E25.0Billable
Congenital adrenogenital disorders associated with enzyme deficiency
Chapter 4: Endocrine, nutritional and metabolic diseases
Inclusion Terms
3 items
Inclusion Terms
- •Congenital adrenal hyperplasia
- •21-Hydroxylase deficiency
- •Salt-losing congenital adrenal hyperplasia
Billable Code
E25.0 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Referenced in Diagnoses
Conditions that use this ICD-10 code in their documentation
View documentation for congenital adrenal hyperplasia
congenital adrenal hyperplasia
View TemplatesCongenital Adrenal Hyperplasia due to 21-hydroxylase deficiency
View documentation for elevated testosterone
elevated testosterone
View TemplatesHyperandrogenism
Additional Information from Parent Codes
The following information may apply to this code from its parent codes in the ICD-10 hierarchy. This information is important for proper coding and classification.
Parent Codes Referenced:
Includes
7 items
Includes
From E25:
- •adrenogenital syndromes, virilizing or feminizing, whether acquired or due to adrenal hyperplasia consequent on inborn enzyme defects in hormone synthesis
- •Female adrenal pseudohermaphroditism
- •Female heterosexual precocious pseudopuberty
- •Male isosexual precocious pseudopuberty
- •Male macrogenitosomia praecox
- •Male sexual precocity with adrenal hyperplasia
- •Male virilization (female)
Excludes1
3 items
Excludes1
From E00-E89:
- •transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Notes
1 item
Notes
From E00-E89:
- •All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.