Search results for Acarbose

187 hits were found for Acarbose

# Family MCID Name MIFTS Score
1
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.601
2
P DBT009 Diabetes Mellitus 64 0.511
3
HYP056 Hypoglycemia 66 0.395
4
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.388
5
HYP066 Hyperglycemia 61 0.383
6
GLC003 Glucose Intolerance 54 0.247
7
HYP060 Hyperinsulinism 54 0.195
8
P DRR001 Diarrhea 57 0.190
9
DMP001 Dumping Syndrome 44 0.185
10
P CRD246 Cardiovascular System Disease 56 0.174
11
P PLY011 Polycystic Ovary Syndrome 56 0.169
12
P CRN300 Coronary Heart Disease 1 63 0.151
13
PRD004 Prediabetes Syndrome 47 0.151
14
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.145
15
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.145
16
P CRN018 Coronary Artery Anomaly 63 0.145
17
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.145
18
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.145
19
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.145
20
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.145
21
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.145
22
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.145
23
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.145
24
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.145
25
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.145
26
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.145
27
ATH013 Atherosclerosis Susceptibility 66 0.138
28
ART140 Arteries, Anomalies of 53 0.138
29
P LVR013 Liver Disease 68 0.131
30
P VSC007 Vascular Disease 63 0.131
31
SYN036 Syncope 45 0.131
32
CRB039 Cerebrovascular Disease 69 0.123
33
ISC004 Ischemia 60 0.123
34
ATX019 Ataxia with Vitamin E Deficiency 48 0.123
35
c HYP595 Hypertension, Essential 84 0.115
36
STR067 Stroke, Ischemic 80 0.115
37
P HRT032 Heart Disease 75 0.115
38
PRP027 Peripheral Vascular Disease 71 0.115
39
ADL002 Adult Syndrome 69 0.115
40
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.115
41
LVR012 Liver Cirrhosis 63 0.115
42
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.107
43
P MYC007 Myocardial Infarction 70 0.107
44
P KDN018 Kidney Disease 70 0.107
45
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.107
46
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.107
47
c RHB024 Rhabdomyosarcoma 2 65 0.107
48
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.107
49
FTT001 Fatty Liver Disease 61 0.107
50
AGN016 Aging 56 0.107
51
HYP043 Hyperandrogenism 48 0.107
52
48X005 48,xyyy 39 0.107
53
c PLY105 Polycystic Ovary Syndrome 1 38 0.107
54
P HPT021 Hepatitis 67 0.098
55
ANG054 Angina Pectoris 66 0.098
56
LPD008 Lipid Metabolism Disorder 62 0.098
57
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.098
58
P HYP750 Hypertriglyceridemia, Familial 61 0.098
59
P INF032 Infertility 57 0.098
60
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.098
61
P NRP001 Neuropathy 56 0.098
62
NNL006 Non-Alcoholic Steatohepatitis 51 0.098
63
HYP081 Hypolipoproteinemia 50 0.098
64
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.098
65
LPT014 Leptin Deficiency or Dysfunction 73 0.087
66
CNG034 Congestive Heart Failure 70 0.087
67
CNS004 Constipation 57 0.087
68
GST033 Gestational Diabetes 57 0.087
69
AMN001 Amenorrhea 54 0.087
70
c MCR113 Microvascular Complications of Diabetes 3 52 0.087
71
ILS001 Ileus 51 0.087
72
ANV001 Anovulation 47 0.087
73
c MCR120 Microvascular Complications of Diabetes 7 47 0.087
74
c MCR130 Microvascular Complications of Diabetes 6 41 0.087
75
c MCR133 Microvascular Complications of Diabetes 4 41 0.087
76
GLC008 Glucose Metabolism Disease 40 0.087
77
PNM003 Pneumatosis Cystoides Intestinalis 30 0.087
78
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.087
79
P NRF023 Neurofibromatosis, Type Ii 76 0.076
80
DFC004 Deficiency Anemia 75 0.076
81
c HYP836 Hypercholesterolemia, Familial, 1 72 0.076
82
P CNR004 Cone-Rod Dystrophy 2 71 0.076
83
c HPT073 Hepatitis C Virus 70 0.076
84
c HPT001 Hepatitis C 63 0.076
85
c ACT068 Acute Cystitis 63 0.076
86
CLT003 Colitis 62 0.076
87
P CTR002 Cataract 60 0.076
88
P GLY013 Glycogen Storage Disease 59 0.076
89
END030 End Stage Renal Failure 58 0.076
90
HMG005 Hemoglobinopathy 55 0.076
91
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.076
92
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.076
93
GLC022 Glucose/galactose Malabsorption 45 0.076
