All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05852 MDDGB15 dystrophy, muscular, dystroglycanopathy (congenital with impaired intellectual development), type B15 (MDDGB15) 618992 AR - - DPM3 - -
03212 MDDGC15;CDG1O dystrophy, muscular, dystroglycanopathy (limb-girdle), type C15 (MDDGC15, CDG1O) 612937 AR 2 2 DPM3 - -
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