46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110)

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.

Language	Label	Description	Also known as
default for all languages	ID_513865687
English	46,XY disorder of sex development due to isolated 17, 20 lyase deficiency	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.