Transmission | Association | Locus | Genes |
Pure form | 1q32 | ? | |
Pure form | 2q31 | ? | |
Pure form | 2q35 | Desmin | |
Pure form | 9q13-22 | ? | |
Autosomal | Pure form | 15q15 | Cardiac actin |
Dominant | Conduction disorders | 1p21.2 | Lamin A/C |
Myopathy | 1p21.2 | Lamin A/C | |
Conduction disorders | 2q14-22 | ? | |
Conduction disorders | 3p22 | ? | |
Conductin disorders + myopathy | 6q23 | ? | |
Sensorineural hearing loss | 6q23-24 | ? | |
Mitral valve prolapsus | 10q21-23 | ? | |
Autosomal recessive | ? | ? | |
X-linked | Xp21 | Dystrophin | |
Barth syndrome | Xq28 | Tafazzin |