'syndrome d'Apert'
(id=331425 ; fe=syndrome d'Apert ; type=1 ; niveau=200 ;
luminosité=50 ;
somme entrante=8658 creation date=2014-06-09 touchdate=2025-12-26 02:12:42.000) ≈ 325 relations sortantes
- syndrome d'Apert --
r_associated #0: 515 / 1 ->
médecine
n1=syndrome d'Apert | n2=médecine | rel=r_associated | relid=0 | w=515
- syndrome d'Apert --
r_associated #0: 386 / 0.75 ->
maladies
n1=syndrome d'Apert | n2=maladies | rel=r_associated | relid=0 | w=386
- syndrome d'Apert --
r_associated #0: 269 / 0.522 ->
ACPS
n1=syndrome d'Apert | n2=ACPS | rel=r_associated | relid=0 | w=269
- syndrome d'Apert --
r_associated #0: 269 / 0.522 ->
acrocéphalosyndactylie d'Apert
n1=syndrome d'Apert | n2=acrocéphalosyndactylie d'Apert | rel=r_associated | relid=0 | w=269
- syndrome d'Apert --
r_associated #0: 269 / 0.522 ->
en:type iii acrocephalosyndactyly
n1=syndrome d'Apert | n2=en:type iii acrocephalosyndactyly | rel=r_associated | relid=0 | w=269
- syndrome d'Apert --
r_associated #0: 268 / 0.52 ->
en:pfeiffer syndrome
n1=syndrome d'Apert | n2=en:pfeiffer syndrome | rel=r_associated | relid=0 | w=268
- syndrome d'Apert --
r_associated #0: 268 / 0.52 ->
maladie
n1=syndrome d'Apert | n2=maladie | rel=r_associated | relid=0 | w=268
- syndrome d'Apert --
r_associated #0: 268 / 0.52 ->
processus pathologique
n1=syndrome d'Apert | n2=processus pathologique | rel=r_associated | relid=0 | w=268
- syndrome d'Apert --
r_associated #0: 267 / 0.518 ->
acro-céphalo-syndactylie de type v
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type v | rel=r_associated | relid=0 | w=267
- syndrome d'Apert --
r_associated #0: 267 / 0.518 ->
en:type i acrocephalosyndactyly
n1=syndrome d'Apert | n2=en:type i acrocephalosyndactyly | rel=r_associated | relid=0 | w=267
- syndrome d'Apert --
r_associated #0: 266 / 0.517 ->
acro-céphalo-syndactylie d'apert
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie d'apert | rel=r_associated | relid=0 | w=266
- syndrome d'Apert --
r_associated #0: 266 / 0.517 ->
Médecine
n1=syndrome d'Apert | n2=Médecine | rel=r_associated | relid=0 | w=266
- syndrome d'Apert --
r_associated #0: 264 / 0.513 ->
acro-céphalo-syndactylie de type 5
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type 5 | rel=r_associated | relid=0 | w=264
- syndrome d'Apert --
r_associated #0: 264 / 0.513 ->
acrocéphalosyndactylie type 5
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type 5 | rel=r_associated | relid=0 | w=264
- syndrome d'Apert --
r_associated #0: 264 / 0.513 ->
en:kurczynski casperson syndrome
n1=syndrome d'Apert | n2=en:kurczynski casperson syndrome | rel=r_associated | relid=0 | w=264
- syndrome d'Apert --
r_associated #0: 263 / 0.511 ->
en:saethre-chotzen syndrome
n1=syndrome d'Apert | n2=en:saethre-chotzen syndrome | rel=r_associated | relid=0 | w=263
- syndrome d'Apert --
r_associated #0: 263 / 0.511 ->
syndrome de Pfeiffer
n1=syndrome d'Apert | n2=syndrome de Pfeiffer | rel=r_associated | relid=0 | w=263
- syndrome d'Apert --
r_associated #0: 262 / 0.509 ->
acrocéphalie-crâne asymétrique et syndactylie modérée
n1=syndrome d'Apert | n2=acrocéphalie-crâne asymétrique et syndactylie modérée | rel=r_associated | relid=0 | w=262
- syndrome d'Apert --
r_associated #0: 262 / 0.509 ->
acrocéphalosyndactylie type i
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type i | rel=r_associated | relid=0 | w=262
- syndrome d'Apert --
r_associated #0: 262 / 0.509 ->
maladie d'apert
n1=syndrome d'Apert | n2=maladie d'apert | rel=r_associated | relid=0 | w=262
- syndrome d'Apert --
r_associated #0: 258 / 0.501 ->
acrocéphalosyndactylie type v
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type v | rel=r_associated | relid=0 | w=258
- syndrome d'Apert --
r_associated #0: 257 / 0.499 ->
acro-céphalo-syndactylie de type 1
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type 1 | rel=r_associated | relid=0 | w=257
- syndrome d'Apert --
r_associated #0: 257 / 0.499 ->
acro-céphalo-syndactylie de type 3
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type 3 | rel=r_associated | relid=0 | w=257
- syndrome d'Apert --
r_associated #0: 257 / 0.499 ->
acro-céphalo-syndactylie de type i
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type i | rel=r_associated | relid=0 | w=257
- syndrome d'Apert --
r_associated #0: 256 / 0.497 ->
acrocéphalosyndactylie, type i
n1=syndrome d'Apert | n2=acrocéphalosyndactylie, type i | rel=r_associated | relid=0 | w=256
- syndrome d'Apert --
r_associated #0: 256 / 0.497 ->
syndrome de Saethre-Chotzen
n1=syndrome d'Apert | n2=syndrome de Saethre-Chotzen | rel=r_associated | relid=0 | w=256
- syndrome d'Apert --
r_associated #0: 193 / 0.375 ->
en:type v acrocephalosyndactyly
n1=syndrome d'Apert | n2=en:type v acrocephalosyndactyly | rel=r_associated | relid=0 | w=193
- syndrome d'Apert --
r_associated #0: 193 / 0.375 ->
médecine
(science)
n1=syndrome d'Apert | n2=médecine (science) | rel=r_associated | relid=0 | w=193
- syndrome d'Apert --
r_associated #0: 192 / 0.373 ->
acrocéphalosyndactylie type 1
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type 1 | rel=r_associated | relid=0 | w=192
- syndrome d'Apert --
r_associated #0: 192 / 0.373 ->
syndrome
n1=syndrome d'Apert | n2=syndrome | rel=r_associated | relid=0 | w=192
- syndrome d'Apert --
r_associated #0: 191 / 0.371 ->
acrocéphalosyndactylie type iii
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type iii | rel=r_associated | relid=0 | w=191
- syndrome d'Apert --
r_associated #0: 186 / 0.361 ->
syndrome d
n1=syndrome d'Apert | n2=syndrome d | rel=r_associated | relid=0 | w=186
- syndrome d'Apert --
r_associated #0: 160 / 0.311 ->
Apert
n1=syndrome d'Apert | n2=Apert | rel=r_associated | relid=0 | w=160
- syndrome d'Apert --
r_associated #0: 155 / 0.301 ->
acrocéphalosyndactylies
n1=syndrome d'Apert | n2=acrocéphalosyndactylies | rel=r_associated | relid=0 | w=155
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
acro-céphalo-syndactylie
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
acro-céphalo-syndactylie de type iii
n1=syndrome d'Apert | n2=acro-céphalo-syndactylie de type iii | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
acrocéphalosyndactylie
n1=syndrome d'Apert | n2=acrocéphalosyndactylie | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
Chotzen
n1=syndrome d'Apert | n2=Chotzen | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
en:apert-crouzon disease
n1=syndrome d'Apert | n2=en:apert-crouzon disease | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 150 / 0.291 ->
syndrome de saethre-chotzen
n1=syndrome d'Apert | n2=syndrome de saethre-chotzen | rel=r_associated | relid=0 | w=150
- syndrome d'Apert --
r_associated #0: 145 / 0.282 ->
en:apert syndrome
n1=syndrome d'Apert | n2=en:apert syndrome | rel=r_associated | relid=0 | w=145
- syndrome d'Apert --
r_associated #0: 135 / 0.262 ->
acrocéphalosyndactylie de type I
n1=syndrome d'Apert | n2=acrocéphalosyndactylie de type I | rel=r_associated | relid=0 | w=135
- syndrome d'Apert --
r_associated #0: 135 / 0.262 ->
FGFR2 gene
n1=syndrome d'Apert | n2=FGFR2 gene | rel=r_associated | relid=0 | w=135
- syndrome d'Apert --
r_associated #0: 130 / 0.252 ->
Crouzon (maladie de)
n1=syndrome d'Apert | n2=Crouzon (maladie de) | rel=r_associated | relid=0 | w=130
- syndrome d'Apert --
r_associated #0: 60 / 0.117 ->
en:orbites étroites
n1=syndrome d'Apert | n2=en:orbites étroites | rel=r_associated | relid=0 | w=60
- syndrome d'Apert --
r_associated #0: 58 / 0.113 ->
en:acrodysplasie
n1=syndrome d'Apert | n2=en:acrodysplasie | rel=r_associated | relid=0 | w=58
- syndrome d'Apert --
r_associated #0: 58 / 0.113 ->
en:Apert's disease
n1=syndrome d'Apert | n2=en:Apert's disease | rel=r_associated | relid=0 | w=58
- syndrome d'Apert --
r_associated #0: 58 / 0.113 ->
en:colobome irien ou choroïdien (rare)
n1=syndrome d'Apert | n2=en:colobome irien ou choroïdien (rare) | rel=r_associated | relid=0 | w=58
- syndrome d'Apert --
r_associated #0: 57 / 0.111 ->
en:nystagmus
n1=syndrome d'Apert | n2=en:nystagmus | rel=r_associated | relid=0 | w=57
- syndrome d'Apert --
r_associated #0: 55 / 0.107 ->
en:FGFR2 en 10q26.13.3
n1=syndrome d'Apert | n2=en:FGFR2 en 10q26.13.3 | rel=r_associated | relid=0 | w=55
- syndrome d'Apert --
