Search results for Sitagliptin

326 hits were found for Sitagliptin

# Family MCID Name MIFTS Score
1
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.900
2
P DBT009 Diabetes Mellitus 64 0.897
3
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.834
4
HYP056 Hypoglycemia 66 0.634
5
HYP066 Hyperglycemia 61 0.353
6
P KDN018 Kidney Disease 72 0.239
7
P TRN020 Turner Syndrome 67 0.215
8
c DBT099 Diabetes Mellitus, Type I 65 0.212
9
FTT001 Fatty Liver Disease 61 0.212
10
GLC003 Glucose Intolerance 54 0.212
11
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.209
12
P LVR013 Liver Disease 68 0.200
13
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.193
14
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.190
15
CNG034 Congestive Heart Failure 69 0.187
16
48X005 48,xyyy 39 0.183
17
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.180
18
ADL002 Adult Syndrome 70 0.180
19
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.180
20
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.180
21
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.180
22
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.180
23
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.180
24
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.180
25
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.180
26
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.180
27
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.180
28
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.180
29
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.176
30
P HRT032 Heart Disease 75 0.176
31
c ACT027 Acute Pancreatitis 60 0.176
32
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.176
33
c RHB024 Rhabdomyosarcoma 2 67 0.169
34
LPP008 Lipoprotein Quantitative Trait Locus 62 0.169
35
P CRD246 Cardiovascular System Disease 57 0.169
36
c MCR113 Microvascular Complications of Diabetes 3 52 0.169
37
c MCR120 Microvascular Complications of Diabetes 7 47 0.169
38
c MCR130 Microvascular Complications of Diabetes 6 41 0.169
39
c MCR133 Microvascular Complications of Diabetes 4 41 0.169
40
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.166
41
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.162
42
ISC004 Ischemia 58 0.162
43
PRD004 Prediabetes Syndrome 47 0.162
44
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.162
45
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.162
46
c CHR684 Chronic Kidney Disease 70 0.158
47
P CRN300 Coronary Heart Disease 1 63 0.150
48
HYP081 Hypolipoproteinemia 51 0.150
49
ATH013 Atherosclerosis Susceptibility 65 0.146
50
LPD008 Lipid Metabolism Disorder 62 0.146
51
P PNC044 Pancreatitis 61 0.146
52
ART140 Arteries, Anomalies of 52 0.146
53
c ACT075 Acute Myocardial Infarction 57 0.141
54
c HYP595 Hypertension, Essential 84 0.137
55
NNL006 Non-Alcoholic Steatohepatitis 54 0.137
56
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.132
57
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.132
58
P MYC007 Myocardial Infarction 70 0.127
59
P PLY011 Polycystic Ovary Syndrome 56 0.127
60
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.122
61
c ACT071 Acute Kidney Failure 60 0.117
62
P NRP001 Neuropathy 56 0.117
63
INT007 Intermediate Coronary Syndrome 55 0.117
64
GST033 Gestational Diabetes 61 0.112
65
P DRR001 Diarrhea 55 0.112
66
P VSC007 Vascular Disease 63 0.106
67
ATX019 Ataxia with Vitamin E Deficiency 42 0.106
68
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.106
69
c PLY105 Polycystic Ovary Syndrome 1 38 0.106
70
CYS001 Cystic Fibrosis 81 0.100
71
P HYP086 Hypothyroidism 69 0.100
72
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.100
73
LNG099 Lung Disease 60 0.100
