| factor v assay | A test used to measure the activity of a blood clotting factor V. This test may be used to evaluate excessive bleeding. Abnormally low factor V assays may be seen in the following conditions: congenital deficiency of factor V, DIC, heparin administration, cirrhosis and primary fibrinolysis. (27 Sep 1997) |
|---|---|
| factor v deficiency | An inherited disorder that results in abnormal blood clotting due to the deficiency of factor V, one of 20 plasma proteins responsible for the maintenance of normal blood clotting. Symptoms include excessive bleeding, bleeding gums, nosebleeds, easy bruising, excessive menstrual bleeding and bleeding into muscle tissue (haematoma) or a joint space (haemarthrosis). Treatment includes the infusion of fresh frozen plasma to restore deficient factor V. (27 Sep 1997) |
| factor V1a | The hexa-amide of cobyrinic acid; a part of the vitamin B12 structure. Synonym: cobyrinamide, cobyrinic hexa-amide, factor V1a. (05 Mar 2000) |
| factor va | <chemical> Activated form of factor v. It is an essential cofactor for the activation of prothrombin catalyzed by factor xa. Chemical name: Blood-coagulation factor Va (12 Dec 1998) |
| factor vii | <chemical> Heat- and storage-stable plasma protein that is activated by tissue thromboplastin to form factor viia in the extrinsic pathway of blood coagulation. The activated form then catalyses the activation of factor x to factor xa. Chemical name: Blood-coagulation factor VII (12 Dec 1998) |
| factor vii assay | A test used to measure the activity of a blood clotting factor VII. This test may be used to evaluate excessive bleeding. Abnormally low factor VII assays may be seen in the following conditions: congenital deficiency of factor VII, fat malabsorption, heparin administration, cirrhosis, vitamin K deficiency and warfarin administration. (27 Sep 1997) |
| factor vii deficiency | An inherited disorder that causes abnormal blood clotting due to the congenital absence of one of the 20 different plasma proteins involved in the coagulation process. Symptoms include bleeding of the gums, nosebleeds, easy bruising, bleeding in muscles or joints and excessive menstrual bleeding. Treatment includes the administration of plasma concentrates of factor VII (extrinsic factor). (27 Sep 1997) |
| factor viia | <enzyme> Activated form of factor vii. Factor viia activates factor x in the extrinsic pathway of blood coagulation. Registry number: EC 3.4.21.21 (12 Dec 1998) |
| factor viii | A coagulation (clotting) factor. Classic haemophilia (haemophilia A) is due to a congenital deficiency in the amount (or activity) of factor VIII. Factor VIII is also known as antihemophiliac factor (AHF) or antihemophiliac globulin (AHG). The gene for factor VIII (that for classic haemophilia) is on the X chromosome so females can be silent carriers without symptoms and males can be haemophiliacs. (12 Dec 1998) |
| factor viii assay | A test used to measure the activity of a blood clotting factor VIII (Von Willebrand factor). This test is usually used to monitor treatment of haemophilia. Abnormally low factor VIII assays may be seen in the following conditions: congenital deficiency of factor VIII (haemophilia), DIC and secondary fibrinolysis. This test may also be performed in the evaluation of Von Willebrand's disease. (27 Sep 1997) |
| factor viii deficiency | A sex-linked genetic disease affecting males that results from a deficiency of clotting factor VIII, a protein factor that is required for normal blood coagulation. Symptoms include easy bruising, bleeding gums, nosebleeds and bleeding into muscle tissue (haematoma) or a joint space (haemarthrosis). Treatment includes the infusion of factor VIII concentrate intravenously to restore this essential factor and normalize blood coagulation. Inheritance: sex-linked. (27 Sep 1997) |
| factor viiia | <chemical> Activated form of factor viii. The b-domain of factor viii is proteolytically cleaved by thrombin to form factor viiia. Factor viiia exists as a non-covalent dimer in a metal-linked (probably calcium) complex and functions as a cofactor in the enzymatic activation of factor x by factor ixa. Factor viiia is similiar in structure and generation to factor va. Chemical name: Blood-coagulation factor VIIIa, procoagulant (12 Dec 1998) |
| factor x | <chemical> Storage-stable glycoprotein blood coagulation factor that can be activated to factor xa by both the intrinsic and extrinsic pathways. A deficiency of factor x, sometimes called stuart-prower factor deficiency, may lead to a systemic coagulation disorder. Chemical name: Blood-coagulation factor X (12 Dec 1998) |
