Newfoundland rod-cone dystrophy (NFRCD)

Genetics

• associated with defects in RLBP1

Clinical manifestations

• retinal dystrophy reminiscent of retinitis punctata albescens but with a substantially lower age at onset & more-rapid & distinctive progression

More general terms

• cone-rod dystrophy (CORD)

Database

• OMIM: https://mirror.omim.org/entry/607476