Search results for Oxcarbazepine

240 hits were found for Oxcarbazepine

# Family MCID Name MIFTS Score
1
P SZR006 Seizure Disorder 58 0.407
2
VSL002 Visual Epilepsy 58 0.366
3
P EPL164 Epilepsy 71 0.357
4
FCL014 Focal Epilepsy 54 0.337
5
P BPL003 Bipolar Disorder 56 0.268
6
c MJR024 Major Affective Disorder 9 41 0.268
7
c MJR022 Major Affective Disorder 8 38 0.268
8
P EXN002 Exanthem 57 0.226
9
SVR097 Severe Cutaneous Adverse Reaction 67 0.179
10
ERY003 Erythema Multiforme 57 0.174
11
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.174
12
ERY066 Erythema Multiforme Major 28 0.174
13
TRG002 Trigeminal Neuralgia 60 0.169
14
P MJR007 Major Affective Disorder 1 43 0.155
15
P NRP001 Neuropathy 56 0.149
16
DBT010 Diabetic Neuropathy 55 0.138
17
c MJR008 Major Affective Disorder 2 34 0.132
18
c MJR003 Major Affective Disorder 6 33 0.132
19
c MJR006 Major Affective Disorder 5 33 0.132
20
c MJR023 Major Affective Disorder 7 33 0.132
21
c MJR004 Major Affective Disorder 4 28 0.132
22
P HYP098 Hypereosinophilic Syndrome 66 0.126
23
ALL026 Allergic Hypersensitivity Disease 64 0.126
24
STT001 Status Epilepticus 59 0.126
25
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.126
26
ADL002 Adult Syndrome 69 0.120
27
c PNS012 Paine Syndrome 61 0.113
28
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.113
29
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.113
30
ALC007 Alcohol Dependence 66 0.106
31
DPR016 Depression 63 0.106
32
P NTR004 Neutropenia 63 0.106
33
P ENC018 Encephalopathy 61 0.106
34
SCH012 Schizoaffective Disorder 50 0.106
35
WTH001 Withdrawal Disorder 48 0.106
36
ATX019 Ataxia with Vitamin E Deficiency 48 0.106
37
c MGR028 Migraine with or Without Aura 1 69 0.098
38
PSY004 Psychotic Disorder 67 0.098
39
P ATS364 Autism 65 0.098
40
P TRN020 Turner Syndrome 65 0.098
41
BNG009 Benign Epilepsy with Centrotemporal Spikes 58 0.098
42
MNT002 Mental Depression 57 0.098
43
OCL069 Ocular Motor Apraxia 51 0.098
44
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.098
45
48X005 48,xyyy 39 0.098
46
CHL079 Children's Interstitial Lung Disease 27 0.098
47
P SCH015 Schizophrenia 75 0.089
48
ANX010 Anxiety 72 0.089
49
P MLT020 Multiple Sclerosis 72 0.089
50
P DMN002 Dementia 67 0.089
51
P PRP019 Peripheral Nervous System Disease 57 0.089
52
P PLY019 Polyneuropathy 56 0.089
53
P EPS030 Episodic Kinesigenic Dyskinesia 1 53 0.089
54
P TRM003 Tremor 53 0.089
55
c BPL002 Bipolar I Disorder 49 0.089
56
P CNR004 Cone-Rod Dystrophy 2 71 0.080
57
P KDN018 Kidney Disease 70 0.080
58
KHL003 Kohlschutter-Tonz Syndrome 64 0.080
59
MDD011 Mood Disorder 62 0.080
60
NTR005 Nutritional Deficiency Disease 61 0.080
61
P HDC001 Headache 57 0.080
62
END040 Endogenous Depression 54 0.080
63
NRT001 Neurotic Disorder 52 0.080
64
P TMP001 Temporal Lobe Epilepsy 50 0.080
65
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.080
66
PST053 Postherpetic Neuralgia 42 0.080
67
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.069
68
AST005 Asthma 77 0.069
69
c HPT073 Hepatitis C Virus 70 0.069
70
P THR014 Thrombocytopenia 68 0.069
71
c ATS007 Autism Spectrum Disorder 67 0.069
72
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.069
73
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 63 0.069
74
DSS008 Disease of Mental Health 57 0.069
75
SCH003 Schizophreniform Disorder 56 0.069
76
P DBT005 Diabetes Insipidus 55 0.069
77
CND002 Conduct Disorder 51 0.069
78
P CHR345 Chronic Pain 50 0.069
79
P MYC033 Myoclonus 46 0.069
