All diseases

7 entries on 1 page. Showing entries 1 - 7.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
01959 CFTD myopathy, congenital, with fiber type disproportion (CFTD) 255310 - 52 51 ACTA1, MYH7, RYR1, SEPN1, TPM2, TPM3 - -
03332 CMD-1S;LVNC-5 cardiomyopathy, dilated, type 1S (CMD-1S, left ventricular noncompaction type 5 (LVNC-5)) 613426 - 0 0 MYH7 - -
01596 CMH-1 cardiomyopathy, hypertrophic, familial, type 1 (CMH-1) 192600 - 0 0 CAV3, MYH6, MYH7, MYLK2 - -
01455 MPD-1 myopathy, distal, type 1 (MPD-1) 160500 - 2 2 MYH7 - -
02755 MSMA myopathy, myosin storage, autosomal dominant (MSMA) 608358 - 0 0 MYH7 - -
04585 MSMB myopathy, myosin storage, autosomal recessive (MSMB) 255160 - 0 0 MYH7 - -
01555 SPMM myopathy, scapuloperoneal, MYH7-related (SPMM) 181430 - 0 0 MYH7 - -
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