Search results for Pravastatin

261 hits were found for Pravastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 58 0.313
2
P CRN018 Coronary Artery Anomaly 68 0.262
3
c CRN300 Coronary Heart Disease 1 64 0.245
4
P HRT032 Heart Disease 74 0.228
5
ISC004 Ischemia 65 0.225
6
ART140 Arteries, Anomalies of 65 0.218
7
P MYC007 Myocardial Infarction 79 0.212
8
ISC006 Ischemic Heart Disease 72 0.212
9
ACQ007 Acquired Immunodeficiency Syndrome 63 0.194
10
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.183
11
P HYP607 Hypercholesterolemia, Familial 79 0.179
12
P DBT009 Diabetes Mellitus 64 0.179
13
P KDN018 Kidney Disease 68 0.171
14
P ART021 Arteriosclerosis 60 0.154
15
P HPT023 Hepatocellular Carcinoma 94 0.145
16
c CHR089 Chronic Kidney Failure 72 0.145
17
URN009 Urinary System Disease 55 0.140
18
END072 Endotheliitis 45 0.140
19
P LVR013 Liver Disease 75 0.135
20
VSC007 Vascular Disease 68 0.130
21
P HPT021 Hepatitis 76 0.124
22
CNG034 Congestive Heart Failure 72 0.124
23
P ADN016 Adenocarcinoma 70 0.124
24
ANG054 Angina Pectoris 66 0.124
25
THR024 Thrombosis 61 0.124
26
SPS003 Spastic Diplegia 54 0.124
27
P LKM002 Leukemia 72 0.118
28
TYP041 Type I 56 0.118
29
CHL061 Childhood Leukemia 55 0.118
30
c LKM061 Leukemia, Acute Myeloid 80 0.112
31
LVR012 Liver Cirrhosis 68 0.112
32
P MYL006 Myeloid Leukemia 68 0.112
33
END030 End Stage Renal Failure 56 0.112
34
ACT118 Acute Non Lymphoblastic Leukemia 32 0.112
35
PSY004 Psychotic Disorder 71 0.106
36
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.106
37
GLC003 Glucose Intolerance 56 0.106
38
P HYP614 Hyperlipidemia, Familial Combined 56 0.106
39
PRP027 Peripheral Vascular Disease 70 0.099
40
ATM095 Autoimmune Disease 64 0.099
41
ANR040 Aneurysm 60 0.099
42
c ACT075 Acute Myocardial Infarction 58 0.099
43
GLC008 Glucose Metabolism Disease 52 0.099
44
P ART022 Arthritis 76 0.092
45
P SCH015 Schizophrenia 69 0.092
46
CNN005 Connective Tissue Disease 64 0.092
47
PLC008 Placenta Disease 61 0.092
48
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.092
49
AST005 Asthma 82 0.084
50
P MCR115 Microvascular Complications of Diabetes 5 71 0.084
51
P MYP004 Myopathy 68 0.084
52
GST050 Gastrointestinal System Disease 64 0.084
53
MYL031 Myeloproliferative Neoplasm 63 0.084
54
HYP066 Hyperglycemia 63 0.084
55
MGK001 Megakaryocytic Leukemia 63 0.084
56
P CMR001 Camurati-Engelmann Disease 61 0.084
57
P NPH012 Nephrotic Syndrome 59 0.084
58
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 59 0.084
59
P MNC007 Monocytic Leukemia 57 0.084
60
RTN018 Retinal Disease 56 0.084
61
c LKM070 Leukemia, Acute Monocytic 55 0.084
62
SCH012 Schizoaffective Disorder 54 0.084
63
ACT098 Acute Erythroid Leukemia 52 0.084
64
INT007 Intermediate Coronary Syndrome 52 0.084
65
c ADL096 Adult Hepatocellular Carcinoma 48 0.084
66
ACT200 Acute Monoblastic Leukemia 46 0.084
67
ACT113 Acute Myeloblastic Leukemia with Maturation 40 0.084
68
ACT114 Acute Myeloblastic Leukemia Without Maturation 31 0.084
69
c ADL093 Adult Acute Monocytic Leukemia 22 0.084
70
P RHM011 Rheumatoid Arthritis 80 0.075
71
DPR016 Depression 72 0.075
72
ANX010 Anxiety 72 0.075
73
P GRF003 Graft-Versus-Host Disease 71 0.075
