genes, neurofibromatosis 1

Preferred Label : genes, neurofibromatosis 1;

MeSH definition : 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.;

MeSH synonym : neurofibromatosis 1 genes; neurofibromatosis 1 gene; nf1 gene; genes, nf 1; gene, nf 1; nf 1 gene; nf 1 genes; nf1 genes; genes, nf1; gene, nf1;

Détails

Origin ID

D016514;

UMLS CUI

C0085113;

Allowable qualifiers
- drug effects [MeSH Qualifier]
- ethics [MeSH Qualifier]
- physiology [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- NF1 Gene [NCIt concept]
- NF1 gene [LOINC component]
Record concept(s)
- genes, neurofibromatosis 1 [MeSH concept]
See also
- neurofibromatosis 1 [MeSH Descriptor]
- neurofibromin 1 [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NF1 Gene [NCIt concept]
- NF1 gene [LOINC component]
- Neurofibromin 1 [OMIM gene]
- neurofibromin 1 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

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