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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
Acquired factor VIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to glycophorin C deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor XII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Protein S deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Vitamin B12 absorption test Procedure site False Body system structure Inferred relationship Existential restriction modifier 1
Drug-induced coagulation inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe hereditary factor VIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary coagulation factor deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Unstable hemoglobin disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Autoimmune pancytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor XIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIC Finding site False Body system structure Inferred relationship Existential restriction modifier
Lupus anticoagulant disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Drug-induced immune thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIB Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor VII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
X chromosome-linked pyridoxine refractory sideroblastic anemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Platelet disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Transient neonatal thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
T activation syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemorrhagic disease of the newborn due to factor II deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIH Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin E disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to gamma glutamyl cysteine synthetase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
X chromosome-linked pyridoxine responsive sideroblastic anemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired coagulation factor deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Mild hereditary factor VIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Failed attempted abortion with afibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
High molecular weight kininogen deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor VIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Immune thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytopenia due to extracorporeal circulation Finding site False Body system structure Inferred relationship Existential restriction modifier
Legal abortion with afibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe combined immunodeficiency disease Finding site True Body system structure Inferred relationship Existential restriction modifier 2
Hereditary factor I deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Illegal abortion with afibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Transient neonatal disorder of coagulation Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor XI deficiency, type II Finding site False Body system structure Inferred relationship Existential restriction modifier
Post infectious thrombocytopenic purpura Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor II deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Moderate hereditary factor VIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor X deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to pyrimidine-5'-nucleotidase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent peripheral T cell maturation Finding site True Body system structure Inferred relationship Existential restriction modifier 1
Thrombocytopenia caused by hypothermia Finding site False Body system structure Inferred relationship Existential restriction modifier
Disseminated intravascular coagulation in newborn Finding site False Body system structure Inferred relationship Existential restriction modifier
Failed attempted abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IID Finding site False Body system structure Inferred relationship Existential restriction modifier
Abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor XI deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired factor V deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Antithrombin III deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent adenosine deaminase Finding site True Body system structure Inferred relationship Existential restriction modifier 1
Factor VII deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor X deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Sex-linked thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Familial multiple factor deficiency syndrome, type V Finding site False Body system structure Inferred relationship Existential restriction modifier
Proaccelerin deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Labile factor deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Placement of choledochal stent Procedure site - Indirect False Body system structure Inferred relationship Existential restriction modifier 1
Factor XI inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary hemolytic anemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor VII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand factor inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to phosphofructokinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired hypoprothrombinemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor V inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor IX deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Secondary cryofibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to hexokinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor V deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor XII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Anticoagulant overdosage Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to triosephosphate isomerase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Adenosine deaminase deficiency Finding site True Body system structure Inferred relationship Existential restriction modifier 2
Hereditary dysfibrinogenemia Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent interleukin-2 production Finding site True Body system structure Inferred relationship Existential restriction modifier 1
Factor XI deficiency, type III Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin E trait Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor XII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Factor VIII inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to reduced nicotinamide adenine dinucleotide diaphorase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Warfarin overdosage Finding site False Body system structure Inferred relationship Existential restriction modifier
Cyclic thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Prekallikrein deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Postpartum coagulation defect with hemorrhage Finding site False Body system structure Inferred relationship Existential restriction modifier
Severe combined immunodeficiency due to absent T cell receptor Finding site True Body system structure Inferred relationship Existential restriction modifier 1
Hereditary factor XI deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Thrombocytopenia due to blood loss Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary factor XIII deficiency disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Hemoglobin C disease Finding site False Body system structure Inferred relationship Existential restriction modifier
Dilutional thrombocytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
von Willebrand disease, type IIE Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glutathione reductase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to glucose phosphate isomerase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to increased adenosine deaminase activity Finding site False Body system structure Inferred relationship Existential restriction modifier
Nezelof's syndrome Finding site True Body system structure Inferred relationship Existential restriction modifier 2
Factor I inhibitor disorder Finding site False Body system structure Inferred relationship Existential restriction modifier
Acquired pancytopenia Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary nonspherocytic hemolytic anemia due to phosphoglycerate kinase deficiency Finding site False Body system structure Inferred relationship Existential restriction modifier
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site False Body system structure Inferred relationship Existential restriction modifier

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