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Metadata
ID DOID:0050985
Name spinocerebellar ataxia type 38
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
Xrefs

OMIM:615957

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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