2008 ICD-9-CM Diagnosis 282.* : Hereditary hemolytic anemias

Free ICD-9-CM Diagnosis Codes Lookup > 2008 > Diseases Of The Blood And Blood-Forming Organs 280-289 > Hereditary hemolytic anemias 282.* > 
2008 ICD-9-CM Diagnosis Code 282 Hereditary hemolytic anemias
includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
2008 ICD-9-CM Diagnosis Code 282.0Hereditary spherocytosis
includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
autosomal dominant trait marked by splenomegaly, jaundice, and fragile, spheroid erythrocytes which are prematurely cleared by the spleen; anemia is usually mild; treatment is splenectomy.
2008 ICD-9-CM Diagnosis Code 282.1Hereditary elliptocytosis
intrinsic defect of erythrocytes inherited as an autosomal dominant trait; erythrocytes assume an oval or elliptical shape.
2008 ICD-9-CM Diagnosis Code 282.2Anemias due to disorders of glutathione metabolism
2008 ICD-9-CM Diagnosis Code 282.3Other hemolytic anemias due to enzyme deficiency
2008 ICD-9-CM Diagnosis Code 282.4 Thalassemias
heterogeneous group of hereditary hemolytic anemias which have in common a decreased rate of synthesis of one or more hemoglobin polypeptide chains.
2008 ICD-9-CM Diagnosis Code 282.41Sickle-cell thalassemia without crisis
2008 ICD-9-CM Diagnosis Code 282.42Sickle-cell thalassemia with crisis
2008 ICD-9-CM Diagnosis Code 282.49Other thalassemia
heterogeneous group of hereditary hemolytic anemias which have in common a decreased rate of synthesis of one or more hemoglobin polypeptide chains.
2008 ICD-9-CM Diagnosis Code 282.5Sickle-cell trait
2008 ICD-9-CM Diagnosis Code 282.6 Sickle-cell disease
disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs; the clinical expression of homozygosity for hemoglobin S.
2008 ICD-9-CM Diagnosis Code 282.60Sickle-cell disease unspecified
disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs; the clinical expression of homozygosity for hemoglobin S.
2008 ICD-9-CM Diagnosis Code 282.61Hb-ss disease without crisis
2008 ICD-9-CM Diagnosis Code 282.62Hb-ss disease with crisis
broad term used to describe several different acute conditions occurring with sickle cell disease, including aplastic crisis, hemolytic crisis, and vasoocclusive crisis.
2008 ICD-9-CM Diagnosis Code 282.63Sickle-cell/hb-c disease without crisis
2008 ICD-9-CM Diagnosis Code 282.64Sickle-cell/hb c disease with crisis
2008 ICD-9-CM Diagnosis Code 282.68Other sickle-cell disease without crisis
2008 ICD-9-CM Diagnosis Code 282.69Other sickle-cell disease with crisis
2008 ICD-9-CM Diagnosis Code 282.7Other hemoglobinopathies
group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
2008 ICD-9-CM Diagnosis Code 282.8Other specified hereditary hemolytic anemias
2008 ICD-9-CM Diagnosis Code 282.9Hereditary hemolytic anemia unspecified
includes hereditary erythrocyte membrane defects, enzyme deficiencies, hemoglobin abnormalities, stem cell defects (paroxysmal nocturnal hemoglobinuria), and alloimmune (Rh) disease of newborn.
 281.*
283.* 