Le Diko - en:brain dopamine-serotonin vesicular transport disease

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Le Diko - en:brain dopamine-serotonin vesicular transport disease

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le dictionnaire d'associations lexicales
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en:brain dopamine-serotonin vesicular transport disease

Nom

Informations lexicales

Langue:anglais

Informations sémantiques

source:wiki

Associations d'idées

68

maladie

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•

cerveau

•

•

en:juvenile amyotrophic lateral sclerosis

•

en:kallman syndrome with heart disease

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

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

•

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

•

en:hall riggs syndrome

•

en:congenital disorder of glycosylation type 2e

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:lethal larsen-like syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:ectodermal dysplasia with blindness syndrome

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

en:oculocutaneous albinism type 6

•

en:moyamoya disease with early onset achalasia

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:braddock syndrome

•

en:deafness and myopia syndrome

•

en:congenital disorder of glycosylation type 1h

•

en:autosomal recessive spastic paraplegia type 39

•

en:robinow-like syndrome

•

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

•

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:autosomal dominant focal dystonia dyt25 type

•

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

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

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

•

en:congenital cataract with ataxia and deafness syndrome

•

en:congenital analbuminemia

•

en:aphalangy and syndactyly with microcephaly syndrome

•

en:bamforth syndrome

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en:congenital disorder of glycosylation type ie

•

en:congenital disorder of glycosylation type id

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

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en:insulin growth factor i deficiency

•

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

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en:bestrophinopathy, autosomal recessive

•

en:split-hand/foot malformation 3

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en:congenital disorder of glycosylation, type if

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en:brain calcification rajab type

•

en:anauxetic dysplasia

•

en:pili torti onychodysplasia syndrome

•

en:late-onset junctional epidermolysis bullosa

•

en:halal syndrome

•

en:fountain syndrome

•

en:craniofacial ulnar renal syndrome

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:heart defects limb shortening

•

en:renal dysplasia - limb defects syndrome

•

en:microcephaly albinism digital anomalies syndrome

•

en:hypomandibular faciocranial dysostosis

•

en:diaphanospondylodysostosis

•

en:manouvrier syndrome

•

en:acrorenal mandibular syndrome

•

en:pelviscapular dysplasia

•

en:najjar syndrome

•

en:familial median cleft of upper and lower lip

•

en:generalized peeling skin syndrome

•

en:cooper jabs syndrome

•

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

•

en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome

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65

en:deafness and myopia syndrome

•

en:pelviscapular dysplasia

•

en:renal dysplasia - limb defects syndrome

•

en:pili torti onychodysplasia syndrome

•

en:ehlers-danlos syndrome kyphoscoliotic and deafness type

•

en:manouvrier syndrome

•

en:brain calcification rajab type

•

en:bamforth syndrome

•

en:yemenite deaf-blind hypopigmentation syndrome

•

en:bestrophinopathy, autosomal recessive

•

en:familial median cleft of upper and lower lip

•

en:primary immunodeficiency syndrome due to p14 deficiency

•

en:lissencephaly type 3 familial fetal akinesia sequence syndrome

•

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

•

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

•

en:diaphanospondylodysostosis

•

en:congenital disorder of glycosylation, type if

•

en:halal syndrome

•

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

•

en:spondyloepiphyseal dysplasia tarda kohn type

•

en:moyamoya disease with early onset achalasia

•

en:braddock syndrome

•

en:zellweger-like syndrome without peroxisomal anomaly

•

en:aphalangy and syndactyly with microcephaly syndrome

•

en:late-onset junctional epidermolysis bullosa

•

en:insulin growth factor i deficiency

•

en:congenital disorder of glycosylation type ie

•

en:kallman syndrome with heart disease

•

en:generalized peeling skin syndrome

•

en:cooper jabs syndrome

•

en:congenital disorder of glycosylation type 2e

•

en:cutaneous photosensitivity and lethal colitis syndrome

•

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

•

en:ectodermal dysplasia with blindness syndrome

•

en:juvenile amyotrophic lateral sclerosis

•

en:congenital analbuminemia

•

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

•

en:congenital cataract with ataxia and deafness syndrome

•

en:robinow-like syndrome

•

en:leukoencephalopathy with metaphyseal chondrodysplasia syndrome

•

en:lethal larsen-like syndrome

•

en:microcephaly albinism digital anomalies syndrome

•

en:heart defects limb shortening

•

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

•

en:mesoaxial synostotic syndactyly with phalangeal reduction syndrome

•

en:fountain syndrome

•

en:congenital disorder of glycosylation type id

•

en:split-hand/foot malformation 3

•

en:anauxetic dysplasia

•

en:hall riggs syndrome

•

en:najjar syndrome

•

en:adducted thumbs and arthrogryposis syndrome christian type

•

en:oculocutaneous albinism type 6

•

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

•

en:autosomal recessive spastic paraplegia type 39

•

en:spondylometaphyseal dysplasia with cone-rod dystrophy syndrome

•

en:cervical hypertrichosis and peripheral neuropathy syndrome

•

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

•

en:autosomal dominant focal dystonia dyt25 type

•

en:congenital disorder of glycosylation type 1h

•

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

•

en:craniofacial ulnar renal syndrome

•

en:acrorenal mandibular syndrome

•

en:hypomandibular faciocranial dysostosis

•

maladie

◀

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

• This page link : https://www.jeuxdemots.org/diko.php?gotermid=9102521 • caches: c1=8 c2=70 c3=66

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