Search results for "[genes] MYH7"

50 hits were found for '[genes] MYH7'

# Family MCID Name MIFTS Score
1
P CRD194 Cardiomyopathy, Familial Hypertrophic 62 20.847
2
c DLT002 Dilated Cardiomyopathy 76 19.654
3
P HRT032 Heart Disease 75 19.654
4
P MYP004 Myopathy 67 19.654
5
P CRD011 Cardiomyopathy 68 18.385
6
SCP008 Scapuloperoneal Syndrome, Myopathic Type 29 18.385
7
LNG097 Liang Distal Myopathy 26 18.385
8
c CRD099 Cardiomyopathy, Dilated, 1e 52 17.021
9
P LFT003 Left Ventricular Noncompaction 50 17.021
10
P RST002 Restrictive Cardiomyopathy 50 17.021
11
P MYS032 Myosin Storage Myopathy 34 17.021
12
c MYP106 Myopathy, Myosin Storage, Autosomal Recessive 23 17.021
13
c MYP105 Myopathy, Myosin Storage, Autosomal Dominant 16 17.021
14
P CNG046 Congenital Fiber-Type Disproportion 50 15.538
15
EBS001 Ebstein Anomaly 45 15.538
16
CNG034 Congestive Heart Failure 72 13.898
17
CNT098 Central Core Disease 65 13.898
18
P VNT002 Ventricular Septal Defect 60 13.898
19
P MSC007 Muscle Hypertrophy 58 13.898
20
WLF001 Wolff-Parkinson-White Syndrome 56 13.898
21
c ART101 Aortic Valve Disease 2 53 13.898
22
OCL008 Oculopharyngeal Muscular Dystrophy 52 13.898
23
c CNG464 Congenital Myopathy 49 13.898
24
SDD007 Sudden Cardiac Death 47 13.898
25
MSC051 Muscular Dystrophy, Rigid Spine, 1 45 13.898
26
END020 Endocardial Fibroelastosis 44 13.898
27
DST004 Distal Muscular Dystrophy 40 13.898
28
c MYH009 Myh7-Related Dilated Cardiomyopathy 21 13.898
29
SCP010 Scapuloperoneal Myopathy 19 13.898
30
c MYH011 Myh7-Related Myosin Storage Myopathy 8 13.898
31
P HLT001 Holt-Oram Syndrome 61 12.036
32
BNF002 Bone Fracture 50 12.036
33
c GLY005 Glycogen Storage Disease Vi 47 12.036
34
P TRC087 Tricuspid Valve Disease 44 12.036
35
DXT001 Dextrocardia 43 12.036
36
PRP009 Peripartum Cardiomyopathy 42 12.036
37
c MYP082 Myopathy, Myofibrillar, 2 39 12.036
38
MYP094 Myopathy, Spheroid Body 38 12.036
39
INT084 Intrinsic Cardiomyopathy 34 12.036
40
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 33 12.036
41
FML304 Familial Isolated Dilated Cardiomyopathy 31 12.036
42
CVL001 Caveolinopathies 26 12.036
43
c SCN022 Scn5a-Related Dilated Cardiomyopathy 22 12.036
44
SCN020 Scn5a-Associated Dilated Cardiomyopathy 17 12.036
45
MYP005 Myopathy of Extraocular Muscle 16 12.036
46
c MYH010 Myh7-Related Familial Hypertrophic Cardiomyopathy 7 12.036
47
c MYH013 Myh7-Related Congenital Fiber-Type Disproportion 5 12.036
48
ATR060 Atrial Standstill, Digenic 51 9.827
49
P ATR081 Atrial Standstill 37 9.827
50
c TPM001 Tpm1-Related Dilated Cardiomyopathy 21 9.827