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Home/Diagnosis/ICD-10 Coding for Congenital Adrenal Hyperplasia

ICD-10 Coding for Congenital Adrenal Hyperplasia

E25.0

Complete ICD-10-CM coding and documentation guide for icd-10 coding for congenital adrenal hyperplasia includes clinical validation requirements, medical necessity guidelines, and coding policies.

Also Known as:
CAH
Adrenogenital Syndrome
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Key Information: ICD-10 Coding for Congenital Adrenal Hyperplasia

Essential facts and insights about ICD-10 Coding for Congenital Adrenal Hyperplasia

Use ICD-10 code E25.0 for congenital adrenogenital disorders associated with enzyme deficiency, ensuring proper documentation in clinical notes.

Primary ICD-10-CM Codes

Congenital adrenogenital disorders associated with enzyme deficiency

Billable Code
E25.0
Billable

Diagnostic Criteria

clinical:
  • • Presence of 21-hydroxylase deficiency confirmed by lab tests
documentation:
  • • Detailed documentation of enzyme deficiency and genetic testing

Applicable To

  • • 21-hydroxylase deficiency

Important Notes

  • • Ensure enzyme deficiency is documented before using E25.0.
Ancillary Codes

Additional codes that may be used with this diagnosis

E27.2

Addisonian crisis

Use for acute adrenal insufficiency related to CAH.

E87.6

Hypokalemia

Use for electrolyte imbalances in salt-wasting CAH.

Frequently Asked Questions

What is the ICD-10 code for congenital adrenal hyperplasia?

The ICD-10 code for congenital adrenal hyperplasia due to 21-hydroxylase deficiency is E25.0. This code is used when enzyme deficiency is confirmed.

How is congenital adrenal hyperplasia documented?

Documentation for congenital adrenal hyperplasia should include specific enzyme deficiency, lab results like elevated 17-OHP, and genetic testing results.

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