ICDcodes.org
FY2027

E25.0Congenital adrenogenital disorders associated with enzyme deficiency

Billable

Is E25.0 billable?

Yes — E25.0 is billable for FY2027. E25.0 is a valid, billable ICD-10-CM code at the highest level of specificity in its branch. E25.0 may be submitted for encounters from October 1, 2026 through September 30, 2027.

E25.0 at a glance

CodeE25.0
DescriptionCongenital adrenogenital disorders associated with enzyme deficiency
BillableYes
Code setICD-10-CM FY2027
Valid for encountersOctober 1, 2026 – September 30, 2027

Which MS-DRGs does E25.0 group to?

E25.0 sits in MDC 10 and helps define the logic of 3 MS-DRGs (version 44, FY2027). Which one a stay actually groups to also depends on procedures and secondary diagnoses.

  • 643Endocrine Disorders with MCCmedical
  • 644Endocrine Disorders with CCmedical
  • 645Endocrine Disorders without CC/MCCmedical

How is E25.0 listed in the Alphabetic Index?

These are the routes through the Alphabetic Index that lead to E25.0. They show the wording a clinician may have documented, which often differs from the Tabular description.

  • Adrenogenitalism, congenital
  • Adrenogenital syndromecongenital
  • Adrenogenital syndromesalt loss
  • Defect, defective3-beta-hydroxysteroid dehydrogenase
  • Defect, defective11-hydroxylase
  • Defect, defective21-hydroxylase
  • Deficiency, deficient3-beta hydroxysteroid dehydrogenase
  • Deficiency, deficient11-hydroxylase
  • Deficiency, deficient21-hydroxylase
  • Hyperadrenocorticismcongenital
  • Macrogenitosomiacongenital (adrenal) (male) (praecox)
  • Masculinizationwith adrenal hyperplasiacongenital (female)

Inclusion terms

Alternative wording in documentation that is classified to E25.0.

  • Congenital adrenal hyperplasia
  • 21-Hydroxylase deficiency
  • Salt-losing congenital adrenal hyperplasia

Excludes1 — never code together — inherited from Chapter 4

The conditions below can never be reported together with E25.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • transitory endocrine and metabolic disorders specific to newborn (P70-P74)

Excludes1 — never code together — inherited from E20-E35

The conditions below can never be reported together with E25.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

Excludes1 — never code together — inherited from E25

The conditions below can never be reported together with E25.0 on the same claim. An Excludes1 note means the two conditions cannot occur in the same patient, so reporting both is a coding error.

  • indeterminate sex and pseudohermaphroditism (Q56)
  • chromosomal abnormalities (Q90-Q99)

How long has E25.0 existed?

E25.0 has been in ICD-10-CM since at least FY2016, the earliest fiscal year on record here.

Derived from the official order files for FY2016–FY2026. FY2017 and FY2020 publish no order file, so those years are not covered.

Which codes are confused with E25.0?

ICD-10-CM declares these codes mutually exclusive with E25.0 — exactly one of each pair can be correct for a given encounter.

Which conditions are coded to E25.0?

What other codes are in the E25 family? (2)