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E25.0 - Congenital adrenogenital disorders associated with enzyme deficiency


The ICD 10 Code for Congenital adrenogenital disorders associated with enzyme deficiency is listed as E25.0.
Additional information concerning this code and description can be found below including ICD 9 crosswalks / GEMS, chapter information, and DRGs where available.

ICD 10 CM Field Value
Diagnosis Code: E25.0
Description: Congenital adrenogenital disorders associated with enzyme deficiency
  • Congenital adrenal hyperplasia
  • 21-Hydroxylase deficiency
  • Salt-losing congenital adrenal hyperplasia
Diagnostic Related Groups
(MS-DRG v30.0)
643 - Endocrine Disorders W Mcc
644 - Endocrine Disorders W Cc
645 - Endocrine Disorders W/o Cc/mcc
Chapter Endocrine, nutritional and metabolic diseases (E00-E89)
Block Disorders of other endocrine glands (E20-E35)
Parent E25 - Adrenogenital disorders
ICD-9-CM Diagnosis Codes General Equivalence Mappings (GEMS):
ICD 9 Dx Code: 255.2 - Adrenogenital disorders (approximate)
ICD-10-CM Siblings (same level / similar specificity) of E25.0:
E25.8 - Other adrenogenital disorders
E25.9 - Adrenogenital disorder, unspecified