Search results for Vigabatrin

457 hits were found for Vigabatrin

# Family MCID Name MIFTS Score
1
WST001 West Syndrome 59 28.369
2
P SZR006 Seizure Disorder 70 19.442
3
FCL014 Focal Epilepsy 53 15.840
4
P TBR001 Tuberous Sclerosis 69 15.125
5
P EPL164 Epilepsy 68 14.947
6
c TBR025 Tuberous Sclerosis 1 84 9.950
7
P ENC018 Encephalopathy 62 9.182
8
LNN001 Lennox-Gastaut Syndrome 61 8.104
9
STT001 Status Epilepticus 59 6.596
10
CCN001 Cocaine Dependence 48 6.407
11
CCN002 Cocaine Abuse 49 5.678
12
CMP006 Complex Partial Epilepsy 36 5.474
13
ERL001 Early Myoclonic Encephalopathy 62 5.304
14
P HYP265 Hypotonia 42 5.154
15
P EXN002 Exanthem 58 4.982
16
P TMP001 Temporal Lobe Epilepsy 49 4.910
17
SCC001 Succinic Semialdehyde Dehydrogenase Deficiency 59 4.877
18
PSY004 Psychotic Disorder 66 4.408
19
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.290
20
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.621
21
PTH003 Pathologic Nystagmus 52 3.509
22
P MYC033 Myoclonus 47 3.412
23
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 3.374
24
BHR001 Behr Syndrome 51 3.325
25
P ERL057 Early Infantile Epileptic Encephalopathy 60 3.318
26
c INF185 Infantile Epilepsy Syndrome 29 3.095
27
c TBR026 Tuberous Sclerosis 2 71 3.029
28
c DVL034 Developmental and Epileptic Encephalopathy 3 44 2.996
29
CRB037 Cerebral Palsy 67 2.996
30
P MVM001 Movement Disease 61 2.975
31
P ENC004 Encephalitis 61 2.898
32
P TRM003 Tremor 48 2.865
33
SPS057 Spasticity 42 2.808
34
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 2.808
35
TRD006 Tardive Dyskinesia 53 2.749
36
DWN001 Down Syndrome 70 2.749
37
LRN003 Learning Disability 49 2.749
38
P OPT006 Optic Nerve Disease 58 2.748
39
BRD001 Brody Myopathy 55 2.742
40
P MCR010 Microcephaly 60 2.563
41
VTR003 Vitreous Detachment 41 2.563
42
VSC002 Vascular Dementia 60 2.563
43
BNS003 Binswanger's Disease 41 2.563
44
ALC007 Alcohol Dependence 66 2.555
45
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 67 2.493
46
P PNC025 Panic Disorder 52 2.493
47
LND001 Landau-Kleffner Syndrome 51 2.493
48
OHT001 Ohtahara Syndrome 38 2.493
49
DRV001 Dravet Syndrome 69 2.444
50
P GLM040 Glioma Susceptibility 1 71 2.402
51
P EPL140 Epilepsy, Idiopathic Generalized 62 2.381
52
CNS004 Constipation 56 2.349
53
ADG002 Audiogenic Seizures 25 2.271
54
P EYD002 Eye Disease 57 2.271
55
DRG003 Drug Dependence 46 2.248
56
VSL002 Visual Epilepsy 39 2.216
57
P ALC033 Alcohol Use Disorder 61 2.205
58
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 2.196
59
PLY183 Polymicrogyria with or Without Vascular-Type Ehlers-Danlos Syndrome 41 2.196
60
PLY024 Polymicrogyria 47 2.196
61
P EPL198 Epilepsy, Myoclonic Juvenile 61 2.192
62
MDD011 Mood Disorder 62 2.189
63
HYP264 Hypertonia 36 2.189
64
P PRK039 Parkinsonism 55 2.177
65
DSS008 Disease of Mental Health 74 2.137
66
P CLR019 Color Blindness 48 2.104
67
PSD088 Pseudobulbar Affect 33 2.104
68
STF001 Stiff-Person Syndrome 58 2.093
69
GNG012 Gingival Overgrowth 49 2.093
70
CRB159 Cerebral Visual Impairment 34 2.026
71
FRS012 First-Degree Atrioventricular Block 39 2.026
72
ATR057 Atrioventricular Block 54 2.026
73
HDN002 Head Injury 44 2.008
74
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.959
75
P NJM001 Nijmegen Breakage Syndrome 76 1.959
76
c TYP009 Type 2 Diabetes Mellitus 92 1.959
77
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 48 1.959
