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Disease • C0019069
Definition
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
Synonyms
Hemophilia A • As, Hemophilia • Hemophilia As • A, Hemophilia • Congenital factor VIII disorder • Hemophilia • hemophilia NOS • Haemophilia • Factor VIII Deficiency • Deficiencies, Factor VIII • Factor VIII Deficiencies • Deficiency, Factor VIII • ANTIHEMOPHILIC FACTOR A DEFICIENCY • AHG DEFICIENCY • Factor VIII Deficiency, Congenital • classical hemophilia • Hemophilia, classical • Hereditary factor VIII deficiency • Classic Hemophilia • Classic Hemophilias • Hemophilias, Classic • Hemophilia, Classic • Functional factor VIII deficiency • Hemophilia, familial • Hemophilia, hereditary • Subhemophilia • ANTIHEMOPHILIC GLOBULIN DEFICIENCY • AUTOSOMAL HEMOPHILIA A • DEFIC FACTOR VIII • FACTOR VIII DEFIC • Cong factor viii diord • Hemophilia A [Disease/Finding] • Factor 8 Deficiency, Congenital • Hemophilia A, Congenital • Congenital Hemophilia As • Hemophilia As, Congenital • Congenital Hemophilia A
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Cyclophosphamide
F8 gene
F9 gene
Hemorrhagic Disorders
Blood Coagulation Disorders, Inherited
Coagulation Protein Disorders
HEMOPHILIA A WITH VASCULAR ABNORMALITY
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