61)
n1=Lester (signe de) | n2=en:mean age at onset 41 years (range 18 to 61) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 45 years
n1=Lester (signe de) | n2=en:mean age at onset 45 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 46.5 years (range 19-64)
n1=Lester (signe de) | n2=en:mean age at onset 46.5 years (range 19-64) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 48 years (range 38 to 64)
n1=Lester (signe de) | n2=en:mean age at onset 48 years (range 38 to 64) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 5 years
n1=Lester (signe de) | n2=en:mean age at onset 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 57-60 years
n1=Lester (signe de) | n2=en:mean age at onset 57-60 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset 66.8 years (range 47-77)
n1=Lester (signe de) | n2=en:mean age at onset 66.8 years (range 47-77) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset for sporadic cjd is 60 years (range, 50 to 70 years)
n1=Lester (signe de) | n2=en:mean age at onset for sporadic cjd is 60 years (range, 50 to 70 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset for variant cjd is 29 years (before age 45 years)
n1=Lester (signe de) | n2=en:mean age at onset for variant cjd is 29 years (before age 45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset is 10.4 years
n1=Lester (signe de) | n2=en:mean age at onset is 10.4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset is 13 years (range 6 to 43)
n1=Lester (signe de) | n2=en:mean age at onset is 13 years (range 6 to 43) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of bone disease is 40 years (range 23-65)
n1=Lester (signe de) | n2=en:mean age at onset of bone disease is 40 years (range 23-65) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of bone fractures, 24 years
n1=Lester (signe de) | n2=en:mean age at onset of bone fractures, 24 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of cerebellar ataxia is 52.8 years
n1=Lester (signe de) | n2=en:mean age at onset of cerebellar ataxia is 52.8 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of dementia is 57 years
n1=Lester (signe de) | n2=en:mean age at onset of dementia is 57 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of hypoglycemia may be delayed (median, 9 months, diagnosis sometimes made in adulthood)
n1=Lester (signe de) | n2=en:mean age at onset of hypoglycemia may be delayed (median, 9 months, diagnosis sometimes made in adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of migraines is 42 years
n1=Lester (signe de) | n2=en:mean age at onset of migraines is 42 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of muscle disease is 42 years (range 24-61)
n1=Lester (signe de) | n2=en:mean age at onset of muscle disease is 42 years (range 24-61) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at onset of proximal muscle weakness, 31 years
n1=Lester (signe de) | n2=en:mean age at onset of proximal muscle weakness, 31 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at resolution of symptoms 10 years
n1=Lester (signe de) | n2=en:mean age at resolution of symptoms 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age at termination 3 to 4 years
n1=Lester (signe de) | n2=en:mean age at termination 3 to 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of death is 34 years
n1=Lester (signe de) | n2=en:mean age of death is 34 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of diagnosis 40 years
n1=Lester (signe de) | n2=en:mean age of diagnosis 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of diagnosis is 40 years (range 11 to 79 years)
n1=Lester (signe de) | n2=en:mean age of diagnosis is 40 years (range 11 to 79 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of diagnosis of renal cell carcinoma is 46 years
n1=Lester (signe de) | n2=en:mean age of diagnosis of renal cell carcinoma is 46 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of diagnosis of uterine leiomyomas is 30 years
n1=Lester (signe de) | n2=en:mean age of diagnosis of uterine leiomyomas is 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 14-24 months
n1=Lester (signe de) | n2=en:mean age of onset 14-24 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 16 to 19 years
n1=Lester (signe de) | n2=en:mean age of onset 16 to 19 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 18 years
n1=Lester (signe de) | n2=en:mean age of onset 18 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 20.6 years
n1=Lester (signe de) | n2=en:mean age of onset 20.6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 21 years (range 14-35 years)
n1=Lester (signe de) | n2=en:mean age of onset 21 years (range 14-35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 22 years (range 5-54)
n1=Lester (signe de) | n2=en:mean age of onset 22 years (range 5-54) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 30 years
n1=Lester (signe de) | n2=en:mean age of onset 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 30 years (range 25-42)
n1=Lester (signe de) | n2=en:mean age of onset 30 years (range 25-42) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 30 years (range first to seventh decade)
n1=Lester (signe de) | n2=en:mean age of onset 30 years (range first to seventh decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 31 years (range 5-60)
n1=Lester (signe de) | n2=en:mean age of onset 31 years (range 5-60) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 34 months
n1=Lester (signe de) | n2=en:mean age of onset 34 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 35-40 years
n1=Lester (signe de) | n2=en:mean age of onset 35-40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 50 to 52 years
n1=Lester (signe de) | n2=en:mean age of onset 50 to 52 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 50.2 years
n1=Lester (signe de) | n2=en:mean age of onset 50.2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset 56 years
n1=Lester (signe de) | n2=en:mean age of onset 56 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset about 62 years (45-79 years)
n1=Lester (signe de) | n2=en:mean age of onset about 62 years (45-79 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset in third decade
n1=Lester (signe de) | n2=en:mean age of onset in third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of onset, 5 years
n1=Lester (signe de) | n2=en:mean age of onset, 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean age of presentation of renal cancer is 50 years, but earlier onset has been reported
n1=Lester (signe de) | n2=en:mean age of presentation of renal cancer is 50 years, but earlier onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean duration of symptoms 4.2 plus or minus 2.4 years
n1=Lester (signe de) | n2=en:mean duration of symptoms 4.2 plus or minus 2.4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mean survival 5 months
n1=Lester (signe de) | n2=en:mean survival 5 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mechanical ventilation may be required
n1=Lester (signe de) | n2=en:mechanical ventilation may be required | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mecp2 mutations are those found in females with rett syndrome (312750)
n1=Lester (signe de) | n2=en:mecp2 mutations are those found in females with rett syndrome (312750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:med is a heterogeneous disorder (see med1 (132400), med2 (600204), med3 (600969), med4 (226900), med5 (608078), and med with diabetes mellitus (226980))
n1=Lester (signe de) | n2=en:med is a heterogeneous disorder (see med1 (132400), med2 (600204), med3 (600969), med4 (226900), med5 (608078), and med with diabetes mellitus (226980)) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:medial onset of end stage renal disease 13 years
n1=Lester (signe de) | n2=en:medial onset of end stage renal disease 13 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age at diagnosis 7 years
n1=Lester (signe de) | n2=en:median age at diagnosis 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age at diagnosis, 59 years
n1=Lester (signe de) | n2=en:median age at diagnosis, 59 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age at onset 23 years
n1=Lester (signe de) | n2=en:median age at onset 23 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age at onset is 21 years
n1=Lester (signe de) | n2=en:median age at onset is 21 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age at onset of puberty is 5.75 years in affected girls and 8.1 years in affected boys
n1=Lester (signe de) | n2=en:median age at onset of puberty is 5.75 years in affected girls and 8.1 years in affected boys | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of diagnosis - 15 years
n1=Lester (signe de) | n2=en:median age of diagnosis - 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of diagnosis is 28 years
n1=Lester (signe de) | n2=en:median age of diagnosis is 28 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of onset of leukoplakia - 7 years (range 1-26 years)
n1=Lester (signe de) | n2=en:median age of onset of leukoplakia - 7 years (range 1-26 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of onset of nail dystrophy - 7 years (range 1-6 years)
n1=Lester (signe de) | n2=en:median age of onset of nail dystrophy - 7 years (range 1-6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of onset of pancytopenia - 10 years (range 1-32 years)
n1=Lester (signe de) | n2=en:median age of onset of pancytopenia - 10 years (range 1-32 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median age of onset of pigmentation - 8 years (range 1-15 years)
n1=Lester (signe de) | n2=en:median age of onset of pigmentation - 8 years (range 1-15 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median life expectancy, 13.4 years
n1=Lester (signe de) | n2=en:median life expectancy, 13.4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median onset of neurologic symptoms is 13 years (range 5 to 28)
n1=Lester (signe de) | n2=en:median onset of neurologic symptoms is 13 years (range 5 to 28) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median onset of proteinuria is 18 years (range 10 to 21)
n1=Lester (signe de) | n2=en:median onset of proteinuria is 18 years (range 10 to 21) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median survival 5.7 years
n1=Lester (signe de) | n2=en:median survival 5.7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:median survival is > 50 years
n1=Lester (signe de) | n2=en:median survival is > 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:medical director review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:medical director review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:medullary thyroid cancer is aggressive and can occur in childhood
n1=Lester (signe de) | n2=en:medullary thyroid cancer is aggressive and can occur in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:meiotic origin >95% maternal, mostly meiosis i
n1=Lester (signe de) | n2=en:meiotic origin >95% maternal, mostly meiosis i | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:melnick-needles syndrome (mns, 309350) is an allelic disorder
n1=Lester (signe de) | n2=en:melnick-needles syndrome (mns, 309350) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mental retardation likely secondary to neonatal hypoxia
n1=Lester (signe de) | n2=en:mental retardation likely secondary to neonatal hypoxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mesomelia becomes more evident with age
n1=Lester (signe de) | n2=en:mesomelia becomes more evident with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:metabolic decompensation, episodic
n1=Lester (signe de) | n2=en:metabolic decompensation, episodic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:metabolic encephalomyopathic crises often triggered by infection
n1=Lester (signe de) | n2=en:metabolic encephalomyopathic crises often triggered by infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:metabolic rate^resting:engrat:pt:^patient:qn
n1=Lester (signe de) | n2=en:metabolic rate^resting:engrat:pt:^patient:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:microdeletion is approximately 1.5mb in length
n1=Lester (signe de) | n2=en:microdeletion is approximately 1.5mb in length | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:middle age onset
n1=Lester (signe de) | n2=en:middle age onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:midline defects
n1=Lester (signe de) | n2=en:midline defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild adult form, with onset after age 13 years, no cardiac involvement, and restricted to muscle involvement with rhabdomyolysis
n1=Lester (signe de) | n2=en:mild adult form, with onset after age 13 years, no cardiac involvement, and restricted to muscle involvement with rhabdomyolysis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild asymmetric regional disease (e.g. 180380.0029)
n1=Lester (signe de) | n2=en:mild asymmetric regional disease (e.g. 180380.0029) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild cases show clinical, biochemical, and mri improvement after the second year of life
n1=Lester (signe de) | n2=en:mild cases show clinical, biochemical, and mri improvement after the second year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild disease course
n1=Lester (signe de) | n2=en:mild disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild disorder
n1=Lester (signe de) | n2=en:mild disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild expression in heterozygous carriers
n1=Lester (signe de) | n2=en:mild expression in heterozygous carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild facial dysmorphism is associated with duplication of the flna gene
n1=Lester (signe de) | n2=en:mild facial dysmorphism is associated with duplication of the flna gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild features such as digital clubbing may be apparent in older heterozygotes
n1=Lester (signe de) | n2=en:mild features such as digital clubbing may be apparent in older heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild involvement of face and arms
n1=Lester (signe de) | n2=en:mild involvement of face and arms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild manifestations in carrier females (cleft lip, cleft tongue)
n1=Lester (signe de) | n2=en:mild manifestations in carrier females (cleft lip, cleft tongue) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild phenotype
n1=Lester (signe de) | n2=en:mild phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild phenotype onset - 11-18 months
n1=Lester (signe de) | n2=en:mild phenotype onset - 11-18 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild symptoms may occur in teenage years
n1=Lester (signe de) | n2=en:mild symptoms may occur in teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mild to severe forms of disease
n1=Lester (signe de) | n2=en:mild to severe forms of disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy
n1=Lester (signe de) | n2=en:milder cases have isolated recurrent daytime sleepiness and/or lapses into sleep without cataplexy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder cases have onset in childhood or adulthood with history of muscle weakness since infancy
n1=Lester (signe de) | n2=en:milder cases have onset in childhood or adulthood with history of muscle weakness since infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder disease with a more favorable prognosis than cmd1u (613694) due to psen1 mutations
n1=Lester (signe de) | n2=en:milder disease with a more favorable prognosis than cmd1u (613694) due to psen1 mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder expression in female heterozygotes
n1=Lester (signe de) | n2=en:milder expression in female heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder form with onset in childhood, absence seizures, and learning difficulties
n1=Lester (signe de) | n2=en:milder form with onset in childhood, absence seizures, and learning difficulties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder manifestations in heterozygous females (broad face, downslanting palpebral fissures, and cleft palate)
n1=Lester (signe de) | n2=en:milder manifestations in heterozygous females (broad face, downslanting palpebral fissures, and cleft palate) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder phenotype associated with aberrant function of a single domain of the zeb2 protein rather than complete haploinsufficiency of zeb2
n1=Lester (signe de) | n2=en:milder phenotype associated with aberrant function of a single domain of the zeb2 protein rather than complete haploinsufficiency of zeb2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:milder, childhood form, with onset by age 4 years, lesser cardiac involvement, and hypoketotic hypoglycemia
n1=Lester (signe de) | n2=en:milder, childhood form, with onset by age 4 years, lesser cardiac involvement, and hypoketotic hypoglycemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mildly progressive
n1=Lester (signe de) | n2=en:mildly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:minimal response to surfactant treatment
n1=Lester (signe de) | n2=en:minimal response to surfactant treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:minimum duplication includes bhlha9 (615416)
n1=Lester (signe de) | n2=en:minimum duplication includes bhlha9 (615416) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:minimum region of duplication is a 9.1-kb region located 40kb 5-prime of the ihh gene
n1=Lester (signe de) | n2=en:minimum region of duplication is a 9.1-kb region located 40kb 5-prime of the ihh gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:miscellaneous
n1=Lester (signe de) | n2=en:miscellaneous | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mliii is a heterogeneous disorder
n1=Lester (signe de) | n2=en:mliii is a heterogeneous disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mode of inheritance is uncertain
n1=Lester (signe de) | n2=en:mode of inheritance is uncertain | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mode of inheritance is unclear
n1=Lester (signe de) | n2=en:mode of inheritance is unclear | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mode of inheritance is unclear, x-linked recessive inheritance could not be ruled out
n1=Lester (signe de) | n2=en:mode of inheritance is unclear, x-linked recessive inheritance could not be ruled out | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:moderate age-related improvement of pancreatic function
n1=Lester (signe de) | n2=en:moderate age-related improvement of pancreatic function | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:momo is an acronym - macrosomia, obesity, macrocrania, ocular abnormalities
n1=Lester (signe de) | n2=en:momo is an acronym - macrosomia, obesity, macrocrania, ocular abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in ashkenazi jews
n1=Lester (signe de) | n2=en:more common in ashkenazi jews | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in females
n1=Lester (signe de) | n2=en:more common in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in females (male:female ratio 4:1)
n1=Lester (signe de) | n2=en:more common in females (male:female ratio 4:1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in males
n1=Lester (signe de) | n2=en:more common in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in men (9:1 male:female ratio)
n1=Lester (signe de) | n2=en:more common in men (9:1 male:female ratio) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in men than women
n1=Lester (signe de) | n2=en:more common in men than women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in women
n1=Lester (signe de) | n2=en:more common in women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more common in women (90%)
n1=Lester (signe de) | n2=en:more common in women (90%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more commonly observed in women
n1=Lester (signe de) | n2=en:more commonly observed in women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more frequent in females
n1=Lester (signe de) | n2=en:more frequent in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more frequent in individuals of asian descent
n1=Lester (signe de) | n2=en:more frequent in individuals of asian descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more frequent in males
n1=Lester (signe de) | n2=en:more frequent in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more prevalent in females
n1=Lester (signe de) | n2=en:more prevalent in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more severe in males than in females
n1=Lester (signe de) | n2=en:more severe in males than in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:more than half of patients develop retinal detachments and/or retinoschisis later in life
n1=Lester (signe de) | n2=en:more than half of patients develop retinal detachments and/or retinoschisis later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:moroccan jewish and ashkenazi jewish families have been described
n1=Lester (signe de) | n2=en:moroccan jewish and ashkenazi jewish families have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mortality approximately 20% in first 2 years
n1=Lester (signe de) | n2=en:mortality approximately 20% in first 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mortality, premature
n1=Lester (signe de) | n2=en:mortality, premature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mosaic distribution of lesions
n1=Lester (signe de) | n2=en:mosaic distribution of lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most (80 to 90%) of cases result from deletions of the sts gene
n1=Lester (signe de) | n2=en:most (80 to 90%) of cases result from deletions of the sts gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most affected infants die in the first month of life
n1=Lester (signe de) | n2=en:most affected infants die in the first month of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most affected infants die shortly after birth from respiratory failure
n1=Lester (signe de) | n2=en:most affected infants die shortly after birth from respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most affected males die of respiratory failure within the first months of life
n1=Lester (signe de) | n2=en:most affected males die of respiratory failure within the first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most affected patients die in childhood
n1=Lester (signe de) | n2=en:most affected patients die in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most become wheelchair-bound late in life
n1=Lester (signe de) | n2=en:most become wheelchair-bound late in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most carrier females have mild mental retardation and subtle facial changes
n1=Lester (signe de) | n2=en:most carrier females have mild mental retardation and subtle facial changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most case are sporadic
n1=Lester (signe de) | n2=en:most case are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases (98%) caused by expanded trinucleotide repeat (cgg)n in the fmr1 gene (309550.0004)
n1=Lester (signe de) | n2=en:most cases (98%) caused by expanded trinucleotide repeat (cgg)n in the fmr1 gene (309550.0004) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are autosomal dominant, recessive inheritance has rarely been reported
n1=Lester (signe de) | n2=en:most cases are autosomal dominant, recessive inheritance has rarely been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are caused by mutation in the phox2b gene
n1=Lester (signe de) | n2=en:most cases are caused by mutation in the phox2b gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are caused by the factor v leiden mutation (r506q, 612309.0001)
n1=Lester (signe de) | n2=en:most cases are caused by the factor v leiden mutation (r506q, 612309.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are de novo occurrences, but rare autosomal dominant inheritance has been reported
n1=Lester (signe de) | n2=en:most cases are de novo occurrences, but rare autosomal dominant inheritance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are isolated
n1=Lester (signe de) | n2=en:most cases are isolated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases are responsive to steroids
n1=Lester (signe de) | n2=en:most cases are responsive to steroids | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases do not have mutations in the mapt gene, but map to chromosome 17q
n1=Lester (signe de) | n2=en:most cases do not have mutations in the mapt gene, but map to chromosome 17q | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases due to de novo mutation
n1=Lester (signe de) | n2=en:most cases due to de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases occur de novo
n1=Lester (signe de) | n2=en:most cases occur de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases result from a de novo mutation
n1=Lester (signe de) | n2=en:most cases result from a de novo mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases result from de novo mutation or deletion of rai1 (607642)
n1=Lester (signe de) | n2=en:most cases result from de novo mutation or deletion of rai1 (607642) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases result from de novo mutations
n1=Lester (signe de) | n2=en:most cases result from de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most cases sporadic
n1=Lester (signe de) | n2=en:most cases sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most children become wheelchair-bound
n1=Lester (signe de) | n2=en:most children become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common age of clinical onset ranges from 16 to 33 years
n1=Lester (signe de) | n2=en:most common age of clinical onset ranges from 16 to 33 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common cancer in men aged 15-40 years
n1=Lester (signe de) | n2=en:most common cancer in men aged 15-40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common disorder of fatty acid oxidation (1/13,000 births)
n1=Lester (signe de) | n2=en:most common disorder of fatty acid oxidation (1/13,000 births) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common episodic ataxia syndrome
n1=Lester (signe de) | n2=en:most common episodic ataxia syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of autosomal dominant hereditary spastic paraplegia (accounts for 40% of spg cases)
n1=Lester (signe de) | n2=en:most common form of autosomal dominant hereditary spastic paraplegia (accounts for 40% of spg cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of bowel obstruction in infancy
n1=Lester (signe de) | n2=en:most common form of bowel obstruction in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of childhood idiopathic epilepsy
n1=Lester (signe de) | n2=en:most common form of childhood idiopathic epilepsy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of congenital methemoglobinemia
n1=Lester (signe de) | n2=en:most common form of congenital methemoglobinemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of inherited, congenital hydrocephalus
n1=Lester (signe de) | n2=en:most common form of inherited, congenital hydrocephalus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common form of porphyria
n1=Lester (signe de) | n2=en:most common form of porphyria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common genetic abnormality is a (gaa)n trinucleotide repeat expansion in intron 1 of the fxn gene (606829.0001)
n1=Lester (signe de) | n2=en:most common genetic abnormality is a (gaa)n trinucleotide repeat expansion in intron 1 of the fxn gene (606829.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common inherited ataxia
n1=Lester (signe de) | n2=en:most common inherited ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common inherited bleeding disorder
n1=Lester (signe de) | n2=en:most common inherited bleeding disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common inherited giant platelet disorder
n1=Lester (signe de) | n2=en:most common inherited giant platelet disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common muscle disease of older persons
n1=Lester (signe de) | n2=en:most common muscle disease of older persons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common mutation is leu276ile (606596.0004)
n1=Lester (signe de) | n2=en:most common mutation is leu276ile (606596.0004) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common subtype of frontotemporal dementia (600274)
n1=Lester (signe de) | n2=en:most common subtype of frontotemporal dementia (600274) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most common terminal deletion syndrome
n1=Lester (signe de) | n2=en:most common terminal deletion syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most frequently affected joints - hands (98%) and feet (88%)
n1=Lester (signe de) | n2=en:most frequently affected joints - hands (98%) and feet (88%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most have onset in first or second decade
n1=Lester (signe de) | n2=en:most have onset in first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most have resolution of symptoms between 6 and 12 months
n1=Lester (signe de) | n2=en:most have resolution of symptoms between 6 and 12 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most individuals are asymptomatic
n1=Lester (signe de) | n2=en:most individuals are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most individuals are wheelchair-bound or bedridden by adolescence
n1=Lester (signe de) | n2=en:most individuals are wheelchair-bound or bedridden by adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most mutations occur de novo
n1=Lester (signe de) | n2=en:most mutations occur de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients appear unaffected in the first year of life
n1=Lester (signe de) | n2=en:most patients appear unaffected in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are asymptomatic
n1=Lester (signe de) | n2=en:most patients are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are asymptomatic and are detected by newborn screening
n1=Lester (signe de) | n2=en:most patients are asymptomatic and are detected by newborn screening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are clinically asymptomatic
n1=Lester (signe de) | n2=en:most patients are clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are clinically asymptomatic and show normal development
n1=Lester (signe de) | n2=en:most patients are clinically asymptomatic and show normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are female
n1=Lester (signe de) | n2=en:most patients are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are from finland
n1=Lester (signe de) | n2=en:most patients are from finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are severely affected
n1=Lester (signe de) | n2=en:most patients are severely affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients are stillborn or die in immediate neonatal period
n1=Lester (signe de) | n2=en:most patients are stillborn or die in immediate neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become seizure-free by age 3 or 4 years
n1=Lester (signe de) | n2=en:most patients become seizure-free by age 3 or 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound after 20 to 30 years
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound after 20 to 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound in adolescence
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound in adolescence or as young adults
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound in adolescence or as young adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound in later childhood
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound in later childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound in the second or third decades
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound in the second or third decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients become wheelchair-bound in the second to fourth decades
n1=Lester (signe de) | n2=en:most patients become wheelchair-bound in the second to fourth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients develop symptoms while on prophylactic vitamin d supplementation in infancy
n1=Lester (signe de) | n2=en:most patients develop symptoms while on prophylactic vitamin d supplementation in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die from heart failure
n1=Lester (signe de) | n2=en:most patients die from heart failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in childhood
n1=Lester (signe de) | n2=en:most patients die in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in early childhood
n1=Lester (signe de) | n2=en:most patients die in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in first years of life
n1=Lester (signe de) | n2=en:most patients die in first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in infancy
n1=Lester (signe de) | n2=en:most patients die in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in infancy features of pseudoxanthoma elasticum, an allelic disorder, have not yet been reported in gaci2 patients (the 4 surviving patients reported as of january 2012 are all age 5 years or less)
n1=Lester (signe de) | n2=en:most patients die in infancy features of pseudoxanthoma elasticum, an allelic disorder, have not yet been reported in gaci2 patients (the 4 surviving patients reported as of january 2012 are all age 5 years or less) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in the first days of life
n1=Lester (signe de) | n2=en:most patients die in the first days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in the first months or years of life
n1=Lester (signe de) | n2=en:most patients die in the first months or years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die in the neonatal period due to respiratory insufficiency
n1=Lester (signe de) | n2=en:most patients die in the neonatal period due to respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die of hepatic failure by 9 months of age
n1=Lester (signe de) | n2=en:most patients die of hepatic failure by 9 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die of renal failure in early adulthood
n1=Lester (signe de) | n2=en:most patients die of renal failure in early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients die within the first year of life
n1=Lester (signe de) | n2=en:most patients die within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients do not learn to sit or walk
n1=Lester (signe de) | n2=en:most patients do not learn to sit or walk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have a family history of fragile x syndrome
n1=Lester (signe de) | n2=en:most patients have a family history of fragile x syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have adult onset of symptoms
n1=Lester (signe de) | n2=en:most patients have adult onset of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have contiguous gene deletion syndrome involving xp22
n1=Lester (signe de) | n2=en:most patients have contiguous gene deletion syndrome involving xp22 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have de novo mutations
n1=Lester (signe de) | n2=en:most patients have de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have involvement of all nails, with more severe changes in the nails of the thumbs and great toes
n1=Lester (signe de) | n2=en:most patients have involvement of all nails, with more severe changes in the nails of the thumbs and great toes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have no bleeding abnormalities
n1=Lester (signe de) | n2=en:most patients have no bleeding abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have pure spastic paraplegia, some have complicated spastic paraplegia
n1=Lester (signe de) | n2=en:most patients have pure spastic paraplegia, some have complicated spastic paraplegia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have recurrent 'flares' of pustular rash with fever, although some develop chronic erythematous plaques without pustules
n1=Lester (signe de) | n2=en:most patients have recurrent 'flares' of pustular rash with fever, although some develop chronic erythematous plaques without pustules | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients have severe streptococcus pneumoniae infections
n1=Lester (signe de) | n2=en:most patients have severe streptococcus pneumoniae infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients lose ambulation 2 years after onset
n1=Lester (signe de) | n2=en:most patients lose ambulation 2 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients need assistance walking or are wheelchair-bound
n1=Lester (signe de) | n2=en:most patients need assistance walking or are wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients need hip replacement by their mid-thirties
n1=Lester (signe de) | n2=en:most patients need hip replacement by their mid-thirties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients present in infancy with anemia
n1=Lester (signe de) | n2=en:most patients present in infancy with anemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients remain ambulatory
n1=Lester (signe de) | n2=en:most patients remain ambulatory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients remain ambulatory in adulthood
n1=Lester (signe de) | n2=en:most patients remain ambulatory in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients require liver transplant in childhood
n1=Lester (signe de) | n2=en:most patients require liver transplant in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients require liver transplantation within the first year of life
n1=Lester (signe de) | n2=en:most patients require liver transplantation within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients require renal transplantation
n1=Lester (signe de) | n2=en:most patients require renal transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients retain ambulation with aids
n1=Lester (signe de) | n2=en:most patients retain ambulation with aids | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most patients show early childhood onset after a period of normal development
n1=Lester (signe de) | n2=en:most patients show early childhood onset after a period of normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most pregnancies with affected fetuses resulted in elective termination
n1=Lester (signe de) | n2=en:most pregnancies with affected fetuses resulted in elective termination | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most remit by 2 months
n1=Lester (signe de) | n2=en:most remit by 2 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most remit by 6 weeks (1-6 months)
n1=Lester (signe de) | n2=en:most remit by 6 weeks (1-6 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most reported cases come from the island of mauritius or nearby islands
n1=Lester (signe de) | n2=en:most reported cases come from the island of mauritius or nearby islands | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most retain independent ambulation
n1=Lester (signe de) | n2=en:most retain independent ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most severe form of gaucher disease
n1=Lester (signe de) | n2=en:most severe form of gaucher disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most severe type of von willebrand disease
n1=Lester (signe de) | n2=en:most severe type of von willebrand disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:most types show autosomal dominant inheritance
n1=Lester (signe de) | n2=en:most types show autosomal dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mother had rubella infection during pregnancy with daughter
n1=Lester (signe de) | n2=en:mother had rubella infection during pregnancy with daughter | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mother who carries the mutation is clinically unaffected
n1=Lester (signe de) | n2=en:mother who carries the mutation is clinically unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor delay
n1=Lester (signe de) | n2=en:motor delay | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor fluctuations
n1=Lester (signe de) | n2=en:motor fluctuations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor impairment more significant than sensory impairment
n1=Lester (signe de) | n2=en:motor impairment more significant than sensory impairment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor neuropathy more prominent than sensory neuropathy
n1=Lester (signe de) | n2=en:motor neuropathy more prominent than sensory neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor skills less affected than cognitive skills
n1=Lester (signe de) | n2=en:motor skills less affected than cognitive skills | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor symptoms are variable
n1=Lester (signe de) | n2=en:motor symptoms are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor symptoms develop later (about 5 years into illness)
n1=Lester (signe de) | n2=en:motor symptoms develop later (about 5 years into illness) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:motor symptoms show mild clinical improvement with levodopa treatment
n1=Lester (signe de) | n2=en:motor symptoms show mild clinical improvement with levodopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mousy odor
n1=Lester (signe de) | n2=en:mousy odor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:movements worsened by anxiety
n1=Lester (signe de) | n2=en:movements worsened by anxiety | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mps1 types are distinguished clinically by age of onset and progression or by mutation(s)
n1=Lester (signe de) | n2=en:mps1 types are distinguished clinically by age of onset and progression or by mutation(s) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mucocutaneous immunodeficiency syndrome may be prominent
n1=Lester (signe de) | n2=en:mucocutaneous immunodeficiency syndrome may be prominent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mulibrey is an acronym (muscle, liver, brain, and eyes)
n1=Lester (signe de) | n2=en:mulibrey is an acronym (muscle, liver, brain, and eyes) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiorgan failure may result from hs
n1=Lester (signe de) | n2=en:multiorgan failure may result from hs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple congenital anomalies
n1=Lester (signe de) | n2=en:multiple congenital anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple gene loci involved in causation of schizophrenia
n1=Lester (signe de) | n2=en:multiple gene loci involved in causation of schizophrenia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple lesions in familial cases
n1=Lester (signe de) | n2=en:multiple lesions in familial cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple mitochondrial dna deletions are found in autosomal dominant pedigrees
n1=Lester (signe de) | n2=en:multiple mitochondrial dna deletions are found in autosomal dominant pedigrees | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple prenatal fractures
n1=Lester (signe de) | n2=en:multiple prenatal fractures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple pterygium syndrome, lethal type
n1=Lester (signe de) | n2=en:multiple pterygium syndrome, lethal type | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple seizures daily at onset
n1=Lester (signe de) | n2=en:multiple seizures daily at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multiple spontaneous abortions in obligate carriers
n1=Lester (signe de) | n2=en:multiple spontaneous abortions in obligate carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:multisystem decompensation in response to viral infection
n1=Lester (signe de) | n2=en:multisystem decompensation in response to viral infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:murcs association
n1=Lester (signe de) | n2=en:murcs association | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:muscle contractions in infancy occur in response to tactile stimulation or crying
n1=Lester (signe de) | n2=en:muscle contractions in infancy occur in response to tactile stimulation or crying | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:muscle involvement shows onset at birth or in infancy
n1=Lester (signe de) | n2=en:muscle involvement shows onset at birth or in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:muscle symptoms precede cardiac symptoms
n1=Lester (signe de) | n2=en:muscle symptoms precede cardiac symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:muscle weakness increases with age
n1=Lester (signe de) | n2=en:muscle weakness increases with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:muscle weakness occurs only in the presence of hyperthyroidism
n1=Lester (signe de) | n2=en:muscle weakness occurs only in the presence of hyperthyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mut- denotes individuals with structurally altered mutase with reduced affinity for adenosylcobalamin (adocbl)
n1=Lester (signe de) | n2=en:mut- denotes individuals with structurally altered mutase with reduced affinity for adenosylcobalamin (adocbl) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mut-0 denotes individuals with cultured fibroblast mutase activity that is undetectable secondary to no functional mutase
n1=Lester (signe de) | n2=en:mut-0 denotes individuals with cultured fibroblast mutase activity that is undetectable secondary to no functional mutase | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutant alleles have 47 to 63 repeats
n1=Lester (signe de) | n2=en:mutant alleles have 47 to 63 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation carriers have an increased risk of developing breast and/or ovarian cancer at an earlier age
n1=Lester (signe de) | n2=en:mutation carriers have an increased risk of developing breast and/or ovarian cancer at an earlier age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation carriers may show toxicity to 5-fluorouracil (5fu)
n1=Lester (signe de) | n2=en:mutation carriers may show toxicity to 5-fluorouracil (5fu) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation found in 1 puerto rican family (last curated august 2014)
n1=Lester (signe de) | n2=en:mutation found in 1 puerto rican family (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in b3gat3 has been found in 1 emirati family and 1 emirati boy
n1=Lester (signe de) | n2=en:mutation in b3gat3 has been found in 1 emirati family and 1 emirati boy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in nola3 found in 1 consanguineous saudi family (as of may 2011)
n1=Lester (signe de) | n2=en:mutation in nola3 found in 1 consanguineous saudi family (as of may 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in npr2 results in gain-of-function
n1=Lester (signe de) | n2=en:mutation in npr2 results in gain-of-function | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in pnpla6 identified in 1 laurence-moon syndrome family (last curated march 2015)
n1=Lester (signe de) | n2=en:mutation in pnpla6 identified in 1 laurence-moon syndrome family (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in rp9 gene in family (607331.0001) likely not pathogenic
n1=Lester (signe de) | n2=en:mutation in rp9 gene in family (607331.0001) likely not pathogenic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in the hcrt gene has been identified in 1 patient
n1=Lester (signe de) | n2=en:mutation in the hcrt gene has been identified in 1 patient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutation in the mass1 gene has been identified in 1 of 48 families with familial febrile seizures linked to 5q14
n1=Lester (signe de) | n2=en:mutation in the mass1 gene has been identified in 1 of 48 families with familial febrile seizures linked to 5q14 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutational analysis revealed that the original weissenbacher-zweymuller patient had non-ophthalmic stickler syndrome (stkl3, 184840)
n1=Lester (signe de) | n2=en:mutational analysis revealed that the original weissenbacher-zweymuller patient had non-ophthalmic stickler syndrome (stkl3, 184840) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations are frequently maternally inherited
n1=Lester (signe de) | n2=en:mutations are frequently maternally inherited | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations have been identified in spanish families
n1=Lester (signe de) | n2=en:mutations have been identified in spanish families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations in the cpo gene cause 3 clinically distinct disorders, hereditary coproporphyria (hcp), 'homozygous' variant hereditary coproporphyria, or harderoporphyria
n1=Lester (signe de) | n2=en:mutations in the cpo gene cause 3 clinically distinct disorders, hereditary coproporphyria (hcp), 'homozygous' variant hereditary coproporphyria, or harderoporphyria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations occur de novo
n1=Lester (signe de) | n2=en:mutations occur de novo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations result in inactivation of nkx3-2 (602183)
n1=Lester (signe de) | n2=en:mutations result in inactivation of nkx3-2 (602183) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:mutations show partial penetrance
n1=Lester (signe de) | n2=en:mutations show partial penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myelodysplastic syndrome developed in 1 of 12 mutation-positive patients
n1=Lester (signe de) | n2=en:myelodysplastic syndrome developed in 1 of 12 mutation-positive patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myoclonic seizures occur on awakening or within 2 hours of awakening
n1=Lester (signe de) | n2=en:myoclonic seizures occur on awakening or within 2 hours of awakening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myoclonus is presenting symptom
n1=Lester (signe de) | n2=en:myoclonus is presenting symptom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myoclonus occurs at rest and with action
n1=Lester (signe de) | n2=en:myoclonus occurs at rest and with action | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myoclonus triggered by action, sudden movements, and inadvertent somatosensory stimuli
n1=Lester (signe de) | n2=en:myoclonus triggered by action, sudden movements, and inadvertent somatosensory stimuli | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:myotilinopathy (609200) is an allelic disorder with overlapping clinical features
n1=Lester (signe de) | n2=en:myotilinopathy (609200) is an allelic disorder with overlapping clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:n-myc oncogene (164840) amplification is associated with poor prognosis
n1=Lester (signe de) | n2=en:n-myc oncogene (164840) amplification is associated with poor prognosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nail changes may be intermittent in some patients
n1=Lester (signe de) | n2=en:nail changes may be intermittent in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nails appear normal at birth, with dystrophic changes developing within the first decade of life
n1=Lester (signe de) | n2=en:nails appear normal at birth, with dystrophic changes developing within the first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nails may be intermittently involved
n1=Lester (signe de) | n2=en:nails may be intermittently involved | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nails, palms, and soles are spared in some patients
n1=Lester (signe de) | n2=en:nails, palms, and soles are spared in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:name sponastrime = spo (spondylo), nas (nasal), strime (striated metaphyses)
n1=Lester (signe de) | n2=en:name sponastrime = spo (spondylo), nas (nasal), strime (striated metaphyses) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:narcolepsy and deafness are the first symptoms
n1=Lester (signe de) | n2=en:narcolepsy and deafness are the first symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:natural aversion to carbohydrates
n1=Lester (signe de) | n2=en:natural aversion to carbohydrates | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:natural aversion to carbohydrates and favoring of protein
n1=Lester (signe de) | n2=en:natural aversion to carbohydrates and favoring of protein | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:near-normoglycemic remission for period of months to years without insulin treatment
n1=Lester (signe de) | n2=en:near-normoglycemic remission for period of months to years without insulin treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nearly 100% penetrance by 60 years of age
n1=Lester (signe de) | n2=en:nearly 100% penetrance by 60 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:negative repeat expansion (reverse anticipation) can occur (approximately 5% of the time)
n1=Lester (signe de) | n2=en:negative repeat expansion (reverse anticipation) can occur (approximately 5% of the time) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal and late-infantile onset
n1=Lester (signe de) | n2=en:neonatal and late-infantile onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal death
n1=Lester (signe de) | n2=en:neonatal death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal death secondary to pulmonary insufficiency
n1=Lester (signe de) | n2=en:neonatal death secondary to pulmonary insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal lethal due to respiratory insufficiency
n1=Lester (signe de) | n2=en:neonatal lethal due to respiratory insufficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal onset
n1=Lester (signe de) | n2=en:neonatal onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal onset of nephrotic syndrome
n1=Lester (signe de) | n2=en:neonatal onset of nephrotic syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal or infant death
n1=Lester (signe de) | n2=en:neonatal or infant death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal sepsis
n1=Lester (signe de) | n2=en:neonatal sepsis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal severe hyperparathyroidism in homozygotes (239200)
n1=Lester (signe de) | n2=en:neonatal severe hyperparathyroidism in homozygotes (239200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neonatal/infantile death in most patients
n1=Lester (signe de) | n2=en:neonatal/infantile death in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuroendocrine recovery occurs in some patients
n1=Lester (signe de) | n2=en:neuroendocrine recovery occurs in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic deterioration is severe after age 2 to 2.5 years
n1=Lester (signe de) | n2=en:neurologic deterioration is severe after age 2 to 2.5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic dysfunction is infrequent and associated with delayed diagnosis
n1=Lester (signe de) | n2=en:neurologic dysfunction is infrequent and associated with delayed diagnosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic features are variable and not progressive
n1=Lester (signe de) | n2=en:neurologic features are variable and not progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic features have been diagnosed in ~30% of cases
n1=Lester (signe de) | n2=en:neurologic features have been diagnosed in ~30% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic features occur in adulthood
n1=Lester (signe de) | n2=en:neurologic features occur in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic features occur later in childhood
n1=Lester (signe de) | n2=en:neurologic features occur later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic findings closely resemble those of huntington disease (hd, 143100)
n1=Lester (signe de) | n2=en:neurologic findings closely resemble those of huntington disease (hd, 143100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic involvement may occur in the absence of visceral involvement
n1=Lester (signe de) | n2=en:neurologic involvement may occur in the absence of visceral involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic signs are present in the neonatal period only
n1=Lester (signe de) | n2=en:neurologic signs are present in the neonatal period only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic signs last hours to days
n1=Lester (signe de) | n2=en:neurologic signs last hours to days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic signs may not be present
n1=Lester (signe de) | n2=en:neurologic signs may not be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic signs onset during adolescence or young adulthood
n1=Lester (signe de) | n2=en:neurologic signs onset during adolescence or young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic symptoms are not always present or may appear late
n1=Lester (signe de) | n2=en:neurologic symptoms are not always present or may appear late | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic symptoms are progressive
n1=Lester (signe de) | n2=en:neurologic symptoms are progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic symptoms may develop decades later
n1=Lester (signe de) | n2=en:neurologic symptoms may develop decades later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurologic symptoms may occur after trauma
n1=Lester (signe de) | n2=en:neurologic symptoms may occur after trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuromuscular forms can present as perinate, infant, child, or adult
n1=Lester (signe de) | n2=en:neuromuscular forms can present as perinate, infant, child, or adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuromuscular, cardiovascular, and infectious symptoms improve with age
n1=Lester (signe de) | n2=en:neuromuscular, cardiovascular, and infectious symptoms improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuropathic, cardiac, leptomeningeal, and ocular predominance may occur
n1=Lester (signe de) | n2=en:neuropathic, cardiac, leptomeningeal, and ocular predominance may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuropathy becomes apparent in childhood
n1=Lester (signe de) | n2=en:neuropathy becomes apparent in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neuropsychiatric manifestations are variable
n1=Lester (signe de) | n2=en:neuropsychiatric manifestations are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:neurotransmitter treatment with l-dopa and serotonin or precursors is effective
n1=Lester (signe de) | n2=en:neurotransmitter treatment with l-dopa and serotonin or precursors is effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:new skin lesions stop appearing before adolescence
n1=Lester (signe de) | n2=en:new skin lesions stop appearing before adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:newborn period is critical for survival
n1=Lester (signe de) | n2=en:newborn period is critical for survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:night blindness from early childhood
n1=Lester (signe de) | n2=en:night blindness from early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nine patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:nine patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nine patients have been reported in detail (as of 14 june 2011)
n1=Lester (signe de) | n2=en:nine patients have been reported in detail (as of 14 june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ninety percent of cases are female
n1=Lester (signe de) | n2=en:ninety percent of cases are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ninety percent of patients with pbg deaminase deficiency are clinically unaffected
n1=Lester (signe de) | n2=en:ninety percent of patients with pbg deaminase deficiency are clinically unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no abdominal symptoms or neurologic symptoms in harderoporphyria
n1=Lester (signe de) | n2=en:no abdominal symptoms or neurologic symptoms in harderoporphyria | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no abnormalities of hair, teeth, or bones
n1=Lester (signe de) | n2=en:no abnormalities of hair, teeth, or bones | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no abnormalities of skin, hair, teeth, or bones
n1=Lester (signe de) | n2=en:no abnormalities of skin, hair, teeth, or bones | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no cardiac or immune defects in patients from the 2 reported families
n1=Lester (signe de) | n2=en:no cardiac or immune defects in patients from the 2 reported families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no chronic or permanent liver damage
n1=Lester (signe de) | n2=en:no chronic or permanent liver damage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no clinical description given for 1 reported patient (last curated december 2013)
n1=Lester (signe de) | n2=en:no clinical description given for 1 reported patient (last curated december 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no clinical details provided by the authors
n1=Lester (signe de) | n2=en:no clinical details provided by the authors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no clinical manifestations
n1=Lester (signe de) | n2=en:no clinical manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no clinical manifestations were noted (incidental laboratory finding)
n1=Lester (signe de) | n2=en:no clinical manifestations were noted (incidental laboratory finding) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no congenital form
n1=Lester (signe de) | n2=en:no congenital form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no consistent disease phenotype
n1=Lester (signe de) | n2=en:no consistent disease phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no consistent dysmorphic facial phenotype
n1=Lester (signe de) | n2=en:no consistent dysmorphic facial phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no dysmorphic features
n1=Lester (signe de) | n2=en:no dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no extraocular findings
n1=Lester (signe de) | n2=en:no extraocular findings | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no family history of
n1=Lester (signe de) | n2=en:no family history of | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no family history, de novo mutations
n1=Lester (signe de) | n2=en:no family history, de novo mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no features consistent with cystic fibrosis found in these patients
n1=Lester (signe de) | n2=en:no features consistent with cystic fibrosis found in these patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no history of familial hypercholesterolemia
n1=Lester (signe de) | n2=en:no history of familial hypercholesterolemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no increased fragility of hair
n1=Lester (signe de) | n2=en:no increased fragility of hair | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no laterality defects
n1=Lester (signe de) | n2=en:no laterality defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no male-to-male transmission
n1=Lester (signe de) | n2=en:no male-to-male transmission | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no mutations reported in la reunion island patients (last curated august 2014)
n1=Lester (signe de) | n2=en:no mutations reported in la reunion island patients (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no neurologic sequelae
n1=Lester (signe de) | n2=en:no neurologic sequelae | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no opportunistic infections
n1=Lester (signe de) | n2=en:no opportunistic infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no peripheral signs of hypothyroidism
n1=Lester (signe de) | n2=en:no peripheral signs of hypothyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no phenotype in heterozygotes
n1=Lester (signe de) | n2=en:no phenotype in heterozygotes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no phenotypic difference between patients who are homozygous or heterozygous for mutations in the spink1 gene
n1=Lester (signe de) | n2=en:no phenotypic difference between patients who are homozygous or heterozygous for mutations in the spink1 gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no phenotypic manifestations
n1=Lester (signe de) | n2=en:no phenotypic manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no preceding skin inflammatory stage
n1=Lester (signe de) | n2=en:no preceding skin inflammatory stage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no predisposition to skin tumor development
n1=Lester (signe de) | n2=en:no predisposition to skin tumor development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no recurrence of nephrotic syndrome after transplantation
n1=Lester (signe de) | n2=en:no recurrence of nephrotic syndrome after transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no response or worsening with acetylcholinesterase inhibitors
n1=Lester (signe de) | n2=en:no response or worsening with acetylcholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no response to phenobarbital
n1=Lester (signe de) | n2=en:no response to phenobarbital | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no situs inversus
n1=Lester (signe de) | n2=en:no situs inversus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no skeletal abnormalities in odontohypophosphatasia
n1=Lester (signe de) | n2=en:no skeletal abnormalities in odontohypophosphatasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no skin abnormalities
n1=Lester (signe de) | n2=en:no skin abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:no systemic manifestations
n1=Lester (signe de) | n2=en:no systemic manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:noise exposure causes more severe hearing loss at high frequencies (2,000 to 8,000 hz)
n1=Lester (signe de) | n2=en:noise exposure causes more severe hearing loss at high frequencies (2,000 to 8,000 hz) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:non-progressive and more severe progressive forms
n1=Lester (signe de) | n2=en:non-progressive and more severe progressive forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:non-progressive or very slowly progressive
n1=Lester (signe de) | n2=en:non-progressive or very slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:non-tender
n1=Lester (signe de) | n2=en:non-tender | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonpenetrance has been observed
n1=Lester (signe de) | n2=en:nonpenetrance has been observed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonprogressive
n1=Lester (signe de) | n2=en:nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonprogressive hepatic form is less frequent
n1=Lester (signe de) | n2=en:nonprogressive hepatic form is less frequent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonprogressive in most patients
n1=Lester (signe de) | n2=en:nonprogressive in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonprogressive or slowly progressive
n1=Lester (signe de) | n2=en:nonprogressive or slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonprogressive or very slowly progressive
n1=Lester (signe de) | n2=en:nonprogressive or very slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonrandom association of following anomalies--v (vertebral anomalies), a (anal atresia), c (cardiovascular anomalies), t (tracheoesophageal fistula), e (esophageal atresia), r (renal anomalies), l (preaxial limb anomalies)
n1=Lester (signe de) | n2=en:nonrandom association of following anomalies--v (vertebral anomalies), a (anal atresia), c (cardiovascular anomalies), t (tracheoesophageal fistula), e (esophageal atresia), r (renal anomalies), l (preaxial limb anomalies) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonreflex epilepsy may occur later in 16 to 38% of patients
n1=Lester (signe de) | n2=en:nonreflex epilepsy may occur later in 16 to 38% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonspecific subtle dysmorphic facial features may be present
n1=Lester (signe de) | n2=en:nonspecific subtle dysmorphic facial features may be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonsyndromic
n1=Lester (signe de) | n2=en:nonsyndromic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nonsyndromic disorder
n1=Lester (signe de) | n2=en:nonsyndromic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nontruncating (missense) lamb2 mutations may display variable phenotypes ranging from a milder variant of pierson syndrome to isolated congenital nephrotic syndrome
n1=Lester (signe de) | n2=en:nontruncating (missense) lamb2 mutations may display variable phenotypes ranging from a milder variant of pierson syndrome to isolated congenital nephrotic syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal - 5 to 37 copies of (ctg)n repeat in dmpk (605377)
n1=Lester (signe de) | n2=en:normal - 5 to 37 copies of (ctg)n repeat in dmpk (605377) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal ability to tolerate heat
n1=Lester (signe de) | n2=en:normal ability to tolerate heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles contain 15 to 50 repeats
n1=Lester (signe de) | n2=en:normal alleles contain 15 to 50 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles contain 6 to 28 repeats
n1=Lester (signe de) | n2=en:normal alleles contain 6 to 28 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles contain up to 30 repeats
n1=Lester (signe de) | n2=en:normal alleles contain up to 30 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles contain up to 44 repeats
n1=Lester (signe de) | n2=en:normal alleles contain up to 44 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles have 10 to 29 repeats and pathologic alleles have 400 to 4,500 repeats
n1=Lester (signe de) | n2=en:normal alleles have 10 to 29 repeats and pathologic alleles have 400 to 4,500 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles have 25 to 44 repeats
n1=Lester (signe de) | n2=en:normal alleles have 25 to 44 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal alleles have 4 to 18 repeats
n1=Lester (signe de) | n2=en:normal alleles have 4 to 18 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal at birth
n1=Lester (signe de) | n2=en:normal at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal birth (finding)
n1=Lester (signe de) | n2=en:normal birth (finding) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal cag repeat length is 7 to 32 triplets
n1=Lester (signe de) | n2=en:normal cag repeat length is 7 to 32 triplets | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal development before onset of seizures
n1=Lester (signe de) | n2=en:normal development before onset of seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal development between episodes
n1=Lester (signe de) | n2=en:normal development between episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal development in first 6-12 months, followed by facial coarsening and progressive delay in physical and mental development
n1=Lester (signe de) | n2=en:normal development in first 6-12 months, followed by facial coarsening and progressive delay in physical and mental development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal development until onset of seizures
n1=Lester (signe de) | n2=en:normal development until onset of seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal female secondary sexual characteristics
n1=Lester (signe de) | n2=en:normal female secondary sexual characteristics | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal fertility
n1=Lester (signe de) | n2=en:normal fertility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal first month
n1=Lester (signe de) | n2=en:normal first month | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal growth and development after 1 year of age
n1=Lester (signe de) | n2=en:normal growth and development after 1 year of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal hemoglobin levels observed in fourth and fifth decades of life, if renal failure not severe
n1=Lester (signe de) | n2=en:normal hemoglobin levels observed in fourth and fifth decades of life, if renal failure not severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal in neonatal period
n1=Lester (signe de) | n2=en:normal in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal intelligence in majority
n1=Lester (signe de) | n2=en:normal intelligence in majority | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal neonatal blood phenylalanine has been reported in rare patients
n1=Lester (signe de) | n2=en:normal neonatal blood phenylalanine has been reported in rare patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal neonatal course
n1=Lester (signe de) | n2=en:normal neonatal course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal range of expanded repeats 9-29, hd range 36-121
n1=Lester (signe de) | n2=en:normal range of expanded repeats 9-29, hd range 36-121 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal sclerae and teeth
n1=Lester (signe de) | n2=en:normal sclerae and teeth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal sialophorin gene
n1=Lester (signe de) | n2=en:normal sialophorin gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:normal sweat electrolytes
n1=Lester (signe de) | n2=en:normal sweat electrolytes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all nails are affected in some patients
n1=Lester (signe de) | n2=en:not all nails are affected in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have a myopathy
n1=Lester (signe de) | n2=en:not all patients have a myopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have all features
n1=Lester (signe de) | n2=en:not all patients have all features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have dysmorphic facial features
n1=Lester (signe de) | n2=en:not all patients have dysmorphic facial features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have facial dysmorphism
n1=Lester (signe de) | n2=en:not all patients have facial dysmorphism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have renal involvement
n1=Lester (signe de) | n2=en:not all patients have renal involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not all patients have skeletal muscle symptoms or mental retardation
n1=Lester (signe de) | n2=en:not all patients have skeletal muscle symptoms or mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not responsive to biotin treatment
n1=Lester (signe de) | n2=en:not responsive to biotin treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:not responsive to steroid treatment
n1=Lester (signe de) | n2=en:not responsive to steroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:noted in early childhood in most patients
n1=Lester (signe de) | n2=en:noted in early childhood in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nova scotian variant (type d) is considered a genetic isolate of npc1 and is associated with a mutation in the npc1 gene (607623.0004)
n1=Lester (signe de) | n2=en:nova scotian variant (type d) is considered a genetic isolate of npc1 and is associated with a mutation in the npc1 gene (607623.0004) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nphp shows autosomal recessive inheritance
n1=Lester (signe de) | n2=en:nphp shows autosomal recessive inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:number of episodes varies from 1 to many (up to 20)
n1=Lester (signe de) | n2=en:number of episodes varies from 1 to many (up to 20) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nutritional risk index:arbitrary concentration:point in time:^patient:quantitative
n1=Lester (signe de) | n2=en:nutritional risk index:arbitrary concentration:point in time:^patient:quantitative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nyctalopia is a later feature of the disorder
n1=Lester (signe de) | n2=en:nyctalopia is a later feature of the disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nystagmus is often the presenting sign
n1=Lester (signe de) | n2=en:nystagmus is often the presenting sign | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:nystagmus may disappear by mid-childhood
n1=Lester (signe de) | n2=en:nystagmus may disappear by mid-childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:obligate female carriers may show mild signs of muscle weakness, especially of the face
n1=Lester (signe de) | n2=en:obligate female carriers may show mild signs of muscle weakness, especially of the face | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:obligatory heterozygotes are clinically unaffected
n1=Lester (signe de) | n2=en:obligatory heterozygotes are clinically unaffected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:observed in individuals of bulgarian roma bowlmaker ethnic group
n1=Lester (signe de) | n2=en:observed in individuals of bulgarian roma bowlmaker ethnic group | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occasional adult onset
n1=Lester (signe de) | n2=en:occasional adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occasional late-onset of symptoms with homozygosity (e.g. 612283.0005 protein c deficiency, homozygous)
n1=Lester (signe de) | n2=en:occasional late-onset of symptoms with homozygosity (e.g. 612283.0005 protein c deficiency, homozygous) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occasionally germ cell tumor arise from extra gonadal site (e.g., mediastinum, retroperitoneum, pineal gland)
n1=Lester (signe de) | n2=en:occasionally germ cell tumor arise from extra gonadal site (e.g., mediastinum, retroperitoneum, pineal gland) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occasionally low-dose insulin required
n1=Lester (signe de) | n2=en:occasionally low-dose insulin required | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs at age 20-50 years
n1=Lester (signe de) | n2=en:occurs at age 20-50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs during pregnancy, most often in the third trimester
n1=Lester (signe de) | n2=en:occurs during pregnancy, most often in the third trimester | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in ~3% pregnancies in western populations
n1=Lester (signe de) | n2=en:occurs in ~3% pregnancies in western populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in 1 in 50,000 newborn males
n1=Lester (signe de) | n2=en:occurs in 1 in 50,000 newborn males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in 2-5 per 10,000 individuals
n1=Lester (signe de) | n2=en:occurs in 2-5 per 10,000 individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in about 1 in 10,000 births
n1=Lester (signe de) | n2=en:occurs in about 1 in 10,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in at least 1 in 55,000 male births (that figure may not include milder variants)
n1=Lester (signe de) | n2=en:occurs in at least 1 in 55,000 male births (that figure may not include milder variants) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in full-term infants
n1=Lester (signe de) | n2=en:occurs in full-term infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in full-term newborns
n1=Lester (signe de) | n2=en:occurs in full-term newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in the absence of trauma
n1=Lester (signe de) | n2=en:occurs in the absence of trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs in women and is triggered by pregnancy or estrogen therapy
n1=Lester (signe de) | n2=en:occurs in women and is triggered by pregnancy or estrogen therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs more frequently in females
n1=Lester (signe de) | n2=en:occurs more frequently in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs most often among black africans
n1=Lester (signe de) | n2=en:occurs most often among black africans | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs most often between 5 and 15 years of age
n1=Lester (signe de) | n2=en:occurs most often between 5 and 15 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs most often in developing countries in tropical regions
n1=Lester (signe de) | n2=en:occurs most often in developing countries in tropical regions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs much more commonly in women
n1=Lester (signe de) | n2=en:occurs much more commonly in women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:occurs on right side in 75% of cases
n1=Lester (signe de) | n2=en:occurs on right side in 75% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ocular abnormalities may be very mild
n1=Lester (signe de) | n2=en:ocular abnormalities may be very mild | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ocular phenotype falls within a spectrum of retinal dystrophy from severe, leber congenital amaurosis, to less severe, juvenile retinitis pigmentosa
n1=Lester (signe de) | n2=en:ocular phenotype falls within a spectrum of retinal dystrophy from severe, leber congenital amaurosis, to less severe, juvenile retinitis pigmentosa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:oculomotor apraxia is not always present
n1=Lester (signe de) | n2=en:oculomotor apraxia is not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:odor of 'sweaty feet'
n1=Lester (signe de) | n2=en:odor of 'sweaty feet' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:oeis is an acronym for omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects
n1=Lester (signe de) | n2=en:oeis is an acronym for omphalocele, exstrophy of the cloaca, imperforate anus, and spinal defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often associated with chiari type i malformation (cm1, 118420)
n1=Lester (signe de) | n2=en:often associated with chiari type i malformation (cm1, 118420) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often associated with klippel-feil anomaly (118100)
n1=Lester (signe de) | n2=en:often associated with klippel-feil anomaly (118100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often associated with syringomyelia (186700)
n1=Lester (signe de) | n2=en:often associated with syringomyelia (186700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often confused with tuberous sclerosis (191000)
n1=Lester (signe de) | n2=en:often confused with tuberous sclerosis (191000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often diagnosed between ages 3-4 months
n1=Lester (signe de) | n2=en:often diagnosed between ages 3-4 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often fatal due in infancy due to intractable diarrhea
n1=Lester (signe de) | n2=en:often fatal due in infancy due to intractable diarrhea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often fatal in utero
n1=Lester (signe de) | n2=en:often fatal in utero | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often identified in newborn period
n1=Lester (signe de) | n2=en:often identified in newborn period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often lethal in infancy
n1=Lester (signe de) | n2=en:often lethal in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often presents with cranial or cervical involvement
n1=Lester (signe de) | n2=en:often presents with cranial or cervical involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often reared as females until puberty
n1=Lester (signe de) | n2=en:often reared as females until puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often refractory to medical therapy
n1=Lester (signe de) | n2=en:often refractory to medical therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often results in death in childhood
n1=Lester (signe de) | n2=en:often results in death in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:often unilateral involvement
n1=Lester (signe de) | n2=en:often unilateral involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:old order amish, african american, and french patients have been described
n1=Lester (signe de) | n2=en:old order amish, african american, and french patients have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:older individuals had moderate to severe hearing loss
n1=Lester (signe de) | n2=en:older individuals had moderate to severe hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:older patients become wheelchair-dependent
n1=Lester (signe de) | n2=en:older patients become wheelchair-dependent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:oligogenic disorder in some patients who carry mutations in more than one neuroendocrine-related gene
n1=Lester (signe de) | n2=en:oligogenic disorder in some patients who carry mutations in more than one neuroendocrine-related gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 3-generation danish family reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one 3-generation danish family reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 3-generation italian family has been described (last curated august 2015)
n1=Lester (signe de) | n2=en:one 3-generation italian family has been described (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 3-generation korean family and one father daughter have been reported (last curated august 2013)
n1=Lester (signe de) | n2=en:one 3-generation korean family and one father daughter have been reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 4-generation caucasian italian family with a heterozygous crybb3 mutation has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one 4-generation caucasian italian family with a heterozygous crybb3 mutation has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 4-generation chinese family has been reported (as of 04/2010)
n1=Lester (signe de) | n2=en:one 4-generation chinese family has been reported (as of 04/2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 5-generation acc family with mutation in bms1 has been described (last curated august 2014)
n1=Lester (signe de) | n2=en:one 5-generation acc family with mutation in bms1 has been described (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 5-generation chinese family reported (last curated november 2014)
n1=Lester (signe de) | n2=en:one 5-generation chinese family reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 7-year-old boy and 2 fetuses have been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:one 7-year-old boy and 2 fetuses have been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one 9-generation family and 1 isolated patient described (last curated march 2014)
n1=Lester (signe de) | n2=en:one 9-generation family and 1 isolated patient described (last curated march 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one amish family has been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:one amish family has been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one ashkenazi jewish family with globozoospermia and spata16 mutation has been described (last curated april 2015)
n1=Lester (signe de) | n2=en:one ashkenazi jewish family with globozoospermia and spata16 mutation has been described (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one boy and 5 unrelated girls have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:one boy and 5 unrelated girls have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one brazilian family with 12 affected individuals reported (last curated february 2014)
n1=Lester (signe de) | n2=en:one brazilian family with 12 affected individuals reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one brother and sister of micmac indian and french-canadian ancestry have been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:one brother and sister of micmac indian and french-canadian ancestry have been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one canadian mennonite family has been reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one canadian mennonite family has been reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one chinese family and 1 unrelated patient have been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:one chinese family and 1 unrelated patient have been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one chinese family has been reported (as of august 2011)
n1=Lester (signe de) | n2=en:one chinese family has been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one chinese family has been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:one chinese family has been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one chinese family with 14 affected individuals has been described (last curated february 2014)
n1=Lester (signe de) | n2=en:one chinese family with 14 affected individuals has been described (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one chinese family with a confirmed mutation has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one chinese family with a confirmed mutation has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one compound heterozygous patient reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one compound heterozygous patient reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous algerian family has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one consanguineous algerian family has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous arab family has been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:one consanguineous arab family has been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous arab family has been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:one consanguineous arab family has been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous arab israeli family has been reported (last curated february, 2013)
n1=Lester (signe de) | n2=en:one consanguineous arab israeli family has been reported (last curated february, 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous caucasian united kingdom family has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one consanguineous caucasian united kingdom family has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous costa rican family has been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one consanguineous costa rican family has been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous egyptian family with 4 affected individuals has been reported (as of december 2011)
n1=Lester (signe de) | n2=en:one consanguineous egyptian family with 4 affected individuals has been reported (as of december 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been found to carry a homozygous mutation in the pclo gene (last curated june 2015)
n1=Lester (signe de) | n2=en:one consanguineous family has been found to carry a homozygous mutation in the pclo gene (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated december 2010)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated december 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated may 2013)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated may 2014)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family has been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:one consanguineous family has been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family of ashkenazi jewish origin has been reported (last cureated may 2012)
n1=Lester (signe de) | n2=en:one consanguineous family of ashkenazi jewish origin has been reported (last cureated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family of indian descent has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one consanguineous family of indian descent has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family with a recessive mutation has been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:one consanguineous family with a recessive mutation has been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous family with homozygosity for a cryab mutation has been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:one consanguineous family with homozygosity for a cryab mutation has been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous israeli bedouin kindred has been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:one consanguineous israeli bedouin kindred has been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous italian family has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one consanguineous italian family has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous moroccan family has been reported (as of january 2012)
n1=Lester (signe de) | n2=en:one consanguineous moroccan family has been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous omani family with a kif7 mutation has been described (last curated january 2016)
n1=Lester (signe de) | n2=en:one consanguineous omani family with a kif7 mutation has been described (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family and 1 unrelated patient have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family and 1 unrelated patient have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been described (last curated march 2015)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been described (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (as of january 2012)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated june 2012)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated june 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family has been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family has been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani family reported (last curated august 2013)
n1=Lester (signe de) | n2=en:one consanguineous pakistani family reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one consanguineous pakistani has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous pakistani reported (last curated july 2015)
n1=Lester (signe de) | n2=en:one consanguineous pakistani reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous saudi arabian family has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one consanguineous saudi arabian family has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous saudi family had additional features of microcephaly, mental retardation, ophthalmoplegia, and syndactyly
n1=Lester (signe de) | n2=en:one consanguineous saudi family had additional features of microcephaly, mental retardation, ophthalmoplegia, and syndactyly | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous saudi family has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one consanguineous saudi family has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous senegalese family has been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:one consanguineous senegalese family has been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous tunisian family has been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:one consanguineous tunisian family has been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one consanguineous turkish family has been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:one consanguineous turkish family has been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family (4 affected members) has been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:one family (4 affected members) has been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and 1 unrelated patient have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:one family and 1 unrelated patient have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and 1 unrelated patient have been reported (last curated january 2011)
n1=Lester (signe de) | n2=en:one family and 1 unrelated patient have been reported (last curated january 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and 1 unrelated patient have been reported (last curated july 2013)
n1=Lester (signe de) | n2=en:one family and 1 unrelated patient have been reported (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and 2 unrelated patients have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:one family and 2 unrelated patients have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and an unrelated patient have been reported (last curated january 2016)
n1=Lester (signe de) | n2=en:one family and an unrelated patient have been reported (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and an unrelated patient have been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:one family and an unrelated patient have been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family and one sporadic case of portuguese descent have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:one family and one sporadic case of portuguese descent have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family described (last curated october 2013)
n1=Lester (signe de) | n2=en:one family described (last curated october 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family from hong kong has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one family from hong kong has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family from punjab, india has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one family from punjab, india has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family from the old order amish has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one family from the old order amish has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family had normal cognitive and neurologic development
n1=Lester (signe de) | n2=en:one family had normal cognitive and neurologic development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been described (last curated august 2015)
n1=Lester (signe de) | n2=en:one family has been described (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported
n1=Lester (signe de) | n2=en:one family has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of 4/2010)
n1=Lester (signe de) | n2=en:one family has been reported (as of 4/2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of april 2012)
n1=Lester (signe de) | n2=en:one family has been reported (as of april 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of august 2010)
n1=Lester (signe de) | n2=en:one family has been reported (as of august 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of curation date may, 2013) onset in infancy
n1=Lester (signe de) | n2=en:one family has been reported (as of curation date may, 2013) onset in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of january 2011)
n1=Lester (signe de) | n2=en:one family has been reported (as of january 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of january 2012)
n1=Lester (signe de) | n2=en:one family has been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of july 2011)
n1=Lester (signe de) | n2=en:one family has been reported (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of june 2011)
n1=Lester (signe de) | n2=en:one family has been reported (as of june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of october 2010)
n1=Lester (signe de) | n2=en:one family has been reported (as of october 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (as of september 2011)
n1=Lester (signe de) | n2=en:one family has been reported (as of september 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:one family has been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated august 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:one family has been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated december 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated december 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one family has been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated january 2010)
n1=Lester (signe de) | n2=en:one family has been reported (last curated january 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated january 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated january 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated june 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated june 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated march 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated march 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one family has been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:one family has been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated may 2012)
n1=Lester (signe de) | n2=en:one family has been reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one family has been reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated november 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:one family has been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated october 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated october 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:one family has been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:one family has been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:one family has been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported and no additional clinical features were provided (last curated june 2013)
n1=Lester (signe de) | n2=en:one family has been reported and no additional clinical features were provided (last curated june 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family has been reported with limited clinical information (last curated october 2014)
n1=Lester (signe de) | n2=en:one family has been reported with limited clinical information (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of algerian descent has been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one family of algerian descent has been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of french-canadian origin has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one family of french-canadian origin has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of french-canadian origin has been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:one family of french-canadian origin has been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of irish traveller descent described (last curated september 2013)
n1=Lester (signe de) | n2=en:one family of irish traveller descent described (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of italian-american descent has been described
n1=Lester (signe de) | n2=en:one family of italian-american descent has been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of mali origin has been reported (last curated january 2013)
n1=Lester (signe de) | n2=en:one family of mali origin has been reported (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of puerto rican descent has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one family of puerto rican descent has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family of sicilian origin has been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:one family of sicilian origin has been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (as of may 2012)
n1=Lester (signe de) | n2=en:one family reported (as of may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (as of november 2011)
n1=Lester (signe de) | n2=en:one family reported (as of november 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated january 2014)
n1=Lester (signe de) | n2=en:one family reported (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated july 2008)
n1=Lester (signe de) | n2=en:one family reported (last curated july 2008) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated june 2009)
n1=Lester (signe de) | n2=en:one family reported (last curated june 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated may 2013)
n1=Lester (signe de) | n2=en:one family reported (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated november 2011)
n1=Lester (signe de) | n2=en:one family reported (last curated november 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported (last curated november 2013)
n1=Lester (signe de) | n2=en:one family reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported with mutation in a heterozygous mutation in dlx5 (last curated october 2014)
n1=Lester (signe de) | n2=en:one family reported with mutation in a heterozygous mutation in dlx5 (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family reported with piezo2 mutation (last curated january 2015)
n1=Lester (signe de) | n2=en:one family reported with piezo2 mutation (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 2 affected brothers has been reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one family with 2 affected brothers has been reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 2 affected fetuses has been reported (as of august 2011)
n1=Lester (signe de) | n2=en:one family with 2 affected fetuses has been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 2 sisters have been reported (as of march 2010)
n1=Lester (signe de) | n2=en:one family with 2 sisters have been reported (as of march 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 3 affected girls has been reported (as of october 2011)
n1=Lester (signe de) | n2=en:one family with 3 affected girls has been reported (as of october 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 3 affected individuals has been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:one family with 3 affected individuals has been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 3 affected males has been reported (as of october 2011)
n1=Lester (signe de) | n2=en:one family with 3 affected males has been reported (as of october 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 3 patients and 1 patient with sporadic disease have been reported (last curated june 2011)
n1=Lester (signe de) | n2=en:one family with 3 patients and 1 patient with sporadic disease have been reported (last curated june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 4 affected sibs has been reported (as of april 2012)
n1=Lester (signe de) | n2=en:one family with 4 affected sibs has been reported (as of april 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 5 affected members has been reported (last curated september 2012)
n1=Lester (signe de) | n2=en:one family with 5 affected members has been reported (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with 6 probands described (as of september 2000)
n1=Lester (signe de) | n2=en:one family with 6 probands described (as of september 2000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a cacna1b mutation has been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one family with a cacna1b mutation has been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a confirmed dcaf8 mutation has been reported (last curated june, 2014)
n1=Lester (signe de) | n2=en:one family with a confirmed dcaf8 mutation has been reported (last curated june, 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a confirmed pathogenic atp2b3 mutation has been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:one family with a confirmed pathogenic atp2b3 mutation has been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a deletion upstream of the lmnb1 gene did not have autonomic symptoms or cerebellar involvement
n1=Lester (signe de) | n2=en:one family with a deletion upstream of the lmnb1 gene did not have autonomic symptoms or cerebellar involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a fatal subacute encephalopathy has been reported
n1=Lester (signe de) | n2=en:one family with a fatal subacute encephalopathy has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with a proven mutation has been reported (last curated november 2015) molecular genetics : caused by mutation in the rna-binding motif protein, x chromosome gene (rbmx, 300199.0001)
n1=Lester (signe de) | n2=en:one family with a proven mutation has been reported (last curated november 2015) molecular genetics : caused by mutation in the rna-binding motif protein, x chromosome gene (rbmx, 300199.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with autosomal dominant inheritance had only progressive bone marrow failure
n1=Lester (signe de) | n2=en:one family with autosomal dominant inheritance had only progressive bone marrow failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with autosomal dominant inheritance has been reported and 1 family with autosomal recessive inheritance has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one family with autosomal dominant inheritance has been reported and 1 family with autosomal recessive inheritance has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with compound heterozygous slc26a5 mutation has been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:one family with compound heterozygous slc26a5 mutation has been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with confirmed cecr1 mutation has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one family with confirmed cecr1 mutation has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with confirmed genetic basis has been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:one family with confirmed genetic basis has been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one family with late-adult onset and cerebellar ataxia has been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one family with late-adult onset and cerebellar ataxia has been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one french family has been reported (as of march 2012)
n1=Lester (signe de) | n2=en:one french family has been reported (as of march 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one french family has been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:one french family has been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one french family has been reported (last curated march 2013)
n1=Lester (signe de) | n2=en:one french family has been reported (last curated march 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one german family has been reported (as of september 2009)
n1=Lester (signe de) | n2=en:one german family has been reported (as of september 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one han chinese family and one german family have been described (last curated april 2015)
n1=Lester (signe de) | n2=en:one han chinese family and one german family have been described (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one indian family has been reported (as of october 2011)
n1=Lester (signe de) | n2=en:one indian family has been reported (as of october 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one individual carried a heterozygous mutation, whereas the other carried a homozygous mutation.
n1=Lester (signe de) | n2=en:one individual carried a heterozygous mutation, whereas the other carried a homozygous mutation. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one israeli arab family has been reported with ptprf mutation (last curated september 2014)
n1=Lester (signe de) | n2=en:one israeli arab family has been reported with ptprf mutation (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one italian family has been described (last curated august 2015)
n1=Lester (signe de) | n2=en:one italian family has been described (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one italian family has been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:one italian family has been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one japanese family has been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:one japanese family has been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one japanese patient has been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:one japanese patient has been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one korean family has been reported (as of november 2011)
n1=Lester (signe de) | n2=en:one korean family has been reported (as of november 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large 3-generation irish family has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one large 3-generation irish family has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large 4-generation uruguayan family reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one large 4-generation uruguayan family reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large consanguineous arab muslim family has been reported (as of september 2011)
n1=Lester (signe de) | n2=en:one large consanguineous arab muslim family has been reported (as of september 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large consanguineous baluchi family from the united arab emirates has been reported with limited clinical information (last curated august 2015)
n1=Lester (signe de) | n2=en:one large consanguineous baluchi family from the united arab emirates has been reported with limited clinical information (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large consanguineous israeli bedouin kindred has been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:one large consanguineous israeli bedouin kindred has been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large consanguineous kindred of israeli muslim descent has been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:one large consanguineous kindred of israeli muslim descent has been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large family has been reported (as of 2008)
n1=Lester (signe de) | n2=en:one large family has been reported (as of 2008) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large family has been reported (last curated june 2013)
n1=Lester (signe de) | n2=en:one large family has been reported (last curated june 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large french family and 1 patient with sporadic occurrence have been reported (last curated january 2013)
n1=Lester (signe de) | n2=en:one large french family and 1 patient with sporadic occurrence have been reported (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large italian kindred has been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:one large italian kindred has been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large spanish family and 1 unrelated patient have been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:one large spanish family and 1 unrelated patient have been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one large swedish family has been reported (as of april 2012)
n1=Lester (signe de) | n2=en:one large swedish family has been reported (as of april 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one lebanese family has been reported
n1=Lester (signe de) | n2=en:one lebanese family has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one likely consanguineous turkish family has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one likely consanguineous turkish family has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one living patient and 1 unrelated fetus have been reported (last curated august, 2014)
n1=Lester (signe de) | n2=en:one living patient and 1 unrelated fetus have been reported (last curated august, 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one male patient has been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:one male patient has been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one of the 2 most common forms of albinism in the world, along with oca2
n1=Lester (signe de) | n2=en:one of the 2 most common forms of albinism in the world, along with oca2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one of the 2 most common forms of oca in the world along with oca1
n1=Lester (signe de) | n2=en:one of the 2 most common forms of oca in the world along with oca1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one of the most common autoimmune diseases
n1=Lester (signe de) | n2=en:one of the most common autoimmune diseases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one pakistani family has been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:one pakistani family has been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one pakistani family has been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:one pakistani family has been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one pakistani family reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one pakistani family reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one pakistani reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one pakistani reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one palestinian family and one lebanese family have been described (last curated march 2016)
n1=Lester (signe de) | n2=en:one palestinian family and one lebanese family have been described (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient (patient a) and 2 sibs have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one patient (patient a) and 2 sibs have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient (patient b) with autosomal recessive inheritance had a more severe phenotype
n1=Lester (signe de) | n2=en:one patient (patient b) with autosomal recessive inheritance had a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient described as having bbs, but with no clinical details has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one patient described as having bbs, but with no clinical details has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient died at 17 months of age
n1=Lester (signe de) | n2=en:one patient died at 17 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient died at age 7 years
n1=Lester (signe de) | n2=en:one patient died at age 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient from a consanguineous lebanese family and one patient from a consanguineous kurdish family have been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:one patient from a consanguineous lebanese family and one patient from a consanguineous kurdish family have been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient had onset at age 4 months after normal development
n1=Lester (signe de) | n2=en:one patient had onset at age 4 months after normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient had onset at birth and a more severe disorder resulting in death at a young age
n1=Lester (signe de) | n2=en:one patient had onset at birth and a more severe disorder resulting in death at a young age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been described (last curated january 2016)
n1=Lester (signe de) | n2=en:one patient has been described (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported
n1=Lester (signe de) | n2=en:one patient has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of april 2011)
n1=Lester (signe de) | n2=en:one patient has been reported (as of april 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of august 2010)
n1=Lester (signe de) | n2=en:one patient has been reported (as of august 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of curation date may, 2013)
n1=Lester (signe de) | n2=en:one patient has been reported (as of curation date may, 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of december 2011)
n1=Lester (signe de) | n2=en:one patient has been reported (as of december 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of february 2012)
n1=Lester (signe de) | n2=en:one patient has been reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of july 2010)
n1=Lester (signe de) | n2=en:one patient has been reported (as of july 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of march 2011)
n1=Lester (signe de) | n2=en:one patient has been reported (as of march 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of may 2011)
n1=Lester (signe de) | n2=en:one patient has been reported (as of may 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (as of sept 2011)
n1=Lester (signe de) | n2=en:one patient has been reported (as of sept 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated january 2010)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated january 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated january 2014)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated july 2013)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated may 2012)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated november 2010)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated november 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated november 2013)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:one patient has been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient has had favorable response to high dose coenzyme q10 supplementation in combination with other medications
n1=Lester (signe de) | n2=en:one patient has had favorable response to high dose coenzyme q10 supplementation in combination with other medications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient reported (last curated november 2012)
n1=Lester (signe de) | n2=en:one patient reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient reported (last curated november 2013)
n1=Lester (signe de) | n2=en:one patient reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient reported with col3a1 mutation (120180.0020)
n1=Lester (signe de) | n2=en:one patient reported with col3a1 mutation (120180.0020) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient reported with slitrk1 mutation (as of january 2010)
n1=Lester (signe de) | n2=en:one patient reported with slitrk1 mutation (as of january 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient showed improvement and was thriving at 46 months of age
n1=Lester (signe de) | n2=en:one patient showed improvement and was thriving at 46 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient studied at molecular level (as of july 2011)
n1=Lester (signe de) | n2=en:one patient studied at molecular level (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient was asymptomatic and detected by neonatal screening
n1=Lester (signe de) | n2=en:one patient was asymptomatic and detected by neonatal screening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient was less severely affected
n1=Lester (signe de) | n2=en:one patient was less severely affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with a de novo mutation has been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:one patient with a de novo mutation has been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with a homozygous mutation has been reported (as of 14 june 2011)
n1=Lester (signe de) | n2=en:one patient with a homozygous mutation has been reported (as of 14 june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with a point mutation in the zbtb18 gene has been reported (last curated november 2013)
n1=Lester (signe de) | n2=en:one patient with a point mutation in the zbtb18 gene has been reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with additional features of fanconi anemia has been reported
n1=Lester (signe de) | n2=en:one patient with additional features of fanconi anemia has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with compound heterozygous pnpla8 mutations has been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:one patient with compound heterozygous pnpla8 mutations has been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with episodic ataxia and later onset has been reported (as of june 2010)
n1=Lester (signe de) | n2=en:one patient with episodic ataxia and later onset has been reported (as of june 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with limited clinical information has been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:one patient with limited clinical information has been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with normal cognition has been reported
n1=Lester (signe de) | n2=en:one patient with normal cognition has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with normal psychomotor development has been reported
n1=Lester (signe de) | n2=en:one patient with normal psychomotor development has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with normal psychomotor development has been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:one patient with normal psychomotor development has been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with severe congenital onset has been reported
n1=Lester (signe de) | n2=en:one patient with severe congenital onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one patient with unrelated german parents has been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:one patient with unrelated german parents has been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one report of a large italian family from sardinia (last curated december 2015)
n1=Lester (signe de) | n2=en:one report of a large italian family from sardinia (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one report of a mother who was mosaic for ring chromosome 14 transmitting it to her 2 sons
n1=Lester (signe de) | n2=en:one report of a mother who was mosaic for ring chromosome 14 transmitting it to her 2 sons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one report of brother and sister from nonconsanguineous parents
n1=Lester (signe de) | n2=en:one report of brother and sister from nonconsanguineous parents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one report of mother and son (last curated august 2012)
n1=Lester (signe de) | n2=en:one report of mother and son (last curated august 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one six-generation family from northern china has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one six-generation family from northern china has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one spanish family has been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:one spanish family has been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one spanish family has been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:one spanish family has been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one swedish patient has been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:one swedish patient has been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one swiss family with 19 affected individuals has been described (last curated february 2014)
n1=Lester (signe de) | n2=en:one swiss family with 19 affected individuals has been described (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one third of patients represent new mutations
n1=Lester (signe de) | n2=en:one third of patients represent new mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one turkish girl has been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:one turkish girl has been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one-third of cases are familial
n1=Lester (signe de) | n2=en:one-third of cases are familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:one-third of cases are sporadic
n1=Lester (signe de) | n2=en:one-third of cases are sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only 1 family had ultrastructural cellular findings of neuronal ceroid lipofuscinosis
n1=Lester (signe de) | n2=en:only 1 family had ultrastructural cellular findings of neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only 10% develop hypertension at 18 years of age or less
n1=Lester (signe de) | n2=en:only 10% develop hypertension at 18 years of age or less | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only 13% develop hypertension at 18 years of age or less
n1=Lester (signe de) | n2=en:only 13% develop hypertension at 18 years of age or less | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only 46,xy individuals are affected
n1=Lester (signe de) | n2=en:only 46,xy individuals are affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only apparent in patients taking eculizumab
n1=Lester (signe de) | n2=en:only apparent in patients taking eculizumab | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only female patients reported (last curated october 2013)
n1=Lester (signe de) | n2=en:only female patients reported (last curated october 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only individuals homozygous for risk or non-risk alleles were studied
n1=Lester (signe de) | n2=en:only individuals homozygous for risk or non-risk alleles were studied | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only some patients showed neurologic involvement
n1=Lester (signe de) | n2=en:only some patients showed neurologic involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:only women have been reported
n1=Lester (signe de) | n2=en:only women have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset - present at birth
n1=Lester (signe de) | n2=en:onset - present at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset <30 months
n1=Lester (signe de) | n2=en:onset <30 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 0-12 hours after birth
n1=Lester (signe de) | n2=en:onset 0-12 hours after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 1-12 years
n1=Lester (signe de) | n2=en:onset 1-12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 1-70 years of age (95% by early 50's)
n1=Lester (signe de) | n2=en:onset 1-70 years of age (95% by early 50's) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 10-20 years of age
n1=Lester (signe de) | n2=en:onset 10-20 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 13 to 63 years of age
n1=Lester (signe de) | n2=en:onset 13 to 63 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 13-15 years
n1=Lester (signe de) | n2=en:onset 13-15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 14 months to 4 years of age
n1=Lester (signe de) | n2=en:onset 14 months to 4 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 2-4 years of age in iia
n1=Lester (signe de) | n2=en:onset 2-4 years of age in iia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 20-55 years of age
n1=Lester (signe de) | n2=en:onset 20-55 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 23 to 30 years
n1=Lester (signe de) | n2=en:onset 23 to 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 3 months of age up to 5 years
n1=Lester (signe de) | n2=en:onset 3 months of age up to 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 30-40 years of age
n1=Lester (signe de) | n2=en:onset 30-40 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 3rd to 4th decade of life
n1=Lester (signe de) | n2=en:onset 3rd to 4th decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 5 to 10 years of age
n1=Lester (signe de) | n2=en:onset 5 to 10 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 5 to 7 years
n1=Lester (signe de) | n2=en:onset 5 to 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 5-30 years
n1=Lester (signe de) | n2=en:onset 5-30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 50 to 65 years
n1=Lester (signe de) | n2=en:onset 50 to 65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 6 months to 2.5 years
n1=Lester (signe de) | n2=en:onset 6 months to 2.5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 6 to 12 months
n1=Lester (signe de) | n2=en:onset 6 to 12 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 6 to 18 months
n1=Lester (signe de) | n2=en:onset 6 to 18 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 6 to 30 years
n1=Lester (signe de) | n2=en:onset 6 to 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 6-13 years
n1=Lester (signe de) | n2=en:onset 6-13 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 7 to 15 months of age
n1=Lester (signe de) | n2=en:onset 7 to 15 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 70-90 years
n1=Lester (signe de) | n2=en:onset 70-90 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset 8-20 years
n1=Lester (signe de) | n2=en:onset 8-20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset about 6 months of age after normal growth and development in the first few months of life
n1=Lester (signe de) | n2=en:onset about 6 months of age after normal growth and development in the first few months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset after age 20 years
n1=Lester (signe de) | n2=en:onset after age 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset after age 40 years
n1=Lester (signe de) | n2=en:onset after age 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset after puberty
n1=Lester (signe de) | n2=en:onset after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset after third decade
n1=Lester (signe de) | n2=en:onset after third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset age 14-28 years
n1=Lester (signe de) | n2=en:onset age 14-28 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset age 15-25 years
n1=Lester (signe de) | n2=en:onset age 15-25 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset age 2 to 7 years
n1=Lester (signe de) | n2=en:onset age 2 to 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset age 20 to 51 years
n1=Lester (signe de) | n2=en:onset age 20 to 51 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset age 32 to 45 years
n1=Lester (signe de) | n2=en:onset age 32 to 45 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ages 2 to 14 years
n1=Lester (signe de) | n2=en:onset ages 2 to 14 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset and diagnosis may occur later (after age 20 years)
n1=Lester (signe de) | n2=en:onset and diagnosis may occur later (after age 20 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset around adolescence in males
n1=Lester (signe de) | n2=en:onset around adolescence in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset around age 2 years
n1=Lester (signe de) | n2=en:onset around age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset around puberty
n1=Lester (signe de) | n2=en:onset around puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset as neonate
n1=Lester (signe de) | n2=en:onset as neonate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 2 to 15 years
n1=Lester (signe de) | n2=en:onset at 2 to 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 2 to 4 years
n1=Lester (signe de) | n2=en:onset at 2 to 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 4 to 10 years
n1=Lester (signe de) | n2=en:onset at 4 to 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 4 to 7 years
n1=Lester (signe de) | n2=en:onset at 4 to 7 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 4 to 9 weeks of age
n1=Lester (signe de) | n2=en:onset at 4 to 9 weeks of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 4 years of age
n1=Lester (signe de) | n2=en:onset at 4 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 5-24 months
n1=Lester (signe de) | n2=en:onset at 5-24 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 6-36 hours of life
n1=Lester (signe de) | n2=en:onset at 6-36 hours of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at 6-9 months
n1=Lester (signe de) | n2=en:onset at 6-9 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at age 10 to 14 years
n1=Lester (signe de) | n2=en:onset at age 10 to 14 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at age 3-5 years
n1=Lester (signe de) | n2=en:onset at age 3-5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at age 36 years
n1=Lester (signe de) | n2=en:onset at age 36 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at age 5 to 15 years
n1=Lester (signe de) | n2=en:onset at age 5 to 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at age 5 years
n1=Lester (signe de) | n2=en:onset at age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at birth or early childhood
n1=Lester (signe de) | n2=en:onset at birth or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at birth or early infancy
n1=Lester (signe de) | n2=en:onset at birth or early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at birth or in first days or life
n1=Lester (signe de) | n2=en:onset at birth or in first days or life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at birth or in first months of life
n1=Lester (signe de) | n2=en:onset at birth or in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at day 1 of life has been reported
