Search results for Rifaximin

329 hits were found for Rifaximin

# Family MCID Name MIFTS Score
1
HPT019 Hepatic Encephalopathy 59 17.912
2
HPT004 Hepatic Coma 43 17.811
3
P ENC018 Encephalopathy 62 16.975
4
IRR002 Irritable Bowel Syndrome 65 14.041
5
LVR012 Liver Cirrhosis 62 12.807
6
P DRR001 Diarrhea 55 12.656
7
P OVR082 Overgrowth Syndrome 42 11.115
8
CRH001 Crohn's Disease 80 8.130
9
PRT036 Peritonitis 65 7.669
10
CNS004 Constipation 56 7.078
11
P HPT021 Hepatitis 68 6.464
12
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 6.279
13
P LVR013 Liver Disease 68 6.067
14
DVR002 Diverticulitis 46 5.764
15
c HPT003 Hepatitis a 63 5.667
16
PRT013 Portal Hypertension 59 5.603
17
DYS015 Dysentery 50 5.281
18
CLT003 Colitis 63 4.725
19
ULC004 Ulcerative Colitis 74 4.704
20
GST050 Gastrointestinal System Disease 55 4.549
21
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 4.377
22
ANT039 Antisynthetase Syndrome 55 4.255
23
c DRR009 Diarrhea 6 46 4.238
24
CRH005 Crohn's Colitis 53 4.215
25
P INF037 Inflammatory Bowel Disease 53 4.089
26
BCT022 Bacterial Infectious Disease 56 4.075
27
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.982
28
NNL006 Non-Alcoholic Steatohepatitis 54 3.944
29
BCT002 Bacterial Vaginosis 53 3.806
30
CLS016 Clostridium Difficile Colitis 49 3.765
31
VRC005 Varicose Veins 59 3.624
32
ALC006 Alcoholic Hepatitis 61 3.566
33
FTT001 Fatty Liver Disease 61 3.550
34
P ALC033 Alcohol Use Disorder 67 3.550
35
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.402
36
HLC007 Helicobacter Pylori Infection 67 3.329
37
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.288
38
PCH007 Pouchitis 42 3.267
39
P CLC063 Celiac Disease 1 66 3.097
40
HPT014 Hepatorenal Syndrome 49 2.972
41
c INF071 Inflammatory Bowel Disease 1 65 2.962
42
c ACT004 Acute Diarrhea 40 2.905
43
ALC007 Alcohol Dependence 65 2.902
44
ESP002 Esophageal Varix 51 2.883
45
RHB024 Rhabdomyosarcoma 2 65 2.809
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.807
47
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.705
48
P SCK005 Sickle Cell Disease 56 2.587
49
P INT068 Intestinal Disease 53 2.537
50
BLN006 Blind Loop Syndrome 34 2.472
51
RSC001 Rosacea 55 2.461
52
c HYP595 Hypertension, Essential 84 2.410
53
P GRF003 Graft-Versus-Host Disease 71 2.405
54
PRT018 Portal Vein Thrombosis 50 2.405
55
c SPN225 Spondyloarthropathy 1 70 2.360
56
IMM167 Immune Deficiency Disease 77 2.336
57
CMM004 Common Variable Immunodeficiency 72 2.336
58
MTH071 Methane Production 25 2.329
59
OCL069 Ocular Motor Apraxia 57 2.272
60
48X005 48,xyyy 39 2.264
61
ALL029 Allergic Disease 61 2.250
62
P GST044 Gastritis 55 2.243
63
c ACT135 Acute Graft Versus Host Disease 51 2.214
64
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.176
65
ADL002 Adult Syndrome 69 2.126
66
P PRK039 Parkinsonism 55 2.019
67
P PRK057 Parkinson Disease, Late-Onset 79 2.019
68
c HPT001 Hepatitis C 61 1.986
69
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 1.904
70
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.904
71
NTR005 Nutritional Deficiency Disease 60 1.904
72
P SLP005 Sleep Disorder 62 1.895
73
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.852
74
P KDN018 Kidney Disease 72 1.852
75
CMP002 Campylobacteriosis 50 1.841
76
ACT058 Active Peptic Ulcer Disease 55 1.829
77
P TRN020 Turner Syndrome 67 1.821
78
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 1.764
79
P ESP024 Esophagitis 60 1.764
80
MCR191 Microscopic Colitis 46 1.706
81
VGN023 Vaginitis 56 1.696
82
GST037 Gastroparesis 52 1.647
83
SHG001 Shigellosis 61 1.626
