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
03445 LGMD-2P;MDDGC-9 dystrophy, muscular, limb-girdle, type 2P (LGMD-2P, dystroglycanopathy C9 (MDDGC-9)) 613818 - 0 0 DAG1 - -
04436 MDDGA-9 dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A9 (MDDGA-9) 616538 - 1 1 DAG1 - -
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