Search results for epilepsy, juvenile myoclonic, susceptibility to

112 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 7.466
2
c EPL084 Epilepsy, Idiopathic Generalized 11 23 4.972
3
c EPL094 Epilepsy, Juvenile Myoclonic 5 21 4.413
4
c MYC070 Myoclonic Epilepsy, Juvenile 1 25 4.133
5
c EPL086 Epilepsy, Idiopathic Generalized 9 24 3.971
6
P EPL164 Epilepsy 65 1.174
7
P ART022 Arthritis 72 0.519
8
NRN002 Neuronitis 39 0.328
9
TMP001 Temporal Lobe Epilepsy 50 0.281
10
MYC033 Myoclonus 41 0.251
11
P NRV007 Nervous System Disease 70 0.251
12
P IDP010 Idiopathic Generalized Epilepsy 58 0.249
13
c CNT035 Central Nervous System Disease 60 0.248
14
FCL014 Focal Epilepsy 55 0.243
15
CRB009 Cerebritis 39 0.241
16
P SZR006 Seizure Disorder 54 0.223
17
P ENC018 Encephalopathy 52 0.220
18
P ATX004 Ataxia 52 0.198
19
STT001 Status Epilepticus 58 0.184
20
P FBR031 Febrile Seizures 49 0.180
21
RTN023 Retinitis 49 0.177
22
ALR002 Al-Raqad Syndrome 29 0.172
23
P CHL002 Childhood Absence Epilepsy 54 0.171
24
P PNC044 Pancreatitis 60 0.165
25
DMN002 Dementia 52 0.161
26
P HYP729 Hypersensitivity Reaction Disease 43 0.160
27
P ENC004 Encephalitis 61 0.153
28
P MYP004 Myopathy 68 0.147
29
P KDN018 Kidney Disease 65 0.146
30
AND005 Androgen Insensitivity Syndrome, Mild 16 0.146
31
P GLM045 Glioma 59 0.144
32
P MSC003 Muscular Atrophy 49 0.143
33
P DYS154 Dystonia 61 0.142
34
P INT063 Intellectual Disability 58 0.141
35
P CRD011 Cardiomyopathy 67 0.139
36
HYP266 Hypoxia 55 0.139
37
P INF037 Inflammatory Bowel Disease 62 0.137
38
P UVT001 Uveitis 57 0.136
39
P TRM003 Tremor 53 0.134
40
P SPN046 Spinal Muscular Atrophy 63 0.134
41
P NRP001 Neuropathy 57 0.133
42
PHY002 Physical Disorder 43 0.133
43
BNS002 Bone Structure Disease 36 0.127
44
P JVN007 Juvenile Absence Epilepsy 43 0.126
45
DRG001 Drug Psychosis 41 0.125
46
c PND001 Pain Disorder 55 0.120
47
HDC001 Headache 53 0.117
48
P MNN013 Meningitis 65 0.116
49
P INF032 Infertility 57 0.116
50
SPS057 Spasticity 42 0.115
51
ADL002 Adult Syndrome 57 0.115
52
P GRV001 Graves' Disease 57 0.114
53
HPT074 Hepatic Adenoma, Somatic 44 0.111
54
P SPN052 Spondyloarthropathy 59 0.110
55
P MYS003 Myasthenia Gravis 67 0.109
56
P TBR001 Tuberous Sclerosis 67 0.107
57
WST001 West Syndrome 58 0.104
58
MYL009 Myelodysplastic Syndrome 71 0.103
59
HNM002 Hinman Syndrome 27 0.100
60
MVM001 Movement Disease 52 0.093
61
MSL001 Measles 58 0.089
62
c EPL133 Epilepsy, Juvenile Absence 1 27 0.089
63
P NPH012 Nephrotic Syndrome 59 0.088
64
BRC012 Brucellosis 61 0.087
65
ATP002 Atopy 61 0.086
66
VSL002 Visual Epilepsy 33 0.083
67
P ASP006 Aspergillosis 60 0.082
68
P CRB042 Cerebellar Ataxia 69 0.082
69
EXF001 Exfoliation Syndrome 57 0.081
70
P MCR010 Microcephaly 58 0.080
71
P PRS038 Personality Disorder 61 0.079
72
P CNJ013 Conjunctivitis 63 0.078
73
PRC002 Paracoccidioidomycosis 52 0.077
74
BRN002 Bronchiolitis 52 0.076
75
CRD119 Cardiac Arrest 59 0.076
76
P TXP001 Toxoplasmosis 60 0.075
77
P ANG001 Angelman Syndrome 62 0.075
78
P PLN008 Peeling Skin Syndrome 49 0.075
79
CCC002 Coccidiosis 49 0.072
80
KHL003 Kohlschutter-Tonz Syndrome 42 0.072
81
BRN028 Brain Cancer 67 0.072
82
P PRP029 Porphyria 59 0.071
83
TNS005 Tonsillitis 56 0.071
84
P ALC004 Alcohol Abuse 57 0.069
85
P OLG002 Oligodendroglioma 55 0.069
86
P RTN008 Retinitis Pigmentosa 80 0.067
87
c EPL098 Epilepsy, Idiopathic Generalized 12 24 0.067
88
P LGH007 Leigh Syndrome 69 0.066
89
P LCH002 Lichen Planus 52 0.064
90
MGL001 Megaloblastic Anemia 49 0.064
91
UND005 Undifferentiated Pleomorphic Sarcoma 44 0.063
92
ADP007 Adie Pupil 35 0.063
93
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 39 0.061
94
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 48 0.060
95
P LYM033 Lymphoproliferative Syndrome 54 0.060
96
INS001 Insulinoma 60 0.060
97
P ACT135 Acute Graft Versus Host Disease 52 0.060
98
NRT004 Neuritis 51 0.059
99
DFC004 Deficiency Anemia 60 0.056
100
KRT006 Keratoconjunctivitis 52 0.056
101
c ATM006 Autoimmune Lymphoproliferative Syndrome 72 0.055
102
c EPL165 Epilepsy, Idiopathic Generalized 14 18 0.055
103
CYS008 Cystic Echinococcosis 44 0.053
104
FBR012 Fabry Disease 71 0.052
105
GNG012 Gingival Overgrowth 51 0.048
106
CRV043 Cervical Dystonia 43 0.047
107
MHR001 Mohr-Tranebjaerg Syndrome 43 0.046
108
MLT077 Multiple Sclerosis, Disease Progression, Modifier of 73 0.045
109
c EPL093 Epilepsy, Idiopathic Generalized 7 15 0.044
110
KRN002 Kearns-Sayre Syndrome 57 0.042
111
PDT025 Pediatric Multiple Sclerosis 37 0.040
112
c PRK020 Parkinson Disease 6, Early Onset 41 0.036
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