Ollier disease

Term ID

DOID:4624

Synonyms

• dyschondroplasia
• Enchondromatosis with haemangiomata
• ENCHONDROMATOSIS, MULTIPLE
• Kast's syndrome
• osteochondromatosis

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

References

• GARD:7251
• ICD10CM:Q78.4
• MESH:D004687
• MIM:166000
• NCI:C3213
• ORDO:296
• SNOMEDCT_US_2023_03_01:46041001
• UMLS_CUI:C0024454

Ontology

Human Disease   ( DOID:4624 )