r_associated #0: 55 / 0.107 ->
Syndrome
n1=syndrome d'Apert | n2=Syndrome | rel=r_associated | relid=0 | w=55
- syndrome d'Apert --
r_associated #0: 54 / 0.105 ->
acrocéphalosyndactylie, type iii
n1=syndrome d'Apert | n2=acrocéphalosyndactylie, type iii | rel=r_associated | relid=0 | w=54
- syndrome d'Apert --
r_associated #0: 54 / 0.105 ->
en:Apert-Crouzon maladie
n1=syndrome d'Apert | n2=en:Apert-Crouzon maladie | rel=r_associated | relid=0 | w=54
- syndrome d'Apert --
r_associated #0: 54 / 0.105 ->
en:exophtalmie
n1=syndrome d'Apert | n2=en:exophtalmie | rel=r_associated | relid=0 | w=54
- syndrome d'Apert --
r_associated #0: 54 / 0.105 ->
en:ophtalmoplégie
n1=syndrome d'Apert | n2=en:ophtalmoplégie | rel=r_associated | relid=0 | w=54
- syndrome d'Apert --
r_associated #0: 53 / 0.103 ->
en:strabisme
n1=syndrome d'Apert | n2=en:strabisme | rel=r_associated | relid=0 | w=53
- syndrome d'Apert --
r_associated #0: 51 / 0.099 ->
ACS I
n1=syndrome d'Apert | n2=ACS I | rel=r_associated | relid=0 | w=51
- syndrome d'Apert --
r_associated #0: 51 / 0.099 ->
ACS
(acro-céphalo-syndactylie)
n1=syndrome d'Apert | n2=ACS (acro-céphalo-syndactylie) | rel=r_associated | relid=0 | w=51
- syndrome d'Apert --
r_associated #0: 50 / 0.097 ->
en:acrocéphalosyndactylie type Ia
n1=syndrome d'Apert | n2=en:acrocéphalosyndactylie type Ia | rel=r_associated | relid=0 | w=50
- syndrome d'Apert --
r_associated #0: 50 / 0.097 ->
en:kératite
n1=syndrome d'Apert | n2=en:kératite | rel=r_associated | relid=0 | w=50
- syndrome d'Apert --
r_associated #0: 49 / 0.095 ->
acrocéphalosyndactylie type Ia
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type Ia | rel=r_associated | relid=0 | w=49
- syndrome d'Apert --
r_associated #0: 47 / 0.091 ->
Apert (syndrome d')
n1=syndrome d'Apert | n2=Apert (syndrome d') | rel=r_associated | relid=0 | w=47
- syndrome d'Apert --
r_associated #0: 46 / 0.089 ->
Apert-Crouzon maladie
n1=syndrome d'Apert | n2=Apert-Crouzon maladie | rel=r_associated | relid=0 | w=46
- syndrome d'Apert --
r_associated #0: 46 / 0.089 ->
en:cataracte
n1=syndrome d'Apert | n2=en:cataracte | rel=r_associated | relid=0 | w=46
- syndrome d'Apert --
r_associated #0: 44 / 0.085 ->
acrodysplasie
n1=syndrome d'Apert | n2=acrodysplasie | rel=r_associated | relid=0 | w=44
- syndrome d'Apert --
r_associated #0: 43 / 0.083 ->
acrobrachycéphalie
n1=syndrome d'Apert | n2=acrobrachycéphalie | rel=r_associated | relid=0 | w=43
- syndrome d'Apert --
r_associated #0: 30 / 0.058 ->
acrocéphalosyndactylie type 3
n1=syndrome d'Apert | n2=acrocéphalosyndactylie type 3 | rel=r_associated | relid=0 | w=30
- syndrome d'Apert --
r_associated #0: 30 / 0.058 ->
en:medicine
n1=syndrome d'Apert | n2=en:medicine | rel=r_associated | relid=0 | w=30
- syndrome d'Apert --
r_associated #0: 23 / 0.045 ->
hypertélorisme
n1=syndrome d'Apert | n2=hypertélorisme | rel=r_associated | relid=0 | w=23
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
acro-céphalo-syndactylies
n1=syndrome d'Apert | n2=acro-céphalo-syndactylies | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
ACS
n1=syndrome d'Apert | n2=ACS | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:absent corpus callosum
n1=syndrome d'Apert | n2=en:absent corpus callosum | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:acrocephalosyndactyly type I
n1=syndrome d'Apert | n2=en:acrocephalosyndactyly type I | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:acrocephaly
n1=syndrome d'Apert | n2=en:acrocephaly | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:and mild syndactyly
n1=syndrome d'Apert | n2=en:and mild syndactyly | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:Chotzen's syndrome
n1=syndrome d'Apert | n2=en:Chotzen's syndrome | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:exomphalos
n1=syndrome d'Apert | n2=en:exomphalos | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:Pfeiffer's syndrome
n1=syndrome d'Apert | n2=en:Pfeiffer's syndrome | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:Saethre-Chotzen's syndrome
n1=syndrome d'Apert | n2=en:Saethre-Chotzen's syndrome | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
en:telecanthus
n1=syndrome d'Apert | n2=en:telecanthus | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle
n1=syndrome d'Apert | n2=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
hypertélorisme-microtie-fente faciale
n1=syndrome d'Apert | n2=hypertélorisme-microtie-fente faciale | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
hypertélorisme, hypospadias, polysyndactylie (syndrome)
n1=syndrome d'Apert | n2=hypertélorisme, hypospadias, polysyndactylie (syndrome) | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
Maladies
n1=syndrome d'Apert | n2=Maladies | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
Saethre-Chotzen (syndrome de)
n1=syndrome d'Apert | n2=Saethre-Chotzen (syndrome de) | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
syndrome de Chotzen
n1=syndrome d'Apert | n2=syndrome de Chotzen | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
syndrome de pfeiffer
n1=syndrome d'Apert | n2=syndrome de pfeiffer | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 20 / 0.039 ->
télécanthus-hypertélorisme-strabisme (syndrome)
n1=syndrome d'Apert | n2=télécanthus-hypertélorisme-strabisme (syndrome) | rel=r_associated | relid=0 | w=20
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
anatomie
n1=syndrome d'Apert | n2=anatomie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
apophysite calcanéenne
n1=syndrome d'Apert | n2=apophysite calcanéenne | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
apophysite tibiale antérieure
n1=syndrome d'Apert | n2=apophysite tibiale antérieure | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
apoplexie utéroplacentaire
n1=syndrome d'Apert | n2=apoplexie utéroplacentaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
brachydactylie-nystagmus-ataxie cérébelleuse
n1=syndrome d'Apert | n2=brachydactylie-nystagmus-ataxie cérébelleuse | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Brünings (position de)
n1=syndrome d'Apert | n2=Brünings (position de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
congénital
n1=syndrome d'Apert | n2=congénital | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
dysostose craniofaciale
n1=syndrome d'Apert | n2=dysostose craniofaciale | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
électro-oculogramme
n1=syndrome d'Apert | n2=électro-oculogramme | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
électronystagmographie
n1=syndrome d'Apert | n2=électronystagmographie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:absent eyebrow
n1=syndrome d'Apert | n2=en:absent eyebrow | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:achromatopsia
n1=syndrome d'Apert | n2=en:achromatopsia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:achromatopsia 1
n1=syndrome d'Apert | n2=en:achromatopsia 1 | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:acrocallosal syndrome
n1=syndrome d'Apert | n2=en:acrocallosal syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:aicardi syndrome
n1=syndrome d'Apert | n2=en:aicardi syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:alacrima
n1=syndrome d'Apert | n2=en:alacrima | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:albinism, ocular
n1=syndrome d'Apert | n2=en:albinism, ocular | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:albinotic fundus
n1=syndrome d'Apert | n2=en:albinotic fundus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:amelogenesis imperfecta pigmented hypomaturation type
n1=syndrome d'Apert | n2=en:amelogenesis imperfecta pigmented hypomaturation type | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:aniridia
n1=syndrome d'Apert | n2=en:aniridia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:ankyloblepharon filiforme adnatum
n1=syndrome d'Apert | n2=en:ankyloblepharon filiforme adnatum | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:anophthalmos
n1=syndrome d'Apert | n2=en:anophthalmos | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:anterior lenticonus
n1=syndrome d'Apert | n2=en:anterior lenticonus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:atresia of nasolacrimal duct
