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Summary Literature (1)
MIM:310500 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1A; CSNB1A

Xenbase Genes: nyx

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010690 - manual digit 1 epithelium
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110870 - congenital stationary night blindness 1A