Cardiomyopathy Update

Cardiomyopathy Update

MedlinePlus sent this bulletin at 04/20/2016 01:10 PM EDT

New on the MedlinePlus Cardiomyopathy page:

Genetics Home Reference: isobutyryl-CoA dehydrogenase deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: keratoderma with woolly hair

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: glycogen storage disease type III

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: neutral lipid storage disease with myopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: primary carnitine deficiency

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: familial hypertrophic cardiomyopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: familial restrictive cardiomyopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: familial dilated cardiomyopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: dilated cardiomyopathy with ataxia syndrome

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: arrhythmogenic right ventricular cardiomyopathy

04/13/2016 02:39 PM EDT

Source: National Library of Medicine - 

Genetics Home Reference: DOLK-congenital disorder of glycosylation

03/15/2016 11:30 PM EDT

Source: National Library of Medicine -