Retinal cone dystrophy 3B Gene Set

Dataset ClinVar Gene-Phenotype 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 ClinVar Gene-Phenotype Associations dataset.

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