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
00141 LGMD-2 dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) - - 182 181 CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG, TRAPPC11 - -
02734 LGMD-2D dystrophy, muscular, limb-girdle, type 2D (LGMD-2D) 608099 - 13 13 SGCA - -
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