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404227002: Hemolysis (observable entity)

Status: current, Primitive. 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 Case insensitive SNOMED CT core
2153874014 Haemolysis en Synonym Active Case insensitive SNOMED CT core
2154897016 Hemolysis en Synonym Active Case insensitive SNOMED CT core

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemolysis Is a Haematologic function false Inferred relationship Some
Haemolysis Is a Erythrocyte destruction true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Autoimmune haemolytic anaemia due to complement Interprets True Haemolysis Inferred relationship Some 3
Primary CD59 deficiency Interprets True Haemolysis Inferred relationship Some 3
Drug-induced immune haemolytic anaemia, immune complex type Interprets True Haemolysis Inferred relationship Some 3
Haemolytic anaemia caused by Bartonella Interprets True Haemolysis Inferred relationship Some 5
Anaemia due to isoimmunisation Interprets True Haemolysis Inferred relationship Some 3
Secondary autoimmune haemolytic anaemia co-occurrent and due to systemic lupus erythematosus Interprets True Haemolysis Inferred relationship Some 3
Idiopathic chronic cold agglutinin disease Interprets True Haemolysis Inferred relationship Some 4
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Haemolysis Inferred relationship Some 4
HNSHA due to phosphofructokinase deficiency Interprets True Haemolysis Inferred relationship Some 3
Duffy isoimmunisation of the newborn Interprets True Haemolysis Inferred relationship Some 4
G-6-PD variant enzyme deficiency anaemia Interprets False Haemolysis Inferred relationship Some 3
HNSHA due to triosephosphate isomerase deficiency Interprets True Haemolysis Inferred relationship Some 3
Kidd isoimmunisation of the newborn Interprets True Haemolysis Inferred relationship Some 4
G-6-PD class V variant anaemia Interprets False Haemolysis Inferred relationship Some 3
Failed attempted termination of pregnancy with intravascular haemolysis Interprets True Haemolysis Inferred relationship Some 1
Haemolytic anaemia due to hexokinase deficiency Interprets False Haemolysis Inferred relationship Some 3
Hapten type low affinity haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 4
Anaemia due to mechanical damage Interprets False Haemolysis Inferred relationship Some 3
Secondary autoimmune haemolytic anaemia co-occurrent and due to lymphoproliferative disorder Interprets True Haemolysis Inferred relationship Some 3
Hemolytic anemia due to glutathione metabolism disorder Interprets True Haemolysis Inferred relationship Some 3
Miscarriage with intravascular hemolysis Interprets True Haemolysis Inferred relationship Some 1
Secondary autoimmune haemolytic anaemia co-occurrent and due to chronic inflammatory disease Interprets True Haemolysis Inferred relationship Some 3
Warm autoimmune haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 4
Lethal haemolytic anaemia and genital anomaly syndrome Interprets True Haemolysis Inferred relationship Some 4
Diarrhoea-negative haemolytic uraemic syndrome Interprets True Haemolysis Inferred relationship Some 6
Secondary autoimmune haemolytic anaemia co-occurrent and due to rheumatic disorder Interprets True Haemolysis Inferred relationship Some 3
Evans syndrome Interprets True Haemolysis Inferred relationship Some 5
Secondary autoimmune haemolytic anaemia co-occurrent and due to ulcerative colitis Interprets True Haemolysis Inferred relationship Some 3
Haemolytic anaemia due to babesiosis Interprets True Haemolysis Inferred relationship Some 4
Chronic haemolytic anaemia Interprets False Haemolysis Inferred relationship Some 3
Haemolytic anaemia due to nonlymphoid neoplasm Interprets True Haemolysis Inferred relationship Some 3
G-6-PD class III variant anaemia Interprets False Haemolysis Inferred relationship Some 3
Secondary warm-type haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 3
Hereditary nonspherocytic haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 3
Maternal autoimmune haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 4
HNSHA due to gamma glutamyl cysteine synthetase deficiency Interprets True Haemolysis Inferred relationship Some 3
Familial haemolytic uraemic syndrome Interprets True Haemolysis Inferred relationship Some 5
Autoimmune haemolytic anaemia due to IgA plus complement Interprets True Haemolysis Inferred relationship Some 4
Traumatic cardiac haemolytic anaemia Interprets False Haemolysis Inferred relationship Some 3
Oroya fever Interprets True Haemolysis Inferred relationship Some 2
Hemolytic anemia due to pyruvate kinase deficiency Interprets False Haemolysis Inferred relationship Some 3
Haemolytic anaemia due to triose phosphate isomerase deficiency Interprets True Haemolysis Inferred relationship Some 3
Illegal termination of pregnancy with intravascular haemolysis Interprets False Haemolysis Inferred relationship Some 1
Congenital nonspherocytic haemolytic anaemia due to inborn error of metabolism Interprets True Haemolysis Inferred relationship Some 4
Anaemia due to enzyme deficiency Interprets False Haemolysis Inferred relationship Some 3
HNSHA due to glucose phosphate isomerase deficiency Interprets True Haemolysis Inferred relationship Some 3
Immediate haemolytic transfusion reaction Interprets True Haemolysis Inferred relationship Some 1
Hereditary haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 3
