Human genes for Ollier disease
Ollier disease [DOID:4624]
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.
Synonyms: Ollier disease, DOID:4624, Ollier disorder, Ollier syndrome, DYSCHONDROPLASIA ...