Concept information
Término preferido
Exostoses, Multiple Hereditary
Notice: Undefined index: in /var/www/html/model/Concept.php on line 545
Tipo
-
mesh:Descriptor
Definición
- 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.
Concepto genérico
Etiquetas alternativas
- Bessel-Hagen Disease
- Chondrodysplasia, Hereditary Deforming
- 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
- Hereditary Multiple Exostoses
- Hereditary Multiple Exostosis
- Multiple Cartilaginous Exostoses
- Multiple Hereditary Exostoses
- Multiple Osteochondromas
- Multiple Osteochondromatosis
- Osteochondromas, Multiple
En otras lenguas
-
francés
-
Aclasie diaphysaire
-
Chondrodysplasie déformante héréditaire
-
Chondrodysplasie héréditaire déformante
-
Maladie de Bessel-Hagen
-
Maladie exostosante multiple
-
Maladie ostéogénique
-
Ostéochondromatose diffuse de Bessel-Hagen
-
Ostéochondromes multiples
URI
http://data.loterre.fr/ark:/67375/JVR-WPXK4HP3-Q
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}