MYH9 has been known to cause an autosomal-dominant disease called MYH9-related disorder (MYH9-RD), characterized by large platelets and thrombocytopenia as well as increased risk of progressive nephropathy, sensorineural deafness, pre-senile cataract, and aberration of liver enzymes29,30. This evidence concerns the gene MYH9 and Thrombocytopenia.