MYH7
MIM.160760 14q12
Pathology
germline mutations in MYH7
- familial hypertrophic cardiomyopathy (MIM.192600)
- familial dilated cardiomyopathy CMD1S (MIM.160760)
- myosin storage myopathy without cardiomyopathy (MIM.608358)
- Laing early-onset distal myopathy or sporadic Laing distal myopathy (MIM.160500) (MPD1) (#15322983#)
See also
MYHs