Concept information
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Neoplastic Syndromes, Hereditary
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Genetic Diseases, Inborn
Heredodegenerative Disorders, Nervous System
...
Nervous System Neoplasms
Peripheral Nervous System Neoplasms
Nerve Sheath Neoplasms
Neurofibroma
...
Nervous System Neoplasms
Peripheral Nervous System Neoplasms
Nerve Sheath Neoplasms
Neurofibroma
Término preferido
Neurofibromatoses
Notice: Undefined index: in /var/www/html/model/Concept.php on line 545
Tipo
-
mesh:Descriptor
Definición
- A group of disorders characterized by an autosomal dominant pattern of inheritance with high rates of spontaneous mutation and multiple neurofibromas or neurilemmomas. NEUROFIBROMATOSIS 1 (generalized neurofibromatosis) accounts for approximately 95% of cases, although multiple additional subtypes (e.g., NEUROFIBROMATOSIS 2, neurofibromatosis 3, etc.) have been described. (From Neurochirurgie 1998 Nov;44(4):267-72)
Concepto genérico
Conceptos específicos
Etiquetas alternativas
- Multiple Neurofibromas
- Neurofibromatosis
- Neurofibromatosis Syndrome
En otras lenguas
-
francés
-
Neurofibromes multiples
URI
http://data.loterre.fr/ark:/67375/JVR-F3PSCGTG-4
{{label}}
{{#each values }} {{! loop through ConceptPropertyValue objects }}
{{#if prefLabel }}
{{/if}}
{{/each}}
{{#if notation }}{{ notation }} {{/if}}{{ prefLabel }}
{{#ifDifferentLabelLang lang }} ({{ lang }}){{/ifDifferentLabelLang}}
{{#if vocabName }}
{{ vocabName }}
{{/if}}