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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 (cell) Is a Blood cell true Inferred relationship Some
Erythrocyte (cell) partie de Blood false Inferred relationship Some
Erythrocyte (cell) partie de Entire body as a whole false Inferred relationship Some
Erythrocyte (cell) partie de Entire hematopoietic system false Additional relationship Some
Erythrocyte (cell) Is a Erythroid cell (cell) true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Hemolytic anemia due to malaria Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization Finding site False Erythrocyte (cell) Inferred relationship Some 3
Secondary autoimmune hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Mechanical haemolytic anaemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Evans syndrome Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic disease of fetus OR newborn due to ABO immunization Finding site False Erythrocyte (cell) Inferred relationship Some 3
Chronic cold agglutinin disease associated with B-cell neoplasm Finding site False Erythrocyte (cell) Inferred relationship Some 3
Primary (idiopathic) autoimmune hemolytic anemia Finding site True Erythrocyte (cell) Inferred relationship Some 3
Drug-induced autoimmune hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Cold autoimmune hemolytic anemia (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 3
Maternal autoimmune hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Duffy isoimmunisation of the newborn Finding site False Erythrocyte (cell) Inferred relationship Some 3
Hemolytic uremic syndrome Finding site True Erythrocyte (cell) Inferred relationship Some 5
Hapten type low affinity hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Kidd isoimmunization of the newborn Finding site False Erythrocyte (cell) Inferred relationship Some 3
Atypical isoimmunization of newborn Finding site False Erythrocyte (cell) Inferred relationship Some 3
Secondary cold-type hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Acquired hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Late anemia due to isoimmunization Finding site False Erythrocyte (cell) Inferred relationship Some 3
Cold agglutinin disease due to and following Epstein-Barr virus infection (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 3
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 6
Thrombotic thrombocytopenic purpura Finding site False Erythrocyte (cell) Inferred relationship Some 6
Autoimmune haemolytic anaemia caused by IgA plus complement Finding site False Erythrocyte (cell) Inferred relationship Some 3
Kell isoimmunization of the newborn Finding site False Erythrocyte (cell) Inferred relationship Some 3
Paroxysmal cold hemoglobinuria Finding site False Erythrocyte (cell) Inferred relationship Some 3
Kernicterus due to isoimmunization Finding site False Erythrocyte (cell) Inferred relationship Some 3
Hapten type high affinity hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Hemolytic anemia caused by Bartonella Finding site False Erythrocyte (cell) Inferred relationship Some 4
Upshaw-Schulman syndrome (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 6
Toxic hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 3
Oroya fever Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare genetic disease characterized by the association of osteosarcoma with limb anomalies (such as bilateral radioulnar synostosis and clinodactyly, as well as other abnormalities of the hands and feet) and erythroid macrocytosis without anemia. There have been no further descriptions in the literature since 1977. Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hereditary cryohydrocytosis with normal stomatin is a rare, hereditary, hemolytic anemia due to a red cell membrane anomaly characterized by fatigue, mild anemia and pseudohyperkalemia due to a potassium leak from the red blood cells. A hallmark of this condition is that red blood cells lyse on storage at 4 degrees centigrade. Finding site True Erythrocyte (cell) Inferred relationship Some 4
A rare, secondary, neonatal autoimmune disease characterized by onset of hemolytic anemia in the neonatal period associated with a positive direct antiglobulin test. Hepatosplenomegaly may be associated. Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare, genetic, hematologic and neurologic disease characterized by chronic, Coombs-negative hemolysis associated with early-onset, relapsing, immune-mediated, inflammatory, axonal or demyelinating, sensory-motor, peripheral polyneuropathy and isolated or recurrent cerebrovascular events (in anterior or posterior circulation). Finding site True Erythrocyte (cell) Inferred relationship Some 4
Congenital hemolytic uremic syndrome (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 6
Rhesus isoimmunization due to anti-Cw Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 5
Rhesus isoimmunisation due to anti-D Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic anemia caused by drugs (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary warm autoimmune hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 4
Post-infectious cold agglutinin disease Finding site False Erythrocyte (cell) Inferred relationship Some 4
Primary warm-type haemolytic anaemia Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 7
Chronic cold agglutinin disease Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hydrops fetalis due to isoimmunization Finding site False Erythrocyte (cell) Inferred relationship Some 5
Anemia caused by alloimmune destruction of transfused red cells Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Finding site False Erythrocyte (cell) Inferred relationship Some 4
Drug-induced immune hemolytic anemia, hapten type Finding site False Erythrocyte (cell) Inferred relationship Some 4
Mixed autoimmune hemolytic anemia is a type of autoimmune hemolytic anemia defined by the presence of both warm and cold autoantibodies, which have a deleterious effect on red blood cells at either body temperature or at lower temperatures. Finding site False Erythrocyte (cell) Inferred relationship Some 4
Acquired thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 7
Diarrhea-associated hemolytic uremic syndrome (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 7
