Search results for myh6

207 hits were found for myh6

# Family MCID Name MIFTS Score
1
c CRD089 Cardiomyopathy, Familial Hypertrophic, 14 27 56.476
2
c ATR022 Atrial Septal Defect 3 29 35.070
3
c CRD096 Cardiomyopathy, Dilated, 1ee 31 33.087
4
c DLT002 Dilated Cardiomyopathy 79 31.688
5
c SCK022 Sick Sinus Syndrome 3 23 31.458
6
P HRT032 Heart Disease 84 30.046
7
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 28.502
8
c ATR087 Atrial Standstill 1 74 24.373
9
P HYP061 Hypertrophic Cardiomyopathy 69 22.440
10
FML304 Familial Isolated Dilated Cardiomyopathy 51 21.272
11
c FML272 Familial Sick Sinus Syndrome 37 18.970
12
PTN001 Patent Foramen Ovale 62 16.142
13
INT276 Interatrial Communication 50 14.673
14
P SCK002 Sick Sinus Syndrome 55 14.312
15
P ATR010 Atrial Heart Septal Defect 58 14.089
16
CNG034 Congestive Heart Failure 69 13.635
17
P MYP004 Myopathy 67 13.298
18
P MYC008 Myocarditis 59 12.424
19
P LFT003 Left Ventricular Noncompaction 57 12.101
20
CRD132 Cardiac Conduction Defect 59 11.424
21
c CRD233 Cardiomyopathy, Dilated, 1b 46 11.372
22
HLT001 Holt-Oram Syndrome 66 10.980
23
WLF001 Wolff-Parkinson-White Syndrome 63 10.677
24
P LNG028 Long Qt Syndrome 63 10.638
25
P CRD119 Cardiac Arrest 68 10.631
26
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 10.530
27
P BRG001 Brugada Syndrome 69 10.530
28
HMP005 Hemiplegia 53 10.384
29
P RST002 Restrictive Cardiomyopathy 54 10.384
30
P HYP055 Hypoplastic Left Heart Syndrome 65 10.261
31
c MYP125 Myopathy, Distal, 1 48 9.227
32
P SCP010 Scapuloperoneal Myopathy 32 9.227
33
P MYC007 Myocardial Infarction 69 8.813
34
BTT016 Batten-Turner Congenital Myopathy 53 8.605
35
LPP008 Lipoprotein Quantitative Trait Locus 65 8.605
36
P DST002 Distal Arthrogryposis 63 8.605
37
P CHR071 Charcot-Marie-Tooth Disease 64 8.605
38
c ART115 Aortic Valve Disease 1 72 8.605
39
c HYP595 Hypertension, Essential 84 8.605
41
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 8.605
42
P MYS079 Miyoshi Muscular Dystrophy 52 8.605
43
TTH006 Tooth Disease 51 8.605
44
HRT011 Heart Septal Defect 49 8.105
45
c PRG126 Progressive Familial Heart Block 59 7.863
46
HRT008 Heart Conduction Disease 44 7.863
47
c LFT021 Left Ventricular Noncompaction 1 44 7.597
48
HYL005 Hyaline Body Myopathy 41 6.854
49
SNT005 Sinoatrial Node Disease 47 6.853
50
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 6.378
51
P TTR001 Tetralogy of Fallot 69 6.339
52
BRT005 Barth Syndrome 55 6.292
53
DBL002 Double Outlet Right Ventricle 57 6.292
54
RSP023 Rasopathy 54 6.232
55
c ART101 Aortic Valve Disease 2 65 6.232
56
P ATR001 Atrioventricular Septal Defect 55 6.232
57
MTR002 Mitral Valve Insufficiency 51 6.232
58
DNN001 Danon Disease 59 6.085
59
KGM001 Kagami-Ogata Syndrome 54 6.085
60
c LNG047 Long Qt Syndrome 2 58 6.085
61
c DFN179 Deafness, Autosomal Recessive 62 29 6.085
62
PLY179 Polyomavirus-Associated Nephropathy 25 6.085
63
c MYS068 Myasthenic Syndrome, Congenital, 20, Presynaptic 42 6.085
64
P MYF003 Myofibrillar Myopathy 50 6.085
65
c MTC143 Mitochondrial Dna Depletion Syndrome 12b 27 6.085
66
c ART119 Arthrogryposis, Distal, Type 5 51 6.085
67
EBS001 Ebstein Anomaly 54 6.085
68
KFM001 Kaufman Oculocerebrofacial Syndrome 55 6.085
69
INT084 Intrinsic Cardiomyopathy 26 6.085
70
c FML001 Familial Atrial Fibrillation 65 6.085
71
c MYS074 Myasthenic Syndrome, Congenital, 12 45 6.085
