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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 Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
12/05/2017
MGI 6.11
The Jackson Laboratory