Congenital vascular defect associated with platelet abnormality and antihemophilic factor deficiency.
D001791:Blood Platelet Disorders; D001792:Blood Platelets; D005169:Factor VIII; D006467:Hemophilia A / Q000235:genetics*; D006474:Hemorrhagic Disorders / Q000235:genetics*; D006801:Humans
C078147:F8 protein, human; D005169:Factor VIII
HEMOPHILIA/genetics; HEMORRHAGIC DIATHESIS/genetics