2010 ICD-9-CM Diagnosis Code 282.3
Other hemolytic anemias due to enzyme deficiency
- Short description: Enzyme defic anemia NEC.
- ICD-9-CM 282.3 is a billable medical code that can be used to indicate a diagnosis on a reimbursement claim, however, 282.3 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 2010 version of ICD-9-CM 282.3.
- More recent version(s) of ICD-9-CM 282.3: 2011 2012 2013 2014 2015.
Convert to ICD-10-CM:
282.3 converts approximately to:
- 2015/16 ICD-10-CM D55.8 Other anemias due to enzyme disorders
Approximate Synonyms
- Anemia due to disorders of glycolytic enzymes
- Anemia due to disorders of nucleotide metabolism
- Anemia due to enzyme deficiency
- Anemia due to enzyme disorder
- Chronic non-spherocytic hemolytic anemia
- Deficiency of pyruvate kinase
- Fumarase deficiency
- Hemolytic anemia due to enzyme deficiency
- Hemolytic anemia due to hexokinase deficiency
- Hemolytic anemia due to pyruvate kinase deficiency
- Hemolytic anemia due to triose phosphate isomerase deficiency
- Hereditary nonspherocytic hemolytic anemia
- Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency
- Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity
- Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency
- Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency
- Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency
- Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity
- Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency
- Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency
- Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency
- Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency
- Triose phosphate isomerase deficiency
Applies To
- Anemia:
- hemolytic nonspherocytic (hereditary), type II
- hexokinase deficiency
- pyruvate kinase [PK] deficiency
- triosephosphate isomerase deficiency
ICD-9-CM Volume 2 Index entries containing back-references to
282.3:
- Anemia 285.9
with
disorder of- anaerobic glycolysis 282.3
pentose phosphate pathway 282.2
- koilonychia 280.9
- 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
- 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
- antineoplastic chemotherapy 285.3
- blood loss (chronic) 280.0
- chemotherapy, antineoplastic 285.3
- 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)
- chemotherapy, antineoplastic 285.3
- 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
- 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
- hexokinase deficiency 282.3
- pyruvate kinase (PK) deficiency 282.3
- triosephosphate isomerase deficiency 282.3
- Deficiency, deficient
- pyruvate kinase (PK) 282.3
- Disorder - see also Disease
- anaerobic glycolysis with anemia 282.3
