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"

161 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 7.953
2
c EPL094 Epilepsy, Juvenile Myoclonic 5 23 4.973
3
P EPL164 Epilepsy 66 1.060
4
P ART022 Arthritis 75 0.495
5
P RHM011 Rheumatoid Arthritis 88 0.381
6
NRN002 Neuronitis 42 0.347
7
P ENC018 Encephalopathy 59 0.327
8
TMP001 Temporal Lobe Epilepsy 51 0.264
9
P IDP010 Idiopathic Generalized Epilepsy 61 0.252
10
FCL014 Focal Epilepsy 56 0.249
11
CRB009 Cerebritis 38 0.241
12
P LPS004 Lupus Erythematosus 63 0.239
13
c SYS001 Systemic Lupus Erythematosus 87 0.232
14
MYC033 Myoclonus 41 0.231
15
PRS047 Prostatitis 56 0.227
16
P SZR006 Seizure Disorder 57 0.218
17
c CNT035 Central Nervous System Disease 59 0.214
18
P NRV007 Nervous System Disease 71 0.213
19
HV1006 Hiv-1 82 0.202
20
P ATX004 Ataxia 53 0.201
21
ALR002 Al-Raqad Syndrome 36 0.199
22
RTN023 Retinitis 49 0.185
23
P PNC044 Pancreatitis 60 0.178
24
P MYP004 Myopathy 67 0.171
25
P FBR031 Febrile Seizures 52 0.170
26
STT001 Status Epilepticus 59 0.167
27
P CHL002 Childhood Absence Epilepsy 56 0.165
28
P ADN016 Adenocarcinoma 69 0.164
29
DMN002 Dementia 64 0.161
30
P ENC004 Encephalitis 61 0.160
31
P GLM045 Glioma 58 0.155
32
P PNM007 Pneumonia 66 0.154
33
JVN033 Juvenile Nasopharyngeal Angiofibroma 39 0.150
34
P NRP001 Neuropathy 60 0.149
35
HYP266 Hypoxia 55 0.147
36
P CRD011 Cardiomyopathy 67 0.145
37
P MSC003 Muscular Atrophy 51 0.141
38
P DYS154 Dystonia 64 0.139
39
WTH001 Withdrawal Disorder 41 0.139
40
P INT063 Intellectual Disability 53 0.137
41
P AST007 Astrocytoma 65 0.136
42
AND005 Androgen Insensitivity Syndrome, Mild 16 0.134
43
SXL003 Sexual Disorder 47 0.133
44
P TRM003 Tremor 54 0.129
45
DRG012 Drug Rash with Eosinophilia and Systemic Symptoms 35 0.128
46
P SPN046 Spinal Muscular Atrophy 63 0.128
47
RSP006 Respiratory System Disease 62 0.128
48
LRN003 Learning Disability 51 0.127
49
P AXN010 Axenfeld-Rieger Syndrome, Type 3 54 0.127
50
PRM097 Primary Immunodeficiency Disease 61 0.123
51
DSS008 Disease of Mental Health 55 0.123
52
P PNC035 Pancreatic Cancer 85 0.122
53
P MNN013 Meningitis 65 0.121
54
SPS057 Spasticity 42 0.121
55
c PND001 Pain Disorder 55 0.121
56
HDC001 Headache 54 0.118
57
P INF032 Infertility 61 0.118
58
WST001 West Syndrome 61 0.116
59
GST045 Gastroenteritis 60 0.115
60
GNG013 Gingivitis 60 0.115
61
P GRV001 Graves' Disease 61 0.115
62
c CRN214 Coronary Heart Disease 5 23 0.115
63
c MYC070 Myoclonic Epilepsy, Juvenile 1 24 0.114
64
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 66 0.114
65
HPT074 Hepatic Adenoma, Somatic 51 0.111
66
P GLB002 Glioblastoma 66 0.109
67
HNM002 Hinman Syndrome 25 0.108
68
MVM001 Movement Disease 54 0.105
69
PHY002 Physical Disorder 44 0.104
70
P SPN052 Spondyloarthropathy 60 0.104
71
P JVN007 Juvenile Absence Epilepsy 37 0.103
72
DRG001 Drug Psychosis 40 0.101
73
FML039 Female Reproductive System Disease 48 0.097
74
P CRN178 Coronary Heart Disease 6 24 0.095
75
CNV018 Convulsions, Familial Infantile, with Paroxysmal Choreoathetosis 44 0.095
76
P PRK057 Parkinson Disease, Late-Onset 72 0.093
77
EXF001 Exfoliation Syndrome 57 0.092
78
WLL006 Wells Syndrome 56 0.091
79
c MCL062 Mucolipidosis Ii Alpha/beta 60 0.091
80
P ESN007 Eosinophilia 61 0.090
81
PRT036 Peritonitis 62 0.089
82
DPH001 Diphtheria 58 0.087
83
