Disease table

A
B
C
D
E
F
G
H
I
J
K
L
M
N
O
P
Q
R
S
T
U
V
W
X
Y
Z

Disease phenotype
OMIM
Gene symbol (chromosome)
protein
Ventricular fibrillation, idiopathic (10.89, 7.7, 10.31, 10.111, 10.116)
SCN5A (3p21)
voltage-gated sodium channel type V alpha

Ventricular fibrillation, paroxysmal familial (10.89, 7.7, 10.31, 10.111, 10.116)
SCN5A (3p21)
voltage-gated sodium channel type V alpha

ventricular tachycardia, catecholaminergic polymorphi (10.85)
CASQ2 (1p13.3-p11)
calsequestrin 2 (cardiac muscle)

Ventricular tachycardia, catecholaminergic polymorphic (10.73, 10.84)
RYR2 (1q42.1-q43)
ryanodine receptor 2

Ventricular tachycardia, stress-induced polymorphic (10.73, 10.84)
RYR2 (1q42.1-q43)
ryanodine receptor 2