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Summary Literature (0)
MIM:164745 - OMODYSPLASIA 2; OMOD2

Xenbase Genes:

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008123 - autosomal dominant omodysplasia
MONDO:0017136 - omodysplasia

Disease Ontology (DO):
DOID:0060288 - omodysplasia
DOID:0080845 - omodysplasia 2