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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 (disorder), Osteochondrodysplasia syndrome (disorder), chondrodystrophy,
Echinobase Genes : gpc-6, sox9, cant1, fgfr3, hspg2, smarcal1, runx2, slc35d1, npr2, hh, col2a1, col1a2, wnt1
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)