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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
Bleeding disorder due to calcium and DAG-regulated guanine exchange factor-1 deficiency Interprets True Haemostatic function Inferred relationship Some 2
Factor X inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Antiphospholipid syndrome Interprets True Haemostatic function Inferred relationship Some 2
Congenital hypofibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Hereditary factor IX deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Acquired afibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Congenital factor IX deficiency variant Interprets True Haemostatic function Inferred relationship Some 2
Purpura of skin co-occurrent and due to vascular fragility Interprets True Haemostatic function Inferred relationship Some 4
Congenital factor IX deficiency with inhibitor Interprets True Haemostatic function Inferred relationship Some 2
Purpura of skin caused by mechanical force Interprets False Haemostatic function Inferred relationship Some 2
Congenital von Willebrand's disease Interprets False Haemostatic function Inferred relationship Some 2
Congenital von Willebrand's disease type I Interprets False Haemostatic function Inferred relationship Some 2
Acquired combined coagulation factor deficiency Interprets True Haemostatic function Inferred relationship Some 2
Pancytopenia with developmental delay syndrome Interprets True Haemostatic function Inferred relationship Some 7
Congenital von Willebrand's disease type II Interprets False Haemostatic function Inferred relationship Some 2
Congenital von Willebrand's disease type III Interprets False Haemostatic function Inferred relationship Some 2
Disseminated intravascular coagulation due to placental abruption Interprets True Haemostatic function Inferred relationship Some 2
Acquired von Willebrand's disease Interprets True Haemostatic function Inferred relationship Some 2
von Willebrand factor inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Factor VIII inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Congenital fibrinogen abnormality Interprets True Haemostatic function Inferred relationship Some 2
Parvoviral aplastic crisis Interprets False Haemostatic function Inferred relationship Some 7
Hypercoagulability syndrome due to glycosylphosphatidylinositol deficiency Interprets True Haemostatic function Inferred relationship Some 2
Humoural immunologic aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 8
Acute idiopathic thrombocytopenic purpura Interprets False Haemostatic function Inferred relationship Some 5
Congenital alpha-2-antiplasmin deficiency Interprets True Haemostatic function Inferred relationship Some 2
Acquired fibrinogen abnormality Interprets True Haemostatic function Inferred relationship Some 2
Thrombocytopenic purpura Interprets True Haemostatic function Inferred relationship Some 4
Acquired thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
X-linked dyserythropoietic anaemia with abnormal platelets and neutropenia Interprets False Haemostatic function Inferred relationship Some 7
Factor I inhibitor disorder Interprets True Haemostatic function Inferred relationship Some 2
Acquired coagulation disorder Interprets True Haemostatic function Inferred relationship Some 2
Transient neonatal thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Purpura fulminans Interprets True Haemostatic function Inferred relationship Some 5
Acquired factor VII deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Secondary cryofibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Hereditary isolated aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 8
Inherited platelet disorder Interprets True Haemostatic function Inferred relationship Some 2
Platelet type pseudo-von Willebrand disease Interprets False Haemostatic function Inferred relationship Some 3
Constitutional aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 7
Glycoprotein Ia defect Interprets False Haemostatic function Inferred relationship Some 2
Glycoprotein Ib defect Interprets True Haemostatic function Inferred relationship Some 2
Uraemic thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Acquired storage pool deficiency (platelets) Interprets True Haemostatic function Inferred relationship Some 3
Acquired factor XIII deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Thrombocytopenia due to massive blood transfusion Interprets True Haemostatic function Inferred relationship Some 3
Cyclooxygenase deficiency Interprets True Haemostatic function Inferred relationship Some 2
Infection-associated purpura Interprets True Haemostatic function Inferred relationship Some 3
Thromboxane synthetase deficiency Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia with AIDS (acquired immunodeficiency syndrome) Interprets True Haemostatic function Inferred relationship Some 8
Acquired platelet disorder Interprets False Haemostatic function Inferred relationship Some 2
