Search results for hcn4

159 hits were found for hcn4

# Family MCID Name MIFTS Score
1
P BRG001 Brugada Syndrome 69 59.637
2
c BRG010 Brugada Syndrome 8 26 57.418
3
c SCK014 Sick Sinus Syndrome 2 29 46.540
4
c FML272 Familial Sick Sinus Syndrome 37 40.113
5
P SCK002 Sick Sinus Syndrome 55 23.397
6
P ATR011 Atrial Fibrillation 66 19.193
7
P HYP061 Hypertrophic Cardiomyopathy 69 16.601
8
P LFT003 Left Ventricular Noncompaction 57 15.976
9
P LNG028 Long Qt Syndrome 63 15.562
10
P HRT032 Heart Disease 84 15.301
11
c DLT002 Dilated Cardiomyopathy 79 13.287
12
ATR057 Atrioventricular Block 54 12.678
13
P CRD119 Cardiac Arrest 68 12.327
14
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 11.632
15
SNT005 Sinoatrial Node Disease 47 10.203
16
RGH001 Right Bundle Branch Block 47 10.132
17
LPP008 Lipoprotein Quantitative Trait Locus 65 9.987
18
HRT008 Heart Conduction Disease 44 8.455
19
RNL012 Renal Tuberculosis 31 7.353
20
c PRG126 Progressive Familial Heart Block 59 7.268
21
EBS001 Ebstein Anomaly 54 7.207
22
SCN049 Second-Degree Atrioventricular Block 34 7.207
23
c LNG053 Long Qt Syndrome 9 43 7.207
24
P ATR010 Atrial Heart Septal Defect 58 7.207
25
c LNG047 Long Qt Syndrome 2 58 7.062
26
ISL151 Isolated Elevated Serum Creatine Phosphokinase Levels 38 7.062
27
c FML001 Familial Atrial Fibrillation 65 7.062
28
THR099 Third-Degree Atrioventricular Block 42 7.062
29
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 7.062
30
c LNG044 Long Qt Syndrome 1 66 7.062
31
P CNG001 Congenital Myasthenic Syndrome 68 7.062
32
c MYS051 Myasthenic Syndrome, Congenital, 5 53 7.062
33
c ATR087 Atrial Standstill 1 74 6.480
34
CRD223 Cardiac Arrhythmia 63 3.446
35
CRD132 Cardiac Conduction Defect 59 3.394
36
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 3.346
37
c BRG005 Brugada Syndrome 1 56 3.126
38
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 2.787
39
CNG034 Congestive Heart Failure 69 2.756
40
P EPL164 Epilepsy 70 1.974
41
P MYC007 Myocardial Infarction 69 1.583
42
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.508
43
ANX010 Anxiety 70 1.487
44
SDD001 Sudden Infant Death Syndrome 60 1.220
45
c HYP522 Hypogonadotropic Hypogonadism 11 with or Without Anosmia 28 1.155
46
RST023 Resting Heart Rate, Variation in 40 1.155
47
SYN036 Syncope 44 1.155
48
ERL001 Early Myoclonic Encephalopathy 63 1.107
49
c ACT075 Acute Myocardial Infarction 55 1.107
50
c INF185 Infantile Epilepsy Syndrome 29 1.107
51
c MYC068 Myoclonic Epilepsy of Infancy 34 1.107
52
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 1.080
53
FCL081 Focal Cortical Dysplasia, Type Ii 59 1.080
54
c TBR025 Tuberous Sclerosis 1 84 1.080
55
P TBR001 Tuberous Sclerosis 69 1.080
56
P PRX010 Paroxysmal Ventricular Fibrillation 25 1.080
57
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.052
58
LFT001 Left Bundle Branch Hemiblock 47 1.021
59
OBS002 Obsessive-Compulsive Disorder 68 1.021
60
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.021
61
P ATT013 Attention Deficit-Hyperactivity Disorder 66 1.021
62
EMB004 Embryonal Carcinoma 55 1.021
63
MDD011 Mood Disorder 62 1.021
64
ART016 Aortic Aneurysm 69 0.695
65
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.695
66
ANR040 Aneurysm 60 0.695
67
P BRS047 Breast Cancer 97 0.602
68
P PNC035 Pancreatic Cancer 86 0.602
69
P MSC005 Muscular Dystrophy 66 0.483
70
P LMB006 Limb-Girdle Muscular Dystrophy 52 0.483
71
P CHR345 Chronic Pain 50 0.412
72
CRD137 Cardiogenic Shock 56 0.385
73
ANX004 Anoxia 40 0.357
74
AGN016 Aging 54 0.326
75
ANG054 Angina Pectoris 65 0.326
76
P MYC084 Mycobacterium Tuberculosis 1 68 0.291
77
ISC004 Ischemia 61 0.291
78
ADR040 Adrenal Gland Pheochromocytoma 45 0.252
79
P PHC003 Pheochromocytoma 70 0.252
80
