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Summary Literature (5)
OMIM:300166 - MICROPHTHALMIA, SYNDROMIC 2; MCOPS2


Xenbase Genes: bcor

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010261 - microphthalmia, syndromic 2
MONDO:0018924 - microphthalmia, Lenz type

Disease Ontology (DO):
DOID:0111809 - syndromic microphthalmia 2
DOID:10629 - microphthalmia