Disease Information | ||||||
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Disease Name | Gene Name | Type | UMLS | Association Type | Score | Source |
Syndrome, Heterotaxy | ACVR2B | disease | C3178805 | Biomarker | 0.7 | disgenet |
Syndrome, Heterotaxy | MMP21 | disease | C3178805 | GeneticVariation | 0.6 | disgenet |
Syndrome, Heterotaxy | MMP21 | disease | C3178805 | Biomarker | 0.6 | disgenet |
Syndrome, Heterotaxy | ZIC3 | disease | C3178805 | Biomarker | 0.52 | disgenet |
Syndrome, Heterotaxy | ZIC3 | disease | C3178805 | GeneticVariation | 0.52 | disgenet |
Syndrome, Heterotaxy | LEFTY2 | disease | C3178805 | Biomarker | 0.5 | disgenet |
Syndrome, Heterotaxy | GDF1 | disease | C3178805 | GeneticVariation | 0.4 | disgenet |
Syndrome, Heterotaxy | GDF1 | disease | C3178805 | Biomarker | 0.4 | disgenet |
Syndrome, Heterotaxy | NODAL | disease | C3178805 | GeneticVariation | 0.4 | disgenet |
Syndrome, Heterotaxy | GDF1 | disease | C3178805 | CausalMutation | 0.4 | disgenet |
Syndrome, Heterotaxy | NODAL | disease | C3178805 | Biomarker | 0.4 | disgenet |
Syndrome, Heterotaxy | CRELD1 | disease | C3178805 | GeneticVariation | 0.31 | disgenet |
Syndrome, Heterotaxy | CRELD1 | disease | C3178805 | Biomarker | 0.31 | disgenet |
Syndrome, Heterotaxy | TDGF1 | disease | C3178805 | Biomarker | 0.3 | disgenet |
Syndrome, Heterotaxy | CFC1 | disease | C3178805 | GeneticVariation | 0.23 | disgenet |
Syndrome, Heterotaxy | CFC1 | disease | C3178805 | Biomarker | 0.23 | disgenet |
Syndrome, Heterotaxy | DNAH11 | disease | C3178805 | GeneticVariation | 0.21 | disgenet |
Syndrome, Heterotaxy | DNAH11 | disease | C3178805 | Biomarker | 0.21 | disgenet |
Syndrome, Heterotaxy | WDR62 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CC2D2A | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | AP1B1 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | DRC1 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CFC1B | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | TMEM67 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | C2orf74 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | DNAI1 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | TBC1D32 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | IFT74 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | RFX3 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CPLANE2 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CEP290 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | BICC1 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | ANKS6 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | FOXH1 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | C1orf127 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | MEGF8 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | DNAH5 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | PCSK5 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CCDC39 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | ARMC4 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | DNAAF3 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | SLIT2 | disease | C3178805 | Biomarker | 0.2 | disgenet |
Syndrome, Heterotaxy | CERS1 | disease | C3178805 | GeneticVariation | 0.1 | disgenet |
Syndrome, Heterotaxy | CERS1 | disease | C3178805 | CausalMutation | 0.1 | disgenet |
Syndrome, Heterotaxy | SHROOM3 | disease | C3178805 | GeneticVariation | 0.01 | disgenet |
Syndrome, Heterotaxy | KCNE1 | disease | C3178805 | GeneticVariation | 0.01 | disgenet |
Syndrome, Heterotaxy | EVC2 | disease | C3178805 | Biomarker | 0.01 | disgenet |
Syndrome, Heterotaxy | CFAP53 | disease | C3178805 | GeneticVariation | 0.01 | disgenet |
Syndrome, Heterotaxy | OTX2 | NA | C3178805 | NA | NA | orphanet |
Syndrome, Heterotaxy | PRRX1 | NA | C3178805 | NA | NA | orphanet |
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