symptom lowerGI anaemia
Codelist metadata
-
Coding system
- SNOMED CT
-
Coding system release
- 37.0.0
-
Organisation
- PHC, University of Oxford
-
Codelist ID
- phc/symptom-lowergi-anaemia
-
Version ID
- 4a1d74f6
Versions
About
No metadata has been provided for this codelist.
Codelists are developed by a broad community of users for individual study purposes, which may or may not meet the needs of other studies. They should not be thought of as universal definitions of a particular condition.
We don't offer any guarantees about what they do or don't identify. Users should carefully check that any codelist meets their needs, and seek clinical input where appropriate.
| code | term |
|---|---|
| 10205009 | Megaloblastic anemia due to exfoliative dermatitis |
| 1052283003 | Restless leg syndrome due to iron deficiency anemia |
| 105599000 | Anemia related to disturbed deoxyribonucleic acid synthesis |
| 10564005 | Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 10619002 | Megaloblastic anemia due to poor nutrition |
| 10741751000119100 | Anemia in mother complicating childbirth |
| 10759351000119103 | Sickle cell anemia in mother complicating childbirth |
| 10762261000119105 | Anemia following acute postoperative blood loss |
| 10806241000119108 | Thalassemia in mother complicating childbirth |
| 10812081000119108 | Iron deficiency anemia in mother complicating childbirth |
| 109998009 | Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia |
| 111407006 | Hemolytic uremic syndrome |
| 111469006 | Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization |
| 111570005 | Anemia due to infection |
| 111571009 | Congenital atransferrinemia |
| 111572002 | Beta zero thalassemia non deletion type |
| 111574001 | Anemia due to copper deficiency |
| 111575000 | Anemia due to membrane defect |
| 111576004 | Acquired stomatocytosis |
| 111577008 | Anemia due to enzyme deficiency |
| 111579006 | Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency |
| 111581008 | Anemia caused by physical agent |
| 1142030006 | Nutritional anemia of pregnancy |
| 1142062009 | Macrocytic anemia of pregnancy |
| 1142083003 | Hemolytic anemia of pregnancy |
| 1142087002 | Congenital megaloblastic anemia due to transcobalamin II deficiency |
| 1148853004 | Iron deficiency anemia following gastrectomy |
| 1148855006 | Iron deficiency anemia due to increased requirement in adolescence |
| 1148856007 | Iron deficiency anemia due to increased requirement in infancy |
| 1148861009 | Iron deficiency anemia due to celiac disease |
| 1148880006 | Non autoimmune hemolytic anemia caused by drug |
| 1148893001 | Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency |
| 1148895008 | Hemolytic anemia due to red cell enolase deficiency |
| 1148897000 | Hemoglobin Paksé disease |
| 1148899002 | Hemoglobin Seal Rock disease |
| 1148914007 | Autosomal dominant sideroblastic anemia |
| 11491000 | Anemia due to niacin deficiency |
| 11503009 | Relative anemia |
| 1153333001 | Pernicious anemia due to autoimmune disorder |
| 1153353002 | Vitamin B12 deficiency anemia following total gastrectomy |
| 1153358006 | Lymphocyte passenger syndrome following organ transplantation |
| 1153380009 | Mechanical hemolysis following insertion of prosthetic heart valve |
| 1153399000 | Homozygous hereditary elliptocytosis |
| 1153403009 | Hereditary iron deficiency anemia |
| 1153409008 | Vitamin B12 deficiency anemia due to chronic atrophic gastritis |
| 115963009 | Regenerative anemia |
| 1171357005 | Vitamin B12 deficiency anemia following gastrectomy |
| 11781007 | Autoimmune hemolytic anemia caused by complement |
| 118791000119106 | Aplastic anemia caused by antineoplastic agent |
| 12189000 | Coombs negative hemolytic anemia |
| 1222681008 | Autoimmune hemolytic anemia, autoimmune thrombocytopenia, primary immunodeficiency syndrome |
| 12238007 | Megaloblastic anemia due to gastrectomy |
| 1237349008 | Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome |
| 1237417007 | Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation |
| 1239371000000103 | Haemoglobin E beta zero thalassaemia |
| 1239381000000101 | Haemoglobin E beta plus thalassaemia |
| 1260217004 | Myelodysplastic neoplasm with low blasts and SF3B1 mutation |
| 1263549001 | Benign intracranial hypertension due to anemia |
| 1269220000 | Anemia suspected |
| 1269225005 | Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency |
| 1269270002 | Infection-related hemolytic uremic syndrome |
| 127034005 | Pancytopenia |
| 127040003 | Sickle cell-hemoglobin SS disease |
| 127041004 | Sickle cell-beta-thalassemia |
| 127042006 | Sickle cell beta plus thalassemia |
| 127043001 | Sickle cell-beta^0^-thalassemia |
| 127044007 | Sickle cell-delta beta^0^-thalassemia |
| 127045008 | Sickle cell anemia with coexistent alpha-thalassemia |
| 127046009 | Sickle cell trait with coexistent alpha-thalassemia |
| 127049002 | Primary (idiopathic) autoimmune hemolytic anemia |
| 127050002 | Secondary autoimmune hemolytic anemia |
| 127052005 | Secondary warm autoimmune hemolytic anemia |
| 127053000 | Post-infectious cold agglutinin disease |
| 127054006 | Cold agglutinin disease due to and following Epstein-Barr virus infection |
| 127055007 | Chronic cold agglutinin disease |
| 127056008 | Chronic cold agglutinin disease associated with B-cell neoplasm |
| 127057004 | Paroxysmal cold hemoglobinuria |
| 127058009 | Paroxysmal cold hemoglobinuria associated with tertiary syphilis |
| 127060006 | Drug-induced immune hemolytic anemia, hapten type |
| 127061005 | Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement |
| 127319005 | Anemia caused by alloimmune destruction of transfused red cells |
| 1285021005 | Fanconi anemia of complementation group C |
| 12907000 | Thiamine-responsive megaloblastic anemia |
| 129638002 | Hemolytic anemia caused by hyperbaric oxygen |
| 13172003 | Chronic idiopathic thrombocytopenic purpura |
| 136281000119109 | Anemia caused by antineoplastic agent |
| 14024008 | Humoral immunologic aplastic anemia |
| 14087004 | Hereditary stomatocytosis |
| 14126008 | Autosomal-linked pyridoxine refractory sideroblastic anemia |
| 14379009 | Dimorphic anemia |
| 14514008 | Anemia due to disturbance of hemoglobin synthesis |
| 15121005 | Hereditary elliptocytosis due to glycophorin C deficiency |
| 15276008 | Drug-induced enzyme deficiency anemia |
| 15326009 | beta^+^ Thalassemia, normal Hb A>2<, type 2 |
| 15332004 | Goats' milk anemia |
| 161456009 | History of iron deficiency anemia |
| 161457000 | History of anemia vitamin B12 deficient |
| 161458005 | History of hemolytic anemia |
| 16360009 | Delta beta thalassemia |
| 16427007 | Delta thalassemia |
| 16623961000119100 | Pancytopenia caused by immunosuppressant |
| 16645003 | Anemia caused by insect venom |
| 16964007 | Hereditary persistence of fetal hemoglobin thalassemia |
| 1801000119106 | Anemia, pre-end stage renal disease on erythropoietin protocol |
| 18273004 | Unstable hemoglobin disease |
| 183005 | Autoimmune pancytopenia |
| 18323000 | Drug-induced immune hemolytic anemia, immune complex type |
| 18637002 | Megaloblastic anemia of premature infant |
| 18662002 | Acquired Heinz body anemia |
| 190996002 | Severe combined immunodeficiency with reticular dysgenesis |
| 191128004 | Iron deficiency anemia due to dietary causes |
| 191136008 | Idiopathic hypochromic anemia |
| 191142007 | Vitamin B12 deficiency anemia due to malabsorption with proteinuria |
| 191146005 | Congenital folate malabsorption anemia |
| 191148006 | Folate deficiency anemia, drug-induced |
| 191149003 | Folate deficiency anemia due to malabsorption |
| 191150003 | Folate deficiency anemia due to liver disorders |
| 191154007 | Combined B12 and folate deficiency anemia |
| 191161006 | Vitamin C deficiency anemia |
| 191169008 | Hereditary elliptocytosis |
| 191170009 | Hemolytic anemia due to glutathione metabolism disorder |
| 191177007 | Hemolytic anemia due to hexokinase deficiency |
| 191179005 | Hemolytic anemia due to triose phosphate isomerase deficiency |
| 191180008 | Anemia due to disorders of nucleotide metabolism |
| 191187006 | Alpha trait thalassemia |
| 191189009 | Beta thalassemia intermedia |
| 191210005 | Primary cold-type hemolytic anemia |
| 191211009 | Primary warm-type hemolytic anemia |
