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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
124302017 Hemostatic function en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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 Only initial character 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
815392011 Hemostatic function (function) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1204583012 Hemostatic function (observable entity) en Fully specified name Active Only initial character 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
190321000077117 hémostase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
190321000077117 hémostase fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

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 Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Amegakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Megakaryocytic thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
May-Hegglin anomaly Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
syndrome d'Epstein Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 4
Montreal platelet syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Mediterranean thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Post-splenectomy thrombocytosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Platelet type pseudo-von Willebrand disease Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Pancytopenia-dysmelia Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 5
Essential thrombocythemia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Parvoviral aplastic crisis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 7
Thrombocytosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplastic anaemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 7
Platelet dysfunction associated with uremia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Aplastic anaemia due to infection Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 8
Hereditary thrombocytopenic disorder (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital dysmegakaryopoietic thrombocytopenia, Paris Trousseau type (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Autoimmune neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Wiskott-Aldrich autosomal dominant variant syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Thrombocytopenia due to sequestration Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Neonatal thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Medich giant platelet syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Attenuated Chédiak-Higashi syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Familial thrombocytosis (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Revesz syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 9
Congenital amegakaryocytic thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired platelet disorder Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Chronic acquired pure red cell aplasia Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 6
Aplastic anemia caused by antineoplastic agent Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 7
X-linked dyserythropoietic anemia with abnormal platelets and neutropenia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 7
Pancytopenia due to IKZF1 mutations Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 6
A rare haemorrhagic disorder due to a platelet anomaly characterised by dysfunctional platelets of abnormally large size, moderate thrombocytopenia, prolonged bleeding time and mild bleeding diathesis (ecchymoses and epistaxis), associated with mitral valve insufficiency. Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Bleeding disorder due to glycoprotein VI deficiency (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Ataxia pancytopenia syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 6
Thrombocytopenia due to severe acute respiratory syndrome coronavirus 2 (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 4
Familial pigmented purpuric eruption (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 5
Fetal thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Fetal hemophilia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Upshaw-Schulman syndrome (disorder) Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Autoimmune thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 5
Acquired thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 5
Drug induced thrombotic thrombocytopenic purpura (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Deficiency of coagulation factor due to vitamin K malabsorption (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Deficiency of coagulation factor due to vitamin K malabsorption in obstructive biliary disease (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Deficiency of factor X due to systemic amyloidosis (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Disorder of fibrinolysis caused by drug (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Fibrinolytic disorder caused by tissue plasminogen activator Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Fibrinolytic disorder caused by urokinase Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Pancytopenia caused by anticonvulsant Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Pancytopenia caused by antithyroid drug (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Vaccine-induced prothrombotic immune thrombocytopenia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
X-linked thrombocytopenia with normal platelets (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired prekallikrein deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Hereditary congenital prekallikrein deficiency (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
DIAPH1-related sensorineural hearing loss-thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Macrothrombocytopenia, lymphedema, developmental delay, facial dysmorphism, camptodactyly syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Hereditary thrombocytopenia with early-onset myelofibrosis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Cytosolic phospholipase-A2 alpha deficiency associated bleeding disorder (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Antepartum hemorrhage with afibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Antepartum hemorrhage with coagulation defect (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Antepartum haemorrhage with hyperfibrinolysis Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Antepartum hemorrhage with coagulation defect - delivered Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Antepartum hemorrhage with coagulation defect - not delivered Interprets False Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Antepartum hemorrhage with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Antepartum hemorrhage with disseminated intravascular coagulation (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Maternal perinatal purpura (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Fetal purpura (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Autosomal dominant thrombocytopenia with platelet secretion defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Severe autosomal recessive macrothrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Thrombocytopenia, anasarca, fever, renal insufficiency, organomegaly syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired antithrombin III deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Premature separation of placenta with coagulation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare genetic coagulation disorder characterized by marked bleeding tendency and posttraumatic bleeding with easy bruising, soft tissue and muscle bleeding, hemarthroses, and menorrhagia due to an increase of soluble thrombomodulin in plasma with subsequent protein C activation and reduction of thrombin generation within a potential thrombus. Abnormal laboratory findings include markedly elevated plasma thrombomodulin, reduced prothrombin consumption, and decreased thrombin generation. Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Congenital autosomal recessive small-platelet thrombocytopenia (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Multifocal lymphangioendotheliomatosis, thrombocytopenia syndrome Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Acquired protein S deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired protein C deficiency Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Acquired heparin cofactor II deficiency (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Intrapartum hemorrhage with coagulation defect Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Parturient hemorrhage associated with hypofibrinogenemia Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Postpartum afibrinogenemia with hemorrhage (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 4
Pigmented purpuric dermatosis (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 5
Lichen aureus Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 6
Progressive pigmentary dermatosis of Schamberg Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 6
Upshaw-Schulman syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 2
Hereditary von Willebrand disease Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Hematopoietic subsyndrome of acute radiation syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Afibrinogenemia following molar pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 4
Afibrinogenemia following ectopic pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 4
Defibrination syndrome following molar pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Defibrination syndrome following ectopic pregnancy (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Postpartum hemolysis-elevated liver enzymes-low platelet count syndrome (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 3
Fanconi anemia of complementation group C Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 7
Mild hereditary factor VIII deficiency disease with high response inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Mild hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe hereditary factor VIII deficiency disease with high response inhibitor (disorder) Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Severe hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Moderate hereditary factor VIII deficiency disease with high response inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1
Moderate hereditary factor VIII deficiency disease with low response inhibitor Interprets True Hemostatic function Inferred relationship Existential restriction modifier (core metadata concept) 1

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