Term Name: dystonia 33
Synonyms:
Definition: A dystonia characterized by a neurologic disorder with onset of focal or generalized dystonia in the first decades of life (from early childhood to adolescence) that has_material_basis_in heterozygous mutation in the EIF2AK2 gene on chromosome 2p22.
Ontology: Human Disease [DOID:0060940]   ( DOID:0060940 )

Relationships
is a type of: autosomal dominant disease autosomal recessive disease dystonia