113 hits were found for 'DMD'

# ++ Fam MCID Name MIFTS Score
1
DCH001 Duchenne Muscular Dystrophy 70 13.887
2
DMD003 Dmd-Associated Dilated Cardiomyopathy 13 13.706
3
DMD004 Dmd-Related Dilated Cardiomyopathy 6 9.869
4
c MSC005 Muscular Dystrophy 54 5.161
5
BCK001 Becker Muscular Dystrophy 62 4.904
6
P DLT002 Dilated Cardiomyopathy 74 3.442
7
DYS032 Dystrophinopathies 44 3.338
8
MSC011 Muscular Dystrophy, Duchenne and Becker Types 19 3.338
9
BRT005 Barth Syndrome 54 2.754
10
c MYP004 Myopathy 52 2.754
11
c SRC016 Sarcoglycanopathies 30 2.754
12
c MCL009 Mcleod Syndrome 28 2.754
13
SPN186 Spinal Cord Injury 63 2.725
14
P CNG030 Congenital Muscular Dystrophy 59 2.725
15
P CNT004 Centronuclear Myopathy 55 2.725
16
DNN001 Danon Disease 51 2.725
17
P MYC008 Myocarditis 51 2.725
18
NRN002 Neuronitis 47 2.725
19
FCL041 Focal Myositis 44 2.725
20
BTH001 Bethlem Myopathy 43 2.725
21
c MYT011 Myotonia 41 2.725
22
c FKY001 Fukuyama Congenital Muscular Dystrophy 39 2.725
23
VCL001 Vacuolar Myopathy 37 2.725
24
DST004 Distal Muscular Dystrophy 32 2.725
25
ALN001 Aland Island Eye Disease 27 2.725
26
CYT006 Cytoplasmic Body Myopathy 24 2.725
27
c RTN058 Retinitis Pigmentosa 3 21 2.725
28
CMP037 Complex Glycerol Kinase Deficiency 19 2.725
29
P MLN008 Melanoma 56 2.392
30
c MNT147 Mental Retardation 51 2.392
31
INT063 Intellectual Disability 42 2.392
32
P RTN008 Retinitis Pigmentosa 76 2.360
33
P MYS003 Myasthenia Gravis 71 2.360
34
LKM002 Leukemia 70 2.360
35
P AST007 Astrocytoma 70 2.360
36
PRT014 Protein S Deficiency 67 2.360
37
MYS005 Myositis 61 2.360
38
PLY041 Polymyositis 61 2.360
39
P DRM010 Dermatomyositis 59 2.360
40
ISC004 Ischemia 57 2.360
41
P HYP040 Hypospadias 56 2.360
42
NRP001 Neuropathy 54 2.360
43
RTN023 Retinitis 53 2.360
44
P MSC003 Muscular Atrophy 51 2.360
45
c MYT002 Myotonic Dystrophy 49 2.360
46
c CTR002 Cataract 48 2.360
47
P NRM005 Neuromuscular Disease 48 2.360
48
RHB003 Rhabdomyosarcoma 48 2.360
49
MSC077 Muscle Eye Brain Disease 35 2.206
50
c NNN003 Noonan Syndrome 73 1.997
51
WLK001 Walker-Warburg Syndrome 45 1.997
52
c LMB006 Limb-Girdle Muscular Dystrophy 55 1.965
53
HYP265 Hypotonia 43 1.965
54
CYS001 Cystic Fibrosis 91 1.927
55
P AMY001 Amyotrophic Lateral Sclerosis 87 1.927
56
P TRN020 Turner Syndrome 71 1.927
57
P CLC005 Celiac Disease 71 1.927
58
P PRM006 Primary Biliary Cirrhosis 69 1.927
59
P SCH015 Schizophrenia 69 1.927
60
ADD001 Addison's Disease 68 1.927
61
MLG056 Malignant Hyperthermia 66 1.927
62
HYP266 Hypoxia 60 1.927
63
c SPN046 Spinal Muscular Atrophy 60 1.927
64
BRN029 Brain Disease 60 1.927
65
PPL022 Papilloma 60 1.927
66
c HYP061 Hypertrophic Cardiomyopathy 59 1.927
67
c HYP086 Hypothyroidism 59 1.927
68
BCL009 B-Cell Chronic Lymphocytic Leukemia 59 1.927
69
CRB037 Cerebral Palsy 58 1.927
70
CHR090 Chronic Lymphocytic Leukemia 56 1.927
71
c BLN003 Blindness 54 1.927
72
c WRD001 Waardenburg's Syndrome 54 1.927
73
GSG001 Gas Gangrene 53 1.927
74
c LTR001 Lateral Sclerosis 52 1.927
75
END072 Endotheliitis 51 1.927
76
EYD002 Eye Disease 50 1.927
77
c GLY013 Glycogen Storage Disease 49 1.927
78
P GLC007 Glaucoma 49 1.927
79
P EMB005 Embryonal Rhabdomyosarcoma 48 1.927
80
c MYP011 Myopathy Congenital 48 1.927
81
P FCS001 Facioscapulohumeral Muscular Dystrophy 46 1.927
82
CRB009 Cerebritis 46 1.927
83
ANL017 Anal Squamous Cell Carcinoma 45 1.927
84
P MYF003 Myofibrillar Myopathy 43 1.927
85
c FML058 Familial Dilated Cardiomyopathy 43 1.927
86
RGD001 Rigid Spine Syndrome 26 1.927
87
MYG003 Myoglobinuria Recurrent 23 1.927
88
WSR001 Was-Related Disorders 22 1.927
89
CNG034 Congestive Heart Failure 74 1.511
90
P BPL003 Bipolar Disorder 76 1.363
91
P MLT019 Multiple Myeloma 76 1.363
92
P CLR023 Colorectal Cancer 66 1.363
93
P MLR004 Malaria 66 1.363
94
SQM006 Squamous Cell Carcinoma 58 1.363
95
SRC014 Sarcoma 54 1.363
96
c MYL007 Myeloma 53 1.363
97
P CRV039 Cervicitis 41 1.363
98
c CRD092 Cardiomyopathy, Dilated, 1w 36 1.363
99
P NGH017 Night Blindness, Congenital Stationary , 1d, Autosomal Recessive 29 1.363
100
BRS089 Breast and Colorectal Cancer 20 1.363
101
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 3 1.363
102
SDD005 Sudden Cardiac Death Multi-Gene Panels 19 0.300
103
THR013 Thoracic Outlet Syndrome 53 0.104
104
ACN002 Acanthosis Nigricans 70 0.085
105
c MNS010 Monosomy Xp21 8 0.085
106
P CNG026 Congenital Heart Defect 65 0.060
107
c HMP007 Hemophilia 64 0.060
108
WST001 West Syndrome 64 0.060
109
MCR037 Macroglossia 49 0.060
110
HYP149 Hyperglycerolemia 38 0.060
111
c ATX010 Ataxia Neuropathy Spectrum 33 0.060
112
FSC006 Fascioscapulohumeral Muscular Dystrophy 2, Digenic 21 0.060
113
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 15 0.060