Search results for Eslicarbazepine acetate

109 hits were found for Eslicarbazepine acetate

# Family MCID Name MIFTS Score
1
P SZR006 Seizure Disorder 70 30.834
2
P EPL164 Epilepsy 68 30.561
3
FCL014 Focal Epilepsy 53 21.483
4
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 12.467
5
ALL029 Allergic Disease 59 11.726
6
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 11.287
7
P NRB001 Neuroblastoma 66 11.276
8
END086 End Stage Renal Disease 52 9.740
9
P EXN002 Exanthem 58 9.611
10
AGN016 Aging 54 8.928
11
GLL048 Glial Tumor 52 8.572
12
GLM045 Glioma 63 8.512
13
GLB002 Glioblastoma 67 8.488
14
VSL002 Visual Epilepsy 39 8.359
15
LPD008 Lipid Metabolism Disorder 62 8.289
16
c MGR028 Migraine with or Without Aura 1 64 7.967
17
CRH001 Crohn's Disease 80 7.841
18
DBT010 Diabetic Neuropathy 54 7.705
19
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 7.702
20
c MJR022 Major Affective Disorder 8 38 7.636
21
c MJR024 Major Affective Disorder 9 41 7.636
22
P BPL003 Bipolar Disorder 56 7.636
23
P ANR048 Aniridia 1 64 7.521
24
MNN043 Meningioma, Familial 79 7.357
25
SCR001 Secretory Meningioma 40 7.357
26
LYM002 Lymphoplasmacyte-Rich Meningioma 35 7.357
27
SPN021 Spinal Meningioma 50 7.357
28
P NRP001 Neuropathy 60 7.055
29
c BPL002 Bipolar I Disorder 47 6.788
30
P GLM040 Glioma Susceptibility 1 71 6.583
31
INT323 Intraocular Pressure Quantitative Trait Locus 64 6.541
32
P LVR013 Liver Disease 69 6.282
33
IMP005 Impotence 52 6.265
34
P BND020 Bone Disease 59 6.206
35
P TRM003 Tremor 48 6.184
36
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 6.139
37
ADL002 Adult Syndrome 70 6.139
38
P HYP086 Hypothyroidism 69 6.017
39
AND005 Androgen Insensitivity Syndrome, Mild 21 6.014
40
P HDC001 Headache 57 5.980
41
P CHR345 Chronic Pain 50 5.890
42
P HYP098 Hypereosinophilic Syndrome 66 5.707
43
P ENC018 Encephalopathy 62 5.521
44
P MCR129 Microvascular Complications of Diabetes 1 68 5.389
45
MLG169 Malignant Astrocytoma 57 5.326
46
TRG002 Trigeminal Neuralgia 61 5.172
47
P TMP001 Temporal Lobe Epilepsy 49 5.103
48
FBR047 Fibromyalgia 58 5.045
49
NSP002 Nasopharyngitis 45 4.989
50
P HPT021 Hepatitis 69 4.896
51
P HYP750 Hypertriglyceridemia, Familial 62 4.806
52
c EPS039 Episodic Pain Syndrome, Familial, 1 42 4.788
53
c PNS012 Paine Syndrome 60 4.760
54
P NRV007 Nervous System Disease 67 4.737
55
PST053 Postherpetic Neuralgia 40 4.724
56
MDD011 Mood Disorder 62 4.450
57
c ACT134 Acute Liver Failure 59 4.441
58
OCL069 Ocular Motor Apraxia 57 4.154
59
P CRD119 Cardiac Arrest 67 4.015
60
P PRP029 Porphyria 60 3.986
61
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 3.983
62
P THY032 Thyroiditis 57 3.975
63
STT001 Status Epilepticus 59 3.869
64
LNN001 Lennox-Gastaut Syndrome 61 3.692
65
DBT002 Diabetic Autonomic Neuropathy 41 3.667
66
c HPT003 Hepatitis a 63 3.462
67
P OLG002 Oligodendroglioma 66 3.447
68
CLF027 Cleft Palate, Isolated 64 3.431
69
ERL001 Early Myoclonic Encephalopathy 62 3.373
70
P PRK039 Parkinsonism 55 3.366
71
P MVM001 Movement Disease 61 3.355
72
APH002 Aphasia 56 3.247
73
P MYC033 Myoclonus 47 3.205
74
ERY003 Erythema Multiforme 56 3.162
75
TRM010 Traumatic Brain Injury 51 3.096
76
STR067 Stroke, Ischemic 80 3.091
77
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 3.031
78
P DYS154 Dystonia 64 3.029
79
HMP009 Haemophilus Influenzae 41 2.952
80
JPN002 Japanese Encephalitis 61 2.864
81
P HYP040 Hypospadias 51 2.817
82
DRV001 Dravet Syndrome 69 2.803
83
P TBR001 Tuberous Sclerosis 69 2.512
84
P EPL198 Epilepsy, Myoclonic Juvenile 61 2.493
85
MYF002 Myofascial Pain Syndrome 46 2.408
86
ERY066 Erythema Multiforme Major 29 2.380
87
OST011 Osteomalacia 52 2.284
88
ATR057 Atrioventricular Block 54 2.151
89
GLS004 Glossopharyngeal Neuralgia 33 2.029
90
CRN309 Cranial Neuralgia 21 1.916
91
PRP083 Porphyria, Acute Intermittent 65 1.832
92
PTH003 Pathologic Nystagmus 52 1.795
93
P TCD001 Tic Disorder 49 1.759
94
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 1.712
95
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.691
96
CLF001 Cleft Lip 53 1.691
97
c MYC068 Myoclonic Epilepsy of Infancy 34 1.560
98
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.527
99
SVR097 Severe Cutaneous Adverse Reaction 69 1.483
100
LRN003 Learning Disability 49 1.342
101
DRG024 Drug Allergy 40 1.289
102
TLR001 Tularemia 56 1.289
103
PHT008 Photosensitive Epilepsy 42 1.264
104
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 45 1.210
105
SCH012 Schizoaffective Disorder 50 1.166
106
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 1.007
107
ANN002 Anencephaly 57 0.894
108
WST001 West Syndrome 59 0.894
109
GNR004 Generalized Anxiety Disorder 55 0.830
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