72
c DYS059 Dystonia 16 47 6.085
73
c LNG044 Long Qt Syndrome 1 66 6.085
74
MBT001 Mobitz Type Ii Atrioventricular Block 34 6.085
75
MSC190 Muscular Disease 36 6.085
76
CNG046 Congenital Fiber-Type Disproportion 52 6.085
77
P PRM001 Primary Cutaneous Amyloidosis 47 6.085
78
P TRC087 Tricuspid Valve Disease 48 6.085
79
P MTR012 Mitral Valve Disease 57 6.085
80
MSC004 Muscle Tissue Disease 21 6.085
81
NNN026 Noonan Syndrome with Multiple Lentigines 65 6.085
82
P CNG001 Congenital Myasthenic Syndrome 68 6.085
83
P PTN014 Patent Ductus Arteriosus 1 59 6.085
84
NRM005 Neuromuscular Disease 63 6.085
85
HRT012 Heart Valve Disease 53 6.085
86
EXT035 Extrinsic Cardiomyopathy 26 6.085
87
P MLG056 Malignant Hyperthermia 65 6.085
88
c BRG005 Brugada Syndrome 1 56 1.925
90
c MGR028 Migraine with or Without Aura 1 64 1.779
91
c CRD093 Cardiomyopathy, Dilated, 1a 54 1.779
92
c CRD069 Cardiomyopathy, Dilated, 1h 41 1.779
93
P ARR023 Arrhythmogenic Right Ventricular Dysplasia, Familial, 9 47 1.258
94
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.258
95
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 1.258
96
HRT038 Heart, Malformation of 36 1.258
97
47X002 47,xyy 48 1.097
98
P MTR003 Mitral Valve Stenosis 53 1.062
99
RFR003 Refractive Error 41 1.062
100
c CRD085 Cardiomyopathy, Familial Hypertrophic, 4 51 1.023
101
ESP021 Esophageal Cancer 84 0.988
102
c LFT018 Left Ventricular Noncompaction 10 25 0.976
103
PLM173 Palmoplantar Hyperkeratosis with Squamous Cell Carcinoma of Skin and 46,xx Sex Reversal 34 0.841
104
SKN022 Skin Squamous Cell Carcinoma 54 0.841
105
PSD011 Pseudovascular Skin Squamous Cell Carcinoma 16 0.841
106
P MYP105 Myopathy, Myosin Storage, Autosomal Dominant 39 0.769
108
c CLR087 Colorectal Cancer 12 34 0.595
109
GST103 Gastric Cancer, Hereditary Diffuse 68 0.595
110
LNG012 Lung Occult Squamous Cell Carcinoma 20 0.595
111
SML009 Small Intestine Adenocarcinoma 57 0.595
112
ESP027 Esophagus Squamous Cell Carcinoma 45 0.595
113
LNG039 Lung Squamous Cell Carcinoma 57 0.595
114
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 60 0.595
115
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.595
116
LNG007 Lung Mixed Small Cell and Squamous Cell Carcinoma 20 0.595
117
P BRS047 Breast Cancer 97 0.573
118
P PNC035 Pancreatic Cancer 86 0.573
119
P ATR011 Atrial Fibrillation 66 0.441
120
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.389
121
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.389
122
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.389
123
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.389
124
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.389
125
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.389
126
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.389
127
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.389
128
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.389
129
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.389
130
CRD223 Cardiac Arrhythmia 63 0.360
131
48X005 48,xyyy 39 0.360
132
P VNT002 Ventricular Septal Defect 58 0.328
133
SNG003 Single Ventricular Heart 30 0.328
134
ATR057 Atrioventricular Block 54 0.294
135
RST023 Resting Heart Rate, Variation in 40 0.294
136
DST006 Diastolic Heart Failure 45 0.294
137
c CRD098 Cardiomyopathy, Familial Restrictive, 3 34 0.254