May-Hegglin anomaly Interprets False Haemostatic function Inferred relationship Some 3
Thrombocytopenia due to alcohol Interprets True Haemostatic function Inferred relationship Some 3
Thrombocytopenia due to sequestration Interprets False Haemostatic function Inferred relationship Some 3
Thrombophilia due to malignant neoplasm Interprets True Haemostatic function Inferred relationship Some 2
Congenital thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Neonatal coagulation disorder Interprets True Haemostatic function Inferred relationship Some 2
Aplastic anaemia due to toxic cause Interprets True Haemostatic function Inferred relationship Some 8
Fanconi's anaemia Interprets False Haemostatic function Inferred relationship Some 7
Pancytopenia Interprets True Haemostatic function Inferred relationship Some 6
Acquired hypoplasminogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Drug-induced immune thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Aplastic anaemia Interprets False Haemostatic function Inferred relationship Some 7
Neonatal thrombocytopenia due to exchange transfusion Interprets True Haemostatic function Inferred relationship Some 3
Idiopathic aplastic anaemia Interprets True Haemostatic function Inferred relationship Some 7
Thrombocytopenia co-occurrent and due to alcoholism Interprets True Haemostatic function Inferred relationship Some 4
Primary ITP (immune thrombocytopenia) Interprets True Haemostatic function Inferred relationship Some 3
Platelet dysfunction associated with uraemia Interprets False Haemostatic function Inferred relationship Some 3
Alloimmune thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Accidental coumarin overdose Interprets False Haemostatic function Inferred relationship Some 2
Catastrophic antiphospholipid syndrome Interprets True Haemostatic function Inferred relationship Some 2
Transient acquired pure red cell aplasia Interprets False Haemostatic function Inferred relationship Some 7
Coumarin overdose of undetermined intent Interprets False Haemostatic function Inferred relationship Some 2
Radiation thrombocytopenia Interprets True Haemostatic function Inferred relationship Some 3
Cryofibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Platelet storage pool defect Interprets True Haemostatic function Inferred relationship Some 3
Accidental warfarin overdose Interprets False Haemostatic function Inferred relationship Some 2
Heparin-induced thrombocytopenia with thrombosis Interprets True Haemostatic function Inferred relationship Some 5
Acquired factor XII deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Familial alpha>2< adrenergic receptor defect in platelets Interprets True Haemostatic function Inferred relationship Some 2
Autoimmune thrombotic thrombocytopenic purpura Interprets False Haemostatic function Inferred relationship Some 9
HELLP syndrome Interprets True Haemostatic function Inferred relationship Some 4
Primary cryofibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Acquired thrombotic thrombocytopenic purpura Interprets False Haemostatic function Inferred relationship Some 9
Thrombophilia due to antiphospholipid antibody Interprets False Haemostatic function Inferred relationship Some 2
Hereditary factor I deficiency disease Interprets True Haemostatic function Inferred relationship Some 2
Haemorrhagic disorder due to hyperheparinaemia Interprets True Haemostatic function Inferred relationship Some 2
WT limb blood syndrome Interprets True Haemostatic function Inferred relationship Some 7
Thrombophilia due to hormone therapy Interprets True Haemostatic function Inferred relationship Some 2
Evans syndrome Interprets True Haemostatic function Inferred relationship Some 7
Illegal termination of pregnancy with defibrination syndrome Interprets False Haemostatic function Inferred relationship Some 2
Aplastic anaemia associated with metabolic alteration Interprets True Haemostatic function Inferred relationship Some 8
Acquired hypofibrinogenaemia Interprets True Haemostatic function Inferred relationship Some 2
Heparin overdose Interprets False Haemostatic function Inferred relationship Some 2
Pancytopenia due to IKZF1 mutations Interprets False Haemostatic function Inferred relationship Some 6
Aplastic anaemia associated with pancreatitis Interprets True Haemostatic function Inferred relationship Some 8
Deficiency of coagulation factor due to liver disease Interprets True Haemostatic function Inferred relationship Some 3
Acquired coagulation factor deficiency Interprets True Haemostatic function Inferred relationship Some 2
Accidental heparin overdose Interprets False Haemostatic function Inferred relationship Some 2
Deficiency of coagulation factor due to vitamin K deficiency Interprets True Haemostatic function Inferred relationship Some 2
Intentional heparin overdose Interprets False Haemostatic function Inferred relationship Some 2

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Reference Sets

Observable entity foundation reference set

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