About   Help   FAQ
Disease Ontology Browser
hereditary multiple exostoses (DOID:206)
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 (2)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
04/18/2017
MGI 6.08
The Jackson Laboratory