Whirlin - CISMeF

Preferred Label : Whirlin;

Symbol : WHRN;

CISMeF acronym : WHRN;

Type : Gene;

Alternative titles and symbols : Cask-interacting protein, 98-kd; CIP98; KIAA1526;

Ensembl ID : ENSG00000095397;

Prefixed ID : *607928;

Details

Origin ID

607928;

UMLS CUI

C1424217;

Automatic exact mappings (from CISMeF team)
- whirlin [ORDO Gene]
- whirlin [HGNC gene]
HGNC gene
- whirlin [HGNC gene]
ORDO concept(s)
- whirlin [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 31 [OMIM Phenotype]
- Usher syndrome, type iid [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DFNB31 gene [LOINC component]
- whirlin [HGNC gene]

Keyword's position in hierarchy(ies) :

You can consult :

All resources
or only the major
or use the search engine

recommendations
documents concerning education
documents for patients