xeroderma pigmentosum, autosomal dominant, mild - CISMeF

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CISMeF

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Xeroderma pigmentosum, autosomal dominant, mildMeSH Supplementary Concept

Preferred Label : xeroderma pigmentosum, autosomal dominant, mild;

Details

Origin ID

C565989;

UMLS CUI

C1860231;

Currated CISMeF NLP mapping
- Xeroderma pigmentosum, autosomal dominant, mild [OMIM Phenotype]
MeSH term(s) associated for indexing
- xeroderma pigmentosum [MeSH Descriptor]
Record concept(s)
- xeroderma pigmentosum, autosomal dominant, mild [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Xeroderma pigmentosum, autosomal dominant, mild [OMIM Phenotype]

Keyword's position in hierarchy(ies) :

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24/05/2025

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