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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
Hemolytic disease of fetus OR newborn due to RhD isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Autoimmune hemolytic anemia caused by complement Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Primary CD59 deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Drug-induced immune hemolytic anemia, immune complex type Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by Bartonella Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Anemia due to isoimmunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Secondary autoimmune hemolytic anemia co-occurrent and due to systemic lupus erythematosus Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Idiopathic chronic cold agglutinin disease Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Duffy isoimmunization of the newborn Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Kidd isoimmunization of the newborn Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Glucose-6-phosphate dehydrogenase deficiency class V variant anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Failed attempted abortion with intravascular hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Hemolytic anemia due to hexokinase deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hapten type low affinity hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Anemia due to mechanical damage Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Secondary autoimmune hemolytic anemia co-occurrent and due to lymphoproliferative disorder Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia due to glutathione metabolism disorder Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Miscarriage with intravascular hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Secondary autoimmune hemolytic anemia co-occurrent and due to chronic inflammatory disease Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Warm autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Lethal hemolytic anemia and genital anomaly syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Diarrhea-negative hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Secondary autoimmune hemolytic anemia co-occurrent and due to rheumatic disorder Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Evans syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Secondary autoimmune hemolytic anemia co-occurrent and due to ulcerative colitis Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia caused by babesiosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Chronic hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia due to nonlymphoid neoplasm Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Glucose-6-phosphate dehydrogenase deficiency class III variant anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Secondary warm-type hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Maternal autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Familial hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Autoimmune hemolytic anemia caused by immunoglobulin A plus complement Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Traumatic cardiac hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Oroya fever Interprets True Hemolysis Inferred relationship Existential restriction modifier 2
Hemolytic anemia due to pyruvate kinase deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia due to triose phosphate isomerase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Illegal abortion with intravascular hemolysis Interprets False Hemolysis Inferred relationship Existential restriction modifier 1
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Anemia due to enzyme deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Immediate hemolytic transfusion reaction Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Hereditary hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic disorder Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Hemolytic anemia due to adenylate kinase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
March hemoglobinuria Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Neonatal autoimmune hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Post-viral paroxysmal cold hemoglobinuria Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Glucose-6-phosphate dehydrogenase deficiency class II variant anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary nonspherocytic hemolytic anemia due to aldolase A deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Anemia due to abnormality extrinsic to the red cell Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Rhesus isoimmunization due to anti-E Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Induced termination of pregnancy complicated by intravascular hemolysis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Secondary paroxysmal cold hemoglobinuria Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic anemia Interprets False Hemolysis Inferred relationship Existential restriction modifier 3
Atypical isoimmunization of newborn Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to glycophorin C deficiency Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis with transient poikilocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Hereditary elliptocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to deficiency of protein 4.1 Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Hereditary elliptocytosis due to alpha spectrin defect Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Atypical hemolytic uremic syndrome Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Primaquine sensitivity anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Delayed hemolysis following artesunate therapy Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Hemolytic disease of fetus due to ABO immunization Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 2
Chronic idiopathic thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 11
Posttransfusion purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Immune thrombocytopenic purpura Interprets False Hemolysis Inferred relationship Existential restriction modifier 11
Post infectious thrombocytopenic purpura Interprets True Hemolysis Inferred relationship Existential restriction modifier 9
Thrombocytopenic purpura due to defective platelet production Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Thrombocytopenic purpura due to platelet consumption Interprets True Hemolysis Inferred relationship Existential restriction modifier 5
Congenital thrombocytopenic purpura Interprets False Hemolysis Inferred relationship Existential restriction modifier 6
Thrombocytopenic purpura associated with metabolic disorder Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Acute idiopathic thrombocytopenic purpura Interprets False Hemolysis Inferred relationship Existential restriction modifier 10
Hemolytic anemia of pregnancy Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic anemia due to red cell enolase deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 4
Hemolytic anemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Interprets False Hemolysis Inferred relationship Existential restriction modifier 4
Non autoimmune hemolytic anemia caused by drug Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Homozygous hereditary elliptocytosis Interprets True Hemolysis Inferred relationship Existential restriction modifier 4
Lymphocyte passenger syndrome following organ transplantation Interprets True Hemolysis Inferred relationship Existential restriction modifier 6
Mechanical hemolysis following insertion of prosthetic heart valve Interprets True Hemolysis Inferred relationship Existential restriction modifier 3
Coombs negative hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Coombs positive hemolytic anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Glucose-6-phosphate dehydrogenase variant enzyme deficiency anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Glucose-6-phosphate dehydrogenase deficiency class V variant anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 1
Glucose-6-phosphate dehydrogenase deficiency class IV variant anemia Interprets True Hemolysis Inferred relationship Existential restriction modifier 1

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This concept is not in any reference sets

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