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Disease Ontology Browser
Ollier disease (DOID:4624)
Alliance: disease page
Synonyms: dyschondroplasia; Enchondromatosis with haemangiomata; ENCHONDROMATOSIS, MULTIPLE; Kast's syndrome; osteochondromatosis
Alt IDs: OMIM:166000, ICD10CM:Q78.4, MESH:D004687, NCI:C3213, ORDO:296, UMLS_CUI:C0024454
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.

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
12/10/2024
MGI 6.24 		The Jackson Laboratory