The National Hemophilia Foundation is dedicated to finding better treatments and cures for inheritable bleeding disorders and to preventing the complications of these disorders through education, advocacy and research. Its programs and initiatives are made possible through the generosity of individuals, corporations and foundations as well as through a cooperative agreement with the Centers for Disease Control and Prevention (CDC).
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51-200 employees
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Non-profit Organizations
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7 Penn Plaza,New York,NY,US
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1948
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Hemophilia, Bleeding Disorders, Von Willebrand Disease
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