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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
Pancytopenia with pancreatitis Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Scott syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Aplastic anemia co-occurrent with human immunodeficiency virus infection Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Acquired inhibitor of coagulation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Pure red cell aplasia, acquired Interprets False Hemostatic function Inferred relationship Existential restriction modifier 7
Ataxia pancytopenia syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 6
Platelet dysfunction caused by drugs Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Cellular immunologic aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Resistance to activated protein C caused by Factor V Leiden Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Anticoagulant overdosage Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombophilia caused by antineoplastic agent therapy Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombophilia due to trauma Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Isolated collagen aggregation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombophilia due to myeloproliferative disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombocytopenia caused by hypothermia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Wiskott-Aldrich syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Primary antiphospholipid syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Primary antiphospholipid syndrome with organ/system involvement Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Primary antiphospholipid syndrome with multisystem involvement Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome with organ/system involvement Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Secondary antiphospholipid syndrome with multisystem involvement Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Chronic idiopathic thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Aplastic anemia due to chronic disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Hemorrhagic disease of the newborn due to factor II deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Thrombophilia due to paroxysmal nocturnal hemoglobinuria Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Aplastic anemia due to infection Interprets False Hemostatic function Inferred relationship Existential restriction modifier 8
Platelet secretory disorder Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Familial platelet syndrome with predisposition to acute myelogenous leukemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Aplastic anemia caused by radiation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Acute purpuric eruption of skin Interprets False Hemostatic function Inferred relationship Existential restriction modifier 4
Acquired factor VIII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired factor XI deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Metabolic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Acquired aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Perinatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Congenital afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Secondary aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Factor XI inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Factor IX inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Bleeding disorder due to glycoprotein VI deficiency Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombophilia due to acquired antithrombin III deficiency Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Doan-Wright syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 6
Glanzmann's thrombasthenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
X-linked congenital dyserythropoietic anemia with thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Platelet procoagulant activity deficiency Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Antiphospholipid syndrome in pregnancy Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Bernard Soulier syndrome Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Induced termination of pregnancy complicated by afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Factor XIII inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Transient neonatal disorder of coagulation Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Warfarin overdosage Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Estren-Dameshek anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Thrombophilia caused by vascular device Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombophilia due to immobilization Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Aplastic anemia caused by antineoplastic agent Interprets False Hemostatic function Inferred relationship Existential restriction modifier 7
Bleeding disorder due to deficiency of calcium and diacylglycerol-regulated guanine nucleotide exchange factor I Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Factor X inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Antiphospholipid syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary factor IX deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital factor IX deficiency variant Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Purpura of skin co-occurrent and due to vascular fragility Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Congenital factor IX deficiency with inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Purpura of skin caused by mechanical force Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease type I Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired combined coagulation factor deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Pancytopenia with developmental delay syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Congenital von Willebrand's disease type II Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital von Willebrand's disease type III Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Disseminated intravascular coagulation due to placental abruption Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired von Willebrand disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
von Willebrand factor inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Factor VIII inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Congenital fibrinogen abnormality Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Parvoviral aplastic crisis Interprets False Hemostatic function Inferred relationship Existential restriction modifier 7
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Humoral immunologic aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Acute idiopathic thrombocytopenic purpura Interprets False Hemostatic function Inferred relationship Existential restriction modifier 5
Congenital alpha-2-antiplasmin deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired fibrinogen abnormality Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Thrombocytopenic purpura Interprets True Hemostatic function Inferred relationship Existential restriction modifier 4
Acquired thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia Interprets False Hemostatic function Inferred relationship Existential restriction modifier 7
Factor I inhibitor disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Acquired coagulation disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Transient neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Purpura fulminans Interprets True Hemostatic function Inferred relationship Existential restriction modifier 5
Acquired factor VII deficiency disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Secondary cryofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Hereditary isolated aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 8
Inherited platelet disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Platelet type pseudo-von Willebrand disease Interprets False Hemostatic function Inferred relationship Existential restriction modifier 3
Constitutional aplastic anemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 7
Glycoprotein Ia defect Interprets False Hemostatic function Inferred relationship Existential restriction modifier 2
Glycoprotein Ib defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier 2
Uremic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3
Acquired storage pool deficiency (platelets) Interprets True Hemostatic function Inferred relationship Existential restriction modifier 3

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