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14089001: Red blood cell count (procedure)

Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
23984019 Red blood cell count en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
23985018 RBC count en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
476071015 RBC - Red blood cell count en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
739997012 Red blood cell count (procedure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

13 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Red blood cell count Is a Blood cell count true Inferred relationship Some
Red blood cell count Is a Red blood cell test false Inferred relationship Some
Red blood cell count Method Investigation - action false Inferred relationship Some
Red blood cell count Has measured component (attribute) Erythrocyte (cell) false Inferred relationship Some
Red blood cell count Has intent Diagnostic intent (qualifier value) false Inferred relationship Some
Red blood cell count Component Hematology observable false Inferred relationship Some
Red blood cell count Component Erythrocyte (cell) true Inferred relationship Some 1
Red blood cell count Has specimen Red blood cell fluid specimen (specimen) false Inferred relationship Some
Red blood cell count Method Evaluation - action false Inferred relationship Some
Red blood cell count Method Measurement - action false Inferred relationship Some 2
Red blood cell count Method Measurement - action true Inferred relationship Some 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Anemia due to and following chemotherapy Interprets False Red blood cell count Inferred relationship Some 2
TEMPI syndrome is a rare multi-systemic disease characterized by the presence of Telangiectasias, Erythrocytosis with elevated erythropoietin levels, Monoclonal gammopathy, Perinephric-fluid collections, and Intrapulmonary shunting. Interprets True Red blood cell count Inferred relationship Some 2
Chuvash erythrocytosis is a rare, genetic, congenital secondary polycythemia disorder characterized by increased hemoglobin, hematocrit and erythropoietin serum levels and normal oxygen affinity, which usually manifests with headache, dizziness, dyspnea and/or plethora. Patients present an increased risk of hemorrhage, thrombosis and early death. Interprets True Red blood cell count 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. Interprets True Red blood cell count Inferred relationship Some 1
A rare constitutional aplastic anemia characterized by progressive trilineage bone marrow failure (with hypocellularity), developmental delay with learning disabilities, and microcephaly. Mild facial dysmorphism and hypotonia have also been reported. Interprets True Red blood cell count Inferred relationship Some 3
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. Interprets True Red blood cell count Inferred relationship Some 3
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). Interprets True Red blood cell count 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. Interprets True Red blood cell count Inferred relationship Some 4
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. Interprets True Red blood cell count Inferred relationship Some 2
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. Interprets True Red blood cell count Inferred relationship Some 2
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. Interprets True Red blood cell count Inferred relationship Some 2
Hereditary isolated aplastic anemia is a rare, genetic, constitutional aplastic anemia disorder characterized by severe peripheral blood pancytopenia and bone marrow hypoplasia in multiple individuals of a family, in the absence of any somatic symptoms. Abnormal bleeding, as well as erythrocyte macrocytosis, is reported and patients usually become transfusion dependent. Interprets True Red blood cell count Inferred relationship Some 2
A rare syndrome with combined immunodeficiency characterized by a variable clinical presentation ranging from asymptomatic individuals to potentially life-threatening, recurrent bacterial infections associated with progressive loss of serum immunoglobulins and B cells. Interprets True Red blood cell count Inferred relationship Some 1
Pancytopenia caused by immunosuppressant Interprets True Red blood cell count Inferred relationship Some 1
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. Interprets True Red blood cell count Inferred relationship Some 1
Hereditary elliptocytosis with transient poikilocytosis Interprets True Red blood cell count Inferred relationship Some 2
Hereditary elliptocytosis Interprets True Red blood cell count Inferred relationship Some 2
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. Interprets True Red blood cell count Inferred relationship Some 7
Anemia due to chronic infectious disease (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Gamma delta beta thalassemia Interprets True Red blood cell count Inferred relationship Some 1
Atypical haemolytic uraemic syndrome Interprets True Red blood cell count Inferred relationship Some 7
Primaquine sensitivity anaemia Interprets True Red blood cell count Inferred relationship Some 1
Megaloblastic anemia due to dihydrofolate reductase deficiency (disorder) Interprets False Red blood cell count Inferred relationship Some 3
Hemolytic disease of fetus due to ABO immunization Interprets True Red blood cell count Inferred relationship Some 3
Anemia due to chronic kidney disease stage 1 Interprets False Red blood cell count Inferred relationship Some 1
Thrombocytopenic purpura Interprets True Red blood cell count Inferred relationship Some 5
Chronic idiopathic thrombocytopenic purpura (disorder) Interprets True Red blood cell count Inferred relationship Some 6
Posttransfusion purpura Interprets True Red blood cell count Inferred relationship Some 7
purpura thrombopénique idiopathique Interprets False Red blood cell count Inferred relationship Some 9
Post infectious thrombocytopenic purpura Interprets True Red blood cell count Inferred relationship Some 7
Thrombocytopenic purpura due to defective platelet production (disorder) Interprets True Red blood cell count Inferred relationship Some 7
Thrombocytopenic purpura due to platelet consumption (disorder) Interprets True Red blood cell count Inferred relationship Some 7
purpura thrombopénique congénital Interprets False Red blood cell count Inferred relationship Some 8
Thrombocytopenic purpura associated with metabolic disorder (disorder) Interprets True Red blood cell count Inferred relationship Some 8
purpura thrombopénique aigu idiopathique Interprets False Red blood cell count Inferred relationship Some 6
Haemolytic anaemia of pregnancy Interprets True Red blood cell count Inferred relationship Some 1
Congenital megaloblastic anemia due to transcobalamin II deficiency (disorder) Interprets True Red blood cell count Inferred relationship Some 5
Macrocytic anaemia of pregnancy Interprets True Red blood cell count Inferred relationship Some 1
Nutritional anaemia of pregnancy Interprets True Red blood cell count Inferred relationship Some 1
Autosomal dominant sideroblastic anemia (disorder) Interprets False Red blood cell count Inferred relationship Some 2
Hemolytic anemia due to red cell enolase deficiency (disorder) Interprets False Red blood cell count Inferred relationship Some 2
Haemoglobin Paksé disease Interprets False Red blood cell count Inferred relationship Some 1
Hemoglobin Seal Rock disease (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Interprets False Red blood cell count Inferred relationship Some 2
Drug-induced non autoimmune haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 2
Iron deficiency anaemia due to coeliac disease Interprets True Red blood cell count Inferred relationship Some 1
Iron deficiency anemia due to increased requirement in adolescence (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Acquired iron deficiency anaemia due to increased requirement in infancy Interprets True Red blood cell count Inferred relationship Some 1
Iron deficiency anemia following gastrectomy (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Anemia caused by antineoplastic agent Interprets True Red blood cell count Inferred relationship Some 1
Pancytopenia caused by anticonvulsant Interprets True Red blood cell count Inferred relationship Some 2
Pancytopenia caused by antithyroid drug (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Anemia due to enzymopathy (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Homozygous hereditary elliptocytosis (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Vitamin B12 deficiency anemia due to chronic atrophic gastritis (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Hereditary iron deficiency anemia Interprets True Red blood cell count Inferred relationship Some 3
Lymphocyte passenger syndrome following organ transplantation Interprets False Red blood cell count Inferred relationship Some 2
Acute sequestration of spleen due to sickle cell thalassemia with crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 4
Acute splenic sequestration due to sickle cell hemoglobin C disease with crisis Interprets False Red blood cell count Inferred relationship Some 4
Mechanical hemolysis following insertion of prosthetic heart valve (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Polycythemia due to HIF2A mutation Interprets True Red blood cell count Inferred relationship Some 1
Vitamin B12 deficiency anemia following total gastrectomy (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Primary familial polycythemia due to erythropoietin receptor mutation Interprets True Red blood cell count Inferred relationship Some 2
Polycythemia due to PHD2 mutation Interprets True Red blood cell count Inferred relationship Some 1
Relative polycythemia due to chronic loss of plasma volume Interprets True Red blood cell count Inferred relationship Some 2
Relative polycythaemia due to acute loss of plasma volume Interprets True Red blood cell count Inferred relationship Some 2
Pernicious anaemia due to autoimmune disorder Interprets True Red blood cell count Inferred relationship Some 2
Aase syndrome Interprets True Red blood cell count Inferred relationship Some 2
Reticulocyte count Is a True Red blood cell count Inferred relationship Some
Hemolytic anemia with emphysema AND cutis laxa Interprets True Red blood cell count Inferred relationship Some 6
Hemolytic anemia caused by hyperbaric oxygen Interprets True Red blood cell count Inferred relationship Some 2
Hemolytic anemia due to hexokinase deficiency Interprets True Red blood cell count Inferred relationship Some 3
Chronic hemolytic anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 3
Autoimmune hemolytic anemia caused by complement Interprets True Red blood cell count Inferred relationship Some 4
Evans syndrome Interprets True Red blood cell count Inferred relationship Some 3
Autoimmune hemolytic anemia caused by immunoglobulin M Interprets True Red blood cell count Inferred relationship Some 4
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Hapten type high affinity hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 3
Hemolytic anemia caused by drugs (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Autoimmune haemolytic anaemia caused by IgA Interprets True Red blood cell count Inferred relationship Some 4
Autoimmune haemolytic anaemia caused by IgA plus complement Interprets True Red blood cell count Inferred relationship Some 2
Hapten type low affinity hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 3
Autoimmune hemolytic anemia caused by immunoglobulin G (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Post-infectious cold agglutinin disease Interprets True Red blood cell count Inferred relationship Some 4
Cold agglutinin disease due to and following Epstein-Barr virus infection (disorder) Interprets True Red blood cell count Inferred relationship Some 3
Chronic cold agglutinin disease Interprets True Red blood cell count Inferred relationship Some 4
Chronic cold agglutinin disease associated with B-cell neoplasm Interprets True Red blood cell count Inferred relationship Some 3
Paroxysmal cold hemoglobinuria Interprets True Red blood cell count Inferred relationship Some 1
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Interprets True Red blood cell count Inferred relationship Some 4
Anemia caused by alloimmune destruction of transfused red cells Interprets True Red blood cell count Inferred relationship Some 4
Primary warm-type haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 1
Secondary warm-type hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Mechanical haemolytic anaemia Interprets True Red blood cell count Inferred relationship Some 1
Toxic hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Secondary autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Acquired haemolytic anaemia associated with AIDS Interprets True Red blood cell count Inferred relationship Some 4
Acquired hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
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. Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Interprets True Red blood cell count Inferred relationship Some 4

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