Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Foramen Ovale, Patent NKX2-5 disease C0016522 GeneticVariation 0.33 disgenet
Foramen Ovale, Patent NKX2-5 disease C0016522 Biomarker 0.33 disgenet
Foramen Ovale, Patent GATA4 disease C0016522 GeneticVariation 0.21 disgenet
Foramen Ovale, Patent GATA4 disease C0016522 Biomarker 0.21 disgenet
Foramen Ovale, Patent NTF3 disease C0016522 Biomarker 0.2 disgenet
Foramen Ovale, Patent CCN1 disease C0016522 Biomarker 0.2 disgenet
Foramen Ovale, Patent UBE2A disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent GDF1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent DVL3 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent AAR2 disease C0016522 GeneticVariation 0.1 disgenet
Foramen Ovale, Patent ASXL1 disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent LTBP4 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent GAA disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent NKX2-1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent ASCC1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PPP1CB disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent FGF14 disease C0016522 GeneticVariation 0.1 disgenet
Foramen Ovale, Patent ACADVL disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent COL11A1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent MAP3K7 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent IGF1R disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent CHST3 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent WDR35 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent FLNC disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent SOS1 disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent NF1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent MYH6 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent ALG12 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent NOTCH1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent DSE disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent RAC1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent B3GAT3 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent HSPA9 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PHGDH disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent GATA6 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PLD1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PEX26 disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent FANCI disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent RPL11 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent STAT1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PIGQ disease C0016522 GeneticVariation 0.1 disgenet
Foramen Ovale, Patent NCAPG2 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent TSFM disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent TALDO1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent FLCN disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent TKT disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent PIGN disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent TMEM94 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent NSD1 disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent MED13L disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent HNRNPK disease C0016522 GeneticVariation 0.1 disgenet
Foramen Ovale, Patent ADNP disease C0016522 CausalMutation 0.1 disgenet
Foramen Ovale, Patent PACS1 disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent NONO disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent TRRAP disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent STAMBP disease C0016522 Biomarker 0.1 disgenet
Foramen Ovale, Patent F5 disease C0016522 GeneticVariation 0.04 disgenet
Foramen Ovale, Patent F2 disease C0016522 GeneticVariation 0.04 disgenet
Foramen Ovale, Patent F5 disease C0016522 Biomarker 0.04 disgenet
Foramen Ovale, Patent ARSD disease C0016522 Biomarker 0.03 disgenet
Foramen Ovale, Patent MTHFR disease C0016522 GeneticVariation 0.02 disgenet
Foramen Ovale, Patent P2RY12 disease C0016522 Biomarker 0.02 disgenet
Foramen Ovale, Patent APOC3 disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent COX8A disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent F3 disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent CHM disease C0016522 Biomarker 0.01 disgenet
Foramen Ovale, Patent MSX2 disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent CHDH disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent RENBP disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent ATP1A2 disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent NPPB disease C0016522 Biomarker 0.01 disgenet
Foramen Ovale, Patent C20orf181 disease C0016522 Biomarker 0.01 disgenet
Foramen Ovale, Patent G6PC3 disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent VWF disease C0016522 Biomarker 0.01 disgenet
Foramen Ovale, Patent CLNK disease C0016522 GeneticVariation 0.01 disgenet
Foramen Ovale, Patent NNT disease C0016522 Biomarker 0.01 disgenet
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