Search results for dmd.1

257 hits were found for dmd.1

# Family MCID Name MIFTS Score
1
DCH001 Duchenne Muscular Dystrophy 79 19.085
2
DMD003 Dmd-Associated Dilated Cardiomyopathy 18 16.232
3
c DMD004 Dmd-Related Dilated Cardiomyopathy 14 14.701
4
c CRD187 Cardiomyopathy, Dilated, 3b 33 11.820
5
BCK001 Becker Muscular Dystrophy 69 6.530
6
P MSC005 Muscular Dystrophy 65 5.110
7
P CRD011 Cardiomyopathy 68 4.029
8
NRM005 Neuromuscular Disease 56 3.780
9
c DLT002 Dilated Cardiomyopathy 76 3.729
10
DST004 Distal Muscular Dystrophy 40 3.668
11
P MYC008 Myocarditis 54 3.651
12
GLY014 Glycerol Kinase Deficiency 44 3.352
13
P MYS005 Myositis 57 3.333
14
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 56 3.333
15
c CNG464 Congenital Myopathy 49 3.333
16
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 44 3.333
17
DYS032 Dystrophinopathies 44 3.112
18
c PRG106 Progressive Muscular Dystrophy 40 3.068
19
FCS012 Facioscapulohumeral Muscular Dystrophy 1 50 3.002
20
c GLY008 Glycogen Storage Disease Ii 59 2.981
21
MLG056 Malignant Hyperthermia 58 2.981
22
c MSC124 Muscular Dystrophy, Congenital 55 2.981
23
P EMR001 Emery-Dreifuss Muscular Dystrophy 55 2.981
24
P MYP101 Myopathy, Centronuclear 54 2.981
25
WLK001 Walker-Warburg Syndrome 52 2.981
26
P CNG046 Congenital Fiber-Type Disproportion 50 2.981
27
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 48 2.981
28
PYL006 Pyloric Stenosis 46 2.981
29
P BTH005 Bethlem Myopathy 1 46 2.981
30
MSC051 Muscular Dystrophy, Rigid Spine, 1 45 2.981
31
ALN001 Aland Island Eye Disease 45 2.981
32
P HYP009 Hypertrophic Pyloric Stenosis 42 2.981
33
RDC010 Reducing Body Myopathy 31 2.981
34
MSC004 Muscle Tissue Disease 34 2.828
35
CHR387 Chromosome Xp21 Deletion Syndrome 27 2.627
36
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 38 2.605
37
FML304 Familial Isolated Dilated Cardiomyopathy 31 2.605
38
NNS032 Non-Syndromic X-Linked Intellectual Disability 28 2.605
39
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 5 2.605
40
EYD002 Eye Disease 61 2.581
41
MSC077 Muscle Eye Brain Disease 57 2.581
42
STR081 Stormorken Syndrome 49 2.581
43
GSG001 Gas Gangrene 49 2.581
44
P MYF003 Myofibrillar Myopathy 42 2.581
45
c MYP082 Myopathy, Myofibrillar, 2 39 2.581
46
MYP100 Myopathy, X-Linked, with Excessive Autophagy 37 2.581
47
c MYP079 Myopathy, Myofibrillar, 5 37 2.581
48
MYT011 Myotonia 36 2.581
49
INT084 Intrinsic Cardiomyopathy 34 2.581
50
SRC016 Sarcoglycanopathies 33 2.581
51
c LCL022 Localized Lipodystrophy 30 2.581
52
CBB005 Cobblestone Lissencephaly 27 2.581
53
c MYG003 Myoglobinuria Recurrent 23 2.581
54
P OTP001 Otopalatodigital Syndrome 21 2.581
55
CYT006 Cytoplasmic Body Myopathy 19 2.581
56
c CRD093 Cardiomyopathy, Dilated, 1a 55 2.108
57
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 54 2.108
58
c MSC120 Muscular Dystrophy, Limb-Girdle, Type 2c 47 2.108
59
c MSC042 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 46 2.108
