Kodex

Code

E25.0

Congenital adrenogenital disorders associated with enzyme deficiency

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Hierarchy

E00-E89 Endocrine, nutritional and metabolic diseases (E00-E89)
- E20-E35 Disorders of other endocrine glands (E20-E35)
  - E25 Adrenogenital disorders
    - E25.0 Congenital adrenogenital disorders associated with enzyme deficiency
    - E25.8 Other adrenogenital disorders
    - E25.9 Adrenogenital disorder, unspecified

Notes

All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.
- E07.0 Hypersecretion of calcitonin
- E34 Other endocrine disorders

Inclusion Terms

E25.0

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

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)

Excludes 1

Q56 Indeterminate sex and pseudohermaphroditism
chromosomal abnormalities (Q90-Q99)
- Q90-Q99 Chromosomal abnormalities, not elsewhere classified (Q90-Q99)

galactorrhea (N64.3)
- N64.3 Galactorrhea not associated with childbirth
gynecomastia (N62)
- N62 Hypertrophy of breast

P70-P74 Transitory endocrine and metabolic disorders specific to newborn (P70-P74)