| 191212002 | Secondary cold-type hemolytic anemia |
| 191213007 | Secondary warm-type hemolytic anemia |
| 191216004 | Non-autoimmune hemolytic anemia |
| 191217008 | Mechanical hemolytic anemia |
| 191218003 | Toxic hemolytic anemia |
| 191222008 | Hemoglobinuria due to hemolysis from external causes |
| 191228007 | Acquired spherocytosis |
| 191229004 | Infantile pyknocytosis |
| 191244003 | Aplastic anemia due to chronic disease |
| 191246001 | Aplastic anemia due to infection |
| 191247005 | Aplastic anemia caused by radiation |
| 191248000 | Aplastic anemia caused by toxic cause |
| 191251007 | Transient hypoplastic anemia |
| 191255003 | Transient acquired pure red cell aplasia |
| 191256002 | Idiopathic aplastic anemia |
| 191260004 | Pyridoxine-responsive sideroblastic anemia |
| 191261000 | Secondary sideroblastic anemia due to disease |
| 191265009 | Anemia in neoplastic disease |
| 191268006 | Chronic anemia |
| 193213003 | Myasthenic syndrome due to pernicious anemia |
| 19442009 | Heterozygous thalassemia |
| 1963002 | Paroxysmal nocturnal hemoglobinuria |
| 199248002 | Iron deficiency anemia of pregnancy |
| 206434001 | Late anemia of newborn due to isoimmunization |
| 21412009 | X chromosome-linked pyridoxine refractory sideroblastic anemia |
| 21914002 | Anemia of thyroid dysfunction |
| 22098000 | Chronic idiopathic autoimmune hemolytic anemia |
| 22347002 | Anemia of gonadal dysfunction |
| 22438006 | Anemia due to disturbance of proliferation AND/OR differentiation of hematopoietic stem cells |
| 22933009 | Glucose-6-phosphate dehydrogenase deficiency class I variant anemia |
| 23371004 | Epsilon gamma delta beta thalassemia |
| 234343008 | Normocytic anemia due to aplasia |
| 234346000 | Dilutional anemia |
| 234347009 | Anemia of chronic disorder |
| 234348004 | Anemia of renal disease |
| 234349007 | Microcytic anemia |
| 234350007 | Neonatal anemia |
| 234352004 | Normocytic anemia due to chronic blood loss |
| 234353009 | Congenital transferrin deficiency |
| 234358000 | Megaloblastic anemia due to dietary causes |
| 234360003 | Vegan's anemia |
| 234361004 | Congenital deficiency of intrinsic factor |
| 234362006 | Biermer's congenital pernicious anemia |
| 234363001 | Selective malabsorption of cyanocobalamin |
| 234364007 | Combined deficiency anemia |
| 234365008 | Thiamine-responsive macrocytosis |
| 234366009 | Alcohol-related sideroblastic anemia |
| 234367000 | Pancytopenia with pancreatitis |
| 234375006 | Transient erythroblastopenia of childhood |
| 234376007 | Acquired red cell aplasia |
| 234380002 | Kell isoimmunization of the newborn |
| 234381003 | Maternal autoimmune hemolytic anemia |
| 234383000 | Homozygous alpha thalassemia |
| 234385007 | Alpha thalassemia-2 trait |
| 234386008 | Hemoglobin Constant Spring trait |
| 234387004 | Hemoglobin Lepore trait |
| 234388009 | Delta-beta-Lepore thalassemia |
| 234389001 | Alpha-beta thalassemia |
| 234390005 | Gamma thalassemia |
| 234391009 | Sickle cell anemia with high hemoglobin F |
| 234392002 | Hemoglobin E/beta thalassemia disease |
| 234402007 | Chronic non-spherocytic hemolytic anemia |
| 234410008 | Hereditary elliptocytosis with transient poikilocytosis |
| 234589002 | Glutathione synthetase deficiency |
| 237617006 | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness |
| 237926007 | Glutathione synthase deficiency without 5-oxoprolinuria |
| 237985009 | Pearson's syndrome |
| 240453002 | Oroya fever |
| 240486003 | Parvoviral aplastic crisis |
| 24620004 | Hemolytic anemia caused by babesiosis |
| 24661004 | Glucose-6-phosphate dehydrogenase deficiency class III variant anemia |
| 24962009 | Anemia due to vitamin E deficiency |
| 24975009 | Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 25251008 | Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency |
| 25266006 | Hereditary spherocytosis due to spectrin deficiency |
| 25443007 | X chromosome-linked pyridoxine responsive sideroblastic anemia |
| 26333003 | Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria |
| 26409005 | Congenital dyserythropoietic anemia, type III |
| 26682008 | Homozygous beta thalassemia |
