RS377700689 LMNA
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Associated Conditions
Familial partial lipodystrophy
Dunnigan type
Mandibuloacral dysplasia with type A lipodystrophy
Congenital muscular dystrophy due to LMNA mutation
Charcot-Marie-Tooth disease type 2B1
Lipoatrophy with Diabetes
Hepatic Steatosis
Hypertrophic Cardiomyopathy
and Leukomelanodermic Papules
Emery-Dreifuss muscular dystrophy
Emery-Dreifuss muscular dystrophy 2
autosomal dominant
Dilated cardiomyopathy 1A
Hutchinson-Gilford syndrome
Lethal tight skin contracture syndrome
Other Variants in LMNA