multiple synostoses syndrome 3

Preferred Label : multiple synostoses syndrome 3;

MeSH note : aks SYNS3; associated with mutation in FGF9;

Origin ID

C567839;

UMLS CUI

C2751826;

Currated CISMeF NLP mapping
- Multiple synostoses syndrome 3 [OMIM Phenotype]
MeSH term(s) associated for indexing
- synostosis [MeSH Descriptor]
Record concept(s)
- multiple synostoses syndrome 3 [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- Multiple synostoses syndrome 3 [OMIM Phenotype]