E22.0
Acromegaly and pituitary gigantism
Risk-adjusting (HCC)Billable code
HCC risk adjustment mapping
CMS-HCC V28
HCC51
Addison's and Cushing's Diseases, Acromegaly, and Other Specified Endocrine Disorders
CMS-HCC ESRD V24
HCC23
Other Significant Endocrine and Metabolic Disorders
RxHCC V08
RXHCC42
Acromegaly and Other Endocrine and Metabolic Disorders
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
This code · E22.0
Inherited from E22Hyperfunction of pituitary gland
Inherited from E20-E35Disorders of other endocrine glands
Inherited from chapter 4Endocrine, nutritional and metabolic diseases
Excludes 1
transitory endocrine and metabolic disorders specific to newborn (P70-P74)
Official Guidelines for E22.0
FY 2026 ›Find E22.0 in the alphabetic index
20 index paths lead to this code
- Acromegaly, acromegalia
- Erdheim's syndrome
- Gigantism
- Launois' syndrome
- Macrospondylitis , acromegalic
- Scaglietti-Dagnini syndrome
- Hypophyseal, hypophysis › gigantism
- Marie's › disease or syndrome
- Overproduction › growth hormone
- Syndrome › costovertebral
- Syndrome › Erdheim's
- Syndrome › Launois'
- Syndrome › Marie's
- Syndrome › pituitary
- Syndrome › Scaglietti-Dagnini
- Arthritis, arthritic › due to or associated with › acromegaly
- Arthritis, arthritic › in › acromegaly
- Arthropathy › in › acromegaly
- Hypersecretion › hormone › growth
- Syndrome › cerebral › gigantism