FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.13  |  FHIR Version n/a  User: [n/a]

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

Start Previous Page 5 of 8 Next End


This concept is not in any reference sets

Back to Start