Search results for Zonisamide

414 hits were found for Zonisamide

# Family MCID Name MIFTS Score
1
P EPL164 Epilepsy 68 20.194
2
P SZR006 Seizure Disorder 70 20.068
3
FCL014 Focal Epilepsy 53 15.469
4
ALC007 Alcohol Dependence 66 9.415
5
c MJR022 Major Affective Disorder 8 38 8.895
6
c MJR024 Major Affective Disorder 9 41 8.895
7
P BPL003 Bipolar Disorder 56 8.895
8
c MGR028 Migraine with or Without Aura 1 64 8.801
9
P TRM003 Tremor 48 8.790
10
WST001 West Syndrome 59 7.891
11
P HDC001 Headache 57 7.624
12
ERL001 Early Myoclonic Encephalopathy 62 7.531
13
c ESS001 Essential Tremor 57 7.060
14
P PRK039 Parkinsonism 55 7.059
15
P MYC033 Myoclonus 47 6.568
16
P EPL140 Epilepsy, Idiopathic Generalized 62 6.418
17
P EXN002 Exanthem 58 6.373
18
P ALC033 Alcohol Use Disorder 61 6.157
19
LNN001 Lennox-Gastaut Syndrome 61 6.126
20
P PRK057 Parkinson Disease, Late-Onset 80 6.114
21
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 5.957
22
STT001 Status Epilepticus 59 5.373
23
ETN001 Eating Disorder 59 5.361
24
NPH009 Nephrolithiasis 54 5.212
25
P MYC026 Myoclonus Epilepsy 35 4.784
26
VSL002 Visual Epilepsy 39 4.775
27
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 4.493
28
MTB004 Metabolic Acidosis 48 4.468
29
ERY003 Erythema Multiforme 56 4.334
30
P EPL198 Epilepsy, Myoclonic Juvenile 61 4.332
31
P DYS154 Dystonia 64 4.322
32
P SCH015 Schizophrenia 74 4.264
33
P MJR007 Major Affective Disorder 1 42 4.230
34
NPH091 Nephrolithiasis, Calcium Oxalate 61 4.190
35
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 4.171
36
SVR097 Severe Cutaneous Adverse Reaction 69 4.171
37
ERY066 Erythema Multiforme Major 29 4.171
38
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.967
39
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.967
40
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.967
41
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.967
42
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.967
43
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.967
44
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.967
45
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.967
46
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.967
47
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.967
48
URL001 Urolithiasis 46 3.911
49
P ENC018 Encephalopathy 62 3.911
50
DBT010 Diabetic Neuropathy 54 3.910
51
SCH012 Schizoaffective Disorder 50 3.828
52
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 3.771
53
PST028 Post-Traumatic Stress Disorder 59 3.763
54
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.599
55
P NRB001 Neuroblastoma 66 3.488
56
P DMN002 Dementia 66 3.465
57
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.421
58
ALL029 Allergic Disease 59 3.274
59
MDD011 Mood Disorder 62 3.254
60
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 3.159
61
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.157
62
P TBR001 Tuberous Sclerosis 69 3.148
63
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.119
64
P CHR345 Chronic Pain 50 3.065
65
PSY004 Psychotic Disorder 66 2.950
66
ACT084 Acute Stress Disorder 54 2.906
67
P ERL057 Early Infantile Epileptic Encephalopathy 60 2.883
68
P MVM001 Movement Disease 61 2.883
69
P TMP001 Temporal Lobe Epilepsy 49 2.866
70
OHT001 Ohtahara Syndrome 38 2.765
71
c PRG011 Progressive Myoclonus Epilepsy 41 2.753
72
P HYP098 Hypereosinophilic Syndrome 66 2.744
73
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 2.645
74
P EPS030 Episodic Kinesigenic Dyskinesia 1 55 2.589
75
CMP006 Complex Partial Epilepsy 36 2.532
76
P MJR001 Major Depressive Disorder 68 2.502
77