n1=syndrome d'Apert | n2=en:atresia of nasolacrimal duct | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:axenfeld anomaly (disorder)
n1=syndrome d'Apert | n2=en:axenfeld anomaly (disorder) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:axenfeld-rieger syndrome
n1=syndrome d'Apert | n2=en:axenfeld-rieger syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:biotinidase deficiency
n1=syndrome d'Apert | n2=en:biotinidase deficiency | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:blue sclera
n1=syndrome d'Apert | n2=en:blue sclera | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:cataract, congenital, cerulean type 1
n1=syndrome d'Apert | n2=en:cataract, congenital, cerulean type 1 | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:chondrodystrophy malacia
n1=syndrome d'Apert | n2=en:chondrodystrophy malacia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:cohen syndrome
n1=syndrome d'Apert | n2=en:cohen syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of choroid
n1=syndrome d'Apert | n2=en:coloboma of choroid | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of optic disc
n1=syndrome d'Apert | n2=en:coloboma of optic disc | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of the eye
n1=syndrome d'Apert | n2=en:coloboma of the eye | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of the eyelid
n1=syndrome d'Apert | n2=en:coloboma of the eyelid | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of the iris
n1=syndrome d'Apert | n2=en:coloboma of the iris | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:coloboma of the retina
n1=syndrome d'Apert | n2=en:coloboma of the retina | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:color blindness, blue
n1=syndrome d'Apert | n2=en:color blindness, blue | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:color blindness, red
n1=syndrome d'Apert | n2=en:color blindness, red | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:color blindness, red-green
n1=syndrome d'Apert | n2=en:color blindness, red-green | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital
n1=syndrome d'Apert | n2=en:congenital | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital ankyloblepharon
n1=syndrome d'Apert | n2=en:congenital ankyloblepharon | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital anomaly of iris
n1=syndrome d'Apert | n2=en:congenital anomaly of iris | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital anomaly of optic nerve
n1=syndrome d'Apert | n2=en:congenital anomaly of optic nerve | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital blindness
n1=syndrome d'Apert | n2=en:congenital blindness | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital cataract
n1=syndrome d'Apert | n2=en:congenital cataract | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital cerebellar cortical atrophy
n1=syndrome d'Apert | n2=en:congenital cerebellar cortical atrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital degeneration of nervous system
n1=syndrome d'Apert | n2=en:congenital degeneration of nervous system | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital ectopic lens
n1=syndrome d'Apert | n2=en:congenital ectopic lens | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital ectopic pupil
n1=syndrome d'Apert | n2=en:congenital ectopic pupil | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital eye disorder
n1=syndrome d'Apert | n2=en:congenital eye disorder | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital fibrosis of the extraocular muscles
n1=syndrome d'Apert | n2=en:congenital fibrosis of the extraocular muscles | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital hypertrophy of retinal pigment epithelium
n1=syndrome d'Apert | n2=en:congenital hypertrophy of retinal pigment epithelium | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital hypoplasia of choroid
n1=syndrome d'Apert | n2=en:congenital hypoplasia of choroid | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital ischemic atrophy of central nervous system structure
n1=syndrome d'Apert | n2=en:congenital ischemic atrophy of central nervous system structure | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital keratoglobus
n1=syndrome d'Apert | n2=en:congenital keratoglobus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital mesh qualifier
n1=syndrome d'Apert | n2=en:congenital mesh qualifier | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital nasolacrimal duct obstruction
n1=syndrome d'Apert | n2=en:congenital nasolacrimal duct obstruction | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital nephrotic syndrome with focal glomerulosclerosis
n1=syndrome d'Apert | n2=en:congenital nephrotic syndrome with focal glomerulosclerosis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital nystagmus
n1=syndrome d'Apert | n2=en:congenital nystagmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital osteodystrophy
n1=syndrome d'Apert | n2=en:congenital osteodystrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital renal atrophy
n1=syndrome d'Apert | n2=en:congenital renal atrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital retinal fold
n1=syndrome d'Apert | n2=en:congenital retinal fold | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital strabismus
n1=syndrome d'Apert | n2=en:congenital strabismus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:congenital syphilitic mucous patches
n1=syndrome d'Apert | n2=en:congenital syphilitic mucous patches | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:cryptophthalmia
n1=syndrome d'Apert | n2=en:cryptophthalmia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:cyclopia
n1=syndrome d'Apert | n2=en:cyclopia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:cytochrome-c oxidase deficiency
n1=syndrome d'Apert | n2=en:cytochrome-c oxidase deficiency | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:deletion 18q syndrome
n1=syndrome d'Apert | n2=en:deletion 18q syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:distichiasis
n1=syndrome d'Apert | n2=en:distichiasis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:duane syndrome
n1=syndrome d'Apert | n2=en:duane syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:dubin-johnson syndrome
n1=syndrome d'Apert | n2=en:dubin-johnson syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:dysosteosclerosis
n1=syndrome d'Apert | n2=en:dysosteosclerosis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:embryonal nuclear cataract (disorder)
n1=syndrome d'Apert | n2=en:embryonal nuclear cataract (disorder) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:epidermolysis bullosa
n1=syndrome d'Apert | n2=en:epidermolysis bullosa | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:eye
n1=syndrome d'Apert | n2=en:eye | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:focal dermal hypoplasia
n1=syndrome d'Apert | n2=en:focal dermal hypoplasia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:fumarase deficiency
n1=syndrome d'Apert | n2=en:fumarase deficiency | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:goniodysgenesis
n1=syndrome d'Apert | n2=en:goniodysgenesis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:growth retardation, alopecia, pseudoanodontia and optic atrophy
n1=syndrome d'Apert | n2=en:growth retardation, alopecia, pseudoanodontia and optic atrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:hereditary vertical
n1=syndrome d'Apert | n2=en:hereditary vertical | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:hypertelorism
n1=syndrome d'Apert | n2=en:hypertelorism | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:hypoplasia of iris
n1=syndrome d'Apert | n2=en:hypoplasia of iris | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:hypoplasia of optic disc
n1=syndrome d'Apert | n2=en:hypoplasia of optic disc | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:irido-corneal dysgenesis
n1=syndrome d'Apert | n2=en:irido-corneal dysgenesis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:irido-corneo-trabecular dysgenesis (disorder)
n1=syndrome d'Apert | n2=en:irido-corneo-trabecular dysgenesis (disorder) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:jacobsen syndrome
