| Source | us.nlm.vsac#0.11.0:null (v4.0.1) |
| resourceType | ValueSet |
| id | 2.16.840.1.113762.1.4.1222.53 |
| canonical | http://cts.nlm.nih.gov/fhir/ValueSet/2.16.840.1.113762.1.4.1222.53 |
| version | 20200414 |
| status | active |
| publisher | HL7 Patient Care WG Steward |
| name | AnemiaConditions |
| title | Anemia Conditions |
| date | 2020-04-14T01:00:20-04:00 |
| experimental | false |
| description | This value set may undergo changes until the HL7 Multiple Chronic Care FHIR IG is formally published in 2024. |
| Usages | (none) |
This value set contains 566 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) |
| 10741751000119100 | http://snomed.info/sct | Anemia in mother complicating childbirth (disorder) |
| 10759351000119103 | http://snomed.info/sct | Sickle cell anemia in mother complicating childbirth (disorder) |
| 10762261000119105 | http://snomed.info/sct | Anemia following acute postoperative blood loss (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) |
| 109998009 | http://snomed.info/sct | Myelodysplastic syndrome with ring sideroblasts and single lineage dysplasia (disorder) |
| 111407006 | http://snomed.info/sct | Hemolytic uremic syndrome (disorder) |
| 111469006 | http://snomed.info/sct | Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization (disorder) |
| 111570005 | http://snomed.info/sct | Anemia due to infection (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) |
| 1142030006 | http://snomed.info/sct | Nutritional anemia of pregnancy (disorder) |
| 1142062009 | http://snomed.info/sct | Macrocytic anemia of pregnancy (disorder) |
| 1142083003 | http://snomed.info/sct | Hemolytic anemia of pregnancy (disorder) |
| 1142087002 | http://snomed.info/sct | Congenital megaloblastic anemia due to transcobalamin II deficiency (disorder) |
| 1148853004 | http://snomed.info/sct | Iron deficiency anemia following gastrectomy (disorder) |
| 1148855006 | http://snomed.info/sct | Iron deficiency anemia due to increased requirement in adolescence (disorder) |
| 1148856007 | http://snomed.info/sct | Iron deficiency anemia due to increased requirement in infancy (disorder) |
| 1148861009 | http://snomed.info/sct | Iron deficiency anemia due to celiac disease (disorder) |
| 1148880006 | http://snomed.info/sct | Non autoimmune hemolytic anemia caused by drug (disorder) |
| 1148893001 | http://snomed.info/sct | Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency (disorder) |
| 1148895008 | http://snomed.info/sct | Hemolytic anemia due to red cell enolase deficiency (disorder) |
| 1148897000 | http://snomed.info/sct | Hemoglobin Paksé disease (disorder) |
| 1148899002 | http://snomed.info/sct | Hemoglobin Seal Rock disease (disorder) |
| 1148914007 | http://snomed.info/sct | Autosomal dominant sideroblastic anemia (disorder) |
| 11491000 | http://snomed.info/sct | Anemia due to niacin deficiency (disorder) |
| 11503009 | http://snomed.info/sct | Relative anemia (disorder) |
| 1153333001 | http://snomed.info/sct | Pernicious anemia due to autoimmune disorder (disorder) |
| 1153353002 | http://snomed.info/sct | Vitamin B12 deficiency anemia following total gastrectomy (disorder) |
| 1153358006 | http://snomed.info/sct | Lymphocyte passenger syndrome following organ transplantation (disorder) |
| 1153380009 | http://snomed.info/sct | Mechanical hemolysis following insertion of prosthetic heart valve (disorder) |
| 1153399000 | http://snomed.info/sct | Homozygous hereditary elliptocytosis (disorder) |
| 1153403009 | http://snomed.info/sct | Hereditary iron deficiency anemia (disorder) |
| 1153409008 | http://snomed.info/sct | Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) |
| 1153413001 | http://snomed.info/sct | Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) |
| 1153415008 | http://snomed.info/sct | Acute sequestration of spleen due to sickle cell hemoglobin C disease with crisis (disorder) |
| 115963009 | http://snomed.info/sct | Regenerative anemia (disorder) |
| 1171357005 | http://snomed.info/sct | Vitamin B12 deficiency anemia following gastrectomy (disorder) |
| 11781007 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by complement (disorder) |
| 118791000119106 | http://snomed.info/sct | Aplastic anemia caused by antineoplastic agent (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) |
| 1237349008 | http://snomed.info/sct | Hydrops, lactic acidosis, sideroblastic anemia, multisystemic failure syndrome (disorder) |
| 1237417007 | http://snomed.info/sct | Carbamoyl-phosphate synthetase 2, aspartate transcarbamylase, and dihydroorotase congenital disorder of glycosylation (disorder) |
| 127034005 | http://snomed.info/sct | Pancytopenia (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) |
| 127060006 | http://snomed.info/sct | Drug-induced immune hemolytic anemia, hapten type (disorder) |
| 127061005 | http://snomed.info/sct | Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement (disorder) |
| 127319005 | http://snomed.info/sct | Anemia caused by alloimmune destruction of transfused red cells (disorder) |
| 12907000 | http://snomed.info/sct | Thiamine-responsive megaloblastic anemia (disorder) |
| 129638002 | http://snomed.info/sct | Hemolytic anemia caused by hyperbaric oxygen (disorder) |
| 13172003 | http://snomed.info/sct | Chronic idiopathic thrombocytopenic purpura (disorder) |
| 136281000119109 | http://snomed.info/sct | Anemia caused by antineoplastic agent (disorder) |
| 14024008 | http://snomed.info/sct | Humoral immunologic aplastic anemia (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) |
| 16623961000119100 | http://snomed.info/sct | Pancytopenia caused by immunosuppressant (disorder) |
| 16645003 | http://snomed.info/sct | Anemia caused by insect venom (disorder) |
| 16964007 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin thalassemia (disorder) |
| 1801000119106 | http://snomed.info/sct | Anemia, pre-end stage renal disease on erythropoietin protocol (disorder) |
| 18273004 | http://snomed.info/sct | Unstable hemoglobin disease (disorder) |
| 183005 | http://snomed.info/sct | Autoimmune pancytopenia (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) |
| 190996002 | http://snomed.info/sct | Severe combined immunodeficiency with reticular dysgenesis (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) |
| 191169008 | http://snomed.info/sct | Hereditary elliptocytosis (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) |
| 191229004 | http://snomed.info/sct | Infantile pyknocytosis (disorder) |
| 191244003 | http://snomed.info/sct | Aplastic anemia due to chronic disease (disorder) |
| 191246001 | http://snomed.info/sct | Aplastic anemia due to infection (disorder) |
| 191247005 | http://snomed.info/sct | Aplastic anemia caused by radiation (disorder) |
| 191248000 | http://snomed.info/sct | Aplastic anemia caused by toxic cause (disorder) |
| 191251007 | http://snomed.info/sct | Transient hypoplastic anemia (disorder) |
| 191255003 | http://snomed.info/sct | Transient acquired pure red cell aplasia (disorder) |
| 191256002 | http://snomed.info/sct | Idiopathic aplastic anemia (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) |
| 199244000 | http://snomed.info/sct | Anemia during pregnancy - baby delivered (disorder) |
| 199245004 | http://snomed.info/sct | Anemia in the puerperium - baby delivered during current episode of care (disorder) |
| 199246003 | http://snomed.info/sct | Anemia during pregnancy - baby not yet delivered (disorder) |
| 199247007 | http://snomed.info/sct | Anemia in the puerperium - baby delivered during previous episode of care (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) |
| 234350007 | http://snomed.info/sct | Neonatal 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) |
| 234367000 | http://snomed.info/sct | Pancytopenia with pancreatitis (disorder) |
| 234375006 | http://snomed.info/sct | Transient erythroblastopenia of childhood (disorder) |
| 234376007 | http://snomed.info/sct | Acquired red cell aplasia (disorder) |
| 234380002 | http://snomed.info/sct | Kell isoimmunization of the newborn (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) |
| 234392002 | http://snomed.info/sct | Hemoglobin E/beta thalassemia disease (disorder) |
| 234410008 | http://snomed.info/sct | Hereditary elliptocytosis with transient poikilocytosis (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) |
| 240486003 | http://snomed.info/sct | Parvoviral aplastic crisis (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) |
| 26409005 | http://snomed.info/sct | Congenital dyserythropoietic anemia, type III (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) |
| 267524009 | http://snomed.info/sct | Constitutional aplastic anemia with malformation (disorder) |
| 267527002 | http://snomed.info/sct | Aplastic anemia due to drugs (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) |
| 273985002 | http://snomed.info/sct | Anemia due to isoimmunization (disorder) |
| 276448005 | http://snomed.info/sct | Idiopathic sideroblastic anemia (disorder) |
| 276578004 | http://snomed.info/sct | Physiological anemia of infancy (disorder) |
| 276580005 | http://snomed.info/sct | Atypical isoimmunization of newborn (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) |
| 28975000 | http://snomed.info/sct | Constitutional aplastic anemia (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) |
| 302873008 | http://snomed.info/sct | Thrombocytopenic purpura (disorder) |
| 303060002 | http://snomed.info/sct | Normocytic anemia following acute bleed (disorder) |
| 30418008 | http://snomed.info/sct | Anemia of adrenal dysfunction (disorder) |
| 30575002 | http://snomed.info/sct | Fanconi's anemia (disorder) |
| 306058006 | http://snomed.info/sct | Aplastic anemia (disorder) |
| 307333004 | http://snomed.info/sct | Rhesus isoimmunization due to anti-D (disorder) |
| 307334005 | http://snomed.info/sct | Rhesus isoimmunization due to anti-c (disorder) |
| 307335006 | http://snomed.info/sct | Rhesus isoimmunization due to anti-E (disorder) |
| 307336007 | http://snomed.info/sct | Rhesus isoimmunization due to anti-Cw (disorder) |
| 307337003 | http://snomed.info/sct | Duffy isoimmunization of the newborn (disorder) |
| 307338008 | http://snomed.info/sct | Kidd isoimmunization of the newborn (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) |
| 328371000119107 | http://snomed.info/sct | Pancytopenia caused by antithyroid drug (disorder) |
| 328381000119105 | http://snomed.info/sct | Pancytopenia caused by anticonvulsant (disorder) |
| 32855007 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin unlinked to beta-globulin gene cluster (disorder) |
| 32858009 | http://snomed.info/sct | Hemolytic disease of fetus OR newborn due to ABO immunization (disorder) |
| 33183004 | http://snomed.info/sct | Post infectious thrombocytopenic purpura (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) |
| 350601000119109 | http://snomed.info/sct | Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder) |
| 350611000119107 | http://snomed.info/sct | Hemolytic disease of fetus due to ABO immunization (disorder) |
| 351181000119103 | http://snomed.info/sct | Anemia due to enzymopathy (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) |
| 373420004 | http://snomed.info/sct | Upshaw-Schulman 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) |
| 387705004 | http://snomed.info/sct | Hemolytic disease of fetus OR newborn due to isoimmunization (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) |
| 398937006 | http://snomed.info/sct | Cold autoimmune hemolytic anemia (disorder) |
| 40108008 | http://snomed.info/sct | Thalassemia (disorder) |
| 402653004 | http://snomed.info/sct | Thrombocytopenic purpura due to defective platelet production (disorder) |
| 402654005 | http://snomed.info/sct | Thrombocytopenic purpura due to platelet consumption (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) |
| 413565006 | http://snomed.info/sct | Aplastic anemia associated with metabolic alteration (disorder) |
| 413566007 | http://snomed.info/sct | Aplastic anemia associated with pancreatitis (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) |
| 415286005 | http://snomed.info/sct | Myelodysplastic syndrome with ring sideroblasts and multilineage dysplasia (disorder) |
| 41614006 | http://snomed.info/sct | Hypoplastic anemia (disorder) |
| 416180004 | http://snomed.info/sct | Hemoglobin SS disease without crisis (disorder) |
| 416826005 | http://snomed.info/sct | Sickle cell-thalassemia disease with crisis (disorder) |
| 417048006 | http://snomed.info/sct | Sickle cell-thalassemia disease without crisis (disorder) |
| 417425009 | http://snomed.info/sct | Hemoglobin SS disease with crisis (disorder) |
| 417626001 | http://snomed.info/sct | Thrombocytopenic purpura associated with metabolic disorder (disorder) |
| 41841004 | http://snomed.info/sct | Sideroblastic anemia (disorder) |
| 420543008 | http://snomed.info/sct | Anemia associated with acquired immunodeficiency syndrome (disorder) |
| 421102007 | http://snomed.info/sct | Aplastic anemia with acquired immunodeficiency syndrome (disorder) |
| 421851008 | http://snomed.info/sct | Acquired hemolytic anemia associated with acquired immunodeficiency syndrome (disorder) |
| 422167001 | http://snomed.info/sct | Mycoplasmal anemia (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) |
| 42601008 | http://snomed.info/sct | Congenital hemolytic anemia (disorder) |
| 428383000 | http://snomed.info/sct | Anemia caused by medication (disorder) |
| 43707008 | http://snomed.info/sct | Anemia caused by heat (disorder) |
| 438476003 | http://snomed.info/sct | Autoimmune thrombotic thrombocytopenic purpura (disorder) |
| 43858000 | http://snomed.info/sct | Secondary aplastic anemia (disorder) |
| 439007008 | http://snomed.info/sct | Acquired thrombotic thrombocytopenic purpura (disorder) |
| 440206000 | http://snomed.info/sct | Hemoglobin SS disease with vasoocclusive crisis (disorder) |
| 441322009 | http://snomed.info/sct | Drug induced thrombotic thrombocytopenic purpura (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) |
| 444108000 | http://snomed.info/sct | Acute sickle cell splenic sequestration crisis (disorder) |
| 444271000 | http://snomed.info/sct | Erythropoietin resistance in anemia of chronic kidney disease (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) |
| 45828008 | http://snomed.info/sct | Anemia in mother complicating pregnancy, childbirth AND/OR puerperium (disorder) |
| 462166006 | http://snomed.info/sct | Fetal anemia (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) |
| 47100003 | http://snomed.info/sct | Anemia of prematurity (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) |
| 48983004 | http://snomed.info/sct | X chromosome-linked sideroblastic anemia (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) |
| 50220002 | http://snomed.info/sct | Cellular immunologic aplastic anemia (disorder) |
| 50253007 | http://snomed.info/sct | Secondary paroxysmal cold hemoglobinuria (disorder) |
| 50715003 | http://snomed.info/sct | Pure red cell aplasia (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) |
| 52951008 | http://snomed.info/sct | Congenital dyserythropoietic anemia (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) |
| 53743006 | http://snomed.info/sct | Anemia following fetal blood loss (disorder) |
| 54006005 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (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) |
| 55907008 | http://snomed.info/sct | Acquired aplastic anemia (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) |
| 57192008 | http://snomed.info/sct | Acute pure red cell aplasia (disorder) |
| 5876000 | http://snomed.info/sct | Acquired pancytopenia (disorder) |
| 59106005 | http://snomed.info/sct | Anemia due to decreased red cell production (disorder) |
| 59548005 | http://snomed.info/sct | Congenital dyserythropoietic anemia, type I (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) |
| 61395005 | http://snomed.info/sct | Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia (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) |
| 62609001 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by immunoglobulin G plus complement (disorder) |
| 62871001 | http://snomed.info/sct | Idiopathic paroxysmal cold hemoglobinuria (disorder) |
| 63565007 | http://snomed.info/sct | Congenital anemia (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) |
| 68870007 | http://snomed.info/sct | Congenital dyserythropoietic anemia, type II (disorder) |
| 68913001 | http://snomed.info/sct | Alpha thalassemia (disorder) |
| 691381000119104 | http://snomed.info/sct | Anemia due to chronic kidney disease stage 1 (disorder) |
| 691401000119104 | http://snomed.info/sct | Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder) |
| 691411000119101 | http://snomed.info/sct | Anemia co-occurrent and due to chronic kidney disease stage 5 (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) |
| 703540008 | http://snomed.info/sct | Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis (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) |
| 713349004 | http://snomed.info/sct | Anemia co-occurrent with human immunodeficiency virus infection (disorder) |
| 713388002 | http://snomed.info/sct | GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder) |
| 713496008 | http://snomed.info/sct | Anemia caused by zidovudine (disorder) |
| 713508003 | http://snomed.info/sct | Aplastic anemia co-occurrent with human immunodeficiency virus infection (disorder) |
| 713533000 | http://snomed.info/sct | Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder) |
| 713910008 | http://snomed.info/sct | Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (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) |
| 71832003 | http://snomed.info/sct | Autoimmune hemolytic anemia caused by immunoglobulin M (disorder) |
| 71855000 | http://snomed.info/sct | Acute megaloblastic anemia secondary to total parenteral nutrition (disorder) |
| 718716008 | http://snomed.info/sct | Autoimmune hemolytic anemia mixed type (disorder) |
| 719019000 | http://snomed.info/sct | WT limb blood syndrome (disorder) |
| 719402008 | http://snomed.info/sct | Lethal hemolytic anemia and genital anomaly syndrome (disorder) |
| 719453009 | http://snomed.info/sct | Congenital dyserythropoietic anemia type IV (disorder) |
| 719816006 | http://snomed.info/sct | X-linked sideroblastic anemia with spinocerebellar ataxia (disorder) |
| 71988008 | http://snomed.info/sct | Aase 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) |
| 720982007 | http://snomed.info/sct | Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (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) |
| 721186001 | http://snomed.info/sct | Megaloblastic anemia due to folate deficiency in prematurity (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) |
| 722207000 | http://snomed.info/sct | Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder) |
| 722475006 | http://snomed.info/sct | X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder) |
| 722721004 | http://snomed.info/sct | Familial hemolytic uremic syndrome (disorder) |
| 72331000119105 | http://snomed.info/sct | Thalassemia in mother complicating pregnancy (disorder) |
| 723512008 | http://snomed.info/sct | Revesz syndrome (disorder) |
| 723623002 | http://snomed.info/sct | Southeast Asian ovalocytosis (disorder) |
| 724138007 | http://snomed.info/sct | Mitochondrial myopathy with sideroblastic anemia syndrome (disorder) |
| 724556004 | http://snomed.info/sct | Iron deficiency anemia due to blood loss (disorder) |
| 724557008 | http://snomed.info/sct | Acquired iron deficiency anemia due to decreased absorption (disorder) |
| 72501006 | http://snomed.info/sct | Anemia caused by arsenic hydride (disorder) |
| 725057008 | http://snomed.info/sct | Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder) |
| 725463007 | http://snomed.info/sct | Severe congenital hypochromic anemia with ringed sideroblasts (disorder) |
| 726669007 | http://snomed.info/sct | Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (disorder) |
| 73073009 | http://snomed.info/sct | Hereditary elliptocytosis due to beta spectrin defect in self-association (disorder) |
| 73162004 | http://snomed.info/sct | Posttransfusion purpura (disorder) |
| 73190000 | http://snomed.info/sct | Epsilon gamma delta beta^0^ thalassemia (disorder) |
| 732960002 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus (disorder) |
| 732962005 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) |
| 732963000 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder (disorder) |
| 732965007 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) |
| 732966008 | http://snomed.info/sct | Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) |
| 734349003 | http://snomed.info/sct | Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (disorder) |
| 735452003 | http://snomed.info/sct | Hereditary vitamin B12 deficiency anemia (disorder) |
| 735453008 | http://snomed.info/sct | Hereditary folate deficiency anemia (disorder) |
| 736024007 | http://snomed.info/sct | Pancytopenia caused by medication (disorder) |
| 737220002 | http://snomed.info/sct | Anemia due to metabolic disorder (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) |
| 75331009 | http://snomed.info/sct | Evans syndrome (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) |
| 765327005 | http://snomed.info/sct | Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (disorder) |
| 765748009 | http://snomed.info/sct | Adult pure red cell aplasia (disorder) |
| 766982000 | http://snomed.info/sct | Hemolytic anemia due to adenylate kinase deficiency (disorder) |
| 767657005 | http://snomed.info/sct | Anemia due to and following chemotherapy (disorder) |
| 768556005 | http://snomed.info/sct | Ataxia pancytopenia syndrome (disorder) |
| 77084001 | http://snomed.info/sct | Immunologic aplastic anemia (disorder) |
| 773489008 | http://snomed.info/sct | Hereditary cryohydrocytosis with normal stomatin (disorder) |
| 774071007 | http://snomed.info/sct | Pancytopenia with developmental delay syndrome (disorder) |
| 774083009 | http://snomed.info/sct | Neonatal autoimmune hemolytic anemia (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) |
| 778027003 | http://snomed.info/sct | Primary CD59 deficiency (disorder) |
| 78129009 | http://snomed.info/sct | Thrombotic thrombocytopenic purpura (disorder) |
| 78209002 | http://snomed.info/sct | Hemolytic uremic syndrome, adult type (disorder) |
| 782759001 | http://snomed.info/sct | X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) |
| 782911008 | http://snomed.info/sct | Hereditary cryohydrocytosis with reduced stomatin (disorder) |
| 783142006 | http://snomed.info/sct | Pancytopenia due to IKAROS family zinc finger 1 mutations (disorder) |
| 783255002 | http://snomed.info/sct | Hereditary isolated aplastic anemia (disorder) |
| 78677008 | http://snomed.info/sct | Anemia due to pantothenic deficiency (disorder) |
| 788865000 | http://snomed.info/sct | Anemia due to chronic infectious disease (disorder) |
| 788944005 | http://snomed.info/sct | Gamma delta beta thalassemia (disorder) |
| 78908001 | http://snomed.info/sct | Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity (disorder) |
| 789660001 | http://snomed.info/sct | Atypical hemolytic uremic syndrome (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) |
| 863953007 | http://snomed.info/sct | Primaquine sensitivity anemia (disorder) |
| 86448001 | http://snomed.info/sct | Anemia due to vitamin B>6< deficiency (disorder) |
| 866092006 | http://snomed.info/sct | Megaloblastic anemia due to dihydrofolate reductase 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) |
| 86986002 | http://snomed.info/sct | Hemolytic disease of fetus OR newborn due to RhD isoimmunization (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) |
| 88854002 | http://snomed.info/sct | Congenital hypoplastic anemia (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) |
| 90414007 | http://snomed.info/sct | Chronic acquired pure red cell aplasia (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) |
| 9764001 | http://snomed.info/sct | Anemia caused by radiation (disorder) |
| D63 | http://hl7.org/fhir/sid/icd-10-cm | Anemia in chronic diseases classified elsewhere |
| D63.0 | http://hl7.org/fhir/sid/icd-10-cm | Anemia in neoplastic disease |
| D63.1 | http://hl7.org/fhir/sid/icd-10-cm | Anemia in chronic kidney disease |
| D63.8 | http://hl7.org/fhir/sid/icd-10-cm | Anemia in other chronic diseases classified elsewhere |
| D64.8 | http://hl7.org/fhir/sid/icd-10-cm | Other specified anemias |
| D64.81 | http://hl7.org/fhir/sid/icd-10-cm | Anemia due to antineoplastic chemotherapy |
| D64.89 | http://hl7.org/fhir/sid/icd-10-cm | Other specified anemias |
| D64.9 | http://hl7.org/fhir/sid/icd-10-cm | Anemia, unspecified |
Produced 08 Sep 2023