n1=Lester (signe de) | n2=en:onset at day 1 of life has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at early age, associated with sudden death in childhood
n1=Lester (signe de) | n2=en:onset at early age, associated with sudden death in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset at or soon after birth
n1=Lester (signe de) | n2=en:onset at or soon after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before 10 years of age in all patients
n1=Lester (signe de) | n2=en:onset before 10 years of age in all patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before 18 months of age
n1=Lester (signe de) | n2=en:onset before 18 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before 50 years of age
n1=Lester (signe de) | n2=en:onset before 50 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before adolescence
n1=Lester (signe de) | n2=en:onset before adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 2 years
n1=Lester (signe de) | n2=en:onset before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 20
n1=Lester (signe de) | n2=en:onset before age 20 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 20 years
n1=Lester (signe de) | n2=en:onset before age 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 3 years
n1=Lester (signe de) | n2=en:onset before age 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 40 years
n1=Lester (signe de) | n2=en:onset before age 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 5 years
n1=Lester (signe de) | n2=en:onset before age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset before age 5 years in the absence of instruction
n1=Lester (signe de) | n2=en:onset before age 5 years in the absence of instruction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 1-3 years
n1=Lester (signe de) | n2=en:onset between 1-3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 10 and 20 years of age
n1=Lester (signe de) | n2=en:onset between 10 and 20 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 12 and 30 years (average 22)
n1=Lester (signe de) | n2=en:onset between 12 and 30 years (average 22) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 13 to 37 years
n1=Lester (signe de) | n2=en:onset between 13 to 37 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 15 and 27 years
n1=Lester (signe de) | n2=en:onset between 15 and 27 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 18 and 65 years
n1=Lester (signe de) | n2=en:onset between 18 and 65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 2 and 4 years of age
n1=Lester (signe de) | n2=en:onset between 2 and 4 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 2 to 20 years
n1=Lester (signe de) | n2=en:onset between 2 to 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 2-5 years
n1=Lester (signe de) | n2=en:onset between 2-5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 28 and 42 years
n1=Lester (signe de) | n2=en:onset between 28 and 42 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 28-32 weeks of gestation
n1=Lester (signe de) | n2=en:onset between 28-32 weeks of gestation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 3 and 11 years of age
n1=Lester (signe de) | n2=en:onset between 3 and 11 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 3 and 6 months of age
n1=Lester (signe de) | n2=en:onset between 3 and 6 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 3 and 8 months of age
n1=Lester (signe de) | n2=en:onset between 3 and 8 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 34 and 51 years of age
n1=Lester (signe de) | n2=en:onset between 34 and 51 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 35-43 years of age
n1=Lester (signe de) | n2=en:onset between 35-43 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 5 and 20 years
n1=Lester (signe de) | n2=en:onset between 5 and 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 5 to 28 years of age
n1=Lester (signe de) | n2=en:onset between 5 to 28 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 6 and 12 months of age
n1=Lester (signe de) | n2=en:onset between 6 and 12 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 6 and 14 years
n1=Lester (signe de) | n2=en:onset between 6 and 14 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 6 and 15 years
n1=Lester (signe de) | n2=en:onset between 6 and 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 6 and 16 years of age
n1=Lester (signe de) | n2=en:onset between 6 and 16 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 6 and 9 months after normal early development
n1=Lester (signe de) | n2=en:onset between 6 and 9 months after normal early development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 7 and 18 years
n1=Lester (signe de) | n2=en:onset between 7 and 18 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 7 and 27 years of age
n1=Lester (signe de) | n2=en:onset between 7 and 27 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 8 and 30 years
n1=Lester (signe de) | n2=en:onset between 8 and 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between 9 and 16 years
n1=Lester (signe de) | n2=en:onset between 9 and 16 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between age 2 and 15 years
n1=Lester (signe de) | n2=en:onset between age 2 and 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between age 30-50 years
n1=Lester (signe de) | n2=en:onset between age 30-50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between age 4 to 7 months
n1=Lester (signe de) | n2=en:onset between age 4 to 7 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 1 to 3 years
n1=Lester (signe de) | n2=en:onset between ages 1 to 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 10 and 25 years
n1=Lester (signe de) | n2=en:onset between ages 10 and 25 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 12 and 20 years
n1=Lester (signe de) | n2=en:onset between ages 12 and 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 16-55
n1=Lester (signe de) | n2=en:onset between ages 16-55 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 2 and 5 years
n1=Lester (signe de) | n2=en:onset between ages 2 and 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between ages 5 and 15 years
n1=Lester (signe de) | n2=en:onset between ages 5 and 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between birth and 3 months of age
n1=Lester (signe de) | n2=en:onset between birth and 3 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between second to sixth decades of life
n1=Lester (signe de) | n2=en:onset between second to sixth decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset between the second and sixth decades
n1=Lester (signe de) | n2=en:onset between the second and sixth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset beyond the second year of life
n1=Lester (signe de) | n2=en:onset beyond the second year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset bimodal, ages 16-22 and ages 57-60
n1=Lester (signe de) | n2=en:onset bimodal, ages 16-22 and ages 57-60 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset birth to 6 months
n1=Lester (signe de) | n2=en:onset birth to 6 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset birth to early childhood
n1=Lester (signe de) | n2=en:onset birth to early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset birth to early infancy
n1=Lester (signe de) | n2=en:onset birth to early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset by 1 year of age
n1=Lester (signe de) | n2=en:onset by 1 year of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset by 3 years of age
n1=Lester (signe de) | n2=en:onset by 3 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset by 7-8 years of age progressing to moderate-to-severe loss of mid and high frequencies during adulthood in a consanguineous iranian family
n1=Lester (signe de) | n2=en:onset by 7-8 years of age progressing to moderate-to-severe loss of mid and high frequencies during adulthood in a consanguineous iranian family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset by age 2 years
n1=Lester (signe de) | n2=en:onset by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset day of life 1-10 in infants fed lactose-containing milk
n1=Lester (signe de) | n2=en:onset day of life 1-10 in infants fed lactose-containing milk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset during childhood (8-10 years of age) progressing to profound deafness by ~50 years of age
n1=Lester (signe de) | n2=en:onset during childhood (8-10 years of age) progressing to profound deafness by ~50 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset during the second/third decade of life with high frequency loss slowly progressing and extending to all frequencies by the fifth/sixth decade of life
n1=Lester (signe de) | n2=en:onset during the second/third decade of life with high frequency loss slowly progressing and extending to all frequencies by the fifth/sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset early childhood
n1=Lester (signe de) | n2=en:onset early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset early in first decade
n1=Lester (signe de) | n2=en:onset early in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset first to seventh decade with 30 to 40 year mode
n1=Lester (signe de) | n2=en:onset first to seventh decade with 30 to 40 year mode | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset from birth
n1=Lester (signe de) | n2=en:onset from birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset from first to third decades of life
n1=Lester (signe de) | n2=en:onset from first to third decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in 1st to 3rd decade of life
n1=Lester (signe de) | n2=en:onset in 1st to 3rd decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence
n1=Lester (signe de) | n2=en:onset in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence or adulthood
n1=Lester (signe de) | n2=en:onset in adolescence or adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence or adulthood has been reported
n1=Lester (signe de) | n2=en:onset in adolescence or adulthood has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence or young adulthood
n1=Lester (signe de) | n2=en:onset in adolescence or young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence or young adulthood has been reported
n1=Lester (signe de) | n2=en:onset in adolescence or young adulthood has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adolescence to early adulthood
n1=Lester (signe de) | n2=en:onset in adolescence to early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in adulthood (third to fourth decade)
n1=Lester (signe de) | n2=en:onset in adulthood (third to fourth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (1 to 7 years) of progressive cardiomyopathy and muscle weakness
n1=Lester (signe de) | n2=en:onset in childhood (1 to 7 years) of progressive cardiomyopathy and muscle weakness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (3 to 10 years)
n1=Lester (signe de) | n2=en:onset in childhood (3 to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (5 to 10 years)
n1=Lester (signe de) | n2=en:onset in childhood (5 to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (6-7 years)
n1=Lester (signe de) | n2=en:onset in childhood (6-7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (ages 1.5 to 7 years)
n1=Lester (signe de) | n2=en:onset in childhood (ages 1.5 to 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (later than in antenatal bartter syndrome 241200)
n1=Lester (signe de) | n2=en:onset in childhood (later than in antenatal bartter syndrome 241200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (mean 6 years)
n1=Lester (signe de) | n2=en:onset in childhood (mean 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (mean age 10 years)
n1=Lester (signe de) | n2=en:onset in childhood (mean age 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range 0.5 to 7 years)
n1=Lester (signe de) | n2=en:onset in childhood (range 0.5 to 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range 1 to 12 years)
n1=Lester (signe de) | n2=en:onset in childhood (range 1 to 12 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range 1 to 9 years)
n1=Lester (signe de) | n2=en:onset in childhood (range 1 to 9 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range 2 to 16 years)
n1=Lester (signe de) | n2=en:onset in childhood (range 2 to 16 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range 4 to 12 years)
n1=Lester (signe de) | n2=en:onset in childhood (range 4 to 12 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range birth to 10 years)
n1=Lester (signe de) | n2=en:onset in childhood (range birth to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range infancy to 10 years)
n1=Lester (signe de) | n2=en:onset in childhood (range infancy to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (range infancy to 14 years)
n1=Lester (signe de) | n2=en:onset in childhood (range infancy to 14 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood (usually before age 5 years)
n1=Lester (signe de) | n2=en:onset in childhood (usually before age 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood of blistering and pigmentary changes
n1=Lester (signe de) | n2=en:onset in childhood of blistering and pigmentary changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or adolescence
n1=Lester (signe de) | n2=en:onset in childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or adolescence (mean age of 6 years, range 1 to 18)
n1=Lester (signe de) | n2=en:onset in childhood or adolescence (mean age of 6 years, range 1 to 18) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or adolescence (median age of 9 years)
n1=Lester (signe de) | n2=en:onset in childhood or adolescence (median age of 9 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or adolescence (range 6 to 15 years)
n1=Lester (signe de) | n2=en:onset in childhood or adolescence (range 6 to 15 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or adolescence in most patients
n1=Lester (signe de) | n2=en:onset in childhood or adolescence in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or as young adult
n1=Lester (signe de) | n2=en:onset in childhood or as young adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or early adolescence
n1=Lester (signe de) | n2=en:onset in childhood or early adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or early adulthood
n1=Lester (signe de) | n2=en:onset in childhood or early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or second decade
n1=Lester (signe de) | n2=en:onset in childhood or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or teenage years (7 to 16 years)
n1=Lester (signe de) | n2=en:onset in childhood or teenage years (7 to 16 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or young adulthood
n1=Lester (signe de) | n2=en:onset in childhood or young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood or youth
n1=Lester (signe de) | n2=en:onset in childhood or youth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood with exacerbation during puberty
n1=Lester (signe de) | n2=en:onset in childhood with exacerbation during puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood, adolescence
n1=Lester (signe de) | n2=en:onset in childhood, adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood, adolescence, and adulthood
n1=Lester (signe de) | n2=en:onset in childhood, adolescence, and adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in childhood, but most noticeable in mid-teens and early adulthood
n1=Lester (signe de) | n2=en:onset in childhood, but most noticeable in mid-teens and early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early adulthood (average 26 years)
n1=Lester (signe de) | n2=en:onset in early adulthood (average 26 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (2-4 years)
n1=Lester (signe de) | n2=en:onset in early childhood (2-4 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (4 to 5 years)
n1=Lester (signe de) | n2=en:onset in early childhood (4 to 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (age 3)
n1=Lester (signe de) | n2=en:onset in early childhood (age 3) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (infancy to 5 years)
n1=Lester (signe de) | n2=en:onset in early childhood (infancy to 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (infancy to 6 years)
n1=Lester (signe de) | n2=en:onset in early childhood (infancy to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood (infancy to age 7 years)
n1=Lester (signe de) | n2=en:onset in early childhood (infancy to age 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood after initial normal development
n1=Lester (signe de) | n2=en:onset in early childhood after initial normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood or adolescence
n1=Lester (signe de) | n2=en:onset in early childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early childhood to puberty
n1=Lester (signe de) | n2=en:onset in early childhood to puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early first decade, although some patients have onset at birth or early in infancy
n1=Lester (signe de) | n2=en:onset in early first decade, although some patients have onset at birth or early in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early infancy
n1=Lester (signe de) | n2=en:onset in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early infancy (2 to 3 months of age)
n1=Lester (signe de) | n2=en:onset in early infancy (2 to 3 months of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early infancy, between 2 weeks and 3 months
n1=Lester (signe de) | n2=en:onset in early infancy, between 2 weeks and 3 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early to late childhood
n1=Lester (signe de) | n2=en:onset in early to late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in early twenties
n1=Lester (signe de) | n2=en:onset in early twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in feet and legs (peroneal distribution)
n1=Lester (signe de) | n2=en:onset in feet and legs (peroneal distribution) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in females ranges from third to seventh decade
n1=Lester (signe de) | n2=en:onset in females ranges from third to seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fifth or sixth decade
n1=Lester (signe de) | n2=en:onset in fifth or sixth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fifties or sixties
n1=Lester (signe de) | n2=en:onset in fifties or sixties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first 2 decades
n1=Lester (signe de) | n2=en:onset in first 2 decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first 2 decades (range 6 to 15 years)
n1=Lester (signe de) | n2=en:onset in first 2 decades (range 6 to 15 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first 2 decades of life
n1=Lester (signe de) | n2=en:onset in first 2 decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first 6 months of life
n1=Lester (signe de) | n2=en:onset in first 6 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first 8 weeks of life
n1=Lester (signe de) | n2=en:onset in first 8 weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first and second decades
n1=Lester (signe de) | n2=en:onset in first and second decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first days of life
n1=Lester (signe de) | n2=en:onset in first days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade
n1=Lester (signe de) | n2=en:onset in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (as early as infancy in some)
n1=Lester (signe de) | n2=en:onset in first decade (as early as infancy in some) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (average 5 years)
n1=Lester (signe de) | n2=en:onset in first decade (average 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (birth to 6 years)
n1=Lester (signe de) | n2=en:onset in first decade (birth to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (birth to age 5 years)
n1=Lester (signe de) | n2=en:onset in first decade (birth to age 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (e.g. 180380.0028)
n1=Lester (signe de) | n2=en:onset in first decade (e.g. 180380.0028) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (range 1 to 7 years)
n1=Lester (signe de) | n2=en:onset in first decade (range 1 to 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade (range 1 to 9 years)
n1=Lester (signe de) | n2=en:onset in first decade (range 1 to 9 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade after normal early development
n1=Lester (signe de) | n2=en:onset in first decade after normal early development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade of life
n1=Lester (signe de) | n2=en:onset in first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decade of life affecting first higher frequencies, then middle to lower frequencies with age
n1=Lester (signe de) | n2=en:onset in first decade of life affecting first higher frequencies, then middle to lower frequencies with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first decades (males)
n1=Lester (signe de) | n2=en:onset in first decades (males) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first few years of life
n1=Lester (signe de) | n2=en:onset in first few years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first hours to days of life
n1=Lester (signe de) | n2=en:onset in first hours to days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first month of life
n1=Lester (signe de) | n2=en:onset in first month of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first months of life
n1=Lester (signe de) | n2=en:onset in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first months or years of life
n1=Lester (signe de) | n2=en:onset in first months or years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first or second decade (range 4 to 13 years)
n1=Lester (signe de) | n2=en:onset in first or second decade (range 4 to 13 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first or second decade (range infancy to teenage years)
n1=Lester (signe de) | n2=en:onset in first or second decade (range infancy to teenage years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first or second decades
n1=Lester (signe de) | n2=en:onset in first or second decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first weeks or months of life
n1=Lester (signe de) | n2=en:onset in first weeks or months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in first weeks to months of life
n1=Lester (signe de) | n2=en:onset in first weeks to months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fourth and fifth decades
n1=Lester (signe de) | n2=en:onset in fourth and fifth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fourth decade
n1=Lester (signe de) | n2=en:onset in fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fourth to fifth decade
n1=Lester (signe de) | n2=en:onset in fourth to fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in fourth to sixth decades
n1=Lester (signe de) | n2=en:onset in fourth to sixth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (1-2 years)
n1=Lester (signe de) | n2=en:onset in infancy (1-2 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (3 months on)
n1=Lester (signe de) | n2=en:onset in infancy (3 months on) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (3 to 7 months)
n1=Lester (signe de) | n2=en:onset in infancy (3 to 7 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (average 4 months, but may be earlier)
n1=Lester (signe de) | n2=en:onset in infancy (average 4 months, but may be earlier) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (first hours to weeks of life)
n1=Lester (signe de) | n2=en:onset in infancy (first hours to weeks of life) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy (first year of life)
n1=Lester (signe de) | n2=en:onset in infancy (first year of life) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy after normal birth and neonatal period
n1=Lester (signe de) | n2=en:onset in infancy after normal birth and neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy after weaning
n1=Lester (signe de) | n2=en:onset in infancy after weaning | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy after weaning from being breast-fed
n1=Lester (signe de) | n2=en:onset in infancy after weaning from being breast-fed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy and early childhood
n1=Lester (signe de) | n2=en:onset in infancy and early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy and third decade had been reported
n1=Lester (signe de) | n2=en:onset in infancy and third decade had been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy of acute hypoglycemic episodes
n1=Lester (signe de) | n2=en:onset in infancy of acute hypoglycemic episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or at birth
n1=Lester (signe de) | n2=en:onset in infancy or at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or childhood
n1=Lester (signe de) | n2=en:onset in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or childhood (range 1 to 13 years)
n1=Lester (signe de) | n2=en:onset in infancy or childhood (range 1 to 13 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or childhood (range 1 to 6 years)
n1=Lester (signe de) | n2=en:onset in infancy or childhood (range 1 to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or early childhood
n1=Lester (signe de) | n2=en:onset in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or early childhood (before age 3 years)
n1=Lester (signe de) | n2=en:onset in infancy or early childhood (before age 3 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or early childhood (birth to 6 years)
n1=Lester (signe de) | n2=en:onset in infancy or early childhood (birth to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or first years of life
n1=Lester (signe de) | n2=en:onset in infancy or first years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or in the first months of life
n1=Lester (signe de) | n2=en:onset in infancy or in the first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy or late childhood
n1=Lester (signe de) | n2=en:onset in infancy or late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy up to 3 years
n1=Lester (signe de) | n2=en:onset in infancy up to 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy was reported in 1 family
n1=Lester (signe de) | n2=en:onset in infancy was reported in 1 family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in infancy, but may not be diagnosed until later in mild cases
n1=Lester (signe de) | n2=en:onset in infancy, but may not be diagnosed until later in mild cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late adulthood
n1=Lester (signe de) | n2=en:onset in late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late adulthood (44 to 73 years)
n1=Lester (signe de) | n2=en:onset in late adulthood (44 to 73 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late childhood (after age 10 years)
n1=Lester (signe de) | n2=en:onset in late childhood (after age 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late childhood or adulthood
n1=Lester (signe de) | n2=en:onset in late childhood or adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late childhood or early teens
n1=Lester (signe de) | n2=en:onset in late childhood or early teens | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late childhood/adolescence (approximately 15 years)
n1=Lester (signe de) | n2=en:onset in late childhood/adolescence (approximately 15 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late infancy
n1=Lester (signe de) | n2=en:onset in late infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late teens to early forties
n1=Lester (signe de) | n2=en:onset in late teens to early forties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late teens to twenties
n1=Lester (signe de) | n2=en:onset in late teens to twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late twenties
n1=Lester (signe de) | n2=en:onset in late twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late twenties to thirties
n1=Lester (signe de) | n2=en:onset in late twenties to thirties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in late-childhood to early adulthood (12 to 20 years)
n1=Lester (signe de) | n2=en:onset in late-childhood to early adulthood (12 to 20 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in lower limbs
n1=Lester (signe de) | n2=en:onset in lower limbs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in males in first to third decade
n1=Lester (signe de) | n2=en:onset in males in first to third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in mid to late childhood
n1=Lester (signe de) | n2=en:onset in mid to late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in mid-adulthood
n1=Lester (signe de) | n2=en:onset in mid-adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in mid-forties
n1=Lester (signe de) | n2=en:onset in mid-forties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in middle age (44 to 60 years)
n1=Lester (signe de) | n2=en:onset in middle age (44 to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in neonatal period or before age 2 years
n1=Lester (signe de) | n2=en:onset in neonatal period or before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in neonatal period or early infancy
n1=Lester (signe de) | n2=en:onset in neonatal period or early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in neonatal period or infancy
n1=Lester (signe de) | n2=en:onset in neonatal period or infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in newborns or infants
n1=Lester (signe de) | n2=en:onset in newborns or infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second and third decades
n1=Lester (signe de) | n2=en:onset in second and third decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second and third decades of life
n1=Lester (signe de) | n2=en:onset in second and third decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second decade
n1=Lester (signe de) | n2=en:onset in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second decade of life progresses from mild to profound hearing loss
n1=Lester (signe de) | n2=en:onset in second decade of life progresses from mild to profound hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second decade or as young adult
n1=Lester (signe de) | n2=en:onset in second decade or as young adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second decade or unilateral involvement indicates a diagnosis of 'progressive cribriform and zosteriform hyperpigmentation' (pczh)
n1=Lester (signe de) | n2=en:onset in second decade or unilateral involvement indicates a diagnosis of 'progressive cribriform and zosteriform hyperpigmentation' (pczh) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second decade, but sometimes earlier
n1=Lester (signe de) | n2=en:onset in second decade, but sometimes earlier | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second half of the first decade of life
n1=Lester (signe de) | n2=en:onset in second half of the first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second or third decades
n1=Lester (signe de) | n2=en:onset in second or third decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second to fifth decade
n1=Lester (signe de) | n2=en:onset in second to fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second to fourth decade
n1=Lester (signe de) | n2=en:onset in second to fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in second to third decades (postlingual)
n1=Lester (signe de) | n2=en:onset in second to third decades (postlingual) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teenage or young adult years
n1=Lester (signe de) | n2=en:onset in teenage or young adult years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teenage years
n1=Lester (signe de) | n2=en:onset in teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teens has been reported
n1=Lester (signe de) | n2=en:onset in teens has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teens or early twenties
n1=Lester (signe de) | n2=en:onset in teens or early twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teens or young adulthood (range 13 to 45 years)
n1=Lester (signe de) | n2=en:onset in teens or young adulthood (range 13 to 45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teens to 20's
n1=Lester (signe de) | n2=en:onset in teens to 20's | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in teens to late twenties (range 14 to 44 years)
n1=Lester (signe de) | n2=en:onset in teens to late twenties (range 14 to 44 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the 3rd decade of life or later
n1=Lester (signe de) | n2=en:onset in the 3rd decade of life or later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first 2 years of life
n1=Lester (signe de) | n2=en:onset in the first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first decade (range birth to 8 years)
n1=Lester (signe de) | n2=en:onset in the first decade (range birth to 8 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first few months of life patients may need lifelong total parenteral nutrition
n1=Lester (signe de) | n2=en:onset in the first few months of life patients may need lifelong total parenteral nutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first hours or days of life
n1=Lester (signe de) | n2=en:onset in the first hours or days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first months of life (3 to 7 months)
n1=Lester (signe de) | n2=en:onset in the first months of life (3 to 7 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the first or second decades of life
n1=Lester (signe de) | n2=en:onset in the first or second decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the fourth to sixth decades (mean 40 years)
n1=Lester (signe de) | n2=en:onset in the fourth to sixth decades (mean 40 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the neonatal period (0-38 days)
n1=Lester (signe de) | n2=en:onset in the neonatal period (0-38 days) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the perinatal period
n1=Lester (signe de) | n2=en:onset in the perinatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the second decade and by age 50 is severe in high and middle frequencies and moderate at low frequencies
n1=Lester (signe de) | n2=en:onset in the second decade and by age 50 is severe in high and middle frequencies and moderate at low frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the second or third decade of life
n1=Lester (signe de) | n2=en:onset in the second or third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the second to fourth decades of life
n1=Lester (signe de) | n2=en:onset in the second to fourth decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in the sixth or seventh decades
n1=Lester (signe de) | n2=en:onset in the sixth or seventh decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in third decade
n1=Lester (signe de) | n2=en:onset in third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in third or fourth decades
n1=Lester (signe de) | n2=en:onset in third or fourth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in third to fifth decade of life
n1=Lester (signe de) | n2=en:onset in third to fifth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in third to fourth decade
n1=Lester (signe de) | n2=en:onset in third to fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in utero in severely affected patients
n1=Lester (signe de) | n2=en:onset in utero in severely affected patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in utero or at birth
n1=Lester (signe de) | n2=en:onset in utero or at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in utero or early infancy
n1=Lester (signe de) | n2=en:onset in utero or early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in utero or in infancy
n1=Lester (signe de) | n2=en:onset in utero or in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in utero, infancy, or early childhood
n1=Lester (signe de) | n2=en:onset in utero, infancy, or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in young adulthood
n1=Lester (signe de) | n2=en:onset in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in young adulthood (range 18 to 23 years)
n1=Lester (signe de) | n2=en:onset in young adulthood (range 18 to 23 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset in young adulthood or adulthood
n1=Lester (signe de) | n2=en:onset in young adulthood or adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset is usually in childhood or adolescence (2 to 18 years)
n1=Lester (signe de) | n2=en:onset is usually in childhood or adolescence (2 to 18 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset late childhood
n1=Lester (signe de) | n2=en:onset late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset may also occur in early infancy, adolescence, or adulthood
n1=Lester (signe de) | n2=en:onset may also occur in early infancy, adolescence, or adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset may be precipitated by viral infection, reye-like episode following ingestion of aspirin
n1=Lester (signe de) | n2=en:onset may be precipitated by viral infection, reye-like episode following ingestion of aspirin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset may be prelingual or in childhood
n1=Lester (signe de) | n2=en:onset may be prelingual or in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset may occur in adulthood
n1=Lester (signe de) | n2=en:onset may occur in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset mid to late adulthood
n1=Lester (signe de) | n2=en:onset mid to late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset occurs earlier in males than females
n1=Lester (signe de) | n2=en:onset occurs earlier in males than females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of abnormal eye movements in early childhood
n1=Lester (signe de) | n2=en:onset of abnormal eye movements in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of acanthosis nigricans correlates with onset of diabetes
n1=Lester (signe de) | n2=en:onset of acanthosis nigricans correlates with onset of diabetes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of acanthosis nigricans in childhood or by puberty
n1=Lester (signe de) | n2=en:onset of acanthosis nigricans in childhood or by puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of achalasia in infancy or early childhood
n1=Lester (signe de) | n2=en:onset of achalasia in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of acne in adolescence, persists into adulthood
n1=Lester (signe de) | n2=en:onset of acne in adolescence, persists into adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of acute encephalopathic attacks in childhood (3 to 7 years)
n1=Lester (signe de) | n2=en:onset of acute encephalopathic attacks in childhood (3 to 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of alopecia in infancy
n1=Lester (signe de) | n2=en:onset of alopecia in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of arthritis in early childhood
n1=Lester (signe de) | n2=en:onset of arthritis in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of ataxia and neuropathy in early twenties
n1=Lester (signe de) | n2=en:onset of ataxia and neuropathy in early twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of ataxia between 1 and 3 years of age
n1=Lester (signe de) | n2=en:onset of ataxia between 1 and 3 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of ataxia in early childhood
n1=Lester (signe de) | n2=en:onset of ataxia in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of ataxia in early childhood (range 15 months to 3 years)
n1=Lester (signe de) | n2=en:onset of ataxia in early childhood (range 15 months to 3 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of ataxia in the fifties
n1=Lester (signe de) | n2=en:onset of ataxia in the fifties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of autoinflammation in infancy or first few years of life
n1=Lester (signe de) | n2=en:onset of autoinflammation in infancy or first few years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of bleeding in infancy or early childhood
n1=Lester (signe de) | n2=en:onset of bleeding in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of bleeding symptoms in childhood or young adulthood
n1=Lester (signe de) | n2=en:onset of bleeding symptoms in childhood or young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of blistering skin in infancy with improvement over time
n1=Lester (signe de) | n2=en:onset of blistering skin in infancy with improvement over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of bone disease in second decade (range 18-44 years)
n1=Lester (signe de) | n2=en:onset of bone disease in second decade (range 18-44 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of bone fragility in childhood
n1=Lester (signe de) | n2=en:onset of bone fragility in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of calf hypotrophy may occur earlier
n1=Lester (signe de) | n2=en:onset of calf hypotrophy may occur earlier | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cardiac involvement later, usually after age 20 years and after skeletal muscle involvement
n1=Lester (signe de) | n2=en:onset of cardiac involvement later, usually after age 20 years and after skeletal muscle involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cardiac symptoms in adolescence
n1=Lester (signe de) | n2=en:onset of cardiac symptoms in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cardiomyopathy may occur several months after birth
n1=Lester (signe de) | n2=en:onset of cardiomyopathy may occur several months after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cataracts in late adolescence
n1=Lester (signe de) | n2=en:onset of cataracts in late adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cholestatic jaundice 2-4 weeks of age and resolved during childhood
n1=Lester (signe de) | n2=en:onset of cholestatic jaundice 2-4 weeks of age and resolved during childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of choreoathetosis in childhood or young adult (6-23 years)
n1=Lester (signe de) | n2=en:onset of choreoathetosis in childhood or young adult (6-23 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of choroideremia in second to third decade
n1=Lester (signe de) | n2=en:onset of choroideremia in second to third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of chronic progressive polyneuropathy in late childhood
n1=Lester (signe de) | n2=en:onset of chronic progressive polyneuropathy in late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of clinical features around puberty
n1=Lester (signe de) | n2=en:onset of clinical features around puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of contractures in utero
n1=Lester (signe de) | n2=en:onset of contractures in utero | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of cough in early adulthood
n1=Lester (signe de) | n2=en:onset of cough in early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of crises in early childhood
n1=Lester (signe de) | n2=en:onset of crises in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of deafness and diabetes in adulthood
n1=Lester (signe de) | n2=en:onset of deafness and diabetes in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of deafness in early childhood
n1=Lester (signe de) | n2=en:onset of deafness in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of dementia in the thirties or forties
n1=Lester (signe de) | n2=en:onset of dementia in the thirties or forties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of diabetes at less than 25 years of age
n1=Lester (signe de) | n2=en:onset of diabetes at less than 25 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of diabetes in neonatal period/ early infancy
n1=Lester (signe de) | n2=en:onset of diabetes in neonatal period/ early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of diabetes in teenage years
n1=Lester (signe de) | n2=en:onset of diabetes in teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of dilated cardiomyopathy less than 3 years
n1=Lester (signe de) | n2=en:onset of dilated cardiomyopathy less than 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease 3-30 years
n1=Lester (signe de) | n2=en:onset of disease 3-30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease 3-8 years
n1=Lester (signe de) | n2=en:onset of disease 3-8 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease 7 months to 3 years
n1=Lester (signe de) | n2=en:onset of disease 7 months to 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease after fourth decade of life
n1=Lester (signe de) | n2=en:onset of disease after fourth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease around 10 years of age
n1=Lester (signe de) | n2=en:onset of disease around 10 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease before 7 years of age
n1=Lester (signe de) | n2=en:onset of disease before 7 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease between 25 and 40 years of age
n1=Lester (signe de) | n2=en:onset of disease between 25 and 40 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease in fourth or fifth decade of life
n1=Lester (signe de) | n2=en:onset of disease in fourth or fifth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease in late childhood
n1=Lester (signe de) | n2=en:onset of disease in late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of disease within the first year of life
n1=Lester (signe de) | n2=en:onset of disease within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of distal muscle weakness in adulthood (range twenties to forties), however, pes cavus or percussion-inducted contractions may be present earlier
n1=Lester (signe de) | n2=en:onset of distal muscle weakness in adulthood (range twenties to forties), however, pes cavus or percussion-inducted contractions may be present earlier | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of dysmorphic features and developmental delay in infancy
n1=Lester (signe de) | n2=en:onset of dysmorphic features and developmental delay in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of dystonia at 12 years
n1=Lester (signe de) | n2=en:onset of dystonia at 12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of dystonia is in childhood
n1=Lester (signe de) | n2=en:onset of dystonia is in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of edema in childhood
n1=Lester (signe de) | n2=en:onset of edema in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of encephalopathy between ages 2 and 3 years
n1=Lester (signe de) | n2=en:onset of encephalopathy between ages 2 and 3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of end-stage renal disease 15 to 20 years after onset
n1=Lester (signe de) | n2=en:onset of end-stage renal disease 15 to 20 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of epiphyseal dysplasia and growth retardation in first 2 years of life
n1=Lester (signe de) | n2=en:onset of epiphyseal dysplasia and growth retardation in first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of episodic liver failure in first 2 years of life
n1=Lester (signe de) | n2=en:onset of episodic liver failure in first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of essential tremor between 16 and 44 years
n1=Lester (signe de) | n2=en:onset of essential tremor between 16 and 44 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of febrile seizures typically between 6 months and 6 years of age
n1=Lester (signe de) | n2=en:onset of febrile seizures typically between 6 months and 6 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of fracture usually when child begins to walk
n1=Lester (signe de) | n2=en:onset of fracture usually when child begins to walk | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of fractures 4-18 months of life
n1=Lester (signe de) | n2=en:onset of fractures 4-18 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of fractures in infancy to early childhood
n1=Lester (signe de) | n2=en:onset of fractures in infancy to early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of gait abnormalities at 8 to 40 years
n1=Lester (signe de) | n2=en:onset of gait abnormalities at 8 to 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of gastrointestinal tumors typically occurs in the second decade
n1=Lester (signe de) | n2=en:onset of gastrointestinal tumors typically occurs in the second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of gaze palsy at birth
n1=Lester (signe de) | n2=en:onset of gaze palsy at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hand involvement at 14 to 60 years
n1=Lester (signe de) | n2=en:onset of hand involvement at 14 to 60 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in adolescence
n1=Lester (signe de) | n2=en:onset of hearing loss in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in childhood
n1=Lester (signe de) | n2=en:onset of hearing loss in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in childhood (range 7 to 13 years)
n1=Lester (signe de) | n2=en:onset of hearing loss in childhood (range 7 to 13 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in first decade of life
n1=Lester (signe de) | n2=en:onset of hearing loss in first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in first or second decade
n1=Lester (signe de) | n2=en:onset of hearing loss in first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in late childhood
n1=Lester (signe de) | n2=en:onset of hearing loss in late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in late childhood or adolescence
n1=Lester (signe de) | n2=en:onset of hearing loss in late childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss in second decade
n1=Lester (signe de) | n2=en:onset of hearing loss in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss prior to or during adolescence
n1=Lester (signe de) | n2=en:onset of hearing loss prior to or during adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hearing loss ranges from childhood to young adulthood
n1=Lester (signe de) | n2=en:onset of hearing loss ranges from childhood to young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hematologic or cns tumors in the first or second decades of life
n1=Lester (signe de) | n2=en:onset of hematologic or cns tumors in the first or second decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hemolytic anemia shortly after birth
n1=Lester (signe de) | n2=en:onset of hemolytic anemia shortly after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hyperpigmentation in early childhood (3 months-6 years) that fades after puberty
n1=Lester (signe de) | n2=en:onset of hyperpigmentation in early childhood (3 months-6 years) that fades after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hyperuricemia or gout in young adulthood
n1=Lester (signe de) | n2=en:onset of hyperuricemia or gout in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of hypoglycemia and hyperinsulinism in the neonatal period
n1=Lester (signe de) | n2=en:onset of hypoglycemia and hyperinsulinism in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of illness often associated with acute infection
n1=Lester (signe de) | n2=en:onset of illness often associated with acute infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of insulin resistance may occur in childhood
n1=Lester (signe de) | n2=en:onset of insulin resistance may occur in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of joint contractures later in life
n1=Lester (signe de) | n2=en:onset of joint contractures later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of joint pain in childhood
n1=Lester (signe de) | n2=en:onset of joint pain in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of kyphosis in childhood
n1=Lester (signe de) | n2=en:onset of kyphosis in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lesions may occur in early childhood or as late as the seventh decade
n1=Lester (signe de) | n2=en:onset of lesions may occur in early childhood or as late as the seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lesions usually in first or second decade of life, but may occur as late as the seventh decade
n1=Lester (signe de) | n2=en:onset of lesions usually in first or second decade of life, but may occur as late as the seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lesions usually in first through fourth decades of life, but may occur as late as the seventh decade
n1=Lester (signe de) | n2=en:onset of lesions usually in first through fourth decades of life, but may occur as late as the seventh decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of linear striations between 5 months and 6 years (only in affected females)
n1=Lester (signe de) | n2=en:onset of linear striations between 5 months and 6 years (only in affected females) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lipodystrophy in early childhood
n1=Lester (signe de) | n2=en:onset of lipodystrophy in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lipodystrophy later in childhood
n1=Lester (signe de) | n2=en:onset of lipodystrophy later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of liver involvement in infancy
n1=Lester (signe de) | n2=en:onset of liver involvement in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lymphedema around puberty
n1=Lester (signe de) | n2=en:onset of lymphedema around puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of lymphedema before puberty
n1=Lester (signe de) | n2=en:onset of lymphedema before puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of macrocephaly in the first year of life
n1=Lester (signe de) | n2=en:onset of macrocephaly in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of major clinical features in young adulthood
n1=Lester (signe de) | n2=en:onset of major clinical features in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of malignancy can occur throughout life
n1=Lester (signe de) | n2=en:onset of malignancy can occur throughout life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of mental impairment in early childhood
n1=Lester (signe de) | n2=en:onset of mental impairment in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of mild symptoms in first or second decade
n1=Lester (signe de) | n2=en:onset of mild symptoms in first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of motor disturbances in childhood
n1=Lester (signe de) | n2=en:onset of motor disturbances in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of muscle weakness around age 5 years
n1=Lester (signe de) | n2=en:onset of muscle weakness around age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of muscle weakness in early childhood, usually before age 10 years
n1=Lester (signe de) | n2=en:onset of muscle weakness in early childhood, usually before age 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of muscle weakness in fifth decade
n1=Lester (signe de) | n2=en:onset of muscle weakness in fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of muscle weakness in late adulthood
n1=Lester (signe de) | n2=en:onset of muscle weakness in late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of myoclonus later in childhood
n1=Lester (signe de) | n2=en:onset of myoclonus later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of nephrotic syndrome and thrombocytopenia in mid-childhood
n1=Lester (signe de) | n2=en:onset of nephrotic syndrome and thrombocytopenia in mid-childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of neurologic disease in early adulthood
n1=Lester (signe de) | n2=en:onset of neurologic disease in early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of neurologic events can occur between 4 and 35 years of age
n1=Lester (signe de) | n2=en:onset of neurologic events can occur between 4 and 35 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of neurologic features is variable, even within the same family (range early childhood to adult)
n1=Lester (signe de) | n2=en:onset of neurologic features is variable, even within the same family (range early childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of neurologic symptoms often by 30 months
n1=Lester (signe de) | n2=en:onset of neurologic symptoms often by 30 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of neuromuscular symptoms between 6 months and 1 year of age
n1=Lester (signe de) | n2=en:onset of neuromuscular symptoms between 6 months and 1 year of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of night blindness varies among patients from early childhood to mid thirties
n1=Lester (signe de) | n2=en:onset of night blindness varies among patients from early childhood to mid thirties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of normal pressure hydrocephalus after age 65 years
n1=Lester (signe de) | n2=en:onset of normal pressure hydrocephalus after age 65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of optic atrophy in childhood
n1=Lester (signe de) | n2=en:onset of optic atrophy in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of optic atrophy in first decade
n1=Lester (signe de) | n2=en:onset of optic atrophy in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of optic atrophy in infancy or early childhood
n1=Lester (signe de) | n2=en:onset of optic atrophy in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of optic neuropathy is usually in early adulthood
n1=Lester (signe de) | n2=en:onset of optic neuropathy is usually in early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of osteoarthritis in teens to early adulthood
n1=Lester (signe de) | n2=en:onset of osteoarthritis in teens to early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of other symptoms in adolescence or early adulthood
n1=Lester (signe de) | n2=en:onset of other symptoms in adolescence or early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of overgrowth in second to third month of life (in some cases)
n1=Lester (signe de) | n2=en:onset of overgrowth in second to third month of life (in some cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of overgrowth in the first year of life (in most cases)
n1=Lester (signe de) | n2=en:onset of overgrowth in the first year of life (in most cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of palmoplantar hyperkeratosis 7-8 years of age
n1=Lester (signe de) | n2=en:onset of palmoplantar hyperkeratosis 7-8 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of parkinsonism in early twenties
n1=Lester (signe de) | n2=en:onset of parkinsonism in early twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of parkinsonism in first decade
n1=Lester (signe de) | n2=en:onset of parkinsonism in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of periodic paralysis (mean) 5 years (range) 8 months to 15 years
n1=Lester (signe de) | n2=en:onset of periodic paralysis (mean) 5 years (range) 8 months to 15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of peripheral neuropathy in the first decade
n1=Lester (signe de) | n2=en:onset of peripheral neuropathy in the first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of peripheral neuropathy or hearing loss in young adulthood (range 16 to 35 years)
n1=Lester (signe de) | n2=en:onset of peripheral neuropathy or hearing loss in young adulthood (range 16 to 35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of peripheral neuropathy ranges from childhood to mid-adulthood
n1=Lester (signe de) | n2=en:onset of peripheral neuropathy ranges from childhood to mid-adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of progressive spastic paraplegia in childhood
n1=Lester (signe de) | n2=en:onset of progressive spastic paraplegia in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of proteinuria in the second to fourth decades
n1=Lester (signe de) | n2=en:onset of proteinuria in the second to fourth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of proteinuria in the third to fourth decades
n1=Lester (signe de) | n2=en:onset of proteinuria in the third to fourth decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of renal dysfunction in early childhood
n1=Lester (signe de) | n2=en:onset of renal dysfunction in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of renal failure in adulthood (range twenties to fifties)
n1=Lester (signe de) | n2=en:onset of renal failure in adulthood (range twenties to fifties) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of scoliosis as early as 2 years of age
n1=Lester (signe de) | n2=en:onset of scoliosis as early as 2 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures around 7 to 12 years
n1=Lester (signe de) | n2=en:onset of seizures around 7 to 12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures at 2-8 days of life
n1=Lester (signe de) | n2=en:onset of seizures at 2-8 days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures before age 2 years
n1=Lester (signe de) | n2=en:onset of seizures before age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures between 2 and 5 years
n1=Lester (signe de) | n2=en:onset of seizures between 2 and 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures between 8 and 11 months of age
n1=Lester (signe de) | n2=en:onset of seizures between 8 and 11 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures between 9 and 12 months of age
n1=Lester (signe de) | n2=en:onset of seizures between 9 and 12 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in first 6 months of life
n1=Lester (signe de) | n2=en:onset of seizures in first 6 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in first months of life
n1=Lester (signe de) | n2=en:onset of seizures in first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in first months of life (usually 4 to 7 months)
n1=Lester (signe de) | n2=en:onset of seizures in first months of life (usually 4 to 7 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in infancy
n1=Lester (signe de) | n2=en:onset of seizures in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in infancy or early childhood
n1=Lester (signe de) | n2=en:onset of seizures in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures in later childhood (5 to 10 years)
n1=Lester (signe de) | n2=en:onset of seizures in later childhood (5 to 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of seizures ranges from 2 to 11 years
n1=Lester (signe de) | n2=en:onset of seizures ranges from 2 to 11 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of sensory neuropathy in later adulthood
n1=Lester (signe de) | n2=en:onset of sensory neuropathy in later adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of skin lesions at birth
n1=Lester (signe de) | n2=en:onset of skin lesions at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of skin manifestations from birth to puberty
n1=Lester (signe de) | n2=en:onset of skin manifestations from birth to puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of sleep terrors between age 4 and 12 years old
n1=Lester (signe de) | n2=en:onset of sleep terrors between age 4 and 12 years old | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of sleepwalking between 4 and 8 years old
n1=Lester (signe de) | n2=en:onset of sleepwalking between 4 and 8 years old | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of slowly progressive spastic paraplegia in first or second decade
n1=Lester (signe de) | n2=en:onset of slowly progressive spastic paraplegia in first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of spastic paraplegia in first year of life
n1=Lester (signe de) | n2=en:onset of spastic paraplegia in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of spasticity by age 2 years
n1=Lester (signe de) | n2=en:onset of spasticity by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of spasticity in childhood
n1=Lester (signe de) | n2=en:onset of spasticity in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms 2-12 months
n1=Lester (signe de) | n2=en:onset of symptoms 2-12 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms 2-4 weeks of age
n1=Lester (signe de) | n2=en:onset of symptoms 2-4 weeks of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms 2-6 years of age
n1=Lester (signe de) | n2=en:onset of symptoms 2-6 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms after age 5
n1=Lester (signe de) | n2=en:onset of symptoms after age 5 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms age 5-30
n1=Lester (signe de) | n2=en:onset of symptoms age 5-30 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms at 2-4 months
n1=Lester (signe de) | n2=en:onset of symptoms at 2-4 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms between ages 3-8 years of age
n1=Lester (signe de) | n2=en:onset of symptoms between ages 3-8 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in adolescence or early adulthood
n1=Lester (signe de) | n2=en:onset of symptoms in adolescence or early adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in childhood
n1=Lester (signe de) | n2=en:onset of symptoms in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in childhood with stiff, painful joints
n1=Lester (signe de) | n2=en:onset of symptoms in childhood with stiff, painful joints | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in early childhood
n1=Lester (signe de) | n2=en:onset of symptoms in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in early childhood in most patients
n1=Lester (signe de) | n2=en:onset of symptoms in early childhood in most patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in fifth decade
n1=Lester (signe de) | n2=en:onset of symptoms in fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in first decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in first or second decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in first or second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in second decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in second or third decade
n1=Lester (signe de) | n2=en:onset of symptoms in second or third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in second or third decade (mean 25 years)
n1=Lester (signe de) | n2=en:onset of symptoms in second or third decade (mean 25 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in second to fifth decades of life
n1=Lester (signe de) | n2=en:onset of symptoms in second to fifth decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in second to third decades of life
n1=Lester (signe de) | n2=en:onset of symptoms in second to third decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in the fourth to sixth decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in the fourth to sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in third to fourth decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in third to fourth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms in third to sixth decade of life
n1=Lester (signe de) | n2=en:onset of symptoms in third to sixth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms less than one year
n1=Lester (signe de) | n2=en:onset of symptoms less than one year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms often associated with nonspecific febrile illness
n1=Lester (signe de) | n2=en:onset of symptoms often associated with nonspecific febrile illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms usually between 12-15 years
n1=Lester (signe de) | n2=en:onset of symptoms usually between 12-15 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms usually in adulthood
n1=Lester (signe de) | n2=en:onset of symptoms usually in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of symptoms within the first 2 decades of life
n1=Lester (signe de) | n2=en:onset of symptoms within the first 2 decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of thrombocytopenia in early childhood
