Neurofibromin 1

Preferred Label : Neurofibromin 1;

Symbol : NF1;

CISMeF acronym : NF1;

Type : Gene;

Alternative titles and symbols : NEUROFIBROMIN;

Ensembl ID : ENSG00000196712;

Prefixed ID : *613113;

Details

Origin ID

613113;

UMLS CUI

C0085113;

Automatic exact mappings (from CISMeF team)
- NF1 Gene [NCIt concept]
- NF1 gene [LOINC component]
- Neurofibromatosis Type 1 [NCIt concept]
- Neurofibromatosis type 1 [ICD-11 Sub-sub category]
- Neurofibromatosis type 1 [ORDO Disease]
- Neurofibromin [NCIt concept]
- Neurofibromin (substance) [SNOMED CT concept]
- neurofibromatosis 1 [DO Concept]
- neurofibromatosis 1 [MeSH Descriptor]
- neurofibromin 1 [ORDO Gene]
- neurofibromin 1 [MeSH concept]
- neurofibromin 1 [MeSH Descriptor]
- neurofibromin 1 [HGNC gene]
HGNC gene
- neurofibromin 1 [HGNC gene]
ORDO concept(s)
- neurofibromin 1 [ORDO Gene]
Phenotypes related
- Juvenile myelomonocytic leukemia [OMIM Phenotype]
- Neurofibromatosis, familial spinal [OMIM Phenotype]
- Neurofibromatosis, type I [OMIM Phenotype]
- Neurofibromatosis-noonan syndrome [OMIM Phenotype]
- Watson syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- NF1 Gene [NCIt concept]
- NF1 gene [LOINC component]
- genes, neurofibromatosis 1 [MeSH concept]
- genes, neurofibromatosis 1 [MeSH Descriptor]
- neurofibromin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients