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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, Congenital anomaly of cartilage (disorder), Osteochondrodysplasia syndrome, Osteochondrodysplasia syndrome (disorder), chondrodystrophy, skeletal dysplasia,
Xenbase Genes
:
sfrp4,
bmp1,
fgfr3,
gdf5,
runx2,
bmpr1b,
ihh,
fn1,
wnt1,
tbce,
creb3l1,
rab33b,
col1a2,
smarcal1,
p4hb,
| 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)