84
GST045 Gastroenteritis 58 1.626
85
c SCL052 Scleroderma, Familial Progressive 60 1.611
86
P SYS005 Systemic Scleroderma 73 1.611
87
HPT009 Hepatopulmonary Syndrome 48 1.611
88
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.604
89
P TRM003 Tremor 50 1.578
90
CLL021 Collagenous Colitis 41 1.569
91
c TYP009 Type 2 Diabetes Mellitus 92 1.563
92
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.563
93
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.563
94
VGN020 Vaginal Disease 48 1.563
95
INT072 Intestinal Pseudo-Obstruction 60 1.513
96
c HPT073 Hepatitis C Virus 71 1.513
97
DFC004 Deficiency Anemia 74 1.513
98
CYT002 Cytokine Deficiency 43 1.513
99
HML018 Homologous Wasting Disease 21 1.513
100
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.449
101
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.449
102
PRS047 Prostatitis 58 1.445
103
P ALZ034 Alzheimer Disease 87 1.380
104
P BRS047 Breast Cancer 97 1.380
105
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.380
106
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.380
107
c PNS012 Paine Syndrome 60 1.380
108
IMM072 Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 1 52 1.380
109
INT319 Intestinal Pseudoobstruction, Neuronal, Chronic Idiopathic, X-Linked 40 1.380
110
TRP004 Tropical Sprue 39 1.380
111
SPR126 Superior Semicircular Canal Dehiscence 41 1.380
112
P ANR048 Aniridia 1 66 1.380
113
LYM012 Lymphoplasmacytic Lymphoma 50 1.380
114
c BNG023 Benign Familial Infantile Epilepsy 57 1.380
115
SCK003 Sickle Cell Anemia 74 1.380
116
HMN044 Human Immunodeficiency Virus Type 1 76 1.380
117
c BLD140 Blood Group, I System 47 1.380
118
VSC044 Visceral Myopathy 50 1.380
119
P HMN038 Human Coronavirus Sensitivity 30 1.380
120
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.380
121
c CNG413 Congenital Short Bowel Syndrome 42 1.380
122
c THR092 Thrombophilia Due to Thrombin Defect 74 1.380
123
WLD007 Waldenstroem's Macroglobulinemia 65 1.380
124
THR024 Thrombosis 56 1.380
125
PLS009 Plasma Cell Neoplasm 64 1.380
126
RCT015 Reactive Arthritis 60 1.380
127
P RCT021 Rectum Cancer 54 1.380
128
ADR007 Adrenoleukodystrophy 74 1.380
129
DFF003 Diffuse Scleroderma 41 1.380
130
VRL011 Viral Infectious Disease 60 1.380
131
P VSC018 Visceral Steatosis 32 1.380
132
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.380
133
P ART022 Arthritis 70 1.380
134
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 1.380
135
P DBT009 Diabetes Mellitus 67 1.380
136
c HMG029 Hemoglobin Se Disease 41 1.380
137
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.380
138
MCR004 Macroglobulinemia 48 1.380
139
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 37 1.380
140
CHL123 Chlamydia 58 1.371
141
P CHL066 Cholangitis 51 1.355
142
P NTR004 Neutropenia 62 1.352
143
c ACT134 Acute Liver Failure 57 1.352
144
c CHR684 Chronic Kidney Disease 74 1.310
145
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 1.275
146
c CHL119 Cholangitis, Primary Sclerosing 57 1.246
147
P SCL009 Sclerosing Cholangitis 46 1.246
148
MST005 Mastitis 52 1.230
149
DVR001 Diverticulitis of Colon 24 1.230
150
P URT039 Urticaria 57 1.230
151
P EXN002 Exanthem 58 1.206
152
ALC009 Alcoholic Liver Cirrhosis 54 1.120
153
P THR014 Thrombocytopenia 66 1.120
154
P PRP019 Peripheral Nervous System Disease 57 1.102
155
P NRP001 Neuropathy 59 1.102
156
DSS032 Disease by Infectious Agent 55 1.084
157
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.065
158
SCH014 Schistosomiasis 56 1.065
159
END086 End Stage Renal Disease 54 1.060
160
