Parkinson Disease 22, Autosomal Dominant

Preferred Label : Parkinson Disease 22, Autosomal Dominant;

NCIt synonyms : PARK22;

NCIt definition : An autosomal dominant subtype of Parkinson disease, caused by mutation(s) in the CHCHD2 gene, encoding coiled-coil-helix-coiled-coil-helix domain-containing protein 2.;

Details

Origin ID

C205643;

Has associated anatomic sites
- Central Nervous System [NCIt concept]
- Nervous System [NCIt concept]
concept_is_in_subset
- Cellosaurus Disease Terminology [NCIt concept]
- Cellosaurus Terminology [NCIt concept]

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