| Term Name: | dystonia 12 |
|---|---|
| Synonyms: | |
| 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. |
| Ontology: | Human Disease [DOID:0090056] ( DOID:0090056 ) |