Scott Syndrome Watchlist (log in to enable) Retrieved 2021-01-23 Source Orphanet Trials — Genes ANO6, ADAM10, ANXA5, KLK3, FLNB, MYH3, ABCB4, PLAG1, PROS1, NPEPPS, MMD, PSAT1, ANO1, ANO10, ANO5 Drugs — Interested in hearing about new therapies? Registered! Scott syndrome is an extremely rare congenital hemorrhagic disorder characterized by hemorrhagic episodes due to impaired platelet coagulant activity.