All diseases

4 entries on 1 page. Showing entries 1 - 4.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01454 CNM1 myopathy, centronuclear, type 1 (CNM1) 160150 AD 44 44 DNM2, MTMR14 - -
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 - - FMR1 - -
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