E72.20
BillableDisorder of urea cycle metabolism, unspecified
Disorder of urea cycle metabolism, unspecified
Coding Notes
Inclusion Terms
Alternative clinical terms for this condition
- Hyperammonemia
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
- •hyperammonemia-hyperornithinemia-homocitrullinemia syndromeE72.4
- •transient hyperammonemia of newbornP74.6
Related Codes(4)
Also Known As / Clinical Terms(97)
SNOMED CT
- Hyperammonaemia9360008
- Hyperammonemia9360008
- Disorder of the urea cycle metabolism36444000
- Disorder of urea cycle36444000
- Alpha-aminoadipic semialdehyde deficiency58558003
- Hyperlysinaemia58558003
- Hyperlysinemia58558003
- Saccharopine dehydrogenase deficiency58558003
- Disorder of lysine and hydroxylysine metabolism237929000
- Lysine and hydroxylysine metabolism disorder237929000
- Hyperlysinuria with hyperammonaemia342553006
- Hyperlysinuria with hyperammonemia342553006
- Periodic hyperlysinaemia with hyperammonaemia342553006
- Periodic hyperlysinemia with hyperammonemia342553006
- Hyperammonemic encephalopathy425522009
- GLUD1 related hyperinsulinism and hyperammonaemia syndrome718106009
- GLUD1 related hyperinsulinism and hyperammonemia syndrome718106009
- Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonaemia syndrome718106009
- Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonemia syndrome718106009
- Hyperinsulinism and hyperammonaemia syndrome718106009
- Hyperinsulinism and hyperammonemia syndrome718106009
- Disorder of liver co-occurrent and due to disorder of urea cycle737203001
- Disorder of liver due to disorder of amino acid metabolism762278005
- CA-VA (carbonic anhydrase VA) deficiency764456001
- CA5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency764456001
- Carbonic anhydrase 5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency764456001
- Carbonic anhydrase VA deficiency764456001
- Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency764456001
- Diazoxide-sensitive diffuse hyperinsulinism1363361006
- Hyperinsulinemic hypoglycaemia, diazoxide-sensitive diffuse form1363361006
- Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form1363361006
UMLS
- Disorder of the urea cycle metabolismC0154246
- Disorder of the urea cycle metabolism (disorder)C0154246
- Disorder of urea cycleC0154246
- Disorder of urea cycle metabolism, unspecifiedC0154246
- Disorder, Urea CycleC0154246
- Disorders of urea cycle metabolismC0154246
- Disorders, Urea CycleC0154246
- Inborn Urea Cycle DisorderC0154246
- Urea Cycle DisorderC0154246
- Urea Cycle DisordersC0154246
- Urea Cycle Disorders, InbornC0154246
- Urea Cycle Metabolism DisorderC0154246
- Urea cycle disorderC0154246
- cycle disorders ureaC0154246
- disorder of the urea cycle metabolismC0154246
- inborn urea cycle disorderC0154246
- of urea cycle disorderC0154246
- urea cycle disorderC0154246
- HyperammonaemiaC0220994
- HyperammonemiaC0220994
- Hyperammonemia (disorder)C0220994
- hyperammonaemiaC0220994
- hyperammonemiaC0220994
Clinical Terms
- Hyperlysinuria with hyperammonaemia
- Carbonic anhydrase VA deficiency
- Diazoxide-sensitive diffuse hyperinsulinism
- Disorders of urea cycle metabolism
- Disorder of lysine and hydroxylysine metabolism
- Hyperammonemia
- Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonaemia syndrome
- Urea cycle disorder
- Periodic hyperlysinaemia with hyperammonaemia
- Disorder of liver co-occurrent and due to disorder of urea cycle
- Lysine and hydroxylysine metabolism disorder
- GLUD1 related hyperinsulinism and hyperammonaemia syndrome
- disorder of the urea cycle metabolism
- Hyperammonemic encephalopathy
- Saccharopine dehydrogenase deficiency
- hyperammonaemia
- Glutamate dehydrogenase 1 related hyperinsulinism and hyperammonemia syndrome
- Carbonic anhydrase 5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- Hyperlysinaemia
- Hyperinsulinemic hypoglycaemia, diazoxide-sensitive diffuse form
- Periodic hyperlysinemia with hyperammonemia
- Hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- Urea Cycle Disorders, Inborn
- Hyperinsulinism and hyperammonaemia syndrome
- CA-VA (carbonic anhydrase VA) deficiency
- Hyperlysinemia
- Disorder of the urea cycle metabolism (disorder)
- GLUD1 related hyperinsulinism and hyperammonemia syndrome
- CA5A related hyperammonemic encephalopathy due to carbonic anhydrase VA deficiency
- Disorder of liver due to disorder of amino acid metabolism
- Alpha-aminoadipic semialdehyde deficiency
- Hyperinsulinemic hypoglycemia, diazoxide-sensitive diffuse form
- Urea Cycle Disorders
- Urea Cycle Metabolism Disorder
- cycle disorders urea
- Disorder of urea cycle
- Hyperinsulinism and hyperammonemia syndrome
- Hyperlysinuria with hyperammonemia
- Disorder, Urea Cycle
- of urea cycle disorder
- Inborn Urea Cycle Disorder
- Disorders, Urea Cycle
- Hyperammonemia (disorder)
Frequently Asked Questions
What is the ICD-10 code for disorder of urea cycle metabolism, unspecified?
The ICD-10-CM code for disorder of urea cycle metabolism, unspecified is E72.20. The full clinical description is "Disorder of urea cycle metabolism, unspecified". E72.20 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.20 mean?
ICD-10-CM code E72.20 represents “Disorder of urea cycle metabolism, unspecified”. 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 E72.20 a billable code?
Yes, E72.20 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.20 in?
E72.20 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.20?
E72.20 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 12 more.
What SNOMED CT codes does E72.20 map to?
E72.20 maps to 11 SNOMED CT concepts: 58558003, 764456001, 1363361006, 737203001, 762278005, and 6 more. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.20?
E72.20 is linked to 2 UMLS Concept Unique Identifiers: C0154246, C0220994. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E72.20 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like disorder of urea cycle metabolism, unspecified 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 E72.20?
There is no direct ICD-11 mapping available for E72.20 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.