Search results for Bosentan

299 hits were found for Bosentan

# Family MCID Name MIFTS Score
1
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.719
2
P PLM037 Pulmonary Hypertension 68 0.601
3
c SCL052 Scleroderma, Familial Progressive 62 0.407
4
c HYP595 Hypertension, Essential 84 0.405
5
P SYS005 Systemic Scleroderma 70 0.321
6
CNN005 Connective Tissue Disease 66 0.266
7
P HRT032 Heart Disease 75 0.227
8
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.221
9
IDP011 Idiopathic Interstitial Pneumonia 63 0.218
10
P PLM036 Pulmonary Fibrosis 61 0.218
11
ESN011 Eisenmenger Syndrome 54 0.218
12
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.212
13
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.212
14
LNG099 Lung Disease 61 0.208
15
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.205
16
RYN005 Raynaud Phenomenon 46 0.184
17
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.180
18
DFF003 Diffuse Scleroderma 42 0.180
19
ADR007 Adrenoleukodystrophy 74 0.177
20
P VSC007 Vascular Disease 63 0.177
21
INT066 Interstitial Lung Disease 59 0.173
22
CNG034 Congestive Heart Failure 70 0.169
23
PLM186 Pulmonary Arterial Hypertension Associated with Portal Hypertension 25 0.161
24
DWN001 Down Syndrome 70 0.138
25
HRT011 Heart Septal Defect 50 0.138
26
PLM189 Pulmonary Arterial Hypertension Associated with Connective Tissue Disease 26 0.138
27
P SRC025 Sarcoidosis 1 70 0.133
28
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.133
29
PLM184 Pulmonary Arterial Hypertension Associated with Congenital Heart Disease 42 0.133
30
SNG003 Single Ventricular Heart 30 0.133
31
P PNM007 Pneumonia 68 0.128
32
LVR012 Liver Cirrhosis 63 0.128
33
HYP266 Hypoxia 56 0.128
34
PRT013 Portal Hypertension 60 0.122
35
BRG013 Buerger Disease 57 0.122
36
47X002 47,xyy 49 0.122
37
ISC004 Ischemia 60 0.116
38
P ATR010 Atrial Heart Septal Defect 60 0.116
39
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.111
40
P TRN020 Turner Syndrome 65 0.111
41
P DBT009 Diabetes Mellitus 64 0.111
43
ACT029 Acute Interstitial Pneumonia 44 0.111
44
MCC013 Mucocutaneous Ulceration, Chronic 39 0.111
45
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.104
46
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.104
47
P KDN018 Kidney Disease 70 0.104
48
TXC005 Toxic Shock Syndrome 61 0.104
49
P VNT002 Ventricular Septal Defect 60 0.104
50
P SCK005 Sickle Cell Disease 50 0.104
51
c SYS001 Systemic Lupus Erythematosus 86 0.097
52
DFC004 Deficiency Anemia 75 0.097
53
SCK003 Sickle Cell Anemia 72 0.097
54
SPR126 Superior Semicircular Canal Dehiscence 40 0.097
55
48X005 48,xyyy 39 0.097
56
c HMG029 Hemoglobin Se Disease 38 0.097
57
c LCL006 Localized Scleroderma 62 0.090
58
P LPS004 Lupus Erythematosus 61 0.090
59
ATM095 Autoimmune Disease 61 0.090
60
P PTN014 Patent Ductus Arteriosus 1 60 0.090
61
PLM012 Pulmonary Sarcoidosis 53 0.090
62
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.090
63
c SRC023 Sarcoidosis 2 43 0.090
64
P RSP003 Respiratory Failure 74 0.082
65
PRP027 Peripheral Vascular Disease 71 0.082
66
ATH013 Atherosclerosis Susceptibility 66 0.082
67
MSC007 Muscle Hypertrophy 63 0.082
68
P VSC011 Vasculitis 62 0.082
69
INT002 Intermittent Claudication 61 0.082
70
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.082
71
P THL005 Thalassemia 60 0.082
72
MXD005 Mixed Connective Tissue Disease 59 0.082
73
P OPT006 Optic Nerve Disease 57 0.082
74
TLN003 Telangiectasis 51 0.082
75
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.082
76
AST005 Asthma 77 0.074
77
MLN008 Melanoma 69 0.074
78
SKN019 Skin Melanoma 67 0.074
79
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.074
80
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.074
81
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.074
82
PLM033 Pulmonary Embolism 59 0.074
83
END030 End Stage Renal Failure 58 0.074
84
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.074
85
P HDC001 Headache 57 0.074
86
P NRP001 Neuropathy 56 0.074
87
PRP080 Peripheral Artery Disease 53 0.074
88
P MTR003 Mitral Valve Stenosis 50 0.074
89
RYN001 Raynaud Disease 49 0.074
90
CRN019 Coronary Artery Vasospasm 46 0.074
91
SYN036 Syncope 45 0.074
92
CYN002 Cyanosis, Transient Neonatal 45 0.074
93
NNS002 Nonspecific Interstitial Pneumonia 45 0.074
94
CYT002 Cytokine Deficiency 44 0.074
95
INT276 Interatrial Communication 42 0.074
96
P PNC035 Pancreatic Cancer 84 0.064
97
c BTT014 Beta-Thalassemia 72 0.064
98
P SLP006 Sleep Apnea 69 0.064
99
c CHR684 Chronic Kidney Disease 66 0.064
100
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.064
101
P MCR115 Microvascular Complications of Diabetes 5 66 0.064
102
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
103
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.064
104
c RHB024 Rhabdomyosarcoma 2 65 0.064
105
APN008 Apnea, Obstructive Sleep 65 0.064
106
LPD008 Lipid Metabolism Disorder 62 0.064
107
c ALP101 Alpha-Thalassemia 62 0.064
108
P HMN010 Hemangioma 61 0.064
109
P MYC008 Myocarditis 59 0.064
110
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.064
111
EXT034 Extrinsic Allergic Alveolitis 58 0.064
112
P OPT009 Optic Neuritis 56 0.064
113
NRT004 Neuritis 53 0.064
114
PRS030 Persistent Fetal Circulation Syndrome 52 0.064
115
c MCR113 Microvascular Complications of Diabetes 3 52 0.064
116
HYP014 Hyperuricemia 51 0.064
117
P CPL006 Capillary Hemangioma 51 0.064
118
P PRC012 Pericardial Effusion 51 0.064
119
SYS003 Systolic Heart Failure 50 0.064
120
HPT009 Hepatopulmonary Syndrome 49 0.064
121
PPL021 Papilledema 48 0.064
122
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.064
123
c MCR120 Microvascular Complications of Diabetes 7 47 0.064
124
c MTR002 Mitral Valve Insufficiency 47 0.064
125
HMP001 Hemopericardium 46 0.064
126
c TRC022 Tricuspid Valve Insufficiency 45 0.064
127
TRP009 Triple X Syndrome 42 0.064
128
c MCR130 Microvascular Complications of Diabetes 6 41 0.064
129
c MCR133 Microvascular Complications of Diabetes 4 41 0.064
130
c MCR112 Microvascular Complications of Diabetes 2 41 0.064
131
c CPL013 Capillary Malformations, Congenital 40 0.064
132
OPT010 Optic Papillitis 39 0.064
133
c CHR682 Chronic Bilirubin Encephalopathy 38 0.064
134
FST001 Foster-Kennedy Syndrome 37 0.064
135
CHR178 Chromosomal Triplication 35 0.064
136
ANX010 Anxiety 72 0.052
137
MLT157 Multiple System Atrophy 1 70 0.052
138
c MGR028 Migraine with or Without Aura 1 69 0.052
139
WRN001 Werner Syndrome 69 0.052
140
BRN024 Bronchitis 68 0.052
141
P TMP003 Temporal Arteritis 67 0.052
142
PRT036 Peritonitis 65 0.052
143
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.052
144
ALL026 Allergic Hypersensitivity Disease 64 0.052
145
P CRN018 Coronary Artery Anomaly 63 0.052
146
c ACT068 Acute Cystitis 63 0.052
147
P HYP055 Hypoplastic Left Heart Syndrome 62 0.052
