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 newborn (P70-P74)
- galactorrhea (N64.3)
- gynecomastia (N62)
- pseudohypoparathyroidism (E20.1)
- 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)
Child Codes (4)
Also Known As / Clinical Terms
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.
Automate ICD-10 Coding With AI
Send clinical text to the AutoICD API and get back structured ICD-10 codes with confidence scores. Integrates into any EHR or billing system in minutes.
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.