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
04292 MDDGA12 dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A12 (MDDGA-12) 615249 AR 1 1 POMK - -
04291 MDDGC12 dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C12 (MDDGC-12) 616094 AR - - POMK - -
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