60
MSC039 Muscular Dystrophy, Congenital Merosin-Deficient 45 2.108
61
c MSC035 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 44 2.108
62
c MNT230 Mental Retardation, X-Linked Syndromic 5 41 2.108
63
c CRD097 Cardiomyopathy, Dilated, 1d 40 2.108
64
c MSC050 Muscular Dystrophy, Congenital, 1b 37 2.108
65
c DLT016 Dilated Cardiomyopathy 1b 36 2.108
66
ALT002 Aleutian Mink Disease 33 2.108
67
c MYT012 Myotonia Congenita, Recessive 32 2.108
68
EXT061 Extracardiac Rhabdomyoma 14 2.108
69
P MYP004 Myopathy 67 0.318
70
MSC012 Muscular Dystrophy, Duchenne and Becker Type 22 0.312
71
P MSC033 Muscle Disorders 52 0.308
72
P MSC003 Muscular Atrophy 50 0.308
73
ATR076 Atrophic Muscular Disease 15 0.308
74
P XLN007 X-Linked Disease 34 0.305
75
MLT021 Multiple System Atrophy 70 0.191
76
NWC001 Newcastle Disease 54 0.149
77
SPN053 Spinal and Bulbar Muscular Atrophy of Kennedy 59 0.110
78
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 42 0.110
79
P HRT032 Heart Disease 75 0.101
80
ACR041 Acromelic Frontonasal Dysostosis 45 0.101
81
BRT030 Birth Defects 43 0.101
82
PRD011 Proud Syndrome 42 0.101
83
CRN212 Craniofacial Dysmorphism, Skeletal Anomalies, and Mental Retardation Syndrome 35 0.101
84
OCL023 Ocular Muscular Dystrophy 13 0.090
85
ATR060 Atrial Standstill, Digenic 51 0.078
86
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 38 0.078
87
P PLM036 Pulmonary Fibrosis 71 0.064
88
P NRV007 Nervous System Disease 71 0.064
89
P LGH007 Leigh Syndrome 70 0.064
90
SKN016 Skin Disease 66 0.064
91
c HMP029 Hemophilia a 63 0.064
92
ISC004 Ischemia 61 0.064
93
P HMP007 Hemophilia 57 0.064
94
P BCK002 Beckwith-Wiedemann Syndrome 56 0.064
95
P INT063 Intellectual Disability 49 0.064
96
LPD004 Lipoid Nephrosis 48 0.064
97
BRD001 Brody Myopathy 47 0.064
98
SKN023 Skin Tag 44 0.064
99
SKN027 Skin Conditions 43 0.064
100
P BLD051 Blood Coagulation Disease 42 0.064
101
SKN005 Skin Atrophy 40 0.064
102
c PRG001 Progressive Muscular Atrophy 39 0.064
103
ALR002 Al-Raqad Syndrome 36 0.064
104
CRT045 Creatine Phosphokinase, Elevated Serum 33 0.064
105
c CRN214 Coronary Heart Disease 5 22 0.064
106
P CRN178 Coronary Heart Disease 6 21 0.064
107
P ISL077 Isolated Hyperckemia 12 0.064
108
P BRS047 Breast Cancer 100 0.045
109
P AST005 Asthma 82 0.045
110
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 80 0.045
111
P SCH015 Schizophrenia 77 0.045
112
STR067 Stroke, Ischemic 75 0.045
113
CNG034 Congestive Heart Failure 72 0.045
114
P INF038 Influenza 72 0.045
115
PRP027 Peripheral Vascular Disease 68 0.045
116
P EPL164 Epilepsy 66 0.045
117
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.045
118
CNT098 Central Core Disease 65 0.045
119
GLN010 Glanzmann Thrombasthenia 63 0.045
120
MLN008 Melanoma 62 0.045
121
c HMP004 Hemophilia B 62 0.045
122
CNN005 Connective Tissue Disease 62 0.045
123
FCT003 Factor X Deficiency 61 0.045
124
VNW001 Von Willebrand's Disease 61 0.045
125
FCT007 Factor Vii Deficiency 61 0.045
