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
03332 CMD1S;LVNC5 cardiomyopathy, dilated, type 1S (CMD-1S, left ventricular noncompaction type 5 (LVNC-5)) 613426 AD 1 2 MYH7 - -
01596 CMH1 cardiomyopathy, hypertrophic, familial, type 1 192600 AD;DD 1 1 CAV3, MYH7, MYLK2 - -
01455 MPD1 myopathy, distal, type 1 (MPD-1) 160500 AD 3 3 MYH7 - -
02755 MSMA myopathy, myosin storage, autosomal dominant (MSMA) 608358 AD 1 1 MYH7 - -
04585 MSMB myopathy, myosin storage, autosomal recessive (MSMB) 255160 AR - - MYH7 - -
01555 SPMM myopathy, scapuloperoneal, MYH7-related (SPMM) 181430 AD - - MYH7 - -
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