Details for Disease -16

DISEASE NAME Hypogonadotropic hypogonadism with absent puberty phenotype
DISEASE CATEGORY (ICD10) Endocrine, nutritional and metabolic diseases
DISEASE ID (ICD10) E23.0
DISEASE ID (OMIM) 228300
36 combinations linked to -16 OLI1396; OLI1397; OLI1398; OLI1399; OLI1400; OLI1401; OLI1402; OLI1403; OLI1404; OLI1405; OLI1406; OLI1407; OLI1408; OLI1409; OLI1410; OLI1411; OLI1412; OLI1413; OLI1414; OLI1416; OLI1417; OLI1418; OLI1419; OLI1420; OLI1421; OLI1422; OLI1423; OLI1424; OLI1425; OLI1426; OLI1427; OLI1428; OLI1429; OLI1430; OLI1431; OLI1415
36 gene combinations linked to -16 FGFR1; POLR3A; AXL; FGFR1; ANOS1; CHD7; CHD7; RNF216; ANOS1; RAB3GAP1; FGFR1; WDR11; KISS1R; PNPLA6; SQSTM1; AMH; CHD7; DMXL2; FGFR1; KL; CHD7; FGFR1; GNRHR; ANOS1; CCDC141; DCC; GNRH1; CHD7; TYRO3; DMXL2; PCSK1; SEMA3A; ANOS1; SMCHD1; FGFR1; IGSF10; SEMA7A; ANOS1; GLI3; AMH; FGFR1; ANOS1; PLXNA1; PNPLA6; HS6ST1; SMCHD1; CHD7; FGFR1; PNPLA6; OTUD4; PROK2; ANOS1; PROP1; IL17RD; RNF216; PNPLA6; SMCHD1; KLB; NDNF; NR0B1; FGFR1; KLB; ANOS1; PNPLA6; ANOS1; DCC; FGFR1; PLXNA1; AMH; ANOS1; AXL; FGF8; ANOS1; DMXL2; RAB3GAP1; CHD7; RAB3GAP2; SPRY4; CHD7; LEPR; RAB3GAP2; FGFR1; OTUD4; FGFR1; SQSTM1; CCDC141; RAB3GAP1; SEMA3A
ORPHANET ID Non-Orphanet disease with DB ID: -16
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