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
05126 LGMD dystrophy, muscular, limb-girdle (LGMD) - - 7596 3751 POPDC3, TCAP, TRAPPC11 - -
00141 LGMD2 dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) - - 314 312 CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG, TRAPPC11 - -
03907 LGMDR18;LGMD2S dystrophy, muscular, limb-girdle, autosomal recessive, type 18 (LGMD2S) 615356 AR 5 2 TRAPPC11 - -
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