Parkinson Disease 19B, Early-Onset

**Semantic type:** Disease or Syndrome

**Definition:** An autosomal recessive subtype of Parkinson disease, caused by mutation(s) in the DNAJC6 gene, encoding putative tyrosine-protein phosphatase auxilin. It is characterized by an onset of Parkinsonism between the third and fifth decades. Mutations(s) in DNAJC6, are also causative in PARK19A.

**Synonyms:** - PARK19B