| DISEASE NAME | Isolated congenital hypogonadotropic hypogonadism |
| DISEASE CATEGORY (ICD10) | Endocrine, nutritional and metabolic diseases |
| DISEASE ID (ICD10) | E23.0 |
| DISEASE ID (OMIM) | N.A. |
| 4 combinations linked to 238666 | OLI036; OLI195; OLI199; OLI396 |
| 3 gene combinations linked to 238666 | PROK2; PROKR2; FGFR1; GNRHR; FGFR1; PROKR2 |
| ORPHANET ID | 238666 |