| DISEASE NAME | Congenital hypogonadotropic hypogonadism |
| DISEASE CATEGORY (ICD10) | Endocrine, nutritional and metabolic diseases |
| DISEASE ID (ICD10) | E23.0 |
| DISEASE ID (OMIM) | N.A. |
| 10 combinations linked to 174590 | OLI018; OLI019; OLI020; OLI650; OLI651; OLI652; OLI653; OLI654; OLI1651; OLI1801 |
| 10 gene combinations linked to 174590 | PLXNA1; SRA1; CHD7; PROK2; RNF216; SRA1; FGFR1; POLR3A; CHD7; PROP1; AMHR2; GNRH1; HS6ST1; PLXNA1; CCDC141; PLXNA1; SEMA3E; FGFR1; NRP1; PLXNA1; PLXNA1; POLR3A |
| ORPHANET ID | 174590 |