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Summary Literature (1)
OMIM:136520 - FOVEAL HYPOPLASIA 1; FVH1

Xenbase Genes: pax6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007628 - foveal hypoplasia 1
MONDO:0016395 - foveal hypoplasia-presenile cataract syndrome