Domain IDSpec Anatomic Site
Concept Class IDBody Structure
Vocabulary ID
SNOMED
help_outline
Systematic Nomenclature of Medicine - Clinical Terms (IHTSDO)
2024-08-01 SNOMED CT International Edition; 2024-09-01 SNOMED CT US Edition; 2024-09-25 SNOMED CT UK Edition
http://www.nlm.nih.gov/research/umls/licensedcontent/umlsknowledgesources.html
Concept ID4218976
Concept code41898006
ValidityValid
ConceptStandard

Language	Synonym Concept
English	Erythrocyte (cell)
Spanish	GR
English	RBC
English	RBC - Red blood cell
English	Red blood cell
English	Red blood corpuscule
Spanish	eritrocito
Spanish	eritrocito (célula)
Spanish	glóbulo rojo

Valid start31-Jan-2002
Valid end31-Dec-2099

Term connections (450)

Relationship	Relates to	Concept id	Vocabulary
Active same_as inactive (SNOMED)	Red blood cell	40461910	SNOMED
Component of	Eosin 5-maleimide labelled red blood cells MFI (mean fluorescence intensity) in blood	37174461	SNOMED
	Eosin 5-maleimide labelled red blood cells control MFI (mean fluorescence intensity) in blood	37174473	SNOMED
	Eosin-5-maleimide cell binding study	44806473	SNOMED
	Erythrocyte color index measurement	4211818	SNOMED
	Hypertonic cryohaemolysis test	44793000	SNOMED
	Isopropanol precipitation test	44805800	SNOMED
	Percentage hypochromic cells	4215550	SNOMED
	Presence of erythrocytes in urine	1077392	SNOMED
	RBC malaria parasitemia count	4270028	SNOMED
	RBCs (red blood cells) in blood smear microscopy qualitative result	37174431	SNOMED
	RBCs (red blood cells) in mid-stream urine microscopy qualitative result	37174433	SNOMED
	Red blood cell count	4030871	SNOMED
	Red blood cell count in CSF	37169735	SNOMED
	Red blood cell count, automated, cerebrospinal fluid	4015172	SNOMED
	Red blood cell count, automated, pleural fluid	4015175	SNOMED
	Red blood cell count, automated, synovial fluid	4015176	SNOMED
	Red blood cell count, automated, urine	4016235	SNOMED
	Red blood cell count, manual, peritoneal fluid	4015173	SNOMED
	Red blood cell maturation age determination	4095339	SNOMED
	Red blood cell membrane protein study	44805798	SNOMED
	Red blood cell morphology	4219640	SNOMED
	Red blood cell size determination	4013087	SNOMED
	Red blood cell test	4098353	SNOMED
	Red cell mean osmotic fragility	4216420	SNOMED
	Reticulocyte haemoglobin content measurement	44806870	SNOMED
	Sample microscopy: red cells	4268415	SNOMED
Finding site of (SNOMED)	A-gamma beta+ HPFH AND beta0 thalassemia in cis	4242755	SNOMED
	Abnormal cation transport syndrome	4120600	SNOMED
	Acquired Heinz body anemia	4088386	SNOMED
	Acquired hemoglobin H disease	4139556	SNOMED
	Acquired hemoglobinopathy	4131125	SNOMED
	Acquired iron deficiency anemia due to decreased absorption	37110336	SNOMED
	Acquired iron deficiency anemia due to increased iron requirement	36713573	SNOMED
	Acquired methemoglobinemia	4170982	SNOMED
	Acquired methemoglobinuria	4167291	SNOMED
	Acquired thrombotic thrombocytopenic purpura	4204900	SNOMED
	Acute sickle cell splenic sequestration crisis	40485018	SNOMED
	Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis	603018	SNOMED
	Acute splenic sequestration of spleen due to sickle cell thalassemia with crisis	607430	SNOMED
	Adenosine deaminase overproduction	4125632	SNOMED
	Adult-onset autosomal recessive sideroblastic anemia	36715009	SNOMED
	Agamma delta beta0 thalassemia	4232474	SNOMED
	Alcohol-related macrocytosis	4120447	SNOMED
	Alpha plus thalassemia	4271753	SNOMED
	Alpha plus thalassemia deletion type	4311397	SNOMED
	Alpha plus thalassemia non deletion type	4311538	SNOMED
	Alpha thalassemia	4287844	SNOMED
	Alpha thalassemia X-linked intellectual disability syndrome	37399441	SNOMED
	Alpha thalassemia-2 trait	4121113	SNOMED
	Alpha thalassemia-mental retardation syndrome	4080702	SNOMED
