E34.321
BillablePrimary insulin-like growth factor-1 (IGF-1) deficiency
Primary insulin-like growth factor-1 (IGF-1) deficiency
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- 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
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- transitory endocrine and metabolic disorders specific to newborn (P70-P74)
- galactorrhea (N64.3)
- gynecomastia (N62)
- pseudohypoparathyroidism (E20.1)
- 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)
Also Known As / Clinical Terms
SNOMED CT
- Laron dwarfism38196001
- Laron syndrome38196001
- Laron-type dwarfism38196001
- Laron-type isolated somatotropin defect38196001
- Laron-type pituitary dwarfism38196001
- Growth hormone receptor absent237838002
- Growth hormone receptor abnormality237839005
- Short stature due to primary acid labile subunit deficiency721074002
- Laron syndrome with immunodeficiency724179008
- Laron-like syndrome724179008
- Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency724179008
- Growth delay due to insulin-like growth factor type 1 deficiency724385009
- Growth delay, deafness, intellectual disability syndrome724385009
- IGF-1 (insulin-like growth factor 1) deficiency724385009
- Primary insulin-like growth factor deficiency724385009
- Hereditary growth hormone deficiency1186807002
UMLS
- Acid-labile subunit gene (IGFALS) defectC5676326
- Dwarfism II, PituitaryC0271568
- Dwarfism IIs, PituitaryC0271568
- Dwarfism, LaronC0271568
- GH Resistance, PrimaryC0271568
- GH-R deficiencyC0271568
- GROWTH HORMONE INSENSITIVITY SYNDROMEC0271568
- GROWTH HORMONE RECEPT DEFICC0271568
- GROWTH HORMONE RECEPTOR DEFICIENCYC0271568
- Growth Hormone Insensitivity SyndromeC0271568
- Growth Hormone Receptor DefectC0271568
- Growth Hormone Receptor DeficiencyC0271568
- Growth hormone receptor defectC0271568
- Growth hormone receptor deficiencyC0271568
- LARON SYNDROMEC0271568
- Laron DwarfismC0271568
- Laron SyndromeC0271568
- Laron Type Dwarfism IC0271568
- Laron dwarfismC0271568
- Laron syndromeC0271568
- Laron type short statureC0271568
- Laron-type dwarfismC0271568
- Laron-type isolated somatotropin defectC0271568
- Laron-type isolated somatotropin defect (disorder)C0271568
- Laron-type pituitary dwarfismC0271568
- Laron-type short statureC0271568
- PITUITARY DWARFISM IIC0271568
- Pituitary Dwarfism IIC0271568
- Pituitary Dwarfism IIsC0271568
- Pituitary dwarfism IIC0271568
- Primary GH ResistanceC0271568
- Primary GH resistanceC0271568
- Primary Growth Hormone ResistanceC0271568
- Primary growth hormone resistanceC0271568
- Severe GH InsensitivityC0271568
- Severe GH insensitivityC0271568
- Syndrome, LaronC0271568
- laron dwarfismC0271568
- laron type dwarfismC0271568
- laron-type dwarfismC0271568
- Growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodiesC5676327
- Growth hormone insensitivity syndrome (GHIS)C5676328
- Insulin-like growth factor 1 gene (IGF1) defectC5674892
- Primary insulin-like growth factor-1 (IGF-1) deficiencyC5674892
- Severe primary insulin-like growth factor-1 deficiency (SPIGFD)C5676329
- Signal transducer and activator of transcription 5B gene (STAT5b) defectC5676330
Frequently Asked Questions
What is the ICD-10 code for primary insulin-like growth factor-1 (igf-1) deficiency?
The ICD-10-CM code for primary insulin-like growth factor-1 (igf-1) deficiency is E34.321. The full clinical description is "Primary insulin-like growth factor-1 (IGF-1) deficiency". E34.321 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E34.321 mean?
ICD-10-CM code E34.321 represents "Primary insulin-like growth factor-1 (IGF-1) deficiency". It is classified under Chapter 4: Endocrine, Nutritional and Metabolic Diseases and is a billable/specific code that can be used on a claim.
Is E34.321 a billable code?
Yes, E34.321 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E34.321 in?
E34.321 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E34.321?
E34.321 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); galactorrhea (N64.3); gynecomastia (N62); and 12 more.
What SNOMED CT codes does E34.321 map to?
E34.321 maps to 7 SNOMED CT concepts: 724385009, 237839005, 237838002, 1186807002, 38196001, and 2 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E34.321?
E34.321 is linked to 7 UMLS Concept Unique Identifiers: C5676326, C0271568, C5676327, C5676328, C5674892, and 2 more. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
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Includes SNOMED Clinical Terms® (SNOMED CT®) used by permission of SNOMED International. Includes content from the UMLS Metathesaurus, courtesy of the U.S. National Library of Medicine.