spinocerebellar ataxia type 36

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Summary

Literature (0)

DOID:0050983 - spinocerebellar ataxia type 36

Disease Ontology Definition:n_a

Synonyms:

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

: nop56

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0013594 - spinocerebellar ataxia type 36

MONDO:0013594 - spinocerebellar ataxia type 36

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

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

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