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"

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

# Family MCID Name MIFTS Score
1
c EMR012 Emery-Dreifuss Muscular Dystrophy 3, Ar 21 12.209
2
P MSC005 Muscular Dystrophy 64 2.422
3
P EMR001 Emery-Dreifuss Muscular Dystrophy 57 1.906
4
P CRD011 Cardiomyopathy 66 0.730
5
P MYP004 Myopathy 67 0.687
6
P LMB006 Limb-Girdle Muscular Dystrophy 54 0.566
7
P CRD132 Cardiac Conduction Defect 35 0.454
8
P NRV007 Nervous System Disease 71 0.438
9
NRM005 Neuromuscular Disease 56 0.403
10
c DLT002 Dilated Cardiomyopathy 75 0.366
11
ALR002 Al-Raqad Syndrome 36 0.354
12
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 41 0.339
13
P LKM002 Leukemia 70 0.337
14
END072 Endotheliitis 41 0.334
15
MSC004 Muscle Tissue Disease 35 0.334
16
PRX075 Proximal Myopathy and Ophthalmoplegia 33 0.333
17
P LPD010 Lipodystrophy 51 0.317
18
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.314
19
ACT049 Acute Disseminated Encephalomyelitis 50 0.286
20
P ALZ034 Alzheimer Disease 92 0.262
21
P MYS005 Myositis 57 0.259
22
INC002 Inclusion Body Myositis 64 0.240
23
P ATR011 Atrial Fibrillation 63 0.235
24
P MYL006 Myeloid Leukemia 67 0.235
25
P PLY019 Polyneuropathy 53 0.234
26
HPT074 Hepatic Adenoma, Somatic 35 0.227
27
P THY032 Thyroiditis 57 0.227
28
MYL009 Myelodysplastic Syndrome 73 0.224
29
SDD007 Sudden Cardiac Death 46 0.223
30
CLP001 Calpainopathy 39 0.222
31
CLL038 Collagen Vi-Related Myopathy 15 0.219
32
P DYS007 Dyskeratosis Congenita 64 0.219
33
SCP008 Scapuloperoneal Syndrome, Myopathic Type 31 0.218
34
INT277 Intellectual Disability-Developmental Delay-Contractures Syndrome 17 0.218
35
HYP266 Hypoxia 55 0.218
36
MLN008 Melanoma 61 0.214
37
P SRC016 Sarcoglycanopathies 34 0.214
38
P CNG001 Congenital Myasthenic Syndrome 52 0.212
39
SCP009 Scapuloperoneal Myopathy, X-Linked Dominant 30 0.209
40
MSC051 Muscular Dystrophy, Rigid Spine, 1 44 0.206
41
P BTH005 Bethlem Myopathy 1 44 0.206
42
MLL018 Miller-Dieker Lissencephaly Syndrome 47 0.202
43
ADN018 Adenoma 59 0.198
44
ORL011 Oral Cancer 53 0.197
45
ATR060 Atrial Standstill, Digenic 51 0.194
46
DFF027 Diffuse Lymphatic Malformation 28 0.192
47
CRN244 Corneal Dystrophy, Schnyder Type 36 0.191
48
P CNG046 Congenital Fiber-Type Disproportion 49 0.186
49
P ORL007 Oral Cavity Cancer 58 0.186
50
ECT006 Ectodermal Dysplasia 46 0.183
51
PRG004 Progeria 54 0.181
52
LPM004 Lipoma 59 0.180
53
OST085 Osteosarcoma, Somatic 63 0.180
54
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 55 0.177
55
P LRY044 Larynx Cancer 48 0.175
56
P PLG001 Pelger-Huet Anomaly 46 0.175
57
MN1001 Mn1 28 0.175
58
ENH001 Enhanced S-Cone Syndrome 44 0.174
59
LKP003 Leukoplakia 44 0.173
60
c HPT015 Hepatitis D 51 0.172
61
ORL012 Oral Leukoplakia 41 0.172
62
SNL007 Senile Cataract 37 0.171
63
MTG002 Mutagen Sensitivity 35 0.170
64
SPR101 Superior Semicircular Canal Dehiscence Syndrome 23 0.170
65
ORC001 Orchitis 35 0.169
66
TTH002 Tooth Agenesis 54 0.169
67
P RPP002 Rippling Muscle Disease 42 0.169
68
MLT001 Multiple Chemical Sensitivity 43 0.168
69
ECT078 Ectodermal Dysplasia 2, Clouston Type 46 0.167
70
DRG002 Drug-Induced Hepatitis 39 0.167
71
OLG001 Oligospermia 39 0.167
72
ALC005 Alcoholic Pancreatitis 35 0.167
73
CLP006 Clopidogrel Resistance 39 0.166
74
TXC020 Toxic Oil Syndrome 38 0.165
75
P ECT062 Ectodermal Dysplasia 10b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 55 0.164
76
ECT061 Ectodermal Dysplasia 10a, Hypohidrotic/hair/nail Type, Autosomal Dominant 37 0.164
77
c ECT058 Ectodermal Dysplasia 11b, Hypohidrotic/hair/tooth Type, Autosomal Recessive 30 0.164
78
c ECT072 Ectodermal Dysplasia 11a, Hypohidrotic/hair/tooth Type, Autosomal Dominant 30 0.164
79
ORL004 Oral Submucous Fibrosis 52 0.164
80
AND001 Anodontia 40 0.164
81
ASB001 Asbestosis 42 0.164
82
c HYP206 Hypohidrotic Ectodermal Dysplasia Autosomal Recessive 26 0.164