Search results for Eslicarbazepine

119 hits were found for Eslicarbazepine

# Family MCID Name MIFTS Score
1
P EPL164 Epilepsy 68 20.917
2
P SZR006 Seizure Disorder 70 20.249
3
FCL014 Focal Epilepsy 53 14.912
4
VSL002 Visual Epilepsy 39 5.460
5
c MJR022 Major Affective Disorder 8 38 4.547
6
c MJR024 Major Affective Disorder 9 41 4.547
7
P BPL003 Bipolar Disorder 56 4.547
8
c BPL002 Bipolar I Disorder 47 4.472
9
P EXN002 Exanthem 58 4.471
10
DBT010 Diabetic Neuropathy 54 4.012
11
P TMP001 Temporal Lobe Epilepsy 49 3.658
12
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 3.650
13
c MGR028 Migraine with or Without Aura 1 64 3.455
14
TRG002 Trigeminal Neuralgia 61 3.394
15
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.389
16
P NRB001 Neuroblastoma 66 2.908
17
AND005 Androgen Insensitivity Syndrome, Mild 21 2.860
18
ADL002 Adult Syndrome 70 2.831
19
FBR047 Fibromyalgia 58 2.815
20
LNN001 Lennox-Gastaut Syndrome 61 2.710
21
CRH001 Crohn's Disease 80 2.653
22
ERL001 Early Myoclonic Encephalopathy 62 2.632
23
NSP002 Nasopharyngitis 45 2.575
24
P MCR129 Microvascular Complications of Diabetes 1 68 2.449
25
P ANR048 Aniridia 1 64 2.449
26
P NRP001 Neuropathy 60 2.449
27
DBT002 Diabetic Autonomic Neuropathy 41 2.449
28
ALL029 Allergic Disease 59 2.437
29
DRV001 Dravet Syndrome 69 2.332
30
LPD008 Lipid Metabolism Disorder 62 2.332
31
P HYP086 Hypothyroidism 69 2.230
32
END086 End Stage Renal Disease 52 2.189
33
P HDC001 Headache 57 2.185
34
P HYP098 Hypereosinophilic Syndrome 66 2.018
35
c PNS012 Paine Syndrome 60 1.912
36
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.912
37
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.912
38
PST053 Postherpetic Neuralgia 40 1.912
39
P NRV007 Nervous System Disease 67 1.912
40
P CRD119 Cardiac Arrest 67 1.909
41
P EPL198 Epilepsy, Myoclonic Juvenile 61 1.865
42
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.821
43
GLB002 Glioblastoma 67 1.821
44
ERY066 Erythema Multiforme Major 29 1.563
45
ERY003 Erythema Multiforme 56 1.563
46
MNN043 Meningioma, Familial 79 1.545
47
P TRM003 Tremor 48 1.545
48
SCR001 Secretory Meningioma 40 1.545
49
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.545
50
SPN021 Spinal Meningioma 50 1.545
51
STT001 Status Epilepticus 59 1.523
52
P CHR345 Chronic Pain 50 1.523
53
CRN309 Cranial Neuralgia 21 1.288
54
c MYC068 Myoclonic Epilepsy of Infancy 34 1.288
55
c ACT134 Acute Liver Failure 59 1.288
56
STR067 Stroke, Ischemic 80 1.288
57
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.288
58
APH002 Aphasia 56 1.288
59
PRP083 Porphyria, Acute Intermittent 65 1.288
60
P HYP750 Hypertriglyceridemia, Familial 62 1.288
61
P GLM040 Glioma Susceptibility 1 71 1.288
62
P PRK039 Parkinsonism 55 1.288
63
P DYS154 Dystonia 64 1.288
64
P MVM001 Movement Disease 61 1.288
65
GLL048 Glial Tumor 52 1.288
66
P LVR013 Liver Disease 69 1.288
67
P OLG002 Oligodendroglioma 66 1.288
68
DFF016 Diffuse Astrocytoma 45 1.288
69
IMP005 Impotence 52 1.288
70
MLG169 Malignant Astrocytoma 57 1.288
71
P BND020 Bone Disease 59 1.288
72
P TCD001 Tic Disorder 49 1.288
73
MDD011 Mood Disorder 62 1.288
74
P PRP029 Porphyria 60 1.288
75
GLS004 Glossopharyngeal Neuralgia 33 1.288
76
P MYC033 Myoclonus 47 1.288
77
GLM045 Glioma 63 1.288
78
MYF002 Myofascial Pain Syndrome 46 1.270
79
P JVN007 Juvenile Absence Epilepsy 47 1.243
80
c EPL133 Epilepsy, Juvenile Absence 1 46 1.243
81
P CHL002 Childhood Absence Epilepsy 63 1.243
82
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.942
83
MSL004 Mesial Temporal Lobe Epilepsy with Hippocampal Sclerosis 26 0.879
84
SNC001 Sunct Headache 28 0.879
85
PHT008 Photosensitive Epilepsy 42 0.879
86
P TBR001 Tuberous Sclerosis 69 0.879
87
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.666
88
SVR097 Severe Cutaneous Adverse Reaction 69 0.666
89
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 0.666
90
P EPL140 Epilepsy, Idiopathic Generalized 62 0.622
91
ANN002 Anencephaly 57 0.622
92
CLF027 Cleft Palate, Isolated 64 0.622
93
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.622
94
ATR057 Atrioventricular Block 54 0.622
95
WST001 West Syndrome 59 0.622
96
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.622
97
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.622
98
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.622
99
OCL069 Ocular Motor Apraxia 57 0.622
100
DRG024 Drug Allergy 40 0.622
101
TRM010 Traumatic Brain Injury 51 0.622
102
SCH012 Schizoaffective Disorder 50 0.622
103
CLF001 Cleft Lip 53 0.622
104
LRN003 Learning Disability 49 0.622
105
P SKL005 Skull Base Meningioma 27 0.622
106
OST011 Osteomalacia 52 0.622
107
P HYP040 Hypospadias 51 0.622
108
JPN002 Japanese Encephalitis 61 0.622
109
LTR003 Lateral Medullary Syndrome 36 0.622
110
GNR004 Generalized Anxiety Disorder 55 0.622
111
TLR001 Tularemia 56 0.622
112
PTH003 Pathologic Nystagmus 52 0.622
113
P ENC018 Encephalopathy 62 0.622
114
EPL230 Epilepsy with Myoclonic-Atonic Seizures 23 0.622
115
HMP009 Haemophilus Influenzae 41 0.622
116
AGN016 Aging 54 0.616
117
c HPT003 Hepatitis a 63 0.616
118
P THY032 Thyroiditis 57 0.616
119
P HPT021 Hepatitis 69 0.616
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