Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Insomnia, Fatal Familial PRNP disease C0206042 AlteredExpression 1 orphanet , disgenet
Insomnia, Fatal Familial PRNP disease C0206042 GeneticVariation 1 orphanet , disgenet
Insomnia, Fatal Familial PRNP disease C0206042 Biomarker 1 orphanet , disgenet
Insomnia, Fatal Familial PRNP disease C0206042 CausalMutation 1 orphanet , disgenet
Insomnia, Fatal Familial GLS disease C0206042 Biomarker 0.02 disgenet
Insomnia, Fatal Familial PRDX2 disease C0206042 GeneticVariation 0.02 disgenet
Insomnia, Fatal Familial C4BPA disease C0206042 GeneticVariation 0.02 disgenet
Insomnia, Fatal Familial CARD14 disease C0206042 GeneticVariation 0.02 disgenet
Insomnia, Fatal Familial ABCB6 disease C0206042 GeneticVariation 0.02 disgenet
Insomnia, Fatal Familial GLS disease C0206042 GeneticVariation 0.02 disgenet
Insomnia, Fatal Familial GFAP disease C0206042 Biomarker 0.01 disgenet
Insomnia, Fatal Familial ZBTB38 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial CSNK2A2 disease C0206042 Biomarker 0.01 disgenet
Insomnia, Fatal Familial MDH1 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial MLKL disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial CHI3L1 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial NDUFB8 disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial TSPO disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial RASA2 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial UQCRC2 disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial COX2 disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial AQP1 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial RYR2 disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial RIPK3 disease C0206042 Biomarker 0.01 disgenet
Insomnia, Fatal Familial MPRIP disease C0206042 Biomarker 0.01 disgenet
Insomnia, Fatal Familial GH1 disease C0206042 Biomarker 0.01 disgenet
Insomnia, Fatal Familial SDHB disease C0206042 AlteredExpression 0.01 disgenet
Insomnia, Fatal Familial MIR146A disease C0206042 GeneticVariation 0.01 disgenet
Insomnia, Fatal Familial PRL disease C0206042 Biomarker 0.01 disgenet
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