All diseases

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

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01562 - myopathy, spheroid body 182920 0 0 MYOT - -
01449 LGMD-1A dystrophy, muscular, limb-girdle, type 1A (LGMD-1A) 159000 0 0 MYOT - -
02832 MFM-3 myopathy, myofibrillar, type 3 (MFM-3) 609200 0 0 MYOT - -