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DOID:0090051 - dystonia 23
Disease Ontology Definition:A focal dystonia characterized by autosomal dominant inheritance of adult-onset cervical dystonia with onset typically in the fourth or fifth decade of life that has_material_basis_in heterozygous mutation in the CACNA1B gene on chromosome 9q34.
Synonyms:
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
focal dystonia (is_a)