Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Hypercholanemia, Familial BAAT disease C1843139 GeneticVariation 0.71 orphanet , disgenet
Hypercholanemia, Familial TJP2 disease C1843139 GermlineCausalMutation 0.71 orphanet , disgenet
Hypercholanemia, Familial TJP2 disease C1843139 GeneticVariation 0.71 orphanet , disgenet
Hypercholanemia, Familial TJP2 disease C1843139 Biomarker 0.71 orphanet , disgenet
Hypercholanemia, Familial BAAT disease C1843139 Biomarker 0.71 orphanet , disgenet
Hypercholanemia, Familial BAAT disease C1843139 GermlineCausalMutation 0.71 orphanet , disgenet
Hypercholanemia, Familial TJP2 disease C1843139 CausalMutation 0.71 orphanet , disgenet
Hypercholanemia, Familial BAAT disease C1843139 CausalMutation 0.71 orphanet , disgenet
Hypercholanemia, Familial EPHX1 disease C1843139 Biomarker 0.6 orphanet , disgenet
Hypercholanemia, Familial EPHX1 disease C1843139 GermlineCausalMutation 0.6 orphanet , disgenet
click here to return to the previous page