Search results for Acarbose

345 hits were found for Acarbose

# Family MCID Name MIFTS Score
1
c TYP009 Type 2 Diabetes Mellitus 92 16.721
2
P DBT009 Diabetes Mellitus 67 13.354
3
HYP066 Hyperglycemia 60 8.950
4
c BLD140 Blood Group, I System 47 8.034
5
HYP056 Hypoglycemia 65 7.546
6
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 7.468
7
GLC003 Glucose Intolerance 53 5.951
8
P PLY011 Polycystic Ovary Syndrome 57 4.775
9
P CRN300 Coronary Heart Disease 1 73 4.726
10
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.385
11
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.385
12
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.385
13
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.385
14
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.385
15
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.385
16
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.385
17
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.385
18
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.385
19
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.385
20
HYP060 Hyperinsulinism 53 4.326
21
PRD004 Prediabetes Syndrome 52 4.210
22
P DRR001 Diarrhea 55 3.839
23
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.765
24
P HRT032 Heart Disease 84 3.709
25
DMP001 Dumping Syndrome 43 3.682
26
SYN036 Syncope 44 3.534
27
LPD008 Lipid Metabolism Disorder 61 3.489
28
ART140 Arteries, Anomalies of 52 3.305
29
LPP008 Lipoprotein Quantitative Trait Locus 65 3.305
30
GST033 Gestational Diabetes 61 3.129
31
FTT001 Fatty Liver Disease 61 3.042
32
AGN016 Aging 54 3.029
33
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.918
34
c TYP008 Type 1 Diabetes Mellitus 77 2.914
35
NNL006 Non-Alcoholic Steatohepatitis 54 2.868
36
P VSC007 Vascular Disease 62 2.827
37
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.815
38
P LVR013 Liver Disease 68 2.778
39
ATH013 Atherosclerosis Susceptibility 63 2.774
40
P INF032 Infertility 60 2.499
41
ISC004 Ischemia 61 2.436
42
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.308
43
HYP043 Hyperandrogenism 47 2.244
44
END072 Endotheliitis 36 2.173
45
48X005 48,xyyy 39 2.144
46
ALC007 Alcohol Dependence 65 2.140
47
P ALC033 Alcohol Use Disorder 67 2.140
48
LVR012 Liver Cirrhosis 62 2.093
49
P HYP750 Hypertriglyceridemia, Familial 62 2.082
50
PLY105 Polycystic Ovary Syndrome 1 39 2.074
51
CNG034 Congestive Heart Failure 69 2.068
52
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.012
53
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.994
54
ADL002 Adult Syndrome 69 1.938
55
RHB024 Rhabdomyosarcoma 2 65 1.938
56
GLC008 Glucose Metabolism Disease 40 1.905
57
P ANR048 Aniridia 1 66 1.777
58
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.777
59
c HYP836 Hypercholesterolemia, Familial, 1 73 1.718
60
PNM003 Pneumatosis Cystoides Intestinalis 32 1.682
61
P GLY013 Glycogen Storage Disease 59 1.653
62
c GLY008 Glycogen Storage Disease Ii 72 1.636
63
P ACN011 Acne 55 1.570
64
c PNS012 Paine Syndrome 60 1.568
65
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.568
66
c DRR009 Diarrhea 6 46 1.568
67
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.568
68
HYP081 Hypolipoproteinemia 49 1.568
69
P TRN020 Turner Syndrome 67 1.568
70
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.568
71
c ACT027 Acute Pancreatitis 60 1.549
72
END086 End Stage Renal Disease 54 1.526
73
ILS001 Ileus 49 1.474
74
c HYP595 Hypertension, Essential 84 1.472
75
CRB039 Cerebrovascular Disease 65 1.472
76
c MCR133 Microvascular Complications of Diabetes 4 41 1.451
77
c MCR113 Microvascular Complications of Diabetes 3 52 1.451
78
c MCR130 Microvascular Complications of Diabetes 6 41 1.451
79
c MCR120 Microvascular Complications of Diabetes 7 47 1.451
80
CLT003 Colitis 63 1.432
81
