| DISEASE NAME | Congenital glaucoma |
| DISEASE CATEGORY (ICD10) | Congenital malformations, deformations and chromosomal abnormalities |
| DISEASE ID (ICD10) | Q15.0 |
| DISEASE ID (OMIM) | 613086; 231300; 600975; 613085; 617272 |
| 9 combinations linked to 98976 | OLI009; OLI010; OLI011; OLI012; OLI169; OLI248; OLI249; OLI767; OLI768 |
| 5 gene combinations linked to 98976 | DPT; FOXC1; NFATC1; DPT; FOXC1; CYP1B1; TEK; CYP1B1; PITX2; CYP1B1; MYOC |
| ORPHANET ID | 98976 |