Lamin A/C
4000
Mandibuloacral dysplasia – 248370
Heart-hand syndrome, Slovenian type – 610140
Cardiomyopathy, dilated, 1A – 115200
Emery-Dreifuss muscular dystrophy 3, autosomal recessive – 616516
Restrictive dermopathy 2 – 619793
Charcot-Marie-Tooth disease, type 2B1 – 605588
Emery-Dreifuss muscular dystrophy 2, autosomal dominant – 181350
Hutchinson-Gilford progeria – 176670
Lipodystrophy, familial partial, type 2 – 151660
Muscular dystrophy, congenital – 613205
Malouf syndrome – 212112