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Summary Literature (0)
DOID:2256 - osteochondrodysplasia

Disease Ontology Definition:A bone development disease that results_in defective development of cartilage or bone.

Synonyms: chondrodystrophy, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome (disorder), Congenital anomaly of cartilage, Osteochondrodysplasia syndrome, skeletal dysplasia, Cartilage Development disorder

Xenbase Genes : sfrp4, bmp1, fgfr3, gdf5, runx2, bmpr1b, ihh, fn1, wnt1, tbce, creb3l1, rab33b, col1a2, smarcal1, p4hb, [+]

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0005516 - osteochondrodysplasia


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

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): bone development disease (is_a), cartilage disease (is_a)