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2007 ICD-9-CM Volume 1 Diagnosis Codes Home > Diseases Of Blood And Blood-Forming Organs 280-289 > Hereditary Hemolytic Anemias 282.* >

2007 ICD-9-CM Diagnosis 282.49

Other thalassemia

This code may be outdated. View the most recent version of ICD-9-CM 282.49

  • A disorder characterized by reduced synthesis of the alpha chains of hemoglobin. The severity of this condition can vary from mild anemia to death, depending on the number of genes deleted.
  • A disorder characterized by reduced synthesis of the beta chains of hemoglobin. There is retardation of hemoglobin A synthesis in the heterozygous form (thalassemia minor), which is asymptomatic, while in the homozygous form (thalassemia major, Cooley's anemia, Mediterranean anemia, erythroblastic anemia), which can result in severe complications and even death, hemoglobin A synthesis is absent.
  • A group of hereditary hemolytic anemias in which there is decreased synthesis of one or more hemoglobin polypeptide chains. There are several genetic types with clinical pictures ranging from barely detectable hematologic abnormality to severe and fatal anemia.
  • 282.49 is a specific code that can be used to specify a diagnosis
  • 282.49 contains 50 index entries
  • View the ICD-9-CM Volume 1 282.* hierarchy

282.49 also known as:

  • Cooley's anemia
  • Hb-Bart's disease
  • Hereditary leptocytosis
  • Mediterranean anemia (with other hemoglobinopathy)
  • Microdrepanocytosis
  • Thalassemia (alpha) (beta) (intermedia) (major) (minima) (minor) (mixed) (trait) (with other hemoglobinopathy)
  • Thalassemia NOS

Index entries containing 282.49:

Alpha thalassemia 282.49
Anemia 285.9
  • Cooley's (erythroblastic) 282.49
  • erythroblastic
    • familial 282.49
  • familial erythroblastic (microcytic) 282.49
  • high A2 282.49
  • leptocytosis (hereditary) 282.49
  • Mediterranean (with hemoglobinopathy) 282.49
  • microcytic (hypochromic) 280.9
    • familial 282.49
  • microdrepanocytosis 282.49
  • Rietti-Greppi-Micheli (thalassemia minor) 282.49
  • target cell (oval) 282.49
  • thalassemia 282.49
Beta thalassemia (major) (minor) (mixed) 282.49
Cooley's anemia (erythroblastic) 282.49
Dameshek's syndrome (erythroblastic anemia) 282.49
Disease, diseased - see also Syndrome
  • Cooley's (erythroblastic anemia) 282.49
  • hemoglobin (Hb) 282.7
    • with thalassemia 282.49
    • abnormal (mixed) NEC 282.7
      • with thalassemia 282.49
    • Bart's 282.49
    • C (Hb-C) 282.7
      • thalassemia 282.49
    • D (Hb-D) 282.7
      • thalassemia 282.49
    • E (Hb-E) 282.7
      • thalassemia 282.49
    • H (Hb-H) 282.49
    • I thalassemia 282.49
  • high fetal gene or hemoglobin thalassemia 282.49
  • Mediterranean (with hemoglobinopathy) 282.49
  • microdrepanocytic 282.49
Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7
  • with thalassemia 282.49
High
  • A2 anemia 282.49
Lepore hemoglobin syndrome 282.49
Leptocytosis, hereditary 282.49
Mediterranean
  • anemia (with other hemoglobinopathy) 282.49
  • disease or syndrome (hemipathic) 282.49
Micheli-Rietti syndrome (thalassemia minor) 282.49
Microdrepanocytosis (thalassemia-Hb-S disease) 282.49
Rietti-Greppi-Micheli anemia or syndrome 282.49
Silvestroni-Bianco syndrome (thalassemia minima) 282.49
Syndrome - see also Disease
  • Dameshek's (erythroblastic anemia) 282.49
  • Lepore hemoglobin 282.49
  • Micheli-Rietti (thalassemia minor) 282.49
  • Rietti-Greppi-Micheli (thalassemia minor) 282.49
  • Silvestroni-Bianco (thalassemia minima) 282.49
Target-oval cell anemia 282.49
Thalassanemia 282.49
Thalassemia (alpha) (beta) (disease) (Hb-C) (Hb-D) (Hb-E) (Hb-H) (Hb-I) (high fetal gene) (high fetal hemoglobin) (intermedia) (major) (minima) (minor) (mixed) (trait) (with other hemoglobinopathy) 282.49Thalassemic variants 282.49
Trait
  • hemoglobin
    • abnormal NEC 282.7
      • with thalassemia 282.49
  • Lepore 282.49
    • with other abnormal hemoglobin NEC 282.49
Variants, thalassemic 282.49