Search results for TMEM43

51 hits were found for TMEM43

# Family MCID Name MIFTS Score
1
c ARR018 Arrhythmogenic Right Ventricular Dysplasia, Familial, 5 45 6.650
2
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 5.222
3
c EMR019 Emery-Dreifuss Muscular Dystrophy 7, Autosomal Dominant 33 4.619
4
P MSC005 Muscular Dystrophy 66 3.398
5
P EMR001 Emery-Dreifuss Muscular Dystrophy 60 3.370
6
P MYP004 Myopathy 70 2.935
7
P HRT032 Heart Disease 75 2.862
8
c DLT002 Dilated Cardiomyopathy 79 2.486
9
P HYP061 Hypertrophic Cardiomyopathy 70 2.422
10
P LNG028 Long Qt Syndrome 66 2.422
11
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 54 2.383
12
P BRG001 Brugada Syndrome 71 2.337
13
P CRD119 Cardiac Arrest 67 2.337
15
P LFT003 Left Ventricular Noncompaction 54 2.337
16
LFT001 Left Bundle Branch Hemiblock 49 1.712
17
c FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 23 1.712
18
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 22 1.712
19
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 22 1.712
20
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 1.653
21
EBS001 Ebstein Anomaly 55 1.653
22
NXS001 Naxos Disease 53 1.653
23
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 53 1.653
24
CRD180 Cardiomyopathy, Dilated, with Woolly Hair and Keratoderma 52 1.653
25
c CRD093 Cardiomyopathy, Dilated, 1a 52 1.653
26
PLM029 Palmoplantar Keratosis 47 1.653
27
P ARR027 Arrhythmogenic Right Ventricular Dysplasia, Familial, 11 47 1.653
28
P FML361 Familial Woolly Hair Syndrome 46 1.653
29
P EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 46 1.653
30
c ARR046 Arrhythmogenic Right Ventricular Dysplasia, Familial, 2 46 1.653
31
c CHR650 Charcot-Marie-Tooth Disease, Axonal, Type 2b1 45 1.653
32
c ARR023 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 45 1.653
33
c ARR050 Arrhythmogenic Right Ventricular Dysplasia, Familial, 8 45 1.653
34
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 45 1.653
35
MYP056 Myopathy, X-Linked, with Postural Muscle Atrophy 44 1.653
36
c ARR024 Arrhythmogenic Right Ventricular Dysplasia, Familial, 12 43 1.653
37
EHL034 Ehlers-Danlos Syndrome, Hypermobility Type 42 1.653
38
c EMR015 Emery-Dreifuss Muscular Dystrophy 5, Autosomal Dominant 42 1.653
39
c EMR014 Emery-Dreifuss Muscular Dystrophy 4, Autosomal Dominant 39 1.653
40
c ARR049 Arrhythmogenic Right Ventricular Dysplasia, Familial, 6 34 1.653
41
c ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 34 1.653
42
c CRD069 Cardiomyopathy, Dilated, 1h 30 1.653
43
INT084 Intrinsic Cardiomyopathy 28 1.653
44
c ATR087 Atrial Standstill 1 75 0.808
45
P RRC004 Rare Cardiomyopathy 44 0.775
46
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.407
47
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.204
48
CRD132 Cardiac Conduction Defect 58 0.144
49
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.072
50
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.072
51
MSC190 Muscular Disease 37 0.072
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