xeroderma pigmentosum, autosomal dominant, mild

Preferred Label : xeroderma pigmentosum, autosomal dominant, mild;

UMLS semantic type : T047 - Disease or Syndrome;

Origin ID

M0566289;

UMLS CUI

C1860231;

Currated CISMeF NLP mapping
- Xeroderma pigmentosum, autosomal dominant, mild [OMIM Phenotype]
Related record
- xeroderma pigmentosum, autosomal dominant, mild [MeSH Supplementary Concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Xeroderma pigmentosum, autosomal dominant, mild [OMIM Phenotype]