All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05475 CMS21 myasthenic syndrome, congenital, type 21, pre-synaptic (CMS-21) 617239 AR - - SLC18A3 - autosomal recessive
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