Forkhead box p2 - CISMeF

" /> Forkhead box p2 - CISMeF

CISMeF

chu

Forkhead box p2OMIM gene

Preferred Label : Forkhead box p2;

Symbol : FOXP2;

CISMeF acronym : FOXP2;

Type : Gene;

Alternative titles and symbols : Trinucleotide repeat-containing gene 10; TNRC10; CAGH44;

Ensembl ID : ENSG00000128573;

Prefixed ID : *605317;

Détails

Origin ID

605317;

UMLS CUI

C1422249;

Automatic exact mappings (from CISMeF team)
- FOXP2 Gene [NCIt concept]
- FOXP2 wt Allele [NCIt concept]
- Forkhead Box Protein P2 [NCIt concept]
- forkhead box P2 [ORDO Gene]
- forkhead box P2 [HGNC gene]
HGNC gene
- forkhead box P2 [HGNC gene]
NCIt concept(s)
- FOXP2 Gene [NCIt concept]
- FOXP2 wt Allele [NCIt concept]
- Forkhead Box Protein P2 [NCIt concept]
ORDO concept(s)
- forkhead box P2 [ORDO Gene]
Phenotypes related
- Speech-language disorder 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FOXP2 Gene [NCIt concept]
- forkhead box P2 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients

Nous contacter.
28/07/2025

[Accueil] [Haut de page]

© CHU de Rouen. Toute utilisation partielle ou totale de ce document doit mentionner la source.

" /> Forkhead box p2 - CISMeF

CISMeF

chu

Forkhead box p2OMIM gene

Preferred Label : Forkhead box p2;

Symbol : FOXP2;

CISMeF acronym : FOXP2;

Type : Gene;

Alternative titles and symbols : Trinucleotide repeat-containing gene 10; TNRC10; CAGH44;

Ensembl ID : ENSG00000128573;

Prefixed ID : *605317;

Détails

Origin ID

605317;

UMLS CUI

C1422249;

Automatic exact mappings (from CISMeF team)
- FOXP2 Gene [NCIt concept]
- FOXP2 wt Allele [NCIt concept]
- Forkhead Box Protein P2 [NCIt concept]
- forkhead box P2 [ORDO Gene]
- forkhead box P2 [HGNC gene]
HGNC gene
- forkhead box P2 [HGNC gene]
NCIt concept(s)
- FOXP2 Gene [NCIt concept]
- FOXP2 wt Allele [NCIt concept]
- Forkhead Box Protein P2 [NCIt concept]
ORDO concept(s)
- forkhead box P2 [ORDO Gene]
Phenotypes related
- Speech-language disorder 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FOXP2 Gene [NCIt concept]
- forkhead box P2 [HGNC gene]

Position du mot-clé dans l'(les) arborescence(s) :

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients

Nous contacter.
28/07/2025

[Accueil] [Haut de page]

© CHU de Rouen. Toute utilisation partielle ou totale de ce document doit mentionner la source.