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"

186 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 7.766
2
c EPL084 Epilepsy, Idiopathic Generalized 11 28 5.140
3
c EPL094 Epilepsy, Juvenile Myoclonic 5 22 4.729
4
c EPL086 Epilepsy, Idiopathic Generalized 9 23 4.154
5
c MYC070 Myoclonic Epilepsy, Juvenile 1 35 3.836
6
P EPL164 Epilepsy 60 1.135
7
P ART022 Arthritis 73 0.512
8
P RHM011 Rheumatoid Arthritis 87 0.389
9
NRN002 Neuronitis 40 0.341
10
P ENC018 Encephalopathy 59 0.300
11
P IDP010 Idiopathic Generalized Epilepsy 61 0.271
12
TMP001 Temporal Lobe Epilepsy 47 0.269
13
FCL014 Focal Epilepsy 55 0.264
14
MYC033 Myoclonus 41 0.262
15
CRB009 Cerebritis 36 0.243
16
P LPS004 Lupus Erythematosus 63 0.241
17
ALR002 Al-Raqad Syndrome 36 0.240
18
c SYS001 Systemic Lupus Erythematosus 87 0.236
19
P SZR006 Seizure Disorder 56 0.228
20
P ATX004 Ataxia 53 0.206
21
PRS047 Prostatitis 56 0.199
22
RTN023 Retinitis 49 0.183
23
P FBR031 Febrile Seizures 53 0.182
24
P CHL002 Childhood Absence Epilepsy 54 0.178
25
STT001 Status Epilepticus 59 0.174
26
DMN002 Dementia 62 0.173
27
P MYP004 Myopathy 67 0.173
28
JVN033 Juvenile Nasopharyngeal Angiofibroma 38 0.167
29
P PNC044 Pancreatitis 62 0.166
30
P PNM007 Pneumonia 67 0.165
31
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.157
32
P ENC004 Encephalitis 60 0.154
33
P GLM045 Glioma 53 0.153
34
P NRV007 Nervous System Disease 71 0.152
35
P AST007 Astrocytoma 66 0.146
36
P DYS154 Dystonia 62 0.145
37
P INT063 Intellectual Disability 46 0.145
38
P TRM003 Tremor 54 0.142
39
P CRD011 Cardiomyopathy 66 0.142
40
P KDN018 Kidney Disease 64 0.142
41
P UVT001 Uveitis 60 0.142
42
WTH001 Withdrawal Disorder 36 0.140
43
P MSC003 Muscular Atrophy 51 0.140
44
P NRP001 Neuropathy 57 0.139
45
c CNT035 Central Nervous System Disease 60 0.139
46
HYP266 Hypoxia 55 0.137
47
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.135
48
ACQ007 Acquired Immunodeficiency Syndrome 60 0.134
49
P MNN013 Meningitis 66 0.132
50
RSP006 Respiratory System Disease 61 0.132
51
LRN003 Learning Disability 49 0.131
52
P SPN046 Spinal Muscular Atrophy 62 0.129
53
WST001 West Syndrome 61 0.126
54
SXL003 Sexual Disorder 45 0.125
55
GNG013 Gingivitis 61 0.124
56
HDC001 Headache 52 0.123
57
P PNC035 Pancreatic Cancer 86 0.121
58
c PND001 Pain Disorder 53 0.120
59
SPS057 Spasticity 41 0.119
60
P SPN052 Spondyloarthropathy 58 0.118
61
RPR002 Reproductive System Disease 45 0.117
62
P INF032 Infertility 61 0.114
63
P TBR001 Tuberous Sclerosis 68 0.111
64
P GLB002 Glioblastoma 65 0.110
65
P GRV001 Graves' Disease 62 0.108
66
BNS002 Bone Structure Disease 37 0.107
67
GST050 Gastrointestinal System Disease 58 0.105
68
DRG001 Drug Psychosis 39 0.104
69
BLD054 Blood Protein Disease 38 0.104
70
GST045 Gastroenteritis 59 0.104
71
P PRK057 Parkinson Disease, Late-Onset 72 0.103
72
PHY002 Physical Disorder 43 0.101
73
P SNS014 Sinusitis 66 0.101
74
HPT074 Hepatic Adenoma, Somatic 35 0.100
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.099
76
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.098
77
RCT015 Reactive Arthritis 65 0.097
78
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.097
79
OTT002 Otitis Media 66 0.096
80
WLL006 Wells Syndrome 57 0.094
81
KRT004 Keratitis 70 0.093
82
PRT036 Peritonitis 65 0.092
83
P ANG001 Angelman Syndrome 62 0.092
84
ECH003 Echinococcosis 53 0.092
85
BRC012 Brucellosis 66 0.091
86
CHL123 Chlamydia 60 0.091
87
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.091
88
c EPL133 Epilepsy, Juvenile Absence 1 25 0.090
89
OTP003 Oto-Palatal-Digital Syndrome 14 0.090
90
GLB015 Glioblastoma Multiforme 63 0.090
91
P CRB042 Cerebellar Ataxia 64 0.090
92
c CRN214 Coronary Heart Disease 5 22 0.090
93
BRN002 Bronchiolitis 56 0.089
94
INT066 Interstitial Lung Disease 60 0.089
95
P NPH012 Nephrotic Syndrome 55 0.088
96
P CRN178 Coronary Heart Disease 6 22 0.088
97
