All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
05351 FCMSU faciocardiomusculoskeletal syndrome, Uruguay type (FCMSU) - - - - FHL1 - -
06842 FCMSU Uruguay faciocardiomusculoskeletal syndrome 300280 XLR - - FHL1 - -
02180 RBMX1A myopathy, reducing body, X-linked, type 1a (RBMX-1A) 300717 XLD - - FHL1 - -
02181 RBMX1B myopathy, reducing body, X-linked, type 1b (RBMX-1B) 300718 XL - - FHL1 - -
02178 SPM myopathy, scapuloperoneal, X-linked dominant (SPM) 300695 XLD 2 2 FHL1 - -
02179 XMPMA;EDMD6 myopathy, X-linked, with postural muscle atrophy (XMPMA, Emery-Dreifuss muscular dystrophy 6 (EDMD-6)) 300696 XLR 9 9 FHL1 - -
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