All diseases

6 entries on 1 page. Showing entries 1 - 6.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01596 CMH1 cardiomyopathy, hypertrophic, familial, type 1 192600 AD;DD 1 1 CAV3, MYH7, MYLK2 - -
01273 hCK hyperCKemia (hCK, elevated serum creatine phosphokinase) 123320 AD 229 277 CAV3, DMD - -
03061 LQT9 QT syndrome, long, type 9 (LQT-9) 611818 AD - - CAV3 - -
03604 MPDT myopathy, distal, Tateyama type 614321 AD - - CAV3 - -
02576 RMD2 disease, muscle, rippling, type 2 606072 AD 85 85 CAV3 - -
02705 RMD2;LGMD1C rippling muscle disease, type 2 (LGMD1C) 607801 AD 4 4 CAV3 - -
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