xeroderma pigmentosum, complementation group E

Preferred Label : xeroderma pigmentosum, complementation group E;

MeSH note : mutation in DDB2;

MeSH synonym : XP, group E; XP5; xeroderma pigmentosum V; XPE;

Details

Origin ID

C564732;

UMLS CUI

C1848411;

Currated CISMeF NLP mapping
- Xeroderma Pigmentosum, Complementation Group E [NCIt concept]
- Xeroderma pigmentosum E [ICD-11 More detail]
- Xeroderma pigmentosum complementation group E [ORDO Disease]
- Xeroderma pigmentosum, complementation group e [OMIM Phenotype]
- Xeroderma pigmentosum, group E (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group E [DO Concept]
- xeroderma pigmentosum group E [Disease (Nov.)]
- xeroderma pigmentosum, group e [SNOMED Notion]
MeSH term(s) associated for indexing
- xeroderma pigmentosum [MeSH Descriptor]
Record concept(s)
- xeroderma pigmentosum, complementation group E [MeSH concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Xeroderma Pigmentosum, Complementation Group E [NCIt concept]
- Xeroderma pigmentosum complementation group E [ORDO Disease]
- Xeroderma pigmentosum, complementation group e [OMIM Phenotype]
- Xeroderma pigmentosum, group E (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group E [DO Concept]
- xeroderma pigmentosum group E [Disease (Nov.)]
- xeroderma pigmentosum, group e [SNOMED Notion]

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