ICD-10-CM Code For Other Hereditary Hemolytic Anemias: Group Overview
The International Classification of Diseases, Tenth Revision, Clinical Modification (ICD-10-CM) code group D58 includes inherited hemolytic anemias other than sickle-cell and thalassemia, such as hereditary spherocytosis, elliptocytosis, and enzyme defects causing chronic hemolysis that result in anemia, jaundice, and splenomegaly. These ICD-10-CM diagnosis codes are used to document clinical presentations of chronic or episodic hemolysis, capture disease severity, organ involvement such as splenic or hepatic effects, and record complications like gallstones or iron overload. Accurate coding within the ICD-10-CM D58 group supports proper claim adjudication, complete clinical documentation, and appropriate reimbursement.
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ICD-10-CM D58: Other Hereditary Hemolytic Anemias Overview
This group represents inherited disorders characterized by premature red blood cell destruction leading to anemia and related sequelae. These diagnoses target the hematologic system and may involve splenic enlargement, jaundice, and varying degrees of hemolysis. Accurate coding matters for reimbursement because it captures disease severity, need for interventions, and supports correct claim adjudication.