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Summary Literature (0)
DOID:0090055 - dystonia 25

Disease Ontology Definition:A multifocal dystonia that is characterized by cervical, laryngeal and hand-forearm dystonia, and has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the GNAL gene on chromosome 18p11.

Synonyms:

Xenbase Genes : gnal

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014033 - dystonia 25


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), multifocal dystonia (is_a)