ICD-10-CM Code E25.8

Other adrenogenital disorders

Version 2020 Billable Code

Valid for Submission

E25.8 is a billable code used to specify a medical diagnosis of other adrenogenital disorders. The code is valid for the year 2020 for the submission of HIPAA-covered transactions. The ICD-10-CM code E25.8 might also be used to specify conditions or terms like achard-thiers syndrome, disorder of androgen receptor, disorder of sexual differentiation, female pseudopuberty, female puberty disorder, feminization-adrenogenital syndrome, etc

ICD-10:E25.8
Short Description:Other adrenogenital disorders
Long Description:Other adrenogenital disorders

Tabular List of Diseases and Injuries

The Tabular List of Diseases and Injuries is a list of ICD-10 codes, organized "head to toe" into chapters and sections with guidance for inclusions, exclusions, descriptions and more. The following references are applicable to the code E25.8:

Inclusion Terms

Inclusion Terms
These terms are the conditions for which that code is to be used. The terms may be synonyms of the code title, or, in the case of "other specified" codes, the terms are a list of the various conditions assigned to that code. The inclusion terms are not necessarily exhaustive. Additional terms found only in the Alphabetic Index may also be assigned to a code.
  • Idiopathic adrenogenital disorder

Use Additional Code

Use Additional Code
The “use additional code” indicates that a secondary code could be used to further specify the patient’s condition. This note is not mandatory and is only used if enough information is available to assign an additional code.
  • code for adverse effect, if applicable, to identify drug T36 T50

Index to Diseases and Injuries

The Index to Diseases and Injuries is an alphabetical listing of medical terms, with each term mapped to one or more ICD-10 code(s). The following references for the code E25.8 are found in the index:


Synonyms

The following clinical terms are approximate synonyms or lay terms that might be used to identify the correct diagnosis code:

  • Achard-Thiers syndrome
  • Disorder of androgen receptor
  • Disorder of sexual differentiation
  • Female pseudopuberty
  • Female puberty disorder
  • Feminization-adrenogenital syndrome
  • Feminizing syndrome of adrenal origin
  • Isosexual precocious pseudopuberty
  • Masculinized female
  • Masculinized female
  • Masculinized female
  • Masculinized female
  • Maternal virilization due to placental aromatase deficiency
  • Precocious pseudopuberty
  • Pseudohermaphrodite, male with adrenocortical disorder
  • Pseudopuberty
  • Pseudo-puberty - feminization
  • Pseudo-puberty - virilization
  • Undervirilization
  • Virilization of female due to SOX9 gene duplication
  • Virilization of female due to SRY gene translocation
  • Virilized female due to gestational hyperandrogenism
  • Virilizing syndrome of adrenal origin

Diagnostic Related Groups

The ICD-10 code E25.8 is grouped in the following groups for version MS-DRG V37.0 What are Diagnostic Related Groups?
The Diagnostic Related Groups (DRGs) are a patient classification scheme which provides a means of relating the type of patients a hospital treats. The DRGs divides all possible principal diagnoses into mutually exclusive principal diagnosis areas referred to as Major Diagnostic Categories (MDC).
applicable from 10/01/2020 through 09/30/2020.

  • 643 - ENDOCRINE DISORDERS WITH MCC
  • 644 - ENDOCRINE DISORDERS WITH CC
  • 645 - ENDOCRINE DISORDERS WITHOUT CC/MCC

Convert E25.8 to ICD-9

  • 255.2 - Adrenogenital disorders (Approximate Flag)

Code Classification

  • Endocrine, nutritional and metabolic diseases (E00–E90)
    • Disorders of other endocrine glands (E20-E35)
      • Adrenogenital disorders (E25)

Code History

  • FY 2016 - New Code, effective from 10/1/2015 through 9/30/2016
    (First year ICD-10-CM implemented into the HIPAA code set)
  • FY 2017 - No Change, effective from 10/1/2016 through 9/30/2017
  • FY 2018 - No Change, effective from 10/1/2017 through 9/30/2018
  • FY 2019 - No Change, effective from 10/1/2018 through 9/30/2019
  • FY 2020 - No Change, effective from 10/1/2019 through 9/30/2020

Information for Patients


Adrenal Gland Disorders

The adrenal glands are small glands located on top of each kidney. They produce hormones that you can't live without, including sex hormones and cortisol. Cortisol helps you respond to stress and has many other important functions.

With adrenal gland disorders, your glands make too much or not enough hormones. In Cushing's syndrome, there's too much cortisol, while with Addison's disease, there is too little. Some people are born unable to make enough cortisol.

Causes of adrenal gland disorders include

  • Genetic mutations
  • Tumors including pheochromocytomas
  • Infections
  • A problem in another gland, such as the pituitary, which helps to regulate the adrenal gland
  • Certain medicines

Treatment depends on which problem you have. Surgery or medicines can treat many adrenal gland disorders.

NIH: National Institute of Child Health and Human Development


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