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Disease Ontology Browser
myoclonic dystonia 11 (DOID:0090034)
Alliance: disease page
Alt IDs: OMIM:159900, ICD10CM:G24.1, ORDO:36899
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.

Disease References using Mouse Models (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.13
The Jackson Laboratory