Search Ontology:
Human Disease
spinocerebellar ataxia type 7
- Term ID
- DOID:0050958
- Synonyms
-
- Definition
- An autosomal dominant cerebellar ataxia that is characterized by ataxia, progressive vision loss, and failure to thrive, has_material_basis_in mutation in the ATXN7 gene. https://rarediseases.info.nih.gov/diseases/4955/spinocerebellar-ataxia-7
- References
- Ontology
- Human Disease ( DOID:0050958 )
- is a type of
-
Show first 5 Terms
Other Pages
Genes Involved
Zebrafish Models