E34.321
BillablePrimary insulin-like growth factor-1 (IGF-1) deficiency
E34.321 is the ICD-10-CM code for Primary insulin-like growth factor-1 (IGF-1) deficiency. It is a billable, specific code valid for reimbursement.
E00-E89 Endocrine, nutritional and metabolic diseases
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)
- •Signal transducer and activator of transcription 5B gene (STAT5b) defect
Frequently asked questions
Source: CMS ICD-10-CM FY2026. For informational purposes only — not medical advice. See our medical disclaimer.
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