Menin 1 - CISMeF

Preferred Label : Menin 1;

Symbol : MEN1;

CISMeF acronym : MEN1;

Type : Gene;

Alternative titles and symbols : Men1 gene; MENIN;

Ensembl ID : ENSG00000133895;

Prefixed ID : *613733;

Details

Origin ID

613733;

UMLS CUI

C0694884;

Automatic exact mappings (from CISMeF team)
- MEN1 Gene [NCIt concept]
- MEN1 gene [LOINC component]
- MEN1 wt Allele [NCIt concept]
- Menin [NCIt concept]
- Multiple endocrine neoplasia type 1 [ORDO Disease]
- Multiple endocrine neoplasia type 1 [ICD-11 More detail]
- Multiple endocrine neoplasia, type 1 (disorder) [SNOMED CT concept]
- menin 1 [ORDO Gene]
- menin 1 [HGNC gene]
- multiple endocrine neoplasia type 1 [MeSH Descriptor]
HGNC gene
- menin 1 [HGNC gene]
ORDO concept(s)
- menin 1 [ORDO Gene]
Phenotypes related
- Multiple endocrine neoplasia, type I [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- MEN1 Gene [NCIt concept]
- MEN1 gene [LOINC component]
- menin 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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