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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

GARD:7251

ICD10CM:Q78.4

MESH:D004687

NCI:C3213

OMIM:166000

ORDO:296

SNOMEDCT_US_2018_03_01:46041001

UMLS_CUI:C0024454

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

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