WT1 transcription factor

Preferred Label : WT1 transcription factor;

Approved symbol HGNC : WT1;

Alias symbols HGNC : NPHS4; WIT-2; WAGR; AWT1; WT-1;

Chromosome HGNC : 11p13;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000184937;

Details

Origin ID

HGNC:12796;

UMLS CUI

C0694898;

Automatic exact mappings (from CISMeF team)
- Nephrotic syndrome, type 4 [OMIM Phenotype]
- WT1 transcription factor [ORDO Gene]
- Wilms tumor 1 [OMIM Phenotype]
- Wilms tumor, aniridia, genitourinary anomalies, and impaired intellectual development syndrome [OMIM Phenotype]
- Wt1 transcription factor [OMIM gene]
NCIt concept
- WT1 Gene [NCIt concept]
OMIM gene
- Wt1 transcription factor [OMIM gene]
Orphanet gene
- WT1 transcription factor [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- WT1 Gene [NCIt concept]
- WT1 gene [LOINC component]
- Wt1 transcription factor [OMIM gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients