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DO Term : dystonia 21 [DOID:0090046] Disease Ontology

Namespace

disease_ontology

Obsolete

false

description

A dystonia characterized by late onset pure torsion dystonia that has_material_basis_in autosomal dominant inheritance of variation in the chromosome region 2q14.3-q21.3.

synonyms:
ORDO:306734,
ICD10CM:G24.1,
614588,
OMIM:614588

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

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