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