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
02594 CMD1L cardiomyopathy, dilated, type 1L (CMD-1L) 606685 - - - SGCD - -
00141 LGMD2 dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) - - 313 311 CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG, TRAPPC11 - -
02350 LGMDR6;LGMD2F dystrophy, muscular, limb-girdle, autosomal recessive, type 6 (LGMD2F) 601287 AR - - SGCD - -
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