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
03531 ATFB12 fibrillation, atrial, familial, type 12 614050 AD - - ABCC9 - -
00358 Cantu osteochondrodysplasia, hypertrichotic (Cantu syndrome) 239850 AD 33 33 ABCC9 - -
02766 CMD1O cardiomyopathy, dilated, type 1O 608569 AD - - ABCC9 - -
06992 IDMYS intellectual disability and myopathy syndrome 619719 AR - - ABCC9 - -
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