ICD Search Engine — ICDMine.com
ICDMine.com › Browse ICD-10-CM Codes › Ch. 4: Endocrine, nutritional and metabolic diseases (E00-E89) › Disorders of other endocrine glands (E20-E35) › E34.32 Genetic causes of short stature › E34.321

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

ICD-10-CM billable/specific code — part of Disorders of other endocrine glands (E20-E35)

Code Details

BillableYes
ChapterChapter 4: Endocrine, nutritional and metabolic diseases (E00-E89)
SectionDisorders of other endocrine glands (E20-E35)
Parent codeE34.32 — Genetic causes of short stature

Coding Notes

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
Want the full interactive search, Excludes1/Excludes2 checking, and Alphabetic Index?
Open the free ICD-10-CM Search Tool →