All diseases

OMIM ID
180020
OMIM term:
RETINAL CONE DYSTROPHY 1; RCD1
Alternative terms:
RETINAL CONE DEGENERATION
CONE DYSTROPHY, AUTOSOMAL DOMINANT
(∗) Location:
6q25-q26  
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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* quick link - http://q.sanger.ac.uk/8nynixjq