MYH9 and autoimmune thrombocytopenic purpura: One patient, initially suspected of having ITP, was confirmed to have MYH9-related thrombocytopenia, two cases initially diagnosed with ITP were confirmed as Bernard-Soulier syndrome, three cases of ITP were reclassified as unspecified inherited thrombocytopenia, and two patients initially suspected as having von Willebrand disease were reclassified as unspecified inherited platelet function disorder.