MNT002 Mental Depression 57 2.502
78
DPR016 Depression 65 2.502
79
c MJR006 Major Affective Disorder 5 32 2.461
80
c MJR023 Major Affective Disorder 7 33 2.461
81
c MJR004 Major Affective Disorder 4 28 2.461
82
c MJR003 Major Affective Disorder 6 32 2.461
83
c MJR008 Major Affective Disorder 2 34 2.461
84
SCH003 Schizophreniform Disorder 55 2.461
85
BLM002 Bulimia Nervosa 57 2.455
86
P MYP006 Myopia 56 2.430
87
PRS063 Paresthesia 39 2.355
88
DRV001 Dravet Syndrome 69 2.335
89
ANN002 Anencephaly 57 2.275
90
c TBR025 Tuberous Sclerosis 1 84 2.270
91
HYP066 Hyperglycemia 61 2.191
92
HYD002 Hydronephrosis 58 2.191
93
CHL068 Cholestasis 61 2.191
94
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.152
95
AND005 Androgen Insensitivity Syndrome, Mild 21 2.152
96
P PTS002 Ptosis 52 2.118
97
MNN017 Mononeuropathy 41 2.118
98
SGC002 Sgce Myoclonus-Dystonia 24 2.118
99
GLL048 Glial Tumor 52 2.109
100
HGH043 High Grade Glioma 45 2.109
101
GLM045 Glioma 63 2.109
102
SPN186 Spinal Cord Injury 61 2.102
103
IMM162 Immunoglobulin E Concentration, Serum 28 2.102
104
P SLP006 Sleep Apnea 69 2.042
105
P NRP001 Neuropathy 60 2.039
106
OCL069 Ocular Motor Apraxia 57 2.006
107
CNS004 Constipation 56 2.006
108
ADL002 Adult Syndrome 70 1.988
109
CRH001 Crohn's Disease 80 1.988
110
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 1.955
111
c PNS012 Paine Syndrome 60 1.955
112
P CHL002 Childhood Absence Epilepsy 63 1.896
113
c SYS001 Systemic Lupus Erythematosus 87 1.865
114
WTH001 Withdrawal Disorder 48 1.865
115
BNR002 Bone Resorption Disease 47 1.865
116
TRD006 Tardive Dyskinesia 53 1.865
117
P LPS004 Lupus Erythematosus 61 1.865
118
P THR014 Thrombocytopenia 66 1.865
119
MTS001 Mutism 44 1.865
120
ANH002 Anhidrosis 46 1.865
121
P CLS010 Cluster Headache 42 1.865
122
ELC001 Elective Mutism 22 1.865
123
c EPL089 Epilepsy, Idiopathic Generalized 4 14 1.769
124
STT041 Stuttering 52 1.769
125
GLC003 Glucose Intolerance 54 1.769
126
P LVR013 Liver Disease 69 1.769
127
PRC013 Pericarditis 53 1.769
128
HYP060 Hyperinsulinism 54 1.769
129
P ANR048 Aniridia 1 64 1.766
130
c MYC068 Myoclonic Epilepsy of Infancy 34 1.665
131
P OVR082 Overgrowth Syndrome 49 1.665
132
CYC008 Cyclic Vomiting Syndrome 46 1.665
133
P MGR001 Migraine Without Aura 49 1.665
134
P RHN004 Rhinitis 57 1.665
135
GNG012 Gingival Overgrowth 49 1.665
136
CRB037 Cerebral Palsy 67 1.665
137
P RNL007 Renal Tubular Acidosis 50 1.655
138
P APL001 Aplastic Anemia 73 1.623
140
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.553
141
PLY068 Polysubstance Abuse 41 1.553
142
TBC004 Tobacco Addiction 63 1.553
143
APN008 Apnea, Obstructive Sleep 67 1.553
144
CCN002 Cocaine Abuse 49 1.553
145
DRG003 Drug Dependence 46 1.553
146
CCN001 Cocaine Dependence 48 1.553
147
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 1.553
148
CYT018 Cytochrome P450 2d6 Variant 26 1.553
149
TRG013 Trigeminal Autonomic Cephalalgia 15 1.549
150
RRH030 Rare Headache 12 1.549
151
SNC001 Sunct Headache 28 1.549
152
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 1.549
153
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 1.549
154
P JVN007 Juvenile Absence Epilepsy 47 1.549
155
HMF011 Hemifacial Spasm, Familial 33 1.549
156
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.549
157
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 1.549
158
c EPL133 Epilepsy, Juvenile Absence 1 46 1.549
159
PRX097 Paroxysmal Dystonia 32 1.549
160
UNV001 Unverricht-Lundborg Syndrome 53 1.549
161
P PLY019 Polyneuropathy 52 1.549
162
CHR073 Choreatic Disease 54 1.549
163
SML011 Smoldering Myeloma 32 1.549
164