78
GLY010 Glycine Encephalopathy 57 1.944
79
P RSP003 Respiratory Failure 74 1.944
80
NRL016 Neural Tube Defects 81 1.906
81
ACR012 Aicardi Syndrome 45 1.906
82
c ATS007 Autism Spectrum Disorder 72 1.857
83
P KDN018 Kidney Disease 72 1.857
84
P DYS154 Dystonia 64 1.857
85
PRV004 Periventricular Leukomalacia 52 1.857
86
MLG169 Malignant Astrocytoma 57 1.857
87
ISC004 Ischemia 61 1.857
88
P OVR082 Overgrowth Syndrome 49 1.793
89
WBR001 Weber Syndrome 38 1.763
90
STR039 Sturge-Weber Syndrome 61 1.763
91
ATS010 Autosomal Recessive Disease 42 1.763
92
47X002 47,xyy 48 1.763
93
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.763
94
AGN016 Aging 54 1.727
95
GLL008 Gilles De La Tourette Syndrome 65 1.727
96
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.727
97
RHB024 Rhabdomyosarcoma 2 67 1.727
98
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.727
99
ADL002 Adult Syndrome 70 1.727
100
c ATM075 Autoimmune Encephalitis 40 1.727
101
MTC005 Mitochondrial Metabolism Disease 45 1.661
102
APH002 Aphasia 56 1.661
103
P OLG002 Oligodendroglioma 66 1.661
104
FST001 Foster-Kennedy Syndrome 39 1.661
105
SCT001 Sciatic Neuropathy 26 1.661
106
ANP009 Anaplastic Oligodendroglioma 41 1.661
107
HYP266 Hypoxia 57 1.661
108
AMN006 Aminoaciduria 37 1.661
109
GLL048 Glial Tumor 52 1.615
110
GLM045 Glioma 63 1.615
111
P ATS364 Autism 69 1.586
112
NRM022 Neurometabolic Disease 24 1.548
113
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.548
114
c SCH051 Schizophrenia 4 32 1.548
116
P HYP111 Hyperprolinemia 45 1.548
117
c HYP248 Hyperprolinemia, Type I 42 1.548
118
IMN001 Iminoglycinuria 41 1.548
119
HRW001 Hair Whorl 35 1.548
120
P BLT016 Bilateral Polymicrogyria 27 1.548
121
GLB002 Glioblastoma 67 1.548
122
P AGN002 Agnosia 54 1.548
123
P HYD006 Hydrocephalus 61 1.548
124
P CHL002 Childhood Absence Epilepsy 63 1.512
125
c MGR028 Migraine with or Without Aura 1 64 1.435
126
P APL001 Aplastic Anemia 73 1.435
128
c INH020 Inherited Metabolic Disorder 48 1.435
129
CLF027 Cleft Palate, Isolated 64 1.420
130
PLY068 Polysubstance Abuse 41 1.420
131
P HYP097 Hyperekplexia 62 1.420
132
P VSC011 Vasculitis 61 1.420
133
ALL029 Allergic Disease 59 1.420
134
HMM003 Hemimegalencephaly 48 1.420
135
5XP001 5-Oxoprolinase Deficiency 30 1.418
136
c MJR022 Major Affective Disorder 8 38 1.353
137
c MJR024 Major Affective Disorder 9 41 1.353
138
P BPL003 Bipolar Disorder 56 1.353
139
P CRD224 Cardiofaciocutaneous Syndrome 1 71 1.268
140
CRP030 Corpus Callosum, Agenesis of, with Facial Anomalies and Cerebellar Ataxia 37 1.268
141
P PRN026 Porencephaly 55 1.268
142
PHT008 Photosensitive Epilepsy 42 1.268
143
P RTN016 Retinal Degeneration 52 1.268
144
P SNS001 Sensorineural Hearing Loss 59 1.268
145
TTN003 Tetanus 65 1.268
146
P SBS003 Substance Abuse 54 1.268
147
P JVN007 Juvenile Absence Epilepsy 47 1.265
148
P ANG001 Angelman Syndrome 65 1.265
149
c EPL133 Epilepsy, Juvenile Absence 1 46 1.265
150
ERY003 Erythema Multiforme 56 1.265
151
P PRP029 Porphyria 60 1.265
152
P CRB088 Cerebral Atrophy 33 1.265
153
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.172
154
SVR097 Severe Cutaneous Adverse Reaction 69 1.172
155
NRR001 Neuroretinitis 42 1.172
156
ERY066 Erythema Multiforme Major 29 1.172
157
RTN023 Retinitis 46 1.172
158
SBP001 Subependymal Giant Cell Astrocytoma 46 1.172
159
