Search results for Alogliptin

101 hits were found for Alogliptin

# Family MCID Name MIFTS Score
1
P DBT009 Diabetes Mellitus 64 0.611
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.601
3
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.519
4
HYP056 Hypoglycemia 66 0.413
5
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.259
6
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.259
7
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.259
8
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.259
9
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.259
10
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.259
11
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.259
12
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.259
13
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.259
14
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.259
15
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.259
16
GST033 Gestational Diabetes 61 0.248
17
LPD008 Lipid Metabolism Disorder 62 0.243
18
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.231
19
HYP066 Hyperglycemia 61 0.218
20
ISC004 Ischemia 58 0.212
21
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.176
22
ATH013 Atherosclerosis Susceptibility 65 0.150
23
HYP060 Hyperinsulinism 54 0.150
24
STR067 Stroke, Ischemic 81 0.140
25
P KDN018 Kidney Disease 72 0.140
26
CRB039 Cerebrovascular Disease 67 0.140
27
c DBT099 Diabetes Mellitus, Type I 65 0.140
28
GLC003 Glucose Intolerance 54 0.140
29
P MYC007 Myocardial Infarction 70 0.118
30
P LVR013 Liver Disease 68 0.118
31
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.118
32
P CRD246 Cardiovascular System Disease 57 0.118
33
INT007 Intermediate Coronary Syndrome 55 0.118
34
c MCR113 Microvascular Complications of Diabetes 3 52 0.118
35
c MCR120 Microvascular Complications of Diabetes 7 47 0.118
36
c MCR130 Microvascular Complications of Diabetes 6 41 0.118
37
c MCR133 Microvascular Complications of Diabetes 4 41 0.118
38
GLC008 Glucose Metabolism Disease 40 0.118
39
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.118
40
P TRN020 Turner Syndrome 67 0.106
41
LPP008 Lipoprotein Quantitative Trait Locus 62 0.106
42
NTR005 Nutritional Deficiency Disease 62 0.106
43
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.106
44
FTT001 Fatty Liver Disease 61 0.106
45
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.106
46
P NRP001 Neuropathy 56 0.106
47
NNL006 Non-Alcoholic Steatohepatitis 54 0.106
48
END086 End Stage Renal Disease 51 0.106
49
NSP002 Nasopharyngitis 43 0.106
50
PRP027 Peripheral Vascular Disease 71 0.092
51
ADL002 Adult Syndrome 70 0.092
52
P VSC007 Vascular Disease 63 0.092
53
c ACT027 Acute Pancreatitis 60 0.092
54
P PLY011 Polycystic Ovary Syndrome 56 0.092
55
AGN016 Aging 56 0.092
56
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.092
57
HYP081 Hypolipoproteinemia 51 0.092
58
P END084 Endocrine System Disease 45 0.092
59
c PLY105 Polycystic Ovary Syndrome 1 38 0.092
60
P PNC035 Pancreatic Cancer 84 0.075
61
c CHR684 Chronic Kidney Disease 70 0.075
62
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.075
63
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.075
64
BLL006 Bullous Pemphigoid 62 0.075
65
P CTR002 Cataract 60 0.075
66
CNS004 Constipation 58 0.075
67
c ACT075 Acute Myocardial Infarction 57 0.075
68
AYM001 Ayme-Gripp Syndrome 57 0.075
69
48X005 48,xyyy 39 0.075
70
P VSC018 Visceral Steatosis 33 0.075
71
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.075
72
P HPT023 Hepatocellular Carcinoma 100 0.053
73
P HRT032 Heart Disease 75 0.053
74
SVR004 Severe Combined Immunodeficiency 73 0.053
75
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.053
76
CNG034 Congestive Heart Failure 69 0.053
77
SVR097 Severe Cutaneous Adverse Reaction 69 0.053
78
ART016 Aortic Aneurysm 69 0.053
79
c MCR129 Microvascular Complications of Diabetes 1 66 0.053
80
P MTR004 Maturity-Onset Diabetes of the Young 65 0.053
81
c ACT068 Acute Cystitis 63 0.053
82
P ENC018 Encephalopathy 61 0.053
83
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.053
84
HPT019 Hepatic Encephalopathy 60 0.053
85
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.053
86
ERY003 Erythema Multiforme 58 0.053
87
P PRP019 Peripheral Nervous System Disease 58 0.053
88
P EXN002 Exanthem 57 0.053
89
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.053
90
P ANG015 Angioedema 57 0.053
91
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.053
92
CRN030 Coronary Stenosis 50 0.053
93
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.053
94
SYN036 Syncope 45 0.053
95
HPT004 Hepatic Coma 45 0.053
96
CRB004 Cerebral Artery Occlusion 45 0.053
97
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.053
98
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.053
99
FRN014 Fournier Gangrene 37 0.053
100
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.053
101
ERY066 Erythema Multiforme Major 30 0.053
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