Pejvakin - CISMeF

Preferred Label : Pejvakin;

Symbol : PJVK;

CISMeF acronym : PJVK;

Type : Gene;

Alternative titles and symbols : Dfnb59 gene;

Ensembl ID : ENSG00000204311;

Prefixed ID : *610219;

Details

Origin ID

610219;

UMLS CUI

C1539285;

Automatic exact mappings (from CISMeF team)
- pejvakin [ORDO Gene]
- pejvakin [HGNC gene]
HGNC gene
- pejvakin [HGNC gene]
ORDO concept(s)
- pejvakin [ORDO Gene]
Phenotypes related
- Deafness, autosomal recessive 59 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- pejvakin [HGNC gene]

Keyword's position in hierarchy(ies) :

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