E72.29
BillableOther disorders of urea cycle metabolism
Other disorders of urea cycle metabolism
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(41)
SNOMED CT
- Hyperammonaemia9360008
- Hyperammonemia9360008
- Hyperaminoaciduria42930003
- Inborn error of amino acid metabolism42930003
- Amino acid acetyltransferase deficiency57119000
- Congenital AGA deficiency57119000
- Hyperammonaemia, type III57119000
- Hyperammonemia, type III57119000
- N-Acetylglutamate synthase deficiency57119000
- N-acetylglutamate synthetase deficiency57119000
- N-acetylglutamate transferase deficiency57119000
- NAGS - N-Acetylglutamate synthase deficiency57119000
- NAGS deficiency57119000
- NAGS-gene related hyperammonaemia type III57119000
- NAGS-gene related hyperammonemia type III57119000
- Deficiency of urease124510004
- CPS1 (carbamoyl-phosphate synthetase 1) deficiency765329008
- CPS1-gene related carbamoyl-phosphate synthetase 1 deficiency765329008
- Carbamoyl-phosphate synthetase 1 deficiency765329008
- Carbamoyl-phosphate synthetase I deficiency765329008
Clinical Terms
- Hyperaminoaciduria
- NAGS - N-Acetylglutamate synthase deficiency
- NAGS deficiency
- NAGS-gene related hyperammonemia type III
- Hyperammonemia
- CPS1-gene related carbamoyl-phosphate synthetase 1 deficiency
- Deficiency of urease
- Hyperammonemia, type III
- CPS1 (carbamoyl-phosphate synthetase 1) deficiency
- Congenital AGA deficiency
- Hyperammonaemia
- Hyperammonaemia, type III
- Carbamoyl-phosphate synthetase I deficiency
- Inborn error of amino acid metabolism
- N-Acetylglutamate synthase deficiency
- NAGS-gene related hyperammonaemia type III
- Amino acid acetyltransferase deficiency
- Carbamoyl-phosphate synthetase 1 deficiency
- N-acetylglutamate transferase deficiency
- N-acetylglutamate synthetase deficiency
Frequently Asked Questions
What is the ICD-10 code for other disorders of urea cycle metabolism?
The ICD-10-CM code for other disorders of urea cycle metabolism is E72.29. The full clinical description is "Other disorders of urea cycle metabolism". E72.29 is a billable/specific code that can be used on insurance claims and medical billing.
What does ICD-10 code E72.29 mean?
ICD-10-CM code E72.29 represents “Other disorders of urea cycle metabolism”. 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 E72.29 a billable code?
Yes, E72.29 is a billable/specific ICD-10-CM code and can be used to indicate a diagnosis on a medical claim.
What chapter is E72.29 in?
E72.29 is in Chapter 4: Endocrine, Nutritional and Metabolic Diseases (codes E00-E89).
What codes cannot be used with E72.29?
E72.29 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 E72.29 map to?
E72.29 maps to 5 SNOMED CT concepts: 57119000, 765329008, 124510004, 42930003, 9360008. SNOMED CT is a clinical terminology used in electronic health records.
What are the UMLS CUIs for E72.29?
E72.29 is linked to 1 UMLS Concept Unique Identifier: C2874261. The UMLS (Unified Medical Language System) integrates multiple biomedical vocabularies maintained by the U.S. National Library of Medicine.
How does E72.29 relate to ICF functioning codes?
ICF (International Classification of Functioning, Disability and Health) codes describe how conditions like other disorders of urea cycle metabolism 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 E72.29?
There is no direct ICD-11 mapping available for E72.29 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.