282.2 GLUTATHIONE DIS ANEMIA


Code Information

Diagnosis Code: 282.2

Short Description: Glutathione dis anemia

Long Description: Anemias due to disorders of glutathione metabolism

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
        • 282.2 Glutathione dis anemia

Code Version: 2015 ICD-9-CM


Synonyms

  • Anemia due to pentose phosphate pathway defect
  • Drug-induced enzyme deficiency anemia
  • Erythrocyte enzyme deficiency
  • Erythrocyte uridine diphosphate galactose-4-epimerase deficiency
  • Favism
  • Glucose phosphate isomerase deficiency
  • Glucose-6-phosphate dehydrogenase deficiency anemia
  • Glucose-6-phosphate dehydrogenase deficiency class I variant anemia
  • Glucose-6-phosphate dehydrogenase deficiency class II variant anemia
  • Glucose-6-phosphate dehydrogenase deficiency class III variant anemia
  • Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia
  • Glucose-6-phosphate dehydrogenase deficiency class V variant anemia
  • Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia
  • Glutathione synthase deficiency without 5-oxoprolinuria
  • Glutathione synthetase deficiency
  • Gluthathione peroxidase deficiency
  • Hemolytic anemia due to glutathione metabolism disorder
  • Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency
  • Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency
  • Leukocyte glucose-6-phosphate dehydrogenase deficiency
  • Muscle phosphofructokinase deficiency
  • Neonatal jaundice with glucose-6-phosphate dehydrogenase deficiency
  • Neutrophil lactoferrin deficiency
  • Pentose disorder

References to Index of Diseases and Injuries

The code 282.2 has the following ICD-9-CM references to the Index of Diseases and Injuries
  • Anemia 285.9
    • with
      • disorder of
        • pentose phosphate pathway 282.2
    • 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
      • nonspherocytic
        • type I 282.2
    • Dacie's (nonspherocytic)
      • type I 282.2
    • deficiency 281.9
      • 6-PGD 282.2
      • 6-phosphogluronic dehydrogenase 282.2
      • enzyme, drug-induced (hemolytic) 282.2
      • erythrocytic glutathione 282.2
      • G-6-PD 282.2
      • GGS-R 282.2
      • glucose-6-phosphate dehydrogenase (G-6-PD) 282.2
      • glutathione peroxidase 282.2
      • glutathione reductase 282.2
      • G SH 282.2
      • pentose phosphate pathway 282.2
    • due to
      • disorder of glutathione metabolism 282.2
      • glutathione metabolism disorder 282.2
      • hexose monophosphate (HMP) shunt deficiency 282.2
    • 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
      • drug-induced 283.0
        • enzyme deficiency 282.2
      • due to
        • enzyme deficiency NEC 282.3
          • drug-induced 282.2
      • nonspherocytic
        • congenital or hereditary NEC 282.3
          • glucose-6-phosphate dehydrogenase deficiency 282.2
          • type I 282.2
        • type I 282.2
    • 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
  • Jaundice (yellow) 782.4
    • fetus or newborn 774.6
      • due to or associated with
        • G-6-PD deficiency 282.2 [774.0]
  • Maldescent, testis 752.51
  • Microstomia (congenital) 744.84
  • Poisoning (acute) - see also Table of Drugs and Chemicals
    • fava bean 282.2
  • Toxicity
    • fava bean 282.2

Crosswalk Information

The code 282.2 converts into the following ICD-10 code(s):
ICD-9 Code ICD-10 Code ICD-10 Description
282.2 Right Arrow D55.0 Anemia due to glucose-6-phosphate dehydrogenase deficiency
D55.1 Anemia due to other disorders of glutathione metabolism
This ICD-9 to ICD-10 data is based on the 2018 General Equivalency Mapping (GEM) files published by the Centers for Medicare & Medicaid Services (CMS) for informational purposes only. The data is not an ICD-10 conversion tool and doesn’t guarantee clinical accuracy.

Similar Codes

ICD-9 Code ICD-9 Description
282.0 Hereditary spherocytosis
282.1 Hereditary elliptocytosis
282.3 Other hemolytic anemias due to enzyme deficiency
282.40 Thalassemia, unspecified
282.41 Sickle-cell thalassemia without crisis
282.42 Sickle-cell thalassemia with crisis
282.43 Alpha thalassemia
282.44 Beta thalassemia
282.45 Delta-beta thalassemia
282.46 Thalassemia minor
282.47 Hemoglobin E-beta thalassemia
282.49 Other thalassemia
282.5 Sickle-cell trait
282.60 Sickle-cell disease, unspecified
282.61 Hb-SS disease without crisis
282.62 Hb-SS disease with crisis
282.63 Sickle-cell/Hb-C disease without crisis
282.64 Sickle-cell/Hb-C disease with crisis
282.68 Other sickle-cell disease without crisis
282.69 Other sickle-cell disease with crisis
282.7 Other hemoglobinopathies
282.8 Other specified hereditary hemolytic anemias
282.9 Hereditary hemolytic anemia, unspecified


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