91689009: Body system structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\Body system structure

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

Descriptions:

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	del af	Entire body as a whole	false	Additional relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Cyclooxygenase deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Thromboxane synthetase deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Giant platelet syndrome	Finding site	False	Body system structure	Inferred relationship	Some
Acquired platelet disorder	Finding site	False	Body system structure	Inferred relationship	Some
Amegakaryocytic thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Megakaryocytic thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
May-Hegglins anomali	Finding site	False	Body system structure	Inferred relationship	Some	2
Montreal platelet syndrome (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
Mediterranean thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
metabolisk trombocytopenisk purpura	Finding site	False	Body system structure	Inferred relationship	Some
Immunbetinget trombocytopenisk purpura	Finding site	False	Body system structure	Inferred relationship	Some
Reactive thrombocytosis	Finding site	False	Body system structure	Inferred relationship	Some
Post-splenectomy thrombocytosis	Finding site	False	Body system structure	Inferred relationship	Some
Radionuclide study of neural receptors	Procedure site	False	Body system structure	Inferred relationship	Some	1
Whole body counter study with vitamin B12	Procedure site	False	Body system structure	Inferred relationship	Some	2
Red cell mass measurement with Cr51	Procedure site	False	Body system structure	Inferred relationship	Some	1
Red cell mass measurement with Tc99m	Procedure site	False	Body system structure	Inferred relationship	Some	1
Abort med afibrinogenæmi	Finding site	False	Body system structure	Inferred relationship	Some
Postpartum afibrinogenemia with hemorrhage	Finding site	False	Body system structure	Inferred relationship	Some
hereditær non-sfærocytisk hæmolytisk anæmi forårsaget af aldolase A-mangel	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary nonspherocytic hemolytic anemia due to glutathione synthetase deficiency (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
SCID due to absent IL-2 receptor	Finding site	True	Body system structure	Inferred relationship	Some	1
Dysfibrinogenemia (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
Kongenit trombocytopenisk purpura	Finding site	False	Body system structure	Inferred relationship	Some
Radionuclide studies in haematology	Procedure site	False	Body system structure	Inferred relationship	Some	1
Radionuclide red cell mass measurement	Procedure site	False	Body system structure	Inferred relationship	Some	1
Perinatal thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Autoimmune neonatal thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Anticoagulant-induced bleeding	Finding site	False	Body system structure	Inferred relationship	Some
Anticoagulant excess without bleeding	Finding site	False	Body system structure	Inferred relationship	Some
Acquired inhibitor of coagulation	Finding site	False	Body system structure	Inferred relationship	Some
Acquired storage pool deficiency (platelets)	Finding site	False	Body system structure	Inferred relationship	Some
Heparin overdose	Finding site	False	Body system structure	Inferred relationship	Some
Accidental heparin overdose	Finding site	False	Body system structure	Inferred relationship	Some
Intentional heparin overdose	Finding site	False	Body system structure	Inferred relationship	Some
overdosis af heparin, uvist med hvilken hensigt	Finding site	False	Body system structure	Inferred relationship	Some
Coumarin overdose	Finding site	False	Body system structure	Inferred relationship	Some
Accidental coumarin overdose	Finding site	False	Body system structure	Inferred relationship	Some
Intentional coumarin overdose	Finding site	False	Body system structure	Inferred relationship	Some
overdosis af cumarin, uvist med hvilken hensigt	Finding site	False	Body system structure	Inferred relationship	Some
Accidental warfarin overdose	Finding site	False	Body system structure	Inferred relationship	Some
tilsigtet overdosis af warfarinnatrium	Finding site	False	Body system structure	Inferred relationship	Some
overdosis af warfarin, uvist med hvilken hensigt	Finding site	False	Body system structure	Inferred relationship	Some
Exhausted platelets	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary nonspherocytic haemolytic anaemia	Finding site	False	Body system structure	Inferred relationship	Some
Thrombocytopenic disorder	Finding site	False	Body system structure	Inferred relationship	Some
Thrombocytopenic purpura	Finding site	False	Body system structure	Inferred relationship	Some
Radionuclide blood cell study	Procedure site	False	Body system structure	Inferred relationship	Some	1
Factor V Leiden mutation	Finding site	False	Body system structure	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Finding site	False	Body system structure	Inferred relationship	Some
Heterozygous Factor V Leiden mutation	Finding site	False	Body system structure	Inferred relationship	Some
Thrombocytopenia due to massive blood transfusion	Finding site	False	Body system structure	Inferred relationship	Some
Idiopathic factor VIII deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Autoimmune factor VIII deficiency (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
Pregnancy-related factor VIII deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Malignancy-related factor VIII deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Platelet sequestration	Finding site	False	Body system structure	Inferred relationship	Some
Thrombocytopenia due to sequestration	Finding site	False	Body system structure	Inferred relationship	Some
Acquired factor IX deficiency disease	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary disorder of cellular element of blood (disorder)	Finding site	True	Body system structure	Inferred relationship	Some	1
Hereditary red blood cell disorder (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary white blood cell disorder (disorder)	Finding site	True	Body system structure	Inferred relationship	Some	1
Blood coagulation disorder with shortened coagulation time	Finding site	False	Body system structure	Inferred relationship	Some
Blood coagulation disorder with prolonged coagulation time	Finding site	False	Body system structure	Inferred relationship	Some
Blood coagulation disorder with shortened bleeding time	Finding site	False	Body system structure	Inferred relationship	Some
Blood coagulation disorder with prolonged bleeding time	Finding site	False	Body system structure	Inferred relationship	Some
Blood coagulation disorder with impaired clot retraction time	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom, type IIF	Finding site	False	Body system structure	Inferred relationship	Some
Hemorrhagic disease of the newborn due to vitamin K deficiency	Finding site	False	Body system structure	Inferred relationship	Some
Pancytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary hemoglobinopathy due to globin chain mutation	Finding site	False	Body system structure	Inferred relationship	Some
Blood coagulation disorder, categorized by value of screening test	Finding site	False	Body system structure	Inferred relationship	Some
Benign gestational thrombocytopenia (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
An autoimmune coagulation disorder characterized by isolated thrombocytopenia (a platelet count <100,000/microL), in the absence of any underlying disorder that may be associated with thrombocytopenia.	Finding site	False	Body system structure	Inferred relationship	Some
Secondary autoimmune thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Alloimmune thrombocytopenia	Finding site	False	Body system structure	Inferred relationship	Some
Alloimmune platelet transfusion refractoriness	Finding site	False	Body system structure	Inferred relationship	Some
Includes true von Willebrand disease with mutation at the VWF locus, as well as mimicking disorders with other mutations (pseudo VWD) and acquired von Willebrand syndrome.	Finding site	False	Body system structure	Inferred relationship	Some
A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a partial, quantitative plasmatic deficiency of an otherwise structurally and functionally normal von Willebrand factor (VWF). The type 1 disease is considered to be the most common form of VWD, caused by mutations in the VWF gene (12p13.3). Transmitted in an autosomal dominant manner.	Finding site	False	Body system structure	Inferred relationship	Some
A form of von Willebrand disease (VWD) with characteristics of a bleeding disorder associated with a qualitative deficiency and functional anomalies of the Willebrand factor (VWF). Depending on the type of functional abnormalities, this form is classified as type 2A, 2B, 2M or 2N. The VWF gene (12p13.3) anomalies that lead to type 2 VWD involve the well-defined functional domains of the VWF protein. Most subtypes of type 2 VWD are transmitted in an autosomal dominant manner except for type 2N and some rare forms of type 2A which are autosomal recessive.	Finding site	False	Body system structure	Inferred relationship	Some
A total or near-total absence of Willebrand factor (VWF) in the plasma and cellular compartments leading to a profound deficiency of plasmatic factor VIII (FVIII). It is the most severe form of von Willebrand disease. Onset usually occurs during the neonatal period or in infancy, but later onset has been reported. The disease is caused by homozygous or compound heterozygous mutations (mainly missense or large mutations) in the VWF gene (12p13.3) that lead to synthesis of a truncated protein or allele silencing. The pattern of inheritance is autosomal recessive.	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 1C	Finding site	False	Body system structure	Inferred relationship	Some
A bleeding disorder with characteristics of mild to moderate mucocutaneous bleeding, which becomes more pronounced during pregnancy or following ingestion of drugs that have anti-platelet activity. This disease is due to hyperresponsive platelets, resulting in thrombocytopenia.	Finding site	False	Body system structure	Inferred relationship	Some
Vitamin K deficiency coagulation disorder	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 1A	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom, type 1^a^	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom type IA	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom type 2A	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 2B	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom type 2B	Finding site	False	Body system structure	Inferred relationship	Some
Acquired hypofibrinogenemia	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Finding site	False	Body system structure	Inferred relationship	Some
Fibrinogen deficiency	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom type 2M	Finding site	False	Body system structure	Inferred relationship	Some
Acquired afibrinogenemia	Finding site	False	Body system structure	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Finding site	False	Body system structure	Inferred relationship	Some
von Willebrands sygdom type 2N	Finding site	False	Body system structure	Inferred relationship	Some
Factor XIII inhibitor disorder	Finding site	False	Body system structure	Inferred relationship	Some
Acquired factor VIII deficiency disease	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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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
4180721000005118	struktur af organsystem	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)