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Echinobase
Summary Literature (0)
DOID:0090055 - dystonia 25

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

Synonyms:

Echinobase Genes : gnal


OMIM:
MIM:615073 - dystonia 25; dyt25

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): multifocal dystonia (is_a)