Disease Information
Disease Name Gene Name Type UMLS Association Type Score Source
Leydig Cell Hypoplasia, Type I LHCGR disease C0266432 GeneticVariation 0.8 orphanet , disgenet
Leydig Cell Hypoplasia, Type I LHCGR disease C0266432 Biomarker 0.8 orphanet , disgenet
Leydig Cell Hypoplasia, Type I LHCGR disease C0266432 AlteredExpression 0.8 orphanet , disgenet
Leydig Cell Hypoplasia, Type I LHCGR disease C0266432 CausalMutation 0.8 orphanet , disgenet
Leydig Cell Hypoplasia, Type I GTF2A1L disease C0266432 CausalMutation 0.1 disgenet
Leydig Cell Hypoplasia, Type I GTF2A1L disease C0266432 GeneticVariation 0.1 disgenet
Leydig Cell Hypoplasia, Type I STON1-GTF2A1L disease C0266432 CausalMutation 0.1 disgenet
Leydig Cell Hypoplasia, Type I STON1-GTF2A1L disease C0266432 GeneticVariation 0.1 disgenet
Leydig Cell Hypoplasia, Type I FSHR disease C0266432 GeneticVariation 0.01 disgenet
Leydig Cell Hypoplasia, Type I EGR4 disease C0266432 Biomarker 0.01 disgenet
Leydig Cell Hypoplasia, Type I LGR6 disease C0266432 GeneticVariation 0.01 disgenet
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