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 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | Endometrial carcinoma, somatic, 608089 (3) | 608089 | 3 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | Ovarian carcinoma, somatic, 167000 (3) | 167000 | 3 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | {Breast cancer, lobular}, 114480 (3) | 114480 | 3 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | Gastric cancer, familial diffuse, with or without cleft lip and/or palate, 137215 (3) | 137215 | 3 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | {Prostate cancer, susceptibility to}, 176807 (3) | 176807 | 3 |
| CDH1 | 16q22.1 | 192090 | REa, D, Ch | Blepharocheilodontic syndrome 1, 119580 (3) | 119580 | 3 |