ANT039 Antisynthetase Syndrome 55 1.371
82
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.371
83
P HYP050 Hyperinsulinemic Hypoglycemia 56 1.361
84
PRT058 Pure Autonomic Failure 58 1.338
85
ANG054 Angina Pectoris 65 1.334
86
PRP027 Peripheral Vascular Disease 71 1.334
87
CNS004 Constipation 56 1.317
88
ALC009 Alcoholic Liver Cirrhosis 54 1.300
89
c MCR115 Microvascular Complications of Diabetes 5 65 1.286
90
P FML011 Familial Adenomatous Polyposis 71 1.263
91
HPT004 Hepatic Coma 43 1.263
92
HPT019 Hepatic Encephalopathy 59 1.263
93
DRM006 Dermatitis 62 1.263
94
P CTR002 Cataract 59 1.263
95
PST011 Pustulosis of Palm and Sole 52 1.243
96
ATN005 Autonomic Dysfunction 45 1.243
97
P ENC018 Encephalopathy 62 1.243
98
P PSR002 Psoriasis 63 1.243
99
P ART022 Arthritis 70 1.231
100
ULC004 Ulcerative Colitis 74 1.223
101
CRH001 Crohn's Disease 80 1.211
102
c HPT001 Hepatitis C 61 1.181
103
INS001 Insulinoma 59 1.153
104
SPN186 Spinal Cord Injury 61 1.153
105
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.128
106
P CRD246 Cardiovascular System Disease 55 1.128
107
P KDN018 Kidney Disease 72 1.128
108
ATN004 Autonomic Neuropathy 42 1.125
109
ACT167 Acute Generalized Exanthematous Pustulosis 38 1.125
110
DBT002 Diabetic Autonomic Neuropathy 40 1.095
111
PRL008 Paralytic Ileus 44 1.095
112
P DMN002 Dementia 65 1.087
113
P RHM011 Rheumatoid Arthritis 81 1.035
114
P MYC007 Myocardial Infarction 69 1.035
115
THY064 Thyroid Hormone Metabolism, Abnormal 28 1.035
116
CYT002 Cytokine Deficiency 43 1.035
117
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.005
118
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 1.001
119
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 1.001
120
P FNG006 Feingold Syndrome 1 61 1.001
121
c ORT011 Orthostatic Hypotension 1 43 1.001
122
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 1.001
123
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 47 1.001
124
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 1.001
125
c HPT003 Hepatitis a 63 1.001
126
P RTN018 Retinal Disease 53 1.001
127
P HPT021 Hepatitis 68 1.001
128
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.997
129
47X002 47,xyy 48 0.997
130
BRT037 Brittle Diabetes 24 0.976
131
INT007 Intermediate Coronary Syndrome 53 0.976
132
DBT010 Diabetic Neuropathy 54 0.976
133
INS024 Insulin-Like Growth Factor I 77 0.955
134
c PRC016 Pre-Eclampsia 64 0.955
135
c BTT014 Beta-Thalassemia 72 0.955
136
BTT017 Beta-Thalassemia Major 53 0.955
137
P THL005 Thalassemia 56 0.955
138
CYS001 Cystic Fibrosis 77 0.931
139
ATM095 Autoimmune Disease 61 0.931
140
SLN001 Silent Myocardial Infarction 32 0.931
141
AMN001 Amenorrhea 53 0.931
142
P MYC008 Myocarditis 59 0.931
143
c CHR684 Chronic Kidney Disease 74 0.931
144
CVT001 Cavitary Optic Disc Anomalies 38 0.906
145
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.906
146
MTH071 Methane Production 25 0.906
147
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.906
148
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.906
149
P KDN017 Kidney Cancer 60 0.906
150
P ECL001 Eclampsia 52 0.906
151
PRT251 Proteinuria, Chronic Benign 58 0.879
152
ADN018 Adenoma 58 0.879
153
INT358 Intestinal Polyposis Syndrome 25 0.879
154
CVD001 Covid-19 58 0.849
155
P SLP006 Sleep Apnea 69 0.849
156
P PLY019 Polyneuropathy 53 0.849
157
HYP266 Hypoxia 56 0.849
158
HYP110 Hyperproinsulinemia 36 0.815
159
ERY003 Erythema Multiforme 56 0.815
160
P HYP086 Hypothyroidism 69 0.815
161
HND002 Hand, Foot and Mouth Disease 50 0.815
162
MTH009 Mouth Disease 57 0.815
163
LYS002 Lysosomal Storage Disease 51 0.815
164
P HYP098 Hypereosinophilic Syndrome 66 0.815
165
NNN035 Non-Insulinoma Pancreatogenous Hypoglycemia Syndrome 21 0.775
166
P PNC044 Pancreatitis 61 0.750
167
LYM042 Lymphocytic Colitis 40 0.722
