1 => Disorder placed on map based on association with a gene; defect unknown
2 => Disorder placed by linkage; no mutation found
3 => Molecular basis known; mutation found in gene
4 => Contiguous gene deletion/duplication syndrome
| Gene Symbol | Chromosomal Location | Gene MIM number | Mapping Method | Phenotype | Phenotype MIM number | Phenotype Mapping Key |
| DNAJC6 | 1p31.3 | 608375 | R, REc | Parkinson disease 19a, juvenile-onset, 615528 (3) | 615528 | 3 |
| DNAJC6 | 1p31.3 | 608375 | R, REc | Parkinson disease 19b, early-onset, 615528 (3) | 615528 | 3 |