All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04318 CMS4A myasthenic syndrome, congenital, type 4A, slow-channel (CMS-4A) 605809 AD;AR 2 2 CHRNE - -
04319 CMS4B myasthenic syndrome, congenital, type 4B, fast-channel (CMS-4B) 616324 AR - - CHRNE - -
01002 CMS4C myasthenic syndrome, congenital, type 4C, associated with acetylcholine receptor deficiency (CMS-4C) 608931 AR 11 - CHRNE - -
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