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41898006: Erythrocyte (cell)

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

Descriptions:

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

37 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte Is a Blood cell true Inferred relationship Existential restriction modifier
Erythrocyte Part of Blood false Inferred relationship Existential restriction modifier
Erythrocyte Part of Entire body as a whole false Inferred relationship Existential restriction modifier
Erythrocyte Part of Entire hematopoietic system false Additional relationship Existential restriction modifier
Erythrocyte Is a Erythroid cell true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hemolytic anemia caused by malaria Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Secondary autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Mechanical hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Evans syndrome Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic disease of fetus OR newborn due to ABO immunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Chronic cold agglutinin disease associated with B-cell neoplasm Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Primary (idiopathic) autoimmune hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Drug-induced autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Cold autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Maternal autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Duffy isoimmunization of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Hapten type low affinity hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Kidd isoimmunization of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Atypical isoimmunization of newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Secondary cold-type hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Acquired hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Late anemia due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Cold agglutinin disease caused by Epstein-Barr virus infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Drug induced thrombotic thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier 6
Thrombotic thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier 6
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Kell isoimmunization of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Kernicterus due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Hapten type high affinity hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by Bartonella Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Upshaw-Schulman syndrome Finding site False Erythrocyte Inferred relationship Existential restriction modifier 6
Toxic hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 3
Oroya fever Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hereditary cryohydrocytosis with normal stomatin Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Neonatal autoimmune hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Primary CD59 deficiency Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Congenital hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 6
Rhesus isoimmunization due to anti-Cw Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia caused by immunoglobulin G Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Rhesus isoimmunization due to anti-D Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic anemia caused by drugs Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary warm autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Post-infectious cold agglutinin disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Primary warm-type hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune thrombotic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Chronic cold agglutinin disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hydrops fetalis due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Anemia caused by alloimmune destruction of transfused red cells Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic disease of newborn co-occurrent and due to ABO immunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Drug-induced immune hemolytic anemia, hapten type Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia mixed type Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Acquired thrombotic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Diarrhea-associated hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Hemolytic disease of fetus OR newborn due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia caused by immunoglobulin M Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia caused by immunoglobulin A Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic uremic syndrome, adult type Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Hemolytic uremic syndrome of childhood Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Rhesus isoimmunization due to anti-c Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Non-autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Acquired hemolytic anemia associated with acquired immunodeficiency syndrome Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Microangiopathic hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic anemia due to infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Hemoglobinuria due to hemolysis from external causes Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Chronic idiopathic autoimmune hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Idiopathic paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Acquired spherocytosis Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Infantile pyknocytosis Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia caused by complement Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Drug-induced immune hemolytic anemia, immune complex type Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Anemia due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Diarrhea-negative hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 7
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemolytic anemia due to nonlymphoid neoplasm Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary warm-type hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Familial hemolytic uremic syndrome Finding site False Erythrocyte Inferred relationship Existential restriction modifier 6
Post-viral paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Rhesus isoimmunization due to anti-E Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Secondary paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier 4
Hemoglobinopathy Toms River Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hereditary persistence of fetal hemoglobin with sickle cell disease syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Autosomal recessive secondary polycythemia not associated with Von Hippel Lindau gene Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Autosomal dominant secondary polycythemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia and neutrophilic dermatosis Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Hereditary cryohydrocytosis with reduced stomatin Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to glycophorin C deficiency Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis with transient poikilocytosis Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Acquired methemoglobinuria Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Drug induced thrombotic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 10
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Thrombotic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 10
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4

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