Search results for dmd.1

114 hits were found for dmd.1

# Family MCID Name MIFTS Score
1
MSC157 Muscular Dystrophy, Duchenne Type 74 19.883
2
c CRD187 Cardiomyopathy, Dilated, 3b 46 16.457
3
MSC152 Muscular Dystrophy, Becker Type 64 6.383
4
P MSC005 Muscular Dystrophy 66 5.362
5
DMD004 Dmd-Related Dilated Cardiomyopathy 9 4.277
6
P MYP004 Myopathy 69 3.679
7
NRM005 Neuromuscular Disease 60 3.648
8
P DLT002 Dilated Cardiomyopathy 76 3.425
9
P MYC008 Myocarditis 58 3.335
10
DST004 Distal Muscular Dystrophy 38 3.335
11
GLY014 Glycerol Kinase Deficiency 47 3.036
12
P LMB006 Limb-Girdle Muscular Dystrophy 55 3.011
13
P MYS005 Myositis 63 2.983
14
WLK001 Walker-Warburg Syndrome 59 2.983
15
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 2.983
16
P CNT004 Centronuclear Myopathy 54 2.983
17
c ATS331 Autosomal Recessive Limb-Girdle Muscular Dystrophy 38 2.983
18
MSC004 Muscle Tissue Disease 39 2.828
19
ADR049 Adrenal Hypoplasia, Congenital 47 2.668
20
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 56 2.615
21
c GLY008 Glycogen Storage Disease Ii 64 2.583
22
c MSC121 Muscular Dystrophy, Limb-Girdle, Type 2a 63 2.583
23
P MLG056 Malignant Hyperthermia 60 2.583
24
RGD003 Rigid Spine Muscular Dystrophy 1 59 2.583
25
c MSC037 Muscular Dystrophy-Dystroglycanopathy , Type a, 4 57 2.583
26
P BTH005 Bethlem Myopathy 1 52 2.583
27
c MYP132 Myopathy, Congenital 51 2.583
28
CNG046 Congenital Fiber-Type Disproportion 48 2.583
29
PYL006 Pyloric Stenosis 47 2.583
30
P HYP009 Hypertrophic Pyloric Stenosis 45 2.583
31
ALN001 Aland Island Eye Disease 39 2.583
32
RDC010 Reducing Body Myopathy 28 2.583
33
DYS032 Dystrophinopathies 43 2.297
34
CHR387 Chromosome Xp21 Deletion Syndrome 35 2.179
35
c ATR087 Atrial Standstill 1 59 2.147
36
c MSC120 Muscular Dystrophy, Limb-Girdle, Type 2c 53 2.147
37
P RTN008 Retinitis Pigmentosa 81 2.109
38
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 59 2.109
39
c CRD093 Cardiomyopathy, Dilated, 1a 58 2.109
40
c MSC035 Muscular Dystrophy-Dystroglycanopathy , Type B, 5 52 2.109
41
MSC077 Muscle Eye Brain Disease 51 2.109
42
GSG001 Gas Gangrene 51 2.109
43
MSC162 Muscular Dystrophy, Congenital Merosin-Deficient, 1a 51 2.109
44
c CRD233 Cardiomyopathy, Dilated, 1b 51 2.109
45
STR081 Stormorken Syndrome 49 2.109
46
c MSC042 Muscular Dystrophy-Dystroglycanopathy , Type B, 6 49 2.109
47
c MSC050 Muscular Dystrophy, Congenital, 1b 45 2.109
48
MCL009 Mcleod Syndrome 45 2.109
49
MYP100 Myopathy, X-Linked, with Excessive Autophagy 44 2.109
50
c MSC116 Muscular Dystrophy, Limb-Girdle, Type 2f 44 2.109
51
P MYF003 Myofibrillar Myopathy 44 2.109
52
MYT011 Myotonia 41 2.109
53
PTT059 Pettigrew Syndrome 40 2.109
54
c CRD097 Cardiomyopathy, Dilated, 1d 40 2.109
55
c MYP082 Myopathy, Myofibrillar, 2 38 2.109
56
c LCL022 Localized Lipodystrophy 36 2.109
57
MCR334 Microcolon 33 2.109
58
ALT002 Aleutian Mink Disease 33 2.109
59
c MYG007 Myoglobinuria, Recurrent 32 2.109
60
CRD235 Cardioneuromyopathy with Hyaline Masses and Nemaline Rods 28 2.109
61
P OTP001 Otopalatodigital Syndrome 21 2.109
62
CYT006 Cytoplasmic Body Myopathy 20 2.109
63
EXT061 Extracardiac Rhabdomyoma 18 2.109
64
P BCK002 Beckwith-Wiedemann Syndrome 58 1.610
65
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 47 1.610
66
BRD001 Brody Myopathy 41 1.610
67
CRT045 Creatine Phosphokinase, Elevated Serum 29 1.610
68
ISL077 Isolated Hyperckemia 23 1.610
69
FML304 Familial Isolated Dilated Cardiomyopathy 36 1.540
70
XLN224 X-Linked Non-Specific Intellectual Disability 21 1.540
71
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 5 1.540
72
INT084 Intrinsic Cardiomyopathy 29 1.491
73
MSC012 Muscular Dystrophy, Duchenne and Becker Type 35 0.439
74
c MYT029 Myotonia Congenita, Autosomal Recessive 32 0.439
75
MSC033 Muscle Disorders 53 0.435
76
ATR076 Atrophic Muscular Disease 6 0.435
77
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.119
78
P BRS047 Breast Cancer 100 0.084
79
P ART022 Arthritis 77 0.084
80
P NRV007 Nervous System Disease 75 0.084
81
SKN016 Skin Disease 68 0.084
82
ISC004 Ischemia 66 0.084
83
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.084
84
SKN027 Skin Conditions 48 0.084
85
AST005 Asthma 83 0.059
86
P INF038 Influenza 77 0.059
87
P OST002 Osteoporosis 75 0.059
88
CNG034 Congestive Heart Failure 74 0.059
89
MLN008 Melanoma 72 0.059
90
P ATS364 Autism 70 0.059
91
P EPL164 Epilepsy 70 0.059
92
c HMP029 Hemophilia a 69 0.059
93
AGN016 Aging 65 0.059
94
HYP266 Hypoxia 61 0.059
95
P HMP007 Hemophilia 61 0.059
96
P CTR002 Cataract 60 0.059
97
P PLY014 Polycystic Kidney Disease 60 0.059
98
P INF032 Infertility 59 0.059
99
IMM158 Immune Suppression 57 0.059
100
WST001 West Syndrome 57 0.059
101
CNS004 Constipation 57 0.059
102
P SCL018 Scoliosis 56 0.059
103
BNF002 Bone Fracture 56 0.059
104
SPS003 Spastic Diplegia 55 0.059
105
HPT082 Hepatic Adenomas, Familial 52 0.059
106
P MYT002 Myotonic Dystrophy 50 0.059
107
ANX004 Anoxia 49 0.059
108
NRR001 Neuroretinitis 46 0.059
109
MCR037 Macroglossia 44 0.059
110
c CHR579 Chiari Malformation Type Ii 42 0.059
111
P HYP265 Hypotonia 40 0.059
112
c TRC078 Trichohepatoenteric Syndrome 2 34 0.059
113
P RNG031 Ring Chromosome Y Syndrome 29 0.059
114
P CYT020 Cytomegalic Congenital Adrenal Hypoplasia 15 0.059
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