126
c ACT075 Acute Myocardial Infarction 60 0.045
127
PLM033 Pulmonary Embolism 60 0.045
128
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.045
129
c HPT003 Hepatitis a 59 0.045
130
P THR015 Thrombophilia 59 0.045
131
P INF032 Infertility 59 0.045
132
PRP030 Purpura 58 0.045
133
CTS003 Coats Disease 57 0.045
134
FCT006 Factor V Deficiency 57 0.045
135
CNS004 Constipation 57 0.045
136
THR024 Thrombosis 57 0.045
137
P HMR003 Hemorrhagic Disease 57 0.045
138
HYP266 Hypoxia 56 0.045
139
P BDD001 Budd-Chiari Syndrome 56 0.045
140
P HMR012 Hemorrhagic Fever 56 0.045
141
P ANT006 Antiphospholipid Syndrome 56 0.045
142
THR004 Thrombocytosis 55 0.045
143
P SCL018 Scoliosis 55 0.045
144
MLN007 Male Infertility 55 0.045
145
P THR005 Thrombotic Thrombocytopenic Purpura 55 0.045
146
c THR092 Thrombophilia Due to Thrombin Defect 54 0.045
147
c THR082 Thrombophilia Due to Activated Protein C Resistance 54 0.045
148
P HYP620 Hypoprothrombinemia 54 0.045
149
c AFB002 Afibrinogenemia, Congenital 54 0.045
150
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 53 0.045
151
FDL002 Food Allergy 53 0.045
152
PRT014 Protein S Deficiency 53 0.045
153
P PLY014 Polycystic Kidney Disease 53 0.045
154
THR016 Thrombophlebitis 53 0.045
155
FCT022 Factor Xi Deficiency, Autosomal Recessive 53 0.045
156
ALL026 Allergic Hypersensitivity Disease 52 0.045
157
PRT011 Protein C Deficiency 52 0.045
158
P SPS003 Spastic Diplegia 52 0.045
159
HNT002 Hantavirus Pulmonary Syndrome 51 0.045
160
P LMB006 Limb-Girdle Muscular Dystrophy 51 0.045
161
IMM136 Immune System Disease 51 0.045
162
DSS009 Disseminated Intravascular Coagulation 51 0.045
163
HPT046 Hepatic Veno-Occlusive Disease 50 0.045
164
INT075 Intracranial Hypertension 50 0.045
165
HPT074 Hepatic Adenoma, Somatic 50 0.045
166
FCT004 Factor Xii Deficiency 50 0.045
167
ANG054 Angina Pectoris 50 0.045
168
MSC072 Muscle Cancer 49 0.045
169
THR104 Thrombophilia Due to Antithrombin Iii Deficiency 49 0.045
170
VNW005 Von Willebrand Disease, Type 1 49 0.045
171
LRN003 Learning Disability 49 0.045
172
PRT018 Portal Vein Thrombosis 49 0.045
173
LMB062 Limb Ischemia 48 0.045
174
P MYT002 Myotonic Dystrophy 48 0.045
175
HYP063 Hypersplenism 48 0.045
176
CRN017 Coronary Thrombosis 48 0.045
177
P AFB001 Afibrinogenemia 48 0.045
178
VND001 Vein Disease 47 0.045
179
PLC007 Placental Abruption 47 0.045
180
PST095 Post-Thrombotic Syndrome 47 0.045
181
HRT007 Heart Cancer 46 0.045
182
SPL012 Splenic Disease 46 0.045
183
HPR003 Heparin-Induced Thrombocytopenia 45 0.045
184
MCR037 Macroglossia 45 0.045
185
P DYS026 Dysfibrinogenemia 45 0.045
186
P ANL018 Analbuminemia 44 0.045
187
SND002 Sneddon Syndrome 44 0.045
188
P RTN014 Retinal Artery Occlusion 44 0.045
189
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.045
190
LKC003 Leukocyte Disease 43 0.045
191
FCT005 Factor Xiii Deficiency 43 0.045
192
NRR001 Neuroretinitis 42 0.045
193
HPT020 Hepatic Vascular Disease 42 0.045
