Home > 2009 ICD-9-CM Diagnosis Codes > Diseases Of The Blood And Blood-Forming Organs 280-289 > Hereditary hemolytic anemias 282-
Specific code 2009 ICD-9-CM Diagnosis Code 282.2
Anemias due to disorders of glutathione metabolism
  • Short description: GLUTATHIONE DIS ANEMIA.
  • ICD-9-CM 282.2 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.2 should only be used for claims with a date of service on or before September 30, 2015. For claims with a date of service on or after October 1, 2015, use an equivalent ICD-10-CM code (or codes).
  • You are viewing the 2009 version of ICD-9-CM 282.2.
  • More recent version(s) of ICD-9-CM 282.2: 2010 2011 2012 2013 2014 2015.
Convert to ICD-10-CM: 282.2 converts approximately to:
  • 2015/16 ICD-10-CM D55.0 Anemia due to glucose-6-phosphate dehydrogenase [G6PD] deficiency
    Or:
  • 2015/16 ICD-10-CM D55.1 Anemia due to other disorders of glutathione metabolism
Approximate Synonyms
  • Anemia due to G6PD deficiency
  • Anemia due to glutathione reductase deficiency
  • Anemia due to pentose phosphate pathway defect
  • Anemia, G6PD deficiency
  • Anemia, glutathione reductase deficiency
  • Drug-induced enzyme deficiency anemia
  • Erythrocyte enzyme deficiency
  • Erythrocyte uridine diphosphate galactose-4-epimerase deficiency
  • Favism
  • G-6-PD class I variant anemia
  • G-6-PD class II variant anemia
  • G-6-PD class III variant anemia
  • G-6-PD class IV variant anemia
  • G-6-PD class V variant anemia
  • G-6-PD variant enzyme deficiency anemia
  • Glucose phosphate isomerase deficiency
  • Glucose-6-phosphate dehydrogenase deficiency anemia
  • Glutathione synthase deficiency without 5-oxoprolinuria
  • Gluthathione peroxidase deficiency
  • Gluthathione synthetase deficiency
  • Hemolytic anemia due to glutathione metabolism disorder
  • Hereditary nonspherocytic hemolytic anemia (HNSHA) due to glutathione reductase deficiency (disorder)
  • Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency
  • HNSHA due to glutathione reductase deficiency
  • Leukocyte glucose-6-phosphate dehydrogenase deficiency
  • Muscle phosphofructokinase deficiency
  • Neonatal jaundice with glucose-6-phosphate dehydrogenase deficiency
  • Neutrophil lactoferrin deficiency
  • Pentose disorder
Applies To
  • Anemia:
    • 6-phosphogluconic dehydrogenase deficiency
    • enzyme deficiency, drug-induced
    • erythrocytic glutathione deficiency
    • glucose-6-phosphate dehydrogenase [G-6-PD] deficiency
    • glutathione-reductase deficiency
    • hemolytic nonspherocytic (hereditary), type I
  • Disorder of pentose phosphate pathway
  • Favism
ICD-9-CM Volume 2 Index entries containing back-references to 282.2:
  • Anemia 285.9
    • with
      • disorder of
        • anaerobic glycolysis 282.3
        • pentose phosphate pathway 282.2
      • koilonychia 280.9
    • 6-phosphogluconic dehydrogenase deficiency 282.2
    • autohemolysis of Selwyn and Dacie (type I) 282.2
    • Baghdad Spring 282.2
    • 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
        • type I 282.2
        • type II 282.3
      • pernicious 281.0
      • spherocytic (see also Spherocytosis) 282.0
    • Dacie's (nonspherocytic)
      • type I 282.2
      • type II 282.3
    • deficiency 281.9
      • 2, 3 diphosphoglycurate mutase 282.3
      • 2, 3 PG 282.3
      • 6-PGD 282.2
      • 6-phosphogluronic dehydrogenase 282.2
      • amino acid 281.4
      • combined B12 and folate 281.3
      • enzyme, drug-induced (hemolytic) 282.2
      • erythrocytic glutathione 282.2
      • folate 281.2
      • folic acid 281.2
      • G-6-PD 282.2
      • GGS-R 282.2
      • glucose-6-phosphate dehydrogenase (G-6-PD) 282.2
      • glucose-phosphate isomerase 282.3
      • glutathione peroxidase 282.2
      • glutathione reductase 282.2
      • glyceraldehyde phosphate dehydrogenase 282.3
      • GPI 282.3
      • G SH 282.2
      • hexokinase 282.3
      • iron (Fe) 280.9
      • nutritional 281.9
        • with
          • poor iron absorption 280.9
          • specified deficiency NEC 281.8
        • due to inadequate dietary iron intake 280.1
        • specified type NEC 281.8
      • of or complicating pregnancy 648.2
      • pentose phosphate pathway 282.2
      • PFK 282.3
      • phosphofructo-aldolase 282.3
      • phosphofructokinase 282.3
      • phosphoglycerate kinase 282.3
      • PK 282.3
      • protein 281.4
      • pyruvate kinase (PK) 282.3
      • TPI 282.3
      • triosephosphate isomerase 282.3
      • vitamin B12 NEC 281.1
    • due to
      • blood loss (chronic) 280.0
      • defect of Embden-Meyerhof pathway glycolysis 282.3
      • disorder of glutathione metabolism 282.2
      • drug - see Anemia, by type (see also Table of Drugs and Chemicals)
      • fetal blood loss 776.5
      • fish tapeworm (D. latum) infestation 123.4
      • glutathione metabolism disorder 282.2
      • hemorrhage (chronic) 280.0
      • hexose monophosphate (HMP) shunt deficiency 282.2
      • impaired absorption 280.9
      • loss of blood (chronic) 280.0
      • myxedema 244.9
      • Necator americanus 126.1
      • prematurity 776.6
      • selective vitamin B12 malabsorption with proteinuria 281.1
    • enzyme deficiency, drug-induced 282.2
    • erythrocytic glutathione deficiency 282.2
    • favism 282.2
    • G-6-PD 282.2
    • glucose-6-phosphate dehydrogenase deficiency 282.2
    • glutathione-reductase deficiency 282.2
    • 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
        • enzyme deficiency 282.2
      • due to
        • cardiac conditions 283.19
        • drugs 283.0
        • enzyme deficiency NEC 282.3
          • drug-induced 282.2
        • 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
        • congenital or hereditary NEC 282.3
          • glucose-6-phosphate dehydrogenase deficiency 282.2
          • pyruvate kinase (PK) deficiency 282.3
          • type I 282.2
          • type II 282.3
        • type I 282.2
        • type II 282.3
      • 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
    • pentose phosphate pathway deficiency 282.2
  • Deficiency, deficient
    • 6-phosphogluconic dehydrogenase (anemia) 282.2
    • erythrocytic glutathione (anemia) 282.2
    • glucose-6-phosphate dehydrogenase anemia 282.2
    • glutathione-reductase (anemia) 282.2
    • hexose monophosphate (HMP) shunt 282.2
  • Disorder - see also Disease
    • pentose phosphate pathway with anemia 282.2
  • Favism (anemia) 282.2
  • Poisoning (acute) - see also Table of Drugs and Chemicals
    • fava bean 282.2
  • Toxicity
    • fava bean 282.2
 282.1 ICD9Data.com 282.3 
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