All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04315 CMS3A myasthenic syndrome, congenital, type 3A, slow-channel (CMS-3A) 616321 AD - - CHRND - -
04316 CMS3B myasthenic syndrome, congenital, type 3B, fast-channel (CMS-3B) 616322 AR - - CHRND - -
04317 CMS3C myasthenic syndrome, congenital, type 3C, associated with acetylcholine receptor deficiency (CMS-3C) 616323 AR - - CHRND - -
00572 LMPS multiple pterygium syndrome, lethal type (LMPS ) 253290 AR 16 16 CHRNA1, CHRND, CHRNG - -
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