Alphabetic Index · main term

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

FY2027Index: An /Alphabetic Index

At the main termD64.9

Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound) is a main term in the FY2027 ICD-10-CM Alphabetic Index (Index to Diseases and Injuries). The Index lists D64.9 for the term on its own. It has 396 subterms and 358 code entries. First-level subterms include with, achlorhydric, achrestic, Addison, agranulocytic, amino-acid-deficiency, aplastic, aregenerative and more. Confirm any code you find here in the Tabular List before you report it.

Subterms 396

with (due to) (in)
- disorder of
  - anaerobic glycolysisD55.29
  - pentose phosphate pathwayD55.1
- koilonychiaD50.9
achlorhydricD50.8
achresticD53.1
Addison (-Biermer) (pernicious)D51.0
agranulocytic see Agranulocytosis
amino-acid-deficiencyD53.0
aplasticD61.9
- congenitalD61.09
- drug-inducedD61.1
- due to
  - drugsD61.1
  - external agents NECD61.2
  - infectionD61.2
  - radiationD61.2
- idiopathicD61.3
- red cell (pure)D60.9
  - chronicD60.0
  - congenitalD61.01
  - specified type NECD60.8
  - transientD60.1
- specified type NECD61.89
- toxicD61.2
aregenerative
- congenitalD61.09
asideroticD50.9
atypical (primary)D64.9
Baghdad springD55.0
Balantidium coliA07.0
Biermer's (pernicious)D51.0
blood loss (chronic)D50.0
- acuteD62
bothriocephalusB70.0[D63.8]
brickmaker'sB76.9[D63.8]
cerebralI67.89
childhoodD58.9
chloroticD50.8
chronic
- blood lossD50.0
- hemolyticD58.9
  - idiopathicD59.9
- simpleD53.9
chronica congenita aregenerativaD61.09
combined system disease NECD51.0[G32.0]
- due to dietary vitamin B12 deficiencyD51.3[G32.0]
complicating pregnancy, childbirth or puerperium see Pregnancy, complicated by (management affected by), anemia
congenitalP61.4
- aplasticD61.09
- due to isoimmunization NOSP55.9
- dyserythropoietic, dyshematopoieticD64.4
- following fetal blood lossP61.3
- Heinz bodyD58.2
- hereditary hemolytic NOSD58.9
- perniciousD51.0
- spherocyticD58.0
Cooley's (erythroblastic)D56.1
cytogenicD51.0
deficiencyD53.9
- 2, 3 diphosphoglycurate mutaseD55.29
- 2, 3 PGD55.29
- 6 phosphogluconate dehydrogenaseD55.1
- 6-PGDD55.1
- amino-acidD53.0
- combined B12 and folateD53.1
- enzymeD55.9
  - drug-induced (hemolytic)D59.2
  - glucose-6-phosphate dehydrogenase (G6PD)D55.0
  - glycolyticD55.29
  - nucleotide metabolismD55.3
  - related to hexose monophosphate (HMP) shunt pathway NECD55.1
  - specified type NECD55.8
- erythrocytic glutathioneD55.1
- folateD52.9
  - dietaryD52.0
  - drug-inducedD52.1
- folic acidD52.9
  - dietaryD52.0
  - drug-inducedD52.1
- G SHD55.1
- GGS-RD55.1
- glucose-6-phosphate dehydrogenaseD55.0
- glutathione reductaseD55.1
- glyceraldehyde phosphate dehydrogenaseD55.29
- G6PDD55.0
- hexokinaseD55.29
- ironD50.9
  - secondary to blood loss (chronic)D50.0
- nutritionalD53.9
  - with
    poor iron absorptionD50.8
    specified deficiency NECD53.8
- phosphofructo-aldolaseD55.29
- phosphoglycerate kinaseD55.29
- PKD55.21
- proteinD53.0
- pyruvate kinaseD55.21
- transcobalamin IID51.2
- triose-phosphate isomeraseD55.29
- vitamin B12 NOSD51.9
  - dietaryD51.3
  - due to
    intrinsic factor deficiencyD51.0
    selective vitamin B12 malabsorption with proteinuriaD51.1
  - perniciousD51.0
  - specified type NECD51.8
Diamond-Blackfan (congenital hypoplastic)D61.01
dibothriocephalusB70.0[D63.8]
dimorphicD53.1
diphasicD53.1
Diphyllobothrium (Dibothriocephalus)B70.0[D63.8]
due to (in) (with)
- antineoplastic chemotherapyD64.81
- blood loss (chronic)D50.0
  - acuteD62
- chemotherapy, antineoplasticD64.81
- chronic disease classified elsewhere NECD63.8
- chronic kidney diseaseD63.1
- deficiency