P VNT002 Ventricular Septal Defect 58 0.252
81
P TMP001 Temporal Lobe Epilepsy 49 0.252
82
HYP005 Hypokalemia 55 0.252
83
PST092 Posttransplant Acute Limbic Encephalitis 29 0.252
84
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.206
85
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.206
86
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.206
87
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.206
88
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.206
89
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.206
90
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.206
91
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.206
92
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.206
93
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.206
94
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.206
95
ANS023 Anus, Imperforate 56 0.206
96
STT001 Status Epilepticus 58 0.206
97
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.206
98
IMP005 Impotence 52 0.206
99
HRT011 Heart Septal Defect 49 0.206
100
DBT002 Diabetic Autonomic Neuropathy 40 0.206
101
ATN004 Autonomic Neuropathy 42 0.206
102
HYP066 Hyperglycemia 60 0.206
103
P TRT010 Teratoma 50 0.206
104
HRT012 Heart Valve Disease 53 0.206
105
CRT028 Cor Triatriatum 25 0.206
106
ATN005 Autonomic Dysfunction 45 0.206
107
P SZR006 Seizure Disorder 69 0.206
108
P MYP004 Myopathy 67 0.206
109
P FBR031 Febrile Seizures 52 0.206
110
P ALZ034 Alzheimer Disease 87 0.146
111
c CRD099 Cardiomyopathy, Dilated, 1e 53 0.146
112
WST005 West Nile Virus 55 0.146
113
CHR515 Chronic Atrial and Intestinal Dysrhythmia 44 0.146
114
CHP002 Chops Syndrome 47 0.146
115
HLX001 Helix Syndrome 47 0.146
116
INT072 Intestinal Pseudo-Obstruction 60 0.146
117
MRF001 Marfan Syndrome 76 0.146
118
c TYP008 Type 1 Diabetes Mellitus 77 0.146
119
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.146
120
c ATS007 Autism Spectrum Disorder 72 0.146
121
P LYS001 Loeys-Dietz Syndrome 65 0.146
122
CHR391 Chromosome 15q24 Deletion Syndrome 33 0.146
123
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.146
124
c BRG004 Brugada Syndrome 4 45 0.146
125
P CLR023 Colorectal Cancer 100 0.146
126
c CRN139 Cornelia De Lange Syndrome 1 61 0.146
127
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.146
128
c BRD016 Bardet-Biedl Syndrome 4 44 0.146
129
WRS002 Warsaw Breakage Syndrome 46 0.146
130
FBR012 Fabry Disease 71 0.146
131
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.146
132
HRW001 Hair Whorl 35 0.146
133
P TTR001 Tetralogy of Fallot 69 0.146
134
ALP095 Alpha Thalassemia-X-Linked Intellectual Disability Syndrome 54 0.146
135
P DRR001 Diarrhea 55 0.146
136
P MTR012 Mitral Valve Disease 57 0.146
137
DBL002 Double Outlet Right Ventricle 57 0.146
138
P MCR010 Microcephaly 59 0.146
139
MTR002 Mitral Valve Insufficiency 51 0.146
140
P CRN015 Cornelia De Lange Syndrome 67 0.146
141
P RTT002 Rett Syndrome 79 0.146
142
c ALP101 Alpha-Thalassemia 62 0.146
143
P ORT004 Orthostatic Intolerance 62 0.146
144
P PTN014 Patent Ductus Arteriosus 1 59 0.146
145
P CRN300 Coronary Heart Disease 1 73 0.146
146
DRV001 Dravet Syndrome 70 0.146
147
NRM005 Neuromuscular Disease 63 0.146
148
P THL005 Thalassemia 56 0.146
149
P NRB001 Neuroblastoma 66 0.146
150
c CNT075 Central Precocious Puberty 53 0.146
151
FML304 Familial Isolated Dilated Cardiomyopathy 51 0.146
152
c FML191 Familial Long Qt Syndrome 54 0.146
153
P PNM007 Pneumonia 64 0.146
154
CHR178 Chromosomal Triplication 34 0.146
155
WRS003 Warsaw Syndrome 11 0.146
156
P DBT009 Diabetes Mellitus 67 0.146
157
P PRC019 Precocious Puberty 49 0.146
158
P SCK005 Sickle Cell Disease 56 0.146
159
IDP034 Idiopathic Central Precocious Puberty 27 0.146
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