All diseases

4 entries on 1 page. Showing entries 1 - 4.
Legend   How to query  

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 - -
00427 MFM1;LGMD1D myopathy, myofibrillar, type 1 (MFM-1, limb-girdle muscular dystrophy 1D (LGMD-1D) 601419 AD;AR 2 - DES - -
00430 MFM1;LGMD2R yopathy, myofibrillar,, type 1 (LGMD2R) 615325 AD;AR - - DES - -
00429 SCPNK scapuloperoneal syndrome, neurogenic, Kaeser type (SCPNK) 181400 AD 5 5 DES - autosomal dominant
Legend   How to query  


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.