Forkhead box n1

Preferred Label : Forkhead box n1;

Symbol : FOXN1;

CISMeF acronym : FOXN1;

Type : Gene;

Alternative titles and symbols : Winged helix nude; WHN;

Ensembl ID : ENSG00000109101;

Prefixed ID : *600838;

Détails

Origin ID

600838;

UMLS CUI

C1421504;

Automatic exact mappings (from CISMeF team)
- FOXN1 Gene [NCIt concept]
- FOXN1 wt Allele [NCIt concept]
- Forkhead Box Protein N1 [NCIt concept]
- forkhead box N1 [ORDO Gene]
- forkhead box N1 [HGNC gene]
HGNC gene
- forkhead box N1 [HGNC gene]
NCIt concept(s)
- FOXN1 Gene [NCIt concept]
- FOXN1 wt Allele [NCIt concept]
- Forkhead Box Protein N1 [NCIt concept]
ORDO concept(s)
- forkhead box N1 [ORDO Gene]
Phenotypes related
- T-cell immunodeficiency, congenital alopecia, and nail dystrophy [OMIM Phenotype]
- T-cell lymphopenia, infantile, with or without nail dystrophy, autosomal dominant [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FOXN1 Gene [NCIt concept]
- forkhead box N1 [HGNC gene]

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