Search results for CASQ2

94 hits were found for CASQ2

# Family MCID Name MIFTS Score
1
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 61.676
2
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 46 49.563
3
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 47.256
4
P CRD119 Cardiac Arrest 68 17.357
5
WLF001 Wolff-Parkinson-White Syndrome 63 13.998
6
c DLT002 Dilated Cardiomyopathy 79 12.704
7
LPP008 Lipoprotein Quantitative Trait Locus 65 11.833
8
P HYP061 Hypertrophic Cardiomyopathy 69 10.650
9
P STR020 Strabismus 56 10.585
10
P BRG001 Brugada Syndrome 69 9.062
11
HRT008 Heart Conduction Disease 44 8.705
12
P LNG028 Long Qt Syndrome 63 8.669
13
c ATR087 Atrial Standstill 1 74 8.101
14
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 61 7.589
15
P JRV004 Jervell and Lange-Nielsen Syndrome 1 56 7.509
16
c LNG047 Long Qt Syndrome 2 58 7.458
17
P LFT003 Left Ventricular Noncompaction 57 7.458
18
c LNG048 Long Qt Syndrome 3 53 7.458
19
P MLG056 Malignant Hyperthermia 65 7.458
20
c SHR030 Short Qt Syndrome 44 7.392
21
c VNT027 Ventricular Tachycardia, Catecholaminergic Polymorphic, 3 34 7.392
22
P TMT001 Timothy Syndrome 55 7.392
23
c ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 45 7.232
24
c FML001 Familial Atrial Fibrillation 65 7.232
25
c LNG044 Long Qt Syndrome 1 66 7.232
26
P CNG001 Congenital Myasthenic Syndrome 68 7.232
27
c MYS051 Myasthenic Syndrome, Congenital, 5 53 7.232
28
CRD132 Cardiac Conduction Defect 59 4.957
29
CRD223 Cardiac Arrhythmia 63 3.704
30
SYN036 Syncope 44 3.418
31
NRL016 Neural Tube Defects 81 2.294
32
SCR020 Sacral Defect with Anterior Meningocele 59 2.294
33
NRL025 Neural Tube Closure Defect 27 2.294
34
ART140 Arteries, Anomalies of 52 1.606
35
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 35 1.523
36
RST023 Resting Heart Rate, Variation in 40 1.523
37
c PRG126 Progressive Familial Heart Block 59 1.473
38
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.284
39
P EYD002 Eye Disease 57 1.284
40
CNG034 Congestive Heart Failure 69 1.258
41
PPL052 Papillomatosis, Confluent and Reticulated 34 1.170
42
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.098
43
P HYP076 Hyperthyroidism 53 1.055
44
P PNC035 Pancreatic Cancer 86 0.777
45
P BRS047 Breast Cancer 97 0.551
46
MYL005 Myelofibrosis 70 0.551
47
P OVR042 Ovarian Cancer 88 0.551
48
BDR001 Bidirectional Tachycardia 14 0.531
49
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.453
50
P ATR011 Atrial Fibrillation 66 0.423
51
P GRV001 Graves' Disease 54 0.423
52
P THY032 Thyroiditis 56 0.423
53
P MYP004 Myopathy 67 0.423
54
P ALZ034 Alzheimer Disease 87 0.392
55
P HRT032 Heart Disease 84 0.392
56
MCH006 Mechanical Strabismus 40 0.358
57
c FML294 Familial Short Qt Syndrome 44 0.358
58
P BLD134 Bladder Cancer 79 0.320
59
c SHR033 Short Qt Syndrome 3 30 0.320
60
OST003 Osteonecrosis 61 0.277
61
c CRD104 Cardiomyopathy, Dilated, 1p 36 0.226
62
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.226
63
c CTC003 Catecholaminergic Polymorphic Ventricular Tachycardia 5 14 0.226
64
c LNG051 Long Qt Syndrome 6 45 0.226
65
c LNG050 Long Qt Syndrome 5 45 0.226
66
c CRD150 Cardiomyopathy, Familial Hypertrophic, 18 25 0.226
67
P ALP106 Alport Syndrome 1, X-Linked 48 0.226
68
VNT025 Ventricular Tachycardia, Catecholaminergic Polymorphic, 5, with or Without Muscle Weakness 19 0.226
69
c CRD085 Cardiomyopathy, Familial Hypertrophic, 4 51 0.226
70
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.226
71
P LMY004 Leiomyosarcoma 62 0.226
72
P CRN300 Coronary Heart Disease 1 73 0.226
73
FML304 Familial Isolated Dilated Cardiomyopathy 51 0.226
74
c FML191 Familial Long Qt Syndrome 54 0.226
75
P MSC005 Muscular Dystrophy 66 0.226
76
P SCH015 Schizophrenia 74 0.160
77
LFT001 Left Bundle Branch Hemiblock 47 0.160
78
c FNC027 Fanconi Anemia, Complementation Group a 81 0.160
79
EBS001 Ebstein Anomaly 54 0.160
80
ING001 Inguinal Hernia 59 0.160
81
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.160
82
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.160
83
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.160
84
ERL052 Early Repolarization Associated with Ventricular Fibrillation 21 0.160
85
CYN002 Cyanosis, Transient Neonatal 43 0.160
86
SNT005 Sinoatrial Node Disease 47 0.160
87
P SCK002 Sick Sinus Syndrome 55 0.160
88
P MTR012 Mitral Valve Disease 57 0.160
89
MSC157 Muscular Dystrophy, Duchenne Type 79 0.160
90
P MYC008 Myocarditis 59 0.160
91
NRM005 Neuromuscular Disease 63 0.160
92
SBC016 Subacute Delirium 42 0.160
93
ALL006 Allergic Asthma 56 0.160
94
P SCK005 Sickle Cell Disease 56 0.160
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