2008 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of The Blood And Blood-Forming Organs 280-289 >
 Other diseases of blood and blood-forming organs- 289 is a non-specific code that cannot be used to specify a diagnosis
Polycythemia secondary- 289.0 is a specific code that can be used to specify a diagnosis
- 289.0 contains 35 index entries
Chronic lymphadenitis- 289.1 is a specific code that can be used to specify a diagnosis
- 289.1 contains 12 index entries
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
Lymphadenitis unspecified except mesenteric- 289.3 is a specific code that can be used to specify a diagnosis
- 289.3 contains 23 index entries
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
Other diseases of spleen- 289.5 is a non-specific code that cannot be used to specify a diagnosis
Disease of spleen unspecified- 289.50 is a specific code that can be used to specify a diagnosis
- 289.50 contains 3 index entries
Chronic congestive splenomegaly- 289.51 is a specific code that can be used to specify a diagnosis
- 289.51 contains 12 index entries
Splenic sequestration- 289.52 is a specific code that can be used to specify a diagnosis
- 289.52 contains 3 index entries
Neutropenic splenomegaly- 289.53 is a specific code that can be used to specify a diagnosis
- 289.53 contains 7 index entries
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. (From Stedman, 25th ed)
- 289.59 is a specific code that can be used to specify a diagnosis
- 289.59 contains 39 index entries
Familial polycythemia- 289.6 is a specific code that can be used to specify a diagnosis
- 289.6 contains 3 index entries
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. (Stedman, 25th ed)
- 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). (Dorland, 27th ed)
- 289.7 is a specific code that can be used to specify a diagnosis
- 289.7 contains 21 index entries
Other specified diseases of blood and blood-forming organs- 289.8 is a non-specific code that cannot be used to specify a diagnosis
Primary hypercoagulable state- 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.
- 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. (Stedman's Med. Dict., 26th ed.)
- An absence or reduced level of Antithrombin III leading to an increased risk for 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. (From Harrison's Principles of Internal Medicine, 12th ed, p1511; Wintrobe's Clinical Hematology, 9th ed, p1523)
- 289.81 is a specific code that can be used to specify a diagnosis
- 289.81 contains 9 index entries
Secondary hypercoagulable state- 289.82 is a specific code that can be used to specify a diagnosis
- 289.82 contains 2 index entries
Myelofibrosis- 289.83 is a specific code that can be used to specify a diagnosis
- 289.83 contains 2 index entries
Other specified diseases of blood and blood-forming organs- A disorder in which the bone marrow is replaced by fibrous tissue.
- 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
- An excess of GAMMA-GLOBULINS in the blood. It is seen frequently in chronic infectious diseases. (Dorland, 27th ed)
- Replacement of the bone marrow by fibrous tissue, occurring in association with a myeloproliferative disorder or secondary to another, unrelated condition. (Dorland, 27th ed)
- 289.89 is a specific code that can be used to specify a diagnosis
- 289.89 contains 26 index entries
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
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