Diko : en:ackerman syndrome

en:ackerman syndrome

Catégories

Nom

Informations lexicales

Langue:anglais

Variantes

›

en:Ackerman syndrome

‹

en:Ackerman syndrome

Définitions

Affection rare associant glaucome juvénile, racines des molaires pyramidales, anomalies digitales et hypotrichie. [Dictionnaire médical de l'Académie de Médecine]

Liens externes

›

umls:C1860167

Associations d'idées

[F]

›

111

•

en:glaucoma

•

syndrome

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome

•

en:timothy syndrome type 2

•

en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome

•

en:steatocystoma multiplex with natal tooth syndrome

•

en:hyperinsulinism due to uncoupling protein 2 deficiency

•

en:aniridia, ptosis, intellectual disability, familial obesity syndrome

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:kallman syndrome with heart disease

•

en:double uterus, hemivagina, renal agenesis syndrome

•

en:congenital analbuminemia

•

en:congenital disorder of glycosylation type 2e

•

en:hypertrichosis and acromegaloid facial appearance syndrome

•

en:diffuse palmoplantar keratoderma and acrocyanosis syndrome

•

en:hypohidrosis due to genetic abnormality of eccrine gland structure and function

•

en:craniofacial ulnar renal syndrome

•

en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency

•

en:absence of fingerprints with congenital milia syndrome

•

en:cooper jabs syndrome

•

en:autosomal dominant palmoplantar keratoderma and congenital alopecia

•

en:hall riggs syndrome

•

en:lethal larsen-like syndrome

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:dyschondrosteosis and nephritis syndrome

•

syndrome d'Ackerman

•

en:moyamoya disease with early onset achalasia

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:hyperinsulinism due to hnf1a deficiency

•

en:hyperinsulinism due to insulin receptor deficiency

•

en:arterial dissection and lentiginosis syndrome

•

en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein

•

en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency

•

en:robinow-like syndrome

•

en:autosomal recessive spastic paraplegia type 39

•

en:congenital disorder of glycosylation type 1h

•

en:familial median cleft of upper and lower lip

•

en:deafness and myopia syndrome

•

en:braddock syndrome

•

en:congenital cataract with ataxia and deafness syndrome

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:oculocutaneous albinism type 6

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:basal epidermolysis bullosa simplex

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:ectodermal dysplasia with blindness syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome

•

en:generalized peeling skin syndrome

•

en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges

•

en:odonto onycho dysplasia with alopecia syndrome

•

en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

•

en:acro-dermato-ungual-lacrimal-tooth syndrome

•

en:congenital disorder of glycosylation, type if

•

en:split-hand/foot malformation 3

•

en:genetic disorder of skin pigmentation

•

en:bestrophinopathy, autosomal recessive

•

en:hair-nail ectodermal dysplasia

•

en:chronic diarrhea with villous atrophy syndrome

•

en:arthrogryposis renal dysfunction cholestasis syndrome

•

en:thoraco-abdominal enteric duplication

•

en:insulin growth factor i deficiency

•

anomalies morphologiques maxillofaciales

•

en:non-androgenic hypertrichosis with genetic disease

•

en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome

•

glaucome

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

•

en:congenital disorder of glycosylation type id

•

en:congenital disorder of glycosylation type ie

•

en:didymosis aplasticosebacea

•

en:distal monosomy 10q syndrome

•

en:familial malignant melanoma of skin

•

glaucoma

•

en:anauxetic dysplasia

•

en:brain calcification rajab type

•

en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:najjar syndrome

•

en:pelviscapular dysplasia

•

en:acrorenal mandibular syndrome

•

en:manouvrier syndrome

•

en:scholte syndrome

•

en:diaphanospondylodysostosis

•

en:hypomandibular faciocranial dysostosis

•

en:pili torti onychodysplasia syndrome

•

en:renal dysplasia - limb defects syndrome

•

en:heart defects limb shortening

•

en:microcephaly albinism digital anomalies syndrome

•

en:fountain syndrome

•

en:tooth malformation

•

en:pterygium colli mental retardation digital anomalies

•

en:late-onset junctional epidermolysis bullosa

•

en:dystrophic epidermolysis bullosa nails only

•

en:hirschsprung disease with type d brachydactyly syndrome

•

malformations maxillo-faciales

•

malformations maxillofaciales

•

en:maxillofacial abnormalities

•

en:halal syndrome

•

en:bamforth syndrome

•

molaires à racine pyramidale avec glaucome juvénile et anomalie de la lèvre supérieure

•

en:Ackerman's syndrome

•

Ackerman (syndrome d')

•

molaires à racine pyramidale avec glaucome juvénile et anomalie de la lèvre supérieure.

