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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, chondrodystrophy, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome (disorder), Congenital anomaly of cartilage, Osteochondrodysplasia syndrome, skeletal dysplasia
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