Search results for KCNQ1

131 hits were found for KCNQ1

# Family MCID Name MIFTS Score
1
c LNG044 Long Qt Syndrome 1 66 7.136
2
P LNG028 Long Qt Syndrome 65 6.926
3
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 6.070
4
c FML001 Familial Atrial Fibrillation 66 4.935
5
c FML191 Familial Long Qt Syndrome 53 4.673
6
c SHR030 Short Qt Syndrome 48 4.647
7
P BCK002 Beckwith-Wiedemann Syndrome 62 4.413
8
P ATR011 Atrial Fibrillation 66 4.380
9
c SHR032 Short Qt Syndrome 2 30 4.233
10
c ATR038 Atrial Fibrillation, Familial, 3 27 4.196
11
c FML294 Familial Short Qt Syndrome 43 3.919
12
P HRT032 Heart Disease 75 3.375
13
SDD001 Sudden Infant Death Syndrome 61 3.218
14
CRD223 Cardiac Arrhythmia 60 3.119
15
c LNG047 Long Qt Syndrome 2 58 2.846
16
P BRG001 Brugada Syndrome 70 2.754
17
SYN036 Syncope 45 2.678
18
PLY012 Polyhydramnios 46 2.675
19
CYS001 Cystic Fibrosis 80 2.626
20
P DBT009 Diabetes Mellitus 64 2.626
21
P CRD119 Cardiac Arrest 67 2.312
22
WLF001 Wolff-Parkinson-White Syndrome 65 2.294
23
c DLT002 Dilated Cardiomyopathy 79 2.234
24
ATR057 Atrioventricular Block 55 2.234
25
HYP005 Hypokalemia 55 2.210
26
P GNG025 Gingival Fibromatosis 51 2.210
27
RRG078 Rare Genetic Deafness 28 2.210
28
MRF001 Marfan Syndrome 75 2.184
29
P SNS001 Sensorineural Hearing Loss 61 2.184
30
P LFT003 Left Ventricular Noncompaction 55 2.184
31
c HYP595 Hypertension, Essential 84 2.120
32
CNG034 Congestive Heart Failure 70 2.120
33
CRD132 Cardiac Conduction Defect 59 1.961
34
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.754
35
c LNG050 Long Qt Syndrome 5 44 1.635
36
c LNG048 Long Qt Syndrome 3 52 1.609
37
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 1.580
38
SNT005 Sinoatrial Node Disease 49 1.580
39
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.545
40
TMT001 Timothy Syndrome 62 1.545
41
P SLV001 Silver-Russell Syndrome 54 1.545
42
c LNG051 Long Qt Syndrome 6 43 1.545
43
c LNG053 Long Qt Syndrome 9 41 1.545
44
c LNG056 Long Qt Syndrome 12 41 1.545
45
c LNG057 Long Qt Syndrome 13 39 1.545
46
c LNG046 Long Qt Syndrome 11 38 1.545
47
P MTR004 Maturity-Onset Diabetes of the Young 66 1.499
48
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 1.499
49
P CNG001 Congenital Myasthenic Syndrome 64 1.499
50
P LPR002 Leopard Syndrome 64 1.499
51
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 1.499
52
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.499
53
c PRG126 Progressive Familial Heart Block 58 1.499
54
c MYS051 Myasthenic Syndrome, Congenital, 5 57 1.499
55
P BNG026 Benign Neonatal Seizures 48 1.499
56
c BRG004 Brugada Syndrome 4 45 1.499
57
c LNG045 Long Qt Syndrome 10 41 1.499
58
HRT008 Heart Conduction Disease 33 1.499
59
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 33 1.499
60
INT084 Intrinsic Cardiomyopathy 29 1.499
61
WLM012 Wilms Tumor Predisposition 26 1.499
62
c BRN108 Branchiootic Syndrome 1 61 0.316
63
GST033 Gestational Diabetes 57 0.135
64
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.123
65
c ATR087 Atrial Standstill 1 74 0.110
66
c MCR113 Microvascular Complications of Diabetes 3 52 0.110
67
HLX001 Helix Syndrome 47 0.110
68
c MCR120 Microvascular Complications of Diabetes 7 47 0.110
69
c MCR130 Microvascular Complications of Diabetes 6 41 0.110
70
c MCR133 Microvascular Complications of Diabetes 4 41 0.110
71
P HYP061 Hypertrophic Cardiomyopathy 66 0.095
72
HYP066 Hyperglycemia 61 0.095
73
ATS010 Autosomal Recessive Disease 48 0.095
74
FBR019 Fibromatosis 44 0.095
75
GRW007 Growth Hormone Deficiency 43 0.095
76
c SHR031 Short Qt Syndrome 1 29 0.095
77
P CLR023 Colorectal Cancer 98 0.078
78
P GST053 Gastric Cancer 83 0.078
79
P EPL164 Epilepsy 71 0.078
80
P MYC007 Myocardial Infarction 70 0.078
81
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.078
82
HYP056 Hypoglycemia 66 0.078
83
c WLM013 Wilms Tumor 1 65 0.078
84
c WLM018 Wilms Tumor 5 62 0.078
85
c WLF013 Wolfram Syndrome 1 58 0.078
86
P SCK002 Sick Sinus Syndrome 55 0.078
87
P RRC004 Rare Cardiomyopathy 44 0.078
90
P HPT023 Hepatocellular Carcinoma 100 0.055
91
DFC004 Deficiency Anemia 75 0.055
92
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.055
93
P NRB001 Neuroblastoma 71 0.055
94
ACR007 Acromegaly 71 0.055
95
P HYP086 Hypothyroidism 68 0.055
96
OST159 Osteogenic Sarcoma 66 0.055
97
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.055
98
P ADN016 Adenocarcinoma 64 0.055
99
P CRN018 Coronary Artery Anomaly 63 0.055
100
P END044 Endometriosis 62 0.055
101
P PRD008 Periodontitis 62 0.055
102
TXC005 Toxic Shock Syndrome 61 0.055
103
ISC004 Ischemia 60 0.055
104
P PTT014 Pitt-Hopkins Syndrome 60 0.055
105
c ACT071 Acute Kidney Failure 59 0.055
106
HLC007 Helicobacter Pylori Infection 59 0.055
107
IRN001 Iron Deficiency Anemia 58 0.055
108
PPT005 Peptic Ulcer Disease 58 0.055
109
P SZR006 Seizure Disorder 58 0.055
110
VSL002 Visual Epilepsy 58 0.055
111
END030 End Stage Renal Failure 58 0.055
112
P INF032 Infertility 57 0.055
113
IRN002 Iron Metabolism Disease 57 0.055
114
P DRR001 Diarrhea 57 0.055
115
c ACT075 Acute Myocardial Infarction 56 0.055
116
P CRD246 Cardiovascular System Disease 56 0.055
117
P PLY011 Polycystic Ovary Syndrome 56 0.055
118
P GST044 Gastritis 55 0.055
119
HYP060 Hyperinsulinism 54 0.055
120
c PRD040 Periodontitis, Chronic 54 0.055
121
ART140 Arteries, Anomalies of 53 0.055
122
P ATR005 Atrophic Gastritis 50 0.055
123
CRN030 Coronary Stenosis 50 0.055
124
THR099 Third-Degree Atrioventricular Block 45 0.055
125
c CRT081 Cortical Dysplasia, Complex, with Other Brain Malformations 7 44 0.055
126
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.055
128
HRM003 Hormone Producing Pituitary Cancer 37 0.055
129
c SHR033 Short Qt Syndrome 3 28 0.055
130
c LNG052 Long Qt Syndrome 8 26 0.055
131
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.055
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