E34.328 Other genetic causes of short stature
The ICD-10-CM code for Other genetic causes of short stature is E34.328 (FY2026). It is a billable, claim-ready diagnosis code.
Classification
- Section
- E20-E35: Disorders of other endocrine glands (E20-E35)
- Category E34
- 23 codes (18 billable)
- FY2026 Status
- Stable since FY2024
Also Known As
ICD-10-CM Alphabetic Index entries that lead to E34.328:
- Dwarfism
- Dwarfism › infantile
- Dwarfism › congenital
- Deficiency, deficient › short stature homeobox gene (SHOX) › with › short stature (idiopathic)
- Short, shortening, shortness › stature (child) (hereditary) (idiopathic) NEC › due to › genetic causes › NPR-2 gene variant
- Short, shortening, shortness › stature (child) (hereditary) (idiopathic) NEC › due to › genetic causes › specified genetic cause NEC
- Short, shortening, shortness › stature (child) (hereditary) (idiopathic) NEC › due to › genetic causes › aggrecan deficiency
- Short, shortening, shortness › stature (child) (hereditary) (idiopathic) NEC › due to › genetic causes › ACAN gene variant
Inclusion Terms
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
U.S. Hospital Utilization
- An estimated 1,185 U.S. inpatient stays in 2023 included E34.328 among the documented diagnoses.
Source: National Inpatient Sample (NIS), Healthcare Cost and Utilization Project (HCUP), Agency for Healthcare Research and Quality, 2016–2023. National survey-weighted estimates.
Official Coding Guidelines
Diabetes mellitus (TOC entry)a. Diabetes mellitus ................................................................................................................... 39
Obesity (TOC entry)b. Obesity .................................................................................................................................. 42
Source: CMS — ICD-10-CM Official Guidelines for Coding and Reporting, FY2026