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Summary Literature (0)
MIM:609218 - FOVEAL HYPOPLASIA 2; FVH2

Xenbase Genes: slc38a8

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012216 - foveal hypoplasia - optic nerve decussation defect - anterior segment dysgenesis syndrome

Disease Ontology (DO):
DOID:0070531 - foveal hypoplasia 2