Term Name: infantile parkinsonism-dystonia 2
Synonyms: Brain dopamine-serotonin vesicular transport disease, PKDYS2
Definition: A movement disease characterized by parkinsonism, dystonia, poor fine motor skills, and autonomic dysfunction including abnormal sweating, cold extremities, and poor sleep that has_material_basis_in homozygous mutation in the SLC18A2 gene on chromosome 10q25.3.
Ontology: Human Disease [DOID:0070490]   ( DOID:0070490 )

Relationships
is a type of: autosomal recessive disease movement disease