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Summary Literature (0)
MIM:615058 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1F; CSNB1F

Xenbase Genes: lrit3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014026 - congenital stationary night blindness 1F
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110864 - congenital stationary night blindness 1F