2006 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > ICD-9-CM Diagnosis 289 Other diseases of blood and blood-forming organs 289 is a non-specific code that cannot be used to specify a diagnosis ICD-9-CM Diagnosis 289.0 Polycythemia secondary 289.0 is a specific code that can be used to specify a diagnosis 289.0 contains 36 index entries ICD-9-CM Diagnosis 289.1 Chronic lymphadenitis 289.1 is a specific code that can be used to specify a diagnosis 289.1 contains 12 index entries ICD-9-CM Diagnosis 289.2 Nonspecific mesenteric lymphadenitis INFLAMMATION of LYMPH NODES in the MESENTERY. 289.2 is a specific code that can be used to specify a diagnosis 289.2 contains 13 index entries ICD-9-CM Diagnosis 289.3 Lymphadenitis unspecified except mesenteric 289.3 is a specific code that can be used to specify a diagnosis 289.3 contains 23 index entries ICD-9-CM Diagnosis 289.4 Hypersplenism Condition characterized by splenomegaly, some reduction in the number of circulating blood cells in the presence of a normal or hyperactive bone marrow, and the potential for reversal by splenectomy. 289.4 is a specific code that can be used to specify a diagnosis 289.4 contains 10 index entries ICD-9-CM Diagnosis 289.5 Other diseases of spleen 289.5 is a non-specific code that cannot be used to specify a diagnosis ICD-9-CM Diagnosis 289.50 Disease of spleen unspecified 289.50 is a specific code that can be used to specify a diagnosis 289.50 contains 3 index entries ICD-9-CM Diagnosis 289.51 Chronic congestive splenomegaly 289.51 is a specific code that can be used to specify a diagnosis 289.51 contains 12 index entries ICD-9-CM Diagnosis 289.52 Splenic sequestration 289.52 is a specific code that can be used to specify a diagnosis 289.52 contains 3 index entries ICD-9-CM Diagnosis 289.59 Other diseases of spleen Insufficiency of arterial or venous blood supply to the spleen due to emboli, thrombi, vascular torsion, or pressure that produces a macroscopic area of necrosis. 289.59 is a specific code that can be used to specify a diagnosis 289.59 contains 39 index entries ICD-9-CM Diagnosis 289.6 Familial polycythemia 289.6 is a specific code that can be used to specify a diagnosis 289.6 contains 3 index entries ICD-9-CM Diagnosis 289.7 Methemoglobinemia A morbid condition due to the presence of sulfmethemoglobin in the blood. It is marked by persistent cyanosis, but the blood count does not reveal any special abnormality in the blood. It is thought to be caused by the action of hydrogen sulfide absorbed from the intestine. The presence of methemoglobin in the blood, resulting in cyanosis. A small amount of methemoglobin is present in the blood normally, but injury or toxic agents convert a larger proportion of hemoglobin into methemoglobin, which does not function reversibly as an oxygen carrier. Methemoglobinemia may be due to a defect in the enzyme NADH methemoglobin reductase (an autosomal recessive trait) or to an abnormality in hemoglobin M (an autosomal dominant trait). 289.7 is a specific code that can be used to specify a diagnosis 289.7 contains 21 index entries ICD-9-CM Diagnosis 289.8 Other specified diseases of blood and blood-forming organs 289.8 is a non-specific code that cannot be used to specify a diagnosis ICD-9-CM Diagnosis 289.81 Primary hypercoagulable state An absence or deficiency in PROTEIN C which leads to impaired regulation of blood coagulation. It is associated with an increased risk of severe or premature thrombosis. An autosomal dominant disorder showing decreased levels of plasma protein S antigen or activity, associated with venous thrombosis and pulmonary embolism. PROTEIN S is a vitamin K-dependent plasma protein that inhibits blood clotting by serving as a cofactor for activated PROTEIN C (also a vitamin K-dependent protein), and the clinical manifestations of its deficiency are virtually identical to those of protein C deficiency. Treatment with heparin for acute thrombotic processes is usually followed by maintenance administration of coumarin drugs for the prevention of recurrent thrombosis. An absence or reduced level of Antithrombin III leading to an increased risk for thrombosis. A hemostatic disorder characterized by a poor anticoagulant response to activated protein C (APC). The activated form of Factor V (Factor Va) is more slowly degraded by activated protein C. Factor V Leiden mutation (R506Q) is the most common cause of APC resistance. 289.81 is a specific code that can be used to specify a diagnosis 289.81 contains 9 index entries ICD-9-CM Diagnosis 289.82 Secondary hypercoagulable state 289.82 is a specific code that can be used to specify a diagnosis 289.82 contains 2 index entries ICD-9-CM Diagnosis 289.89 Other specified diseases of blood and blood-forming organs A partial or complete replacement of the bone marrow stroma by fibrous tissue. It can be a primary bone marrow lesion as part of the chronic myeloproliferative disorders (chronic idiopathic myelofibrosis), a manifestation of acute myeloid leukemia (acute panmyelosis with myelofibrosis), or a secondary phenomenon due to bone marrow involvement by a metastatic tumor (e.g., metastatic breast carcinoma). --2003 A disorder in which the bone marrow is replaced by fibrous tissue. An excess of GAMMA-GLOBULINS in the blood. It is seen frequently in chronic infectious diseases. Replacement of the bone marrow by fibrous tissue, occurring in association with a myeloproliferative disorder or secondary to another, unrelated condition. 289.89 is a specific code that can be used to specify a diagnosis 289.89 contains 27 index entries ICD-9-CM Diagnosis 289.9 Unspecified diseases of blood and blood-forming organs Disorders of the blood and blood forming tissues. 289.9 is a specific code that can be used to specify a diagnosis 289.9 contains 23 index entries