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41898006: Erythrocyte (cell)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
69909016 Erythrocyte en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
69911013 Red blood cell en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
69912018 RBC en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
69913011 Red blood corpuscule en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
493141011 RBC - Red blood cell en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
778737018 Erythrocyte (cell) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

37 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte Is a Blood cell true Inferred relationship Some
Erythrocyte Part of Blood false Inferred relationship Some
Erythrocyte Part of Entire body as a whole false Inferred relationship Some
Erythrocyte Part of Entire hematopoietic system false Additional relationship Some
Erythrocyte Is a Erythroid cell (cell) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte Inferred relationship Some 4
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder) Finding site True Erythrocyte Inferred relationship Some 9
Familial haemolytic uraemic syndrome Finding site True Erythrocyte Inferred relationship Some 8
Hereditary elliptocytosis due to alpha spectrin defect Finding site True Erythrocyte Inferred relationship Some 4
Gamma delta beta thalassemia Finding site True Erythrocyte Inferred relationship Some 3
Atypical haemolytic uraemic syndrome Finding site True Erythrocyte Inferred relationship Some 5
Primaquine sensitivity anaemia Finding site True Erythrocyte Inferred relationship Some 3
Post-artesunate delayed haemolysis Finding site True Erythrocyte Inferred relationship Some 1
Moderate deficiency of glucose-6-phosphate dehydrogenase (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Hemolytic disease of fetus due to ABO immunization Finding site True Erythrocyte Inferred relationship Some 6
Fetal hemoglobinopathy Finding site True Erythrocyte Inferred relationship Some 1
Thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Some 6
Chronic idiopathic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Some 3
Posttransfusion purpura Finding site True Erythrocyte Inferred relationship Some 2
Immune thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Some 5
Post infectious thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Some 2
Thrombocytopenic purpura due to defective platelet production (disorder) Finding site True Erythrocyte Inferred relationship Some 2
Thrombocytopenic purpura due to platelet consumption (disorder) Finding site True Erythrocyte Inferred relationship Some 2
Congenital thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Some 5
Thrombocytopenic purpura associated with metabolic disorder (disorder) Finding site True Erythrocyte Inferred relationship Some 5
Acute idiopathic thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Some 11
Severe deficiency of glucose-6-phosphate dehydrogenase (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Haemolytic anaemia of pregnancy Finding site True Erythrocyte Inferred relationship Some 3
Macrocytic anaemia of pregnancy Finding site True Erythrocyte Inferred relationship Some 3
Nutritional anaemia of pregnancy Finding site True Erythrocyte Inferred relationship Some 3
Idiopathic paroxysmal cold hemoglobinuria Finding site True Erythrocyte Inferred relationship Some 5
Deficiency of glucose-6-phosphate dehydrogenase with normal enzyme activity (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Hemoglobin C beta thalassemia (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Hemolytic anemia due to red cell enolase deficiency (disorder) Finding site False Erythrocyte Inferred relationship Some 5
Haemoglobin Paksé disease Finding site True Erythrocyte Inferred relationship Some 2
Hemoglobin Seal Rock disease (disorder) Finding site True Erythrocyte Inferred relationship Some 2
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Finding site False Erythrocyte Inferred relationship Some 5
Drug-induced non autoimmune haemolytic anaemia Finding site False Erythrocyte Inferred relationship Some 5
Homozygous hereditary elliptocytosis (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Lymphocyte passenger syndrome following organ transplantation Finding site False Erythrocyte Inferred relationship Some 1
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) Finding site True Erythrocyte Inferred relationship Some 3
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis Finding site True Erythrocyte Inferred relationship Some 3
Mechanical hemolysis following insertion of prosthetic heart valve (disorder) Finding site True Erythrocyte Inferred relationship Some 5
Polycythemia due to HIF2A mutation Finding site True Erythrocyte Inferred relationship Some 2
Primary familial polycythemia due to erythropoietin receptor mutation Finding site True Erythrocyte Inferred relationship Some 3
Polycythemia due to PHD2 mutation Finding site True Erythrocyte Inferred relationship Some 2
Relative polycythemia due to chronic loss of plasma volume Finding site True Erythrocyte Inferred relationship Some 3
Relative polycythaemia due to acute loss of plasma volume Finding site True Erythrocyte Inferred relationship Some 3
Anemia caused by alloimmune destruction of transfused red cells Finding site True Erythrocyte Inferred relationship Some 2
Hemoglobin C crystals (finding) Finding site True Erythrocyte Inferred relationship Some 1
Hemoglobin SC crystals (finding) Finding site True Erythrocyte Inferred relationship Some 1
Multiple paraganglioma associated with polycythaemia Finding site True Erythrocyte Inferred relationship Some 4
Upshaw-Schulman syndrome (disorder) Finding site True Erythrocyte Inferred relationship Some 8
Hemolytic uremic syndrome with diacylglycerol kinase epsilon deficiency (disorder) Finding site True Erythrocyte Inferred relationship Some 8
Infection-related hemolytic uremic syndrome (disorder) Finding site True Erythrocyte Inferred relationship Some 9
Glutathione synthetase deficiency Finding site True Erythrocyte Inferred relationship Some 5
Glutathione synthase deficiency without 5-oxoprolinuria Finding site True Erythrocyte Inferred relationship Some 5
Methemoglobinemia due to nitrate poisoning (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Haemoglobin D beta plus thalassaemia Finding site True Erythrocyte Inferred relationship Some 1
Haemoglobin E beta plus thalassaemia Finding site True Erythrocyte Inferred relationship Some 1
Haemoglobin C beta plus thalassaemia Finding site True Erythrocyte Inferred relationship Some 1
Hemoglobin E beta zero thalassemia Finding site True Erythrocyte Inferred relationship Some 1
Hemoglobin D beta zero thalassemia (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Haemoglobin C beta zero thalassaemia Finding site True Erythrocyte Inferred relationship Some 1
Delta beta thalassemia trait (disorder) Finding site True Erythrocyte Inferred relationship Some 1
Glutathione synthase deficiency with 5-oxoprolinuria Finding site True Erythrocyte Inferred relationship Some 5
Atypical haemolytic uraemic syndrome with complement gene abnormality Finding site True Erythrocyte Inferred relationship Some 10
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Finding site True Erythrocyte Inferred relationship Some 10

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