Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Syndrome, Kallmann's WDR11 disease C0162809 GermlineCausalMutation 0.74 orphanet , disgenet
Syndrome, Kallmann's WDR11 disease C0162809 AlteredExpression 0.74 orphanet , disgenet
Syndrome, Kallmann's WDR11 disease C0162809 Biomarker 0.74 orphanet , disgenet
Syndrome, Kallmann's PROKR2 disease C0162809 Biomarker 0.7 orphanet , disgenet
Syndrome, Kallmann's PROKR2 disease C0162809 GermlineCausalMutation 0.7 orphanet , disgenet
Syndrome, Kallmann's PROKR2 disease C0162809 GeneticVariation 0.7 orphanet , disgenet
Syndrome, Kallmann's ANOS1 disease C0162809 GeneticVariation 0.7 orphanet , disgenet
Syndrome, Kallmann's ANOS1 disease C0162809 GermlineCausalMutation 0.7 orphanet , disgenet
Syndrome, Kallmann's ANOS1 disease C0162809 Biomarker 0.7 orphanet , disgenet
Syndrome, Kallmann's CHD7 disease C0162809 GeneticVariation 0.6 orphanet , disgenet
Syndrome, Kallmann's PROK2 disease C0162809 GeneticVariation 0.6 orphanet , disgenet
Syndrome, Kallmann's FGFR1 disease C0162809 GermlineCausalMutation 0.6 orphanet , disgenet
Syndrome, Kallmann's CHD7 disease C0162809 GermlineCausalMutation 0.6 orphanet , disgenet
Syndrome, Kallmann's PROK2 disease C0162809 GermlineCausalMutation 0.6 orphanet , disgenet
Syndrome, Kallmann's FGFR1 disease C0162809 GeneticVariation 0.6 orphanet , disgenet
Syndrome, Kallmann's FGFR1 disease C0162809 Biomarker 0.6 orphanet , disgenet
Syndrome, Kallmann's CHD7 disease C0162809 Biomarker 0.6 orphanet , disgenet
Syndrome, Kallmann's PROK2 disease C0162809 Biomarker 0.6 orphanet , disgenet
Syndrome, Kallmann's CHD7 disease C0162809 AlteredExpression 0.6 orphanet , disgenet
Syndrome, Kallmann's FGF8 disease C0162809 GeneticVariation 0.56 orphanet , disgenet
Syndrome, Kallmann's FGF8 disease C0162809 Biomarker 0.56 orphanet , disgenet
Syndrome, Kallmann's FGF8 disease C0162809 GermlineCausalMutation 0.56 orphanet , disgenet
Syndrome, Kallmann's SOX10 disease C0162809 Biomarker 0.55 orphanet , disgenet
Syndrome, Kallmann's SOX10 disease C0162809 GeneticVariation 0.55 orphanet , disgenet
Syndrome, Kallmann's SOX10 disease C0162809 GermlineCausalMutation 0.55 orphanet , disgenet
Syndrome, Kallmann's KISS1R disease C0162809 GermlineCausalMutation 0.52 disgenet
Syndrome, Kallmann's KISS1R disease C0162809 Biomarker 0.52 disgenet
Syndrome, Kallmann's KISS1R disease C0162809 GeneticVariation 0.52 disgenet
Syndrome, Kallmann's TACR3 disease C0162809 GermlineCausalMutation 0.5 orphanet , disgenet
Syndrome, Kallmann's TACR3 disease C0162809 Biomarker 0.5 orphanet , disgenet
Syndrome, Kallmann's SEMA3A disease C0162809 AlteredExpression 0.36 orphanet , disgenet
Syndrome, Kallmann's SEMA3A disease C0162809 Biomarker 0.36 orphanet , disgenet
Syndrome, Kallmann's SEMA3A disease C0162809 GeneticVariation 0.36 orphanet , disgenet
Syndrome, Kallmann's SEMA3A disease C0162809 GermlineCausalMutation 0.36 orphanet , disgenet
Syndrome, Kallmann's NSMF disease C0162809 GermlineCausalMutation 0.34 disgenet
Syndrome, Kallmann's NSMF disease C0162809 GeneticVariation 0.34 disgenet
Syndrome, Kallmann's NSMF disease C0162809 Biomarker 0.34 disgenet
Syndrome, Kallmann's CCDC141 disease C0162809 GermlineCausalMutation 0.32 orphanet , disgenet
Syndrome, Kallmann's CCDC141 disease C0162809 GeneticVariation 0.32 orphanet , disgenet
Syndrome, Kallmann's CCDC141 disease C0162809 SusceptibilityMutation 0.32 orphanet , disgenet
Syndrome, Kallmann's HESX1 disease C0162809 GermlineCausalMutation 0.31 orphanet , disgenet
Syndrome, Kallmann's HESX1 disease C0162809 GeneticVariation 0.31 orphanet , disgenet
Syndrome, Kallmann's FEZF1 disease C0162809 GermlineCausalMutation 0.31 orphanet , disgenet
Syndrome, Kallmann's FEZF1 disease C0162809 GeneticVariation 0.31 orphanet , disgenet
Syndrome, Kallmann's FGF17 disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's SPRY4 disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's SOX3 disease C0162809 GermlineCausalMutation 0.3 disgenet
Syndrome, Kallmann's SOX2 disease C0162809 GermlineCausalMutation 0.3 disgenet
Syndrome, Kallmann's FLRT3 disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's OTX2 disease C0162809 GermlineCausalMutation 0.3 disgenet
Syndrome, Kallmann's IL17RD disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's HS6ST1 disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's DCC disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's DUSP6 disease C0162809 GermlineCausalMutation 0.3 orphanet , disgenet
Syndrome, Kallmann's ARNT2 disease C0162809 GermlineCausalMutation 0.3 disgenet
Syndrome, Kallmann's GNRHR disease C0162809 Biomarker 0.29 disgenet
Syndrome, Kallmann's GNRHR disease C0162809 GeneticVariation 0.29 disgenet
Syndrome, Kallmann's GNRH1 disease C0162809 GeneticVariation 0.26 disgenet
Syndrome, Kallmann's GNRH1 disease C0162809 Biomarker 0.26 disgenet
Syndrome, Kallmann's CSHL1 disease C0162809 Biomarker 0.2 disgenet
