xeroderma pigmentosum, complementation group G

Preferred Label : xeroderma pigmentosum, complementation group G;

MeSH note : mutation in ERCC5;

MeSH synonym : xeroderma pigmentosum VII;

Détails

Origin ID

C562593;

UMLS CUI

C0268141;

Automatic exact mappings (from CISMeF team)
- DNA Repair Protein Complementing XP-G Cells [NCIt concept]
Currated CISMeF NLP mapping
- Xeroderma Pigmentosum, Complementation Group G [NCIt concept]
- Xeroderma pigmentosum G [ICD-11 More detail]
- Xeroderma pigmentosum complementation group G [HPO term]
- Xeroderma pigmentosum complementation group G [ORDO Disease]
- Xeroderma pigmentosum, complementation group g [OMIM Phenotype]
- Xeroderma pigmentosum, group G (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group G [Disease (Nov.)]
- xeroderma pigmentosum group G [DO Concept]
- xeroderma pigmentosum, group g [SNOMED Notion]
MeSH term(s) associated for indexing
- xeroderma pigmentosum [MeSH Descriptor]
Record concept(s)
- xeroderma pigmentosum, complementation group G [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Xeroderma Pigmentosum, Complementation Group G [NCIt concept]
- Xeroderma pigmentosum complementation group G [HPO term]
- Xeroderma pigmentosum complementation group G [ORDO Disease]
- Xeroderma pigmentosum, complementation group g [OMIM Phenotype]
- Xeroderma pigmentosum, group G (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group G [DO Concept]
- xeroderma pigmentosum group G [Disease (Nov.)]
- xeroderma pigmentosum, group g [SNOMED Notion]

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