D55.1
Anemia due to other disorders of glutathione metabolism
HCC risk adjustment mapping
CMS-HCC ESRD V24
Coagulation Defects and Other Specified Hematological Disorders
Coding notes
Excludes 1 never coded together · Excludes 2 may co-exist
Anemia (due to) enzyme deficiencies, except G6PD, related to the hexose monophosphate [HMP] shunt pathway Anemia (due to) hemolytic nonspherocytic (hereditary), type I
drug-induced enzyme deficiency anemia (D59.2)
autoimmune disease (systemic) NOS (M35.9) certain conditions originating in the perinatal period (P00-P96) complications of pregnancy, childbirth and the puerperium (O00-O9A) congenital malformations, deformations and chromosomal abnormalities (Q00-Q99) endocrine, nutritional and metabolic diseases (E00-E88) human immunodeficiency virus [HIV] disease (B20) injury, poisoning and certain other consequences of external causes (S00-T88) neoplasms (C00-D49) symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified (R00-R94)
Official Guidelines for D55.1
FY 2026 ›Find D55.1 in the alphabetic index
14 index paths lead to this code
- Anemia › erythrocytic glutathione deficiency
- Anemia › glutathione-reductase deficiency
- Disorder › pentose phosphate pathway with anemia
- Anemia › deficiency › 6 phosphogluconate dehydrogenase
- Anemia › deficiency › 6-PGD
- Anemia › deficiency › erythrocytic glutathione
- Anemia › deficiency › G SH
- Anemia › deficiency › GGS-R
- Anemia › deficiency › glutathione reductase
- Anemia › with › disorder of › pentose phosphate pathway
- Anemia › deficiency › enzyme › related to hexose monophosphate shunt pathway NEC
- Anemia › due to › disorder of › glutathione metabolism
- Anemia › hemolytic › nonspherocytic › type › I
- Anemia › hemolytic › nonspherocytic › congenital or hereditary NEC › type › I