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
05595 CS Cockayne syndrome (CS) - - 9 9 ERCC6, ERCC8 - -
00612 CSA Cockayne syndrome, type A (CSA) 216400 AR 6 3 ERCC8 - -
00139 ID intellectual disability (ID) - - 2694 2376 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 553 more - -
00613 UVSS2 UV-sensitive syndrome, type 2 (UVSS-2) 614621 AR - - ERCC8 - -
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