myoclonic dystonia 15 Disease Ontology Browser

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Disease Ontology Browser

myoclonic dystonia 15 (DOID:0090035)
Alliance: disease page
Alt IDs: OMIM:607488, ORDO:210566
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.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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