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Search results for KCNE2

153 hits were found for KCNE2

# Family MCID Name MIFTS Score
1
c LNG051 Long Qt Syndrome 6 45 49.309
2
c ATR039 Atrial Fibrillation, Familial, 4 21 37.511
3
c LNG044 Long Qt Syndrome 1 66 34.431
4
P LNG028 Long Qt Syndrome 64 32.822
5
c FML001 Familial Atrial Fibrillation 65 27.722
6
c FML191 Familial Long Qt Syndrome 55 24.777
7
CRD223 Cardiac Arrhythmia 63 23.210
8
P ATR011 Atrial Fibrillation 66 18.767
9
c DLT002 Dilated Cardiomyopathy 78 14.763
10
P HRT032 Heart Disease 81 14.601
11
P BRG001 Brugada Syndrome 69 13.275
12
ATR057 Atrioventricular Block 54 12.543
13
c LNG048 Long Qt Syndrome 3 53 12.304
14
c LNG047 Long Qt Syndrome 2 59 12.091
15
P HYP061 Hypertrophic Cardiomyopathy 69 12.062
16
c LNG050 Long Qt Syndrome 5 46 11.240
17
SDD001 Sudden Infant Death Syndrome 60 10.914
18
LPP008 Lipoprotein Quantitative Trait Locus 65 10.914
19
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 10.279
20
c SHR030 Short Qt Syndrome 44 10.202
21
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 10.021
23
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 8.652
24
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 61 7.904
25
P TMT001 Timothy Syndrome 55 7.717
26
c LNG056 Long Qt Syndrome 12 41 7.473
27
c OST080 Osteogenesis Imperfecta, Type Ii 56 6.884
28
c LNG057 Long Qt Syndrome 13 40 6.884
29
INT084 Intrinsic Cardiomyopathy 27 6.884
30
c DFN269 Deafness, Autosomal Recessive 98 35 6.884
31
c LNG053 Long Qt Syndrome 9 42 6.884
32
c LNG045 Long Qt Syndrome 10 41 6.884
33
c LNG046 Long Qt Syndrome 11 39 6.884
34
c BRG003 Brugada Syndrome 3 36 6.884
35
c MYS051 Myasthenic Syndrome, Congenital, 5 53 6.884
36
P CNG001 Congenital Myasthenic Syndrome 68 6.884
37
HRT008 Heart Conduction Disease 44 6.884
38
SYN036 Syncope 45 6.138
39
CRD132 Cardiac Conduction Defect 60 4.963
40
P ALP008 Alopecia 54 3.752
41
P HYP086 Hypothyroidism 69 3.752
42
P MYC007 Myocardial Infarction 70 3.667
43
DWR001 Dwarfism 44 3.171
44
P GST044 Gastritis 55 3.007
45
P LTH003 Lethal Congenital Contracture Syndrome 41 2.965
46
DFC004 Deficiency Anemia 74 2.951
47
ISC004 Ischemia 61 2.724
48
c TYP009 Type 2 Diabetes Mellitus 92 2.638
49
P DBT009 Diabetes Mellitus 67 2.638
50
c BRN108 Branchiootic Syndrome 1 62 2.525
51
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.350
52
GTR002 Goiter 53 2.350
53
HYP266 Hypoxia 57 2.350
54
HLC007 Helicobacter Pylori Infection 67 2.242
55
c ACT075 Acute Myocardial Infarction 56 2.242
56
ADN018 Adenoma 59 2.242
57
GRW007 Growth Hormone Deficiency 46 2.126
58
ATH013 Atherosclerosis Susceptibility 63 2.126
59
P GNG025 Gingival Fibromatosis 47 2.126
60
FBR019 Fibromatosis 42 2.126
61
c HYP836 Hypercholesterolemia, Familial, 1 73 2.001
62
FTT001 Fatty Liver Disease 62 2.001
63
P LVR013 Liver Disease 69 2.001
64
BNG006 Benign Familial Neonatal Epilepsy 55 2.001
65
ACR007 Acromegaly 70 2.001
66
IRN001 Iron Deficiency Anemia 58 2.001
67
HRM003 Hormone Producing Pituitary Cancer 33 2.001
68
IRN002 Iron Metabolism Disease 57 2.001
69
HYP056 Hypoglycemia 65 2.001
70
P GST053 Gastric Cancer 83 1.862
71
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.862
72
P HPT023 Hepatocellular Carcinoma 96 1.704
73
GST040 Gastric Adenocarcinoma 67 1.704
74
P CRD119 Cardiac Arrest 67 1.667
75
HLX001 Helix Syndrome 48 1.516
76
DWN001 Down Syndrome 70 1.502
77
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.493
78
HYP005 Hypokalemia 55 1.318
79
c FML294 Familial Short Qt Syndrome 43 1.179
80
ART140 Arteries, Anomalies of 53 1.179
81
c ATR038 Atrial Fibrillation, Familial, 3 29 1.179