n1=Lester (signe de) | n2=en:onset of thrombocytopenia in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of thrombosis by age 2 years
n1=Lester (signe de) | n2=en:onset of thrombosis by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of tremor usually before onset of seizures
n1=Lester (signe de) | n2=en:onset of tremor usually before onset of seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of tumors usually in adulthood
n1=Lester (signe de) | n2=en:onset of tumors usually in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of vision loss in young adulthood (<20 years)
n1=Lester (signe de) | n2=en:onset of vision loss in young adulthood (<20 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of visual dysfunction in early childhood
n1=Lester (signe de) | n2=en:onset of visual dysfunction in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of visual loss in childhood (around age 5 years)
n1=Lester (signe de) | n2=en:onset of visual loss in childhood (around age 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of visual loss in the first decade
n1=Lester (signe de) | n2=en:onset of visual loss in the first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset of visual loss in the first or second decades
n1=Lester (signe de) | n2=en:onset of visual loss in the first or second decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset often begins in childhood or adolescence
n1=Lester (signe de) | n2=en:onset often begins in childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset often in late adolescence
n1=Lester (signe de) | n2=en:onset often in late adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset precipitated by fasting or illness
n1=Lester (signe de) | n2=en:onset precipitated by fasting or illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset prenatally or at birth
n1=Lester (signe de) | n2=en:onset prenatally or at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from 2 days to 7 months (most at 2-3 months)
n1=Lester (signe de) | n2=en:onset ranges from 2 days to 7 months (most at 2-3 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from birth to age 4 years
n1=Lester (signe de) | n2=en:onset ranges from birth to age 4 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from childhood (severe phenotype) to adulthood (limited phenotype)
n1=Lester (signe de) | n2=en:onset ranges from childhood (severe phenotype) to adulthood (limited phenotype) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from childhood to adulthood
n1=Lester (signe de) | n2=en:onset ranges from childhood to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from childhood to young adulthood
n1=Lester (signe de) | n2=en:onset ranges from childhood to young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from early childhood to adulthood (usually before age 15)
n1=Lester (signe de) | n2=en:onset ranges from early childhood to adulthood (usually before age 15) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from first to third decade
n1=Lester (signe de) | n2=en:onset ranges from first to third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset ranges from young adulthood to sixties
n1=Lester (signe de) | n2=en:onset ranges from young adulthood to sixties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset second decade of life
n1=Lester (signe de) | n2=en:onset second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset soon after birth
n1=Lester (signe de) | n2=en:onset soon after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset soon after birth or within the first year of life
n1=Lester (signe de) | n2=en:onset soon after birth or within the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset typically in childhood although onset in late adolescence or early adulthood has been reported
n1=Lester (signe de) | n2=en:onset typically in childhood although onset in late adolescence or early adulthood has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually after age 40
n1=Lester (signe de) | n2=en:onset usually after age 40 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually after viral-like infection
n1=Lester (signe de) | n2=en:onset usually after viral-like infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually associated with febrile illness
n1=Lester (signe de) | n2=en:onset usually associated with febrile illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually at 2 to 6 months of age
n1=Lester (signe de) | n2=en:onset usually at 2 to 6 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually at birth
n1=Lester (signe de) | n2=en:onset usually at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually at birth, but may occur later
n1=Lester (signe de) | n2=en:onset usually at birth, but may occur later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually before age 10 years
n1=Lester (signe de) | n2=en:onset usually before age 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually before age 40 years
n1=Lester (signe de) | n2=en:onset usually before age 40 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually before age 40 years (range 15 to 55)
n1=Lester (signe de) | n2=en:onset usually before age 40 years (range 15 to 55) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually between 30 and 50 years of age
n1=Lester (signe de) | n2=en:onset usually between 30 and 50 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually by age 2 years
n1=Lester (signe de) | n2=en:onset usually by age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in adolescence
n1=Lester (signe de) | n2=en:onset usually in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in adulthood
n1=Lester (signe de) | n2=en:onset usually in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in adulthood although childhood onset has been reported
n1=Lester (signe de) | n2=en:onset usually in adulthood although childhood onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood
n1=Lester (signe de) | n2=en:onset usually in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood (1 to 9 years of age)
n1=Lester (signe de) | n2=en:onset usually in childhood (1 to 9 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood (infancy to teens)
n1=Lester (signe de) | n2=en:onset usually in childhood (infancy to teens) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood (range 17 months to 39 years)
n1=Lester (signe de) | n2=en:onset usually in childhood (range 17 months to 39 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood (range 6 months to 16 years)
n1=Lester (signe de) | n2=en:onset usually in childhood (range 6 months to 16 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood (range infancy to late childhood)
n1=Lester (signe de) | n2=en:onset usually in childhood (range infancy to late childhood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood after bcg vaccination
n1=Lester (signe de) | n2=en:onset usually in childhood after bcg vaccination | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in childhood or adolescence
n1=Lester (signe de) | n2=en:onset usually in childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in early adolescence
n1=Lester (signe de) | n2=en:onset usually in early adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in early childhood
n1=Lester (signe de) | n2=en:onset usually in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in early childhood (but can range from infancy to adulthood)
n1=Lester (signe de) | n2=en:onset usually in early childhood (but can range from infancy to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in early childhood, although ranges from birth to adulthood
n1=Lester (signe de) | n2=en:onset usually in early childhood, although ranges from birth to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first decade
n1=Lester (signe de) | n2=en:onset usually in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first month of life
n1=Lester (signe de) | n2=en:onset usually in first month of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first or second decade (mean 10 years)
n1=Lester (signe de) | n2=en:onset usually in first or second decade (mean 10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first or second decades
n1=Lester (signe de) | n2=en:onset usually in first or second decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first to third decade of life
n1=Lester (signe de) | n2=en:onset usually in first to third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in first year of life
n1=Lester (signe de) | n2=en:onset usually in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy
n1=Lester (signe de) | n2=en:onset usually in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy although later onset may occur
n1=Lester (signe de) | n2=en:onset usually in infancy although later onset may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy or childhood
n1=Lester (signe de) | n2=en:onset usually in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy or early childhood
n1=Lester (signe de) | n2=en:onset usually in infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy or early childhood (9 months to 6 years)
n1=Lester (signe de) | n2=en:onset usually in infancy or early childhood (9 months to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in infancy or up to 2 years of age although later onset has been reported ('late-infantile')
n1=Lester (signe de) | n2=en:onset usually in infancy or up to 2 years of age although later onset has been reported ('late-infantile') | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in late adolescence or early adulthood (range 15 to 45 years)
n1=Lester (signe de) | n2=en:onset usually in late adolescence or early adulthood (range 15 to 45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in late infancy or childhood (1 to 6 years)
n1=Lester (signe de) | n2=en:onset usually in late infancy or childhood (1 to 6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in mid-teens, average 15 years (range 2 to 20 years)
n1=Lester (signe de) | n2=en:onset usually in mid-teens, average 15 years (range 2 to 20 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in second decade
n1=Lester (signe de) | n2=en:onset usually in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in second decade (may occur earlier)
n1=Lester (signe de) | n2=en:onset usually in second decade (may occur earlier) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in second decade of life, although earlier and later onset have been reported
n1=Lester (signe de) | n2=en:onset usually in second decade of life, although earlier and later onset have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in second or third decades
n1=Lester (signe de) | n2=en:onset usually in second or third decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in the first 4 years of life
n1=Lester (signe de) | n2=en:onset usually in the first 4 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in the first decade (range 0.8 to 5 years)
n1=Lester (signe de) | n2=en:onset usually in the first decade (range 0.8 to 5 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in the neck
n1=Lester (signe de) | n2=en:onset usually in the neck | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in the neonatal period although later onset has been reported
n1=Lester (signe de) | n2=en:onset usually in the neonatal period although later onset has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in the third decade (range 11 to 50 years)
n1=Lester (signe de) | n2=en:onset usually in the third decade (range 11 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in third decade of life
n1=Lester (signe de) | n2=en:onset usually in third decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in third or fourth decade
n1=Lester (signe de) | n2=en:onset usually in third or fourth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually in young adulthood
n1=Lester (signe de) | n2=en:onset usually in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset usually within first weeks of life
n1=Lester (signe de) | n2=en:onset usually within first weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within first 2 years
n1=Lester (signe de) | n2=en:onset within first 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within first 2 years of life
n1=Lester (signe de) | n2=en:onset within first 2 years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within first 3 months of life
n1=Lester (signe de) | n2=en:onset within first 3 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within first 6 months of life
n1=Lester (signe de) | n2=en:onset within first 6 months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within first year of life
n1=Lester (signe de) | n2=en:onset within first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:onset within the first decade of life
n1=Lester (signe de) | n2=en:onset within the first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ophthalmologic signs onset in first to sixth decade
n1=Lester (signe de) | n2=en:ophthalmologic signs onset in first to sixth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:opportunistic infections
n1=Lester (signe de) | n2=en:opportunistic infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:oral contraceptives may also cause symptoms
n1=Lester (signe de) | n2=en:oral contraceptives may also cause symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:oral supplementation with ubiquinone does not result in major clinical improvement
n1=Lester (signe de) | n2=en:oral supplementation with ubiquinone does not result in major clinical improvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:original phenotype description based on patients from la reunion island in the indian ocean off the east coast of africa where the incidence is 1/1,500 births
n1=Lester (signe de) | n2=en:original phenotype description based on patients from la reunion island in the indian ocean off the east coast of africa where the incidence is 1/1,500 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ossification evident 2-8 months following swelling
n1=Lester (signe de) | n2=en:ossification evident 2-8 months following swelling | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ossification occurs spontaneously during childhood
n1=Lester (signe de) | n2=en:ossification occurs spontaneously during childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other features of neurofibromatosis type i (nf1, 162200) may or may not be present
n1=Lester (signe de) | n2=en:other features of neurofibromatosis type i (nf1, 162200) may or may not be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other half show head circumference more retarded than height
n1=Lester (signe de) | n2=en:other half show head circumference more retarded than height | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other muscle become involved about 5 years after onset
n1=Lester (signe de) | n2=en:other muscle become involved about 5 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other tumors may also occur
n1=Lester (signe de) | n2=en:other tumors may also occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other variants of waardenburg syndrome include waardenburg syndrome type 1 (193500), waardenburg syndrome type 3 (148820), and waardenburg syndrome type 4 (277580)
n1=Lester (signe de) | n2=en:other variants of waardenburg syndrome include waardenburg syndrome type 1 (193500), waardenburg syndrome type 3 (148820), and waardenburg syndrome type 4 (277580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other variants of waardenburg syndrome include waardenburg syndrome type 2 (193510), waardenburg syndrome type 3 (148820), and waardenburg syndrome type 4 (277580)
n1=Lester (signe de) | n2=en:other variants of waardenburg syndrome include waardenburg syndrome type 2 (193510), waardenburg syndrome type 3 (148820), and waardenburg syndrome type 4 (277580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:other visual functions, including visual acuity, visual field, and color vision, are usually normal in these patients
n1=Lester (signe de) | n2=en:other visual functions, including visual acuity, visual field, and color vision, are usually normal in these patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:otopalatodigital syndrome type i (opd1, 311300) is an allelic disorder
n1=Lester (signe de) | n2=en:otopalatodigital syndrome type i (opd1, 311300) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:otopalatodigital syndrome type ii (opd2, 304120) is an allelic disorder
n1=Lester (signe de) | n2=en:otopalatodigital syndrome type ii (opd2, 304120) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:otopalatodigital syndrome type ii (opd2, 304120) is an allelic disorder with a more severe, frequently lethal phenotype
n1=Lester (signe de) | n2=en:otopalatodigital syndrome type ii (opd2, 304120) is an allelic disorder with a more severe, frequently lethal phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overall course less severe compared to patients with cfh (134370) mutations
n1=Lester (signe de) | n2=en:overall course less severe compared to patients with cfh (134370) mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overall prevalence is between 0.5 and 14 per 100,000 people per year
n1=Lester (signe de) | n2=en:overall prevalence is between 0.5 and 14 per 100,000 people per year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlap with obsessive-compulsive disorder (ocd, 164230)
n1=Lester (signe de) | n2=en:overlap with obsessive-compulsive disorder (ocd, 164230) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlap with tourette syndrome (137580)
n1=Lester (signe de) | n2=en:overlap with tourette syndrome (137580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlapping clinical spectrum and allelic to masa syndrome (303350)
n1=Lester (signe de) | n2=en:overlapping clinical spectrum and allelic to masa syndrome (303350) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlapping features of digeorge syndrome
n1=Lester (signe de) | n2=en:overlapping features of digeorge syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlapping features with barber-say syndrome (209885)
n1=Lester (signe de) | n2=en:overlapping features with barber-say syndrome (209885) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:overlapping pathologic features with x-linked myopathy with excessive autophagy (xmea, 310440)
n1=Lester (signe de) | n2=en:overlapping pathologic features with x-linked myopathy with excessive autophagy (xmea, 310440) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pain in lower limb
n1=Lester (signe de) | n2=en:pain in lower limb | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pain is noted to feel cold
n1=Lester (signe de) | n2=en:pain is noted to feel cold | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pain is relieved by antiinflammatory medication
n1=Lester (signe de) | n2=en:pain is relieved by antiinflammatory medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pain most commonly affects the trunk, extremities, pelvic region, buttocks
n1=Lester (signe de) | n2=en:pain most commonly affects the trunk, extremities, pelvic region, buttocks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pain tends to occur later in the day
n1=Lester (signe de) | n2=en:pain tends to occur later in the day | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:painful cramping following ischemic exercise test
n1=Lester (signe de) | n2=en:painful cramping following ischemic exercise test | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pancreatic endocrine abnormalities reported in 1 family only
n1=Lester (signe de) | n2=en:pancreatic endocrine abnormalities reported in 1 family only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:parental somatic mosaicism in 2 cases produced mild phenotype in the patients
n1=Lester (signe de) | n2=en:parental somatic mosaicism in 2 cases produced mild phenotype in the patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:parietal foramina-2 (pfm2, 609597) are caused by mutations in the alx4 gene (605420)
n1=Lester (signe de) | n2=en:parietal foramina-2 (pfm2, 609597) are caused by mutations in the alx4 gene (605420) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:paris-trousseau thrombocytopenia can occur in jacobsen syndrome (147791) in which similar platelet defects are accompanied by facial dysmorphism, cardiac defects, mental retardation, and deletion at 11q23
n1=Lester (signe de) | n2=en:paris-trousseau thrombocytopenia can occur in jacobsen syndrome (147791) in which similar platelet defects are accompanied by facial dysmorphism, cardiac defects, mental retardation, and deletion at 11q23 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:part of 'dent disease complex'
n1=Lester (signe de) | n2=en:part of 'dent disease complex' | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:part of 'dent disease complex' (see 300009)
n1=Lester (signe de) | n2=en:part of 'dent disease complex' (see 300009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:partial deficiency of hypoxanthine phosphoribosyltransferase (hprt, 78% activity)
n1=Lester (signe de) | n2=en:partial deficiency of hypoxanthine phosphoribosyltransferase (hprt, 78% activity) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:partial factor viii deficiency in heterozygous carriers
n1=Lester (signe de) | n2=en:partial factor viii deficiency in heterozygous carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:partial laminin alpha-2 deficiency results in milder phenotype
n1=Lester (signe de) | n2=en:partial laminin alpha-2 deficiency results in milder phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:partial or absent response to steroid treatment
n1=Lester (signe de) | n2=en:partial or absent response to steroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:partially responsive to laser treatment
n1=Lester (signe de) | n2=en:partially responsive to laser treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:paternal age effect
n1=Lester (signe de) | n2=en:paternal age effect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:paternal anticipation bias
n1=Lester (signe de) | n2=en:paternal anticipation bias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic alleles contain 52 to 86 repeats
n1=Lester (signe de) | n2=en:pathogenic alleles contain 52 to 86 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic alleles contain 71 to 1,300 repeats
n1=Lester (signe de) | n2=en:pathogenic alleles contain 71 to 1,300 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic alleles contain 75-11,000 repeats
n1=Lester (signe de) | n2=en:pathogenic alleles contain 75-11,000 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic alleles contain greater than 41 repeats
n1=Lester (signe de) | n2=en:pathogenic alleles contain greater than 41 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic alleles have 19 to 33 repeats
n1=Lester (signe de) | n2=en:pathogenic alleles have 19 to 33 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pathogenic cag repeat length is 51 to 78 triplets
n1=Lester (signe de) | n2=en:pathogenic cag repeat length is 51 to 78 triplets | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient b had a more severe phenotype
n1=Lester (signe de) | n2=en:patient b had a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient b is 1 child born of unrelated scandinavian parents with a more severe phenotype with onset in the neonatal period
n1=Lester (signe de) | n2=en:patient b is 1 child born of unrelated scandinavian parents with a more severe phenotype with onset in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient b presented with asymptomatic increased serum creatine kinase and no clinical muscle symptoms
n1=Lester (signe de) | n2=en:patient b presented with asymptomatic increased serum creatine kinase and no clinical muscle symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient satisfaction with healthcare delivery:score:pt:^patient:qn
n1=Lester (signe de) | n2=en:patient satisfaction with healthcare delivery:score:pt:^patient:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient with factor ix leyden variants (see, e.g., 300746.0001) have bleeding in childhood that improves or resolves after puberty
n1=Lester (signe de) | n2=en:patient with factor ix leyden variants (see, e.g., 300746.0001) have bleeding in childhood that improves or resolves after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patient with truncating mutations are more likely to develop neurologic abnormalities
n1=Lester (signe de) | n2=en:patient with truncating mutations are more likely to develop neurologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients achieve ambulation
n1=Lester (signe de) | n2=en:patients achieve ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are 46,xy individuals who may be phenotypically female
n1=Lester (signe de) | n2=en:patients are 46,xy individuals who may be phenotypically female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are born with normal head circumference
n1=Lester (signe de) | n2=en:patients are born with normal head circumference | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are often asymptomatic
n1=Lester (signe de) | n2=en:patients are often asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are often misdiagnosed with spherocytosis
n1=Lester (signe de) | n2=en:patients are often misdiagnosed with spherocytosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are often of mediterranean origin
n1=Lester (signe de) | n2=en:patients are often of mediterranean origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are prone to impaired thermoregulation
n1=Lester (signe de) | n2=en:patients are prone to impaired thermoregulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are severely disabled as adults
n1=Lester (signe de) | n2=en:patients are severely disabled as adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are susceptible to sepsis and dehydration
n1=Lester (signe de) | n2=en:patients are susceptible to sepsis and dehydration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients are typically blind by second or third decade of life, but pace of visual deterioration is highly variable
n1=Lester (signe de) | n2=en:patients are typically blind by second or third decade of life, but pace of visual deterioration is highly variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients become wheelchair-bound about 10 years after onset
n1=Lester (signe de) | n2=en:patients become wheelchair-bound about 10 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients become wheelchair-bound as adults
n1=Lester (signe de) | n2=en:patients become wheelchair-bound as adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients between 30 and 60 years have discomfort with prolonged standing
n1=Lester (signe de) | n2=en:patients between 30 and 60 years have discomfort with prolonged standing | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients can be divided into 2 groups based on whether typical hand anomalies are present
n1=Lester (signe de) | n2=en:patients can be divided into 2 groups based on whether typical hand anomalies are present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients can have als, ftd, or both
n1=Lester (signe de) | n2=en:patients can have als, ftd, or both | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients can have multiple seizure types
n1=Lester (signe de) | n2=en:patients can have multiple seizure types | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients develop acute symptoms under physiologic stress due to illness
n1=Lester (signe de) | n2=en:patients develop acute symptoms under physiologic stress due to illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients develop aortic dissection with little or no aortic enlargement
n1=Lester (signe de) | n2=en:patients develop aortic dissection with little or no aortic enlargement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients develop multiple tumors
n1=Lester (signe de) | n2=en:patients develop multiple tumors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients die in infancy due to infectious complications
n1=Lester (signe de) | n2=en:patients die in infancy due to infectious complications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients do not exhibit ophthalmoplegia
n1=Lester (signe de) | n2=en:patients do not exhibit ophthalmoplegia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients do not exhibit skin pigmentation changes
n1=Lester (signe de) | n2=en:patients do not exhibit skin pigmentation changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients do not have clinical hypothyroidism
n1=Lester (signe de) | n2=en:patients do not have clinical hypothyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients do not have ectopia lentis
n1=Lester (signe de) | n2=en:patients do not have ectopia lentis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients exhibit no signs of ocular or cutaneous albinism
n1=Lester (signe de) | n2=en:patients exhibit no signs of ocular or cutaneous albinism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients frequently have additional malformations or abnormalities, especially in the hepatobiliary and gastrointestinal systems
n1=Lester (signe de) | n2=en:patients frequently have additional malformations or abnormalities, especially in the hepatobiliary and gastrointestinal systems | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients from 4 unrelated families have been reported (as of october 2011)
n1=Lester (signe de) | n2=en:patients from 4 unrelated families have been reported (as of october 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients from old order amish community and turkey have been reported
n1=Lester (signe de) | n2=en:patients from old order amish community and turkey have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients gradually develop tolerance to carbohydrates over time
n1=Lester (signe de) | n2=en:patients gradually develop tolerance to carbohydrates over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have a distinctive shallow u-shaped audiogram
n1=Lester (signe de) | n2=en:patients have a distinctive shallow u-shaped audiogram | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have increased numbers and earlier onset of neurofibromas compared to patients with neurofibromatosis-1 due to point mutations
n1=Lester (signe de) | n2=en:patients have increased numbers and earlier onset of neurofibromas compared to patients with neurofibromatosis-1 due to point mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have no abnormalities of hair, teeth, or bone
n1=Lester (signe de) | n2=en:patients have no abnormalities of hair, teeth, or bone | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have normal aldosterone/renin ratios and 24-hour urine aldosterone levels
n1=Lester (signe de) | n2=en:patients have normal aldosterone/renin ratios and 24-hour urine aldosterone levels | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have normal levels of vitamin a, beta-carotene, and zinc
n1=Lester (signe de) | n2=en:patients have normal levels of vitamin a, beta-carotene, and zinc | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have normal pituitary function
n1=Lester (signe de) | n2=en:patients have normal pituitary function | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients have severe anemia requiring regular transfusions for normal activity
n1=Lester (signe de) | n2=en:patients have severe anemia requiring regular transfusions for normal activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients in whom echocardiography has been performed have a normal heart, heart valves, and aortic root
n1=Lester (signe de) | n2=en:patients in whom echocardiography has been performed have a normal heart, heart valves, and aortic root | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients look as if they have protein deficiency or malnutrition
n1=Lester (signe de) | n2=en:patients look as if they have protein deficiency or malnutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may be asymptomatic, but are at risk for metabolic decompensation
n1=Lester (signe de) | n2=en:patients may be asymptomatic, but are at risk for metabolic decompensation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may become totally dependent for all activities of daily living
n1=Lester (signe de) | n2=en:patients may become totally dependent for all activities of daily living | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may become ventilator-dependent
n1=Lester (signe de) | n2=en:patients may become ventilator-dependent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may become wheelchair-bound
n1=Lester (signe de) | n2=en:patients may become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may become wheelchair-bound after about 12 years
n1=Lester (signe de) | n2=en:patients may become wheelchair-bound after about 12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may become wheelchair-bound as adults
n1=Lester (signe de) | n2=en:patients may become wheelchair-bound as adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may die in infancy or childhood due to respiratory failure
n1=Lester (signe de) | n2=en:patients may die in infancy or childhood due to respiratory failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have a combination phenotype of pmc and hypp (see 603967.0005)
n1=Lester (signe de) | n2=en:patients may have a combination phenotype of pmc and hypp (see 603967.0005) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have benign course until late adulthood
n1=Lester (signe de) | n2=en:patients may have benign course until late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have either dementia or motor neuron disease or both
n1=Lester (signe de) | n2=en:patients may have either dementia or motor neuron disease or both | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have head and neck paragangliomas only, adrenal or extraadrenal pheochromocytomas only, or both
n1=Lester (signe de) | n2=en:patients may have head and neck paragangliomas only, adrenal or extraadrenal pheochromocytomas only, or both | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have recurrent infections due to immunosuppressive therapy
n1=Lester (signe de) | n2=en:patients may have recurrent infections due to immunosuppressive therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may have seizures only, dyskinesia only, or both
n1=Lester (signe de) | n2=en:patients may have seizures only, dyskinesia only, or both | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may or may not have dysmorphic features
n1=Lester (signe de) | n2=en:patients may or may not have dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may present with autoimmune features or primary immunodeficiency
n1=Lester (signe de) | n2=en:patients may present with autoimmune features or primary immunodeficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may present with either renal or neurologic symptoms
n1=Lester (signe de) | n2=en:patients may present with either renal or neurologic symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may present with recurrent illnesses or infections, or shock
n1=Lester (signe de) | n2=en:patients may present with recurrent illnesses or infections, or shock | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may require implantable cardioverter defibrillators
n1=Lester (signe de) | n2=en:patients may require implantable cardioverter defibrillators | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may show both optic neuropathy and dystonia or only 1 disorder
n1=Lester (signe de) | n2=en:patients may show both optic neuropathy and dystonia or only 1 disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may show intermittent signs of improvement
n1=Lester (signe de) | n2=en:patients may show intermittent signs of improvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients may show normal development
n1=Lester (signe de) | n2=en:patients may show normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients need lifelong total parenteral nutrition
n1=Lester (signe de) | n2=en:patients need lifelong total parenteral nutrition | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients need support with walking or are wheelchair-bound
n1=Lester (signe de) | n2=en:patients need support with walking or are wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients of brazilian origin have a pure cerebellar atrophy
n1=Lester (signe de) | n2=en:patients of brazilian origin have a pure cerebellar atrophy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients of mexican or amerindian origin have a complicated phenotype with additional neurologic features
n1=Lester (signe de) | n2=en:patients of mexican or amerindian origin have a complicated phenotype with additional neurologic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often become wheelchair-bound
n1=Lester (signe de) | n2=en:patients often become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often become wheelchair-bound 3 to 4 decades after onset
n1=Lester (signe de) | n2=en:patients often become wheelchair-bound 3 to 4 decades after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often have a more severe and complicated phenotype in addition to peo
n1=Lester (signe de) | n2=en:patients often have a more severe and complicated phenotype in addition to peo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often have other clinical symptoms resulting from dysfunction of the autonomic nervous system
n1=Lester (signe de) | n2=en:patients often have other clinical symptoms resulting from dysfunction of the autonomic nervous system | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often nonambulatory by the mid-twenties
n1=Lester (signe de) | n2=en:patients often nonambulatory by the mid-twenties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often require cardiac transplantation
n1=Lester (signe de) | n2=en:patients often require cardiac transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients often require implantation of a pacemaker
n1=Lester (signe de) | n2=en:patients often require implantation of a pacemaker | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients older than 60 years have severe degenerative arthritis in the feet
n1=Lester (signe de) | n2=en:patients older than 60 years have severe degenerative arthritis in the feet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients present at birth with respiratory distress or poor head control
n1=Lester (signe de) | n2=en:patients present at birth with respiratory distress or poor head control | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients present with groin pain
n1=Lester (signe de) | n2=en:patients present with groin pain | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients remain ambulatory
n1=Lester (signe de) | n2=en:patients remain ambulatory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients require achilles tendon lengthening in first or second decade of life
n1=Lester (signe de) | n2=en:patients require achilles tendon lengthening in first or second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients retain ambulation even after long disease course
n1=Lester (signe de) | n2=en:patients retain ambulation even after long disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients show sorbitol and glycerol intolerance
n1=Lester (signe de) | n2=en:patients show sorbitol and glycerol intolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients usually require total thyroidectomy
n1=Lester (signe de) | n2=en:patients usually require total thyroidectomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients walk on tips of toes with dorsal foot deviated laterally
n1=Lester (signe de) | n2=en:patients walk on tips of toes with dorsal foot deviated laterally | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients who acquire ability to walk may lose it
n1=Lester (signe de) | n2=en:patients who acquire ability to walk may lose it | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with a more severe phenotype have been reported with mutations in more than 1 lqts-related gene
n1=Lester (signe de) | n2=en:patients with a more severe phenotype have been reported with mutations in more than 1 lqts-related gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with abcb4 mutations benefit from ursodeoxycholic acid (udca) treatment
n1=Lester (signe de) | n2=en:patients with abcb4 mutations benefit from ursodeoxycholic acid (udca) treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with adult onset present with psychiatric features
n1=Lester (signe de) | n2=en:patients with adult onset present with psychiatric features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with atypical form have milder disease, with onset in the first months of life and increased survival
n1=Lester (signe de) | n2=en:patients with atypical form have milder disease, with onset in the first months of life and increased survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with autosomal dominant inheritance and a single gdap1 mutation have a less severe course with later onset
n1=Lester (signe de) | n2=en:patients with autosomal dominant inheritance and a single gdap1 mutation have a less severe course with later onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with contiguous gene deletion of 8q24 have more severe features
n1=Lester (signe de) | n2=en:patients with contiguous gene deletion of 8q24 have more severe features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with glaucoma have nonsense or truncating sbf2 mutations (607697.0002)
n1=Lester (signe de) | n2=en:patients with glaucoma have nonsense or truncating sbf2 mutations (607697.0002) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with hemophilia b(m) variants (see, e.g., 300746.0030) also have prolonged pt
n1=Lester (signe de) | n2=en:patients with hemophilia b(m) variants (see, e.g., 300746.0030) also have prolonged pt | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with homozygous mutations display mild palmoplantar keratoderma and woolly hair in addition to arvd
n1=Lester (signe de) | n2=en:patients with homozygous mutations display mild palmoplantar keratoderma and woolly hair in addition to arvd | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with homozygous mutations have a more severe disorder
n1=Lester (signe de) | n2=en:patients with homozygous mutations have a more severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with homozygous or compound heterozygous mutations have more severe renal glucose wasting than those with heterozygous mutations
n1=Lester (signe de) | n2=en:patients with homozygous or compound heterozygous mutations have more severe renal glucose wasting than those with heterozygous mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with homozygous, compound heterozygous, and heterozygous mutation have been reported
n1=Lester (signe de) | n2=en:patients with homozygous, compound heterozygous, and heterozygous mutation have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with later onset do not have dysmorphic features
n1=Lester (signe de) | n2=en:patients with later onset do not have dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with later onset have better prognosis
n1=Lester (signe de) | n2=en:patients with later onset have better prognosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with longer disease duration show motor neuron involvement
n1=Lester (signe de) | n2=en:patients with longer disease duration show motor neuron involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with meb have less severe features and longer survival
n1=Lester (signe de) | n2=en:patients with meb have less severe features and longer survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with meb may acquire ability to walk and a few words
n1=Lester (signe de) | n2=en:patients with meb may acquire ability to walk and a few words | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with medication-resistant hypertension require bilateral adrenalectomy
n1=Lester (signe de) | n2=en:patients with medication-resistant hypertension require bilateral adrenalectomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with more severe phenotype have been reported with mutations in more than 1 lqt-related gene
n1=Lester (signe de) | n2=en:patients with more severe phenotype have been reported with mutations in more than 1 lqt-related gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with more severe phenotype have been reported with mutations in more than 1 lqts-related gene
n1=Lester (signe de) | n2=en:patients with more severe phenotype have been reported with mutations in more than 1 lqts-related gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with mutation in the nhlrc1 gene have slightly longer survival
n1=Lester (signe de) | n2=en:patients with mutation in the nhlrc1 gene have slightly longer survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with neurologic manifestations and sox10 mutations have the neurologic variant (pcwh, 609136)
n1=Lester (signe de) | n2=en:patients with neurologic manifestations and sox10 mutations have the neurologic variant (pcwh, 609136) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with null mutations have neonatal onset within 72 hours of birth
n1=Lester (signe de) | n2=en:patients with null mutations have neonatal onset within 72 hours of birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with null mutations in (ctsd) show a more severe phenotype with onset at birth ('congenital ncl') and early death within days
n1=Lester (signe de) | n2=en:patients with null mutations in (ctsd) show a more severe phenotype with onset at birth ('congenital ncl') and early death within days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with recessive mutations have a more severe phenotype
n1=Lester (signe de) | n2=en:patients with recessive mutations have a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with residual enzyme activity have childhood or adult onset
n1=Lester (signe de) | n2=en:patients with residual enzyme activity have childhood or adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with t2 deficiency and urinary abnormalities may be asymptomatic
n1=Lester (signe de) | n2=en:patients with t2 deficiency and urinary abnormalities may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with the autosomal recessive disorder have a more severe phenotype
n1=Lester (signe de) | n2=en:patients with the autosomal recessive disorder have a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with total c4 deficiency are homozygous for double null c4 haplotype
n1=Lester (signe de) | n2=en:patients with total c4 deficiency are homozygous for double null c4 haplotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients with variant cjd are homozygous for met129 polymorphism (176640.0005)
n1=Lester (signe de) | n2=en:patients with variant cjd are homozygous for met129 polymorphism (176640.0005) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:patients younger than 30 years complain only that they cannot run fast
n1=Lester (signe de) | n2=en:patients younger than 30 years complain only that they cannot run fast | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pavm more frequent in hht1 than hht2
n1=Lester (signe de) | n2=en:pavm more frequent in hht1 than hht2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pavms occur more frequently in hereditary hemorrhagic telangiectasia 1 (hht1) than hht2
n1=Lester (signe de) | n2=en:pavms occur more frequently in hereditary hemorrhagic telangiectasia 1 (hht1) than hht2 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pcd is a distinct disorder from premature chromatid separation (pcs, 176430), which occurs in all chromosomes
n1=Lester (signe de) | n2=en:pcd is a distinct disorder from premature chromatid separation (pcs, 176430), which occurs in all chromosomes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pcs is a distinct disorder from premature centromere division (pcd, 212790), which affects only the x chromosome
n1=Lester (signe de) | n2=en:pcs is a distinct disorder from premature centromere division (pcd, 212790), which affects only the x chromosome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:peak age of onset in second decade
n1=Lester (signe de) | n2=en:peak age of onset in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:peak age of onset in second decade (range childhood to 50 years)
n1=Lester (signe de) | n2=en:peak age of onset in second decade (range childhood to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:peak age of onset in second decade (range childhood to 76 years)
n1=Lester (signe de) | n2=en:peak age of onset in second decade (range childhood to 76 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pectus carinatum present in obligate carrier mothers
n1=Lester (signe de) | n2=en:pectus carinatum present in obligate carrier mothers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pedigrees compatible with autosomal dominant inheritance have been reported
n1=Lester (signe de) | n2=en:pedigrees compatible with autosomal dominant inheritance have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pedigrees consistent with autosomal dominant and autosomal recessive inheritance have been described
n1=Lester (signe de) | n2=en:pedigrees consistent with autosomal dominant and autosomal recessive inheritance have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pelizaeus-merzbacher disease (pmd, 312080) is an allelic disorder
n1=Lester (signe de) | n2=en:pelizaeus-merzbacher disease (pmd, 312080) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance 86% by 50 years of age
n1=Lester (signe de) | n2=en:penetrance 86% by 50 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance by age 50 is 93% in female mutation carriers and 68% in male mutation carriers
n1=Lester (signe de) | n2=en:penetrance by age 50 is 93% in female mutation carriers and 68% in male mutation carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance estimated to be 80%
n1=Lester (signe de) | n2=en:penetrance estimated to be 80% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance is usually complete by age 65 years
n1=Lester (signe de) | n2=en:penetrance is usually complete by age 65 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance of 70 to 80% over a lifetime in heterozygous mutation carriers
n1=Lester (signe de) | n2=en:penetrance of 70 to 80% over a lifetime in heterozygous mutation carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:penetrance of disease is complete between 30 and 40 years of age
n1=Lester (signe de) | n2=en:penetrance of disease is complete between 30 and 40 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:peo is not always present
n1=Lester (signe de) | n2=en:peo is not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:percentages based on review of 51 published cases (pmid 24891339)
n1=Lester (signe de) | n2=en:percentages based on review of 51 published cases (pmid 24891339) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:performing laboratory medical director:id:pt:facility:nom
n1=Lester (signe de) | n2=en:performing laboratory medical director:id:pt:facility:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:performing laboratory name:identifier:point in time:facility:nominal
n1=Lester (signe de) | n2=en:performing laboratory name:identifier:point in time:facility:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:performing laboratory phone:tele:pt:facility:nom
n1=Lester (signe de) | n2=en:performing laboratory phone:tele:pt:facility:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:performing laboratory:addr:pt:facility:nom
n1=Lester (signe de) | n2=en:performing laboratory:addr:pt:facility:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:perinatal death
n1=Lester (signe de) | n2=en:perinatal death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:perinatal lethal
n1=Lester (signe de) | n2=en:perinatal lethal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:perinatal lethality
n1=Lester (signe de) | n2=en:perinatal lethality | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:periodic paralysis triggered by exercise, rest following exercise, prolonged periods of rest, and stress
n1=Lester (signe de) | n2=en:periodic paralysis triggered by exercise, rest following exercise, prolonged periods of rest, and stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:periodontium is less severely affected than in papillon-lefevre syndrome
n1=Lester (signe de) | n2=en:periodontium is less severely affected than in papillon-lefevre syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:peripheral neuropathy occurs in adulthood
n1=Lester (signe de) | n2=en:peripheral neuropathy occurs in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:periventricular heterotopia (300049) is an allelic disorder
n1=Lester (signe de) | n2=en:periventricular heterotopia (300049) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:persistence of febrile seizures beyond age 6 years
n1=Lester (signe de) | n2=en:persistence of febrile seizures beyond age 6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:persistent bleeding after injury or surgery
n1=Lester (signe de) | n2=en:persistent bleeding after injury or surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:persistent bleeding after trauma
n1=Lester (signe de) | n2=en:persistent bleeding after trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:persistent exposure to fructose leads to chronic liver and kidney complications
n1=Lester (signe de) | n2=en:persistent exposure to fructose leads to chronic liver and kidney complications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phace is an acronym for posterior fossa brain malformation, large facial hemangiomas, arterial anomalies, cardiac anomalies and aortic coarctation, and eye abnormalities
n1=Lester (signe de) | n2=en:phace is an acronym for posterior fossa brain malformation, large facial hemangiomas, arterial anomalies, cardiac anomalies and aortic coarctation, and eye abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype combines features of hirschsprung disease (142623), charcot-marie-tooth disease type 1 (cmt1b, 118200), waardenburg-shah syndrome (277580), and central dysmyelinating leukodystrophy (312080)
n1=Lester (signe de) | n2=en:phenotype combines features of hirschsprung disease (142623), charcot-marie-tooth disease type 1 (cmt1b, 118200), waardenburg-shah syndrome (277580), and central dysmyelinating leukodystrophy (312080) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype is classically defined as aplasia cutis and transverse limb defects
n1=Lester (signe de) | n2=en:phenotype is classically defined as aplasia cutis and transverse limb defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype is due to hypomorphic nonmosaic mutation in the ebp gene
n1=Lester (signe de) | n2=en:phenotype is due to hypomorphic nonmosaic mutation in the ebp gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype is indistinguishable from congenital cytomegalovirus (cmv) infection
n1=Lester (signe de) | n2=en:phenotype is indistinguishable from congenital cytomegalovirus (cmv) infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype is worsened by cold temperature
n1=Lester (signe de) | n2=en:phenotype is worsened by cold temperature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype may be exacerbated by maltreatment in childhood
n1=Lester (signe de) | n2=en:phenotype may be exacerbated by maltreatment in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype may be influenced by maternal alcohol consumption during pregnancy
n1=Lester (signe de) | n2=en:phenotype may be influenced by maternal alcohol consumption during pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype may be oligogenic in some patients who carry mutations in more than one hh-associated gene
n1=Lester (signe de) | n2=en:phenotype may be oligogenic in some patients who carry mutations in more than one hh-associated gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype may or may not be consistent within a family.
n1=Lester (signe de) | n2=en:phenotype may or may not be consistent within a family. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotype range from typical parkinson disease (168600) to dementia with lewy bodies (127750)
n1=Lester (signe de) | n2=en:phenotype range from typical parkinson disease (168600) to dementia with lewy bodies (127750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic heterogeneity
n1=Lester (signe de) | n2=en:phenotypic heterogeneity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap between neurofibromatosis type 1 (162200) and noonan syndrome (163950)
n1=Lester (signe de) | n2=en:phenotypic overlap between neurofibromatosis type 1 (162200) and noonan syndrome (163950) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with albright hereditary osteodystrophy (aho, 103580) and smith-magenis syndrome (sms, 182290)
n1=Lester (signe de) | n2=en:phenotypic overlap with albright hereditary osteodystrophy (aho, 103580) and smith-magenis syndrome (sms, 182290) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with charcot-marie-tooth disease 2b (cmt2b, 600882)
n1=Lester (signe de) | n2=en:phenotypic overlap with charcot-marie-tooth disease 2b (cmt2b, 600882) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with currarino syndrome (176450)
n1=Lester (signe de) | n2=en:phenotypic overlap with currarino syndrome (176450) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with cytochrome c oxidase deficiency (220110)
n1=Lester (signe de) | n2=en:phenotypic overlap with cytochrome c oxidase deficiency (220110) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with denys-drash syndrome (194080).
n1=Lester (signe de) | n2=en:phenotypic overlap with denys-drash syndrome (194080). | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with desbuquois dysplasia (251450)
n1=Lester (signe de) | n2=en:phenotypic overlap with desbuquois dysplasia (251450) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with fhm1 (141500) and sca6 (183086)
n1=Lester (signe de) | n2=en:phenotypic overlap with fhm1 (141500) and sca6 (183086) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with frontotemporal dementia (600274)
n1=Lester (signe de) | n2=en:phenotypic overlap with frontotemporal dementia (600274) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with hereditary sensory and autonomic neuropathy type i (hsan1, 162400)
n1=Lester (signe de) | n2=en:phenotypic overlap with hereditary sensory and autonomic neuropathy type i (hsan1, 162400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with munke syndrome (602849) due to a mutation in the fgfr3 gene (p250r, 134934.0014)
n1=Lester (signe de) | n2=en:phenotypic overlap with munke syndrome (602849) due to a mutation in the fgfr3 gene (p250r, 134934.0014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with neurofibromatosis 1 (nf1, 162200)
n1=Lester (signe de) | n2=en:phenotypic overlap with neurofibromatosis 1 (nf1, 162200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with noonan syndrome 3 (609942) or cardiofaciocutaneous syndrome (115150)
n1=Lester (signe de) | n2=en:phenotypic overlap with noonan syndrome 3 (609942) or cardiofaciocutaneous syndrome (115150) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with parkinson disease
n1=Lester (signe de) | n2=en:phenotypic overlap with parkinson disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with pkan neuroaxonal dystrophy (nbia1, 234200)
n1=Lester (signe de) | n2=en:phenotypic overlap with pkan neuroaxonal dystrophy (nbia1, 234200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with revesz syndrome (268130)
n1=Lester (signe de) | n2=en:phenotypic overlap with revesz syndrome (268130) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with thrombotic thrombocytopenic purpura (ttp, 274150)
n1=Lester (signe de) | n2=en:phenotypic overlap with thrombotic thrombocytopenic purpura (ttp, 274150) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with wagr syndrome (194072), frasier syndrome (136680)
n1=Lester (signe de) | n2=en:phenotypic overlap with wagr syndrome (194072), frasier syndrome (136680) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic overlap with xeroderma pigmentosum (see, e.g., 278700)
n1=Lester (signe de) | n2=en:phenotypic overlap with xeroderma pigmentosum (see, e.g., 278700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic similarities to angelman syndrome (105830)
n1=Lester (signe de) | n2=en:phenotypic similarities to angelman syndrome (105830) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic similarities to costello syndrome (218040)
n1=Lester (signe de) | n2=en:phenotypic similarities to costello syndrome (218040) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic similarities to leigh syndrome (256000)
n1=Lester (signe de) | n2=en:phenotypic similarities to leigh syndrome (256000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic similarities to noonan syndrome (163950)
n1=Lester (signe de) | n2=en:phenotypic similarities to noonan syndrome (163950) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variability
n1=Lester (signe de) | n2=en:phenotypic variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variability has been described, with some patients exhibiting partial and others complete hypogonadotropic hypogonadism
n1=Lester (signe de) | n2=en:phenotypic variability has been described, with some patients exhibiting partial and others complete hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variability within families and among patients carrying the same mutation
n1=Lester (signe de) | n2=en:phenotypic variability within families and among patients carrying the same mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variability within families and among patients carrying the same mutation appears to be due to the oligogenic nature of the disorder, with some patients having mutations in more than 1 neuroendocrine-related gene
n1=Lester (signe de) | n2=en:phenotypic variability within families and among patients carrying the same mutation appears to be due to the oligogenic nature of the disorder, with some patients having mutations in more than 1 neuroendocrine-related gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variability, intrafamilial
n1=Lester (signe de) | n2=en:phenotypic variability, intrafamilial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variation
n1=Lester (signe de) | n2=en:phenotypic variation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variation (may affect language expression, reception, and/or articulation)
n1=Lester (signe de) | n2=en:phenotypic variation (may affect language expression, reception, and/or articulation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypic variation in severity and symptoms
n1=Lester (signe de) | n2=en:phenotypic variation in severity and symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypically indistinguishable from hemophilia a (306700)
n1=Lester (signe de) | n2=en:phenotypically indistinguishable from hemophilia a (306700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:phenotypically mild form of joubert syndrome
n1=Lester (signe de) | n2=en:phenotypically mild form of joubert syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:physical features are apparent at birth
n1=Lester (signe de) | n2=en:physical features are apparent at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:physiologic decreased plasma cholinesterase activity in pregnancy, the puerperium, and newborns
n1=Lester (signe de) | n2=en:physiologic decreased plasma cholinesterase activity in pregnancy, the puerperium, and newborns | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pigment does not develop with age
n1=Lester (signe de) | n2=en:pigment does not develop with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pigmentary abnormalities apparent at birth or in infancy
n1=Lester (signe de) | n2=en:pigmentary abnormalities apparent at birth or in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pigmentation not always butterfly-shaped
n1=Lester (signe de) | n2=en:pigmentation not always butterfly-shaped | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pigmented spots appear in infancy through childhood and fade in adulthood
n1=Lester (signe de) | n2=en:pigmented spots appear in infancy through childhood and fade in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:plantar contractures become apparent with onset of ambulation
n1=Lester (signe de) | n2=en:plantar contractures become apparent with onset of ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:plasma cholinesterase measurement
n1=Lester (signe de) | n2=en:plasma cholinesterase measurement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pmp22 (601097) and rai1 (607642) are included in smallest region of overlap
n1=Lester (signe de) | n2=en:pmp22 (601097) and rai1 (607642) are included in smallest region of overlap | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pneumocytosis carinii infection (12 to 42%)
n1=Lester (signe de) | n2=en:pneumocytosis carinii infection (12 to 42%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poland syndrome can be associated with moebius syndrome (157900)
n1=Lester (signe de) | n2=en:poland syndrome can be associated with moebius syndrome (157900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:polg mutations account for approximately 45% of all peo cases
n1=Lester (signe de) | n2=en:polg mutations account for approximately 45% of all peo cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:polyhydramnios
n1=Lester (signe de) | n2=en:polyhydramnios | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:polyps occur in teens
n1=Lester (signe de) | n2=en:polyps occur in teens | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor gonadotropin response to gonadotropin releasing hormone (gnrh)
n1=Lester (signe de) | n2=en:poor gonadotropin response to gonadotropin releasing hormone (gnrh) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor or no response to glucocorticoid treatment
n1=Lester (signe de) | n2=en:poor or no response to glucocorticoid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor outcome
n1=Lester (signe de) | n2=en:poor outcome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to acetylcholinesterase inhibitors
n1=Lester (signe de) | n2=en:poor response to acetylcholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to acetylcholinesterase inhibitors or cholinergic agents
n1=Lester (signe de) | n2=en:poor response to acetylcholinesterase inhibitors or cholinergic agents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to g-csf treatment
n1=Lester (signe de) | n2=en:poor response to g-csf treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to l-dopa
n1=Lester (signe de) | n2=en:poor response to l-dopa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to levodopa treatment
n1=Lester (signe de) | n2=en:poor response to levodopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:poor response to the c5 inhibitor eculizumab
n1=Lester (signe de) | n2=en:poor response to the c5 inhibitor eculizumab | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:positive family history in 12-33% patients
n1=Lester (signe de) | n2=en:positive family history in 12-33% patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:positive response to treatment with growth hormone
n1=Lester (signe de) | n2=en:positive response to treatment with growth hormone | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible autosomal dominant (165199) and autosomal recessive (258650) forms
n1=Lester (signe de) | n2=en:possible autosomal dominant (165199) and autosomal recessive (258650) forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible autosomal dominant form 165199 and x-linked form, cmtx5 311070
