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404227002: Hemolysis (observable entity)

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

Descriptions:

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

0 descendants.

Expanded Value Set

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

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