E72.21
BillableArgininemia
Argininemia
Coding Notes
Excludes 1
Codes that cannot be used together with this code (mutual exclusion)
- •transitory endocrine and metabolic disorders specific to newbornP70-P74
- •androgen insensitivity syndromeE34.5
- •congenital adrenal hyperplasiaE25.0
- •hemolytic anemias attributable to enzyme disordersD55
- •Marfan syndromeQ87.4
- •5-alpha-reductase deficiencyE29.1
- disorders of:
- •aromatic amino-acid metabolismE70
- •branched-chain amino-acid metabolismE71.0-E71.2
- •fatty-acid metabolismE71.3
- •purine and pyrimidine metabolismE79
- •gout (M1A.-,M10
- •disorders of ornithine metabolismE72.4
Related Codes(4)
Also Known As / Clinical Terms(74)
SNOMED CT
- ARG1-gene related arginase deficiency23501004
- ARGI deficiency23501004
- Arginase 1-gene related arginase deficiency23501004
- Arginase deficiency23501004
- Argininaemia23501004
- Argininemia23501004
- Deficiency of arginase23501004
- Hyperargininaemia23501004
- Hyperargininemia23501004
- Deficiency of arginine deiminase124520009
- Deficiency of arginine dihydrolase124520009
UMLS
- ARG1 DEFICIENCYC0268548
- ARG1 DeficienciesC0268548
- ARG1 DeficiencyC0268548
- ARG1 deficiencyC0268548
- ARG1-gene related arginase deficiencyC0268548
- ARGI deficiencyC0268548
- ARGINASE DEFIC DISC0268548
- ARGINASE DEFICIENCYC0268548
- ARGININEMIAC0268548
- Arginase 1 deficiencyC0268548
- Arginase 1-gene related arginase deficiencyC0268548
- Arginase DeficienciesC0268548
- Arginase DeficiencyC0268548
- Arginase Deficiency DiseaseC0268548
- Arginase Deficiency DiseasesC0268548
- Arginase deficiencyC0268548
- Arginase deficiency (disorder)C0268548
- Arginase deficiency diseaseC0268548
- ArgininaemiaC0268548
- ArgininemiaC0268548
- DEFIC DIS ARGINASEC0268548
- Deficiencies, ARG1C0268548
- Deficiencies, ArginaseC0268548
- Deficiency Disease, ArginaseC0268548
- Deficiency Diseases, ArginaseC0268548
- Deficiency of arginaseC0268548
- Deficiency, ARG1C0268548
- Deficiency, ArginaseC0268548
- HYPERARGININEMIAC0268548
- HyperargininaemiaC0268548
- HyperargininemiaC0268548
- HyperargininemiasC0268548
- arginase deficiencyC0268548
- argininaemiaC0268548
- argininemiaC0268548
- hyperargininaemiaC0268548
- hyperargininemiaC0268548
Clinical Terms
- Arginase Deficiency Disease
- Deficiencies, ARG1
- ARGINASE DEFIC DIS
- Argininaemia
- Arginase 1 deficiency
- Deficiency, Arginase
- Arginase Deficiencies
- ARG1 DEFICIENCY
- Hyperargininemias
- Deficiency Diseases, Arginase
- Arginase 1-gene related arginase deficiency
- ARG1 Deficiencies
- Hyperargininemia
- ARGI deficiency
- Deficiencies, Arginase
- Arginase Deficiency
- Arginase Deficiency Diseases
- Deficiency of arginine dihydrolase
- ARG1-gene related arginase deficiency
- Arginase deficiency (disorder)
- Deficiency Disease, Arginase
- DEFIC DIS ARGINASE
- hyperargininaemia
- Deficiency, ARG1
- Deficiency of arginase
- Deficiency of arginine deiminase
Frequently Asked Questions
What is the ICD-10 code for argininemia?
The ICD-10-CM code for argininemia is E72.21. The full clinical description is "Argininemia". E72.21 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.21 mean?
ICD-10-CM code E72.21 represents “Argininemia”. 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 E72.21 a billable code?
Yes, E72.21 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.21 in?
E72.21 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.21?
E72.21 has Excludes1 notes indicating codes that cannot be used together with it, including: transitory endocrine and metabolic disorders specific to newborn (P70-P74); androgen insensitivity syndrome (E34.5-); congenital adrenal hyperplasia (E25.0); and 10 more.
What SNOMED CT codes does E72.21 map to?
E72.21 maps to 2 SNOMED CT concepts: 23501004, 124520009. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.21?
E72.21 is linked to 1 UMLS Concept Unique Identifier: C0268548. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E72.21 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like argininemia 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 E72.21?
There is no direct ICD-11 mapping available for E72.21 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.