xeroderma pigmentosum, complementation group C

Preferred Label : xeroderma pigmentosum, complementation group C;

MeSH note : mutation in XPC gene;

MeSH synonym : XP3; xeroderma pigmentosum III; XPCC; XP, group C;

Details

Origin ID

C567886;

UMLS CUI

C2752147;

Currated CISMeF NLP mapping
- XPC complex subunit, DNA damage recognition and repair factor [ORDO Gene]
- Xeroderma Pigmentosum, Complementation Group C [NCIt concept]
- Xeroderma pigmentosum C [ICD-11 More detail]
- Xeroderma pigmentosum complementation group C [ORDO Disease]
- Xeroderma pigmentosum, Complementation group C [OMIM Phenotype]
- Xeroderma pigmentosum, group C (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group C [Disease (Nov.)]
- xeroderma pigmentosum group C [DO Concept]
- xeroderma pigmentosum, group c [SNOMED Notion]
MeSH term(s) associated for indexing
- xeroderma pigmentosum [MeSH Descriptor]
Record concept(s)
- xeroderma pigmentosum, complementation group C [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- XPC complex subunit, DNA damage recognition and repair factor [ORDO Gene]
- Xeroderma Pigmentosum, Complementation Group C [NCIt concept]
- Xeroderma pigmentosum complementation group C [ORDO Disease]
- Xeroderma pigmentosum, Complementation group C [OMIM Phenotype]
- Xeroderma pigmentosum, group C (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group C [DO Concept]
- xeroderma pigmentosum group C [Disease (Nov.)]
- xeroderma pigmentosum, group c [SNOMED Notion]

Keyword's position in hierarchy(ies) :

Main resources

You can consult :

recommendations
documents concerning education
documents for patients