74848003: Hemostatic function (observable entity)

SNOMED CT Concept\Observable entity (observable entity)\Any function or property that is not mainly morphologic or structural, including both measurable and observable features and physiologic actions\Hematologic function\Hemostatic 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
Hemostatic function	Is a	Hematologic function	true	Inferred relationship	Some

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Acquired storage pool deficiency (platelets)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Acquired factor XIII deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Thrombocytopenia due to massive blood transfusion	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Cyclooxygenase deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Infection-associated purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Thromboxane synthetase deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Aplastic anemia with AIDS (acquired immunodeficiency syndrome)	Interprets	True	Hemostatic function	Inferred relationship	Some	8
Acquired platelet disorder	Interprets	False	Hemostatic function	Inferred relationship	Some	2
May-Hegglin anomaly	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Thrombocytopenia caused by alcohol (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Thrombocytopenia due to sequestration	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Thrombophilia due to malignant neoplasm	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Congenital thrombocytopenia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Neonatal coagulation disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Aplastic anemia caused by toxic cause	Interprets	True	Hemostatic function	Inferred relationship	Some	8
Fanconi's anemia	Interprets	False	Hemostatic function	Inferred relationship	Some	7
Pancytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	6
Acquired hypoplasminogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Drug-induced immune thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Aplastic anaemia	Interprets	False	Hemostatic function	Inferred relationship	Some	7
Neonatal thrombocytopenia due to exchange transfusion	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Idiopathic aplastic anaemia	Interprets	True	Hemostatic function	Inferred relationship	Some	7
Thrombocytopaenia co-occurrent and due to alcoholism	Interprets	True	Hemostatic function	Inferred relationship	Some	4
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.	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Platelet dysfunction associated with uremia (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Alloimmune thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Accidental coumarin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Catastrophic antiphospholipid syndrome (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Transient acquired pure red cell aplasia	Interprets	False	Hemostatic function	Inferred relationship	Some	7
Coumarin overdose of undetermined intent	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Radiation thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Cryofibrinogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Platelet storage pool defect	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Accidental warfarin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Heparin-induced thrombocytopenia with thrombosis	Interprets	True	Hemostatic function	Inferred relationship	Some	5
Acquired factor XII deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Familial alpha>2< adrenergic receptor defect in platelets	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Autoimmune thrombotic thrombocytopenic purpura (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	9
HELLP syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	4
Primary cryofibrinogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Acquired thrombotic thrombocytopenic purpura (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	9
thrombophilie due aux anticorps antiphospholipides	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Hereditary factor I deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hemorrhagic disorder due to hyperheparinemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
A rare constitutional aplastic anemia disorder characterized by severe hypo/aplastic anemia or pancytopenia associated with skeletal anomalies (such as radial/ulnar defects and hand/digit abnormalities) and an increased risk of leukemia. There have been no further descriptions in the literature since 1995.	Interprets	True	Hemostatic function	Inferred relationship	Some	7
Thrombophilia due to hormone therapy	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Evans syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	7
Illegal abortion with defibrination syndrome	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Aplastic anemia associated with metabolic alteration (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	8
Acquired hypofibrinogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Heparin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
A rare syndrome with combined immunodeficiency characterized by a variable clinical presentation ranging from asymptomatic individuals to potentially life-threatening, recurrent bacterial infections associated with progressive loss of serum immunoglobulins and B cells.	Interprets	False	Hemostatic function	Inferred relationship	Some	6
Aplastic anemia associated with pancreatitis (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	8
Deficiency of coagulation factor due to liver disease	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Acquired coagulation factor deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Accidental heparin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Deficiency of coagulation factor due to vitamin K deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Intentional heparin overdose (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Pancytopenia caused by immunosuppressant	Interprets	True	Hemostatic function	Inferred relationship	Some	7
Acquired factor II deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Antibody mediated acquired pure red cell aplasia caused by erythropoiesis stimulating agent (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	7
surdose d'héparine d'intention indéterminée	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Coumarin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Medich giant platelet syndrome (MGPS) is a platelet granule disorder characterized by thrombocytopenia with giant platelets resulting in easy bleeding.	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Intentional coumarin overdose	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Hereditary factor XI deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Platelet dense granule deficiency	Interprets	False	Hemostatic function	Inferred relationship	Some	2
surdose intentionnelle de warfarine sodique	Interprets	False	Hemostatic function	Inferred relationship	Some	2
surdose de warfarin d'intention indéterminée	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Hemorrhagic disease of the newborn due to vitamin K deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Immunoglobulin A vasculitis	Interprets	False	Hemostatic function	Inferred relationship	Some	5
Acquired thrombophilia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Thrombophilia due to acquired protein C deficiency	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Gardner-Diamond syndrome (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
A rare syndromic renal disorder characterized by renal, neurologic and thyroid disease, associated with thrombocytopenia. There have been no further descriptions in the literature since 1978.	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Thrombocytopenia due to diminished platelet production	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Purpura of skin and/or skin-associated mucous membrane co-occurrent and due to coagulation disorder (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
A rare isolated constitutional thrombocytopenia characterized by abnormally large platelets.	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Hereditary thrombocytopenic disorder (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Thrombocytopenia caused by drugs (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Pancytopenia due to antineoplastic chemotherapy (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	7
Neonatal purpura fulminans due to homozygous protein C deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	5
A rare acquired aplastic anaemia characterised by a severe normocytic anaemia with normal peripheral leukocyte and platelet counts, reticulocytopenia, high serum ferritin and transferrin saturation levels and isolated, almost complete absence of erythroblasts in the bone marrow with normal granulopoiesis and megakaryopoiesis. It presents with signs of severe anaemia (fatigue, lethargy, pallor, intolerance of physical exercise and exertional dyspnoea) in the absence of haemorrhagic symptoms.	Interprets	False	Hemostatic function	Inferred relationship	Some	7
Mixed cryofibrinogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Drug-induced coagulation inhibitor disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Chédiak-Higashi syndrome	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Consumption coagulopathy caused by snake venom	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Atypical haemolytic uraemic syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	10
Platelet secretory disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Bernard Soulier syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Doan-Wright syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	6
Fanconi's anemia	Interprets	True	Hemostatic function	Inferred relationship	Some	7
dysfonctionnement plaquettaire médicamenteux	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Platelet procoagulant activity deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Platelet dysfunction caused by aspirin (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Platelet dense granule deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Autoimmune pancytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	5
Chédiak-Higashi syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Acquired PF-3 disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Glycoprotein Ia defect	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Amegakaryocytic thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	2

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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
190321000077117	hémostase	fr	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Switzerland NRC maintained Module