endothelial dystrophy, congenital hereditary, with nail hypoplasia

Preferred Label : endothelial dystrophy, congenital hereditary, with nail hypoplasia;

Origin ID

C565591;

UMLS CUI

C1856970;

Currated CISMeF NLP mapping
- Endothelial dystrophy, congenital hereditary, with nail hypoplasia [OMIM Phenotype]
MeSH term(s) associated for indexing
- corneal dystrophies, hereditary [MeSH Descriptor]
- nail diseases [MeSH Descriptor]
Record concept(s)
- endothelial dystrophy, congenital hereditary, with nail hypoplasia [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Endothelial dystrophy, congenital hereditary, with nail hypoplasia [OMIM Phenotype]