	Alpha trait thalassemia	4098749	SNOMED
	Alpha zero thalassemia	4278816	SNOMED
	Alpha-beta thalassemia	4122931	SNOMED
	Alpha-thalassemia intellectual disability syndrome linked to chromosome 16	42539413	SNOMED
	Alpha/beta lipoproteinemia	4120601	SNOMED
	Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome	36715351	SNOMED
	Anemia caused by alloimmune destruction of transfused red cells	4132085	SNOMED
	Anemia caused by zidovudine	37018722	SNOMED
	Anemia due to nuclear maturation defect	42596489	SNOMED Veterinary
	Anemia due to unknown or multiple mechanisms	4009305	SNOMED
	Anemia in chronic kidney disease stage 4	37398911	SNOMED
	Anemia in chronic kidney disease stage 5	37395652	SNOMED
	Atypical hemolytic uremic syndrome	37312165	SNOMED
	Atypical hemolytic uremic syndrome with anti-factor H antibodies	1244954	SNOMED
	Atypical hemolytic uremic syndrome with complement gene abnormality	1244936	SNOMED
	Autoimmune thrombotic thrombocytopenic purpura	4230266	SNOMED
	Autosomal dominant secondary polycythemia	37204525	SNOMED
	Autosomal recessive congenital methemoglobinemia	35624651	SNOMED
	Autosomal recessive congenital methemoglobinemia type I	35624653	SNOMED
	Autosomal recessive congenital methemoglobinemia type II	35624652	SNOMED
	Autosomal recessive secondary polycythemia not associated with VHL (Von Hippel Lindau) gene	37204848	SNOMED
	Beta plus thalassemia	4196206	SNOMED
	Beta plus thalassemia normal hemoglobin A-2 type 1 silent	4187256	SNOMED
	Beta thalassemia	4278669	SNOMED
	Beta thalassemia X-linked thrombocytopenia syndrome	37397537	SNOMED
	Beta thalassemia intermedia	4100992	SNOMED
	Beta thalassemia trait	4149681	SNOMED
	Beta zero thalassemia	4315393	SNOMED
	Beta zero thalassemia deletion type	4099005	SNOMED
	Beta zero thalassemia non deletion type	4009304	SNOMED
	Blood group deletion syndrome	4120459	SNOMED
	Chicken anaemia virus infection	42599372	SNOMED Veterinary
	Chorea acanthocytosis syndrome	4097680	SNOMED
	Chronic idiopathic autoimmune hemolytic anemia	4318674	SNOMED
	Chronic idiopathic thrombocytopenic purpura	318397	SNOMED
	Chronic non-spherocytic hemolytic anemia	4125630	SNOMED
	Chuvash erythrocytosis	36674691	SNOMED
	Congenital dyserythropoietic anemia	4204062	SNOMED
	Congenital dyserythropoietic anemia type IV	36714288	SNOMED
	Congenital dyserythropoietic anemia, type I	4241982	SNOMED
	Congenital dyserythropoietic anemia, type II	4286660	SNOMED
	Congenital dyserythropoietic anemia, type III	4097214	SNOMED
	Congenital elliptocytosis	4076717	SNOMED
	Congenital hemolytic anemia	4175331	SNOMED
	Congenital hemolytic uremic syndrome	40481595	SNOMED
	Congenital methemoglobinaema with defective methemoglobin-reducing system	4122934	SNOMED
	Congenital methemoglobinemia	4146093	SNOMED
	Congenital methemoglobinemia with abnormal methemoglobins	4120456	SNOMED
	Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism	4178677	SNOMED
	Congenital pure red cell aplasia	4120453	SNOMED
	Congenital thrombocytopenic purpura	437242	SNOMED
	Cystic fibrosis with gastritis and megaloblastic anemia syndrome	36714965	SNOMED
	Cytochrome b-3 deficiency	4130065	SNOMED
	Deficiency anemia associated with AIDS	4227834	SNOMED
	Deficiency of glucose-6-phosphate dehydrogenase	4050620	SNOMED
	Deficiency of glucose-6-phosphate dehydrogenase with normal enzyme activity	606652	SNOMED
	Deficiency of glutathione reductase (NAD(P)H)	4050151	SNOMED
	Deficiency of hexokinase	4049579	SNOMED
	Dehydrated hereditary stomatocytosis	37399453	SNOMED
	Delayed hemolytic transfusion reaction	4307962	SNOMED
	Delta beta thalassemia	4038772	SNOMED
	Delta beta thalassemia trait	1245854	SNOMED
	Delta beta zero thalassemia	4297017	SNOMED
	Delta thalassemia	4039785	SNOMED
