Search results for Pravastatin

311 hits were found for Pravastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 65 0.303
2
c CRN018 Coronary Artery Anomaly 74 0.251
3
c CRN300 Coronary Heart Disease 1 62 0.244
4
c HRT032 Heart Disease 76 0.231
5
c MYC007 Myocardial Infarction 78 0.211
6
ISC004 Ischemia 67 0.208
7
ART140 Arteries, Anomalies of 67 0.208
8
ISC006 Ischemic Heart Disease 72 0.202
9
ACQ007 Acquired Immunodeficiency Syndrome 66 0.190
10
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.190
11
c HYP607 Hypercholesterolemia, Familial 82 0.180
12
c CRD246 Cardiovascular System Disease 57 0.176
13
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.172
14
c KDN018 Kidney Disease 71 0.172
15
c DBT009 Diabetes Mellitus 67 0.165
16
P PRC016 Pre-Eclampsia 61 0.145
17
c ART021 Arteriosclerosis 61 0.145
18
c HPT023 Hepatocellular Carcinoma 97 0.136
19
P CHR089 Chronic Kidney Failure 73 0.136
20
VSC007 Vascular Disease 72 0.136
21
c LVR013 Liver Disease 77 0.132
22
ANG054 Angina Pectoris 70 0.132
23
URN009 Urinary System Disease 59 0.132
25
c ADN016 Adenocarcinoma 71 0.122
26
c LKM002 Leukemia 72 0.117
27
CNG034 Congestive Heart Failure 71 0.117
28
THR024 Thrombosis 64 0.117
29
SPS003 Spastic Diplegia 49 0.117
30
P LKM061 Leukemia, Acute Myeloid 83 0.111
31
ALL026 Allergic Hypersensitivity Disease 68 0.111
32
c MYL006 Myeloid Leukemia 68 0.111
33
LVR012 Liver Cirrhosis 67 0.106
34
END030 End Stage Renal Failure 60 0.106
35
ACT118 Acute Non Lymphoblastic Leukemia 33 0.106
36
PSY004 Psychotic Disorder 74 0.100
37
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.100
38
PLC008 Placenta Disease 59 0.100
39
GLC003 Glucose Intolerance 59 0.100
40
P ACT075 Acute Myocardial Infarction 57 0.100
41
c HYP614 Hyperlipidemia, Familial Combined 56 0.100
42
PRP080 Peripheral Artery Disease 56 0.100
43
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.100
44
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.100
45
AST005 Asthma 81 0.093
46
PRP027 Peripheral Vascular Disease 72 0.093
47
ATM095 Autoimmune Disease 68 0.093
48
c MYP004 Myopathy 65 0.093
49
GLC008 Glucose Metabolism Disease 54 0.093
50
c ART022 Arthritis 78 0.086
51
c SCH015 Schizophrenia 73 0.086
52
CRB039 Cerebrovascular Disease 70 0.086
53
CNN005 Connective Tissue Disease 67 0.086
54
P ACT210 Acute Respiratory Distress Syndrome 66 0.086
55
c PLY014 Polycystic Kidney Disease 63 0.086
56
P ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.086
57
c NPH012 Nephrotic Syndrome 59 0.086
58
P ACT071 Acute Kidney Failure 54 0.086
59
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.086
60
DPR016 Depression 73 0.079
61
c PNM007 Pneumonia 72 0.079
62
c MCR115 Microvascular Complications of Diabetes 5 71 0.079
63
GST050 Gastrointestinal System Disease 67 0.079
64
HYP066 Hyperglycemia 65 0.079
65
MGK001 Megakaryocytic Leukemia 64 0.079
66
MYL031 Myeloproliferative Neoplasm 64 0.079
67
GST049 Gastrointestinal System Cancer 62 0.079
68
c CMR001 Camurati-Engelmann Disease 62 0.079
69
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 59 0.079
70
c ECL001 Eclampsia 59 0.079
71
RTN018 Retinal Disease 58 0.079
72
P LKM070 Leukemia, Acute Monocytic 57 0.079
73
c MNC007 Monocytic Leukemia 57 0.079
74
SCH012 Schizoaffective Disorder 54 0.079
75
INT007 Intermediate Coronary Syndrome 50 0.079
76
ACT098 Acute Erythroid Leukemia 50 0.079
77
ACT200 Acute Monoblastic Leukemia 48 0.079
78
GST071 Gastrointestinal Carcinoma 46 0.079
