Diagnosis Code: E25.0

Short Description: Congenital adrenogenital disorders assoc w enzyme deficiency

Long Description: Congenital adrenogenital disorders associated with enzyme deficiency

The code E25.0 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Disorders of other endocrine glands (E20-E35)
    • Adrenogenital disorders (E25)
      • E25.0 Congenital adrenogenital disorders assoc w enzyme deficiency

Code Version: 2022 ICD-10-CM

Synonyms

• 17 alpha-Hydroxyprogesterone aldolase deficiency
• 3 beta-Hydroxysteroid dehydrogenase deficiency
• 3-Beta-hydroxy-delta-5-C27-steroid dehydrogenase deficiency
• 46,XY disorder of sex development
• 46,XY disorder of sex development due to isolated 17,20-lyase deficiency
• Adrenal virilism
• Adrenal virilism
• Adrenal virilism
• Adrenal virilism
• Adrenal virilism
• Aldosterone deficiency
• CAH - desmolase deficiency
• Cholesterol monooxygenase deficiency
• Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
• Congenital adrenal hyperplasia
• Congenital adrenal hyperplasia due to 21-hydroxylase deficiency non-classic form
• Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency
• Congenital adrenal hypoplasia, X-linked
• Congenital hypoplasia of adrenal gland
• Congenital lipoid adrenal hyperplasia due to STAR deficiency
• Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency classic form
• Congenital lipoid adrenal hyperplasia due to steroidogenic acute regulatory protein deficiency non classic form
• Corticosterone 18-monooxygenase deficiency
• Deficiency of 3alpha-hydroxysteroid dehydrogenase
• Deficiency of 3beta-hydroxysteroid dehydrogenase
• Deficiency of steroid 11-beta-monooxygenase
• Deficiency of steroid 21-monooxygenase
• Disorder of cholesterol catabolism
• Disorder of cholesterol metabolism
• Female pseudohermaphroditism
• Female pseudohermaphroditism due to congenital adrenal hyperplasia
• Fetal endocrine disorder
• Fetal virilism
• Hyperandrogenism due to non-classic 21-hydroxylase deficiency
• Hypertension due to congenital adrenal hyperplasia
• Late onset congenital adrenal hyperplasia
• Male pseudohermaphroditism
• Male pseudohermaphroditism due to congenital adrenal hyperplasia
• Mild steroid 21-hydroxylase deficiency
• Moderate steroid 21-hydroxylase deficiency
• Pseudohermaphrodite, female with adrenocortical disorder
• Pseudohermaphroditism due to congenital adrenal hyperplasia
• Salt-losing congenital adrenal hyperplasia
• Salt-losing congenital adrenal hyperplasia with virilism
• Severe steroid 21-hydroxylase deficiency
• Steroid 21-monooxygenase deficiency, salt wasting type
• Steroid 21-monooxygenase deficiency, simple virilizing type
• Synthetic defect of bile acids
• Virilization-adrenogenital syndrome
• Virilizing syndrome of adrenal origin
• Virilizing syndrome of adrenal origin

Diagnostic Related Group(s)

The code E25.0 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Endocrine Disorders With Mcc (643)
• Endocrine Disorders With Cc (644)
• Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E25.0 has the following ICD-10-CM references to the Index of Diseases and Injuries

• Inclusion Terms:
  • Congenital adrenal hyperplasia
  • 21-Hydroxylase deficiency
  • Salt-losing congenital adrenal hyperplasia

Crosswalk Information

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This page was last updated on: 10/1/2023

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