80
SBC016 Subacute Delirium 44 0.069
81
49X006 49, Xxxxy Syndrome 41 0.069
82
CNT106 Centralopathic Epilepsy 36 0.069
83
CYT018 Cytochrome P450 2d6 Variant 27 0.069
84
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 69 0.056
85
P HYP086 Hypothyroidism 68 0.056
86
OBS002 Obsessive-Compulsive Disorder 68 0.056
87
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.056
88
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.056
89
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.056
90
P HYP069 Hyperparathyroidism 62 0.056
91
P EPL198 Epilepsy, Myoclonic Juvenile 62 0.056
92
P PRP029 Porphyria 62 0.056
93
P EPL140 Epilepsy, Idiopathic Generalized 61 0.056
94
DRM006 Dermatitis 61 0.056
95
ERL001 Early Myoclonic Encephalopathy 61 0.056
96
SPN186 Spinal Cord Injury 60 0.056
97
P PTN014 Patent Ductus Arteriosus 1 60 0.056
98
ETN001 Eating Disorder 59 0.056
99
c ESS001 Essential Tremor 56 0.056
100
P SBS003 Substance Abuse 54 0.056
101
PNC001 Pancytopenia 54 0.056
102
P PNC025 Panic Disorder 53 0.056
103
PTH003 Pathologic Nystagmus 51 0.056
104
SMT006 Somatoform Disorder 51 0.056
105
c SCN007 Secondary Hyperparathyroidism 50 0.056
106
INP001 Inappropriate Adh Syndrome 49 0.056
107
47X002 47,xyy 49 0.056
108
RDC002 Radiculopathy 48 0.056
109
DNT045 Dental Anomalies and Short Stature 48 0.056
110
SMT001 Somatization Disorder 48 0.056
111
DRG024 Drug Allergy 43 0.056
112
PRS063 Paresthesia 43 0.056
113
SPS057 Spasticity 41 0.056
114
NNT008 Neonatal Abstinence Syndrome 38 0.056
115
SNC001 Sunct Headache 23 0.056
116
PRX022 Paroxysmal Choreoathetosis 23 0.056
117
P CLR023 Colorectal Cancer 98 0.040
118
P BRS047 Breast Cancer 96 0.040
119
c HYP595 Hypertension, Essential 84 0.040
120
P GLM040 Glioma Susceptibility 1 81 0.040
121
INS024 Insulin-Like Growth Factor I 79 0.040
122
c ART115 Aortic Valve Disease 1 75 0.040
123
DFC004 Deficiency Anemia 75 0.040
124
GLB015 Glioblastoma Multiforme 75 0.040
125
P APL001 Aplastic Anemia 74 0.040
126
END057 Endometrial Cancer 74 0.040
127
BRN028 Brain Cancer 73 0.040
128
P NRB001 Neuroblastoma 71 0.040
129
WLS001 Wilson Disease 70 0.040
130
RCK004 Rickets 69 0.040
131
P OLG002 Oligodendroglioma 67 0.040
132
P HPT021 Hepatitis 67 0.040
133
P PRP003 Porphyria Cutanea Tarda 67 0.040
134
FCT007 Factor Vii Deficiency 66 0.040
135
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.040
136
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.040
137
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.040
138
P DYS154 Dystonia 65 0.040
139
P PRS038 Personality Disorder 65 0.040
140
P DBT009 Diabetes Mellitus 64 0.040
141
NRM005 Neuromuscular Disease 63 0.040
142
P GLM045 Glioma 63 0.040
143
c HPT001 Hepatitis C 63 0.040
144
P HML002 Hemolytic Anemia 62 0.040
145
c FNC043 Fanconi Anemia, Complementation Group E 62 0.040
146
TXC005 Toxic Shock Syndrome 61 0.040
147
P MVM001 Movement Disease 61 0.040
148
HYP066 Hyperglycemia 61 0.040
149
P LPS004 Lupus Erythematosus 61 0.040
150
P ATR010 Atrial Heart Septal Defect 60 0.040
151
WST001 West Syndrome 60 0.040
152
HYD002 Hydronephrosis 59 0.040
153
P BND020 Bone Disease 59 0.040
154
GRD007 Grade Iii Astrocytoma 59 0.040
155
P PRD006 Prader-Willi Syndrome 59 0.040
156
ADN018 Adenoma 58 0.040
157
CMP010 Complex Regional Pain Syndrome 58 0.040
158
P INF032 Infertility 57 0.040
159
VSC002 Vascular Dementia 57 0.040
160
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.040
161
P ALP008 Alopecia 56 0.040
162
