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Summary Literature (0)
MIM:613830 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1D; CSNB1D

Xenbase Genes: slc24a1

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013450 - congenital stationary night blindness 1D
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110868 - congenital stationary night blindness 1D