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Summary Literature (1)
MIM:206900 - MICROPHTHALMIA, SYNDROMIC 3; MCOPS3

Xenbase Genes: sox2, six6

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008799 - anophthalmia/microphthalmia-esophageal atresia syndrome

Disease Ontology (DO):
DOID:0111801 - syndromic microphthalmia 3
DOID:10629 - microphthalmia