ICD-10-CM Diagnosis Code E25.0
Effective Date: 10/01/2015 To 09/30/2025Congenital adrenogenital disorders associated with enzyme deficiency
CMS-HCC-V24 | CMS-HCC-V28 | RxHCC | Age | Gender | Maternity | Acute or Chronic | MCC |
---|---|---|---|---|---|---|---|
23 | -- | 43 | -- | -- | -- | Acute | No |
Applicable To for E25.0:
Back-references to E25.0
Adrenogenital syndrome E25.9
Adrenogenitalism, congenital E25.0
Defect, defective Q89.9
Deficiency, deficient
Hyperadrenocorticism E24.9
Hyperfunction
Hyperplasia, hyperplastic
Macrogenitosomia(adrenal) (male) (praecox) E25.9
Masculinization(female) with adrenal hyperplasia E25.9
Precocity, sexual(constitutional) (cryptogenic) (female) (idiopathic) (male) E30.1
Pseudohermaphroditism Q56.3
Syndrome see also Disease
Virilism(adrenal) E25.9
Virilization(female) (suprarenal) E25.9
- congenital E25.0
- salt loss E25.0
- 11-hydroxylase E25.0
- 21-hydroxylase E25.0
- 3-beta-hydroxysteroid dehydrogenase E25.0
- 11-hydroxylase E25.0
- 21-hydroxylase E25.0
- 3-beta hydroxysteroid dehydrogenase E25.0
- congenital E25.0
- congenital E25.0
- congenital E25.0
- with adrenal hyperplasia E25.9
- congenital E25.0
- congenital E25.0
- female see also Disorder, adrenogenital Q56.2
- adrenal(congenital) E25.0
- adrenal(congenital) E25.0
- adrenogenital E25.9
- congenital, associated with enzyme deficiency E25.0
- congenital, associated with enzyme deficiency E25.0
- congenital E25.0
- congenital E25.0
Related Medications for
E25.0
Chapter, Section and Diagnosis Prefix for
E25.0