xeroderma pigmentosum, complementation group E

Preferred Label : xeroderma pigmentosum, complementation group E;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0565032;

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 [Disease (Nov.)]
- xeroderma pigmentosum group E [DO Concept]
- xeroderma pigmentosum, group e [SNOMED Notion]
Related record
- xeroderma pigmentosum, complementation group E [MeSH Supplementary 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]