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 - congenital stationary night blindness autosomal dominant 1

MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):

DOID:0110862 - congenital stationary night blindness autosomal dominant 1