Search Ontology:
Human Disease
autosomal dominant cerebellar ataxia
- Term ID
- DOID:1441
- Synonyms
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- spinocerebellar ataxia
- Definition
- A cerebellar ataxia that has_material_basis_in autosomal dominant inheritance. (2)
- References
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- MESH:D020754
- MIM:PS164400
- NCI:C82341
- ORDO:94
- SNOMEDCT_US_2023_03_01:129609000
- UMLS_CUI:C0087012
- Ontology
- Human Disease ( DOID:1441 )
- is a type of
-
- has subtype
Other Pages
Genes Involved
Zebrafish Models