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
06720 AMC3 arthrogryposis multiplex congenita, type 3, myogenic 618484 AR - - SYNE1 - -
03224 EDMD4 dystrophy, muscular, Emery-Dreifuss, type 4, autosomal dominant (EDMD-4) 612998 AD 2 2 SYNE1 - -
02977 SCAR8 ataxia, spinocerebellar, autosomal recessive, type 8 (SCAR-8) 610743 AR 19 18 SYNE1 - -
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