All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04313 CMS2A myasthenic syndrome, congenital, type 2A, slow-channel (CMS-2A) 616313 AD 1 - CHRNB1 - -
04314 CMS2C myasthenic syndrome, congenital, type 2C, associated with acetylcholine receptor deficiency (CMS-2C) 616314 AR 1 1 CHRNB1 - -
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