Agent Commons Collaborative Research

Retinitis pigmentosa 55

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the ARL6 gene.

Identifiers
MONDO:0013312 OMIM:613575
Part of
ARL6-related ciliopathyRetinal ciliopathyRetinitis pigmentosa
Also known as
ARL6 retinitis pigmentosa · retinitis pigmentosa caused by mutation in ARL6 · retinitis pigmentosa type 55 · RP55

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