148
c ATM011 Autoimmune Hepatitis 62 0.052
149
P DRM010 Dermatomyositis 61 0.052
150
CHL068 Cholestasis 60 0.052
151
VRC005 Varicose Veins 60 0.052
152
NTH001 Netherton Syndrome 60 0.052
153
PRT058 Pure Autonomic Failure 59 0.052
154
LNG108 Langerhans Cell Histiocytosis 58 0.052
155
P PLY041 Polymyositis 57 0.052
156
BRN056 Bronchopulmonary Dysplasia 57 0.052
157
AGN016 Aging 56 0.052
158
RHM027 Rheumatic Disease 56 0.052
159
P INF037 Inflammatory Bowel Disease 56 0.052
160
HYP005 Hypokalemia 55 0.052
161
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.052
162
P HST010 Histiocytosis 53 0.052
163
ART140 Arteries, Anomalies of 53 0.052
164
ACR041 Acromelic Frontonasal Dysostosis 52 0.052
165
TRC062 Tricuspid Atresia 52 0.052
166
ESP002 Esophageal Varix 51 0.052
167
P OPN001 Open-Angle Glaucoma 49 0.052
168
ENT004 Enthesopathy 48 0.052
169
P RNL015 Renal Hypertension 48 0.052
170
LMT001 Limited Scleroderma 47 0.052
171
PRT019 Protein-Losing Enteropathy 46 0.052
172
DST006 Diastolic Heart Failure 44 0.052
173
c HYP543 Hypoplastic Left Heart Syndrome 1 40 0.052
174
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.052
175
RRS014 Rare Surgical Neurologic Disease 32 0.052
176
UNV002 Univentricular Heart 28 0.052
177
CYT018 Cytochrome P450 2d6 Variant 27 0.052
178
IDP092 Idiopathic/heritable Pulmonary Arterial Hypertension 25 0.052
179
CLF033 Cleft Mitral Valve 18 0.052
180
P BRS047 Breast Cancer 96 0.037
181
MYL069 Myeloma, Multiple 85 0.037
182
c DLT002 Dilated Cardiomyopathy 79 0.037
183
CNN003 Conn's Syndrome 79 0.037
184
IMM167 Immune Deficiency Disease 78 0.037
185
P SCH015 Schizophrenia 75 0.037
186
c ATR087 Atrial Standstill 1 74 0.037
187
CRH001 Crohn's Disease 74 0.037
188
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.037
189
P MLT020 Multiple Sclerosis 72 0.037
190
P EPL164 Epilepsy 71 0.037
191
P OST001 Osteopetrosis 71 0.037
192
c HPT073 Hepatitis C Virus 70 0.037
193
MYL009 Myelodysplastic Syndrome 70 0.037
194
P TTR001 Tetralogy of Fallot 69 0.037
195
ADL002 Adult Syndrome 69 0.037
196
P INF038 Influenza 68 0.037
197
PSY004 Psychotic Disorder 67 0.037
198
HYP056 Hypoglycemia 66 0.037
199
P HYP098 Hypereosinophilic Syndrome 66 0.037
200
c HMP029 Hemophilia a 65 0.037
201
P ART005 Arteriovenous Malformation 65 0.037
202
P MNN013 Meningitis 65 0.037
203
P ATS364 Autism 65 0.037
204
P HRP006 Herpes Simplex 65 0.037
205
c DPH024 Diaphragmatic Hernia, Congenital 64 0.037
206
c ART101 Aortic Valve Disease 2 63 0.037
207
KND001 Kindler Syndrome 63 0.037
208
P ADL010 Adult Respiratory Distress Syndrome 63 0.037
209
c HPT001 Hepatitis C 63 0.037
210
P NTR004 Neutropenia 63 0.037
211
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.037
212
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.037
213
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.037
214
RHM001 Rheumatic Fever 61 0.037
215
P PNC044 Pancreatitis 61 0.037
216
ACQ007 Acquired Immunodeficiency Syndrome 60 0.037
217
HRP004 Herpes Zoster 60 0.037
218
APP008 Appendicitis 60 0.037
219
c ACT027 Acute Pancreatitis 59 0.037
220
c ACT071 Acute Kidney Failure 59 0.037
221
P SZR006 Seizure Disorder 58 0.037
222
VSL002 Visual Epilepsy 58 0.037
223
CNS004 Constipation 57 0.037
224
P END033 Endocarditis 57 0.037
225
P UVT001 Uveitis 57 0.037
226
P DRR001 Diarrhea 57 0.037
227
THR024 Thrombosis 56 0.037
228
P BPL003 Bipolar Disorder 56 0.037
