ERCC excision repair 5, endonuclease

Preferred Label : ERCC excision repair 5, endonuclease;

Approved symbol HGNC : ERCC5;

Name synonyms HGNC : Cockayne syndrome;

Chromosome HGNC : 13q33.1;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000134899;

Détails

Origin ID

HGNC:3437;

UMLS CUI

C1333359;

Automatic exact mappings (from CISMeF team)
- Cockayne Syndrome [NCIt concept]
- Cockayne Syndrome [Radlex concept]
- Cockayne syndrome [ICD-11 More detail]
- Cockayne syndrome [PASCAL descriptor]
- Cockayne syndrome [DO Concept]
- Cockayne syndrome [ORDO Disease]
- Cockayne syndrome (disorder) [SNOMED CT concept]
- Cockayne syndrome a [OMIM Phenotype]
- Cockayne's syndrome [MedDRA Preferred Term]
- Congenital malformation syndromes predominantly associated with short stature [ICD-10 Sub-category]
- ERCC excision repair 5, endonuclease [ORDO Gene]
- Ercc excision repair 5, endonuclease [OMIM gene]
- cockayne syndrome [SNOMED Notion]
- cockayne syndrome [MeSH concept]
- cockayne syndrome [MeSH Descriptor]
NCIt concept
- ERCC5 Gene [NCIt concept]
OMIM gene
- Ercc excision repair 5, endonuclease [OMIM gene]
Orphanet gene
- ERCC excision repair 5, endonuclease [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- ERCC5 Gene [NCIt concept]
- Ercc excision repair 5, endonuclease [OMIM gene]

Position du mot-clé dans l'(les) arborescence(s) :

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