disease has feature bone benign neoplasm Ollier disease https://github.com/monarch-initiative/mondo/issues/4948 https://github.com/monarch-initiative/mondo/issues/9097 https://rarediseases.info.nih.gov/diseases/7251/ollier-disease https://www.malacards.org/card/enchondromatosis_multiple_ollier_type dyschondroplasia 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. GARD:0007251 multiple enchondromatosis enchondromatosis Ollier disease ICD10CM:Q78.4 osteochondromatosis NANDO:2201015 MONDO:0008145 NANDO:2200049 Orphanet:296 MEDGEN:41775 NORD:1526 MedDRA:10014642 SCTID:268274005 Ollier type enchondromatosis multiple cartilaginous enchondroses OMIM:166000 UMLS:C0014084 Ollier's disease enchondromatosis, multiple, Ollier type NCIT:C3008 icd11.foundation:1648299787 DOID:4624 hereditary neoplastic syndrome skeletal dysplasia bone neoplasm obsolete primary bone dysplasia with disorganized development of skeletal components overgrowth syndrome developmental defect during embryogenesis disorder of development or morphogenesis hereditary disorder of connective tissue