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
03868 CMD1KK;CMH22;RCM4 cardiomyopathy, dilated, type 1KK (CMD-1KK, hypertrophic type 22 (CHM-22), restrictive (RCM-4)) 615248 AD - - MYPN - autosomal dominant
06080 NEM11 Nemaline myopathy 11, autosomal recessive 617336 AR - - MYPN - -
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