Espin - CISMeF

Preferred Label : Espin;

Symbol : ESPN;

CISMeF acronym : ESPN;

Type : Gene;

Alternative titles and symbols : Espin, mouse, homolog of;

Ensembl ID : ENSG00000187017;

Prefixed ID : *606351;

Details

Origin ID

606351;

UMLS CUI

C1421921;

Automatic exact mappings (from CISMeF team)
- espin [ORDO Gene]
- espin [HGNC gene]
HGNC gene
- espin [HGNC gene]
NCIt concept(s)
- ESPN Gene [NCIt concept]
- ESPN wt Allele [NCIt concept]
- Espin [NCIt concept]
ORDO concept(s)
- espin [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 36, with or without vestibular involvement [OMIM Phenotype]
- Usher syndrome, type 1m [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ESPN Gene [NCIt concept]
- espin [HGNC gene]

Keyword's position in hierarchy(ies) :

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