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Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency
MeSH Supplementary Concept Data 2024
Details
Concepts
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
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Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency
Preferred
Concept UI
M0564129
Registry Number
0
Terms
Myasthenic Syndrome, Congenital, with Facial Dysmorphism, associated with Acetylcholine Receptor Deficiency
Preferred Term
Term UI
T828747
Date
08/28/2012
LexicalTag
NON
ThesaurusID
OMIM (2013)
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