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Summary Literature (0)
OMIM:610125 - MICROPHTHALMIA, SYNDROMIC 5; MCOPS5


Xenbase Genes: otx2

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0012413 - syndromic microphthalmia type 5

Disease Ontology (DO):
DOID:0111806 - syndromic microphthalmia 5
DOID:10629 - microphthalmia