74
P ANG015 Angioedema 57 0.100
75
c FML035 Familial Hyperlipidemia 55 0.100
76
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.100
77
END086 End Stage Renal Disease 51 0.100
78
49X006 49, Xxxxy Syndrome 41 0.100
79
CHL079 Children's Interstitial Lung Disease 26 0.100
80
DWN001 Down Syndrome 70 0.093
81
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.093
82
P LCT001 Lactic Acidosis 51 0.093
83
c PRM038 Primary Agammaglobulinemia 44 0.093
84
P HPT023 Hepatocellular Carcinoma 100 0.086
85
STR067 Stroke, Ischemic 81 0.086
86
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.086
87
DFC004 Deficiency Anemia 70 0.086
88
CRB039 Cerebrovascular Disease 67 0.086
89
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.086
90
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.086
91
c ACT068 Acute Cystitis 63 0.086
92
P PSR002 Psoriasis 62 0.086
93
LVR012 Liver Cirrhosis 62 0.086
94
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.086
95
CNS004 Constipation 58 0.086
96
P HDC001 Headache 57 0.086
97
HYP266 Hypoxia 57 0.086
98
DBT010 Diabetic Neuropathy 54 0.086
99
PST011 Pustulosis of Palm and Sole 52 0.086
100
CYT002 Cytokine Deficiency 42 0.086
101
ACT088 Acute Insulin Response 41 0.086
102
GLC008 Glucose Metabolism Disease 40 0.086
103
P VSC018 Visceral Steatosis 33 0.086
104
c LKM061 Leukemia, Acute Myeloid 84 0.079
105
P PRK057 Parkinson Disease, Late-Onset 78 0.079
106
P RSP003 Respiratory Failure 74 0.079
107
P CNR004 Cone-Rod Dystrophy 2 73 0.079
108
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.079
109
c LKM063 Leukemia, Chronic Myeloid 72 0.079
110
PRP027 Peripheral Vascular Disease 71 0.079
111
P LKM062 Leukemia, Acute Lymphoblastic 69 0.079
112
P LYM118 Lymphoma 68 0.079
113
P LKM002 Leukemia 68 0.079
114
SKN016 Skin Disease 63 0.079
115
c HPT001 Hepatitis C 62 0.079
116
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.079
117
c SVR001 Severe Acute Respiratory Syndrome 62 0.079
118
ATM095 Autoimmune Disease 62 0.079
119
P MYL006 Myeloid Leukemia 60 0.079
120
P ALC033 Alcohol Use Disorder 58 0.079
121
P EXN002 Exanthem 57 0.079
122
P SBS003 Substance Abuse 55 0.079
123
HYP060 Hyperinsulinism 54 0.079
124
GST037 Gastroparesis 54 0.079
125
LYM040 Lymphoblastic Lymphoma 54 0.079
126
BNR002 Bone Resorption Disease 48 0.079
127
LYM019 Lymphosarcoma 46 0.079
128
ATN004 Autonomic Neuropathy 45 0.079
129
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.079
130
ATM052 Autoimmune Disease 1 37 0.079
131
FST010 Fasting Hypoglycemia 35 0.079
132
c CHR064 Chronic Monocytic Leukemia 33 0.079
133
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.079
134
P PNC035 Pancreatic Cancer 84 0.071
135
c ATR087 Atrial Standstill 1 75 0.071
136
c HYP836 Hypercholesterolemia, Familial, 1 73 0.071
137
HMN044 Human Immunodeficiency Virus Type 1 71 0.071
138
P HPT021 Hepatitis 67 0.071
139
P DMN002 Dementia 66 0.071
140
MSC007 Muscle Hypertrophy 64 0.071
141
ACQ007 Acquired Immunodeficiency Syndrome 60 0.071
142
P INF032 Infertility 57 0.071
143
c PSR017 Psoriasis 2 53 0.071
144
c PSR023 Psoriasis 1 52 0.071
145
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.071
146
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.071
147
c PSR032 Psoriasis 11 47 0.071
148
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.071
149
P END084 Endocrine System Disease 45 0.071
150
CVD001 Covid-19 44 0.071
151
MDD018 Middle East Respiratory Syndrome 43 0.071
152
c PSR028 Psoriasis 7 42 0.071
153
c PSR018 Psoriasis 13 41 0.071
154
C1N001 C1 Inhibitor Deficiency 39 0.071
155
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.071
156
P LNG032 Lung Cancer 98 0.061
157
P GLM040 Glioma Susceptibility 1 81 0.061
