Retinitis pigmentosa 59

MONDO:0013468

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

25 clinical trials for this condition and its sub-types, 0 tagged with Retinitis pigmentosa 59 itself.

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Part of

↑ Retinitis pigmentosa (89) ↑ DHDDS-CDG (1) ↑ DHDDS-related syndrome (0)

Including sub-types (25) Tagged with Retinitis pigmentosa 59 (0)

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