74848003: Hemostatic function (observable entity)

SNOMED CT Concept\Observable entity\Function (observable entity)\Hematologic function\Hemostatic function

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

Descriptions:

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
Thrombocytopenia due to blood loss	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Factor IX deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary thrombocytopenia with normal platelets	Interprets	True	Hemostatic function	Inferred relationship	Some	2
von Willebrand disease, type IIB	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Dysfibrinogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2A	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Mild hereditary factor IX deficiency disease with inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to increase in anti-8a (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Platelet disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Gamma chain defect dysfibrinogenaemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Pseudo von Willebrand disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Passovoy factor deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary von Willebrand disease type 2	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hypoplasminogenaemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Purpura due to prolonged vomiting and/or coughing (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Postpartum afibrinogenemia with hemorrhage	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Mild hereditary factor IX deficiency disease without inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Wiskott-Aldrich autosomal dominant variant syndrome (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Familial multiple factor deficiency syndrome, type VI	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial thrombocytosis (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Moderate hereditary factor VIII deficiency disease without inhibitor (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Itching purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Kasabach-Merritt syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Protein S deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Thrombocytopenic disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hyperfibrinogenemia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Post infectious thrombocytopenic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Thrombocytopenia due to extracorporeal circulation (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Primary non-thrombocytopenic purpura (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Blood coagulation disorder with shortened bleeding time	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Montreal platelet syndrome (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Deficiency of naturally occurring coagulation factor inhibitor	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Giant platelet syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Factor XI deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Platelet membrane defect	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Blood coagulation disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hemorrhagic disorder due to increase in anti-9a	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Drug induced thrombotic thrombocytopenic purpura (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	8
maladie de Von Willebrand,type 1	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Cyclic thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Factor XI deficiency, type III	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Acquired purpura fulminans (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	4
Prothrombin complex deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Moderate hereditary factor VIII deficiency disease (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Factor VII deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
abortus provocatus non lege artis met afibrinogenemie	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Hereditary von Willebrand disease type 3	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Blood coagulation disorder complicating pregnancy (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hereditary hypoplasminogenemia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Secondary thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Idiopathic factor VIII deficiency (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Mixed alpha granule and dense body deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Stellate pseudoscar in senile purpura (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Hereditary factor II deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Secondary autoimmune thrombocytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Failed attempted abortion with defibrination syndrome (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial hemorrhagic diathesis	Interprets	True	Hemostatic function	Inferred relationship	Some	1
dermite ocre	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Multiple sclerosis, ichthyosis, factor VIII deficiency syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	3
GATA binding protein 1 related thrombocytopenia with dyserythropoiesis (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Macrothrombocytopenia with mitral valve insufficiency	Interprets	False	Hemostatic function	Inferred relationship	Some	3
Failed attempted abortion with afibrinogenemia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Blood coagulation disorder with prolonged bleeding time	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Mediterranean thrombocytopenia	Interprets	False	Hemostatic function	Inferred relationship	Some	2
parodontitis gelijktijdig met syndroom van Chédiak-Higashi	Interprets	False	Hemostatic function	Inferred relationship	Some	3
maladie de von Willebrand type 2M	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Hereditary factor X deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
maladie de von Willebrand type 2B	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Blood coagulation disorder complicating childbirth	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hemophilia	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Chronic acquired pure red cell aplasia	Interprets	False	Hemostatic function	Inferred relationship	Some	6
Homozygous prothrombin G20210A mutation (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Familial multiple factor deficiency syndrome, type I (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Late onset diffuse bleeding diathesis secondary to vitamin K deficient hemorrhagic disease of fetus and newborn (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Steroid purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Acquired factor IX deficiency disease	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Haemorrhagic disorder due to increase in anti-10a	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Non-thrombocytopenic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Postpartum coagulation defects	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Postpartum fibrinolysis with hemorrhage	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Acquired pancytopenia	Interprets	True	Hemostatic function	Inferred relationship	Some	5
maladie de von Willebrand, type IIE	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Fibrinogen abnormality	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Miscarriage with defibrination syndrome	Interprets	True	Hemostatic function	Inferred relationship	Some	1
maladie de von Willebrand, type IIA	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Antiprothrombin disorder	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Radioulnar synostosis with amegakaryocytic thrombocytopenia syndrome (disorder)	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Capillary fragility abnormality	Interprets	True	Hemostatic function	Inferred relationship	Some	3
Thrombocytopenia due to extracorporeal circulation of blood	Interprets	True	Hemostatic function	Inferred relationship	Some	2
maladie de von Willebrand, type IIF	Interprets	False	Hemostatic function	Inferred relationship	Some	1
Neonatal antiphospholipid syndrome (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Acquired PF-3 disease	Interprets	False	Hemostatic function	Inferred relationship	Some	2
Autosomal dominant deficiency of plasminogen	Interprets	True	Hemostatic function	Inferred relationship	Some	1
High molecular weight kininogen deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
pancytopenie-dysmeliesyndroom	Interprets	False	Hemostatic function	Inferred relationship	Some	5
Autoimmune factor VIII deficiency	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Secondary non-thrombocytopenic purpura	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Platelet factor V deficiency (factor V Quebec)	Interprets	True	Hemostatic function	Inferred relationship	Some	1
Hyperglobulinemic purpura (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	2
Hereditary thrombophilia (disorder)	Interprets	True	Hemostatic function	Inferred relationship	Some	1

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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
124304016	Hemostatic function, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
124305015	Hemostasis, NOS	en	Synonym (core metadata concept)	Inactive	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	Entire term case insensitive (core metadata concept)	SNOMED CT core
124308018	Haemostasis, NOS	en	Synonym (core metadata concept)	Inactive	Only initial character case insensitive (core metadata concept)	SNOMED CT core
124309014	Haemostatic function, NOS	en	Synonym (core metadata concept)	Inactive	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	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
815392011	Hemostatic function (function)	en	Fully specified name	Inactive	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
7557891000172118	hemostatische functie	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7557901000172119	bloedstolling	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7557911000172116	stolling van bloed	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)
7557921000172114	hemostase	nl	Synonym (core metadata concept)	Active	Entire term case insensitive (core metadata concept)	Belgian module (core metadata concept)