| DISEASE NAME | Familial hemophagocytic lymphohistiocytosis |
| DISEASE CATEGORY (ICD10) | Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism |
| DISEASE ID (ICD10) | D76.1 |
| DISEASE ID (OMIM) | 267700; 603552; 603553; 608898; 613101 |
| 25 combinations linked to 540 | OLI522; OLI523; OLI524; OLI525; OLI526; OLI527; OLI528; OLI529; OLI530; OLI531; OLI532; OLI533; OLI534; OLI535; OLI536; OLI537; OLI538; OLI539; OLI540; OLI541; OLI542; OLI543; OLI544; OLI545; OLI546 |
| 6 gene combinations linked to 540 | STXBP2; UNC13D; PRF1; UNC13D; PRF1; STXBP2; STX11; UNC13D; STX11; STXBP2; RAB27A; STXBP2 |
| ORPHANET ID | 540 |