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 25 1.045
161
CNG034 Congestive Heart Failure 69 1.028
162
CLN019 Colonic Disease 47 1.025
163
ISC004 Ischemia 61 1.003
164
P HML001 Hemolytic-Uremic Syndrome 52 0.980
165
c VRL010 Viral Hepatitis 52 0.980
166
CHL014 Cholera 62 0.980
167
BRN004 Brain Edema 54 0.980
168
SPN051 Spondylitis 51 0.980
169
TXC005 Toxic Shock Syndrome 62 0.980
170
INF009 Inflammatory Spondylopathy 30 0.980
172
c ACT027 Acute Pancreatitis 60 0.956
173
47X002 47,xyy 48 0.956
174
CYS001 Cystic Fibrosis 77 0.930
175
P END046 Endometritis 46 0.930
176
P LCT002 Lactose Intolerance 52 0.930
177
c ACT071 Acute Kidney Failure 60 0.930
178
HMP009 Haemophilus Influenzae 41 0.930
179
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 54 0.901
180
P HML002 Hemolytic Anemia 62 0.901
181
GST040 Gastric Adenocarcinoma 66 0.901
182
PST030 Postcholecystectomy Syndrome 33 0.901
183
P INF038 Influenza 68 0.901
184
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.894
185
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.894
186
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.894
187
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.894
188
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.894
189
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.894
190
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.894
191
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.894
192
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.894
193
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.894
194
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.894
195
c INF145 Infantile Liver Failure Syndrome 1 44 0.894
196
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.894
197
HYP081 Hypolipoproteinemia 49 0.894
198
DMP001 Dumping Syndrome 43 0.894
199
P HRT032 Heart Disease 84 0.894
200
CRB009 Cerebritis 43 0.894
201
SYS003 Systolic Heart Failure 49 0.894
202
PRS011 Persian Gulf Syndrome 35 0.894
203
HYP056 Hypoglycemia 65 0.894
204
END072 Endotheliitis 36 0.894
205
P RST001 Restless Legs Syndrome 52 0.870
206
NSS002 Neisseria Meningitidis Infection 47 0.870
207
MCS002 Mucositis 55 0.834
208
GST023 Gastric Ulcer 52 0.834
209
ERY003 Erythema Multiforme 56 0.792
210
SVR097 Severe Cutaneous Adverse Reaction 68 0.792
211
ERY066 Erythema Multiforme Major 29 0.792
212
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.792
213
P CLR023 Colorectal Cancer 100 0.752
214
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.737
215
ENT011 Enterocolitis 55 0.737
216
CHD004 Chudley-Mccullough Syndrome 47 0.737
217
PRS036 Parasitic Protozoa Infectious Disease 44 0.737
218
P MVM001 Movement Disease 61 0.737
219
P DYS154 Dystonia 64 0.737
220
CHR073 Choreatic Disease 53 0.737
221
P PNM007 Pneumonia 64 0.737
222
PYD002 Pyoderma 49 0.737
223
PYD001 Pyoderma Gangrenosum 53 0.737
224
P PNC044 Pancreatitis 61 0.462
225
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.454
226
P CNR004 Cone-Rod Dystrophy 2 75 0.454
227
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.454
228
P ADN016 Adenocarcinoma 63 0.454
229
CLN015 Colon Adenocarcinoma 64 0.454
230
ATX019 Ataxia with Vitamin E Deficiency 44 0.454
231
STM006 Stomach Disease 47 0.454
232
P LYM118 Lymphoma 69 0.441
233
P LKM002 Leukemia 66 0.441
234
LYM019 Lymphosarcoma 46 0.441
235
P HDC001 Headache 56 0.400
236
P CLS010 Cluster Headache 42 0.377
237
ASP007 Aspiration Pneumonia 49 0.326
238
c GLL024 Gallbladder Disease 1 53 0.267
239
PPT005 Peptic Ulcer Disease 58 0.267
240
GST092 Gastroesophageal Reflux 60 0.231
241
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.231
