platelet-type bleeding disorder 9 (Q32146449)

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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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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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