n1=Lester (signe de) | n2=en:possible autosomal dominant form 165199 and x-linked form, cmtx5 311070 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible autosomal recessive form 258650 and x-linked form cmtx5 311070
n1=Lester (signe de) | n2=en:possible autosomal recessive form 258650 and x-linked form cmtx5 311070 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible benefit from treatment with 3,4-diaminopyridine and salbutamol
n1=Lester (signe de) | n2=en:possible benefit from treatment with 3,4-diaminopyridine and salbutamol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible defect of a specific lipase in the pathway of free fatty acid oxidation
n1=Lester (signe de) | n2=en:possible defect of a specific lipase in the pathway of free fatty acid oxidation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible favorable response to ketogenic diet
n1=Lester (signe de) | n2=en:possible favorable response to ketogenic diet | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible genetic heterogeneity (linkage to xp22 in some families)
n1=Lester (signe de) | n2=en:possible genetic heterogeneity (linkage to xp22 in some families) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible gonadal mosaicism in one report
n1=Lester (signe de) | n2=en:possible gonadal mosaicism in one report | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible increase of aneuploidy in offspring
n1=Lester (signe de) | n2=en:possible increase of aneuploidy in offspring | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible x-linked dominant inheritance
n1=Lester (signe de) | n2=en:possible x-linked dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible x-linked inheritance
n1=Lester (signe de) | n2=en:possible x-linked inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possible x-linked recessive inheritance
n1=Lester (signe de) | n2=en:possible x-linked recessive inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possibly allelic to cohen syndrome (216550)
n1=Lester (signe de) | n2=en:possibly allelic to cohen syndrome (216550) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:possibly x-linked recessive inheritance
n1=Lester (signe de) | n2=en:possibly x-linked recessive inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:postlingual onset
n1=Lester (signe de) | n2=en:postlingual onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:preaxial involvement in approximately 60% of patients
n1=Lester (signe de) | n2=en:preaxial involvement in approximately 60% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by fatigue or alcohol
n1=Lester (signe de) | n2=en:precipitated by fatigue or alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by febrile illness and fasting
n1=Lester (signe de) | n2=en:precipitated by febrile illness and fasting | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by fever
n1=Lester (signe de) | n2=en:precipitated by fever | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by general anesthesia
n1=Lester (signe de) | n2=en:precipitated by general anesthesia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by infection, fasting, or intercurrent illness
n1=Lester (signe de) | n2=en:precipitated by infection, fasting, or intercurrent illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by mechanical compression or pressure on nerve
n1=Lester (signe de) | n2=en:precipitated by mechanical compression or pressure on nerve | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitated by sleep deprivation
n1=Lester (signe de) | n2=en:precipitated by sleep deprivation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitating factors - ingestion of wheat gluten, rye, and/or barley
n1=Lester (signe de) | n2=en:precipitating factors - ingestion of wheat gluten, rye, and/or barley | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitating factors include viral illness and pregnancy
n1=Lester (signe de) | n2=en:precipitating factors include viral illness and pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:precipitation by pregnancy
n1=Lester (signe de) | n2=en:precipitation by pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:predisposition to neoplasia
n1=Lester (signe de) | n2=en:predisposition to neoplasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:predominantly occurs in young males with a high rate of atopic disease
n1=Lester (signe de) | n2=en:predominantly occurs in young males with a high rate of atopic disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:predominantly occurs in young males with high rate of atopic disease
n1=Lester (signe de) | n2=en:predominantly occurs in young males with high rate of atopic disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:preferably treated with iodine supplementation rather than thyroid hormone replacement
n1=Lester (signe de) | n2=en:preferably treated with iodine supplementation rather than thyroid hormone replacement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prelingual onset
n1=Lester (signe de) | n2=en:prelingual onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prelingual onset in males
n1=Lester (signe de) | n2=en:prelingual onset in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:premature aging syndrome
n1=Lester (signe de) | n2=en:premature aging syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:premature death may occur
n1=Lester (signe de) | n2=en:premature death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal diagnosis available
n1=Lester (signe de) | n2=en:prenatal diagnosis available | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal diagnosis by ultrasound
n1=Lester (signe de) | n2=en:prenatal diagnosis by ultrasound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal history of maternal diabetes in 35% of cases
n1=Lester (signe de) | n2=en:prenatal history of maternal diabetes in 35% of cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal onset
n1=Lester (signe de) | n2=en:prenatal onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal onset or onset at birth
n1=Lester (signe de) | n2=en:prenatal onset or onset at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal onset or onset in infancy
n1=Lester (signe de) | n2=en:prenatal onset or onset in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal or neonatal onset
n1=Lester (signe de) | n2=en:prenatal or neonatal onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal or perinatal death
n1=Lester (signe de) | n2=en:prenatal or perinatal death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prenatal or perinatal lethality in hemizygous males
n1=Lester (signe de) | n2=en:prenatal or perinatal lethality in hemizygous males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:preponderance of affected females (80%) to males
n1=Lester (signe de) | n2=en:preponderance of affected females (80%) to males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presence of 4 major features or 3 major and 2 minor features establishes the diagnosis
n1=Lester (signe de) | n2=en:presence of 4 major features or 3 major and 2 minor features establishes the diagnosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presence of additional features is variable
n1=Lester (signe de) | n2=en:presence of additional features is variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death
n1=Lester (signe de) | n2=en:presence of severe midfacial and limb defects and birth length less than 37cm associated with stillborn or early infant death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:present at birth
n1=Lester (signe de) | n2=en:present at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:present in infancy in all affected individuals
n1=Lester (signe de) | n2=en:present in infancy in all affected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:present in jewish yemenite population
n1=Lester (signe de) | n2=en:present in jewish yemenite population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation after 18 months
n1=Lester (signe de) | n2=en:presentation after 18 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation after 6 months
n1=Lester (signe de) | n2=en:presentation after 6 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation at 3-6 weeks of age
n1=Lester (signe de) | n2=en:presentation at 3-6 weeks of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation between 6-18 months
n1=Lester (signe de) | n2=en:presentation between 6-18 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in adults - episodic or nocturnal diarrhea, flatulence, weight loss, iron deficiency anemia, macrocytic anemia, coagulopathy, vitamin d deficiency
n1=Lester (signe de) | n2=en:presentation in adults - episodic or nocturnal diarrhea, flatulence, weight loss, iron deficiency anemia, macrocytic anemia, coagulopathy, vitamin d deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in childhood includes waddling gait and knee pain/stiffness
n1=Lester (signe de) | n2=en:presentation in childhood includes waddling gait and knee pain/stiffness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in children - diarrhea, constipation (rarely), short stature, pubertal delay, rickets, iron and folate deficiency with anemia
n1=Lester (signe de) | n2=en:presentation in children - diarrhea, constipation (rarely), short stature, pubertal delay, rickets, iron and folate deficiency with anemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in early childhood
n1=Lester (signe de) | n2=en:presentation in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in first year of life
n1=Lester (signe de) | n2=en:presentation in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presentation in infants - impaired growth, diarrhea, abdominal distention, vomiting
n1=Lester (signe de) | n2=en:presentation in infants - impaired growth, diarrhea, abdominal distention, vomiting | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presenting symptoms - recurrent uti, polyuria/polydipsia, hematuria, and abacterial leukocyturia
n1=Lester (signe de) | n2=en:presenting symptoms - recurrent uti, polyuria/polydipsia, hematuria, and abacterial leukocyturia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presenting symptoms in the upper body
n1=Lester (signe de) | n2=en:presenting symptoms in the upper body | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents as early-onset strokes in 43% of patients
n1=Lester (signe de) | n2=en:presents as early-onset strokes in 43% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents at 2 to 3 months of age
n1=Lester (signe de) | n2=en:presents at 2 to 3 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents at a later age than sporadic wilms tumor
n1=Lester (signe de) | n2=en:presents at a later age than sporadic wilms tumor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents at a later stage than sporadic wilms tumor
n1=Lester (signe de) | n2=en:presents at a later stage than sporadic wilms tumor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents at birth or early childhood
n1=Lester (signe de) | n2=en:presents at birth or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents with 4 types of painful episodes - (1) birth crisis, babies are born red and stiff (2) rectal crisis, triggered by defecation or emotional factors (3) ocular crisis (4) mandibular crisis, triggered by eating or yawning
n1=Lester (signe de) | n2=en:presents with 4 types of painful episodes - (1) birth crisis, babies are born red and stiff (2) rectal crisis, triggered by defecation or emotional factors (3) ocular crisis (4) mandibular crisis, triggered by eating or yawning | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presents with inguinal hernia (prepubertal) or primary amenorrhea (post pubertal)
n1=Lester (signe de) | n2=en:presents with inguinal hernia (prepubertal) or primary amenorrhea (post pubertal) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:presumed autosomal dominant with incomplete penetrance
n1=Lester (signe de) | n2=en:presumed autosomal dominant with incomplete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence 1 in 1,250
n1=Lester (signe de) | n2=en:prevalence 1 in 1,250 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence 1 in 8000
n1=Lester (signe de) | n2=en:prevalence 1 in 8000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence 1-2% in northern european populations
n1=Lester (signe de) | n2=en:prevalence 1-2% in northern european populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence 1/10,000-1/15,000 female births
n1=Lester (signe de) | n2=en:prevalence 1/10,000-1/15,000 female births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence approximately 1 in 4,000 males
n1=Lester (signe de) | n2=en:prevalence approximately 1 in 4,000 males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence estimated at 1 in 50,000
n1=Lester (signe de) | n2=en:prevalence estimated at 1 in 50,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence estimated at 1 in 86,000
n1=Lester (signe de) | n2=en:prevalence estimated at 1 in 86,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in caucasians is 1 in 1,000,000
n1=Lester (signe de) | n2=en:prevalence in caucasians is 1 in 1,000,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in finland is 1 in 25,000
n1=Lester (signe de) | n2=en:prevalence in finland is 1 in 25,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in norway is 1 in 80,000
n1=Lester (signe de) | n2=en:prevalence in norway is 1 in 80,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in poland is 1 in 129,000
n1=Lester (signe de) | n2=en:prevalence in poland is 1 in 129,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in sardinia is 1 in 14,000
n1=Lester (signe de) | n2=en:prevalence in sardinia is 1 in 14,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in slovenia is 1 in 43,000
n1=Lester (signe de) | n2=en:prevalence in slovenia is 1 in 43,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in taiwan is 1 in 132,000
n1=Lester (signe de) | n2=en:prevalence in taiwan is 1 in 132,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence in the finnish population of 5.8 per million
n1=Lester (signe de) | n2=en:prevalence in the finnish population of 5.8 per million | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence is estimated to be 1 in 1,100,000
n1=Lester (signe de) | n2=en:prevalence is estimated to be 1 in 1,100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence is estimated to be 1 in 150,000
n1=Lester (signe de) | n2=en:prevalence is estimated to be 1 in 150,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence much higher in whites than blacks
n1=Lester (signe de) | n2=en:prevalence much higher in whites than blacks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 0.5 to 1 in 1,000
n1=Lester (signe de) | n2=en:prevalence of 0.5 to 1 in 1,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 0.6 to 10 per 100,000 individuals
n1=Lester (signe de) | n2=en:prevalence of 0.6 to 10 per 100,000 individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 1,429 in tanzania
n1=Lester (signe de) | n2=en:prevalence of 1 in 1,429 in tanzania | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 1,500
n1=Lester (signe de) | n2=en:prevalence of 1 in 1,500 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 10,000 african-americans
n1=Lester (signe de) | n2=en:prevalence of 1 in 10,000 african-americans | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 10,000 caucasians
n1=Lester (signe de) | n2=en:prevalence of 1 in 10,000 caucasians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 100,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 150 to 1 in 1,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 150 to 1 in 1,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 150,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 150,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 2,833 in zimbabwe
n1=Lester (signe de) | n2=en:prevalence of 1 in 2,833 in zimbabwe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 200,000 to 1 in 800,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 200,000 to 1 in 800,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 227 hopi indians
n1=Lester (signe de) | n2=en:prevalence of 1 in 227 hopi indians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 240 zuni indians
n1=Lester (signe de) | n2=en:prevalence of 1 in 240 zuni indians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 28,000 african-americans
n1=Lester (signe de) | n2=en:prevalence of 1 in 28,000 african-americans | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 28,000 caucasians
n1=Lester (signe de) | n2=en:prevalence of 1 in 28,000 caucasians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 3,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 3,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 3,900 in south africa
n1=Lester (signe de) | n2=en:prevalence of 1 in 3,900 in south africa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 30,000 in northern europe
n1=Lester (signe de) | n2=en:prevalence of 1 in 30,000 in northern europe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 300,000 in quebec
n1=Lester (signe de) | n2=en:prevalence of 1 in 300,000 in quebec | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 40,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 40,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 40,000 among caucasians
n1=Lester (signe de) | n2=en:prevalence of 1 in 40,000 among caucasians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 40,000 to 1 in 80,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 40,000 to 1 in 80,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 50,000-70,000 live births
n1=Lester (signe de) | n2=en:prevalence of 1 in 50,000-70,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 6,000 to 1 in 10,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 6,000 to 1 in 10,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 7,900 in cameroon
n1=Lester (signe de) | n2=en:prevalence of 1 in 7,900 in cameroon | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 1 in 70,000
n1=Lester (signe de) | n2=en:prevalence of 1 in 70,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 19 in 1,000,000 in sweden
n1=Lester (signe de) | n2=en:prevalence of 19 in 1,000,000 in sweden | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 2-7% in english-speaking preschool children
n1=Lester (signe de) | n2=en:prevalence of 2-7% in english-speaking preschool children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of 7 in 100,000 live births
n1=Lester (signe de) | n2=en:prevalence of 7 in 100,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of approximately 1 in 2000 individuals
n1=Lester (signe de) | n2=en:prevalence of approximately 1 in 2000 individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of essential tremor ranges from 0.4 to 6% in the general population
n1=Lester (signe de) | n2=en:prevalence of essential tremor ranges from 0.4 to 6% in the general population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of homozygous c4a deficiency in sle 10-15x higher than general population
n1=Lester (signe de) | n2=en:prevalence of homozygous c4a deficiency in sle 10-15x higher than general population | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of in 1 in 8,000
n1=Lester (signe de) | n2=en:prevalence of in 1 in 8,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of sleep terrors about 3% in children
n1=Lester (signe de) | n2=en:prevalence of sleep terrors about 3% in children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of sleep terrors less than 1% in adults
n1=Lester (signe de) | n2=en:prevalence of sleep terrors less than 1% in adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of sleepwalking about 3% in adults
n1=Lester (signe de) | n2=en:prevalence of sleepwalking about 3% in adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of sleepwalking up to 26% in childhood
n1=Lester (signe de) | n2=en:prevalence of sleepwalking up to 26% in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence of true hypoprothrombinemia is 1 in 2 million
n1=Lester (signe de) | n2=en:prevalence of true hypoprothrombinemia is 1 in 2 million | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence ranges from 1 in 12,000 to 1 in 50,000
n1=Lester (signe de) | n2=en:prevalence ranges from 1 in 12,000 to 1 in 50,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalence rates average 10-20% of the general population over age 60
n1=Lester (signe de) | n2=en:prevalence rates average 10-20% of the general population over age 60 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent among european, particularly spanish, gypsies (r1109x, 608206.0006)
n1=Lester (signe de) | n2=en:prevalent among european, particularly spanish, gypsies (r1109x, 608206.0006) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent among individuals of east asian descent
n1=Lester (signe de) | n2=en:prevalent among individuals of east asian descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent among patients of asian descent, particularly japanese
n1=Lester (signe de) | n2=en:prevalent among patients of asian descent, particularly japanese | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent among the amish
n1=Lester (signe de) | n2=en:prevalent among the amish | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in arabic, turkish, armenian, and sephardic jewish populations
n1=Lester (signe de) | n2=en:prevalent in arabic, turkish, armenian, and sephardic jewish populations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in ashkenazi jews
n1=Lester (signe de) | n2=en:prevalent in ashkenazi jews | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in bulgarian gypsies
n1=Lester (signe de) | n2=en:prevalent in bulgarian gypsies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in newfoundland
n1=Lester (signe de) | n2=en:prevalent in newfoundland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in north africa
n1=Lester (signe de) | n2=en:prevalent in north africa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in old order amish of lancaster county, pennsylvania and saulteaux/ojibway indians of canada
n1=Lester (signe de) | n2=en:prevalent in old order amish of lancaster county, pennsylvania and saulteaux/ojibway indians of canada | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in quebec
n1=Lester (signe de) | n2=en:prevalent in quebec | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in sweden
n1=Lester (signe de) | n2=en:prevalent in sweden | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prevalent in the old order amish in the u.s. and in finland
n1=Lester (signe de) | n2=en:prevalent in the old order amish in the u.s. and in finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:primarily diagnosed in females
n1=Lester (signe de) | n2=en:primarily diagnosed in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:primary teeth affected greater than secondary teeth
n1=Lester (signe de) | n2=en:primary teeth affected greater than secondary teeth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prodromal symptoms include nasal congestion, dry throat, severe fatigue, vertigo, and headache
n1=Lester (signe de) | n2=en:prodromal symptoms include nasal congestion, dry throat, severe fatigue, vertigo, and headache | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:profound dementia and death usually occurs by age 50 years
n1=Lester (signe de) | n2=en:profound dementia and death usually occurs by age 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prognosis good
n1=Lester (signe de) | n2=en:prognosis good | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progresses through puberty, then stabilizes
n1=Lester (signe de) | n2=en:progresses through puberty, then stabilizes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progresses to involve upper limbs
n1=Lester (signe de) | n2=en:progresses to involve upper limbs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression in adulthood
n1=Lester (signe de) | n2=en:progression in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression more frequent in men than women
n1=Lester (signe de) | n2=en:progression more frequent in men than women | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression of disease stops at a best-corrected visual acuity of 0.2 (20/100) to 0.1 (20/200)
n1=Lester (signe de) | n2=en:progression of disease stops at a best-corrected visual acuity of 0.2 (20/100) to 0.1 (20/200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression of phenotype with age
n1=Lester (signe de) | n2=en:progression of phenotype with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression of the disorder is precipitated by viral symptoms
n1=Lester (signe de) | n2=en:progression of the disorder is precipitated by viral symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progression to profound hearing loss affecting all frequencies
n1=Lester (signe de) | n2=en:progression to profound hearing loss affecting all frequencies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive
n1=Lester (signe de) | n2=en:progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive cerebellar ataxia
n1=Lester (signe de) | n2=en:progressive cerebellar ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive clinical course with onset in childhood
n1=Lester (signe de) | n2=en:progressive clinical course with onset in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive deafness
n1=Lester (signe de) | n2=en:progressive deafness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive degenerative hip disease requiring replacement in 2nd to 4th decade
n1=Lester (signe de) | n2=en:progressive degenerative hip disease requiring replacement in 2nd to 4th decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disease
n1=Lester (signe de) | n2=en:progressive disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disease is seen in some patients
n1=Lester (signe de) | n2=en:progressive disease is seen in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disease with onset in infancy
n1=Lester (signe de) | n2=en:progressive disease with onset in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder
n1=Lester (signe de) | n2=en:progressive disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder due to secondary myopathy
n1=Lester (signe de) | n2=en:progressive disorder due to secondary myopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder regarding both neurologic and renal symptoms
n1=Lester (signe de) | n2=en:progressive disorder regarding both neurologic and renal symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder that may become stable in young adulthood
n1=Lester (signe de) | n2=en:progressive disorder that may become stable in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder, usually with rapid, relentless course
n1=Lester (signe de) | n2=en:progressive disorder, usually with rapid, relentless course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive disorder, with older patients exhibiting more severe symptoms
n1=Lester (signe de) | n2=en:progressive disorder, with older patients exhibiting more severe symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive neurologic deterioration if untreated
n1=Lester (signe de) | n2=en:progressive neurologic deterioration if untreated | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive or slowly progressive
n1=Lester (signe de) | n2=en:progressive or slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive renal disorder
n1=Lester (signe de) | n2=en:progressive renal disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive sclerosis with age
n1=Lester (signe de) | n2=en:progressive sclerosis with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive skeletal dysplasia
n1=Lester (signe de) | n2=en:progressive skeletal dysplasia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:progressive, with full manifestations at puberty
n1=Lester (signe de) | n2=en:progressive, with full manifestations at puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:prominent psychiatric symptoms
n1=Lester (signe de) | n2=en:prominent psychiatric symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:protein c deficiency is found in 3-4% of patients with venous thromboembolism
n1=Lester (signe de) | n2=en:protein c deficiency is found in 3-4% of patients with venous thromboembolism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:protein s deficiency is found in 2-3% of patients with thromboembolism
n1=Lester (signe de) | n2=en:protein s deficiency is found in 2-3% of patients with thromboembolism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:protracted course
n1=Lester (signe de) | n2=en:protracted course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:protracted disease course
n1=Lester (signe de) | n2=en:protracted disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:provoked by crying or emotional upset
n1=Lester (signe de) | n2=en:provoked by crying or emotional upset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pseudoarylsulfatase a deficiency is an allelic disorder with reduced levels of arsa activity, but no neurologic manifestations
n1=Lester (signe de) | n2=en:pseudoarylsulfatase a deficiency is an allelic disorder with reduced levels of arsa activity, but no neurologic manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pseudomembrane formation triggered by injury, infection, irritation, surgery
n1=Lester (signe de) | n2=en:pseudomembrane formation triggered by injury, infection, irritation, surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:psychiatric symptoms may be the presenting sign
n1=Lester (signe de) | n2=en:psychiatric symptoms may be the presenting sign | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:psychomotor delay may already be apparent at onset of seizures
n1=Lester (signe de) | n2=en:psychomotor delay may already be apparent at onset of seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ptosis is usually presenting feature
n1=Lester (signe de) | n2=en:ptosis is usually presenting feature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pulsatile headache lasts hours to days
n1=Lester (signe de) | n2=en:pulsatile headache lasts hours to days | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pulse generator system for tympanic treatment of inner ear endolymphatic fluid
n1=Lester (signe de) | n2=en:pulse generator system for tympanic treatment of inner ear endolymphatic fluid | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pyogenic arthritis, pyoderma gangrenosum and acne
n1=Lester (signe de) | n2=en:pyogenic arthritis, pyoderma gangrenosum and acne | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:pyridoxine responsive individuals often have milder manifestations than those not responsive
n1=Lester (signe de) | n2=en:pyridoxine responsive individuals often have milder manifestations than those not responsive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:quinidine therapy may be effective
n1=Lester (signe de) | n2=en:quinidine therapy may be effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:radioresistant dna synthesis
n1=Lester (signe de) | n2=en:radioresistant dna synthesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:range of onset 11 to 50 years
n1=Lester (signe de) | n2=en:range of onset 11 to 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapid disease progression
n1=Lester (signe de) | n2=en:rapid disease progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapid disease progression from ages 40 to 50 years
n1=Lester (signe de) | n2=en:rapid disease progression from ages 40 to 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapid progression in adolescence
n1=Lester (signe de) | n2=en:rapid progression in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapid progression to disability
n1=Lester (signe de) | n2=en:rapid progression to disability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive
n1=Lester (signe de) | n2=en:rapidly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive (6-24 months)
n1=Lester (signe de) | n2=en:rapidly progressive (6-24 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive course
n1=Lester (signe de) | n2=en:rapidly progressive course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive deterioration (in some patients)
n1=Lester (signe de) | n2=en:rapidly progressive deterioration (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive disorder
n1=Lester (signe de) | n2=en:rapidly progressive disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive episodes
n1=Lester (signe de) | n2=en:rapidly progressive episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive neonatal onset with early death
n1=Lester (signe de) | n2=en:rapidly progressive neonatal onset with early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive to persistent vegetative state or death
n1=Lester (signe de) | n2=en:rapidly progressive to persistent vegetative state or death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rapidly progressive, but slower than creutzfeldt-jakob disease (123400)
n1=Lester (signe de) | n2=en:rapidly progressive, but slower than creutzfeldt-jakob disease (123400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare adult cases reported
n1=Lester (signe de) | n2=en:rare adult cases reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare adult onset
n1=Lester (signe de) | n2=en:rare adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare autosomal dominant inheritance has been reported
n1=Lester (signe de) | n2=en:rare autosomal dominant inheritance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare disorder
n1=Lester (signe de) | n2=en:rare disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare patients with homozygous null mutations have most severe disease
n1=Lester (signe de) | n2=en:rare patients with homozygous null mutations have most severe disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare spontaneous improvement occurs (8%)
n1=Lester (signe de) | n2=en:rare spontaneous improvement occurs (8%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rare survival to teens
n1=Lester (signe de) | n2=en:rare survival to teens | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rarely produces clinical jaundice
n1=Lester (signe de) | n2=en:rarely produces clinical jaundice | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rarely reported in infants
n1=Lester (signe de) | n2=en:rarely reported in infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rarely, patients may be asymptomatic
n1=Lester (signe de) | n2=en:rarely, patients may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rarely, patients with childhood-onset may lose the renal phosphate-wasting defect
n1=Lester (signe de) | n2=en:rarely, patients with childhood-onset may lose the renal phosphate-wasting defect | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rash, edema, and arthralgia may occur during crisis
n1=Lester (signe de) | n2=en:rash, edema, and arthralgia may occur during crisis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ratio female to male, 19:10 in index family
n1=Lester (signe de) | n2=en:ratio female to male, 19:10 in index family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reason for lab test:type:pt:bld.dot:nom
n1=Lester (signe de) | n2=en:reason for lab test:type:pt:bld.dot:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recessive inheritance has been reported
n1=Lester (signe de) | n2=en:recessive inheritance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recessive inheritance is rare
n1=Lester (signe de) | n2=en:recessive inheritance is rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrence is possible
n1=Lester (signe de) | n2=en:recurrence is possible | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrence of symptoms after cholecystectomy
n1=Lester (signe de) | n2=en:recurrence of symptoms after cholecystectomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent acute episodes
n1=Lester (signe de) | n2=en:recurrent acute episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent acute episodes of neurologic deterioration associated with febrile illnesses
n1=Lester (signe de) | n2=en:recurrent acute episodes of neurologic deterioration associated with febrile illnesses | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent bacterial infection
n1=Lester (signe de) | n2=en:recurrent bacterial infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent bacterial infections beginning in childhood
n1=Lester (signe de) | n2=en:recurrent bacterial infections beginning in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent bacterial infections with onset in the first or second year of life
n1=Lester (signe de) | n2=en:recurrent bacterial infections with onset in the first or second year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent bacterial, viral, and fungal infections
n1=Lester (signe de) | n2=en:recurrent bacterial, viral, and fungal infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent cholestatic episodes in puberty, following surgery or severe trauma, and pregnancy
n1=Lester (signe de) | n2=en:recurrent cholestatic episodes in puberty, following surgery or severe trauma, and pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent episodes of liver failure during intercurrent infections
n1=Lester (signe de) | n2=en:recurrent episodes of liver failure during intercurrent infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent febrile crises preceded by chills and accompanied by headache and bilateral cervical lymphadenopathy
n1=Lester (signe de) | n2=en:recurrent febrile crises preceded by chills and accompanied by headache and bilateral cervical lymphadenopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:recurrent febrile crises with lymphadenopathy, hepatosplenomegaly, vomiting, and diarrhea
n1=Lester (signe de) | n2=en:recurrent febrile crises with lymphadenopathy, hepatosplenomegaly, vomiting, and diarrhea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced exercise tolerance
n1=Lester (signe de) | n2=en:reduced exercise tolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced fertility
n1=Lester (signe de) | n2=en:reduced fertility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced fetal movement
n1=Lester (signe de) | n2=en:reduced fetal movement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced life expectancy
n1=Lester (signe de) | n2=en:reduced life expectancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced life expectancy, death by 10 years of age in 70% of patients
n1=Lester (signe de) | n2=en:reduced life expectancy, death by 10 years of age in 70% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced longevity
n1=Lester (signe de) | n2=en:reduced longevity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance (75%)
n1=Lester (signe de) | n2=en:reduced penetrance (75%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance (89%)
n1=Lester (signe de) | n2=en:reduced penetrance (89%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance (about 60%)
n1=Lester (signe de) | n2=en:reduced penetrance (about 60%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance (approximately 54%)
n1=Lester (signe de) | n2=en:reduced penetrance (approximately 54%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance (approximately 87%)
n1=Lester (signe de) | n2=en:reduced penetrance (approximately 87%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance has been reported
n1=Lester (signe de) | n2=en:reduced penetrance has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance in females
n1=Lester (signe de) | n2=en:reduced penetrance in females | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced penetrance, estimated to be 15% at 60 years, 21% at 70 years, and 32% at 80 years
n1=Lester (signe de) | n2=en:reduced penetrance, estimated to be 15% at 60 years, 21% at 70 years, and 32% at 80 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reduced zinc in affected mother's breast milk is unresponsive to oral zinc supplementation
n1=Lester (signe de) | n2=en:reduced zinc in affected mother's breast milk is unresponsive to oral zinc supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab name:identifier:time reported elsewhere:reference lab test:nominal
n1=Lester (signe de) | n2=en:reference lab name:identifier:time reported elsewhere:reference lab test:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test identifier:id:xxx:reference lab test:nom
n1=Lester (signe de) | n2=en:reference lab test identifier:id:xxx:reference lab test:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test method:type:time reported elsewhere:reference lab test:narrative
n1=Lester (signe de) | n2=en:reference lab test method:type:time reported elsewhere:reference lab test:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test name:type:time reported elsewhere:reference lab test:nominal
n1=Lester (signe de) | n2=en:reference lab test name:type:time reported elsewhere:reference lab test:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test number and name:identifier:time reported elsewhere:reference lab test:nominal
n1=Lester (signe de) | n2=en:reference lab test number and name:identifier:time reported elsewhere:reference lab test:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test reference range:finding:time reported elsewhere:reference lab test:nominal
n1=Lester (signe de) | n2=en:reference lab test reference range:finding:time reported elsewhere:reference lab test:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reference lab test results:finding:time reported elsewhere:reference lab test:narrative
n1=Lester (signe de) | n2=en:reference lab test results:finding:time reported elsewhere:reference lab test:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:regional, racial, and ethnic clustering has been noted
n1=Lester (signe de) | n2=en:regional, racial, and ethnic clustering has been noted | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:regression in infancy (in some patients)
n1=Lester (signe de) | n2=en:regression in infancy (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relapsing-remitting course
n1=Lester (signe de) | n2=en:relapsing-remitting course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relationship of rare neuropsychiatric signs to histidinemia is unclear
n1=Lester (signe de) | n2=en:relationship of rare neuropsychiatric signs to histidinemia is unclear | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively benign course
n1=Lester (signe de) | n2=en:relatively benign course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively benign course after acute episodes in childhood
n1=Lester (signe de) | n2=en:relatively benign course after acute episodes in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively mild course
n1=Lester (signe de) | n2=en:relatively mild course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively mild cutis laxa, associated with severe vascular abnormalities
n1=Lester (signe de) | n2=en:relatively mild cutis laxa, associated with severe vascular abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively mild phenotype
n1=Lester (signe de) | n2=en:relatively mild phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatively slow progression
n1=Lester (signe de) | n2=en:relatively slow progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relatives with multiple small congenital pigmented nevi
n1=Lester (signe de) | n2=en:relatives with multiple small congenital pigmented nevi | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:relief is achieved by cooling or by elevating the extremities
n1=Lester (signe de) | n2=en:relief is achieved by cooling or by elevating the extremities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:renal anomalies are not always present
n1=Lester (signe de) | n2=en:renal anomalies are not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:renal dysfunction normalizes in the first year of life
n1=Lester (signe de) | n2=en:renal dysfunction normalizes in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:renal failure in second or third decade
n1=Lester (signe de) | n2=en:renal failure in second or third decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:renal involvement and coloboma may not be present
n1=Lester (signe de) | n2=en:renal involvement and coloboma may not be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:repeat expansions range from 70 to over 1,000 (normal 5 to 30 repeats)
n1=Lester (signe de) | n2=en:repeat expansions range from 70 to over 1,000 (normal 5 to 30 repeats) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:repeat is unstable if > 52 repeats
n1=Lester (signe de) | n2=en:repeat is unstable if > 52 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:repeat tracts may expand as patient ages (somatic instability)
n1=Lester (signe de) | n2=en:repeat tracts may expand as patient ages (somatic instability) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported cases all sporadic
n1=Lester (signe de) | n2=en:reported cases all sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in 1 family (last curated may 2013)
n1=Lester (signe de) | n2=en:reported in 1 family (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in 2 sibs (february 1991)
n1=Lester (signe de) | n2=en:reported in 2 sibs (february 1991) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in a large hutterite family
n1=Lester (signe de) | n2=en:reported in a large hutterite family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in individuals of amish or mennonite descent
n1=Lester (signe de) | n2=en:reported in individuals of amish or mennonite descent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in individuals of french canadian origin
n1=Lester (signe de) | n2=en:reported in individuals of french canadian origin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in individuals of jewish moroccan ancestry
n1=Lester (signe de) | n2=en:reported in individuals of jewish moroccan ancestry | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in individuals of sephardic jewish ancestry
n1=Lester (signe de) | n2=en:reported in individuals of sephardic jewish ancestry | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported in the ohio amish anabaptist community
n1=Lester (signe de) | n2=en:reported in the ohio amish anabaptist community | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reported patients are asymptomatic
n1=Lester (signe de) | n2=en:reported patients are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:resembles intrauterine torch infection but without intrauterine infection
n1=Lester (signe de) | n2=en:resembles intrauterine torch infection but without intrauterine infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:resembles pseudo-torch syndrome (251290)
n1=Lester (signe de) | n2=en:resembles pseudo-torch syndrome (251290) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:residual neurologic deficits are slowly progressive
n1=Lester (signe de) | n2=en:residual neurologic deficits are slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:resource identifier:uri:pt:study:nom
n1=Lester (signe de) | n2=en:resource identifier:uri:pt:study:nom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:respiratory distress may be precipitated by viral respiratory infection
n1=Lester (signe de) | n2=en:respiratory distress may be precipitated by viral respiratory infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:response to acetazolamide
n1=Lester (signe de) | n2=en:response to acetazolamide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:response to benadryl (diphenhydramine)
n1=Lester (signe de) | n2=en:response to benadryl (diphenhydramine) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:response to zinc supplementation
n1=Lester (signe de) | n2=en:response to zinc supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:responsive to high-dose biotin or biotin/thiamine treatment
n1=Lester (signe de) | n2=en:responsive to high-dose biotin or biotin/thiamine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:responsive to oral mannose therapy
n1=Lester (signe de) | n2=en:responsive to oral mannose therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:responsive to thiazide diuretics
n1=Lester (signe de) | n2=en:responsive to thiazide diuretics | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:responsive to treatment
n1=Lester (signe de) | n2=en:responsive to treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:responsive to vitamin b12 therapy
n1=Lester (signe de) | n2=en:responsive to vitamin b12 therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:results in severe motor disability and loss of independent ambulation
n1=Lester (signe de) | n2=en:results in severe motor disability and loss of independent ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reticulate acropigmentation of kitamura (hyperpigmentation found primarily in hands and feet)
n1=Lester (signe de) | n2=en:reticulate acropigmentation of kitamura (hyperpigmentation found primarily in hands and feet) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:reticulate hyperpigmentation onset birth - 2 years
n1=Lester (signe de) | n2=en:reticulate hyperpigmentation onset birth - 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:retinal arteriolar tortuosity develops in adolescence and is progressive
n1=Lester (signe de) | n2=en:retinal arteriolar tortuosity develops in adolescence and is progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:retinal degeneration not always present
n1=Lester (signe de) | n2=en:retinal degeneration not always present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:retinal hemorrhages usually resolve without sequelae
n1=Lester (signe de) | n2=en:retinal hemorrhages usually resolve without sequelae | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:retinal holes were present in an asymptomatic female carrier
n1=Lester (signe de) | n2=en:retinal holes were present in an asymptomatic female carrier | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:retinitis punctata albescens and macular degeneration starting in late childhood to early teens
n1=Lester (signe de) | n2=en:retinitis punctata albescens and macular degeneration starting in late childhood to early teens | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:rickets and premature primary tooth loss occur in childhood
n1=Lester (signe de) | n2=en:rickets and premature primary tooth loss occur in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:right side affected greater than left side
n1=Lester (signe de) | n2=en:right side affected greater than left side | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk factors for development of tgct - family history, cryptorchidism (219050), testicular feminization (300068), klinefelter syndrome, previous tgct, gonadal dysgenesis
n1=Lester (signe de) | n2=en:risk factors for development of tgct - family history, cryptorchidism (219050), testicular feminization (300068), klinefelter syndrome, previous tgct, gonadal dysgenesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk haplotype found in dutch families
n1=Lester (signe de) | n2=en:risk haplotype found in dutch families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of affected offspring in maternal translocation carrier - 4-10%
n1=Lester (signe de) | n2=en:risk of affected offspring in maternal translocation carrier - 4-10% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of affected offspring in paternal translocation carrier - 0-7%
n1=Lester (signe de) | n2=en:risk of affected offspring in paternal translocation carrier - 0-7% | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of death due to cardiac dysfunction
n1=Lester (signe de) | n2=en:risk of death due to cardiac dysfunction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of sudden death
n1=Lester (signe de) | n2=en:risk of sudden death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of sudden death due to cardiac arrhythmias
n1=Lester (signe de) | n2=en:risk of sudden death due to cardiac arrhythmias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of sudden death due to cardiac defects
n1=Lester (signe de) | n2=en:risk of sudden death due to cardiac defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of sudden death in childhood due to cardiac arrest
n1=Lester (signe de) | n2=en:risk of sudden death in childhood due to cardiac arrest | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of sudden death with exertion
n1=Lester (signe de) | n2=en:risk of sudden death with exertion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:risk of thromboembolic stroke
n1=Lester (signe de) | n2=en:risk of thromboembolic stroke | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:saddle-back st-segment elevation shows beat-to-beat and day-to-day variability
n1=Lester (signe de) | n2=en:saddle-back st-segment elevation shows beat-to-beat and day-to-day variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sando (607459) is a phenotypic variant of autosomal recessive peo
n1=Lester (signe de) | n2=en:sando (607459) is a phenotypic variant of autosomal recessive peo | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sca8 is caused by bidirectional transcription on chromosome 13q21 involving complementary repeat expansion in atxn8 (613289) and atxn8-opposite strand (603680)
n1=Lester (signe de) | n2=en:sca8 is caused by bidirectional transcription on chromosome 13q21 involving complementary repeat expansion in atxn8 (613289) and atxn8-opposite strand (603680) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:scalp hair quality improves during pregnancy
n1=Lester (signe de) | n2=en:scalp hair quality improves during pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:scarf is an acronym - skeletal abnormalities, cutis laxa/craniosynostosis, ambiguous genitalia, retardation, and facial abnormalities
n1=Lester (signe de) | n2=en:scarf is an acronym - skeletal abnormalities, cutis laxa/craniosynostosis, ambiguous genitalia, retardation, and facial abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seasonal variation in severity of skin symptoms reported by some patients
n1=Lester (signe de) | n2=en:seasonal variation in severity of skin symptoms reported by some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:second most common form of usher syndrome type i
n1=Lester (signe de) | n2=en:second most common form of usher syndrome type i | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:secondary features include arterial hypertension and renal involvement
n1=Lester (signe de) | n2=en:secondary features include arterial hypertension and renal involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:secondary hemorrhage
n1=Lester (signe de) | n2=en:secondary hemorrhage | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:secondary prevention, avoid smoking, alcohol, and oxidants
n1=Lester (signe de) | n2=en:secondary prevention, avoid smoking, alcohol, and oxidants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:secondary tumors develop within the skin lesions
n1=Lester (signe de) | n2=en:secondary tumors develop within the skin lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:secretory diarrhea begins prenatally
n1=Lester (signe de) | n2=en:secretory diarrhea begins prenatally | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see (277600) for a phenotypically similar autosomal recessive form
n1=Lester (signe de) | n2=en:see (277600) for a phenotypically similar autosomal recessive form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see (608328) for a phenotypically similar autosomal dominant form
n1=Lester (signe de) | n2=en:see (608328) for a phenotypically similar autosomal dominant form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 123000 for an autosomal dominant form due to mutation in ankh (605145)
n1=Lester (signe de) | n2=en:see 123000 for an autosomal dominant form due to mutation in ankh (605145) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 171060.0005 for patients with homozygous abcb4 mutations and unaffected heterozygous family members
n1=Lester (signe de) | n2=en:see 171060.0005 for patients with homozygous abcb4 mutations and unaffected heterozygous family members | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 177850 for description of heterozygous phenotype
n1=Lester (signe de) | n2=en:see 177850 for description of heterozygous phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 218400 for an autosomal recessive form caused by mutation in gja1 (121014.0021)
n1=Lester (signe de) | n2=en:see 218400 for an autosomal recessive form caused by mutation in gja1 (121014.0021) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 255160 for an autosomal recessive form
n1=Lester (signe de) | n2=en:see 255160 for an autosomal recessive form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 607731 for an autosomal recessive form
n1=Lester (signe de) | n2=en:see 607731 for an autosomal recessive form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see 609888 for a discussion on leprosy susceptibility
n1=Lester (signe de) | n2=en:see 609888 for a discussion on leprosy susceptibility | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also a childhood-onset form (114100)
n1=Lester (signe de) | n2=en:see also a childhood-onset form (114100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also adult-onset stiff person syndrome (184850)
n1=Lester (signe de) | n2=en:see also adult-onset stiff person syndrome (184850) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also an adult-onset form (213600)
n1=Lester (signe de) | n2=en:see also an adult-onset form (213600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also antenatal bartter syndrome type 1 (601678) and bartter syndrome type 2 (241200)
n1=Lester (signe de) | n2=en:see also antenatal bartter syndrome type 1 (601678) and bartter syndrome type 2 (241200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also antenatal bartter syndrome type 1 (601678), bartter syndrome type 2 (241200), bartter syndrome 3 (607364), and bartter syndrome 4b digenic (613090)
n1=Lester (signe de) | n2=en:see also antenatal bartter syndrome type 1 (601678), bartter syndrome type 2 (241200), bartter syndrome 3 (607364), and bartter syndrome 4b digenic (613090) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also antley-bixler syndrome (abs) with normal steroidogenesis (207410)
n1=Lester (signe de) | n2=en:see also antley-bixler syndrome (abs) with normal steroidogenesis (207410) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant fmf (134610), caused by heterozygous mutations in the mefv gene
n1=Lester (signe de) | n2=en:see also autosomal dominant fmf (134610), caused by heterozygous mutations in the mefv gene | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant form (128230)
n1=Lester (signe de) | n2=en:see also autosomal dominant form (128230) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant form (160800), which is less common and less severe
n1=Lester (signe de) | n2=en:see also autosomal dominant form (160800), which is less common and less severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant form (176860)
n1=Lester (signe de) | n2=en:see also autosomal dominant form (176860) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant giant axonal neuropathy (610100)
n1=Lester (signe de) | n2=en:see also autosomal dominant giant axonal neuropathy (610100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant hypophosphatemic rickets (193100)
n1=Lester (signe de) | n2=en:see also autosomal dominant hypophosphatemic rickets (193100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant lutheran-null phenotype (111150)
n1=Lester (signe de) | n2=en:see also autosomal dominant lutheran-null phenotype (111150) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant peoa1 (157640)
n1=Lester (signe de) | n2=en:see also autosomal dominant peoa1 (157640) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant robinow syndrome (180700)
n1=Lester (signe de) | n2=en:see also autosomal dominant robinow syndrome (180700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal dominant sick sinus syndrome (163800)
n1=Lester (signe de) | n2=en:see also autosomal dominant sick sinus syndrome (163800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal form, 146450, and another x-linked form, 300633
n1=Lester (signe de) | n2=en:see also autosomal form, 146450, and another x-linked form, 300633 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal form, 146450, and another x-linked form, 300758
n1=Lester (signe de) | n2=en:see also autosomal form, 146450, and another x-linked form, 300758 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive bh4-dependent hyperphenylalaninemia (233910), an allelic disorder with a more severe phenotype
n1=Lester (signe de) | n2=en:see also autosomal recessive bh4-dependent hyperphenylalaninemia (233910), an allelic disorder with a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive familial mediterranean fever (fmf, 249100)
n1=Lester (signe de) | n2=en:see also autosomal recessive familial mediterranean fever (fmf, 249100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive form (255700), which is more common and more severe
n1=Lester (signe de) | n2=en:see also autosomal recessive form (255700), which is more common and more severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive form (612304)
n1=Lester (signe de) | n2=en:see also autosomal recessive form (612304) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive peob (258450)
n1=Lester (signe de) | n2=en:see also autosomal recessive peob (258450) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive robinow syndrome (268310)
n1=Lester (signe de) | n2=en:see also autosomal recessive robinow syndrome (268310) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also autosomal recessive sick sinus syndrome (sss1, 608567)
n1=Lester (signe de) | n2=en:see also autosomal recessive sick sinus syndrome (sss1, 608567) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also benign familial infantile convulsions (bfic1, 601764)
n1=Lester (signe de) | n2=en:see also benign familial infantile convulsions (bfic1, 601764) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also benign familial neonatal-infantile convulsions (bfnis, 607745), which shows some phenotypic similarities
n1=Lester (signe de) | n2=en:see also benign familial neonatal-infantile convulsions (bfnis, 607745), which shows some phenotypic similarities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also benign neonatal epilepsy (ebn1, 121200)
n1=Lester (signe de) | n2=en:see also benign neonatal epilepsy (ebn1, 121200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also cblc (277400)
n1=Lester (signe de) | n2=en:see also cblc (277400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also cbld (277410)
n1=Lester (signe de) | n2=en:see also cbld (277410) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also chromosome 2q32-q33 deletion syndrome (612313)
n1=Lester (signe de) | n2=en:see also chromosome 2q32-q33 deletion syndrome (612313) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also cmtx1 (302800) and cmt3x (302802)
n1=Lester (signe de) | n2=en:see also cmtx1 (302800) and cmt3x (302802) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also cmtx1 (302800) and cmtx2 (302801)
n1=Lester (signe de) | n2=en:see also cmtx1 (302800) and cmtx2 (302801) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also congenital stiff person syndrome (149400)
n1=Lester (signe de) | n2=en:see also congenital stiff person syndrome (149400) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also crigler-najjar syndrome type i (218800) which is also due to mutations in ugt1 (191740)
n1=Lester (signe de) | n2=en:see also crigler-najjar syndrome type i (218800) which is also due to mutations in ugt1 (191740) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also da2b (601680), which is an allelic disorder
n1=Lester (signe de) | n2=en:see also da2b (601680), which is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also dent disease 2 (300555)
n1=Lester (signe de) | n2=en:see also dent disease 2 (300555) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also distal hmn2a (158590)
n1=Lester (signe de) | n2=en:see also distal hmn2a (158590) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also dominant deb (131750), an allelic disorder with a less severe phenotype
n1=Lester (signe de) | n2=en:see also dominant deb (131750), an allelic disorder with a less severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also dominant deb (131750), an allelic disorder with a similar phenotype
n1=Lester (signe de) | n2=en:see also dominant deb (131750), an allelic disorder with a similar phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also dyggve-melchior-clausen disease (223800)
n1=Lester (signe de) | n2=en:see also dyggve-melchior-clausen disease (223800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also dyssegmental dysplasia, silverman-handmaker type (224410)
n1=Lester (signe de) | n2=en:see also dyssegmental dysplasia, silverman-handmaker type (224410) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also ecyt2 (263400) and ecyt3 (609820)
n1=Lester (signe de) | n2=en:see also ecyt2 (263400) and ecyt3 (609820) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also erythrocytosis 1 (ecyt1, 133100)
n1=Lester (signe de) | n2=en:see also erythrocytosis 1 (ecyt1, 133100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also facial hemihypertrophy (133900)
n1=Lester (signe de) | n2=en:see also facial hemihypertrophy (133900) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also familial cold autoinflammatory syndrome (120100), an allelic disorder with overlapping features
n1=Lester (signe de) | n2=en:see also familial cold autoinflammatory syndrome (120100), an allelic disorder with overlapping features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also familial developmental dysphasia (600117)
n1=Lester (signe de) | n2=en:see also familial developmental dysphasia (600117) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also febrile seizures (feb1, 121210)
n1=Lester (signe de) | n2=en:see also febrile seizures (feb1, 121210) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also french-canadian type of leigh syndrome (220111)
n1=Lester (signe de) | n2=en:see also french-canadian type of leigh syndrome (220111) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also gaucher disease type iii (231000), which is much less severe
n1=Lester (signe de) | n2=en:see also gaucher disease type iii (231000), which is much less severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also glanzmann thrombasthenia due to mutations in integrin alpha 2b (273800)
n1=Lester (signe de) | n2=en:see also glanzmann thrombasthenia due to mutations in integrin alpha 2b (273800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also glut1ds2 (612126), an allelic disorder with a less severe phenotype
n1=Lester (signe de) | n2=en:see also glut1ds2 (612126), an allelic disorder with a less severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also griscelli syndrome type 1 (214450) for a similar disorder without immunological abnormalities and griscelli syndrome type 3 (609227) for a similar disorder without neurologic or immunologic abnormalities
n1=Lester (signe de) | n2=en:see also griscelli syndrome type 1 (214450) for a similar disorder without immunological abnormalities and griscelli syndrome type 3 (609227) for a similar disorder without neurologic or immunologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also griscelli syndrome, type 1 (214450) for a similar disorder with characteristic neurologic disease and griscelli syndrome, type 2 (607624) for a similar disorder with characteristic immunodeficiency/hemophagocytic syndrome.