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 40 1.172
160
CRB009 Cerebritis 43 1.166
161
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.106
162
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.106
163
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.106
164
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.106
165
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.106
166
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.106
167
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.106
168
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.106
169
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.106
170
c HYP595 Hypertension, Essential 85 1.106
171
GLC003 Glucose Intolerance 54 1.106
172
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.106
173
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.106
174
HYP060 Hyperinsulinism 54 1.106
175
AND005 Androgen Insensitivity Syndrome, Mild 21 1.106
176
c RTN047 Retinitis Pigmentosa 18 46 1.069
177
c EXD008 Exudative Vitreoretinopathy 1 71 1.069
178
WTH001 Withdrawal Disorder 48 1.069
179
ALX003 Alexander Disease 61 1.069
180
GYR004 Gyrate Atrophy of Choroid and Retina 58 1.069
181
P OLV001 Olivopontocerebellar Atrophy 51 1.069
182
48X005 48,xyyy 39 1.069
183
P RTN008 Retinitis Pigmentosa 80 1.069
184
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 61 1.069
185
P LSS002 Lissencephaly 50 1.069
186
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.069
187
P LVR013 Liver Disease 69 1.069
188
ACT078 Acute Porphyria 49 1.069
189
HYP144 Hyperacusis 23 1.069
190
PHN003 Phenylketonuria 76 0.957
191
ANG018 Angiomyolipoma 46 0.957
192
NPH009 Nephrolithiasis 54 0.957
193
HYP056 Hypoglycemia 65 0.957
194
P FBR031 Febrile Seizures 52 0.957
195
c DVL112 Developmental and Epileptic Encephalopathy 89 24 0.931
196
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.828
197
ANX004 Anoxia 40 0.828
198
BTN003 Biotinidase Deficiency 62 0.828
199
P FRG001 Fragile X Syndrome 70 0.828
200
c LSS005 Lissencephaly 1 57 0.828
201
OTT002 Otitis Media 71 0.828
202
MYC080 Myoclonic Epilepsy of Unverricht and Lundborg 53 0.828
203
SBC001 Subacute Sclerosing Panencephalitis 53 0.828
204
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.828
205
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.828
206
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.828
207
P SCL018 Scoliosis 57 0.828
208
TRM010 Traumatic Brain Injury 51 0.828
209
P MYP004 Myopathy 67 0.828
210
P ALP008 Alopecia 54 0.828
211
P DVL113 Developmental and Epileptic Encephalopathy 43 0.828
212
c CRT089 Cortical Dysplasia, Complex, with Other Brain Malformations 10 39 0.828
213
IMP005 Impotence 52 0.828
214
P BND020 Bone Disease 59 0.828
215
P RTN018 Retinal Disease 53 0.828
216
P ACT028 Acute Closed-Angle Glaucoma 32 0.828
217
P PRC019 Precocious Puberty 47 0.828
218
P HDC001 Headache 57 0.828
219
NRN016 Neuronal Migration Disorders 40 0.828
220
STX005 Stxbp1 Encephalopathy 23 0.828
221
P ALZ034 Alzheimer Disease 87 0.676
222
P RTT002 Rett Syndrome 79 0.676
223
CRD223 Cardiac Arrhythmia 63 0.676
224
LYM007 Lymphangioleiomyomatosis 68 0.676
225
ANX010 Anxiety 70 0.676
226
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 55 0.676
227
MTB004 Metabolic Acidosis 48 0.676
228
c MCR115 Microvascular Complications of Diabetes 5 65 0.676
229
