has material basis in germline mutation in CHCHD2 Parkinson disease late-onset Parkinson disease Parkinson disease 22, autosomal dominant https://www.malacards.org/card/parkinson_disease_22_autosomal_dominant CHCHD2 Parkinson disease Parkinson disease caused by mutation in CHCHD2 PARK22 Parkinson disease 22, autosomal dominant Parkinson disease 22, autosomal dominant; PARK22 Any Parkinson disease in which the cause of the disease is a mutation in the CHCHD2 gene. OMIM:616710 UMLS:C4225238 MONDO:0014742 MEDGEN:907886 DOID:0080504 GARD:0025012