74848003: Hemostatic function (observable entity)

SNOMED CT Concept\Observable entity\Any function or property that is not mainly morphologic or structural, including both measurable and observable features and physiologic actions\Hematologic function\Haemostatic function

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
Haemostatic function	Is a	Hematologic function	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Hereditary thrombophilia (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Cryofibrinogenemic purpura (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Idiopatisk trombocytopenisk purpura	Interprets	False	Haemostatic function	Inferred relationship	Some	4
Stasis purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Purpura due to increased intravascular pressure (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Cryoglobulinemic purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Heterozygous protein S deficiency (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Acquired red cell aplasia	Interprets	False	Haemostatic function	Inferred relationship	Some	6
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Hereditary factor XIII A subunit deficiency (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Exhausted platelets	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Alpha-2-antiplasmin deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Postpartum coagulation defect with hemorrhage	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Autoimmune neonatal thrombocytopenia	Interprets	False	Haemostatic function	Inferred relationship	Some	3
Blood coagulation disorder with impaired clot retraction time	Interprets	True	Haemostatic function	Inferred relationship	Some	1
afibrinogenæmi efter molagraviditet OG/ELLER ektopisk graviditet	Interprets	False	Haemostatic function	Inferred relationship	Some	1
Factor XI deficiency, type II	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor IX deficiency disease without inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Megakaryocytic aplasia	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Neonatal thrombocytopenia due to platelet alloimmunization (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
von Willebrands sygdom type 2A	Interprets	False	Haemostatic function	Inferred relationship	Some	1
Heterozygous prothrombin G20210A mutation (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to increase in anti-11a	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Fibrinolytic bleeding syndrome	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Purpura annularis telangiectodes of Majocchi	Interprets	True	Haemostatic function	Inferred relationship	Some	3
Induced termination of pregnancy complicated by defibrination syndrome (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Senile purpura (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Familial multiple factor deficiency syndrome, type II	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Qualitative platelet disorder (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Constitutional aplastic anemia with malformation	Interprets	True	Haemostatic function	Inferred relationship	Some	6
Factor VIII deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Combined coagulation factor deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Fibrinolysis - postpartum	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor XIII deficiency disease	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type IV	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Hereditary elevated factor XI (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
kunstigt fremkaldt purpura	Interprets	False	Haemostatic function	Inferred relationship	Some	2
Embolic purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Severe hereditary factor VIII deficiency disease without inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Miscarriage with afibrinogenemia (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Autoimmune pancytopenia	Interprets	False	Haemostatic function	Inferred relationship	Some	5
Posttransfusion purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	3
Systemic fibrinogenolysis	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary combined coagulation factor deficiency (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
post partum-koagulationsdefekter, barn født med postnatalt problem	Interprets	False	Haemostatic function	Inferred relationship	Some	1
Hereditary antithrombin III deficiency (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Thrombophilia associated with pregnancy	Interprets	True	Haemostatic function	Inferred relationship	Some	1
von Willebrands sygdom, trombocyttype	Interprets	False	Haemostatic function	Inferred relationship	Some	1
Hereditary hyperfibrinogenemia (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Thrombocytopathy, asplenia and miosis (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	3
Hypofibrinogenaemia	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Neonatal trombocytopeni associeret med maternel idiopatisk trombocytopenisk purpura	Interprets	False	Haemostatic function	Inferred relationship	Some	2
Thrombotic thrombocytopenic purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	8
Hyperheparinemia	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary elevated factor VIII (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Dysplasminogenemia	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor VII deficiency disease (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Pregnancy-related factor VIII deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Eczematid-like purpura of Doucas and Kapetanakis	Interprets	True	Haemostatic function	Inferred relationship	Some	4
Hereditary factor XII deficiency disease	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Waldenstrom's hypergammaglobulinemic purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Acquired platelet function disorder	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Dysproteinemic purpura (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Afibrinogenaemia - postpartum	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Purpuric disorder (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Severe hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Factor XI deficiency, type I	Interprets	True	Haemostatic function	Inferred relationship	Some	1
von Willebrands sygdom type IIG	Interprets	False	Haemostatic function	Inferred relationship	Some	1
Legal abort med defibrineringssyndrom	Interprets	False	Haemostatic function	Inferred relationship	Some	1
A rare inherited bleeding disorder due to the reduction in activity and antigen levels of both factor V (FV) and factor VIII (FVIII) and characterized by mild-to-moderate bleeding symptoms.	Interprets	True	Haemostatic function	Inferred relationship	Some	1
MYH9-related disease (MYH9-RD) is an inherited giant platelet disorder with a complex phenotype characterized by congenital thrombocytopenia and possible subsequent manifestations of sensorineural hearing loss, presenile cataracts, elevation of liver enzymes, and/or progressive nephropathy often leading to end-stage renal disease (ESRD). Epstein syndrome, Fechtner syndrome, May-Hegglin anomaly and Sebastian syndrome, previously described as distinct disorders, represent some of the different clinical presentations of MYH9-RD.	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Hereditary von Willebrand disease type 2N (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Thrombocytosis	Interprets	False	Haemostatic function	Inferred relationship	Some	2
Amegakaryocytic thrombocytopenia	Interprets	False	Haemostatic function	Inferred relationship	Some	2
Post partum-koagulationsdefekter med postnatalt problem	Interprets	False	Haemostatic function	Inferred relationship	Some	1
A rare life-threatening genetic coagulation disorder with characteristics of an increased risk of blood clot formation in several members of a family due to a thrombomodulin gene mutation. Patients may manifest with venous thromboembolic disease, premature myocardial infarction and/or arterial thrombosis.	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type V	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Dense body defect	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Transient neonatal thrombocytopenia due to exchange transfusion	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Prekallikrein deficiency	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Anticoagulant-induced bleeding	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Primary thrombocytopenia	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Disseminated intravascular coagulation in newborn	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Protein C deficiency disease	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to circulating anticoagulants	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hypodysfibrinogenemia	Interprets	True	Haemostatic function	Inferred relationship	Some	1
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%	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary von Willebrand disease type 1A	Interprets	True	Haemostatic function	Inferred relationship	Some	1
A rare genetic syndrome with limb reduction defects with characteristics of thrombocytosis, unilateral transverse limb defects (ranging from absence of phalanges to absence of hand or forearm) and splenomegaly.	Interprets	True	Haemostatic function	Inferred relationship	Some	4
An isolated constitutional thrombocytopenia characterized by an isolated and severe decrease in the number of platelets and megakaryocytes during the first years of life that develops into bone marrow failure with pancytopenia later in childhood.	Interprets	False	Haemostatic function	Inferred relationship	Some	2
Mild hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary dysplasminogenemia	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	1
Aplastic anemia associated with pregnancy (disorder)	Interprets	True	Haemostatic function	Inferred relationship	Some	6
Purpura simplex	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Benign primary hypergammaglobulinemic purpura	Interprets	True	Haemostatic function	Inferred relationship	Some	2
Mild disease manifests factor VIII activity of greater than 5% of normal	Interprets	True	Haemostatic function	Inferred relationship	Some	1

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Id	Description	Lang	Type	Status	Case?	Module
124302017	Hemostatic function	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
124306019	Blood coagulation	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
124307011	Blood clotting	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
124310016	Hemostasis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502831011	Haemostasis	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
502832016	Haemostatic function	en	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
1204583012	Hemostatic function (observable entity)	en	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT core
2009011000005117	hæmostasefunktion	da	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Danish module (core metadata concept)