Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hyperkeratosis lenticularis perstans APOE disease C0263420 GeneticVariation 0.09 disgenet
Hyperkeratosis lenticularis perstans APOE disease C0263420 Biomarker 0.09 disgenet
Hyperkeratosis lenticularis perstans LPL disease C0263420 Biomarker 0.04 disgenet
Hyperkeratosis lenticularis perstans LDLR disease C0263420 Biomarker 0.04 disgenet
Hyperkeratosis lenticularis perstans LPL disease C0263420 GeneticVariation 0.04 disgenet
Hyperkeratosis lenticularis perstans LDLR disease C0263420 GeneticVariation 0.04 disgenet
Hyperkeratosis lenticularis perstans LDLR disease C0263420 AlteredExpression 0.04 disgenet
Hyperkeratosis lenticularis perstans CETP disease C0263420 Biomarker 0.02 disgenet
Hyperkeratosis lenticularis perstans CETP disease C0263420 AlteredExpression 0.02 disgenet
Hyperkeratosis lenticularis perstans CR2 disease C0263420 AlteredExpression 0.01 disgenet
Hyperkeratosis lenticularis perstans HLP disease C0263420 Biomarker 0.01 disgenet
Hyperkeratosis lenticularis perstans LCAT disease C0263420 Biomarker 0.01 disgenet
Hyperkeratosis lenticularis perstans EGFR disease C0263420 AlteredExpression 0.01 disgenet
Hyperkeratosis lenticularis perstans NPPA disease C0263420 GeneticVariation 0.01 disgenet
Hyperkeratosis lenticularis perstans PDLIM7 disease C0263420 GeneticVariation 0.01 disgenet
Hyperkeratosis lenticularis perstans OLR1 disease C0263420 AlteredExpression 0.01 disgenet
Hyperkeratosis lenticularis perstans APOA5 disease C0263420 GeneticVariation 0.01 disgenet
Hyperkeratosis lenticularis perstans LPA disease C0263420 Biomarker 0.01 disgenet
Hyperkeratosis lenticularis perstans NPPB disease C0263420 GeneticVariation 0.01 disgenet
Hyperkeratosis lenticularis perstans APOC3 disease C0263420 GeneticVariation 0.01 disgenet
Hyperkeratosis lenticularis perstans MAPK8 disease C0263420 AlteredExpression 0.01 disgenet
Hyperkeratosis lenticularis perstans CD40 disease C0263420 AlteredExpression 0.01 disgenet
Hyperkeratosis lenticularis perstans APOB disease C0263420 GeneticVariation 0.01 disgenet
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