E25.0
E25.0: Congenital adrenogenital disorders associated with enzyme deficiency
Billable / specific codeICD-10-CM
E25.0 is a billable, specific ICD-10-CM code for congenital adrenogenital disorders associated with enzyme deficiency. It is valid for submission on a claim.
Check E25.0 with the rest of the claim: free scrubberInclusion terms
Alternative wordings a physician may use in the chart for this same code.
- Congenital adrenal hyperplasia
- 21-Hydroxylase deficiency
- Salt-losing congenital adrenal hyperplasia
Other codes that can never be billed with E25.0
Their own Excludes1 notes name this code, so the conflict is not listed above.
Risk adjustment
No CMS-HCC V28 category: this code does not change a RAF score.
Medicare coverage
E25.0 is named in 6 Medicare coverage policies: 6 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.
- A55336Billing and Coding: Retroperitoneal Ultrasound
- A56421Billing and Coding: CT of the Abdomen and Pelvis
- A56619Billing and Coding: Nerve Conduction Studies and Electromyography
- A57204Billing and Coding: MRI and CT Scans of the Head and Neck
Alphabetic index entries that lead here
- Adrenogenitalism, congenital
- Adrenogenital syndrome›congenital
- Adrenogenital syndrome›salt loss
- Defect, defective›11-hydroxylase
- Defect, defective›21-hydroxylase
- Defect, defective›3-beta-hydroxysteroid dehydrogenase
- Deficiency, deficient›11-hydroxylase
- Deficiency, deficient›21-hydroxylase
- Deficiency, deficient›3-beta hydroxysteroid dehydrogenase
- Hyperadrenocorticism›congenital
- Macrogenitosomia›congenital
- Masculinization with adrenal hyperplasia›congenital
Code history
Unchanged in every release from FY2024 to FY2027.