n1=syndrome d'Apert | n2=en:jacobsen syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:juvenile gangliosidosis gm1
n1=syndrome d'Apert | n2=en:juvenile gangliosidosis gm1 | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:leber congenital amaurosis
n1=syndrome d'Apert | n2=en:leber congenital amaurosis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:leber hereditary optic atrophy
n1=syndrome d'Apert | n2=en:leber hereditary optic atrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:left atrial endocardial fibroelastosis
n1=syndrome d'Apert | n2=en:left atrial endocardial fibroelastosis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:macrophthalmus
n1=syndrome d'Apert | n2=en:macrophthalmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:maleformatio ectodermalis generalisata of bafverstedt
n1=syndrome d'Apert | n2=en:maleformatio ectodermalis generalisata of bafverstedt | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:manifest-latent nystagmus
n1=syndrome d'Apert | n2=en:manifest-latent nystagmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:megophthalmos
n1=syndrome d'Apert | n2=en:megophthalmos | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:mental retardation
n1=syndrome d'Apert | n2=en:mental retardation | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:microcephaly-capillary malformation syndrome
n1=syndrome d'Apert | n2=en:microcephaly-capillary malformation syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:microcornea
n1=syndrome d'Apert | n2=en:microcornea | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:microphakia
n1=syndrome d'Apert | n2=en:microphakia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:microphthalmos
n1=syndrome d'Apert | n2=en:microphthalmos | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:microspherophakia
n1=syndrome d'Apert | n2=en:microspherophakia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:mucolipidosis type iv
n1=syndrome d'Apert | n2=en:mucolipidosis type iv | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4
n1=syndrome d'Apert | n2=en:muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies) type a, 4 | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:mydriasis, congenital
n1=syndrome d'Apert | n2=en:mydriasis, congenital | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:myoclonic
n1=syndrome d'Apert | n2=en:myoclonic | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:myotubular myopathy with type i atrophy
n1=syndrome d'Apert | n2=en:myotubular myopathy with type i atrophy | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:myxomatosis of cardiac valve
n1=syndrome d'Apert | n2=en:myxomatosis of cardiac valve | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:neonatal jaundice
n1=syndrome d'Apert | n2=en:neonatal jaundice | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:neuronal ceroid lipofuscinosis
n1=syndrome d'Apert | n2=en:neuronal ceroid lipofuscinosis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:neuronal ceroid lipofuscinosis type 3
n1=syndrome d'Apert | n2=en:neuronal ceroid lipofuscinosis type 3 | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:night blindness, congenital stationary
n1=syndrome d'Apert | n2=en:night blindness, congenital stationary | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:nystagmus and other irregular eye movements
n1=syndrome d'Apert | n2=en:nystagmus and other irregular eye movements | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:nystagmuses
n1=syndrome d'Apert | n2=en:nystagmuses | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:nystaxis
n1=syndrome d'Apert | n2=en:nystaxis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:ocular motility disorders
n1=syndrome d'Apert | n2=en:ocular motility disorders | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:open eye
n1=syndrome d'Apert | n2=en:open eye | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:ophthalmology
n1=syndrome d'Apert | n2=en:ophthalmology | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:optic nerve hypoplasia
n1=syndrome d'Apert | n2=en:optic nerve hypoplasia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:orbital separation diminished
n1=syndrome d'Apert | n2=en:orbital separation diminished | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:pelizaeus-merzbacher disease
n1=syndrome d'Apert | n2=en:pelizaeus-merzbacher disease | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:persistent hyperplastic primary vitreous
n1=syndrome d'Apert | n2=en:persistent hyperplastic primary vitreous | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:persistent pupillary membranes
n1=syndrome d'Apert | n2=en:persistent pupillary membranes | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:peutz-jeghers syndrome
n1=syndrome d'Apert | n2=en:peutz-jeghers syndrome | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:phosphoenolpyruvate carboxykinase deficiency
n1=syndrome d'Apert | n2=en:phosphoenolpyruvate carboxykinase deficiency | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:polycoria
n1=syndrome d'Apert | n2=en:polycoria | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:porokeratosis of mibelli
n1=syndrome d'Apert | n2=en:porokeratosis of mibelli | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:porokeratosis, disseminated superficial actinic
n1=syndrome d'Apert | n2=en:porokeratosis, disseminated superficial actinic | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:posterior embryotoxon
n1=syndrome d'Apert | n2=en:posterior embryotoxon | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:posterior lenticonus
n1=syndrome d'Apert | n2=en:posterior lenticonus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:primary hyperoxaluria type i
n1=syndrome d'Apert | n2=en:primary hyperoxaluria type i | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:pulmonary alveolar proteinosis, congenital
n1=syndrome d'Apert | n2=en:pulmonary alveolar proteinosis, congenital | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:retinal dysplasia
n1=syndrome d'Apert | n2=en:retinal dysplasia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:schindler disease, type i
n1=syndrome d'Apert | n2=en:schindler disease, type i | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:spherophakia
n1=syndrome d'Apert | n2=en:spherophakia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:synophrys
n1=syndrome d'Apert | n2=en:synophrys | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:talantropia
n1=syndrome d'Apert | n2=en:talantropia | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:type ii acrocephalopolysyndactyly
n1=syndrome d'Apert | n2=en:type ii acrocephalopolysyndactyly | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:X-linked
n1=syndrome d'Apert | n2=en:X-linked | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
en:x-linked dyskeratosis congenita
n1=syndrome d'Apert | n2=en:x-linked dyskeratosis congenita | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
épreuve rotatoire multifréquentielle
n1=syndrome d'Apert | n2=épreuve rotatoire multifréquentielle | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
flutter oculaire
n1=syndrome d'Apert | n2=flutter oculaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Frenzel (nystagmus de)
n1=syndrome d'Apert | n2=Frenzel (nystagmus de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
gaze nystagmus
n1=syndrome d'Apert | n2=gaze nystagmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
globe oculaire
n1=syndrome d'Apert | n2=globe oculaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
globes oculaires
n1=syndrome d'Apert | n2=globes oculaires | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Hallpike (manoeuvre de)
n1=syndrome d'Apert | n2=Hallpike (manoeuvre de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Harris (nystagmus ataxique de)
n1=syndrome d'Apert | n2=Harris (nystagmus ataxique de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Hennebert (signe d')
n1=syndrome d'Apert | n2=Hennebert (signe d') | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
héréditaire
n1=syndrome d'Apert | n2=héréditaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
