| DISEASE NAME | Meckel syndrome |
| DISEASE CATEGORY (ICD10) | Congenital malformations, deformations and chromosomal abnormalities |
| DISEASE ID (ICD10) | Q61.9 |
| DISEASE ID (OMIM) | 615397; 249000; 603194; 607361; 611134; 611561; 612284; 613885; 609345; 614209; 617562 |
| 3 combinations linked to 564 | OLI1371; OLI215; OLI216 |
| 3 gene combinations linked to 564 | KIF14; TMEM67; CC2D2A; NPHP3; CC2D2A; PKHD1 |
| ORPHANET ID | 564 |