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
00144 CSS3 Coffin-Siris syndrome 3 614608 - 0 0 SMARCB1 - -
00145 RTPS1 Rhabdoid tumor predisposition syndrome 1 609322 - 0 0 SMARCB1 - -
00146 SWNTS1 Schwannomatosis-1, susceptibility to 162091 - 0 0 SMARCB1 - -
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