| hemophilia B |
Haemophilia B (also spelled Hemophilia B or H?ophilia B) is a blood clotting disorder caused by a mutation of the Factor IX gene. It is the second most common form of haemophilia, rarer than haemophilia A. It is sometimes called Christmas disease after Stephen Christmas, the first patient described with this disease. In addition, the first report of its identification was published in the Christmas edition of the British Medical Journal. ...
출처: en.wikipedia.org/wiki/Hemophilia_B
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| hemophiliac |
Haemophilia or hemophilia is the name of any of several hereditary genetic illnesses that impair the body's ability to control bleeding. Genetic deficiencies (or, very rarely, an autoimmune disorder) cause lowered plasma clotting factor activity so as to compromise blood-clotting; when a blood vessel is injured, a scab will not form and the vessel can continue to bleed excessively for a very long period of time. ...
출처: en.wikipedia.org/wiki/Hemophiliac
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| hemophilia |
Group of hereditary disorders in which affected individuals fail to make enough of certain proteins needed to form blood clots.
출처: www.stjude.org/glossary
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| hemophilia |
An inherited disease that affects mostly males and prevents normal blood clotting. It is treated by lifelong injections of a synthetic version of the clotting factor lacking in persons with the disease.
출처: www.amfar.org/cgi-bin/iowa/bridge.html
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| hemophilia |
Any of several hereditary blood-coagulation disorders in which the blood fails to clot normally because of a deficiency or abnormality of one of the clotting factors. Hemophilia, a recessive trait associated with the X-chromosome, is manifested almost exclusively in males. [Heritage]
출처: www.antiquusmorbus.com/English/EnglishH.htm
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