41898006: Erythrocyte (cell)

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

\Body system structure\Structure of hematological system (body structure)\Blood cell\Erythrocyte

\Cell\Entire 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	Some
Erythrocyte	del af	Blood	false	Inferred relationship	Some
Erythrocyte	del af	Entire body as a whole	false	Inferred relationship	Some
Erythrocyte	del af	Entire hematopoietic system	false	Additional relationship	Some
Erythrocyte	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	Inferred relationship	Some	4
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Secondary autoimmune hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Mechanical haemolytic anaemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Evans syndrome	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hemolytic disease of fetus OR newborn due to ABO immunization	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Chronic cold agglutinin disease associated with B-cell neoplasm	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Primary (idiopathic) autoimmune hemolytic anemia	Finding site	True	Erythrocyte	Inferred relationship	Some	3
Drug-induced autoimmune hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Cold autoimmune hemolytic anemia (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Maternal autoimmune hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Duffy isoimmunisation of the newborn	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Hemolytic uremic syndrome	Finding site	True	Erythrocyte	Inferred relationship	Some	5
Hapten type low affinity hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Kidd isoimmunization of the newborn	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Atypical isoimmunization of newborn	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Secondary cold-type hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Acquired hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Late anemia due to isoimmunization	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Cold agglutinin disease due to and following Epstein-Barr virus infection (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Drug induced thrombotic thrombocytopenic purpura (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	6
Thrombotic thrombocytopenic purpura	Finding site	False	Erythrocyte	Inferred relationship	Some	6
Autoimmune haemolytic anaemia caused by IgA plus complement	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Kell isoimmunization of the newborn	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Paroxysmal cold hemoglobinuria	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Kernicterus due to isoimmunization	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Hapten type high affinity hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Hemolytic anemia caused by Bartonella	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Upshaw-Schulman syndrome (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	6
Toxic hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	3
Oroya fever	Finding site	True	Erythrocyte	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	Inferred relationship	Some	1
A rare hereditary haemolytic anaemia due to a red cell membrane anomaly characterised by fatigue, mild anaemia and pseudohyperkalaemia 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. There is evidence this disease is caused by heterozygous mutation in the SLC4A1 gene on chromosome 17q21.	Finding site	True	Erythrocyte	Inferred relationship	Some	4
A very 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	Inferred relationship	Some	1
A rare genetic haematologic and neurologic disease characterised by chronic Coombs-negative haemolysis. The disease is 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	Inferred relationship	Some	4
Congenital hemolytic uremic syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	6
Rhesus isoimmunization due to anti-Cw	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune hemolytic anemia caused by immunoglobulin G (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	5
Rhesus isoimmunisation due to anti-D	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hemolytic anemia caused by drugs (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary warm autoimmune hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Post-infectious cold agglutinin disease	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Primary warm-type haemolytic anaemia	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune thrombotic thrombocytopenic purpura (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Chronic cold agglutinin disease	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hydrops fetalis due to isoimmunization	Finding site	False	Erythrocyte	Inferred relationship	Some	5
Anemia caused by alloimmune destruction of transfused red cells	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Paroxysmal cold hemoglobinuria associated with tertiary syphilis	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Drug-induced immune hemolytic anemia, hapten type	Finding site	False	Erythrocyte	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	Inferred relationship	Some	4
Acquired thrombotic thrombocytopenic purpura (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Diarrhea-associated hemolytic uremic syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Hemolytic disease of fetus OR newborn due to isoimmunization (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune hemolytic anemia caused by immunoglobulin M	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune haemolytic anaemia caused by IgA	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hemolytic uremic syndrome, adult type	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Hemolytic uremic syndrome of childhood	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Rhesus isoimmunization due to anti-c	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Non-autoimmune hemolytic anemia	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Acquired haemolytic anaemia associated with AIDS	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Microangiopathic hemolytic anemia	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Hemolytic anemia due to infection	Finding site	False	Erythrocyte	Inferred relationship	Some	5
Haemoglobinuria due to haemolysis from external causes	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune hemolytic anemia (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Chronic idiopathic autoimmune hemolytic anemia	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Idiopathic paroxysmal cold hemoglobinuria	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Acquired spherocytosis	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Infantile pyknocytosis (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Autoimmune hemolytic anemia caused by complement	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Drug-induced immune haemolytic anaemia, immune complex type	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Anaemia due to isoimmunisation	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Diarrhea-negative hemolytic uremic syndrome (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	7
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder)	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Hemolytic anemia due to nonlymphoid neoplasm	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary warm-type haemolytic anaemia	Finding site	False	Erythrocyte	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	Inferred relationship	Some	6
Post-viral paroxysmal cold hemoglobinuria	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Rhesus isoimmunisation due to anti-E	Finding site	False	Erythrocyte	Inferred relationship	Some	4
Secondary paroxysmal cold hemoglobinuria	Finding site	False	Erythrocyte	Inferred relationship	Some	4
A rare genetic haemoglobinopathy disorder due to a defect in the gama subunit of the fetal haemoglobin and characterised by neonatal cyanosis, low haemoglobin oxygen saturation levels without arterial hypoxaemia, moderate anaemia and reticulocytosis, not associated with heart or lung disease. Symptoms progressively subside within the first months of life. Can be caused by heterozygous mutation in the HBG2 gene on chromosome 11p15.5.	Finding site	True	Erythrocyte	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.	Finding site	True	Erythrocyte	Inferred relationship	Some	1
A rare hereditary haematologic disease characterised by an increase in haemoglobin, haematocrit and erythrocyte mass resulting in plethora or ruddy complexion, headache, dizziness, tinnitus and exertional dyspnoea. In some cases, thrombophlebitis and arthralgia have also been reported.	Finding site	True	Erythrocyte	Inferred relationship	Some	1
A rare genetic hematologic disease characterized by increased levels of serum hemoglobin, hematocrit 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	Inferred relationship	Some	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	Some	3
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. Caused by mutation in the GATA1 gene on chromosome Xp11.	Finding site	True	Erythrocyte	Inferred relationship	Some	5
A rare hemolytic anemia characterized by a 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. There is evidence the disease is caused by heterozygous mutation in the SLC2A1 gene on chromosome 1p34.	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Hereditary elliptocytosis due to glycophorin C deficiency	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Hereditary elliptocytosis with transient poikilocytosis	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Acquired methemoglobinuria	Finding site	True	Erythrocyte	Inferred relationship	Some	2
Drug induced thrombotic thrombocytopenic purpura (disorder)	Finding site	True	Erythrocyte	Inferred relationship	Some	10
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Hereditary elliptocytosis due to deficiency of protein 4.1	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Hereditary elliptocytosis due to abnormal protein 4.1	Finding site	True	Erythrocyte	Inferred relationship	Some	4
Thrombotic thrombocytopenic purpura	Finding site	True	Erythrocyte	Inferred relationship	Some	10
Hereditary elliptocytosis due to beta spectrin defect in self-association	Finding site	True	Erythrocyte	Inferred relationship	Some	4

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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
2794491000005115	Erytrocyt	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)