RS267607613 LMNA
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Associated Conditions
Primary familial hypertrophic cardiomyopathy
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Charcot-Marie-Tooth disease
Cardiomyopathy
Monogenic diabetes
Primary dilated cardiomyopathy
Charcot-Marie-Tooth disease type 2B1
Emery-Dreifuss muscular dystrophy 3
autosomal recessive
Primary familial hypertrophic cardiomyopathy
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2
Other Variants in LMNA