	Delta zero thalassemia	4267282	SNOMED
	Delta-beta-Lepore thalassemia	4122930	SNOMED
	Diarrhea-associated hemolytic uremic syndrome	4190190	SNOMED
	Diarrhea-negative hemolytic uremic syndrome	4159967	SNOMED
	Dominant beta-thalassemia	37396761	SNOMED
	Double heterozygous sickling disorder	4049095	SNOMED
	Drug induced thrombotic thrombocytopenic purpura	4258261	SNOMED
	Drug-induced immune hemolytic anemia	4131918	SNOMED
	Drug-induced methemoglobinemia	4098157	SNOMED
	Epsilon gamma delta beta thalassemia	4052711	SNOMED
	Epsilon gamma delta beta0 thalassemia	4248254	SNOMED
	Erythrocyte enzyme deficiency	4125629	SNOMED
	Erythrocyte membrane abnormality	4122936	SNOMED
	Erythrocytosis	4130681	SNOMED
	Erythrocytosis caused by low atmospheric pressure	4093608	SNOMED
	Erythrocytosis due to alveolar hypoventilation	4249398	SNOMED
	Erythrocytosis due to autotransfusion	4103465	SNOMED
	Erythrocytosis due to cardiovascular disease	4151360	SNOMED
	Erythrocytosis due to cerebellar hemangioma	4049332	SNOMED
	Erythrocytosis due to cyanotic congenital heart disease	4131130	SNOMED
	Erythrocytosis due to defective oxygen transport	4234995	SNOMED
	Erythrocytosis due to endocrine disorder	4197910	SNOMED
	Erythrocytosis due to hepatoma	4175334	SNOMED
	Erythrocytosis due to hydronephrosis	4312942	SNOMED
	Erythrocytosis due to polycythemia vera	4189309	SNOMED
	Erythrocytosis due to pulmonary disease	4301874	SNOMED
	Erythrocytosis due to renal cyst	4216559	SNOMED
	Erythrocytosis due to renal tumor	4185407	SNOMED
	Erythrocytosis due to tissue hypoxemia	4055357	SNOMED
	Erythrocytosis due to uterine myoma	4142351	SNOMED
	Erythropoiesis stimulating agent induced antibody mediated acquired pure red cell aplasia	45770674	SNOMED
	Familial erythrocytosis	433741	SNOMED
	Familial erythrocytosis due to diphosphoglycerate mutase deficiency	4130682	SNOMED
	Familial hemolytic uremic syndrome	36717581	SNOMED
	Familial methemoglobinemia	4101131	SNOMED
	Familial polycythemia vera	4131920	SNOMED
	Familial pseudohyperkalemia	37397197	SNOMED
	Favism	4098744	SNOMED
	Feline infectious anaemia	42572621	SNOMED Veterinary
	Fetal hemoglobinopathy	618636	SNOMED
	Gaisbock's syndrome	4167506	SNOMED
	Gamma delta beta thalassemia	37311954	SNOMED
	Gamma thalassemia	4122932	SNOMED
	Glucose phosphate isomerase deficiency	4121117	SNOMED
	Glutathione synthase deficiency with 5-oxoprolinuria	4192278	SNOMED
	Glutathione synthase deficiency without 5-oxoprolinuria	4035266	SNOMED
	Glutathione synthetase deficiency	4121287	SNOMED
	HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency	4254249	SNOMED
	HNSHA due to NADH diaphorase deficiency	4171026	SNOMED
	HNSHA due to NADH-methemoglobin reductase deficiency	4320919	SNOMED
	HNSHA due to aldolase A deficiency	4009787	SNOMED
	HNSHA due to decreased adenosine deaminase activity	4193514	SNOMED
	HNSHA due to diphosphoglycerate mutase deficiency	4265915	SNOMED
	HNSHA due to gamma glutamyl cysteine synthetase deficiency	4101917	SNOMED
	HNSHA due to glucose phosphate isomerase deficiency	4181143	SNOMED
	HNSHA due to glutathione reductase deficiency	4178731	SNOMED
	HNSHA due to glutathione synthetase deficiency	4009788	SNOMED
	HNSHA due to hexokinase deficiency	4174701	SNOMED
	HNSHA due to phosphofructokinase deficiency	4187034	SNOMED
	HNSHA due to phosphoglycerate kinase deficiency	4242111	SNOMED
	HNSHA due to pyrimidine-5'-nucleotidase deficiency	4145277	SNOMED
	HNSHA due to triosephosphate isomerase deficiency	4258685	SNOMED
	HPFH A gamma beta+ thalassemia	4213820	SNOMED
	HPFH deletion type	4311673	SNOMED
	HPFH linked to beta-globulin gene cluster	4231453	SNOMED
	HPFH nondeletion type	4206913	SNOMED
	HPFH unlinked to beta-globulin gene cluster	4140101	SNOMED
