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

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