ICD 10 CM Index: Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)
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Anemia (essential) (general) (hemoglobin deficiency) (infantile) (primary) (profound)
ICD 10 Code is D64.9.
- with (due to) (in)
- 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
- idiopathic D61.3
- red cell (pure) D60.9
- 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
- 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 D55.2
- 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
- erythrocytic glutathione D55.1
- folate D52.9
- folic acid D52.9
- 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
- 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
- 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
- dietary vitamin B12 deficiency D51.3
- disorder of
- 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
- 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 (congenital pancytopenia) D61.09
- favism D55.0
- fish tapeworm infestation (D. latum) B70.0
- 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
- acute D59.9
- autoimmune D59.10
- chronic D58.9
- idiopathic D59.9
- cold type (primary) (secondary) (symptomatic) D59.12
- congenital (spherocytic), See Spherocytosis
- due to
- familial D58.9
- hereditary D58.9
- 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
- primary
- secondary D59.4
- specified type NEC (hereditary) D58.8
- Stransky-Regala type D58.8, See also Hemoglobinopathy
- symptomatic D59.4
- toxic D59.4
- warm type (primary) (secondary) (symptomatic) D59.11
- hemorrhagic (chronic) D50.0
- acute D62
- Herrick's D57.1
- hexokinase deficiency D55.2
- 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
- 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
- Joseph-Diamond-Blackfan (congenital hypoplastic) D61.01
- Lederer's (hemolytic) D59.19
- leukoerythroblastic D61.82
- macrocytic D53.9
- 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
- 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
- nonspherocytic hemolytic, See Anemia, hemolytic, nonspherocytic
- normocytic (infectional) D64.9
- nutritional (deficiency) D53.9
- 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
- postoperative (postprocedural)
- postpartum O90.81
- pressure D64.89
- progressive D64.9
- 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
- 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
- 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)
- specified type NEC D64.3
- sideropenic (refractory) D50.9
- 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
- von Jaksch's D64.89
- Witts' (achlorhydric anemia) D50.8