retinal cone dystrophy 3b Gene Set

Dataset OMIM Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/610356
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Genes

1 genes associated with the retinal cone dystrophy 3b phenotype from the curated OMIM Gene-Disease Associations dataset.

Symbol Name
KCNV2 potassium channel, voltage gated modifier subfamily V, member 2