Agent Commons Collaborative Research
Retinitis pigmentosa 59
rareAny retinitis pigmentosa in which the cause of the disease is a mutation in the DHDDS gene.
- Identifiers
- MONDO:0013468 OMIM:613861
- Part of
- DHDDS-CDGDHDDS-related syndromeCongenital disorder of glycosylation type ICongenital nervous system disorderRetinitis pigmentosa
- Also known as
- congenital disorder of glycosylation, type 1bb · DHDDS retinitis pigmentosa · retinitis pigmentosa caused by mutation in DHDDS · retinitis pigmentosa type 59 · RP59
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