E34.32
Non-billableGenetic causes of short stature
Genetic causes of short stature
This is a header/category code. For billing purposes, use a more specific child code from the list below.
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •galactorrheaN64.3
- •gynecomastiaN62
- •pseudohypoparathyroidismE20.1
- •achondroplastic short statureQ77.4
- •hypochondroplastic short statureQ77.4
- •nutritional short statureE45
- •pituitary short statureE23.0
- •progeriaE34.8
- •renal short statureN25.0
- •Russell-Silver syndromeQ87.19
- •short-limbed stature with immunodeficiencyD82.2
- •short stature (child)R62.52
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
- •short stature NOSR62.52
Child Codes (4)
Related Codes(3)
Also Known As / Clinical Terms(1)
Frequently Asked Questions
What is the ICD-10 code for genetic causes of short stature?
The ICD-10-CM code for genetic causes of short stature is E34.32. The full clinical description is "Genetic causes of short stature". E34.32 is a non-billable header code. Use a more specific child code for billing purposes.
What does ICD-10 code E34.32 mean?
ICD-10-CM code E34.32 represents “Genetic causes of short stature”. It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a non-billable header code. Use a more specific child code for billing purposes.
Is E34.32 a billable code?
No, E34.32 is a non-billable header code. You need to use one of its more specific child codes for billing. There are 4 child codes under E34.32.
What chapter is E34.32 in?
E34.32 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E34.32?
E34.32 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 12 more.
What are the subcategories under E34.32?
E34.32 has 4 child codes, including: E34.321 (Primary insulin-like growth factor-1 (IGF-1) deficiency), E34.322 (Insulin-like growth factor-1 (IGF-1) resistance), E34.328 (Other genetic causes of short stature), E34.329 (Unspecified genetic causes of short stature).
What are the UMLS CUIs for E34.32?
E34.32 is linked to 1 UMLS Concept Unique Identifier: C5674891. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E34.32 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like genetic causes of short stature affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.
What is the ICD-11 equivalent of E34.32?
There is no direct ICD-11 mapping available for E34.32 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.