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Summary Literature (0)
MIM:601349 - MICROPHTHALMIA, SYNDROMIC 8; MCOPS8

Xenbase Genes: snx3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011045 - MMEP syndrome

Disease Ontology (DO):
DOID:0111803 - syndromic microphthalmia 8