Search results for DSG2

67 hits were found for DSG2

# Family MCID Name MIFTS Score
1
c ARR028 Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 43 6.699
2
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 63 5.949
3
c ATR087 Atrial Standstill 1 74 4.120
4
c DLT002 Dilated Cardiomyopathy 79 4.005
5
c CRD108 Cardiomyopathy, Dilated, 1bb 20 3.571
6
P RRC004 Rare Cardiomyopathy 44 3.450
7
P PMP001 Pemphigus 55 2.872
8
P HRT032 Heart Disease 75 2.805
9
P INF037 Inflammatory Bowel Disease 56 2.805
10
P CRD119 Cardiac Arrest 67 2.480
11
P LNG028 Long Qt Syndrome 65 2.429
12
P RST002 Restrictive Cardiomyopathy 56 2.429
13
FML304 Familial Isolated Dilated Cardiomyopathy 40 2.400
14
c ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 45 2.369
15
KRT009 Keratosis 53 2.333
16
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 2.290
17
SKN016 Skin Disease 63 2.290
18
PMP006 Pemphigus Vulgaris, Familial 58 2.290
19
P LFT003 Left Ventricular Noncompaction 55 2.290
20
P KRT005 Keratoacanthoma 48 2.290
21
LFT001 Left Bundle Branch Hemiblock 49 1.675
22
PMP004 Pemphigus Foliaceus 43 1.675
23
RTT001 Ritter's Disease 43 1.675
24
c FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 24 1.675
25
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 23 1.675
26
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 23 1.675
27
P BRG001 Brugada Syndrome 70 1.619
28
c FML001 Familial Atrial Fibrillation 66 1.619
29
P LPR002 Leopard Syndrome 64 1.619
30
c BNG091 Benign Chronic Pemphigus 59 1.619
31
CLL003 Cellulitis 54 1.619
32
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 51 1.619
33
IMP004 Impetigo 49 1.619
34
PLM029 Palmoplantar Keratosis 47 1.619
35
P ARR023 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 45 1.619
36
c ARR027 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 45 1.619
37
c ARR050 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 45 1.619
38
c ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 45 1.619
39
c ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 44 1.619
40
PRN049 Paraneoplastic Pemphigus 43 1.619
41
c ARR024 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 42 1.619
42
P BLL007 Bullous Skin Disease 40 1.619
43
c ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 36 1.619
44
c ARR049 Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 34 1.619
45
c ARR047 Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 34 1.619
46
INT084 Intrinsic Cardiomyopathy 29 1.619
47
SHP001 Shipyard Eye 29 1.619
48
P HYP061 Hypertrophic Cardiomyopathy 66 0.165
49
c CRD233 Cardiomyopathy, Dilated, 1b 48 0.134
50
CRD132 Cardiac Conduction Defect 59 0.116
51
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.095
52
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.095
53
CRD223 Cardiac Arrhythmia 60 0.095
54
SYS003 Systolic Heart Failure 50 0.095
55
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.067
56
P MYP004 Myopathy 64 0.067
57
P ADN016 Adenocarcinoma 64 0.067
58
SQM006 Squamous Cell Carcinoma 60 0.067
59
PLM010 Pulmonary Edema 55 0.067
60
P ICH004 Ichthyosis 54 0.067
61
P MYS079 Miyoshi Muscular Dystrophy 53 0.067
62
P RNL017 Renal Oncocytoma 53 0.067
63
P TRT010 Teratoma 51 0.067
64
P PLN008 Peeling Skin Syndrome 44 0.067
65
c PLN018 Peeling Skin Syndrome 2 38 0.067
66
c CHR020 Chronic Interstitial Cystitis 37 0.067
67
EXF002 Exfoliative Ichthyosis 22 0.067
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