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
01562 - myopathy, spheroid body 182920 AD - - MYOT - -
01449 LGMD1A dystrophy, muscular, limb-girdle, type 1A (LGMD-1A) 159000 - 1 1 MYOT - -
02832 MFM3 myopathy, myofibrillar, type 3 (MFM-3) 609200 AD - - MYOT - -
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