Search results for emery-dreifuss muscular dystrophy, ar

54 hits were found for emery-dreifuss muscular dystrophy, ar

# Family MCID Name MIFTS Score
1
c EMR020 Emery-Dreifuss Muscular Dystrophy 3, Autosomal Recessive 25 14.838
2
P MSC005 Muscular Dystrophy 66 2.904
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 53 2.214
4
c EMR017 Emery-Dreifuss Muscular Dystrophy 1, X-Linked 29 0.904
5
P EMR004 Emery-Dreifuss Muscular Dystrophy, X-Linked 29 0.899
6
c EMR018 Emery-Dreifuss Muscular Dystrophy 2, Autosomal Dominant 43 0.845
7
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 32 0.769
8
P LMB006 Limb-Girdle Muscular Dystrophy 55 0.738
9
P MYP004 Myopathy 69 0.717
10
P MYT002 Myotonic Dystrophy 50 0.542
11
MSC165 Muscular Dystrophy, Congenital, Lmna-Related 59 0.509
12
P CRD132 Cardiac Conduction Defect 53 0.467
13
ANR038 Anorexia Nervosa 1 21 0.465
14
P DLT002 Dilated Cardiomyopathy 76 0.431
15
ALR002 Al-Raqad Syndrome 30 0.402
16
P NRV007 Nervous System Disease 75 0.396
17
c MSC112 Muscular Dystrophy, Limb-Girdle, Type 1b 40 0.389
18
NRM005 Neuromuscular Disease 60 0.383
19
P LPD010 Lipodystrophy 57 0.372
20
c MYT021 Myotonic Dystrophy 1 68 0.323
21
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.301
22
P MYS005 Myositis 63 0.285
23
ALP046 Alport Syndrome, X-Linked 74 0.277
24
TTR025 Tetraamelia Syndrome, Autosomal Recessive 40 0.272
25
HPT082 Hepatic Adenomas, Familial 52 0.256
26
P FML012 Familial Partial Lipodystrophy 53 0.253
27
c ALZ056 Alzheimer Disease 3 41 0.249
28
P CRV039 Cervicitis 49 0.249
29
P ANX007 Anauxetic Dysplasia 1 36 0.247
30
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 40 0.245
31
INC002 Inclusion Body Myositis 64 0.242
32
P PLY019 Polyneuropathy 58 0.230
33
P ATR011 Atrial Fibrillation 68 0.230
34
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.229
35
SCP012 Scapuloperoneal Myopathy, Myh7-Related 24 0.227
36
P CNT004 Centronuclear Myopathy 54 0.221
37
CLL038 Collagen Vi-Related Myopathy 15 0.220
38
P CNG001 Congenital Myasthenic Syndrome 55 0.219
39
P DYS007 Dyskeratosis Congenita 68 0.216
40
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 35 0.216
41
ATR057 Atrioventricular Block 52 0.213
42
P PLG001 Pelger-Huet Anomaly 48 0.213
43
c MSC050 Muscular Dystrophy, Congenital, 1b 45 0.210
44
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 54 0.205
45
CNG046 Congenital Fiber-Type Disproportion 48 0.179
46
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.176
47
c CRD233 Cardiomyopathy, Dilated, 1b 51 0.174
48
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 57 0.157
49
c MCL062 Mucolipidosis Ii Alpha/beta 58 0.155
50
c ATR087 Atrial Standstill 1 59 0.154
51
PCT003 Pectus Excavatum 44 0.153
52
P AXN002 Axenfeld-Rieger Syndrome 53 0.141
53
ACT049 Acute Disseminated Encephalomyelitis 52 0.140
54
LTH045 Lutheran Suppressor, X-Linked 41 0.137
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