Search results for emery-dreifuss muscular dystrophy, ar

167 hits were found for emery-dreifuss muscular dystrophy, ar

# Family MCID Name MIFTS Score
1
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 23 13.676
2
P MSC005 Muscular Dystrophy 65 2.009
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 1.502
4
P CRD011 Cardiomyopathy 68 0.530
5
P MYP004 Myopathy 67 0.497
6
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.471
7
P MYT002 Myotonic Dystrophy 48 0.390
8
BCK001 Becker Muscular Dystrophy 69 0.383
9
c DLT002 Dilated Cardiomyopathy 76 0.300
10
P CRD132 Cardiac Conduction Defect 43 0.285
11
P NRV007 Nervous System Disease 71 0.277
12
NRM005 Neuromuscular Disease 56 0.272
13
c PRG106 Progressive Muscular Dystrophy 40 0.263
14
P LPD010 Lipodystrophy 55 0.260
15
RTN023 Retinitis 50 0.248
16
MSC004 Muscle Tissue Disease 34 0.236
17
SDD007 Sudden Cardiac Death 47 0.224
18
ALR002 Al-Raqad Syndrome 36 0.221
19
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.212
20
PRX075 Proximal Myopathy and Ophthalmoplegia 41 0.203
21
ATR057 Atrioventricular Block 49 0.195
22
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 39 0.194
23
TTR016 Tetra-Amelia Syndrome 36 0.193
24
P MYS005 Myositis 57 0.192
25
P ATR011 Atrial Fibrillation 66 0.190
26
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 44 0.185
27
HPT074 Hepatic Adenoma, Somatic 50 0.181
28
SCP008 Scapuloperoneal Syndrome, Myopathic Type 29 0.177
29
c MSC124 Muscular Dystrophy, Congenital 55 0.173
30
INC002 Inclusion Body Myositis 66 0.172
31
WLK001 Walker-Warburg Syndrome 52 0.171
32
P FML012 Familial Partial Lipodystrophy 52 0.170
33
NTR003 Natural Killer Cell Leukemia 47 0.169
34
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 48 0.169
35
c MSC120 Muscular Dystrophy, Limb-Girdle, Type 2c 47 0.168
36
ATR060 Atrial Standstill, Digenic 51 0.164
37
P HRT032 Heart Disease 75 0.163
38
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 55 0.162
39
P ALZ034 Alzheimer Disease 92 0.161
40
P PLY019 Polyneuropathy 56 0.160
41
P DYS007 Dyskeratosis Congenita 63 0.153
42
AND005 Androgen Insensitivity Syndrome, Mild 16 0.152
43
MSC077 Muscle Eye Brain Disease 57 0.150
44
P CNG001 Congenital Myasthenic Syndrome 55 0.149
45
CLL038 Collagen Vi-Related Myopathy 16 0.149
46
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 54 0.148
47
SRC016 Sarcoglycanopathies 33 0.144
48
c MSC119 Muscular Dystrophy, Limb-Girdle, Type 2h 41 0.142
49
P RSP003 Respiratory Failure 71 0.142
50
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 29 0.142
51
P HYP055 Hypoplastic Left Heart Syndrome 61 0.141
52
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 0.140
53
ACT049 Acute Disseminated Encephalomyelitis 49 0.138
54
CNG034 Congestive Heart Failure 72 0.135
55
P MSC007 Muscle Hypertrophy 58 0.132
56
P SLP006 Sleep Apnea 61 0.132
57
c CRD099 Cardiomyopathy, Dilated, 1e 52 0.131
58
MLG056 Malignant Hyperthermia 58 0.130
59
P VNT002 Ventricular Septal Defect 60 0.127
60
RTN018 Retinal Disease 53 0.125
61
MLL018 Miller-Dieker Lissencephaly Syndrome 45 0.123
62
OBS061 Obstructive Sleep Apnea 66 0.122
63
P HYP263 Hypersomnia 40 0.121
64
c ACT075 Acute Myocardial Infarction 60 0.119
65
P STR022 Stargardt Disease 56 0.118
66
PLM129 Pulmonary Disease, Chronic Obstructive 63 0.118
67
PTN001 Patent Foramen Ovale 55 0.114
68
P MYF003 Myofibrillar Myopathy 42 0.114
69
P LNG028 Long Qt Syndrome 64 0.114
70
c MYP072 Myopathy, Myofibrillar, 1 39 0.114
71
P ORL007 Oral Cavity Cancer 59 0.114
72
P LFT003 Left Ventricular Noncompaction 50 0.113
73
c CNG012 Congenital Generalized Lipodystrophy 44 0.112
74
P CNG046 Congenital Fiber-Type Disproportion 50 0.112
75
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.110
76
PLM033 Pulmonary Embolism 60 0.110
77
STR046 Stargardt Macular Degeneration 29 0.109
78
PRP009 Peripartum Cardiomyopathy 42 0.109
79
ISC006 Ischemic Heart Disease 68 0.108
80
CHG001 Chagas Disease 67 0.108
