|Name||platelet-type bleeding disorder 9|
|Definition||An inherited blood coagulation disease characterized by autosomal dominant inheritance of mild thrombocytopenia, mild alpha-granue deficiency, defective platelet adhesion that has material basis in mutation in the ITGA2 gene on chromosome 5q11.2.
collagen platelet receptor deficiency [EXACT]
glycoprotein Ia deficiency [EXACT]
GP Ia deficiency [EXACT]