| 267513007 | Deficiency anemias |
| 267517008 | Vitamin B12 deficiency anemia due to dietary causes |
| 267518003 | Folate deficiency anemia due to dietary causes |
| 267524009 | Constitutional aplastic anemia with malformation |
| 267527002 | Aplastic anemia due to drugs |
| 267530009 | Acute posthemorrhagic anemia |
| 269175006 | Beta thalassemia trait |
| 2694001 | Myelophthisic anemia |
| 26944003 | Acute megaloblastic anemia due to dialysis |
| 27080008 | Beta zero thalassemia deletion type |
| 271737000 | Anemia |
| 27342004 | Anemia of pregnancy |
| 27366005 | Megaloblastic anemia due to hemodialysis |
| 273985002 | Anemia due to isoimmunization |
| 275538002 | History of anemia |
| 276448005 | Idiopathic sideroblastic anemia |
| 276578004 | Physiological anemia of infancy |
| 276579007 | Late anemia of newborn |
| 276580005 | Atypical isoimmunization of newborn |
| 27798002 | Megaloblastic anemia due to impaired absorption of folate |
| 278363000 | Alcoholic macrocytosis |
| 28147001 | Hemolytic anemia caused by Clostridium welchii |
| 2835000 | Traumatic cardiac hemolytic anemia |
| 286928002 | Deficiency anemias, excluding iron |
| 28975000 | Constitutional aplastic anemia |
| 290246007 | Sideropenic anemia with reticuloendothelial siderosis |
| 291262006 | Simple chronic anemia |
| 29177004 | Anemia due to pentose phosphate pathway defect |
| 29551000 | Anemia caused by oxygen |
| 300980002 | Normocytic anemia |
| 301317008 | Hereditary nonspherocytic hemolytic anemia |
| 302873008 | Thrombocytopenic purpura |
| 303060002 | Normocytic anemia following acute bleed |
| 30418008 | Anemia of adrenal dysfunction |
| 30575002 | Fanconi's anemia |
| 306058006 | Aplastic anemia |
| 307333004 | Rhesus isoimmunization due to anti-D |
| 307334005 | Rhesus isoimmunization due to anti-c |
| 307335006 | Rhesus isoimmunization due to anti-E |
| 307336007 | Rhesus isoimmunization due to anti-Cw |
| 307337003 | Duffy isoimmunization of the newborn |
| 307338008 | Kidd isoimmunization of the newborn |
| 307343001 | Acquired hemoglobin H disease |
| 307726001 | Anemia in ovarian carcinoma |
| 309742004 | Drug-induced autoimmune hemolytic anemia |
| 310647000 | Anemia secondary to renal failure |
| 31206006 | Refractory megaloblastic anemia |
| 313291009 | Anemia during the puerperium |
| 31820007 | Anemia of endocrine disorder |
| 32094009 | Megaloblastic anemia caused by fish tapeworm |
| 322699009 | Intracorpuscular hemolytic anemia |
| 323666000 | Anemia due to intrinsic red cell abnormality |
| 32648007 | Mild hereditary spherocytosis due to spectrin deficiency |
| 3272007 | Stomatocytosis |
| 328301000119102 | Pancytopenia due to antineoplastic chemotherapy |
| 328371000119107 | Pancytopenia caused by antithyroid drug |
| 328381000119105 | Pancytopenia caused by anticonvulsant |
| 32855007 | Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster |
| 32858009 | Hemolytic disease of fetus OR newborn due to ABO immunization |
| 33183004 | Post infectious thrombocytopenic purpura |
| 33491002 | Autoimmune hemolytic anemia caused by immunoglobulin A plus complement |
| 33905008 | Hereditary spherocytosis due to deficiency of protein 4.2 |
| 34194007 | Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency |
| 34247008 | Anemia due to mechanical damage |
| 34629009 | Anemia due to zinc deficiency |
| 34852006 | Glucose-6-phosphate dehydrogenase deficiency class II variant anemia |
| 34925000 | Megaloblastic anemia due to inborn errors of metabolism |
| 350601000119109 | Hemolytic disease of newborn co-occurrent and due to ABO immunization |
| 350611000119107 | Hemolytic disease of fetus due to ABO immunization |
| 351181000119103 | Anemia due to enzymopathy |
| 35703006 | Post-viral paroxysmal cold hemoglobinuria |
| 3571004 | Megaloblastic anemia due to pancreatic insufficiency |
| 35778001 | Megaloblastic anemia due to error of folate metabolism |
| 360495000 | Familial megaloblastic anemia |
| 363041004 | Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism |
| 36467003 | Alpha plus thalassemia |
| 36472007 | Sickle cell-thalassemia disease |
