74848003: hemostase (waarneembare entiteit)

SNOMED CT Concept\Observable entity\Function (observable entity)\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
Hereditary thrombophilia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Cryofibrinogenemic purpura (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
idiopathische trombocytopenische purpura	Interprets	False	Hemostatic function	Inferred relationship	Some	4
Stasis purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Purpura due to increased intravascular pressure (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Cryoglobulinaemic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Heterozygous protein S deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Acquired red cell aplasia	Interprets	False	Hemostatic function	Inferred relationship	Some	6
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hereditary factor XIII A subunit deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Exhausted platelets	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Alpha-2-antiplasmin deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Postpartum coagulation defect with hemorrhage	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Autoimmune neonatal thrombocytopenia	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Blood coagulation disorder with impaired clot retraction time (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
afibrinogenemie na molazwangerschap en/of ectopische zwangerschap	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Factor XI deficiency, type II	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor IX deficiency disease without inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Megakaryocytic aplasia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Neonatal thrombocytopenia due to platelet alloimmunization (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
ziekte van von Willebrand type 2A	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Heterozygous prothrombin G20210A mutation (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to increase in anti-11a	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Fibrinolytic bleeding syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Purpura annularis telangiectodes of Majocchi (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Induced termination of pregnancy complicated by defibrination syndrome (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Senile purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Familial multiple factor deficiency syndrome, type II	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Qualitative platelet disorder (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Constitutional aplastic anemia with malformation	Interprets	True	Hemostatic function	Inferred relationship	Some	6
Factor VIII deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Combined coagulation factor deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Fibrinolysis - postpartum	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor IX deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor XIII deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type IV	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hereditary elevated factor XI (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
nagebootste purpura (aandoening)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Embolic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Severe hereditary factor VIII deficiency disease without inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Miscarriage with afibrinogenemia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Autoimmune pancytopenia	Interprets	False	Hemostatic function	Inferred relationship	Some	5
Posttransfusion purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Systemic fibrinogenolysis	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary combined coagulation factor deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
stollingsstoornis post partum - bevallen met postpartaal probleem (aandoening)	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Hereditary antithrombin III deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Thrombophilia associated with pregnancy	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Platelet type von Willebrand's disease	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Hereditary hyperfibrinogenemia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Moderate hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Thrombocytopathy, asplenia and miosis (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Hypofibrinogenaemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
neonatale trombocytopenie door maternale idiopathische trombocytopenische purpura (aandoening)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Thrombotic thrombocytopenic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	8
Hyperheparinemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary elevated factor VIII (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Dysplasminogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor VII deficiency disease (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Pregnancy-related factor VIII deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Eczematid-like purpura of Doucas and Kapetanakis	Interprets	True	Hemostatic function	Inferred relationship	Some	4
Hereditary factor XII deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Waldenstrom's hypergammaglobulinaemic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Acquired platelet function disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Dysproteinemic purpura (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Afibrinogenaemia - postpartum	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Purpuric disorder (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Severe hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Factor XI deficiency, type I	Interprets	True	Hemostatic function	Inferred relationship	Some	1
ziekte van von Willebrand type 2A subtype IIG	Interprets	False	Hemostatic function	Inferred relationship	Some	1
abortus provocatus lege artis met verbruikscoagulopathie (aandoening)	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Combined deficiency of factor V and factor VIII (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
MYH9 related disease	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hereditary von Willebrand disease type 2N (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Thrombocytosis	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Amegakaryocytic thrombocytopenia	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Postpartum coagulation defects with postnatal problem	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial thrombomodulin anomalies (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type V	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Dense body defect	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Transient neonatal thrombocytopenia due to exchange transfusion	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Prekallikrein deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Anticoagulant-induced bleeding	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Primary thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Disseminated intravascular coagulation in newborn	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Protein C deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to circulating anticoagulants	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hypodysfibrinogenaemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Severe hereditary factor VIII deficiency disease (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary von Willebrand disease type 1A	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Thrombocythemia with distal limb defect (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	4
Congenital amegakaryocytic thrombocytopenia (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Mild hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary dysplasminogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary factor VIII deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Aplastic anemia associated with pregnancy (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	6
Purpura simplex	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Benign primary hypergammaglobulinemic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Mild hereditary factor VIII deficiency disease (disorder)	Interprets	True	Hemostatic 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
12348791000146119	hemostatische functie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12380141000146116	stolling van bloed	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12380151000146118	hemostase	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12380161000146115	bloedstolling	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)
12494491000146119	hemostase (waarneembare entiteit)	nl	Fully specified name	Active	Entire term case insensitive (core metadata concept)	SNOMED CT Netherlands NRC maintained module (core metadata concept)