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Summary Literature (0)
OMIM:610444 - NIGHT BLINDNESS, CONGENITAL STATIONARY, AUTOSOMAL DOMINANT 3; CSNBAD3


Xenbase Genes: gnat1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012497 - congenital stationary night blindness autosomal dominant 3
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110715 - congenital stationary night blindness autosomal dominant 3