E25.0 - Congenital adrenogenital disorders associated with enzyme deficiency
- Applicable to Congenital adrenogenital disorders associated with enzyme deficiency
- The 2025 edition of ICD10-CM E25.0 became effective on October 1, 2024.
- This is the American ICD10-CM version of E25.0 - other international versions of ICD10 E25.0 may differ.
- E25.0 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
Inclusion terms help to clarify and specify the conditions or diseases covered by a particular ICD-10-CM code.
Inclusion Term:
- Congenital adrenal hyperplasia
- 21-Hydroxylase deficiency
- Salt-losing congenital adrenal hyperplasia
Billable/Specific Code
The following codes above E25.0 contain annotation back-references that may be applicable to E25.0:
- Chapter: E00-E89 - Endocrine, nutritional and metabolic diseases
- Section: E20-E35 - Disorders of other endocrine glands
- Category: E25 - Adrenogenital disorders
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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