Term Name:	autosomal recessive spinocerebellar ataxia 22
Synonyms:	SCAR22
Definition:	An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the VWA3B gene on chromosome 2q11.2.
Ontology:	Human Disease [DOID:0111614]   ( DOID:0111614 )