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
00156 CSS syndrome, Coffin-Siris (CSS) - - 225 189 ARID1A, ARID1B, ARID2, DPF2, SMARCA4, SMARCB1, SMARCE1, SOX11 - -
05386 CSS5 syndrome, Coffin-Siris, type 5 (CSS5) 616938 AD 0 0 SMARCE1 - autosomal dominant
02638 meningioma meningioma, familial, susceptibility to 607174 AD 65 65 MN1, NF2, PDGFB, PTEN, SMARCE1, SUFU - -
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