E34.32 - Genetic causes of short stature
- Applicable to Genetic causes of short stature
- The 2025 edition of ICD10-CM E34.32 became effective on October 1, 2024.
- This is the American ICD10-CM version of E34.32 - other international versions of ICD10 E34.32 may differ.
- E34.32 is a Non-Billable / Non-Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- E34.32 Code should not be used for billing or reimbursement purposes as there are multiple ICD-10 CM codes below it that contain a greater level of detail.
- E34.32 - Genetic causes of short stature
- E34.32 - Genetic causes of short stature
- 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
Non-Billable/Non-Specific Code
The following codes above E34.32 contain annotation back-references that may be applicable to E34.32:
- Chapter: E00-E89 - Endocrine, nutritional and metabolic diseases
- Section: E20-E35 - Disorders of other endocrine glands
- Category: E34 - Other endocrine disorders
Browse other similar CM codes:
Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.
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