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

The MalaCard for "epilepsy, juvenile myoclonic, susceptibility to" has been retired.
Searching MalaCards for entries containing "epilepsy, juvenile myoclonic, susceptibility to"

180 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 7.721
2
c EPL084 Epilepsy, Idiopathic Generalized 11 23 5.103
3
c EPL094 Epilepsy, Juvenile Myoclonic 5 23 4.699
4
c MYC070 Myoclonic Epilepsy, Juvenile 1 24 4.174
5
c EPL086 Epilepsy, Idiopathic Generalized 9 24 4.125
6
P EPL164 Epilepsy 66 1.137
7
P ART022 Arthritis 75 0.508
8
P RHM011 Rheumatoid Arthritis 88 0.385
9
P ENC018 Encephalopathy 59 0.335
10
NRN002 Neuronitis 42 0.331
11
TMP001 Temporal Lobe Epilepsy 51 0.279
12
P IDP010 Idiopathic Generalized Epilepsy 61 0.264
13
FCL014 Focal Epilepsy 56 0.264
14
MYC033 Myoclonus 41 0.241
15
CRB009 Cerebritis 38 0.237
16
P LPS004 Lupus Erythematosus 63 0.233
17
P SZR006 Seizure Disorder 57 0.228
18
c SYS001 Systemic Lupus Erythematosus 87 0.227
19
c CNT035 Central Nervous System Disease 59 0.220
20
P NRV007 Nervous System Disease 71 0.213
21
PRS047 Prostatitis 56 0.193
22
HV1006 Hiv-1 82 0.190
23
P ATX004 Ataxia 53 0.189
24
ALR002 Al-Raqad Syndrome 36 0.182
25
P FBR031 Febrile Seizures 52 0.177
26
STT001 Status Epilepticus 59 0.175
27
RTN023 Retinitis 49 0.174
28
P CHL002 Childhood Absence Epilepsy 56 0.172
29
P PNC044 Pancreatitis 60 0.163
30
P MYP004 Myopathy 67 0.161
31
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.160
32
DMN002 Dementia 64 0.156
33
P PNM007 Pneumonia 66 0.151
34
P ENC004 Encephalitis 61 0.149
35
P ADN016 Adenocarcinoma 69 0.146
36
P GLM045 Glioma 58 0.142
37
P MSC003 Muscular Atrophy 51 0.140
38
P AST007 Astrocytoma 65 0.138
39
HYP266 Hypoxia 55 0.137
40
WTH001 Withdrawal Disorder 41 0.136
41
P DYS154 Dystonia 64 0.135
42
P INT063 Intellectual Disability 53 0.135
43
P NRP001 Neuropathy 60 0.134
44
P CRD011 Cardiomyopathy 67 0.133
45
LRN003 Learning Disability 51 0.128
46
P SPN046 Spinal Muscular Atrophy 63 0.128
47
P TRM003 Tremor 54 0.127
48
SXL003 Sexual Disorder 47 0.125
49
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.125
50
RSP006 Respiratory System Disease 62 0.122
51
AND005 Androgen Insensitivity Syndrome, Mild 16 0.120
52
DSS008 Disease of Mental Health 55 0.119
53
P MNN013 Meningitis 65 0.117
54
WST001 West Syndrome 61 0.117
55
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.116
56
HDC001 Headache 54 0.116
57
PRM097 Primary Immunodeficiency Disease 61 0.116
58
c PND001 Pain Disorder 55 0.115
59
P INF032 Infertility 61 0.114
60
P GRV001 Graves' Disease 61 0.113
61
GNG013 Gingivitis 60 0.112
62
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.111
63
P PNC035 Pancreatic Cancer 85 0.110
64
SPS057 Spasticity 42 0.110
65
P JVN007 Juvenile Absence Epilepsy 37 0.106
66
P SPN052 Spondyloarthropathy 60 0.105
67
MVM001 Movement Disease 54 0.103
68
P GLB002 Glioblastoma 66 0.100
69
PHY002 Physical Disorder 44 0.099
70
GST045 Gastroenteritis 60 0.098
71
c CRN214 Coronary Heart Disease 5 23 0.094
72
HPT074 Hepatic Adenoma, Somatic 51 0.093
73
FML039 Female Reproductive System Disease 48 0.092
74
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.092
75
P PRK057 Parkinson Disease, Late-Onset 72 0.090
76
HNM002 Hinman Syndrome 25 0.090
77
RCT015 Reactive Arthritis 62 0.090
78
DRG001 Drug Psychosis 40 0.089
79
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.088
80
c EPL133 Epilepsy, Juvenile Absence 1 26 0.088
81
EXF001 Exfoliation Syndrome 57 0.087
82
P CRN178 Coronary Heart Disease 6 24 0.087
83
WLL006 Wells Syndrome 56 0.085
84
P ASP006 Aspergillosis 60 0.084
85
TRM010 Traumatic Brain Injury 52 0.083
86
OCL009 Ocular Cancer 62 0.083
87
P ANG001 Angelman Syndrome 61 0.083
88
P CRB042 Cerebellar Ataxia 64 0.082
89
PRT036 Peritonitis 62 0.082
90
OST017 Osteomyelitis 59 0.082
91
KRT004 Keratitis 70 0.081
92
