E34.322
BillableInsulin-like growth factor-1 (IGF-1) resistance
Insulin-like growth factor-1 (IGF-1) resistance
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Genetic syndrome with resistance to insulin-like growth factor-1
- Insulin-like growth factor-1 receptor (IGF-1R) defect
- Post-insulin-like growth factor-1 receptor signaling defect
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •galactorrheaN64.3
- •gynecomastiaN62
- •pseudohypoparathyroidismE20.1
- •achondroplastic short statureQ77.4
- •hypochondroplastic short statureQ77.4
- •nutritional short statureE45
- •pituitary short statureE23.0
- •progeriaE34.8
- •renal short statureN25.0
- •Russell-Silver syndromeQ87.19
- •short-limbed stature with immunodeficiencyD82.2
- •short stature (child)R62.52
- short stature in specific dysmorphic syndromes - code to syndrome - see Alphabetical Index
- •short stature NOSR62.52
Related Codes(3)
Also Known As / Clinical Terms(44)
SNOMED CT
- Growth delay due to insulin-like growth factor 1 resistance715625007
- Growth delay due to insulin-like growth factor I resistance715625007
- IGF-1 (insulin-like growth factor 1) resistance715625007
- Somatomedin C resistance715625007
- Short stature due to partial GHR (growth hormone receptor) deficiency783098009
- Short stature due to partial growth hormone receptor deficiency783098009
- Short stature co-occurrent and due to endocrine disorder368331000119100
UMLS
- Genetic syndrome with resistance to insulin-like growth factor-1C5676331
- Growth delay due to insulin-like growth factor 1 resistanceC1849157
- Growth delay due to insulin-like growth factor I resistanceC1849157
- Growth delay due to insulin-like growth factor I resistance (disorder)C1849157
- IGF-1 (insulin-like growth factor 1) resistanceC1849157
- IGF-I RESISTANCEC1849157
- IGF-I ResistanceC1849157
- IGF1RESC1849157
- INSULIN-LIKE GROWTH FACTOR I, RESISTANCE TOC1849157
- Insulin Growth Factor I ResistanceC1849157
- Insulin-Like Growth Factor I, Resistance ToC1849157
- Insulin-like growth factor-1 (IGF-1) resistanceC1849157
- SOMATOMEDIN, END-ORGAN INSENSITIVITY TOC1849157
- SOMATOMEDIN-C, RESISTANCE TOC1849157
- Somatomedin C resistanceC1849157
- Somatomedin C, Resistance ToC1849157
- Somatomedin, End-Organ Insensitivity ToC1849157
- Insulin-like growth factor-1 receptor (IGF-1R) defectC5676332
- Post-insulin-like growth factor-1 receptor signaling defectC5676333
Clinical Terms
- IGF-I RESISTANCE
- Insulin-Like Growth Factor I, Resistance To
- Short stature due to partial GHR (growth hormone receptor) deficiency
- Growth delay due to insulin-like growth factor I resistance
- Genetic syndrome with resistance to insulin-like growth factor-1
- Growth delay due to insulin-like growth factor I resistance (disorder)
- Somatomedin, End-Organ Insensitivity To
- Post-insulin-like growth factor-1 receptor signaling defect
- SOMATOMEDIN-C, RESISTANCE TO
- Insulin Growth Factor I Resistance
- Short stature due to partial growth hormone receptor deficiency
- Short stature co-occurrent and due to endocrine disorder
- Growth delay due to insulin-like growth factor 1 resistance
- IGF-1 (insulin-like growth factor 1) resistance
- IGF1RES
- Somatomedin C resistance
- Somatomedin C, Resistance To
- Insulin-like growth factor-1 receptor (IGF-1R) defect
Frequently Asked Questions
What is the ICD-10 code for insulin-like growth factor-1 (igf-1) resistance?
The ICD-10-CM code for insulin-like growth factor-1 (igf-1) resistance is E34.322. The full clinical description is "Insulin-like growth factor-1 (IGF-1) resistance". E34.322 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E34.322 mean?
ICD-10-CM code E34.322 represents “Insulin-like growth factor-1 (IGF-1) resistance”. 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 E34.322 a billable code?
Yes, E34.322 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E34.322 in?
E34.322 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E34.322?
E34.322 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 E34.322 map to?
E34.322 maps to 3 SNOMED CT concepts: 715625007, 368331000119100, 783098009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E34.322?
E34.322 is linked to 4 UMLS Concept Unique Identifiers: C5676331, C1849157, C5676332, C5676333. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E34.322 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like insulin-like growth factor-1 (igf-1) resistance 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 E34.322?
There is no direct ICD-11 mapping available for E34.322 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.