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2006 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.* >

2006 ICD-9-CM Diagnosis 289.89

Other specified diseases of blood and blood-forming organs

View the most recent version of ICD-9-CM 289.89

  • 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
  • View the ICD-9-CM Volume 1 289.* hierarchy

Alternate Terminology

  • Hypergammaglobulinemia
  • Myelofibrosis
  • 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 289.89Hyperprothrombinemia 289.89
                        Insufficiency, insufficient
                        • pseudocholinesterase 289.89
                          Lipophagocytosis 289.89
                            Macrocytosis 289.89
                              Metaplasia
                              • myelogenous 289.89
                                • myeloid 289.89
                                  • agnogenic
                                    • megakaryocytic
                                    Myelosclerosis 289.89
                                    • with myeloid metaplasia (M9961/1)
                                      • disseminated, of nervous system 340
                                        • megakaryocytic (M9961/1)
                                          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