n1=Lester (signe de) | n2=en:see also griscelli syndrome, type 1 (214450) for a similar disorder with characteristic neurologic disease and griscelli syndrome, type 2 (607624) for a similar disorder with characteristic immunodeficiency/hemophagocytic syndrome. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also hmn2b (608634)
n1=Lester (signe de) | n2=en:see also hmn2b (608634) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also infantile (600649) and late-onset (255110) cpt ii deficiency
n1=Lester (signe de) | n2=en:see also infantile (600649) and late-onset (255110) cpt ii deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also isolated pneumothorax (173600), an allelic disorder that may represent a mild form of the bhd syndrome
n1=Lester (signe de) | n2=en:see also isolated pneumothorax (173600), an allelic disorder that may represent a mild form of the bhd syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also junctional eb with pyloric atresia (226730)
n1=Lester (signe de) | n2=en:see also junctional eb with pyloric atresia (226730) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also later childhood-onset form (300718)
n1=Lester (signe de) | n2=en:see also later childhood-onset form (300718) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also leptin deficiency (614962) and summary information in bmiq1 (606641)
n1=Lester (signe de) | n2=en:see also leptin deficiency (614962) and summary information in bmiq1 (606641) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also lethal neonatal (608836) and adult forms (255110)
n1=Lester (signe de) | n2=en:see also lethal neonatal (608836) and adult forms (255110) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also mmab (251110)
n1=Lester (signe de) | n2=en:see also mmab (251110) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also more severe phenotype peeling skin syndrome (270300)
n1=Lester (signe de) | n2=en:see also more severe phenotype peeling skin syndrome (270300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also muckle-wells syndrome (191900), an allelic disorder with overlapping features
n1=Lester (signe de) | n2=en:see also muckle-wells syndrome (191900), an allelic disorder with overlapping features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also oca1a (203100)
n1=Lester (signe de) | n2=en:see also oca1a (203100) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also oca1b, or 'yellow albinism,' an allelic disorder with residual tyrosinase activity and some pigmentation
n1=Lester (signe de) | n2=en:see also oca1b, or 'yellow albinism,' an allelic disorder with residual tyrosinase activity and some pigmentation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also optic atrophy 1 (165500), an allelic disorder without deafness
n1=Lester (signe de) | n2=en:see also optic atrophy 1 (165500), an allelic disorder without deafness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also optic atrophy with deafness (125250), an allelic disorder
n1=Lester (signe de) | n2=en:see also optic atrophy with deafness (125250), an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pachyonychia congenita, type 3 (pc1, 167200)
n1=Lester (signe de) | n2=en:see also pachyonychia congenita, type 3 (pc1, 167200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also park6 (605909), park7 (606324), and park9 (606693) for autosomal recessive disorders with overlapping phenotypes
n1=Lester (signe de) | n2=en:see also park6 (605909), park7 (606324), and park9 (606693) for autosomal recessive disorders with overlapping phenotypes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also peeling skin syndrome, acral type (609796)
n1=Lester (signe de) | n2=en:see also peeling skin syndrome, acral type (609796) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also perinatal lethal variant (608013), which is more severe
n1=Lester (signe de) | n2=en:see also perinatal lethal variant (608013), which is more severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pfm3 on chromosome 4q21-q23 (609566)
n1=Lester (signe de) | n2=en:see also pfm3 on chromosome 4q21-q23 (609566) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pgl1 (168000)
n1=Lester (signe de) | n2=en:see also pgl1 (168000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pgl2 (601650), pgl3 (605373), and pgl4 (115310)
n1=Lester (signe de) | n2=en:see also pgl2 (601650), pgl3 (605373), and pgl4 (115310) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pseudohypoparathyroidism type ia (103580)
n1=Lester (signe de) | n2=en:see also pseudohypoparathyroidism type ia (103580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pseudohypoparathyroidism type ia (php1a, 103580)
n1=Lester (signe de) | n2=en:see also pseudohypoparathyroidism type ia (php1a, 103580) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pseudohypoparathyroidism type ib (603233) and ic (612462)
n1=Lester (signe de) | n2=en:see also pseudohypoparathyroidism type ib (603233) and ic (612462) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also pseudopseudohypoparathyroidism (612463)
n1=Lester (signe de) | n2=en:see also pseudopseudohypoparathyroidism (612463) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also recessive deb (226600), an allelic disorder with a more severe phenotype
n1=Lester (signe de) | n2=en:see also recessive deb (226600), an allelic disorder with a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also severe, early-onset form (300717)
n1=Lester (signe de) | n2=en:see also severe, early-onset form (300717) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also simplex eb with pyloric atresia (612138)
n1=Lester (signe de) | n2=en:see also simplex eb with pyloric atresia (612138) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also simpson-golabi-behmel syndrome 1 (sgbs1, 312870)
n1=Lester (signe de) | n2=en:see also simpson-golabi-behmel syndrome 1 (sgbs1, 312870) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also the autosomal recessive form (243000)
n1=Lester (signe de) | n2=en:see also the autosomal recessive form (243000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also the homozygous state, mosaic variegated aneuploidy (mva, 257300)
n1=Lester (signe de) | n2=en:see also the homozygous state, mosaic variegated aneuploidy (mva, 257300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also the lethal neonatal (608836) and infantile (600649) forms
n1=Lester (signe de) | n2=en:see also the lethal neonatal (608836) and infantile (600649) forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also the non-herlitz type of jeb (226650), a less severe disorder
n1=Lester (signe de) | n2=en:see also the non-herlitz type of jeb (226650), a less severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also the x-linked form (300291)
n1=Lester (signe de) | n2=en:see also the x-linked form (300291) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also two x-linked forms 300633 and 300758
n1=Lester (signe de) | n2=en:see also two x-linked forms 300633 and 300758 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked (310400) and autosomal dominant (160150) forms
n1=Lester (signe de) | n2=en:see also x-linked (310400) and autosomal dominant (160150) forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked alpha-thalassemia/mental retardation syndrome (301040)
n1=Lester (signe de) | n2=en:see also x-linked alpha-thalassemia/mental retardation syndrome (301040) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked dominant form (300652)
n1=Lester (signe de) | n2=en:see also x-linked dominant form (300652) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked edmd (310300)
n1=Lester (signe de) | n2=en:see also x-linked edmd (310300) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked leigh syndrome (312170)
n1=Lester (signe de) | n2=en:see also x-linked leigh syndrome (312170) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see also x-linked nephrocalcinosis (310468), x-linked recessive hypophosphatemic rickets (300554), and low-molecular-weight proteinuria with nephrocalcinosis (308990)
n1=Lester (signe de) | n2=en:see also x-linked nephrocalcinosis (310468), x-linked recessive hypophosphatemic rickets (300554), and low-molecular-weight proteinuria with nephrocalcinosis (308990) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see cmt4a (214400) for autosomal recessive demyelinating forms
n1=Lester (signe de) | n2=en:see cmt4a (214400) for autosomal recessive demyelinating forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see ebn1 (121200) for an autosomal dominant form
n1=Lester (signe de) | n2=en:see ebn1 (121200) for an autosomal dominant form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see entry 104300 for general information on alzheimer disease
n1=Lester (signe de) | n2=en:see entry 104300 for general information on alzheimer disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see joubert syndrome 7 (611560), an allelic disorder with a less severe phenotype
n1=Lester (signe de) | n2=en:see joubert syndrome 7 (611560), an allelic disorder with a less severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see myotonic dystonia 1 (dm1, 160900) for a disorder with a similar phenotype
n1=Lester (signe de) | n2=en:see myotonic dystonia 1 (dm1, 160900) for a disorder with a similar phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see pkd1 (601313) due to mutation in polycystin 1 (601313), pkd2 (173910) due to mutation in polycystin 2 (173910), and pkd3 (600666)
n1=Lester (signe de) | n2=en:see pkd1 (601313) due to mutation in polycystin 1 (601313), pkd2 (173910) due to mutation in polycystin 2 (173910), and pkd3 (600666) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see recessive form optb4 (611490)
n1=Lester (signe de) | n2=en:see recessive form optb4 (611490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see speech-language disorder 1 602081 and familial developmental dysphasia 600117 for similar disorders
n1=Lester (signe de) | n2=en:see speech-language disorder 1 602081 and familial developmental dysphasia 600117 for similar disorders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:see the more common methemoglobinemia types i and ii (250800)
n1=Lester (signe de) | n2=en:see the more common methemoglobinemia types i and ii (250800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seen more frequently in infants of diabetic mothers
n1=Lester (signe de) | n2=en:seen more frequently in infants of diabetic mothers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:segmental distribution often affecting 1 limb
n1=Lester (signe de) | n2=en:segmental distribution often affecting 1 limb | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure frequency decreases during early childhood
n1=Lester (signe de) | n2=en:seizure frequency decreases during early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure onset after 3 months
n1=Lester (signe de) | n2=en:seizure onset after 3 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure onset at a mean of 14 months (range 6 to 36 months)
n1=Lester (signe de) | n2=en:seizure onset at a mean of 14 months (range 6 to 36 months) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure onset between 3 and 11 years
n1=Lester (signe de) | n2=en:seizure onset between 3 and 11 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure onset in first months or years of life
n1=Lester (signe de) | n2=en:seizure onset in first months or years of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizure severity and frequency tend to improve with age
n1=Lester (signe de) | n2=en:seizure severity and frequency tend to improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures and cognitive involvement are variable findings
n1=Lester (signe de) | n2=en:seizures and cognitive involvement are variable findings | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures and dystonia peak during childhood
n1=Lester (signe de) | n2=en:seizures and dystonia peak during childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are easily controlled by medications
n1=Lester (signe de) | n2=en:seizures are easily controlled by medications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are fever-sensitive
n1=Lester (signe de) | n2=en:seizures are fever-sensitive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are followed by drowsiness in most cases
n1=Lester (signe de) | n2=en:seizures are followed by drowsiness in most cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are often refractory
n1=Lester (signe de) | n2=en:seizures are often refractory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are poorly responsive to treatment
n1=Lester (signe de) | n2=en:seizures are poorly responsive to treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are provoked by immersion in hot or warm water
n1=Lester (signe de) | n2=en:seizures are provoked by immersion in hot or warm water | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are refractory
n1=Lester (signe de) | n2=en:seizures are refractory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are refractory to medication
n1=Lester (signe de) | n2=en:seizures are refractory to medication | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are refractory to treatment
n1=Lester (signe de) | n2=en:seizures are refractory to treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are responsive to pyridoxine treatment
n1=Lester (signe de) | n2=en:seizures are responsive to pyridoxine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are sensitive to hyperventilation
n1=Lester (signe de) | n2=en:seizures are sensitive to hyperventilation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are usually intractable
n1=Lester (signe de) | n2=en:seizures are usually intractable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are usually refractory
n1=Lester (signe de) | n2=en:seizures are usually refractory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures are usually refractory at first
n1=Lester (signe de) | n2=en:seizures are usually refractory at first | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures become nearly continuous
n1=Lester (signe de) | n2=en:seizures become nearly continuous | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures easily controlled by medications
n1=Lester (signe de) | n2=en:seizures easily controlled by medications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures last about 30 seconds to 3 minutes
n1=Lester (signe de) | n2=en:seizures last about 30 seconds to 3 minutes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may be precipitated by sleep deprivation, alcohol consumption, or flashing lights
n1=Lester (signe de) | n2=en:seizures may be precipitated by sleep deprivation, alcohol consumption, or flashing lights | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may be refractory
n1=Lester (signe de) | n2=en:seizures may be refractory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may be refractory to treatment
n1=Lester (signe de) | n2=en:seizures may be refractory to treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may be triggered by infection
n1=Lester (signe de) | n2=en:seizures may be triggered by infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may improve with age
n1=Lester (signe de) | n2=en:seizures may improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may occur upon awakening or at any time during the day
n1=Lester (signe de) | n2=en:seizures may occur upon awakening or at any time during the day | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may occur with illness
n1=Lester (signe de) | n2=en:seizures may occur with illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may persist into adulthood
n1=Lester (signe de) | n2=en:seizures may persist into adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may remit in adolescence
n1=Lester (signe de) | n2=en:seizures may remit in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may remit later in childhood
n1=Lester (signe de) | n2=en:seizures may remit later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures may remit with age (in some patients)
n1=Lester (signe de) | n2=en:seizures may remit with age (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause
n1=Lester (signe de) | n2=en:seizures occur in absence of intracranial infection or defined pathologic or traumatic cause | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures occur upon awakening
n1=Lester (signe de) | n2=en:seizures occur upon awakening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures precipitated by fatigue or alcohol
n1=Lester (signe de) | n2=en:seizures precipitated by fatigue or alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures recur in 33% of patients
n1=Lester (signe de) | n2=en:seizures recur in 33% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures remit by age 5 years
n1=Lester (signe de) | n2=en:seizures remit by age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures remit in early childhood
n1=Lester (signe de) | n2=en:seizures remit in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures remit in later childhood
n1=Lester (signe de) | n2=en:seizures remit in later childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures remit spontaneously by age 5 years
n1=Lester (signe de) | n2=en:seizures remit spontaneously by age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures resolve by 4 months of age
n1=Lester (signe de) | n2=en:seizures resolve by 4 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures tend to become more focal with age
n1=Lester (signe de) | n2=en:seizures tend to become more focal with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures tend to occur upon awakening
n1=Lester (signe de) | n2=en:seizures tend to occur upon awakening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures tend to remit later in childhood
n1=Lester (signe de) | n2=en:seizures tend to remit later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures usually occur in the first months of life
n1=Lester (signe de) | n2=en:seizures usually occur in the first months of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures usually remit in adolescence
n1=Lester (signe de) | n2=en:seizures usually remit in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures usually remit spontaneously by 12 months of age
n1=Lester (signe de) | n2=en:seizures usually remit spontaneously by 12 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seizures, recurrent, refractory
n1=Lester (signe de) | n2=en:seizures, recurrent, refractory | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sensorineural hearing loss may be presenting feature
n1=Lester (signe de) | n2=en:sensorineural hearing loss may be presenting feature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sensory loss is rapidly progressive and severe
n1=Lester (signe de) | n2=en:sensory loss is rapidly progressive and severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:serum triglycerides decrease with age
n1=Lester (signe de) | n2=en:serum triglycerides decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 01:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 01:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 02:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 02:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 03:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 03:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 04:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 04:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 05:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 05:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 06:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 06:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 07:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 07:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 08:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 08:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 09:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 09:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 10:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 10:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 11:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 11:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 12:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 12:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 13:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 13:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 14:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 14:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 15:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 15:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 16:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 16:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 17:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 17:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 18:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 18:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 19:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 19:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 20:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 20:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 21:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 21:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 22:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 22:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 23:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 23:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 24:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 24:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 25:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 25:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 26:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 26:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 27:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 27:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 28:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 28:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 29:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 29:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 30:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 30:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 31:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 31:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 32:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 32:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 33:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 33:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 34:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 34:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 35:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 35:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 36:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 36:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 37:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 37:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 38:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 38:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 39:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 39:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 40:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 40:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 41:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 41:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 42:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 42:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 43:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 43:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 44:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 44:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 45:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 45:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 46:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 46:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 47:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 47:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 48:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 48:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 49:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 49:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 50:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 50:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 51:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 51:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 52:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 52:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 53:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 53:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 54:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 54:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 55:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 55:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 56:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 56:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 57:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 57:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 58:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 58:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 59:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 59:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 60:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 60:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 61:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 61:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 62:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 62:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 63:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 63:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 64:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 64:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 65:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 65:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 66:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 66:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 67:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 67:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 68:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 68:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 69:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 69:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 70:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 70:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 71:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 71:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 72:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 72:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 73:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 73:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 74:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 74:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 75:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 75:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 76:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 76:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 77:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 77:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 78:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 78:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 79:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 79:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:service comment 80:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:service comment 80:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seven patients from 4 families in israel have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:seven patients from 4 families in israel have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seven patients reported (as of march 2011)
n1=Lester (signe de) | n2=en:seven patients reported (as of march 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seventy percent of cases are stillborn
n1=Lester (signe de) | n2=en:seventy percent of cases are stillborn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:seventy percent of cases have associated anomalies
n1=Lester (signe de) | n2=en:seventy percent of cases have associated anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:several forms of autosomal recessive spastic paraplegia (see 270800)
n1=Lester (signe de) | n2=en:several forms of autosomal recessive spastic paraplegia (see 270800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe ambulatory restriction
n1=Lester (signe de) | n2=en:severe ambulatory restriction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe clinical course
n1=Lester (signe de) | n2=en:severe clinical course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe course
n1=Lester (signe de) | n2=en:severe course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe disorder
n1=Lester (signe de) | n2=en:severe disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe epilepsy may lead to early death
n1=Lester (signe de) | n2=en:severe epilepsy may lead to early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe form with onset at 3 to 4 months of age and severe developmental delay
n1=Lester (signe de) | n2=en:severe form with onset at 3 to 4 months of age and severe developmental delay | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe hearing loss by age 50 years
n1=Lester (signe de) | n2=en:severe hearing loss by age 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe heat intolerance
n1=Lester (signe de) | n2=en:severe heat intolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe hypertension develops in childhood
n1=Lester (signe de) | n2=en:severe hypertension develops in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe infantile cases usually die by 6 months
n1=Lester (signe de) | n2=en:severe infantile cases usually die by 6 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe infantile form presents before 6 months
n1=Lester (signe de) | n2=en:severe infantile form presents before 6 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe infections in untreated patients with neutropenia
n1=Lester (signe de) | n2=en:severe infections in untreated patients with neutropenia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe involvement of legs
n1=Lester (signe de) | n2=en:severe involvement of legs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe neurodegenerative course resulting in a comatose state or death
n1=Lester (signe de) | n2=en:severe neurodegenerative course resulting in a comatose state or death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe phenotype
n1=Lester (signe de) | n2=en:severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe phenotype onset - neonate
n1=Lester (signe de) | n2=en:severe phenotype onset - neonate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe volume depletion
n1=Lester (signe de) | n2=en:severe volume depletion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severe, early-onset, usually within the first days of life, with cardiomyopathy and early death
n1=Lester (signe de) | n2=en:severe, early-onset, usually within the first days of life, with cardiomyopathy and early death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severely affected individuals may carry 2 mutated alleles
n1=Lester (signe de) | n2=en:severely affected individuals may carry 2 mutated alleles | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severity of clinical phenotype varies both within and between kindreds
n1=Lester (signe de) | n2=en:severity of clinical phenotype varies both within and between kindreds | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severity of hematologic disorder decreases with advancing age
n1=Lester (signe de) | n2=en:severity of hematologic disorder decreases with advancing age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severity of phenotype is not related to residual enzyme activity
n1=Lester (signe de) | n2=en:severity of phenotype is not related to residual enzyme activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severity of phenotype may vary with x-inactivation patterns and/or mutation type
n1=Lester (signe de) | n2=en:severity of phenotype may vary with x-inactivation patterns and/or mutation type | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:severity of skin symptoms may vary within families
n1=Lester (signe de) | n2=en:severity of skin symptoms may vary within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sex ratio - 2 females to 1 male
n1=Lester (signe de) | n2=en:sex ratio - 2 females to 1 male | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sex ratio - 2.3 males-to-1 female
n1=Lester (signe de) | n2=en:sex ratio - 2.3 males-to-1 female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sex ratio of 4-4.5 males to 1 female
n1=Lester (signe de) | n2=en:sex ratio of 4-4.5 males to 1 female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sexual infantilism
n1=Lester (signe de) | n2=en:sexual infantilism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:shields classification -
n1=Lester (signe de) | n2=en:shields classification - | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:short is an acronym for short stature, hyperextensibility of joints/hernia, ocular depression, rieger anomaly, teething delay
n1=Lester (signe de) | n2=en:short is an acronym for short stature, hyperextensibility of joints/hernia, ocular depression, rieger anomaly, teething delay | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:short limbs become more apparent during childhood
n1=Lester (signe de) | n2=en:short limbs become more apparent during childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:short stepped shuffling gait
n1=Lester (signe de) | n2=en:short stepped shuffling gait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:short survival (less than 10 years after onset)
n1=Lester (signe de) | n2=en:short survival (less than 10 years after onset) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:short umbilical cord
n1=Lester (signe de) | n2=en:short umbilical cord | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sib a developed symptoms after routine mmr vaccination
n1=Lester (signe de) | n2=en:sib a developed symptoms after routine mmr vaccination | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sib b did not receive mmr vaccination and was asymptomatic in infancy
n1=Lester (signe de) | n2=en:sib b did not receive mmr vaccination and was asymptomatic in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:significant clinical overlap with sotos syndrome (117550)
n1=Lester (signe de) | n2=en:significant clinical overlap with sotos syndrome (117550) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:significant number of patients are stillborn or die in neonatal period
n1=Lester (signe de) | n2=en:significant number of patients are stillborn or die in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:significant phenotypic variability
n1=Lester (signe de) | n2=en:significant phenotypic variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:signs and symptoms depend on tumor location and activity
n1=Lester (signe de) | n2=en:signs and symptoms depend on tumor location and activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar clinical phenotype to edsiii (130020)
n1=Lester (signe de) | n2=en:similar clinical phenotype to edsiii (130020) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar disorder to x-linked pelizaeus-merzbacher disease (pmd, 312080)
n1=Lester (signe de) | n2=en:similar disorder to x-linked pelizaeus-merzbacher disease (pmd, 312080) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar phenotype to juvenile neuronal ceroid lipofuscinosis 3 (cln3, 204200)
n1=Lester (signe de) | n2=en:similar phenotype to juvenile neuronal ceroid lipofuscinosis 3 (cln3, 204200) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar phenotype to x-linked hypophosphatemia (xlh, 307800)
n1=Lester (signe de) | n2=en:similar phenotype to x-linked hypophosphatemia (xlh, 307800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar to infantile neuroaxonal dystrophy (inad, 256600)
n1=Lester (signe de) | n2=en:similar to infantile neuroaxonal dystrophy (inad, 256600) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:similar to spondylometaphyseal dysplasia, type a4 (609052) but without anterior tonguing of vertebrae
n1=Lester (signe de) | n2=en:similar to spondylometaphyseal dysplasia, type a4 (609052) but without anterior tonguing of vertebrae | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:simple febrile seizures usually remit by age 6 years
n1=Lester (signe de) | n2=en:simple febrile seizures usually remit by age 6 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:single lesions in sporadic cases
n1=Lester (signe de) | n2=en:single lesions in sporadic cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:single mitochondrial dna deletions are found in sporadic kss patients
n1=Lester (signe de) | n2=en:single mitochondrial dna deletions are found in sporadic kss patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:single umbilical artery
n1=Lester (signe de) | n2=en:single umbilical artery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sister of affected male siblings had mild learning disabilities and obesity
n1=Lester (signe de) | n2=en:sister of affected male siblings had mild learning disabilities and obesity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six affected individuals, including 5 fetuses from interrupted pregnancies and 1 term birth have been reported (last curated april 2016)
n1=Lester (signe de) | n2=en:six affected individuals, including 5 fetuses from interrupted pregnancies and 1 term birth have been reported (last curated april 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six genetically confirmed patients have been reported (as of december 2009)
n1=Lester (signe de) | n2=en:six genetically confirmed patients have been reported (as of december 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients from 1 saudi arabian family have been reported (last curated december 2011)
n1=Lester (signe de) | n2=en:six patients from 1 saudi arabian family have been reported (last curated december 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients from 4 families have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:six patients from 4 families have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients have been reported (5/18/2011)
n1=Lester (signe de) | n2=en:six patients have been reported (5/18/2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients have been reported (as of july 2011)
n1=Lester (signe de) | n2=en:six patients have been reported (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients have been reported (as of october 2011)
n1=Lester (signe de) | n2=en:six patients have been reported (as of october 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:six patients reported (last curated march 2015)
n1=Lester (signe de) | n2=en:six patients reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:size of deletion varies from cytogenetically visible deletions to undetectable cytogenetic deletions
n1=Lester (signe de) | n2=en:size of deletion varies from cytogenetically visible deletions to undetectable cytogenetic deletions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skeletal abnormalities are variable
n1=Lester (signe de) | n2=en:skeletal abnormalities are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skeletal and endocrine features have not been fully characterized in all of the patients reported
n1=Lester (signe de) | n2=en:skeletal and endocrine features have not been fully characterized in all of the patients reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skeletal and facial features are variable
n1=Lester (signe de) | n2=en:skeletal and facial features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skeletal features are variably present
n1=Lester (signe de) | n2=en:skeletal features are variably present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skewed x-inactivation in carriers
n1=Lester (signe de) | n2=en:skewed x-inactivation in carriers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skewed x-inactivation, with complete skewing in some individuals
n1=Lester (signe de) | n2=en:skewed x-inactivation, with complete skewing in some individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin abnormalities can be present at birth or appear later in infancy or childhood
n1=Lester (signe de) | n2=en:skin abnormalities can be present at birth or appear later in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin abnormalities tend to decrease with age
n1=Lester (signe de) | n2=en:skin abnormalities tend to decrease with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin and hair abnormalities apparent at birth
n1=Lester (signe de) | n2=en:skin and hair abnormalities apparent at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin appears normal at birth, with development of generalized ichthyosis in childhood
n1=Lester (signe de) | n2=en:skin appears normal at birth, with development of generalized ichthyosis in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin blistering and photosensitivity improve in adulthood
n1=Lester (signe de) | n2=en:skin blistering and photosensitivity improve in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin changes are progressive in childhood
n1=Lester (signe de) | n2=en:skin changes are progressive in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin changes have onset in childhood
n1=Lester (signe de) | n2=en:skin changes have onset in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin erythroderma may resolve early, leaving atrophic lesions
n1=Lester (signe de) | n2=en:skin erythroderma may resolve early, leaving atrophic lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesion appear shortly after birth and tend to disappear in young adulthood
n1=Lester (signe de) | n2=en:skin lesion appear shortly after birth and tend to disappear in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions are fully penetrant by second decade
n1=Lester (signe de) | n2=en:skin lesions are fully penetrant by second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions are primarily trauma-induced but occasionally appear spontaneously
n1=Lester (signe de) | n2=en:skin lesions are primarily trauma-induced but occasionally appear spontaneously | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions exacerbated by heat, exercise (sweating), and sunlight
n1=Lester (signe de) | n2=en:skin lesions exacerbated by heat, exercise (sweating), and sunlight | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions improve in the summer
n1=Lester (signe de) | n2=en:skin lesions improve in the summer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions manifest in the first year of life
n1=Lester (signe de) | n2=en:skin lesions manifest in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions on back, face, nape of neck, and waist tend to be mild
n1=Lester (signe de) | n2=en:skin lesions on back, face, nape of neck, and waist tend to be mild | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions resolve between 6 months and 2 years of age
n1=Lester (signe de) | n2=en:skin lesions resolve between 6 months and 2 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions tend to occur on distal extremities or at elbows and knees
n1=Lester (signe de) | n2=en:skin lesions tend to occur on distal extremities or at elbows and knees | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin lesions worsen with heat or sun exposure
n1=Lester (signe de) | n2=en:skin lesions worsen with heat or sun exposure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin manifestation less frequently observed in cold climates
n1=Lester (signe de) | n2=en:skin manifestation less frequently observed in cold climates | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin manifestations appear in infancy or childhood and are gradually progressive until the mid-to-late second decade of life
n1=Lester (signe de) | n2=en:skin manifestations appear in infancy or childhood and are gradually progressive until the mid-to-late second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin manifestations are more severe and of later onset than papillon-lefevre syndrome
n1=Lester (signe de) | n2=en:skin manifestations are more severe and of later onset than papillon-lefevre syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin manifestations may not be present
n1=Lester (signe de) | n2=en:skin manifestations may not be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin neoplasia may appear later in life
n1=Lester (signe de) | n2=en:skin neoplasia may appear later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin peeling exacerbated by heat, friction, and humidity
n1=Lester (signe de) | n2=en:skin peeling exacerbated by heat, friction, and humidity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:skin wrinkling improves with age
n1=Lester (signe de) | n2=en:skin wrinkling improves with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slc25a4 mutations account for approximately 4% of all peo cases
n1=Lester (signe de) | n2=en:slc25a4 mutations account for approximately 4% of all peo cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sleep disturbance or sleep apnea (obstructive, central, or mixed)
n1=Lester (signe de) | n2=en:sleep disturbance or sleep apnea (obstructive, central, or mixed) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sleep terrors usually remit during adolescence
n1=Lester (signe de) | n2=en:sleep terrors usually remit during adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sleepwalking triggered by alcohol, sleep deprivation, stress
n1=Lester (signe de) | n2=en:sleepwalking triggered by alcohol, sleep deprivation, stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sleepwalking usually remits in adolescence
n1=Lester (signe de) | n2=en:sleepwalking usually remits in adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slight increased risk for malignancy
n1=Lester (signe de) | n2=en:slight increased risk for malignancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slight male predominance (3:2)
n1=Lester (signe de) | n2=en:slight male predominance (3:2) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slightly increased female:male ratio (1.4:1 to 2:1)
n1=Lester (signe de) | n2=en:slightly increased female:male ratio (1.4:1 to 2:1) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slow course of functional deterioration compared to severity of mri findings
n1=Lester (signe de) | n2=en:slow course of functional deterioration compared to severity of mri findings | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slow or nonprogressive
n1=Lester (signe de) | n2=en:slow or nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slow progression
n1=Lester (signe de) | n2=en:slow progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slow progression without marked disability
n1=Lester (signe de) | n2=en:slow progression without marked disability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slow, progressive growth, then stable
n1=Lester (signe de) | n2=en:slow, progressive growth, then stable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slowly or non-progressive
n1=Lester (signe de) | n2=en:slowly or non-progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slowly or nonprogressive
n1=Lester (signe de) | n2=en:slowly or nonprogressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slowly progressive disease
n1=Lester (signe de) | n2=en:slowly progressive disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slowly progressive moleculr basis : caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0003)
n1=Lester (signe de) | n2=en:slowly progressive moleculr basis : caused by mutation in the apoptosis-inducing factor, mitochondrion-associated, 1 gene (aifm1, 300169.0003) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:slowly progressive or nonprogressive course
n1=Lester (signe de) | n2=en:slowly progressive or nonprogressive course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:small placenta
n1=Lester (signe de) | n2=en:small placenta | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:smaller repeat lengths in younger generations (reverse anticipation)
n1=Lester (signe de) | n2=en:smaller repeat lengths in younger generations (reverse anticipation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:solitary disease is more common in males
n1=Lester (signe de) | n2=en:solitary disease is more common in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:somatic mosaicism has been observed in some patients
n1=Lester (signe de) | n2=en:somatic mosaicism has been observed in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:somatic mutations occur in adrenal tumor tissue (601639.0001)
n1=Lester (signe de) | n2=en:somatic mutations occur in adrenal tumor tissue (601639.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:somatic or germline mosaicism may occur
n1=Lester (signe de) | n2=en:somatic or germline mosaicism may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some affected family members are asymptomatic
n1=Lester (signe de) | n2=en:some affected family members are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some affected individuals have normal subsequent development
n1=Lester (signe de) | n2=en:some affected individuals have normal subsequent development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some boys with premutations (55 to 200 repeats) may show milder features, including autistic features
n1=Lester (signe de) | n2=en:some boys with premutations (55 to 200 repeats) may show milder features, including autistic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some carrier females have episodes of significant hyperammonemia in infancy or childhood
n1=Lester (signe de) | n2=en:some carrier females have episodes of significant hyperammonemia in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some carrier females have mild features
n1=Lester (signe de) | n2=en:some carrier females have mild features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some carrier females may manifest mild symptoms
n1=Lester (signe de) | n2=en:some carrier females may manifest mild symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some familial occurrence, most de novo aberrations
n1=Lester (signe de) | n2=en:some familial occurrence, most de novo aberrations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some families have axonal cmt (cmt2m)
n1=Lester (signe de) | n2=en:some families have axonal cmt (cmt2m) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features are variable
n1=Lester (signe de) | n2=en:some features are variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features are variable, even within families
n1=Lester (signe de) | n2=en:some features are variable, even within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features are variably expressed
n1=Lester (signe de) | n2=en:some features are variably expressed | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features are variably present
n1=Lester (signe de) | n2=en:some features are variably present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features may be progressive
n1=Lester (signe de) | n2=en:some features may be progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features may be variable
n1=Lester (signe de) | n2=en:some features may be variable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features not found in all patients
n1=Lester (signe de) | n2=en:some features not found in all patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some features occur in adolescence, including migraine, seizures, and psychiatric disorders
n1=Lester (signe de) | n2=en:some features occur in adolescence, including migraine, seizures, and psychiatric disorders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some female carriers are more mildly affected
n1=Lester (signe de) | n2=en:some female carriers are more mildly affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some female heterozygotes express phenotypic features (e.g., coarse facies, mild mental retardation)
n1=Lester (signe de) | n2=en:some female heterozygotes express phenotypic features (e.g., coarse facies, mild mental retardation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some female patients can conceive after administration of gonadotropins
n1=Lester (signe de) | n2=en:some female patients can conceive after administration of gonadotropins | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some females are affected
n1=Lester (signe de) | n2=en:some females are affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some females have only deafness and ovarian dysgenesis without neurologic abnormalities
n1=Lester (signe de) | n2=en:some females have only deafness and ovarian dysgenesis without neurologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some heterozygotes exhibit a mild phenotype of cutaneous syndactyly between the second and third toes
n1=Lester (signe de) | n2=en:some heterozygotes exhibit a mild phenotype of cutaneous syndactyly between the second and third toes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some heterozygotes may have increased urinary excretion of cystine and may develop stones
n1=Lester (signe de) | n2=en:some heterozygotes may have increased urinary excretion of cystine and may develop stones | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some heterozygous carriers exhibit accelerated age-related hearing loss
n1=Lester (signe de) | n2=en:some heterozygous carriers exhibit accelerated age-related hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some heterozygous carriers may have mild manifestations
n1=Lester (signe de) | n2=en:some heterozygous carriers may have mild manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some heterozygous cpt2 mutation carriers may be symptomatic
n1=Lester (signe de) | n2=en:some heterozygous cpt2 mutation carriers may be symptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some individuals may be clinically asymptomatic
n1=Lester (signe de) | n2=en:some individuals may be clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some laboratory abnormalities may fluctuate or improve with time
n1=Lester (signe de) | n2=en:some laboratory abnormalities may fluctuate or improve with time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some male patients exhibit some degree of spermatogenesis, hence the designation 'fertile eunuch syndrome' has been used
n1=Lester (signe de) | n2=en:some male patients exhibit some degree of spermatogenesis, hence the designation 'fertile eunuch syndrome' has been used | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some more severely affected patients may die in infancy
n1=Lester (signe de) | n2=en:some more severely affected patients may die in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some mutation carriers have mild features of frontonasal dysplasia (613451)
n1=Lester (signe de) | n2=en:some mutation carriers have mild features of frontonasal dysplasia (613451) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some mutations have been found in homozygosity and the phenotype is more severe than that of the heterozygous parents
n1=Lester (signe de) | n2=en:some mutations have been found in homozygosity and the phenotype is more severe than that of the heterozygous parents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients acquire late ambulation
n1=Lester (signe de) | n2=en:some patients acquire late ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients are asymptomatic and detected only by newborn screening
n1=Lester (signe de) | n2=en:some patients are asymptomatic and detected only by newborn screening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients are asymptomatic and diagnosed incidentally
n1=Lester (signe de) | n2=en:some patients are asymptomatic and diagnosed incidentally | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients are clinically unaffected.
n1=Lester (signe de) | n2=en:some patients are clinically unaffected. | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients become bedridden
n1=Lester (signe de) | n2=en:some patients become bedridden | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients become wheelchair-bound
n1=Lester (signe de) | n2=en:some patients become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients become wheelchair-bound in second decade
n1=Lester (signe de) | n2=en:some patients become wheelchair-bound in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients born in consanguineous families may carry homozygous mutations, but the phenotype does not appear to be more severe
n1=Lester (signe de) | n2=en:some patients born in consanguineous families may carry homozygous mutations, but the phenotype does not appear to be more severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients can attend special school
n1=Lester (signe de) | n2=en:some patients can attend special school | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients can be treated with large doses of vitamin d and calcium
n1=Lester (signe de) | n2=en:some patients can be treated with large doses of vitamin d and calcium | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients can hold menial jobs
n1=Lester (signe de) | n2=en:some patients can hold menial jobs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients carry heterozygous mutations
n1=Lester (signe de) | n2=en:some patients carry heterozygous mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients develop diabetes mellitus as adolescents
n1=Lester (signe de) | n2=en:some patients develop diabetes mellitus as adolescents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients develop ophthalmoplegia in middle age
n1=Lester (signe de) | n2=en:some patients develop ophthalmoplegia in middle age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not achieve independent ambulation
n1=Lester (signe de) | n2=en:some patients do not achieve independent ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not develop renal failure
n1=Lester (signe de) | n2=en:some patients do not develop renal failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not develop stroke
n1=Lester (signe de) | n2=en:some patients do not develop stroke | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not have bone disease
n1=Lester (signe de) | n2=en:some patients do not have bone disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not have dysmorphic features
n1=Lester (signe de) | n2=en:some patients do not have dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not have thin corpus callosum
n1=Lester (signe de) | n2=en:some patients do not have thin corpus callosum | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not manifest renal disease in the first decade of life
n1=Lester (signe de) | n2=en:some patients do not manifest renal disease in the first decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not reach end-stage renal failure
n1=Lester (signe de) | n2=en:some patients do not reach end-stage renal failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients do not show neurologic abnormalities or dysmorphic features
n1=Lester (signe de) | n2=en:some patients do not show neurologic abnormalities or dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients exhibit features of more than 1 type of cardiomyopathy
n1=Lester (signe de) | n2=en:some patients exhibit features of more than 1 type of cardiomyopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients exhibit minimal central lesions with severe peripheral lesions, and vice-versa
n1=Lester (signe de) | n2=en:some patients exhibit minimal central lesions with severe peripheral lesions, and vice-versa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients experience later reversal of hypogonadotropic hypogonadism
n1=Lester (signe de) | n2=en:some patients experience later reversal of hypogonadotropic hypogonadism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients experience respiratory infections in association with episodes of jaundice in childhood
n1=Lester (signe de) | n2=en:some patients experience respiratory infections in association with episodes of jaundice in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a contiguous gene defect involving both the cyp21a2 (613815) and the tnxb (600985) genes
n1=Lester (signe de) | n2=en:some patients have a contiguous gene defect involving both the cyp21a2 (613815) and the tnxb (600985) genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a contiguous gene syndrome due to loss of adjacent genes (sts, 308100 and kal1, 300836) on xp22.3 via deletions and translocations
n1=Lester (signe de) | n2=en:some patients have a contiguous gene syndrome due to loss of adjacent genes (sts, 308100 and kal1, 300836) on xp22.3 via deletions and translocations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a crouzon-like appearance
n1=Lester (signe de) | n2=en:some patients have a crouzon-like appearance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a milder nonprogressive phenotype
n1=Lester (signe de) | n2=en:some patients have a milder nonprogressive phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a more severe phenotype and have febrile and afebrile seizures after childhood (gefs+)
n1=Lester (signe de) | n2=en:some patients have a more severe phenotype and have febrile and afebrile seizures after childhood (gefs+) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a secreted but biologically inactive mutant leptin
n1=Lester (signe de) | n2=en:some patients have a secreted but biologically inactive mutant leptin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have a severe phenotype with neurologic manifestations beginning at birth
n1=Lester (signe de) | n2=en:some patients have a severe phenotype with neurologic manifestations beginning at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have additional neurologic involvement
n1=Lester (signe de) | n2=en:some patients have additional neurologic involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have an attenuated phenotype
n1=Lester (signe de) | n2=en:some patients have an attenuated phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have an atypical phenotype with a more protracted disease course resulting in death in middle age
n1=Lester (signe de) | n2=en:some patients have an atypical phenotype with a more protracted disease course resulting in death in middle age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have asymptomatic hypocalcemia
n1=Lester (signe de) | n2=en:some patients have asymptomatic hypocalcemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have cessation of seizures at a mean of 12 years
n1=Lester (signe de) | n2=en:some patients have cessation of seizures at a mean of 12 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have deletions or duplications of chromosome 2p25.3 encompassing several genes
n1=Lester (signe de) | n2=en:some patients have deletions or duplications of chromosome 2p25.3 encompassing several genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have isolated cfeom
n1=Lester (signe de) | n2=en:some patients have isolated cfeom | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have juvenile-onset myoclonic epilepsy
n1=Lester (signe de) | n2=en:some patients have juvenile-onset myoclonic epilepsy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have later onset and more variable phenotype (mngie)
n1=Lester (signe de) | n2=en:some patients have later onset and more variable phenotype (mngie) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have later onset of the disorder as young adults
n1=Lester (signe de) | n2=en:some patients have later onset of the disorder as young adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have lethal fetal akinesia with death in utero
n1=Lester (signe de) | n2=en:some patients have lethal fetal akinesia with death in utero | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have milder persistent blistering
n1=Lester (signe de) | n2=en:some patients have milder persistent blistering | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have milder phenotype with later onset of symptoms, in second to third decades of life
n1=Lester (signe de) | n2=en:some patients have milder phenotype with later onset of symptoms, in second to third decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have no clinical symptoms and are detected by routine newborn screening
n1=Lester (signe de) | n2=en:some patients have no clinical symptoms and are detected by routine newborn screening | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have no manifestations
n1=Lester (signe de) | n2=en:some patients have no manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have no neurologic abnormalities
n1=Lester (signe de) | n2=en:some patients have no neurologic abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have no or mild manifestations and normal development
n1=Lester (signe de) | n2=en:some patients have no or mild manifestations and normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have only ambiguous genitalia or other evidence of disordered steroidogenesis
n1=Lester (signe de) | n2=en:some patients have only ambiguous genitalia or other evidence of disordered steroidogenesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have only ocular involvement or only oral involvement
n1=Lester (signe de) | n2=en:some patients have only ocular involvement or only oral involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have only plantar surface involvement
n1=Lester (signe de) | n2=en:some patients have only plantar surface involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have onset at birth or in early infancy, whereas other have onset in late childhood or adolescence
n1=Lester (signe de) | n2=en:some patients have onset at birth or in early infancy, whereas other have onset in late childhood or adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have onset in second decade of life
n1=Lester (signe de) | n2=en:some patients have onset in second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have persistence of seizures to adulthood, but then show remission
n1=Lester (signe de) | n2=en:some patients have persistence of seizures to adulthood, but then show remission | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have resolution of symptoms in first year of life
n1=Lester (signe de) | n2=en:some patients have resolution of symptoms in first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients have subclinical exocrine pancreatic deficiency
n1=Lester (signe de) | n2=en:some patients have subclinical exocrine pancreatic deficiency | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may be asymptomatic
n1=Lester (signe de) | n2=en:some patients may be asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may be asymptomatic and have only short telomeres
n1=Lester (signe de) | n2=en:some patients may be asymptomatic and have only short telomeres | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may be asymptomatic if diagnosed early and properly managed during metabolic crises
n1=Lester (signe de) | n2=en:some patients may be asymptomatic if diagnosed early and properly managed during metabolic crises | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may be clinically asymptomatic
n1=Lester (signe de) | n2=en:some patients may be clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may become bedridden 10 to 20 years after onset
n1=Lester (signe de) | n2=en:some patients may become bedridden 10 to 20 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may become wheelchair-bound
n1=Lester (signe de) | n2=en:some patients may become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may benefit from coenzyme q10 treatment
n1=Lester (signe de) | n2=en:some patients may benefit from coenzyme q10 treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may develop concurrent failure to thrive and dyslipidemia
n1=Lester (signe de) | n2=en:some patients may develop concurrent failure to thrive and dyslipidemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may develop interictal progressive ataxia
n1=Lester (signe de) | n2=en:some patients may develop interictal progressive ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may die from cardiomyopathy in the first or second decade of life
n1=Lester (signe de) | n2=en:some patients may die from cardiomyopathy in the first or second decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may die in infancy, whereas others survive into adulthood and are only mildly affected or essentially clinically asymptomatic
n1=Lester (signe de) | n2=en:some patients may die in infancy, whereas others survive into adulthood and are only mildly affected or essentially clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have a milder phenotype
n1=Lester (signe de) | n2=en:some patients may have a milder phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have a more protracted disorder with neurodegeneration
n1=Lester (signe de) | n2=en:some patients may have a more protracted disorder with neurodegeneration | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have isolated cardiac involvement
n1=Lester (signe de) | n2=en:some patients may have isolated cardiac involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have isolated myokymia
n1=Lester (signe de) | n2=en:some patients may have isolated myokymia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have normal brain imaging
n1=Lester (signe de) | n2=en:some patients may have normal brain imaging | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have normal development until onset of seizures in infancy
n1=Lester (signe de) | n2=en:some patients may have normal development until onset of seizures in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have normal psychomotor development
n1=Lester (signe de) | n2=en:some patients may have normal psychomotor development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have residual muscle weakness
n1=Lester (signe de) | n2=en:some patients may have residual muscle weakness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may have unilateral involvement, may be able to raise the eye above midline, or may not have ptosis--these patients are classified as having cfeom3 (cfeom3b)
n1=Lester (signe de) | n2=en:some patients may have unilateral involvement, may be able to raise the eye above midline, or may not have ptosis--these patients are classified as having cfeom3 (cfeom3b) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may live to adulthood
n1=Lester (signe de) | n2=en:some patients may live to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may lose independent ambulation
n1=Lester (signe de) | n2=en:some patients may lose independent ambulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may need surgery or renal transplant
n1=Lester (signe de) | n2=en:some patients may need surgery or renal transplant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may not achieve walking
n1=Lester (signe de) | n2=en:some patients may not achieve walking | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may not have recurrent infections
n1=Lester (signe de) | n2=en:some patients may not have recurrent infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may not present until adulthood
n1=Lester (signe de) | n2=en:some patients may not present until adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may present with adult-onset small fiber neuropathy
n1=Lester (signe de) | n2=en:some patients may present with adult-onset small fiber neuropathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may present with myopathic features
n1=Lester (signe de) | n2=en:some patients may present with myopathic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may present with transient neonatal hypotonia, and then later develop classic pmc in childhood
n1=Lester (signe de) | n2=en:some patients may present with transient neonatal hypotonia, and then later develop classic pmc in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may respond to thiamine treatment
n1=Lester (signe de) | n2=en:some patients may respond to thiamine treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show a favorable response to oral coenzyme q10 supplementation
n1=Lester (signe de) | n2=en:some patients may show a favorable response to oral coenzyme q10 supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show deterioration with infections
n1=Lester (signe de) | n2=en:some patients may show deterioration with infections | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show mild decrease in head circumference over time
n1=Lester (signe de) | n2=en:some patients may show mild decrease in head circumference over time | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show neurologic improvement late in life
n1=Lester (signe de) | n2=en:some patients may show neurologic improvement late in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show normal early development before seizure onset
n1=Lester (signe de) | n2=en:some patients may show normal early development before seizure onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients may show response to immunosuppressive agents
n1=Lester (signe de) | n2=en:some patients may show response to immunosuppressive agents | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients never achieve sitting
n1=Lester (signe de) | n2=en:some patients never achieve sitting | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients never achieve walking or running
n1=Lester (signe de) | n2=en:some patients never achieve walking or running | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients never gain ambulation or become wheelchair-bound
n1=Lester (signe de) | n2=en:some patients never gain ambulation or become wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients present with apparent nonsyndromic dilated cardiomyopathy in early childhood
n1=Lester (signe de) | n2=en:some patients present with apparent nonsyndromic dilated cardiomyopathy in early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients present with spasticity, whereas others present with cerebellar ataxia
n1=Lester (signe de) | n2=en:some patients present with spasticity, whereas others present with cerebellar ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients report cyclical changes in severity of symptoms
n1=Lester (signe de) | n2=en:some patients report cyclical changes in severity of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients report increased tolerance to heat
n1=Lester (signe de) | n2=en:some patients report increased tolerance to heat | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients report seasonal variation in symptoms
n1=Lester (signe de) | n2=en:some patients report seasonal variation in symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients require cardiac transplantation
n1=Lester (signe de) | n2=en:some patients require cardiac transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients require insulin for treatment
n1=Lester (signe de) | n2=en:some patients require insulin for treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients respond to acetazolamide
n1=Lester (signe de) | n2=en:some patients respond to acetazolamide | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show a favorable response to sulfonylurea treatment
n1=Lester (signe de) | n2=en:some patients show a favorable response to sulfonylurea treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show delayed development from birth
n1=Lester (signe de) | n2=en:some patients show delayed development from birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show improvement during summer or with fever
n1=Lester (signe de) | n2=en:some patients show improvement during summer or with fever | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show improvement in muscle power in the teenage years
n1=Lester (signe de) | n2=en:some patients show improvement in muscle power in the teenage years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show infantile onset
