"DOID:0111614"^^ . "An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in VWA3B on chromosome 2q11.2."^^ . . . "autosomal recessive spinocerebellar ataxia 22"^^ . . "OMIM:616948"^^ . "SCAR22"@en . "disease_ontology"^^ .