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91689009: Body system structure (body structure)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
151907017 Organ system en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
509587013 Body system structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
12681000077117 structure d'un système corporel fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

32409 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Body system structure Is a Anatomical structure true Inferred relationship Existential restriction modifier (core metadata concept)
Body system structure partie de Entire body as a whole (body structure) false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Abscess of external nose Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Mediterranean macrothrombocytopenia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type VI (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Thalassemia-hemoglobin C disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Primary cryofibrinogenemia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Illegal abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA due to diphosphoglycerate mutase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary sideroblastic anemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Defibrination syndrome following molar AND/OR ectopic pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia due to hypersplenism (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Acquired factor XIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type III Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Acquired coagulation factor inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorders involving the elements of blood coagulation, including platelets, coagulation factors and inhibitors, and the fibrinolytic system. Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type II Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytosis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Legal abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin D disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome, type IV Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disseminated intravascular coagulation Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
May Hegglin syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial hemorrhagic diathesis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Blood coagulation disorder due to liver disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia (HNSHA) due to reduced nicotinamide adenine dinucleotide (NADH)-methemoglobin reductase deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
von Willebrand disease, type IIG Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Posttransfusion purpura (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Heparin-induced thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin D trait Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Factor II deficiency (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Acquired thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
HNSHA (hereditary nonspherocytic hemolytic anemia) due to pyruvate kinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemoglobin M disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Evans syndrome (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Haemoglobin C trait Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Protein C deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Factor X deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Canine infectious cyclic thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hyperheparinemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Conjunctivorhinostomy with insertion of stent Procedure site - Indirect (attribute) False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Mixed cryofibrinogenaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Familial multiple factor deficiency syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Red cell survival study Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Neonatal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Insertion of biliary stent by ERCP Procedure site - Indirect (attribute) False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Familial multiple factor deficiency syndrome, type I (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Afibrinogenemia following molar AND/OR ectopic pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Coagulation factor deficiency syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
von Willebrand disease, type IIA Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia due to non-immune destruction Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Factor XI deficiency, type I Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary elliptocytosis due to alpha spectrin defect Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary factor V deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Factor IX inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal thrombocytopenia due to exchange transfusion Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Haemophilia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary pyropoikilocytosis Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Factor X inhibitor disorder (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Neonatal coagulation disorder (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Disorder involving the fibrinolytic system Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hypoplasminogenemia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary hypoplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal dominant deficiency of plasminogen Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Acquired hypoplasminogenaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Dysplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary dysplasminogenaemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Autosomal recessive SCID (severe combined immunodeficiency disease) Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Complement component deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary disorder of immune system Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
séquelles d'affections classées par appareil touché Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Isotope B12 with iron absorption Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Isotope static scan lymph node Procedure site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Hemolytic anemia due to glutathione metabolism disorder Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hämolytische Anämie durch Mangel der erythrozytären Pyruvatkinase Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Haemolytic anaemia due to triose phosphate isomerase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to circulating anticoagulants Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to antithrombinemia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to hyperheparinemia Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to increase in anti-VIIIa Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to increase in anti-9a Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to increase in anti-10a Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hemorrhagic disorder due to increase in anti-11a Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of coagulation factor due to liver disease Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Deficiency of coagulation factor due to vitamin K deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Acquired factor II deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Thrombocytopenia due to extracorporeal circulation of blood Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Hereditary eosinophilia Finding site True Body system structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Afibrinogenemia following abortive pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Defibrination syndrome following abortive pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Postpartum coagulation defects - delivered with postnatal problem Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
trouble de la coagulation du post-partum conséquences postnatales Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Transient neonatal thrombocytopenia due to exchange transfusion Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder) Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)
Transient neonatal thrombocytopenia due to isoimmunisation Finding site False Body system structure Inferred relationship Existential restriction modifier (core metadata concept)

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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