Search results for epilepsy, juvenile myoclonic, susceptibility to

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

# Family MCID Name MIFTS Score
1
c EPL100 Epilepsy, Generalized, with Febrile Seizures Plus, Type 5 47 7.724
2
c EPL084 Epilepsy, Idiopathic Generalized 11 22 5.091
3
c EPL094 Epilepsy, Juvenile Myoclonic 5 23 4.694
4
c MYC070 Myoclonic Epilepsy, Juvenile 1 24 4.146
5
c EPL086 Epilepsy, Idiopathic Generalized 9 24 4.120
6
P EPL164 Epilepsy 66 1.146
7
P ENC018 Encephalopathy 59 0.337
8
NRN002 Neuronitis 41 0.326
9
TMP001 Temporal Lobe Epilepsy 50 0.277
10
P IDP010 Idiopathic Generalized Epilepsy 61 0.264
11
FCL014 Focal Epilepsy 55 0.258
12
MYC033 Myoclonus 42 0.247
13
CRB009 Cerebritis 39 0.236
14
P SZR006 Seizure Disorder 56 0.227
15
c CNT035 Central Nervous System Disease 60 0.218
16
P NRV007 Nervous System Disease 71 0.215
17
P CLR023 Colorectal Cancer 97 0.195
18
P ATX004 Ataxia 53 0.193
19
ALR002 Al-Raqad Syndrome 36 0.191
20
STT001 Status Epilepticus 59 0.177
21
P FBR031 Febrile Seizures 53 0.175
22
RTN023 Retinitis 50 0.172
23
P CHL002 Childhood Absence Epilepsy 55 0.171
24
P PNC044 Pancreatitis 61 0.162
25
P HPT023 Hepatocellular Carcinoma 92 0.162
26
GST053 Gastric Cancer 78 0.162
27
P AXN010 Axenfeld-Rieger Syndrome, Type 3 55 0.161
28
DMN002 Dementia 65 0.160
29
P MYP004 Myopathy 67 0.159
30
SQM006 Squamous Cell Carcinoma 70 0.152
31
P ENC004 Encephalitis 63 0.149
32
P ADN016 Adenocarcinoma 69 0.148
33
P GLM045 Glioma 60 0.144
34
P MSC003 Muscular Atrophy 50 0.143
35
HYP266 Hypoxia 56 0.138
36
P CRD011 Cardiomyopathy 68 0.137
37
P DYS154 Dystonia 65 0.135
38
P AST007 Astrocytoma 65 0.134
39
P NRP001 Neuropathy 59 0.133
40
P INT063 Intellectual Disability 49 0.133
41
P SPN046 Spinal Muscular Atrophy 65 0.131
42
AND005 Androgen Insensitivity Syndrome, Mild 16 0.130
43
P TRM003 Tremor 54 0.130
44
P KDN018 Kidney Disease 66 0.129
45
LRN003 Learning Disability 49 0.129
46
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.123
47
DSS008 Disease of Mental Health 52 0.119
48
ORL011 Oral Cancer 56 0.118
49
P LTR001 Lateral Sclerosis 53 0.117
50
P TBR001 Tuberous Sclerosis 67 0.115
51
P INF032 Infertility 59 0.114
52
SPS057 Spasticity 42 0.114
53
HDC001 Headache 54 0.114
54
c PND001 Pain Disorder 54 0.111
55
WST001 West Syndrome 57 0.110
56
P GRV001 Graves' Disease 59 0.105
57
P GLB002 Glioblastoma 68 0.103
58
P JVN007 Juvenile Absence Epilepsy 40 0.103
59
HPT074 Hepatic Adenoma, Somatic 50 0.094
60
BRN028 Brain Cancer 70 0.094
61
c CRN214 Coronary Heart Disease 5 22 0.093
62
HNM002 Hinman Syndrome 25 0.091
63
HMP009 Haemophilus Influenzae 45 0.089
64
PHY002 Physical Disorder 43 0.089
65
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 41 0.088
66
EXF001 Exfoliation Syndrome 57 0.087
67
ORL015 Oral Squamous Cell Carcinoma 57 0.087
68
c EPL133 Epilepsy, Juvenile Absence 1 26 0.087
69
P CRN178 Coronary Heart Disease 6 21 0.087
70
P NPH012 Nephrotic Syndrome 59 0.086
71
