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74848003: Hemostatic function (observable entity)

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

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

28 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Haemostatic function Is a Haematologic function true Inferred relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Thrombocytopenic purpura due to platelet consumption Interprets True Haemostatic function Inferred relationship Some 3
Severe hereditary factor IX deficiency disease without inhibitor Interprets True Haemostatic function Inferred relationship Some 1
Essential thrombocythaemia Interprets False Haemostatic function Inferred relationship Some 2
Refractory thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Hereditary hyperhomocysteinemia Interprets True Haemostatic function Inferred relationship Some 1
Hereditary factor XIII B subunit deficiency Interprets True Haemostatic function Inferred relationship Some 1
Hereditary coagulation factor deficiency Interprets True Haemostatic function Inferred relationship Some 1
Transient neonatal thrombocytopenia due to isoimmunisation Interprets True Haemostatic function Inferred relationship Some 2
Vitamin K deficiency coagulation disorder Interprets True Haemostatic function Inferred relationship Some 1
Thrombophilia Interprets True Haemostatic function Inferred relationship Some 1
Reactive thrombocytosis Interprets True Haemostatic function Inferred relationship Some 2
Homozygous Factor V Leiden mutation Interprets True Haemostatic function Inferred relationship Some 1
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 2
Coagulation factor deficiency syndrome Interprets True Haemostatic function Inferred relationship Some 1
Hermansky-Pudlak syndrome Interprets True Haemostatic function Inferred relationship Some 3
Kaolin induced coagulation Is a True Haemostatic function Inferred relationship Some
Acquired haemophilia Interprets True Haemostatic function Inferred relationship Some 1
Aplastic anaemia due to drugs Interprets True Haemostatic function Inferred relationship Some 8
Acquired factor V deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Systemic lupus erythematosus-associated antiphospholipid syndrome Interprets True Haemostatic function Inferred relationship Some 3
Perinatal purpura Interprets False Haemostatic function Inferred relationship Some 3
Heparin-induced thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Bleeding diathesis due to thromboxane synthesis deficiency Interprets True Haemostatic function Inferred relationship Some 4
Congenital factor IX deficiency without inhibitor Interprets True Haemostatic function Inferred relationship Some 2
Neonatal thrombocytopenia Interprets False Haemostatic function Inferred relationship Some 3
Bleeding diathesis due to collagen receptor defect Interprets True Haemostatic function Inferred relationship Some 2
Congenital plasminogen activator inhibitor deficiency type 1 Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to acquired protein S deficiency Interprets False Haemostatic function Inferred relationship Some 2
Thrombocytopenia due to hypersplenism Interprets True Haemostatic function Inferred relationship Some 3
Immune thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 4
Factor V inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Acquired factor X deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to drug therapy Interprets True Haemostatic function Inferred relationship Some 2
Pancytopenia due to medicine Interprets True Haemostatic function Inferred relationship Some 1
Hereditary dysfibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Severe fever with thrombocytopenia syndrome virus Interprets True Haemostatic function Inferred relationship Some 6
Immunologic aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 7
Vascular haemostatic disease Interprets True Haemostatic function Inferred relationship Some 3
Thrombocytopenia with AIDS (acquired immunodeficiency syndrome) Interprets True Haemostatic function Inferred relationship Some 3
Acquired coagulation factor inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Hereditary combined deficiency of vitamin K-dependent clotting factors Interprets True Haemostatic function Inferred relationship Some 2
Platelet dysfunction due to aspirin Interprets False Haemostatic function Inferred relationship Some 2
Thrombocytopenia due to defective platelet production Interprets True Haemostatic function Inferred relationship Some 3
Pancytopenia with pancreatitis Interprets True Haemostatic function Inferred relationship Some 7
Scott syndrome Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia co-occurrent with HIV infection Interprets True Haemostatic function Inferred relationship Some 8
Acquired inhibitor of coagulation Interprets True Haemostatic function Inferred relationship Some 2
Pure red cell aplasia, acquired Interprets False Haemostatic function Inferred relationship Some 7
Ataxia pancytopenia syndrome Interprets False Haemostatic function Inferred relationship Some 6
Platelet dysfunction due to drugs Interprets False Haemostatic function Inferred relationship Some 3
