Diagnosis Code: 282.7

Short Description: Hemoglobinopathies NEC

Long Description: Other hemoglobinopathies

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
      • 282.7 Hemoglobinopathies NEC

Code Version: 2015 ICD-9-CM

Synonyms

• A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis
• Acquired Heinz body anemia
• Acquired hemoglobinopathy
• Arthropathy secondary to hemoglobinopathy
• Decreased erythrocyte life span
• Double heterozygous sickling disorder
• Heinz bodies
• Hematopoietic maturation arrest
• Hemoglobin A1c above reference range
• Hemoglobin C disease
• Hemoglobin C trait
• Hemoglobin D disease
• Hemoglobin D trait
• Hemoglobin E disease
• Hemoglobin E trait
• Hemoglobin low
• Hemoglobin O-Arab trait
• Hemoglobin very high
• Hemoglobin Zurich disease
• Hemoglobinopathy
• Hemoglobinopathy with cyanosis
• Hemoglobinopathy with erythrocytosis
• Hereditary hemoglobinopathy
• Hereditary hemoglobinopathy due to globin chain mutation
• Hereditary persistence of fetal hemoglobin
• Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia
• Hereditary persistence of fetal hemoglobin deletion type
• Hereditary persistence of fetal hemoglobin delta beta^0^ thalassemia
• Hereditary persistence of fetal hemoglobin G gamma beta^+^ thalassemia
• Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster
• Hereditary persistence of fetal hemoglobin, nondeletion type
• Heterozygous hemoglobinopathy
• High affinity hemoglobin
• Homozygous hemoglobinopathy
• Increased erythrocyte destruction
• Increased heme-heme interaction
• Low affinity hemoglobin
• Mixed hemoglobin disorder
• Osteonecrosis due to hemoglobinopathy
• Red blood cell destruction finding
• Sickle cell retinopathy
• Thalassemia-hemoglobin C disease
• Unstable hemoglobin disease

References to Index of Diseases and Injuries

The code 282.7 has the following ICD-9-CM references to the Index of Diseases and Injuries

• Abnormal, abnormality, abnormalities - see also Anomaly
  • hemoglobin (see also Disease, hemoglobin) 282.7
    • trait - see Trait, hemoglobin, abnormal

• Anemia 285.9
  • congenital (following fetal blood loss) 776.5
    • Heinz-body 282.7
  • Heinz-body, congenital 282.7
  • hemolytic 283.9
    • Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7

• Arthritis, arthritic (acute) (chronic) (subacute) 716.9
  • due to or associated with
    • hemoglobinopathy NEC (see also Disease, hemoglobin) 282.7 [713.2]

• Disease, diseased - see also Syndrome
  • hemoglobin (Hb) 282.7
    • with thalassemia 282.49
    • abnormal (mixed) NEC 282.7
      • with thalassemia 282.49
    • AS genotype 282.5
    • Bart's 282.43
    • C (Hb-C) 282.7
      • with other abnormal hemoglobin NEC 282.7
      • elliptocytosis 282.7
      • Hb-S (without crisis) 282.63
        • with
          • crisis 282.64
          • vaso-occlusive pain 282.64
      • sickle-cell (without crisis) 282.63
        • with
          • crisis 282.64
          • vaso-occlusive pain 282.64
      • thalassemia 282.49
    • constant spring 282.7
    • D (Hb-D) 282.7
      • with other abnormal hemoglobin NEC 282.7
      • Hb-S (without crisis) 282.68
        • with crisis 282.69
      • sickle-cell (without crisis) 282.68
        • with crisis 282.69
      • thalassemia 282.49
    • E (Hb-E) 282.7
      • with other abnormal hemoglobin NEC 282.7
      • Hb-S� (without crisis) 282.68
        • with crisis 282.69
      • sickle-cell� (without crisis) 282.68
        • with crisis 282.69
      • thalassemia 282.47
    • elliptocytosis 282.7
    • F (Hb-F) 282.7
    • G (Hb-G) 282.7
    • H (Hb-H) 282.43
    • hereditary persistence, fetal (HPFH) ("Swiss variety") 282.7
    • high fetal gene 282.7
    • I thalassemia 282.49
    • M 289.7
    • S - see also Disease, sickle-cell, Hb-S
      • thalassemia (without crisis) 282.41
        • with
          • crisis 282.42
          • vaso-occlusive pain 282.42
    • spherocytosis 282.7
    • unstable, hemolytic 282.7
    • Zurich (Hb-Zurich) 282.7
  • hemolytic (fetus) (newborn) 773.2
    • unstable hemoglobin 282.7
  • HPFH (hereditary persistence of fetal hemoglobin) ("Swiss variety") 282.7
  • unstable hemoglobin hemolytic 282.7

• Elliptocytosis (congenital) (hereditary) 282.1
  • Hb-C (disease) 282.7
  • hemoglobin disease 282.7

• Findings, (abnormal), without diagnosis (examination) (laboratory test) 796.4
  • hematocrit
    • elevated 282.7
  • hemoglobin
    • elevated 282.7

• Heinz-body anemia, congenital 282.7

• Hemoglobin - see also condition
  • fetal, hereditary persistence 282.7

• Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7
  • with thalassemia 282.49
  • sickle-cell 282.60
    • with thalassemia (without crisis) 282.41
      • with
        • crisis 282.42
        • vaso-occlusive pain 282.42

• Persistence, persistent (congenital) 759.89
  • fetal
    • hemoglobin (hereditary) ("Swiss variety") 282.7
  • hemoglobin, fetal (hereditary) (HPFH) 282.7

• Spherocytosis (congenital) (familial) (hereditary) 282.0
  • hemoglobin disease 282.7

• Trait
  • hemoglobin
    • abnormal NEC 282.7
      • with thalassemia 282.46
    • C (see also Disease, hemoglobin, C) 282.7
      • with elliptocytosis 282.7

Crosswalk Information

The code 282.7 converts into the following ICD-10 code(s):

Similar Codes

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

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