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Summary Literature (0)
DOID:0060465 - fibrochondrogenesis


Disease Ontology Definition:An osteochondrodysplasia that is characterized by shortened long bones in the arms and legs that are unusually wide at the ends, flattened vertebrae with a characteristic pinched or pear shape, and a very narrow chest in infants with short, wide ribs and a round and prominent abdomen.

Synonyms:

Xenbase Genes : col11a2, col11a1

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0016068 - fibrochondrogenesis

OMIM:
OMIM:228520 - FIBROCHONDROGENESIS 1; FBCG1
OMIM:614524 - FIBROCHONDROGENESIS 2; FBCG2

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

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