Cerebroretinal microangiopathy with calcifications and cysts 2

Any Coats plus syndrome in which the cause of the disease is a mutation in the STN1 gene.

Also known as: Coats plus syndrome caused by mutation in STN1, STN1 Coats plus syndrome, cerebroretinal microangiopathy with calcifications and cysts 2, cerebroretinal microangiopathy with calcifications and cysts type 2, CRMCC2

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