Search results for kcnq4

119 hits were found for kcnq4

# Family MCID Name MIFTS Score
1
ATS251 Autosomal Dominant Non-Syndromic Sensorineural Deafness Type Dfna 38 64.063
2
c DFN190 Deafness, Autosomal Dominant 2a 37 49.458
3
DFN001 Dfna2 Nonsyndromic Hearing Loss 12 36.019
4
P NNS072 Nonsyndromic Hearing Loss 40 29.776
5
P SNS001 Sensorineural Hearing Loss 59 22.680
6
RRG078 Rare Genetic Deafness 29 21.199
7
NNS044 Non-Syndromic Genetic Deafness 30 20.821
8
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 14.791
9
c NNS007 Nonsyndromic Deafness 33 14.243
10
c BRN108 Branchiootic Syndrome 1 62 13.071
11
P LNG028 Long Qt Syndrome 64 10.903
12
c LNG044 Long Qt Syndrome 1 66 10.386
13
DFN245 Deafness, Autosomal Recessive 4, with Enlarged Vestibular Aqueduct 50 9.465
14
c ATS005 Autosomal Dominant Nonsyndromic Deafness 24 9.465
15
c DFN136 Deafness, Autosomal Dominant 9 44 9.378
16
MNR012 Meniere Disease 56 7.612
17
P BRN042 Branchiootic Syndrome 41 7.612
18
P BNG026 Benign Neonatal Seizures 49 7.343
19
c DFN118 Deafness, Autosomal Dominant 44 27 6.692
20
c DFN107 Deafness, Autosomal Dominant 10 40 6.692
21
c DFN353 Deafness, Autosomal Dominant 12 38 6.692
22
c DFN351 Deafness, Autosomal Dominant 6 42 6.692
23
c DFN137 Deafness, Autosomal Dominant 13 32 6.692
24
c DFN117 Deafness, Autosomal Dominant 15 38 6.692
25
P YLN002 Y-Linked Monogenic Disease 17 6.692
26
c DFN099 Deafness, Autosomal Dominant 2b 30 6.692
27
c DFN255 Deafness, Autosomal Dominant 64 26 6.692
28
P USH001 Usher Syndrome 64 6.692
29
c FML001 Familial Atrial Fibrillation 65 6.692
30
c DFN189 Deafness, Autosomal Dominant 25 39 6.692
31
c DFN149 Deafness, Autosomal Dominant 18 25 6.692
32
c DFN200 Deafness, Autosomal Dominant 17 43 6.692
33
c DFN354 Deafness, Autosomal Dominant 20 41 6.692
34
c DFN165 Deafness, Autosomal Recessive 14 19 6.692
35
c DFN148 Deafness, Autosomal Dominant 16 29 6.692
36
c DFN094 Deafness, Autosomal Dominant 28 31 6.692
37
c DFN097 Deafness, Autosomal Recessive 1a 46 6.692
38
c DFN155 Deafness, Autosomal Dominant 41 34 6.692
39
c DFN128 Deafness, Autosomal Dominant 36 39 6.692
40
ACT032 Acute Hemorrhagic Leukoencephalitis 33 6.692
41
c DFN166 Deafness, Autosomal Recessive 17 23 6.692
42
P WRD001 Waardenburg's Syndrome 60 6.692
43
P INN002 Inner Ear Disease 50 6.692
44
ADT003 Auditory System Disease 49 6.692
45
VST004 Vestibular Disease 40 6.692
46
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 6.692
47
PRP028 Peripheral Vertigo 37 6.692
48
HLX001 Helix Syndrome 48 3.771
49
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 3.693
50
HRN029 Hearing Loss, Noise-Induced 37 3.117
51
c WLF013 Wolfram Syndrome 1 60 2.723
52
P VSC007 Vascular Disease 63 2.365
53
P ALC033 Alcohol Use Disorder 61 2.226
