- includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
282 Hereditary hemolytic anemias convert 282 to ICD-10
282.0 Hereditary spherocytosis convert 282.0 to ICD-10- 282.1 Hereditary elliptocytosis convert 282.1 to ICD-10
- 282.2 Anemias due to disorders of glutathione metabolism convert 282.2 to ICD-10
- 282.3 Other hemolytic anemias due to enzyme deficiency convert 282.3 to ICD-10
- 282.4 Thalassemias convert 282.4 to ICD-10
282.41 Sickle-cell thalassemia without crisis convert 282.41 to ICD-10- 282.42 Sickle-cell thalassemia with crisis convert 282.42 to ICD-10
282.49 Other thalassemia convert 282.49 to ICD-10- 282.5 Sickle-cell trait convert 282.5 to ICD-10
- 282.6 Sickle-cell disease convert 282.6 to ICD-10
- 282.60 … unspecified convert 282.60 to ICD-10
- 282.61 Hb-ss disease without crisis convert 282.61 to ICD-10
- 282.62 Hb-ss disease with crisis convert 282.62 to ICD-10
- 282.63 Sickle-cell/hb-c disease without crisis convert 282.63 to ICD-10
- 282.64 Sickle-cell/hb c disease with crisis convert 282.64 to ICD-10
- 282.68 Other sickle-cell disease without crisis convert 282.68 to ICD-10
- 282.69 Other sickle-cell disease with crisis convert 282.69 to ICD-10
- 282.7 Other hemoglobinopathies convert 282.7 to ICD-10
- 282.8 Other specified hereditary hemolytic anemias convert 282.8 to ICD-10
- 282.9 Hereditary hemolytic anemia unspecified convert 282.9 to ICD-10