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DOID:0090042 - torsion dystonia 17
Disease Ontology Definition:A dystonia characterized by autosomal recessive inheritance of progressive dystonia, dysphonia, dysarthria and neck torticollis that has_material_basis_in variation in the chromosome region 20p11.2-q13.12.
Synonyms:
Echinobase Genes :
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
dystonia (is_a)