genes, neurofibromatosis 2

Preferred Label : genes, neurofibromatosis 2;

MeSH definition : Tumor suppressor genes located on the long arm of human chromosome 22. Mutation or loss of these genes causes NEUROFIBROMATOSIS 2.;

MeSH synonym : genes, nf 2; gene, nf 2; genes, nf2; nf 2 gene; nf 2 genes; nf2 genes; neurofibromatosis 2 genes; gene, neurofibromatosis 2; neurofibromatosis 2 gene; gene, nf2; nf2 gene;

Details

Origin ID

D016515;

UMLS CUI

C0085114;

Allowable qualifiers
- drug effects [MeSH Qualifier]
- ethics [MeSH Qualifier]
- physiology [MeSH Qualifier]
- radiation effects [MeSH Qualifier]
Automatic exact mappings (from CISMeF team)
- NF2 Gene [NCIt concept]
- NF2 gene [LOINC component]
Record concept(s)
- genes, neurofibromatosis 2 [MeSH concept]
See also
- neurofibromatosis 2 [MeSH Descriptor]
- neurofibromin 2 [MeSH Descriptor]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NF2 Gene [NCIt concept]
- NF2 gene [LOINC component]
- NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [HGNC gene]
- Nf2, moesin-ezrin-radixin-like (merlin) tumor suppressor [OMIM gene]

Keyword's position in hierarchy(ies) :

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