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 |
| ALPL | 1p36.12 | 171760 | S, H, Fd, F, A | Hypophosphatasia, infantile, 241500 (3) | 241500 | 3 |
| ALPL | 1p36.12 | 171760 | S, H, Fd, F, A | Hypophosphatasia, childhood, 241510 (3) | 241510 | 3 |
| ALPL | 1p36.12 | 171760 | S, H, Fd, F, A | Odontohypophosphatasia, 146300 (3) | 146300 | 3 |
| ALPL | 1p36.12 | 171760 | S, H, Fd, F, A | Hypophosphatasia, adult, 146300 (3) | 146300 | 3 |