Congenital stationary night blindness, type 2A Gene Set

Dataset ClinVar Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.omim.org/entry/300071
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Genes

1 genes associated with the Congenital stationary night blindness, type 2A phenotype from the curated ClinVar Gene-Phenotype Associations dataset.

Symbol Name
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit