Search results for "[genes] RYR2"

28 hits were found for '[genes] RYR2'

# Family MCID Name MIFTS Score
1
P HRT032 Heart Disease 76 21.207
2
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 49 21.207
3
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 58 19.837
4
c DLT002 Dilated Cardiomyopathy 75 18.366
5
ARR030 Arrhythmogenic Right Ventricular Dysplasia 2 29 18.366
6
P CRD011 Cardiomyopathy 67 16.766
7
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 16.766
8
c LNG044 Long Qt Syndrome 1 67 14.996
9
CRD119 Cardiac Arrest 63 14.996
10
CNT098 Central Core Disease 66 12.987
11
P ATR011 Atrial Fibrillation 64 12.987
12
MLG056 Malignant Hyperthermia 57 12.987
13
P LFT003 Left Ventricular Noncompaction 49 12.987
14
VNT011 Ventricular Fibrillation, Familial, 1 43 12.987
15
P SDD001 Sudden Infant Death Syndrome 61 10.603
16
P MSC033 Muscle Disorders 52 10.603
17
c VNT029 Ventricular Tachycardia, Catecholaminergic Polymorphic, 4 41 10.603
18
CYC008 Cyclic Vomiting Syndrome 38 10.603
19
c VNT010 Ventricular Tachycardia, Catecholaminergic Polymorphic, 2 36 10.603
20
CNG032 Congenital Structural Myopathy 29 10.603
21
ARR005 Arrhythmogenic Right Ventricular Dysplasia/cardiomyopathy 2 13 10.603
22
P CRD194 Cardiomyopathy, Familial Hypertrophic 64 7.498
23
HRT008 Heart Conduction Disease 43 7.498
24
INT084 Intrinsic Cardiomyopathy 35 7.498
25
FML213 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Right Dominant Form 24 7.498
26
FML214 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Biventricular Form 23 7.498
27
FML215 Familial Isolated Arrhythmogenic Ventricular Dysplasia, Left Dominant Form 23 7.498
28
c RYR003 Ryr2-Related Catecholaminergic Polymorphic Ventricular Tachycardia 6 7.498