242
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.231
243
c ACT068 Acute Cystitis 61 0.231
244
FBR047 Fibromyalgia 58 0.231
245
ATN004 Autonomic Neuropathy 42 0.231
246
GRD001 Giardiasis 46 0.188
247
P END033 Endocarditis 58 0.188
248
LYM042 Lymphocytic Colitis 40 0.188
249
HPT085 Hepatitis, Fulminant Viral 33 0.188
250
STT001 Status Epilepticus 58 0.188
251
P URN019 Urinary Tract Infection 49 0.188
252
c INH020 Inherited Metabolic Disorder 47 0.188
253
c ATM011 Autoimmune Hepatitis 62 0.188
254
ACR007 Acromegaly 70 0.188
255
P INT143 Interstitial Cystitis 59 0.188
256
P CYS018 Cystitis 59 0.188
257
PRM236 Primary Biliary Cholangitis 62 0.188
258
FNC002 Functional Diarrhea 39 0.188
259
MGC001 Megacolon 48 0.188
260
P SZR006 Seizure Disorder 69 0.188
261
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.188
262
BDD001 Budd-Chiari Syndrome 62 0.133
263
MYL069 Myeloma, Multiple 77 0.133
264
WLS001 Wilson Disease 70 0.133
265
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.133
266
MLD018 Mild Cognitive Impairment 48 0.133
267
DPH021 Diaphragm Disease 42 0.133
268
NDL024 Nodal Marginal Zone Lymphoma 37 0.133
269
c MGR028 Migraine with or Without Aura 1 64 0.133
270
P LPR021 Leprosy 3 71 0.133
271
P CRG003 Crigler-Najjar Syndrome, Type I 64 0.133
272
HYP025 Hyperphosphatemia 47 0.133
273
ISC015 Ischemic Colitis 43 0.133
274
P SCL018 Scoliosis 57 0.133
275
DRG024 Drug Allergy 40 0.133
276
SPP012 Suppressor of Tumorigenicity 11 19 0.133
277
INT051 Intussusception 53 0.133
278
ATM095 Autoimmune Disease 61 0.133
279
c SYS001 Systemic Lupus Erythematosus 86 0.133
280
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.133
281
BLR028 Biliary Atresia, Extrahepatic 36 0.133
282
P SJG008 Sjogren Syndrome 61 0.133
283
RBS001 Rabies 58 0.133
284
HSH003 Hashimoto Thyroiditis 60 0.133
285
P EPL164 Epilepsy 70 0.133
286
AVD001 Avoidant Personality Disorder 49 0.133
287
P PRS038 Personality Disorder 65 0.133
288
P BND020 Bone Disease 60 0.133
289
ALV002 Alveolar Echinococcosis 56 0.133
290
BLR001 Biliary Atresia 55 0.133
291
PNC001 Pancytopenia 52 0.133
292
CHL068 Cholestasis 61 0.133
293
LPD008 Lipid Metabolism Disorder 61 0.133
294
P END044 Endometriosis 62 0.133
295
NPH009 Nephrolithiasis 54 0.133
296
HYP063 Hypersplenism 52 0.133
297
TRC003 Trichomoniasis 53 0.133
298
CRY003 Cryptosporidiosis 55 0.133
299
QDR001 Quadriplegia 49 0.133
300
TYP007 Typhoid Fever 63 0.133
301
P HYP086 Hypothyroidism 69 0.133
302
c ACT036 Acute Cholangitis 35 0.133
303
ASC003 Ascending Cholangitis 25 0.133
304
ECH003 Echinococcosis 52 0.133
305
TXC001 Toxic Megacolon 37 0.133
306
MGL001 Megaloblastic Anemia 59 0.133
307
NRG002 Neurogenic Bladder 55 0.133
308
JPN002 Japanese Encephalitis 61 0.133
309
ONC002 Onchocerciasis 50 0.133
310
LYM017 Lyme Disease 63 0.133
311
HYP066 Hyperglycemia 60 0.133
312
P ECT006 Ectodermal Dysplasia 62 0.133
313
MDD011 Mood Disorder 62 0.133
314
PLG002 Plague 58 0.133
315
OMN001 Omenn Syndrome 63 0.133
316
ATN005 Autonomic Dysfunction 45 0.133
317
P THY032 Thyroiditis 56 0.133
318
DYS073 Dysphagia 53 0.133
319
HYP266 Hypoxia 56 0.133
320
INT075 Intracranial Hypertension 52 0.133
321
YLL002 Yellow Fever 61 0.133
322
HYP005 Hypokalemia 55 0.133
323
SPN186 Spinal Cord Injury 61 0.133
324
P LPS004 Lupus Erythematosus 61 0.133
325
CHC001 Chickenpox 56 0.133
326
ILS001 Ileus 49 0.133
327
HNS001 Hansen's Disease 32 0.133
328
RFR013 Refractory Celiac Disease 33 0.133
329
CNG491 Congenital Portosystemic Shunt 17 0.133
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