1 => The disorder is placed on the map based on its association with a gene, but the underlying defect is not known
2 => The disorder has been placed on the map by linkage; no mutation has been found
3 => The molecular basis for the disorder is known; a mutation has been found in the gene
4 => A contiguous gene deletion or duplication syndrome, multiple genes are deleted or duplicated causing the phenotype
| 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 |