P MLN007 Male Infertility 56 0.040
163
PTN001 Patent Foramen Ovale 56 0.040
164
PRP030 Purpura 55 0.040
165
TRD006 Tardive Dyskinesia 55 0.040
166
NRL004 Neuroleptic Malignant Syndrome 55 0.040
167
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.040
168
P MYP006 Myopia 55 0.040
169
P ANT006 Antiphospholipid Syndrome 54 0.040
170
HYP060 Hyperinsulinism 54 0.040
171
GLS001 Gliosarcoma 54 0.040
172
P RST001 Restless Legs Syndrome 54 0.040
173
P ANG015 Angioedema 54 0.040
174
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.040
175
SNS003 Sensory Peripheral Neuropathy 53 0.040
176
BRD004 Borderline Personality Disorder 53 0.040
177
TRM010 Traumatic Brain Injury 53 0.040
178
IMP005 Impotence 52 0.040
179
GNT002 Giant Cell Glioblastoma 52 0.040
181
MYL001 Myelitis 51 0.040
182
P FBR031 Febrile Seizures 51 0.040
183
SPP010 Suppressor of Tumorigenicity 3 51 0.040
184
PNG002 Pain Agnosia 51 0.040
185
c ACT134 Acute Liver Failure 51 0.040
186
c PRM108 Primary Progressive Multiple Sclerosis 51 0.040
187
HRT011 Heart Septal Defect 50 0.040
188
P AST007 Astrocytoma 50 0.040
189
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.040
190
TRC010 Trichotillomania 50 0.040
191
LRN003 Learning Disability 49 0.040
192
CRY004 Cryoglobulinemia 49 0.040
193
BNR002 Bone Resorption Disease 48 0.040
194
HYP043 Hyperandrogenism 48 0.040
195
CCN002 Cocaine Abuse 48 0.040
196
SXL003 Sexual Disorder 48 0.040
197
P JVN007 Juvenile Absence Epilepsy 48 0.040
198
P ATS011 Autosomal Dominant Nocturnal Frontal Lobe Epilepsy 48 0.040
199
FCL012 Facial Paralysis 48 0.040
200
P NRV006 Nervous System Cancer 48 0.040
201
DYS009 Dysthymic Disorder 48 0.040
202
PRP007 Priapism 48 0.040
203
SPC010 Speech and Communication Disorders 47 0.040
204
P ERY008 Erythromelalgia 47 0.040
205
SRT004 Serotonin Syndrome 46 0.040
206
INT067 Interstitial Nephritis 46 0.040
207
c CNT033 Central Nervous System Cancer 46 0.040
208
P TRN034 Transverse Myelitis 46 0.040
209
GLL048 Glial Tumor 45 0.040
210
c MLG068 Malignant Glioma 45 0.040
211
MXD026 Mixed Glioma 45 0.040
212
GRN017 Granulocytopenia 44 0.040
213
PRM003 Premature Ejaculation 44 0.040
214
c PRM038 Primary Agammaglobulinemia 43 0.040
215
ANP009 Anaplastic Oligodendroglioma 43 0.040
216
BSL009 Basal Ganglia Calcification 41 0.040
217
RDN001 Reading Disorder 40 0.040
218
c EPL133 Epilepsy, Juvenile Absence 1 39 0.040
219
MLN003 Melancholia 39 0.040
220
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 39 0.040
221
OCL066 Oculogyric Crisis 38 0.040
222
P CRB088 Cerebral Atrophy 38 0.040
223
OLG006 Oligoastrocytoma 35 0.040
224
FXD003 Fixed Drug Eruption 35 0.040
225
c ADL008 Adult Oligodendroglioma 35 0.040
227
PHN011 Phenytoin Toxicity 33 0.040
228
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.040
229
GLS004 Glossopharyngeal Neuralgia 33 0.040
230
RRS014 Rare Surgical Neurologic Disease 32 0.040
231
ANP008 Anaplastic Oligoastrocytoma 30 0.040
232
PRG074 Progressive Myoclonus Epilepsy, Lafora Type 29 0.040
233
PRR019 Perioral Myoclonia with Absences 28 0.040
234
EXF003 Exfoliative Dermatitis 27 0.040
235
EXT059 External Auditory Canal, Bilateral Atresia of, with Congenital Vertical Talus 27 0.040
236
ANT078 Antipyrine Metabolism 24 0.040
237
JVN026 Jeavons Syndrome 24 0.040
238
NTL003 Notalgia Paresthetica 20 0.040
239
RSM003 Rasmussen Subacute Encephalitis 19 0.040
240
RSM002 Rasmussen Johnsen Thomsen Syndrome 17 0.040
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