E25.8
BillableOther adrenogenital disorders
Other adrenogenital disorders
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Idiopathic adrenogenital disorder
Includes
Conditions included under this code
- 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)
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
Use Additional Code
Additional codes that should follow this code
Related Codes(2)
ICD-11 Equivalents(1)
ICD-11 Equivalents
View full mappingCorresponding ICD-11 codes from the WHO crosswalk mapping
Also Known As / Clinical Terms(82)
SNOMED CT
- Androgen receptor abnormal9979004
- Disorder of androgen receptor9979004
- Virilising syndrome of adrenal origin17318002
- Virilizing syndrome of adrenal origin17318002
- Precocious female puberty19911007
- Female pseudopuberty21731004
- Female puberty disorder23886002
- Achard-Thiers syndrome34041001
- Diabetic-bearded woman syndrome34041001
- Isosexual precocious pseudopuberty35567006
- Disorder of sexual differentiation39179006
- Feminisation-adrenogenital syndrome237747002
- Feminising syndrome of adrenal origin237747002
- Feminization-adrenogenital syndrome237747002
- Feminizing syndrome of adrenal origin237747002
- Pseudohermaphrodite, male with adrenocortical disorder237748007
- Undervirilisation237807003
- Undervirilization237807003
- Pseudo-puberty - virilisation237819006
- Pseudo-puberty - virilization237819006
- Pseudo-puberty - feminisation237820000
- Pseudo-puberty - feminization237820000
- Masculinised female271602007
- Masculinized female271602007
- Virilized XX gestational hyperandrogenism426898004
- Virilized female due to gestational hyperandrogenism426898004
- Maternal virilisation due to placental aromatase deficiency427627006
- Maternal virilization due to placental aromatase deficiency427627006
- Virilisation of female due to SOX9 gene duplication443898004
- Virilization of female due to SOX9 gene duplication443898004
- Virilisation of female due to SRY gene translocation444058005
- Virilization of female due to SRY gene translocation444058005
- Gonadotropin independent precocious puberty736606009
- Peripheral precocious puberty736606009
- Precocious pseudopuberty736606009
- Adrenogenital disorder caused by drug1142059006
- Drug-induced adrenogenital disorder1142059006
- Idiopathic adrenogenital disorder1217054001
- Iatrogenic adrenogenital disorder1217060001
UMLS
Clinical Terms
- Pseudohermaphrodite, male with adrenocortical disorder
- Female puberty disorder
- Undervirilization
- Adrenogenital disorder caused by drug
- Feminization-adrenogenital syndrome
- Virilized XX gestational hyperandrogenism
- Idiopathic adrenogenital disorder (disorder)
- Pseudo-puberty - virilization
- Isosexual precocious pseudopuberty
- Virilisation of female due to SRY gene translocation
- Virilizing syndrome of adrenal origin
- Precocious pseudopuberty
- Pseudo-puberty - virilisation
- Idiopathic adrenogenital disorder
- Feminizing syndrome of adrenal origin
- Precocious female puberty
- Maternal virilisation due to placental aromatase deficiency
- Masculinized female
- Virilization of female due to SRY gene translocation
- Iatrogenic adrenogenital disorder
- Androgen receptor abnormal
- Female pseudopuberty
- Feminisation-adrenogenital syndrome
- Pseudo-puberty - feminization
- Virilized female due to gestational hyperandrogenism
- Drug-induced adrenogenital disorder
- Undervirilisation
- Peripheral precocious puberty
- Gonadotropin independent precocious puberty
- Disorder of androgen receptor
- Virilising syndrome of adrenal origin
- Feminising syndrome of adrenal origin
- Virilisation of female due to SOX9 gene duplication
- Diabetic-bearded woman syndrome
- Maternal virilization due to placental aromatase deficiency
- Disorder of sexual differentiation
- Pseudo-puberty - feminisation
- Masculinised female
- Virilization of female due to SOX9 gene duplication
- Achard-Thiers syndrome
Frequently Asked Questions
What is the ICD-10 code for other adrenogenital disorders?
The ICD-10-CM code for other adrenogenital disorders is E25.8. The full clinical description is "Other adrenogenital disorders". E25.8 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E25.8 mean?
ICD-10-CM code E25.8 represents “Other adrenogenital disorders”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E25.8 a billable code?
Yes, E25.8 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E25.8 in?
E25.8 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E25.8?
E25.8 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 2 more.
Are additional codes required with E25.8?
Yes, when using E25.8, also report: adverse effect, if applicable, to identify drug (T36-T50 with fifth or sixth character 5).
What SNOMED CT codes does E25.8 map to?
E25.8 maps to 22 SNOMED CT concepts: 34041001, 1142059006, 9979004, 39179006, 21731004, and 17 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E25.8?
E25.8 is linked to 2 UMLS Concept Unique Identifiers: C1384854, C0348459. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E25.8 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other adrenogenital disorders affect a person's functioning — body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E25.8?
E25.8 maps to the ICD-11 code: 5A71.Z (Adrenogenital disorders, unspecified).
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.