E34.321

Billable

Primary insulin-like growth factor-1 (IGF-1) deficiency

Primary insulin-like growth factor-1 (IGF-1) deficiency

Status

Billable / Specific

Block

E20-E35

Parent Code

E34.32

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)

Related Codes(3)
E34.322

Insulin-like growth factor-1 (IGF-1) resistance

BillableE34.328

Other genetic causes of short stature

BillableE34.329

Unspecified genetic causes of short stature

Billable
Also Known As / Clinical Terms(104)

SNOMED CT

UMLS

Clinical Terms

  • Laron Dwarfism
  • GH-R deficiency
  • Growth Hormone Insensitivity Syndrome
  • Severe GH Insensitivity
  • Primary insulin-like growth factor deficiency
  • Primary Growth Hormone Resistance
  • Laron syndrome with immunodeficiency
  • Laron-type dwarfism
  • Growth hormone receptor absent
  • Acid-labile subunit gene (IGFALS) defect
  • Laron Syndrome
  • Laron-type short stature
  • Short stature due to primary acid labile subunit deficiency
  • Growth Hormone Receptor Deficiency
  • Dwarfism IIs, Pituitary
  • Growth delay due to insulin-like growth factor type 1 deficiency
  • GROWTH HORMONE RECEPT DEFIC
  • Growth hormone gene 1 (GH1) defect with growth hormone neutralizing antibodies
  • Growth Hormone Receptor Defect
  • Laron Type Dwarfism I
  • Syndrome, Laron
  • Pituitary Dwarfism II
  • Laron-type pituitary dwarfism
  • Insulin-like growth factor 1 gene (IGF1) defect
  • Primary GH Resistance
  • laron type dwarfism
  • Hereditary growth hormone deficiency
  • GH Resistance, Primary
  • IGF-1 (insulin-like growth factor 1) deficiency
  • Laron-like syndrome
  • Growth hormone receptor abnormality
  • Growth delay, deafness, intellectual disability syndrome
  • Dwarfism, Laron
  • Laron-type isolated somatotropin defect (disorder)
  • Laron type short stature
  • Pituitary Dwarfism IIs
  • Severe primary insulin-like growth factor-1 deficiency (SPIGFD)
  • Laron-type isolated somatotropin defect
  • Dwarfism II, Pituitary
  • Growth hormone insensitivity syndrome (GHIS)
  • Short stature due to STAT5b (signal transducer and activator of transcription 5b) deficiency
  • Signal transducer and activator of transcription 5B gene (STAT5b) defect
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.

How does E34.321 relate to ICF functioning codes?

ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like primary insulin-like growth factor-1 (igf-1) deficiency affect a person's functioning: body functions, activities, participation, and environmental factors. AutoICD provides ICF Core Sets for 12+ conditions and can map clinical text to ICF categories automatically. Browse the ICF directory to explore functioning codes.

What is the ICD-11 equivalent of E34.321?

There is no direct ICD-11 mapping available for E34.321 in the WHO crosswalk tables. This may mean the concept is classified differently in ICD-11. Use the ICD-10 to ICD-11 converter to search for related codes.

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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.