autosomal recessive spinocerebellar ataxia 21 Disease Ontology Browser

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Disease Ontology Browser

autosomal recessive spinocerebellar ataxia 21 (DOID:0111155)
Alliance: disease page
Synonyms: acute infantile liver failure-cerebellar ataxia-peripheral sensory motor neuropathy syndrome; autosomal recessive spinocerebellar ataxia 21 with hepatopathy; SCAR21
Alt IDs: OMIM:616719, ORDO:466794
Definition: An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous or compound heterozygous mutation in the SCYL1 gene on chromosome 11q13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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