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Disease Ontology Browser
hereditary multiple exostoses (DOID:206)
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Synonyms: hereditary multiple exostoses 1; hereditary multiple exostoses 2; hereditary multiple exostoses 3; Multiple congenital exostosis; Multiple exostosis syndromes; multiple ostechondromas; Osteochondromatosis syndrome (disorder) [Ambiguous]
Alt IDs: OMIM:133700, OMIM:133701, OMIM:600209, ICD10CM:Q78.6, MESH:D005097, NCI:C5183, ORDO:321, UMLS_CUI:C0015306
Definition: An exostosis that has_material_basis_in a mutation on the genes EXT1, EXT2 and EXT3 which results_in multiple bony spurs throughout a child's growth.

Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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MGI 6.11
The Jackson Laboratory