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91689009: Body system structure (body structure)

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

Descriptions:

Id Description Lang Type Status Case? Module
151907017 Organ system en Synonym Active Entire term case insensitive SNOMED CT core module
509587013 Body system structure en Synonym Active Entire term case insensitive SNOMED CT core module
835054011 Body system structure (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module

31131 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
Body system structure Part of Entire body as a whole false Additional relationship Existential restriction modifier
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
Abscess of external nose Finding site False Body system structure Inferred relationship Existential restriction modifier 2
Mediterranean macrothrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type VI Finding site False Body system structure Inferred relationship Existential restriction modifier
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Thalassemia-hemoglobin C disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Primary cryofibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Illegal abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to diphosphoglycerate mutase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary sideroblastic anemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Defibrination syndrome following molar AND/OR ectopic pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytopenia due to hypersplenism Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor XIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type III Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired coagulation factor inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Blood coagulation disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type II Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin-ankyrin interaction Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytosis Finding site False Body system structure Inferred relationship Existential restriction modifier
Legal abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin D disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type IV Finding site False Body system structure Inferred relationship Existential restriction modifier
Disseminated intravascular coagulation Finding site False Body system structure Inferred relationship Existential restriction modifier
May Hegglin syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial hemorrhagic diathesis Finding site False Body system structure Inferred relationship Existential restriction modifier
Blood coagulation disorder due to liver disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide-methemoglobin reductase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIG Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to beta spectrin defect in self-association Finding site False Body system structure Inferred relationship Existential restriction modifier
Posttransfusion purpura Finding site False Body system structure Inferred relationship Existential restriction modifier
Heparin-induced thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin D trait Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor II deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyruvate kinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary methemoglobinemia due to globin chain mutation Finding site False Body system structure Inferred relationship Existential restriction modifier
Evans syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to abnormal protein 4.1 Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin C trait Finding site False Body system structure Inferred relationship Existential restriction modifier
Protein C deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor X deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to decreased adenosine deaminase activity Finding site False Body system structure Inferred relationship Existential restriction modifier
Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura Finding site False Body system structure Inferred relationship Existential restriction modifier
Canine infectious cyclic thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hyperheparinemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Conjunctivorhinostomy with insertion of stent Procedure site - Indirect False Body system structure Inferred relationship Existential restriction modifier 3
Mixed cryofibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Red cell survival study Procedure site False Body system structure Inferred relationship Existential restriction modifier 2
Neonatal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Insertion of biliary stent by endoscopic retrograde cholangiopancreatography Procedure site - Indirect False Body system structure Inferred relationship Existential restriction modifier 2
Familial multiple factor deficiency syndrome, type I Finding site False Body system structure Inferred relationship Existential restriction modifier
Afibrinogenemia following molar AND/OR ectopic pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier
Coagulation factor deficiency syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIA Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytopenia due to non-immune destruction Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor XI deficiency, type I Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to alpha spectrin defect Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor V deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor IX inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Neonatal thrombocytopenia due to exchange transfusion Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemophilia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary pyropoikilocytosis Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor X inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Neonatal coagulation disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Disorder involving the fibrinolytic system Finding site False Body system structure Inferred relationship Existential restriction modifier
Hypoplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary hypoplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Autosomal dominant deficiency of plasminogen Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired hypoplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Dysplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary dysplasminogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Autosomal recessive severe combined immunodeficiency disease Finding site True Body system structure Inferred relationship Existential restriction modifier 2
Complement component deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier 2
Congenital nonspherocytic hemolytic anemia due to inborn error of metabolism Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary disorder of immune system Finding site True Body system structure Inferred relationship Existential restriction modifier 1
Sequelae of disorders classified by disorder-system Finding site False Body system structure Inferred relationship Existential restriction modifier 1
Isotope B12 with iron absorption Procedure site False Body system structure Inferred relationship Existential restriction modifier 1
Isotope static scan lymph node Procedure site False Body system structure Inferred relationship Existential restriction modifier 2
Hemolytic anemia due to glutathione metabolism disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemolytic anemia due to pyruvate kinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemolytic anemia due to triose phosphate isomerase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to circulating anticoagulants Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to antithrombinemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to hyperheparinemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to increase in anti-8a Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to increase in anti-9a Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to increase in anti-10a Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disorder due to increase in anti-11a Finding site False Body system structure Inferred relationship Existential restriction modifier
Deficiency of coagulation factor due to liver disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Deficiency of coagulation factor due to vitamin K deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor II deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytopenia due to extracorporeal circulation of blood Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary eosinophilia Finding site True Body system structure Inferred relationship Existential restriction modifier 3
Afibrinogenemia following abortive pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier
Defibrination syndrome following abortive pregnancy Finding site False Body system structure Inferred relationship Existential restriction modifier
Postpartum coagulation defects - delivered with postnatal problem Finding site False Body system structure Inferred relationship Existential restriction modifier
Postpartum coagulation defects with postnatal problem Finding site False Body system structure Inferred relationship Existential restriction modifier
Transient neonatal thrombocytopenia due to exchange transfusion Finding site False Body system structure Inferred relationship Existential restriction modifier
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Transient neonatal thrombocytopenia due to isoimmunization Finding site False Body system structure Inferred relationship Existential restriction modifier

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