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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:0016068 - fibrochondrogenesis |
| MIM:228520 - FIBROCHONDROGENESIS 1; FBCG1 |
| MIM:614524 - FIBROCHONDROGENESIS 2; FBCG2 |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
osteochondrodysplasia (is_a)