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

The MalaCard for "epilepsy, juvenile myoclonic, susceptibility to, 5" has been retired.
Searching MalaCards for entries containing "epilepsy, juvenile myoclonic, susceptibility to, 5"

168 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 7.944
2
c EPL094 Epilepsy, Juvenile Myoclonic 5 22 5.012
3
P EPL164 Epilepsy 60 1.063
4
P ART022 Arthritis 73 0.500
5
P RHM011 Rheumatoid Arthritis 87 0.388
6
NRN002 Neuronitis 40 0.359
7
P ENC018 Encephalopathy 59 0.299
8
ALR002 Al-Raqad Syndrome 36 0.266
9
P IDP010 Idiopathic Generalized Epilepsy 61 0.261
10
TMP001 Temporal Lobe Epilepsy 47 0.255
11
MYC033 Myoclonus 41 0.254
12
FCL014 Focal Epilepsy 55 0.251
13
CRB009 Cerebritis 36 0.251
14
P LPS004 Lupus Erythematosus 63 0.247
15
c SYS001 Systemic Lupus Erythematosus 87 0.244
16
PRS047 Prostatitis 56 0.234
17
P ATX004 Ataxia 53 0.221
18
P SZR006 Seizure Disorder 56 0.219
19
RTN023 Retinitis 49 0.198
20
P MYP004 Myopathy 67 0.184
21
P PNC044 Pancreatitis 62 0.182
22
DMN002 Dementia 62 0.179
23
P FBR031 Febrile Seizures 53 0.177
24
P CHL002 Childhood Absence Epilepsy 54 0.173
25
P AXN010 Axenfeld-Rieger Syndrome, Type 3 52 0.169
26
P PNM007 Pneumonia 67 0.168
27
STT001 Status Epilepticus 59 0.167
28
P GLM045 Glioma 53 0.166
29
P ENC004 Encephalitis 60 0.164
30
P NRV007 Nervous System Disease 71 0.160
31
JVN033 Juvenile Nasopharyngeal Angiofibroma 38 0.159
32
P NRP001 Neuropathy 57 0.158
33
P CRD011 Cardiomyopathy 66 0.158
34
P KDN018 Kidney Disease 64 0.157
35
P DYS154 Dystonia 62 0.151
36
P INT063 Intellectual Disability 46 0.148
37
HYP266 Hypoxia 55 0.148
38
P TRM003 Tremor 54 0.147
39
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 34 0.144
40
P AST007 Astrocytoma 66 0.143
41
P MSC003 Muscular Atrophy 51 0.143
42
WTH001 Withdrawal Disorder 36 0.142
43
c CNT035 Central Nervous System Disease 60 0.141
44
ACQ007 Acquired Immunodeficiency Syndrome 60 0.140
45
P MNN013 Meningitis 66 0.136
46
P UVT001 Uveitis 60 0.135
47
RSP006 Respiratory System Disease 61 0.135
48
SPS057 Spasticity 41 0.133
49
P PNC035 Pancreatic Cancer 86 0.132
50
P SPN046 Spinal Muscular Atrophy 62 0.132
51
SXL003 Sexual Disorder 45 0.131
52
LRN003 Learning Disability 49 0.130
53
c PND001 Pain Disorder 53 0.129
54
GNG013 Gingivitis 61 0.127
55
HDC001 Headache 52 0.126
56
WST001 West Syndrome 61 0.124
57
GST045 Gastroenteritis 59 0.122
58
RPR002 Reproductive System Disease 45 0.120
59
P GLB002 Glioblastoma 65 0.118
60
P INF032 Infertility 61 0.118
61
BNS002 Bone Structure Disease 37 0.117
62
P SPN052 Spondyloarthropathy 58 0.115
63
GST050 Gastrointestinal System Disease 58 0.115
64
c EPL084 Epilepsy, Idiopathic Generalized 11 28 0.114
65
DRG001 Drug Psychosis 39 0.112
66
P GRV001 Graves' Disease 62 0.111
67
HPT074 Hepatic Adenoma, Somatic 35 0.110
68
c CRN214 Coronary Heart Disease 5 22 0.110
69
c MYC070 Myoclonic Epilepsy, Juvenile 1 35 0.110
70
P TBR001 Tuberous Sclerosis 68 0.109
71
P SNS014 Sinusitis 66 0.108
72
BLD054 Blood Protein Disease 38 0.106
73
P PRK057 Parkinson Disease, Late-Onset 72 0.106
74
PHY002 Physical Disorder 43 0.105
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 42 0.104
76
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 32 0.101
77
PRT036 Peritonitis 65 0.100
78
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 42 0.100
79
WLL006 Wells Syndrome 57 0.099
80
P CRB042 Cerebellar Ataxia 64 0.097
81
P CRN178 Coronary Heart Disease 6 22 0.096
82
BRC012 Brucellosis 66 0.095
83
OTT002 Otitis Media 66 0.094
84
BRN002 Bronchiolitis 56 0.094
