All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03876 FANCQ Fanconi anemia, complementation group Q (FANCQ) 615272 AR 2 2 ERCC4 - -
00139 ID intellectual disability (ID) - - 2351 2050 AAAS, AARS2, ABCD1, ABCD4, ABHD5, ACAD9, ACO2, ACOX1, ACSF3, ACSL4, ACTB, ACTG1, ADAMTS10, ADAR, ADCK3, ADSL, AFF2, AGA, AGTR2, AHI1, 543 more - -
00717 XFEPS progeroid syndrome, XFE (XFEPS) 610965 AR - - ERCC4 - -
00716 XPF xeroderma pigmentosum, complementation group F (XPF) 278760 AR 1 1 ERCC4 - -
Legend   How to query