2026 ICD-10-CM Diagnosis Code E34.322Insulin-like growth factor-1 (IGF-1) resistance

ICD-10-CM CodesE00–E89E20-E35E34

ICD-10-CM E34.322
CMSSource: CMS FY 2026 ICD-10-CM dataset · Effective Oct 1, 2025 – Sep 30, 2026

E34.322 is a billable ICD-10-CM diagnosis code for insulin-like growth factor-1 (IGF-1) resistance. It is valid on HIPAA claims for fiscal year 2026 (October 1, 2025 through September 30, 2026) and groups to MS-DRG 643 through 645. Coders also document this condition as growth delay due to insulin-like growth factor I resistance. In AHRQ's Clinical Classifications Software (CCSR), this diagnosis falls under Other specified and unspecified endocrine disorders.

Code Identity

ICD-10-CM Code
E34.322
Billable Status
Yes — Valid for Submission
Code Describes
Insulin-like growth factor-1 (IGF-1) resistance
Short Description
Insulin-like growth factor-1 (IGF-1) resistance
Same as the full description in the CMS dataset.
Parent Code
Genetic causes of short stature

Code Classification

ChapterE00–E89Endocrine, nutritional and metabolic diseases
SectionE20-E35Disorders of other endocrine glands
CategoryE34Other endocrine disorders
This CodeE34.322Insulin-like growth factor-1 (IGF-1) resistance

Approximate SynonymsGuidance

Alternate terms and clinical phrases that map to this code.

  • Growth delay due to insulin-like growth factor I resistance
  • Short stature co-occurrent and due to endocrine disorder
  • Short stature due to partial growth hormone receptor deficiency

Tabular List NotesGuidance

Coding notes and annotation back-references applicable to this code.

Inclusion Terms

  • Genetic syndrome with resistance to insulin-like growth factor-1
  • Insulin-like growth factor-1 receptor (IGF-1R) defect
  • Post-insulin-like growth factor-1 receptor signaling defect

Index to Diseases and InjuriesGuidance

External Cause of Injuries IndexGuidance

References for this code in the External Cause of Injuries Index.

    • Short, shortening, shortness
      • stature (child) (hereditary) (idiopathic) NEC
        • due to
          • genetic causes
            • genetic syndrome with resistance to insulin-like growth factor-1
    • Short, shortening, shortness
      • stature (child) (hereditary) (idiopathic) NEC
        • due to
          • genetic causes
            • insulin-like growth factor-1 receptor (IGF-1R) defect
    • Short, shortening, shortness
      • stature (child) (hereditary) (idiopathic) NEC
        • due to
          • genetic causes
            • insulin-like growth factor-1 (IGF-1) resistance
    • Short, shortening, shortness
      • stature (child) (hereditary) (idiopathic) NEC
        • due to
          • genetic causes
            • post-insulin-like growth factor-1 receptor signaling defect

Clinical ClassificationClinical

AHRQ’s CCSR groups this code into broader clinical categories.

CCSR END015
Other specified and unspecified endocrine disorders
Default principal diagnosis: inpatient Yes · outpatient Yes

Patient EducationClinical

Growth Disorders

Does your child seem much shorter - or much taller - than other kids his or her age? It could be normal. Some children may be small for their age but still be developing normally. Some children are short or tall because their parents are.

Read the full article at MedlinePlus

Courtesy of MedlinePlus, a service of the U.S. National Library of Medicine.

Code History & ChangesHistory

Replacement E34.322 replaces the following previously assigned code(s):

  • E34.3 - Short stature due to endocrine disorder
FY 2023AddedAdded to the ICD-10-CM code setEffective October 1, 2022.
FY 2024–2025No changes
FY 2026CurrentCurrent code set, no changesEffective October 1, 2025 through September 30, 2026.

Questions About E34.322Overview

Is E34.322 (Genetic causes of short stature) a billable code?

Yes. This is a billable ICD-10-CM code, specific enough to report insulin-like growth factor-1 (IGF-1) resistance on HIPAA-covered claims from October 1, 2025 through September 30, 2026.

What MS-DRG does E34.322 group to?

When insulin-like growth factor-1 (IGF-1) resistance is the principal diagnosis on an inpatient stay, it groups to MS-DRG 643, 644, 645, with relative weights from 0.7683 to 1.6461 depending on complications. Higher weights mean higher Medicare reimbursement.

Footnotes

[1] Chronic - a chronic condition code indicates a condition lasting 12 months or longer and its effect on the patient based on one or both of the following criteria:

  • The condition results in the need for ongoing intervention with medical products,treatment, services, and special equipment
  • The condition places limitations on self-care, independent living, and social interactions.