HNSHA due to glutathione reductase deficiency Interprets True Haemolysis Inferred relationship Some 3
HNSHA due to pyrimidine-5'-nucleotidase deficiency Interprets True Haemolysis Inferred relationship Some 3
Haemolytic disorder Interprets True Haemolysis Inferred relationship Some 1
Haemolytic anaemia due to adenylate kinase deficiency Interprets True Haemolysis Inferred relationship Some 3
March haemoglobinuria Interprets True Haemolysis Inferred relationship Some 1
Neonatal autoimmune haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 4
Post-viral paroxysmal cold haemoglobinuria Interprets True Haemolysis Inferred relationship Some 3
G-6-PD class II variant anaemia Interprets False Haemolysis Inferred relationship Some 3
Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency Interprets False Haemolysis Inferred relationship Some 3
Anaemia due to abnormality extrinsic to the red cell Interprets False Haemolysis Inferred relationship Some 3
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets True Haemolysis Inferred relationship Some 4
HNSHA due to glutathione synthetase deficiency Interprets True Haemolysis Inferred relationship Some 3
Rhesus isoimmunisation due to anti-E Interprets True Haemolysis Inferred relationship Some 3
Induced termination of pregnancy complicated by intravascular haemolysis Interprets True Haemolysis Inferred relationship Some 1
Secondary paroxysmal cold haemoglobinuria Interprets True Haemolysis Inferred relationship Some 3
Haemolytic anaemia Interprets False Haemolysis Inferred relationship Some 3
Atypical isoimmunisation of newborn Interprets True Haemolysis Inferred relationship Some 4
Hereditary elliptocytosis due to glycophorin C deficiency Interprets True Haemolysis Inferred relationship Some 3
Hereditary elliptocytosis with transient poikilocytosis Interprets True Haemolysis Inferred relationship Some 1
Hereditary elliptocytosis Interprets True Haemolysis Inferred relationship Some 4
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Interprets True Haemolysis Inferred relationship Some 3
Hereditary elliptocytosis due to deficiency of protein 4.1 Interprets True Haemolysis Inferred relationship Some 3
Hereditary elliptocytosis due to abnormal protein 4.1 Interprets True Haemolysis Inferred relationship Some 3
Hereditary elliptocytosis due to beta spectrin defect in self-association Interprets True Haemolysis Inferred relationship Some 3
Alport syndrome, intellectual disability, midface hypoplasia, elliptocytosis syndrome Interprets True Haemolysis Inferred relationship Some 6
Hereditary elliptocytosis due to alpha spectrin defect Interprets True Haemolysis Inferred relationship Some 3
Atypical haemolytic uraemic syndrome Interprets True Haemolysis Inferred relationship Some 6
Primaquine sensitivity anaemia Interprets True Haemolysis Inferred relationship Some 4
Post-artesunate delayed haemolysis Interprets True Haemolysis Inferred relationship Some 3
Haemolytic disease of fetus due to ABO immunisation Interprets True Haemolysis Inferred relationship Some 4
Thrombocytopenic purpura Interprets True Haemolysis Inferred relationship Some 2
Chronic idiopathic thrombocytopenic purpura Interprets True Haemolysis Inferred relationship Some 11
Posttransfusion purpura Interprets True Haemolysis Inferred relationship Some 5
Idiopathic thrombocytopenic purpura Interprets False Haemolysis Inferred relationship Some 11
Post infectious thrombocytopenic purpura Interprets True Haemolysis Inferred relationship Some 9
Thrombocytopenic purpura due to defective platelet production Interprets True Haemolysis Inferred relationship Some 5
Thrombocytopenic purpura due to platelet consumption Interprets True Haemolysis Inferred relationship Some 5
Congenital thrombocytopenic purpura Interprets False Haemolysis Inferred relationship Some 6
Thrombocytopenic purpura associated with metabolic disorder Interprets True Haemolysis Inferred relationship Some 6
Acute idiopathic thrombocytopenic purpura Interprets False Haemolysis Inferred relationship Some 10
Haemolytic anaemia of pregnancy Interprets True Haemolysis Inferred relationship Some 4
Haemolytic anaemia due to red cell enolase deficiency Interprets False Haemolysis Inferred relationship Some 4
Haemolytic anaemia due to glyceraldehyde-3-phosphate dehydrogenase deficiency Interprets False Haemolysis Inferred relationship Some 4
Drug-induced non autoimmune haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 3
Homozygous hereditary elliptocytosis Interprets True Haemolysis Inferred relationship Some 4
Lymphocyte passenger syndrome following organ transplantation Interprets True Haemolysis Inferred relationship Some 6
Mechanical haemolysis due to prosthetic valve Interprets True Haemolysis Inferred relationship Some 3
Coombs negative haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 1
Coombs positive haemolytic anaemia Interprets True Haemolysis Inferred relationship Some 1
G-6-PD variant enzyme deficiency anaemia Interprets True Haemolysis Inferred relationship Some 1
G-6-PD class V variant anaemia Interprets True Haemolysis Inferred relationship Some 1
G-6-PD class IV variant anaemia Interprets True Haemolysis Inferred relationship Some 1
G-6-PD class I variant anaemia Interprets True Haemolysis Inferred relationship Some 1

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Reference Sets

Observable entity foundation reference set

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