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Summary Literature (0)
MIM:617763 - SHORT STATURE, HEARING LOSS, RETINITIS PIGMENTOSA, AND DISTINCTIVE FACIES; SHRF

Xenbase Genes: exosc2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0044634 - retinitis pigmentosa-hearing loss-premature aging-short stature-facial dysmorphism syndrome