All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01088 LGMD-2O;MDDGC-3 dystrophy, muscular, limb-girdle, type 2O (LGMD-2O, dystroglycanopathy C3 (MDDGC-3)) 613157 - 0 0 POMGNT1 - -
00073 MDDGA-3;MEB;WWS dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A3 (MDDGA-3, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB)) 253280 - 0 0 POMGNT1 - -
03738 MDDGA-8 dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A8 (MDDGA-8) 614830 - 1 1 POMGNT2 - -
01087 MDDGB-3 dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B3 (MDDGB-3) 613151 - 0 0 POMGNT1 - -
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