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DOID:4624 - Ollier disease
Disease Ontology Definition:A syndrome that is characterized by an asymmetric distribution of cartilagenous tumors, which may lead to skeletal deformities and limb-length discrepancy. This condition primarily affects the long bones and cartilage of the joints of the arms and legs, specifically the area where the shaft and head of a long bone meet.
Synonyms: DYSCHONDROPLASIA, ENCHONDROMATOSIS, MULTIPLE, Enchondromatosis with haemangiomata, Kast's syndrome, OSTEOCHONDROMATOSIS,
Xenbase Genes
:
pth1r,
idh2,
idh1
| MONDO:0008145 - Ollier disease |
Other Model Organisms: Alliance, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
syndrome (is_a)