Search results for "[genes] MYH7"

47 hits were found for '[genes] MYH7'

# Family MCID Name MIFTS Score
1
P CRD011 Cardiomyopathy 59 21.097
2
P HYP061 Hypertrophic Cardiomyopathy 55 21.097
3
P MYP004 Myopathy 54 19.890
4
c CRD194 Cardiomyopathy, Familial Hypertrophic 52 19.890
5
c DLT002 Dilated Cardiomyopathy 72 17.225
6
P RST002 Restrictive Cardiomyopathy 52 17.225
7
P MYS032 Myosin Storage Myopathy 31 17.225
8
LNG097 Liang Distal Myopathy 28 17.225
9
c MYP106 Myopathy, Myosin Storage, Autosomal Recessive 21 17.225
10
c MYP105 Myopathy, Myosin Storage, Autosomal Dominant 18 17.225
11
CNG034 Congestive Heart Failure 64 15.725
12
P LFT003 Left Ventricular Noncompaction 50 15.725
13
c CRD099 Cardiomyopathy, Dilated, 1e 39 15.725
14
SCP008 Scapuloperoneal Syndrome, Myopathic Type 28 15.725
15
c CNG401 Congenital Heart Disease 64 14.064
16
EBS001 Ebstein Anomaly 43 14.064
17
c CNG464 Congenital Myopathy 42 14.064
18
SDD007 Sudden Cardiac Death 39 14.064
19
SCP010 Scapuloperoneal Myopathy 24 14.064
20
WLF001 Wolff-Parkinson-White Syndrome 59 12.180
21
P VNT002 Ventricular Septal Defect 51 12.180
22
P CNG046 Congenital Fiber-Type Disproportion 51 12.180
23
OCL008 Oculopharyngeal Muscular Dystrophy 50 12.180
24
c ART101 Aortic Valve Disease 2 45 12.180
25
DST004 Distal Muscular Dystrophy 32 12.180
26
c MYH009 Myh7-Related Dilated Cardiomyopathy 23 12.180
27
CNT098 Central Core Disease 59 9.945
28
P HRT032 Heart Disease 58 9.945
29
c ART115 Aortic Valve Disease 1 47 9.945
30
END020 Endocardial Fibroelastosis 43 9.945
31
c GLY005 Glycogen Storage Disease Vi 41 9.945
32
c MYP082 Myopathy, Myofibrillar, 2 38 9.945
33
BNF002 Bone Fracture 37 9.945
34
P TRC087 Tricuspid Valve Disease 37 9.945
35
c MYP078 Myopathy, Myofibrillar, 3 37 9.945
36
MYP094 Myopathy, Spheroid Body 36 9.945
37
INT084 Intrinsic Cardiomyopathy 29 9.945
38
CVL001 Caveolinopathies 26 9.945
39
c SCN022 Scn5a-Related Dilated Cardiomyopathy 18 9.945
40
MYP005 Myopathy of Extraocular Muscle 17 9.945
41
SCN020 Scn5a-Associated Dilated Cardiomyopathy 15 9.945
42
c MYH011 Myh7-Related Myosin Storage Myopathy 8 9.945
43
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 33 7.032
44
FML304 Familial Isolated Dilated Cardiomyopathy 30 7.032
45
CLS026 Classic Multiminicore Myopathy 14 7.032
46
c MYH010 Myh7-Related Familial Hypertrophic Cardiomyopathy 7 7.032
47
c MYH013 Myh7-Related Congenital Fiber-Type Disproportion 5 7.032