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Endplate Acetylcholinesterase Deficiency MeSH Supplementary Concept Data 2022


MeSH Supplementary
Endplate Acetylcholinesterase Deficiency
Unique ID
C566415
RDF Unique Identifier
http://id.nlm.nih.gov/mesh/C566415
Entry Term(s)
Congenital Myasthenic Syndrome Type Ic
Engel Congenital Myasthenic Syndrome
Myasthenic Syndrome, Congenital, Engel Type
Registry Number
0
Heading Mapped to
*Myasthenic Syndromes, Congenital
Frequency
8
Date of Entry
2012/11/05
Endplate Acetylcholinesterase Deficiency Preferred
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