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Summary Literature (0)
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 Disease Ontology (on Monarch Initiative):
MONDO:0008145 - Ollier disease

OMIM:
OMIM:166000 - ENCHONDROMATOSIS, MULTIPLE, OLLIER TYPE

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): syndrome (is_a)