MeSH Browser

MeSH Supplementary: Myasthenic Syndrome, Congenital, Associated with Facial Dysmorphism
Unique ID: C563830
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563830
Registry Numbers: 0
Heading Mapped to: *Blepharoptosis; *Myasthenic Syndromes, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 1955/01/01

Myasthenic Syndrome, Congenital, Associated with Facial Dysmorphism MeSH Supplementary Concept Data 2025