56
MTN003 Motion Sickness 51 1.899
57
c DFN114 Deafness, Autosomal Recessive 67 35 1.899
58
BNG006 Benign Familial Neonatal Epilepsy 55 1.839
59
P EPL164 Epilepsy 68 1.592
61
P PLM037 Pulmonary Hypertension 72 1.454
62
c DPH024 Diaphragmatic Hernia, Congenital 64 1.300
63
PRT037 Pertussis 65 1.126
64
ACS001 Acoustic Neuroma 56 1.126
65
NRL005 Neurilemmoma 60 1.126
66
P ALZ034 Alzheimer Disease 87 0.919
67
P EPL140 Epilepsy, Idiopathic Generalized 62 0.919
68
CRD223 Cardiac Arrhythmia 63 0.919
69
P SCH015 Schizophrenia 74 0.919
70
c ATR087 Atrial Standstill 1 74 0.919
71
c BRN131 Branchiootorenal Syndrome 1 45 0.919
72
ATR057 Atrioventricular Block 54 0.919
73
c LNG047 Long Qt Syndrome 2 59 0.919
74
P BRN006 Branchiootorenal Syndrome 50 0.919
75
c PRC016 Pre-Eclampsia 65 0.919
76
c DLT002 Dilated Cardiomyopathy 78 0.919
77
IMP005 Impotence 52 0.919
78
P HYP086 Hypothyroidism 69 0.919
79
P SCK002 Sick Sinus Syndrome 55 0.919
80
IRR002 Irritable Bowel Syndrome 65 0.919
81
MST020 Mast Cell Activation Syndrome 28 0.919
82
c GLM047 Glioma Susceptibility 3 33 0.803
83
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.803
84
c GLM025 Glioma Susceptibility 2 30 0.803
85
c GLM043 Glioma Susceptibility 9 30 0.803
86
P GLM040 Glioma Susceptibility 1 71 0.803
87
MNN043 Meningioma, Familial 79 0.803
88
P OLG002 Oligodendroglioma 66 0.803
89
GLM045 Glioma 63 0.803
90
P BRS047 Breast Cancer 98 0.779
91
c USH036 Usher Syndrome, Type I 61 0.650
92
AGN016 Aging 54 0.650
93
c DFN159 Deafness, Autosomal Dominant 5 31 0.650
94
ALC007 Alcohol Dependence 66 0.650
95
c LNG050 Long Qt Syndrome 5 46 0.650
96
c DFN178 Deafness, Autosomal Recessive 59 32 0.650
97
c SZR022 Seizures, Benign Familial Neonatal, 1 43 0.650
98
ERM002 Ear Malformation 36 0.650
99
P NRB001 Neuroblastoma 66 0.650
100
HYP066 Hyperglycemia 61 0.650
101
P RTN016 Retinal Degeneration 52 0.650
102
HYP005 Hypokalemia 55 0.650
103
PPT005 Peptic Ulcer Disease 58 0.650
104
CNS004 Constipation 56 0.650
105
c BSL007 Basal Cell Carcinoma 68 0.650
106
P RNL007 Renal Tubular Acidosis 50 0.650
107
P ECL001 Eclampsia 52 0.650
108
P DRR001 Diarrhea 55 0.650
109
NNS008 Nonsyndromic Hearing Loss and Deafness, Dfna3 16 0.650
110
P FBR031 Febrile Seizures 52 0.650
111
HYP266 Hypoxia 57 0.650
112
c DFN027 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 3 14 0.650
113
c CNT101 Central Congenital Hypothyroidism 36 0.650
114
CNV009 Convulsions Benign Familial Neonatal Dominant Form 31 0.650
115
P OVR042 Ovarian Cancer 88 0.551
116
P PNC035 Pancreatic Cancer 86 0.551
117
MYL005 Myelofibrosis 71 0.551
118
NRL016 Neural Tube Defects 81 0.430
119
P RNL017 Renal Oncocytoma 54 0.430
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