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Summary Literature (0)
MIM:610445 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 1; CSNBAD1

Xenbase Genes: rho, rho.2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012498 - serosa of appendix
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110862 - congenital stationary night blindness autosomal dominant 1