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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
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte (cell) Inferred relationship Some 4
A rare constitutional hemolytic anemia that is characterized by the association of Alport syndrome, midface hypoplasia, intellectual deficit and elliptocytosis. It has been described in two families. The syndrome is transmitted as an X-linked trait is caused by a contiguous gene deletion in Xq22.3 involving several genes including COL4A5, FACL4 and AMMECR1. Finding site True Erythrocyte (cell) Inferred relationship Some 9
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 True Erythrocyte (cell) Inferred relationship Some 8
Hereditary elliptocytosis due to alpha spectrin defect Finding site True Erythrocyte (cell) Inferred relationship Some 4
Gamma delta beta thalassemia Finding site True Erythrocyte (cell) Inferred relationship Some 3
Atypical haemolytic uraemic syndrome Finding site True Erythrocyte (cell) Inferred relationship Some 5
Primaquine sensitivity anaemia Finding site True Erythrocyte (cell) Inferred relationship Some 3
Post-artesunate delayed haemolysis Finding site True Erythrocyte (cell) Inferred relationship Some 1
Moderate deficiency of glucose-6-phosphate dehydrogenase (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemolytic disease of fetus due to ABO immunization Finding site True Erythrocyte (cell) Inferred relationship Some 6
Fetal hemoglobinopathy Finding site True Erythrocyte (cell) Inferred relationship Some 1
Thrombocytopenic purpura Finding site True Erythrocyte (cell) Inferred relationship Some 6
Chronic idiopathic thrombocytopenic purpura (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 3
Posttransfusion purpura Finding site True Erythrocyte (cell) Inferred relationship Some 2
purpura thrombopénique idiopathique Finding site False Erythrocyte (cell) Inferred relationship Some 5
Post infectious thrombocytopenic purpura Finding site True Erythrocyte (cell) Inferred relationship Some 2
Thrombocytopenic purpura due to defective platelet production (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 2
Thrombocytopenic purpura due to platelet consumption (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 2
purpura thrombopénique congénital Finding site False Erythrocyte (cell) Inferred relationship Some 5
Thrombocytopenic purpura associated with metabolic disorder (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 5
purpura thrombopénique aigu idiopathique Finding site False Erythrocyte (cell) Inferred relationship Some 11
Severe deficiency of glucose-6-phosphate dehydrogenase (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Haemolytic anaemia of pregnancy Finding site True Erythrocyte (cell) Inferred relationship Some 3
Macrocytic anaemia of pregnancy Finding site True Erythrocyte (cell) Inferred relationship Some 3
Nutritional anaemia of pregnancy Finding site True Erythrocyte (cell) Inferred relationship Some 3
Idiopathic paroxysmal cold hemoglobinuria Finding site True Erythrocyte (cell) Inferred relationship Some 5
Deficiency of glucose-6-phosphate dehydrogenase with normal enzyme activity (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemoglobin C beta thalassemia (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemolytic anemia due to red cell enolase deficiency (disorder) Finding site False Erythrocyte (cell) Inferred relationship Some 5
Haemoglobin Paksé disease Finding site True Erythrocyte (cell) Inferred relationship Some 2
Hemoglobin Seal Rock disease (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 2
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Finding site False Erythrocyte (cell) Inferred relationship Some 5
Drug-induced non autoimmune haemolytic anaemia Finding site False Erythrocyte (cell) Inferred relationship Some 5
Homozygous hereditary elliptocytosis (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Lymphocyte passenger syndrome following organ transplantation Finding site False Erythrocyte (cell) Inferred relationship Some 1
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 3
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis Finding site True Erythrocyte (cell) Inferred relationship Some 3
Mechanical hemolysis following insertion of prosthetic heart valve (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 5
Polycythemia due to HIF2A mutation Finding site True Erythrocyte (cell) Inferred relationship Some 2
Primary familial polycythemia due to erythropoietin receptor mutation Finding site True Erythrocyte (cell) Inferred relationship Some 3
Polycythemia due to PHD2 mutation Finding site True Erythrocyte (cell) Inferred relationship Some 2
Relative polycythemia due to chronic loss of plasma volume Finding site True Erythrocyte (cell) Inferred relationship Some 3
Relative polycythaemia due to acute loss of plasma volume Finding site True Erythrocyte (cell) Inferred relationship Some 3
Anemia caused by alloimmune destruction of transfused red cells Finding site True Erythrocyte (cell) Inferred relationship Some 2
