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E34.328

E34.328: Other genetic causes of short stature

Billable / specific codeICD-10-CM

E34.328 is a billable, specific ICD-10-CM code for other genetic causes of short stature. It is valid for submission on a claim.

Check E34.328 with the rest of the claim: free scrubber

Inclusion terms

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

  • Short stature due to ACAN gene variant
  • Short stature due to aggrecan deficiency
  • Short stature due to NPR-2 gene variant

Excludes1 inherited from the categories above E34.328

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

E34.328 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

  • Dwarfism
  • Dwarfism›congenital
  • Dwarfism›infantile
  • Deficiency, deficient›short stature homeobox gene›with›short stature(idiopathic)
  • Short, shortening, shortness›stature NEC›due to›genetic causes›ACAN gene variant
  • Short, shortening, shortness›stature NEC›due to›genetic causes›aggrecan deficiency
  • Short, shortening, shortness›stature NEC›due to›genetic causes›NPR-2 gene variant
  • Short, shortening, shortness›stature NEC›due to›genetic causes›specified genetic cause NEC

Code history

Unchanged in every release from FY2024 to FY2027.

Other codes under E34.32

ICD-10-CMFY2027· effective October 1, 2026

Loaded directly from the CMS/NCHS ICD-10-CM public-domain release: see data sources and our editorial policy. If this page disagrees with the CMS tabular list, this page is wrong. Reference information for professional coders; not medical or billing advice.