112 hits were found for 'DMD'

# Family MCID Name MIFTS Score
1
DCH001 Duchenne Muscular Dystrophy 78 13.897
2
DMD003 Dmd-Associated Dilated Cardiomyopathy 21 13.710
3
c DMD004 Dmd-Related Dilated Cardiomyopathy 10 9.872
4
c MSC005 Muscular Dystrophy 62 5.179
5
BCK001 Becker Muscular Dystrophy 69 4.914
6
P DLT002 Dilated Cardiomyopathy 82 3.448
7
DYS032 Dystrophinopathies 47 3.410
8
MSC011 Muscular Dystrophy, Duchenne and Becker Types 24 3.344
9
BRT005 Barth Syndrome 62 2.759
10
P MYP004 Myopathy 58 2.759
11
MCL009 Mcleod Syndrome 30 2.759
12
c SRC016 Sarcoglycanopathies 28 2.759
13
P CNG030 Congenital Muscular Dystrophy 72 2.730
14
P CNT004 Centronuclear Myopathy 65 2.730
15
NRN002 Neuronitis 64 2.730
16
DNN001 Danon Disease 57 2.730
17
P MYC008 Myocarditis 56 2.730
18
SPN186 Spinal Cord Injury 52 2.730
19
BTH001 Bethlem Myopathy 51 2.730
20
c FKY001 Fukuyama Congenital Muscular Dystrophy 40 2.730
21
FCL041 Focal Myositis 40 2.730
22
ALN001 Aland Island Eye Disease 36 2.730
23
DST004 Distal Muscular Dystrophy 34 2.730
24
VCL001 Vacuolar Myopathy 30 2.730
25
MYT011 Myotonia 29 2.730
26
c RTN058 Retinitis Pigmentosa 3 28 2.730
27
CYT006 Cytoplasmic Body Myopathy 22 2.730
28
CMP037 Complex Glycerol Kinase Deficiency 17 2.730
29
P MLN008 Melanoma 65 2.397
30
P INT063 Intellectual Disability 51 2.397
31
P RTN008 Retinitis Pigmentosa 81 2.365
32
P MYS003 Myasthenia Gravis 79 2.365
33
P LKM002 Leukemia 79 2.365
34
P AST007 Astrocytoma 72 2.365
35
P DRM010 Dermatomyositis 70 2.365
36
MYS005 Myositis 67 2.365
37
PRT014 Protein S Deficiency 66 2.365
38
ISC004 Ischemia 64 2.365
39
RTN023 Retinitis 61 2.365
40
NRP001 Neuropathy 61 2.365
41
P HYP040 Hypospadias 59 2.365
42
NRM005 Neuromuscular Disease 55 2.365
43
c MYT002 Myotonic Dystrophy 54 2.365
44
RHB003 Rhabdomyosarcoma 54 2.365
45
PLY041 Polymyositis 54 2.365
46
c CTR002 Cataract 53 2.365
47
P MSC003 Muscular Atrophy 52 2.365
48
MNT147 Mental Retardation 35 2.365
49
MSC077 Muscle Eye Brain Disease 38 2.210
50
c NNN003 Noonan Syndrome 77 2.001
51
WLK001 Walker-Warburg Syndrome 48 2.001
52
c LMB006 Limb-Girdle Muscular Dystrophy 57 1.969
53
CYS001 Cystic Fibrosis 103 1.931
54
P AMY001 Amyotrophic Lateral Sclerosis 100 1.931
55
P SCH015 Schizophrenia 77 1.931
56
P TRN020 Turner Syndrome 77 1.931
57
ADD001 Addison's Disease 75 1.931
58
P PRM006 Primary Biliary Cirrhosis 74 1.931
59
P CLC005 Celiac Disease 73 1.931
60
c HYP086 Hypothyroidism 68 1.931
61
GSG001 Gas Gangrene 66 1.931
62
MLG056 Malignant Hyperthermia 65 1.931
63
PPL022 Papilloma 64 1.931
64
CRB037 Cerebral Palsy 64 1.931
65
c CHR090 Chronic Lymphocytic Leukemia 63 1.931
66
c SPN046 Spinal Muscular Atrophy 63 1.931
67
BRN029 Brain Disease 62 1.931
68
c HYP061 Hypertrophic Cardiomyopathy 61 1.931
69
EYD002 Eye Disease 60 1.931
70
P GLC007 Glaucoma 58 1.931
71
CRB009 Cerebritis 56 1.931
72
c LTR001 Lateral Sclerosis 55 1.931
73
c GLY013 Glycogen Storage Disease 55 1.931
74
P EMB005 Embryonal Rhabdomyosarcoma 55 1.931
75
P BCL009 B-Cell Chronic Lymphocytic Leukemia 54 1.931
76
c WRD001 Waardenburg's Syndrome 53 1.931
77
P FCS001 Facioscapulohumeral Muscular Dystrophy 47 1.931
78
c MYF003 Myofibrillar Myopathy 47 1.931
79
END072 Endotheliitis 47 1.931
80
ANL017 Anal Squamous Cell Carcinoma 46 1.931
81
HYP266 Hypoxia 43 1.931
82
c MYP011 Myopathy Congenital 42 1.931
83
c BLN003 Blindness 37 1.931
84
c FML058 Familial Dilated Cardiomyopathy 35 1.931
85
HYP265 Hypotonia 30 1.931
86
WSR001 Was-Related Disorders 28 1.931
87
RGD001 Rigid Spine Syndrome 21 1.931
88
MYG003 Myoglobinuria Recurrent 21 1.931
89
CNG034 Congestive Heart Failure 81 1.514
90
P MLT019 Multiple Myeloma 89 1.365
91
P BPL003 Bipolar Disorder 80 1.365
92
P CLR023 Colorectal Cancer 73 1.365
93
P MLR004 Malaria 73 1.365
94
SRC014 Sarcoma 63 1.365
95
SQM006 Squamous Cell Carcinoma 61 1.365
96
c MYL007 Myeloma 59 1.365
97
P CRV039 Cervicitis 52 1.365
98
c CRD092 Cardiomyopathy, Dilated, 1w 45 1.365
99
P BRS089 Breast and Colorectal Cancer 22 1.365
100
SYM016 Symptomatic Form of Muscular Dystrophy of Duchenne and Becker in Female Carriers 6 1.365
101
SDD005 Sudden Cardiac Death Multi-Gene Panels 21 0.300
102
THR013 Thoracic Outlet Syndrome 54 0.104
103
ACN002 Acanthosis Nigricans 73 0.085
104
c MNS010 Monosomy Xp21 20 0.085
105
P CNG026 Congenital Heart Defect 73 0.060
106
c HMP007 Hemophilia 68 0.060
107
WST001 West Syndrome 64 0.060
108
P ATX010 Ataxia Neuropathy Spectrum 44 0.060
109
SYN053 Syndromic Diarrhea 42 0.060
110
HYP149 Hyperglycerolemia 41 0.060
111
FSC006 Fascioscapulohumeral Muscular Dystrophy 2, Digenic 29 0.060
112
ADR026 Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism 24 0.060