n1=Lester (signe de) | n2=en:some patients show infantile onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show no bleeding abnormalities
n1=Lester (signe de) | n2=en:some patients show no bleeding abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show normal development until onset of disorder
n1=Lester (signe de) | n2=en:some patients show normal development until onset of disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show onset in childhood
n1=Lester (signe de) | n2=en:some patients show onset in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show onset later in childhood
n1=Lester (signe de) | n2=en:some patients show onset later in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show rapid disease progression
n1=Lester (signe de) | n2=en:some patients show rapid disease progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients show significant clinical improvement with riboflavin supplementation
n1=Lester (signe de) | n2=en:some patients show significant clinical improvement with riboflavin supplementation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients survive infancy
n1=Lester (signe de) | n2=en:some patients survive infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with 2 opa1 mutations have a more severe phenotype with earlier onset
n1=Lester (signe de) | n2=en:some patients with 2 opa1 mutations have a more severe phenotype with earlier onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with advanced loss of vision have normal eog
n1=Lester (signe de) | n2=en:some patients with advanced loss of vision have normal eog | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with heterozygous mutations may be symptomatic
n1=Lester (signe de) | n2=en:some patients with heterozygous mutations may be symptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with hypertrophic cardiomyopathy progress to a dilated phenotype with severe heart failure
n1=Lester (signe de) | n2=en:some patients with hypertrophic cardiomyopathy progress to a dilated phenotype with severe heart failure | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with onset of severe disease in infancy are diagnosed with leber congenital amaurosis, whereas other patients with childhood onset of less severe retinal dystrophy are diagnosed with retinitis pigmentosa
n1=Lester (signe de) | n2=en:some patients with onset of severe disease in infancy are diagnosed with leber congenital amaurosis, whereas other patients with childhood onset of less severe retinal dystrophy are diagnosed with retinitis pigmentosa | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some patients with vitelliform macular dystrophy are homozygous or compound heterozygous for mutations in best1, with their heterozygous relatives showing milder forms of eye disease
n1=Lester (signe de) | n2=en:some patients with vitelliform macular dystrophy are homozygous or compound heterozygous for mutations in best1, with their heterozygous relatives showing milder forms of eye disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some pedigrees are consistent with autosomal dominant inheritance
n1=Lester (signe de) | n2=en:some pedigrees are consistent with autosomal dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some people with a cnnm2 mutation are asymptomatic
n1=Lester (signe de) | n2=en:some people with a cnnm2 mutation are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some phenotypic overlap with alpers syndrome (mtdps4a, 203700)
n1=Lester (signe de) | n2=en:some phenotypic overlap with alpers syndrome (mtdps4a, 203700) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some phenotypic overlap with rett syndrome (312750)
n1=Lester (signe de) | n2=en:some phenotypic overlap with rett syndrome (312750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some response to l-dopa therapy
n1=Lester (signe de) | n2=en:some response to l-dopa therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:some tumors may be microsatellite instable and carry somatic mutations in msh mismatch repair genes
n1=Lester (signe de) | n2=en:some tumors may be microsatellite instable and carry somatic mutations in msh mismatch repair genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sparing of some nails in some individuals
n1=Lester (signe de) | n2=en:sparing of some nails in some individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spastic paraplegia 2 (spg2, 312920) is an allelic disorder
n1=Lester (signe de) | n2=en:spastic paraplegia 2 (spg2, 312920) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spasticity is slowly progressive
n1=Lester (signe de) | n2=en:spasticity is slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spasticity occurs before parkinsonism
n1=Lester (signe de) | n2=en:spasticity occurs before parkinsonism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:specific features may vary, but syndactyly and renal/anogenital malformations are cardinal features
n1=Lester (signe de) | n2=en:specific features may vary, but syndactyly and renal/anogenital malformations are cardinal features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spectrum of laterality defects
n1=Lester (signe de) | n2=en:spectrum of laterality defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spectrum of malformations resulting from impaired midline cleavage of the embryonic forebrain
n1=Lester (signe de) | n2=en:spectrum of malformations resulting from impaired midline cleavage of the embryonic forebrain | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spinal involvement improves with age
n1=Lester (signe de) | n2=en:spinal involvement improves with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spinal tumors are necessary for diagnosis
n1=Lester (signe de) | n2=en:spinal tumors are necessary for diagnosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:splenectomy increases thrombotic risk in these patients
n1=Lester (signe de) | n2=en:splenectomy increases thrombotic risk in these patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous bleeding is rare
n1=Lester (signe de) | n2=en:spontaneous bleeding is rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous chromosomal instability with multiple rearrangements, especially chromosome 7 and 14
n1=Lester (signe de) | n2=en:spontaneous chromosomal instability with multiple rearrangements, especially chromosome 7 and 14 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous improvement or resolution of skin creases in childhood
n1=Lester (signe de) | n2=en:spontaneous improvement or resolution of skin creases in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous resolution by 12 months of age with no recurrence later in life
n1=Lester (signe de) | n2=en:spontaneous resolution by 12 months of age with no recurrence later in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous resolution of seizures by 12 months of age
n1=Lester (signe de) | n2=en:spontaneous resolution of seizures by 12 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous resolution usually after 12 months of age
n1=Lester (signe de) | n2=en:spontaneous resolution usually after 12 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous resorption (rare)
n1=Lester (signe de) | n2=en:spontaneous resorption (rare) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous reversal of gnrh deficiency may occur in some patients
n1=Lester (signe de) | n2=en:spontaneous reversal of gnrh deficiency may occur in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneous tumor regression may occur
n1=Lester (signe de) | n2=en:spontaneous tumor regression may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spontaneously resolves by 5 to 6 months of age
n1=Lester (signe de) | n2=en:spontaneously resolves by 5 to 6 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sporadic cases often single lesions versus multiple lesions in familial cases
n1=Lester (signe de) | n2=en:sporadic cases often single lesions versus multiple lesions in familial cases | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sporadic occurrence
n1=Lester (signe de) | n2=en:sporadic occurrence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sporadic occurrence is associated with advanced paternal age
n1=Lester (signe de) | n2=en:sporadic occurrence is associated with advanced paternal age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sporadic or acquired pct precipitated by alcohol, estrogens, iron, and polychlorinated cyclic hydrocarbons
n1=Lester (signe de) | n2=en:sporadic or acquired pct precipitated by alcohol, estrogens, iron, and polychlorinated cyclic hydrocarbons | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:spots occur in 95% of patients but can be absent
n1=Lester (signe de) | n2=en:spots occur in 95% of patients but can be absent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stable or slowly progressive course
n1=Lester (signe de) | n2=en:stable or slowly progressive course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stage ii, rapid developmental regression (onset 1-4 years)
n1=Lester (signe de) | n2=en:stage ii, rapid developmental regression (onset 1-4 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stage iii, pseudostationary period (onset 2-10 years)
n1=Lester (signe de) | n2=en:stage iii, pseudostationary period (onset 2-10 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stage iv, late motor deterioration (when ambulation ceases)
n1=Lester (signe de) | n2=en:stage iv, late motor deterioration (when ambulation ceases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:static or slowly progressive
n1=Lester (signe de) | n2=en:static or slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:static, nonprogressive disorder
n1=Lester (signe de) | n2=en:static, nonprogressive disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stickler syndrome (108300) and marshall syndrome share several characteristics such as midface hypoplasia, high myopia, and sensorineural hearing loss
n1=Lester (signe de) | n2=en:stickler syndrome (108300) and marshall syndrome share several characteristics such as midface hypoplasia, high myopia, and sensorineural hearing loss | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stillbirth
n1=Lester (signe de) | n2=en:stillbirth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stillborn or death in infancy
n1=Lester (signe de) | n2=en:stillborn or death in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stillborn or death shortly after birth
n1=Lester (signe de) | n2=en:stillborn or death shortly after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stillborn or infantile death usual in prenatal form
n1=Lester (signe de) | n2=en:stillborn or infantile death usual in prenatal form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:stillborn or lethal in the neonatal period
n1=Lester (signe de) | n2=en:stillborn or lethal in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:striking intrafamilial variability
n1=Lester (signe de) | n2=en:striking intrafamilial variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subclavian artery supply disruption in embryogenesis has been suggested as etiology
n1=Lester (signe de) | n2=en:subclavian artery supply disruption in embryogenesis has been suggested as etiology | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subset of patients have cytochrome c oxidase deficiency (see 220110)
n1=Lester (signe de) | n2=en:subset of patients have cytochrome c oxidase deficiency (see 220110) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subset of patients have french-canadian leigh syndrome (220111)
n1=Lester (signe de) | n2=en:subset of patients have french-canadian leigh syndrome (220111) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subset of patients have leigh syndrome (256000)
n1=Lester (signe de) | n2=en:subset of patients have leigh syndrome (256000) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtle facial phenotype compared to other types of hpe
n1=Lester (signe de) | n2=en:subtle facial phenotype compared to other types of hpe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtle personality and behavioral changes are presenting signs
n1=Lester (signe de) | n2=en:subtle personality and behavioral changes are presenting signs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtype 3a comprises myoclonus and dementia
n1=Lester (signe de) | n2=en:subtype 3a comprises myoclonus and dementia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtype 3b comprises horizontal supranuclear gaze palsy and aggressive systemic disease
n1=Lester (signe de) | n2=en:subtype 3b comprises horizontal supranuclear gaze palsy and aggressive systemic disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtype 3c (231005) comprises cardiovascular calcifications
n1=Lester (signe de) | n2=en:subtype 3c (231005) comprises cardiovascular calcifications | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:subtype of migraine with aura
n1=Lester (signe de) | n2=en:subtype of migraine with aura | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:successful treatment with oral isotretinoin
n1=Lester (signe de) | n2=en:successful treatment with oral isotretinoin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden cardiac death frequent in affected families
n1=Lester (signe de) | n2=en:sudden cardiac death frequent in affected families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden cardiac death in some families
n1=Lester (signe de) | n2=en:sudden cardiac death in some families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death
n1=Lester (signe de) | n2=en:sudden death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death due to cardiac arrhythmia may occur
n1=Lester (signe de) | n2=en:sudden death due to cardiac arrhythmia may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death due to cardiomyopathy
n1=Lester (signe de) | n2=en:sudden death due to cardiomyopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death in affected females occurs in the forties
n1=Lester (signe de) | n2=en:sudden death in affected females occurs in the forties | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death in affected males occurs in teens
n1=Lester (signe de) | n2=en:sudden death in affected males occurs in teens | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death may occur
n1=Lester (signe de) | n2=en:sudden death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death secondary to impaction of medulla oblongata
n1=Lester (signe de) | n2=en:sudden death secondary to impaction of medulla oblongata | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden death within first days of life
n1=Lester (signe de) | n2=en:sudden death within first days of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden infant death may occur
n1=Lester (signe de) | n2=en:sudden infant death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:sudden infantile death may occur
n1=Lester (signe de) | n2=en:sudden infantile death may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:supervisor review:impression/interpretation of study:point in time:to be specified in another part of the message:nominal
n1=Lester (signe de) | n2=en:supervisor review:impression/interpretation of study:point in time:to be specified in another part of the message:nominal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:surgical intervention is not always curative
n1=Lester (signe de) | n2=en:surgical intervention is not always curative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival 30 to 40 years after onset
n1=Lester (signe de) | n2=en:survival 30 to 40 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival greater than one year rare
n1=Lester (signe de) | n2=en:survival greater than one year rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival past infancy is rare
n1=Lester (signe de) | n2=en:survival past infancy is rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival to 10 years
n1=Lester (signe de) | n2=en:survival to 10 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival to 20 years in severe form
n1=Lester (signe de) | n2=en:survival to 20 years in severe form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival to 20s-60s in iib
n1=Lester (signe de) | n2=en:survival to 20s-60s in iib | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival to 5-15 years of age
n1=Lester (signe de) | n2=en:survival to 5-15 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survival to advanced age
n1=Lester (signe de) | n2=en:survival to advanced age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:surviving infants develop severe nonbullous ichthyosiform erythroderma
n1=Lester (signe de) | n2=en:surviving infants develop severe nonbullous ichthyosiform erythroderma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:surviving males are postzygotic mosaic for ebp mutations
n1=Lester (signe de) | n2=en:surviving males are postzygotic mosaic for ebp mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survivors develop dysautonomia-like symptoms
n1=Lester (signe de) | n2=en:survivors develop dysautonomia-like symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survivors have mental retardation, spasticity, and adducted thumbs (masa syndrome findings (303350))
n1=Lester (signe de) | n2=en:survivors have mental retardation, spasticity, and adducted thumbs (masa syndrome findings (303350)) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:survivors may develop renal insufficiency and hepatic dysfunction
n1=Lester (signe de) | n2=en:survivors may develop renal insufficiency and hepatic dysfunction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:susceptibility to infections start in the first year of life
n1=Lester (signe de) | n2=en:susceptibility to infections start in the first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:susceptibility to infections starts in the first week of life
n1=Lester (signe de) | n2=en:susceptibility to infections starts in the first week of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:swelling starts to fade by age 30 years and gradually becomes unremarkable
n1=Lester (signe de) | n2=en:swelling starts to fade by age 30 years and gradually becomes unremarkable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptom onset at birth or infancy arnold-chiari type ii is uniquely associated with myelomeninogocele (182940)
n1=Lester (signe de) | n2=en:symptom onset at birth or infancy arnold-chiari type ii is uniquely associated with myelomeninogocele (182940) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptom onset ranges from infancy to adulthood
n1=Lester (signe de) | n2=en:symptom onset ranges from infancy to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptomatic female carriers have been described in 1 japanese family
n1=Lester (signe de) | n2=en:symptomatic female carriers have been described in 1 japanese family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptomatic if > 200 repeats
n1=Lester (signe de) | n2=en:symptomatic if > 200 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms aggravated by fatigue, exertion, sleep deprivation, emotion, hunger
n1=Lester (signe de) | n2=en:symptoms aggravated by fatigue, exertion, sleep deprivation, emotion, hunger | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms ameliorate with age
n1=Lester (signe de) | n2=en:symptoms ameliorate with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms appear in early childhood and are progressive
n1=Lester (signe de) | n2=en:symptoms appear in early childhood and are progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms are aggravated by febrile illness
n1=Lester (signe de) | n2=en:symptoms are aggravated by febrile illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms are not apparent at rest
n1=Lester (signe de) | n2=en:symptoms are not apparent at rest | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms are not relieved by alcohol
n1=Lester (signe de) | n2=en:symptoms are not relieved by alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms are often responsive to alcohol
n1=Lester (signe de) | n2=en:symptoms are often responsive to alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms are responsive to cobalamin treatment
n1=Lester (signe de) | n2=en:symptoms are responsive to cobalamin treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms begin focally, later segmental or generalized
n1=Lester (signe de) | n2=en:symptoms begin focally, later segmental or generalized | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms benefit from sleep
n1=Lester (signe de) | n2=en:symptoms benefit from sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms can be prevented by strict dietary restriction
n1=Lester (signe de) | n2=en:symptoms can be prevented by strict dietary restriction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms develop immediately after birth
n1=Lester (signe de) | n2=en:symptoms develop immediately after birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms highly variable - rapidly progressive course leading to hepatic failure versus acute hepatic crisis
n1=Lester (signe de) | n2=en:symptoms highly variable - rapidly progressive course leading to hepatic failure versus acute hepatic crisis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms improve during the summer
n1=Lester (signe de) | n2=en:symptoms improve during the summer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms improve following sleep
n1=Lester (signe de) | n2=en:symptoms improve following sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms improve with age, resulting in woolly hair with almost normal hair density
n1=Lester (signe de) | n2=en:symptoms improve with age, resulting in woolly hair with almost normal hair density | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms induced by strenuous exercise
n1=Lester (signe de) | n2=en:symptoms induced by strenuous exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms may be aggravated by acute illness
n1=Lester (signe de) | n2=en:symptoms may be aggravated by acute illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms may be exacerbated by pregnancy or trauma
n1=Lester (signe de) | n2=en:symptoms may be exacerbated by pregnancy or trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms may be exacerbated in women during pregnancy or by oral contraceptives (see 614972)
n1=Lester (signe de) | n2=en:symptoms may be exacerbated in women during pregnancy or by oral contraceptives (see 614972) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms may be precipitated by infection
n1=Lester (signe de) | n2=en:symptoms may be precipitated by infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms may decrease after age 30 years
n1=Lester (signe de) | n2=en:symptoms may decrease after age 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms must occur for 6 months including 1 month of characteristic symptoms (e.g. delusions) to make diagnosis
n1=Lester (signe de) | n2=en:symptoms must occur for 6 months including 1 month of characteristic symptoms (e.g. delusions) to make diagnosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms noted at 2-3 years
n1=Lester (signe de) | n2=en:symptoms noted at 2-3 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms occur only during pregnancy (usual onset after 6 weeks gestation)
n1=Lester (signe de) | n2=en:symptoms occur only during pregnancy (usual onset after 6 weeks gestation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms occur only during sleep
n1=Lester (signe de) | n2=en:symptoms occur only during sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms of zinc deficiency occur only in exclusively breastfed infants
n1=Lester (signe de) | n2=en:symptoms of zinc deficiency occur only in exclusively breastfed infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms often decrease or remit with age
n1=Lester (signe de) | n2=en:symptoms often decrease or remit with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms often improve gradually with age
n1=Lester (signe de) | n2=en:symptoms often improve gradually with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by alcohol, caffeine, fatigue, stress, exertion, ovulation, menstruation
n1=Lester (signe de) | n2=en:symptoms precipitated by alcohol, caffeine, fatigue, stress, exertion, ovulation, menstruation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by exercise and excitement
n1=Lester (signe de) | n2=en:symptoms precipitated by exercise and excitement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by stress, exertion, fatigue, alcohol
n1=Lester (signe de) | n2=en:symptoms precipitated by stress, exertion, fatigue, alcohol | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by sudden movement, stress, exertion, exercise, fatigue, caffeine, alcohol, cigarettes
n1=Lester (signe de) | n2=en:symptoms precipitated by sudden movement, stress, exertion, exercise, fatigue, caffeine, alcohol, cigarettes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by sudden movement, stress, exertion, fatigue
n1=Lester (signe de) | n2=en:symptoms precipitated by sudden movement, stress, exertion, fatigue | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by sudden movement, stress, exertion, fatigue, illness
n1=Lester (signe de) | n2=en:symptoms precipitated by sudden movement, stress, exertion, fatigue, illness | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by sudden movement, stress, exertion, fatigue' attacks typically last for hours
n1=Lester (signe de) | n2=en:symptoms precipitated by sudden movement, stress, exertion, fatigue' attacks typically last for hours | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms precipitated by sudden movements
n1=Lester (signe de) | n2=en:symptoms precipitated by sudden movements | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms present as acute metabolic and clinical decompensation associated with infection
n1=Lester (signe de) | n2=en:symptoms present as acute metabolic and clinical decompensation associated with infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms present from infancy or early childhood
n1=Lester (signe de) | n2=en:symptoms present from infancy or early childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms progress with worsening myopathy
n1=Lester (signe de) | n2=en:symptoms progress with worsening myopathy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms relieved by ovarian suppression
n1=Lester (signe de) | n2=en:symptoms relieved by ovarian suppression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms relieved by progesterone antagonist (in some patients)
n1=Lester (signe de) | n2=en:symptoms relieved by progesterone antagonist (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms relieved by serotonin antagonist (in some patients)
n1=Lester (signe de) | n2=en:symptoms relieved by serotonin antagonist (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms remain focal
n1=Lester (signe de) | n2=en:symptoms remain focal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms resolve over weeks to months with usually no residual symptoms between attacks
n1=Lester (signe de) | n2=en:symptoms resolve over weeks to months with usually no residual symptoms between attacks | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms show insidious onset in the late first through third decades
n1=Lester (signe de) | n2=en:symptoms show insidious onset in the late first through third decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms tend to improve with age
n1=Lester (signe de) | n2=en:symptoms tend to improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms typically begin in childhood
n1=Lester (signe de) | n2=en:symptoms typically begin in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually appear in adulthood
n1=Lester (signe de) | n2=en:symptoms usually appear in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually induced only by strenuous exercise
n1=Lester (signe de) | n2=en:symptoms usually induced only by strenuous exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually last 30-60 minutes
n1=Lester (signe de) | n2=en:symptoms usually last 30-60 minutes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually manifest in childhood including waddling gait and painful, stiff joints
n1=Lester (signe de) | n2=en:symptoms usually manifest in childhood including waddling gait and painful, stiff joints | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually occur in adults
n1=Lester (signe de) | n2=en:symptoms usually occur in adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms usually resolve without treatment
n1=Lester (signe de) | n2=en:symptoms usually resolve without treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms vary according to location of tumor
n1=Lester (signe de) | n2=en:symptoms vary according to location of tumor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms vary from asymptomatic patients to patients with metabolic acidosis
n1=Lester (signe de) | n2=en:symptoms vary from asymptomatic patients to patients with metabolic acidosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:symptoms worsen with fatigue and exercise
n1=Lester (signe de) | n2=en:symptoms worsen with fatigue and exercise | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:syncope
n1=Lester (signe de) | n2=en:syncope | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:syndromic forms of dense granule only platelet storage pool deficiencies (delta-spd) include hermansky-pudlak syndrome (203300) and chediak-hygashi syndrome (214500)
n1=Lester (signe de) | n2=en:syndromic forms of dense granule only platelet storage pool deficiencies (delta-spd) include hermansky-pudlak syndrome (203300) and chediak-hygashi syndrome (214500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:systemic amyloid deposition may occur
n1=Lester (signe de) | n2=en:systemic amyloid deposition may occur | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:systemic granulomatous disease
n1=Lester (signe de) | n2=en:systemic granulomatous disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:systemic iron overload due to ineffective erythropoiesis
n1=Lester (signe de) | n2=en:systemic iron overload due to ineffective erythropoiesis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:t-cell lymphopenia is more severe early in life
n1=Lester (signe de) | n2=en:t-cell lymphopenia is more severe early in life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:teeth may undergo post-eruptive changes
n1=Lester (signe de) | n2=en:teeth may undergo post-eruptive changes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:telangiectases persist in adulthood
n1=Lester (signe de) | n2=en:telangiectases persist in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:telangiectasia become evident between the second and eighth year of life
n1=Lester (signe de) | n2=en:telangiectasia become evident between the second and eighth year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:temperature instability
n1=Lester (signe de) | n2=en:temperature instability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tendency to lighter pigmentation than unaffected relatives
n1=Lester (signe de) | n2=en:tendency to lighter pigmentation than unaffected relatives | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:term infants generally die within hours of birth, but 1 patient was kept alive for 13 months with ventilatory support
n1=Lester (signe de) | n2=en:term infants generally die within hours of birth, but 1 patient was kept alive for 13 months with ventilatory support | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the acronym midas is microphthalmia, dermal aplasia, sclerocornea
n1=Lester (signe de) | n2=en:the acronym midas is microphthalmia, dermal aplasia, sclerocornea | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the characteristic changes in the spine resolve by adolescence
n1=Lester (signe de) | n2=en:the characteristic changes in the spine resolve by adolescence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the familial form of pityriasis rubra pilaris is generally resistant to treatment and persists
n1=Lester (signe de) | n2=en:the familial form of pityriasis rubra pilaris is generally resistant to treatment and persists | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the frequency is estimated at 1/20,000 to 1/50,000 births
n1=Lester (signe de) | n2=en:the frequency is estimated at 1/20,000 to 1/50,000 births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the lower the s-ado:saicar ratio, the more severe the phenotype
n1=Lester (signe de) | n2=en:the lower the s-ado:saicar ratio, the more severe the phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the majority of female heterozygotes reveal ophthalmologic abnormalities - multiple, micropunctate, gray lens opacities or single, dense posterior cataract
n1=Lester (signe de) | n2=en:the majority of female heterozygotes reveal ophthalmologic abnormalities - multiple, micropunctate, gray lens opacities or single, dense posterior cataract | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the majority of patients (~95%) have 1 of 3 mtdna point mutations (g3460a 516000.0001, g11778a 516003.0001, or t14484c 516006.0001)
n1=Lester (signe de) | n2=en:the majority of patients (~95%) have 1 of 3 mtdna point mutations (g3460a 516000.0001, g11778a 516003.0001, or t14484c 516006.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the most studied group is efe pygmies from ituri forest in northeast zaire
n1=Lester (signe de) | n2=en:the most studied group is efe pygmies from ituri forest in northeast zaire | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the mttl1 c.3243a-g transition (590050.0001) is the most common mutation
n1=Lester (signe de) | n2=en:the mttl1 c.3243a-g transition (590050.0001) is the most common mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the presence of an hspa9 variant (dbsnp rs10117) in trans may be required for expression of the clinical phenotype (pseudodominant inheritance)
n1=Lester (signe de) | n2=en:the presence of an hspa9 variant (dbsnp rs10117) in trans may be required for expression of the clinical phenotype (pseudodominant inheritance) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:the relationship of central core disease to moderate multiminicore with hand involvement is unclear, for a description of classic multiminicore disease, see 602771
n1=Lester (signe de) | n2=en:the relationship of central core disease to moderate multiminicore with hand involvement is unclear, for a description of classic multiminicore disease, see 602771 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:therapy is placement of implantable cardioverter defibrillator (icd)
n1=Lester (signe de) | n2=en:therapy is placement of implantable cardioverter defibrillator (icd) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:therapy-induced dyskinesias
n1=Lester (signe de) | n2=en:therapy-induced dyskinesias | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:there are several subtypes
n1=Lester (signe de) | n2=en:there are several subtypes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thiamine supplementation may be beneficial
n1=Lester (signe de) | n2=en:thiamine supplementation may be beneficial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thin, fine hair described in few individuals
n1=Lester (signe de) | n2=en:thin, fine hair described in few individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:this patient died at age 2 years
n1=Lester (signe de) | n2=en:this patient died at age 2 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:this patient died at age 8 months
n1=Lester (signe de) | n2=en:this patient died at age 8 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:this specific disorder has been described in 1 family (ke)
n1=Lester (signe de) | n2=en:this specific disorder has been described in 1 family (ke) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thoracic abnormalities tend to improve with age
n1=Lester (signe de) | n2=en:thoracic abnormalities tend to improve with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thorax anomaly ameliorates with age (in some patients)
n1=Lester (signe de) | n2=en:thorax anomaly ameliorates with age (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:those who survive initial acute episode have no recurrence of hepatic involvement, but may have persistent hypotonia
n1=Lester (signe de) | n2=en:those who survive initial acute episode have no recurrence of hepatic involvement, but may have persistent hypotonia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:those with intermediate repeat expansions show reduced penetrance
n1=Lester (signe de) | n2=en:those with intermediate repeat expansions show reduced penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:those with larger deletions of chromosome 2q23.1 tend to have more dysmorphic features
n1=Lester (signe de) | n2=en:those with larger deletions of chromosome 2q23.1 tend to have more dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three affected sibs have been reported
n1=Lester (signe de) | n2=en:three affected sibs have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three amish patients have been reported (as of february 2012)
n1=Lester (signe de) | n2=en:three amish patients have been reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three distinct clinical forms - endemic (equatorial africa), sporadic, and immunodeficiency-associated (e.g., hiv infection)
n1=Lester (signe de) | n2=en:three distinct clinical forms - endemic (equatorial africa), sporadic, and immunodeficiency-associated (e.g., hiv infection) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families described (last curated january 2014)
n1=Lester (signe de) | n2=en:three families described (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (as of 28 june 2011)
n1=Lester (signe de) | n2=en:three families have been reported (as of 28 june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (as of december 2011)
n1=Lester (signe de) | n2=en:three families have been reported (as of december 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (as of september 2011)
n1=Lester (signe de) | n2=en:three families have been reported (as of september 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (last curated april 2011)
n1=Lester (signe de) | n2=en:three families have been reported (last curated april 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (last curated august 2012)
n1=Lester (signe de) | n2=en:three families have been reported (last curated august 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (last curated july 2013)
n1=Lester (signe de) | n2=en:three families have been reported (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (last curated november 2010)
n1=Lester (signe de) | n2=en:three families have been reported (last curated november 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families have been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:three families have been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three families of ashkenazi jewish descent have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:three families of ashkenazi jewish descent have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three fetuses from 1 family have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:three fetuses from 1 family have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three forms of cjd: acquired (including variant), sporadic, and inherited
n1=Lester (signe de) | n2=en:three forms of cjd: acquired (including variant), sporadic, and inherited | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three girls from 2 unrelated families have been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:three girls from 2 unrelated families have been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three main clinical forms
n1=Lester (signe de) | n2=en:three main clinical forms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three main phenotypes
n1=Lester (signe de) | n2=en:three main phenotypes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three major clinical forms are apparent
n1=Lester (signe de) | n2=en:three major clinical forms are apparent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three males in 1 family have been reported (last curated august 2012)
n1=Lester (signe de) | n2=en:three males in 1 family have been reported (last curated august 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three out of 4 reported patients died (last curated may 2014)
n1=Lester (signe de) | n2=en:three out of 4 reported patients died (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients (2 related) reported (last curated march 2013)
n1=Lester (signe de) | n2=en:three patients (2 related) reported (last curated march 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients (2 sisters and 1 unrelated female) have been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:three patients (2 sisters and 1 unrelated female) have been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients from 1 french canadian family have been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:three patients from 1 french canadian family have been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients from 1 mexican family has been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:three patients from 1 mexican family has been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients from 2 families have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:three patients from 2 families have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients from 2 unrelated families have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:three patients from 2 unrelated families have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients from 2 unrelated families have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:three patients from 2 unrelated families have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been described (last curated january 2013)
n1=Lester (signe de) | n2=en:three patients have been described (last curated january 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported
n1=Lester (signe de) | n2=en:three patients have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported (as of august 2011)
n1=Lester (signe de) | n2=en:three patients have been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported (as of february 2012)
n1=Lester (signe de) | n2=en:three patients have been reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported (as of november 2010)
n1=Lester (signe de) | n2=en:three patients have been reported (as of november 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported (as of october 2009)
n1=Lester (signe de) | n2=en:three patients have been reported (as of october 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:three patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients in one family have been reported (as of october 2011), and only one mutation carrier exhibited mental retardation and ataxia
n1=Lester (signe de) | n2=en:three patients in one family have been reported (as of october 2011), and only one mutation carrier exhibited mental retardation and ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients reported, one with a wdpcp mutation (last curated january 2015)
n1=Lester (signe de) | n2=en:three patients reported, one with a wdpcp mutation (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three patients with sox 18 mutations from 2 unrelated families have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:three patients with sox 18 mutations from 2 unrelated families have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three sibs born of consanguineous arab parents have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:three sibs born of consanguineous arab parents have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three sibs from one consanguineous turkish family with an slc9a1 mutation has been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:three sibs from one consanguineous turkish family with an slc9a1 mutation has been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three sibs in one consanguineous iranian family have been described (last curated march 2015)
n1=Lester (signe de) | n2=en:three sibs in one consanguineous iranian family have been described (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three stages of disease progression - stage 1 (subclinical), stage 2 (early myoclonic), stage 3 (disabling myoclonic)
n1=Lester (signe de) | n2=en:three stages of disease progression - stage 1 (subclinical), stage 2 (early myoclonic), stage 3 (disabling myoclonic) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three subtypes of pfeiffer syndrome have been described - type 1: 'mild' autosomal dominant
n1=Lester (signe de) | n2=en:three subtypes of pfeiffer syndrome have been described - type 1: 'mild' autosomal dominant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three times more common in males
n1=Lester (signe de) | n2=en:three times more common in males | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three type of cystinosis are recognized - infantile nephropathic (219800), juvenile or adolescent nephropathic (219900), and adult nonnephropathic (219750)
n1=Lester (signe de) | n2=en:three type of cystinosis are recognized - infantile nephropathic (219800), juvenile or adolescent nephropathic (219900), and adult nonnephropathic (219750) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three types of cystinosis are recognized
n1=Lester (signe de) | n2=en:three types of cystinosis are recognized | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three types of pct: type i (176090) sporadic, presents in adults: types ii and iii (176100) familial, presents in childhood
n1=Lester (signe de) | n2=en:three types of pct: type i (176090) sporadic, presents in adults: types ii and iii (176100) familial, presents in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated caucasian patients have been reported (as of january 2012)
n1=Lester (signe de) | n2=en:three unrelated caucasian patients have been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated consanguineous families (libyan, egyptian, and pakistani origin) have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:three unrelated consanguineous families (libyan, egyptian, and pakistani origin) have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (as of june 2011)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (as of june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated june 2012)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated june 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated families have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:three unrelated families have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated french families have been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:three unrelated french families have been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated girls have been reported (as of july 2011)
n1=Lester (signe de) | n2=en:three unrelated girls have been reported (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated males have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:three unrelated males have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated january 2010)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated january 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated july 2013)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients have been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:three unrelated patients have been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated patients with the same de novo mutation have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:three unrelated patients with the same de novo mutation have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three unrelated probands have been reported (last curated january 2016)
n1=Lester (signe de) | n2=en:three unrelated probands have been reported (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:three variants distinguished by age of onset - infantile ( onset before age 2), juvenile (onset in childhood), and adult
n1=Lester (signe de) | n2=en:three variants distinguished by age of onset - infantile ( onset before age 2), juvenile (onset in childhood), and adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thromboembolism is the most common cause of death
n1=Lester (signe de) | n2=en:thromboembolism is the most common cause of death | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thrombosis triggered by pregnancy, oral contraceptives, trauma, surgery
n1=Lester (signe de) | n2=en:thrombosis triggered by pregnancy, oral contraceptives, trauma, surgery | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:thyroid carcinoma
n1=Lester (signe de) | n2=en:thyroid carcinoma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:time of analysis:tmstp:pt:xxx:qn
n1=Lester (signe de) | n2=en:time of analysis:tmstp:pt:xxx:qn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:toe-walking gait
n1=Lester (signe de) | n2=en:toe-walking gait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tooth agenesis ranges from 1 missing tooth to marked oligodontia
n1=Lester (signe de) | n2=en:tooth agenesis ranges from 1 missing tooth to marked oligodontia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:torso and upper body remain normal in shape and contour
n1=Lester (signe de) | n2=en:torso and upper body remain normal in shape and contour | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:toxicologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:toxicologist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:transfusion of plasma, which has apoc-ii, causes decrease in plasma triglycerides
n1=Lester (signe de) | n2=en:transfusion of plasma, which has apoc-ii, causes decrease in plasma triglycerides | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:trauma may accelerate symptoms
n1=Lester (signe de) | n2=en:trauma may accelerate symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:trauma, anxiety, and/or stress can precipitate or aggravate edema
n1=Lester (signe de) | n2=en:trauma, anxiety, and/or stress can precipitate or aggravate edema | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:trauma, im injection, surgery can be foci of ectopic ossification
n1=Lester (signe de) | n2=en:trauma, im injection, surgery can be foci of ectopic ossification | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with betaine, especially for pyridoxine nonresponders
n1=Lester (signe de) | n2=en:treatment with betaine, especially for pyridoxine nonresponders | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with bh4 is effective
n1=Lester (signe de) | n2=en:treatment with bh4 is effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with coq10 may result in some clinical improvement
n1=Lester (signe de) | n2=en:treatment with coq10 may result in some clinical improvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with dichloroacetate (dca) prolongs survival
n1=Lester (signe de) | n2=en:treatment with dichloroacetate (dca) prolongs survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with enzyme replacement therapy
n1=Lester (signe de) | n2=en:treatment with enzyme replacement therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with folinic acid offers some benefit for anemia and seizure control
n1=Lester (signe de) | n2=en:treatment with folinic acid offers some benefit for anemia and seizure control | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with hematopoietic stem cell transplant if diagnosed at < 24 months of age
n1=Lester (signe de) | n2=en:treatment with hematopoietic stem cell transplant if diagnosed at < 24 months of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with levodopa is not effective
n1=Lester (signe de) | n2=en:treatment with levodopa is not effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with oral coenzyme q may ameliorate symptoms
n1=Lester (signe de) | n2=en:treatment with oral coenzyme q may ameliorate symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with oral folic acid can ameliorate, resolve, or prevent clinical symptoms and myelination defects
n1=Lester (signe de) | n2=en:treatment with oral folic acid can ameliorate, resolve, or prevent clinical symptoms and myelination defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with oral steroids can restore hearing during episodes of hearing loss and tinnitus
n1=Lester (signe de) | n2=en:treatment with oral steroids can restore hearing during episodes of hearing loss and tinnitus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with polyethylene glycol-modified bovine ada, bone marrow transplantation, and/or gene therapy
n1=Lester (signe de) | n2=en:treatment with polyethylene glycol-modified bovine ada, bone marrow transplantation, and/or gene therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with riboflavin has been helpful in some patients
n1=Lester (signe de) | n2=en:treatment with riboflavin has been helpful in some patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with serine and glycine replacement may alleviate features if started at birth
n1=Lester (signe de) | n2=en:treatment with serine and glycine replacement may alleviate features if started at birth | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with sulfonylurea can be effective
n1=Lester (signe de) | n2=en:treatment with sulfonylurea can be effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with tnf inhibitors may be beneficial
n1=Lester (signe de) | n2=en:treatment with tnf inhibitors may be beneficial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:treatment with vitamin d and phosphate is effective
n1=Lester (signe de) | n2=en:treatment with vitamin d and phosphate is effective | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tremor is aggravated by emotional stress
n1=Lester (signe de) | n2=en:tremor is aggravated by emotional stress | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tremor is aggravated by low glucose or light
n1=Lester (signe de) | n2=en:tremor is aggravated by low glucose or light | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tremor may be elicited by movement or postural maintenance
n1=Lester (signe de) | n2=en:tremor may be elicited by movement or postural maintenance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tremors develop after seizures
n1=Lester (signe de) | n2=en:tremors develop after seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:triggered by exercise, fasting, or other metabolic stresses
n1=Lester (signe de) | n2=en:triggered by exercise, fasting, or other metabolic stresses | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:triggered by minor head trauma
n1=Lester (signe de) | n2=en:triggered by minor head trauma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:triggered by pregnancy, drugs, chemotherapy, cancer, bone marrow transplantation, infection
n1=Lester (signe de) | n2=en:triggered by pregnancy, drugs, chemotherapy, cancer, bone marrow transplantation, infection | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:triggered by use of antibiotics (24% of cases) and nonsteroidal antiinflammatory drugs (18% of cases)
n1=Lester (signe de) | n2=en:triggered by use of antibiotics (24% of cases) and nonsteroidal antiinflammatory drugs (18% of cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:triggers are variable, even within a family
n1=Lester (signe de) | n2=en:triggers are variable, even within a family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:trp2 (langer-giedion syndrome, 150230) is a microdeletion syndrome involving deletions of both the trps1 (604386) and ext1 (608177) genes
n1=Lester (signe de) | n2=en:trp2 (langer-giedion syndrome, 150230) is a microdeletion syndrome involving deletions of both the trps1 (604386) and ext1 (608177) genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:trps2 (langer-giedion syndrome, 150230) is a microdeletion syndrome involving deletions of both trps1 (190350) and ext1 (608177) genes
n1=Lester (signe de) | n2=en:trps2 (langer-giedion syndrome, 150230) is a microdeletion syndrome involving deletions of both trps1 (190350) and ext1 (608177) genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:truncating mutations in crebbp found in 10% of patients
n1=Lester (signe de) | n2=en:truncating mutations in crebbp found in 10% of patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tumor predisposition syndrome
n1=Lester (signe de) | n2=en:tumor predisposition syndrome | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tumor suppressor genes
n1=Lester (signe de) | n2=en:tumor suppressor genes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tumors are microsatellite stable
n1=Lester (signe de) | n2=en:tumors are microsatellite stable | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tumors may show spontaneous regression
n1=Lester (signe de) | n2=en:tumors may show spontaneous regression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:tumors usually develop between 40 and 60 years of age
n1=Lester (signe de) | n2=en:tumors usually develop between 40 and 60 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:twelve or more lesions per eye in individuals over 60 years of age
n1=Lester (signe de) | n2=en:twelve or more lesions per eye in individuals over 60 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:twenty-five percent of affected babies are stillborn
n1=Lester (signe de) | n2=en:twenty-five percent of affected babies are stillborn | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:twinning due to superfetation
n1=Lester (signe de) | n2=en:twinning due to superfetation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two adult sibs have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:two adult sibs have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two affected females have been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:two affected females have been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two affected sibs have been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:two affected sibs have been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two alpha-globin genes - 5-prime or alpha-2 and 3-prime or alpha-1
n1=Lester (signe de) | n2=en:two alpha-globin genes - 5-prime or alpha-2 and 3-prime or alpha-1 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two arab muslim families have been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:two arab muslim families have been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two autosomal dominant families have been reported (as of may 2011)
n1=Lester (signe de) | n2=en:two autosomal dominant families have been reported (as of may 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two brothers in a french family have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:two brothers in a french family have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two chinese sisters and one chinese woman have been described (last curated april 2014)
n1=Lester (signe de) | n2=en:two chinese sisters and one chinese woman have been described (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two clinical forms - type i (deficiency of b5r is isolated to erythrocytes) and type ii (deficiency of b5r in all cell types)
n1=Lester (signe de) | n2=en:two clinical forms - type i (deficiency of b5r is isolated to erythrocytes) and type ii (deficiency of b5r in all cell types) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two clinical presentations - solely neurologic form and a neurologic-multivisceral form
n1=Lester (signe de) | n2=en:two clinical presentations - solely neurologic form and a neurologic-multivisceral form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two complementation groups - pcca (secondary to defects in the alpha chain of pcc, 232000) and pccbc (secondary to defects in the beta subunit of pcc, 232050)
n1=Lester (signe de) | n2=en:two complementation groups - pcca (secondary to defects in the alpha chain of pcc, 232000) and pccbc (secondary to defects in the beta subunit of pcc, 232050) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous families with 2 patients each have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:two consanguineous families with 2 patients each have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous families with two affected sibs each have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:two consanguineous families with two affected sibs each have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous lebanese families have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:two consanguineous lebanese families have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous pakistan families have been described
n1=Lester (signe de) | n2=en:two consanguineous pakistan families have been described | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous turkish families have been reported (as of august 2011)
n1=Lester (signe de) | n2=en:two consanguineous turkish families have been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two consanguineous turkish families have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:two consanguineous turkish families have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two different phenotypes exist - severe phenotype (early infantile onset, epileptic encephalopathy and often cardiomyopathy) and mild phenotype (more variable clinical presentation)
n1=Lester (signe de) | n2=en:two different phenotypes exist - severe phenotype (early infantile onset, epileptic encephalopathy and often cardiomyopathy) and mild phenotype (more variable clinical presentation) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families described (last curated july 2013)
n1=Lester (signe de) | n2=en:two families described (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families described (last curated november 2013)
n1=Lester (signe de) | n2=en:two families described (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families each with two affected children have been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:two families each with two affected children have been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families from the tamil nedu region of eastern india have been described (last curated november 2015)
n1=Lester (signe de) | n2=en:two families from the tamil nedu region of eastern india have been described (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (as of 6/2011)
n1=Lester (signe de) | n2=en:two families have been reported (as of 6/2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (as of curation date april 2014)
n1=Lester (signe de) | n2=en:two families have been reported (as of curation date april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (as of june 2011)
n1=Lester (signe de) | n2=en:two families have been reported (as of june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (as of may 2011)
n1=Lester (signe de) | n2=en:two families have been reported (as of may 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:two families have been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated december 2010)
n1=Lester (signe de) | n2=en:two families have been reported (last curated december 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated december 2013)
n1=Lester (signe de) | n2=en:two families have been reported (last curated december 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:two families have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:two families have been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:two families have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families have been reported (september 2010)
n1=Lester (signe de) | n2=en:two families have been reported (september 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families of canadian origin have been reported (last curated may 2012)
n1=Lester (signe de) | n2=en:two families of canadian origin have been reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families of french-canadian origin have been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:two families of french-canadian origin have been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families reported (last curated february 2013)
n1=Lester (signe de) | n2=en:two families reported (last curated february 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families reported (last curated september 2012)
n1=Lester (signe de) | n2=en:two families reported (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families with confirmed adra2b mutations have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two families with confirmed adra2b mutations have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two families with different phenotypes have been reported (as of september 2010)
n1=Lester (signe de) | n2=en:two families with different phenotypes have been reported (as of september 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two fetuses from terminated pregnancies in 1 family have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:two fetuses from terminated pregnancies in 1 family have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two fetuses have been reported (as of august 2011)
n1=Lester (signe de) | n2=en:two fetuses have been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two forms: iia (severe) and iib (mild)
n1=Lester (signe de) | n2=en:two forms: iia (severe) and iib (mild) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two japanese brothers have been reported (as of september 2011)
n1=Lester (signe de) | n2=en:two japanese brothers have been reported (as of september 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two japanese families have been reported (as of february 2012)
n1=Lester (signe de) | n2=en:two japanese families have been reported (as of february 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two japanese patients have been reported (last curated march 2013)
n1=Lester (signe de) | n2=en:two japanese patients have been reported (last curated march 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two jordanian sibs have been reported (last curated november 2014)
n1=Lester (signe de) | n2=en:two jordanian sibs have been reported (last curated november 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two loci control synthesis of c4, c4a (120810) and c4b (120820)
n1=Lester (signe de) | n2=en:two loci control synthesis of c4, c4a (120810) and c4b (120820) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two loci described - eec1 (129900) and eec3 (604292)
n1=Lester (signe de) | n2=en:two loci described - eec1 (129900) and eec3 (604292) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two main groups defined by age at onset: childhood (1 to 3 years) and onset after puberty
n1=Lester (signe de) | n2=en:two main groups defined by age at onset: childhood (1 to 3 years) and onset after puberty | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two main phenotypes, early-onset with neurologic defects and early-adult onset with gout
n1=Lester (signe de) | n2=en:two main phenotypes, early-onset with neurologic defects and early-adult onset with gout | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two main phenotypes, metabolic and neurologic
n1=Lester (signe de) | n2=en:two main phenotypes, metabolic and neurologic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two main phenotypes, severe and mild
n1=Lester (signe de) | n2=en:two main phenotypes, severe and mild | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two main presentations
n1=Lester (signe de) | n2=en:two main presentations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two mother and child pairs have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:two mother and child pairs have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two of 3 patients became wheelchair-bound
n1=Lester (signe de) | n2=en:two of 3 patients became wheelchair-bound | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two of 6 patients became wheelchair-bound by age 20 years
n1=Lester (signe de) | n2=en:two of 6 patients became wheelchair-bound by age 20 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two pairs of sisters described from two canadian dariusleut hutterite families (last curated september 2013)
n1=Lester (signe de) | n2=en:two pairs of sisters described from two canadian dariusleut hutterite families (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two pakistani families have been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:two pakistani families have been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two pakistani families reported (last curated july 2014)
n1=Lester (signe de) | n2=en:two pakistani families reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two pakistani families with a homozygous crybb3 mutation have been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:two pakistani families with a homozygous crybb3 mutation have been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients from 1 italian family have been reported (as of april 2010)
n1=Lester (signe de) | n2=en:two patients from 1 italian family have been reported (as of april 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients from spain have been reported (as of january 2012)
n1=Lester (signe de) | n2=en:two patients from spain have been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients have been reported
n1=Lester (signe de) | n2=en:two patients have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients have been reported (as of august 2010)
n1=Lester (signe de) | n2=en:two patients have been reported (as of august 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients have been reported (as of august 2011)
n1=Lester (signe de) | n2=en:two patients have been reported (as of august 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients in one ashkenzai jewish family described (last curated june 2014)
n1=Lester (signe de) | n2=en:two patients in one ashkenzai jewish family described (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients reported (last curated may 2013)
n1=Lester (signe de) | n2=en:two patients reported (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients required liver transplantation
n1=Lester (signe de) | n2=en:two patients required liver transplantation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients with a wws phenotype have been reported
n1=Lester (signe de) | n2=en:two patients with a wws phenotype have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients with heterozygous prickle1 mutations and limited clinical and familial details have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:two patients with heterozygous prickle1 mutations and limited clinical and familial details have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients with point mutations in rad21 have been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:two patients with point mutations in rad21 have been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two patients without cardiomyopathy or cataracts have been reported
n1=Lester (signe de) | n2=en:two patients without cardiomyopathy or cataracts have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two peaks of onset, childhood and adult
n1=Lester (signe de) | n2=en:two peaks of onset, childhood and adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two presentations - rapid, fatal disorder of infancy and slowly progressive muscular disorder of childhood
n1=Lester (signe de) | n2=en:two presentations - rapid, fatal disorder of infancy and slowly progressive muscular disorder of childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two probands have been reported
n1=Lester (signe de) | n2=en:two probands have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two related patients have been reported (as of november 2010)
n1=Lester (signe de) | n2=en:two related patients have been reported (as of november 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two siblings of consanguineous turkish parents have been reported
n1=Lester (signe de) | n2=en:two siblings of consanguineous turkish parents have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs and an unrelated fetus have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:two sibs and an unrelated fetus have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs born of consanguineous moroccan parents have been reported (last curated may 2012)
n1=Lester (signe de) | n2=en:two sibs born of consanguineous moroccan parents have been reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs died before 2 years of age
n1=Lester (signe de) | n2=en:two sibs died before 2 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs each from unrelated saudi arabian families reported (last curated may 2014)
n1=Lester (signe de) | n2=en:two sibs each from unrelated saudi arabian families reported (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs from a consanguineous syrian family have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:two sibs from a consanguineous syrian family have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated july 2013)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated july 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated may 2013)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated november 2012)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs have been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:two sibs have been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sibs, a boy and a girl, have been reported (as of july 2009)
n1=Lester (signe de) | n2=en:two sibs, a boy and a girl, have been reported (as of july 2009) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sisters born of consanguineous palestinian parents have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:two sisters born of consanguineous palestinian parents have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sisters have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:two sisters have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sisters have been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:two sisters have been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two sisters, born of consanguineous moroccan parents, have been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:two sisters, born of consanguineous moroccan parents, have been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two subtypes - seminoma and nonseminoma
n1=Lester (signe de) | n2=en:two subtypes - seminoma and nonseminoma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two subtypes based on pathologic findings of 'balloon cells' - type iia, absence of balloon cells and type iib, presence of balloon cells
n1=Lester (signe de) | n2=en:two subtypes based on pathologic findings of 'balloon cells' - type iia, absence of balloon cells and type iib, presence of balloon cells | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two subtypes noninflammatory type a and inflammatory type b
n1=Lester (signe de) | n2=en:two subtypes noninflammatory type a and inflammatory type b | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two subtypes, episodic (85% of patients) and chronic (15%)
n1=Lester (signe de) | n2=en:two subtypes, episodic (85% of patients) and chronic (15%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two thirds of patients are female
n1=Lester (signe de) | n2=en:two thirds of patients are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two types - lethal neonatal and less severe, late onset
n1=Lester (signe de) | n2=en:two types - lethal neonatal and less severe, late onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two types - one with premature ovarian failure (bpes type 1) and one without pof (bpes type 2)
n1=Lester (signe de) | n2=en:two types - one with premature ovarian failure (bpes type 1) and one without pof (bpes type 2) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two types - severe infantile form (type i) and milder form (type ii)
n1=Lester (signe de) | n2=en:two types - severe infantile form (type i) and milder form (type ii) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two types of platelet gpiv deficiency - type i, absence gpiv on monocytes (173510.0005) and type ii, presence gpiv on monocytes (173510.0001)
n1=Lester (signe de) | n2=en:two types of platelet gpiv deficiency - type i, absence gpiv on monocytes (173510.0005) and type ii, presence gpiv on monocytes (173510.0001) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two types, type i or type a (classical cockayne syndrome, 216400) and type ii or type b (severe cockayne syndrome, 133540)