79
ACT113 Acute Myeloblastic Leukemia with Maturation 43 0.079
80
P PRC031 Preeclampsia/eclampsia 1 41 0.079
81
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.079
82
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.079
83
P ADL093 Adult Acute Monocytic Leukemia 22 0.079
84
c RHM011 Rheumatoid Arthritis 82 0.070
85
c HPT021 Hepatitis 74 0.070
86
ANX010 Anxiety 73 0.070
87
c GRF003 Graft-Versus-Host Disease 72 0.070
88
MYL009 Myelodysplastic Syndrome 71 0.070
89
DSS008 Disease of Mental Health 70 0.070
90
LNG099 Lung Disease 70 0.070
91
c ATR011 Atrial Fibrillation 69 0.070
92
OBS002 Obsessive-Compulsive Disorder 69 0.070
93
c ART023 Arthropathy 68 0.070
94
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.070
95
c MJR001 Major Depressive Disorder 67 0.070
96
P HPT003 Hepatitis a 66 0.070
97
c ENC018 Encephalopathy 65 0.070
98
RHM027 Rheumatic Disease 65 0.070
99
MNT002 Mental Depression 65 0.070
100
MDD011 Mood Disorder 65 0.070
101
JNT002 Joint Disorders 64 0.070
102
BCT022 Bacterial Infectious Disease 63 0.070
103
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.070
104
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.070
105
END040 Endogenous Depression 59 0.070
106
HYP060 Hyperinsulinism 57 0.070
107
c PNC025 Panic Disorder 57 0.070
108
P SVR005 Severe Pre-Eclampsia 55 0.070
109
PST021 Postpartum Depression 55 0.070
110
GNR004 Generalized Anxiety Disorder 55 0.070
111
HLL004 Hellp Syndrome 52 0.070
112
c CLL015 Collagen Disease 52 0.070
113
PRD004 Prediabetes Syndrome 51 0.070
114
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.070
115
ART004 Aortic Atherosclerosis 45 0.070
116
c BRS047 Breast Cancer 100 0.061
117
c LNG032 Lung Cancer 99 0.061
118
P SYS001 Systemic Lupus Erythematosus 88 0.061
119
c ALZ034 Alzheimer Disease 88 0.061
120
ESP021 Esophageal Cancer 84 0.061
121
STR067 Stroke, Ischemic 84 0.061
122
CRH001 Crohn's Disease 79 0.061
123
GST053 Gastric Cancer 78 0.061
124
P HYP595 Hypertension, Essential 77 0.061
125
c MLT020 Multiple Sclerosis 76 0.061
126
PLM001 Pulmonary Tuberculosis 74 0.061
127
KWS002 Kawasaki Disease 72 0.061
128
P JVN004 Juvenile Myelomonocytic Leukemia 70 0.061
129
c PLM036 Pulmonary Fibrosis 70 0.061
130
c LYM118 Lymphoma 69 0.061
131
c LPS004 Lupus Erythematosus 69 0.061
132
P SML038 Small Cell Cancer of the Lung 69 0.061
133
DMN002 Dementia 69 0.061
134
c VSC011 Vasculitis 67 0.061
135
GST045 Gastroenteritis 65 0.061
136
c CHR285 Chronic Myelomonocytic Leukemia 65 0.061
137
c ADL010 Adult Respiratory Distress Syndrome 64 0.061
138
RSP006 Respiratory System Disease 64 0.061
139
HMR039 Hemorrhage, Intracerebral 62 0.061
140
c INT068 Intestinal Disease 62 0.061
141
CRH005 Crohn's Colitis 61 0.061
142
c SML001 Small Cell Carcinoma 61 0.061
143
NWB001 Newborn Respiratory Distress Syndrome 61 0.061
144
c ANT006 Antiphospholipid Syndrome 60 0.061
145
CHL068 Cholestasis 60 0.061
146
P VRL010 Viral Hepatitis 60 0.061
147
DMY004 Demyelinating Disease 60 0.061
148
PLM010 Pulmonary Edema 60 0.061
149
BRN106 Burns 59 0.061
150
TRN015 Transient Cerebral Ischemia 59 0.061
151
ILT001 Ileitis 59 0.061
152
LYM019 Lymphosarcoma 59 0.061
153
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.061
154
ESP023 Esophageal Disease 59 0.061
155
PRN019 Perinatal Necrotizing Enterocolitis 58 0.061
156
P MCR113 Microvascular Complications of Diabetes 3 58 0.061
157
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.061
