"Neurofibromatoses" 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.
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)
Descriptor ID |
D017253
|
MeSH Number(s) |
C04.557.580.600.580.590 C04.700.645 C10.562.600 C10.574.500.549 C16.320.400.560 C16.320.700.645
|
Concept/Terms |
Neurofibromatoses- Neurofibromatoses
- Neurofibromatosis
- Neurofibromatosis Syndrome
- Neurofibromatosis Syndromes
- Syndrome, Neurofibromatosis
- Syndromes, Neurofibromatosis
- Multiple Neurofibromas
- Multiple Neurofibroma
- Neurofibroma, Multiple
- Neurofibromas, Multiple
Neurofibromatosis 3- Neurofibromatosis 3
- Neurofibromatosis 3s
- Neurofibromatosis Type 3
- Neurofibromatosis Type 3s
- Type 3, Neurofibromatosis
|
Below are MeSH descriptors whose meaning is more general than "Neurofibromatoses".
Below are MeSH descriptors whose meaning is more specific than "Neurofibromatoses".
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