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Summary Literature (0)
MIM:300915 - MICROPHTHALMIA, SYNDROMIC 13; MCOPS13

Xenbase Genes: hmgb3

Human Disease Resource: OMIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010485 - X-linked colobomatous microphthalmia-microcephaly-intellectual disability-short stature syndrome

Disease Ontology (DO):
DOID:0111811 - syndromic microphthalmia 13