Search results for KCNE2

74 hits were found for KCNE2

# Family MCID Name MIFTS Score
1
c LNG051 Long Qt Syndrome 6 44 5.311
2
P LNG028 Long Qt Syndrome 66 4.343
3
c ATR039 Atrial Fibrillation, Familial, 4 21 4.283
4
c FML001 Familial Atrial Fibrillation 65 3.885
5
CRD223 Cardiac Arrhythmia 60 3.642
6
P ATR011 Atrial Fibrillation 66 3.518
7
P HRT032 Heart Disease 75 3.368
8
c FML191 Familial Long Qt Syndrome 53 3.338
9
c LNG044 Long Qt Syndrome 1 66 3.325
10
c DLT002 Dilated Cardiomyopathy 79 2.488
11
P BRG001 Brugada Syndrome 71 2.488
12
P HYP061 Hypertrophic Cardiomyopathy 70 2.457
13
ATR057 Atrioventricular Block 55 2.423
14
CNG034 Congestive Heart Failure 69 2.382
15
c LNG048 Long Qt Syndrome 3 53 2.382
17
c LNG047 Long Qt Syndrome 2 58 1.871
18
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 1.813
19
c LNG050 Long Qt Syndrome 5 46 1.813
20
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.779
21
c SHR030 Short Qt Syndrome 46 1.738
22
WLF001 Wolff-Parkinson-White Syndrome 66 1.684
23
P CNG001 Congenital Myasthenic Syndrome 66 1.684
24
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 1.684
25
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.684
26
TMT001 Timothy Syndrome 61 1.684
27
c MYS051 Myasthenic Syndrome, Congenital, 5 57 1.684
28
c OST080 Osteogenesis Imperfecta, Type Ii 54 1.684
29
SNT005 Sinoatrial Node Disease 49 1.684
30
c LNG056 Long Qt Syndrome 12 42 1.684
31
c LNG045 Long Qt Syndrome 10 42 1.684
32
c LNG053 Long Qt Syndrome 9 41 1.684
33
c LNG057 Long Qt Syndrome 13 40 1.684
34
c LNG046 Long Qt Syndrome 11 39 1.684
35
c BRG003 Brugada Syndrome 3 39 1.684
36
c DFN269 Deafness, Autosomal Recessive 98 35 1.684
37
HRT008 Heart Conduction Disease 32 1.684
38
INT084 Intrinsic Cardiomyopathy 28 1.684
39
SYN036 Syncope 45 0.171
40
CRD132 Cardiac Conduction Defect 58 0.129
41
P GST053 Gastric Cancer 83 0.091
42
DFC004 Deficiency Anemia 70 0.091
43
P HYP086 Hypothyroidism 69 0.091
44
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.091
45
c BRN108 Branchiootic Syndrome 1 62 0.091
46
P GST044 Gastritis 56 0.091
47
P ALP008 Alopecia 54 0.091
48
P HPT023 Hepatocellular Carcinoma 100 0.064
49
c HYP836 Hypercholesterolemia, Familial, 1 73 0.064
50
ACR007 Acromegaly 71 0.064
51
P MYC007 Myocardial Infarction 70 0.064
52
GST040 Gastric Adenocarcinoma 70 0.064
53
P LVR013 Liver Disease 68 0.064
54
HYP056 Hypoglycemia 66 0.064
55
ATH013 Atherosclerosis Susceptibility 65 0.064
56
P DBT009 Diabetes Mellitus 64 0.064
57
P ADN016 Adenocarcinoma 64 0.064
58
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.064
59
FTT001 Fatty Liver Disease 61 0.064
60
IRN001 Iron Deficiency Anemia 59 0.064
61
ADN018 Adenoma 59 0.064
62
HLC007 Helicobacter Pylori Infection 59 0.064
63
IRN002 Iron Metabolism Disease 57 0.064
64
c ACT075 Acute Myocardial Infarction 57 0.064
65
HYP266 Hypoxia 57 0.064
66
GTR002 Goiter 53 0.064
67
P GNG025 Gingival Fibromatosis 50 0.064
68
HLX001 Helix Syndrome 47 0.064
69
GRW007 Growth Hormone Deficiency 46 0.064
70
DWR001 Dwarfism 44 0.064
71
FBR019 Fibromatosis 41 0.064
72
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.064
73
P LTH003 Lethal Congenital Contracture Syndrome 40 0.064
74
HRM003 Hormone Producing Pituitary Cancer 37 0.064
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