All diseases

OMIM ID
193220
OMIM term:
VITREORETINOCHOROIDOPATHY; VRCP
Alternative terms:
VITREORETINOCHOROIDOPATHY, AUTOSOMAL DOMINANT; ADVIRC
VITREORETINOCHOROIDOPATHY WITH MICROCORNEA, GLAUCOMA, AND CATARACT
VITREORETINOCHOROIDOPATHY, AUTOSOMAL DOMINANT, WITH NANOPHTHALMOS MICROCORNEA, ROD-CONE DYSTROPHY, CATARACT, AND POSTERIOR STAPHYLOMA, INCLUDED; MRCS, INCLUDED
(∗) Location:
11q12.3  
(†) Associated OMIM genes:
BEST1  
(‡) Associated MGI genes:

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