spinocerebellar ataxia type 15

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Summary

Literature (0)

DOID:0050965 - spinocerebellar ataxia type 15

Disease Ontology Definition:An autosomal dominant cerebellar ataxia that is characterized by progressive ataxia, nystagmus, dysarthria and dysphagia, has_material_basis_in mutation in the ITPR1 gene.

Synonyms: spinocerebellar ataxia type 16

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

: itpr1

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011694 - spinocerebellar ataxia type 15/16

MONDO:0011694 - spinocerebellar ataxia type 15/16

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant cerebellar ataxia (is_a)