| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1029.322 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1029.322 |
| version | 20210605 |
| status | active |
| publisher | Joint Commission |
| name | Anemia |
| title | Anemia |
| date | 2021-06-05T01:01:30-04:00 |
| experimental | false |
| Usages | (none) |
This value set contains 379 concepts
| Code | System | Display |
| 10205009 | http://snomed.info/sct | Megaloblastic anemia due to exfoliative dermatitis (disorder) |
| 105599000 | http://snomed.info/sct | Anemia related to disturbed deoxyribonucleic acid synthesis (disorder) |
| 10564005 | http://snomed.info/sct | Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) |
| 10619002 | http://snomed.info/sct | Megaloblastic anemia due to poor nutrition (disorder) |
| 10759351000119103 | http://snomed.info/sct | Sickle cell anemia in mother complicating childbirth (disorder) |
| 10806241000119108 | http://snomed.info/sct | Thalassemia in mother complicating childbirth (disorder) |
| 10812081000119108 | http://snomed.info/sct | Iron deficiency anemia in mother complicating childbirth (disorder) |
| 109996008 | http://snomed.info/sct | Myelodysplastic syndrome: Refractory anemia, without ringed sideroblasts, without excess blasts (disorder) |
| 109998009 | http://snomed.info/sct | Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (disorder) |
| 110000005 | http://snomed.info/sct | Refractory anemia with excess blasts in transformation (disorder) |
| 111407006 | http://snomed.info/sct | Hemolytic uremic syndrome (disorder) |
| 111571009 | http://snomed.info/sct | Congenital atransferrinemia (disorder) |
| 111572002 | http://snomed.info/sct | Beta zero thalassemia non deletion type (disorder) |
| 111574001 | http://snomed.info/sct | Anemia due to copper deficiency (disorder) |
| 111575000 | http://snomed.info/sct | Anemia due to membrane defect (disorder) |
| 111576004 | http://snomed.info/sct | Acquired stomatocytosis (disorder) |
| 111577008 | http://snomed.info/sct | Anemia due to enzyme deficiency (disorder) |
| 111579006 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder) |
| 111581008 | http://snomed.info/sct | Anemia caused by physical agent (disorder) |
| 11491000 | http://snomed.info/sct | Anemia due to niacin deficiency (disorder) |
| 11503009 | http://snomed.info/sct | Relative anemia (disorder) |
| 115963009 | http://snomed.info/sct | Regenerative anemia (disorder) |
| 11781007 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by complement (disorder) |
| 119641000119103 | http://snomed.info/sct | Homozygous hemoglobin H constant spring thalassemia (disorder) |
| 119691000119106 | http://snomed.info/sct | Hemoglobin C/beta thalassemia disease (disorder) |
| 119701000119106 | http://snomed.info/sct | Hemoglobin D/beta thalassemia disease (disorder) |
| 12189000 | http://snomed.info/sct | Coombs negative hemolytic anemia (disorder) |
| 12238007 | http://snomed.info/sct | Megaloblastic anemia due to gastrectomy (disorder) |
| 127040003 | http://snomed.info/sct | Sickle cell-hemoglobin SS disease (disorder) |
| 127041004 | http://snomed.info/sct | Sickle cell-beta-thalassemia (disorder) |
| 127042006 | http://snomed.info/sct | Sickle cell beta plus thalassemia (disorder) |
| 127043001 | http://snomed.info/sct | Sickle cell-beta^0^-thalassemia (disorder) |
| 127044007 | http://snomed.info/sct | Sickle cell-delta beta^0^-thalassemia (disorder) |
| 127045008 | http://snomed.info/sct | Sickle cell anemia with coexistent alpha-thalassemia (disorder) |
| 127046009 | http://snomed.info/sct | Sickle cell trait with coexistent alpha-thalassemia (disorder) |
| 127049002 | http://snomed.info/sct | Primary (idiopathic) autoimmune hemolytic anemia (disorder) |
| 127050002 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia (disorder) |
| 127052005 | http://snomed.info/sct | Secondary warm autoimmune hemolytic anemia (disorder) |
| 127053000 | http://snomed.info/sct | Post-infectious cold agglutinin disease (disorder) |
| 127054006 | http://snomed.info/sct | Cold agglutinin disease caused by Epstein-Barr virus infection (disorder) |
| 127055007 | http://snomed.info/sct | Chronic cold agglutinin disease (disorder) |
| 127056008 | http://snomed.info/sct | Chronic cold agglutinin disease associated with B-cell neoplasm (disorder) |
