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Summary Literature (1)
DOID:0050950 - autosomal recessive cerebellar ataxia


Disease Ontology Definition:A cerebellar ataxia that has_material_basis_in autosomal recessive inheritance.

Synonyms:


In Mondo Disease Ontology:
MONDO:0015244 - autosomal recessive cerebellar ataxia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Xenbase Genes : slc9a1, tubb2b, atm, vps13d, ca8, grid2, uba5, ano10, atcay, stub1, setx, tdp2, vldlr, pmpca, twnk, [+]

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): autosomal recessive disease (is_a), cerebellar ataxia (is_a), hereditary ataxia (is_a)