Search results for KCNE1

72 hits were found for KCNE1

# Family MCID Name MIFTS Score
1
P LNG028 Long Qt Syndrome 65 6.148
2
c LNG050 Long Qt Syndrome 5 44 4.539
3
c JRV002 Jervell and Lange-Nielsen Syndrome 2 29 4.367
4
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 4.337
5
c LNG044 Long Qt Syndrome 1 66 4.291
6
c FML191 Familial Long Qt Syndrome 53 3.144
7
P ATR011 Atrial Fibrillation 66 3.106
8
P BRG001 Brugada Syndrome 70 2.962
9
c FML001 Familial Atrial Fibrillation 66 2.936
10
P HRT032 Heart Disease 75 2.877
11
c LNG047 Long Qt Syndrome 2 58 2.506
12
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 2.457
13
P SNS001 Sensorineural Hearing Loss 61 2.429
14
c DLT002 Dilated Cardiomyopathy 79 2.398
15
c SHR030 Short Qt Syndrome 48 2.398
16
ATR057 Atrioventricular Block 55 2.362
17
CRD223 Cardiac Arrhythmia 60 1.904
18
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.772
19
HRN029 Hearing Loss, Noise-Induced 37 1.772
20
c LNG051 Long Qt Syndrome 6 43 1.695
21
WLF001 Wolff-Parkinson-White Syndrome 65 1.641
22
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 1.641
23
P CNG001 Congenital Myasthenic Syndrome 64 1.641
24
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 1.641
25
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.641
26
TMT001 Timothy Syndrome 62 1.641
27
c MYS051 Myasthenic Syndrome, Congenital, 5 57 1.641
28
P LFT003 Left Ventricular Noncompaction 55 1.641
29
c LNG048 Long Qt Syndrome 3 52 1.641
30
ADT003 Auditory System Disease 50 1.641
31
VLV047 Volvulus of Midgut 50 1.641
32
c DYS141 Dyskeratosis Congenita, Autosomal Dominant 1 47 1.641
33
VST004 Vestibular Disease 41 1.641
34
c LNG053 Long Qt Syndrome 9 41 1.641
35
c LNG056 Long Qt Syndrome 12 41 1.641
36
c LNG057 Long Qt Syndrome 13 39 1.641
37
c LNG096 Long Qt Syndrome 15 39 1.641
38
PRP028 Peripheral Vertigo 39 1.641
39
c LNG046 Long Qt Syndrome 11 38 1.641
40
c LNG098 Long Qt Syndrome 14 38 1.641
41
HRT008 Heart Conduction Disease 33 1.641
42
INT084 Intrinsic Cardiomyopathy 29 1.641
43
c ATS005 Autosomal Dominant Nonsyndromic Deafness 27 1.641
44
MCK004 Meckel's Diverticulitis 21 1.641
45
CRD132 Cardiac Conduction Defect 59 0.246
46
c BRN108 Branchiootic Syndrome 1 61 0.227
47
SYN036 Syncope 45 0.208
48
c ATR087 Atrial Standstill 1 74 0.161
49
P RRC004 Rare Cardiomyopathy 44 0.161
50
HLX001 Helix Syndrome 47 0.114
51
P CRD119 Cardiac Arrest 67 0.093
52
P HYP061 Hypertrophic Cardiomyopathy 66 0.093
53
HYP066 Hyperglycemia 61 0.093
54
HYP005 Hypokalemia 55 0.093
55
c SHR032 Short Qt Syndrome 2 30 0.093
56
c SHR031 Short Qt Syndrome 1 29 0.093
57
RRG078 Rare Genetic Deafness 28 0.093
58
c HYP836 Hypercholesterolemia, Familial, 1 72 0.066
59
P NRB001 Neuroblastoma 71 0.066
60
CNG034 Congestive Heart Failure 70 0.066
61
P SLP006 Sleep Apnea 69 0.066
62
P INF038 Influenza 68 0.066
63
SDD001 Sudden Infant Death Syndrome 61 0.066
64
c ACT075 Acute Myocardial Infarction 56 0.066
65
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.066
66
P CRD246 Cardiovascular System Disease 56 0.066
67
c NNS007 Nonsyndromic Deafness 47 0.066
68
c FML294 Familial Short Qt Syndrome 43 0.066
69
HTR003 Heterotaxy 39 0.066
70
c PRG020 Paragangliomas 3 38 0.066
71
c SHR033 Short Qt Syndrome 3 28 0.066
72
ERL052 Early Repolarization Associated with Ventricular Fibrillation 22 0.066
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