| 127057004 | http://snomed.info/sct | Paroxysmal cold hemoglobinuria (disorder) |
| 127058009 | http://snomed.info/sct | Paroxysmal cold hemoglobinuria associated with tertiary syphilis (disorder) |
| 127061005 | http://snomed.info/sct | Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement (disorder) |
| 12907000 | http://snomed.info/sct | Thiamine-responsive megaloblastic anemia (disorder) |
| 129638002 | http://snomed.info/sct | Hemolytic anemia caused by hyperbaric oxygen (disorder) |
| 14087004 | http://snomed.info/sct | Hereditary stomatocytosis (disorder) |
| 14126008 | http://snomed.info/sct | Autosomal-linked pyridoxine refractory sideroblastic anemia (disorder) |
| 14379009 | http://snomed.info/sct | Dimorphic anemia (disorder) |
| 14514008 | http://snomed.info/sct | Anemia due to disturbance of hemoglobin synthesis (disorder) |
| 15121005 | http://snomed.info/sct | Hereditary elliptocytosis due to glycophorin C deficiency (disorder) |
| 15276008 | http://snomed.info/sct | Drug-induced enzyme deficiency anemia (disorder) |
| 15326009 | http://snomed.info/sct | beta^+^ Thalassemia, normal Hb A>2<, type 2 (disorder) |
| 15332004 | http://snomed.info/sct | Goats' milk anemia (disorder) |
| 16360009 | http://snomed.info/sct | Delta beta thalassemia (disorder) |
| 16427007 | http://snomed.info/sct | Delta thalassemia (disorder) |
| 16645003 | http://snomed.info/sct | Anemia caused by insect venom (disorder) |
| 1801000119106 | http://snomed.info/sct | Anemia, pre-end stage renal disease on erythropoietin protocol (disorder) |
| 18323000 | http://snomed.info/sct | Drug-induced immune hemolytic anemia, immune complex type (disorder) |
| 18637002 | http://snomed.info/sct | Megaloblastic anemia of premature infant (disorder) |
| 18662002 | http://snomed.info/sct | Acquired Heinz body anemia (disorder) |
| 191128004 | http://snomed.info/sct | Iron deficiency anemia due to dietary causes (disorder) |
| 191136008 | http://snomed.info/sct | Idiopathic hypochromic anemia (disorder) |
| 191142007 | http://snomed.info/sct | Vitamin B12 deficiency anemia due to malabsorption with proteinuria (disorder) |
| 191146005 | http://snomed.info/sct | Congenital folate malabsorption anemia (disorder) |
| 191148006 | http://snomed.info/sct | Folate deficiency anemia, drug-induced (disorder) |
| 191149003 | http://snomed.info/sct | Folate deficiency anemia due to malabsorption (disorder) |
| 191150003 | http://snomed.info/sct | Folate deficiency anemia due to liver disorders (disorder) |
| 191154007 | http://snomed.info/sct | Combined B12 and folate deficiency anemia (disorder) |
| 191161006 | http://snomed.info/sct | Vitamin C deficiency anemia (disorder) |
| 191170009 | http://snomed.info/sct | Hemolytic anemia due to glutathione metabolism disorder (disorder) |
| 191177007 | http://snomed.info/sct | Hemolytic anemia due to hexokinase deficiency (disorder) |
| 191179005 | http://snomed.info/sct | Hemolytic anemia due to triose phosphate isomerase deficiency (disorder) |
| 191180008 | http://snomed.info/sct | Anemia due to disorders of nucleotide metabolism (disorder) |
| 191187006 | http://snomed.info/sct | Alpha trait thalassemia (disorder) |
| 191189009 | http://snomed.info/sct | Beta thalassemia intermedia (disorder) |
| 191210005 | http://snomed.info/sct | Primary cold-type hemolytic anemia (disorder) |
| 191211009 | http://snomed.info/sct | Primary warm-type hemolytic anemia (disorder) |
| 191212002 | http://snomed.info/sct | Secondary cold-type hemolytic anemia (disorder) |
| 191213007 | http://snomed.info/sct | Secondary warm-type hemolytic anemia (disorder) |
| 191216004 | http://snomed.info/sct | Non-autoimmune hemolytic anemia (disorder) |
| 191217008 | http://snomed.info/sct | Mechanical hemolytic anemia (disorder) |
| 191218003 | http://snomed.info/sct | Toxic hemolytic anemia (disorder) |
| 191222008 | http://snomed.info/sct | Hemoglobinuria due to hemolysis from external causes (disorder) |
| 191228007 | http://snomed.info/sct | Acquired spherocytosis (disorder) |
| 191247005 | http://snomed.info/sct | Aplastic anemia caused by radiation (disorder) |
| 191248000 | http://snomed.info/sct | Aplastic anemia caused by toxic cause (disorder) |
| 191260004 | http://snomed.info/sct | Pyridoxine-responsive sideroblastic anemia (disorder) |
