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Summary Literature (0)
MIM:184840 - OTOSPONDYLOMEGAEPIPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; OSMEDA

Xenbase Genes: col11a2

Human Disease Resource: MIM

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0008490 - otospondylomegaepiphyseal dysplasia, autosomal dominant

Disease Ontology (DO):
DOID:0080046 - Stickler syndrome
DOID:0080677 - otospondylomegaepiphyseal dysplasia, autosomal dominant