Disease-gene associations mined from literature

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,  Ollier diseases ...

Linkouts:  OMIM #1 #2