Search results for KCND3
46 hits were found for KCND3
# |
|
Family |
MCID |
Name |
MIFTS |
Score |
1 |
|
c
|
SPN095 |
Spinocerebellar Ataxia 19 |
32 |
5.967 |
|
2 |
|
c
|
SPN247 |
Spinocerebellar Ataxia Type 19/22 |
36 |
5.253 |
|
3 |
|
c
|
BRG012 |
Brugada Syndrome 9 |
31 |
4.301 |
|
4 |
|
P
|
BRG001 |
Brugada Syndrome |
71 |
4.283 |
|
5 |
|
P
|
LNG028 |
Long Qt Syndrome |
66 |
3.209 |
|
6 |
|
P
|
ATS308 |
Autosomal Dominant Cerebellar Ataxia |
60 |
2.791 |
|
7 |
|
c
|
DLT002 |
Dilated Cardiomyopathy |
79 |
2.620 |
|
8 |
|
P
|
ATR011 |
Atrial Fibrillation |
66 |
2.620 |
|
9 |
|
c
|
HRD026 |
Hereditary Ataxia |
48 |
2.620 |
|
10 |
|
P
|
DYS154 |
Dystonia |
65 |
2.581 |
|
11 |
|
P
|
EPS003 |
Episodic Ataxia |
59 |
2.534 |
|
12 |
|
|
RGH001 |
Right Bundle Branch Block |
48 |
2.534 |
|
13 |
|
P
|
CNG001 |
Congenital Myasthenic Syndrome |
66 |
1.792 |
|
14 |
|
c
|
LNG044 |
Long Qt Syndrome 1 |
66 |
1.792 |
|
15 |
|
c
|
FML001 |
Familial Atrial Fibrillation |
65 |
1.792 |
|
16 |
|
P
|
CTC001 |
Catecholaminergic Polymorphic Ventricular Tachycardia |
63 |
1.792 |
|
17 |
|
c
|
EPS042 |
Episodic Ataxia, Type 1 |
60 |
1.792 |
|
18 |
|
c
|
LNG047 |
Long Qt Syndrome 2 |
58 |
1.792 |
|
19 |
|
c
|
MYS051 |
Myasthenic Syndrome, Congenital, 5 |
57 |
1.792 |
|
20 |
|
c
|
SPN311 |
Spinocerebellar Ataxia 13 |
50 |
1.792 |
|
21 |
|
|
SNT005 |
Sinoatrial Node Disease |
49 |
1.792 |
|
22 |
|
c
|
SHR030 |
Short Qt Syndrome |
46 |
1.792 |
|
23 |
|
c
|
BRG007 |
Brugada Syndrome 5 |
39 |
1.792 |
|
24 |
|
c
|
SPN102 |
Spinocerebellar Ataxia 30 |
34 |
1.792 |
|
25 |
|
|
HRT008 |
Heart Conduction Disease |
32 |
1.792 |
|
26 |
|
c
|
SPS115 |
Spastic Paraplegia 41, Autosomal Dominant |
29 |
1.792 |
|
27 |
|
|
INT084 |
Intrinsic Cardiomyopathy |
28 |
1.792 |
|
28 |
|
c
|
CRB217 |
Cerebellar Ataxia Type 42 |
23 |
1.792 |
|
29 |
|
c
|
CRB222 |
Cerebellar Ataxia Type 9 |
22 |
1.792 |
|
30 |
|
c
|
CRB219 |
Cerebellar Ataxia Type 41 |
22 |
1.792 |
|
31 |
|
|
ATX038 |
Ataxia and Polyneuropathy, Adult-Onset |
45 |
0.220 |
|
32 |
|
|
ALC028 |
Alacrima, Achalasia, and Mental Retardation Syndrome |
64 |
0.147 |
|
33 |
|
c
|
VNT034 |
Ventricular Fibrillation, Paroxysmal Familial, 1 |
67 |
0.104 |
|
34 |
|
|
VSL002 |
Visual Epilepsy |
59 |
0.104 |
|
35 |
|
|
ERL052 |
Early Repolarization Associated with Ventricular Fibrillation |
22 |
0.104 |
|
36 |
|
c
|
EPL184 |
Epileptic Encephalopathy, Early Infantile, 6 |
70 |
0.073 |
|
37 |
|
P
|
ATT013 |
Attention Deficit-Hyperactivity Disorder |
65 |
0.073 |
|
38 |
|
P
|
ENC018 |
Encephalopathy |
61 |
0.073 |
|
39 |
|
|
CRD223 |
Cardiac Arrhythmia |
60 |
0.073 |
|
40 |
|
|
CRD132 |
Cardiac Conduction Defect |
58 |
0.073 |
|
41 |
|
P
|
STR020 |
Strabismus |
55 |
0.073 |
|
42 |
|
|
APR001 |
Apraxia |
52 |
0.073 |
|
43 |
|
P
|
MYC033 |
Myoclonus |
46 |
0.073 |
|
44 |
|
|
SYN036 |
Syncope |
45 |
0.073 |
|
45 |
|
|
MCH006 |
Mechanical Strabismus |
42 |
0.073 |
|
46 |
|
P
|
CRB059 |
Cerebellar Degeneration |
37 |
0.073 |
|