DxCodebookFY2027 · Oct 1, 2026 – Sep 30, 2027

Category · FY2027

E25 Adrenogenital disorders

  • Header · not billable

E25 is not billable. The category heads 3 billable codes in FY2027: the 3 codes directly below it.

Index → code

  • Virilism (adrenal) → E25.9
  • Adrenogenital syndrome → E25.9
  • Adrenogenitalism, congenital → E25.0
Billable codes
3
Subdivisions
3
CC / MCC codes
0 / 0
HCC V28 codes
0
New FY2027
0
Index entries
46

Codes in E25

  1. E25.0
    Congenital adrenogenital disorders associated with enzyme deficiency
    Billable
    Inclusion terms 3

    Inclusion terms

    • Congenital adrenal hyperplasia
    • 21-Hydroxylase deficiency
    • Salt-losing congenital adrenal hyperplasia
  2. E25.8
    Other adrenogenital disorders
    Billable
    Inclusion terms 1, Use additional code 1

    Inclusion terms

    • Idiopathic adrenogenital disorder

    Use additional code

    • code for adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5) T36 T50
  3. E25.9
    Adrenogenital disorder, unspecified
    Billable
    Inclusion terms 1

    Inclusion terms

    • Adrenogenital syndrome NOS

Sources of each column.

Instructions

At E25

Includes

  • adrenogenital syndromes, virilizing or feminizing, whether acquired or due to adrenal hyperplasia consequent on inborn enzyme defects in hormone synthesis
  • Female adrenal pseudohermaphroditism
  • Female heterosexual precocious pseudopuberty
  • Male isosexual precocious pseudopuberty
  • Male macrogenitosomia praecox
  • Male sexual precocity with adrenal hyperplasia
  • Male virilization (female)

Excludes1

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

Notes that also apply

Block E20-E35 instructions (Excludes1 2): printed on the block page.

Chapter 4 instructions (Notes 1, Excludes1 1): printed on the chapter 4 page.

Index entries

  • Adrenogenitalism, congenital → E25.0
  • Adrenogenital syndrome → E25.9
  • Macrogenitosomia (adrenal) (male) (praecox) → E25.9
  • Masculinization (female) with adrenal hyperplasia → E25.9
  • Virilism (adrenal) → E25.9
  • Virilization (female) (suprarenal) → E25.9
  • Adrenogenital syndromecongenital → E25.0
  • Adrenogenital syndromesalt loss → E25.0
  • Defect, defective3-beta-hydroxysteroid dehydrogenase → E25.0
  • Defect, defective11-hydroxylase → E25.0
  • Defect, defective21-hydroxylase → E25.0
  • Deficiency, deficient3-beta hydroxysteroid dehydrogenase → E25.0
  • Deficiency, deficient11-hydroxylase → E25.0
  • Deficiency, deficient21-hydroxylase → E25.0
  • Hyperadrenocorticismcongenital → E25.0
  • Macrogenitosomia (adrenal) (male) (praecox)congenital → E25.0
  • Masculinization (female) with adrenal hyperplasiacongenital → E25.0
  • Virilism (adrenal)congenital → E25.0
  • Virilization (female) (suprarenal)congenital → E25.0
  • Adrenogenital syndromeacquired → E25.8
  • Pseudohermaphroditismadrenal → E25.8
  • Pseudopuberty, precociousfemale heterosexual → E25.8
  • Pseudopuberty, precociousmale isosexual → E25.8
  • Disorder (of)adrenogenital → E25.9
  • Precocity, sexual (constitutional) (cryptogenic) (female) (idiopathic) (male)with adrenal hyperplasia → E25.9
  • Syndromeadrenogenital → E25.9
  • Hyperplasia, hyperplasticadrenal (capsule) (cortex) (gland)congenital → E25.0
  • Precocity, sexual (constitutional) (cryptogenic) (female) (idiopathic) (male)with adrenal hyperplasiacongenital → E25.0
  • Pseudohermaphroditismfemaleadrenal (congenital) → E25.0
  • Syndromeadrenogenitalcongenital, associated with enzyme deficiency → E25.0
  • Disorder (of)adrenogenitaldrug-induced → E25.8
  • Disorder (of)adrenogenitaliatrogenic → E25.8
  • Disorder (of)adrenogenitalidiopathic → E25.8
  • Pseudohermaphroditismfemalewith adrenocortical disorder → E25.8
  • Pseudohermaphroditismmaleadrenal → E25.8
  • Hyperfunctionadrenal cortex, not associated with Cushing's syndromevirilism → E25.9
  • Hyperfunctionadrenal cortex, not associated with Cushing's syndromevirilismcongenital → E25.0
  • Hyperplasia, hyperplasticadrenal (capsule) (cortex) (gland)congenitalsalt-losing → E25.0
  • Pseudohermaphroditismmalewithadrenocortical disorder → E25.8
  • Puberty (development state)prematuredue toadrenal cortical hyperfunction → E25.8

6 more, longer entries are not listed; the search box finds them by word.

NCHS Alphabetic Index. Index first, then the Tabular List.

Hierarchy