2009 ICD-9-CM Diagnosis 284.* : Aplastic anemia

Free ICD-9-CM Diagnosis Codes Lookup > 2009 > Diseases Of The Blood And Blood-Forming Organs 280-289 > Aplastic anemia 284.* > 
2009 ICD-9-CM Diagnosis Code 284 Aplastic anemia
2009 ICD-9-CM Diagnosis Code 284.0 Constitutional aplastic anemia
familial or idiopathic form, usually fatal; Fanconi's anemia presents before age 10, marked by microcephaly, skin discolorations, and sexual and mental retardation.
2009 ICD-9-CM Diagnosis Code 284.01Constitutional red blood cell aplasia
familial or idiopathic form, usually fatal; Fanconi's anemia presents before age 10, marked by microcephaly, skin discolorations, and sexual and mental retardation.
2009 ICD-9-CM Diagnosis Code 284.09Other constitutional aplastic anemia
A rare and often fatal inherited disease in which the bone marrow fails to produce red blood cells, white blood cells, platelets, or a combination of these cells. The disease may transform into myelodysplastic syndrome or leukemia.
Fanconi anemia (FA) is an autosomal recessive genetic disorder characterised clinically by progressive bone marrow failure, skeletal deformities and a predisposition to neoplasia. Patient cells manifest an extreme chromosomal instability and hypersensitivity to polyfunctional alkylating agents. It is assumed that the basic defect is related to the repair of DNA damage, in particular that of so-called DNA crosslinks. Currently there are eight complementation groups in FA (FA-A-FA-H) which indicates that at least eight independent genes can lead to FA. Three of these genes have been identified: FANCA, FANCC and FANCG. (from PMID 10472548)
2009 ICD-9-CM Diagnosis Code 284.1Pancytopenia
2009 ICD-9-CM Diagnosis Code 284.2Myelophthisis
2009 ICD-9-CM Diagnosis Code 284.8 Other specified aplastic anemias
2009 ICD-9-CM Diagnosis Code 284.81Other specified aplastic anemias
2009 ICD-9-CM Diagnosis Code 284.89Red cell aplasia (acquired)(adult) (with thymoma)
2009 ICD-9-CM Diagnosis Code 284.9Aplastic anemia unspecified
anemia associated with a fatty, hypocellular bone marrow and global dyshematopoiesis; can be idiopathic or due to microbial, metabolic, autoimmune, or other abnormality.
A condition in which the bone marrow is unable to produce blood cells.
Anemia resulting from bone marrow failure (aplastic or hypoplastic bone marrow). The production of erythroblasts and red cells is markedly decreased, and it may be associated with decreased production of granulocytes (granulocytopenia) and platelets (thrombocytopenia) as well. Aplastic anemia may be idiopathic or secondary due to bone marrow damage by toxins, radiation, or immunologic factors. -- 2004
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