Exostoses, Multiple Hereditary
"Exostoses, Multiple Hereditary" is a descriptor in the National Library of Medicine's controlled vocabulary thesaurus,
MeSH (Medical Subject Headings). Descriptors are arranged in a hierarchical structure,
which enables searching at various levels of specificity.
Hereditary disorder transmitted by an autosomal dominant gene and characterized by multiple exostoses (multiple osteochondromas) near the ends of long bones. The genetic abnormality results in a defect in the osteoclastic activity at the metaphyseal ends of the bone during the remodeling process in childhood or early adolescence. The metaphyses develop benign, bony outgrowths often capped by cartilage. A small number undergo neoplastic transformation.
| Descriptor ID |
D005097
|
| MeSH Number(s) |
C04.557.450.565.575.610.615.325 C04.700.330 C05.116.099.708.670.615.325 C05.116.540.310.500 C16.320.700.330
|
| Concept/Terms |
Exostoses, Multiple Hereditary- Exostoses, Multiple Hereditary
- Hereditary Exostoses, Multiple
- Chondrodysplasia, Hereditary Deforming
- Chondrodysplasias, Hereditary Deforming
- Deforming Chondrodysplasia, Hereditary
- Deforming Chondrodysplasias, Hereditary
- Hereditary Deforming Chondrodysplasia
- Hereditary Deforming Chondrodysplasias
- Diaphyseal Aclasis
- Aclases, Diaphyseal
- Aclasis, Diaphyseal
- Diaphyseal Aclases
- Exostoses, Familial
- Exostoses, Hereditary Multiple
- Multiple Exostoses, Hereditary
- Exostoses, Multiple
- Multiple Exostoses
- Exostoses, Multiple Cartilaginous
- Cartilaginous Exostoses, Multiple
- Exostoses, Multiple, Type I
- Exostosis, Familial
- Familial Exostosis
- Exostosis, Hereditary Multiple
- Multiple Exostosis, Hereditary
- Exostosis, Multiple
- Multiple Exostosis
- Exostosis, Multiple Cartilaginous
- Cartilaginous Exostosis, Multiple
- Multiple Cartilaginous Exostosis
- Familial Exostoses
- Hereditary Multiple Exostoses
- Hereditary Multiple Exostosis
- Multiple Cartilaginous Exostoses
- Multiple Hereditary Exostoses
- Multiple Osteochondromas
- Multiple Osteochondroma
- Osteochondroma, Multiple
- Multiple Osteochondromatosis
- Osteochondromas, Multiple
- Bessel-Hagen Disease
|
Below are MeSH descriptors whose meaning is more general than "Exostoses, Multiple Hereditary".
- Diseases [C]
- Neoplasms [C04]
- Neoplasms by Histologic Type [C04.557]
- Neoplasms, Connective and Soft Tissue [C04.557.450]
- Neoplasms, Connective Tissue [C04.557.450.565]
- Neoplasms, Bone Tissue [C04.557.450.565.575]
- Osteochondroma [C04.557.450.565.575.610]
- Osteochondromatosis [C04.557.450.565.575.610.615]
- Exostoses, Multiple Hereditary [C04.557.450.565.575.610.615.325]
- Neoplastic Syndromes, Hereditary [C04.700]
- Exostoses, Multiple Hereditary [C04.700.330]
- Musculoskeletal Diseases [C05]
- Bone Diseases [C05.116]
- Bone Diseases, Developmental [C05.116.099]
- Osteochondrodysplasias [C05.116.099.708]
- Osteochondroma [C05.116.099.708.670]
- Osteochondromatosis [C05.116.099.708.670.615]
- Exostoses, Multiple Hereditary [C05.116.099.708.670.615.325]
- Hyperostosis [C05.116.540]
- Exostoses [C05.116.540.310]
- Exostoses, Multiple Hereditary [C05.116.540.310.500]
- Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16]
- Genetic Diseases, Inborn [C16.320]
- Neoplastic Syndromes, Hereditary [C16.320.700]
- Exostoses, Multiple Hereditary [C16.320.700.330]
Below are MeSH descriptors whose meaning is more specific than "Exostoses, Multiple Hereditary".
This graph shows the total number of publications written about "Exostoses, Multiple Hereditary" by people in this website by year, and whether "Exostoses, Multiple Hereditary" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2011 | 1 | 0 | 1 |
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Below are the most recent publications written about "Exostoses, Multiple Hereditary" by people in Profiles.
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Development of genu valgum after removal of osteochondromas from the proximal tibia. J Pediatr Orthop B. 2016 Nov; 25(6):582-6.
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EXT2-positive multiple hereditary osteochondromas with some features suggestive of metachondromatosis. Skeletal Radiol. 2012 May; 41(5):607-10.
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Autism and multiple exostoses associated with an X;8 translocation occurring within the GRPR gene and 3' to the SDC2 gene. Hum Mol Genet. 1997 Aug; 6(8):1241-50.
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Musculoskeletal applications of three-dimensional surface reconstructions. Orthop Clin North Am. 1985 Jul; 16(3):543-55.