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Metadata
DOID DOID:0090056
Name dystonia 12
Definition A dystonia characterized by autosomal dominant inheritance of asymmetric dystonia and parkinsonism with abrupt onset in young adulthood that has_material_basis_in heterozygous mutation in the ATP1A3 gene on chromosome 19q13.
Xrefs

ICD10CM:G24.1

OMIM:128235

ORDO:71517

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is_a dystonia

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