| ICD-10-CM-2023 > D50-D89 > D55-D59 > D58 |
D55-D59 | Hemolytic anemias | |
D58 | Other hereditary hemolytic anemias | |
Excl1.: | hemolytic anemia of the newborn (P55.-) | |
D58.0 | Hereditary spherocytosis | |
Info: | Acholuric (familial) jaundice Congenital (spherocytic) hemolytic icterus Minkowski-Chauffard syndrome | |
D58.1 | Hereditary elliptocytosis | |
Info: | Elliptocytosis (congenital) Ovalocytosis (congenital) (hereditary) | |
D58.2 | Other hemoglobinopathies | |
Info: | Abnormal hemoglobin NOS Congenital Heinz body anemia Hb-C disease Hb-D disease Hb-E disease Hemoglobinopathy NOS Unstable hemoglobin hemolytic disease | |
Excl1.: | familial polycythemia (D75.0) Hb-M disease (D74.0) hemoglobin E-beta thalassemia (D56.5) hereditary persistence of fetal hemoglobin [HPFH] (D56.4) high-altitude polycythemia (D75.1) methemoglobinemia (D74.-) other hemoglobinopathies with thalassemia (D56.8) | |
D58.8 | Other specified hereditary hemolytic anemias | |
Info: | Stomatocytosis | |
D58.9 | Hereditary hemolytic anemia, unspecified | |
|
ICD-10-CM-2023 Code Search Engine and PCS-2023 Code Search Engine |