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) - - 2695 2377 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00123 MDDGA1;MEB;WWS dystrophy-dystroglycanopathy, muscular, (congenital with brain and eye anomalies), type A1 (WWS, MEB) 236670 AR 1 1 POMT1 - -
01101 MDDGB1 dystrophy-dystroglycanopathy, muscular, (congenital with mental retardation), type B1 613155 AR 1 1 POMT1 - -
01102 MDDGC1;LGMDR11;LGMD2K dystrophy-dystroglycanopathy, muscular, (limb-girdle), type C1 (LGMDR11, LGMD2K) 609308 AR 1 1 POMT1 - -
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