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
00959 - dysplasia, otodental, chromsome deletion syndrome - - - - FADD, FGF3 - -
03421 - Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations 613759 AR - - FADD - -
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