Search Ontology:
Human Disease
spinocerebellar ataxia type 37
- Term ID
- DOID:0050984
- Synonyms
-
- Definition
- An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia and dysarthria, presenting in mid-adulthood, and has_material_basis_in mutation to the DAB1 gene. https://www.omim.org/entry/615945
- References
- Ontology
- Human Disease ( DOID:0050984 )
- is a type of
-
Other Pages
Genes Involved
Zebrafish Models