Search results for epilepsy, juvenile myoclonic, susceptibility to

100 hits were found for epilepsy, juvenile myoclonic, susceptibility to

# Family MCID Name MIFTS Score
1
c EPL209 Epilepsy, Idiopathic Generalized 10 55 9.052
2
c EPL084 Epilepsy, Idiopathic Generalized 11 20 5.493
3
P EPL198 Epilepsy, Myoclonic Juvenile 29 5.451
4
c EPL205 Epilepsy, Idiopathic Generalized 13 17 5.051
5
c EPL086 Epilepsy, Idiopathic Generalized 9 20 4.605
6
c MYC085 Myoclonic Epilepsy, Juvenile 3 14 4.396
7
c MYC086 Myoclonic Epilepsy, Juvenile 4 17 4.097
8
c EPL093 Epilepsy, Idiopathic Generalized 7 23 2.815
9
c EPL186 Epilepsy, Juvenile Myoclonic 9 17 2.662
10
P EPL164 Epilepsy 70 1.454
11
P ENC018 Encephalopathy 58 0.446
12
TMP001 Temporal Lobe Epilepsy 54 0.372
13
NRN002 Neuronitis 43 0.364
14
FCL014 Focal Epilepsy 56 0.328
15
AGN016 Aging 65 0.323
16
P EPL140 Epilepsy, Idiopathic Generalized 58 0.321
17
MYC033 Myoclonus 40 0.314
18
c CNT035 Central Nervous System Disease 65 0.312
19
P NRV007 Nervous System Disease 75 0.310
20
P SZR006 Seizure Disorder 55 0.297
21
c BLD140 Blood Group, I System 37 0.286
22
CRB009 Cerebritis 41 0.275
23
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.260
24
P DBT009 Diabetes Mellitus 72 0.248
25
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.231
26
STT001 Status Epilepticus 60 0.225
27
P FBR031 Febrile Seizures 52 0.222
28
P ANR048 Aniridia 1 68 0.221
29
ANR038 Anorexia Nervosa 1 21 0.220
30
BLD137 Blood Group--Ahonen 17 0.218
31
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.215
32
P CHL002 Childhood Absence Epilepsy 56 0.212
33
RTN023 Retinitis 52 0.196
34
ALR002 Al-Raqad Syndrome 30 0.190
35
P MLT020 Multiple Sclerosis 85 0.185
36
ANX010 Anxiety 72 0.183
37
DMN002 Dementia 68 0.180
38
P PNC044 Pancreatitis 64 0.178
39
P ENC004 Encephalitis 66 0.176
40
P CRV039 Cervicitis 49 0.172
41
P TRM003 Tremor 54 0.171
42
P DYS154 Dystonia 61 0.163
43
P MSC003 Muscular Atrophy 55 0.163
44
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.159
45
MGR028 Migraine with or Without Aura 1 55 0.158
46
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.158
47
P MYP004 Myopathy 69 0.158
48
P SPN046 Spinal Muscular Atrophy 63 0.153
49
P NRP001 Neuropathy 63 0.152
50
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.150
51
P KDN018 Kidney Disease 69 0.147
52
HYP266 Hypoxia 61 0.146
53
P TBR001 Tuberous Sclerosis 69 0.144
54
MLR020 Malaria, Mild 23 0.138
55
P JVN007 Juvenile Absence Epilepsy 42 0.138
56
SPS057 Spasticity 41 0.135
57
HDC001 Headache 55 0.132
58
c EPL133 Epilepsy, Juvenile Absence 1 31 0.129
59
P MNN013 Meningitis 71 0.128
60
HPT082 Hepatic Adenomas, Familial 52 0.125
61
P INF032 Infertility 59 0.124
62
ALP046 Alport Syndrome, X-Linked 74 0.121
63
WST001 West Syndrome 57 0.119
64
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.115
65
P GRV001 Graves' Disease 62 0.113
66
P NPH012 Nephrotic Syndrome 60 0.104
67
c BRN108 Branchiootic Syndrome 1 47 0.103
68
P MCR010 Microcephaly 57 0.098
69
ACR006 Aceruloplasminemia 65 0.096
70
BLD163 Blood Group, Dombrock System 23 0.092
71
P ANG001 Angelman Syndrome 61 0.089
72
PRP016 Paraplegia 53 0.089
73
P RTN008 Retinitis Pigmentosa 81 0.088
74
P PRS038 Personality Disorder 65 0.088
75
c PNS012 Paine Syndrome 52 0.084
76
CRD119 Cardiac Arrest 63 0.083
77
P PRP029 Porphyria 62 0.082
78
P HMP006 Hemiplegic Migraine 49 0.081
79
P HYP061 Hypertrophic Cardiomyopathy 65 0.078
80
P LPD010 Lipodystrophy 57 0.077
81
MVM001 Movement Disease 40 0.073
82
INS001 Insulinoma 66 0.072
83
LGH007 Leigh Syndrome 68 0.072
84
c EPL098 Epilepsy, Idiopathic Generalized 12 18 0.069
85
c LBR014 Leber Congenital Amaurosis 4 48 0.069
86
MLT157 Multiple System Atrophy 1 65 0.069
87
P ALC004 Alcohol Abuse 63 0.069
88
c EPL165 Epilepsy, Idiopathic Generalized 14 18 0.069
89
P MTC133 Mitochondrial Myopathy 53 0.068
90
c ESS001 Essential Tremor 58 0.068
91
P NGH001 Night Blindness 51 0.065
92
P PHT010 Photoparoxysmal Response 1 31 0.064
93
SPN331 Spondyloocular Syndrome 34 0.061
94
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.059
95
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.057
96
FBR012 Fabry Disease 72 0.056
97
PRP083 Porphyria, Acute Intermittent 60 0.056
98
CRV043 Cervical Dystonia 45 0.050
99
MHR001 Mohr-Tranebjaerg Syndrome 39 0.049
100
DMN031 Dementia, Lewy Body 66 0.047
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