Anemia(essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)

Anemia(essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)

D64.9

with(due to) (in)

disorder of

anaerobic glycolysis

D55.29

pentose phosphate pathway

D55.1

koilonychia

D50.9

achlorhydric

D50.8

achrestic

D53.1

Addison(-Biermer) (pernicious)

D51.0

agranulocytic

See: Agranulocytosis

amino-acid-deficiency

D53.0

aplastic

D61.9

congenital

D61.09

drug-induced

D61.1

due to

drugs

D61.1

external agents NEC

D61.2

infection

D61.2

radiation

D61.2

idiopathic

D61.3

red cell(pure)

D60.9

chronic

D60.0

congenital

D61.01

specified type NEC

D60.8

transient

D60.1

specified type NEC

D61.89

toxic

D61.2

aregenerative

congenital

D61.09

asiderotic

D50.9

atypical(primary)

D64.9

Baghdad spring

D55.0

Balantidium coli

A07.0

Biermer's(pernicious)

D51.0

blood loss(chronic)

D50.0

acute

D62

bothriocephalus

B70.0

Manifestation: D63.8

brickmaker's

B76.9

Manifestation: D63.8

cerebral

I67.89

childhood

D58.9

chlorotic

D50.8

chronic

blood loss

D50.0

hemolytic

D58.9

idiopathic

D59.9

simple

D53.9

chronica congenita aregenerativa

D61.09

combined system disease NEC

D51.0

Manifestation: G32.0

due to dietary vitamin B12 deficiency

D51.3

Manifestation: G32.0

complicating pregnancy, childbirth or puerperium

See: Pregnancy, complicated by (management affected by), anemia

congenital

P61.4

aplastic

D61.09

due to isoimmunization NOS

P55.9

dyserythropoietic, dyshematopoietic

D64.4

following fetal blood loss

P61.3

Heinz body

D58.2

hereditary hemolytic NOS

D58.9

pernicious

D51.0

spherocytic

D58.0

Cooley's(erythroblastic)

D56.1

cytogenic

D51.0

deficiency

D53.9

2, 3 diphosphoglycurate mutase

D55.29

2, 3 PG

D55.29

6 phosphogluconate dehydrogenase

D55.1

6-PGD

D55.1

amino-acid

D53.0

combined B12 and folate

D53.1

enzyme

D55.9

drug-induced(hemolytic)

D59.2

glucose-6-phosphate dehydrogenase(G6PD)

D55.0

glycolytic

D55.29

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

G SH

D55.1

GGS-R

D55.1

glucose-6-phosphate dehydrogenase

D55.0

glutathione reductase

D55.1

glyceraldehyde phosphate dehydrogenase

D55.29

G6PD

D55.0

hexokinase

D55.29

iron

D50.9

secondary to blood loss(chronic)

D50.0

nutritional

D53.9

with

poor iron absorption

D50.8

specified deficiency NEC

D53.8

phosphofructo-aldolase

D55.29

phosphoglycerate kinase

D55.29

PK

D55.21

protein

D53.0

pyruvate kinase

D55.21

transcobalamin II

D51.2

triose-phosphate isomerase

D55.29

vitamin B12 NOS

D51.9

dietary

D51.3

due to

intrinsic factor deficiency

D51.0

selective vitamin B12 malabsorption with proteinuria

D51.1

pernicious

D51.0

specified type NEC

D51.8

Diamond-Blackfan(congenital hypoplastic)

D61.01

dibothriocephalus

B70.0

Manifestation: D63.8

dimorphic

D53.1

diphasic

D53.1

Diphyllobothrium(Dibothriocephalus)

B70.0

Manifestation: D63.8

due to(in) (with)

antineoplastic chemotherapy

D64.81

blood loss(chronic)

D50.0

acute

D62

chemotherapy, antineoplastic

D64.81

chronic disease classified elsewhere NEC

D63.8

chronic kidney disease

D63.1

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 B12 deficiency

D51.3

disorder of

glutathione metabolism

D55.1

nucleotide metabolism

D55.3

drug

See: Anemia, by type

See also: Table of Drugs and Chemicals

end stage renal disease

D63.1

enzyme disorder

D55.9

fetal blood loss

P61.3

fish tapeworm(D. latum) infestation

B70.0

Manifestation: D63.8

hemorrhage(chronic)

D50.0

acute

D62

impaired absorption

D50.9

loss of blood(chronic)

D50.0

acute

D62

myxedema

E03.9

Manifestation: D63.8

Necator americanus

B76.1

Manifestation: D63.8

prematurity

P61.2

selective vitamin B12 malabsorption with proteinuria

D51.1

transcobalamin II deficiency

D51.2

Dyke-Young type(secondary) (symptomatic)

D59.19

dyserythropoietic(congenital)

D64.4

dyshematopoietic(congenital)

D64.4

Egyptian

B76.9

Manifestation: D63.8

elliptocytosis

See: Elliptocytosis

enzyme-deficiency, drug-induced

D59.2

epidemic

B76.9

See also: Ancylostomiasis

Manifestation: D63.8

erythroblastic

familial

D56.1

newborn

P55.9

See also: Disease, hemolytic

of childhood

D56.1

erythrocytic glutathione deficiency

D55.1

erythropoietin-resistant anemia(EPO resistant anemia)

D63.1

Faber's(achlorhydric anemia)

D50.9

factitious(self-induced blood letting)

D50.0

familial erythroblastic

D56.1

Fanconi('s)

D61.03

favism

D55.0

fish tapeworm(D. latum) infestation

B70.0

Manifestation: D63.8

folate(folic acid) deficiency

D52.9

glucose-6-phosphate dehydrogenase(G6PD) deficiency

D55.0

glutathione-reductase deficiency

D55.1

goat's milk

D52.0

granulocytic

See: Agranulocytosis

Heinz body, congenital

D58.2

hemolytic

D58.9

acquired

D59.9

with hemoglobinuria NEC

D59.6

autoimmune NEC

D59.19

infectious

D59.4

specified type NEC

D59.8

toxic

D59.4

acute

D59.9

due to enzyme deficiency specified type NEC

D55.8

Lederer's

D59.19

autoimmune

D59.10

cold

D59.12

drug-induced

D59.0

mixed

D59.13

warm

D59.11

chronic

D58.9

idiopathic

D59.9

cold type(primary) (secondary) (symptomatic)

D59.12

congenital(spherocytic)

See: Spherocytosis

due to

cardiac conditions

D59.4

drugs(nonautoimmune)

D59.2

autoimmune

D59.0

enzyme disorder

D55.9

drug-induced

D59.2

presence of shunt or other internal prosthetic device

D59.4