Hem`o*phil"i*a(h`m*fl"* or hm`*fl"*), n. [NL., fr. Gr. a"i^ma, blood + filei^n to love.] (Med.) A condition characterized by a tendency to profuse and uncontrollable hemorrhage from the slightest wounds; it is caused by an absence or abnormality of a clotting factor in the blood, and is a recessive genetic disease linked to the X-chromosome, and therefore usually occurs only in males; there are several specific forms. It may be treated by administering purified clotting factor. It was formerly termed Hematophilia.
[1913 Webster +PJC]
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