82
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 1.021
83
P NRB001 Neuroblastoma 66 1.021
84
P EPL164 Epilepsy 68 1.021
85
PPT005 Peptic Ulcer Disease 58 1.021
87
P SCH015 Schizophrenia 74 0.834
88
P CRN300 Coronary Heart Disease 1 73 0.834
89
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.834
90
GRG001 Greig Cephalopolysyndactyly Syndrome 64 0.834
91
c LNG098 Long Qt Syndrome 14 42 0.834
92
c LNG096 Long Qt Syndrome 15 41 0.834
93
CNG034 Congestive Heart Failure 69 0.834
94
P SCK002 Sick Sinus Syndrome 55 0.834
96
CHR178 Chromosomal Triplication 34 0.834
97
P SZR006 Seizure Disorder 70 0.589
98
SDD004 Sudden Arrhythmia Death Syndrome 22 0.589
99
P THY054 Thyrotoxic Periodic Paralysis 50 0.589
100
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.589
101
P ALP106 Alport Syndrome 1, X-Linked 47 0.589
102
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.589
103
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.589
104
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.589
105
P PHC003 Pheochromocytoma 69 0.589
106
c ATR087 Atrial Standstill 1 74 0.589
107
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.589
108
c MGR028 Migraine with or Without Aura 1 64 0.589
109
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.589
110
c MCR115 Microvascular Complications of Diabetes 5 65 0.589
111
P FML023 Familial Hemiplegic Migraine 53 0.589
112
SNT005 Sinoatrial Node Disease 47 0.589
113
c GRV008 Graves Disease 1 54 0.589
114
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.589
115
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.589
116
P LWD006 Low Density Lipoprotein Cholesterol Level Quantitative Trait Locus 6 13 0.589
117
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.589
118
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.589
119
P MJR001 Major Depressive Disorder 68 0.589
120
c BRG008 Brugada Syndrome 6 32 0.589
121
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 46 0.589
122
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.589
123
c NTR047 Neutropenia, Severe Congenital, 1, Autosomal Dominant 37 0.589
124
c ATR026 Atrial Fibrillation, Familial, 1 21 0.589
125
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.589
126
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.589
127
WLF001 Wolff-Parkinson-White Syndrome 65 0.589
128
c SHR032 Short Qt Syndrome 2 32 0.589
129
ADR040 Adrenal Gland Pheochromocytoma 46 0.589
130
P TRM003 Tremor 48 0.589
131
P PRD021 Periodic Paralysis 41 0.589
132
P TRN020 Turner Syndrome 67 0.589
133
MNT002 Mental Depression 57 0.589
134
HRT012 Heart Valve Disease 53 0.589
135
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.589
136
P MGR003 Migraine with Aura 52 0.589
137
P MGR001 Migraine Without Aura 49 0.589
138
TXC005 Toxic Shock Syndrome 62 0.589
139
P HYP076 Hyperthyroidism 53 0.589
140
c ACT071 Acute Kidney Failure 60 0.589
141
GST037 Gastroparesis 52 0.589
142
P GND004 Gonadal Dysgenesis 47 0.589
143
QDR001 Quadriplegia 50 0.589
144
P BNG026 Benign Neonatal Seizures 49 0.589
145
DPR016 Depression 65 0.589
146
CNV009 Convulsions Benign Familial Neonatal Dominant Form 31 0.589
147
P PRX010 Paroxysmal Ventricular Fibrillation 26 0.589
148
P ATS364 Autism 69 0.482
149
P BRS047 Breast Cancer 98 0.482
150
c LKM061 Leukemia, Acute Myeloid 83 0.482
151
P PNC035 Pancreatic Cancer 86 0.482
152
P LKM062 Leukemia, Acute Lymphoblastic 69 0.482
153
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.482
The MalaCards human disease database index: 1-9 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
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