Hemoglobin C crystals (finding) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemoglobin SC crystals (finding) Finding site True Erythrocyte (cell) Inferred relationship Some 1
A rare, endocrine disease characterized by early onset of polycythemia, and later occurring multiple paraganglioma. Clinical presentation includes hypertension, headaches, fatigue, nausea, anxiety, and high concentration of red blood cells, leading to increased risk of stroke and pulmonary thromboembolism. Finding site True Erythrocyte (cell) Inferred relationship Some 4
Upshaw-Schulman syndrome (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 8
A rare genetic hemolytic uremic syndrome (HUS) characterized by infantile onset of relapsing episodes of microangiopathic hemolytic anemia, thrombocytopenia, and acute kidney injury. The episodes are often preceded by viral infections. Affected individuals typically present persistent hypertension, hematuria, and proteinuria (sometimes in the nephrotic range) and develop chronic kidney disease with age. Finding site True Erythrocyte (cell) Inferred relationship Some 8
A rare type of hemolytic uremic syndrome (HUS) characterized by the triad of hemolytic anemia due to generalized thrombotic microangiopathy, thrombocytopenia, and acute kidney injury, and most commonly occurring after acute gastroenteritis due to Shiga toxin-producing enterohemorrhagic Escherichia coli or Shigella dysenteriae. Other infectious causes of HUS include Streptococcus pneumoniae, HIV, Mycoplasma pneumoniae, Histoplasmosis, and Coxsackie virus. Finding site True Erythrocyte (cell) Inferred relationship Some 9
A rare disorder characterized by hemolytic anemia, associated with metabolic acidosis and 5-oxoprolinuria in moderate forms, and with progressive neurological symptoms and recurrent bacterial infections in the most severe forms. Finding site True Erythrocyte (cell) Inferred relationship Some 5
Glutathione synthase deficiency without 5-oxoprolinuria Finding site True Erythrocyte (cell) Inferred relationship Some 5
Methemoglobinemia due to nitrate poisoning (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Haemoglobin D beta plus thalassaemia Finding site True Erythrocyte (cell) Inferred relationship Some 1
Haemoglobin E beta plus thalassaemia Finding site True Erythrocyte (cell) Inferred relationship Some 1
Haemoglobin C beta plus thalassaemia Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemoglobin E beta zero thalassemia Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemoglobin D beta zero thalassemia (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Haemoglobin C beta zero thalassaemia Finding site True Erythrocyte (cell) Inferred relationship Some 1
Delta beta thalassemia trait (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Glutathione synthase deficiency with 5-oxoprolinuria Finding site True Erythrocyte (cell) Inferred relationship Some 5
Atypical haemolytic uraemic syndrome with complement gene abnormality Finding site True Erythrocyte (cell) Inferred relationship Some 10
Atypical haemolytic uraemic syndrome with anti-factor H antibodies Finding site True Erythrocyte (cell) Inferred relationship Some 10
Presence of erythrocytes in urine (observable entity) Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell count, automated, cerebrospinal fluid Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell count, manual, peritoneal fluid Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell count, automated, pleural fluid Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell count, automated, urine (procedure) Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell count, automated, synovial fluid Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell morphology Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell size determination Component True Erythrocyte (cell) Inferred relationship Some 1
Red blood cell maturation age determination Component True Erythrocyte (cell) Inferred relationship Some 1
A rare multiple congenital anomalies/dysmorphic syndrome characterized by global developmental delay, moderate to severe intellectual disability, language delay and asymptomatic persistence of fetal hemoglobin. Joint laxity and microcephaly are commonly observed. Majority of the patients present with variable dysmorphic features (including strabismus, downslanting palpebral fissures, anteverted nose with small nares and full tip, external ear anomalies, thin upper lip and everted lower lip). Behavior problems including anxiety, recurrent hand flapping/biting and attention deficit can also be observed. Finding site True Erythrocyte (cell) Inferred relationship Some 2
Beta thalassemia major in mother complicating pregnancy Finding site True Erythrocyte (cell) Inferred relationship Some 1
Beta thalassemia trait in mother complicating pregnancy (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 2
Alpha thalassemia trait in mother complicating pregnancy (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hemoglobin Iraq-Halabja trait (disorder) Finding site True Erythrocyte (cell) Inferred relationship Some 1
Hereditary pyropoikilocytosis Finding site True Erythrocyte (cell) Inferred relationship Some 4

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