Diko : en:teebi kaurah syndrome

en:teebi kaurah syndrome

Catégories

Nom

Informations lexicales

Langue:anglais

Informations sémantiques

Liens externes

›

umls:C2931373

Associations d'idées

[F]

›

syndrome

•

en:timothy syndrome type 2

•

en:ectodermal dysplasia with blindness syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:lethal larsen-like syndrome

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:congenital disorder of glycosylation type 2e

•

en:hall riggs syndrome

•

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

•

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

•

en:basal epidermolysis bullosa simplex

•

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:adducted thumbs and arthrogryposis syndrome christian type

•

en:aphalangy and syndactyly with microcephaly syndrome

•

en:congenital analbuminemia

•

en:double uterus, hemivagina, renal agenesis syndrome

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:diffuse palmoplantar keratoderma and acrocyanosis syndrome

•

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

•

en:moyamoya disease with early onset achalasia

•

en:x-linked intellectual disability with ataxia and apraxia syndrome

•

en:x-linked intellectual disability with acromegaly and hyperactivity syndrome

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:autosomal dominant focal dystonia dyt25 type

•

en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome

•

en:arterial dissection and lentiginosis syndrome

•

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

•

en:robinow-like syndrome

•

en:juvenile amyotrophic lateral sclerosis

•

en:autosomal recessive spastic paraplegia type 39

•

en:dyschondrosteosis and nephritis syndrome

•

en:congenital disorder of glycosylation type 1h

•

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:hypertrichosis and acromegaloid facial appearance syndrome

•

en:porencephaly

•

en:non-androgenic hypertrichosis with genetic disease

•

en:brain calcification rajab type

•

en:fountain syndrome

•

en:pterygium colli mental retardation digital anomalies

•

en:bamforth syndrome

•

en:halal syndrome

•

en:late-onset junctional epidermolysis bullosa

•

en:brain malformation, congenital heart disease, postaxial polydactyly syndrome

•

en:pili torti onychodysplasia syndrome

•

en:anauxetic dysplasia

•

en:congenital disorder of glycosylation, type if

•

en:heart defects limb shortening

•

en:split-hand/foot malformation 3

•

en:genetic disorder of skin pigmentation

•

en:bestrophinopathy, autosomal recessive

•

en:nails, malformed

•

en:arthrogryposis renal dysfunction cholestasis syndrome

•

en:thoraco-abdominal enteric duplication

•

en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome

•

en:insulin growth factor i deficiency

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:renal dysplasia - limb defects syndrome

•

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

•

en:familial median cleft of upper and lower lip

•

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:congenital cerebral ventriculomegaly

•

en:generalized peeling skin syndrome

•

en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome

•

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

•

en:microcephaly albinism digital anomalies syndrome

•

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

•

en:najjar syndrome

•

en:pelviscapular dysplasia

•

en:acrorenal mandibular syndrome

•

en:manouvrier syndrome

•

en:scholte syndrome

•

en:diaphanospondylodysostosis

•

en:hypomandibular faciocranial dysostosis

•

en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome

◀

‹

en:congenital disorder of glycosylation type 1h

•

en:autosomal dominant palmoplantar keratoderma and congenital alopecia

•

en:kallman syndrome with heart disease

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:congenital cataract with ataxia and deafness syndrome

•

en:manouvrier syndrome

•

en:split-hand/foot malformation 3

•

en:bamforth syndrome

•

en:pterygium colli mental retardation digital anomalies

•

en:diaphanospondylodysostosis

•

en:generalized peeling skin syndrome

•

en:acrorenal mandibular syndrome

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

en:basal epidermolysis bullosa simplex

•

en:braddock syndrome

•

en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome

•

en:familial median cleft of upper and lower lip

•

en:nails, malformed

•

en:microcephaly albinism digital anomalies syndrome

•

en:scholte syndrome

•

en:double uterus, hemivagina, renal agenesis syndrome

•

en:moyamoya disease with early onset achalasia

•

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

•

en:x-linked intellectual disability with corpus callosum agenesis and spastic quadriparesis syndrome

•

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

•

en:craniofacial ulnar renal syndrome

•

en:anauxetic dysplasia

•

en:heart defects limb shortening

•

en:thoraco-abdominal enteric duplication

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

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

•

en:oculocutaneous albinism type 6

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:arterial dissection and lentiginosis syndrome

•

en:lethal larsen-like syndrome

•

en:hall riggs syndrome

•

en:megalencephaly, polymicrogyria, postaxial polydactyly, hydrocephalus syndrome

•

en:late-onset junctional epidermolysis bullosa

•

en:brain malformation, congenital heart disease, postaxial polydactyly syndrome

•

en:congenital disorder of glycosylation, type if

•

en:polyneuropathy, hearing loss, ataxia, retinitis pigmentosa, cataract syndrome

•

en:brain calcification rajab type

•

en:najjar syndrome

•

en:pili torti onychodysplasia syndrome

•

en:pelviscapular dysplasia

•

en:deafness and myopia syndrome

•

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

•

en:diffuse palmoplantar keratoderma and acrocyanosis syndrome

•

en:congenital analbuminemia

•

en:congenital disorder of glycosylation type 2e

•

en:autosomal dominant focal dystonia dyt25 type

•

en:non-androgenic hypertrichosis with genetic disease

•

en:bestrophinopathy, autosomal recessive

•

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

•

en:cooper jabs syndrome

•

en:timothy syndrome type 2

•

en:aphalangy and syndactyly with microcephaly syndrome

•

en:ectodermal dysplasia with blindness syndrome

•

en:dyschondrosteosis and nephritis syndrome

•

en:autosomal recessive spastic paraplegia type 39

•

en:robinow-like syndrome

•

en:arthrogryposis renal dysfunction cholestasis syndrome

•

en:halal syndrome

•

en:fountain syndrome

•

en:renal dysplasia - limb defects syndrome

•

en:congenital cerebral ventriculomegaly

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:juvenile amyotrophic lateral sclerosis

•

en:x-linked intellectual disability with acromegaly and hyperactivity syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

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

•

en:hypomandibular faciocranial dysostosis

•

en:absence of fingerprints with congenital milia syndrome

•

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

•

en:porencephaly

•

en:hypertrichosis and acromegaloid facial appearance syndrome

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:x-linked intellectual disability with ataxia and apraxia syndrome

•

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

•

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

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:genetic disorder of skin pigmentation

•

en:insulin growth factor i deficiency

•

syndrome

•

absence d'empreintes digitales avec syndrome de milia congénital

◀

• Mathieu Lafourcade • LIRMM (données libres en Creative Commons) •

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=9102744 • caches: c1=44 c2=308 c3=104

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