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Metadata
ID	DOID:0111614
Name	autosomal recessive spinocerebellar ataxia 22
Definition	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2. https://www.ncbi.nlm.nih.gov/pubmed/26157035
Xrefs	OMIM:616948
Synonyms	SCAR22 [EXACT]
Parent Relationships	is_a autosomal recessive cerebellar ataxia