158
P INF071 Inflammatory Bowel Disease 1 57 0.061
159
STM006 Stomach Disease 56 0.061
160
c MSC033 Muscle Disorders 56 0.061
161
LNG031 Lung Benign Neoplasm 56 0.061
162
c INF037 Inflammatory Bowel Disease 56 0.061
163
ENT011 Enterocolitis 55 0.061
164
MYL004 Myelodysplastic Myeloproliferative Cancer 54 0.061
165
c PRM002 Primary Hyperoxaluria 54 0.061
166
CLC006 Calcinosis 53 0.061
167
P ADL096 Adult Hepatocellular Carcinoma 48 0.061
168
CRB085 Cerebral Hemorrhage 46 0.061
169
P MCR120 Microvascular Complications of Diabetes 7 46 0.061
170
P MCR130 Microvascular Complications of Diabetes 6 43 0.061
171
P MCR133 Microvascular Complications of Diabetes 4 43 0.061
172
BRN039 Bronchial Neoplasm 43 0.061
173
SCH003 Schizophreniform Disorder 43 0.061
174
P HYP794 Hyperoxaluria, Primary, Type I 43 0.061
175
RSP007 Respiratory Distress Syndrome, Infant 38 0.061
176
P TRC078 Trichohepatoenteric Syndrome 2 35 0.061
177
MYL074 Myelodysplastic Syndrome with Excess Blasts 33 0.061
178
BRN097 Brainstem Auditory Evoked Responses 26 0.061
179
MNS002 Mini Stroke 25 0.061
180
c PRS040 Prostate Cancer 93 0.050
181
MYL069 Myeloma, Multiple 85 0.050
182
INS024 Insulin-Like Growth Factor I 83 0.050
183
HMN044 Human Immunodeficiency Virus Type 1 75 0.050
184
c INF038 Influenza 75 0.050
185
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.050
186
P HPT073 Hepatitis C Virus 73 0.050
187
c AMY004 Amyloidosis 69 0.050
188
P HPT001 Hepatitis C 69 0.050
189
VRL011 Viral Infectious Disease 69 0.050
190
SKN016 Skin Disease 68 0.050
191
OST003 Osteonecrosis 67 0.050
192
c PRP003 Porphyria Cutanea Tarda 67 0.050
193
HSH003 Hashimoto Thyroiditis 67 0.050
194
P CHR417 Chronic Graft Versus Host Disease 67 0.050
195
P MCR129 Microvascular Complications of Diabetes 1 66 0.050
196
c PRP019 Peripheral Nervous System Disease 66 0.050
197
P CNT035 Central Nervous System Disease 65 0.050
198
CRB011 Cerebrotendinous Xanthomatosis 65 0.050
199
c HRM001 Hermansky-Pudlak Syndrome 64 0.050
200
c NRP001 Neuropathy 63 0.050
201
AGN016 Aging 63 0.050
202
ERY003 Erythema Multiforme 63 0.050
203
P ACT073 Acute Leukemia 62 0.050
204
c MYS005 Myositis 62 0.050
205
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.050
206
c PRP029 Porphyria 60 0.050
207
P PCH015 Pachyonychia Congenita 1 60 0.050
208
c HMR003 Hemorrhagic Disease 59 0.050
209
HMT018 Hematopoietic Stem Cell Transplantation 59 0.050
210
c OCL002 Oculocutaneous Albinism 58 0.050
211
c HYP750 Hypertriglyceridemia, Familial 58 0.050
212
NRT004 Neuritis 58 0.050
213
CRT016 Carotid Artery Disease 58 0.050
214
BLD053 Blood Platelet Disease 56 0.050
215
CYS039 Cystic Kidney Disease 55 0.050
216
MSC190 Muscular Disease 55 0.050
217
XNT003 Xanthomatosis 54 0.050
218
IDP024 Idiopathic Inflammatory Myopathy 52 0.050
219
P HRM005 Hermansky-Pudlak Syndrome 1 51 0.050
220
c BLD051 Blood Coagulation Disease 51 0.050
221
P HRM008 Hermansky-Pudlak Syndrome 5 51 0.050
222
CHL061 Childhood Leukemia 51 0.050
223
SKN027 Skin Conditions 51 0.050
224
MLR006 Male Reproductive Organ Cancer 50 0.050
225
c FML035 Familial Hyperlipidemia 50 0.050
226
P HRM006 Hermansky-Pudlak Syndrome 3 50 0.050
227
AMN002 Amino Acid Metabolic Disorder 49 0.050
228
P HNT004 Huntington Disease-Like 2 48 0.050
229
ALB002 Albinism 48 0.050
230
STR089 Storage Pool Platelet Disease 48 0.050
231
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.050
232
PGM003 Pigmentation Disease 48 0.050
233
