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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Other Diseases Of Blood And Blood-Forming Organs 289.* > 2007 ICD-9-CM Diagnosis 289.89 Other specified diseases of blood and blood-forming organs This code may be outdated. View the most recent version of ICD-9-CM 289.89 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 View the ICD-9-CM Volume 1 289.* hierarchy 289.89 also known as: Hypergammaglobulinemia Pseudocholinesterase deficiency Index entries containing 289.89: Anemia 285.9 osteosclerotic 289.89 Blood disease 289.9 specified NEC 289.89 Decrease, decreased fragility of erythrocytes 289.89 Deficiency, deficient pseudocholinesterase 289.89 Degeneration, degenerative reticuloendothelial system 289.89 Disease, diseased - see also Syndrome blood (-forming organs) 289.9 specified NEC 289.89 Dysfunction hemoglobin 289.89 Dysplasia - see also Anomaly erythroid NEC 289.89 myeloid NEC 289.89 Esterapenia 289.89 Hypergammaglobulinemia 289.89 monoclonal, benign (BMH) 273.1 polyclonal 273.0 Waldenström's 273.0 Hyperprothrombinemia 289.89 Insufficiency, insufficient pseudocholinesterase 289.89 Lipophagocytosis 289.89 Macrocytosis 289.89 Metaplasia myelogenous 289.89 myeloid 289.89 agnogenic 238.76 megakaryocytic 238.76 Myelosclerosis 289.89 with myeloid metaplasia (M9961/1) 238.76 disseminated, of nervous system 340 megakaryocytic (M9961/1) 238.79 Necrosis, necrotic bone (see also Osteomyelitis) 730.1 marrow 289.89 Nitrosohemoglobinemia 289.89 Normoblastosis 289.89 Osteomyelofibrosis 289.89 Osteomyelosclerosis 289.89 Osteosclerotic anemia 289.89 Sensitivity, sensitization - see also Allergy suxamethonium 289.89 Syndrome - see also Disease hypercoagulation NEC 289.89