Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 24
- Term ID
- DOID:0111615
- Synonyms
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- SCAR24
- Definition
- An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the UBA5 gene on chromosome 3q22.1. https://www.ncbi.nlm.nih.gov/pubmed/26872069
- References
- Ontology
- Human Disease ( DOID:0111615 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models