- D55.1 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 D55.1 became effective on October 1, 2022.
- This is the American ICD-10-CM version of D55.1 – other international versions of ICD-10 D55.1 may differ.
ICD-10-CM D55.1 is grouped within Diagnostic Related Group(s):
Applicable To
- Anemia (due to) enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway
- Anemia (due to) hemolytic nonspherocytic (hereditary), type I
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 D55.1:
- pentose phosphate pathway > disorder of D55.29
- 6 phosphogluconate dehydrogenase > deficiency D53.9
- 6-PGD > deficiency D53.9
- related to hexose monophosphate shunt pathway NEC (HMP) > enzyme D55.9
- erythrocytic glutathione > deficiency D53.9
- G SH > deficiency D53.9
- GGS-R > deficiency D53.9
- glutathione reductase > deficiency D53.9
- disorder of > due to (in) (with) D64.81
- glutathione metabolism > disorder of D55.1
- erythrocytic glutathione deficiency > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- glutathione-reductase deficiency > Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) D64.9
- type > congenital or hereditary NEC D55.8
- I > type D55.1
- type > nonspherocytic D55.8
- I > type D55.1
- pentose phosphate pathway with anemia > Disorder (of)