hereditary multiple exostoses
Sign in to saveAlso known as Multiple congenital exostosis, Multiple exostosis syndromes, Osteochondromatosis syndrome (disorder) [Ambiguous], hereditary multiple exostoses 1, hereditary multiple exostoses 2, hereditary multiple exostoses 3, multiple ostechondromas, Osteochondromatosis syndrome
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
In the Vinony graph
Within Vinony's link graph, hereditary multiple exostoses is referenced by 76 other articles, and connects out to World Health Organization, International Standard Book Number and autism.
It sits within the topics Proteoglycan metabolism disorders, Rare diseases and Skeletal disorders.
Its subject is documented across 11 Wikipedia language editions.
Research
1,747 papers- Multiple hereditary exostoses and enchondromatosis.Best practice & research. Clinical rheumatology · 2020
- Multiple Hereditary Exostoses.Radiologic technology · 2016
- Hereditary multiple exostoses and enchondromatosis.Best practice & research. Clinical rheumatology · 2008
- Hereditary Multiple Exostoses: New Insights into Pathogenesis, Clinical Complications, and Potential Treatments.Current osteoporosis reports · 2017
- Multiple Hereditary Exostoses-Family "Bone History" Revealed.Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases · 2022
via PubMed
Wikidata facts
Show 7 more facts
- symptoms and signs
- exostosis
- Commons category
- Hereditary multiple exostoses
- NCI Thesaurus ID
- C5183
- health specialty
- medical genetics
- exact match
- www.orpha.net/ORDO/Orphanet_321
- genetic association
- EXT1
- on focus list of Wikimedia project
- WikiProject Medicine
via Wikidata · CC0