|
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
![Genes associated with this Disease Ontology entry or its descendents or its corresponding OMIM entries](img/icons/info1.png)
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)