E25.0
Billable codeCongenital adrenogenital disorders associated with enzyme deficiency
The ICD-10 code for congenital adrenogenital disorders associated with enzyme deficiency is E25.0.
Clinical notes
Also known as
Alternate wording, synonyms, or specific conditions that fall under this code, listed to help confirm you've picked the right one.
- Congenital adrenal hyperplasia
- 21-Hydroxylase deficiency
- Salt-losing congenital adrenal hyperplasia
Documentation support
General coding-documentation guidance — not a substitute for payer-specific requirements or professional coding judgment.
- •As a general rule, code to the highest level of specificity supported by the documentation in the medical record.
Related codes in this category
- E25.8Other adrenogenital disorders
- E25.9Adrenogenital disorder, unspecified
- E25.0Congenital adrenogenital disorders associated with enzyme deficiency
ICD-9-CM equivalent
Informational only — GEM mappings are approximate, not guaranteed one-to-one equivalents. Verify before use in billing.
- 2552Approximate match
Associated MS-DRGs
E25.0 can serve as the principal diagnosis for these Medicare Severity Diagnosis-Related Groups.
Informational only — actual DRG assignment also depends on procedures, complications/comorbidities (CC/MCC), discharge status, and payer-specific rules not reflected here.