Search results for epilepsy, juvenile myoclonic, susceptibility to, 5

87 hits were found for epilepsy, juvenile myoclonic, susceptibility to, 5

# Family MCID Name MIFTS Score
1
c EPL209 Epilepsy, Idiopathic Generalized 10 55 9.234
2
c EPL205 Epilepsy, Idiopathic Generalized 13 17 5.379
3
P EPL164 Epilepsy 70 1.353
4
P ENC018 Encephalopathy 58 0.438
5
NRN002 Neuronitis 43 0.381
6
AGN016 Aging 65 0.354
7
TMP001 Temporal Lobe Epilepsy 54 0.350
8
c BLD140 Blood Group, I System 37 0.317
9
P NRV007 Nervous System Disease 75 0.314
10
c CNT035 Central Nervous System Disease 65 0.312
11
FCL014 Focal Epilepsy 56 0.304
12
P EPL140 Epilepsy, Idiopathic Generalized 58 0.301
13
MYC033 Myoclonus 40 0.297
14
P SZR006 Seizure Disorder 55 0.281
15
CRB009 Cerebritis 41 0.279
16
P DBT009 Diabetes Mellitus 72 0.272
17
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 63 0.261
18
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.248
19
P ANR048 Aniridia 1 68 0.247
20
ANR038 Anorexia Nervosa 1 21 0.246
21
BLD137 Blood Group--Ahonen 17 0.244
22
ATX038 Ataxia and Polyneuropathy, Adult-Onset 38 0.242
23
STT001 Status Epilepticus 60 0.213
24
ALR002 Al-Raqad Syndrome 30 0.210
25
P FBR031 Febrile Seizures 52 0.210
26
RTN023 Retinitis 52 0.207
27
ANX010 Anxiety 72 0.200
28
P CHL002 Childhood Absence Epilepsy 56 0.198
29
P PNC044 Pancreatitis 64 0.194
30
P MLT020 Multiple Sclerosis 85 0.190
31
DMN002 Dementia 68 0.189
32
P ENC004 Encephalitis 66 0.186
33
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.182
34
P CRV039 Cervicitis 49 0.182
35
P NRP001 Neuropathy 63 0.174
36
P MYP004 Myopathy 69 0.171
37
P TRM003 Tremor 54 0.170
38
P KDN018 Kidney Disease 69 0.170
39
P DYS154 Dystonia 61 0.165
40
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 37 0.165
41
P MSC003 Muscular Atrophy 55 0.162
42
HYP266 Hypoxia 61 0.160
43
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.158
44
MGR028 Migraine with or Without Aura 1 55 0.157
45
P SPN046 Spinal Muscular Atrophy 63 0.151
46
HPT082 Hepatic Adenomas, Familial 52 0.148
47
SPS057 Spasticity 41 0.147
48
ALP046 Alport Syndrome, X-Linked 74 0.144
49
HDC001 Headache 55 0.141
50
P TBR001 Tuberous Sclerosis 69 0.141
51
P MNN013 Meningitis 71 0.136
52
P INF032 Infertility 59 0.134
53
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 40 0.120
54
P GRV001 Graves' Disease 62 0.114
55
c EPL086 Epilepsy, Idiopathic Generalized 9 20 0.113
56
c BRN108 Branchiootic Syndrome 1 47 0.110
57
P MCR010 Microcephaly 57 0.105
58
P NPH012 Nephrotic Syndrome 60 0.105
59
BLD163 Blood Group, Dombrock System 23 0.102
60
ACR006 Aceruloplasminemia 65 0.101
61
PRP016 Paraplegia 53 0.096
62
P RTN008 Retinitis Pigmentosa 81 0.094
63
c PNS012 Paine Syndrome 52 0.089
64
CRD119 Cardiac Arrest 63 0.089
65
P PRS038 Personality Disorder 65 0.089
66
P ANG001 Angelman Syndrome 61 0.087
67
MVM001 Movement Disease 40 0.083
68
P HYP061 Hypertrophic Cardiomyopathy 65 0.082
69
P PRP029 Porphyria 62 0.082
70
P HMP006 Hemiplegic Migraine 49 0.080
71
INS001 Insulinoma 66 0.078
72
P LPD010 Lipodystrophy 57 0.077
73
MLT157 Multiple System Atrophy 1 65 0.076
74
LGH007 Leigh Syndrome 68 0.073
75
c LBR014 Leber Congenital Amaurosis 4 48 0.073
76
P MTC133 Mitochondrial Myopathy 53 0.069
77
c ESS001 Essential Tremor 58 0.069
78
P ALC004 Alcohol Abuse 63 0.067
79
P NGH001 Night Blindness 51 0.066
80
P PHT010 Photoparoxysmal Response 1 31 0.063
81
SPN331 Spondyloocular Syndrome 34 0.062
82
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 54 0.060
83
UND005 Undifferentiated Pleomorphic Sarcoma 59 0.059
84
FBR012 Fabry Disease 72 0.059
85
PRP083 Porphyria, Acute Intermittent 60 0.059
86
DMN031 Dementia, Lewy Body 66 0.050
87
CRV043 Cervical Dystonia 45 0.050
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