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Summary Literature (0)
DOID:0090051 - dystonia 23


Disease Ontology Definition:A focal dystonia characterized by adult-onset cervical dystonia typically in the fourth or fifth decade of life that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the CACNA1B gene on chromosome 9q34.

Synonyms:

Xenbase Genes : cacna1b

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013928 - dystonia 23


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), focal dystonia (is_a)