Radioulnar synostosis with amegakaryocytic thrombocytopenia 2

Any radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome in which the cause of the disease is a mutation in the MECOM gene.

Also known as: MECOM radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome, RUSAT2, radio-ulnar synostosis-amegakaryocytic thrombocytopenia syndrome caused by mutation in MECOM, radioulnar synostosis with amegakaryocytic thrombocytopenia 2, radioulnar synostosis with amegakaryocytic thrombocytopenia 2; RUSAT2, radioulnar synostosis with amegakaryocytic thrombocytopenia type 2

77 clinical trials for this condition and its sub-types.