hypertrophic cardiomyopathy, familial, mid-left ventricular chamber type 2, ventricular myosin regulatory light chain-2 mutation associated

Genetics

• associated with defects in MYL2

More general terms

• familial hypertrophic cardiomyopathy

Additional terms

• myosin regulatory light chain (MRLC)

Database

• OMIM: https://mirror.omim.org/entry/608758