All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
06366 MRMV4 Mirror movements 4 618264 AD - - NTN1 - -
03150 MYPCN myopathy, congenital, Compton-North (MYPCN) 612540 AR 4 4 CNTN1 - -
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