41898006: Erythrocyte (cell)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\...

\Body system structure\Hematological system structure (body structure)\Blood cell\Erythrocyte

\Cell\Entire cell (cell)\...

\Erythroid cell (cell)\Erythrocyte

\Blood cell\Erythrocyte

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

Descriptions:

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
Anemia due to blood loss	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Hypochromic microcytic anemia with iron overload (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemolytic anemia caused by Bartonella	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Haemolytic anaemia due to babesiosis	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Mycoplasmal anemia (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hemolytic anemia due to infection	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anemia due to infection	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hemolytic anemia caused by Clostridium welchii	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Oroya fever	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Hemolytic anemia due to malaria	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Anemia following acute postoperative blood loss (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Anaemia co-occurrent and due to chronic kidney disease stage 3	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia co-occurrent with human immunodeficiency virus infection (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia caused by zidovudine (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Aplastic anaemia co-occurrent with human immunodeficiency virus infection	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Dehydrated hereditary stomatocytosis (DHS) is a rare haemolytic anaemia characterised by a decreased red cell osmotic fragility due to a defect in cation permeability, resulting in red cell dehydration and mild to moderate compensated haemolysis. Pseudohyperkalaemia (loss of potassium ions from red cells on storage at room temperature) is sometimes observed.	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Alpha thalassemia X-linked intellectual disability syndrome (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Dominant beta-thalassemia (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Familial pseudohyperkalemia (FP) is an inherited, mild, non-hemolytic subtype of hereditary stomatocytosis that is associated with a temperature-dependent anomaly in red cell membrane permeability to potassium that leads to high in vitro potassium levels in samples stored below 37°C. FP is not associated with additional hematological abnormalities, although affected individuals may show some mild abnormalities like macrocytosis.	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Beta thalassemia X-linked thrombocytopenia syndrome	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Autosomal recessive sideroblastic anemia (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Anemia co-occurrent and due to chronic kidney disease stage 4 (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Anemia co-occurrent and due to chronic kidney disease stage 5 (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Telangiectasia, erythrocytosis, monoclonal gammopathy, perinephric fluid collections and intrapulmonary shunting syndrome (disorder)	Finding site	True	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)
Lethal hemolytic anemia and genital anomaly syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Congenital dyserythropoietic anemia type IV (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Adult-onset autosomal recessive sideroblastic anemia	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Cystic fibrosis with gastritis and megaloblastic anemia syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Megaloblastic anemia due to folate deficiency due to increased requirement (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Megaloblastic anaemia due to folate deficiency in pregnancy and lactation	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Megaloblastic anemia due to folate deficiency in prematurity (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	5
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
X-linked congenital dyserythropoietic anemia with thrombocytopenia (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Polycythemia neonatorum due to inherited disorder of erythropoietin production	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	2
Polycythemia neonatorum following blood transfusion (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Overhydrated hereditary stomatocytosis (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Pancreatic insufficiency, dyserythropoietic anemia, calvarial hyperostosis syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	6
Familial haemolytic uraemic syndrome	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Southeast Asian ovalocytosis	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
A rare severe neurodegenerative disorder that is considered one of the phenocopies of Huntington Disease (HD) affecting patients of African descent and characterized by a triad of movement (chorea, oculomotor, parkinsonism), psychiatric (prominently sadness, irritability and anxiety), and cognitive abnormalities (early cognitive decline and subcortical-like dementia).	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
McLeod neuroacanthocytosis syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
Iron deficiency anaemia due to blood loss	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Acquired iron deficiency anemia due to decreased absorption (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
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)
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune haemolytic anaemia co-occurrent and due to rheumatic disorder	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)
Hemoglobin M disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassaemia intermedia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Haemoglobin Bart's hydrops syndrome	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
A>gamma< beta^+^ HPFH AND beta^0^ thalassemia in cis	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemoglobin D trait	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
beta^+^ Thalassemia, normal Hb A>2<, type 2	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Delta beta thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sickle cell trait (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Delta thalassemia (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary persistence of fetal hemoglobin thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Unstable hemoglobin disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Heterozygous thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Double heterozygous sickling disorder	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Epsilon gamma delta beta thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemoglobin E disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell-hemoglobin D disease (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Homozygous beta thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Beta zero thalassemia deletion type	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary persistence of foetal haemoglobin (HPF) unlinked to beta-globulin gene cluster	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sickle cell-hemoglobin C disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Alpha plus thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Sickle cell-thalassemia disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	4
HPFH A gamma beta^+^ thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassaemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemoglobin E trait	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Sickle cell-hemoglobin E disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Thalassemia with other hemoglobinopathy (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Beta plus thalassaemia normal haemoglobin A>2< type 1 silent	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemoglobin H disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Haemoglobin C disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Hereditary persistence of fetal hemoglobin delta beta plus thalassemia (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
HPFH nondeletion type	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary persistence of fetal haemoglobin G gamma beta plus thalassaemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia-hemoglobin C disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Delta zero thalassemia (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Beta thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Alpha zero thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hemoglobin D disease	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Alpha thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hb Lepore thalassaemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Epsilon gamma delta beta^0^ thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassemia major	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Haemoglobin C trait	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	1
Delta beta zero thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Beta plus thalassemia	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Thalassaemia syndrome	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Alpha plus thalassemia non deletion type (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3
Hereditary persistence of foetal haemoglobin (HPFH) deletion type	Finding site	True	Erythrocyte	Inferred relationship	Existential restriction modifier (core metadata concept)	3

Start Previous Page 11 of 14 Next End

This concept is not in any reference sets

Back to Start

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