ICD-10-CM Alphabetic Index to Diseases and Injuries

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

Default code: D64.9. Follow the subterms below to reach a more specific code.

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
brickmaker's B76.9
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
due to dietary vitamin B12 deficiency D51.3
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
dimorphic D53.1
diphasic D53.1
Diphyllobothrium (Dibothriocephalus) B70.0
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
hemorrhage (chronic) D50.0
acute D62
impaired absorption D50.9
loss of blood (chronic) D50.0
acute D62
myxedema E03.9
Necator americanus B76.1
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
elliptocytosis — see Elliptocytosis
enzyme-deficiency, drug-induced D59.2
epidemic B76.9 — see also Ancylostomiasis
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
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
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
mixed type (primary) (secondary) (symptomatic) D59.13
nonautoimmune D59.4
drug-induced D59.2
nonspherocytic
congenital or hereditary NEC D55.8
glucose-6-phosphate dehydrogenase deficiency D55.0
pyruvate kinase deficiency D55.21
type
I D55.1
II D55.29
type
I D55.1
II D55.29
primary
autoimmune
cold type D59.12
mixed type D59.13
warm type D59.11
secondary D59.4
autoimmune
cold type D59.12
mixed type D59.13
warm type D59.11
specified (hereditary) type NEC D58.8
Stransky-Regala type D58.8 — see also Hemoglobinopathy
symptomatic D59.4
autoimmune
cold type D59.12
mixed type D59.13
warm type D59.11
toxic D59.4
warm type (primary) (secondary) (symptomatic) D59.11
hemorrhagic (chronic) D50.0
acute D62
Herrick's D57.1
hexokinase deficiency D55.29
hookworm B76.9
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 D63.0 — see also Neoplasm
intertropical D63.8 — see also Ancylostomiasis
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) D59.19
leukoerythroblastic D61.82
macrocytic D53.9
nutritional D52.0
tropical D52.8
malarial B54 — see also Malaria
malignant (progressive) D51.0
malnutrition D53.9
marsh B54 — see also Malaria
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
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 B54 — see also Malaria
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 (acute) blood loss D62
chronic blood loss D50.0
specified NEC D64.89
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 D55.21
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
target cell D64.89
thalassemia D56.9
thrombocytopenic — see Thrombocytopenia
toxic D61.2
tropical B76.9
macrocytic D52.8
tuberculous A18.89
vegan D51.3
vitamin
B6-responsive D64.3
B12 deficiency (dietary) pernicious D51.0
von Jaksch's D64.89
Witts' (achlorhydric anemia) D50.8