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Summary Literature (0)
MIM:193220 - VITREORETINOCHOROIDOPATHY; VRCP

Xenbase Genes: best1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008662 - autosomal dominant vitreoretinochoroidopathy
MONDO:0016979 - MRCS syndrome

Disease Ontology (DO):
DOID:0111569 - autosomal dominant vitreoretinochoroidopathy