NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A Gene Set

Dataset CTD Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link http://ctdbase.org/detail.go?type=disease&acc=OMIM:300071
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Genes

1 genes/proteins associated with the disease NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A from the curated CTD Gene-Disease Associations dataset.

Symbol Name Standardized Value
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit 2.88009