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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
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

32681 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 Some
Body system structure partie de Entire body as a whole false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Acquired factor VIII deficiency disease Finding site False Body system structure Inferred relationship Some
Hereditary elliptocytosis due to glycophorin C deficiency Finding site False Body system structure Inferred relationship Some
Acquired factor XII deficiency disease Finding site False Body system structure Inferred relationship Some
Protein S deficiency disease Finding site False Body system structure Inferred relationship Some
Vitamin B12 absorption test Procedure site False Body system structure Inferred relationship Some 1
Drug-induced coagulation inhibitor disorder Finding site False Body system structure Inferred relationship Some
A severe form of hemophilia A characterized by a large deficiency of factor VIII (biological activity <1 IU/dL) leading to frequent spontaneous hemorrhage and abnormal bleeding as a result of minor injuries, or following trauma, surgery or tooth extraction. It primarily affects males but may also be observed in female carriers of disease-causing mutations. Finding site False Body system structure Inferred relationship Some
Hereditary coagulation factor deficiency Finding site False Body system structure Inferred relationship Some
Unstable hemoglobin disease Finding site False Body system structure Inferred relationship Some
Autoimmune pancytopenia Finding site False Body system structure Inferred relationship Some
Factor XIII deficiency disease Finding site False Body system structure Inferred relationship Some
von Willebrand disease, type IIC Finding site False Body system structure Inferred relationship Some
Lupus anticoagulant disorder Finding site False Body system structure Inferred relationship Some
Drug-induced immune thrombocytopenia Finding site False Body system structure Inferred relationship Some
von Willebrand disease, type IIB Finding site False Body system structure Inferred relationship Some
Acquired factor VII deficiency disease Finding site False Body system structure Inferred relationship Some
X chromosome-linked pyridoxine refractory sideroblastic anemia Finding site False Body system structure Inferred relationship Some
Platelet disorder Finding site False Body system structure Inferred relationship Some
Transient neonatal thrombocytopenia Finding site False Body system structure Inferred relationship Some
T activation syndrome Finding site False Body system structure Inferred relationship Some
Hemorrhagic disease of the newborn due to factor II deficiency Finding site False Body system structure Inferred relationship Some
von Willebrand disease, type IIH Finding site False Body system structure Inferred relationship Some
Hemoglobin E disease Finding site False Body system structure Inferred relationship Some
HNSHA due to gamma glutamyl cysteine synthetase deficiency Finding site False Body system structure Inferred relationship Some
X chromosome-linked pyridoxine responsive sideroblastic anemia Finding site False Body system structure Inferred relationship Some
Acquired coagulation factor deficiency Finding site False Body system structure Inferred relationship Some
A mild form of haemophilia A characterised by a small deficiency of factor VIII (biological activity between 5 and 40 IU/dL) leading to abnormal bleeding as a result of minor injuries or following surgery or tooth extraction. Spontaneous haemorrhages do not occur. Patients may be also labelled as having mild haemophilia A if they have a FVIII >40 IU/dL and a DNA change in the F8 gene and one of the following: (i) a family member with the same DNA change and FVIII of <40 IU/dL, and the DNA change is found in <1% of the population; and (ii) the international databases list the DNA change as being associated with haemophilia A and <40 IU/dL FVIII. The condition may affect males and female carriers of disease-causing mutations. Finding site False Body system structure Inferred relationship Some
Failed attempted abortion with afibrinogenemia (disorder) Finding site False Body system structure Inferred relationship Some
High molecular weight kininogen deficiency Finding site False Body system structure Inferred relationship Some
Hereditary factor VIII deficiency disease Finding site False Body system structure Inferred relationship Some
Immune thrombocytopenia Finding site False Body system structure Inferred relationship Some
Thrombocytopenia due to extracorporeal circulation (disorder) Finding site False Body system structure Inferred relationship Some
Legal abortion with afibrinogenemia Finding site False Body system structure Inferred relationship Some
Severe combined immunodeficiency disease Finding site True Body system structure Inferred relationship Some 2
Hereditary factor I deficiency disease Finding site False Body system structure Inferred relationship Some
Illegal abortion with afibrinogenemia Finding site False Body system structure Inferred relationship Some
Transient neonatal disorder of coagulation Finding site False Body system structure Inferred relationship Some
Factor XI deficiency, type II Finding site False Body system structure Inferred relationship Some
Post infectious thrombocytopenic purpura Finding site False Body system structure Inferred relationship Some
Hereditary factor II deficiency disease Finding site False Body system structure Inferred relationship Some
Moderate disease manifests factor VIII activity of 2% to 5% of normal Finding site False Body system structure Inferred relationship Some
Acquired factor X deficiency disease Finding site False Body system structure Inferred relationship Some
HNSHA due to pyrimidine-5'-nucleotidase deficiency Finding site False Body system structure Inferred relationship Some
Severe combined immunodeficiency due to absent peripheral T cell maturation (disorder) Finding site True Body system structure Inferred relationship Some 1
Thrombocytopenia due to hypothermia Finding site False Body system structure Inferred relationship Some
Disseminated intravascular coagulation in newborn Finding site False Body system structure Inferred relationship Some
Failed attempted abortion with defibrination syndrome (disorder) Finding site False Body system structure Inferred relationship Some
von Willebrand disease, type IID Finding site False Body system structure Inferred relationship Some
Abortion with defibrination syndrome Finding site False Body system structure Inferred relationship Some
Acquired factor XI deficiency disease Finding site False Body system structure Inferred relationship Some
Acquired factor V deficiency disease Finding site False Body system structure Inferred relationship Some
Antithrombin III deficiency Finding site False Body system structure Inferred relationship Some
Severe combined immunodeficiency due to absent adenosine deaminase (disorder) Finding site True Body system structure Inferred relationship Some 1
Factor VII deficiency Finding site False Body system structure Inferred relationship Some
Hereditary factor X deficiency disease Finding site False Body system structure Inferred relationship Some
Sex-linked thrombocytopenia Finding site False Body system structure Inferred relationship Some
Familial multiple factor deficiency syndrome, type V Finding site False Body system structure Inferred relationship Some
Proaccelerin deficiency Finding site False Body system structure Inferred relationship Some
Labile factor deficiency Finding site False Body system structure Inferred relationship Some
Placement of choledochal stent Procedure site - Indirect (attribute) False Body system structure Inferred relationship Some 1
Factor XI inhibitor disorder Finding site False Body system structure Inferred relationship Some
Hereditary haemolytic anaemia Finding site False Body system structure Inferred relationship Some
Hereditary factor VII deficiency disease (disorder) Finding site False Body system structure Inferred relationship Some
von Willebrand factor inhibitor disorder Finding site False Body system structure Inferred relationship Some
HNSHA due to phosphofructokinase deficiency Finding site False Body system structure Inferred relationship Some
Acquired hypoprothrombinemia Finding site False Body system structure Inferred relationship Some
Factor V inhibitor disorder Finding site False Body system structure Inferred relationship Some
Hereditary factor IX deficiency disease Finding site False Body system structure Inferred relationship Some
Secondary cryofibrinogenemia Finding site False Body system structure Inferred relationship Some
HNSHA due to hexokinase deficiency Finding site False Body system structure Inferred relationship Some
Factor V deficiency Finding site False Body system structure Inferred relationship Some
Hereditary factor XII deficiency disease Finding site False Body system structure Inferred relationship Some
Anticoagulant overdosage (disorder) Finding site False Body system structure Inferred relationship Some
HNSHA due to triosephosphate isomerase deficiency Finding site False Body system structure Inferred relationship Some
Adenosine deaminase deficiency Finding site True Body system structure Inferred relationship Some 2
Hereditary dysfibrinogenemia (disorder) Finding site False Body system structure Inferred relationship Some
Severe combined immunodeficiency due to absent interleukin-2 production (disorder) Finding site True Body system structure Inferred relationship Some 1
Factor XI deficiency, type III Finding site False Body system structure Inferred relationship Some
Hemoglobin E trait Finding site False Body system structure Inferred relationship Some
Factor XII deficiency disease Finding site False Body system structure Inferred relationship Some
Factor VIII inhibitor disorder (disorder) Finding site False Body system structure Inferred relationship Some
HNSHA due to NADH diaphorase deficiency Finding site False Body system structure Inferred relationship Some
Warfarin overdosage Finding site False Body system structure Inferred relationship Some
Cyclic thrombocytopenia Finding site False Body system structure Inferred relationship Some
Prekallikrein deficiency Finding site False Body system structure Inferred relationship Some
Postpartum coagulation defect with hemorrhage Finding site False Body system structure Inferred relationship Some
Severe combined immunodeficiency due to absent T cell receptor (disorder) Finding site True Body system structure Inferred relationship Some 1
Hereditary factor XI deficiency disease Finding site False Body system structure Inferred relationship Some
Thrombocytopenia due to blood loss Finding site False Body system structure Inferred relationship Some
Hereditary factor XIII deficiency disease Finding site False Body system structure Inferred relationship Some
Hemoglobin C disease Finding site False Body system structure Inferred relationship Some
Dilutional thrombocytopenia Finding site False Body system structure Inferred relationship Some
von Willebrand disease, type IIE Finding site False Body system structure Inferred relationship Some
HNSHA due to glutathione reductase deficiency Finding site False Body system structure Inferred relationship Some
HNSHA due to glucose phosphate isomerase deficiency Finding site False Body system structure Inferred relationship Some
A rare genetic haematologic disease characterised by mild chronic haemolytic anaemia (due to highly elevated adenosine deaminase activity in red blood cells resulting in their premature destruction), elevated reticulocyte count, splenomegaly and mild hyperbilirubinaemia. Other cells and tissues are not affected. Finding site False Body system structure Inferred relationship Some
Nezelof's syndrome (disorder) Finding site True Body system structure Inferred relationship Some 2
Factor I inhibitor disorder Finding site False Body system structure Inferred relationship Some
Acquired pancytopenia Finding site False Body system structure Inferred relationship Some
HNSHA due to phosphoglycerate kinase deficiency Finding site False Body system structure Inferred relationship Some
Hereditary elliptocytosis due to deficiency of protein 4.1 Finding site False Body system structure Inferred relationship Some

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Reference Sets

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

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