P MDL005 Medulloblastoma 77 0.084
72
OCL009 Ocular Cancer 59 0.082
73
ADT003 Auditory System Disease 40 0.080
74
P PLN008 Peeling Skin Syndrome 45 0.080
75
P LYM033 Lymphoproliferative Syndrome 56 0.080
76
P CRB042 Cerebellar Ataxia 63 0.080
77
PPL022 Papilloma 55 0.079
78
GLB015 Glioblastoma Multiforme 63 0.078
79
HYP711 Hypotonia, Ataxia, and Delayed Development Syndrome 26 0.077
80
P MCR010 Microcephaly 58 0.077
81
DDN006 Duodenitis 42 0.076
82
CRD119 Cardiac Arrest 61 0.076
83
P PRS038 Personality Disorder 62 0.076
84
OPT006 Optic Nerve Disease 52 0.076
85
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 43 0.075
86
SPT004 Septic Arthritis 60 0.074
87
P ANG001 Angelman Syndrome 61 0.073
88
c DWL002 Dowling-Degos Disease 1 49 0.072
89
P RTN008 Retinitis Pigmentosa 80 0.072
90
P PRP029 Porphyria 59 0.071
91
P FNC043 Fanconi Anemia, Complementation Group E 55 0.068
92
P OLG002 Oligodendroglioma 56 0.068
93
P LGH007 Leigh Syndrome 70 0.067
94
NRN005 Neuronal Ceroid-Lipofuscinoses 42 0.066
95
GLM004 Gliomatosis Cerebri 49 0.066
96
MGL001 Megaloblastic Anemia 50 0.065
97
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.065
98
P GST044 Gastritis 56 0.064
99
SFT003 Soft Tissue Sarcoma 57 0.064
100
GNG004 Ganglioglioma 50 0.063
101
SLC006 Silicosis 53 0.062
102
P CRN035 Cranial Nerve Palsy 46 0.062
103
P GCH001 Gaucher's Disease 62 0.062
104
P TRT010 Teratoma 52 0.061
105
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 34 0.061
106
SQM013 Squamous Cell Carcinoma, Head and Neck 70 0.060
107
c INV001 Invasive Aspergillosis 47 0.060
108
INS001 Insulinoma 61 0.060
109
P NGH001 Night Blindness 48 0.057
110
KRT009 Keratosis 52 0.056
111
P EPN002 Ependymoma 53 0.056
112
BCT002 Bacterial Vaginosis 52 0.055
113
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.055
114
TTR016 Tetra-Amelia Syndrome 36 0.054
115
P FML011 Familial Adenomatous Polyposis 68 0.054
116
BRN032 Brain Glioma 48 0.054
117
LPT001 Leptospirosis 62 0.053
118
PPT005 Peptic Ulcer Disease 58 0.052
119
ASP003 Aseptic Meningitis 51 0.052
120
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.052
121
ADP007 Adie Pupil 34 0.051
122
BRN022 Bronchiectasis 50 0.051
123
EPL101 Epilepsy, Idiopathic Generalized, Suscpetibility to, 12 18 0.050
124
P UVL004 Uveal Melanoma 60 0.050
125
P LRY044 Larynx Cancer 57 0.049
126
PTZ001 Peutz-Jeghers Syndrome 71 0.049
127
ALB002 Albinism 46 0.048
128
P CNT044 Central Nervous System Primitive Neuroectodermal Neoplasm 30 0.047
129
MCR013 Microphthalmia 60 0.046
130
TNG003 Tongue Cancer 58 0.046
131
ANG018 Angiomyolipoma 46 0.045
132
P PNL012 Penile Cancer 58 0.043
133
MHR001 Mohr-Tranebjaerg Syndrome 41 0.042
134
PLM020 Pleomorphic Xanthoastrocytoma 42 0.041
135
P SLD010 Sialidosis, Type I 54 0.040
136
c NRV012 Nervous System Benign Neoplasm 31 0.040
137
DDN010 Duodenum Cancer 43 0.040
138
OCL001 Ocular Albinism 42 0.038
139
GLY031 Glycoproteinosis 28 0.036
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