	Hb Lepore thalassemia	4290233	SNOMED
	HbE (haemoglobin E) beta plus thalassaemia	3657472	SNOMED
	HbE (haemoglobin E) beta zero thalassaemia	3657471	SNOMED
	Hemoglobin Bart's hydrops syndrome	4200254	SNOMED
	Hemoglobin C beta plus thalassemia	1246707	SNOMED
	Hemoglobin C beta thalassemia	606961	SNOMED
	Hemoglobin C beta zero thalassemia	1246708	SNOMED
	Hemoglobin C crystals	4287329	SNOMED
	Hemoglobin C disease	4176425	SNOMED
	Hemoglobin C trait	4296149	SNOMED
	Hemoglobin C/beta thalassemia disease	760845	SNOMED
	Hemoglobin Constant Spring trait	4125628	SNOMED
	Hemoglobin D beta plus thalassemia	1246709	SNOMED
	Hemoglobin D beta zero thalassemia	1246710	SNOMED
	Hemoglobin D disease	4280961	SNOMED
	Hemoglobin D trait	4252396	SNOMED
	Hemoglobin D/beta thalassemia disease	765176	SNOMED
	Hemoglobin E beta plus thalassemia	1246711	SNOMED
	Hemoglobin E beta zero thalassemia	1246712	SNOMED
	Hemoglobin E disease	4094597	SNOMED
	Hemoglobin E trait	4262394	SNOMED
	Hemoglobin E/beta thalassemia disease	4120455	SNOMED
	Hemoglobin H constant spring thalassemia	40491316	SNOMED
	Hemoglobin H disease	4168911	SNOMED
	Hemoglobin Lepore trait	4121114	SNOMED
	Hemoglobin M disease	4327189	SNOMED
	Hemoglobin O-Arab trait	40484201	SNOMED
	Hemoglobin Paksé disease	602960	SNOMED
	Hemoglobin S sickling disorder with crisis	4216915	SNOMED
	Hemoglobin S sickling disorder without crisis	4166115	SNOMED
	Hemoglobin SC crystals	4246377	SNOMED
	Hemoglobin SS disease with crisis	26942	SNOMED
	Hemoglobin SS disease with vasoocclusive crisis	4209085	SNOMED
	Hemoglobin SS disease without crisis	30683	SNOMED
	Hemoglobin Seal Rock disease	606952	SNOMED
	Hemoglobin Zurich disease	4100994	SNOMED
	Hemoglobinemia	4049428	SNOMED
	Hemoglobinopathy	432868	SNOMED
	Hemoglobinopathy Toms River	37204287	SNOMED
	Hemoglobinopathy with cyanosis	4223384	SNOMED
	Hemoglobinopathy with erythrocytosis	4327329	SNOMED
	Hemolytic anemia associated with chronic inflammatory disease	4077896	SNOMED
	Hemolytic anemia associated with lymphoproliferative disorder	4281372	SNOMED
	Hemolytic anemia associated with rheumatic disorder	4009790	SNOMED
	Hemolytic anemia associated with systemic lupus erythematosus	4320480	SNOMED
	Hemolytic anemia associated with ulcerative colitis	4005188	SNOMED
	Hemolytic anemia caused by Bartonella	4297024	SNOMED
	Hemolytic anemia caused by Clostridium welchii	4151502	SNOMED
	Hemolytic anemia due to adenylate kinase deficiency	35624317	SNOMED
	Hemolytic anemia due to babesiosis	4085853	SNOMED
	Hemolytic anemia due to erythrocyte adenosine deaminase overproduction	4203291	SNOMED
	Hemolytic anemia due to glutathione metabolism disorder	23988	SNOMED
	Hemolytic anemia due to infection	4297537	SNOMED
	Hemolytic anemia due to malaria	4298975	SNOMED
	Hemolytic anemia due to pyruvate kinase deficiency	4098746	SNOMED
	Hemolytic anemia due to triose phosphate isomerase deficiency	4100991	SNOMED
	Hemolytic anemia of pregnancy	606061	SNOMED
	Hemolytic disease of fetus due to ABO immunization	601103	SNOMED
	Hemolytic transfusion reaction	4218193	SNOMED
	Hemolytic uremic syndrome	197253	SNOMED
	Hemolytic uremic syndrome of childhood	4267646	SNOMED
	Hemolytic uremic syndrome with DGKE deficiency	37167956	SNOMED
	Hemolytic uremic syndrome, adult type	4302298	SNOMED
	Hereditary acanthocytosis	4034180	SNOMED
	Hereditary cryohydrocytosis with normal stomatin	36676579	SNOMED
	Hereditary cryohydrocytosis with reduced stomatin	37204308	SNOMED
	Hereditary elliptocytosis	22288	SNOMED
	Hereditary elliptocytosis due to abnormal protein 4.1	4327824	SNOMED
	Hereditary elliptocytosis due to alpha spectrin defect	4228681	SNOMED
	Hereditary elliptocytosis due to beta spectrin defect in self-association	4218794	SNOMED
