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Summary Literature (0)
DOID:0060288 - omodysplasia

Disease Ontology Definition:An osteochondrodysplasia that is characterized by severe limb shortening and facial dysmorphism.

Synonyms:

Xenbase Genes : gpc6

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


Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): osteochondrodysplasia (is_a)