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84054007: Erythrocyte destruction, function (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1204973017 Erythrocyte destruction, function (observable entity) en Fully specified name Active Case insensitive SNOMED CT core
139376010 Erythrocyte destruction en Synonym Active Case insensitive SNOMED CT core
2671877018 Erythrocyte destruction, function en Synonym Active Case insensitive SNOMED CT core

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Erythrocyte destruction Is a Blood cell destruction, function true Inferred relationship Some
Erythrocyte destruction Is a Haematologic function false Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Haemolysis Is a True Erythrocyte destruction Inferred relationship Some
Mechanical haemolysis due to cardiovascular prosthetic patch Interprets False Erythrocyte destruction Inferred relationship Some
Miscarriage with intravascular hemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Illegal termination of pregnancy with intravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Legal termination of pregnancy with intravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Induced termination of pregnancy complicated by intravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Red blood cell destruction finding Interprets True Erythrocyte destruction Inferred relationship Some 1
Intravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Increased erythrocyte destruction Interprets True Erythrocyte destruction Inferred relationship Some 1
Extravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Decreased erythrocyte destruction Interprets True Erythrocyte destruction Inferred relationship Some 1
Haemoglobinuria Interprets False Erythrocyte destruction Inferred relationship Some
Abnormal erythrocyte destruction Interprets True Erythrocyte destruction Inferred relationship Some 1
Kernicterus due to isoimmunisation Interprets False Erythrocyte destruction Inferred relationship Some
Traumatic cardiac haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Warm autoimmune haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Acquired haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia due to nonlymphoid neoplasm Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia due to erythrocyte adenosine deaminase overproduction Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to IgG Interprets False Erythrocyte destruction Inferred relationship Some
Idiopathic chronic cold agglutinin disease Interprets False Erythrocyte destruction Inferred relationship Some
Severe hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to complement Interprets False Erythrocyte destruction Inferred relationship Some
Coombs negative haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Drug-induced enzyme deficiency anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Hydrops fetalis due to isoimmunisation Interprets False Erythrocyte destruction Inferred relationship Some
Drug-induced immune haemolytic anaemia, immune complex type Interprets False Erythrocyte destruction Inferred relationship Some
Chronic idiopathic autoimmune haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD class I variant anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia due to babesiosis Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD class III variant anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Mild hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to gamma glutamyl cysteine synthetase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia caused by Clostridium welchii Interprets False Erythrocyte destruction Inferred relationship Some
Anaemia due to pentose phosphate pathway defect Interprets False Erythrocyte destruction Inferred relationship Some
Mild hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic disease of fetus OR newborn due to ABO immunisation Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to IgA plus complement Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary spherocytosis due to deficiency of protein 4.2 Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to pyrimidine-5'-nucleotidase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Anaemia due to mechanical damage Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD class II variant anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Post-viral paroxysmal cold haemoglobinuria Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic uraemic syndrome of childhood Interprets False Erythrocyte destruction Inferred relationship Some
Immediate haemolytic transfusion reaction Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia due to infection Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic transfusion reaction Interprets False Erythrocyte destruction Inferred relationship Some
Polyagglutinable erythrocyte syndrome Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to phosphofructokinase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to hexokinase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Hapten type low affinity haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Anaemia due to abnormality extrinsic to the red cell Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to triosephosphate isomerase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Failed attempted termination of pregnancy with intravascular haemolysis Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary spherocytosis due to combined deficiency of spectrin AND ankyrin Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to NADH diaphorase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Secondary paroxysmal cold haemoglobinuria Interprets False Erythrocyte destruction Inferred relationship Some
Microangiopathic haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to glutathione reductase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to glucose phosphate isomerase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary spherocytosis Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia with emphysema AND cutis laxa Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to diphosphoglycerate mutase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Glucose-6-phosphate dehydrogenase deficiency anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to IgG plus complement Interprets False Erythrocyte destruction Inferred relationship Some
Idiopathic paroxysmal cold haemoglobinuria Interprets False Erythrocyte destruction Inferred relationship Some
Antibody-mediated anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Late anaemia due to isoimmunisation Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary spherocytosis due to beta spectrin defect Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to IgM Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA (hereditary nonspherocytic haemolytic anaemia) due to pyruvate kinase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Coombs positive haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Evans syndrome Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia caused by Bartonella Interprets False Erythrocyte destruction Inferred relationship Some
Severe hereditary spherocytosis due to spectrin deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia caused by malaria Interprets False Erythrocyte destruction Inferred relationship Some
Thrombotic thrombocytopenic purpura Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic uraemic syndrome, adult type Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD class V variant anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic anaemia due to drugs Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD class IV variant anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Delayed haemolytic transfusion reaction Interprets False Erythrocyte destruction Inferred relationship Some
Hapten type high affinity haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
G-6-PD variant enzyme deficiency anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic disease of fetus OR newborn due to Rh isoimmunisation Interprets False Erythrocyte destruction Inferred relationship Some
Autoimmune haemolytic anaemia due to IgA Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic uraemic syndrome Interprets False Erythrocyte destruction Inferred relationship Some
Haemolytic disease of the newborn due to non-ABO, non-Rh isoimmunisation Interprets False Erythrocyte destruction Inferred relationship Some
Anaemia due to enzyme deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Hereditary nonspherocytic haemolytic anaemia due to aldolase A deficiency Interprets False Erythrocyte destruction Inferred relationship Some
HNSHA due to glutathione synthetase deficiency Interprets False Erythrocyte destruction Inferred relationship Some
Primary (idiopathic) autoimmune haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Secondary autoimmune haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Secondary warm autoimmune haemolytic anaemia Interprets False Erythrocyte destruction Inferred relationship Some
Post-infectious cold agglutinin disease Interprets False Erythrocyte destruction Inferred relationship Some

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Reference Sets

Observable entity foundation reference set

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