xeroderma pigmentosum, complementation group F

Preferred Label : xeroderma pigmentosum, complementation group F;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0562892;

UMLS CUI

C0268140;

Automatic exact mappings (from CISMeF team)
- DNA Repair Endonuclease XPF [NCIt concept]
- ERCC excision repair 4, endonuclease catalytic subunit [ORDO Gene]
Currated CISMeF NLP mapping
- Xeroderma Pigmentosum, Complementation Group F [NCIt concept]
- Xeroderma pigmentosum F [ICD-11 More detail]
- Xeroderma pigmentosum complementation group F [ORDO Disease]
- Xeroderma pigmentosum, complementation group f [OMIM Phenotype]
- Xeroderma pigmentosum, group F (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group F [Disease (Nov.)]
- xeroderma pigmentosum group F [DO Concept]
- xeroderma pigmentosum, group f [SNOMED Notion]
Related record
- xeroderma pigmentosum, complementation group F [MeSH Supplementary Concept]
Semantic type(s)
- Congenital Abnormality [UMLS semantic type]
UMLS correspondences (same concept)
- Xeroderma Pigmentosum, Complementation Group F [NCIt concept]
- Xeroderma pigmentosum complementation group F [ORDO Disease]
- Xeroderma pigmentosum, complementation group f [OMIM Phenotype]
- Xeroderma pigmentosum, group F (disorder) [SNOMED CT concept]
- xeroderma pigmentosum group F [DO Concept]
- xeroderma pigmentosum group F [Disease (Nov.)]
- xeroderma pigmentosum, group f [SNOMED Notion]