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Summary Literature (0)
MIM:614565 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1E; CSNB1E

Xenbase Genes: gpr179

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013807 - congenital stationary night blindness 1E
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110869 - congenital stationary night blindness 1E