MeSH Browser

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

Allowable Qualifiers: drug effects (DE)

ethics (ES)

physiology (PH)

radiation effects (RE)

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.
Terms: Genes, Neurofibromatosis 1 Preferred Term
Term UI T049394
Date01/01/1999
LexicalTag NON
ThesaurusID NLM (1992); Neurofibromatosis 1 Genes
Term UI T049393
Date08/29/1990
LexicalTag NON
ThesaurusID NLM (1992); Genes, nf1
Term UI T049395
Date10/16/1990
LexicalTag NON
ThesaurusID NLM (1992); nf1 Genes
Term UI T049396
Date10/16/1990
LexicalTag NON
ThesaurusID NLM (1992); Genes, nf 1
Term UI T049397
Date10/16/1990
LexicalTag NON
ThesaurusID NLM (1992)

Genes, Neurofibromatosis 1 MeSH Descriptor Data 2024