| 36568005 | Hemolytic uremic syndrome of childhood |
| 36919001 | Anemia caused by lead |
| 371046004 | Traumatic hemolytic anemia |
| 371315009 | Iron deficiency anemia secondary to inadequate dietary iron intake |
| 37272000 | Rh deficiency syndrome |
| 373420004 | Upshaw-Schulman syndrome |
| 373421000 | Diarrhea-associated hemolytic uremic syndrome |
| 373422007 | Diarrhea-negative hemolytic uremic syndrome |
| 37370005 | Megaloblastic anemia caused by drugs |
| 38689004 | Hemolytic anemia due to infection |
| 387702001 | Perinatal anemia |
| 387705004 | Hemolytic disease of fetus OR newborn due to isoimmunization |
| 387745008 | Sports anemia |
| 38911009 | Hereditary hemolytic anemia |
| 389214003 | Ghosal hematodiaphyseal dysplasia |
| 38970002 | Doan-Wright syndrome |
| 39586009 | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia |
| 3978000 | Warm autoimmune hemolytic anemia |
| 398937006 | Cold autoimmune hemolytic anemia |
| 40108008 | Thalassemia |
| 402653004 | Thrombocytopenic purpura due to defective platelet production |
| 402654005 | Thrombocytopenic purpura due to platelet consumption |
| 40387008 | Polyagglutinable erythrocyte syndrome |
| 413532003 | Anemia due to blood loss |
| 413533008 | Anemia due to chronic blood loss |
| 413565006 | Aplastic anemia associated with metabolic alteration |
| 413566007 | Aplastic anemia associated with pancreatitis |
| 413567003 | Aplastic anemia associated with pregnancy |
| 413603009 | Autoimmune hemolytic anemia |
| 41387000 | Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency |
| 41462006 | Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells |
| 41614006 | Hypoplastic anemia |
| 416180004 | Hemoglobin SS disease without crisis |
| 417048006 | Sickle cell-thalassemia disease without crisis |
| 417626001 | Thrombocytopenic purpura associated with metabolic disorder |
| 41841004 | Sideroblastic anemia |
| 420543008 | Anemia associated with acquired immunodeficiency syndrome |
| 421102007 | Aplastic anemia with acquired immunodeficiency syndrome |
| 421851008 | Acquired hemolytic anemia associated with acquired immunodeficiency syndrome |
| 422167001 | Mycoplasmal anemia |
| 42461002 | Anemia caused by copper |
| 42484009 | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency |
| 42601008 | Congenital hemolytic anemia |
| 428383000 | Anemia caused by medication |
| 429208004 | History of aplastic anemia |
| 429217004 | History of autoimmune hemolytic anemia |
| 43707008 | Anemia caused by heat |
| 43742007 | Pericarditis associated with severe chronic anemia |
| 438476003 | Autoimmune thrombotic thrombocytopenic purpura |
| 43858000 | Secondary aplastic anemia |
| 439007008 | Acquired thrombotic thrombocytopenic purpura |
| 441322009 | Drug induced thrombotic thrombocytopenic purpura |
| 441482006 | History of sickle cell anemia |
| 441586006 | History of Fanconi anemia |
| 441638006 | History of Diamond-Blackfan anemia |
| 44206008 | Hapten type low affinity hemolytic anemia |
| 44288006 | Anemia due to abnormality extrinsic to the red cell |
| 444271000 | Erythropoietin resistance in anemia of chronic kidney disease |
| 44452003 | Normocytic hypochromic anemia |
| 444976001 | Congenital hemolytic uremic syndrome |
| 44641000 | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency |
| 44666001 | Microcytic hypochromic anemia |
| 447117006 | Hemoglobin H constant spring thalassemia |
| 44910003 | Megaloblastic anemia due to decreased intake of vitamin B>12< |
| 45098004 | Anemia due to multiple mechanisms |
| 45828008 | Anemia in mother complicating pregnancy, childbirth AND/OR puerperium |
| 462166006 | Fetal anemia |
| 46737006 | Normocytic normochromic anemia |
| 46760003 | Estren-Dameshek anemia |
| 47047009 | Thalassemia with other hemoglobinopathy |
| 47084006 | Beta plus thalassemia normal hemoglobin A>2< type 1 silent |
| 47100003 | Anemia of prematurity |
| 47516005 | Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin |
| 47526003 | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency |
| 47844003 | Megaloblastic anemia due to chronic hemolytic anemia |
| 4854004 | Acquired hemolytic anemia |
