Classical hemophilia
Deficiency factor VIII with functional defect)
Hemophilia NOS
Hemophilia A
An inherited deficiency of coagulation factor viii characterized by the tendency to spontaneous or exaggerated post-traumatic hemorrhage. Inherited as an x-linked recessive disease, hemophilia a is the most common hemophilia, occurring in approximately 1 in 10,000 male births.
Classic hemophilia resulting from a deficiency of factor viii; an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
The classic hemophilia resulting from a deficiency of factor viii. It is an inherited disorder of blood coagulation characterized by a permanent tendency to hemorrhage.
capillary fragility (hereditary) (D69.8)
factor VIII deficiency NOS (D66)
factor VIII deficiency with functional defect (D66)