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Summary Literature (0)
MIM:613216 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1C; CSNB1C

Xenbase Genes: trpm1

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0013183 - congenital stationary night blindness 1C
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110867 - congenital stationary night blindness 1C