E34.321 - Primary insulin-like growth factor-1 (IGF-1) deficiency

  • Applicable to Primary insulin-like growth factor-1 (IGF-1) deficiency
  • The 2025 edition of ICD10-CM E34.321 became effective on October 1, 2024.
  • This is the American ICD10-CM version of E34.321 - other international versions of ICD10 E34.321 may differ.
  • E34.321 is a Billable / Specific ICD10-CM code that can be used to indicate a diagnosis for reimbursement purposes.

 Inclusion Term

  • 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

The following codes above E34.321 contain annotation back-references that may be applicable to E34.321:

Chapter: E00-E89 Endocrine, nutritional and metabolic diseases

Section: E20-E35 Disorders of other endocrine glands

Category: E34 Other endocrine disorders

deficiency icd 10
 
primary icd 10
 
growth icd 10
 
Billable/Specific Code

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