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DOID:0090035 - myoclonic dystonia 15
Disease Ontology Definition:A myoclonic dystonia that is characterized by jerky movements of the upper limbs, hands, and axial muscles, and has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 18p11.
Synonyms:
Xenbase Genes :
MONDO:0011844 - myoclonic dystonia 15 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee