Red blood cell (RBC) tests Under review

Coding system: SNOMED CT (UK Clinical Edition)
Coding system release: 39.2.0
Organisation: OpenSAFELY
Codelist ID: opensafely/red-blood-cell-rbc-tests
Version ID: 17bcafa1
Number of codes included: 6

Versions

17bcafa1 Under review
Created: 15 Dec 2024 at 22:33
576a859e Published
Created: 15 Feb 2021 at 13:48

Description

A SNOMED CT codelist for patients receiving monitoring of red blood cell (RBC) tests.

Methodology

We searched for the team "red blood cell", and included all codes relating to measurement.

Signed off by

Richard Croker, (April 20, 2021)
Brian MacKenna, (April 21, 2021)

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
1022451000000103	Red blood cell count
14089001	Red blood cell count
142831004	Red blood cell count
165428005	Red blood cell count NOS
365625004	Finding of red blood cell count
537891000000106	Red blood cell count NOS

This page shows the search terms that were used to build the codelist. Concepts that match the search terms, but which were excluded, are in faint grey.

1022451000000103

Included 0 out of 0 matching concepts.

Show matching concepts

red blood cell count

Included 6 out of 436 matching concepts.

Show matching concepts

Aase syndrome (71988008)
Acquired aplastic anemia (55907008)
Acquired hemolytic anemia (4854004)
Acquired hemolytic anemia associated with acquired immunodeficiency syndrome (421851008)
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (713533000)
Acquired iron deficiency anemia due to decreased absorption (724557008)
Acquired iron deficiency anemia due to increased iron requirement (717948004)
Acquired pancytopenia (5876000)
Acquired red cell aplasia (234376007)
Acquired spherocytosis (191228007)
Acquired thiamine deficiency anemia (721295000)
Acquired thrombotic thrombocytopenic purpura (439007008)
Acute megaloblastic anemia due to dialysis (26944003)
Acute pure red cell aplasia (57192008)
Adult pure red cell aplasia (765748009)
Alpha plus thalassemia deletion type (86242003)
Alpha plus thalassemia non deletion type (85422000)
Alpha thalassemia X-linked intellectual disability syndrome (715342005)
Alpha-thalassemia intellectual disability syndrome linked to chromosome 16 (734349003)
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (720982007)
Anemia caused by alloimmune destruction of transfused red cells (127319005)
Anemia caused by antineoplastic agent (136281000119109)
Anemia caused by heat (43707008)
Anemia caused by lead (36919001)
Anemia caused by zidovudine (713496008)
Anemia co-occurrent and due to chronic kidney disease stage 4 (691401000119104)
Anemia co-occurrent and due to chronic kidney disease stage 5 (691411000119101)
Anemia co-occurrent with human immunodeficiency virus infection (713349004)
Anemia due to abnormality extrinsic to the red cell (44288006)
Anemia due to enzyme deficiency (111577008)
Anemia due to mechanical damage (34247008)
Anemia due to membrane defect (111575000)
Anemia due to pentose phosphate pathway defect (29177004)
Anemia following fetal blood loss (53743006)
Anemia of prematurity (47100003)
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (713910008)
Antibody-mediated anemia (66309005)
Aplastic anemia (306058006)
Aplastic anemia associated with metabolic alteration (413565006)
Aplastic anemia associated with pancreatitis (413566007)
Aplastic anemia associated with pregnancy (413567003)
Aplastic anemia caused by antineoplastic agent (118791000119106)
Aplastic anemia caused by radiation (191247005)
Aplastic anemia caused by toxic cause (191248000)
Aplastic anemia co-occurrent with human immunodeficiency virus infection (713508003)
Aplastic anemia due to chronic disease (191244003)
Aplastic anemia due to drugs (267527002)
Aplastic anemia due to infection (191246001)
Aplastic anemia with acquired immunodeficiency syndrome (421102007)
Aplastic anemia, intellectual disability, dwarfism syndrome (1332385000)
Ataxia pancytopenia syndrome (768556005)
Atypical hemolytic uremic syndrome (789660001)
Atypical hemolytic uremic syndrome with anti-factor H antibodies (1295220004)
Atypical hemolytic uremic syndrome with complement gene abnormality (1293264009)
Atypical isoimmunization of newborn (276580005)
Autoimmune hemolytic anemia (413603009)
Autoimmune hemolytic anemia caused by complement (11781007)
Autoimmune hemolytic anemia caused by immunoglobulin A (91411007)
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement (33491002)
Autoimmune hemolytic anemia caused by immunoglobulin G (5603006)
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement (62609001)
Autoimmune hemolytic anemia caused by immunoglobulin M (71832003)
Autoimmune hemolytic anemia mixed type (718716008)
Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement (127061005)
Autoimmune pancytopenia (183005)
Autoimmune thrombotic thrombocytopenic purpura (438476003)
Autosomal dominant secondary polycythemia (783202008)
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene (783766005)
Cellular immunologic aplastic anemia (50220002)
Central nervous system calcification, deafness, tubular acidosis, anemia syndrome (726669007)
Chronic acquired pure red cell aplasia (90414007)
Chronic cold agglutinin disease (127055007)
Chronic cold agglutinin disease associated with B-cell neoplasm (127056008)
Chronic hemolytic anemia (707480001)
Chronic idiopathic autoimmune hemolytic anemia (22098000)
Chronic idiopathic thrombocytopenic purpura (13172003)
Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis (703540008)
Chuvash erythrocytosis (770407006)
Cold agglutinin disease due to and following Epstein-Barr virus infection (127054006)
Cold autoimmune hemolytic anemia (398937006)
Congenital anemia (63565007)
Congenital atransferrinemia (111571009)
Congenital dyserythropoietic anemia (52951008)
Congenital dyserythropoietic anemia type IV (719453009)
Congenital dyserythropoietic anemia, type I (59548005)
Congenital dyserythropoietic anemia, type II (68870007)
Congenital dyserythropoietic anemia, type III (26409005)
Congenital hemolytic anemia (42601008)
Congenital hemolytic uremic syndrome (444976001)
Congenital hypoplastic anemia (88854002)
Congenital megaloblastic anemia due to transcobalamin II deficiency (1142087002)
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (363041004)
Congenital sideroblastic anemia, B-cell immunodeficiency, periodic fever, developmental delay syndrome (765327005)
Congenital transferrin deficiency (234353009)
Constitutional aplastic anemia (28975000)
Constitutional aplastic anemia with malformation (267524009)
Coombs negative hemolytic anemia (12189000)
Coombs positive hemolytic anemia (74789008)
Count of nucleated red blood cells in blood (58571000237106)
Count of red blood cells in cerebrospinal fluid (16901000237101)
Count of red blood cells in fluid (15141000237109)
Count of red blood cells in urine (43331000237105)
Diarrhea-associated hemolytic uremic syndrome (373421000)
Diarrhea-negative hemolytic uremic syndrome (373422007)
Doan-Wright syndrome (38970002)
Drug induced thrombotic thrombocytopenic purpura (441322009)
Drug-induced autoimmune hemolytic anemia (309742004)
Drug-induced enzyme deficiency anemia (15276008)
Drug-induced immune hemolytic anemia, hapten type (127060006)
Drug-induced immune hemolytic anemia, immune complex type (18323000)
Duffy isoimmunization of the newborn (307337003)
Epsilon gamma delta beta^0^ thalassemia (73190000)
Erythrocytosis (127062003)
Erythrocytosis caused by low atmospheric pressure (25881005)
Erythrocytosis due to alveolar hypoventilation (40679002)
Erythrocytosis due to autotransfusion (25601009)
Erythrocytosis due to cardiovascular disease (28319009)
Erythrocytosis due to cerebellar hemangioma (15466007)
Erythrocytosis due to cyanotic congenital heart disease (127063008)
Erythrocytosis due to defective oxygen transport (90501009)
Erythrocytosis due to endocrine disorder (80511004)
Erythrocytosis due to hepatoma (42616006)
Erythrocytosis due to hydronephrosis (9426002)
Erythrocytosis due to polycythemia vera (414127000)
Erythrocytosis due to pulmonary disease (78578005)
Erythrocytosis due to renal cyst (71716005)
Erythrocytosis due to renal tumor (43918003)
Erythrocytosis due to tissue hypoxemia (19588001)
Erythrocytosis due to uterine myoma (34397005)
Estren-Dameshek anemia (46760003)
Evans syndrome (75331009)
Familial erythrocytosis (17342003)
Familial erythrocytosis due to diphosphoglycerate mutase deficiency (127065001)
Familial hemolytic uremic syndrome (722721004)
Familial megaloblastic anemia (360495000)
Familial polycythemia vera (127066000)
Fanconi anemia of complementation group C (1285021005)
Fanconi's anemia (30575002)
Finding of red blood cell count (365625004)
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (713388002)
Gaisbock's syndrome (48250002)
Gamma delta beta thalassemia (788944005)
Ghosal hematodiaphyseal dysplasia (389214003)
Glucose-6-phosphate dehydrogenase deficiency anemia (62403005)
Glucose-6-phosphate dehydrogenase deficiency class I variant anemia (22933009)
Glucose-6-phosphate dehydrogenase deficiency class II variant anemia (34852006)
Glucose-6-phosphate dehydrogenase deficiency class III variant anemia (24661004)
Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia (82003006)
Glucose-6-phosphate dehydrogenase deficiency class V variant anemia (80963002)
Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia (86859003)
Glutathione synthase deficiency with 5-oxoprolinuria (39112005)
Glutathione synthase deficiency without 5-oxoprolinuria (237926007)
Glutathione synthetase deficiency (234589002)
Hapten type high affinity hemolytic anemia (86225009)
Hapten type low affinity hemolytic anemia (44206008)
Hematopoietic subsyndrome of acute radiation syndrome (723489005)
Hemoglobin Bart's hydrops syndrome (5300004)
Hemoglobinopathy with erythrocytosis (75063005)
Hemoglobinuria due to hemolysis from external causes (191222008)
Hemolytic anemia (61261009)
Hemolytic anemia caused by Bartonella (76366001)
Hemolytic anemia caused by Clostridium welchii (28147001)
Hemolytic anemia caused by drugs (81711008)
Hemolytic anemia caused by hyperbaric oxygen (129638002)
Hemolytic anemia due to adenylate kinase deficiency (766982000)
Hemolytic anemia due to babesiosis (24620004)
Hemolytic anemia due to glutathione metabolism disorder (191170009)
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency (1148893001)
Hemolytic anemia due to hexokinase deficiency (191177007)
Hemolytic anemia due to infection (38689004)
Hemolytic anemia due to malaria (77663007)
Hemolytic anemia due to nonlymphoid neoplasm (4939006)
Hemolytic anemia due to red cell enolase deficiency (1148895008)
Hemolytic anemia due to triose phosphate isomerase deficiency (191179005)
Hemolytic anemia of pregnancy (1142083003)
Hemolytic anemia with emphysema AND cutis laxa (60805002)
Hemolytic disease of fetus OR newborn due to ABO immunization (32858009)
Hemolytic disease of fetus OR newborn due to RhD isoimmunization (86986002)
Hemolytic disease of fetus OR newborn due to isoimmunization (387705004)
Hemolytic disease of fetus due to ABO immunization (350611000119107)
Hemolytic disease of newborn co-occurrent and due to ABO immunization (350601000119109)
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization (111469006)
Hemolytic uremic syndrome (111407006)
Hemolytic uremic syndrome of childhood (36568005)
Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (1269225005)
Hemolytic uremic syndrome, adult type (78209002)
Hereditary cryohydrocytosis with normal stomatin (773489008)
Hereditary cryohydrocytosis with reduced stomatin (782911008)
Hereditary elliptocytosis (191169008)
Hereditary elliptocytosis due to abnormal protein 4.1 (75443009)
Hereditary elliptocytosis due to alpha spectrin defect (8857001)
Hereditary elliptocytosis due to beta spectrin defect in self-association (73073009)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction (66262001)
Hereditary elliptocytosis due to deficiency of protein 4.1 (5994005)
Hereditary elliptocytosis due to glycophorin C deficiency (15121005)
Hereditary elliptocytosis with transient poikilocytosis (234410008)
Hereditary hemolytic anemia (38911009)
Hereditary iron deficiency anemia (1153403009)
Hereditary isolated aplastic anemia (783255002)
Hereditary nonspherocytic hemolytic anemia (301317008)
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity (78908001)
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency (62268000)
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency (25251008)
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency (52413004)
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency (52212006)
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (111579006)
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency (42484009)
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity (5315003)
Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency (41387000)
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency (59644002)
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency (34194007)
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency (74703006)
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency (47526003)
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency (44641000)
Hereditary spherocytosis (55995005)
Hereditary spherocytosis due to beta spectrin defect (69981004)
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (47516005)
Hereditary spherocytosis due to deficiency of protein 4.2 (33905008)
Hereditary spherocytosis due to spectrin deficiency (25266006)
Hereditary stomatocytosis (14087004)
High oxygen affinity hemoglobin polycythemia (3947004)
Homozygous hereditary elliptocytosis (1153399000)
Humoral immunologic aplastic anemia (14024008)
Hypochromic microcytic anemia with iron overload (711161006)
Hypochromic red blood cells percent count in blood (1111581000000104)
Hypoplastic anemia (41614006)
Idiopathic aplastic anemia (191256002)
Idiopathic chronic cold agglutinin disease (6398009)
Idiopathic erythrocytosis (285777008)
Idiopathic paroxysmal cold hemoglobinuria (62871001)
Idiopathic sideroblastic anemia (276448005)
Immature reticulocyte fraction (991641000000108)
Immature reticulocyte fraction (413042008)
Immunologic aplastic anemia (77084001)
Inappropriate secondary erythrocytosis (44456000)
Infantile pyknocytosis (191229004)
Infection-related hemolytic uremic syndrome (1269270002)
Intracorpuscular hemolytic anemia (322699009)
Iron deficiency anemia (87522002)
Iron deficiency anemia due to blood loss (724556004)
Iron deficiency anemia due to celiac disease (1148861009)
Iron deficiency anemia due to dietary causes (191128004)
Iron deficiency anemia due to increased requirement in adolescence (1148855006)
Iron deficiency anemia due to increased requirement in infancy (1148856007)
Iron deficiency anemia during maternal intrapartum period (1287713006)
Iron deficiency anemia following gastrectomy (1148853004)
Iron deficiency anemia of pregnancy (199248002)
Iron deficiency anemia secondary to inadequate dietary iron intake (371315009)
Iron-refractory iron deficiency anemia (722005000)
Juvenile type megaloblastic anemia (49284006)
Kell isoimmunization of the newborn (234380002)
Kidd isoimmunization of the newborn (307338008)
Late anemia due to isoimmunization (68361004)
Late anemia of newborn (276579007)
Late anemia of newborn due to isoimmunization (206434001)
Lethal hemolytic anemia and genital anomaly syndrome (719402008)
Lymphocyte passenger syndrome following organ transplantation (1153358006)
Macrocytic anemia of pregnancy (1142062009)
Maternal autoimmune hemolytic anemia (234381003)
Mechanical hemolysis following insertion of prosthetic heart valve (1153380009)
Mechanical hemolytic anemia (191217008)
Megaloblastic anemia due to alcoholism (87810006)
Megaloblastic anemia due to blind loop syndrome (60164003)
Megaloblastic anemia due to celiac disease (6659005)
Megaloblastic anemia due to congenital deficiency of intrinsic factor (60504009)
Megaloblastic anemia due to disease of small intestine (82895008)
Megaloblastic anemia due to error of cobalamin metabolism (68700003)
Megaloblastic anemia due to error of folate metabolism (35778001)
Megaloblastic anemia due to folate deficiency due to increased requirement (721184003)
Megaloblastic anemia due to folate deficiency in pregnancy and lactation (721185002)
Megaloblastic anemia due to folate deficiency in prematurity (721186001)
Megaloblastic anemia due to impaired absorption of folate (27798002)
Megaloblastic anemia due to inborn errors of metabolism (34925000)
Megaloblastic anemia due to pregnancy (91217009)
Megaloblastic anemia due to tropical sprue (87806008)
Megaloblastic anemia, thiamine-responsive, with diabetes mellitus and sensorineural deafness (237617006)
Microangiopathic hemolytic anemia (51071000)
Microcytic anemia (234349007)
Microcytic hypochromic anemia (44666001)
Microcytic normochromic anemia (4984008)
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (24975009)
Mild hereditary spherocytosis due to spectrin deficiency (32648007)
Mitochondrial myopathy with sideroblastic anemia syndrome (724138007)
Multiple paraganglioma associated with polycythemia (1197217007)
Neonatal anemia (234350007)
Neonatal autoimmune hemolytic anemia (774083009)
Neonatal polycythemia (32984002)
Neonatal polycythemia due to intra-uterine growth retardation (737210007)
Neonatal polycythemia due to placental insufficiency (737209002)
Non autoimmune hemolytic anemia caused by drug (1148880006)
Non-autoimmune hemolytic anemia (191216004)
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (725057008)
Nucleated red blood cell count (1022461000000100)
Nucleated red blood cell count (142837000)
Nucleated red blood cell count procedure (165426009)
Nucleated red blood cell count result (825851000000109)
Nutritional anemia of pregnancy (1142030006)
Oroya fever (240453002)
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (722207000)
Pancytopenia (127034005)
Pancytopenia caused by anticonvulsant (328381000119105)
Pancytopenia caused by antidiabetic drug (328391000119108)
Pancytopenia caused by antithyroid drug (328371000119107)
Pancytopenia caused by colchicine (328321000119106)
Pancytopenia caused by immunosuppressant (16623961000119100)
Pancytopenia caused by medication (736024007)
Pancytopenia caused by non-steroidal anti-inflammatory agent (328331000119109)
Pancytopenia due to IKAROS family zinc finger 1 mutations (783142006)
Pancytopenia due to antineoplastic chemotherapy (328301000119102)
Pancytopenia with developmental delay syndrome (774071007)
Pancytopenia with pancreatitis (234367000)
Paroxysmal cold hemoglobinuria (127057004)
Paroxysmal cold hemoglobinuria associated with tertiary syphilis (127058009)
Parvoviral aplastic crisis (240486003)
Percent count of high ribonucleic acid reticulocyte in blood (57381000237103)
Percent count of low ribonucleic acid reticulocyte in blood (56101000237106)
Percent count of medium ribonucleic acid reticulocyte in blood (53291000237102)
Percent count of reticulocytes in blood (57711000237107)
Percent of immature reticulocyte in blood (2381000237106)
Percentage hypochromic cells (993901000000100)
Percentage hypochromic cells (395015001)
Percentage nucleated red blood cells (1015551000000102)
Percentage reticulocyte count (1019541000000102)
Perinatal anemia (387702001)
Pernicious anemia due to autoimmune disorder (1153333001)
Physiological anemia of infancy (276578004)
Plummer-Vinson syndrome (80126007)
Polyagglutinable erythrocyte syndrome (40387008)
Polycythemia due to HIF2A mutation (1153352007)
Polycythemia due to PHD2 mutation (1153350004)
Polycythemia due to cyanotic heart disease (191372008)
Polycythemia due to cyanotic respiratory disease (191373003)
Polycythemia due to donor twin transfusion (38697006)
Polycythemia due to maternal-fetal transfusion (76873001)
Polycythemia neonatorum due to inherited disorder of erythropoietin production (722585009)
Polycythemia neonatorum following blood transfusion (722586005)
Post infectious thrombocytopenic purpura (33183004)
Post-infectious cold agglutinin disease (127053000)
Post-viral paroxysmal cold hemoglobinuria (35703006)
Postpartum iron deficiency anemia (10755381000119108)
Posttransfusion purpura (73162004)
Primaquine sensitivity anemia (863953007)
Primary (idiopathic) autoimmune hemolytic anemia (127049002)
Primary CD59 deficiency (778027003)
Primary cold-type hemolytic anemia (191210005)
Primary familial polycythemia due to erythropoietin receptor mutation (1153349004)
Primary warm-type hemolytic anemia (191211009)
Pseudo polycythemia due to acute loss of plasma volume (1153342008)
Pseudo polycythemia due to chronic loss of plasma volume (1153343003)
Pseudo-polycythemia (389148008)
Pure red cell aplasia (50715003)
Red blood cell count (1022451000000103)
Red blood cell count (14089001)
Red blood cell count (142831004)
Red blood cell count NOS (537891000000106)
Red blood cell count NOS (165428005)
Red blood cell count above reference range (165424007)
Red blood cell count below reference range (165423001)
Red blood cell count borderline low (165422006)
Red blood cell count borderline raised (165425008)
Red blood cell count outside reference range (165427000)
Red blood cell count within reference range (165421004)
Red blood cell count, automated, cerebrospinal fluid (104111000)
Red blood cell count, automated, pleural fluid (104118006)
Red blood cell count, automated, synovial fluid (104125004)
Red blood cell count, automated, urine (104122001)
Red blood cell count, manual, peritoneal fluid (104114008)
Red blood cell malaria parasitemia count (401327001)
Relative polycythemia (389147003)
Reticulocyte count (993441000000109)
Reticulocyte count (45995003)
Reticulocyte count in blood (1108051000000105)
Reticulocyte count outside reference range (165685003)
Reticulocyte count within reference range (165686002)
Reticulocyte count, flow cytometry (104153004)
Reticulocyte count, hematocrit adjusted (121100002)
Reticulocyte count, manual (104152009)
Reticulocyte percent count (313639004)
Reticulocyte production index (1110451000000102)
Reticulocytopenia (124961001)
Reticulocytosis (46049004)
Reticulocytosis after B12 (170824004)
Revesz syndrome (723512008)
Rhesus isoimmunization due to anti-Cw (307336007)
Rhesus isoimmunization due to anti-D (307333004)
Rhesus isoimmunization due to anti-E (307335006)
Rhesus isoimmunization due to anti-c (307334005)
Secondary aplastic anemia (43858000)
Secondary autoimmune hemolytic anemia (127050002)
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (732962005)
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder (732963000)
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (732965007)
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus (732960002)
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (732966008)
Secondary cold-type hemolytic anemia (191212002)
Secondary paroxysmal cold hemoglobinuria (50253007)
Secondary polycythemia (44865000)
Secondary polycythemia with excess erythropoietin (367328005)
Secondary polycythemia without excess erythropoietin (234400004)
Secondary warm autoimmune hemolytic anemia (127052005)
Secondary warm-type hemolytic anemia (191213007)
Selective malabsorption of cyanocobalamin (234363001)
Severe combined immunodeficiency with reticular dysgenesis (190996002)
Severe congenital hypochromic anemia with ringed sideroblasts (725463007)
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin (10564005)
Severe hereditary spherocytosis due to spectrin deficiency (77413008)
Sideropenic anemia with reticuloendothelial siderosis (290246007)
Stress polycythemia (36874002)
Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome (718614004)
Thalassemia in mother complicating childbirth (10806241000119108)
Thalassemia in mother complicating pregnancy (72331000119105)
Thiamine-responsive megaloblastic anemia (12907000)
Thrombocytopenic purpura (302873008)
Thrombocytopenic purpura associated with metabolic disorder (417626001)
Thrombocytopenic purpura due to defective platelet production (402653004)
Thrombocytopenic purpura due to platelet consumption (402654005)
Thrombotic thrombocytopenic purpura (78129009)
Toxic hemolytic anemia (191218003)
Transient acquired pure red cell aplasia (191255003)
Transient erythroblastopenia of childhood (234375006)
Transient hypoplastic anemia (191251007)
Traumatic cardiac hemolytic anemia (2835000)
Traumatic hemolytic anemia (371046004)
Unstable hemoglobin disease (18273004)
Upshaw-Schulman syndrome (373420004)
Vitamin B12 deficiency anemia due to chronic atrophic gastritis (1153409008)
Vitamin B12 deficiency anemia following gastrectomy (1171357005)
Vitamin B12 deficiency anemia following total gastrectomy (1153353002)
WT limb blood syndrome (719019000)
Warm autoimmune hemolytic anemia (3978000)
X chromosome-linked pyridoxine refractory sideroblastic anemia (21412009)
X chromosome-linked pyridoxine responsive sideroblastic anemia (25443007)
X chromosome-linked sideroblastic anemia (48983004)
X-linked congenital dyserythropoietic anemia with thrombocytopenia (722475006)
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (782759001)
X-linked sideroblastic anemia with spinocerebellar ataxia (719816006)

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