| 48553001 | Hemoglobin H disease |
| 48580008 | Anemia due to starvation |
| 48983004 | X chromosome-linked sideroblastic anemia |
| 49284006 | Juvenile type megaloblastic anemia |
| 4939006 | Hemolytic anemia due to nonlymphoid neoplasm |
| 49472006 | Megaloblastic anemia due to vitamin B>12< deficiency |
| 49708008 | Anemia of chronic renal failure |
| 4984008 | Microcytic normochromic anemia |
| 50220002 | Cellular immunologic aplastic anemia |
| 50253007 | Secondary paroxysmal cold hemoglobinuria |
| 50715003 | Pure red cell aplasia |
| 51071000 | Microangiopathic hemolytic anemia |
| 51667002 | Anemia due to riboflavin deficiency |
| 52212006 | Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency |
| 52413004 | Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency |
| 52565000 | Non megaloblastic anemia associated with nutritional deficiency |
| 52951008 | Congenital dyserythropoietic anemia |
| 5300004 | Hemoglobin Bart's hydrops syndrome |
| 5315003 | Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity |
| 53165003 | Megaloblastic anemia |
| 53743006 | Anemia following fetal blood loss |
| 54006005 | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia |
| 5430006 | Megaloblastic anemia due to total parenteral nutrition |
| 54698001 | Megaloblastic anemia due to Zollinger-Ellison syndrome |
| 55907008 | Acquired aplastic anemia |
| 55995005 | Hereditary spherocytosis |
| 5603006 | Autoimmune hemolytic anemia caused by immunoglobulin G |
| 56205004 | Hereditary persistence of fetal hemoglobin, nondeletion type |
| 57192008 | Acute pure red cell aplasia |
| 5876000 | Acquired pancytopenia |
| 59106005 | Anemia due to decreased red cell production |
| 59548005 | Congenital dyserythropoietic anemia, type I |
| 59644002 | Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency |
| 5967006 | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis |
| 5994005 | Hereditary elliptocytosis due to deficiency of protein 4.1 |
| 60138009 | Anemia of pituitary deficiency |
| 60164003 | Megaloblastic anemia due to blind loop syndrome |
| 60504009 | Megaloblastic anemia due to congenital deficiency of intrinsic factor |
| 60805002 | Hemolytic anemia with emphysema AND cutis laxa |
| 61261009 | Hemolytic anemia |
| 61395005 | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia |
| 61777009 | Thalassemia-hemoglobin C disease |
| 62074008 | Delta zero thalassemia |
| 62268000 | Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency |
| 62389006 | Acute megaloblastic anemia due to severe illness |
| 62403005 | Glucose-6-phosphate dehydrogenase deficiency anemia |
| 62609001 | Autoimmune hemolytic anemia caused by immunoglobulin G plus complement |
| 62871001 | Idiopathic paroxysmal cold hemoglobinuria |
| 63565007 | Congenital anemia |
| 6398009 | Idiopathic chronic cold agglutinin disease |
| 65959000 | Beta thalassemia |
| 66055002 | Alpha zero thalassemia |
| 66262001 | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction |
| 66309005 | Antibody-mediated anemia |
| 6659005 | Megaloblastic anemia due to celiac disease |
| 66612000 | Nutritional anemia |
| 67894009 | Megaloblastic anemia due to increased requirements |
| 68361004 | Late anemia due to isoimmunization |
| 68700003 | Megaloblastic anemia due to error of cobalamin metabolism |
| 68870007 | Congenital dyserythropoietic anemia, type II |
| 68913001 | Alpha thalassemia |
| 691381000119104 | Anemia due to chronic kidney disease stage 1 |
| 691401000119104 | Anemia co-occurrent and due to chronic kidney disease stage 4 |
| 691411000119101 | Anemia co-occurrent and due to chronic kidney disease stage 5 |
| 691421000119108 | Anemia co-occurrent and due to chronic kidney disease stage 3 |
| 69216008 | Hb Lepore thalassemia |
| 69574002 | Anemia of parathyroid dysfunction |
| 697908003 | Pulmonary arterial hypertension associated with chronic hemolytic anemia |
| 69981004 | Hereditary spherocytosis due to beta spectrin defect |
| 703135009 | Anemia in malignant neoplastic disease |
| 703540008 | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis |
| 707323002 | Anemia co-occurrent and due to chronic kidney disease |
