Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)
D64.9 with (due to) (in)
disorder of
anaerobic glycolysis
D55.2 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 [D63.8] brickmaker's
B76.9 [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 [G32.0] due to dietary vitamin B12 deficiency
D51.3 [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
D55.2 2, 3 PG
D55.2 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
D55.2 nucleotide metabolism
D55.3 related to hexose monophosphate shunt pathway NEC (HMP)
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
D55.2 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 phosphofructo-aldolase
D55.2 phosphoglycerate kinase
D55.2 PK
D55.2 protein
D53.0 pyruvate kinase
D55.2 transcobalamin II
D51.2 triose-phosphate isomerase
D55.2 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 [D63.8] dimorphic
D53.1 diphasic
D53.1 Diphyllobothrium (Dibothriocephalus)
B70.0 [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 infestation (D.latum)
B70.0 [D63.8] hemorrhage (chronic)
D50.0 acute
D62 impaired absorption
D50.9 loss of blood (chronic)
D50.0 acute
D62 myxedema
E03.9 [D63.8] Necator americanus
B76.1 [D63.8] prematurity
P61.2 selective vitamin B12 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 Elliptocytosis enzyme-deficiency, drug-induced
D59.2 epidemic --see also Ancylostomiasis
B76.9 [D63.8] erythroblastic
familial
D56.1 newborn --see also Disease, hemolytic
P55.9 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 (congenital pancytopenia)
D61.09 favism
D55.0 fish tapeworm infestation (D. latum)
B70.0 [D63.8] folate deficiency (folic acid)
D52.9 glucose-6-phosphate dehydrogenase deficiency (G6PD)
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
D59.1 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
D59.1 autoimmune
D59.1 drug-induced
D59.0 chronic
D58.9 idiopathic
D59.9 cold type (secondary) (symptomatic)
D59.1 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 familial
D58.9 hereditary
D58.9 due to enzyme disorder
D55.9 specified type NEC
D55.8 specified type NEC
D58.8 idiopathic (chronic)
D59.9 mechanical
D59.4 microangiopathic
D59.4 nonautoimmune
D59.4 drug-induced
D59.2 nonspherocytic
congenital or hereditary NEC
D55.8 glucose-6-phosphate dehydrogenase deficiency
D55.0 pyruvate kinase deficiency
D55.2 type
I
D55.1 II
D55.2 type
I
D55.1 II
D55.2 secondary
D59.4 autoimmune
D59.1 specified type NEC (hereditary)
D58.8 Stransky-Regala type --see also Hemoglobinopathy
D58.8 symptomatic
D59.4 autoimmune
D59.1 toxic
D59.4 warm type (secondary) (symptomatic)
D59.1 hemorrhagic (chronic)
D50.0 acute
D62 Herrick's
D57.1 hexokinase deficiency
D55.2 hookworm
B76.9 [D63.8] hypochromic (idiopathic) (microcytic) (normoblastic)
D50.9 due to blood loss (chronic)
D50.0 acute
D62 familial sex-linked
D64.0 pyridoxine-responsive
D64.3 sideroblastic, sex-linked
D64.0 hypoplasia, red blood cells
D61.9 congenital or familial
D61.01 hypoplastic (idiopathic)
D61.9 congenital or familial (of childhood)
D61.01 hypoproliferative (refractive)
D61.9 idiopathic
D64.9 aplastic
D61.3 hemolytic, chronic
D59.9 in (due to) (with)
chronic kidney disease
D63.1 end stage renal disease
D63.1 failure, kidney (renal)
D63.1 neoplastic disease --see also Neoplasm
D63.0 intertropical --see also Ancylostomiasis
D63.8 iron deficiency
D50.9 secondary to blood loss (chronic)
