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84054007: Erythrocyte destruction, function (observable entity)

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
139376010 Erythrocyte destruction en Synonym Active Entire term case insensitive SNOMED CT core module
139377018 Erythrocyte destruction, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
825817011 Erythrocyte destruction (function) en Fully specified name Inactive Only initial character case insensitive SNOMED CT core module
1204973017 Erythrocyte destruction, function (observable entity) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2671877018 Erythrocyte destruction, function en Synonym Active Entire term case insensitive SNOMED CT core module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte destruction, function Is a Hematologic function false Inferred relationship Existential restriction modifier
Erythrocyte destruction, function Is a Blood cell destruction, function true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Red blood cell destruction finding Interprets True Erythrocyte destruction, function Inferred relationship Existential restriction modifier 1
Intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Increased erythrocyte destruction Interprets True Erythrocyte destruction, function Inferred relationship Existential restriction modifier 1
Extravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Decreased erythrocyte destruction Interprets True Erythrocyte destruction, function Inferred relationship Existential restriction modifier 1
Hemoglobinuria Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Abnormal erythrocyte destruction Interprets True Erythrocyte destruction, function Inferred relationship Existential restriction modifier 1
Hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolysis Is a True Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Mechanical hemolysis due to cardiovascular prosthetic patch Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Miscarriage with intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Illegal abortion with intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Legal abortion with intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Induced termination of pregnancy complicated by intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Kernicterus due to isoimmunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Traumatic cardiac hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Warm autoimmune hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Acquired hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia due to nonlymphoid neoplasm Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by immunoglobulin G Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Idiopathic chronic cold agglutinin disease Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by complement Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Coombs negative hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Drug-induced enzyme deficiency anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hydrops fetalis due to isoimmunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Drug-induced immune hemolytic anemia, immune complex type Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Chronic idiopathic autoimmune hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class I variant anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia caused by babesiosis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class III variant anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia caused by Clostridium welchii Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Anemia due to pentose phosphate pathway defect Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Mild hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic disease of fetus OR newborn due to ABO immunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to deficiency of protein 4.2 Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Anemia due to mechanical damage Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class II variant anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Post-viral paroxysmal cold hemoglobinuria Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic uremic syndrome of childhood Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Immediate hemolytic transfusion reaction Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia due to infection Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic transfusion reaction Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Polyagglutinable erythrocyte syndrome Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hapten type low affinity hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Anemia due to abnormality extrinsic to the red cell Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Failed attempted abortion with intravascular hemolysis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Secondary paroxysmal cold hemoglobinuria Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Microangiopathic hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary spherocytosis Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia with emphysema AND cutis laxa Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Idiopathic paroxysmal cold hemoglobinuria Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Antibody-mediated anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Late anemia due to isoimmunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary spherocytosis due to beta spectrin defect Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by immunoglobulin M Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Coombs positive hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Evans syndrome Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia caused by Bartonella Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Severe hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia caused by malaria Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Thrombotic thrombocytopenic purpura Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic uremic syndrome, adult type Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class V variant anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic anemia caused by drugs Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Delayed hemolytic transfusion reaction Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hapten type high affinity hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic disease of fetus OR newborn due to RhD isoimmunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Autoimmune hemolytic anemia caused by immunoglobulin A Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic uremic syndrome Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Anemia due to enzyme deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Primary (idiopathic) autoimmune hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Secondary autoimmune hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Secondary warm autoimmune hemolytic anemia Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier
Post-infectious cold agglutinin disease Interprets False Erythrocyte destruction, function Inferred relationship Existential restriction modifier

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