| DISEASE NAME | Hypogonadotropic hypogonadism with Fertile Eunuch phenotype |
| DISEASE CATEGORY (ICD10) | Endocrine, nutritional and metabolic diseases |
| DISEASE ID (ICD10) | E23.0 |
| DISEASE ID (OMIM) | 228300 |
| 8 combinations linked to -14 | OLI1376; OLI1377; OLI1378; OLI1379; OLI1380; OLI1381; OLI1382; OLI1383 |
| 8 gene combinations linked to -14 | FGFR1; LEPR; KL; POLR3B; TBC1D20; DCC; FGFR1; DMXL2; GNRHR; LEPR; CHD7; POLR3A; CCDC141; GLI3; GNRHR; CCDC141; FGFR1; FGFR1; RAB3GAP2 |
| ORPHANET ID | Non-Orphanet disease with DB ID: -14 |