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Ontology Browser
Term:
Parkinsonism-Dystonia, Childhood-Onset, 3 (DOID:9001163)
Annotations: Rat: (1) Mouse: (1) Human: (3) Chinchilla: (1) Bonobo: (1) Dog: (1) Squirrel: (1) Pig: (1) Naked Mole-rat: (1) Green Monkey: (1)
Parent Terms Term With Siblings Child Terms
atypical dopamine transporter deficiency syndrome 
classic dopamine transporter deficiency syndrome  
infantile parkinsonism-dystonia 2  
Parkinsonism-Dystonia, Childhood-Onset, 3  
An autosomal recessive neurodegenerative disorder with onset in infancy or early childhood. Caused by homozygous or compound heterozygous mutation in the WARS2 gene on chromosome 1p12.

Synonyms
Exact Synonyms: PKDYS3
Broad Synonyms: WARS2-RELATED CONDITION ;   WARS2-RELATED DISORDER
Primary IDs: OMIM:619738
Definition Sources: OMIM:619738

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