Specific code 2011 ICD-9-CM Diagnosis Code 282.7
Other hemoglobinopathies
  • Short description: Hemoglobinopathies NEC.
  • ICD-9-CM 282.7 will be replaced by an equivalent ICD-10-CM code (or codes) when the United States transitions from ICD-9-CM to ICD-10-CM on October 1, 2015.
  • ICD-9-CM 282.7 is a billable medical code that can be used to specify a diagnosis on a reimbursement claim.
  • You are viewing the 2011 version of ICD-9-CM 282.7.
  • More recent version(s) of ICD-9-CM 282.7: 2012 2013 2014.
Disease Synonyms
  • 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
  • Hemoglobinopathy, hereditary
  • 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 nondeletion type
  • Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster
  • Heterozygous hemoglobinopathy
  • Hgb C disease
  • Hgb C trait
  • Hgb D disease
  • Hgb D trait
  • Hgb E disease
  • Hgb E trait
  • 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
282.7 Excludes
  • familial polycythemia (289.6)
  • hemoglobin M [Hb-M] disease (289.7)
  • high-oxygen-affinity hemoglobin (289.0)
Applies To
  • Abnormal hemoglobin NOS
  • Congenital Heinz-body anemia
  • Disease:
    • hemoglobin C [Hb-C]
    • hemoglobin D [Hb-D]
    • hemoglobin E [Hb-E]
    • hemoglobin Zurich [Hb-Zurich]
  • Hemoglobinopathy NOS
  • Hereditary persistence of fetal hemoglobin [HPFH]
  • Unstable hemoglobin hemolytic disease
Convert to ICD-10-CM: 282.7 converts approximately to:
  • 2014 ICD-10-CM D56.4 Hereditary persistence of fetal hemoglobin [HPFH]
    Or:
  • 2014 ICD-10-CM D58.2 Other hemoglobinopathies
ICD-9-CM Volume 2 Index entries containing back-references to 282.7:
  • 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
      • aplastic 284.01
      • due to isoimmunization NEC 773.2
      • Heinz-body 282.7
      • hereditary hemolytic NEC 282.9
      • nonspherocytic
      • pernicious 281.0
      • spherocytic (see also Spherocytosis) 282.0
    • Heinz-body, congenital 282.7
    • hemolytic 283.9
      • acquired 283.9
        • with hemoglobinuria NEC 283.2
        • autoimmune (cold type) (idiopathic) (primary) (secondary) (symptomatic) (warm type) 283.0
        • due to
          • cold reactive antibodies 283.0
          • drug exposure 283.0
          • warm reactive antibodies 283.0
        • fragmentation 283.19
        • idiopathic (chronic) 283.9
        • infectious 283.19
        • non-autoimmune 283.10
        • toxic 283.19
        • traumatic cardiac 283.19
      • acute 283.9
        • due to enzyme deficiency NEC 282.3
        • fetus or newborn (see also Disease, hemolytic) 773.2
        • Lederer's (acquired infectious hemolytic anemia) 283.19
      • autoimmune (acquired) 283.0
      • chronic 282.9
      • cold type (secondary) (symptomatic) 283.0
      • congenital (spherocytic) (see also Spherocytosis) 282.0
        • nonspherocytic - see Anemia, hemolytic, nonspherocytic, congenital
      • drug-induced 283.0
      • due to
        • cardiac conditions 283.19
        • drugs 283.0
        • enzyme deficiency NEC 282.3
        • presence of shunt or other internal prosthetic device 283.19
        • thrombotic thrombocytopenic purpura 446.6
      • elliptocytotic (see also Elliptocytosis) 282.1
      • familial 282.9
      • hereditary 282.9
        • due to enzyme deficiency NEC 282.3
        • specified NEC 282.8
      • idiopathic (chronic) 283.9
      • infectious (acquired) 283.19
      • mechanical 283.19
      • microangiopathic 283.19
      • nonautoimmune 283.10
      • nonspherocytic
      • of or complicating pregnancy 648.2
      • resulting from presence of shunt or other internal prosthetic device 283.19
      • secondary 283.19
      • sickle-cell - see Disease, sickle-cell
      • Stransky-Regala type (Hb-E) (see also Disease, hemoglobin) 282.7
      • symptomatic 283.19
      • toxic (acquired) 283.19
      • uremic (adult) (child) 283.11
      • warm type (secondary) (symptomatic) 283.0
  • Disease, diseased - see also Syndrome
    • hemoglobin (Hb) 282.7
      • with thalassemia 282.49
      • abnormal (mixed) NEC 282.7
      • AS genotype 282.5
      • Bart's 282.49
      • C (Hb-C) 282.7
        • with other abnormal hemoglobin NEC 282.7
        • elliptocytosis 282.7
        • Hb-S (without crisis) 282.63
        • sickle-cell (without crisis) 282.63
        • 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
        • sickle-cell (without crisis) 282.68
        • thalassemia 282.49
      • E (Hb-E) 282.7
        • with other abnormal hemoglobin NEC 282.7
        • Hb-S (without crisis) 282.68
        • sickle-cell (without crisis) 282.68
        • thalassemia 282.49
      • elliptocytosis 282.7
      • F (Hb-F) 282.7
      • G (Hb-G) 282.7
      • H (Hb-H) 282.49
      • 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
      • spherocytosis 282.7
      • unstable, hemolytic 282.7
      • Zurich (Hb-Zurich) 282.7
    • hemolytic (fetus) (newborn) 773.2
      • autoimmune (cold type) (warm type) 283.0
      • due to or with
        • incompatibility
          • ABO (blood group) 773.1
          • blood (group) (Duffy) (Kell) (Kidd) (Lewis) (M) (S) NEC 773.2
          • Rh (blood group) (factor) 773.0
        • Rh negative mother 773.0
      • 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
  • Heinz-body anemia, congenital 282.7
  • Hemoglobin - see also condition
    • fetal, hereditary persistence 282.7
  • Hemoglobinopathy (mixed) (see also Disease, hemoglobin) 282.7
  • Persistence, persistent (congenital) 759.89
    • fetal
      • circulation 747.83
      • form of cervix (uteri) 752.49
      • hemoglobin (hereditary) ("Swiss variety") 282.7
      • pulmonary hypertension 747.83
    • hemoglobin, fetal (hereditary) (HPFH) 282.7
  • Spherocytosis (congenital) (familial) (hereditary) 282.0
    • hemoglobin disease 282.7
  • Trait
    • hemoglobin
      • abnormal NEC 282.7
      • C (see also Disease, hemoglobin, C) 282.7
        • with elliptocytosis 282.7
      • S (Hb-S) 282.5
ICD-9-CM codes are used in medical billing and coding to describe diseases, injuries, symptoms and conditions. ICD-9-CM 282.7 is one of thousands of ICD-9-CM codes used in healthcare. Although ICD-9-CM and CPT codes are largely numeric, they differ in that CPT codes describe medical procedures and services. Can't find a code? Start at the root of ICD-9-CM, check the 2011 ICD-9-CM Index or use the search engine at the top of this page to lookup any code.