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
07088 DEE90 encephalopathy, developmental and epileptic, type 90 301058 XLD;XLR - - FGF13 - -
07089 XLID110 intellectual developmental disorder, X-linked type 110 301095 XLR - - FGF13 - -
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