- E72.19 is a billable/specific ICD-10-CM code that can be used to indicate a diagnosis for reimbursement purposes.
- The 2024 edition of ICD-10-CM E72.19 became effective on October 1, 2022.
- This is the American ICD-10-CM version of E72.19 – other international versions of ICD-10 E72.19 may differ.
ICD-10-CM E72.19 is grouped within Diagnostic Related Group(s):
- 642 Inborn and other disorders of metabolism
Applicable To
- Cystathioninuria
- Methioninemia
- Sulfite oxidase deficiency
Code History
- 2016 (effective 10/1/2015): New code (first year of non-draft ICD-10-CM)
- 2016 (effective 10/1/2015): No change
- 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
- 2024 (effective 10/1/2022): No change
Diagnosis Index entries containing back-references to E72.19:
- sulfite oxidase > Deficiency, deficient
- oast-house-urine > Disease, diseased
- amino-acid > Disorder (of)
- cystathioninuria > amino-acid E72.19
- other specified > sulfur-bearing E72.10
- cystathionine > metabolism E88.9
- homocystine > metabolism E88.9
- methionine > metabolism E88.9
- methionine > Malabsorption K90.9