All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00139 ID intellectual disability (ID) - - 2355 2054 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 543 more - -
00279 MDDGA7 dystrophy, muscular, dystroglycanopathy (congenital with brain and eye anomalies), type A7 (MDDGA-7) 614643 AR 26 26 ISPD - -
04526 MDDGC7;LGMD2U dystrophy, muscular, dystroglycanopathy, type C7 (MDDGC-7, limb-girdle muscular dystrophy type 2U (LGMD-2U)) 616052 AR - - ISPD - -
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