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74848003: Hemostatic function (observable entity)

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

Descriptions:

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

48 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hemostatic function Is a Hematologic function true Inferred relationship Existential restriction modifier
Inbound Relationships Type Active Source Characteristic Refinability Group
Hereditary thrombophilia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Cryofibrinogenemic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Immune thrombocytopenic purpura Interprets False Hemostatic function Inferred relationship Existential restriction modifier 4
Stasis purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Purpura due to increased intravascular pressure Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Cryoglobulinemic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Heterozygous protein S deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Acquired red cell aplasia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 6
Early onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary factor XIII A subunit deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Exhausted platelets Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Alpha-2-antiplasmin deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Postpartum coagulation defect with hemorrhage Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Autoimmune neonatal thrombocytopenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Blood coagulation disorder with impaired clot retraction time Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Afibrinogenemia following molar AND/OR ectopic pregnancy Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Factor XI deficiency, type II Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor IX deficiency disease without inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Megakaryocytic aplasia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Neonatal thrombocytopenia due to platelet alloimmunization Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
von Willebrand disease type 2A Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Heterozygous prothrombin G20210A mutation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to increase in anti-11a Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Fibrinolytic bleeding syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Purpura annularis telangiectodes of Majocchi Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Induced termination of pregnancy complicated by defibrination syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Senile purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Familial multiple factor deficiency syndrome, type II Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Qualitative platelet disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Constitutional aplastic anemia with malformation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Factor VIII deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Combined coagulation factor deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Fibrinolysis - postpartum Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor IX deficiency disease with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor XIII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome, type IV Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Classic onset hemorrhagic disease of newborn due to vitamin K deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary elevated factor XI Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Factitious purpura Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Embolic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Severe hereditary factor VIII deficiency disease without inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Miscarriage with afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Autoimmune pancytopenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 5
Posttransfusion purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Systemic fibrinogenolysis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary combined coagulation factor deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Postpartum coagulation defects - delivered with postnatal problem Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary antithrombin III deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Thrombophilia associated with pregnancy Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Platelet type von Willebrand's disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary hyperfibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Moderate hereditary factor VIII deficiency disease with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Thrombocytopathy, asplenia and miosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Neonatal thrombocytopenia associated with maternal idiopathic thrombocytopenic purpura Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombotic thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Hyperheparinemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary elevated factor VIII Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Dysplasminogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor VII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Pregnancy-related factor VIII deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Eczematid-like purpura of Doucas and Kapetanakis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Hereditary factor XII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Waldenstrom's hypergammaglobulinemic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired platelet function disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Dysproteinemic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Afibrinogenemia - postpartum Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor VIII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Purpuric disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Severe hereditary factor VIII deficiency disease with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Factor XI deficiency, type I Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
von Willebrand disease, type IIG Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Legal abortion with defibrination syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 1
Combined deficiency of factor V and factor VIII Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Myosin heavy chain 9 non muscle related disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary von Willebrand disease type 2N Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Thrombocytosis Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Amegakaryocytic thrombocytopenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Postpartum coagulation defects with postnatal problem Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Familial thrombomodulin anomalies Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Familial multiple factor deficiency syndrome, type V Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Dense body defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Transient neonatal thrombocytopenia due to exchange transfusion Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Prekallikrein deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Anticoagulant-induced bleeding Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Primary thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Disseminated intravascular coagulation in newborn Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Protein C deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hemorrhagic disorder due to circulating anticoagulants Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hypodysfibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Severe hereditary factor VIII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary von Willebrand disease type 1A Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Thrombocythemia with distal limb defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Congenital amegakaryocytic thrombocytopenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Mild hereditary factor VIII deficiency disease with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary dysplasminogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Hereditary factor VIII deficiency disease with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1
Aplastic anemia associated with pregnancy Interprets True Hemostatic function Inferred relationship Existential restriction modifier 6
Purpura simplex Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Benign primary hypergammaglobulinemic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Mild hereditary factor VIII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 1

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