158
P RHM011 Rheumatoid Arthritis 80 0.061
159
IMM167 Immune Deficiency Disease 78 0.061
160
GLB015 Glioblastoma Multiforme 75 0.061
161
LPT014 Leptin Deficiency or Dysfunction 74 0.061
162
P GRF003 Graft-Versus-Host Disease 72 0.061
163
MYL009 Myelodysplastic Syndrome 70 0.061
164
c PNC108 Pancreatitis, Hereditary 70 0.061
165
SVR097 Severe Cutaneous Adverse Reaction 69 0.061
166
ANG054 Angina Pectoris 66 0.061
167
KHL003 Kohlschutter-Tonz Syndrome 65 0.061
168
P MTR004 Maturity-Onset Diabetes of the Young 65 0.061
169
P ADN016 Adenocarcinoma 64 0.061
170
c HPT003 Hepatitis a 62 0.061
171
c LPM012 Lipomatosis, Multiple 60 0.061
172
c ACT073 Acute Leukemia 58 0.061
173
ERY003 Erythema Multiforme 58 0.061
174
P CND004 Candidiasis 58 0.061
175
P PRP019 Peripheral Nervous System Disease 58 0.061
176
c CHR417 Chronic Graft Versus Host Disease 57 0.061
177
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.061
178
ORL005 Oral Candidiasis 56 0.061
179
P PLY019 Polyneuropathy 56 0.061
180
HYP005 Hypokalemia 55 0.061
181
PLM010 Pulmonary Edema 54 0.061
182
THY030 Thyroid Gland Disease 52 0.061
183
c ACT135 Acute Graft Versus Host Disease 52 0.061
184
CLR109 Colorectal Adenocarcinoma 51 0.061
185
VLV011 Vulvovaginal Candidiasis 49 0.061
186
47X002 47,xyy 49 0.061
187
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.061
188
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.061
189
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.061
190
TRP009 Triple X Syndrome 42 0.061
191
MNN017 Mononeuropathy 42 0.061
192
DBT002 Diabetic Autonomic Neuropathy 41 0.061
193
HRW001 Hair Whorl 36 0.061
194
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.061
195
ERY066 Erythema Multiforme Major 30 0.061
196
HML018 Homologous Wasting Disease 22 0.061
197
CNN003 Conn's Syndrome 79 0.050
198
P OST002 Osteoporosis 74 0.050
199
ANX010 Anxiety 73 0.050
200
c HPT073 Hepatitis C Virus 72 0.050
201
ACR007 Acromegaly 71 0.050
202
WRN001 Werner Syndrome 69 0.050
203
P ART022 Arthritis 69 0.050
204
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.050
205
P MCR115 Microvascular Complications of Diabetes 5 66 0.050
206
c MCR129 Microvascular Complications of Diabetes 1 66 0.050
207
P ATR011 Atrial Fibrillation 66 0.050
208
c FML001 Familial Atrial Fibrillation 65 0.050
209
TBC004 Tobacco Addiction 64 0.050
210
P FRD001 Friedreich Ataxia 64 0.050
211
c LPD015 Lipodystrophy, Familial Partial, Type 2 64 0.050
212
c ALP101 Alpha-Thalassemia 62 0.050
213
NTR005 Nutritional Deficiency Disease 62 0.050
214
VRL011 Viral Infectious Disease 61 0.050
215
c WLF013 Wolfram Syndrome 1 60 0.050
216
P WLF004 Wolfram Syndrome 60 0.050
217
P SNS001 Sensorineural Hearing Loss 60 0.050
218
P THL005 Thalassemia 60 0.050
219
VSL002 Visual Epilepsy 59 0.050
220
IRN001 Iron Deficiency Anemia 59 0.050
221
ADN018 Adenoma 59 0.050
222
PPT005 Peptic Ulcer Disease 59 0.050
223
ERY029 Erythermalgia, Primary 58 0.050
224
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.050
225
IRN002 Iron Metabolism Disease 57 0.050
226
P RHN004 Rhinitis 57 0.050
227
P SZR006 Seizure Disorder 56 0.050
228
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.050
229
P PTT006 Pituitary Adenoma 55 0.050
230
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 55 0.050
231
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.050
232
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 55 0.050
233
c GLL024 Gallbladder Disease 1 53 0.050
234
c INF145 Infantile Liver Failure Syndrome 1 50 0.050
235
SYS003 Systolic Heart Failure 49 0.050
236
LPT006 Leptin Receptor Deficiency 48 0.050
237
RNL077 Renal Fibrosis 47 0.050
238
PPL001 Papillary Adenoma 44 0.050
239
