mandibulofacial dysostosis with ptosis, autosomal dominant

Preferred Label : mandibulofacial dysostosis with ptosis, autosomal dominant;

Origin ID

C564267;

UMLS CUI

C1842349;

Currated CISMeF NLP mapping
- Mandibulofacial dysostosis with ptosis, autosomal dominant [OMIM Phenotype]
MeSH term(s) associated for indexing
- blepharoptosis [MeSH Descriptor]
- mandibulofacial dysostosis [MeSH Descriptor]
Record concept(s)
- mandibulofacial dysostosis with ptosis, autosomal dominant [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Mandibulofacial dysostosis with ptosis, autosomal dominant [OMIM Phenotype]