whirlin - CISMeF

Preferred Label : whirlin;

Approved symbol HGNC : WHRN;

Alias symbols HGNC : PDZD7B; USH2D; CIP98;

Chromosome HGNC : 9q32;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000095397;

Details

Origin ID

HGNC:16361;

UMLS CUI

C1424217;

Automatic exact mappings (from CISMeF team)
- Usher syndrome, type iid [OMIM Phenotype]
- Whirlin [OMIM gene]
- whirlin [ORDO Gene]
OMIM gene
- Whirlin [OMIM gene]
Orphanet gene
- whirlin [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- DFNB31 gene [LOINC component]
- Whirlin [OMIM gene]

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