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Summary Literature (0)
DOID:0111615 - autosomal recessive spinocerebellar ataxia 24


Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in UBA5 on chromosome 3q22.1.

Synonyms: SCAR24

Xenbase Genes : uba5


OMIM:
OMIM:617133 - SPINOCEREBELLAR ATAXIA, AUTOSOMAL RECESSIVE 24; SCAR24

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal recessive cerebellar ataxia (is_a)