myasthenic syndrome, congenital, associated with facial dysmorphism

Preferred Label : myasthenic syndrome, congenital, associated with facial dysmorphism;

Origin ID

C563830;

UMLS CUI

C3502061;

MeSH term(s) associated for indexing
- blepharoptosis [MeSH Descriptor]
- myasthenic syndromes, congenital [MeSH Descriptor]
Record concept(s)
- myasthenic syndrome, congenital, associated with facial dysmorphism [MeSH concept]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]