	Hereditary elliptocytosis due to beta spectrin-ankyrin interaction	4281394	SNOMED
	Hereditary elliptocytosis due to deficiency of protein 4.1	4243676	SNOMED
	Hereditary elliptocytosis due to glycophorin C deficiency	4034711	SNOMED
	Hereditary elliptocytosis with transient poikilocytosis	4125633	SNOMED
	Hereditary hemoglobin S	4214191	SNOMED
	Hereditary hemoglobinopathy	4144746	SNOMED
	Hereditary hemoglobinopathy due to globin chain mutation	4130066	SNOMED
	Hereditary hemolytic anemia	28396	SNOMED
	Hereditary methemoglobinemia, enzymatic type	4048203	SNOMED
	Hereditary nonspherocytic hemolytic anemia	4115393	SNOMED
	Hereditary persistence of fetal hemoglobin	4098015	SNOMED
	Hereditary persistence of fetal hemoglobin G gamma beta plus thalassemia	4264017	SNOMED
	Hereditary persistence of fetal hemoglobin delta beta plus thalassemia	4203904	SNOMED
	Hereditary persistence of fetal hemoglobin thalassemia	4061151	SNOMED
	Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome	37204550	SNOMED
	Hereditary pyropoikilocytosis	4312021	SNOMED
	Hereditary red blood cell disorder	4214409	SNOMED
	Hereditary sideroblastic anemia	4269075	SNOMED
	Hereditary spherocytosis	24909	SNOMED
	Hereditary spherocytosis due to beta spectrin defect	4320651	SNOMED
	Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	4168441	SNOMED
	Hereditary spherocytosis due to deficiency of protein 4.2	4144956	SNOMED
	Hereditary spherocytosis due to spectrin deficiency	4099224	SNOMED
	Hereditary stomatocytosis	4031827	SNOMED
	Heterozygous hemoglobinopathy	4047524	SNOMED
	Heterozygous thalassemia	4023612	SNOMED
	High affinity hemoglobin	4122933	SNOMED
	High oxygen affinity hemoglobin polycythemia	4190447	SNOMED
	Homozygous alpha thalassemia	4120454	SNOMED
	Homozygous beta thalassemia	4132431	SNOMED
	Homozygous hemoglobin H constant spring thalassemia	760844	SNOMED
	Homozygous hemoglobinopathy	4048205	SNOMED
	Homozygous hereditary elliptocytosis	607421	SNOMED
	Idiopathic chronic cold agglutinin disease	4273847	SNOMED
	Idiopathic erythrocytosis	4112805	SNOMED
	Idiopathic methemoglobinemia	4103123	SNOMED
	Idiopathic paroxysmal cold hemoglobinuria	4271197	SNOMED
	Immediate hemolytic transfusion reaction	4277354	SNOMED
	Inappropriate secondary erythrocytosis	4195320	SNOMED
	Infection-related hemolytic uremic syndrome	37167983	SNOMED
	Infectious avian anaemia	42599242	SNOMED Veterinary
	Infective hemolytic anemia	4098756	SNOMED
	Intraerythrocytic parasitosis by Entopolypoides	4243187	SNOMED
	Intraerythrocytic parasitosis by Nuttallia	4003500	SNOMED
	Iron deficiency without anemia	4120446	SNOMED
	Lethal hemolytic anemia and genital anomaly syndrome	36714258	SNOMED
	Low affinity hemoglobin	4121116	SNOMED
	Macrocytic anemia of pregnancy	606052	SNOMED
	Macrocytic hypochromic anemia	42596487	SNOMED Veterinary
	Macrocytic normochromic anemia	42596488	SNOMED Veterinary
	Macrocytosis - no anemia	4125489	SNOMED
	Majeed syndrome	45766392	SNOMED
	McLeod neuroacanthocytosis syndrome	37110098	SNOMED
	Mechanical hemolysis following insertion of prosthetic heart valve	600662	SNOMED
	Megaloblastic anemia due to folate deficiency due to increased requirement	36715492	SNOMED
	Megaloblastic anemia due to folate deficiency in pregnancy and lactation	36715493	SNOMED
	Megaloblastic anemia due to folate deficiency in prematurity	36715494	SNOMED
	Methemoglobin reductase deficiency	4120457	SNOMED
	Methemoglobinemia	432882	SNOMED
	Methemoglobinemia due to nitrate poisoning	4231981	SNOMED
	Microangiopathic hemolytic anemia	4198102	SNOMED
	Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	4093515	SNOMED
	Mild hereditary spherocytosis due to spectrin deficiency	4138560	SNOMED
	Mixed hemoglobin disorder	4295183	SNOMED
