
2007 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 2007 version of ICD-9-CM 282.2.
- More recent version(s) of ICD-9-CM 282.2: 2008 2009 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
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

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

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