Last update 01 Nov 2024

Cardiomyopathy, Familial Hypertrophic, 14

Basic Info

Synonyms
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 14, CMH14, Cardiomyopathy, Familial Hypertrophic, 14
+ [2]
Introduction
An autosomal dominant subtype of familial hypertrophic cardiomyopathy caused by mutation(s) in the MYH6 gene, encoding myosin-6.

Related

100 Clinical Results associated with Cardiomyopathy, Familial Hypertrophic, 14
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100 Translational Medicine associated with Cardiomyopathy, Familial Hypertrophic, 14
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0 Patents (Medical) associated with Cardiomyopathy, Familial Hypertrophic, 14
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1
Literatures (Medical) associated with Cardiomyopathy, Familial Hypertrophic, 14
01 Aug 2011European Journal of Human GeneticsQ2 · BIOLOGY
Clinical utility gene card for: hypertrophic cardiomyopathy (type 1–14)
Q2 · BIOLOGY

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