All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01946 - myopathy, Miyoshi 254130 - - - DYSF - -
02603 DMAT myopathy, distal, with anterior tibial onset (DMAT) 606768 - - - DYSF - -
00141 LGMD-2 dystrophy, muscular, limb-girdle, autosomal recessive, type 2 (LGMD-2) - - - - CAPN3, DYSF, FKRP, FKTN, SGCA, SGCB, SGCD, SGCG - -
01943 LGMD-2B dystrophy, muscular, limb-girdle, type 2B (LGMD-2B) 253601 - - - DYSF - -
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