Ollier disease

Disease Export to PDF
Name:
Ollier disease
Description:
A rare primary bone dysplasia characterized by multiple enchondromas (benign cartilage-forming tumors). The lesions are generally unilateral or asymmetrically distributed. The most common affected site is the appendicular skeleton.
ORPHAcode:
296
Synonyms:
Dyschondroplasia
XREF(s):
Analyte(s):
Created:
13 May 2019 - 01:02
Changed:
22 Jun 2023 - 16:14