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Descriptor English: Genes, Neurofibromatosis 1
Descriptor Spanish: Genes de Neurofibromatosis 1
Descriptor genes de la neurofibromatosis 1
Entry term(s) genes nf1
Scope note: Genes supresores de tumores localizados en el brazo largo del cromosoma 17 humano, en la región 17q11.2. La mutación de estos genes causa la NEUROFIBROMATOSIS 1, el síndrome de Watson y el síndrome LEOPARD.
Descriptor Portuguese: Genes da Neurofibromatose 1
Descriptor French: Gènes nf1
Entry term(s): Gene, nf 1
Gene, nf1
Genes, nf 1
Genes, nf1
Neurofibromatosis 1 Gene
Neurofibromatosis 1 Genes
nf 1 Gene
nf 1 Genes
nf1 Gene
nf1 Genes
Tree number(s): G05.360.340.024.340.375.249.340
G05.360.340.024.340.415.400.340
RDF Unique Identifier: https://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.
Allowable Qualifiers: DE drug effects
ES ethics
PH physiology
RE radiation effects
Previous Indexing: Neurofibromatosis 1/genetics (1987-1991)
Public MeSH Note: 92
History Note: 92
Related: Neurofibromatosis 1 MeSH
Neurofibromin 1 MeSH
DeCS ID: 30086
Unique ID: D016514
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 1992/01/01
Date of Entry: 1991/06/21
Revision Date: 2008/07/08
Genes, Neurofibromatosis 1 - Preferred
Concept UI M0025208
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.
Preferred term Genes, Neurofibromatosis 1
Entry term(s) Gene, nf 1
Gene, nf1
Genes, nf 1
Genes, nf1
Neurofibromatosis 1 Gene
Neurofibromatosis 1 Genes
nf 1 Gene
nf 1 Genes
nf1 Gene
nf1 Genes



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