ICD-10-CM Code for Primary insulin-like growth factor-1 (IGF-1) deficiency E34.321
ICD-10 code E34.321 for Primary insulin-like growth factor-1 (IGF-1) deficiency is a medical classification as listed by WHO under the range - Endocrine, nutritional and metabolic diseases .
Primary insulin-like growth factor-1 (IGF-1) deficiency
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
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
E34.3
Excludes1: achondroplastic short stature (Q77.4)
hypochondroplastic short stature (Q77.4)
nutritional short stature (E45)
pituitary short stature (E23.0)
progeria (E34.8)
renal short stature (N25.0)
Russell-Silver syndrome (Q87.19)
short-limbed stature with immunodeficiency (D82.2)
short stature (child) (R62.52)
short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
short stature NOS (R62.52)
E34
Excludes1: pseudohypoparathyroidism (E20.1)
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