E34.321
Primary insulin-like growth factor-1 (IGF-1) deficiency
Applicable To
-
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
Details
-
E34.321 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
-
ICD-10-CM E34.321 is a new 2023 ICD-10-CM code that became effective on October 1, 2022.
-
This is the American ICD-10-CM version of E34.321 – other international versions of ICD-10 E34.321 may differ.