# |
|
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 |
|