Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Ollier disease

MONDO:0008145

A rare primary bone dysplasia disorder characterized by the development of multiple mainly unilateral or asymmetrically distributed enchondromas throughout the metaphyses of the long bones.

Also known as: Ollier disease, Ollier type enchondromatosis, Ollier's disease, dyschondroplasia, osteochondromatosis, enchondromatosis, enchondromatosis, multiple, Ollier type, multiple cartilaginous enchondroses

1440 clinical trials for this condition and its sub-types, 3 tagged with Ollier disease itself.

Follow this condition to get notified about new trials

Where it sits in the disease tree

Browse by category →
Sort by