	Moderate deficiency of glucose-6-phosphate dehydrogenase	618728	SNOMED
	Multiple paraganglioma associated with polycythemia	37162690	SNOMED
	Neonatal autoimmune hemolytic anemia	36674478	SNOMED
	Neonatal hemolysis with systemic bacterial infection	42539567	SNOMED
	Neonatal polycythemia	439140	SNOMED
	Neonatal polycythemia due to intra-uterine growth retardation	42537679	SNOMED
	Neonatal polycythemia due to placental insufficiency	42537678	SNOMED
	Non-anemic red cell disorder	4122921	SNOMED
	Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase	37110727	SNOMED
	Nucleated erythrocytosis	42599417	SNOMED Veterinary
	Nutritional anemia of pregnancy	606027	SNOMED
	Oroya fever	4347537	SNOMED
	Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome	37116373	SNOMED
	Overhydrated hereditary stomatocytosis	36716203	SNOMED
	Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome	36716259	SNOMED
	Phosphatidylcholine-sterol acyltransferase deficiency	4176854	SNOMED
	Phosphoglycerokinase deficiency	4120458	SNOMED
	Polycythemia due to HIF2A mutation	607388	SNOMED
	Polycythemia due to PHD2 mutation	607386	SNOMED
	Polycythemia due to cyanotic heart disease	4103122	SNOMED
	Polycythemia due to cyanotic respiratory disease	4098151	SNOMED
	Polycythemia due to donor twin transfusion	4305235	SNOMED
	Polycythemia due to maternal-fetal transfusion	4297988	SNOMED
	Polycythemia neonatorum due to inherited disorder of erythropoietin production	36716548	SNOMED
	Polycythemia neonatorum following blood transfusion	36716549	SNOMED
	Post infectious thrombocytopenic purpura	4140545	SNOMED
	Post-artesunate delayed hemolysis	3655917	SNOMED
	Posttransfusion purpura	4247776	SNOMED
	Primaquine sensitivity anemia	3661615	SNOMED
	Primary (idiopathic) autoimmune hemolytic anemia	4131915	SNOMED
	Primary (idiopathic) warm autoimmune hemolytic anemia	4130679	SNOMED
	Primary CD59 deficiency	36674519	SNOMED
	Primary familial polycythemia due to erythropoietin receptor mutation	607385	SNOMED
	Pseudo-polycythemia	4308045	SNOMED
	Red blood cell disorder	432739	SNOMED
	Red blood cell sequestration in liver	4316361	SNOMED
	Relative polycythemia	4308044	SNOMED
	Relative polycythemia due to acute loss of plasma volume	607378	SNOMED
	Relative polycythemia due to chronic loss of plasma volume	607379	SNOMED
	Rh deficiency syndrome	4290596	SNOMED
	Secondary polycythemia	435790	SNOMED
	Secondary polycythemia with excess erythropoietin	4273627	SNOMED
	Secondary polycythemia without excess erythropoietin	4122935	SNOMED
	Severe deficiency of glucose-6-phosphate dehydrogenase	605090	SNOMED
	Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin	4021466	SNOMED
	Severe hereditary spherocytosis due to spectrin deficiency	4298813	SNOMED
	Sickle cell anemia in mother complicating childbirth	45757146	SNOMED
	Sickle cell anemia with coexistent alpha-thalassemia	4131914	SNOMED
	Sickle cell anemia with high hemoglobin F	4121115	SNOMED
	Sickle cell beta plus thalassemia	4130678	SNOMED
	Sickle cell trait	25518	SNOMED
	Sickle cell trait in mother complicating childbirth	45757147	SNOMED
	Sickle cell trait in mother complicating pregnancy	45773070	SNOMED
	Sickle cell trait with coexistent alpha-thalassemia	4130189	SNOMED
	Sickle cell-Hemoglobin O Arab disease	4130190	SNOMED
	Sickle cell-beta-thalassemia	4130067	SNOMED
	Sickle cell-beta0-thalassemia	4130068	SNOMED
	Sickle cell-delta beta0-thalassemia	4131913	SNOMED
	Sickle cell-hemoglobin C disease	24006	SNOMED
	Sickle cell-hemoglobin C disease with crisis	443721	SNOMED
	Sickle cell-hemoglobin C disease without crisis	443726	SNOMED
	Sickle cell-hemoglobin D disease	4103763	SNOMED
	Sickle cell-hemoglobin D disease with crisis	4167364	SNOMED
