| DISEASE NAME | Hypogonadotropic hypogonadism with partial puberty phenotype |
| DISEASE CATEGORY (ICD10) | Endocrine, nutritional and metabolic diseases |
| DISEASE ID (ICD10) | E23.0 |
| DISEASE ID (OMIM) | 228300 |
| 12 combinations linked to -15 | OLI1384; OLI1385; OLI1386; OLI1387; OLI1388; OLI1389; OLI1390; OLI1391; OLI1392; OLI1393; OLI1394; OLI1395 |
| 12 gene combinations linked to -15 | ARHGAP35; IL17RD; SMCHD1; TCF12; GNRHR; PROP1; KLB; PROP1; GNRHR; IGSF10; NDNF; SOX10; KLB; SOX10; CCDC141; TCF12; AMH; ANOS1; CUL4A; PNPLA6; ANOS1; TCF12; CCDC141; DMXL2; FGFR1; NDNF; FGFR1; OTUD4; PROKR2; FGFR1; POLR3B; SMCHD1; SQSTM1; IGSF10; TACR3 |
| ORPHANET ID | Non-Orphanet disease with DB ID: -15 |