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DOID:0090046 - dystonia 21
Disease Ontology Definition:A dystonia characterized by autosomal dominant inheritance of late onset pure torsion dystonia that has_material_basis_in variation in the chromosome region 2q14.3-q21.3.
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)