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DOID:0070558 - autosomal recessive spinocerebellar ataxia 34
Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the CA8 gene on chromosome 8q12.1.
Synonyms: CAMRQ3, CAMRQ syndrome 3, cerebellar ataxia and mental retardation with or without quadrupedal locomotion 3, cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome 3, cerebellar ataxia, mental retardation, and disequilibrium syndrome 3, cerebellar ataxia, mental retardation, and dysequilibrium syndrome 3, SCAR34, spinocerebellar ataxia, autosomal recessive 34
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),
cerebellar ataxia, impaired intellectual development, and dysequilibrium syndrome (is_a)