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 1.549
165
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 39 1.549
166
P HMF004 Hemifacial Spasm 38 1.549
167
HRN029 Hearing Loss, Noise-Induced 37 1.542
168
FBR047 Fibromyalgia 58 1.542
169
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.542
170
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.528
171
c SPN383 Spinocerebellar Ataxia 42 33 1.499
172
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.499
173
c HMC039 Hemochromatosis, Type 1 73 1.418
174
HMC038 Hemochromatosis, Neonatal 33 1.418
175
MYC079 Myoclonic Epilepsy of Lafora 64 1.418
176
PHT008 Photosensitive Epilepsy 42 1.418
177
P NRC002 Narcolepsy 56 1.418
178
NSP002 Nasopharyngitis 45 1.418
179
IMP005 Impotence 52 1.296
180
MTC004 Mitochondrial Encephalomyopathy 42 1.295
181
P ATS364 Autism 69 1.263
182
EPL095 Epilepsy with Myoclonic Absences 13 1.263
183
SXL003 Sexual Disorder 49 1.263
184
c TYP009 Type 2 Diabetes Mellitus 92 1.263
185
c DVL034 Developmental and Epileptic Encephalopathy 3 44 1.263
186
P DBT009 Diabetes Mellitus 67 1.263
187
HYP034 Hypertensive Encephalopathy 43 1.263
188
P MGR003 Migraine with Aura 52 1.263
189
PRP030 Purpura 54 1.263
190
P DST107 Distal Renal Tubular Acidosis 48 1.263
191
CVD001 Covid-19 57 1.228
192
CMP034 Complete Androgen Insensitivity Syndrome 55 1.199
193
GLB002 Glioblastoma 67 1.193
194
P ENC004 Encephalitis 61 1.094
195
c ATR087 Atrial Standstill 1 74 1.060
196
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.060
197
IMM003 Immunoglobulin Alpha Deficiency 44 1.060
198
c CRB217 Cerebellar Ataxia Type 42 23 1.060
199
INT075 Intracranial Hypertension 53 1.060
200
HRT011 Heart Septal Defect 49 1.060
201
HYP005 Hypokalemia 55 1.060
202
CRB004 Cerebral Artery Occlusion 45 1.060
203
ASP007 Aspiration Pneumonia 49 1.060
204
c ACT027 Acute Pancreatitis 60 1.060
205
P ATR010 Atrial Heart Septal Defect 58 1.060
206
P NRN021 Neuronal Ceroid Lipofuscinosis 65 1.060
207
INT066 Interstitial Lung Disease 60 1.060
208
PHR003 Pharyngitis 58 1.060
209
P DRR001 Diarrhea 55 1.060
210
OLG006 Oligoastrocytoma 34 1.060
211
c BRN108 Branchiootic Syndrome 1 62 1.052
212
MYF002 Myofascial Pain Syndrome 46 1.052
213
P DYS193 Dystonia 11, Myoclonic 55 1.039
214
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.039
215
c DYS056 Dystonia 12 63 1.039
216
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.039
217
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.039
218
RHB024 Rhabdomyosarcoma 2 67 1.015
219
P GLM040 Glioma Susceptibility 1 71 1.015
220
MXD026 Mixed Glioma 45 1.015
221
P MCR010 Microcephaly 60 0.979
222
PTH003 Pathologic Nystagmus 52 0.979
223
P HYP265 Hypotonia 42 0.979
224
PST053 Postherpetic Neuralgia 40 0.979
225
P RTT002 Rett Syndrome 79 0.848
226
ACR012 Aicardi Syndrome 45 0.848
227
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 0.848
228
P DVL113 Developmental and Epileptic Encephalopathy 43 0.848
229
P VSC007 Vascular Disease 63 0.848
230
P HYD006 Hydrocephalus 61 0.848
231
HMP005 Hemiplegia 54 0.848
232
CRB039 Cerebrovascular Disease 66 0.848
233
PLY024 Polymicrogyria 47 0.848
234
P FBR031 Febrile Seizures 52 0.848
235
P RST001 Restless Legs Syndrome 52 0.807
236
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.692
237
BTN003 Biotinidase Deficiency 62 0.692
238
ANR007 Anorexia Nervosa 60 0.692
239
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 45 0.692
240
P BND018 Band Heterotopia 53 0.692
241
OBS002 Obsessive-Compulsive Disorder 68 0.692
242
SGM008 Segmental Dystonia 28 0.692
243
CRV043 Cervical Dystonia 46 0.692
244
c ATS007 Autism Spectrum Disorder 72 0.692
