Certain infectious and parasitic diseases

WHO’s ICD-10 version for 2007
Anemia-------continued
- complicating pregnancy, childbirth or
puerperium O99.0
- congenital P61.4
- - due to isoimmunization NEC P55.9
- - dyserythropoietic, dyshematopoietic D64.4
- - following fetal blood loss P61.3
- - Heinz body D58.2
- - hereditary hemolytic NEC D58.9
- Cooley's (erythroblastic) D56.1
- deficiency D53.9
- - amino-acid D53.0
- - 2,3-diphosphoglycerate mutase (2,3-PG)
D55.2
- - enzyme D55.9
- - - drug-induced (hemolytic) D59.2
- - - glucose-6-phosphate dehydrogenase
(G6PD) D55.0
- - - glycolytic D55.2
- - - nucleotide metabolism D55.3
- - - related to hexose monophosphate (HMP)
shunt pathway NEC D55.1
- - - specified type NEC D55.8
- - erythrocytic glutathione D55.1
- - folate D52.9
- - - dietary D52.0
- - - drug-induced D52.1
- - folic acid D52.9
- - - dietary D52.0
- - - drug-induced D52.1
- - GSH D55.1
- - GGS-R D55.1
- - glucose-6-phosphate dehydrogenase
(G6PD) D55.0
- - glutathione reductase (GGS-R) D55.1
- - glyceraldehyde phosphate dehydrogenase D55.2
- - G6PD D55.0
- - hexokinase D55.2
- - iron D50.9
- - - secondary to blood loss (chronic) D50.0
- - nutritional D53.9
- - - with
- - - - poor iron absorption D50.8
- - - - specified deficiency NEC D53.8
- - 2,3-PG D55.2
- - 6-PGD D55.1
- - phosphofructo-aldolase D55.2
- - 6-phosphogluconate dehydrogenase (6-
PGD) D55.1
- - phosphoglycerate kinase (PK) D55.2
- - PK D55.2
- - protein D53.0
- - pyruvate kinase D55.2
- - transcobalamin II D51.2
- - triose-phosphate isomerase D55.2
- - vitamin B 12 D51.9
- - - dietary D51.3
- - - due to
Anemia-------continued
- - - - intrinsic factor deficiency D51.0
- - - - selective vitamin B 12 malabsorption
with proteinuria D51.1
- - - specified type NEC D51.8
- Diamond-Blackfan D61.0
- dimorphic D53.1
- diphasic D53.1
- Diphyllobothrium (Dibothriocephalus)
B70.0† D63.8*
- drepanocytic (see also Disease, sickle-cell) D57.1
- due to
- - deficiency
- - - amino-acid D53.0
- - - copper D53.8
- - - folate (folic acid) D52.9
- - - - dietary D52.0
- - - - drug-induced D52.1
- - - molybdenum D53.8
- - - protein D53.0
- - - zinc D53.8
- - dietary vitamin B 12 deficiency D51.3
- - disorder of
- - - glutathione metabolism D55.1
- - - nucleotide metabolism D55.3
- - enzyme disorder D55.9
- - fetal blood loss P61.3
- - hemorrhage (chronic) D50.0
- - - acute D62
- - loss of blood (chronic) D50.0
- - - acute D62
- - myxedema E03.9† D63.8*
- - prematurity P61.2
- - selective vitamin B 12 malabsorption
with proteinuria D51.1
- - transcobalamin II deficiency D51.2
- Dyke-Young type (secondary) (symptomatic)
D59.1
- dyserythropoietic (congenital) D64.4
- dyshematopoietic (congenital) D64.4
- Egyptian B76.9† D63.8*
- elliptocytosis (see also Elliptocytosis) D58.1
- enzyme-deficiency, drug-induced D59.2
- erythroblastic
- - familial D56.1
- - fetus or newborn (see also Disease,
hemolytic) P55.9
- - of childhood D56.1
- erythrocytic glutathione deficiency D55.1
- essential D64.9
- familial erythroblastic D56.1
- Fanconi's D61.0
- favism D55.0
- fetus or newborn P61.4
- - due to
- - - ABO (antibodies) (isoimmunization)
(maternal/fetal incompatibility) P55.1
- - - Rh (antibodies) (isoimmunization)
(maternal/fetal incompatibility) P55.0
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