229
c ACT075 Acute Myocardial Infarction 56 0.037
230
P CRD246 Cardiovascular System Disease 56 0.037
231
DBL002 Double Outlet Right Ventricle 56 0.037
232
P MYS005 Myositis 56 0.037
233
c BCT007 Bacterial Meningitis 55 0.037
234
LMB062 Limb Ischemia 55 0.037
235
CPL003 Capillary Leak Syndrome 55 0.037
236
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.037
237
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.037
238
P ATR001 Atrioventricular Septal Defect 55 0.037
239
FCT001 Factor Viii Deficiency 55 0.037
240
PLM010 Pulmonary Edema 55 0.037
241
P ANT006 Antiphospholipid Syndrome 54 0.037
242
P MYM013 Moyamoya Disease 1 54 0.037
243
P ART021 Arteriosclerosis 54 0.037
244
PRT082 Preterm Premature Rupture of the Membranes 54 0.037
245
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.037
246
MRG003 Marginal Zone B-Cell Lymphoma 53 0.037
247
ALC009 Alcoholic Liver Cirrhosis 53 0.037
248
HRT012 Heart Valve Disease 53 0.037
249
KRT009 Keratosis 53 0.037
250
P ACT105 Acute Mountain Sickness 52 0.037
251
OLG003 Oligohydramnios 52 0.037
252
P HMP007 Hemophilia 51 0.037
253
SPP010 Suppressor of Tumorigenicity 3 51 0.037
254
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.037
255
FSC004 Fasciitis 50 0.037
256
P OVR082 Overgrowth Syndrome 50 0.037
257
MTB004 Metabolic Acidosis 50 0.037
258
DDN011 Duodenal Atresia 49 0.037
259
CYT005 Cytomegalovirus Retinitis 49 0.037
260
BHR001 Behr Syndrome 49 0.037
261
CRY004 Cryoglobulinemia 49 0.037
262
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.037
263
CLC006 Calcinosis 48 0.037
264
ATX019 Ataxia with Vitamin E Deficiency 48 0.037
265
BNN003 Bone Inflammation Disease 48 0.037
266
ESN015 Eosinophilic Fasciitis 47 0.037
267
c BCT013 Bacterial Pneumonia 47 0.037
268
RNL077 Renal Fibrosis 47 0.037
269
RTN023 Retinitis 46 0.037
270
URT010 Ureteral Obstruction 46 0.037
271
PRL019 Prolidase Deficiency 46 0.037
272
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.037
273
CRB004 Cerebral Artery Occlusion 44 0.037
274
P MJR007 Major Affective Disorder 1 43 0.037
275
NRR001 Neuroretinitis 43 0.037
276
P CLL015 Collagen Disease 42 0.037
277
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.037
278
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.037
279
c MJR024 Major Affective Disorder 9 41 0.037
280
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 39 0.037
281
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.037
282
c MJR022 Major Affective Disorder 8 38 0.037
283
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.037
284
c PLM167 Pulmonary Venoocclusive Disease 2, Autosomal Recessive 36 0.037
285
c MJR008 Major Affective Disorder 2 34 0.037
286
DXR001 Doxorubicin Induced Cardiomyopathy 33 0.037
287
c MJR003 Major Affective Disorder 6 33 0.037
288
c MJR006 Major Affective Disorder 5 33 0.037
289
c MJR023 Major Affective Disorder 7 33 0.037
290
c MJR004 Major Affective Disorder 4 28 0.037
291
PLS031 Plastic Bronchitis 27 0.037
292
MST020 Mast Cell Activation Syndrome 27 0.037
293
CRT028 Cor Triatriatum 27 0.037
294
CMP035 Complete Atrioventricular Canal 26 0.037
295
PRQ002 Paraquat Poisoning 25 0.037
296
UNL013 Unilateral Absence of a Pulmonary Artery 21 0.037
297
DBL010 Double-Orifice Mitral Valve 18 0.037
298
CTN020 Cutaneous Sclerosis 17 0.037
299
c INF055 Infectious Myocarditis 17 0.037
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