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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
69909016 Erythrocyte en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character case insensitive (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
493142016 Red blood cells en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
493143014 Red cells en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
778737018 Erythrocyte (cell) en Fully specified name Active Only initial character case insensitive (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 Existential restriction modifier (core metadata concept)
Erythrocyte partie de Blood false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte partie de Entire body as a whole (body structure) false Inferred relationship Existential restriction modifier (core metadata concept)
Erythrocyte partie de Entire haematopoietic system false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Erythrocyte Is a Erythroid cell (cell) true Inferred relationship Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hemolytic anemia due to malaria Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Haemolytic disease of the newborn due to non-ABO, non-Rh isoimmunisation Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Secondary autoimmune haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Mechanical haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Evans syndrome (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic disease of fetus OR newborn due to ABO immunization (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Chronic cold agglutinin disease associated with B-cell neoplasm (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Primary (idiopathic) autoimmune hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Drug-induced autoimmune hemolytic anemia (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Cold autoimmune haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Maternal autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Duffy isoimmunization of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Haemolytic uraemic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 5
Hapten type low affinity hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Kidd isoimmunisation of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Atypical isoimmunization of newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Secondary cold-type hemolytic anemia (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Acquired hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Late anemia due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Cold agglutinin disease due to and following Epstein-Barr virus infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 6
Thrombotic thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 6
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Kell isoimmunization of the newborn Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Kernicterus due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Hapten type high affinity hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Hemolytic anemia caused by Bartonella Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Upshaw-Schulman syndrome (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 6
Toxic hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
Oroya fever Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Osteosarcoma, limb anomalies, erythroid macrocytosis syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary cryohydrocytosis with normal stomatin Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Neonatal autoimmune hemolytic anemia (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Primary CD59 deficiency Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital hemolytic uremic syndrome (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 6
Rhesus isoimmunization due to anti-Cw Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 5
Rhesus isoimmunisation due to anti-D Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic anemia caused by drugs (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary warm autoimmune haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Post-infectious cold agglutinin disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Primary warm-type haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Chronic cold agglutinin disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hydrops fetalis due to isoimmunization Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 5
Anemia caused by alloimmune destruction of transfused red cells (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Drug-induced immune hemolytic anemia, hapten type Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune hemolytic anemia mixed type Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Diarrhea-associated hemolytic uremic syndrome (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune hemolytic anemia caused by immunoglobulin M Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune haemolytic anaemia caused by IgA Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic uremic syndrome, adult type Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Hemolytic uremic syndrome of childhood Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Rhesus isoimmunisation due to anti-c Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Non-autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Acquired hemolytic anemia associated with AIDS (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Microangiopathic hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic anemia due to infection Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 5
Haemoglobinuria due to haemolysis from external causes Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune hemolytic anemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Chronic idiopathic autoimmune hemolytic anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Idiopathic paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Acquired spherocytosis Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Infantile pyknocytosis Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Autoimmune hemolytic anemia caused by complement (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Drug-induced immune haemolytic anaemia, immune complex type Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Anemia due to isoimmunization (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Diarrhea-negative hemolytic uremic syndrome (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 7
Secondary autoimmune haemolytic anaemia co-occurrent and due to rheumatic disorder Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hemolytic anemia due to nonlymphoid neoplasm Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary warm-type haemolytic anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Familial haemolytic uraemic syndrome Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 6
Post-viral paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Rhesus isoimmunisation due to anti-E Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Secondary paroxysmal cold hemoglobinuria Finding site False Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Haemoglobinopathy Toms River Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary persistence of fetal haemoglobin with sickle cell disease syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive secondary polycythaemia not associated with VHL (Von Hippel Lindau) gene Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal dominant secondary polycythemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 1
An extremely rare genetic multisystemic disorder with characteristics of chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia, which may be accompanied by neutrophilic dermatosis. The disease can be associated with fever, joint pain, delayed bone age, growth failure, short adult stature, and development of flexion contractures. Other reported manifestations include failure to thrive, hepatomegaly, neutropenia, and transient cholestatic jaundice. The clinical course is chronic. Caused by a mutation in LPIN2 (18p11.31), which encodes phosphatidate phosphatase LPIN2 (Lipin-2), important in lipid metabolism. Follows an autosomal recessive pattern of inheritance. Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 5
Hereditary cryohydrocytosis with reduced stomatin Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to glycophorin C deficiency Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis with transient poikilocytosis (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Acquired methemoglobinuria (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 2
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 10
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4
Thrombotic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 10
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte Inferred relationship Existential restriction modifier (core metadata concept) 4

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