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) - - - - CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG - -
01944 LGMD-2C;SCARMD dystrophy, muscular, limb-girdle, type 2C (LGMD-2C, severe autosomal recessive muscular dystrophy, North African type (SCARMD)) 253700 - - - SGCG - -
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