|OBO ID: DOID:0050985|
|Term Name:||spinocerebellar ataxia type 38||Search Ontology:|
|Definition:||An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and nystagmus, presenting in mid-adulthood, and has_material_basis_in mutation to the ELOVL5 gene. https://www.omim.org/entry/615957|
|Ontology:||Human Disease (DOID:0050985)|
|is a type of:||
OTHER spinocerebellar ataxia type 38 PAGES
ZEBRAFISH MODELS No data available
PHENOTYPE No data available
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