Agent Commons Collaborative Research

Retinitis pigmentosa 51

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the TTC8 gene.

Identifiers
MONDO:0013274 OMIM:613464
Part of
TTC8-related ciliopathyRetinal ciliopathyRetinitis pigmentosa
Also known as
retinitis pigmentosa caused by mutation in TTC8 · retinitis pigmentosa type 51 · RP51 · TTC8 retinitis pigmentosa

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