Syndrome, Kallmann's GHRH disease C0162809 Biomarker 0.2 disgenet
Syndrome, Kallmann's KISS1 disease C0162809 Biomarker 0.2 disgenet
Syndrome, Kallmann's NR5A1 disease C0162809 Biomarker 0.2 disgenet
Syndrome, Kallmann's SERPINA4 disease C0162809 GeneticVariation 0.1 disgenet
Syndrome, Kallmann's SERPINA4 disease C0162809 Biomarker 0.1 disgenet
Syndrome, Kallmann's STS disease C0162809 Biomarker 0.07 disgenet
Syndrome, Kallmann's STS disease C0162809 GeneticVariation 0.07 disgenet
Syndrome, Kallmann's NR0B1 disease C0162809 Biomarker 0.05 disgenet
Syndrome, Kallmann's NR0B1 disease C0162809 AlteredExpression 0.05 disgenet
Syndrome, Kallmann's NR0B1 disease C0162809 GeneticVariation 0.05 disgenet
Syndrome, Kallmann's PRKAR2A disease C0162809 Biomarker 0.03 disgenet
Syndrome, Kallmann's PRKAR2A disease C0162809 GeneticVariation 0.03 disgenet
Syndrome, Kallmann's FN1 disease C0162809 Biomarker 0.03 disgenet
Syndrome, Kallmann's FN1 disease C0162809 GeneticVariation 0.03 disgenet
Syndrome, Kallmann's ACKR3 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's ACKR3 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's BRS3 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's BRS3 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's GPR42 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's CXCR6 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's GPR42 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's SEMA7A disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's ADRA1A disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's SSTR4 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's LPAR2 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's ADRA2B disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's ADRA2B disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's SSTR4 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's CXCR6 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's ADRA1A disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's LPAR2 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's TUBB3 disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's BRD2 disease C0162809 AlteredExpression 0.02 disgenet
Syndrome, Kallmann's IHH disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's EDNRA disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's EDNRA disease C0162809 GeneticVariation 0.02 disgenet
Syndrome, Kallmann's PLXNA1 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's BRD2 disease C0162809 Biomarker 0.02 disgenet
Syndrome, Kallmann's LINC01672 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's EMX1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's NRP1 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's SCEL disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's LEPR disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's AMH disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's NTRK1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's PRL disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's PALM2AKAP2 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's POMC disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's CD55 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's EBF2 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's CD44 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's ROBO1 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's EMX2 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's GLI3 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's NTN1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's ANOS2P disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's RMRP disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's SIX3 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's RN7SL263P disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's RMST disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's PROP1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's FGF1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's PCSK1 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's SHOX disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's TSHZ1 disease C0162809 AlteredExpression 0.01 disgenet
Syndrome, Kallmann's NRP2 disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's SEMA3E disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's AXL disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's NT5E disease C0162809 Biomarker 0.01 disgenet
Syndrome, Kallmann's PAX2 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's ANK1 disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's LEP disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's NDN disease C0162809 GeneticVariation 0.01 disgenet
Syndrome, Kallmann's NDNF NA C0162809 NA NA orphanet
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