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
Jervell and Lange-Nielsen syndrome (10.91, 7.19)
KCNE1 (21q22.1-q22.2)
potassium voltage-gated channel, Isk-related family, member 1

jervell and lange-nielsen syndrome (10.99, 10.87, 7.17, 7.16, 10.103, 10.97)
KCNQ1 (11p15.5)
potassium voltage-gated channel, KQT-like subfamily, member 1