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Summary Literature (0)
MIM:163500 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 2; CSNBAD2

Xenbase Genes: pde6b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008099 - congenital stationary night blindness autosomal dominant 2
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110863 - congenital stationary night blindness autosomal dominant 2