myICD10.com Logo
21-hydroxylase deficiency

Medical Definition

A classic form of congenital adrenal hyperplasia that is characterized by severe 21-hydroxylase deficiency, resulting in glucocorticoid and mineralocorticoid deficiency, without clinically significant salt wasting, and androgen excess, which causes virilization in female infants.
Related Codes (1)
Code
Description
Billable
Details
E25.0Congenital adrenogenital disorders associated with enzyme deficiency

Rows per page

Page 1 of 1