| Descriptor English: | Exostoses, Multiple Hereditary | ||||||
| Descriptor Spanish: |
Exostosis Múltiple Hereditaria
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| Descriptor Portuguese: | Exostose Múltipla Hereditária | ||||||
| Descriptor French: | Maladie des exostoses multiples | ||||||
| Entry term(s): |
Aclases, Diaphyseal Aclasis, Diaphyseal Bessel-Hagen Disease Cartilaginous Exostoses, Multiple Cartilaginous Exostosis, Multiple Chondrodysplasia, Hereditary Deforming Chondrodysplasias, Hereditary Deforming Deforming Chondrodysplasia, Hereditary Deforming Chondrodysplasias, Hereditary Diaphyseal Aclases Diaphyseal Aclasis Exostoses, Familial Exostoses, Hereditary Multiple Exostoses, Multiple Exostoses, Multiple Cartilaginous Exostoses, Multiple, Type I Exostosis, Familial Exostosis, Hereditary Multiple Exostosis, Multiple Exostosis, Multiple Cartilaginous Familial Exostoses Familial Exostosis Hereditary Deforming Chondrodysplasia Hereditary Deforming Chondrodysplasias Hereditary Exostoses, Multiple Hereditary Multiple Exostoses Hereditary Multiple Exostosis Multiple Cartilaginous Exostoses Multiple Cartilaginous Exostosis Multiple Exostoses Multiple Exostoses, Hereditary Multiple Exostosis Multiple Exostosis, Hereditary Multiple Hereditary Exostoses Multiple Osteochondroma Multiple Osteochondromas Multiple Osteochondromatosis Osteochondroma, Multiple Osteochondromas, Multiple |
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| Tree 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 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D005097 | ||||||
| Scope note: | 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. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Exostoses (1966-1967) |
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| Public MeSH Note: | 90; was EXOSTOSES, MULTIPLE 1968-89 |
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| Online Note: | use EXOSTOSES, MULTIPLE HEREDITARY to search EXOSTOSES, MULTIPLE 1968-89 |
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| History Note: | 90; was EXOSTOSES, MULTIPLE 1968-89 |
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| DeCS ID: | 28249 | ||||||
| Unique ID: | D005097 | ||||||
| NLM Classification: | WE 250 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1968/01/01 | ||||||
| Date of Entry: | 1999/01/01 | ||||||
| Revision Date: | 2013/07/08 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms
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Exostoses, Multiple Hereditary
- Preferred
| Concept UI |
M0008037 |
| Scope note | 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. |
| Preferred term | Exostoses, Multiple Hereditary |
| Entry term(s) |
Aclases, Diaphyseal Aclasis, Diaphyseal Bessel-Hagen Disease Cartilaginous Exostoses, Multiple Cartilaginous Exostosis, Multiple Chondrodysplasia, Hereditary Deforming Chondrodysplasias, Hereditary Deforming Deforming Chondrodysplasia, Hereditary Deforming Chondrodysplasias, Hereditary Diaphyseal Aclases Diaphyseal Aclasis Exostoses, Familial Exostoses, Hereditary Multiple Exostoses, Multiple Exostoses, Multiple Cartilaginous Exostoses, Multiple, Type I Exostosis, Familial Exostosis, Hereditary Multiple Exostosis, Multiple Exostosis, Multiple Cartilaginous Familial Exostoses Familial Exostosis Hereditary Deforming Chondrodysplasia Hereditary Deforming Chondrodysplasias Hereditary Exostoses, Multiple Hereditary Multiple Exostoses Hereditary Multiple Exostosis Multiple Cartilaginous Exostoses Multiple Cartilaginous Exostosis Multiple Exostoses Multiple Exostoses, Hereditary Multiple Exostosis Multiple Exostosis, Hereditary Multiple Hereditary Exostoses Multiple Osteochondroma Multiple Osteochondromas Multiple Osteochondromatosis Osteochondroma, Multiple Osteochondromas, Multiple |
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