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Summary Literature (0)
MIM:257270 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 1B; CSNB1B

Xenbase Genes: grm6

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0009758 - abdominal ganglion
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110865 - congenital stationary night blindness 1B