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
00139 ID intellectual disability (ID) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01102 LGMD-2K;MDDGC-1 dystrophy, muscular, limb-girdle, type 2K (LGMD-2K, dystroglycanopathy C1 (MDDGC-1)) 609308 - - - POMT1 - -
00123 MDDGA-1;MEB;WWS dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A1 (MDDGA-1, Walker-Warburg syndrome (WWS), muscle-eye-brain disease (MEB)) 236670 - - - POMT1 - -
01101 MDDGB-1 dystrophy, muscular, dystroglycanopathy (congenital with mental retardation), type B1 (MDDGB-1) 613155 - - - POMT1 - -
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