RS150645079 LMNA
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Associated Conditions
Cardiomyopathy
Charcot-Marie-Tooth disease type 2
Mandibuloacral dysplasia with type A lipodystrophy
Familial partial lipodystrophy
Dunnigan type
Congenital muscular dystrophy due to LMNA mutation
Hutchinson-Gilford syndrome
Dilated cardiomyopathy 1A
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Other Variants in LMNA