MTR014 Motor Neuron Disease 57 0.087
98
PPL022 Papilloma 54 0.087
99
P CNJ013 Conjunctivitis 65 0.087
100
OST017 Osteomyelitis 60 0.087
101
KHL003 Kohlschutter-Tonz Syndrome 35 0.087
102
CYT008 Cytomegalovirus Infection 51 0.087
103
SXD001 Sex Differentiation Disease 39 0.085
104
OPT006 Optic Nerve Disease 47 0.084
105
EXF001 Exfoliation Syndrome 56 0.083
106
P RTT002 Rett Syndrome 77 0.082
107
P OLG002 Oligodendroglioma 55 0.082
108
DPH001 Diphtheria 55 0.082
109
P AGG001 Aggressive Periodontitis 49 0.081
110
P PLN008 Peeling Skin Syndrome 45 0.080
111
NRN005 Neuronal Ceroid-Lipofuscinoses 48 0.080
112
c ANT034 Anterior Uveitis 49 0.080
113
P TMP003 Temporal Arteritis 61 0.080
114
BCT004 Bacteriuria 48 0.079
115
P ALP009 Alopecia Areata 62 0.079
116
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.078
117
P MCR010 Microcephaly 60 0.077
118
P ESN007 Eosinophilia 61 0.077
119
TNS005 Tonsillitis 58 0.077
120
P PRS038 Personality Disorder 60 0.077
121
P LGH007 Leigh Syndrome 70 0.076
122
MXD005 Mixed Connective Tissue Disease 63 0.076
123
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.076
124
P GST044 Gastritis 64 0.076
125
P LCH002 Lichen Planus 61 0.075
126
P MMP001 Mumps 56 0.075
127
c ACT210 Acute Respiratory Distress Syndrome 55 0.075
128
P HYP061 Hypertrophic Cardiomyopathy 64 0.074
129
ADT003 Auditory System Disease 49 0.074
130
OBS001 Obstructive Jaundice 47 0.074
131
P ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.074
132
P PRP029 Porphyria 56 0.073
133
P HYP265 Hypotonia 39 0.073
134
GLM004 Gliomatosis Cerebri 48 0.072
135
FSC004 Fasciitis 47 0.072
136
CRD119 Cardiac Arrest 63 0.072
137
P ACT135 Acute Graft Versus Host Disease 52 0.071
138
LYM027 Lymphopenia 54 0.071
139
P RTN008 Retinitis Pigmentosa 78 0.071
140
PRS045 Prostatic Hypertrophy 44 0.069
141
MLT021 Multiple System Atrophy 71 0.069
142
APH001 Aphthous Stomatitis 62 0.069
143
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.069
144
ADL030 Adult-Onset Still's Disease 57 0.069
145
HYP043 Hyperandrogenism 46 0.067
146
VSC047 Vascular Malformation 45 0.067
147
P DYS021 Dysautonomia 47 0.067
148
c MLG068 Malignant Glioma 49 0.067
149
P HYP076 Hyperthyroidism 59 0.066
150
ORL013 Oral Lichen Planus 53 0.066
151
c CHR417 Chronic Graft Versus Host Disease 50 0.065
152
EXT034 Extrinsic Allergic Alveolitis 58 0.065
153
FRB001 Farber Lipogranulomatosis 54 0.065
154
P LRY016 Laryngeal Carcinoma 60 0.064
155
P CRN035 Cranial Nerve Palsy 44 0.062
156
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.062
157
INS001 Insulinoma 60 0.061
158
GRF001 Graft-Versus-Host Disease, Protection Against 54 0.061
159
PLM014 Pleomorphic Adenoma 51 0.061
160
CRB090 Cerebral Hypoxia 45 0.061
161
SLP001 Sleeping Sickness 48 0.061
162
ANG050 Angiocentric Glioma 29 0.061
163
GYN001 Gynecomastia 49 0.060
164
GNC003 Geniculate Herpes Zoster 34 0.060
165
MYM001 Myoma 51 0.059
166
LYM052 Lymphomatoid Papulosis 45 0.059
167
ASP003 Aseptic Meningitis 51 0.059
168
SPH001 Sapho Syndrome 48 0.058
169
FBR012 Fabry Disease 68 0.058
170
OLV001 Olivopontocerebellar Atrophy 53 0.057
171
P BRS053 Breast Fibroadenoma 44 0.057
172
PDT035 Pediatric Systemic Lupus Erythematosus 40 0.057
173
NCR007 Necrotizing Fasciitis 43 0.056
174
BHC003 Behcet Syndrome 60 0.056
175
MHR001 Mohr-Tranebjaerg Syndrome 43 0.055
176
c PRK020 Parkinson Disease 6, Early Onset 46 0.055
177
CMP034 Complete Androgen Insensitivity Syndrome 42 0.055
178
c SML034 Small Cell Neuroendocrine Carcinoma 41 0.054
179
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 56 0.054
180
GND002 Gender Identity Disorder 44 0.053
181
TNG003 Tongue Cancer 59 0.053
182
VGT001 Vogt-Koyanagi-Harada Disease 54 0.053
183
EPL101 Epilepsy, Idiopathic Generalized, Suscpetibility to, 12 24 0.052
184
P LYD001 Leydig Cell Tumor 40 0.050
185
IDP064 Idiopathic Neutropenia 43 0.049
186
EST004 Estrogen Excess 36 0.049