has material basis in germline mutation in ATP1A3 dystonia 12 https://github.com/monarch-initiative/mondo/issues/4521 https://github.com/monarch-initiative/mondo/issues/6752 NANDO:1200523 dystonia 12 rapid-onset dystonia-parkinsonism NANDO:1200524 OMIM:128235 DOID:0090056 dystonic disorder caused by mutation in ATP1A3 dystonia-12 SCTID:702323008 DYT-ATP1A3 Rapid-onset dystonia-parkinsonism (RDP) is a very rare movement disorder, characterized by the abrupt onset of parkinsonism and dystonia, often triggered by physical or psychological stress. RDP MEDGEN:358384 dystonia type 12 UMLS:C1868681 Orphanet:71517 dystonia-Parkinsonism, rapid-onset ATP1A3 dystonic disorder MESH:C538001 MONDO:0007496 NCIT:C157577 GARD:0009628 DYT12 combined dystonia parkinsonian disorder inherited dystonia ATP1A3-associated neurological disorder