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DO Term : myoclonic dystonia 15 [DOID:0090035] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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:
  • ORDO:210566,
  • OMIM:607488,
  • 607488
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents