Genes, Neurofibromatosis 2
"Genes, Neurofibromatosis 2" 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 22. Mutation or loss of these genes causes NEUROFIBROMATOSIS 2.
Descriptor ID |
D016515
|
MeSH Number(s) |
G05.360.340.024.340.375.249.345 G05.360.340.024.340.415.400.345
|
Concept/Terms |
Genes, Neurofibromatosis 2- Genes, Neurofibromatosis 2
- Genes, nf 2
- Gene, nf 2
- nf 2 Gene
- nf 2 Genes
- nf2 Genes
- Neurofibromatosis 2 Genes
- Gene, Neurofibromatosis 2
- Neurofibromatosis 2 Gene
- Genes, nf2
- Gene, nf2
- nf2 Gene
|
Below are MeSH descriptors whose meaning is more general than "Genes, Neurofibromatosis 2".
Below are MeSH descriptors whose meaning is more specific than "Genes, Neurofibromatosis 2".
This graph shows the total number of publications written about "Genes, Neurofibromatosis 2" by people in this website by year, and whether "Genes, Neurofibromatosis 2" was a major or minor topic of these publications.
To see the data from this visualization as text,
click here.
Below are the most recent publications written about "Genes, Neurofibromatosis 2" by people in Profiles.