E34.328
Other genetic causes of short stature
Billable FY2026 2025-10-01 → 2026-09-30
Exclusions 15 never code together
E34.3code
Excludes1
- achondroplastic short stature (Q77.4)Q77.4
- hypochondroplastic short stature (Q77.4)Q77.4
- nutritional short stature (E45)E45
- pituitary short stature (E23.0)E23.0
- progeria (E34.8)E34.8
- renal short stature (N25.0)N25.0
- Russell-Silver syndrome (Q87.19)Q87.19
- short-limbed stature with immunodeficiency (D82.2)D82.2
- short stature (child) (R62.52)R62.52
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
- short stature NOS (R62.52)R62.52
E00-E89chapter
Excludes1
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)P70-P74
Excludes1 — never code together. The excluded condition and this one are mutually exclusive.
Instructional notes 4
E34.328code
Inclusion terms
- Short stature due to ACAN gene variant
- Short stature due to aggrecan deficiency
- Short stature due to NPR-2 gene variant
E00-E89chapter
Notes
- 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.E05.8E07.0E16-E31E34.-
Index entries leading here 3
Alongside this code 3 same parent — E34.32
Additional references
AHA Coding Clinic® Licence required
Official coding advice for this code. Published by the American Hospital Association. Not included in this installation.