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n. 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.

n. Alternative spelling of haemophilia.

n. 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.

n. In pathology, a congenital morbid condition characterized by a tendency to bleed immoderately from any insignificant wound, or even spontaneously. Also called hematophilia, hemorrhaphilia, and hemorrhagic diathesis.

n. congenital tendency to uncontrolled bleeding; usually affects males and is transmitted from mother to son

"The division includes inpatient and outpatient services, the Apheresis program, the Transfusion Medicine program and clinical research programs in hemophilia, sickle cell disease, thalassemia and bone marrow failure."

sex-linked disorder    blood disease    blood disorder   

hematophilia   

angiohemophilia    vascular hemophilia    classical haemophilia    classical hemophilia    hemophilia a    hemophilia b    Christmas disease    haemophilia a    von willebrand's disease    haemophilia b   

Emilia    Lilia   

leukopenia    endometriosis    thrombocytopenia    hemolysis    widowerhood    thrombophlebitis    plt    osteoporosis    reproval    choriocarcinoma