Disease Term Disease ID Gene Symbol Classification References Source
Hyperandrogenism, Nonclassic Type, due to 21-Hydroxylase Deficiency C1859995 CYP21A2 Causal Pathogenic evidence from ClinVar - ClinVar
Hyperandrogenism C0206081 BMPR2 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations 22825968 -
Hyperandrogenism due to cortisone reductase deficiency 168588 H6PD Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -
HSD11B1 Unknown Evidence from: GenCC, GWAS, ClinVar (non-pathogenic), CBGDA, or Text Mining associations - -