  - amino-acidD53.0
  - copperD53.8
  - folate (folic acid)D52.9
    dietaryD52.0
    drug-inducedD52.1
  - molybdenumD53.8
  - proteinD53.0
  - zincD53.8
- dietary vitamin B12 deficiencyD51.3
- disorder of
  - glutathione metabolismD55.1
  - nucleotide metabolismD55.3
- drug see Anemia, by type · see also Table of Drugs and Chemicals
- end stage renal diseaseD63.1
- enzyme disorderD55.9
- fetal blood lossP61.3
- fish tapeworm (D. latum) infestationB70.0[D63.8]
- hemorrhage (chronic)D50.0
  - acuteD62
- impaired absorptionD50.9
- loss of blood (chronic)D50.0
  - acuteD62
- myxedemaE03.9[D63.8]
- Necator americanusB76.1[D63.8]
- prematurityP61.2
- selective vitamin B12 malabsorption with proteinuriaD51.1
- transcobalamin II deficiencyD51.2
Dyke-Young type (secondary) (symptomatic)D59.19
dyserythropoietic (congenital)D64.4
dyshematopoietic (congenital)D64.4
EgyptianB76.9[D63.8]
elliptocytosis see Elliptocytosis
enzyme-deficiency, drug-inducedD59.2
epidemic see also AncylostomiasisB76.9[D63.8]
erythroblastic
- familialD56.1
- newborn see also Disease, hemolyticP55.9
- of childhoodD56.1
erythrocytic glutathione deficiencyD55.1
erythropoietin-resistant anemia (EPO resistant anemia)D63.1
Faber's (achlorhydric anemia)D50.9
factitious (self-induced blood letting)D50.0
familial erythroblasticD56.1
Fanconi ('s)D61.03
favismD55.0
fish tapeworm (D. latum) infestationB70.0[D63.8]
folate (folic acid) deficiencyD52.9
glucose-6-phosphate dehydrogenase (G6PD) deficiencyD55.0
glutathione-reductase deficiencyD55.1
goat's milkD52.0
granulocytic see Agranulocytosis
Heinz body, congenitalD58.2
hemolyticD58.9
- acquiredD59.9
  - with hemoglobinuria NECD59.6
  - autoimmune NECD59.19
  - infectiousD59.4
  - specified type NECD59.8
  - toxicD59.4
- acuteD59.9
  - due to enzyme deficiency specified type NECD55.8
  - Lederer'sD59.19
- autoimmuneD59.10
  - coldD59.12
  - drug-inducedD59.0
  - mixedD59.13
  - warmD59.11
- chronicD58.9
  - idiopathicD59.9
- cold type (primary) (secondary) (symptomatic)D59.12
- congenital (spherocytic) see Spherocytosis
- due to
  - cardiac conditionsD59.4
  - drugs (nonautoimmune)D59.2
    autoimmuneD59.0
  - enzyme disorderD55.9
    drug-inducedD59.2
  - presence of shunt or other internal prosthetic deviceD59.4
- familialD58.9
- hereditaryD58.9
  - due to enzyme disorderD55.9
    specified type NECD55.8
  - specified type NECD58.8
- idiopathic (chronic)D59.9
- mechanicalD59.4
- microangiopathicD59.4
- mixed type (primary) (secondary) (symptomatic)D59.13
- nonautoimmuneD59.4
  - drug-inducedD59.2
- nonspherocytic
  - congenital or hereditary NECD55.8
    glucose-6-phosphate dehydrogenase deficiencyD55.0
    pyruvate kinase deficiencyD55.21
    type
    ID55.1
    IID55.29
  - type
    ID55.1
    IID55.29
- primary
  - autoimmune
    cold typeD59.12
    mixed typeD59.13
    warm typeD59.11
- secondaryD59.4
  - autoimmune
    cold typeD59.12
    mixed typeD59.13
    warm typeD59.11
- specified (hereditary) type NECD58.8
- Stransky-Regala type see also HemoglobinopathyD58.8
- symptomaticD59.4
  - autoimmune
    cold typeD59.12
    mixed typeD59.13
    warm typeD59.11
- toxicD59.4
- warm type (primary) (secondary) (symptomatic)D59.11
hemorrhagic (chronic)D50.0
- acuteD62
Herrick'sD57.1
hexokinase deficiencyD55.29
hookwormB76.9[D63.8]
hypochromic (idiopathic) (microcytic) (normoblastic)D50.9
- due to blood loss (chronic)D50.0
  - acuteD62
- familial sex-linkedD64.0
- pyridoxine-responsiveD64.3
- sideroblastic, sex-linkedD64.0
hypoplasia, red blood cellsD61.9
- congenital or familialD61.01
hypoplastic (idiopathic)D61.9
- congenital or familial (of childhood)D61.01
hypoproliferative (refractive)D61.9
idiopathicD64.9