94
c PRM038 Primary Agammaglobulinemia 43 0.076
95
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.076
96
CHL079 Children's Interstitial Lung Disease 27 0.076
97
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.062
98
ULC004 Ulcerative Colitis 73 0.062
99
P FML011 Familial Adenomatous Polyposis 72 0.062
100
DWN001 Down Syndrome 70 0.062
101
c GLY008 Glycogen Storage Disease Ii 70 0.062
102
P MCR115 Microvascular Complications of Diabetes 5 66 0.062
103
c MCR129 Microvascular Complications of Diabetes 1 66 0.062
104
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.062
105
MSC007 Muscle Hypertrophy 63 0.062
106
c HPT003 Hepatitis a 63 0.062
107
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.062
108
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.062
109
P ENC018 Encephalopathy 61 0.062
110
LNG099 Lung Disease 61 0.062
111
VRL011 Viral Infectious Disease 61 0.062
112
HPT019 Hepatic Encephalopathy 60 0.062
113
INS001 Insulinoma 60 0.062
114
c ACT027 Acute Pancreatitis 59 0.062
115
PRT058 Pure Autonomic Failure 59 0.062
116
P SZR006 Seizure Disorder 58 0.062
117
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.062
118
VSL002 Visual Epilepsy 58 0.062
119
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.062
120
HYP005 Hypokalemia 55 0.062
121
MCL006 Macular Retinal Edema 55 0.062
122
ALC009 Alcoholic Liver Cirrhosis 53 0.062
123
P RTN018 Retinal Disease 52 0.062
124
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.062
125
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.062
126
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 49 0.062
127
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.062
128
DBT006 Diabetic Macular Edema 48 0.062
129
SXL003 Sexual Disorder 48 0.062
130
PRL008 Paralytic Ileus 44 0.062
131
ATN004 Autonomic Neuropathy 44 0.062
132
HPT004 Hepatic Coma 43 0.062
133
IDP033 Idiopathic Edema 43 0.062
134
c ORT011 Orthostatic Hypotension 1 43 0.062
135
DBT002 Diabetic Autonomic Neuropathy 41 0.062
136
c MCR112 Microvascular Complications of Diabetes 2 41 0.062
137
RDN001 Reading Disorder 40 0.062
138
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.062
139
c ORT012 Orthostatic Hypotension 2 27 0.062
140
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.062
141
P CLR023 Colorectal Cancer 98 0.044
142
P PNC035 Pancreatic Cancer 84 0.044
143
CYS001 Cystic Fibrosis 80 0.044
144
INS024 Insulin-Like Growth Factor I 79 0.044
145
CRH001 Crohn's Disease 74 0.044
146
c BTT014 Beta-Thalassemia 72 0.044
147
P OCL013 Oculodentodigital Dysplasia 69 0.044
148
P SLP006 Sleep Apnea 69 0.044
149
P HYP086 Hypothyroidism 68 0.044
150
c CHR684 Chronic Kidney Disease 66 0.044
151
P HYP098 Hypereosinophilic Syndrome 66 0.044
152
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.044
153
P PSR002 Psoriasis 62 0.044
154
TRN015 Transient Cerebral Ischemia 62 0.044
155
DRM006 Dermatitis 61 0.044
156
c GLY060 Glycogen Storage Disease Ia 61 0.044
157
P PNC044 Pancreatitis 61 0.044
158
ATM095 Autoimmune Disease 61 0.044
159
SPN186 Spinal Cord Injury 60 0.044
160
P THL005 Thalassemia 60 0.044
161
P MYC008 Myocarditis 59 0.044
162
ADN018 Adenoma 58 0.044
163
PMP006 Pemphigus Vulgaris, Familial 58 0.044
164
ERY003 Erythema Multiforme 57 0.044
165
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.044
166
P PLY019 Polyneuropathy 56 0.044
167
MTH009 Mouth Disease 56 0.044
168
INT007 Intermediate Coronary Syndrome 55 0.044
169
DBT010 Diabetic Neuropathy 55 0.044
170
P PMP001 Pemphigus 55 0.044
171
PST011 Pustulosis of Palm and Sole 52 0.044
172
LYS002 Lysosomal Storage Disease 52 0.044
173
HND002 Hand, Foot and Mouth Disease 51 0.044
174
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.044
175
47X002 47,xyy 49 0.044
176
ATN005 Autonomic Dysfunction 47 0.044
177
P END084 Endocrine System Disease 44 0.044
178
CYT002 Cytokine Deficiency 44 0.044
179
c HYP272 Hypercholesterolemia, Familial, 3 43 0.044
180
LYM042 Lymphocytic Colitis 41 0.044
181
CVT001 Cavitary Optic Disc Anomalies 38 0.044
182
HYP110 Hyperproinsulinemia 38 0.044
183
SLN001 Silent Myocardial Infarction 31 0.044
184
THY064 Thyroid Hormone Metabolism, Abnormal 30 0.044
185
MTH071 Methane Production 26 0.044
186
INT358 Intestinal Polyposis Syndrome 25 0.044
187
BRT037 Brittle Diabetes 25 0.044
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