D50.0 acute
D62 specified type NEC
D50.8 Joseph-Diamond-Blackfan (congenital hypoplastic)
D61.01 Lederer's (hemolytic)
D59.1 leukoerythroblastic
D61.82 macrocytic
D53.9 nutritional
D52.0 tropical
D52.8 malarial --see also Malaria
B54 [D63.8] malignant (progressive)
D51.0 malnutrition
D53.9 marsh --see also Malaria
B54 [D63.8] Mediterranean (with other hemoglobinopathy)
D56.9 megaloblastic
D53.1 combined B12 and folate deficiency
D53.1 hereditary
D51.1 nutritional
D52.0 orotic aciduria
D53.0 refractory
D53.1 specified type NEC
D53.1 megalocytic
D53.1 microcytic (hypochromic)
D50.9 due to blood loss (chronic)
D50.0 acute
D62 familial
D56.8 microdrepanocytosis
D57.40 microelliptopoikilocytic (Rietti-Greppi- Micheli)
D56.9 miner's
B76.9 [D63.8] myelodysplastic
D46.9 myelofibrosis
D75.81 myelogenous
D64.89 myelopathic
D64.89 myelophthisic
D61.82 myeloproliferative
D47.Z9 newborn
P61.4 due to
ABO (antibodies, isoimmunization, maternal/fetal incompatibility)
P55.1 Rh (antibodies, isoimmunization, maternal/fetal incompatibility)
P55.0 following fetal blood loss
P61.3 posthemorrhagic (fetal)
P61.3 nonspherocytic hemolytic
--see Anemia, hemolytic, nonspherocytic normocytic (infectional)
D64.9 due to blood loss (chronic)
D50.0 acute
D62 myelophthisic
D61.82 nutritional (deficiency)
D53.9 with
poor iron absorption
D50.8 specified deficiency NEC
D53.8 megaloblastic
D52.0 of prematurity
P61.2 orotaciduric (congenital) (hereditary)
D53.0 osteosclerotic
D64.89 ovalocytosis (hereditary)
--see Elliptocytosis paludal --see also Malaria
B54 [D63.8] pernicious (congenital) (malignant) (progressive)
D51.0 pleochromic
D64.89 of sprue
D52.8 posthemorrhagic (chronic)
D50.0 acute
D62 newborn
P61.3 postoperative (postprocedural)
due to blood loss (acute)
D62 chronic blood loss
D50.0 specified NEC
D64.9 postpartum
O90.81 pressure
D64.89 progressive
D64.9 malignant
D51.0 pernicious
D51.0 protein-deficiency
D53.0 pseudoleukemica infantum
D64.89 pure red cell
D60.9 congenital
D61.01 pyridoxine-responsive
D64.3 pyruvate kinase deficiency
D55.2 refractory
D46.4 with
excess of blasts
D46.20 1 (RAEB 1)
D46.21 2 (RAEB 2)
D46.22 in transformation (RAEB T)
--see Leukemia, acute myeloblastic hemochromatosis
D46.1 sideroblasts (ring) (RARS)
D46.1 megaloblastic
D53.1 sideroblastic
D46.1 sideropenic
D50.9 without ring sideroblasts, so stated
D46.0 without sideroblasts without excess of blasts
D46.0 Rietti-Greppi-Micheli
D56.9 scorbutic
D53.2 secondary to
blood loss (chronic)
D50.0 acute
D62 hemorrhage (chronic)
D50.0 acute
D62 semiplastic
D61.89 sickle-cell --see Disease, sickle-cell
sideroblastic
D64.3 hereditary
D64.0 hypochromic, sex-linked
D64.0 pyridoxine-responsive NEC
D64.3 refractory
D46.1 secondary (due to)
disease
D64.1 drugs and toxins
D64.2 specified type NEC
D64.3 sideropenic (refractory)
D50.9 due to blood loss (chronic)
D50.0 acute
D62 simple chronic
D53.9 specified type NEC
D64.89 spherocytic (hereditary)
--see Spherocytosis splenic
D64.89 splenomegalic
D64.89 stomatocytosis
D58.8 syphilitic (acquired) (late)
A52.79 [D63.8] target cell
D64.89 thalassemia
D56.9 thrombocytopenic
--see Thrombocytopenia toxic
D61.2 tropical
B76.9 [D63.8] macrocytic
D52.8 tuberculous
A18.89 [D63.8] vegan
D51.3 vitamin
B6-responsive
D64.3 B12 deficiency pernicious (dietary)
D51.0 von Jaksch's
D64.89 Witts' (achlorhydric anemia)
D50.8