81
P MYC008 Myocarditis 54 0.108
82
P LRY044 Larynx Cancer 57 0.108
83
PRC012 Pericardial Effusion 51 0.107
84
NNL002 Nonalcoholic Steatohepatitis 50 0.107
85
ANV001 Anovulation 44 0.107
86
SYS003 Systolic Heart Failure 43 0.107
87
SYN036 Syncope 47 0.106
88
c CRD093 Cardiomyopathy, Dilated, 1a 55 0.106
89
P PTN002 Patent Ductus Arteriosus 52 0.105
90
ALS001 Alstrom Syndrome 53 0.105
91
CHR066 Chronic Fatigue Syndrome 64 0.104
92
END030 End Stage Renal Failure 55 0.104
93
P PMP005 Pemphigus Vulgaris 51 0.104
94
CRD137 Cardiogenic Shock 46 0.104
95
LKP003 Leukoplakia 38 0.103
96
c CRD097 Cardiomyopathy, Dilated, 1d 40 0.103
97
BNN003 Bone Inflammation Disease 44 0.103
98
ENH001 Enhanced S-Cone Syndrome 44 0.103
99
TTR001 Tetralogy of Fallot 71 0.102
100
c HPT015 Hepatitis D 52 0.102
101
INT007 Intermediate Coronary Syndrome 50 0.102
102
PLM010 Pulmonary Edema 54 0.102
103
c RTN070 Retinitis Pigmentosa 9 35 0.102
104
P ATR001 Atrioventricular Septal Defect 52 0.102
105
c FML001 Familial Atrial Fibrillation 58 0.101
106
c MYP102 Myopathy, Centronuclear, Autosomal Recessive 32 0.101
107
VNT011 Ventricular Fibrillation, Familial, 1 41 0.101
108
DBT062 Diabetic Foot Ulcers 51 0.101
109
P RST002 Restrictive Cardiomyopathy 50 0.101
110
P HYP120 Hypoaldosteronism 36 0.101
111
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 60 0.100
112
HYP006 Hypertensive Heart Disease 50 0.100
113
MYP100 Myopathy, X-Linked, with Excessive Autophagy 37 0.100
114
P HYP065 Hyperaldosteronism 50 0.100
115
HPT014 Hepatorenal Syndrome 46 0.100
116
DST006 Diastolic Heart Failure 46 0.100
117
c VNT013 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1 48 0.099
118
c LNG044 Long Qt Syndrome 1 62 0.099
119
PRD004 Prediabetes Syndrome 43 0.099
120
MLT001 Multiple Chemical Sensitivity 43 0.099
121
c LCL006 Localized Scleroderma 61 0.098
122
BRT005 Barth Syndrome 52 0.098
123
P ABD016 Abdominal Obesity-Metabolic Syndrome 41 0.098
124
CHR476 Chronic Angina 26 0.098
125
MTG002 Mutagen Sensitivity 36 0.098
126
P HLT001 Holt-Oram Syndrome 61 0.098
127
SNL007 Senile Cataract 37 0.098
128
DRR010 Darier Disease 60 0.098
129
P RNL015 Renal Hypertension 48 0.098
130
P RNV001 Renovascular Hypertension 47 0.098
131
c MLG069 Malignant Hypertension 47 0.098
132
c LPD037 Lipodystrophy, Familial Partial, 2 52 0.097
133
EBS001 Ebstein Anomaly 45 0.097
134
NPH004 Nephropathia Epidemica 40 0.097
135
ALC005 Alcoholic Pancreatitis 36 0.097
136
ALC009 Alcoholic Liver Cirrhosis 49 0.097
137
FTL021 Fetal Macrosomia 41 0.097
138
OLG001 Oligospermia 36 0.097
139
VNB005 Van Buchem Disease 49 0.096
140
MCR191 Microscopic Colitis 47 0.096
141
P MTR012 Mitral Valve Disease 58 0.096
142
c ART115 Aortic Valve Disease 1 50 0.096
143
c SHR030 Short Qt Syndrome 44 0.096
144
c FML191 Familial Long Qt Syndrome 42 0.096
145
ACN002 Acanthosis Nigricans 57 0.095
146
PRC013 Pericarditis 51 0.095
147
c PST041 Posterior Urethral Valves 47 0.095
148
RNL097 Renal Artery Disease 43 0.095
149
ART031 Aortic Coarctation 43 0.095
150
TXC020 Toxic Oil Syndrome 39 0.095
151
P MYS032 Myosin Storage Myopathy 34 0.095
152
CLR063 Colorblindness, Deutan 31 0.095
153
RNL104 Renal Hypodysplasia 29 0.095
154
c ART101 Aortic Valve Disease 2 53 0.094
155
P RNL100 Renal Hypodysplasia/aplasia 1 53 0.094
156
c ALZ036 Alzheimer Disease, Type 3 53 0.094
157
GSG001 Gas Gangrene 49 0.094
158
CNT046 Central Nervous System Vasculitis 46 0.094
159
END020 Endocardial Fibroelastosis 44 0.094
160
ASB001 Asbestosis 42 0.094
161
BRN107 Branchiootorenal Syndrome 1, with or Without Cataracts 42 0.094
162
DRG002 Drug-Induced Hepatitis 40 0.094
163
P BRN042 Branchiootic Syndrome 39 0.094
164
P ACQ009 Acquired Metabolic Disease 38 0.094
165
c FML250 Familial Progressive Cardiac Conduction Defect 28 0.094
166
c CRD091 Cardiomyopathy, Dilated, 1dd 26 0.094
167
BRN121 Branchiootorenal/branchiootic Syndrome 18 0.094
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