85
KRT004 Keratitis 70 0.094
86
P ESN007 Eosinophilia 61 0.093
87
RCT015 Reactive Arthritis 65 0.093
88
KHL003 Kohlschutter-Tonz Syndrome 35 0.092
89
DPH001 Diphtheria 55 0.092
90
INT066 Interstitial Lung Disease 60 0.092
91
MTR014 Motor Neuron Disease 57 0.091
92
OTP003 Oto-Palatal-Digital Syndrome 14 0.091
93
ECH003 Echinococcosis 53 0.090
94
GLB015 Glioblastoma Multiforme 63 0.090
95
c PRK024 Parkinson Disease, Juvenile, Type 2 49 0.089
96
P NPH012 Nephrotic Syndrome 55 0.089
97
c EPL133 Epilepsy, Juvenile Absence 1 25 0.089
98
P ANG001 Angelman Syndrome 62 0.088
99
EXF001 Exfoliation Syndrome 56 0.088
100
P CNJ013 Conjunctivitis 65 0.088
101
P RTT002 Rett Syndrome 77 0.087
102
SXD001 Sex Differentiation Disease 39 0.086
103
P MCR010 Microcephaly 60 0.086
104
CYT008 Cytomegalovirus Infection 51 0.085
105
P HYP265 Hypotonia 39 0.085
106
P ALP009 Alopecia Areata 62 0.085
107
P PLN008 Peeling Skin Syndrome 45 0.085
108
PPL022 Papilloma 54 0.084
109
OPT006 Optic Nerve Disease 47 0.083
110
c JVN024 Juvenile Hereditary Hemochromatosis 30 0.080
111
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 30 0.080
112
TNS005 Tonsillitis 58 0.080
113
P RTN008 Retinitis Pigmentosa 78 0.080
114
ADT003 Auditory System Disease 49 0.080
115
P HYP061 Hypertrophic Cardiomyopathy 64 0.079
116
NRN005 Neuronal Ceroid-Lipofuscinoses 48 0.079
117
P AGG001 Aggressive Periodontitis 49 0.079
118
BCT004 Bacteriuria 48 0.078
119
P GST044 Gastritis 64 0.078
120
c ANT034 Anterior Uveitis 49 0.077
121
P MMP001 Mumps 56 0.077
122
c ACT210 Acute Respiratory Distress Syndrome 55 0.077
123
P PRS038 Personality Disorder 60 0.076
124
APH001 Aphthous Stomatitis 62 0.076
125
P LGH007 Leigh Syndrome 70 0.076
126
FSC004 Fasciitis 47 0.075
127
MLT021 Multiple System Atrophy 71 0.075
128
GLM004 Gliomatosis Cerebri 48 0.074
129
MXD005 Mixed Connective Tissue Disease 63 0.074
130
P LCH002 Lichen Planus 61 0.073
131
CRD119 Cardiac Arrest 63 0.073
132
P PRP029 Porphyria 56 0.073
133
PRS045 Prostatic Hypertrophy 44 0.072
134
OBS001 Obstructive Jaundice 47 0.072
135
P DYS021 Dysautonomia 47 0.072
136
c MLG068 Malignant Glioma 49 0.071
137
VSC047 Vascular Malformation 45 0.071
138
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 33 0.070
139
P HYP076 Hyperthyroidism 59 0.070
140
P ACT135 Acute Graft Versus Host Disease 52 0.069
141
LYM027 Lymphopenia 54 0.069
142
HYP043 Hyperandrogenism 46 0.069
143
INS001 Insulinoma 60 0.069
144
ADL030 Adult-Onset Still's Disease 57 0.069
145
c CHR417 Chronic Graft Versus Host Disease 50 0.068
146
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 35 0.068
147
EXT034 Extrinsic Allergic Alveolitis 58 0.066
148
GYN001 Gynecomastia 49 0.064
149
MYM001 Myoma 51 0.064
150
P CRN035 Cranial Nerve Palsy 44 0.063
151
P LRY016 Laryngeal Carcinoma 60 0.063
152
LYM052 Lymphomatoid Papulosis 45 0.063
153
PLM014 Pleomorphic Adenoma 51 0.062
154
OLV001 Olivopontocerebellar Atrophy 53 0.062
155
GNC003 Geniculate Herpes Zoster 34 0.061
156
FBR012 Fabry Disease 68 0.060
157
ASP003 Aseptic Meningitis 51 0.060
158
ANG050 Angiocentric Glioma 29 0.060
159
NCR007 Necrotizing Fasciitis 43 0.058
160
BHC003 Behcet Syndrome 60 0.058
161
P BRS053 Breast Fibroadenoma 44 0.058
162
MHR001 Mohr-Tranebjaerg Syndrome 43 0.057
163
c PRK020 Parkinson Disease 6, Early Onset 46 0.056
164
GND002 Gender Identity Disorder 44 0.055
165
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 56 0.053
166
TNG003 Tongue Cancer 59 0.053
167
P LYD001 Leydig Cell Tumor 40 0.053
168
IDP064 Idiopathic Neutropenia 43 0.049