Congenital myasthenic syndrome (CMS) is a group of genetic disorders of impaired neuromuscular transmission at the motor endplate characterized by fatigable muscle weakness.

Synonyms: CMS

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Term information

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ICD-10:G70.2
OMIM:603034
OMIM:614198
OMIM:616330
OMIM:615120
OMIM:617143
OMIM:616314
OMIM:616313
OMIM:614750
MeSH:D020294
UMLS:C0751882
OMIM:254300
OMIM:601462
OMIM:608930
OMIM:608931
OMIM:254190
OMIM:616040
OMIM:605809
OMIM:616321
OMIM:616325
OMIM:616324
OMIM:616720
OMIM:616323
OMIM:616224
OMIM:616322
OMIM:610542
OMIM:616228
OMIM:617239
OMIM:616227
OMIM:616304
OMIM:616326
OMIM:254210

notation

ORPHA:590