Search results for "[genes] MYH7"

49 hits were found for '[genes] MYH7'

# Family MCID Name MIFTS Score
1
P MYP004 Myopathy 50 24.204
2
P CNG401 Congenital Heart Disease 68 22.095
3
P HYP061 Hypertrophic Cardiomyopathy 56 22.095
4
c DLT002 Dilated Cardiomyopathy 73 20.962
5
P CRD011 Cardiomyopathy 53 20.962
6
c CRD194 Cardiomyopathy, Familial Hypertrophic 55 19.763
7
LNG097 Liang Distal Myopathy 29 17.115
8
MSC004 Muscle Tissue Disease 23 17.115
9
CNG034 Congestive Heart Failure 65 15.624
10
c CRD099 Cardiomyopathy, Dilated, 1e 45 15.624
11
P LFT003 Left Ventricular Noncompaction 44 15.624
12
P RST002 Restrictive Cardiomyopathy 38 15.624
13
INT084 Intrinsic Cardiomyopathy 27 15.624
14
c MYP106 Myopathy, Myosin Storage, Autosomal Recessive 20 15.624
15
EBS001 Ebstein Anomaly 42 13.974
16
SDD007 Sudden Cardiac Death 36 13.974
17
SCP008 Scapuloperoneal Syndrome, Myopathic Type 26 13.974
18
SCP010 Scapuloperoneal Myopathy 22 13.974
19
WLF001 Wolff-Parkinson-White Syndrome 60 12.102
20
OCL008 Oculopharyngeal Muscular Dystrophy 51 12.102
21
P VNT002 Ventricular Septal Defect 50 12.102
22
P CNG046 Congenital Fiber-Type Disproportion 48 12.102
23
c ART101 Aortic Valve Disease 2 46 12.102
24
PRP009 Peripartum Cardiomyopathy 38 12.102
25
DST004 Distal Muscular Dystrophy 32 12.102
26
FML304 Familial Isolated Dilated Cardiomyopathy 31 12.102
27
c FML154 Familial Restrictive Cardiomyopathy 29 12.102
28
c MYH009 Myh7-Related Dilated Cardiomyopathy 20 12.102
29
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 20 12.102
30
HYL005 Hyaline Body Myopathy 12 12.102
31
P NNN008 Noonan Syndrome 1 62 9.881
32
CNT098 Central Core Disease 60 9.881
33
P HLT001 Holt-Oram Syndrome 58 9.881
34
END020 Endocardial Fibroelastosis 43 9.881
35
c ART115 Aortic Valve Disease 1 43 9.881
36
c GLY005 Glycogen Storage Disease Vi 42 9.881
37
BNF002 Bone Fracture 39 9.881
38
P TRC087 Tricuspid Valve Disease 35 9.881
39
ORB013 Orbital Disease 33 9.881
40
ATS008 Autosomal Dominant Disease 31 9.881
41
CVL001 Caveolinopathies 25 9.881
42
c SCN022 Scn5a-Related Dilated Cardiomyopathy 20 9.881
43
MYP005 Myopathy of Extraocular Muscle 19 9.881
44
SCN020 Scn5a-Associated Dilated Cardiomyopathy 16 9.881
45
c MYH011 Myh7-Related Myosin Storage Myopathy 16 9.881
46
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 35 6.987
47
CLS026 Classic Multiminicore Myopathy 17 6.987
48
c MYH010 Myh7-Related Familial Hypertrophic Cardiomyopathy 8 6.987
49
c MYH013 Myh7-Related Congenital Fiber-Type Disproportion 5 6.987