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

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