| 191261000 | http://snomed.info/sct | Secondary sideroblastic anemia due to disease (disorder) |
| 191262007 | http://snomed.info/sct | Secondary sideroblastic anemia caused by drugs and toxins (disorder) |
| 191265009 | http://snomed.info/sct | Anemia in neoplastic disease (disorder) |
| 191268006 | http://snomed.info/sct | Chronic anemia (disorder) |
| 19442009 | http://snomed.info/sct | Heterozygous thalassemia (disorder) |
| 1963002 | http://snomed.info/sct | Paroxysmal nocturnal hemoglobinuria (disorder) |
| 199248002 | http://snomed.info/sct | Iron deficiency anemia of pregnancy (disorder) |
| 21412009 | http://snomed.info/sct | X chromosome-linked pyridoxine refractory sideroblastic anemia (disorder) |
| 21914002 | http://snomed.info/sct | Anemia of thyroid dysfunction (disorder) |
| 22098000 | http://snomed.info/sct | Chronic idiopathic autoimmune hemolytic anemia (disorder) |
| 22347002 | http://snomed.info/sct | Anemia of gonadal dysfunction (disorder) |
| 22438006 | http://snomed.info/sct | Anemia due to disturbance of proliferation AND/OR differentiation of hematopoietic stem cells (disorder) |
| 22933009 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency class I variant anemia (disorder) |
| 23371004 | http://snomed.info/sct | Epsilon gamma delta beta thalassemia (disorder) |
| 234343008 | http://snomed.info/sct | Normocytic anemia due to aplasia (disorder) |
| 234346000 | http://snomed.info/sct | Dilutional anemia (disorder) |
| 234347009 | http://snomed.info/sct | Anemia of chronic disorder (disorder) |
| 234348004 | http://snomed.info/sct | Anemia of renal disease (disorder) |
| 234349007 | http://snomed.info/sct | Microcytic anemia (disorder) |
| 234352004 | http://snomed.info/sct | Normocytic anemia due to chronic blood loss (disorder) |
| 234353009 | http://snomed.info/sct | Congenital transferrin deficiency (disorder) |
| 234358000 | http://snomed.info/sct | Megaloblastic anemia due to dietary causes (disorder) |
| 234360003 | http://snomed.info/sct | Vegan's anemia (disorder) |
| 234361004 | http://snomed.info/sct | Congenital deficiency of intrinsic factor (disorder) |
| 234362006 | http://snomed.info/sct | Biermer's congenital pernicious anemia (disorder) |
| 234363001 | http://snomed.info/sct | Selective malabsorption of cyanocobalamin (disorder) |
| 234364007 | http://snomed.info/sct | Combined deficiency anemia (disorder) |
| 234365008 | http://snomed.info/sct | Thiamine-responsive macrocytosis (disorder) |
| 234366009 | http://snomed.info/sct | Alcohol-related sideroblastic anemia (disorder) |
| 234381003 | http://snomed.info/sct | Maternal autoimmune hemolytic anemia (disorder) |
| 234383000 | http://snomed.info/sct | Homozygous alpha thalassemia (disorder) |
| 234385007 | http://snomed.info/sct | Alpha thalassemia-2 trait (disorder) |
| 234386008 | http://snomed.info/sct | Hemoglobin Constant Spring trait (disorder) |
| 234387004 | http://snomed.info/sct | Hemoglobin Lepore trait (disorder) |
| 234388009 | http://snomed.info/sct | Delta-beta-Lepore thalassemia (disorder) |
| 234389001 | http://snomed.info/sct | Alpha-beta thalassemia (disorder) |
| 234390005 | http://snomed.info/sct | Gamma thalassemia (disorder) |
| 234391009 | http://snomed.info/sct | Sickle cell anemia with high hemoglobin F (disorder) |
| 237617006 | http://snomed.info/sct | Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (disorder) |
| 237985009 | http://snomed.info/sct | Pearson's syndrome (disorder) |
| 240453002 | http://snomed.info/sct | Oroya fever (disorder) |
| 24620004 | http://snomed.info/sct | Hemolytic anemia caused by babesiosis (disorder) |
| 24661004 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency class III variant anemia (disorder) |
| 24962009 | http://snomed.info/sct | Anemia due to vitamin E deficiency (disorder) |
| 24975009 | http://snomed.info/sct | Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) |
| 25251008 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (disorder) |
| 25266006 | http://snomed.info/sct | Hereditary spherocytosis due to spectrin deficiency (disorder) |
| 25443007 | http://snomed.info/sct | X chromosome-linked pyridoxine responsive sideroblastic anemia (disorder) |
| 26333003 | http://snomed.info/sct | Megaloblastic anemia due to vitamin B>12< malabsorption with proteinuria (disorder) |
| 26682008 | http://snomed.info/sct | Homozygous beta thalassemia (disorder) |
| 267513007 | http://snomed.info/sct | Deficiency anemias (disorder) |
| 267517008 | http://snomed.info/sct | Vitamin B12 deficiency anemia due to dietary causes (disorder) |
| 267518003 | http://snomed.info/sct | Folate deficiency anemia due to dietary causes (disorder) |
| 267530009 | http://snomed.info/sct | Acute posthemorrhagic anemia (disorder) |
| 269175006 | http://snomed.info/sct | Beta thalassemia trait (disorder) |
| 2694001 | http://snomed.info/sct | Myelophthisic anemia (disorder) |
| 26944003 | http://snomed.info/sct | Acute megaloblastic anemia due to dialysis (disorder) |
| 27080008 | http://snomed.info/sct | Beta zero thalassemia deletion type (disorder) |
| 271737000 | http://snomed.info/sct | Anemia (disorder) |
| 27342004 | http://snomed.info/sct | Anemia of pregnancy (disorder) |
| 27366005 | http://snomed.info/sct | Megaloblastic anemia due to hemodialysis (disorder) |
| 276448005 | http://snomed.info/sct | Idiopathic sideroblastic anemia (disorder) |
| 27798002 | http://snomed.info/sct | Megaloblastic anemia due to impaired absorption of folate (disorder) |
| 278363000 | http://snomed.info/sct | Alcoholic macrocytosis (disorder) |
| 28147001 | http://snomed.info/sct | Hemolytic anemia caused by Clostridium welchii (disorder) |
| 2835000 | http://snomed.info/sct | Traumatic cardiac hemolytic anemia (disorder) |
| 286928002 | http://snomed.info/sct | Deficiency anemias, excluding iron (disorder) |
| 290246007 | http://snomed.info/sct | Sideropenic anemia with reticuloendothelial siderosis (disorder) |
| 291262006 | http://snomed.info/sct | Simple chronic anemia (disorder) |
| 29177004 | http://snomed.info/sct | Anemia due to pentose phosphate pathway defect (disorder) |
| 29551000 | http://snomed.info/sct | Anemia caused by oxygen (disorder) |
| 300980002 | http://snomed.info/sct | Normocytic anemia (disorder) |
| 301317008 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia (disorder) |
| 30418008 | http://snomed.info/sct | Anemia of adrenal dysfunction (disorder) |
| 30575002 | http://snomed.info/sct | Fanconi's anemia (disorder) |
| 307343001 | http://snomed.info/sct | Acquired hemoglobin H disease (disorder) |
| 307726001 | http://snomed.info/sct | Anemia in ovarian carcinoma (disorder) |
| 309742004 | http://snomed.info/sct | Drug-induced autoimmune hemolytic anemia (disorder) |
| 310647000 | http://snomed.info/sct | Anemia secondary to renal failure (disorder) |
| 31206006 | http://snomed.info/sct | Refractory megaloblastic anemia (disorder) |
| 313291009 | http://snomed.info/sct | Anemia during the puerperium (disorder) |
| 31820007 | http://snomed.info/sct | Anemia of endocrine disorder (disorder) |
| 32094009 | http://snomed.info/sct | Megaloblastic anemia caused by fish tapeworm (disorder) |
| 322699009 | http://snomed.info/sct | Intracorpuscular hemolytic anemia (disorder) |
| 323666000 | http://snomed.info/sct | Anemia due to intrinsic red cell abnormality (disorder) |
| 32648007 | http://snomed.info/sct | Mild hereditary spherocytosis due to spectrin deficiency (disorder) |
| 3272007 | http://snomed.info/sct | Stomatocytosis (disorder) |
| 328301000119102 | http://snomed.info/sct | Pancytopenia due to antineoplastic chemotherapy (disorder) |
| 32855007 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) |
| 33491002 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by immunoglobulin A plus complement (disorder) |
| 33905008 | http://snomed.info/sct | Hereditary spherocytosis due to deficiency of protein 4.2 (disorder) |
| 34194007 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (disorder) |
| 34247008 | http://snomed.info/sct | Anemia due to mechanical damage (disorder) |
| 34629009 | http://snomed.info/sct | Anemia due to zinc deficiency (disorder) |
| 34852006 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency class II variant anemia (disorder) |
| 34925000 | http://snomed.info/sct | Megaloblastic anemia due to inborn errors of metabolism (disorder) |
| 35703006 | http://snomed.info/sct | Post-viral paroxysmal cold hemoglobinuria (disorder) |
| 3571004 | http://snomed.info/sct | Megaloblastic anemia due to pancreatic insufficiency (disorder) |
| 35778001 | http://snomed.info/sct | Megaloblastic anemia due to error of folate metabolism (disorder) |
| 360495000 | http://snomed.info/sct | Familial megaloblastic anemia (disorder) |
| 363041004 | http://snomed.info/sct | Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) |
| 36467003 | http://snomed.info/sct | Alpha plus thalassemia (disorder) |
| 36472007 | http://snomed.info/sct | Sickle cell-thalassemia disease (disorder) |
| 36568005 | http://snomed.info/sct | Hemolytic uremic syndrome of childhood (disorder) |
| 36919001 | http://snomed.info/sct | Anemia caused by lead (disorder) |
| 371046004 | http://snomed.info/sct | Traumatic hemolytic anemia (disorder) |
| 371315009 | http://snomed.info/sct | Iron deficiency anemia secondary to inadequate dietary iron intake (disorder) |
| 37272000 | http://snomed.info/sct | Rh deficiency syndrome (disorder) |
| 373421000 | http://snomed.info/sct | Diarrhea-associated hemolytic uremic syndrome (disorder) |
| 373422007 | http://snomed.info/sct | Diarrhea-negative hemolytic uremic syndrome (disorder) |
| 37370005 | http://snomed.info/sct | Megaloblastic anemia caused by drugs (disorder) |
| 38689004 | http://snomed.info/sct | Hemolytic anemia due to infection (disorder) |
| 387702001 | http://snomed.info/sct | Perinatal anemia (disorder) |
| 387745008 | http://snomed.info/sct | Sports anemia (disorder) |
| 38911009 | http://snomed.info/sct | Hereditary hemolytic anemia (disorder) |
| 389214003 | http://snomed.info/sct | Ghosal hematodiaphyseal dysplasia (disorder) |
| 38970002 | http://snomed.info/sct | Doan-Wright syndrome (disorder) |
| 39586009 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin A gamma beta^+^ thalassemia (disorder) |
| 3978000 | http://snomed.info/sct | Warm autoimmune hemolytic anemia (disorder) |
| 398623004 | http://snomed.info/sct | Myelodysplastic syndrome with excess blasts (disorder) |
| 398937006 | http://snomed.info/sct | Cold autoimmune hemolytic anemia (disorder) |
| 40108008 | http://snomed.info/sct | Thalassemia (disorder) |
| 40387008 | http://snomed.info/sct | Polyagglutinable erythrocyte syndrome (disorder) |
| 413532003 | http://snomed.info/sct | Anemia due to blood loss (disorder) |
| 413533008 | http://snomed.info/sct | Anemia due to chronic blood loss (disorder) |
| 413567003 | http://snomed.info/sct | Aplastic anemia associated with pregnancy (disorder) |
| 413603009 | http://snomed.info/sct | Autoimmune hemolytic anemia (disorder) |
| 41387000 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency (disorder) |
| 41462006 | http://snomed.info/sct | Anemia due to disturbance of proliferation AND/OR differentiation of erythroid precursor cells (disorder) |
| 415283002 | http://snomed.info/sct | Myelodysplastic syndrome with excess blasts-1 (disorder) |
| 415284008 | http://snomed.info/sct | Myelodysplastic syndrome with excess blasts-2 (disorder) |
| 41614006 | http://snomed.info/sct | Hypoplastic anemia (disorder) |
| 416180004 | http://snomed.info/sct | Hemoglobin SS disease without crisis (disorder) |
| 417048006 | http://snomed.info/sct | Sickle cell-thalassemia disease without crisis (disorder) |
| 41841004 | http://snomed.info/sct | Sideroblastic anemia (disorder) |
| 420543008 | http://snomed.info/sct | Anemia associated with acquired immunodeficiency syndrome (disorder) |
| 421851008 | http://snomed.info/sct | Acquired hemolytic anemia associated with acquired immunodeficiency syndrome (disorder) |
| 42461002 | http://snomed.info/sct | Anemia caused by copper (disorder) |
| 42484009 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (disorder) |
| 424988008 | http://snomed.info/sct | Anemia caused by substance (disorder) |
| 428383000 | http://snomed.info/sct | Anemia caused by medication (disorder) |
| 43707008 | http://snomed.info/sct | Anemia caused by heat (disorder) |
| 44206008 | http://snomed.info/sct | Hapten type low affinity hemolytic anemia (disorder) |
| 44288006 | http://snomed.info/sct | Anemia due to abnormality extrinsic to the red cell (disorder) |
| 44452003 | http://snomed.info/sct | Normocytic hypochromic anemia (disorder) |
| 444976001 | http://snomed.info/sct | Congenital hemolytic uremic syndrome (disorder) |
| 44641000 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (disorder) |
