ICD-10-CM Diagnosis Code (2025)
Official Description for E34.321
Primary insulin-like growth factor-1 (IGF-1) deficiency
Coding Notes & Guidelines for E34.321
Inclusion Terms
- 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
Parent Code (Less Specific):
About ICD-10-CM Code E34.321 (Primary insulin-like growth factor-1)
ICD-10-CM code E34.321 is a billable or specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes. The 2025 edition of ICD-10-CM E34.321 became effective on October 1, 2024.
This page provides detailed information about E34.321 - Primary insulin-like growth factor-1 (IGF-1) deficiency. It includes common terminology, coding guidelines such as "Includes," "Excludes1," and "Excludes2" notes, and information on required 7th characters. Utilizing this information correctly is essential for accurate medical coding and claims submission for conditions like Primary insulin-like growth factor-1.