Search results for Carbenoxolone

84 hits were found for Carbenoxolone

# Family MCID Name MIFTS Score
1
GST023 Gastric Ulcer 53 0.423
2
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.331
3
P DDN001 Duodenal Ulcer 52 0.331
4
PPT005 Peptic Ulcer Disease 59 0.257
5
HYP005 Hypokalemia 55 0.137
6
ISC004 Ischemia 58 0.125
7
VSL002 Visual Epilepsy 59 0.112
8
P SZR006 Seizure Disorder 56 0.112
9
P GST044 Gastritis 56 0.112
10
HYP060 Hyperinsulinism 54 0.112
11
P EPL164 Epilepsy 71 0.097
12
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.097
13
P MYP004 Myopathy 70 0.097
14
P HRP006 Herpes Simplex 65 0.097
15
ALL026 Allergic Hypersensitivity Disease 62 0.097
16
BRN071 Brain Injury 49 0.097
17
CRB004 Cerebral Artery Occlusion 45 0.097
18
GLB015 Glioblastoma Multiforme 75 0.079
19
P NRB001 Neuroblastoma 72 0.079
20
P GLM045 Glioma 63 0.079
21
ATM095 Autoimmune Disease 62 0.079
22
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.079
23
APP015 Apparent Mineralocorticoid Excess 58 0.079
24
TRM010 Traumatic Brain Injury 51 0.079
25
P TMP001 Temporal Lobe Epilepsy 50 0.079
26
GLL048 Glial Tumor 45 0.079
27
P PSD003 Pseudohypoaldosteronism 44 0.079
28
P MYG005 Myoglobinuria 44 0.079
29
ALL014 Allergic Encephalomyelitis 38 0.079
30
ADG002 Audiogenic Seizures 25 0.079
31
P CLR023 Colorectal Cancer 99 0.056
32
P GST053 Gastric Cancer 83 0.056
33
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.056
34
c HYP836 Hypercholesterolemia, Familial, 1 73 0.056
35
ULC004 Ulcerative Colitis 73 0.056
36
P KDN018 Kidney Disease 72 0.056
37
P MLT020 Multiple Sclerosis 72 0.056
38
P SRC025 Sarcoidosis 1 70 0.056
39
P HYP098 Hypereosinophilic Syndrome 67 0.056
40
TTN003 Tetanus 65 0.056
41
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.056
42
P ADN016 Adenocarcinoma 64 0.056
43
P MVM001 Movement Disease 63 0.056
44
TRN015 Transient Cerebral Ischemia 63 0.056
45
DPR016 Depression 63 0.056
46
CLT003 Colitis 62 0.056
47
P HYP750 Hypertriglyceridemia, Familial 62 0.056
48
P ESP024 Esophagitis 62 0.056
49
FTT001 Fatty Liver Disease 61 0.056
50
SPN186 Spinal Cord Injury 60 0.056
51
c LPM012 Lipomatosis, Multiple 60 0.056
52
STT001 Status Epilepticus 60 0.056
53
c ACT071 Acute Kidney Failure 60 0.056
54
P CYS018 Cystitis 59 0.056
55
P GLL022 Guillain-Barre Syndrome 59 0.056
56
P DNG005 Dengue Virus 59 0.056
57
ADN018 Adenoma 59 0.056
58
P PLY017 Polyarteritis Nodosa 58 0.056
59
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.056
60
c ESS001 Essential Tremor 56 0.056
61
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.056
62
GNT003 Genital Herpes 54 0.056
63
GLC003 Glucose Intolerance 54 0.056
64
P TRM003 Tremor 54 0.056
65
DMY004 Demyelinating Disease 52 0.056
66
PPT001 Peptic Esophagitis 52 0.056
67
PNG002 Pain Agnosia 51 0.056
68
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.056
69
STM007 Stomatitis 50 0.056
70
P ATR005 Atrophic Gastritis 50 0.056
71
VCC001 Vaccinia 49 0.056
72
GLC106 Glucocorticoid Resistance, Generalized 48 0.056
73
DRY001 Dry Eye Syndrome 47 0.056
74
STM006 Stomach Disease 47 0.056
75
ACT003 Acute Kidney Tubular Necrosis 45 0.056
76
P CHR345 Chronic Pain 44 0.056
77
PTT037 Pituitary Tumors 44 0.056
78
PLM005 Pleomorphic Lipoma 40 0.056
79
BLR002 Bile Reflux 39 0.056
80
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.056
81
BLN010 Balanitis 37 0.056
82
GNT167 Genetic Obesity 33 0.056
83
GST039 Gastroduodenitis 31 0.056
84
c RNG024 Ring Chromosome 8 26 0.056
Content
Loading form....