E34.321
Billable
ChapterE00–E89
Ranksubcategory
Official Description
Primary insulin-like growth factor-1 (IGF-1) deficiency
Metadata & Insights
- •Billable/specific code (valid for reimbursement).
- •Chapter 4: Endocrine, Nutritional and Metabolic Diseases (E00-E89).
Instructional Notes
Includes
- Acid-labile subunit gene (IGFALS) defect
- Growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodies
- Growth hormone insensitivity syndrome (GHIS)
- Insulin-like growth factor 1 gene (IGF1) defect
- Laron type short stature
- Severe primary insulin-like growth factor-1 deficiency (SPIGFD)
General instructions are available for the parent sections:
Clinical Hierarchy
BillableHas subcodes
Applicable Ancestor Context
The following parent sections contain instructions or notes that apply to E34.321:
Code History
- FY 2022: This code replaced E34.3 (Short stature due to endocrine disorder)
MS-DRG Classification
This code is grouped within the following Diagnosis Related Group(s) for clinical reimbursement:
Cross Reference
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