All diseases

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00570 CMS1A myasthenic syndrome, congenital, type 1A, slow-channel (CMS-1A) 601462 AD 1 1 CHRNA1 - -
00571 CMS1B myasthenic syndrome, congenital, type 1B, fast-channel (CMS-1B) 608930 AD;AR 0 0 CHRNA1 - -
00572 LMPS multiple pterygium syndrome, lethal type (LMPS ) 253290 AR 16 16 CHRNA1, CHRND, CHRNG - -
Legend   How to query