Catalog

46,XY disorder of sex development due to isolated 17, 20 lyase deficiency

No MMS code

Link to WHO Definition

46,XY disorder of sex development due to isolated 17, 20 lyase deficiency – http://id.who.int/icd/entity/513865687

This refers to disorder of sex development due to a rare endocrine and autosomal recessive genetic disorder which is characterised by a complete or partial loss of 17,20-lyase activity and, in turn, impaired production of the androgen and estrogen sex steroids.