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
04436 MDDGA9 dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A9 616538 AR 1 1 DAG1 - -
03445 MDDGC9;LGMDR16;LGMD2P dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C9 (LGMDR16, LGMD2P) 613818 AR - - DAG1 - -
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