Diagnosis Code: E34.321

Short Description: Primary insulin-like growth factor-1 (IGF-1) deficiency

Long Description: Primary insulin-like growth factor-1 (IGF-1) deficiency

The code E34.321 is VALID for claim submission

Code Classification:

• Endocrine, nutritional and metabolic diseases (E00–E89)
  • Disorders of other endocrine glands (E20-E35)
    • Other endocrine disorders (E34)
      • E34.321 Primary insulin-like growth factor-1 (IGF-1) deficiency

Code Version: 2022 ICD-10-CM

Synonyms

• Growth delay due to insulin-like growth factor type 1 deficiency
• Growth hormone receptor abnormality
• Growth hormone receptor absent
• Hereditary growth hormone deficiency
• Laron syndrome with immunodeficiency
• Laron-type isolated somatotropin defect
• Short stature due to primary acid labile subunit deficiency

Diagnostic Related Group(s)

The code E34.321 is grouped in the following Diagnostic Related Group(s) (MS-DRG v39.0)

• Endocrine Disorders With Mcc (643)
• Endocrine Disorders With Cc (644)
• Endocrine Disorders Without Cc/mcc (645)

References to Index of Diseases and Injuries

The code E34.321 has the following ICD-10-CM references to the Index of Diseases and Injuries

• 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

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This page was last updated on: 10/1/2023

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