| 44666001 | http://snomed.info/sct | Microcytic hypochromic anemia (disorder) |
| 447117006 | http://snomed.info/sct | Hemoglobin H constant spring thalassemia (disorder) |
| 44910003 | http://snomed.info/sct | Megaloblastic anemia due to decreased intake of vitamin B>12< (disorder) |
| 45098004 | http://snomed.info/sct | Anemia due to multiple mechanisms (disorder) |
| 46737006 | http://snomed.info/sct | Normocytic normochromic anemia (disorder) |
| 46760003 | http://snomed.info/sct | Estren-Dameshek anemia (disorder) |
| 47047009 | http://snomed.info/sct | Thalassemia with other hemoglobinopathy (disorder) |
| 47084006 | http://snomed.info/sct | Beta plus thalassemia normal hemoglobin A>2< type 1 silent (disorder) |
| 47516005 | http://snomed.info/sct | Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (disorder) |
| 47526003 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (disorder) |
| 47844003 | http://snomed.info/sct | Megaloblastic anemia due to chronic hemolytic anemia (disorder) |
| 4854004 | http://snomed.info/sct | Acquired hemolytic anemia (disorder) |
| 48553001 | http://snomed.info/sct | Hemoglobin H disease (disorder) |
| 48580008 | http://snomed.info/sct | Anemia due to starvation (disorder) |
| 49284006 | http://snomed.info/sct | Juvenile type megaloblastic anemia (disorder) |
| 4939006 | http://snomed.info/sct | Hemolytic anemia due to nonlymphoid neoplasm (disorder) |
| 49472006 | http://snomed.info/sct | Megaloblastic anemia due to vitamin B>12< deficiency (disorder) |
| 49708008 | http://snomed.info/sct | Anemia of chronic renal failure (disorder) |
| 4984008 | http://snomed.info/sct | Microcytic normochromic anemia (disorder) |
| 50253007 | http://snomed.info/sct | Secondary paroxysmal cold hemoglobinuria (disorder) |
| 51071000 | http://snomed.info/sct | Microangiopathic hemolytic anemia (disorder) |
| 51667002 | http://snomed.info/sct | Anemia due to riboflavin deficiency (disorder) |
| 52212006 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (disorder) |
| 52413004 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (disorder) |
| 52565000 | http://snomed.info/sct | Non megaloblastic anemia associated with nutritional deficiency (disorder) |
| 5300004 | http://snomed.info/sct | Hemoglobin Bart's hydrops syndrome (disorder) |
| 5315003 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (disorder) |
| 53165003 | http://snomed.info/sct | Megaloblastic anemia (disorder) |
| 5430006 | http://snomed.info/sct | Megaloblastic anemia due to total parenteral nutrition (disorder) |
| 54698001 | http://snomed.info/sct | Megaloblastic anemia due to Zollinger-Ellison syndrome (disorder) |
| 55995005 | http://snomed.info/sct | Hereditary spherocytosis (disorder) |
| 5603006 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) |
| 56205004 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin, nondeletion type (disorder) |
| 59106005 | http://snomed.info/sct | Anemia due to decreased red cell production (disorder) |
| 59644002 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency (disorder) |
| 5967006 | http://snomed.info/sct | A gamma beta^+^ hereditary persistence of fetal hemoglobin AND beta^0^ thalassemia in cis (disorder) |
| 5994005 | http://snomed.info/sct | Hereditary elliptocytosis due to deficiency of protein 4.1 (disorder) |
| 60138009 | http://snomed.info/sct | Anemia of pituitary deficiency (disorder) |
| 60164003 | http://snomed.info/sct | Megaloblastic anemia due to blind loop syndrome (disorder) |
| 60504009 | http://snomed.info/sct | Megaloblastic anemia due to congenital deficiency of intrinsic factor (disorder) |
| 60805002 | http://snomed.info/sct | Hemolytic anemia with emphysema AND cutis laxa (disorder) |
| 61261009 | http://snomed.info/sct | Hemolytic anemia (disorder) |
| 61777009 | http://snomed.info/sct | Thalassemia-hemoglobin C disease (disorder) |
| 62074008 | http://snomed.info/sct | Delta zero thalassemia (disorder) |
| 62268000 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (disorder) |
| 62389006 | http://snomed.info/sct | Acute megaloblastic anemia due to severe illness (disorder) |
| 62403005 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency anemia (disorder) |
| 62871001 | http://snomed.info/sct | Idiopathic paroxysmal cold hemoglobinuria (disorder) |