SXL003 Sexual Disorder 49 0.676
230
GMM004 Gamma-Amino Butyric Acid Metabolism Disorder 27 0.676
231
P PRD006 Prader-Willi Syndrome 61 0.676
232
PRP001 Propionic Acidemia 65 0.676
233
TRT020 Tritanopia 50 0.676
234
GLT007 Glutathione Synthetase Deficiency 48 0.676
235
IMM162 Immunoglobulin E Concentration, Serum 28 0.676
236
CLB010 Coloboma of Macula 53 0.676
237
HPT004 Hepatic Coma 43 0.676
238
SPC030 Specific Language Disorder 25 0.676
239
HYP066 Hyperglycemia 61 0.676
240
MNT002 Mental Depression 57 0.676
241
P HRD018 Hair Disease 44 0.676
242
c VRL007 Viral Encephalitis 50 0.676
243
FBR047 Fibromyalgia 58 0.676
244
KDN015 Kidney Angiomyolipoma 46 0.676
245
P UVT001 Uveitis 57 0.676
246
HPT019 Hepatic Encephalopathy 59 0.676
247
PRM003 Premature Ejaculation 44 0.676
248
RTN020 Retinal Vascular Disease 46 0.676
249
ACQ001 Acquired Color Blindness 31 0.676
250
MNN009 Meningoencephalitis 48 0.676
251
MCR013 Microphthalmia 60 0.676
252
P CNJ013 Conjunctivitis 66 0.676
253
BNG009 Benign Epilepsy with Centrotemporal Spikes 60 0.676
254
P SCL015 Scleritis 48 0.676
255
QDR001 Quadriplegia 50 0.676
256
HYP080 Hypogonadism 50 0.676
258
STX004 Stxbp1 Encephalopathy with Epilepsy 15 0.676
259
P NRF002 Neurofibromatosis 57 0.676
260
EXT039 Extrapontine Myelinolysis 18 0.676
261
P CRB059 Cerebellar Degeneration 36 0.676
262
P CNG515 Congenital Zika Syndrome 19 0.676
263
PYR016 Pyridoxine Deficiency 29 0.676
264
MSL001 Measles 61 0.676
265
c DWL002 Dowling-Degos Disease 1 58 0.591
266
JMP002 Jumping Frenchmen of Maine 21 0.591
267
c 3MT007 3-Methylglutaconic Aciduria 37 0.591
268
c 3MT023 3-Methylglutaconic Aciduria, Type Ix 24 0.591
269
P NRP001 Neuropathy 60 0.591
270
PRX097 Paroxysmal Dystonia 32 0.591
271
HYP005 Hypokalemia 55 0.591
272
c ACT027 Acute Pancreatitis 60 0.591
273
P PNC044 Pancreatitis 61 0.591
274
P FML187 Familial Hypertension 34 0.591
275
CHR178 Chromosomal Triplication 34 0.591
276
RBN014 Robin Sequence with Cleft Mandible and Limb Anomalies 36 0.545
277
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.545
278
CMR002 Coumarin Resistance 59 0.545
279
ANT039 Antisynthetase Syndrome 55 0.545
280
HGH043 High Grade Glioma 45 0.545
281
MXD026 Mixed Glioma 45 0.545
282
CHL079 Children's Interstitial Lung Disease 26 0.545
283
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.545
284
FTL073 Fetal Anticonvulsant Syndrome 23 0.478
285
GRW007 Growth Hormone Deficiency 46 0.478
286
c MYC068 Myoclonic Epilepsy of Infancy 34 0.478
287
LBR025 Lobar Holoprosencephaly 47 0.478
288
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.478
289
c RRP028 Rare Epilepsy 17 0.478
290
CLS049 Classic Phenylketonuria 41 0.478
291
PTR034 Paternal Uniparental Disomy 19 0.478
292
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 0.478
293
FRG010 Fragile X Tremor/ataxia Syndrome 44 0.478
294
c MLT128 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 2 50 0.478
295
ANN002 Anencephaly 57 0.478
296
P RTN209 Retinoschisis 1, X-Linked, Juvenile 60 0.478
297
MYC072 Myoclonic Epilepsy Associated with Ragged-Red Fibers 45 0.478
298
P BND018 Band Heterotopia 53 0.478
299
FRY006 Fryns Microphthalmia Syndrome 52 0.478
300
OBS002 Obsessive-Compulsive Disorder 68 0.478
301
P OST002 Osteoporosis 76 0.478
302
c EPS042 Episodic Ataxia, Type 1 58 0.478
303
P CNR004 Cone-Rod Dystrophy 2 74 0.478
304
