myoclonic dystonia 15

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Summary

Literature (0)

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 Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries

:

Mondo Disease Ontology (on Monarch Initiative):

MONDO:0011844 - myoclonic dystonia 15

MONDO:0011844 - myoclonic dystonia 15

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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

Parent(s): autosomal dominant disease (is_a), myoclonic dystonia (is_a)