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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
MIM:615073 - dystonia 25; dyt25 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
multifocal dystonia (is_a)