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Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency MeSH Supplementary Concept Data 2022


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 Number
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 Preferred
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