245
APH002 Aphasia 56 0.692
246
c RNG029 Ring Chromosome 14 Syndrome 31 0.692
247
MCR237 Macrocephaly/megalencephaly Syndrome, Autosomal Recessive 40 0.692
248
PHN003 Phenylketonuria 76 0.692
249
OST159 Osteogenic Sarcoma 66 0.692
250
c HYP836 Hypercholesterolemia, Familial, 1 73 0.692
251
P KBK002 Kabuki Syndrome 1 65 0.692
252
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.692
253
TRM010 Traumatic Brain Injury 51 0.692
254
RPD005 Rapidly Involuting Congenital Hemangioma 46 0.692
255
P RNG032 Ring Chromosome 39 0.692
256
P MYP004 Myopathy 67 0.692
257
GNG004 Ganglioglioma 53 0.692
258
CLF001 Cleft Lip 53 0.692
259
LRN003 Learning Disability 49 0.692
260
P BLT016 Bilateral Polymicrogyria 27 0.692
261
P GST044 Gastritis 55 0.692
262
c VRL007 Viral Encephalitis 50 0.692
263
OST011 Osteomalacia 52 0.692
264
RYS001 Reye Syndrome 49 0.692
265
c INH020 Inherited Metabolic Disorder 48 0.692
266
P SLP005 Sleep Disorder 61 0.692
267
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 0.692
268
LPD008 Lipid Metabolism Disorder 62 0.692
269
P TCD001 Tic Disorder 49 0.692
270
P ACT028 Acute Closed-Angle Glaucoma 32 0.692
271
AMN003 Amnestic Disorder 54 0.692
272
GNR004 Generalized Anxiety Disorder 55 0.692
273
SCN067 Scn1a Seizure Disorders 12 0.692
274
GRN017 Granulocytopenia 42 0.692
275
HYP056 Hypoglycemia 65 0.692
276
HDN002 Head Injury 44 0.692
277
P MTC069 Mitochondrial Disorders 57 0.692
278
P MGL013 Megalencephaly 45 0.692
279
ATN005 Autonomic Dysfunction 46 0.692
280
PRP068 Propriospinal Myoclonus 12 0.692
281
CTR172 Citrullinemia, Classic 65 0.571
282
P ESN008 Eosinophilic Pneumonia 50 0.571
283
NRL004 Neuroleptic Malignant Syndrome 52 0.571
284
P RSP003 Respiratory Failure 74 0.571
285
P PNM007 Pneumonia 67 0.571
286
AGN016 Aging 54 0.501
287
c TBR026 Tuberous Sclerosis 2 71 0.501
288
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.501
289
c HYP595 Hypertension, Essential 85 0.501
290
CMR002 Coumarin Resistance 59 0.501
291
ANT039 Antisynthetase Syndrome 55 0.501
292
CNT033 Central Nervous System Cancer 47 0.501
293
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.501
294
P NRV006 Nervous System Cancer 48 0.501
295
CHL079 Children's Interstitial Lung Disease 26 0.501
296
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.501
297
PRX035 Paroxysmal Dyskinesia 30 0.489
298
MTC196 Mitochondrial Disease with Epilepsy 9 0.489
299
MTC005 Mitochondrial Metabolism Disease 45 0.489
300
SCN061 Scn8a Encephalopathy 13 0.489
301
NRM022 Neurometabolic Disease 24 0.489
302
RRM016 Rare Movement Disorder 15 0.489
303
c ACT134 Acute Liver Failure 59 0.489
304
c EPS035 Episodic Ataxia, Type 2 63 0.489
305
P FRG001 Fragile X Syndrome 70 0.489
306
CRD223 Cardiac Arrhythmia 63 0.489
307
CRD132 Cardiac Conduction Defect 60 0.489
308
ANX010 Anxiety 70 0.489
309
END057 Endometrial Cancer 72 0.489
310
P MYS005 Myositis 56 0.489
311
P OST002 Osteoporosis 76 0.489
312
CLF027 Cleft Palate, Isolated 64 0.489
313
CRT072 Creutzfeldt-Jakob Disease 68 0.489
314
DND001 Dandy-Walker Syndrome 49 0.489
315
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.489
316
P ALT001 Alternating Hemiplegia of Childhood 57 0.489
317
FCL022 Focal Dystonia 42 0.489
318
MLR004 Malaria 80 0.489
319
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.489
320
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.489
321
CYN002 Cyanosis, Transient Neonatal 43 0.489
322
P URN019 Urinary Tract Infection 49 0.489
323
FNG001 Finger Agnosia 19 0.489
324
P ATR011 Atrial Fibrillation 66 0.489
325
P SML001 Small Cell Carcinoma 52 0.489
326
LMB024 Limbic Encephalitis 43 0.489