194
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.045
195
SPC010 Speech and Communication Disorders 41 0.045
196
ESP002 Esophageal Varix 41 0.045
197
P PRP034 Purpura Fulminans 41 0.045
198
LCH001 Leech Infestation 40 0.045
199
KRN001 Korean Hemorrhagic Fever 39 0.045
200
ISC015 Ischemic Colitis 39 0.045
201
MNN021 Meningococcemia 39 0.045
202
P HYP265 Hypotonia 38 0.045
203
BRN026 Branch Retinal Artery Occlusion 38 0.045
204
FMR003 Femoral Neuropathy 38 0.045
205
PRP028 Peripheral Vertigo 38 0.045
206
BLD054 Blood Protein Disease 37 0.045
207
c CHR579 Chiari Malformation Type Ii 37 0.045
208
WTH001 Withdrawal Disorder 37 0.045
209
c INH004 Inherited Blood Coagulation Disease 36 0.045
210
NTR005 Nutritional Deficiency Disease 36 0.045
211
INT078 Intracranial Thrombosis 36 0.045
212
BLT003 Blue Toe Syndrome 35 0.045
213
GNT005 Giant Hemangioma 35 0.045
214
FRN014 Fournier Gangrene 35 0.045
215
SGT001 Sagittal Sinus Thrombosis 35 0.045
216
RDN001 Reading Disorder 34 0.045
217
HPT081 Hepatic Infarction 34 0.045
218
SPN185 Spinal Cord Infarction 34 0.045
219
PLM013 Pulmonary Immaturity 34 0.045
220
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.045
221
ANG049 Angioedema Induced by Ace Inhibitors 34 0.045
222
ALP043 Alpha-2-Plasmin Inhibitor Deficiency 33 0.045
223
CLD011 Cold Urticaria 33 0.045
224
ANT013 Anterior Spinal Artery Syndrome 33 0.045
225
MRN001 Marantic Endocarditis 32 0.045
226
P HRT017 Heart Tumor 32 0.045
227
P CHR084 Chromosomal Disease 32 0.045
228
SBN001 Subendocardial Myocardial Infarction 32 0.045
229
INT010 Intracranial Embolism 32 0.045
230
QLT001 Qualitative Platelet Defect 32 0.045
231
INT050 Intestinal Impaction 31 0.045
232
ALC001 Alcohol-Related Birth Defect 31 0.045
233
CRB132 Cerebral Sinovenous Thrombosis 31 0.045
234
CPM001 Cap Myopathy 30 0.045
235
VSC008 Vascular Hemostatic Disease 30 0.045
236
VTM003 Vitamin Metabolic Disorder 30 0.045
237
c TRC078 Trichohepatoenteric Syndrome 2 29 0.045
238
PRM243 Primary Bone Cancer 29 0.045
239
FSH003 Fish Allergy 29 0.045
240
c AST037 Asthma 1 28 0.045
241
ANT022 Anterior Cranial Fossa Meningioma 28 0.045
242
WRT002 Writing Disorder 27 0.045
243
HNM002 Hinman Syndrome 25 0.045
244
P MYP095 Myopathy, Distal, 4 25 0.045
245
INT076 Intracranial Sinus Thrombosis 24 0.045
246
c CRD153 Cardiomyopathy, Dilated, 2b 24 0.045
247
SNG003 Single Ventricular Heart 22 0.045
248
CRB017 Cerebral Falx Meningioma 21 0.045
249
c MYP112 Myopathy, Distal, 3 20 0.045
250
c CRN173 Coronary Heart Disease 8 18 0.045
251
c CRN176 Coronary Heart Disease 9 18 0.045
252
c MYP116 Myopathy, Distal, 5 15 0.045
253
HRT029 Heart Tumor of the Child 15 0.045
254
CGL001 Coagulation Protein Disease 14 0.045
255
c DLT001 Delta Chain Disease 13 0.045
256
c GTD003 Gatad1-Related Dilated Cardiomyopathy 10 0.045
257
CRD048 Cardiomyopathy with or Without Skeletal Myopathy 9 0.045
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