|  D58 |  | Other hereditary hemolytic anemias  | 
	
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		| 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 |  | Hereditary hemolytic anemia, unspecified |  |