Hemolytic disease of fetus OR newborn due to isoimmunization (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune hemolytic anemia caused by immunoglobulin M Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune haemolytic anaemia caused by IgA Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic uremic syndrome, adult type Finding site True Erythrocyte (cell) Inferred relationship Some 7
Hemolytic uremic syndrome of childhood Finding site True Erythrocyte (cell) Inferred relationship Some 7
Rhesus isoimmunization due to anti-c Finding site False Erythrocyte (cell) Inferred relationship Some 4
Non-autoimmune hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 4
Acquired haemolytic anaemia associated with AIDS Finding site False Erythrocyte (cell) Inferred relationship Some 4
Microangiopathic hemolytic anemia Finding site True Erythrocyte (cell) Inferred relationship Some 4
Hemolytic anemia due to infection Finding site False Erythrocyte (cell) Inferred relationship Some 5
Haemoglobinuria due to haemolysis from external causes Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune hemolytic anemia (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Chronic idiopathic autoimmune hemolytic anemia Finding site True Erythrocyte (cell) Inferred relationship Some 4
Idiopathic paroxysmal cold hemoglobinuria Finding site False Erythrocyte (cell) Inferred relationship Some 4
Acquired spherocytosis Finding site False Erythrocyte (cell) Inferred relationship Some 4
Infantile pyknocytosis (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Autoimmune hemolytic anemia caused by complement Finding site False Erythrocyte (cell) Inferred relationship Some 4
Drug-induced immune hemolytic anemia, immune complex type Finding site False Erythrocyte (cell) Inferred relationship Some 4
Anaemia due to isoimmunisation Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Diarrhea-negative hemolytic uremic syndrome (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 7
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemolytic anemia due to nonlymphoid neoplasm Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary warm-type hemolytic anemia Finding site False Erythrocyte (cell) Inferred relationship Some 4
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Finding site False Erythrocyte (cell) Inferred relationship Some 6
Post-viral paroxysmal cold hemoglobinuria Finding site False Erythrocyte (cell) Inferred relationship Some 4
Rhesus isoimmunization due to anti-E Finding site False Erythrocyte (cell) Inferred relationship Some 4
Secondary paroxysmal cold hemoglobinuria Finding site False Erythrocyte (cell) Inferred relationship Some 4
Hemoglobinopathy Toms River is a rare, genetic hemoglobinopathy disorder, due to a defect in the gamma subunit of the fetal hemoglobin, characterized by neonatal cyanosis, low hemoglobin oxygen saturation levels without arterial hypoxemia, moderate anemia and reticulocytosis, not associated with heart or lung disease. Symptoms progressively subside within the first months of life. Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare, genetic, hemoglobinopathy characterized by generally mild clinical phenotype, high fetal hemoglobin levels and mild microcytosis and hypochromia. In some cases, acute sickle cell disease manifestations were reported, namely acute chest syndrome and acute pain crisis. The genotype is characterized by the combination of an HbS and HbF allele; symptoms depend on the degree of HbF:HbS expressivity with patients with more than 35% pancellular HbF expression being asymptomatic. Symptomatic patients have heterocellular expression of HbF. Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare, hereditary, hematologic disease characterized by an increase in hemoglobin, hematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnea. In some cases, thrombophlebitis and arthralgia have also been reported. Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare, genetic, haematologic disease characterised by increased levels of serum haemoglobin, haematocrit and erythrocyte mass, associated with elevated or inappropriately normal erythropoietin serum levels, occurring in various members of a family and with autosomal dominant inheritance. Finding site True Erythrocyte (cell) Inferred relationship Some 1
Majeed syndrome is a rare genetic multisystemic disorder characterised by chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anaemia, which may be accompanied by neutrophilic dermatosis. Finding site True Erythrocyte (cell) Inferred relationship Some 3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia is a rare, genetic, constitutional dyserythropoietic anemia disorder characterized by moderate to severe anemia without thrombocytopenia, variable degrees of neutropenia, and bone marrow biopsy findings of trilineage dysplasia and hypocellularity of erythroid and granulocytic lineages. Peripheral blood findings include anisocytosis, macrocytosis, poikilocytosis, elliptocytes, and fragmented erythrocytes. Finding site True Erythrocyte (cell) Inferred relationship Some 5
A rare hemolytic anemia characterized by combination of neurologic features, such as psychomotor delay, seizures, variable movement disorders, and hemolytic anemia with stomatocytosis, resulting in cation-leaky erythrocytes, pseudohyperkalemia, hemolytic crises and hepatosplenomegaly. Cataracts are also a presenting feature. Finding site True Erythrocyte (cell) Inferred relationship Some 4
Hereditary elliptocytosis due to glycophorin C deficiency Finding site True Erythrocyte (cell) Inferred relationship Some 4
Hereditary elliptocytosis with transient poikilocytosis Finding site True Erythrocyte (cell) Inferred relationship Some 4
Acquired methemoglobinuria Finding site True Erythrocyte (cell) Inferred relationship Some 2
Drug induced thrombotic thrombocytopenic purpura (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 10
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site True Erythrocyte (cell) Inferred relationship Some 4
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site True Erythrocyte (cell) Inferred relationship Some 4
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site True Erythrocyte (cell) Inferred relationship Some 4
Thrombotic thrombocytopenic purpura Finding site True Erythrocyte (cell) Inferred relationship Some 10
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte (cell) Inferred relationship Some 4

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