DMP001 Dumping Syndrome 44 0.050
240
NSP002 Nasopharyngitis 43 0.050
241
FNC007 Functioning Pituitary Adenoma 43 0.050
242
DRG024 Drug Allergy 42 0.050
243
EXC002 Exocrine Pancreatic Insufficiency 42 0.050
244
c WLF009 Wolfram Syndrome 2 42 0.050
245
RST023 Resting Heart Rate, Variation in 41 0.050
246
RDN001 Reading Disorder 40 0.050
247
PTT003 Pituitary-Dependent Cushing's Disease 39 0.050
248
P ALZ034 Alzheimer Disease 88 0.035
249
P GST053 Gastric Cancer 83 0.035
250
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.035
251
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.035
252
P PHC003 Pheochromocytoma 71 0.035
253
P MYP004 Myopathy 70 0.035
254
CRB037 Cerebral Palsy 69 0.035
255
P OCL013 Oculodentodigital Dysplasia 69 0.035
256
ALL003 Allergic Rhinitis 67 0.035
257
P HYP098 Hypereosinophilic Syndrome 67 0.035
258
P PLM036 Pulmonary Fibrosis 65 0.035
259
P PRD008 Periodontitis 64 0.035
260
TRN015 Transient Cerebral Ischemia 63 0.035
261
c OPT053 Optic Atrophy 1 63 0.035
262
CLT003 Colitis 62 0.035
263
P HYP750 Hypertriglyceridemia, Familial 62 0.035
264
BLL006 Bullous Pemphigoid 62 0.035
265
P ART023 Arthropathy 62 0.035
266
SPN186 Spinal Cord Injury 60 0.035
267
ACN002 Acanthosis Nigricans 60 0.035
268
ORL011 Oral Cancer 60 0.035
269
INS001 Insulinoma 60 0.035
270
STF001 Stiff-Person Syndrome 60 0.035
271
STT001 Status Epilepticus 60 0.035
272
P MYC008 Myocarditis 59 0.035
273
P BND020 Bone Disease 59 0.035
274
THY029 Thyroid Carcinoma 59 0.035
275
PRT058 Pure Autonomic Failure 59 0.035
276
P INT070 Intestinal Obstruction 58 0.035
277
P BCL017 B-Cell Lymphoma 58 0.035
278
EYD002 Eye Disease 58 0.035
279
c DWL002 Dowling-Degos Disease 1 58 0.035
280
PMP006 Pemphigus Vulgaris, Familial 57 0.035
281
CHL067 Cholecystitis 57 0.035
282
VSC002 Vascular Dementia 57 0.035
283
PHR003 Pharyngitis 57 0.035
284
P PYL005 Pyelonephritis 56 0.035
285
ALL006 Allergic Asthma 56 0.035
286
MCL006 Macular Retinal Edema 55 0.035
287
LMB062 Limb Ischemia 55 0.035
288
P MLN007 Male Infertility 55 0.035
289
P PMP001 Pemphigus 54 0.035
290
TND005 Tendinitis 54 0.035
291
CLL003 Cellulitis 54 0.035
292
CLR030 Clear Cell Renal Cell Carcinoma 53 0.035
293
P LCH002 Lichen Planus 53 0.035
294
P SHR001 Short Bowel Syndrome 53 0.035
295
P THY032 Thyroiditis 52 0.035
296
OCL069 Ocular Motor Apraxia 51 0.035
297
c PNC106 Pancreatic Agenesis 1 51 0.035
298
TRM010 Traumatic Brain Injury 51 0.035
299
c HNT004 Huntington Disease-Like 2 50 0.035
300
CRT013 Carotid Stenosis 50 0.035
301
PLC008 Placenta Disease 50 0.035
302
ENT004 Enthesopathy 49 0.035
303
HYP043 Hyperandrogenism 48 0.035
304
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.035
305
PNC034 Pancreas Disease 48 0.035
306
ADR040 Adrenal Gland Pheochromocytoma 46 0.035
307
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.035
308
OVR063 Overnutrition 44 0.035
309
c HYP272 Hypercholesterolemia, Familial, 3 44 0.035
310
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.035
311
CRB086 Cerebral Aneurysms 40 0.035
312
ASP030 Aspirin Resistance 39 0.035
313
ENT001 Enterocele 39 0.035
314
c HNT011 Huntington Disease-Like 3 38 0.035
315
P FML187 Familial Hypertension 37 0.035
316
FRN014 Fournier Gangrene 37 0.035
317
HYP114 Hypertensive Nephropathy 36 0.035
318
FXD003 Fixed Drug Eruption 35 0.035
319
AMR003 Amaurosis Fugax 34 0.035
320
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.035
321
GNT167 Genetic Obesity 33 0.035
322
KDN013 Kidney Hypertrophy 32 0.035
323
DFF031 Diffuse Alveolar Hemorrhage 30 0.035
324
FNT004 Fainting 30 0.035
325
BRT037 Brittle Diabetes 25 0.035
326
c DMN005 Diamond-Blackfan Anemia 2 25 0.035
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