281833003: Entire hematological system (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure (body structure)\Anatomical structure\Body system structure\Structure of hematological system (body structure)\Entire hematological system (body 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
Entire hematological system (body structure)	Is a	Body system structure	false	Inferred relationship	Some
Entire hematological system (body structure)	del af	Entire body as a whole	false	Additional relationship	Some
Entire hematological system (body structure)	Is a	Structure of hematological system (body structure)	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Intentional coumarin overdose	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
overdosis af cumarin, uvist med hvilken hensigt	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Accidental warfarin overdose	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
tilsigtet overdosis af warfarinnatrium	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
overdosis af warfarin, uvist med hvilken hensigt	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Factor V Leiden mutation	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Homozygous Factor V Leiden mutation	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Heterozygous Factor V Leiden mutation	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Idiopathic factor VIII deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Autoimmune factor VIII deficiency (disorder)	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Pregnancy-related factor VIII deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Malignancy-related factor VIII deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Antibody screen (procedure)	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hemolysin detection, cold	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hemolysin detection, warm	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired factor IX deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
RBC antibody detection, warm with titration	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood coagulation disorder with shortened coagulation time	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood coagulation disorder with prolonged coagulation time	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood coagulation disorder with shortened bleeding time	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood coagulation disorder with prolonged bleeding time	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood coagulation disorder with impaired clot retraction time	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Deficiency of pyruvate kinase	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Deficiency of adenylate kinase	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom, type IIF	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hemorrhagic disease of the newborn due to vitamin K deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Infusion of dextran (procedure)	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-hemoglobin SS disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-beta-thalassemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell beta plus thalassaemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-beta^0^-thalassemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-delta beta^0^-thalassemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell trait with coexistent alpha-thalassemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-hemoglobin Lepore disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Sickle cell-Hemoglobin O Arab disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Apheresis	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	2
Blood coagulation disorder, categorized by value of screening test	Finding site	False	Entire hematological system (body 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	Entire hematological system (body 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	Entire hematological system (body 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	Entire hematological system (body 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	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 1B	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 1C	Finding site	False	Entire hematological system (body 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	Entire hematological system (body structure)	Inferred relationship	Some
Vitamin K deficiency coagulation disorder	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 1A	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom, type 1^a^	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type IA	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 2A	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type 2A	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 2B	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type 2B	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired hypofibrinogenemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 2M	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Fibrinogen deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type 2M	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired afibrinogenemia	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary von Willebrand disease type 2N (disorder)	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type 2N	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Antibody identification, RBC, albumin	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Chronic idiopathic thrombocytopenic purpura	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Hemolysin detection, cold, quantitative	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Purpura fulminans	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Anti-human globulin test, enzyme technique, titer	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Factor XIII inhibitor disorder	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired factor VIII deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired factor XII deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Protein S deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Akroangiodermatit	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Stasis purpura	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Vitamin B12 absorption test	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Vitamin B12 isotope studies	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	2
Indirect Coombs test	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Drug-induced coagulation inhibitor disorder (disorder)	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Severe disease manifests factor VIII activity of less than 1%, except in the U.K. and Italy, where severe disease includes factor VIII activity levels of less than 2%	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Hereditary coagulation factor deficiency	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Compatibility test, crossmatch, screening for compatible unit, saline and/or high protein	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood unit collection for directed donation, donor	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Fresh frozen plasma preparation	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
RBC antibody detection, cold with titration	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Factor XIII deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Packed red blood cell preparation, sedimentation (procedure)	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
RBC antibody detection with saline	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type IIC	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Lupus anticoagulant disorder	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
von Willebrands sygdom type IIB	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Therapeutic plasmapheresis using plasma as the major replacement fluid (procedure)	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	2
Blood typing, ABO, Rho(D) and RBC antibody screening	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Acquired factor VII deficiency disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Red cell iron utilization study	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Antibody detection, RBC, saline, high protein and anti-human globulin technique	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Plasmapheresis	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	2
Vascular hemostatic disease	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Allergisk purpura	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Blood group typing B	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Miscarriage with afibrinogenemia (disorder)	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some
Plasma radioiron turnover rate	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Hemoglobin S disease without crisis	Finding site	False	Entire hematological system (body structure)	Inferred relationship	Some	1
Blood donor rejection, clerical	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some
Antibody detection, RBC, enzyme, 1 stage technique, including anti-human globulin	Procedure site	False	Entire hematological system (body structure)	Inferred relationship	Some

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Id	Description	Lang	Type	Status	Case?	Module
2528953015	Entire hematological system (body structure)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2532372011	Entire haematological system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2532373018	Entire hematological system	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
4629991000005119	hæmatologiske system som helhed	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)