Search Ontology:
Human Disease
spinocerebellar ataxia type 30
- Term ID
- DOID:0050979
- Synonyms
-
- 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
- References
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- GARD:4950
- MIM:613371
- Ontology
- Human Disease ( DOID:0050979 )
- is a type of
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