dyschromatosis universalis hereditaria 2

Preferred Label : dyschromatosis universalis hereditaria 2;

Origin ID

C567194;

UMLS CUI

C2675183;

Currated CISMeF NLP mapping
- Dyschromatosis universalis hereditaria 2 [OMIM Phenotype]
MeSH term(s) associated for indexing
- pigmentation disorders [MeSH Descriptor]
- skin diseases, genetic [MeSH Descriptor]
Record concept(s)
- dyschromatosis universalis hereditaria 2 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Dyschromatosis universalis hereditaria 2 [OMIM Phenotype]