168
IMP005 Impotence 52 0.722
169
c TYP028 Type 1 Diabetes Mellitus 2 49 0.666
170
P GST053 Gastric Cancer 82 0.595
171
c GLY060 Glycogen Storage Disease Ia 63 0.595
172
c HPT073 Hepatitis C Virus 71 0.595
173
PMP006 Pemphigus Vulgaris, Familial 58 0.595
174
ANV001 Anovulation 46 0.595
175
P PMP001 Pemphigus 55 0.595
176
P CNR004 Cone-Rod Dystrophy 2 75 0.496
177
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.496
178
c HYP272 Hypercholesterolemia, Familial, 3 46 0.496
179
TRN015 Transient Cerebral Ischemia 62 0.496
180
P PNC035 Pancreatic Cancer 86 0.496
181
STR067 Stroke, Ischemic 79 0.496
182
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 32 0.496
183
AND005 Androgen Insensitivity Syndrome, Mild 21 0.496
184
P LCT001 Lactic Acidosis 50 0.476
185
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.422
186
P CLR023 Colorectal Cancer 100 0.382
187
HRT040 Hirata Disease 38 0.360
188
LPT014 Leptin Deficiency or Dysfunction 77 0.337
189
OCL069 Ocular Motor Apraxia 57 0.285
190
ATS010 Autosomal Recessive Disease 42 0.285
191
P MYC084 Mycobacterium Tuberculosis 1 68 0.285
192
FST010 Fasting Hypoglycemia 33 0.285
193
c PCH010 Pachyonychia Congenita 3 43 0.255
194
c DWL002 Dowling-Degos Disease 1 58 0.255
195
MLT157 Multiple System Atrophy 1 69 0.255
196
DYS015 Dysentery 50 0.255
197
SVR001 Severe Acute Respiratory Syndrome 68 0.255
198
CNN005 Connective Tissue Disease 66 0.255
199
HYP005 Hypokalemia 55 0.255
200
PPT005 Peptic Ulcer Disease 58 0.255
201
INT043 Intestinal Disaccharidase Deficiency 25 0.255
202
THY029 Thyroid Carcinoma 54 0.255
203
P ALZ034 Alzheimer Disease 87 0.220
204
P SPP010 Suppressor of Tumorigenicity 3 51 0.220
205
BCT022 Bacterial Infectious Disease 56 0.220
206
ACT088 Acute Insulin Response 39 0.220
207
CHL014 Cholera 62 0.220
208
BRN024 Bronchitis 67 0.220
209
P INT068 Intestinal Disease 53 0.220
210
P PRP019 Peripheral Nervous System Disease 57 0.220
211
HYP026 Hypoglycemic Coma 37 0.220
212
KRT009 Keratosis 52 0.220
213
PRN014 Paronychia 50 0.220
214
P NRP001 Neuropathy 59 0.220
215
LYS028 Lysosomal Glycogen Storage Disease 18 0.220
216
P OVR082 Overgrowth Syndrome 42 0.220
217
P BLD134 Bladder Cancer 79 0.180
218
P SRC025 Sarcoidosis 1 70 0.180
219
HLX001 Helix Syndrome 47 0.180
220
ESP020 Esophageal Atresia 60 0.180
221
PLY150 Polykaryocytosis Inducer 29 0.180
222
ACN002 Acanthosis Nigricans 56 0.180
223
P KRB001 Krabbe Disease 69 0.180
224
VLV047 Volvulus of Midgut 55 0.180
225
ISC015 Ischemic Colitis 43 0.180
226
CLR109 Colorectal Adenocarcinoma 50 0.180
227
DSM002 Desmosterolosis 39 0.180
228
P KLZ004 Kala-Azar 1 41 0.180
229
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.180
231
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.180
232
P URN019 Urinary Tract Infection 49 0.180
233
GT001 Gout 63 0.180
234
CHL068 Cholestasis 61 0.180
235
ENT004 Enthesopathy 51 0.180
236
DNT012 Dental Caries 53 0.180
237
P HYP069 Hyperparathyroidism 62 0.180
238
P GRV001 Graves' Disease 54 0.180
239
P BRS044 Breast Adenocarcinoma 58 0.180
240
BLR008 Bilirubin Metabolic Disorder 57 0.180
241
c SCN007 Secondary Hyperparathyroidism 51 0.180
242
P SKN015 Skin Carcinoma 71 0.180
243
GTL001 Gitelman Syndrome 65 0.180
244
SKN012 Skin Carcinoma in Situ 20 0.180
245
P INS002 in Situ Carcinoma 53 0.180
246
P NRB001 Neuroblastoma 66 0.180
247
P MYP004 Myopathy 67 0.180
248
MYT011 Myotonia 38 0.180
249
LSH001 Leishmaniasis 63 0.180
251
PST021 Postpartum Depression 50 0.180
252
GRW007 Growth Hormone Deficiency 47 0.180
253
P HYP083 Hypopituitarism 52 0.180
254
P DBT005 Diabetes Insipidus 54 0.180
255
P PRD021 Periodic Paralysis 42 0.180
256
P PRS040 Prostate Cancer 95 0.127
257
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.127
258
c GLL024 Gallbladder Disease 1 53 0.127
259
WLF002 Wolf-Hirschhorn Syndrome 57 0.127
260
P PLM037 Pulmonary Hypertension 69 0.127
261
EPD015 Epidemic Typhus 44 0.127
262
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.127
263
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.127
264
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.127
265
P INF037 Inflammatory Bowel Disease 53 0.127
266
P CHR071 Charcot-Marie-Tooth Disease 64 0.127
267
RCK004 Rickets 65 0.127
268
PMP014 Pemphigoid 49 0.127
269
c MGR028 Migraine with or Without Aura 1 64 0.127
270
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.127
271
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.127
272
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.127
273
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.127
274
P LPR021 Leprosy 3 71 0.127
275
P ANP001 Anaplastic Large Cell Lymphoma 61 0.127
276
MTB004 Metabolic Acidosis 48 0.127
277
CLS016 Clostridium Difficile Colitis 49 0.127
278
P SLM003 Salmonellosis 54 0.127
279
CLR108 Colorectal Adenoma 63 0.127
280
HMN044 Human Immunodeficiency Virus Type 1 76 0.127
281
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.127
282
PPL052 Papillomatosis, Confluent and Reticulated 34 0.127
283
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.127
284
P LNG064 Lung Cancer Susceptibility 3 70 0.127
285
P MTR004 Maturity-Onset Diabetes of the Young 66 0.127
286
FRG010 Fragile X Tremor/ataxia Syndrome 43 0.127
287
FBR012 Fabry Disease 71 0.127
288
P RSP003 Respiratory Failure 74 0.127
289
CRD223 Cardiac Arrhythmia 63 0.127
290
STF001 Stiff-Person Syndrome 57 0.127
291
KRT019 Keratitis, Hereditary 66 0.127
292
HMP005 Hemiplegia 53 0.127
293
DFC004 Deficiency Anemia 74 0.127
294
c ACT068 Acute Cystitis 61 0.127
295
GLB002 Glioblastoma 67 0.127
296
NPH009 Nephrolithiasis 54 0.127
297
P CNJ013 Conjunctivitis 66 0.127
298
OVR063 Overnutrition 42 0.127
299
IRN002 Iron Metabolism Disease 56 0.127
300
HYP014 Hyperuricemia 51 0.127
301
CRB037 Cerebral Palsy 67 0.127
302
MNT002 Mental Depression 56 0.127
303
KLB003 Klebsiella Pneumonia 49 0.127
304
EXC002 Exocrine Pancreatic Insufficiency 42 0.127
305
FCL012 Facial Paralysis 49 0.127
306
P DDN001 Duodenal Ulcer 53 0.127
307
TTH006 Tooth Disease 51 0.127
308
GST023 Gastric Ulcer 52 0.127
309
IRN001 Iron Deficiency Anemia 58 0.127
310
CHL004 Cholelithiasis 48 0.127
311
FNC002 Functional Diarrhea 39 0.127
312
DBT008 Diabetic Angiopathy 47 0.127
313
FML035 Familial Hyperlipidemia 55 0.127
314
P NNT058 Neonatal Diabetes 52 0.127
315
SKN016 Skin Disease 62 0.127
316
P CRV031 Cervical Adenocarcinoma 48 0.127
317
c GLY006 Glycogen Storage Disease Viii 34 0.127
318
PLG002 Plague 58 0.127
319
KRN002 Kearns-Sayre Syndrome 63 0.127
320
P NSP012 Nasopharyngeal Carcinoma 60 0.127
321
CRN020 Coronary Restenosis 39 0.127
322
CRN030 Coronary Stenosis 50 0.127
323
IDP033 Idiopathic Edema 41 0.127
324
P DYS021 Dysautonomia 38 0.127
325
INT042 Internuclear Ophthalmoplegia 32 0.127
326
MLT006 Multidrug-Resistant Tuberculosis 47 0.127
327
SYS003 Systolic Heart Failure 49 0.127
328
P EYD002 Eye Disease 57 0.127
329
P HDC001 Headache 56 0.127
330
BLL006 Bullous Pemphigoid 61 0.127
331
IMP004 Impetigo 48 0.127
332
VSC002 Vascular Dementia 59 0.127
333
c HRD088 Hereditary Neuropathies 34 0.127
334
FTD001 Foot Drop 36 0.127
335
OST012 Osteoarthritis 77 0.127
336
ANT024 Anthrax Disease 58 0.127
337
GST039 Gastroduodenitis 37 0.127
338
GST050 Gastrointestinal System Disease 55 0.127
339
P HMR005 Hemorrhoid 49 0.127
340
IRR002 Irritable Bowel Syndrome 65 0.127
341
DBT018 Diabetic Mastopathy 18 0.127
342
HNS001 Hansen's Disease 32 0.127
343
PHS018 Phosphorylase Kinase Deficiency 37 0.127
344
ACN019 Acanthamoeba Keratitis 30 0.127
345
P PRM227 Primary Orthostatic Hypotension 23 0.127
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