PRS042 Prostate Disease 47 0.050
234
P PCH012 Pachyonychia Congenita 2 47 0.050
235
NPH010 Nephrosclerosis 46 0.050
236
BRN080 Brain Ischemia 43 0.050
237
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.050
238
P HRM009 Hermansky-Pudlak Syndrome 6 43 0.050
239
P MCR112 Microvascular Complications of Diabetes 2 42 0.050
240
P INH004 Inherited Blood Coagulation Disease 41 0.050
241
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.050
242
P HNT011 Huntington Disease-Like 3 40 0.050
243
MSC004 Muscle Tissue Disease 39 0.050
244
P HRM011 Hermansky-Pudlak Syndrome 8 39 0.050
245
P HRM012 Hermansky-Pudlak Syndrome 9 37 0.050
246
HYP114 Hypertensive Nephropathy 37 0.050
247
P HRM007 Hermansky-Pudlak Syndrome 4 36 0.050
248
P HRM010 Hermansky-Pudlak Syndrome 7 34 0.050
249
DLT018 Dilution, Pigmentary 31 0.050
250
P HYP805 Hypercholesterolemia, Autosomal Dominant, 3 29 0.050
251
LYM053 Lymphomatous Thyroiditis 27 0.050
252
HYP213 Hypomelanotic Disorder 26 0.050
253
HML018 Homologous Wasting Disease 25 0.050
254
AMN012 Aminoacidopathies 25 0.050
255
P HYP163 Hyperlipidemia Type 3 22 0.050
256
INB001 Inborn Amino Acid Metabolism Disorder 16 0.050
257
c PLM037 Pulmonary Hypertension 77 0.035
258
c NRV007 Nervous System Disease 72 0.035
259
c PSR002 Psoriasis 67 0.035
260
CHL123 Chlamydia 66 0.035
261
c CRD119 Cardiac Arrest 66 0.035
262
c DRM010 Dermatomyositis 66 0.035
263
c END044 Endometriosis 65 0.035
264
QFV001 Q Fever 63 0.035
265
c CND004 Candidiasis 63 0.035
266
c HST010 Histiocytosis 63 0.035
267
HYP266 Hypoxia 63 0.035
268
PRM236 Primary Biliary Cholangitis 63 0.035
269
BRN002 Bronchiolitis 62 0.035
270
PRP030 Purpura 62 0.035
271
MXD005 Mixed Connective Tissue Disease 61 0.035
272
ING001 Inguinal Hernia 61 0.035
273
NRM005 Neuromuscular Disease 61 0.035
274
ALL006 Allergic Asthma 61 0.035
275
c GST044 Gastritis 61 0.035
276
ATH013 Atherosclerosis Susceptibility 61 0.035
277
c NTR004 Neutropenia 61 0.035
278
c INF032 Infertility 60 0.035
279
c FCL005 Focal Segmental Glomerulosclerosis 60 0.035
280
BRN012 Bronchiolitis Obliterans 60 0.035
281
SQM006 Squamous Cell Carcinoma 59 0.035
282
c PLY041 Polymyositis 59 0.035
283
IMP005 Impotence 58 0.035
284
c ICH004 Ichthyosis 57 0.035
285
c GLM045 Glioma 56 0.035
286
LYM024 Lymphatic System Disease 55 0.035
287
NNL002 Nonalcoholic Steatohepatitis 55 0.035
288
c PRM006 Primary Biliary Cirrhosis 54 0.035
289
PNG002 Pain Agnosia 54 0.035
290
HDN002 Head Injury 52 0.035
291
P FCL025 Focal Segmental Glomerulosclerosis 1 52 0.035
292
c MTC133 Mitochondrial Myopathy 52 0.035
293
PST011 Pustulosis of Palm and Sole 50 0.035
294
ASP030 Aspirin Resistance 46 0.035
295
MYC005 Myocardial Stunning 46 0.035
296
CRB004 Cerebral Artery Occlusion 46 0.035
297
c PRP034 Purpura Fulminans 46 0.035
298
CRB086 Cerebral Aneurysms 44 0.035
299
BLN006 Blind Loop Syndrome 43 0.035
300
CHL147 Chlamydia Pneumonia 42 0.035
301
SCR011 Scrapie 42 0.035
302
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.035
303
CRT004 Carotid Artery Thrombosis 37 0.035
304
PRM087 Premature Chromatid Separation Trait 36 0.035
305
MYT011 Myotonia 34 0.035
306
P ICH023 Ichthyosis, Acquired 34 0.035
307
DFC001 Defective Apolipoprotein B-100 32 0.035
308
SLN001 Silent Myocardial Infarction 24 0.035
309
IND009 Indeterminate Cell Histiocytosis 21 0.035
310
DST081 Distal Trisomy 11q 20 0.035
311
VSC009 Vascular Skin Disease 20 0.035
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