marie's ataxia
61Erythrokeratodermia variabilis — Classification and external resources OMIM 133200 Erythrokeratodermia variabilis (also known as Erythrokeratodermia figurata variabilis, Keratosis extremitatum progrediens, Keratosis palmoplantaris transgrediens et progrediens, [1] …
62Vohwinkel syndrome — Classification and external resources OMIM 124500 DiseasesDB 32216 eMedicine …
63Hallermann–Streiff syndrome — Classification and external resources ICD 9 756.0 OMIM 234100 DiseasesDB …
64Hereditary elliptocytosis — Classification and external resources Blood smear showing elliptocytes ICD 10 D …
65Nonsyndromic deafness — is hearing loss that is not associated with other signs and symptoms. In contrast, syndromic deafness involves hearing loss that occurs with abnormalities in other parts of the body. Genetic changes are related to the following types of… …
66Adrenoleukodystrophy — Classification and external resources T2 weighted axial scan at the level of the caudate heads demonstrates marked loss of posterior white matter, with reduced volume and increased signal intensity. The anterior white matter is spared. Features… …
67Rett syndrome — Classification and external resources ICD 10 F84.2 ICD 9 330.8 …
68Primidone — Systematic (IUPAC) name 5 ethyl 5 phenyl hexahydropyrimidine 4,6 dione Clinical data Pregnancy cat. D …
69Chromosome 11 (human) — Chromosome 11 Chart Chromosome 11 is one of the 23 pairs of chromosomes in humans. Humans normally have two copies of this chromosome. Chromosome 11 spans about 134.5 million base pairs (the building material of DNA) and represents between 4 and… …
70Ataxie — En médecine, l ataxie (du grec ataxiā, signifiant « désordre ») est une pathologie neuromusculaire qui consiste en un manque de coordination fine des mouvements volontaires. Elle n est pas liée à une déficience physique des muscles mais …
