Xeroderma Pigmentosum, Type G-Cockayne Syndrome

Preferred Label : Xeroderma Pigmentosum, Type G-Cockayne Syndrome;

CISMeF synonym : Xpg/Cs; xeroderma pigmentosum, type G/Cockayne syndrome;

MeSH synonym : Xpg-Cs;

Détails

Origin ID

C566879;

UMLS CUI

C1968561;

Automatic exact mappings (from CISMeF team)
- DNA Repair Protein Complementing XP-G Cells [NCIt concept]
- ERCC5 wt Allele [NCIt concept]
- Ercc excision repair 5, endonuclease [OMIM gene]
- Xeroderma pigmentosum, complementation group g [OMIM Phenotype]
MeSH term(s) associated for indexing
- cockayne syndrome [MeSH Descriptor]
- xeroderma pigmentosum [MeSH Descriptor]
Record concept(s)
- Xeroderma Pigmentosum, Type G-Cockayne Syndrome [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]

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