Human genes for platelet-type bleeding disorder 9
Platelet-type bleeding disorder 9 [DOID:0111045]
A blood platelet 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.
Synonyms: platelet-type bleeding disorder 9, DOID:0111045, platelettype bleeding disorder 9, BDPLT9, collagen platelet receptor deficiency ...