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Summary Literature (0)
MIM:610427 - CONE-ROD SYNAPTIC DISORDER, CONGENITAL NONPROGRESSIVE; CRSD

Xenbase Genes: cabp4

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012490 - cone-rod synaptic disorder, congenital nonprogressive
MONDO:0016293 - congenital stationary night blindness