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Summary Literature (6)
DOID:2256 - osteochondrodysplasia


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

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


In Mondo Disease Ontology:
MONDO:0005516 - osteochondrodysplasia

Human Disease Resources: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee

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

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Parent(s): bone development disease (is_a)