Sry-box 11 - CISMeF

Preferred Label : Sry-box 11;

Symbol : SOX11;

CISMeF acronym : SOX11;

Type : Gene;

Alternative titles and symbols : Sry-related hmg-box gene 11;

Ensembl ID : ENSG00000176887;

Prefixed ID : *600898;

Détails

Origin ID

600898;

UMLS CUI

C1420318;

Automatic exact mappings (from CISMeF team)
- SOX11 Gene [NCIt concept]
- SOX11 wt Allele [NCIt concept]
- SRY-box transcription factor 11 [ORDO Gene]
- SRY-box transcription factor 11 [HGNC gene]
- Transcription Factor SOX-11 [NCIt concept]
HGNC gene
- SRY-box transcription factor 11 [HGNC gene]
NCIt concept(s)
- SOX11 Gene [NCIt concept]
- SOX11 wt Allele [NCIt concept]
- Transcription Factor SOX-11 [NCIt concept]
ORDO concept(s)
- SRY-box transcription factor 11 [ORDO Gene]
Phenotypes related
- Intellectual developmental disorder with microcephaly and with or without ocular malformations or hypogonadotropic hypogonadism [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SOX11 Gene [NCIt concept]
- SRY-box transcription factor 11 [HGNC gene]

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

Vous pouvez consulter :

recommendations
documents concerning education
documents for patients