D55.29
Anemia due to other disorders of glycolytic enzymes
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
Hexokinase deficiency anemia Triose-phosphate isomerase deficiency anemia
disorders of glycolysis not associated with anemia (E74.81-)
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 D55.29
FY 2026 ›Find D55.29 in the alphabetic index
13 index paths lead to this code
- Anemia › hexokinase deficiency
- Disorder › anaerobic glycolysis with anemia
- Anemia › deficiency › 2, 3 diphosphoglycurate mutase
- Anemia › deficiency › 2, 3 PG
- Anemia › deficiency › glyceraldehyde phosphate dehydrogenase
- Anemia › deficiency › hexokinase
- Anemia › deficiency › phosphofructo-aldolase
- Anemia › deficiency › phosphoglycerate kinase
- Anemia › deficiency › triose-phosphate isomerase
- Anemia › with › disorder of › anaerobic glycolysis
- Anemia › deficiency › enzyme › glycolytic
- Anemia › hemolytic › nonspherocytic › type › II
- Anemia › hemolytic › nonspherocytic › congenital or hereditary NEC › type › II