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
07106 AMC6 arthrogryposis multiplex congenita, type 6 619334 AR - - NEB - -
05837 NEBDM Nebulin related distal myopathy - AD;AR;SMo 10 8 NEB skeletal muscle -
04164 NEM myopathy, nemaline (NEM) - - 471 470 CFL2, KLHL40, KLHL41, NEB - -
01963 NEM2 myopathy, nemaline, type 2 (NEM2) 256030 AR 11 11 NEB - -
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