Genes, Neurofibromatosis 1
"Genes, Neurofibromatosis 1" 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.
Tumor suppressor genes located on the long arm of human chromosome 17 in the region 17q11.2. Mutation of these genes is thought to cause NEUROFIBROMATOSIS 1, Watson syndrome, and LEOPARD syndrome.
| Descriptor ID |
D016514
|
| MeSH Number(s) |
G05.360.340.024.340.375.249.340 G05.360.340.024.340.415.400.340
|
| Concept/Terms |
Genes, Neurofibromatosis 1- Genes, Neurofibromatosis 1
- Genes, nf 1
- Gene, nf 1
- nf 1 Gene
- nf 1 Genes
- nf1 Genes
- Neurofibromatosis 1 Genes
- Neurofibromatosis 1 Gene
- Genes, nf1
- Gene, nf1
- nf1 Gene
|
Below are MeSH descriptors whose meaning is more general than "Genes, Neurofibromatosis 1".
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This graph shows the total number of publications written about "Genes, Neurofibromatosis 1" by people in this website by year, and whether "Genes, Neurofibromatosis 1" was a major or minor topic of these publications.
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| Year | Major Topic | Minor Topic | Total |
|---|
| 2005 | 1 | 0 | 1 |
| 2008 | 0 | 1 | 1 |
| 2019 | 0 | 1 | 1 |
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Below are the most recent publications written about "Genes, Neurofibromatosis 1" by people in Profiles.