Deaf1 transcription factor

Preferred Label : Deaf1 transcription factor;

Symbol : DEAF1;

CISMeF acronym : DEAF1;

Type : Gene;

Alternative titles and symbols : Deaf1, drosophila, homolog of; Suppressin; Zinc finger mynd domain-containing protein 5; SPN; ZMYND5; Deformed epidermal autoregulatory factor 1 homolog;

Ensembl ID : ENSG00000177030;

Prefixed ID : *602635;

Details

Origin ID

602635;

UMLS CUI

C1422833;

Automatic exact mappings (from CISMeF team)
- DEAF1 transcription factor [ORDO Gene]
- DEAF1 transcription factor [HGNC gene]
- SPN Gene [NCIt concept]
- Solitary Pulmonary Nodule [NCIt concept]
- Special Populations Networks [NCIt concept]
- suppressin [MeSH concept]
- suppressin [MeSH Supplementary Concept]
HGNC gene
- DEAF1 transcription factor [HGNC gene]
ORDO concept(s)
- DEAF1 transcription factor [ORDO Gene]
Phenotypes related
- Neurodevelopmental disorder with hypotonia and impaired expressive language and with or without seizures [OMIM Phenotype]
- Vulto-van silfhout-de vries syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DEAF1 transcription factor [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients