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404227002: Hemolysis (observable entity)

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2004. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
2148056014 Hemolysis (observable entity) en Fully specified name Active Entire term case insensitive SNOMED CT core module
2153874014 Haemolysis en Synonym Active Entire term case insensitive SNOMED CT core module
2154897016 Hemolysis en Synonym Active Entire term case insensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemolysis Is a Hematologic function false Inferred relationship Existential restriction modifier
Hemolysis Is a Erythrocyte destruction, function true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Acidified glycerol lysis test Component False Hemolysis Inferred relationship Existential restriction modifier
Traumatic hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Glucose-6-phosphate dehydrogenase deficiency class I variant anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Congenital hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Hemolytic anemia with emphysema AND cutis laxa Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Nonspherocytic hemolytic anemia due to deficiency of adenosinetriphosphatase Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Rhesus isoimmunization due to anti-Cw Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Antibody-mediated anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Autoimmune hemolytic anemia caused by immunoglobulin G Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Coombs negative hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Primary (idiopathic) autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary spherocytosis due to beta spectrin defect Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Upshaw-Schulman syndrome Interprets False Hemolysis Inferred relationship Existential restriction modifier 7
Hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Primary cold-type hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Acquired hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Acquired hemolytic anemia co-occurrent with human immunodeficiency virus infection Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Rhesus isoimmunization due to anti-D Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by drugs Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Late anemia due to isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic transfusion reaction Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Secondary warm autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Post-infectious cold agglutinin disease Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Intracorpuscular hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Primary warm-type hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Cold agglutinin disease caused by Epstein-Barr virus infection Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hapten type high affinity hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Autoimmune thrombotic thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Drug-induced enzyme deficiency anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Chronic cold agglutinin disease Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Drug induced thrombotic thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 7
Hydrops fetalis due to isoimmunization Interprets False Hemolysis Inferred relationship Existential restriction modifier 4
Kell isoimmunization of the newborn Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Anemia caused by alloimmune destruction of transfused red cells Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Paroxysmal cold hemoglobinuria Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic disease of newborn co-occurrent and due to ABO immunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Congenital hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Mechanical hemolysis due to cardiovascular prosthetic patch Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Neonatal hemolysis co-occurrent and due to systemic bacterial infection Interprets True Hemolysis Inferred relationship Existential restriction modifier 2
Paroxysmal cold hemoglobinuria associated with tertiary syphilis Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Secondary autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Intravascular hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Drug-induced immune hemolytic anemia, hapten type Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Autoimmune hemolytic anemia, categorized by antibody class AND/OR complement Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary spherocytosis due to spectrin deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia mixed type Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Acquired thrombotic thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Hereditary spherocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Diarrhea-associated hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Hemolytic disease of fetus OR newborn due to isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic disease of the newborn due to non-ABO, non-Rh isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Chronic cold agglutinin disease associated with B-cell neoplasm Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Anemia due to pentose phosphate pathway defect Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by malaria Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Autoimmune hemolytic anemia caused by immunoglobulin M Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Autoimmune hemolytic anemia caused by immunoglobulin A Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Secondary cold-type hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic uremic syndrome, adult type Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Legal abortion with intravascular hemolysis Interprets False Hemolysis Inferred relationship Existential restriction modifier 1
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic uremic syndrome of childhood Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Drug-induced autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Rhesus isoimmunization due to anti-c Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by Clostridium welchii Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Non-autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Polyagglutinable erythrocyte syndrome Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Mechanical hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Acquired hemolytic anemia associated with acquired immunodeficiency syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Glucose-6-phosphate dehydrogenase deficiency anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Toxic hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Thrombotic thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 7
Coombs positive hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Microangiopathic hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary spherocytosis due to deficiency of protein 4.2 Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Kernicterus due to isoimmunization Interprets False Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic anemia due to infection Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemoglobinuria due to hemolysis from external causes Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic disease of fetus OR newborn due to ABO immunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Extravascular hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Chronic idiopathic autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Idiopathic paroxysmal cold hemoglobinuria Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Autoimmune hemolytic anemia caused by immunoglobulin G plus complement Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Cold autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Severe hereditary spherocytosis due to spectrin deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic anemia caused by hyperbaric oxygen Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Acquired spherocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Mild hereditary spherocytosis due to spectrin deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Delayed hemolytic transfusion reaction Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Infantile pyknocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Intravascular hemolysis following abortive pregnancy Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Hemolytic disease of fetus OR newborn due to RhD isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4

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