Search Ontology:
Human Disease
autosomal recessive spinocerebellar ataxia 25
- Term ID
- DOID:0080259
- Synonyms
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- SCAR25
- Definition
- An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the ATG5 gene on chromosome 6q21. https://www.ncbi.nlm.nih.gov/pubmed/26812546
- References
- Ontology
- Human Disease ( DOID:0080259 )
- is a type of
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Other Pages
Genes Involved
Zebrafish Models