retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description disease cluster belonging to disease group vision (Genetic Association Database)
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Genes

1 genes associated with the disease retinitis pigmentosa; leber congenital amaurosis; usher syndrome type i in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
CDHR1 cadherin-related family member 1