Diagnosis Code: 282.49

Short Description: Thalassemia NEC

Long Description: Other thalassemia

Code Classification:

• Diseases of the blood and blood-forming organs (280–289)
  • Diseases of the blood and blood-forming organs (280-289)
    • 282 Hereditary hemolytic anemias
      • 282.49 Thalassemia NEC

Code Version: 2015 ICD-9-CM

Synonyms

• ^A^gamma delta beta^0^ thalassemia
• A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis
• Acquired hemoglobin H disease
• alpha Thalassemia
• Alpha thalassemia-2 trait
• Alpha thalassemia-mental retardation syndrome
• Alpha trait thalassemia
• alpha^+^ Thalassemia
• alpha^+^ Thalassemia, deletion type
• alpha^+^ Thalassemia, nondeletion type
• alpha^0^ Thalassemia
• Alpha-beta thalassemia
• beta Thalassemia
• Beta thalassemia intermedia
• Beta thalassemia trait
• beta^+^ Thalassemia
• beta^+^ Thalassemia, normal Hb A>2<, type 1, silent
• beta^+^ Thalassemia, normal Hb A>2<, type 2
• beta^0^ Thalassemia
• beta^0^ Thalassemia, deletion type
• beta^0^ Thalassemia, nondeletion type
• delta beta Thalassemia
• delta beta^0^ Thalassemia
• delta Thalassemia
• delta^0^ Thalassemia
• Delta-beta-Lepore thalassemia
• epsilon gamma delta beta Thalassemia
• epsilon gamma delta beta^0^ Thalassemia
• Gamma thalassemia
• Hb Lepore thalassemia
• Hemoglobin Bart's hydrops syndrome
• Hemoglobin Constant Spring trait
• Hemoglobin E/beta thalassemia disease
• Hemoglobin H disease
• Hemoglobin Lepore trait
• Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster
• Hereditary persistence of fetal hemoglobin thalassemia
• Heterozygous thalassemia
• Homozygous alpha thalassemia
• Homozygous beta thalassemia
• Leptocytosis
• Leptospirosis icterohemorrhagica
• Sickle cell anemia with coexistent alpha-thalassemia
• Sickle cell trait with coexistent alpha-thalassemia
• Sickle cell-beta^+^-thalassemia
• Sickle cell-beta^0^-thalassemia
• Sickle cell-beta-thalassemia
• Sickle cell-delta beta^0^-thalassemia
• Sickle cell-thalassemia disease
• Thalassemia
• Thalassemia intermedia
• Thalassemia major
• Thalassemia syndrome
• Thalassemia with other hemoglobinopathy

References to Index of Diseases and Injuries

The code 282.49 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Anemia 285.9
  • Mediterranean� 282.40
    • with hemoglobinopathy 282.49
  • microcytic (hypochromic) 280.9
    • familial 282.49

• Dameshek's syndrome (erythroblastic anemia) 282.49

• Disease, diseased - see also Syndrome
  • hemoglobin (Hb) 282.7
    • with thalassemia 282.49
    • abnormal (mixed) NEC 282.7
      • with thalassemia 282.49
    • C (Hb-C) 282.7
      • thalassemia 282.49
    • D (Hb-D) 282.7
      • thalassemia 282.49
    • I thalassemia 282.49
  • Mediterranean 282.40
    • with hemoglobinopathy 282.49

• Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7
  • with thalassemia 282.49

• Mediterranean
  • anemia� 282.40
    • with other hemoglobinopathy 282.49
  • disease or syndrome (hemopathic) 282.40
    • with other hemoglobinopathy 282.49

• Syndrome - see also Disease
  • Dameshek's (erythroblastic anemia) 282.49

• Thalassemia (disease)�� 282.40
  • with other hemoglobinopathy 282.49
  • dominant 282.49
  • hemoglobin
    • C (Hb-C) 282.49
    • D (Hb-D) 282.49
    • E (Hb-E) 282.49
    • H (Hb-H) 282.49
    • I (Hb-I) 282.49
  • mixed 282.49
  • specified NEC 282.49

• Thalassemic variants 282.49

• Trait
  • Lepore 282.46
    • with other abnormal hemoglobin NEC 282.49

• Variants, thalassemic 282.49

Crosswalk Information

The code 282.49 converts into the following ICD-10 code(s):

Similar Codes

This page was last updated on: 10/1/2014

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