exostosis hereditary multiple osteochondromas https://github.com/monarch-initiative/mondo/issues/6750 https://rarediseases.info.nih.gov/diseases/7035/hereditary-multiple-osteochondromas https://www.malacards.org/card/exostoses_multiple_type_i https://www.malacards.org/card/hereditary_multiple_exostoses HMO NORD:1233 exostoses, multiple GARD:0007035 NANDO:2201015 NANDO:2201014 MESH:D005097 osteochondromatosis syndrome hereditary multiple exostoses multiple cartilaginous exostoses UMLS:C0015306 MEDGEN:4612 hereditary multiple exostosis NCIT:C5183 SCTID:716742001 hereditary multiple exostoses 1 hereditary multiple exostoses 2 osteochondromatosis syndrome (disorder) [ambiguous] MONDO:0005508 SCTID:254044004 This term's classification was reviewed in the context of the Strategic Refinement project (2023) and was determined to be excluded from the 'metabolic disease' (MONDO:0005066) ontology branch (https://orcid.org/0000-0002-1780-5230) hereditary multiple exostoses 3 icd11.foundation:1578364807 OMIMPS:133700 Orphanet:321 DOID:206 EXT NANDO:2200049 Bessel-Hagen disease icd11.foundation:146330302 A bone neoplasm characterized by development of two or more cartilage capped bony outgrowths (osteochondromas) of the long bones. multiple exostoses hereditary neoplastic syndrome bone neoplasm obsolete primary bone dysplasia with disorganized development of skeletal components hereditary disorder of connective tissue