Neurofibromin 2

Preferred Label : Neurofibromin 2;

Symbol : NF2;

CISMeF acronym : NF2;

Type : Gene;

Alternative titles and symbols : Schwannomin; MERLIN; SCH;

Ensembl ID : ENSG00000186575;

Prefixed ID : *607379;

Details

Origin ID

607379;

UMLS CUI

C0085114;

Automatic exact mappings (from CISMeF team)
- Falco columbarius (organism) [SNOMED CT concept]
- Full NF2-related schwannomatosis [ORDO Disease]
- Merlin [NCIt concept]
- Merlin (substance) [SNOMED CT concept]
- NF2 Gene [NCIt concept]
- NF2 gene [LOINC component]
- NF2 wt Allele [NCIt concept]
- NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [ORDO Gene]
- NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [HGNC gene]
- Neurofibromatosis Type 2 [NCIt concept]
- Neurofibromatosis type 2 (disorder) [SNOMED CT concept]
- Spindle Cell Hemangioma [NCIt concept]
- Supracervical Hysterectomy [NCIt concept]
- Synovial Chondrosarcoma [NCIt concept]
- neurofibromatosis 2 [DO Concept]
- neurofibromin 2 [MeSH Descriptor]
- neurofibromin 2 [MeSH concept]
- spindle cell hemangioma [DO Concept]
- suprachiasmatic nucleus [UBERON concept]
HGNC gene
- NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [HGNC gene]
NCIt concept(s)
- Merlin [NCIt concept]
- NF2 Gene [NCIt concept]
- NF2 wt Allele [NCIt concept]
ORDO concept(s)
- NF2, moesin-ezrin-radixin like (MERLIN) tumor suppressor [ORDO Gene]
Phenotypes related
- Meningioma, familial, susceptibility to [OMIM Phenotype]
- Neurofibromatosis, type II [OMIM Phenotype]
- Schwannomatosis 1 [OMIM Phenotype]
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]
- genes, neurofibromatosis 2 [MeSH concept]
- genes, neurofibromatosis 2 [MeSH Descriptor]

Keyword's position in hierarchy(ies) :

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