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Summary Literature (1)
MIM:610356 - RETINAL CONE DYSTROPHY 3B; RCD3B

Xenbase Genes: kcnv2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012475 - cone dystrophy with supernormal rod response

Disease Ontology (DO):
DOID:0050795 - cone dystrophy
DOID:0081022 - retinal cone dystrophy 3B