Term Name: | infantile parkinsonism-dystonia 2 |
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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 ) |