hyporéflectivité vestibulaire
n1=syndrome d'Apert | n2=hyporéflectivité vestibulaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
indice de fixation oculaire
n1=syndrome d'Apert | n2=indice de fixation oculaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
isolé
n1=syndrome d'Apert | n2=isolé | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Lenoble-Aubineau (syndrome de)
n1=syndrome d'Apert | n2=Lenoble-Aubineau (syndrome de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
lié
n1=syndrome d'Apert | n2=lié | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
loucher sur
n1=syndrome d'Apert | n2=loucher sur | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
maladie de l'oeil
n1=syndrome d'Apert | n2=maladie de l'oeil | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
manoeuvre de Hallpike
n1=syndrome d'Apert | n2=manoeuvre de Hallpike | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
microphtalmie avec anomalies associées
n1=syndrome d'Apert | n2=microphtalmie avec anomalies associées | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
mouvement d'oscillation involontaire
n1=syndrome d'Apert | n2=mouvement d'oscillation involontaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
mouvement oscillatoire
n1=syndrome d'Apert | n2=mouvement oscillatoire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
mouvements involontaires des yeux
n1=syndrome d'Apert | n2=mouvements involontaires des yeux | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
mouvements oscillatoires
n1=syndrome d'Apert | n2=mouvements oscillatoires | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
muscles de l'oeil
n1=syndrome d'Apert | n2=muscles de l'oeil | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
myopie forte (génétique)
n1=syndrome d'Apert | n2=myopie forte (génétique) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
névrite vestibulaire
n1=syndrome d'Apert | n2=névrite vestibulaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
non précisé, nystagmus
n1=syndrome d'Apert | n2=non précisé, nystagmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nosologie
n1=syndrome d'Apert | n2=nosologie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Nyssen-van Bogaert (syndrome de)
n1=syndrome d'Apert | n2=Nyssen-van Bogaert (syndrome de) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmométrie
n1=syndrome d'Apert | n2=nystagmométrie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus
n1=syndrome d'Apert | n2=nystagmus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus (zone de moindre)
n1=syndrome d'Apert | n2=nystagmus (zone de moindre) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus congénital
n1=syndrome d'Apert | n2=nystagmus congénital | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus congénital essentiel
n1=syndrome d'Apert | n2=nystagmus congénital essentiel | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus congénital isolé
n1=syndrome d'Apert | n2=nystagmus congénital isolé | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus de défaut d'usage
n1=syndrome d'Apert | n2=nystagmus de défaut d'usage | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus de fixation
n1=syndrome d'Apert | n2=nystagmus de fixation | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus de positionnement
n1=syndrome d'Apert | n2=nystagmus de positionnement | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus dissocié
n1=syndrome d'Apert | n2=nystagmus dissocié | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus et autres anomalies des mouvements oculaires
n1=syndrome d'Apert | n2=nystagmus et autres anomalies des mouvements oculaires | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus et autres mouvements oculaires irréguliers
n1=syndrome d'Apert | n2=nystagmus et autres mouvements oculaires irréguliers | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus héréditaire vertical
n1=syndrome d'Apert | n2=nystagmus héréditaire vertical | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus idiopathique
n1=syndrome d'Apert | n2=nystagmus idiopathique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus latent
n1=syndrome d'Apert | n2=nystagmus latent | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus lié au sexe
n1=syndrome d'Apert | n2=nystagmus lié au sexe | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus manifeste
n1=syndrome d'Apert | n2=nystagmus manifeste | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus myoclonies
n1=syndrome d'Apert | n2=nystagmus myoclonies | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus pathologique
n1=syndrome d'Apert | n2=nystagmus pathologique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus pathologiques
n1=syndrome d'Apert | n2=nystagmus pathologiques | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus post-optocinétique
n1=syndrome d'Apert | n2=nystagmus post-optocinétique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
nystagmus see-saw
n1=syndrome d'Apert | n2=nystagmus see-saw | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
oculaire
n1=syndrome d'Apert | n2=oculaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
oeil
n1=syndrome d'Apert | n2=oeil | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
œil
n1=syndrome d'Apert | n2=œil | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
ophtalmologie
n1=syndrome d'Apert | n2=ophtalmologie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
optocinétique
n1=syndrome d'Apert | n2=optocinétique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
oscillation
n1=syndrome d'Apert | n2=oscillation | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
oscillations
n1=syndrome d'Apert | n2=oscillations | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
oscillopsie
n1=syndrome d'Apert | n2=oscillopsie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
pathologie
n1=syndrome d'Apert | n2=pathologie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
pendulaire (épreuve)
n1=syndrome d'Apert | n2=pendulaire (épreuve) | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
prépondérance directionnelle
n1=syndrome d'Apert | n2=prépondérance directionnelle | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
réflexe physiologique
n1=syndrome d'Apert | n2=réflexe physiologique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
réflexe vestibulo-oculomoteur
n1=syndrome d'Apert | n2=réflexe vestibulo-oculomoteur | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
saccadé
n1=syndrome d'Apert | n2=saccadé | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
sexe
n1=syndrome d'Apert | n2=sexe | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
signe clinique
n1=syndrome d'Apert | n2=signe clinique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
signe clinique en neurologie
n1=syndrome d'Apert | n2=signe clinique en neurologie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndactylie
n1=syndrome d'Apert | n2=syndactylie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
Syndrome d'Apert
n1=syndrome d'Apert | n2=Syndrome d'Apert | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome d'apert
n1=syndrome d'Apert | n2=syndrome d'apert | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de « un et demi »
n1=syndrome d'Apert | n2=syndrome de « un et demi » | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de El-Sahy-Waters
n1=syndrome d'Apert | n2=syndrome de El-Sahy-Waters | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de Joubert
n1=syndrome d'Apert | n2=syndrome de Joubert | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de Lenoble-Aubineau
n1=syndrome d'Apert | n2=syndrome de Lenoble-Aubineau | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de Marinesco-Sjögren
n1=syndrome d'Apert | n2=syndrome de Marinesco-Sjögren | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de Ohdo
n1=syndrome d'Apert | n2=syndrome de Ohdo | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome de Peters plus
n1=syndrome d'Apert | n2=syndrome de Peters plus | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome des fentes médianes
n1=syndrome d'Apert | n2=syndrome des fentes médianes | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome du vermis
