All diseases

3 entries on 1 page. Showing entries 1 - 3.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
03531 ATFB-12 fibrillation, atrial, familial, type 12 (ATFB-12) 614050 - - - ABCC9 - -
00358 Cantu Cantu syndrome (osteochondrodysplasia, hypertrichotic) 239850 - - - ABCC9 - -
02766 CMD-1O cardiomyopathy, dilated, type 1O (CMD-1O) 608569 - - - ABCC9 - -
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