symptom lowerGI anaemia
- 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
- 4a1d74f6
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.