Search results for Glimepiride

156 hits were found for Glimepiride

# Family MCID Name MIFTS Score
1
OBS288 Obsolete: Glimepiride Toxicity 1 2.854
2
P OBS318 Obsolete: Susceptibility to Hypoglycemia Due to Glimepiride Treatment 1 2.854
3
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.931
4
P DBT009 Diabetes Mellitus 66 0.885
5
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 61 0.854
6
HYP056 Hypoglycemia 68 0.703
7
HYP066 Hyperglycemia 63 0.296
8
LPD008 Lipid Metabolism Disorder 64 0.225
9
P TRN020 Turner Syndrome 66 0.198
10
ATH013 Atherosclerosis Susceptibility 68 0.192
11
P CRN018 Coronary Artery Anomaly 67 0.192
12
P HYP724 Hyperlipoproteinemia, Type Iii 74 0.180
13
P KDN018 Kidney Disease 73 0.180
14
P CRN300 Coronary Heart Disease 1 59 0.180
15
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 0.180
16
c RHB024 Rhabdomyosarcoma 2 64 0.173
17
HYP081 Hypolipoproteinemia 51 0.173
18
ADL002 Adult Syndrome 62 0.166
19
c LPD015 Lipodystrophy, Familial Partial, Type 2 60 0.159
20
GLC003 Glucose Intolerance 55 0.159
21
P MYC007 Myocardial Infarction 74 0.152
22
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 82 0.144
23
P HRT032 Heart Disease 78 0.144
24
CNG034 Congestive Heart Failure 69 0.144
25
P DBT085 Diabetes Mellitus, Insulin-Dependent 68 0.144
26
48X005 48,xyyy 37 0.144
27
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.136
28
ART140 Arteries, Anomalies of 60 0.136
29
c MCR113 Microvascular Complications of Diabetes 3 55 0.136
30
c MCR120 Microvascular Complications of Diabetes 7 48 0.136
31
c BDY007 Body Mass Index Quantitative Trait Locus 1 43 0.136
32
c MCR130 Microvascular Complications of Diabetes 6 42 0.136
33
c MCR133 Microvascular Complications of Diabetes 4 42 0.136
34
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.136
35
CRB039 Cerebrovascular Disease 71 0.127
36
ISC004 Ischemia 62 0.127
37
P NRP001 Neuropathy 57 0.127
38
STR067 Stroke, Ischemic 82 0.118
39
c HYP595 Hypertension, Essential 87 0.107
40
P MCR115 Microvascular Complications of Diabetes 5 67 0.107
41
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 62 0.107
42
INS001 Insulinoma 60 0.107
43
END030 End Stage Renal Failure 60 0.107
44
THR024 Thrombosis 58 0.107
45
CYT002 Cytokine Deficiency 46 0.107
46
ATX019 Ataxia with Vitamin E Deficiency 46 0.107
47
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 36 0.107
48
P BDY004 Body Mass Index Quantitative Trait Locus 11 78 0.096
49
PRP027 Peripheral Vascular Disease 72 0.096
50
P HPT021 Hepatitis 69 0.096
51
c MCR129 Microvascular Complications of Diabetes 1 67 0.096
52
P MTR004 Maturity-Onset Diabetes of the Young 66 0.096
53
P VSC007 Vascular Disease 65 0.096
54
MSC007 Muscle Hypertrophy 65 0.096
55
c ACT068 Acute Cystitis 63 0.096
56
P CTR002 Cataract 62 0.096
57
c FML035 Familial Hyperlipidemia 56 0.096
58
HYP060 Hyperinsulinism 55 0.096
59
P DRR001 Diarrhea 55 0.096
60
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.096
61
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 54 0.096
62
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.096
63
c BDY021 Body Mass Index Quantitative Trait Locus 20 50 0.096
64
c BDY005 Body Mass Index Quantitative Trait Locus 9 49 0.096
65
PRD004 Prediabetes Syndrome 49 0.096
66
c BDY010 Body Mass Index Quantitative Trait Locus 4 48 0.096
67
c BDY015 Body Mass Index Quantitative Trait Locus 12 48 0.096
68
c BDY019 Body Mass Index Quantitative Trait Locus 18 48 0.096
69
c BDY011 Body Mass Index Quantitative Trait Locus 10 47 0.096
70
c BDY017 Body Mass Index Quantitative Trait Locus 14 46 0.096
71
c BDY006 Body Mass Index Quantitative Trait Locus 8 45 0.096
72
c BDY012 Body Mass Index Quantitative Trait Locus 7 45 0.096
73
DWN001 Down Syndrome 70 0.083
74
ANG054 Angina Pectoris 66 0.083
75
