autosomal recessive spinocerebellar ataxia 11

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Summary

Literature (0)

DOID:0080063 - autosomal recessive spinocerebellar ataxia 11

Disease Ontology Definition:An autosomal recessive cerebellar ataxia that has_material_basis_in homozygous mutation in the SYT14 gene on chromosome 1q32.

Synonyms: SCAR11

Xenbase Genes Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

: syt14

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013645 - autosomal recessive spinocerebellar ataxia 11

MONDO:0013645 - autosomal recessive spinocerebellar ataxia 11

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)