Disease-gene associations mined from literature

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,  GP Ia deficiency ...