E34.322

E34.322: Insulin-like growth factor-1 (IGF-1) resistance

Billable / specific codeICD-10-CM

E34.322 is a billable, specific ICD-10-CM code for insulin-like growth factor-1 (igf-1) resistance. It is valid for submission on a claim.

Check E34.322 with the rest of the claim: free scrubber

Inclusion terms

Alternative wordings a physician may use in the chart for this same code.

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

Excludes1 inherited from the categories above E34.322

A category’s note binds every code beneath it.

Written on E34.3: Short stature due to endocrine disorder

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)

Written on E34: Other endocrine disorders

pseudohypoparathyroidism (E20.1)

Risk adjustment

No CMS-HCC V28 category: this code does not change a RAF score.

Medicare coverage

E34.322 is named in 1 Medicare coverage policy: 1 listing it as supporting medical necessity. Which one applies depends on your Medicare contractor.

A57204Billing and Coding: MRI and CT Scans of the Head and Neck

Alphabetic index entries that lead here

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(IGF-1R)
Short, shortening, shortness›stature NEC›due to›genetic causes›insulin-like growth factor-1 resistance(IGF-1)
Short, shortening, shortness›stature NEC›due to›genetic causes›post-insulin-like growth factor-1 receptor signaling defect

Code history

Unchanged in every release from FY2024 to FY2027.