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
00428 CMD1I cardiomyopathy, dilated, type 1I (CMD-1I) 604765 AD 1 1 DES - -
00430 LGMD2R dystrophy, muscular, limb-girdle, type 2R (LGMD-2R) 615325 - 0 0 DES - -
00427 MFM1;LGMD1D myopathy, myofibrillar, type 1 (MFM-1, limb-girdle muscular dystrophy 1D (LGMD-1D) 601419 AD;AR 0 0 DES - -
00429 SCPNK scapuloperoneal syndrome, neurogenic, Kaeser type (SCPNK) 181400 AD 5 5 DES - autosomal dominant
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