Table 5.
Disease | Hereditary Mode | Gene |
---|---|---|
Chronic atrial and intestinal dysrhythmia syndrome (CAID) | AD | SGOL1 |
Histiocytoid cardiomyopathy (HCM) | XD/AR | MT-CYB, NDUFB11 |
Limb girdle muscular dystrophy (LGMD) | AR | BVES |
Intellectual disability/arrhythmic syndrome | AR | GNB5 |
Intellectual disability/cardiac hypertrophy/congestive heart failure syndrome | XR | CLIC2 |
Recurrent metabolic myogenic brain crisis/rhabdomyolysis/arrhythmia/intellectual disability syndrome | AR | TANGO2 |
Progressive sensorineural hearing loss/hypertrophic cardiomyopathy syndrome | AD | MYO6 |
Sinoatrial node dysfunction and deafness (SANDD) | AR | CACNA1D |
AD—autosomal dominant inheritance; AR—autosomal recessive inheritance; XD—X-linked dominant inheritance; DR—X-linked recessive inheritance.