All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
02603 DMAT myopathy, distal, with anterior tibial onset (DMAT) 606768 - 7 7 DYSF - -
00141 LGMD-2 dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) - - 182 181 CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG, TRAPPC11 - -
01943 LGMD2B dystrophy, muscular, limb-girdle, type 2B (LGMD2B) 253601 AR 27 28 DYSF - -
01946 MMD dystrophy, muscular, Miyoshi (MMD) - - 328 313 DYSF - -
05547 MMD-1 dystrophy, muscular, Miyoshi type 1(MMD-1) 254130 - 0 0 DYSF - autosomal recessive
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