E34.321✓ Billable
Primary insulin-like growth factor-1 (IGF-1) deficiency
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
Also Indexed As(ICD-10-CM Alphabetic Index)
These clinical terms, synonyms, and manifestations all map to E34.321 in the official ICD-10-CM Alphabetic Index.
Dwarfism, Laron-typeShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, Laron-typeShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, acid-labile subunit gene (IGFALS) defectShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodiesShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, growth hormone insensitivity syndrome (GHIS)Short, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, insulin-like growth factor 1 gene (IGF1) defectShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, primary insulin-like growth factor-1 (IGF-1) deficiencyShort, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, severe primary insulin-like growth factor-1 deficiency (SPIGFD)Short, shortening, shortness, stature (child) (hereditary) (idiopathic) NEC, due to, genetic causes, signal transducer and activator of transcription 5B gene (STAT5b) defect
Code Hierarchy
┌4Endocrine, nutritional and metabolic diseases (E00-E89)├E20-E35Disorders of other endocrine glands (E20-E35)├E34Other endocrine disorders
└E34.321Primary insulin-like growth factor-1 (IGF-1) deficiency
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