n1=syndrome d'Apert | n2=syndrome du vermis | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome neuropathie, ataxie, rétinite pigmentaire
n1=syndrome d'Apert | n2=syndrome neuropathie, ataxie, rétinite pigmentaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome vestibulaire
n1=syndrome d'Apert | n2=syndrome vestibulaire | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome vestibulaire central
n1=syndrome d'Apert | n2=syndrome vestibulaire central | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
syndrome vestibulaire périphérique
n1=syndrome d'Apert | n2=syndrome vestibulaire périphérique | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
trouble de la vision
n1=syndrome d'Apert | n2=trouble de la vision | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
trouble de la vue
n1=syndrome d'Apert | n2=trouble de la vue | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
vertige
n1=syndrome d'Apert | n2=vertige | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
vertige de positionnement
n1=syndrome d'Apert | n2=vertige de positionnement | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
vertige positionnel
n1=syndrome d'Apert | n2=vertige positionnel | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
vidéonystagmographie
n1=syndrome d'Apert | n2=vidéonystagmographie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
vidéonystagmoscopie
n1=syndrome d'Apert | n2=vidéonystagmoscopie | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 10 / 0.019 ->
yeux
n1=syndrome d'Apert | n2=yeux | rel=r_associated | relid=0 | w=10
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
apophysite
n1=syndrome d'Apert | n2=apophysite | rel=r_associated | relid=0 | w=5
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
crânio-sténose
n1=syndrome d'Apert | n2=crânio-sténose | rel=r_associated | relid=0 | w=5
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
crâniosténose
n1=syndrome d'Apert | n2=crâniosténose | rel=r_associated | relid=0 | w=5
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
craniosténose
n1=syndrome d'Apert | n2=craniosténose | rel=r_associated | relid=0 | w=5
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
en:acrobrachykephaly
n1=syndrome d'Apert | n2=en:acrobrachykephaly | rel=r_associated | relid=0 | w=5
- syndrome d'Apert --
r_associated #0: 5 / 0.01 ->
en:craniosynostosis
n1=syndrome d'Apert | n2=en:craniosynostosis | rel=r_associated | relid=0 | w=5
| ≈ 149 relations entrantes
- médecine ---
r_associated #0: 389 -->
syndrome d'Apert
n1=médecine | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=389
- maladies ---
r_associated #0: 267 -->
syndrome d'Apert
n1=maladies | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=267
- acrocéphalosyndactylie ---
r_associated #0: 189 -->
syndrome d'Apert
n1=acrocéphalosyndactylie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=189
- acrocéphalosyndactylie de type I ---
r_associated #0: 152 -->
syndrome d'Apert
n1=acrocéphalosyndactylie de type I | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=152
- acro-céphalo-syndactylie ---
r_associated #0: 141 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=141
- FGFR2 gene ---
r_associated #0: 135 -->
syndrome d'Apert
n1=FGFR2 gene | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=135
- Crouzon (maladie de) ---
r_associated #0: 130 -->
syndrome d'Apert
n1=Crouzon (maladie de) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=130
- hypertélorisme ---
r_associated #0: 100 -->
syndrome d'Apert
n1=hypertélorisme | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=100
- en:hypertelorism ---
r_associated #0: 99 -->
syndrome d'Apert
n1=en:hypertelorism | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=99
- ACS
(acro-céphalo-syndactylie) ---
r_associated #0: 85 -->
syndrome d'Apert
n1=ACS (acro-céphalo-syndactylie) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=85
- acrocéphalosyndactylies ---
r_associated #0: 67 -->
syndrome d'Apert
n1=acrocéphalosyndactylies | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=67
- en:nystagmus ---
r_associated #0: 65 -->
syndrome d'Apert
n1=en:nystagmus | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=65
- nystagmus ---
r_associated #0: 64 -->
syndrome d'Apert
n1=nystagmus | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=64
- acro-céphalo-syndactylies ---
r_associated #0: 61 -->
syndrome d'Apert
n1=acro-céphalo-syndactylies | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=61
- syndrome ---
r_associated #0: 56 -->
syndrome d'Apert
n1=syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=56
- syndrome de saethre-chotzen ---
r_associated #0: 56 -->
syndrome d'Apert
n1=syndrome de saethre-chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=56
- syndrome de Saethre-Chotzen ---
r_associated #0: 52 -->
syndrome d'Apert
n1=syndrome de Saethre-Chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=52
- syndrome de pfeiffer ---
r_associated #0: 45 -->
syndrome d'Apert
n1=syndrome de pfeiffer | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=45
- télécanthus-hypertélorisme-strabisme (syndrome) ---
r_associated #0: 44 -->
syndrome d'Apert
n1=télécanthus-hypertélorisme-strabisme (syndrome) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=44
- acro-céphalo-syndactylie de type i ---
r_associated #0: 42 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type i | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=42
- syndrome de Pfeiffer ---
r_associated #0: 42 -->
syndrome d'Apert
n1=syndrome de Pfeiffer | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=42
- Médecine ---
r_associated #0: 41 -->
syndrome d'Apert
n1=Médecine | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=41
- ACS ---
r_associated #0: 40 -->
syndrome d'Apert
n1=ACS | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- ACS I ---
r_associated #0: 40 -->
syndrome d'Apert
n1=ACS I | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- Syndrome de Saethre-Chotzen ---
r_associated #0: 40 -->
syndrome d'Apert
n1=Syndrome de Saethre-Chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- en:ophtalmoplégie ---
r_associated #0: 40 -->
syndrome d'Apert
n1=en:ophtalmoplégie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- hypertélorisme, hypospadias, polysyndactylie (syndrome) ---
r_associated #0: 40 -->
syndrome d'Apert
n1=hypertélorisme, hypospadias, polysyndactylie (syndrome) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- hypertélorisme-microtie-fente faciale ---
r_associated #0: 40 -->
syndrome d'Apert
n1=hypertélorisme-microtie-fente faciale | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- médecine
(science) ---
r_associated #0: 40 -->
syndrome d'Apert
n1=médecine (science) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- syndrome de Chotzen ---
r_associated #0: 40 -->
syndrome d'Apert
n1=syndrome de Chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=40
- en:Apert-Crouzon maladie ---
r_associated #0: 39 -->
syndrome d'Apert
n1=en:Apert-Crouzon maladie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=39
- en:Chotzen's syndrome ---
r_associated #0: 39 -->
syndrome d'Apert
n1=en:Chotzen's syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=39
- Saethre-Chotzen (syndrome de) ---
r_associated #0: 37 -->
syndrome d'Apert
n1=Saethre-Chotzen (syndrome de) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=37
- en:telecanthus ---
r_associated #0: 37 -->
syndrome d'Apert
n1=en:telecanthus | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=37
- nystagmus héréditaire vertical ---
r_associated #0: 36 -->
syndrome d'Apert
n1=nystagmus héréditaire vertical | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=36
- ACPS ---
r_associated #0: 35 -->
syndrome d'Apert
n1=ACPS | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=35
- en:Apert's disease ---
r_associated #0: 35 -->
syndrome d'Apert
n1=en:Apert's disease | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=35
- en:type iii acrocephalosyndactyly ---
r_associated #0: 35 -->
syndrome d'Apert
n1=en:type iii acrocephalosyndactyly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=35
- acrocéphalosyndactylie, type iii ---
r_associated #0: 34 -->
syndrome d'Apert
