he·mo·phil·i·a

[hee-muh-fil-ee-uh, -feel-yuh, hem-uh-]
noun
any of several X-linked genetic disorders, symptomatic chiefly in males, in which excessive bleeding occurs owing to the absence or abnormality of a clotting factor in the blood.

Origin:
1850–55; < Neo-Latin; see hemo-, -philia

Dictionary.com Unabridged
Based on the Random House Dictionary, © Random House, Inc. 2013.
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Collins
World English Dictionary
haemophilia or hemophilia (ˌhiːməʊˈfɪlɪə, ˌhɛm-, ˌhiːməʊˈfɪlɪə, ˌhɛm-) [Click for IPA pronunciation guide]
 
n
an inheritable disease, usually affecting only males but transmitted by women to their male children, characterized by loss or impairment of the normal clotting ability of blood so that a minor wound may result in fatal bleeding
 
hemophilia or hemophilia
 
n
 
haemo'philioid or hemophilia
 
adj
 
hemo'philioid or hemophilia
 
adj

Collins English Dictionary - Complete & Unabridged 10th Edition
2009 © William Collins Sons & Co. Ltd. 1979, 1986 © HarperCollins
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00:10
Hemophilia is always a great word to know.
So is lollapalooza. Does it mean:
an arrangement of five objects, as trees, in a square or rectangle, one at each corner and one in the middle.
an extraordinary or unusual thing, person, or event; an exceptional example or instance.
Etymonline
Word Origin & History

hemophilia
1854 (in Anglicized form hæmophily), from Ger. hämophile, coined in Mod.L. in 1828 by Ger. physician Johann Lucas Schönlein (1793-1864), from Gk. haima "blood" (see -emia) + philia "to love," related to philos "loving."
Online Etymology Dictionary, © 2010 Douglas Harper
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American Heritage
Medical Dictionary

hemophilia he·mo·phil·i·a (hē'mə-fĭl'ē-ə, -fēl'yə)
n.
Any of several hereditary blood-coagulation disorders, manifested almost exclusively in males, in which the blood fails to clot normally because of a deficiency or an abnormality of one of the clotting factors.

The American Heritage® Stedman's Medical Dictionary
Copyright © 2002, 2001, 1995 by Houghton Mifflin Company. Published by Houghton Mifflin Company.
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American Heritage
Science Dictionary
hemophilia   (hē'mə-fĭl'ē-ə)  Pronunciation Key 
Any of several hereditary coagulation disorders, seen almost exclusively in males, in which the blood fails to clot normally because of a deficiency or an abnormality of one of the clotting factors.
The American Heritage® Science Dictionary
Copyright © 2002. Published by Houghton Mifflin. All rights reserved.
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American Heritage
Cultural Dictionary
hemophilia [(hee-muh-fil-ee-uh, hee-muh-feel-yuh)]

A hereditary disease caused by a deficiency of a substance in the blood that aids in clotting. Hemophiliacs can bleed to death even from small cuts and bruises, because their blood has largely lost the ability to clot.

Note: Queen Victoria of Britain, whose descendants have been kings and queens of several countries in Europe, carried the gene for hemophilia, which has turned up repeatedly in royal families since her lifetime. Her great-grandson, the heir to the throne of Russia, suffered from the disease, and his parents fell under the influence of the monk Grigori Rasputin in hopes of a miraculous cure. The resulting chaos in the government of Russia helped bring on the Russian Revolution and the establishment of the Soviet Union.
The American Heritage® New Dictionary of Cultural Literacy, Third Edition
Copyright © 2005 by Houghton Mifflin Company.
Published by Houghton Mifflin Company. All rights reserved.
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Example sentences
The disease is similar to hemophilia, except bleeding into joints is less common.
Hemophilia causes delayed bleeding, which can occur spontaneously or after an injury.
Hemophilia is a rare genetic condition in which the blood doesn't clot normally.
Hemophilia is an inherited bleeding disorder in which the blood does not clot properly.
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