CRT072 Creutzfeldt-Jakob Disease 68 0.478
305
GST092 Gastroesophageal Reflux 61 0.478
306
HMN044 Human Immunodeficiency Virus Type 1 78 0.478
307
P PLM037 Pulmonary Hypertension 72 0.478
308
HYP017 Hypophosphatemia 49 0.478
309
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.478
310
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.478
311
CYN002 Cyanosis, Transient Neonatal 43 0.478
312
P MLT140 Multiple Congenital Anomalies-Hypotonia-Seizures Syndrome 38 0.478
313
P PRV006 Pervasive Developmental Disorder 52 0.478
314
ADT001 Auditory Agnosia 26 0.478
315
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 0.478
316
HMN047 Human Cytomegalovirus Infection 57 0.478
317
VRB001 Verbal Auditory Agnosia 18 0.478
318
P ANT088 Anterior Segment Dysgenesis 55 0.478
319
P PRV002 Periventricular Nodular Heterotopia 52 0.478
320
P CNG010 Congenital Stationary Night Blindness 56 0.478
321
IMM167 Immune Deficiency Disease 78 0.478
322
MYC079 Myoclonic Epilepsy of Lafora 64 0.478
323
LGH007 Leigh Syndrome 70 0.478
324
CNT106 Centralopathic Epilepsy 33 0.478
325
KRT019 Keratitis, Hereditary 66 0.478
326
IGR001 Ige Responsiveness, Atopic 59 0.478
327
SGW002 Segawa Syndrome, Autosomal Recessive 44 0.478
328
INT333 Intellectual Developmental Disorder with Autism and Speech Delay 29 0.478
329
P LKM062 Leukemia, Acute Lymphoblastic 69 0.478
330
CMB044 Combined Oxidative Phosphorylation Deficiency 14 33 0.478
331
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 0.478
332
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.478
333
P MJR001 Major Depressive Disorder 68 0.478
334
GBT001 Gaba-Transaminase Deficiency 37 0.478
335
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 18 0.478
336
PRP083 Porphyria, Acute Intermittent 65 0.478
337
CHR081 Choroideremia 58 0.478
338
MLL018 Miller-Dieker Lissencephaly Syndrome 52 0.478
339
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 52 0.478
340
DBF001 D-Bifunctional Protein Deficiency 55 0.478
341
EPL199 Epilepsy, Progressive Myoclonic, 4, with or Without Renal Failure 36 0.478
342
P STR020 Strabismus 56 0.478
343
P HNT016 Huntington Disease 73 0.478
344
NVS017 Nevus, Epidermal 66 0.478
346
P ANR048 Aniridia 1 64 0.478
347
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 50 0.478
348
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.478
350
CMB008 Combined Oxidative Phosphorylation Deficiency 34 0.478
351
P HYP730 Hypogonadotropic Hypogonadism 53 0.478
352
MLY001 Molybdenum Cofactor Deficiency 40 0.478
353
PRT037 Pertussis 65 0.478
354
PRX001 Peroxisomal Disease 46 0.478
355
SCT002 Scotoma 42 0.478
356
P MSC003 Muscular Atrophy 52 0.478
357
P HLP001 Holoprosencephaly 69 0.478
358
URM002 Uremia 47 0.478
359
P RHB003 Rhabdomyosarcoma 66 0.478
360
SPC005 Speech Disorder 45 0.478
361
P HMC002 Homocystinuria 53 0.478
362
CLF001 Cleft Lip 53 0.478
363
INT075 Intracranial Hypertension 53 0.478
364
c PRG011 Progressive Myoclonus Epilepsy 41 0.478
365
MCH006 Mechanical Strabismus 40 0.478
366
CNT015 Central Sleep Apnea 46 0.478
367
CRB001 Cerebral Lymphoma 36 0.478
368
RRG018 Rare Genetic Epilepsy 9 0.478
369
NNT008 Neonatal Abstinence Syndrome 40 0.478
370
P HYP098 Hypereosinophilic Syndrome 66 0.478
371
CRY020 Cryptogenic Late-Onset Epileptic Spasms 9 0.478
372
LWG005 Low-Grade Astrocytoma 38 0.478
373
P MTH008 Methylmalonic Acidemia 52 0.478