n1=acrocéphalosyndactylie, type iii | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:Saethre-Chotzen's syndrome ---
r_associated #0: 34 -->
syndrome d'Apert
n1=en:Saethre-Chotzen's syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:acrodysplasie ---
r_associated #0: 34 -->
syndrome d'Apert
n1=en:acrodysplasie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:colobome irien ou choroïdien (rare) ---
r_associated #0: 34 -->
syndrome d'Apert
n1=en:colobome irien ou choroïdien (rare) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:orbites étroites ---
r_associated #0: 34 -->
syndrome d'Apert
n1=en:orbites étroites | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:type v acrocephalosyndactyly ---
r_associated #0: 34 -->
syndrome d'Apert
n1=en:type v acrocephalosyndactyly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- nystagmus lié au sexe ---
r_associated #0: 34 -->
syndrome d'Apert
n1=nystagmus lié au sexe | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- nystagmus myoclonies ---
r_associated #0: 34 -->
syndrome d'Apert
n1=nystagmus myoclonies | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=34
- en:Pfeiffer's syndrome ---
r_associated #0: 33 -->
syndrome d'Apert
n1=en:Pfeiffer's syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=33
- hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle ---
r_associated #0: 33 -->
syndrome d'Apert
n1=hernie diaphragmatique, exomphalocèle, absence de corps calleux, hypertélorisme, myopie et surdité neurosensorielle | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=33
- acro-céphalo-syndactylie de type iii ---
r_associated #0: 32 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type iii | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- acrocéphalie-crâne asymétrique et syndactylie modérée ---
r_associated #0: 32 -->
syndrome d'Apert
n1=acrocéphalie-crâne asymétrique et syndactylie modérée | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- acrocéphalosyndactylie d'Apert ---
r_associated #0: 32 -->
syndrome d'Apert
n1=acrocéphalosyndactylie d'Apert | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- acrocéphalosyndactylie type i ---
r_associated #0: 32 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type i | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- acrocéphalosyndactylie type v ---
r_associated #0: 32 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type v | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- en:FGFR2 en 10q26.13.3 ---
r_associated #0: 32 -->
syndrome d'Apert
n1=en:FGFR2 en 10q26.13.3 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- en:pfeiffer syndrome ---
r_associated #0: 32 -->
syndrome d'Apert
n1=en:pfeiffer syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- nystagmus congénital isolé ---
r_associated #0: 32 -->
syndrome d'Apert
n1=nystagmus congénital isolé | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=32
- Chotzen ---
r_associated #0: 31 -->
syndrome d'Apert
n1=Chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=31
- acro-céphalo-syndactylie d'apert ---
r_associated #0: 31 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie d'apert | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=31
- acrocéphalosyndactylie type iii ---
r_associated #0: 31 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type iii | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=31
- en:strabisme ---
r_associated #0: 31 -->
syndrome d'Apert
n1=en:strabisme | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=31
- Apert-Crouzon maladie ---
r_associated #0: 30 -->
syndrome d'Apert
n1=Apert-Crouzon maladie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=30
- en:absent corpus callosum ---
r_associated #0: 30 -->
syndrome d'Apert
n1=en:absent corpus callosum | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=30
- en:acrocéphalosyndactylie type Ia ---
r_associated #0: 30 -->
syndrome d'Apert
n1=en:acrocéphalosyndactylie type Ia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=30
- Maladies ---
r_associated #0: 29 -->
syndrome d'Apert
n1=Maladies | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=29
- acrocéphalosyndactylie type 1 ---
r_associated #0: 29 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type 1 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=29
- Apert (syndrome d') ---
r_associated #0: 28 -->
syndrome d'Apert
n1=Apert (syndrome d') | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- acro-céphalo-syndactylie de type 3 ---
r_associated #0: 28 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type 3 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- acro-céphalo-syndactylie de type 5 ---
r_associated #0: 28 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type 5 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- acrocéphalosyndactylie type 5 ---
r_associated #0: 28 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type 5 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- en:acrocephaly ---
r_associated #0: 28 -->
syndrome d'Apert
n1=en:acrocephaly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- en:apert-crouzon disease ---
r_associated #0: 28 -->
syndrome d'Apert
n1=en:apert-crouzon disease | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- en:cataracte ---
r_associated #0: 28 -->
syndrome d'Apert
n1=en:cataracte | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- en:type i acrocephalosyndactyly ---
r_associated #0: 28 -->
syndrome d'Apert
n1=en:type i acrocephalosyndactyly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=28
- acrocéphalosyndactylie type 3 ---
r_associated #0: 27 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type 3 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:acrocephalosyndactyly type I ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:acrocephalosyndactyly type I | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:and mild syndactyly ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:and mild syndactyly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:apert syndrome ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:apert syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:exomphalos ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:exomphalos | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:exophtalmie ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:exophtalmie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:kératite ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:kératite | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- en:saethre-chotzen syndrome ---
r_associated #0: 27 -->
syndrome d'Apert
n1=en:saethre-chotzen syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=27
- acro-céphalo-syndactylie de type 1 ---
r_associated #0: 26 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type 1 | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=26
- acro-céphalo-syndactylie de type v ---
r_associated #0: 26 -->
syndrome d'Apert
n1=acro-céphalo-syndactylie de type v | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=26
- en:kurczynski casperson syndrome ---
r_associated #0: 26 -->
syndrome d'Apert
n1=en:kurczynski casperson syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=26
- syndrome d ---
r_associated #0: 26 -->
syndrome d'Apert
n1=syndrome d | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=26
- en:strabismus syndrome ---
r_associated #0: 25 -->
syndrome d'Apert
n1=en:strabismus syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=25
- en:talantropia ---
r_associated #0: 25 -->
syndrome d'Apert
n1=en:talantropia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=25
- en:nystaxis ---
r_associated #0: 24 -->
syndrome d'Apert
n1=en:nystaxis | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=24
- acrocéphalosyndactylie, type i ---
r_associated #0: 23 -->
syndrome d'Apert
n1=acrocéphalosyndactylie, type i | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=23
- en:acrocephalosyndactyly ---
r_associated #0: 23 -->
syndrome d'Apert
n1=en:acrocephalosyndactyly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=23
- télécanthus ---
r_associated #0: 23 -->
syndrome d'Apert
n1=télécanthus | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=23
