Term Name: | spinocerebellar ataxia type 38 |
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Synonyms: | |
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. |
Ontology: | Human Disease [DOID:0050985] ( DOID:0050985 ) |