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ICD-10 diagnosis code

E25.0 Congenital adrenogenital disorders associated with enzyme deficiency

This page in Swedish

E25.0 is the ICD-10 code for Congenital adrenogenital disorders associated with enzyme deficiency. It is a four-character subcategory of E25 (Adrenogenital disorders), the most specific level in the WHO edition. It belongs to the block E20–E35 (Disorders of other endocrine glands) in Chapter IV, Endocrine, nutritional and metabolic diseases.

Code type
Subcategory (4 characters)
Chapter
IV · E00–E90
Classification
WHO ICD-10, 2019 version

What E25.0 includes

Conditions and terms that are coded here.

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

E25.0 in national editions

Countries report with their own edition of ICD-10. Most keep the WHO code and add more specific codes beneath it.

SwedenICD-10-SE

E25.0Kongenitala adrenogenitala rubbningar förenade med enzymbrist

  • E25.0ABinjurebarkshyperplasi, kongenital, med saltförlust
  • E25.0BBinjurebarkshyperplasi, kongenital, med enzymbrist
  • E25.0CBinjurebarkshyperplasi, sent debuterande form (icke klassisk form)
  • E25.0DMacrogenitosomia praecox
NorwayICD-10-NO

E25.0Medfødt adrenogenital forstyrrelse i tilknytning til enzymmangel

DenmarkICD-10-DK

DE250Medfødt adrenogenitalt syndrom med enzymdefekt

  • DE250BMedfødt 21-hydroxylasemangel
  • DE250CMedfødt salttabende binyrebarkhyperplasi
  • DE250DMedfødt binyrebarkhyperplasi
FinlandICD-10-FI

E25.0Synnynnäiset adrenogenitaaliset häiriöt, joihin liittyy entsyymivajaus

  • E25.00Suolanmenetystä aiheuttava synnynnäinen lisämunuaisen liikakasvu
  • E25.01Muu tai määrittämätön synnynnäinen lisämunuaisen liikakasvu
GermanyICD-10-GM

E25.0Angeborene adrenogenitale Störungen in Verbindung mit Enzymmangel

  • E25.0021-Hydroxylase-Mangel [AGS Typ 3], klassische Form
  • E25.0121-Hydroxylase-Mangel [AGS Typ 3], Late-onset-Form
  • E25.08Sonstige angeborene adrenogenitale Störungen in Verbindung mit Enzymmangel
  • E25.09Angeborene adrenogenitale Störung in Verbindung mit Enzymmangel, nicht näher bezeichnet
FranceICD-10-FR

E25.0Anomalies génitosurrénaliennes congénitales liées à un déficit enzymatique

NetherlandsICD-10-NL

E25.0congenitale adrenogenitale aandoeningen samenhangend met

United StatesICD-10-CM

E25.0Congenital adrenogenital disorders associated with enzyme deficiency

Based on the World Health Organization’s International Statistical Classification of Diseases and Related Health Problems, 10th revision (ICD-10), 2019 version, and the national editions published by each country’s health authority. This page is a reference, not coding advice; follow your national coding rules when you report.

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