All diseases

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

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00156 CSS Coffin-Siris syndrome (CSS) - - 285 255 ARID1A, ARID1B, ARID2, DPF2, SMARCA4, SMARCB1, SMARCC2, SMARCE1, SOX11 - -
04112 CSS9;MRD27 Coffin-Siris syndrome, type 9 (CSS9, mental retardation, autosomal dominant syndrome, type 27 (MRD27)) 615866 AD 3 2 SOX11 - -
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