All diseases

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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05266 LGMDR25;LGMD2X dystrophy, muscular, limb-girdle, autosomal recessive, type 25 (LGMD2X) 616812 AR 2 2 BVES - -
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