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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
G-6-PD class V variant anemia Interprets False Red blood cell count Inferred relationship Some 1
Hemolytic anemia caused by drugs (disorder) Interprets False Red blood cell count Inferred relationship Some 1
G-6-PD class IV variant anemia Interprets False Red blood cell count Inferred relationship Some 1
Anaemia due to diabetes mellitus Interprets False Red blood cell count Inferred relationship Some 1
G-6-PD variant enzyme deficiency anemia Interprets False Red blood cell count Inferred relationship Some 1
Autoimmune haemolytic anaemia caused by IgA Interprets False Red blood cell count Inferred relationship Some 1
Primary (idiopathic) autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Chronic cold agglutinin disease Interprets False Red blood cell count Inferred relationship Some 1
Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement Interprets True Red blood cell count Inferred relationship Some 1
Hemolytic anemia caused by hyperbaric oxygen Interprets False Red blood cell count Inferred relationship Some 1
Primary cold-type hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Secondary cold-type hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Neonatal anemia Interprets True Red blood cell count Inferred relationship Some 1
Maternal autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Familial megaloblastic anemia Interprets True Red blood cell count Inferred relationship Some 1
Diarrhea-associated hemolytic uremic syndrome (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Perinatal anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Cold autoimmune hemolytic anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Autoimmune hemolytic anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Acute sickle cell splenic sequestration crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Fetal anemia Interprets False Red blood cell count Inferred relationship Some 1
Anaemia in chronic kidney disease Interprets False Red blood cell count Inferred relationship Some 1
Anaemia co-occurrent and due to chronic kidney disease stage 3 Interprets False Red blood cell count Inferred relationship Some 1
Microangiopathic hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Hereditary spherocytosis Interprets True Red blood cell count Inferred relationship Some 1
Hemolytic anemia due to triose phosphate isomerase deficiency Interprets True Red blood cell count Inferred relationship Some 1
Traumatic hemolytic anemia (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Chronic hemolytic anemia (disorder) Interprets False 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 False Red blood cell count Inferred relationship Some 8
Hemolytic anemia associated with chronic inflammatory disease Interprets False Red blood cell count Inferred relationship Some 1
Secondary paroxysmal cold hemoglobinuria Interprets True Red blood cell count Inferred relationship Some 1
HNSHA due to glutathione reductase deficiency Interprets True Red blood cell count Inferred relationship Some 1
Hemolytic anemia associated with lymphoproliferative disorder Interprets False Red blood cell count Inferred relationship Some 1
Hemolytic anemia associated with rheumatic disorder Interprets False Red blood cell count Inferred relationship Some 1
Sickle cell-hemoglobin SS disease Interprets False Red blood cell count Inferred relationship Some 1
Secondary warm autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Interprets False Red blood cell count Inferred relationship Some 1
Hemolytic anemia due to hexokinase deficiency Interprets False Red blood cell count Inferred relationship Some 1
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Interprets False Red blood cell count Inferred relationship Some 1
Aplastic anemia associated with pregnancy (disorder) Interprets True Red blood cell count Inferred relationship Some 2
Hemoglobin SS disease without crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Hemoglobin SS disease with crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 1
Hemoglobin SS disease with vasoocclusive crisis (disorder) Interprets False Red blood cell count Inferred relationship Some 1
A rare syndromic, inherited form of sideroblastic anemia characterized by mild to moderate anemia (with hypochromia and microcytosis) and early-onset, non- or slowly progressive spinocerebellar ataxia. Interprets True Red blood cell count Inferred relationship Some 4
IRIDA (Iron-refractory iron deficiency anemia) syndrome is a rare autosomal recessive iron metabolism disorder characterized by iron deficiency anemia (hypochromic, microcytic) that is often unresponsive to oral iron intake and partially responsive to parenteral iron treatment. Interprets True Red blood cell count Inferred relationship Some 4
Sickle cell anaemia in mother complicating childbirth Interprets False Red blood cell count Inferred relationship Some 1
Anemia due to pentose phosphate pathway defect Interprets False Red blood cell count Inferred relationship Some 1
HNSHA due to pyrimidine-5'-nucleotidase deficiency Interprets True Red blood cell count Inferred relationship Some 1
HNSHA due to phosphofructokinase deficiency Interprets True Red blood cell count Inferred relationship Some 1
Hypoplastic anemia Interprets True Red blood cell count Inferred relationship Some 2
HNSHA due to decreased adenosine deaminase activity Interprets True Red blood cell count Inferred relationship Some 1
Congenital atransferrinemia Interprets True Red blood cell count Inferred relationship Some 1
Anemia due to enzyme deficiency Interprets True Red blood cell count Inferred relationship Some 1
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets False Red blood cell count Inferred relationship Some 1
Congenital transferrin deficiency Interprets True Red blood cell count Inferred relationship Some 1
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism Interprets True Red blood cell count Inferred relationship Some 1
Acquired haemolytic anaemia associated with AIDS Interprets False Red blood cell count Inferred relationship Some 1
Anemia following acute postoperative blood loss (disorder) Interprets False Red blood cell count Inferred relationship Some 2
Drug-induced immune hemolytic anemia, immune complex type Interprets True Red blood cell count Inferred relationship Some 1