- en:diaphragmatic hernia ---
r_associated #0: 22 -->
syndrome d'Apert
n1=en:diaphragmatic hernia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=22
- en:nystagmuses ---
r_associated #0: 22 -->
syndrome d'Apert
n1=en:nystagmuses | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=22
- maladie ---
r_associated #0: 22 -->
syndrome d'Apert
n1=maladie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=22
- processus pathologique ---
r_associated #0: 22 -->
syndrome d'Apert
n1=processus pathologique | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=22
- Apert ---
r_associated #0: 21 -->
syndrome d'Apert
n1=Apert | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- Pfeiffer (syndrome de) ---
r_associated #0: 21 -->
syndrome d'Apert
n1=Pfeiffer (syndrome de) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- acrocéphalie ---
r_associated #0: 21 -->
syndrome d'Apert
n1=acrocéphalie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- acrocéphalosyndactylie type Ia ---
r_associated #0: 21 -->
syndrome d'Apert
n1=acrocéphalosyndactylie type Ia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- acrodysplasie ---
r_associated #0: 21 -->
syndrome d'Apert
n1=acrodysplasie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- caryotype ---
r_associated #0: 21 -->
syndrome d'Apert
n1=caryotype | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- colobome de l'iris avec ptosis, hypertélorisme et retard mental ---
r_associated #0: 21 -->
syndrome d'Apert
n1=colobome de l'iris avec ptosis, hypertélorisme et retard mental | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- en:acrodysplasia ---
r_associated #0: 21 -->
syndrome d'Apert
n1=en:acrodysplasia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- en:skull asymetry ---
r_associated #0: 21 -->
syndrome d'Apert
n1=en:skull asymetry | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=21
- Syndrome ---
r_associated #0: 20 -->
syndrome d'Apert
n1=Syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=20
- acrobrachycéphalie ---
r_associated #0: 15 -->
syndrome d'Apert
n1=acrobrachycéphalie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=15
- chotzen ---
r_associated #0: 15 -->
syndrome d'Apert
n1=chotzen | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=15
- en:acrobrachykephaly ---
r_associated #0: 15 -->
syndrome d'Apert
n1=en:acrobrachykephaly | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=15
- Caryotype ---
r_associated #0: 10 -->
syndrome d'Apert
n1=Caryotype | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- Hypertélorisme ---
r_associated #0: 10 -->
syndrome d'Apert
n1=Hypertélorisme | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- Nyssen-van Bogaert (syndrome de) ---
r_associated #0: 10 -->
syndrome d'Apert
n1=Nyssen-van Bogaert (syndrome de) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- apophysite calcanéenne ---
r_associated #0: 10 -->
syndrome d'Apert
n1=apophysite calcanéenne | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- apophysite tibiale antérieure ---
r_associated #0: 10 -->
syndrome d'Apert
n1=apophysite tibiale antérieure | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- apoplexie utéroplacentaire ---
r_associated #0: 10 -->
syndrome d'Apert
n1=apoplexie utéroplacentaire | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:X-linked ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:X-linked | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:and sensorineural deafness ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:and sensorineural deafness | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:caryotype ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:caryotype | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:congenital ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:congenital | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:facial clefting syndrome ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:facial clefting syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:hereditary vertical ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:hereditary vertical | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:hypospadias ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:hypospadias | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:iris coloboma with ptosis ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:iris coloboma with ptosis | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:microtia ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:microtia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:myoclonic ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:myoclonic | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:myopia ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:myopia | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- en:polysyndactyly syndrome ---
r_associated #0: 10 -->
syndrome d'Apert
n1=en:polysyndactyly syndrome | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hernie diaphragmatique ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hernie diaphragmatique | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertensinase ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertensinase | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertensine ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertensine | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertensinogène ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertensinogène | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertension ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertension | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertension abdominale ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertension abdominale | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- hypertension artérielle ---
r_associated #0: 10 -->
syndrome d'Apert
n1=hypertension artérielle | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- maladie d'apert ---
r_associated #0: 10 -->
syndrome d'Apert
n1=maladie d'apert | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- maladie de Crouzon ---
r_associated #0: 10 -->
syndrome d'Apert
n1=maladie de Crouzon | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- omphalocèle ---
r_associated #0: 10 -->
syndrome d'Apert
n1=omphalocèle | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécardiographie ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécardiographie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécardiophone ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécardiophone | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- téléclitoridie ---
r_associated #0: 10 -->
syndrome d'Apert
n1=téléclitoridie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécobalt ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécobalt | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécobalt-thérapie ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécobalt-thérapie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- téléconsultation ---
r_associated #0: 10 -->
syndrome d'Apert
n1=téléconsultation | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécrâne ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécrâne | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télécæsiothérapie ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télécæsiothérapie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télédermatologie ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télédermatologie | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télédiastole ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télédiastole | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- télédétection ---
r_associated #0: 10 -->
syndrome d'Apert
n1=télédétection | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=10
- Chotzen (syndrome de) ---
r_associated #0: 5 -->
syndrome d'Apert
n1=Chotzen (syndrome de) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=5
- nystagmus (zone de moindre) ---
r_associated #0: 5 -->
syndrome d'Apert
n1=nystagmus (zone de moindre) | n2=syndrome d'Apert | rel=r_associated | relid=0 | w=5
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