| 6398009 | http://snomed.info/sct | Idiopathic chronic cold agglutinin disease (disorder) |
| 65959000 | http://snomed.info/sct | Beta thalassemia (disorder) |
| 66055002 | http://snomed.info/sct | Alpha zero thalassemia (disorder) |
| 66262001 | http://snomed.info/sct | Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (disorder) |
| 66309005 | http://snomed.info/sct | Antibody-mediated anemia (disorder) |
| 6659005 | http://snomed.info/sct | Megaloblastic anemia due to celiac disease (disorder) |
| 66612000 | http://snomed.info/sct | Nutritional anemia (disorder) |
| 67894009 | http://snomed.info/sct | Megaloblastic anemia due to increased requirements (disorder) |
| 68361004 | http://snomed.info/sct | Late anemia due to isoimmunization (disorder) |
| 68700003 | http://snomed.info/sct | Megaloblastic anemia due to error of cobalamin metabolism (disorder) |
| 68913001 | http://snomed.info/sct | Alpha thalassemia (disorder) |
| 691421000119108 | http://snomed.info/sct | Anemia co-occurrent and due to chronic kidney disease stage 3 (disorder) |
| 69216008 | http://snomed.info/sct | Hb Lepore thalassemia (disorder) |
| 69574002 | http://snomed.info/sct | Anemia of parathyroid dysfunction (disorder) |
| 69981004 | http://snomed.info/sct | Hereditary spherocytosis due to beta spectrin defect (disorder) |
| 703135009 | http://snomed.info/sct | Anemia in malignant neoplastic disease (disorder) |
| 707323002 | http://snomed.info/sct | Anemia co-occurrent and due to chronic kidney disease (disorder) |
| 707324008 | http://snomed.info/sct | Anemia co-occurrent and due to end stage renal disease (disorder) |
| 707480001 | http://snomed.info/sct | Chronic hemolytic anemia (disorder) |
| 711161006 | http://snomed.info/sct | Hypochromic microcytic anemia with iron overload (disorder) |
| 713533000 | http://snomed.info/sct | Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder) |
| 715342005 | http://snomed.info/sct | Alpha thalassemia X-linked intellectual disability syndrome (disorder) |
| 715526002 | http://snomed.info/sct | Dehydrated hereditary stomatocytosis (disorder) |
| 716682000 | http://snomed.info/sct | Dominant beta-thalassemia (disorder) |
| 717050005 | http://snomed.info/sct | Autosomal recessive sideroblastic anemia (disorder) |
| 717254007 | http://snomed.info/sct | Familial pseudohyperkalemia (disorder) |
| 717946000 | http://snomed.info/sct | Megaloblastic anemia due to vitamin B12 deficiency secondary to intestinal disease (disorder) |
| 717947009 | http://snomed.info/sct | Vitamin B12 deficiency anemia caused by drug (disorder) |
| 717948004 | http://snomed.info/sct | Acquired iron deficiency anemia due to increased iron requirement (disorder) |
| 718196002 | http://snomed.info/sct | Beta thalassemia X-linked thrombocytopenia syndrome (disorder) |
| 71855000 | http://snomed.info/sct | Acute megaloblastic anemia secondary to total parenteral nutrition (disorder) |
| 719402008 | http://snomed.info/sct | Lethal hemolytic anemia and genital anomaly syndrome (disorder) |
| 720401009 | http://snomed.info/sct | Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder) |
| 720465002 | http://snomed.info/sct | Adult-onset autosomal recessive sideroblastic anemia (disorder) |
| 721184003 | http://snomed.info/sct | Megaloblastic anemia due to folate deficiency due to increased requirement (disorder) |
| 721185002 | http://snomed.info/sct | Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder) |
| 721295000 | http://snomed.info/sct | Acquired thiamine deficiency anemia (disorder) |
| 722005000 | http://snomed.info/sct | Iron-refractory iron deficiency anemia (disorder) |
| 722125003 | http://snomed.info/sct | Overhydrated hereditary stomatocytosis (disorder) |
| 722721004 | http://snomed.info/sct | Familial hemolytic uremic syndrome (disorder) |
| 72331000119105 | http://snomed.info/sct | Thalassemia in mother complicating pregnancy (disorder) |
| 72501006 | http://snomed.info/sct | Anemia caused by arsenic hydride (disorder) |
| 73073009 | http://snomed.info/sct | Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) |
| 73190000 | http://snomed.info/sct | Epsilon gamma delta beta^0^ thalassemia (disorder) |
| 73891003 | http://snomed.info/sct | Acute megaloblastic anemia caused by nitrous oxide (disorder) |
