FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.21  |  FHIR Version n/a  User: [n/a]

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
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 9
Familial hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 8
Hereditary elliptocytosis due to alpha spectrin defect Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Gamma delta beta thalassemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Atypical hemolytic uremic syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Primaquine sensitivity anemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Delayed hemolysis following artesunate therapy Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Moderate deficiency of glucose-6-phosphate dehydrogenase Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hemolytic disease of fetus due to ABO immunization Finding site True Erythrocyte Inferred relationship Existential restriction modifier 6
Fetal hemoglobinopathy Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 6
Chronic idiopathic thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Posttransfusion purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Immune thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Post infectious thrombocytopenic purpura Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Thrombocytopenic purpura due to defective platelet production Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Thrombocytopenic purpura due to platelet consumption Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Congenital thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Thrombocytopenic purpura associated with metabolic disorder Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Acute idiopathic thrombocytopenic purpura Finding site False Erythrocyte Inferred relationship Existential restriction modifier 11
Severe deficiency of glucose-6-phosphate dehydrogenase Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hemolytic anemia of pregnancy Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Macrocytic anemia of pregnancy Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Nutritional anemia of pregnancy Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Idiopathic paroxysmal cold hemoglobinuria Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Deficiency of glucose-6-phosphate dehydrogenase with normal enzyme activity Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hemoglobin C beta thalassemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hemolytic anemia due to red cell enolase deficiency Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Hemoglobin Paksé disease Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Hemoglobin Seal Rock disease Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Non autoimmune hemolytic anemia caused by drug Finding site False Erythrocyte Inferred relationship Existential restriction modifier 5
Homozygous hereditary elliptocytosis Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Lymphocyte passenger syndrome following organ transplantation Finding site False Erythrocyte Inferred relationship Existential restriction modifier 1
Acute sequestration of spleen due to sickle cell thalassemia with crisis Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Acute sequestration of spleen due to sickle cell hemoglobin C disease with crisis Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Mechanical hemolysis following insertion of prosthetic heart valve Finding site True Erythrocyte Inferred relationship Existential restriction modifier 5
Polycythemia due to HIF2A mutation Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Primary familial polycythemia due to erythropoietin receptor mutation Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Polycythemia due to PHD2 mutation Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Pseudo polycythemia due to chronic loss of plasma volume Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Pseudo polycythemia due to acute loss of plasma volume Finding site True Erythrocyte Inferred relationship Existential restriction modifier 3
Anemia caused by alloimmune destruction of transfused red cells Finding site True Erythrocyte Inferred relationship Existential restriction modifier 2
Hemoglobin C crystals Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Hemoglobin SC crystals Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Multiple paraganglioma associated with polycythemia Finding site True Erythrocyte Inferred relationship Existential restriction modifier 4
Upshaw-Schulman syndrome Finding site True Erythrocyte Inferred relationship Existential restriction modifier 8
Hypertonic cryohaemolysis test Component False Erythrocyte Inferred relationship Existential restriction modifier
Haemoglobin E beta zero thalassaemia (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Haemoglobin E beta plus thalassaemia (disorder) Finding site True Erythrocyte Inferred relationship Existential restriction modifier 1
Red blood cell count NOS Component False Erythrocyte Inferred relationship Existential restriction modifier
Hematocrit - PCV - NOS (procedure) Component False Erythrocyte Inferred relationship Existential restriction modifier
Mean corpuscular hemoglobin NOS (procedure) Component False Erythrocyte Inferred relationship Existential restriction modifier
Mean corpuscular hemoglobin concentration (MCHC) - NOS (procedure) Component False Erythrocyte Inferred relationship Existential restriction modifier
Mean corpuscular volume - NOS Component False Erythrocyte Inferred relationship Existential restriction modifier
Red blood cell size NOS Component False Erythrocyte Inferred relationship Existential restriction modifier
Eosin-5-maleimide cell binding study Component True Erythrocyte Inferred relationship Existential restriction modifier 2
Reticulocyte haemoglobin content measurement Component True Erythrocyte Inferred relationship Existential restriction modifier 2
Hypertonic cryohaemolysis test Component True Erythrocyte Inferred relationship Existential restriction modifier 2
Red blood cell membrane protein study Component True Erythrocyte Inferred relationship Existential restriction modifier 2
Isopropanol precipitation test Component True Erythrocyte Inferred relationship Existential restriction modifier 1
Eosin-5-maleimide cell binding study Component False Erythrocyte Inferred relationship Existential restriction modifier
Reticulocyte haemoglobin content measurement Component False Erythrocyte Inferred relationship Existential restriction modifier
Red blood cell membrane protein study Component False Erythrocyte Inferred relationship Existential restriction modifier
Isopropanol precipitation test Component False Erythrocyte Inferred relationship Existential restriction modifier
Red blood cell pyruvate kinase screening test Component True Erythrocyte Inferred relationship Existential restriction modifier 2
Erythropoiesis stimulating agent induced antibody mediated acquired pure red cell aplasia Finding site False Erythrocyte Inferred relationship Existential restriction modifier
Recurrent anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier
[X]Other megaloblastic anaemias, not elsewhere classified Finding site False Erythrocyte Inferred relationship Existential restriction modifier
[X]Aplastic and other anaemias Finding site False Erythrocyte Inferred relationship Existential restriction modifier
[X]Other dietary vitamin B12 deficiency anaemia Finding site False Erythrocyte Inferred relationship Existential restriction modifier
[X]Other iron deficiency anaemias Finding site False Erythrocyte Inferred relationship Existential restriction modifier
[X]Haemolytic anaemias Finding site False Erythrocyte Inferred relationship Existential restriction modifier
Count of red blood cells in cerebrospinal fluid (observable entity) Component True Erythrocyte Inferred relationship Existential restriction modifier 1
Control mean fluorescence intensity of eosin 5-maleimide labelled red blood cells in blood (observable entity) Component True Erythrocyte Inferred relationship Existential restriction modifier 1
Qualitative result of red blood cells in blood smear microscopy (observable entity) Component True Erythrocyte Inferred relationship Existential restriction modifier 1
Mean fluorescence intensity of eosin 5-maleimide labelled red blood cells in blood (observable entity) Component True Erythrocyte Inferred relationship Existential restriction modifier 1
Qualitative result of red blood cells in mid-stream urine microscopy (observable entity) Component True Erythrocyte Inferred relationship Existential restriction modifier 1

Start Previous Page 14 of 14


This concept is not in any reference sets

Back to Start