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Genes, Neurofibromatosis 1 MeSH Descriptor Data 2021


MeSH Heading
Genes, Neurofibromatosis 1
Tree Number(s)
G05.360.340.024.340.375.249.340
G05.360.340.024.340.415.400.340
Unique ID
D016514
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/D016514
Scope Note
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.
Entry Term(s)
Genes, nf 1
Genes, nf1
Neurofibromatosis 1 Genes
nf1 Genes
Previous Indexing
Neurofibromatosis 1/genetics (1987-1991)
See Also
Neurofibromatosis 1
Neurofibromin 1
Public MeSH Note
92
History Note
92
Date Established
1992/01/01
Date of Entry
1991/06/21
Revision Date
2008/07/08
Genes, Neurofibromatosis 1 Preferred
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