Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Anencephaly TRIM36 disease C0002902 GeneticVariation 0.61 disgenet
Anencephaly TRIM36 disease C0002902 Biomarker 0.61 disgenet
Anencephaly MTHFR disease C0002902 GeneticVariation 0.44 orphanet , disgenet
Anencephaly MTHFR disease C0002902 SusceptibilityMutation 0.44 orphanet , disgenet
Anencephaly MTHFR disease C0002902 Biomarker 0.44 orphanet , disgenet
Anencephaly VANGL2 disease C0002902 Biomarker 0.4 orphanet , disgenet
Anencephaly VANGL2 disease C0002902 SusceptibilityMutation 0.4 orphanet , disgenet
Anencephaly THAS disease C0002902 Biomarker 0.3 disgenet
Anencephaly EFNA5 disease C0002902 Biomarker 0.2 disgenet
Anencephaly LMO4 disease C0002902 Biomarker 0.2 disgenet
Anencephaly CECR2 disease C0002902 Biomarker 0.2 disgenet
Anencephaly FUZ disease C0002902 GeneticVariation 0.13 disgenet
Anencephaly FUZ disease C0002902 Biomarker 0.13 disgenet
Anencephaly MKS1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly KIAA0586 disease C0002902 Biomarker 0.1 disgenet
Anencephaly VANGL1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly TMEM216 disease C0002902 Biomarker 0.1 disgenet
Anencephaly CEP55 disease C0002902 Biomarker 0.1 disgenet
Anencephaly TMEM231 disease C0002902 Biomarker 0.1 disgenet
Anencephaly HOXD13 disease C0002902 Biomarker 0.1 disgenet
Anencephaly CCL2 disease C0002902 Biomarker 0.1 disgenet
Anencephaly TMEM107 disease C0002902 Biomarker 0.1 disgenet
Anencephaly RPGRIP1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly TMEM67 disease C0002902 Biomarker 0.1 disgenet
Anencephaly KIF7 disease C0002902 Biomarker 0.1 disgenet
Anencephaly CEP290 disease C0002902 Biomarker 0.1 disgenet
Anencephaly CC2D2A disease C0002902 Biomarker 0.1 disgenet
Anencephaly B9D2 disease C0002902 Biomarker 0.1 disgenet
Anencephaly WDPCP disease C0002902 Biomarker 0.1 disgenet
Anencephaly TBXT disease C0002902 Biomarker 0.1 disgenet
Anencephaly RPGRIP1L disease C0002902 Biomarker 0.1 disgenet
Anencephaly TCTN2 disease C0002902 Biomarker 0.1 disgenet
Anencephaly DACT1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly B9D1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly B4GAT1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly CSPP1 disease C0002902 Biomarker 0.1 disgenet
Anencephaly AFP disease C0002902 Biomarker 0.02 disgenet
Anencephaly AFP disease C0002902 AlteredExpression 0.02 disgenet
Anencephaly HLA-B disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly TUBGCP2 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly GOLGA4 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly CELSR1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly CASP8 disease C0002902 Biomarker 0.01 disgenet
Anencephaly PRKACB disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly LMNB1 disease C0002902 Biomarker 0.01 disgenet
Anencephaly COMT disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly BMP4 disease C0002902 AlteredExpression 0.01 disgenet
Anencephaly IRF6 disease C0002902 Biomarker 0.01 disgenet
Anencephaly SCRIB disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly MSX2 disease C0002902 Biomarker 0.01 disgenet
Anencephaly MTHFD1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly HOXA10 disease C0002902 AlteredExpression 0.01 disgenet
Anencephaly MIR212 disease C0002902 Biomarker 0.01 disgenet
Anencephaly MTRR disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly PCMT1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly FOXN1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly FOLH1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly CUL4B disease C0002902 AlteredExpression 0.01 disgenet
Anencephaly ABO disease C0002902 Biomarker 0.01 disgenet
Anencephaly CASP3 disease C0002902 AlteredExpression 0.01 disgenet
Anencephaly WIPI1 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly CXCL6 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly DVL3 disease C0002902 GeneticVariation 0.01 disgenet
Anencephaly MIR451A disease C0002902 AlteredExpression 0.01 disgenet
Anencephaly FAP disease C0002902 GeneticVariation 0.01 disgenet
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