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
05551 CMH26;RCM5 cardiomyopathy, hypertrophic, type 26 (CMD-26); cardiomyopathy, restrictive, type 5 (RCM-5) 617047 AD - - FLNC - autosomal dominant
02855 MFM5 myopathy, myofibrillar, type 5 (MFM-5, filamin C related) 609524 AD 1 - FLNC - -
03535 MPD4 myopathy, distal, type 4 (MPD-4) 614065 AD - - FLNC - -
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