All diseases

2 entries on 1 page. Showing entries 1 - 2.

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00156 CSS Coffin-Siris syndrome (CSS) - 220 188 ARID1A, ARID1B, ARID2, SMARCA4, SMARCB1, SMARCE1 - -
05387 CSS-6 Coffin-Siris syndrome, type 3 (CSS-6) 617808 0 0 ARID2 - autosomal dominant