Visualize Submit Comment

Metadata
ID	DOID:0080064
Name	autosomal recessive spinocerebellar ataxia 17
Definition	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CWF19L1 gene on chromosome 10q24. https://www.ncbi.nlm.nih.gov/pubmed/26197978
Xrefs	OMIM:616127
Synonyms	SCAR17 [EXACT]
Parent Relationships	is_a autosomal recessive cerebellar ataxia