| 74703006 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (disorder) |
| 74789008 | http://snomed.info/sct | Coombs positive hemolytic anemia (disorder) |
| 75443009 | http://snomed.info/sct | Hereditary elliptocytosis due to abnormal protein 4.1 (disorder) |
| 75451007 | http://snomed.info/sct | Thalassemia major (disorder) |
| 76336008 | http://snomed.info/sct | Delta beta zero thalassemia (disorder) |
| 76366001 | http://snomed.info/sct | Hemolytic anemia caused by Bartonella (disorder) |
| 77413008 | http://snomed.info/sct | Severe hereditary spherocytosis due to spectrin deficiency (disorder) |
| 77607006 | http://snomed.info/sct | Drug-induced sideroblastic anemia (disorder) |
| 77663007 | http://snomed.info/sct | Hemolytic anemia caused by malaria (disorder) |
| 78209002 | http://snomed.info/sct | Hemolytic uremic syndrome, adult type (disorder) |
| 78677008 | http://snomed.info/sct | Anemia due to pantothenic deficiency (disorder) |
| 78908001 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity (disorder) |
| 78997000 | http://snomed.info/sct | Megaloblastic anemia due to vegetarianism (disorder) |
| 79035003 | http://snomed.info/sct | Anemia due to unknown mechanism (disorder) |
| 79592006 | http://snomed.info/sct | Beta plus thalassemia (disorder) |
| 80126007 | http://snomed.info/sct | Plummer-Vinson syndrome (disorder) |
| 80875006 | http://snomed.info/sct | Achlorhydric anemia (disorder) |
| 80963002 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency class V variant anemia (disorder) |
| 81711008 | http://snomed.info/sct | Hemolytic anemia caused by drugs (disorder) |
| 82003006 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia (disorder) |
| 82430007 | http://snomed.info/sct | Acute megaloblastic anemia (disorder) |
| 82895008 | http://snomed.info/sct | Megaloblastic anemia due to disease of small intestine (disorder) |
| 82980005 | http://snomed.info/sct | Anemia due to diabetes mellitus (disorder) |
| 83414005 | http://snomed.info/sct | Macrocytic anemia (disorder) |
| 84027009 | http://snomed.info/sct | Pernicious anemia (disorder) |
| 84188003 | http://snomed.info/sct | Thalassemia syndrome (disorder) |
| 85422000 | http://snomed.info/sct | Alpha plus thalassemia non deletion type (disorder) |
| 85557000 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin deletion type (disorder) |
| 85570009 | http://snomed.info/sct | Anemia due to vitamin A deficiency (disorder) |
| 85649008 | http://snomed.info/sct | Megaloblastic anemia due to folate deficiency (disorder) |
| 85746008 | http://snomed.info/sct | Anemia due to protein deficiency (disorder) |
| 862001 | http://snomed.info/sct | Anemia caused by chlorate (disorder) |
| 86225009 | http://snomed.info/sct | Hapten type high affinity hemolytic anemia (disorder) |
| 86242003 | http://snomed.info/sct | Alpha plus thalassemia deletion type (disorder) |
| 86325007 | http://snomed.info/sct | Non megaloblastic anemia due to alcoholism (disorder) |
| 86448001 | http://snomed.info/sct | Anemia due to vitamin B>6< deficiency (disorder) |
| 86715000 | http://snomed.info/sct | Beta zero thalassemia (disorder) |
| 86859003 | http://snomed.info/sct | Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia (disorder) |
| 87522002 | http://snomed.info/sct | Iron deficiency anemia (disorder) |
| 87806008 | http://snomed.info/sct | Megaloblastic anemia due to tropical sprue (disorder) |
| 87810006 | http://snomed.info/sct | Megaloblastic anemia due to alcoholism (disorder) |
| 87994004 | http://snomed.info/sct | Xerocytosis (disorder) |
| 8857001 | http://snomed.info/sct | Hereditary elliptocytosis due to alpha spectrin defect (disorder) |
| 89459006 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin linked to beta-globulin gene cluster (disorder) |
| 89810003 | http://snomed.info/sct | ^A^gamma delta beta^0^ thalassemia (disorder) |
| 90175006 | http://snomed.info/sct | Secondary acquired sideroblastic anemia (disorder) |
| 91217009 | http://snomed.info/sct | Megaloblastic anemia due to pregnancy (disorder) |
| 91411007 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by immunoglobulin A (disorder) |
| 934007 | http://snomed.info/sct | Thalassemia intermedia (disorder) |
| 9434008 | http://snomed.info/sct | Hereditary pyropoikilocytosis (disorder) |
Produced 08 Sep 2023