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) - - - - AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 515 more - -
01018 MRD-16 mental retardation, autosomal dominant, type 16 (MRD-16) 614609 - - - SMARCA4 - -
01017 RTPS-2 tumor, rhabdoid, predisposition syndrome, type 2 (RTPS-2) 613325 - - - SMARCA4 - -
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