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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
General
cone-rod dystrophy (CORD)
Database Correlations
OMIM 607476
References
OMIM :accession 607476