E34.322
Insulin-like growth factor-1 (IGF-1) resistance
This code does not map to a risk-adjusting HCC in the loaded models.
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
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
achondroplastic short stature (Q77.4) hypochondroplastic short stature (Q77.4) nutritional short stature (E45) pituitary short stature (E23.0) progeria (E34.8) renal short stature (N25.0) Russell-Silver syndrome (Q87.19) short-limbed stature with immunodeficiency (D82.2) short stature (child) (R62.52) short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index short stature NOS (R62.52)
pseudohypoparathyroidism (E20.1)
transitory endocrine and metabolic disorders specific to newborn (P70-P74)
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.
Official Guidelines for E34.322
FY 2026 ›Find E34.322 in the alphabetic index
4 index paths lead to this code
- Short, shortening, shortness › stature NEC › due to › genetic causes › genetic syndrome with resistance to insulin-like growth factor-1
- Short, shortening, shortness › stature NEC › due to › genetic causes › insulin-like growth factor-1 receptor defect
- Short, shortening, shortness › stature NEC › due to › genetic causes › insulin-like growth factor-1 resistance
- Short, shortening, shortness › stature NEC › due to › genetic causes › post-insulin-like growth factor-1 receptor signaling defect