Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
PEHO syndrome ZNHIT3 disease C1850055 CausalMutation 0.73 orphanet , disgenet
PEHO syndrome ZNHIT3 disease C1850055 GeneticVariation 0.73 orphanet , disgenet
PEHO syndrome ZNHIT3 disease C1850055 AlteredExpression 0.73 orphanet , disgenet
PEHO syndrome ZNHIT3 disease C1850055 Biomarker 0.73 orphanet , disgenet
PEHO syndrome ZNHIT3 disease C1850055 GermlineCausalMutation 0.73 orphanet , disgenet
PEHO syndrome KIF1A disease C1850055 GermlineCausalMutation 0.42 orphanet , disgenet
PEHO syndrome KIF1A disease C1850055 GeneticVariation 0.42 orphanet , disgenet
PEHO syndrome KIF1A disease C1850055 CausalMutation 0.42 orphanet , disgenet
PEHO syndrome CCDC88A disease C1850055 GeneticVariation 0.32 disgenet
PEHO syndrome CCDC88A disease C1850055 Biomarker 0.32 disgenet
PEHO syndrome HESX1 disease C1850055 GeneticVariation 0.01 disgenet
PEHO syndrome VPS53 disease C1850055 GeneticVariation 0.01 disgenet
PEHO syndrome RARS2 disease C1850055 GeneticVariation 0.01 disgenet
PEHO syndrome SEPSECS disease C1850055 GeneticVariation 0.01 disgenet
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