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
00052 FANCQ Fanconi anemia, complementation group Q 615272 - 0 0 ERCC4 - -
00051 XFEPS XFE PROGEROID SYNDROME 610965 - 0 0 ERCC4 - -
00053 XPF Xeroderma pigmentosum, group F 278760 - 0 0 ERCC4 - -
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