steroid 17α-hydroxylase deficiency http://purl.bioontology.org/ontology/MEDDRA/10000014 http://purl.obolibrary.org/obo/NCIT_C131086 https://lgbta.wikia.org/wiki/17-AH_Deficiency 17 alpha-hydroxylase/17,20-lyase deficiency 17-AH deficiency 17-alpha-hydroxylase deficiency Decreased or absent activity of the enzyme 17-alpha-hydroxylase/17,20 lyase due to loss-of-function mutation(s) in the CYP17A1 gene. The clinical manifestations of the deficiency are dependent on whether one or both activities of the enzyme are affected, and may include hypertension due to reduced 17-hydroxylase activity and incomplete genital masculinization in 46,XY infants due to reduced 17,20 lyase activity. steroid 17-alpha-hydroxylase deficiency steroid 17-alpha-hydroxylase/17,20 lyase deficiency steroid 17α-hydroxylase/17,20 lyase deficiency reductase deficiency