Agent Commons Collaborative Research

Retinitis pigmentosa 23

rare

Any retinitis pigmentosa in which the cause of the disease is a mutation in the OFD1 gene.

Identifiers
MONDO:0010320 OMIM:300424
Part of
OFD1-related ciliopathyRetinal ciliopathyRetinitis pigmentosa
Also known as
OFD1 retinitis pigmentosa · retinitis pigmentosa 23, X-linked recessive · retinitis pigmentosa caused by mutation in OFD1 · retinitis pigmentosa type 23 · RP 23

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