Search Ontology:
Human Disease

spinocerebellar ataxia 44

Term ID
DOID:0080286
Synonyms
Definition
An autosomal dominant cerebellar ataxia that has_material_basis_in heterozygous mutation in the GRM1 gene on chromosome 6q24. https://pubmed.ncbi.nlm.nih.gov/28886343/
References
Ontology
Human Disease   ( DOID:0080286 )
Relationships
is a type of
Other Pages
Genes Involved
Zebrafish Models