| DISEASE NAME | Amelogenesis imperfecta |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | K00.5 |
| DISEASE ID (OMIM) | 130900; 204650; 204700; 301200; 301201; 612529; 613211; 614832; 615887; 616221; 616270; 104500; 104510; 104530; 617217 |
| 8 combinations linked to 88661 | OLI521; OLI1641; OLI1642; OLI1733; OLI1734; OLI1735; OLI1736; OLI1737 |
| 8 gene combinations linked to 88661 | AMELX; LAMA3; ENAM; LAMA3; COL17A1; RELT; COL17A1; LAMA3; AMELX; WNT10A; ACP4; WNT10A; FAM83H; WDR72; DLX3; WNT10A |
| ORPHANET ID | 88661 |