138
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.254
139
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.254
140
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 39 0.254
141
c CRD097 Cardiomyopathy, Dilated, 1d 47 0.254
142
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.254
143
SQM006 Squamous Cell Carcinoma 59 0.254
144
P HYP076 Hyperthyroidism 53 0.254
145
P MSC005 Muscular Dystrophy 66 0.254
146
FML293 Familial Isolated Restrictive Cardiomyopathy 42 0.254
147
CHR103 Charge Syndrome 65 0.208
148
c MSC179 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 10 40 0.208
149
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.208
150
c PLM164 Pulmonary Hypertension, Primary, 1 80 0.208
151
P EPL164 Epilepsy 70 0.208
152
ISC004 Ischemia 61 0.208
153
SVR004 Severe Combined Immunodeficiency 71 0.208
154
P NTR004 Neutropenia 62 0.208
155
c CRD080 Cardiomyopathy, Dilated, 1g 42 0.208
156
PLY100 Polyploidy 36 0.208
157
P PRS040 Prostate Cancer 95 0.147
158
c TYP009 Type 2 Diabetes Mellitus 92 0.147
159
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.147
160
P ATX030 Ataxia-Telangiectasia 80 0.147
161
RGH009 Right Atrial Isomerism 57 0.147
162
c CRD062 Cardiomyopathy, Familial Hypertrophic, 7 32 0.147
163
P GST053 Gastric Cancer 82 0.147
164
TRC062 Tricuspid Atresia 54 0.147
165
c DVL072 Developmental and Epileptic Encephalopathy 47 25 0.147
166
P PLM037 Pulmonary Hypertension 69 0.147
167
c CNG616 Congenital Heart Defects, Multiple Types, 7 21 0.147
168
P PRN062 Pr Interval, Variation in 9 0.147
169
c CLR131 Ciliary Dyskinesia, Primary, 1 62 0.147
170
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.147
171
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.147
172
CLN044 Colon Adenoma 44 0.147
173
ORL015 Oral Squamous Cell Carcinoma 43 0.147
174
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.147
175
P KBK002 Kabuki Syndrome 1 66 0.147
176
c DMN023 Diamond-Blackfan Anemia 1 68 0.147
177
P NNN008 Noonan Syndrome 1 76 0.147
178
P ALG028 Alagille Syndrome 1 73 0.147
179
c BRD014 Bardet-Biedl Syndrome 2 53 0.147
180
c CNG520 Congenital Heart Defects, Multiple Types, 6 29 0.147
181
c CRD091 Cardiomyopathy, Dilated, 1dd 43 0.147
182
PRP009 Peripartum Cardiomyopathy 54 0.147
183
FBR012 Fabry Disease 71 0.147
184
HYP060 Hyperinsulinism 53 0.147
185
LPD008 Lipid Metabolism Disorder 61 0.147
186
ADN018 Adenoma 58 0.147
187
OVR063 Overnutrition 42 0.147
188
IRN002 Iron Metabolism Disease 56 0.147
189
TLN003 Telangiectasis 51 0.147
190
P DMN001 Diamond-Blackfan Anemia 73 0.147
191
HMS001 Hemosiderosis 48 0.147
192
DPH001 Diphtheria 59 0.147
193
c ACT071 Acute Kidney Failure 60 0.147
194
CCC002 Coccidiosis 50 0.147
195
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.147
196
P ORT004 Orthostatic Intolerance 62 0.147
197
P CRN300 Coronary Heart Disease 1 73 0.147
198
c CHR684 Chronic Kidney Disease 74 0.147
199
SPN186 Spinal Cord Injury 61 0.147
200
HTR003 Heterotaxy 44 0.147
201
P PRM011 Primary Ciliary Dyskinesia 69 0.147
202
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.147
203
P FML187 Familial Hypertension 34 0.147
204
ORL011 Oral Cancer 60 0.147
205
c PSD047 Pseudo-Turner Syndrome 52 0.147
206
P RRH023 Rare Hereditary Hemochromatosis 53 0.147
207
SHN001 Shone Complex 15 0.147
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