| factor x assay | A test used to measure the activity of a blood clotting factor X. This test may be used to evaluate excessive bleeding. Abnormally low factor X assays may be seen in the following conditions: congenital deficiency of factor X, fat malabsorption, heparin administration, cirrhosis, vitamin K deficiency and warfarin administration. (27 Sep 1997) |
| factor x deficiency | Blood coagulation disorder usually inherited as an autosomal recessive trait, though it can be acquired. It is characterised by defective activity in both the intrinsic and extrinsic pathways, impaired thromboplastin time, and impaired prothrombin consumption. (12 Dec 1998) |
Synonyms : Blood Coagulation Factor VII, Activated, Activated Factor VII, Factor VIIa, Coagulation, VIIa, Coagulation Factor
Synonyms : Blood Coagulation Factor VIII, F VIII-C, Factor VIII-Heavy Chain, Factor VIIIC, Hemofil, Hemofil HM, Hemofil M, Hemophil, Humate-P, Hyate-C, Hyatt-C, Monoclate, F VIII C, Factor VIII Heavy Chain, Factor VIII, Coagulation, Humate P, HumateP, Hyate C, HyateC, Hyatt C
Synonyms : Blood Coagulation Factor VIII, Activated, Activated Factor VIII, Factor VIII, Thrombin Activated, Factor VIIIa, Coagulation, Thrombin-Activated Factor VIII, VIIIa, Coagulation Factor
Synonyms : Blood Coagulation Factor X, Stuart Prower Factor, Factor X, Coagulation, X, Coagulation Factor
Synonyms : Deficiency, Factor X, Deficiency, Stuart-Prower, Deficiency, Stuart-Prower Factor, Stuart-Prower Deficiency, Stuart-Prower Factor Deficiency, Deficiencies, Factor X, Deficiency, Stuart Prower, Deficiency, Stuart Prower Factor, Factor X Deficiencies
| factor XII |
Hageman factor: coagulation factor whose deficiency results in prolongation of clotting time of venous blood
출처: wordnet.princeton.edu/perl/webwn
|
|---|---|
| factor XIII |
fibrinase: in the clotting of blood thrombin catalyzes factor XIII into its active form (fibrinase) which causes fibrin to form a stable clot
출처: wordnet.princeton.edu/perl/webwn
|
| facts of life |
reproduction: the sexual activity of conceiving and bearing offspring
출처: wordnet.princeton.edu/perl/webwn
|
| factitious |
not produced by natural forces; "brokers created a factitious demand for stocks"
출처: wordnet.princeton.edu/perl/webwn
|
| factor |
anything that contributes causally to a result; "a number of factors determined the outcome" component: an abstract part of something; "jealousy was a component of his character"; "two constituents of a musical composition are melody and harmony"; "the grammatical elements of a sentence"; "a key factor in her success"; "humor: an effective ingredient of a speech" any of the numbers (or symbols) that form a product when multiplied together divisor: one of two or more integers that can be exactly divided into another integer; "what are the 4 factors of 6?" agent: a businessman who buys or sells for another in exchange for a commission an independent variable in statistics gene: (genetics) a segment of DNA that is involved in producing a polypeptide chain; it can include regions preceding and following the coding DNA as well as introns between the exons; it is considered a unit of heredity; "genes were formerly called factors" resolve into factors; "a quantum computer can factor the number 15"
출처: wordnet.princeton.edu/perl/webwn
|
| FACT | coagulation factor whose absence is associated with hemophilia B |
|---|---|
| FACT | the constant value of the ratio of two proportional quantities x and y |
| FACT | the ratio of the breaking stress of a structure to the estimated maximum stress in ordinary use |
| FACT | resolve into factors |
| FACT | a coagulation factor |
| FACT | a coagulation factor formed in the kidney under the influence of vitamin K |
| FACT | a coagulation factor (trade name Hemofil) whose absence is associated with hemophilia A |
| FACT | coagulation factor that is converted to an enzyme that converts prothrombin to thrombin in a reaction that depends on calcium ions and other coagulation factors |
| FACT | coagulation factor whose deficiency results in a hemorrhagic tendency |
| FACT | coagulation factor whose deficiency results in prolongation of clotting time of venous blood |
| FACT | in the clotting of blood thrombin catalyzes factor XIII into its active form (fibrinase) which causes fibrin to form a stable clot |
| FACT | the product of all the integers up to and including a given integer |