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 )

Relationships
is a type of: autosomal dominant disease dystonia