All diseases

5 entries on 1 page. Showing entries 1 - 5.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05351 FCMSU syndrome, faciocardiomusculoskeletal, Uruguay type (FCMSU) - - 0 0 FHL1 - -
02180 RBMX-1A myopathy, reducing body, X-linked, type 1a (RBMX-1A) 300717 - 0 0 FHL1 - -
02181 RBMX-1B myopathy, reducing body, X-linked, type 1b (RBMX-1B) 300718 - 0 0 FHL1 - -
02178 SPM myopathy, scapuloperoneal, X-linked dominant (SPM) 300695 - 2 2 FHL1 - -
02179 XMPMA;EDMD-6 myopathy, X-linked, with postural muscle atrophy (XMPMA, Emery-Dreifuss muscular dystrophy 6 (EDMD-6)) 300696 - 9 9 FHL1 - -
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