(Q32146449)
English
platelet-type bleeding disorder 9
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
- glycoprotein Ia deficiency
- BDPLT9
- GP Ia deficiency
- BLEEDING DISORDER, PLATELET-TYPE, 9
- Bleeding diathesis due to integrin alpha2-beta1 deficiency
- BLEEDING DISORDER, PLATELET-TYPE, 9; BDPLT9
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