327
PPL058 Papilloma of Choroid Plexus 55 0.489
328
NRL016 Neural Tube Defects 81 0.489
329
CNT106 Centralopathic Epilepsy 33 0.489
330
c DVL038 Developmental and Epileptic Encephalopathy 7 46 0.489
331
LPT014 Leptin Deficiency or Dysfunction 78 0.489
332
SPN424 Spinocerebellar Ataxia 42, Early-Onset, Severe, with Neurodevelopmental Deficits 26 0.489
333
c EPL098 Epilepsy, Idiopathic Generalized 12 29 0.489
334
STF001 Stiff-Person Syndrome 58 0.489
335
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 0.489
336
TRG002 Trigeminal Neuralgia 61 0.489
337
c SZR022 Seizures, Benign Familial Neonatal, 1 43 0.489
338
P HYP750 Hypertriglyceridemia, Familial 62 0.489
339
DMN031 Dementia, Lewy Body 65 0.489
340
MLD001 Melioidosis 67 0.489
341
P PTN014 Patent Ductus Arteriosus 1 59 0.489
342
DSS032 Disease by Infectious Agent 55 0.489
344
PRT037 Pertussis 65 0.489
345
DRG024 Drug Allergy 40 0.489
346
DYS004 Dyscalculia 35 0.489
347
BRN004 Brain Edema 54 0.489
348
P VSC011 Vasculitis 61 0.489
349
P ALP008 Alopecia 54 0.489
350
47X002 47,xyy 48 0.489
351
SYN036 Syncope 45 0.489
352
SPS087 Spasmus Nutans 21 0.489
353
UNC021 Unclassified Cardiomyopathy 10 0.489
354
SKN016 Skin Disease 63 0.489
355
P OLG002 Oligodendroglioma 66 0.489
356
BNG006 Benign Familial Neonatal Epilepsy 55 0.489
357
P LCT001 Lactic Acidosis 51 0.489
358
P AGN002 Agnosia 54 0.489
359
CNN005 Connective Tissue Disease 67 0.489
360
P PRD008 Periodontitis 64 0.489
361
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.489
362
P NTR004 Neutropenia 63 0.489
363
ASP003 Aseptic Meningitis 50 0.489
364
NRG002 Neurogenic Bladder 55 0.489
365
LND001 Landau-Kleffner Syndrome 51 0.489
366
RFL002 Reflex Epilepsy 41 0.489
367
PPL022 Papilloma 53 0.489
368
DYS006 Dysembryoplastic Neuroepithelial Tumor 32 0.489
369
MYM001 Myoma 54 0.489
370
SQM002 Squamous Cell Papilloma 46 0.489
371
P HYP086 Hypothyroidism 69 0.489
372
P ANG015 Angioedema 56 0.489
373
DPH001 Diphtheria 59 0.489
374
ATN004 Autonomic Neuropathy 42 0.489
375
P HYP040 Hypospadias 51 0.489
376
SPS004 Spastic Quadriplegia 40 0.489
377
TTN003 Tetanus 65 0.489
378
HYP043 Hyperandrogenism 48 0.489
379
MNN009 Meningoencephalitis 48 0.489
380
P FNC004 Fanconi Syndrome 60 0.489
381
CNG034 Congestive Heart Failure 69 0.489
382
MCL006 Macular Retinal Edema 57 0.489
383
P PRP019 Peripheral Nervous System Disease 58 0.489
384
P SBS003 Substance Abuse 54 0.489
385
INP001 Inappropriate Adh Syndrome 48 0.489
386
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 0.489
387
GST037 Gastroparesis 52 0.489
388
P URT039 Urticaria 58 0.489
389
DBT004 Diabetic Polyneuropathy 50 0.489
390
QDR001 Quadriplegia 50 0.489
391
P BNG026 Benign Neonatal Seizures 49 0.489
393
P MYC008 Myocarditis 59 0.489
394
P EPS003 Episodic Ataxia 59 0.489
395
HNS001 Hansen's Disease 32 0.489
396
OPS006 Opsoclonus-Myoclonus Syndrome 48 0.489
397
SPL018 Splenomegaly 49 0.489
399
P CRB088 Cerebral Atrophy 33 0.489
400
NRN016 Neuronal Migration Disorders 40 0.489
402
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 0.489
403
DYS073 Dysphagia 53 0.489
404
P CRB059 Cerebellar Degeneration 36 0.489
405
CYT002 Cytokine Deficiency 43 0.489
406
CNV009 Convulsions Benign Familial Neonatal Dominant Form 31 0.489
408
PRN029 Parainfluenza Virus Type 3 32 0.489
409
CHR178 Chromosomal Triplication 34 0.489
410
PST047 Post-Traumatic Epilepsy 20 0.489
411
PSD088 Pseudobulbar Affect 33 0.489
412
c ATM075 Autoimmune Encephalitis 40 0.489
413
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.489
414
PCH002 Pachygyria 32 0.489
Content
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