Human genes for dystonia 12
Dystonia 12 [DOID:0090056]
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.
Synonyms: dystonia 12, DOID:0090056