n1=Lester (signe de) | n2=en:two types, type i or type a (classical cockayne syndrome, 216400) and type ii or type b (severe cockayne syndrome, 133540) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated boys have been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:two unrelated boys have been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated boys reported with relatively mild phenotype (last curated may 2012)
n1=Lester (signe de) | n2=en:two unrelated boys reported with relatively mild phenotype (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated chinese families have been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:two unrelated chinese families have been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated chinese families have been reported (last curated november 2013)
n1=Lester (signe de) | n2=en:two unrelated chinese families have been reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families (saudi arabian and israeli palestinian) have been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families (saudi arabian and israeli palestinian) have been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families have been reported (last curated january 2016)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families have been reported (last curated january 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated consanguineous families have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:two unrelated consanguineous families have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families and 1 isolated patient have been reported (last curated june 2012)
n1=Lester (signe de) | n2=en:two unrelated families and 1 isolated patient have been reported (last curated june 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (as of july 2011)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (as of july 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (as of october 2010)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (as of october 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated august 2013)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated december 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated december 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated february 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated february 2016)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated february 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated january 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated july 2012)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated july 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated june 2012)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated june 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated june 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated june 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated march 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated march 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated may 2013)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated may 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated may 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated may 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated november 2012)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated november 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated november 2013)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated november 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated november 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated november 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated october 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated october 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated september 2012)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported (last curated september 2015)
n1=Lester (signe de) | n2=en:two unrelated families have been reported (last curated september 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported to have hpca mutations
n1=Lester (signe de) | n2=en:two unrelated families have been reported to have hpca mutations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families have been reported, 1 showing autosomal dominant inheritance and 1 showing autosomal recessive inheritance (last curated february 2014)
n1=Lester (signe de) | n2=en:two unrelated families have been reported, 1 showing autosomal dominant inheritance and 1 showing autosomal recessive inheritance (last curated february 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families of european descent have been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:two unrelated families of european descent have been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated families, one north african descent and one of italian descent, have been reported (last curated august 2014)
n1=Lester (signe de) | n2=en:two unrelated families, one north african descent and one of italian descent, have been reported (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated girls reported (last curated october 2013)
n1=Lester (signe de) | n2=en:two unrelated girls reported (last curated october 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated individuals have been reported (last curated january 2014)
n1=Lester (signe de) | n2=en:two unrelated individuals have been reported (last curated january 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated japanese families have been reported (last curated september 2014)
n1=Lester (signe de) | n2=en:two unrelated japanese families have been reported (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated japanese patients have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two unrelated japanese patients have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated japanese patients have been reported (last curated may 2012)
n1=Lester (signe de) | n2=en:two unrelated japanese patients have been reported (last curated may 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated men have been reported (last curated march 2016)
n1=Lester (signe de) | n2=en:two unrelated men have been reported (last curated march 2016) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients had multiple congenital anomalies and died in early infancy
n1=Lester (signe de) | n2=en:two unrelated patients had multiple congenital anomalies and died in early infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported
n1=Lester (signe de) | n2=en:two unrelated patients have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (as of august 2010)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (as of august 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (as of january 2012)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (as of june 2011)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (as of june 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (as of may 2011)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (as of may 2011) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated april 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated april 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated april 2014)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated april 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated april 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated april 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated august 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated august 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated august 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated december 2010)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated december 2010) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated december 2012)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated december 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated december 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated december 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated february 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated february 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated january 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated january 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated july 2014)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated july 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated july 2014) onset in infancy or childhood
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated july 2014) onset in infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated july 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated july 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated june 2012)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated june 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated june 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated june 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated june 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated june 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated march 2014)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated march 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated may 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated may 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated october 2012)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated october 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated october 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated october 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated october 2015)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated october 2015) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported (last curated september 2013)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported (last curated september 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported, 1 with normal neurologic development and the other with profound neurologic abnormalities (last curated august 2014)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported, 1 with normal neurologic development and the other with profound neurologic abnormalities (last curated august 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients have been reported, but nadk2 mutation has only been confirmed in 1 patient (last curated september 2014)
n1=Lester (signe de) | n2=en:two unrelated patients have been reported, but nadk2 mutation has only been confirmed in 1 patient (last curated september 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients reported (last curated september 2012)
n1=Lester (signe de) | n2=en:two unrelated patients reported (last curated september 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with classic eds and a mutation in col1a1 (120150.0059) has been reported
n1=Lester (signe de) | n2=en:two unrelated patients with classic eds and a mutation in col1a1 (120150.0059) has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with confirmed mutations have been reported (as of january 2012)
n1=Lester (signe de) | n2=en:two unrelated patients with confirmed mutations have been reported (as of january 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with different phenotypes have been reported (as of march 2012)
n1=Lester (signe de) | n2=en:two unrelated patients with different phenotypes have been reported (as of march 2012) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with epileptic encephalopathy have been reported
n1=Lester (signe de) | n2=en:two unrelated patients with epileptic encephalopathy have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with pathogenic csf2rb mutations have been reported (last curated december 2014)
n1=Lester (signe de) | n2=en:two unrelated patients with pathogenic csf2rb mutations have been reported (last curated december 2014) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two unrelated patients with slightly different phenotypes have been reported (last curated august 2013)
n1=Lester (signe de) | n2=en:two unrelated patients with slightly different phenotypes have been reported (last curated august 2013) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:two-step mutation hypothesis (germline mutation followed by somatic mutation or two sequential somatic mutations)
n1=Lester (signe de) | n2=en:two-step mutation hypothesis (germline mutation followed by somatic mutation or two sequential somatic mutations) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 1 - associated with osteogenesis imperfecta (125490)
n1=Lester (signe de) | n2=en:type 1 - associated with osteogenesis imperfecta (125490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 1 porencephaly is usually unilateral and results from destructive lesions
n1=Lester (signe de) | n2=en:type 1 porencephaly is usually unilateral and results from destructive lesions | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2 - hereditary opalescent dentin, not associated with bone defect (125490)
n1=Lester (signe de) | n2=en:type 2 - hereditary opalescent dentin, not associated with bone defect (125490) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2 porencephaly is usually symmetrical and results from developmental malformation
n1=Lester (signe de) | n2=en:type 2 porencephaly is usually symmetrical and results from developmental malformation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2: cloverleaf skull, elbow ankylosis, early demise, sporadic
n1=Lester (signe de) | n2=en:type 2: cloverleaf skull, elbow ankylosis, early demise, sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2a is characterized by deficiency of high molecular weight monomers
n1=Lester (signe de) | n2=en:type 2a is characterized by deficiency of high molecular weight monomers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2b is characterized by increased affinity for platelet glycoprotein 1b
n1=Lester (signe de) | n2=en:type 2b is characterized by increased affinity for platelet glycoprotein 1b | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2cb is characterized by defective binding affinity for collagen types i and iii
n1=Lester (signe de) | n2=en:type 2cb is characterized by defective binding affinity for collagen types i and iii | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2m is characterized by decreased platelet adhesion in the presence of high molecular weight monomers
n1=Lester (signe de) | n2=en:type 2m is characterized by decreased platelet adhesion in the presence of high molecular weight monomers | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2n is characterized by decreased binding affinity for factor viii
n1=Lester (signe de) | n2=en:type 2n is characterized by decreased binding affinity for factor viii | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 2n shows autosomal recessive inheritance
n1=Lester (signe de) | n2=en:type 2n shows autosomal recessive inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 3 - brandywine isolate opalescent dentin (125500)
n1=Lester (signe de) | n2=en:type 3 - brandywine isolate opalescent dentin (125500) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type 3: craniosynostosis, early demise, sporadic
n1=Lester (signe de) | n2=en:type 3: craniosynostosis, early demise, sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type a characterized by progressive myoclonic epilepsy
n1=Lester (signe de) | n2=en:type a characterized by progressive myoclonic epilepsy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type b characterized by dementia, motor disturbances, and facial dyskinesia
n1=Lester (signe de) | n2=en:type b characterized by dementia, motor disturbances, and facial dyskinesia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i b5r endemic in athabascan indians, navajo indians, and yakutsk natives of siberia
n1=Lester (signe de) | n2=en:type i b5r endemic in athabascan indians, navajo indians, and yakutsk natives of siberia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i has most severe manifestations by age 4-5 years
n1=Lester (signe de) | n2=en:type i has most severe manifestations by age 4-5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i is infantile-onset, severe
n1=Lester (signe de) | n2=en:type i is infantile-onset, severe | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i onset at 8 to 15 months of age after normal development
n1=Lester (signe de) | n2=en:type i onset at 8 to 15 months of age after normal development | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i patients have undetectable aprt activity and are homozygous or compound heterozygous for null alleles
n1=Lester (signe de) | n2=en:type i patients have undetectable aprt activity and are homozygous or compound heterozygous for null alleles | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type i sialidosis (cherry-red spot/myoclonus syndrome ) - mild disease, no dysmorphic features, onset in second decade
n1=Lester (signe de) | n2=en:type i sialidosis (cherry-red spot/myoclonus syndrome ) - mild disease, no dysmorphic features, onset in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type ii is adult-onset (kanzaki disease, 609242)
n1=Lester (signe de) | n2=en:type ii is adult-onset (kanzaki disease, 609242) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type ii is progressive and leads to shortened lifespan
n1=Lester (signe de) | n2=en:type ii is progressive and leads to shortened lifespan | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type ii patients are usually japanese and have significant aprt activity (10-25%)
n1=Lester (signe de) | n2=en:type ii patients are usually japanese and have significant aprt activity (10-25%) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type ii sialidosis - severe disease, dysmorphic features, variable onset (congenital or hydropic (in utero), infantile (1-12 months), juvenile (2-20 years))
n1=Lester (signe de) | n2=en:type ii sialidosis - severe disease, dysmorphic features, variable onset (congenital or hydropic (in utero), infantile (1-12 months), juvenile (2-20 years)) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type iia tends to have more severe phenotype with earlier onset
n1=Lester (signe de) | n2=en:type iia tends to have more severe phenotype with earlier onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type iii is intermediate form
n1=Lester (signe de) | n2=en:type iii is intermediate form | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type iiia has both liver and muscle involvement
n1=Lester (signe de) | n2=en:type iiia has both liver and muscle involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:type iiib liver involvement only (15% of all cases)
n1=Lester (signe de) | n2=en:type iiib liver involvement only (15% of all cases) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:types of psoriasis include - plaque, guttate, erythrodermic, pustular
n1=Lester (signe de) | n2=en:types of psoriasis include - plaque, guttate, erythrodermic, pustular | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:typical attacks last from seconds to minutes, but longer occurrences have been reported
n1=Lester (signe de) | n2=en:typical attacks last from seconds to minutes, but longer occurrences have been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:typical onset in adulthood
n1=Lester (signe de) | n2=en:typical onset in adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:typically no physical features of albright hereditary osteodystrophy (aho)
n1=Lester (signe de) | n2=en:typically no physical features of albright hereditary osteodystrophy (aho) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:typically sporadic occurrence
n1=Lester (signe de) | n2=en:typically sporadic occurrence | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:u-shaped pattern of temperature-dependent potassium flux (in some patients)
n1=Lester (signe de) | n2=en:u-shaped pattern of temperature-dependent potassium flux (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:u.s. frequency higher in blacks than whites
n1=Lester (signe de) | n2=en:u.s. frequency higher in blacks than whites | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:udp-galactose-4-epimerase deficiency in circulating blood cells only ('peripheral' or 'mild' form, usually asymptomatic)
n1=Lester (signe de) | n2=en:udp-galactose-4-epimerase deficiency in circulating blood cells only ('peripheral' or 'mild' form, usually asymptomatic) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ullrich congenital muscular dystrophy (254090) is an allelic disorder with autosomal recessive inheritance and a more severe phenotype
n1=Lester (signe de) | n2=en:ullrich congenital muscular dystrophy (254090) is an allelic disorder with autosomal recessive inheritance and a more severe phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ultrarapid metabolizers have multiple copies of the cyp2d6 gene (124030.0007)
n1=Lester (signe de) | n2=en:ultrarapid metabolizers have multiple copies of the cyp2d6 gene (124030.0007) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ultrasound detection in second trimester of pregnancy
n1=Lester (signe de) | n2=en:ultrasound detection in second trimester of pregnancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:unaffected individuals carry 3 to 14 repeats, whereas affected individuals carry 650 to 2,500 repeats
n1=Lester (signe de) | n2=en:unaffected individuals carry 3 to 14 repeats, whereas affected individuals carry 650 to 2,500 repeats | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:unbalanced chromosomal translocation carrier have thin body habitus, shallow orbital ridges, arched eyebrows, exophthalmia, ptosis, bilateral ophthalmoplegia, thin upper lip, kyphosis, pectus excavatum, and mental retardation
n1=Lester (signe de) | n2=en:unbalanced chromosomal translocation carrier have thin body habitus, shallow orbital ridges, arched eyebrows, exophthalmia, ptosis, bilateral ophthalmoplegia, thin upper lip, kyphosis, pectus excavatum, and mental retardation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:uncommon and rare features seen in the most severely affected patients
n1=Lester (signe de) | n2=en:uncommon and rare features seen in the most severely affected patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:uncommon disorder
n1=Lester (signe de) | n2=en:uncommon disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:uniparental disomy
n1=Lester (signe de) | n2=en:uniparental disomy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:unusual cabbage-like odor
n1=Lester (signe de) | n2=en:unusual cabbage-like odor | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:unusual skill with jigsaw puzzle
n1=Lester (signe de) | n2=en:unusual skill with jigsaw puzzle | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:up to 25% of patients are asymptomatic or mildly affected, suggesting incomplete penetrance
n1=Lester (signe de) | n2=en:up to 25% of patients are asymptomatic or mildly affected, suggesting incomplete penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:up to 50% of patients may have various additional congenital anomalies
n1=Lester (signe de) | n2=en:up to 50% of patients may have various additional congenital anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:up to 60% of female mutation carriers develop lobular breast cancer
n1=Lester (signe de) | n2=en:up to 60% of female mutation carriers develop lobular breast cancer | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:upper limb involvement in first decade
n1=Lester (signe de) | n2=en:upper limb involvement in first decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:upper limb involvement may occur later
n1=Lester (signe de) | n2=en:upper limb involvement may occur later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:upper limb involvement occur later
n1=Lester (signe de) | n2=en:upper limb involvement occur later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:upper limb involvement usually occurs later
n1=Lester (signe de) | n2=en:upper limb involvement usually occurs later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:upper urinary tract usually normal
n1=Lester (signe de) | n2=en:upper urinary tract usually normal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:urinalysis specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative
n1=Lester (signe de) | n2=en:urinalysis specialist review:impression/interpretation of study:point in time:to be specified in another part of the message:narrative | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:urine turns dark on standing and alkalinization
n1=Lester (signe de) | n2=en:urine turns dark on standing and alkalinization | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:user syndrome type ii (congenital moderate-severe deafness, normal vestibular dysfunction, and onset of retinitis pigmentosa in late second to early third decade) - 3 loci
n1=Lester (signe de) | n2=en:user syndrome type ii (congenital moderate-severe deafness, normal vestibular dysfunction, and onset of retinitis pigmentosa in late second to early third decade) - 3 loci | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:ush3 cases account for 40% of all usher patients in finland
n1=Lester (signe de) | n2=en:ush3 cases account for 40% of all usher patients in finland | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usher syndrome type i (congenital profound deafness, absent vestibular function, and prepubertal onset of retinitis pigmentosa) - 7 loci
n1=Lester (signe de) | n2=en:usher syndrome type i (congenital profound deafness, absent vestibular function, and prepubertal onset of retinitis pigmentosa) - 7 loci | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usher syndrome type iii (postlingual progressive deafness, variable vestibular dysfunction, and progressive retinitis pigmentosa with variable age of onset) - 1 locus
n1=Lester (signe de) | n2=en:usher syndrome type iii (postlingual progressive deafness, variable vestibular dysfunction, and progressive retinitis pigmentosa with variable age of onset) - 1 locus | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usual age of onset in the 20s and 30s
n1=Lester (signe de) | n2=en:usual age of onset in the 20s and 30s | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usual onset before age 6 years and death by age 20
n1=Lester (signe de) | n2=en:usual onset before age 6 years and death by age 20 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usual onset under age 30 years
n1=Lester (signe de) | n2=en:usual onset under age 30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually a manifestation of the carney complex (cnc1, 1609890)
n1=Lester (signe de) | n2=en:usually a manifestation of the carney complex (cnc1, 1609890) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually a sporadic disorder
n1=Lester (signe de) | n2=en:usually a sporadic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually adult onset
n1=Lester (signe de) | n2=en:usually adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually affects children
n1=Lester (signe de) | n2=en:usually affects children | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually asymptomatic
n1=Lester (signe de) | n2=en:usually asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually begins in feet and legs (peroneal distribution)
n1=Lester (signe de) | n2=en:usually begins in feet and legs (peroneal distribution) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually begins in feet and legs (peroneal distribution), but may progress to upper limbs
n1=Lester (signe de) | n2=en:usually begins in feet and legs (peroneal distribution), but may progress to upper limbs | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually clinically asymptomatic
n1=Lester (signe de) | n2=en:usually clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually death in utero or rarely in neonatal period
n1=Lester (signe de) | n2=en:usually death in utero or rarely in neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually fatal
n1=Lester (signe de) | n2=en:usually fatal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually fatal by age 5 years
n1=Lester (signe de) | n2=en:usually fatal by age 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually fatal in first 2 decades
n1=Lester (signe de) | n2=en:usually fatal in first 2 decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually fatal in infancy
n1=Lester (signe de) | n2=en:usually fatal in infancy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually fatal within the first few weeks of life
n1=Lester (signe de) | n2=en:usually fatal within the first few weeks of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually favorable response to treatment
n1=Lester (signe de) | n2=en:usually favorable response to treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually follows a static course or is slowly progressive
n1=Lester (signe de) | n2=en:usually follows a static course or is slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually lethal in the neonatal period
n1=Lester (signe de) | n2=en:usually lethal in the neonatal period | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually no increased fragility of hair
n1=Lester (signe de) | n2=en:usually no increased fragility of hair | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually occurs in children younger than 5 years
n1=Lester (signe de) | n2=en:usually occurs in children younger than 5 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually occurs in young adulthood
n1=Lester (signe de) | n2=en:usually occurs in young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually occurs in young adults
n1=Lester (signe de) | n2=en:usually occurs in young adults | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually poor response to steroid treatment
n1=Lester (signe de) | n2=en:usually poor response to steroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually presents in third to fourth decade (but onset can range from childhood to elderly)
n1=Lester (signe de) | n2=en:usually presents in third to fourth decade (but onset can range from childhood to elderly) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually progressive
n1=Lester (signe de) | n2=en:usually progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually shows early age at onset (range 1 to 7 years, mean 4.6 years)
n1=Lester (signe de) | n2=en:usually shows early age at onset (range 1 to 7 years, mean 4.6 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually sporadic
n1=Lester (signe de) | n2=en:usually sporadic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually sporadic disorder resulting from de novo 22q11.2 deletion
n1=Lester (signe de) | n2=en:usually sporadic disorder resulting from de novo 22q11.2 deletion | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually sporadic, but 1-2% of cases are familial
n1=Lester (signe de) | n2=en:usually sporadic, but 1-2% of cases are familial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually sporadic, few cases described with autosomal dominant inheritance
n1=Lester (signe de) | n2=en:usually sporadic, few cases described with autosomal dominant inheritance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:usually symptomatic in adulthood with history of weakness since infancy or childhood
n1=Lester (signe de) | n2=en:usually symptomatic in adulthood with history of weakness since infancy or childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:uterine leiomyomata are found in hereditary leiomyomatosis and renal cell cancer syndrome (150800)
n1=Lester (signe de) | n2=en:uterine leiomyomata are found in hereditary leiomyomatosis and renal cell cancer syndrome (150800) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variability in age of onset and severity of disease
n1=Lester (signe de) | n2=en:variability in age of onset and severity of disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variability in extent of dislocation of lens and/or displacement of pupil, both within families and between eyes in a single individual
n1=Lester (signe de) | n2=en:variability in extent of dislocation of lens and/or displacement of pupil, both within families and between eyes in a single individual | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable abnormalities
n1=Lester (signe de) | n2=en:variable abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at diagnosis
n1=Lester (signe de) | n2=en:variable age at diagnosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset
n1=Lester (signe de) | n2=en:variable age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (8 to 62 years)
n1=Lester (signe de) | n2=en:variable age at onset (8 to 62 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (birth to adolescence)
n1=Lester (signe de) | n2=en:variable age at onset (birth to adolescence) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (birth to adult)
n1=Lester (signe de) | n2=en:variable age at onset (birth to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (childhood to adult)
n1=Lester (signe de) | n2=en:variable age at onset (childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (childhood to adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (childhood to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (childhood to age 50)
n1=Lester (signe de) | n2=en:variable age at onset (childhood to age 50) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (earliest reported 7 years)
n1=Lester (signe de) | n2=en:variable age at onset (earliest reported 7 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (infant to adult)
n1=Lester (signe de) | n2=en:variable age at onset (infant to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (late childhood to adult)
n1=Lester (signe de) | n2=en:variable age at onset (late childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 10 to 50 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 10 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 14 to 50 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 14 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 15 to 60 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 15 to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 2 to 48 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 2 to 48 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 2 to 59 years, mean 24 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 2 to 59 years, mean 24 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 25 to 78 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 25 to 78 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 4 to 40 years, mostly in first or second decade)
n1=Lester (signe de) | n2=en:variable age at onset (range 4 to 40 years, mostly in first or second decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 6 to 54 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 6 to 54 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 8 to 60 years, mean 32)
n1=Lester (signe de) | n2=en:variable age at onset (range 8 to 60 years, mean 32) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range 9 to 78 years)
n1=Lester (signe de) | n2=en:variable age at onset (range 9 to 78 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range adolescence to late adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range adolescence to late adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range birth to 60 years)
n1=Lester (signe de) | n2=en:variable age at onset (range birth to 60 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range birth to teenage years)
n1=Lester (signe de) | n2=en:variable age at onset (range birth to teenage years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range childhood to adult)
n1=Lester (signe de) | n2=en:variable age at onset (range childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range childhood to adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range childhood to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range childhood to late adult)
n1=Lester (signe de) | n2=en:variable age at onset (range childhood to late adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range childhood to mid-sixties)
n1=Lester (signe de) | n2=en:variable age at onset (range childhood to mid-sixties) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range first to fourth decade)
n1=Lester (signe de) | n2=en:variable age at onset (range first to fourth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range first to third decade)
n1=Lester (signe de) | n2=en:variable age at onset (range first to third decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range from early childhood to mid-adult)
n1=Lester (signe de) | n2=en:variable age at onset (range from early childhood to mid-adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range infancy to 30 years)
n1=Lester (signe de) | n2=en:variable age at onset (range infancy to 30 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range infancy to adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range infancy to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range infancy to late adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range infancy to late adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range infancy to young adult)
n1=Lester (signe de) | n2=en:variable age at onset (range infancy to young adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range late infancy to adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range late infancy to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range prenatal to mid-adulthood)
n1=Lester (signe de) | n2=en:variable age at onset (range prenatal to mid-adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range teenage to adult years)
n1=Lester (signe de) | n2=en:variable age at onset (range teenage to adult years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (range teens to late adult)
n1=Lester (signe de) | n2=en:variable age at onset (range teens to late adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset (usually 20 to 30 years of age)
n1=Lester (signe de) | n2=en:variable age at onset (usually 20 to 30 years of age) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset from childhood to adulthood
n1=Lester (signe de) | n2=en:variable age at onset from childhood to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of arrhythmia (range 12 to 59 years)
n1=Lester (signe de) | n2=en:variable age at onset of arrhythmia (range 12 to 59 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of neuropathy (range first to sixth decade)
n1=Lester (signe de) | n2=en:variable age at onset of neuropathy (range first to sixth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of seizures
n1=Lester (signe de) | n2=en:variable age at onset of seizures | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of symptoms (from childhood to the sixth decade of life)
n1=Lester (signe de) | n2=en:variable age at onset of symptoms (from childhood to the sixth decade of life) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of symptoms, from second to fifth decade of life
n1=Lester (signe de) | n2=en:variable age at onset of symptoms, from second to fifth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset of symptoms, ranging from the second to seventh decades of life
n1=Lester (signe de) | n2=en:variable age at onset of symptoms, ranging from the second to seventh decades of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, but most often in the first 2 decades
n1=Lester (signe de) | n2=en:variable age at onset, but most often in the first 2 decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, but usually in childhood
n1=Lester (signe de) | n2=en:variable age at onset, but usually in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, early childhood to adult
n1=Lester (signe de) | n2=en:variable age at onset, early childhood to adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, first to second decades
n1=Lester (signe de) | n2=en:variable age at onset, first to second decades | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, from birth to ninth decade
n1=Lester (signe de) | n2=en:variable age at onset, from birth to ninth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, from first decade to fourth or fifth decade of life
n1=Lester (signe de) | n2=en:variable age at onset, from first decade to fourth or fifth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, infancy to adulthood
n1=Lester (signe de) | n2=en:variable age at onset, infancy to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, most often in second decade
n1=Lester (signe de) | n2=en:variable age at onset, most often in second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, mostly in third decade (range teenage years to fourth decade)
n1=Lester (signe de) | n2=en:variable age at onset, mostly in third decade (range teenage years to fourth decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, range from infancy to adulthood
n1=Lester (signe de) | n2=en:variable age at onset, range from infancy to adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, range infancy to adult
n1=Lester (signe de) | n2=en:variable age at onset, range infancy to adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, ranges from third to fifth decade of life
n1=Lester (signe de) | n2=en:variable age at onset, ranges from third to fifth decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, ranging from 18 months to 27 years
n1=Lester (signe de) | n2=en:variable age at onset, ranging from 18 months to 27 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, ranging from childhood to adult
n1=Lester (signe de) | n2=en:variable age at onset, ranging from childhood to adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, ranging from childhood to late adulthood
n1=Lester (signe de) | n2=en:variable age at onset, ranging from childhood to late adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, ranging from prelingual at birth to fifth decade
n1=Lester (signe de) | n2=en:variable age at onset, ranging from prelingual at birth to fifth decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, usually first or second decade
n1=Lester (signe de) | n2=en:variable age at onset, usually first or second decade | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, usually in first decade, but can occur later
n1=Lester (signe de) | n2=en:variable age at onset, usually in first decade, but can occur later | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age at onset, with cataract noted in early childhood in some patients and in the third to sixth decade of life in other patients
n1=Lester (signe de) | n2=en:variable age at onset, with cataract noted in early childhood in some patients and in the third to sixth decade of life in other patients | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset
n1=Lester (signe de) | n2=en:variable age of onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (20 to 35 years old)
n1=Lester (signe de) | n2=en:variable age of onset (20 to 35 years old) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (6 to 35 years)
n1=Lester (signe de) | n2=en:variable age of onset (6 to 35 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (7-59 years)
n1=Lester (signe de) | n2=en:variable age of onset (7-59 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (childhood to adult)
n1=Lester (signe de) | n2=en:variable age of onset (childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (childhood to adulthood)
n1=Lester (signe de) | n2=en:variable age of onset (childhood to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (childhood to young adulthood)
n1=Lester (signe de) | n2=en:variable age of onset (childhood to young adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (first to third decades)
n1=Lester (signe de) | n2=en:variable age of onset (first to third decades) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (infancy to 63 years)
n1=Lester (signe de) | n2=en:variable age of onset (infancy to 63 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range 1 to 30 years)
n1=Lester (signe de) | n2=en:variable age of onset (range 1 to 30 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range 1-40 years)
n1=Lester (signe de) | n2=en:variable age of onset (range 1-40 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range 13 to 67 years, median 48 years)
n1=Lester (signe de) | n2=en:variable age of onset (range 13 to 67 years, median 48 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range 4 months to 45 years)
n1=Lester (signe de) | n2=en:variable age of onset (range 4 months to 45 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range 4 to 47 years)
n1=Lester (signe de) | n2=en:variable age of onset (range 4 to 47 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range early childhood to adult)
n1=Lester (signe de) | n2=en:variable age of onset (range early childhood to adult) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset (range first to third decade)
n1=Lester (signe de) | n2=en:variable age of onset (range first to third decade) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset of parkinsonism (first decade to adulthood)
n1=Lester (signe de) | n2=en:variable age of onset of parkinsonism (first decade to adulthood) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset of renal manifestations
n1=Lester (signe de) | n2=en:variable age of onset of renal manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset, from 6 to 50 years of age
n1=Lester (signe de) | n2=en:variable age of onset, from 6 to 50 years of age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset, from early childhood to seventh decade of life
n1=Lester (signe de) | n2=en:variable age of onset, from early childhood to seventh decade of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable age of onset, ranging from 11 to 50 years
n1=Lester (signe de) | n2=en:variable age of onset, ranging from 11 to 50 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable cardiac defects
n1=Lester (signe de) | n2=en:variable cardiac defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable cardiac phenotype
n1=Lester (signe de) | n2=en:variable cardiac phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable cataract phenotypes within a family
n1=Lester (signe de) | n2=en:variable cataract phenotypes within a family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical features
n1=Lester (signe de) | n2=en:variable clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical phenotype
n1=Lester (signe de) | n2=en:variable clinical phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical presentation
n1=Lester (signe de) | n2=en:variable clinical presentation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical presentation ranging from acute onset to normal adult
n1=Lester (signe de) | n2=en:variable clinical presentation ranging from acute onset to normal adult | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical presentation that may change with age
n1=Lester (signe de) | n2=en:variable clinical presentation that may change with age | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable clinical severity
n1=Lester (signe de) | n2=en:variable clinical severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable degree of severity of widening and deviation of fifth fingers, both within and between affected individuals
n1=Lester (signe de) | n2=en:variable degree of severity of widening and deviation of fifth fingers, both within and between affected individuals | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable disease course
n1=Lester (signe de) | n2=en:variable disease course | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable disease severity
n1=Lester (signe de) | n2=en:variable disease severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable distribution, may be focal, segmental, multifocal, or generalized
n1=Lester (signe de) | n2=en:variable distribution, may be focal, segmental, multifocal, or generalized | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable duration (minutes to hours)
n1=Lester (signe de) | n2=en:variable duration (minutes to hours) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable dysmorphic features
n1=Lester (signe de) | n2=en:variable dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expression
n1=Lester (signe de) | n2=en:variable expression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expression and severity
n1=Lester (signe de) | n2=en:variable expression and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expression in females otopalatodigital syndrome type i (opd1, 311300) is an allelic disorder
n1=Lester (signe de) | n2=en:variable expression in females otopalatodigital syndrome type i (opd1, 311300) is an allelic disorder | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expression of features
n1=Lester (signe de) | n2=en:variable expression of features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity
n1=Lester (signe de) | n2=en:variable expressivity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity in families
n1=Lester (signe de) | n2=en:variable expressivity in families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity of each feature
n1=Lester (signe de) | n2=en:variable expressivity of each feature | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity within a family
n1=Lester (signe de) | n2=en:variable expressivity within a family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity, even within families
n1=Lester (signe de) | n2=en:variable expressivity, even within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable expressivity, some patients may be clinically asymptomatic
n1=Lester (signe de) | n2=en:variable expressivity, some patients may be clinically asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable extraneurologic features
n1=Lester (signe de) | n2=en:variable extraneurologic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable facial dysmorphic features
n1=Lester (signe de) | n2=en:variable facial dysmorphic features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable features
n1=Lester (signe de) | n2=en:variable features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable features and severity
n1=Lester (signe de) | n2=en:variable features and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable features present
n1=Lester (signe de) | n2=en:variable features present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable frequency (2 per day up to 1 per month)
n1=Lester (signe de) | n2=en:variable frequency (2 per day up to 1 per month) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable frequency (daily to monthly)
n1=Lester (signe de) | n2=en:variable frequency (daily to monthly) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable frequency (weekly to yearly)
n1=Lester (signe de) | n2=en:variable frequency (weekly to yearly) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable frequency and duration of episodes
n1=Lester (signe de) | n2=en:variable frequency and duration of episodes | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable frequency and severity
n1=Lester (signe de) | n2=en:variable frequency and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable heat tolerance
n1=Lester (signe de) | n2=en:variable heat tolerance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable ictal semiology
n1=Lester (signe de) | n2=en:variable ictal semiology | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable infectious phenotype
n1=Lester (signe de) | n2=en:variable infectious phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable involvement of hematologic parameters
n1=Lester (signe de) | n2=en:variable involvement of hematologic parameters | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable locations
n1=Lester (signe de) | n2=en:variable locations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable manifestation of features
n1=Lester (signe de) | n2=en:variable manifestation of features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable manifestations
n1=Lester (signe de) | n2=en:variable manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable neurologic phenotype
n1=Lester (signe de) | n2=en:variable neurologic phenotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable neuroradiologic findings
n1=Lester (signe de) | n2=en:variable neuroradiologic findings | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable number of nails involved
n1=Lester (signe de) | n2=en:variable number of nails involved | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable onset of seizures from neonatal to first year of life
n1=Lester (signe de) | n2=en:variable onset of seizures from neonatal to first year of life | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable onset, from infancy to young adulthood
n1=Lester (signe de) | n2=en:variable onset, from infancy to young adulthood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable pattern of body involvement although symptoms may predominate in upper or lower body
n1=Lester (signe de) | n2=en:variable pattern of body involvement although symptoms may predominate in upper or lower body | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable penetrance
n1=Lester (signe de) | n2=en:variable penetrance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable penetrance and expressivity
n1=Lester (signe de) | n2=en:variable penetrance and expressivity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable penetrance of these features
n1=Lester (signe de) | n2=en:variable penetrance of these features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype (myotonia may or may not be present)
n1=Lester (signe de) | n2=en:variable phenotype (myotonia may or may not be present) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype (range from completely female to males with mild undermasculinization)
n1=Lester (signe de) | n2=en:variable phenotype (range from completely female to males with mild undermasculinization) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype and severity
n1=Lester (signe de) | n2=en:variable phenotype and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype depending on residual enzyme activity
n1=Lester (signe de) | n2=en:variable phenotype depending on residual enzyme activity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype ranging from woolly to sparse hair, even within a single family
n1=Lester (signe de) | n2=en:variable phenotype ranging from woolly to sparse hair, even within a single family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype within and between oi5 families
n1=Lester (signe de) | n2=en:variable phenotype within and between oi5 families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype within families
n1=Lester (signe de) | n2=en:variable phenotype within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype within families ranging from woolly hair to hypotrichosis
n1=Lester (signe de) | n2=en:variable phenotype within families ranging from woolly hair to hypotrichosis | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype, particularly with regard to cortical malformations
n1=Lester (signe de) | n2=en:variable phenotype, particularly with regard to cortical malformations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotype, some patients have very mild symptoms
n1=Lester (signe de) | n2=en:variable phenotype, some patients have very mild symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotypic expression
n1=Lester (signe de) | n2=en:variable phenotypic expression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotypic expression within same individual in each eye (in some patients)
n1=Lester (signe de) | n2=en:variable phenotypic expression within same individual in each eye (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable phenotypic features cataloged depending on development of fetus or infant
n1=Lester (signe de) | n2=en:variable phenotypic features cataloged depending on development of fetus or infant | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable presentation
n1=Lester (signe de) | n2=en:variable presentation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable presentation and evolution of symptoms
n1=Lester (signe de) | n2=en:variable presentation and evolution of symptoms | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable presentation and manifestations
n1=Lester (signe de) | n2=en:variable presentation and manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable presentation of clinical features
n1=Lester (signe de) | n2=en:variable presentation of clinical features | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable progression
n1=Lester (signe de) | n2=en:variable progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable progression rate
n1=Lester (signe de) | n2=en:variable progression rate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable response to acetazolamide and carbamazepine
n1=Lester (signe de) | n2=en:variable response to acetazolamide and carbamazepine | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable response to acetylcholinesterase inhibitors
n1=Lester (signe de) | n2=en:variable response to acetylcholinesterase inhibitors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable response to levodopa treatment
n1=Lester (signe de) | n2=en:variable response to levodopa treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable response to steroid treatment
n1=Lester (signe de) | n2=en:variable response to steroid treatment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable response to vitamin b12 therapy
n1=Lester (signe de) | n2=en:variable response to vitamin b12 therapy | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity (in patients with hsan2d)
n1=Lester (signe de) | n2=en:variable severity (in patients with hsan2d) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity (mild symptoms to severe handicap)
n1=Lester (signe de) | n2=en:variable severity (mild symptoms to severe handicap) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity and progression
n1=Lester (signe de) | n2=en:variable severity and progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity between patients and between eyes (in some patients)
n1=Lester (signe de) | n2=en:variable severity between patients and between eyes (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity in symptoms among affected individuals within a family as well as among families with same mutation
n1=Lester (signe de) | n2=en:variable severity in symptoms among affected individuals within a family as well as among families with same mutation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity of brain malformations
n1=Lester (signe de) | n2=en:variable severity of brain malformations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity of clinical and radiologic manifestations
n1=Lester (signe de) | n2=en:variable severity of clinical and radiologic manifestations | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity of phenotype and other features may be present
n1=Lester (signe de) | n2=en:variable severity of phenotype and other features may be present | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity of scaling and palmoplantar keratoderma
n1=Lester (signe de) | n2=en:variable severity of scaling and palmoplantar keratoderma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity ranging from asymptomatic euthyroid to severe hypothyroidism
n1=Lester (signe de) | n2=en:variable severity ranging from asymptomatic euthyroid to severe hypothyroidism | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity that correlates with rate and magnitude of neuronal protein accumulation
n1=Lester (signe de) | n2=en:variable severity that correlates with rate and magnitude of neuronal protein accumulation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, correlates with age at onset
n1=Lester (signe de) | n2=en:variable severity, correlates with age at onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, even within families
n1=Lester (signe de) | n2=en:variable severity, even within families | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, intrafamilial
n1=Lester (signe de) | n2=en:variable severity, intrafamilial | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, ranging from 'typical' to 'severe' disease
n1=Lester (signe de) | n2=en:variable severity, ranging from 'typical' to 'severe' disease | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, ranging from central severe to peripheral to transient
n1=Lester (signe de) | n2=en:variable severity, ranging from central severe to peripheral to transient | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable severity, some patients have a protracted course with little neurologic involvement
n1=Lester (signe de) | n2=en:variable severity, some patients have a protracted course with little neurologic involvement | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable survival
n1=Lester (signe de) | n2=en:variable survival | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variable survival (some neonatal lethality)
n1=Lester (signe de) | n2=en:variable survival (some neonatal lethality) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variably expressivity
n1=Lester (signe de) | n2=en:variably expressivity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variably severity
n1=Lester (signe de) | n2=en:variably severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variant at may present with dystonia only
n1=Lester (signe de) | n2=en:variant at may present with dystonia only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variant lesch-nyhan, 1.5-8% hprt activity with neurologic abnormalities, but no self-injurious behavior
n1=Lester (signe de) | n2=en:variant lesch-nyhan, 1.5-8% hprt activity with neurologic abnormalities, but no self-injurious behavior | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:variation in slc24a5 has also been associated with variation in skin color (shep4)
n1=Lester (signe de) | n2=en:variation in slc24a5 has also been associated with variation in skin color (shep4) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vasculitic symptoms are associated with cold exposure (in some patients)
n1=Lester (signe de) | n2=en:vasculitic symptoms are associated with cold exposure (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vast majority of heterozygotes are asymptomatic
n1=Lester (signe de) | n2=en:vast majority of heterozygotes are asymptomatic | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:venous malformations previously referred to as angiomas or hemangiomas
n1=Lester (signe de) | n2=en:venous malformations previously referred to as angiomas or hemangiomas | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vertical eye movement abnormalities appear before horizontal eye movement abnormalities
n1=Lester (signe de) | n2=en:vertical eye movement abnormalities appear before horizontal eye movement abnormalities | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:very few patients reported
n1=Lester (signe de) | n2=en:very few patients reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:very low occurrence of retinal, hepatic, pancreatic, and renal anomalies
n1=Lester (signe de) | n2=en:very low occurrence of retinal, hepatic, pancreatic, and renal anomalies | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:very rare
n1=Lester (signe de) | n2=en:very rare | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:very slow progression
n1=Lester (signe de) | n2=en:very slow progression | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:very variable phenotype, with some patients having many features and others only a few
n1=Lester (signe de) | n2=en:very variable phenotype, with some patients having many features and others only a few | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vhl type 1 - renal carcinoma and hemangioblastoma
n1=Lester (signe de) | n2=en:vhl type 1 - renal carcinoma and hemangioblastoma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vhl type 2a - hemangioblastoma and pheochromocytoma
n1=Lester (signe de) | n2=en:vhl type 2a - hemangioblastoma and pheochromocytoma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vhl type 2b - renal carcinoma and pheochromocytoma
n1=Lester (signe de) | n2=en:vhl type 2b - renal carcinoma and pheochromocytoma | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:vhl type 2c - pheochromocytoma only
n1=Lester (signe de) | n2=en:vhl type 2c - pheochromocytoma only | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:virtually all patients are female
n1=Lester (signe de) | n2=en:virtually all patients are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:virtually all patients with this condition are female
n1=Lester (signe de) | n2=en:virtually all patients with this condition are female | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visceral manifestations are less apparent
n1=Lester (signe de) | n2=en:visceral manifestations are less apparent | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visceral multicentric involvement has a poorer prognosis than solitary lesions limited to the skin
n1=Lester (signe de) | n2=en:visceral multicentric involvement has a poorer prognosis than solitary lesions limited to the skin | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual acuity better than anticipated from ophthalmoscopic appearance
n1=Lester (signe de) | n2=en:visual acuity better than anticipated from ophthalmoscopic appearance | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual acuity varies considerably, depending on the presence of secondary defects such as retinal exudates or detachment
n1=Lester (signe de) | n2=en:visual acuity varies considerably, depending on the presence of secondary defects such as retinal exudates or detachment | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual acuity varies from 20/20 to no light perception
n1=Lester (signe de) | n2=en:visual acuity varies from 20/20 to no light perception | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual and hearing loss are slowly progressive
n1=Lester (signe de) | n2=en:visual and hearing loss are slowly progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual field and color defects invariably present only in patients with advanced loss of vision
n1=Lester (signe de) | n2=en:visual field and color defects invariably present only in patients with advanced loss of vision | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual impairment is present at birth and is progressive
n1=Lester (signe de) | n2=en:visual impairment is present at birth and is progressive | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:visual symptoms present by late childhood
n1=Lester (signe de) | n2=en:visual symptoms present by late childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:waddling gait
n1=Lester (signe de) | n2=en:waddling gait | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:waddling gait noted at age 15-20 months
n1=Lester (signe de) | n2=en:waddling gait noted at age 15-20 months | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:waddling gait, often presenting sign in second year
n1=Lester (signe de) | n2=en:waddling gait, often presenting sign in second year | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:waddling gate
n1=Lester (signe de) | n2=en:waddling gate | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:walking delay
n1=Lester (signe de) | n2=en:walking delay | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:warm weather and alcohol are alleviating factors
n1=Lester (signe de) | n2=en:warm weather and alcohol are alleviating factors | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wasting of hands often occurs first
n1=Lester (signe de) | n2=en:wasting of hands often occurs first | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wasting of the hands is the first and most prominent manifestation
n1=Lester (signe de) | n2=en:wasting of the hands is the first and most prominent manifestation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:waxing and waning cardiomyopathy (in some patients)
n1=Lester (signe de) | n2=en:waxing and waning cardiomyopathy (in some patients) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:weakness during pregnancy in some affected females has been reported
n1=Lester (signe de) | n2=en:weakness during pregnancy in some affected females has been reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wheelchair use at 20-30 years
n1=Lester (signe de) | n2=en:wheelchair use at 20-30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wheelchair use by 10-30 years
n1=Lester (signe de) | n2=en:wheelchair use by 10-30 years | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wheelchair-bound after 2 decades of disease onset
n1=Lester (signe de) | n2=en:wheelchair-bound after 2 decades of disease onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wheelchair-bound average 12 years after onset
n1=Lester (signe de) | n2=en:wheelchair-bound average 12 years after onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:when present, onset of vestibular dysfunction in childhood
n1=Lester (signe de) | n2=en:when present, onset of vestibular dysfunction in childhood | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide clinical variability
n1=Lester (signe de) | n2=en:wide clinical variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide phenotypic variability
n1=Lester (signe de) | n2=en:wide phenotypic variability | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide phenotypic variability and severity
n1=Lester (signe de) | n2=en:wide phenotypic variability and severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide phenotypic variation
n1=Lester (signe de) | n2=en:wide phenotypic variation | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide range of onset from childhood to adult (10 to 50 years)
n1=Lester (signe de) | n2=en:wide range of onset from childhood to adult (10 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide range of severity between affected members of the same family
n1=Lester (signe de) | n2=en:wide range of severity between affected members of the same family | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide spectrum of severity
n1=Lester (signe de) | n2=en:wide spectrum of severity | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:wide variability in severity of limb defects
n1=Lester (signe de) | n2=en:wide variability in severity of limb defects | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:women affected more than men (3:2)
n1=Lester (signe de) | n2=en:women affected more than men (3:2) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:women are more often affected
n1=Lester (signe de) | n2=en:women are more often affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:women may be mildly affected
n1=Lester (signe de) | n2=en:women may be mildly affected | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worldwide frequency of 1 in 100,000 infants
n1=Lester (signe de) | n2=en:worldwide frequency of 1 in 100,000 infants | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worldwide frequency of 1 in 2,000,000
n1=Lester (signe de) | n2=en:worldwide frequency of 1 in 2,000,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worldwide incidence of 1 in 185,000 live births
n1=Lester (signe de) | n2=en:worldwide incidence of 1 in 185,000 live births | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worldwide prevalence of 1/100,000
n1=Lester (signe de) | n2=en:worldwide prevalence of 1/100,000 | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worsening of hand weakness with cold (in some)
n1=Lester (signe de) | n2=en:worsening of hand weakness with cold (in some) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:worsening of symptoms during sleep
n1=Lester (signe de) | n2=en:worsening of symptoms during sleep | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:x-linked inheritance could not be ruled out
n1=Lester (signe de) | n2=en:x-linked inheritance could not be ruled out | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:x-linked mental retardation-hypotonic facies syndrome (309580) is an allelic disorder without alpha-thalassemia
n1=Lester (signe de) | n2=en:x-linked mental retardation-hypotonic facies syndrome (309580) is an allelic disorder without alpha-thalassemia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:x-linked recessive cytochrome b-negative cgd
n1=Lester (signe de) | n2=en:x-linked recessive cytochrome b-negative cgd | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:xy karyotype
n1=Lester (signe de) | n2=en:xy karyotype | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:young adult onset
n1=Lester (signe de) | n2=en:young adult onset | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:young adult onset (range 13 to 50 years)
n1=Lester (signe de) | n2=en:young adult onset (range 13 to 50 years) | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:young-adult onset (18-30 years) of sensory ataxia
n1=Lester (signe de) | n2=en:young-adult onset (18-30 years) of sensory ataxia | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:younger onset rarely reported
n1=Lester (signe de) | n2=en:younger onset rarely reported | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:z allele most common, only in caucasians
n1=Lester (signe de) | n2=en:z allele most common, only in caucasians | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
en:zinc deficiency in breastfed offspring resolves after weaning
n1=Lester (signe de) | n2=en:zinc deficiency in breastfed offspring resolves after weaning | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
figuré
n1=Lester (signe de) | n2=figuré | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
irrésistible
n1=Lester (signe de) | n2=irrésistible | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
létale
n1=Lester (signe de) | n2=létale | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
léthal
n1=Lester (signe de) | n2=léthal | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
meurtrier
n1=Lester (signe de) | n2=meurtrier | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
qui entraîne la mort
n1=Lester (signe de) | n2=qui entraîne la mort | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
séduction
n1=Lester (signe de) | n2=séduction | rel=r_associated | relid=0 | w=5
- Lester (signe de) --
r_associated #0: 5 / 0.083 ->
sublétal
n1=Lester (signe de) | n2=sublétal | rel=r_associated | relid=0 | w=5
| ≈ 16 relations entrantes
- léthalité ---
r_associated #0: 37 -->
Lester (signe de)
n1=léthalité | n2=Lester (signe de) | rel=r_associated | relid=0 | w=37
- létalité ---
r_associated #0: 31 -->
Lester (signe de)
n1=létalité | n2=Lester (signe de) | rel=r_associated | relid=0 | w=31
- signe de Lester ---
r_associated #0: 28 -->
Lester (signe de)
n1=signe de Lester | n2=Lester (signe de) | rel=r_associated | relid=0 | w=28
- en:Lester's sign ---
r_associated #0: 25 -->
Lester (signe de)
n1=en:Lester's sign | n2=Lester (signe de) | rel=r_associated | relid=0 | w=25
- léthal ---
r_associated #0: 21 -->
Lester (signe de)
n1=léthal | n2=Lester (signe de) | rel=r_associated | relid=0 | w=21
- Lester ---
r_associated #0: 20 -->
Lester (signe de)
n1=Lester | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- Létalité ---
r_associated #0: 20 -->
Lester (signe de)
n1=Létalité | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- mort ---
r_associated #0: 20 -->
Lester (signe de)
n1=mort | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- médecine ---
r_associated #0: 20 -->
Lester (signe de)
n1=médecine | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- onycho-ostéodysplasie ---
r_associated #0: 20 -->
Lester (signe de)
n1=onycho-ostéodysplasie | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- signe ---
r_associated #0: 20 -->
Lester (signe de)
n1=signe | n2=Lester (signe de) | rel=r_associated | relid=0 | w=20
- en:lethal ---
r_associated #0: 15 -->
Lester (signe de)
n1=en:lethal | n2=Lester (signe de) | rel=r_associated | relid=0 | w=15
- létal ---
r_associated #0: 15 -->
Lester (signe de)
n1=létal | n2=Lester (signe de) | rel=r_associated | relid=0 | w=15
- en:deadliness ---
r_associated #0: 10 -->
Lester (signe de)
n1=en:deadliness | n2=Lester (signe de) | rel=r_associated | relid=0 | w=10
- en:lester's sign ---
r_associated #0: 10 -->
Lester (signe de)
n1=en:lester's sign | n2=Lester (signe de) | rel=r_associated | relid=0 | w=10
- Létal ---
r_associated #0: 5 -->
Lester (signe de)
n1=Létal | n2=Lester (signe de) | rel=r_associated | relid=0 | w=5
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