Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Leydig Cell Hypoplasia, Type II LHCGR disease C2673497 CausalMutation 0.42 orphanet , disgenet
Leydig Cell Hypoplasia, Type II LHCGR disease C2673497 Biomarker 0.42 orphanet , disgenet
Leydig Cell Hypoplasia, Type II LHCGR disease C2673497 GeneticVariation 0.42 orphanet , disgenet
Leydig Cell Hypoplasia, Type II STON1-GTF2A1L disease C2673497 CausalMutation 0.1 disgenet
Leydig Cell Hypoplasia, Type II GTF2A1L disease C2673497 CausalMutation 0.1 disgenet
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