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Summary Literature (1)
MIM:300071 - NIGHT BLINDNESS, CONGENITAL STATIONARY, TYPE 2A; CSNB2A

Xenbase Genes: cacna1f

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010241 - congenital stationary night blindness 2A
MONDO:0016293 - congenital stationary night blindness

Disease Ontology (DO):
DOID:0110871 - congenital stationary night blindness 2A