2026 ICD-10-CM Diagnosis Code E34.322Insulin-like growth factor-1 (IGF-1) resistance
ICD-10-CM Codes›E00–E89›E20-E35›E34
- Billable — Valid for Submission
- Chronic Condition
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
Code Classification
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
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.
Index to Diseases and InjuriesGuidance
Alphabetical index entries that point to this code.
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.
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
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.