•

syndrome d

•

Ackerman

•

glaucome juvénile avec anomalie de la lèvre supérieure et des racines dentaires

•

processus pathologique

•

affection

◀

‹

106

anomalies morphologiques maxillofaciales

•

en:maxillofacial abnormalities

•

malformations maxillofaciales

•

malformations maxillo-faciales

•

glaucoma

•

en:glaucoma

•

glaucome

•

en:dystrophic epidermolysis bullosa nails only

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:oculocutaneous albinism type 6

•

en:brain calcification rajab type

•

en:scholte syndrome

•

en:distal monosomy 10q syndrome

•

en:insulin growth factor i deficiency

•

en:braddock syndrome

•

en:timothy syndrome type 2

•

en:congenital disorder of glycosylation type 2e

•

en:robinow-like syndrome

•

en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome

•

en:bestrophinopathy, autosomal recessive

•

en:anauxetic dysplasia

•

en:ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis

•

en:fountain syndrome

•

en:acro-dermato-ungual-lacrimal-tooth syndrome

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:autosomal dominant palmoplantar keratoderma and congenital alopecia

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:congenital cataract with ataxia and deafness syndrome

•

en:deafness and myopia syndrome

•

en:congenital disorder of glycosylation type 1h

•

en:acute infantile liver failure due to synthesis defect of mitochondrial deoxyribonucleic acid encoded protein

•

en:moyamoya disease with early onset achalasia

•

en:heart defects limb shortening

•

en:didymosis aplasticosebacea

•

en:odonto onycho dysplasia with alopecia syndrome

•

en:genetic disorder of skin pigmentation

•

en:congenital disorder of glycosylation, type if

•

en:hirschsprung disease with type d brachydactyly syndrome

•

en:generalized peeling skin syndrome

•

en:anonychia-onychodystrophy with hypoplasia or absence of distal phalanges

•

en:absence of fingerprints with congenital milia syndrome

•

en:craniofacial ulnar renal syndrome

•

en:kallman syndrome with heart disease

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:autosomal recessive spastic paraplegia type 39

•

en:renal dysplasia - limb defects syndrome

•

en:thoraco-abdominal enteric duplication

•

en:halal syndrome

•

en:pterygium colli mental retardation digital anomalies

•

en:bamforth syndrome

•

en:hypertrichosis and acromegaloid facial appearance syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:dyschondrosteosis and nephritis syndrome

•

en:aniridia, ptosis, intellectual disability, familial obesity syndrome

•

en:dentinogenesis imperfecta, short stature, hearing loss, intellectual disability syndrome

•

en:hyperinsulinism due to uncoupling protein 2 deficiency

•

en:cooper jabs syndrome

•

en:non-androgenic hypertrichosis with genetic disease

•

en:diaphanospondylodysostosis

•

en:congenital disorder of glycosylation type ie

•

en:lethal larsen-like syndrome

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:arterial dissection and lentiginosis syndrome

•

en:hyperinsulinism due to insulin receptor deficiency

•

en:late-onset junctional epidermolysis bullosa

•

en:steatocystoma multiplex with natal tooth syndrome

•

en:congenital analbuminemia

•

en:hypohidrosis due to genetic abnormality of eccrine gland structure and function

•

en:najjar syndrome

•

en:acrorenal mandibular syndrome

•

en:hypotrichosis-osteolysis-periodontitis-palmoplantar keratoderma syndrome

•

en:chronic diarrhea with villous atrophy syndrome

•

en:arthrogryposis renal dysfunction cholestasis syndrome

•

en:familial malignant melanoma of skin

•

en:manouvrier syndrome

•

en:pili torti onychodysplasia syndrome

•

en:diffuse palmoplantar keratoderma and acrocyanosis syndrome

•

en:ectodermal dysplasia with blindness syndrome

•

en:palmoplantar keratoderma, 46,xx sex reversal, predisposition to squamous cell carcinoma syndrome

•

en:hyperinsulinism due to hnf1a deficiency

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

en:microcephaly albinism digital anomalies syndrome

•

en:split-hand/foot malformation 3

•

en:hair-nail ectodermal dysplasia

•

en:pulmonary fibrosis, hepatic hyperplasia, bone marrow hypoplasia syndrome

•

en:hypomandibular faciocranial dysostosis

•

en:congenital disorder of glycosylation type id

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

•

en:tooth malformation

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:mendelian susceptibility to mycobacterial disease due to complete interleukin 12 subunit beta deficiency

•

en:pelviscapular dysplasia

•

en:familial median cleft of upper and lower lip

•

en:double uterus, hemivagina, renal agenesis syndrome

•

en:hall riggs syndrome

•

en:basal epidermolysis bullosa simplex

•

en:glycogen storage disease with severe cardiomyopathy due to glycogenin deficiency

•

syndrome

•

Glasgow (score de)

•

Glaucome

•

absence d'empreintes digitales avec syndrome de milia congénital

•

glaucome à pression normale

•

glaucome à angle ouvert

•

glaucome à angle fermé

◀

Synonymes et quasi-synonymes

›

molaires à racine pyramidale avec glaucome juvénile et anomalie de la lèvre supérieure

•

Ackerman (syndrome d')

•

molaires à racine pyramidale avec glaucome juvénile et anomalie de la lèvre supérieure.

•

glaucome juvénile avec anomalie de la lèvre supérieure et des racines dentaires

Génériques

[F] [H]

›

en:syndrome

•

affection

•

syndrome d

•

processus pathologique

•

syndrome

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons - C0 domaine public) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=8621279 • caches: c1=14 c2=121 c3=108

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