Search results for mybpc3

159 hits were found for mybpc3

# Family MCID Name MIFTS Score
1
P HYP061 Hypertrophic Cardiomyopathy 69 95.111
2
c ATR087 Atrial Standstill 1 74 83.368
3
FML304 Familial Isolated Dilated Cardiomyopathy 49 74.358
4
c CRD085 Cardiomyopathy, Familial Hypertrophic, 4 50 64.626
5
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 46.012
6
P LFT003 Left Ventricular Noncompaction 57 45.540
7
c LFT018 Left Ventricular Noncompaction 10 28 45.361
8
c DLT002 Dilated Cardiomyopathy 78 43.694
9
CRD132 Cardiac Conduction Defect 60 27.675
10
P LNG028 Long Qt Syndrome 64 22.227
11
c CRD233 Cardiomyopathy, Dilated, 1b 46 20.988
12
P HRT032 Heart Disease 81 18.846
13
c PRG126 Progressive Familial Heart Block 58 16.300
14
HRT008 Heart Conduction Disease 44 16.300
15
P CRD119 Cardiac Arrest 67 16.298
16
DSS008 Disease of Mental Health 74 15.345
17
WLF001 Wolff-Parkinson-White Syndrome 65 14.237
18
P RST002 Restrictive Cardiomyopathy 54 14.127
19
P MYP004 Myopathy 67 13.646
20
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 13.313
21
P ATR011 Atrial Fibrillation 66 12.948
22
P BRG001 Brugada Syndrome 69 12.899
23
DST006 Diastolic Heart Failure 45 12.507
24
LPP008 Lipoprotein Quantitative Trait Locus 65 11.993
25
c ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 43 11.339
27
c CRD069 Cardiomyopathy, Dilated, 1h 42 9.908
28
c CRD093 Cardiomyopathy, Dilated, 1a 53 9.908
29
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 9.465
30
DNN001 Danon Disease 59 8.887
31
NNN026 Noonan Syndrome with Multiple Lentigines 65 8.887
32
c BRG005 Brugada Syndrome 1 54 8.018
33
P DST002 Distal Arthrogryposis 65 7.735
34
BRT005 Barth Syndrome 56 7.548
35
c LNG047 Long Qt Syndrome 2 59 7.304
36
EBS001 Ebstein Anomaly 55 7.304
37
c LNG044 Long Qt Syndrome 1 66 7.304
38
c MTC143 Mitochondrial Dna Depletion Syndrome 12b 27 6.714
39
RSP023 Rasopathy 53 6.714
40
INT084 Intrinsic Cardiomyopathy 27 6.714
41
c FML346 Familial Adenomatous Polyposis 1 65 6.714
42
c ART101 Aortic Valve Disease 2 66 6.714
43
c LTH026 Lethal Congenital Contracture Syndrome 4 33 6.714
44
TRC078 Trichohepatoenteric Syndrome 2 34 6.714
45
MTR002 Mitral Valve Insufficiency 52 6.714
46
SYN036 Syncope 45 3.957
47
47X002 47,xyy 48 3.858
48
MSC007 Muscle Hypertrophy 64 3.734
49
CNG034 Congestive Heart Failure 69 2.684
50
ART140 Arteries, Anomalies of 53 2.497
51
SYS003 Systolic Heart Failure 49 2.396
52
P MYC008 Myocarditis 59 2.349
53
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 2.258
54
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 2.205
55
VCS001 Vici Syndrome 57 2.173
56
TRN015 Transient Cerebral Ischemia 63 2.173
57
c CRD219 Cardiomyopathy, Infantile Hypertrophic 34 2.047
58
MTC150 Mitochondrial Complex V Deficiency, Mitochondrial Type 1 29 2.047
59
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.955
60
FBR012 Fabry Disease 70 1.908
61
P PTN014 Patent Ductus Arteriosus 1 59 1.750
62
HMP001 Hemopericardium 47 1.667
63
P PRC012 Pericardial Effusion 50 1.667
64
ATR057 Atrioventricular Block 54 1.563
65
P NNN008 Noonan Syndrome 1 77 1.318
66
c PSD047 Pseudo-Turner Syndrome 52 1.318
67
c CRD099 Cardiomyopathy, Dilated, 1e 53 1.318
68
P HRS035 Hirschsprung Disease 1 66 1.304
70
P NRP001 Neuropathy 60 1.304
71
NRT004 Neuritis 53 1.304
72
P PRP019 Peripheral Nervous System Disease 58 1.304
73
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 1.179
74
c CRD061 Cardiomyopathy, Familial Hypertrophic, 13 31 1.179
75
NTH001 Netherton Syndrome 61 1.179
76
P AMY004 Amyloidosis 70 1.179
77
CNG506 Congenital Amyoplasia 27 1.021
78
SDD004 Sudden Arrhythmia Death Syndrome 22 1.021
79
P ALZ034 Alzheimer Disease 87 1.021
80
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.021
81
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.021
82
c CRD232 Cardiomyopathy, Familial Hypertrophic, 6 37 1.021
