Search results for DSC2

56 hits were found for DSC2

# Family MCID Name MIFTS Score
1
P ARR027 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 47 7.547
2
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 5.062
3
c ATR087 Atrial Standstill 1 75 3.410
4
c DLT002 Dilated Cardiomyopathy 79 3.119
5
P HRT032 Heart Disease 75 2.856
6
P HYP061 Hypertrophic Cardiomyopathy 70 2.619
7
P CRD119 Cardiac Arrest 67 2.414
8
P LNG028 Long Qt Syndrome 66 2.414
9
P ECT006 Ectodermal Dysplasia 62 2.332
10
P PMP001 Pemphigus 54 2.332
11
NXS001 Naxos Disease 53 2.332
12
PLM137 Palmoplantar Keratoderma and Woolly Hair 34 2.332
13
c ARR023 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 45 1.752
14
c PGM011 Pigmented Nodular Adrenocortical Disease, Primary, 2 27 1.752
15
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 52 1.707
16
c FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 23 1.707
17
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 22 1.707
18
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 22 1.707
19
P BRG001 Brugada Syndrome 71 1.649
20
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.649
21
DRR014 Darier-White Disease 60 1.649
22
c BNG091 Benign Chronic Pemphigus 58 1.649
23
P LFT003 Left Ventricular Noncompaction 54 1.649
24
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 1.649
25
LFT001 Left Bundle Branch Hemiblock 49 1.649
26
DYS064 Dystonia 3, Torsion, X-Linked 47 1.649
27
ECT007 Ectodermal Dysplasia/skin Fragility Syndrome 47 1.649
28
PLM029 Palmoplantar Keratosis 47 1.649
29
P FML361 Familial Woolly Hair Syndrome 46 1.649
30
c ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 46 1.649
31
c ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 45 1.649
32
c ARR050 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 45 1.649
33
c ARR028 Arrhythmogenic Right Ventricular Dysplasia, Familial, 10 44 1.649
34
c ARR024 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 43 1.649
35
P HRD018 Hair Disease 43 1.649
36
PRN049 Paraneoplastic Pemphigus 42 1.649
37
RTT001 Ritter's Disease 41 1.649
38
P BLL007 Bullous Skin Disease 41 1.649
39
c ARR049 Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 34 1.649
40
c ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 34 1.649
41
c ARR047 Arrhythmogenic Right Ventricular Dysplasia, Familial, 3 33 1.649
42
NVS007 Nevus of Ota 28 1.649
43
INT084 Intrinsic Cardiomyopathy 28 1.649
44
P RRC004 Rare Cardiomyopathy 44 0.940
45
c CRD099 Cardiomyopathy, Dilated, 1e 51 0.099
46
c CRD233 Cardiomyopathy, Dilated, 1b 45 0.099
47
ESP021 Esophageal Cancer 90 0.070
48
P GST053 Gastric Cancer 83 0.070
49
SQM006 Squamous Cell Carcinoma 60 0.070
50
DNG002 Dengue Hemorrhagic Fever 60 0.070
51
P MYC008 Myocarditis 59 0.070
52
VLV032 Vulva Cancer 59 0.070
53
CRD132 Cardiac Conduction Defect 58 0.070
54
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.070
55
CTR188 Cataract 46, Juvenile-Onset, with or Without Arrhythmic Cardiomyopathy 21 0.070
56
ERL027 Early-Onset Non-Syndromic Cataract 10 0.070
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