Details for Disease 619

DISEASE NAME Primary ovarian failure
DISEASE CATEGORY (ICD10) Endocrine, nutritional and metabolic diseases
DISEASE ID (ICD10) E28.3
DISEASE ID (OMIM) 233300; 300510; 614324; 618078; 618117; 618723
48 combinations linked to 619 OLI090; OLI091; OLI092; OLI093; OLI094; OLI095; OLI1039; OLI1040; OLI1041; OLI1042; OLI1043; OLI1044; OLI1045; OLI1046; OLI1047; OLI1048; OLI1049; OLI1050; OLI1051; OLI1052; OLI1053; OLI1054; OLI1055; OLI1056; OLI1057; OLI1058; OLI1059; OLI1060; OLI1061; OLI1062; OLI1063; OLI1064; OLI1065; OLI1066; OLI1067; OLI1068; OLI1069; OLI1070; OLI1071; OLI1722; OLI1723; OLI1724; OLI1725; OLI1726; OLI1727; OLI1728; OLI1729; OLI1730
48 gene combinations linked to 619 APC2; ATG2A; COL6A1; KPNA2; LARS2; RBBP8; RIPK1; THBS2; ATM; NCOR2; POLG; HK3; LGR4; VWF; ID1; TEX15; TUBA8; ATR; POLG; NOTCH2; SAMD11; TP53; ERBB3; LARS2; POLG; PLEC; RAD52; RBBP8; ATG4C; ATM; PRIM1; KMT2D; NBN; SAMD11; APC2; COL6A2; LRP5; BMP15; GDF9; NOBOX; STAG3; LHCGR; REC8; AGRN; VLDLR; FANCA; TP63; DMRT3; RELN; AKAP9; HDAC5; HK3; SAMD11; CCNB1IP1; MLH3; CYP21A2; MSH4; COL6A2; SAMD11; GPR137C; RELN; GDF9; REC8; FOXL2; GALT; BMP15; SMC1B; NOBOX; SMC1B; FIGLA; GDF9; BMP15; NOBOX; FSHR; SMC1B; MSH4; MSH5; GDF9; SPIDR; BMP15; FOXL2; FOXL2; MSH4; FOXL2; NR5A1; BMPR2; FOXL2; FOXL2; PGRMC1; MSH4; MSH5; PGRMC1; ANAPC1; ATR; LARS2; MLH3; POLE; ADAMTS16; ATM; BLM; CYP21A2; FSHR; MCM9; NCOR2; RAD52; RAD54L; RYR3; ERBB4; PKP1; RYR3; SAMD11; FIGLA; NCOR2; NOBOX; NR5A1; NOTCH3; TRRAP; VWF; ATG4C; NOTCH4; RMI1; SAMD11; ADAMTS5; NR5A1; RAD50; SYNE1; ADAMTS4; DHCR24; FSHR; RAD52
ORPHANET ID 619

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