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Metadata
ID DOID:0080062
Name autosomal recessive spinocerebellar ataxia 13
Definition An autosomal recessive cerebellar ataxia that is characterized by delayed psychomotor development beginning in infancy and that has_material_basis_in homozygous mutation in the GRM1 gene on chromosome 6q24.
https://www.ncbi.nlm.nih.gov/pubmed/22901947
Xrefs

OMIM:614831

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is_a autosomal recessive cerebellar ataxia

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