haemophilia A

(redirected from Factor VIII deficiency)
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Related to Factor VIII deficiency: factor IX deficiency, Factor VII deficiency
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Synonyms for haemophilia A

hemophilia caused by a congenital deficiency of factor VIII

References in periodicals archive ?
Haemophilia A is a bleeding disease characterized by coagulation factor VIII deficiency, an important protein factor in blood's clotting process.
Hemophilia A, also known as factor VIII deficiency or classic hemophilia, is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
The most common coagulopathy diagnosed was factor VIII deficiency, in 39 patients, followed by activated protein C resistance, in 23 patients, and a deficiency in methylenetetrahydrofolate reductase, also in 23 patients.
Hemophilia A, also called as classical hemophilia or factor VIII deficiency hemophilia, is caused by deficiency of clotting factor VIII.
Antihemophilic Factor/von Willebrand Factor Complex (Human), Alphanate(R), is indicated for the prevention and control of bleeding in patients with Factor VIII deficiency due to hemophilia A or acquired Factor VIII deficiency.
ADVATE[Antihemophilic Factor (Recombinant)] is a recombinant antihemophilic factor indicated for use in children and adults with hemophilia A (congenital factor VIII deficiency or classic hemophilia) for:
ADVATE is a recombinant antihemophilic factor indicated for use in children and adults with hemophilia A (congenital factor VIII deficiency or classic hemophilia) for:
About hemophilia A Hemophilia A, also called Factor VIII deficiency or classic hemophilia, is a genetic disorder caused by missing or defective Factor VIII, a clotting protein.
Hemophilia A is caused by a factor VIII deficiency and occurs in ~1 out of every 5,000 male births.
About Hemophilia A Hemophilia A, also known as factor VIII deficiency or classic hemophilia, is a largely inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
Hemophilia A, also known as factor VIII deficiency or classic hemophilia is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
About Hemophilia A, Hemophilia B, and Neutralizing Antibodies ("Inhibitors") Hemophilia A, also known as factor VIII deficiency or classic hemophilia, is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
Hemophilia A, also known as factor VIII deficiency or classical hemophilia is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
About Hemophilia A Hemophilia A, also known as factor VIII deficiency or classic hemophilia, is largely an inherited bleeding disorder in which one of the proteins needed to form blood clots in the body is missing or reduced.
Avigen also intends to use Cellmate for potential future products using AAV vector to deliver genes to correct Factor VIII deficiency associated with hemophilia A and to correct symptoms of Parkinson's Disease.