dystonia 12 (DOID:0090056)
Alliance: disease page
Alt IDs: OMIM:128235, ICD10CM:G24.1, MESH:C538001, ORDO:71517
Definition: A dystonia that is characterized by asymmetric dystonia and parkinsonism with abrupt onset in young adulthood that has_material_basis_in autosomal dominant inheritance of heterozygous mutation in the gene encoding the alpha-3 subunit of the N,K-ATPase (ATP1A3) on chromosome 19q13.