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.083
76
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.083
77
P HYP750 Hypertriglyceridemia, Familial 62 0.083
78
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.083
79
NTR005 Nutritional Deficiency Disease 61 0.083
80
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 61 0.083
81
P FTT008 Fatty Liver Disease, Nonalcoholic 1 58 0.083
82
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.083
83
MCL006 Macular Retinal Edema 52 0.083
84
PRP080 Peripheral Artery Disease 51 0.083
85
MCL027 Macular Dystrophy, Dominant Cystoid 47 0.083
86
DBT006 Diabetic Macular Edema 46 0.083
87
MNG006 Monogenic Diabetes 45 0.083
88
c MCR112 Microvascular Complications of Diabetes 2 42 0.083
89
RDN001 Reading Disorder 42 0.083
90
RTN004 Retinal Microaneurysm 41 0.083
91
P LVR013 Liver Disease 71 0.068
92
c FNC043 Fanconi Anemia, Complementation Group E 64 0.068
93
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 63 0.068
94
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.068
95
FTT001 Fatty Liver Disease 63 0.068
96
TRN015 Transient Cerebral Ischemia 62 0.068
97
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.068
98
P PNC044 Pancreatitis 61 0.068
99
PRT058 Pure Autonomic Failure 60 0.068
100
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.068
101
INT002 Intermittent Claudication 60 0.068
102
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 0.068
103
P EXN002 Exanthem 58 0.068
104
INT007 Intermediate Coronary Syndrome 58 0.068
105
P PRN023 Prion Disease 57 0.068
106
c VRL010 Viral Hepatitis 56 0.068
107
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 56 0.068
108
HYP005 Hypokalemia 55 0.068
109
NNL006 Non-Alcoholic Steatohepatitis 53 0.068
110
DYS014 Dyspepsia 51 0.068
111
LMB062 Limb Ischemia 50 0.068
112
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 49 0.068
113
GLC008 Glucose Metabolism Disease 47 0.068
114
DMP001 Dumping Syndrome 44 0.068
115
SYN046 Syndrome of Inappropriate Antidiuretic Hormone 44 0.068
116
ATN004 Autonomic Neuropathy 43 0.068
117
c HYP555 Hypertriglyceridemia, Transient Infantile 38 0.068
118
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.068
119
c DRR009 Diarrhea 6 32 0.068
120
c CHR465 Chronic Diarrhea Due to Guanylate Cyclase 2c Overactivity 21 0.068
121
P HPT023 Hepatocellular Carcinoma 99 0.048
122
P PNC035 Pancreatic Cancer 86 0.048
123
AST005 Asthma 80 0.048
124
P BLD134 Bladder Cancer 79 0.048
125
ANX010 Anxiety 75 0.048
126
c HYP836 Hypercholesterolemia, Familial, 1 74 0.048
127
LPT014 Leptin Deficiency or Dysfunction 72 0.048
128
P HYP098 Hypereosinophilic Syndrome 67 0.048
129
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.048
130
P SKN015 Skin Carcinoma 67 0.048
131
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 65 0.048
132
P OCL013 Oculodentodigital Dysplasia 65 0.048
133
P VSC011 Vasculitis 64 0.048
134
CHL068 Cholestasis 61 0.048
135
c ACT027 Acute Pancreatitis 60 0.048
136
P HDC001 Headache 59 0.048
137
CNS004 Constipation 59 0.048
138
AGN016 Aging 58 0.048
139
c LKM060 Leukemia, Acute Lymphoblastic 3 57 0.048
140
PRP030 Purpura 56 0.048
141
P ART021 Arteriosclerosis 56 0.048
142
P LCH002 Lichen Planus 55 0.048
143
HMC014 Homocysteinemia 54 0.048
144
P HMC002 Homocystinuria 52 0.048
145
BNR002 Bone Resorption Disease 51 0.048
146
HYP080 Hypogonadism 51 0.048
147
CRD137 Cardiogenic Shock 50 0.048
148
47X002 47,xyy 49 0.048
149
THR013 Thoracic Outlet Syndrome 49 0.048
150
ART004 Aortic Atherosclerosis 47 0.048
151
c HYP272 Hypercholesterolemia, Familial, 3 44 0.048
152
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 44 0.048
153
TRP009 Triple X Syndrome 42 0.048
154
HYP064 Hypogonadotropism 40 0.048
155
CRB004 Cerebral Artery Occlusion 38 0.048
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