	Sickle cell-hemoglobin D disease without crisis	4166099	SNOMED
	Sickle cell-hemoglobin E disease	4264046	SNOMED
	Sickle cell-hemoglobin E disease with crisis	4219568	SNOMED
	Sickle cell-hemoglobin E disease without crisis	4211932	SNOMED
	Sickle cell-hemoglobin Lepore disease	4131126	SNOMED
	Sickle cell-hemoglobin SS disease	22281	SNOMED
	Sickle cell-thalassemia disease	315523	SNOMED
	Sickle cell-thalassemia disease with crisis	443738	SNOMED
	Sickle cell-thalassemia disease without crisis	321263	SNOMED
	Sickling disorder due to hemoglobin S	4213628	SNOMED
	Southeast Asian ovalocytosis	37109777	SNOMED
	Stokvis' disease	4211545	SNOMED
	Stress polycythemia	4285372	SNOMED
	Sulfhemoglobinemia	4137763	SNOMED
	TEMPI syndrome	36713680	SNOMED
	Thalassemia	30978	SNOMED
	Thalassemia in mother complicating childbirth	45757189	SNOMED
	Thalassemia in mother complicating pregnancy	45773071	SNOMED
	Thalassemia intermedia	4247579	SNOMED
	Thalassemia major	4327045	SNOMED
	Thalassemia syndrome	4222774	SNOMED
	Thalassemia with other hemoglobinopathy	4188474	SNOMED
	Thalassemia-hemoglobin C disease	4264909	SNOMED
	Thrombocytopenic purpura	4119134	SNOMED
	Thrombocytopenic purpura associated with metabolic disorder	4214947	SNOMED
	Thrombocytopenic purpura due to defective platelet production	4299560	SNOMED
	Thrombocytopenic purpura due to platelet consumption	4292531	SNOMED
	Thrombotic thrombocytopenic purpura	4301602	SNOMED
	Toxic methemoglobinemia with cyanosis	4131911	SNOMED
	Triose phosphate isomerase deficiency	4125631	SNOMED
	Unstable hemoglobin disease	4082253	SNOMED
	Upshaw-Schulman syndrome	4159966	SNOMED
	Uridine monophosphate hydrolase deficiency	4121119	SNOMED
	Vaso-occlusive pain episode in sickle cell disease	35626024	SNOMED
	Vitamin E deficiency anemia	4098743	SNOMED
	X chromosome-linked pyridoxine refractory sideroblastic anemia	4060269	SNOMED
	X chromosome-linked pyridoxine responsive sideroblastic anemia	4102056	SNOMED
	X chromosome-linked sideroblastic anemia	40599994	SNOMED
	X-linked congenital dyserythropoietic anemia with thrombocytopenia	36716460	SNOMED
	X-linked dyserythropoietic anemia with abnormal platelets and neutropenia	37204236	SNOMED
	X-linked sideroblastic anemia with spinocerebellar ataxia	36714533	SNOMED
	[X]Haemolytic anaemias	44796118	SNOMED
	[X]Other dietary vitamin B12 deficiency anaemia	44799845	SNOMED
	[X]Other iron deficiency anaemias	44794389	SNOMED
	[X]Other megaloblastic anaemias, not elsewhere classified	44794616	SNOMED
	beta+ Thalassemia normal Hb A-2 type 2	4035988	SNOMED
	von Jaksch's anemia	4120449	SNOMED
Has Module	SNOMED CT core	40642539	SNOMED
Has inherent (SNOMED)	Magnesium, red blood cell molar concentration in blood	37160145	SNOMED
	RBC (red blood cell) magnesium level	37393147	SNOMED
Has status	Primitive	40642538	SNOMED
Is a	Blood cell	4272801	SNOMED
	Erythroid cell	4212984	SNOMED
Non-standard to Standard map (OMOP)	Erythrocyte	4218976	SNOMED
Relative to of (SNOMED)	Percentage reticulocyte count	37393631	SNOMED
	Reticulocyte percent count in blood	37174474	SNOMED
Specimen source topography of (SNOMED)	Erythrocyte specimen	4000622	SNOMED
	Erythrocyte specimen from blood donor	4046282	SNOMED
	Erythrocyte specimen from blood product	4048851	SNOMED
	Erythrocyte specimen from patient	4048852	SNOMED
	Red blood cell fluid specimen	4105828	SNOMED
Standard to Non-standard map (OMOP)	ERYTHROCYTES	37539543	CDISC
	Erythrocyte	4218976	SNOMED
	Red blood cell	3166692	Nebraska Lexicon
	Red blood cell	40461910	SNOMED
	Red blood corpuscule	3488306	Nebraska Lexicon
Subsumes	Abnormal red blood cell	4264114	SNOMED
	Leptocyte	4123835	SNOMED
	Nucleated red blood cell	4104363	SNOMED
	Reticulocyte	4199752	SNOMED
	Siderocyte	4264922	SNOMED

