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Metadata
ID DOID:0050979
Name spinocerebellar ataxia type 30
Definition An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene.
https://www.omim.org/entry/613371
Xrefs

GARD:4950

OMIM:613371

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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