| DISEASE NAME | Non-Syndromic genetic keratoconus |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | 148300; 617928 |
| 23 combinations linked to -21 | OLI1672; OLI1673; OLI1674; OLI1675; OLI1677; OLI1678; OLI1679; OLI1680; OLI1681; OLI1682; OLI1683; OLI1684; OLI1685; OLI1686; OLI1687; OLI1688; OLI1689; OLI1690; OLI1691; OLI1692; OLI1693; OLI1694; OLI1695 |
| 23 gene combinations linked to -21 | LOXHD1; NDRG1; ZNF469; COL4A3; COL8A2; MMP1; MMP2; LOXL2; PIKFYVE; PPIP5K2; SLC8A3; LOXHD1; TTN; COL2A1; COL4A4; COL6A3; TTN; ARG1; COL23A1; COL4A2; DUXA; HSPG2; CDH23; CDHR1; CPSF3; EML6; SLC4A4; IDUA; INPPL1; ITGB4; ZEB1; CDH23; CDHR1; GUCY2D; INPPL1; CPAMD8; HSPG2; IMPG2; IDUA; INPPL1; ITGB4; SPARC; TTN; KRT19; KRT7; APEX1; IDUA; COL6A5; GRHL1; SLC4A4; COL9A3; EML6; TTN; COL6A6; LOXHD1; LRP1B; PIK3CG; SLC4A11; ALDH1A2; CDHR1; LRP1B; COL8A2; GALNT14; IPO5; ADAMTS8; ADAMTS9; ADAMTS7; COL5A3; DOCK9; EML6; IDUA; LOXL1; ZNF469 |
| ORPHANET ID | Non-Orphanet disease with DB ID: -21 |