Search results for "emery-dreifuss muscular dystrophy, ar"

The MalaCard for "emery-dreifuss muscular dystrophy, ar" has been retired.
Searching MalaCards for entries containing "emery-dreifuss muscular dystrophy, ar"

77 hits were found for 'emery-dreifuss muscular dystrophy, ar'

# Family MCID Name MIFTS Score
1
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 21 13.828
2
P MSC005 Muscular Dystrophy 64 2.406
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 1.878
4
P CRD011 Cardiomyopathy 67 0.649
5
P MYP004 Myopathy 67 0.579
6
P LMB006 Limb-Girdle Muscular Dystrophy 50 0.539
7
c DLT002 Dilated Cardiomyopathy 75 0.344
8
P CRD132 Cardiac Conduction Defect 40 0.339
9
P NRV007 Nervous System Disease 71 0.326
10
c HRT021 Heart Block, Progressive, Type Ia 47 0.310
11
NRM005 Neuromuscular Disease 57 0.304
12
P LPD010 Lipodystrophy 52 0.296
13
MSC004 Muscle Tissue Disease 36 0.286
14
ALR002 Al-Raqad Syndrome 36 0.259
15
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 34 0.244
16
P MYS005 Myositis 56 0.227
17
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.225
18
PRX075 Proximal Myopathy and Ophthalmoplegia 43 0.220
19
c ATS330 Autosomal Recessive Limb-Girdle Muscular Dystrophy 43 0.211
20
INC002 Inclusion Body Myositis 63 0.210
21
ACT049 Acute Disseminated Encephalomyelitis 49 0.208
22
ATR060 Atrial Standstill, Digenic 53 0.200
23
P ATR011 Atrial Fibrillation 64 0.199
24
P ALZ034 Alzheimer Disease 93 0.196
25
P PLY019 Polyneuropathy 54 0.195
26
HPT074 Hepatic Adenoma, Somatic 51 0.192
27
SDD007 Sudden Cardiac Death 46 0.187
28
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 54 0.187
29
SCP008 Scapuloperoneal Syndrome, Myopathic Type 29 0.185
30
P DYS007 Dyskeratosis Congenita 63 0.184
31
TTR016 Tetra-Amelia Syndrome 36 0.184
32
CLL038 Collagen Vi-Related Myopathy 16 0.182
33
ATR057 Atrioventricular Block 49 0.180
34
c MSC121 Muscular Dystrophy, Limb-Girdle, Type 2a 51 0.179
35
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 29 0.177
36
AND005 Androgen Insensitivity Syndrome, Mild 16 0.176
37
P CNG001 Congenital Myasthenic Syndrome 53 0.175
38
c MSC113 Muscular Dystrophy, Limb-Girdle, Type 2b 54 0.174
39
c MSC119 Muscular Dystrophy, Limb-Girdle, Type 2h 40 0.170
40
SRC016 Sarcoglycanopathies 34 0.165
41
P MYS033 Miyoshi Muscular Dystrophy 1 42 0.163
42
MSC051 Muscular Dystrophy, Rigid Spine, 1 43 0.158
43
P BTH005 Bethlem Myopathy 1 46 0.152
44
MLL018 Miller-Dieker Lissencephaly Syndrome 45 0.148
45
P ORL007 Oral Cavity Cancer 58 0.139
46
P CNG046 Congenital Fiber-Type Disproportion 48 0.137
47
ECT006 Ectodermal Dysplasia 47 0.136
48
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.131
49
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.131
50
GLB001 Gilbert Syndrome 61 0.130
51
NTR003 Natural Killer Cell Leukemia 47 0.130
52
P PLG001 Pelger-Huet Anomaly 45 0.129
53
P LRY044 Larynx Cancer 59 0.129
54
P RPP002 Rippling Muscle Disease 41 0.129
55
ENH001 Enhanced S-Cone Syndrome 45 0.128
56
c HPT015 Hepatitis D 52 0.127
57
LKP003 Leukoplakia 41 0.126
58
ORC001 Orchitis 34 0.124
59
ALC009 Alcoholic Liver Cirrhosis 48 0.124
60
SNL007 Senile Cataract 38 0.124
61
MLT001 Multiple Chemical Sensitivity 43 0.123
62
TTH002 Tooth Agenesis 55 0.123
63
MTG002 Mutagen Sensitivity 36 0.123
64
ECT078 Ectodermal Dysplasia 2, Clouston Type 45 0.122
65
ALC005 Alcoholic Pancreatitis 36 0.122
66
OLG001 Oligospermia 39 0.122
67
CLP006 Clopidogrel Resistance 39 0.121
68
ASB001 Asbestosis 42 0.121
69
TXC020 Toxic Oil Syndrome 39 0.120
70
ECT070 Ectodermal Dysplasia 1, Hypohidrotic, X-Linked 38 0.120
71
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 58 0.118
72
ORL004 Oral Submucous Fibrosis 51 0.118
73
DRG002 Drug-Induced Hepatitis 39 0.118
74
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 36 0.118
75
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 30 0.118
76
c ECT072 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant 29 0.118
77
c HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 25 0.118