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

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

# Family MCID Name MIFTS Score
1
c EPL100 Epilepsy, Generalized, with Febrile Seizures Plus, Type 5 47 7.956
2
c EPL094 Epilepsy, Juvenile Myoclonic 5 23 4.969
3
P EPL164 Epilepsy 66 1.068
4
NRN002 Neuronitis 41 0.340
5
P ENC018 Encephalopathy 59 0.328
6
TMP001 Temporal Lobe Epilepsy 50 0.263
7
P IDP010 Idiopathic Generalized Epilepsy 61 0.251
8
FCL014 Focal Epilepsy 55 0.243
9
CRB009 Cerebritis 39 0.239
10
MYC033 Myoclonus 42 0.236
11
P SZR006 Seizure Disorder 56 0.216
12
P NRV007 Nervous System Disease 71 0.215
13
c CNT035 Central Nervous System Disease 60 0.211
14
P CLR023 Colorectal Cancer 97 0.208
15
ALR002 Al-Raqad Syndrome 36 0.205
16
P ATX004 Ataxia 53 0.203
17
RTN023 Retinitis 50 0.182
18
GST053 Gastric Cancer 78 0.177
19
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.176
20
P PNC044 Pancreatitis 61 0.175
21
P HPT023 Hepatocellular Carcinoma 92 0.175
22
STT001 Status Epilepticus 59 0.170
23
P FBR031 Febrile Seizures 53 0.169
24
P MYP004 Myopathy 67 0.167
25
SQM006 Squamous Cell Carcinoma 70 0.166
26
P ADN016 Adenocarcinoma 69 0.164
27
P CHL002 Childhood Absence Epilepsy 55 0.163
28
DMN002 Dementia 65 0.163
29
P ENC004 Encephalitis 63 0.157
30
P GLM045 Glioma 60 0.156
31
P CRD011 Cardiomyopathy 68 0.147
32
P NRP001 Neuropathy 59 0.147
33
HYP266 Hypoxia 56 0.147
34
P KDN018 Kidney Disease 66 0.144
35
P MSC003 Muscular Atrophy 50 0.143
36
AND005 Androgen Insensitivity Syndrome, Mild 16 0.142
37
P DYS154 Dystonia 65 0.138
38
P INT063 Intellectual Disability 49 0.136
39
P AST007 Astrocytoma 65 0.132
40
P TRM003 Tremor 54 0.131
41
P SPN046 Spinal Muscular Atrophy 65 0.130
42
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.126
43
LRN003 Learning Disability 49 0.126
44
ORL011 Oral Cancer 56 0.125
45
SPS057 Spasticity 42 0.124
46
DSS008 Disease of Mental Health 52 0.123
47
P LTR001 Lateral Sclerosis 53 0.121
48
c PND001 Pain Disorder 54 0.117
49
P INF032 Infertility 59 0.117
50
HDC001 Headache 54 0.115
51
HPT074 Hepatic Adenoma, Somatic 50 0.114
52
P TBR001 Tuberous Sclerosis 67 0.112
53
HNM002 Hinman Syndrome 25 0.112
54
c CRN214 Coronary Heart Disease 5 22 0.112
55
P GLB002 Glioblastoma 68 0.110
56
WST001 West Syndrome 57 0.110
57
P GRV001 Graves' Disease 59 0.107
58
c MYC070 Myoclonic Epilepsy, Juvenile 1 24 0.104
59
P JVN007 Juvenile Absence Epilepsy 40 0.100
60
HMP009 Haemophilus Influenzae 45 0.096
61
P CRN178 Coronary Heart Disease 6 21 0.095
62
BRN028 Brain Cancer 70 0.095
63
PHY002 Physical Disorder 43 0.092
64
ORL015 Oral Squamous Cell Carcinoma 57 0.092
65
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.090
66
EXF001 Exfoliation Syndrome 57 0.090
67
P MDL005 Medulloblastoma 77 0.086
68
ADT003 Auditory System Disease 40 0.085
69
P LYM033 Lymphoproliferative Syndrome 56 0.085
70
P NPH012 Nephrotic Syndrome 59 0.084
71
P PLN008 Peeling Skin Syndrome 45 0.084
72
OCL009 Ocular Cancer 59 0.084
73
c EPL133 Epilepsy, Juvenile Absence 1 26 0.083
74
P CRB042 Cerebellar Ataxia 63 0.083
75
P MCR010 Microcephaly 58 0.080
76
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.080
77
GLB015 Glioblastoma Multiforme 63 0.079
78
DDN006 Duodenitis 42 0.078
79
PPL022 Papilloma 55 0.078
80
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.077
81
OPT006 Optic Nerve Disease 52 0.077
82
CRD119 Cardiac Arrest 61 0.076
83
P PRS038 Personality Disorder 62 0.076
84
P RTN008 Retinitis Pigmentosa 80 0.076
85
c DWL002 Dowling-Degos Disease 1 49 0.075
86
KRT009 Keratosis 52 0.074
87
SPT004 Septic Arthritis 60 0.074
88
P PRP029 Porphyria 59 0.073
89
P ANG001 Angelman Syndrome 61 0.071
90
P FNC043 Fanconi Anemia, Complementation Group E 55 0.070
91
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.069
92
SFT003 Soft Tissue Sarcoma 57 0.068
93
GLM004 Gliomatosis Cerebri 49 0.067
94
P LGH007 Leigh Syndrome 70 0.067
95
MGL001 Megaloblastic Anemia 50 0.067
96
TTR016 Tetra-Amelia Syndrome 36 0.067
97
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.066
98
P OLG002 Oligodendroglioma 56 0.066
99
INS001 Insulinoma 61 0.066
100
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.066
101
NRN005 Neuronal Ceroid-Lipofuscinoses 42 0.064
102
P GST044 Gastritis 56 0.064
103
GNG004 Ganglioglioma 50 0.063
104
P TRT010 Teratoma 52 0.063
105
P CRN035 Cranial Nerve Palsy 46 0.063
106
ADP007 Adie Pupil 34 0.061
107
SLC006 Silicosis 53 0.061
108
P FML011 Familial Adenomatous Polyposis 68 0.060
109
P GCH001 Gaucher's Disease 62 0.060
110
BCT002 Bacterial Vaginosis 52 0.058
111
P NGH001 Night Blindness 48 0.057
112
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.057
113
LPT001 Leptospirosis 62 0.056
114
BRN032 Brain Glioma 48 0.056
115
P EPN002 Ependymoma 53 0.055
116
P UVL004 Uveal Melanoma 60 0.054
117
ASP003 Aseptic Meningitis 51 0.054
118
PPT005 Peptic Ulcer Disease 58 0.053
119
MCR013 Microphthalmia 60 0.052
120
ALB002 Albinism 46 0.051
121
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.051
122
BRN022 Bronchiectasis 50 0.050
123
ANG018 Angiomyolipoma 46 0.048
124
TNG003 Tongue Cancer 58 0.046
125
PLM020 Pleomorphic Xanthoastrocytoma 42 0.043
126
P PNL012 Penile Cancer 58 0.043
127
MHR001 Mohr-Tranebjaerg Syndrome 41 0.042
128
c NRV012 Nervous System Benign Neoplasm 31 0.042
129
DDN010 Duodenum Cancer 43 0.042
130
OCL001 Ocular Albinism 42 0.039
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