Other disorders of urea cycle metabolism (2025)

  1. ICD-10-CM Codes
  2. E00-E89
  3. E70-E88
  4. E72-
  5. 2025 ICD-10-CM Diagnosis Code E72.29

Other disorders of urea cycle metabolism (1)

Other disorders of urea cycle metabolism

    2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 Billable/Specific Code
  • E72.29 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
  • The 2025 edition of ICD-10-CM E72.29 became effective on October 1, 2024.
  • This is the American ICD-10-CM version of E72.29 - other international versions of ICD-10 E72.29 may differ.

The following code(s) above E72.29 contain annotation back-references

Annotation Back-References

In this context, annotation back-references refer to codes that contain:

  • Applicable To annotations, or
  • Code Also annotations, or
  • Code First annotations, or
  • Excludes1 annotations, or
  • Excludes2 annotations, or
  • Includes annotations, or
  • Note annotations, or
  • Use Additional annotations

that may be applicable to E72.29:

  • E00-E89

    2025 ICD-10-CM Range E00-E89

    Endocrine, nutritional and metabolic diseases

    Note

    • All neoplasms, whether functionally active or not, are classified in Chapter 2. Appropriate codes in this chapter (i.e. E05.8, E07.0, E16-E31, E34.-) may be used as additional codes to indicate either functional activity by neoplasms and ectopic endocrine tissue or hyperfunction and hypofunction of endocrine glands associated with neoplasms and other conditions classified elsewhere.

    Type 1 Excludes

    • transitory endocrine and metabolic disorders specific to newborn (P70-P74)

    Endocrine, nutritional and metabolic diseases
  • E70-E88

    2025 ICD-10-CM Range E70-E88

    Metabolic disorders

    Type 1 Excludes

    • androgen insensitivity syndrome (E34.5-)
    • congenital adrenal hyperplasia (E25.0)
    • hemolytic anemias attributable to enzyme disorders (D55.-)
    • Marfan syndrome (Q87.4-)
    • 5-alpha-reductase deficiency (E29.1)

    Type 2 Excludes

    • Ehlers-Danlos syndromes (Q79.6-)

    Metabolic disorders
  • E72

    ICD-10-CM Diagnosis Code E72

    Other disorders of amino-acid metabolism

      2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 Non-Billable/Non-Specific Code

    Type 1 Excludes

    • disorders of:
    • aromatic amino-acid metabolism (E70.-)
    • branched-chain amino-acid metabolism (E71.0-E71.2)
    • fatty-acid metabolism (E71.3)
    • purine and pyrimidine metabolism (E79.-)
    • gout (M1A.-, M10.-)
    Other disorders of amino-acid metabolism
  • E72.2

    ICD-10-CM Diagnosis Code E72.2

    Disorders of urea cycle metabolism

      2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 Non-Billable/Non-Specific Code

    Type 1 Excludes

    • disorders of ornithine metabolism (E72.4)
    Disorders of urea cycle metabolism

Approximate Synonyms

  • Congenital hyperammonemia, type i
  • Deficiency, carbamyl phosphate synthetase
  • Deficiency, n acetylglutamate synthetase
  • Hyperammonemia, type iii

ICD-10-CM E72.29 is grouped within Diagnostic Related Group(s) (MS-DRG v42.0):

  • 642 Inborn and other disorders of metabolism

Convert E72.29 to ICD-9-CM

Code History

  • 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
  • 2017 (effective 10/1/2016): No change
  • 2018 (effective 10/1/2017): No change
  • 2019 (effective 10/1/2018): No change
  • 2020 (effective 10/1/2019): No change
  • 2021 (effective 10/1/2020): No change
  • 2022 (effective 10/1/2021): No change
  • 2023 (effective 10/1/2022): No change
  • 2024 (effective 10/1/2023): No change
  • 2025 (effective 10/1/2024): No change

Diagnosis Index entries containing back-references to E72.29:

  • Disorder (of) - see also Disease
    • urea cycle metabolism E72.20

      ICD-10-CM Diagnosis Code E72.20

      Disorder of urea cycle metabolism, unspecified

        2016 2017 2018 2019 2020 2021 2022 2023 2024 2025 Billable/Specific Code

      Applicable To

      • Hyperammonemia

      Type 1 Excludes

      • hyperammonemia-hyperornithinemia-homocitrullinemia syndrome E72.4
      • transient hyperammonemia of newborn (P74.6)
      • other specified E72.29

ICD-10-CM Codes Adjacent To E72.29

E72.1 Disorders of sulfur-bearing amino-acid metabolism

E72.10 …… unspecified

E72.11 Homocystinuria

E72.12 Methylenetetrahydrofolate reductase deficiency

E72.19 Other disorders of sulfur-bearing amino-acid metabolism

E72.2 Disorders of urea cycle metabolism

E72.20 Disorder of urea cycle metabolism, unspecified

E72.21 Argininemia

E72.22 Arginosuccinic aciduria

E72.23 Citrullinemia

E72.29 Other disorders of urea cycle metabolism

E72.3 Disorders of lysine and hydroxylysine metabolism

E72.4 Disorders of ornithine metabolism

E72.5 Disorders of glycine metabolism

E72.50 Disorder of glycine metabolism, unspecified

E72.51 Non-ketotic hyperglycinemia

E72.52 Trimethylaminuria

E72.53 Primary hyperoxaluria

E72.59 Other disorders of glycine metabolism

E72.8 Other specified disorders of amino-acid metabolism

E72.81 Disorders of gamma aminobutyric acid metabolism

Reimbursement claims with a date of service on or after October 1, 2015 require the use of ICD-10-CM codes.

Other disorders of urea cycle metabolism (2025)

References

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