D58 |
 |
Other hereditary hemolytic anemias |
| |
| Excludes1 |
hemolytic anemia of the newborn (P55.-)
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D58.0 |
 |
Hereditary spherocytosis |
| |
| Acholuric (familial) jaundice | | Congenital (spherocytic) hemolytic icterus | | Minkowski-Chauffard syndrome |
|
|
| |
D58.1 |
 |
Hereditary elliptocytosis |
| |
| Elliptocytosis (congenital) | | Ovalocytosis (congenital) (hereditary) |
|
|
| |
D58.2 |
 |
Other hemoglobinopathies |
| |
| Abnormal hemoglobin NOS | | Congenital Heinz body anemia | | Hb-C disease | | Hb-D disease | | Hb-E disease | | Hemoglobinopathy NOS | | Unstable hemoglobin hemolytic disease |
| Excludes1 |
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)
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|
|
| |
D58.8 |
 |
Other specified hereditary hemolytic anemias |
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|
|
| |
D58.9 |
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Hereditary hemolytic anemia, unspecified |
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