Search results for "[genes] MYH7"

49 hits were found for '[genes] MYH7'

# Family MCID Name MIFTS Score
1
P CRD194 Cardiomyopathy, Familial Hypertrophic 64 21.987
2
P CRD011 Cardiomyopathy 67 20.859
3
c DLT002 Dilated Cardiomyopathy 75 19.666
4
P MYP004 Myopathy 67 19.666
5
P HRT032 Heart Disease 76 18.396
6
P MYS032 Myosin Storage Myopathy 33 18.396
7
c MYP105 Myopathy, Myosin Storage, Autosomal Dominant 17 18.396
8
LNG097 Liang Distal Myopathy 27 17.031
9
c MYP106 Myopathy, Myosin Storage, Autosomal Recessive 23 17.031
10
CNG034 Congestive Heart Failure 71 15.547
11
P RST002 Restrictive Cardiomyopathy 50 15.547
12
P LFT003 Left Ventricular Noncompaction 49 15.547
13
c CRD099 Cardiomyopathy, Dilated, 1e 42 15.547
14
SCP008 Scapuloperoneal Syndrome, Myopathic Type 29 15.547
15
c CNG464 Congenital Myopathy 50 13.906
16
P CNG046 Congenital Fiber-Type Disproportion 48 13.906
17
SDD007 Sudden Cardiac Death 46 13.906
18
EBS001 Ebstein Anomaly 44 13.906
19
SCP010 Scapuloperoneal Myopathy 17 13.906
20
c LNG044 Long Qt Syndrome 1 67 12.043
21
CNT098 Central Core Disease 66 12.043
22
P VNT002 Ventricular Septal Defect 59 12.043
23
P MSC007 Muscle Hypertrophy 59 12.043
24
WLF001 Wolff-Parkinson-White Syndrome 57 12.043
25
c ART101 Aortic Valve Disease 2 55 12.043
26
OCL008 Oculopharyngeal Muscular Dystrophy 51 12.043
27
END020 Endocardial Fibroelastosis 44 12.043
28
DST004 Distal Muscular Dystrophy 40 12.043
29
c MYH011 Myh7-Related Myosin Storage Myopathy 8 12.043
30
ATR060 Atrial Standstill, Digenic 53 9.833
31
c GLY005 Glycogen Storage Disease Vi 48 9.833
32
BNF002 Bone Fracture 47 9.833
33
P TRC087 Tricuspid Valve Disease 44 9.833
34
DXT001 Dextrocardia 44 9.833
35
PRP009 Peripartum Cardiomyopathy 41 9.833
36
c MYP082 Myopathy, Myofibrillar, 2 37 9.833
37
MYP094 Myopathy, Spheroid Body 37 9.833
38
INT084 Intrinsic Cardiomyopathy 35 9.833
39
CVL001 Caveolinopathies 27 9.833
40
c MYH009 Myh7-Related Dilated Cardiomyopathy 21 9.833
41
MYP005 Myopathy of Extraocular Muscle 15 9.833
42
MSC051 Muscular Dystrophy, Rigid Spine, 1 43 6.953
43
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 33 6.953
44
FML304 Familial Isolated Dilated Cardiomyopathy 30 6.953
45
c SCN022 Scn5a-Related Dilated Cardiomyopathy 22 6.953
46
c TPM001 Tpm1-Related Dilated Cardiomyopathy 20 6.953
47
SCN020 Scn5a-Associated Dilated Cardiomyopathy 17 6.953
48
c MYH010 Myh7-Related Familial Hypertrophic Cardiomyopathy 7 6.953
49
c MYH013 Myh7-Related Congenital Fiber-Type Disproportion 4 6.953