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DOID:0111617 - autosomal recessive spinocerebellar ataxia 6
Disease Ontology Definition:An autosomal recessive cerebellar ataxia characterized by onset in infancy of nonprogressive cerebellar ataxia without intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in a region on chromosome 20q11-q13.
Synonyms: SCAR6, autosomal recessive spinocerebellar ataxia type 6, infantile-onset autosomal recessive nonprogressive cerebellar ataxia,
Xenbase Genes
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Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal recessive cerebellar ataxia (is_a)