Search results for "[genes] MYH7"

47 hits were found for '[genes] MYH7'

# Family MCID Name MIFTS Score
1
P CRD011 Cardiomyopathy 68 21.097
2
P HYP061 Hypertrophic Cardiomyopathy 63 21.097
3
P MYP004 Myopathy 66 19.890
4
c CRD194 Cardiomyopathy, Familial Hypertrophic 55 19.890
5
c DLT002 Dilated Cardiomyopathy 74 17.225
6
P RST002 Restrictive Cardiomyopathy 48 17.225
7
P MYS032 Myosin Storage Myopathy 31 17.225
8
LNG097 Liang Distal Myopathy 26 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 72 15.725
12
P LFT003 Left Ventricular Noncompaction 49 15.725
13
c CRD099 Cardiomyopathy, Dilated, 1e 38 15.725
14
SCP008 Scapuloperoneal Syndrome, Myopathic Type 25 15.725
15
c CNG401 Congenital Heart Disease 70 14.064
16
c CNG464 Congenital Myopathy 48 14.064
17
SDD007 Sudden Cardiac Death 47 14.064
18
EBS001 Ebstein Anomaly 44 14.064
19
SCP010 Scapuloperoneal Myopathy 26 14.064
20
P VNT002 Ventricular Septal Defect 59 12.180
21
WLF001 Wolff-Parkinson-White Syndrome 57 12.180
22
c ART101 Aortic Valve Disease 2 54 12.180
23
P CNG046 Congenital Fiber-Type Disproportion 47 12.180
24
OCL008 Oculopharyngeal Muscular Dystrophy 47 12.180
25
DST004 Distal Muscular Dystrophy 42 12.180
26
c MYH009 Myh7-Related Dilated Cardiomyopathy 22 12.180
27
P HRT032 Heart Disease 68 9.945
28
CNT098 Central Core Disease 67 9.945
29
c ART115 Aortic Valve Disease 1 54 9.945
30
BNF002 Bone Fracture 47 9.945
31
c GLY005 Glycogen Storage Disease Vi 46 9.945
32
P TRC087 Tricuspid Valve Disease 45 9.945
33
END020 Endocardial Fibroelastosis 40 9.945
34
c MYP082 Myopathy, Myofibrillar, 2 37 9.945
35
c MYP078 Myopathy, Myofibrillar, 3 37 9.945
36
INT084 Intrinsic Cardiomyopathy 37 9.945
37
MYP094 Myopathy, Spheroid Body 35 9.945
38
CVL001 Caveolinopathies 25 9.945
39
c SCN022 Scn5a-Related Dilated Cardiomyopathy 22 9.945
40
MYP005 Myopathy of Extraocular Muscle 19 9.945
41
SCN020 Scn5a-Associated Dilated Cardiomyopathy 17 9.945
42
c MYH011 Myh7-Related Myosin Storage Myopathy 12 9.945
43
FML304 Familial Isolated Dilated Cardiomyopathy 34 7.032
44
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 33 7.032
45
CLS026 Classic Multiminicore Myopathy 16 7.032
46
c MYH010 Myh7-Related Familial Hypertrophic Cardiomyopathy 9 7.032
47
c MYH013 Myh7-Related Congenital Fiber-Type Disproportion 6 7.032