All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

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 - -
00756 MRD-15 mental retardation, autosomal dominant, type 15 (MRD-15) 614608 - - - SMARCB1 - -
00755 RTPS-1 tumor, rhabdoid, predisposition syndrome, type 1 (RTPS-1) 609322 - - - SMARCB1 - -
00436 SWNTS-1 Schwannomatosis, type 1 (SWNTS-1) 162091 - - - LZTR1, NF2, SMARCB1 - -
Legend   How to query