Any inherited bleeding disorder, platelet-type in which the cause of the disease is a mutation in the CD36 gene.
Comprehensive, easy-to-understand information about this condition
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factor VII and Factor VIII, combined deficiency of
MONDO:0007595
gray platelet syndrome
MONDO:0007686
primary release disorder of platelets
MONDO:0008309
platelet-type von Willebrand disease
MONDO:0008332
platelet-type bleeding disorder 16
MONDO:0008552
platelet-type bleeding disorder 17
MONDO:0008553