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74848003: Hemostatic function (observable entity)

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

Descriptions:

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

28 descendants. Search Descendants:

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
Mild hereditary factor VIII deficiency disease (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary platelet function disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Postinfective immunoglobulin A vasculitis (disorder) Interprets False Hemostatic function Inferred relationship Some 3
Blood coagulation disorder, categorized by value of screening test Interprets True Hemostatic function Inferred relationship Some 1
Factor X deficiency Interprets True Hemostatic function Inferred relationship Some 1
Thrombocytopenic purpura due to defective platelet production (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Homozygous protein S deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Factor I deficiency disease (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Transient neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Thrombocytopenia due to non-immune destruction Interprets True Hemostatic function Inferred relationship Some 2
A disintegrin and metalloproteinase with thrombospondin type 1 motif 13 deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Defect of purinergic receptor p2y G protein-coupled 12 (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Gray platelet syndrome Interprets True Hemostatic function Inferred relationship Some 1
Purpura rheumatica Interprets False Hemostatic function Inferred relationship Some 2
Hemorrhagic disease due to alpha-1-antitrypsin Pittsburgh mutation Interprets True Hemostatic function Inferred relationship Some 1
von Willebrand disease, type IIC Interprets False Hemostatic function Inferred relationship Some 1
Lupus anticoagulant disorder Interprets True Hemostatic function Inferred relationship Some 1
Thrombocytopenic purpura associated with metabolic disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Antithrombin III deficiency Interprets True Hemostatic function Inferred relationship Some 1
White platelet syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2M Interprets True Hemostatic function Inferred relationship Some 1
Hereditary heparin cofactor II deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Thromboxane generation defect Interprets True Hemostatic function Inferred relationship Some 1
Pigmented purpuric lichenoid dermatitis of Gougerot and Blum Interprets True Hemostatic function Inferred relationship Some 1
Hereditary von Willebrand disease type 2B Interprets True Hemostatic function Inferred relationship Some 1
DK phocomelia syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Amegakaryocytic thrombocytopenia with congenital malformation Interprets True Hemostatic function Inferred relationship Some 3
Hereditary factor V deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
Anti-factor II disorder Interprets True Hemostatic function Inferred relationship Some 1
Anticoagulant excess without bleeding Interprets True Hemostatic function Inferred relationship Some 1
von Willebrand disease type IA Interprets False Hemostatic function Inferred relationship Some 1
Radial aplasia-thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Some 2
Factor XIII deficiency disease Interprets True Hemostatic function Inferred relationship Some 1
Blood coagulation disorder due to liver disease Interprets True Hemostatic function Inferred relationship Some 1
Severe hereditary factor IX deficiency disease with inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Haemorrhagic disorder due to antithrombinaemia Interprets True Hemostatic function Inferred relationship Some 1
Alpha chain defect dysfibrinogenemia Interprets True Hemostatic function Inferred relationship Some 1
Familial multiple factor deficiency syndrome, type III Interprets True Hemostatic function Inferred relationship Some 1
Upshaw-Schulman syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 8
Congenital thrombocytopenic purpura Interprets False Hemostatic function Inferred relationship Some 3
Hereditary von Willebrand disease type 1B Interprets True Hemostatic function Inferred relationship Some 1
Factor II deficiency Interprets True Hemostatic function Inferred relationship Some 1
Contact purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Homozygous protein C deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Sex-linked thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Revesz syndrome (disorder) Interprets False Hemostatic function Inferred relationship Some 8
Mild hereditary factor VIII deficiency disease without inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
von Willebrand disorder Interprets True Hemostatic function Inferred relationship Some 1
Megakaryocytic thrombocytopenia Interprets False Hemostatic function Inferred relationship Some 2
Purpura pigmentosa chronica Interprets True Hemostatic function Inferred relationship Some 2
Acute haemorrhagic oedema of childhood Interprets False Hemostatic function Inferred relationship Some 3
Clothing purpura (disorder) Interprets True Hemostatic function Inferred relationship Some 2
von Willebrand disease, type IIH Interprets False Hemostatic function Inferred relationship Some 1
Legal abortion with afibrinogenemia Interprets False Hemostatic function Inferred relationship Some 1
MYH9 macrothrombocytopenia syndrome Interprets False Hemostatic function Inferred relationship Some 1
Secondary cutaneous vasculitis (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Afibrinogenemia Interprets True Hemostatic function Inferred relationship Some 1
Heterozygous protein C deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Thrombocytopenic purpura due to platelet consumption (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Severe hereditary factor IX deficiency disease without inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Essential thrombocythemia (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Refractory thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Hereditary hyperhomocysteinemia (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary factor XIII B subunit deficiency (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary coagulation factor deficiency Interprets True Hemostatic function Inferred relationship Some 1
Transient neonatal thrombocytopenia due to isoimmunisation Interprets True Hemostatic function Inferred relationship Some 2
Vitamin K deficiency coagulation disorder Interprets True Hemostatic function Inferred relationship Some 1
Thrombophilia Interprets True Hemostatic function Inferred relationship Some 1
Reactive thrombocytosis Interprets True Hemostatic function Inferred relationship Some 2
Homozygous Factor V Leiden mutation Interprets True Hemostatic function Inferred relationship Some 1
Neonatal thrombocytopenia due to idiopathic maternal thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 2
Coagulation factor deficiency syndrome Interprets True Hemostatic function Inferred relationship Some 1
Hermansky-Pudlak syndrome Interprets True Hemostatic function Inferred relationship Some 3
Acquired hemophilia Interprets True Hemostatic function Inferred relationship Some 1
Aplastic anemia due to drugs Interprets True Hemostatic function Inferred relationship Some 8
Acquired factor V deficiency disease Interprets True Hemostatic function Inferred relationship Some 2
Systemic lupus erythematosus-associated antiphospholipid syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Perinatal purpura Interprets False Hemostatic function Inferred relationship Some 3
Heparin-induced thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 3
Bleeding diathesis due to thromboxane synthesis deficiency Interprets True Hemostatic function Inferred relationship Some 4
Congenital factor IX deficiency without inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Neonatal thrombocytopenia Interprets False Hemostatic function Inferred relationship Some 3
Bleeding diathesis due to collagen receptor defect Interprets True Hemostatic function Inferred relationship Some 2
Congenital plasminogen activator inhibitor deficiency type 1 (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Thrombophilia due to acquired protein S deficiency Interprets False Hemostatic function Inferred relationship Some 2
Thrombocytopenia due to hypersplenism Interprets True Hemostatic function Inferred relationship Some 3
Immune thrombocytopenia Interprets True Hemostatic function Inferred relationship Some 4
Factor V inhibitor disorder Interprets True Hemostatic function Inferred relationship Some 2
Acquired factor X deficiency disease Interprets True Hemostatic function Inferred relationship Some 2
Thrombophilia caused by drug therapy Interprets False Hemostatic function Inferred relationship Some 2
Pancytopenia caused by medication (disorder) Interprets True Hemostatic function Inferred relationship Some 1
Hereditary dysfibrinogenemia (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Severe fever with thrombocytopenia syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 6
Immunologic aplastic anemia Interprets True Hemostatic function Inferred relationship Some 7
Vascular hemostatic disease Interprets True Hemostatic function Inferred relationship Some 3
Thrombocytopenia with acquired immunodeficiency syndrome (disorder) Interprets True Hemostatic function Inferred relationship Some 3
Acquired coagulation factor inhibitor disorder (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Hereditary combined deficiency of vitamin K-dependent clotting factors (disorder) Interprets True Hemostatic function Inferred relationship Some 2
Platelet dysfunction caused by aspirin (disorder) Interprets False Hemostatic function Inferred relationship Some 2
Thrombocytopenia due to defective platelet production Interprets True Hemostatic function Inferred relationship Some 3
Pancytopenia with pancreatitis Interprets True Hemostatic function Inferred relationship Some 7

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