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Summary Literature (0)
DOID:0090034 - myoclonic dystonia 11


Disease Ontology Definition:A myoclonic dystonia characterized by autosomal dominant inheritance and association with psychiatric disorder that has_material_basis_in heterozygous mutation in the SGCE gene on chromosome 7q21.

Synonyms:

Xenbase Genes : sgce, drd2

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008044 - myoclonic dystonia 11

OMIM:
OMIM:159900 - DYSTONIA 11, MYOCLONIC; DYT11

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

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