Retinitis pigmentosa 59

Any retinitis pigmentosa in which the cause of the disease is a mutation in the DHDDS gene.

Also known as: DHDDS retinitis pigmentosa, RP59, congenital disorder of glycosylation, type 1bb, retinitis pigmentosa 59, retinitis pigmentosa caused by mutation in DHDDS, retinitis pigmentosa type 59, congenital disorder of glycosylation, type Ibb

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