P CRB042 Cerebellar Ataxia 64 0.087
84
RCT015 Reactive Arthritis 62 0.087
85
P LYM033 Lymphoproliferative Syndrome 53 0.086
86
TRM010 Traumatic Brain Injury 52 0.086
87
P PLN008 Peeling Skin Syndrome 47 0.085
88
OCL009 Ocular Cancer 62 0.085
89
BRC012 Brucellosis 65 0.084
90
c EPL133 Epilepsy, Juvenile Absence 1 26 0.084
91
ADT003 Auditory System Disease 51 0.083
92
KRT004 Keratitis 70 0.082
93
SXD001 Sex Differentiation Disease 40 0.081
94
P HMN010 Hemangioma 60 0.081
95
P CNJ013 Conjunctivitis 65 0.080
96
P MCR010 Microcephaly 58 0.080
97
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 37 0.080
98
P ANG001 Angelman Syndrome 61 0.080
99
BRN002 Bronchiolitis 56 0.079
100
OPT006 Optic Nerve Disease 51 0.079
101
GLB015 Glioblastoma Multiforme 62 0.079
102
MTR014 Motor Neuron Disease 59 0.079
103
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.079
104
OTT002 Otitis Media 66 0.079
105
INT309 Intellectual Developmental Disorder with Persistence of Fetal Hemoglobin 29 0.078
106
P RTN008 Retinitis Pigmentosa 79 0.078
107
P OVR049 Ovarian Disease 55 0.078
108
CYT008 Cytomegalovirus Infection 51 0.078
109
PPL022 Papilloma 55 0.077
110
P RTT002 Rett Syndrome 78 0.076
111
P PRS038 Personality Disorder 61 0.075
112
APH001 Aphthous Stomatitis 62 0.074
113
c INF067 Inflammatory Bowel Disease 10 51 0.074
114
P PRP029 Porphyria 58 0.073
115
P HYP265 Hypotonia 39 0.072
116
CRD119 Cardiac Arrest 63 0.072
117
c ANT034 Anterior Uveitis 49 0.071
118
TNS005 Tonsillitis 58 0.071
119
ECH003 Echinococcosis 53 0.067
120
FSC004 Fasciitis 46 0.067
121
NRN005 Neuronal Ceroid-Lipofuscinoses 52 0.067
122
ATS001 Autistic Disorder 59 0.067
123
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 36 0.067
124
KHL003 Kohlschutter-Tonz Syndrome 37 0.066
125
MLT021 Multiple System Atrophy 71 0.066
126
INS001 Insulinoma 59 0.066
127
P LGH007 Leigh Syndrome 70 0.066
128
GLM004 Gliomatosis Cerebri 53 0.066
129
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 34 0.065
130
VSC047 Vascular Malformation 45 0.064
131
P DYS021 Dysautonomia 47 0.064
132
P ATX030 Ataxia-Telangiectasia 76 0.064
133
P CRN035 Cranial Nerve Palsy 43 0.064
134
P ACT135 Acute Graft Versus Host Disease 53 0.064
135
BCT004 Bacteriuria 47 0.064
136
MGL016 Megaloblastic Anemia-1, Finnish Type 46 0.063
137
CHR066 Chronic Fatigue Syndrome 64 0.061
138
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 49 0.061
139
c CHR417 Chronic Graft Versus Host Disease 50 0.060
140
HYP043 Hyperandrogenism 48 0.059
141
P MNC007 Monocytic Leukemia 55 0.058
142
LYM027 Lymphopenia 54 0.058
143
FRB001 Farber Lipogranulomatosis 51 0.057
144
OBS001 Obstructive Jaundice 48 0.054
145
FBR012 Fabry Disease 69 0.054
146
SCB001 Scabies 45 0.052
147
MYM001 Myoma 51 0.052
148
NCR007 Necrotizing Fasciitis 45 0.051
149
GYN001 Gynecomastia 49 0.050
150
PRS045 Prostatic Hypertrophy 44 0.050
151
ASP003 Aseptic Meningitis 51 0.048
152
P BRS053 Breast Fibroadenoma 46 0.047
153
SPN035 Spindle Cell Sarcoma 47 0.047
154
ANG050 Angiocentric Glioma 28 0.047
155
BNN001 Bannayan-Riley-Ruvalcaba Syndrome 54 0.046
156
P LYD001 Leydig Cell Tumor 44 0.046
157
GND002 Gender Identity Disorder 44 0.041
158
EST004 Estrogen Excess 38 0.039
159
BHC003 Behcet Syndrome 61 0.039
160
IDP064 Idiopathic Neutropenia 45 0.036
161
c PRK020 Parkinson Disease 6, Early Onset 47 0.035