Cellular immunologic aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 8
Resistance to activated protein C due to Factor V Leiden Interprets True Haemostatic function Inferred relationship Some 2
Anticoagulant overdosage Interprets False Haemostatic function Inferred relationship Some 2
Thrombophilia due to antineoplastic agent therapy Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to trauma Interprets True Haemostatic function Inferred relationship Some 2
Isolated collagen aggregation defect Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to myeloproliferative disorder Interprets True Haemostatic function Inferred relationship Some 2
Thrombocytopenia due to hypothermia Interprets True Haemostatic function Inferred relationship Some 4
Wiskott-Aldrich syndrome Interprets True Haemostatic function Inferred relationship Some 3
Primary antiphospholipid syndrome Interprets True Haemostatic function Inferred relationship Some 2
Primary antiphospholipid syndrome with organ/system involvement Interprets False Haemostatic function Inferred relationship Some 2
Hereditary thrombophilia due to congenital histidine-rich (poly-L) glycoprotein deficiency Interprets True Haemostatic function Inferred relationship Some 2
Primary antiphospholipid syndrome with multisystem involvement Interprets True Haemostatic function Inferred relationship Some 2
Secondary antiphospholipid syndrome Interprets True Haemostatic function Inferred relationship Some 2
Secondary antiphospholipid syndrome with organ/system involvement Interprets False Haemostatic function Inferred relationship Some 2
Secondary antiphospholipid syndrome with multisystem involvement Interprets True Haemostatic function Inferred relationship Some 2
Chronic idiopathic thrombocytopenic purpura Interprets True Haemostatic function Inferred relationship Some 5
Aplastic anaemia due to chronic disease Interprets True Haemostatic function Inferred relationship Some 8
Haemorrhagic disease of the newborn due to factor II deficiency Interprets True Haemostatic function Inferred relationship Some 4
Thrombophilia due to paroxysmal nocturnal haemoglobinuria Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia due to infection Interprets False Haemostatic function Inferred relationship Some 8
Platelet secretory disorder Interprets False Haemostatic function Inferred relationship Some 2
Familial platelet syndrome with predisposition to acute myelogenous leukaemia Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia due to radiation Interprets True Haemostatic function Inferred relationship Some 8
Acute purpuric eruption of skin Interprets False Haemostatic function Inferred relationship Some 4
Acquired factor VIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Acquired factor XI deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Metabolic purpura Interprets True Haemostatic function Inferred relationship Some 3
Acquired aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 7
Perinatal thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Congenital afibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Secondary aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 7
Factor XI inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Factor IX inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Bleeding disorder due to glycoprotein VI deficiency Interprets False Haemostatic function Inferred relationship Some 2
Thrombophilia due to acquired antithrombin III deficiency Interprets False Haemostatic function Inferred relationship Some 2
Doan-Wright syndrome Interprets False Haemostatic function Inferred relationship Some 6
Glanzmann's thrombasthenia Interprets True Haemostatic function Inferred relationship Some 2
X-linked congenital dyserythropoietic anaemia with thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 7
Platelet procoagulant activity deficiency Interprets False Haemostatic function Inferred relationship Some 2
Antiphospholipid syndrome in pregnancy Interprets True Haemostatic function Inferred relationship Some 2
Bernard Soulier syndrome Interprets False Haemostatic function Inferred relationship Some 3
Induced termination of pregnancy complicated by afibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Factor XIII inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Transient neonatal disorder of coagulation Interprets True Haemostatic function Inferred relationship Some 2
Warfarin overdosage Interprets False Haemostatic function Inferred relationship Some 2
Estren-Dameshek anaemia Interprets True Haemostatic function Inferred relationship Some 7
Thrombophilia caused by vascular device Interprets True Haemostatic function Inferred relationship Some 2
Thrombophilia due to immobilisation Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia caused by antineoplastic agent Interprets False Haemostatic function Inferred relationship Some 7
Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency Interprets True Haemostatic function Inferred relationship Some 2

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Reference Sets

Observable entity foundation reference set

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