| 707324008 | Anemia co-occurrent and due to end stage renal disease |
| 707480001 | Chronic hemolytic anemia |
| 711161006 | Hypochromic microcytic anemia with iron overload |
| 713349004 | Anemia co-occurrent with human immunodeficiency virus infection |
| 713388002 | GATA binding protein 1 related thrombocytopenia with dyserythropoiesis |
| 713496008 | Anemia caused by zidovudine |
| 713508003 | Aplastic anemia co-occurrent with human immunodeficiency virus infection |
| 713533000 | Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection |
| 713910008 | Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent |
| 715342005 | Alpha thalassemia X-linked intellectual disability syndrome |
| 715526002 | Dehydrated hereditary stomatocytosis |
| 716682000 | Dominant beta-thalassemia |
| 717050005 | Autosomal recessive sideroblastic anemia |
| 717254007 | Familial pseudohyperkalemia |
| 717946000 | Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease |
| 717947009 | Vitamin B12 deficiency anemia caused by drug |
| 717948004 | Acquired iron deficiency anemia due to increased iron requirement |
| 718196002 | Beta thalassemia X-linked thrombocytopenia syndrome |
| 71832003 | Autoimmune hemolytic anemia caused by immunoglobulin M |
| 71855000 | Acute megaloblastic anemia secondary to total parenteral nutrition |
| 718716008 | Autoimmune hemolytic anemia mixed type |
| 719019000 | WT limb blood syndrome |
| 719402008 | Lethal hemolytic anemia and genital anomaly syndrome |
| 719453009 | Congenital dyserythropoietic anemia type IV |
| 719816006 | X-linked sideroblastic anemia with spinocerebellar ataxia |
| 71988008 | Aase syndrome |
| 720401009 | Cystic fibrosis with gastritis and megaloblastic anemia syndrome |
| 720465002 | Adult-onset autosomal recessive sideroblastic anemia |
| 720982007 | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome |
| 721184003 | Megaloblastic anemia due to folate deficiency due to increased requirement |
| 721185002 | Megaloblastic anemia due to folate deficiency in pregnancy and lactation |
| 721186001 | Megaloblastic anemia due to folate deficiency in prematurity |
| 721295000 | Acquired thiamine deficiency anemia |
| 722005000 | Iron-refractory iron deficiency anemia |
| 722125003 | Overhydrated hereditary stomatocytosis |
| 722207000 | Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome |
| 722475006 | X-linked congenital dyserythropoietic anemia with thrombocytopenia |
| 722721004 | Familial hemolytic uremic syndrome |
| 72331000119105 | Thalassemia in mother complicating pregnancy |
| 723489005 | Hematopoietic subsyndrome of acute radiation syndrome |
| 723512008 | Revesz syndrome |
| 723623002 | Southeast Asian ovalocytosis |
| 724138007 | Mitochondrial myopathy with sideroblastic anemia syndrome |
| 724556004 | Iron deficiency anemia due to blood loss |
| 724557008 | Acquired iron deficiency anemia due to decreased absorption |
| 72501006 | Anemia caused by arsenic hydride |
| 725057008 | Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase |
| 725463007 | Severe congenital hypochromic anemia with ringed sideroblasts |
| 726669007 | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome |
| 73073009 | Hereditary elliptocytosis due to beta spectrin defect in self-association |
| 73162004 | Posttransfusion purpura |
| 73190000 | Epsilon gamma delta beta^0^ thalassemia |
| 732960002 | Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus |
| 732962005 | Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease |
| 732963000 | Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder |
| 732965007 | Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder |
| 732966008 | Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis |
| 734349003 | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 |
| 735452003 | Hereditary vitamin B12 deficiency anemia |
| 735453008 | Hereditary folate deficiency anemia |
| 736024007 | Pancytopenia caused by medication |
| 737220002 | Anemia due to metabolic disorder |
| 73891003 | Acute megaloblastic anemia caused by nitrous oxide |
| 74703006 | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency |
| 74789008 | Coombs positive hemolytic anemia |
| 75331009 | Evans syndrome |
| 75443009 | Hereditary elliptocytosis due to abnormal protein 4.1 |
| 75451007 | Thalassemia major |
| 76336008 | Delta beta zero thalassemia |
| 76366001 | Hemolytic anemia caused by Bartonella |
| 765327005 | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome |
| 765748009 | Adult pure red cell aplasia |
| 766982000 | Hemolytic anemia due to adenylate kinase deficiency |
| 767657005 | Anemia due to and following chemotherapy |
| 768556005 | Ataxia pancytopenia syndrome |
| 77084001 | Immunologic aplastic anemia |
| 772169008 | Hemolytic uremic syndrome suspected |
| 773489008 | Hereditary cryohydrocytosis with normal stomatin |
| 774071007 | Pancytopenia with developmental delay syndrome |
| 774083009 | Neonatal autoimmune hemolytic anemia |
| 77413008 | Severe hereditary spherocytosis due to spectrin deficiency |
| 77607006 | Drug-induced sideroblastic anemia |
| 77663007 | Hemolytic anemia caused by malaria |
| 778027003 | Primary CD59 deficiency |
| 78129009 | Thrombotic thrombocytopenic purpura |
| 78209002 | Hemolytic uremic syndrome, adult type |
| 782759001 | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia |
| 782911008 | Hereditary cryohydrocytosis with reduced stomatin |
| 783142006 | Pancytopenia due to IKAROS family zinc finger 1 mutations |
| 783255002 | Hereditary isolated aplastic anemia |
| 78677008 | Anemia due to pantothenic deficiency |
| 788865000 | Anemia due to chronic infectious disease |
| 788944005 | Gamma delta beta thalassemia |
| 78908001 | Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity |
| 789660001 | Atypical hemolytic uremic syndrome |
| 78997000 | Megaloblastic anemia due to vegetarianism |
| 79035003 | Anemia due to unknown mechanism |
| 79592006 | Beta plus thalassemia |
| 80126007 | Plummer-Vinson syndrome |
| 80875006 | Achlorhydric anemia |
| 80963002 | Glucose-6-phosphate dehydrogenase deficiency class V variant anemia |
| 81711008 | Hemolytic anemia caused by drugs |
| 82003006 | Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia |
| 820601000000103 | Refractory anaemia with multilineage dysplasia |
| 82430007 | Acute megaloblastic anemia |
| 82895008 | Megaloblastic anemia due to disease of small intestine |
| 82980005 | Anemia due to diabetes mellitus |
| 83414005 | Macrocytic anemia |
| 84027009 | Pernicious anemia |
| 84188003 | Thalassemia syndrome |
| 85422000 | Alpha plus thalassemia non deletion type |
| 85557000 | Hereditary persistence of fetal hemoglobin deletion type |
| 85570009 | Anemia due to vitamin A deficiency |
| 85649008 | Megaloblastic anemia due to folate deficiency |
| 85746008 | Anemia due to protein deficiency |
| 862001 | Anemia caused by chlorate |
| 86225009 | Hapten type high affinity hemolytic anemia |
| 86242003 | Alpha plus thalassemia deletion type |
| 86325007 | Non megaloblastic anemia due to alcoholism |
| 863953007 | Primaquine sensitivity anemia |
| 86448001 | Anemia due to vitamin B>6< deficiency |
| 866092006 | Megaloblastic anemia due to dihydrofolate reductase deficiency |
| 866381000000109 | Recurrent anaemia |
| 86715000 | Beta zero thalassemia |
| 86859003 | Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia |
| 86986002 | Hemolytic disease of fetus OR newborn due to RhD isoimmunization |
| 87522002 | Iron deficiency anemia |
| 87806008 | Megaloblastic anemia due to tropical sprue |
| 87810006 | Megaloblastic anemia due to alcoholism |
| 87994004 | Xerocytosis |
| 8857001 | Hereditary elliptocytosis due to alpha spectrin defect |
| 88854002 | Congenital hypoplastic anemia |
| 89459006 | Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster |
| 89810003 | ^A^gamma delta beta^0^ thalassemia |
| 90175006 | Secondary acquired sideroblastic anemia |
| 90414007 | Chronic acquired pure red cell aplasia |
| 91217009 | Megaloblastic anemia due to pregnancy |
| 91411007 | Autoimmune hemolytic anemia caused by immunoglobulin A |
| 934007 | Thalassemia intermedia |
| 9434008 | Hereditary pyropoikilocytosis |
| 9764001 | Anemia caused by radiation |
Codes not in the full codelist are in faint grey.