83
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.021
84
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.021
85
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.021
86
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.021
87
c LFT021 Left Ventricular Noncompaction 1 44 1.021
88
c LFT017 Left Ventricular Noncompaction 8 27 1.021
89
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.021
90
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.021
91
c CRD056 Cardiomyopathy, Familial Hypertrophic, 11 27 1.021
92
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.021
93
P RTN024 Retinoblastoma 73 1.021
94
NRM005 Neuromuscular Disease 63 1.021
95
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.021
96
DYS032 Dystrophinopathies 47 1.021
97
P MTC069 Mitochondrial Disorders 57 1.021
98
CMP017 Camptocormism 26 1.021
99
P CRN300 Coronary Heart Disease 1 73 0.834
100
MSC152 Muscular Dystrophy, Becker Type 69 0.834
101
MSC157 Muscular Dystrophy, Duchenne Type 79 0.834
102
c ART144 Arthrogryposis, Distal, Type 1a 60 0.834
103
c ART060 Arthrogryposis, Distal, Type 1b 33 0.834
104
LPT014 Leptin Deficiency or Dysfunction 78 0.834
105
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 52 0.834
106
P ANR048 Aniridia 1 64 0.834
107
P ART018 Aortic Valve Insufficiency 52 0.834
108
P MSC005 Muscular Dystrophy 67 0.834
109
P VNT002 Ventricular Septal Defect 58 0.834
110
P EYD002 Eye Disease 57 0.834
111
CNG065 Congenital Contractures 25 0.834
112
P ATS364 Autism 69 0.589
113
ATR024 Atrial Fibrillation and Stroke 22 0.589
114
SNG003 Single Ventricular Heart 30 0.589
115
CRD223 Cardiac Arrhythmia 63 0.589
116
AGN016 Aging 54 0.589
117
MRF001 Marfan Syndrome 76 0.589
118
c MYT021 Myotonic Dystrophy 1 68 0.589
119
PPL052 Papillomatosis, Confluent and Reticulated 34 0.589
120
c OPT053 Optic Atrophy 1 62 0.589
121
c PRG042 Progressive Familial Heart Block, Type Ia 66 0.589
122
HYD038 Hydrops Fetalis, Nonimmune 59 0.589
123
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.589
124
c CRD079 Cardiomyopathy, Familial Hypertrophic, 9 39 0.589
125
c CRD148 Cardiomyopathy, Familial Hypertrophic, 16 23 0.589
126
c ATS007 Autism Spectrum Disorder 72 0.589
127
ART074 Aortic Dissection 53 0.589
128
c 3MT007 3-Methylglutaconic Aciduria 37 0.589
129
SNT005 Sinoatrial Node Disease 47 0.589
130
PTC001 Potocki-Shaffer Syndrome 41 0.589
131
P ENC069 Encephalopathy, Progressive, Early-Onset, with Brain Edema and/or Leukoencephalopathy, 1 25 0.589
132
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 0.589
133
P SRC025 Sarcoidosis 1 71 0.589
134
c EXS020 Exostoses, Multiple, Type Ii 38 0.589
135
c BRD014 Bardet-Biedl Syndrome 2 53 0.589
136
c DVL099 Developmental and Epileptic Encephalopathy 75 27 0.589
137
MDD018 Middle East Respiratory Syndrome 44 0.589
138
GNT082 Genetic Neuromuscular Disease 10 0.589
139
P TRM003 Tremor 48 0.589
140
P THR014 Thrombocytopenia 66 0.589
141
HRT011 Heart Septal Defect 49 0.589
142
NRN001 Neuroendocrine Carcinoma 47 0.589
143
PRP009 Peripartum Cardiomyopathy 55 0.589
144
c MTC088 Mitochondrial Dna Depletion Syndrome 13 43 0.589
145
LFT001 Left Bundle Branch Hemiblock 47 0.589
146
TLN003 Telangiectasis 51 0.589
147
P NTR004 Neutropenia 63 0.589
148
P VSC007 Vascular Disease 63 0.589
149
P GLY013 Glycogen Storage Disease 60 0.589
150
LYS002 Lysosomal Storage Disease 51 0.589
151
P SCK002 Sick Sinus Syndrome 55 0.589
152
P MYT002 Myotonic Dystrophy 51 0.589
153
P HYP055 Hypoplastic Left Heart Syndrome 65 0.589
154
CLP006 Clopidogrel Resistance 44 0.589
155
P SCK005 Sickle Cell Disease 56 0.589
156
P OST028 Osteochondroma 45 0.589
157
P BRS047 Breast Cancer 98 0.573
158
P PNC035 Pancreatic Cancer 86 0.573
159
CLL010 Cellular Ependymoma 57 0.573
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