| Metadata | |
|---|---|
| ID | DOID:4624 |
| Name | Ollier disease |
| 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. http://en.wikipedia.org/wiki/Ollier_disease, http://rarediseases.info.nih.gov/GARD/Condition/7251/Ollier_disease.aspx |
| Xrefs |
SNOMEDCT_US_2023_03_01:46041001 |
| Subsets |
DO_rare_slim NCIthesaurus |
| Synonyms |
DYSCHONDROPLASIA [EXACT] Enchondromatosis with haemangiomata [EXACT] ENCHONDROMATOSIS, MULTIPLE [EXACT] Kast's syndrome [EXACT] OSTEOCHONDROMATOSIS [EXACT] |
| Parent Relationships |
is_a syndrome |