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Metadata
ID DOID:0080286
Name spinocerebellar ataxia 44
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/
Xrefs

OMIM:617691

Parent Relationships

is_a autosomal dominant cerebellar ataxia

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