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Summary Literature (0)
MIM:616079 - RETINAL DYSTROPHY WITH INNER RETINAL DYSFUNCTION AND GANGLION CELL ABNORMALITIES; RDGCA

Xenbase Genes: itm2b

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0014483 - retinal dystrophy with inner retinal dysfunction and ganglion cell anomalies