has material basis in germline mutation in PLA2G6 late-onset Parkinson disease autosomal recessive Parkinson disease 14 https://www.malacards.org/card/parkinson_disease_14_autosomal_recessive PARK14 A rare neurodegenerative disease usually presenting before the age of 30 and which is characterized by dystonia, L-dopa-responsive parkinsonism, pyramidal signs and rapid cognitive decline. GARD:0012568 PLA2G6 hereditary late onset Parkinson disease autosomal recessive Parkinson disease type 14 Parkinson disease 14, autosomal recessive SCTID:720466001 MONDO:0013060 MESH:C567844 hereditary late onset Parkinson disease caused by mutation in PLA2G6 dystonia-parkinsonism, Paisan-Ruiz type PLA2G6-related dystonia-parkinsonism OMIM:612953 MEDGEN:414488 DOID:0060900 UMLS:C2751842 Orphanet:199351 PLA2G6-associated neurodegeneration obsolete persistent combined dystonia