374
BNG006 Benign Familial Neonatal Epilepsy 55 0.478
375
P LCT001 Lactic Acidosis 51 0.478
376
ADN018 Adenoma 59 0.478
377
AGR002 Agoraphobia 45 0.478
378
ACT084 Acute Stress Disorder 54 0.478
379
OST012 Osteoarthritis 77 0.478
380
P NGH001 Night Blindness 52 0.478
381
SPP007 Suppression Amblyopia 38 0.478
382
AMB002 Amblyopia 50 0.478
383
RCK004 Rickets 68 0.478
384
ASP007 Aspiration Pneumonia 49 0.478
385
P KLP003 Klippel-Feil Syndrome 47 0.478
386
OST011 Osteomalacia 52 0.478
387
P DMN002 Dementia 66 0.478
388
GT001 Gout 64 0.478
389
P NTR004 Neutropenia 63 0.478
390
P OPT009 Optic Neuritis 57 0.478
391
DYS009 Dysthymic Disorder 52 0.478
392
ATY001 Atypical Depressive Disorder 45 0.478
393
FTS001 Fetishism 24 0.478
394
NRT004 Neuritis 53 0.478
395
P HYP086 Hypothyroidism 69 0.478
396
HYP030 Hypoactive Sexual Desire Disorder 41 0.478
397
P MTC010 Mitochondrial Dna Depletion Syndrome 47 0.478
398
CYT005 Cytomegalovirus Retinitis 50 0.478
399
P HYP040 Hypospadias 51 0.478
400
SPS004 Spastic Quadriplegia 40 0.478
401
VYR001 Voyeurism 21 0.478
402
ASP004 Asphyxia Neonatorum 50 0.478
403
DSS009 Disseminated Intravascular Coagulation 57 0.478
404
VTM033 Vitamin K Deficiency Bleeding 48 0.478
405
HYP043 Hyperandrogenism 48 0.478
406
EXH001 Exhibitionism 25 0.478
407
BRN024 Bronchitis 67 0.478
408
CRB039 Cerebrovascular Disease 66 0.478
409
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.478
410
P OVR046 Ovarian Cyst 46 0.478
411
PRP030 Purpura 54 0.478
412
GNG013 Gingivitis 59 0.478
413
ANP005 Anaplastic Astrocytoma 57 0.478
414
P TCD001 Tic Disorder 49 0.478
415
c GM2006 Gm2 Gangliosidosis 46 0.478
416
UNV001 Unverricht-Lundborg Syndrome 53 0.478
417
PDP001 Pedophilia 29 0.478
418
SCH003 Schizophreniform Disorder 55 0.478
419
TXC008 Toxic Optic Neuropathy 27 0.478
420
SCL003 Social Phobia 48 0.478
421
CHR073 Choreatic Disease 54 0.478
422
GNR004 Generalized Anxiety Disorder 55 0.478
423
PST028 Post-Traumatic Stress Disorder 59 0.478
424
P MNN013 Meningitis 65 0.478
425
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.478
426
SCN067 Scn1a Seizure Disorders 12 0.478
427
TBL023 Tubulinopathies 31 0.478
428
XLN247 X-Linked Congenital Retinoschisis 20 0.478
429
FRS020 Fars2 Deficiency 8 0.478
430
RFR003 Refractive Error 41 0.478
431
P EPS003 Episodic Ataxia 59 0.478
432
HRN003 Heroin Dependence 44 0.478
433
HRP009 Herpes Simplex Encephalitis 58 0.478
434
HYP231 Hypothalamic Hamartomas 35 0.478
435
DPR016 Depression 65 0.478
436
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 0.478
440
P MTC069 Mitochondrial Disorders 57 0.478
441
P CHR345 Chronic Pain 50 0.478
442
ATN005 Autonomic Dysfunction 46 0.478
443
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.478
445
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 0.478
446
P HYP263 Hypersomnia 41 0.478
447
c CNG439 Congenital Lymphedema 30 0.478
448
CDK006 Cdkl5 Deficiency Disorder 30 0.478
449
CYT006 Cytoplasmic Body Myopathy 18 0.478
450
MLN046 Melanoma-Associated Retinopathy 24 0.478
451
P MYC026 Myoclonus Epilepsy 35 0.478
452
OCL024 Ocular Neuromyotonia 12 0.478
453
PST047 Post-Traumatic Epilepsy 20 0.478
454
ALL014 Allergic Encephalomyelitis 34 0.478
455
SBC016 Subacute Delirium 43 0.478
456
PCH002 Pachygyria 32 0.478
457
P GNG009 Gangliosidosis 44 0.478
Content
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