P PLN008 Peeling Skin Syndrome 47 0.080
93
P LYM033 Lymphoproliferative Syndrome 53 0.080
94
PPL022 Papilloma 55 0.080
95
OTT002 Otitis Media 66 0.080
96
P CNJ013 Conjunctivitis 65 0.080
97
BRC012 Brucellosis 65 0.080
98
OPT006 Optic Nerve Disease 51 0.079
99
SXD001 Sex Differentiation Disease 40 0.078
100
CYT008 Cytomegalovirus Infection 51 0.078
101
P HMN010 Hemangioma 60 0.078
102
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.078
103
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.077
104
GLB015 Glioblastoma Multiforme 62 0.077
105
MTR014 Motor Neuron Disease 59 0.077
106
DPH001 Diphtheria 58 0.077
107
ADT003 Auditory System Disease 51 0.076
108
P OVR049 Ovarian Disease 55 0.076
109
P MCR010 Microcephaly 58 0.075
110
P PRS038 Personality Disorder 61 0.075
111
P ESN007 Eosinophilia 61 0.075
112
BRN002 Bronchiolitis 56 0.075
113
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.073
114
c ANT034 Anterior Uveitis 49 0.073
115
P RTN008 Retinitis Pigmentosa 79 0.073
116
CRD119 Cardiac Arrest 63 0.073
117
P PRP029 Porphyria 58 0.072
118
P RTT002 Rett Syndrome 78 0.072
119
c INF067 Inflammatory Bowel Disease 10 51 0.071
120
P OLG002 Oligodendroglioma 55 0.069
121
NRN005 Neuronal Ceroid-Lipofuscinoses 52 0.069
122
P LGH007 Leigh Syndrome 70 0.067
123
ECH003 Echinococcosis 53 0.067
124
APH001 Aphthous Stomatitis 62 0.067
125
TNS005 Tonsillitis 58 0.067
126
P TMP003 Temporal Arteritis 60 0.066
127
ATS001 Autistic Disorder 59 0.066
128
P ACT135 Acute Graft Versus Host Disease 53 0.065
129
BCT004 Bacteriuria 47 0.065
130
P HYP265 Hypotonia 39 0.065
131
GLM004 Gliomatosis Cerebri 53 0.064
132
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.064
133
KHL003 Kohlschutter-Tonz Syndrome 37 0.064
134
FSC004 Fasciitis 46 0.064
135
P CRN035 Cranial Nerve Palsy 43 0.062
136
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.061
137
INS001 Insulinoma 59 0.060
138
VSC047 Vascular Malformation 45 0.059
139
P DYS021 Dysautonomia 47 0.059
140
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.059
141
MLT021 Multiple System Atrophy 71 0.059
142
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.059
143
LYM027 Lymphopenia 54 0.058
144
HYP043 Hyperandrogenism 48 0.058
145
FRB001 Farber Lipogranulomatosis 51 0.058
146
CHR066 Chronic Fatigue Syndrome 64 0.058
147
c CHR417 Chronic Graft Versus Host Disease 50 0.057
148
P ATX030 Ataxia-Telangiectasia 76 0.056
149
c GCH015 Gaucher Disease, Type I 66 0.056
150
c ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.056
151
P EPN002 Ependymoma 53 0.056
152
SLP001 Sleeping Sickness 48 0.055
153
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.054
154
OBS001 Obstructive Jaundice 48 0.054
155
P MNC007 Monocytic Leukemia 55 0.052
156
FBR012 Fabry Disease 69 0.051
157
UND005 Undifferentiated Pleomorphic Sarcoma 43 0.051
158
EPL101 Epilepsy, Idiopathic Generalized, Suscpetibility to, 12 19 0.050
159
NCR007 Necrotizing Fasciitis 45 0.048
160
MYM001 Myoma 51 0.047
161
P BRS053 Breast Fibroadenoma 46 0.047
162
GYN001 Gynecomastia 49 0.047
163
ANG050 Angiocentric Glioma 28 0.047
164
CMP034 Complete Androgen Insensitivity Syndrome 42 0.046
165
ASP003 Aseptic Meningitis 51 0.046
166
PRS045 Prostatic Hypertrophy 44 0.046
167
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 54 0.046
168
SCB001 Scabies 45 0.045
169
c SML034 Small Cell Neuroendocrine Carcinoma 40 0.044
170
SPN035 Spindle Cell Sarcoma 47 0.043
171
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.042
172
c INT064 Intermediate Uveitis 52 0.042
173
P LYD001 Leydig Cell Tumor 44 0.042
174
GND002 Gender Identity Disorder 44 0.041
175
EST004 Estrogen Excess 38 0.039
176
PLM019 Pleomorphic Liposarcoma 44 0.038
177
BHC003 Behcet Syndrome 61 0.038
178
VGT001 Vogt-Koyanagi-Harada Disease 52 0.037
179
IDP064 Idiopathic Neutropenia 45 0.034
180
c PRK020 Parkinson Disease 6, Early Onset 47 0.034