MeSH Browser

MeSH Supplementary: Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency
Unique ID: C563829
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C563829
Registry Numbers: 0
Heading Mapped to: Receptors, Cholinergic / deficiency; *Craniofacial Abnormalities; *Myasthenic Syndromes, Congenital
Frequency: 0
Date of Entry: 2012/11/05
Revision Date: 2013/11/06

Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency MeSH Supplementary Concept Data 2025