All diseases

4 entries on 1 page. Showing entries 1 - 4.
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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 - -
05387 CSS6 Coffin-Siris syndrome, type 6 (CSS6) 617808 AD 3 3 ARID2 - autosomal dominant
02209 MRX101 mental retardation, X-linked, type 101 (MRX101) 300928 XLR 5 5 MID2 - -
04494 SCAR18 ataxia, spinocerebellar, autosomal recessive, type 18 (SCAR-18) 616204 AR - - GRID2 - -
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