| DISEASE NAME | Rare congenital non-syndromic heart malformation |
| DISEASE CATEGORY (ICD10) | None |
| DISEASE ID (ICD10) | N.A. |
| DISEASE ID (OMIM) | 231300; 600975; 613085; 613086; 617272 |
| 2 combinations linked to 88991 | OLI1072; OLI248 |
| 2 gene combinations linked to 88991 | FGFR1; STARD3; DPT; FOXC1; NFATC1 |
| ORPHANET ID | 88991 |