Visualize Submit Comment
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

MIM:617691

Parent Relationships

is_a autosomal dominant cerebellar ataxia

Add an item to the term tracker