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
00262 FXS fragile-X syndrome (FXS) 300624 XLD 4 2 FMR1 - -
02172 FXTAS Fragile X tremor/ataxia syndrome (FXTAS) 300623 XLD 1 1 FMR1 - -
02257 POF1 ovarian failure, premature, type 1 (POF-1) 311360 XL 0 0 FMR1 - -
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