2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 >
 Hereditary hemolytic anemias- Hemolytic anemia due to various intrinsic defects of the erythrocyte.
- 282 is a non-specific code that cannot be used to specify a diagnosis
Hereditary spherocytosis- A familial congenital hemolytic anemia characterized by numerous abnormally shaped erythrocytes which are generally spheroidal. The erythrocytes have increased osmotic fragility and are abnormally permeable to sodium ions.
- Hemolytic anemia due to various intrinsic defects of the erythrocyte.
- 282.0 is a specific code that can be used to specify a diagnosis
- 282.0 contains 13 index entries
Hereditary elliptocytosis- An intrinsic defect of erythrocytes inherited as an autosomal dominant trait. The erythrocytes assume an oval or elliptical shape.
- 282.1 is a specific code that can be used to specify a diagnosis
- 282.1 contains 8 index entries
Anemias due to disorders of glutathione metabolism- Hemolytic anemia due to the ingestion of fava beans or after inhalation of pollen from the Vicia fava plant by persons with glucose-6-phosphate dehydrogenase deficient erythrocytes.
- 282.2 is a specific code that can be used to specify a diagnosis
- 282.2 contains 41 index entries
Other hemolytic anemias due to enzyme deficiency- 282.3 is a specific code that can be used to specify a diagnosis
- 282.3 contains 30 index entries
Thalassemias- A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
- 282.4 is a non-specific code that cannot be used to specify a diagnosis
Sickle-cell thalassemia without crisis- 282.41 is a specific code that can be used to specify a diagnosis
- 282.41 contains 6 index entries
Sickle-cell thalassemia with crisis- 282.42 is a specific code that can be used to specify a diagnosis
- 282.42 contains 12 index entries
Other thalassemia- A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
- A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
- A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
- 282.49 is a specific code that can be used to specify a diagnosis
- 282.49 contains 50 index entries
Sickle-cell trait- The condition of being heterozygous for hemoglobin S.
- 282.5 is a specific code that can be used to specify a diagnosis
- 282.5 contains 10 index entries
Sickle-cell disease- A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.
- 282.6 is a non-specific code that cannot be used to specify a diagnosis
Sickle-cell disease unspecified- A disease characterized by chronic hemolytic anemia, episodic painful crises, and pathologic involvement of many organs. It is the clinical expression of homozygosity for hemoglobin S.
- 282.60 is a specific code that can be used to specify a diagnosis
- 282.60 contains 13 index entries
Hb-ss disease without crisis- 282.61 is a specific code that can be used to specify a diagnosis
- 282.61 contains 10 index entries
Hb-ss disease with crisis- 282.62 is a specific code that can be used to specify a diagnosis
- 282.62 contains 5 index entries
Sickle-cell/hb-c disease without crisis- One of the sickle cell disorders characterized by the presence of both hemoglobin S and hemoglobin C. It is similar to, but less severe than sickle cell anemia.
- 282.63 is a specific code that can be used to specify a diagnosis
- 282.63 contains 5 index entries
Sickle-cell/hb c disease with crisis- 282.64 is a specific code that can be used to specify a diagnosis
- 282.64 contains 11 index entries
Other sickle-cell disease without crisis- 282.68 is a specific code that can be used to specify a diagnosis
- 282.68 contains 8 index entries
Other sickle-cell disease with crisis- 282.69 is a specific code that can be used to specify a diagnosis
- 282.69 contains 9 index entries
Other hemoglobinopathies- A disease characterized by compensated hemolysis with a normal hemoglobin level or a mild to moderate anemia. There may be intermittent abdominal discomfort, splenomegaly, and slight jaundice.
- A group of inherited disorders characterized by structural alterations within the hemoglobin molecule.
- Hemoglobins characterized by structural alterations within the molecule. The alteration can be either absence, addition or substitution of one or more amino acids in the globin part of the molecule at selected positions in the polypeptide chains.
- 282.7 is a specific code that can be used to specify a diagnosis
- 282.7 contains 38 index entries
Other specified hereditary hemolytic anemias- 282.8 is a specific code that can be used to specify a diagnosis
- 282.8 contains 5 index entries
Hereditary hemolytic anemia unspecified- Hemolytic anemia due to various intrinsic defects of the erythrocyte.
- 282.9 is a specific code that can be used to specify a diagnosis
- 282.9 contains 6 index entries
|
|
|
