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Summary Literature (0)
MIM:615524 - MICROPHTHALMIA, SYNDROMIC 12; MCOPS12

Xenbase Genes: rarb

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0011010 - Matthew-Wood syndrome
MONDO:0014229 - microphthalmia, syndromic 12

Disease Ontology (DO):
DOID:0111800 - syndromic microphthalmia 12