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Summary Literature (0)
MIM:300895 - OHDO SYNDROME, X-LINKED; OHDOX

Xenbase Genes: med12

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0010477 - blepharophimosis - intellectual disability syndrome, MKB type

Disease Ontology (DO):
DOID:0060289 - Ohdo syndrome