- D53.0 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 D53.0 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D53.0 – other international versions of ICD-10 D53.0 may differ.
ICD-10-CM D53.0 is grouped within Diagnostic Related Group(s):
Applicable To
- Amino-acid deficiency anemia
- Orotaciduric anemia
Type 1 Excludes
- Lesch-Nyhan syndrome (E79.1)
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 D53.0:
- anemia > orotic (congenital) (hereditary) (pyrimidine deficiency) E79.8
- anemia > Amino-acid disorder E72.9
- amino-acid-deficiency > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- amino-acid > deficiency D53.9
- protein > deficiency D53.9
- deficiency > due to (in) (with) D64.81
- amino-acid > deficiency D53.0
- protein > deficiency D53.0
- orotic aciduria > megaloblastic D53.1
- orotaciduric (congenital) (hereditary) > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- protein-deficiency > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- anemia > protein E46
- anemia > Orotaciduria, oroticaciduria (congenital) (hereditary) (pyrimidine deficiency) E79.8