License Agreement

In order to use the SNOMED International SNOMED CT Browser and HemOnc, please accept the following license agreement:

SNOMED INTERNATIONAL SNOMED CT LICENSE AGREEMENT

SNOMED International SNOMED CT Browser includes SNOMED Clinical Terms® (SNOMED CT®) which is used by permission of the SNOMED International. All rights reserved. SNOMED CT® was originally created by the College of American Pathologists.
“SNOMED”, “SNOMED CT” and “SNOMED Clinical Terms” are registered trademarks of the SNOMED International (www.snomed.org)

Use of SNOMED CT in SNOMED International SNOMED CT Browser is governed by the conditions of the following SNOMED CT license issued by SNOMED International:

The meaning of the terms “Affiliate”, or “Data Analysis System”, “Data Creation System”, “Derivative”, “End User”, “Extension”, “Member”, “Non-Member Territory”, “SNOMED CT” and “SNOMED CT Content” are as defined in the SNOMED International Affiliate License Agreement (see on the SNOMED International web site).
Information about Affiliate Licensing is available athttp://www.snomed.org/snomed-ct/get-snomed-ct. Individuals or organizations wishing to register as SNOMED International Affiliates can register at mlds.ihtsdotools.org, subject to acceptance of the Affiliate License Agreement (see on the SNOMED International web site).
The current list of SNOMED International Member Territories can be viewed at www.snomed.org/members. Countries not included in that list are "Non-Member Territories".
End Users, that do not hold an SNOMED International Affiliate License, may access SNOMED CT® using SNOMED International SNOMED CT Browser subject to acceptance of and adherence to the following sub-license limitations:
1. The sub-licensee is only permitted to access SNOMED CT® using this software (or service) for the purpose of exploring and evaluating the terminology.
2. The sub-licensee is not permitted the use of this software as part of a system that constitutes a SNOMED CT "Data Creation System" or "Data Analysis System", as defined in the SNOMED International Affiliate License. This means that the sub-licensee must not use SNOMED International SNOMED CT Browser to add or copy SNOMED CT identifiers into any type of record system, database or document.
3. The sub-licensee is not permitted to translate or modify SNOMED CT Content or Derivatives.
4. The sub-licensee is not permitted to distribute or share SNOMED CT Content or Derivatives.
SNOMED International Affiliates may use SNOMED International SNOMED CT Browser as part of a "Data Creation System" or "Data Analysis System" subject to the following conditions:
1. The SNOMED International Affiliate, using SNOMED International SNOMED CT Browsermust accept full responsibility for any reporting and fees due for use or deployment of such a system in a Non-Member Territory.
2. The SNOMED International Affiliate must not useSNOMED International SNOMED CT Browser to access or interact with SNOMED CT in any way that is not permitted by the Affiliate License Agreement.
3. In the event of termination of the Affiliate License Agreement, the use ofSNOMED International SNOMED CT Browser will be subject to the End User limitations noted in 4.

HemOnc license agreement

The HemOnc Vocabulary is a derivative product of HemOnc.org, which is wholly owned and operated by HemOnc.org LLC. Use of the HemOnc Vocabulary is governed by the conditions of this License Agreement issued by HemOnc.org LLC:

The meaning of the terms “Data Analysis System”, “Data Creation System”, and “License” is defined below.
If you are already holding a HemOnc ontology License, you are subject to the terms and conditions of the License for the version of the HemOnc Vocabulary which was provided to you. If you wish to obtain this version of the HemOnc Vocabulary, you are subject to the following limitations.
If you currently do not hold a HemOnc ontology License, you may access the HemOnc Vocabulary subject to acceptance of and adherence to the following limitations:
1. You are permitted to access HemOnc using this software for the purpose of exploring and evaluating the terminology.
2. You are permitted to use HemOnc as part of a system that constitutes a Data Analysis System, as defined below.
3. You are not permitted the use of HemOnc as part of a system that constitutes a Data Creation System, as defined below. This means that you must not use HemOnc identifiers in any type of system intended for direct or indirect patient care.
4. If you share the Licensed Material with a third party, attribution of the HemOnc vocabulary must be given to HemOnc.org LLC, with a URI or hyperlink to HemOnc.org provided if reasonably possible. Use of HemOnc by a third party would be limited to a Data Analysis System and a copy of this License Agreement must be supplied to the third party.
5. You may not use HemOnc as a substitute for formal medical training, substitute it for independent clinical judgment, and construe it as offering medical advice.

If you wish to utilize the vocabulary for purposes other than specified here, contact us by emailing licensing@hemonc.org.

You agree to indemnify and hold HemOnc.org LLC and all parties who have contributed to HemOnc.org and this derivative product harmless from and against all claims, liability, losses, damages, costs, and expenses, including--but not limited to--legal fees

Definitions

Data Analysis System: a computer system that is used to analyze records or other data, but not if that system is also a Data Creation System

Data Creation System: a computer system that is used to create records or other data that is encoded using HemOnc, for the purposes of facilitating patient care

License: the separate CC BY-NC-SA 4.0 license to the full HemOnc ontology

Details

Term connections (450)

Athena – OHDSI Vocabularies Repository

License Agreement

SNOMED INTERNATIONAL SNOMED CT LICENSE AGREEMENT

HemOnc license agreement