All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
00054 COFS3 Cerebrooculofacioskeletal syndrome 3 616570 - 0 0 ERCC5 - -
00055 XPG Xeroderma pigmentosum, group G 278780 - 0 0 ERCC5 - -
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