- aplasticD61.3
- hemolytic, chronicD59.9
in (due to) (with)
- chronic kidney diseaseD63.1
- end stage renal diseaseD63.1
- failure, kidney (renal)D63.1
- neoplastic disease see also NeoplasmD63.0
intertropical see also AncylostomiasisD63.8
iron deficiencyD50.9
- secondary to blood loss (chronic)D50.0
  - acuteD62
- specified type NECD50.8
Joseph-Diamond-Blackfan (congenital hypoplastic)D61.01
Lederer's (hemolytic)D59.19
leukoerythroblasticD61.82
macrocyticD53.9
- nutritionalD52.0
- tropicalD52.8
malarial see also MalariaB54[D63.8]
malignant (progressive)D51.0
malnutritionD53.9
marsh see also MalariaB54[D63.8]
Mediterranean (with other hemoglobinopathy)D56.9
megaloblasticD53.1
- combined B12 and folate deficiencyD53.1
- hereditaryD51.1
- nutritionalD52.0
- orotic aciduriaD53.0
- refractoryD53.1
- specified type NECD53.1
megalocyticD53.1
microcytic (hypochromic)D50.9
- due to blood loss (chronic)D50.0
  - acuteD62
- familialD56.8
microdrepanocytosisD57.40
microelliptopoikilocytic (Rietti-Greppi- Micheli)D56.9
miner'sB76.9[D63.8]
myelodysplasticD46.9
myelofibrosisD75.81
myelogenousD64.89
myelopathicD64.89
myelophthisicD61.82
myeloproliferativeD47.Z9
newbornP61.4
- due to
  - ABO (antibodies, isoimmunization, maternal/fetal incompatibility)P55.1
  - Rh (antibodies, isoimmunization, maternal/fetal incompatibility)P55.0
- following fetal blood lossP61.3
- posthemorrhagic (fetal)P61.3
nonspherocytic hemolytic see Anemia, hemolytic, nonspherocytic
normocytic (infectional)D64.9
- due to blood loss (chronic)D50.0
  - acuteD62
- myelophthisicD61.82
nutritional (deficiency)D53.9
- with
  - poor iron absorptionD50.8
  - specified deficiency NECD53.8
- megaloblasticD52.0
of prematurityP61.2
orotaciduric (congenital) (hereditary)D53.0
osteoscleroticD64.89
ovalocytosis (hereditary) see Elliptocytosis
paludal see also MalariaB54[D63.8]
pernicious (congenital) (malignant) (progressive)D51.0
pleochromicD64.89
- of sprueD52.8
posthemorrhagic (chronic)D50.0
- acuteD62
- newbornP61.3
postoperative (postprocedural)
- due to (acute) blood lossD62
  - chronic blood lossD50.0
- specified NECD64.89
postpartumO90.81
pressureD64.89
progressiveD64.9
- malignantD51.0
- perniciousD51.0
protein-deficiencyD53.0
pseudoleukemica infantumD64.89
pure red cellD60.9
- congenitalD61.01
pyridoxine-responsiveD64.3
pyruvate kinase deficiencyD55.21
refractoryD46.4
- with
  - excess of blastsD46.20
    1 (RAEB 1)D46.21
    2 (RAEB 2)D46.22
    in transformation (RAEB T) see Leukemia, acute myeloblastic
  - hemochromatosisD46.1
  - sideroblasts (ring) (RARS)D46.1
- megaloblasticD53.1
- sideroblasticD46.1
- sideropenicD50.9
- without ring sideroblasts, so statedD46.0
- without sideroblasts without excess of blastsD46.0
Rietti-Greppi-MicheliD56.9
scorbuticD53.2
secondary to
- blood loss (chronic)D50.0
  - acuteD62
- hemorrhage (chronic)D50.0
  - acuteD62
semiplasticD61.89
sickle-cell see Disease, sickle-cell
sideroblasticD64.3
- hereditaryD64.0
- hypochromic, sex-linkedD64.0
- pyridoxine-responsive NECD64.3
- refractoryD46.1
- secondary (due to)
  - diseaseD64.1
  - drugs and toxinsD64.2
- specified type NECD64.3
sideropenic (refractory)D50.9
- due to blood loss (chronic)D50.0
  - acuteD62
simple chronicD53.9
specified type NECD64.89
spherocytic (hereditary) see Spherocytosis
splenicD64.89
splenomegalicD64.89
stomatocytosisD58.8
syphilitic (acquired) (late)A52.79[D63.8]
target cellD64.89
thalassemiaD56.9
thrombocytopenic see Thrombocytopenia
toxicD61.2
tropicalB76.9[D63.8]
- macrocyticD52.8
tuberculousA18.89[D63.8]
veganD51.3
vitamin
- B6-responsiveD64.3
- B12 deficiency (dietary) perniciousD51.0
von Jaksch'sD64.89
Witts' (achlorhydric anemia)D50.8