Hapten type low affinity hemolytic anemia Interprets False Red blood cell count Inferred relationship Some 1
Microcytic hypochromic anemia Interprets True Red blood cell count Inferred relationship Some 1
Hapten type high affinity hemolytic anemia Interprets False Red blood cell count Inferred relationship Some 1
Drug-induced immune hemolytic anemia Interprets False Red blood cell count Inferred relationship Some 1
Drug-induced immune hemolytic anemia, hapten type Interprets True Red blood cell count Inferred relationship Some 1
Drug-induced autoimmune hemolytic anemia Interprets True Red blood cell count Inferred relationship Some 1
Hypochromic microcytic anemia with iron overload (disorder) Interprets True Red blood cell count Inferred relationship Some 1
Acquired thiamine deficiency anemia (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Megaloblastic anemia due to folate deficiency due to increased requirement (disorder) Interprets True Red blood cell count Inferred relationship Some 6
Megaloblastic anemia due to folate deficiency in pregnancy and lactation (disorder) Interprets True Red blood cell count Inferred relationship Some 6
Megaloblastic anemia due to folate deficiency in prematurity (disorder) Interprets True Red blood cell count Inferred relationship Some 6
Doan-Wright syndrome Interprets True Red blood cell count Inferred relationship Some 3
Thrombotic thrombocytopenic purpura Interprets True Red blood cell count Inferred relationship Some 4
Pancytopenia with pancreatitis Interprets True Red blood cell count Inferred relationship Some 4
Upshaw-Schulman syndrome (disorder) Interprets False Red blood cell count Inferred relationship Some 4
Autoimmune thrombotic thrombocytopenic purpura (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Acquired thrombotic thrombocytopenic purpura (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Drug induced thrombotic thrombocytopenic purpura (disorder) Interprets True Red blood cell count Inferred relationship Some 4
Pancytopenia due to antineoplastic chemotherapy (disorder) Interprets True Red blood cell count Inferred relationship Some 5
Acquired pancytopenia Interprets True Red blood cell count Inferred relationship Some 3
Pancytopenia Interprets True Red blood cell count Inferred relationship Some 3
Pancytopenia-dysmelia Interprets False Red blood cell count Inferred relationship Some 3
Overhydrated hereditary stomatocytosis (OHSt) is a disorder of red cell membrane permeability to monovalent cations and is characterized clinically by hemolytic anemia. Interprets True Red blood cell count Inferred relationship Some 4
Hemolytic disease of newborn co-occurrent and due to ABO immunization (disorder) Interprets True Red blood cell count Inferred relationship Some 7
Haemolytic uraemic syndrome with either a family history of haemolytic uraemic syndrome or a genetic mutation known to cause haemolytic uraemic syndrome, or both. Interprets True Red blood cell count Inferred relationship Some 11
Southeast Asian ovalocytosis (SAO) is a rare hereditary red cell membrane defect characterized by the presence of oval-shaped erythrocytes and with most patients being asymptomatic or occasionally manifesting with mild symptoms such as pallor, jaundice, anemia and gallstones. Interprets False Red blood cell count Inferred relationship Some 4
Mitochondrial myopathy and sideroblastic anemia belongs to the heterogeneous family of metabolic myopathies. It is characterized by progressive exercise intolerance manifesting in childhood, onset of sideroblastic anemia around adolescence, lactic acidemia, and mitochondrial myopathy. Interprets True Red blood cell count Inferred relationship Some 4
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase (disorder) Interprets True Red blood cell count Inferred relationship Some 7
STEAP3/TSAP6-related sideroblastic anemia is a very rare severe non-syndromic hypochromic anemia, which is characterized by transfusion-dependent hypochromic, poorly regenerative anemia, iron overload, resembling non-syndromic sideroblastic anemia except for increased erythrocyte protoporphyrin levels. Interprets True Red blood cell count Inferred relationship Some 2
Iron deficiency anemia due to blood loss (disorder) Interprets True Red blood cell count Inferred relationship Some 5
Acquired iron deficiency anemia due to decreased absorption (disorder) Interprets True Red blood cell count Inferred relationship Some 5
A rare genetic neurological disorder characterized by early-onset progressive leukoencephalopathy, severe developmental delay, early-onset or congenital deafness (only few cases reported without hearing loss), and visual impairment. All patients manifest calcifications in brain and spinal cord. Cognitive impairment, seizures, hypotonia, spastic tetraplegia or quadriplegia are observed in the majority of the patients. Variable features may include microcephaly and anemia. Interprets True Red blood cell count Inferred relationship Some 4
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease (disorder) Interprets False Red blood cell count Inferred relationship Some 10
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Interprets False Red blood cell count Inferred relationship Some 10
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder (disorder) Interprets False Red blood cell count Inferred relationship Some 10
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis (disorder) Interprets False Red blood cell count Inferred relationship Some 10
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus Interprets False Red blood cell count Inferred relationship Some 9
A rare developmental defect during embryogenesis, a contiguous gene deletion syndrome, is a form of alpha-thalassemia characterized by microcytosis, hypochromia, normal hemoglobin (Hb) level or mild anemia, associated with developmental abnormalities. Interprets True Red blood cell count Inferred relationship Some 9
Hereditary vitamin B12 deficiency anemia (disorder) Interprets False Red blood cell count Inferred relationship Some 4
Hereditary folate deficiency anemia (disorder) Interprets False Red blood cell count Inferred relationship Some 4
Pancytopenia caused by medication (disorder) Interprets True Red blood cell count Inferred relationship Some 6
Pericarditis associated with severe chronic anemia Interprets False Red blood cell count Inferred relationship Some 3

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