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From NeuroLex
| Created
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5 October 2007 +
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| CurationStatus
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uncurated +
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| DefiningCitation
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Adams et al., Principles of Neurology, 6th ed, p1016 +
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| Definition
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A group of disorders characterized by an a … 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 (MeSH). tosis 3, etc.) have been described (MeSH).
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| DefinitionSource
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MeSH +
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| Id
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birnlex_12605 +
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| Label
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Neurofibromatosis +
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| Modification dateThis property is a special property in this wiki.
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30 May 2009 04:29:01 +
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| ModifiedDate
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30 May 2009 +
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| SuperCategory
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Neurofibroma +
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| Synonym
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Neurofibromatosis Syndrome +,
Multiple Neurofibromas +
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| Categories |
Neurofibroma
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