74
P ATR011 Atrial Fibrillation 68 0.075
75
P ART023 Arthropathy 67 0.075
76
CRB039 Cerebrovascular Disease 67 0.075
77
OBS002 Obsessive-Compulsive Disorder 66 0.075
78
P MJR001 Major Depressive Disorder 65 0.075
79
MDD011 Mood Disorder 63 0.075
80
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.075
81
P ENC018 Encephalopathy 62 0.075
82
RHM027 Rheumatic Disease 62 0.075
83
P PLY014 Polycystic Kidney Disease 60 0.075
84
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.075
85
JNT002 Joint Disorders 59 0.075
86
P HYP724 Hyperlipoproteinemia, Type Iii 58 0.075
87
MNT002 Mental Depression 57 0.075
88
P PNC025 Panic Disorder 55 0.075
89
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.075
90
c ACT071 Acute Kidney Failure 54 0.075
91
GNR004 Generalized Anxiety Disorder 53 0.075
92
PRP080 Peripheral Artery Disease 53 0.075
93
P CLL015 Collagen Disease 52 0.075
94
ART004 Aortic Atherosclerosis 47 0.075
95
ENT004 Enthesopathy 46 0.075
96
PRD004 Prediabetes Syndrome 45 0.075
97
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.075
98
CRB009 Cerebritis 41 0.075
99
P BRS047 Breast Cancer 100 0.065
100
P LNG032 Lung Cancer 98 0.065
101
P ALZ034 Alzheimer Disease 87 0.065
102
c SYS001 Systemic Lupus Erythematosus 86 0.065
103
CRH001 Crohn's Disease 78 0.065
104
P MLT020 Multiple Sclerosis 78 0.065
105
ESP021 Esophageal Cancer 77 0.065
106
GST053 Gastric Cancer 77 0.065
107
P LYM118 Lymphoma 70 0.065
108
MYL009 Myelodysplastic Syndrome 70 0.065
109
P PNM007 Pneumonia 69 0.065
110
c SML038 Small Cell Cancer of the Lung 68 0.065
111
P LPS004 Lupus Erythematosus 68 0.065
112
DMN002 Dementia 68 0.065
113
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.065
114
VSC011 Vasculitis 65 0.065
115
GST045 Gastroenteritis 64 0.065
116
P INT068 Intestinal Disease 64 0.065
117
AGN016 Aging 64 0.065
118
VRL011 Viral Infectious Disease 63 0.065
119
P CHR285 Chronic Myelomonocytic Leukemia 62 0.065
120
c HPT003 Hepatitis a 61 0.065
121
c VRL010 Viral Hepatitis 59 0.065
122
c PRC016 Pre-Eclampsia 59 0.065
123
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.065
124
P SML001 Small Cell Carcinoma 58 0.065
125
DMY004 Demyelinating Disease 57 0.065
126
HMT018 Hematopoietic Stem Cell Transplantation 57 0.065
127
P ECL001 Eclampsia 57 0.065
128
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.065
129
BRN106 Burns 56 0.065
130
HYP060 Hyperinsulinism 56 0.065
131
ILT001 Ileitis 56 0.065
132
ESP023 Esophageal Disease 56 0.065
133
TRN015 Transient Cerebral Ischemia 56 0.065
134
LYM019 Lymphosarcoma 55 0.065
135
c INF071 Inflammatory Bowel Disease 1 53 0.065
136
P INF037 Inflammatory Bowel Disease 53 0.065
137
MYL004 Myelodysplastic Myeloproliferative Cancer 53 0.065
138
P PRM002 Primary Hyperoxaluria 53 0.065
139
STM006 Stomach Disease 52 0.065
140
CLC006 Calcinosis 51 0.065
141
CHL128 Childhood Hepatocellular Carcinoma 49 0.065
142
RFR010 Refractory Anemia 49 0.065
143
P BRN120 Bronchus Cancer 49 0.065
144
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.065
145
PDT001 Pediatric Lymphoma 45 0.065
146
SCH003 Schizophreniform Disorder 43 0.065
147
c HYP794 Hyperoxaluria, Primary, Type I 41 0.065
148
c ADL001 Adult Lymphoma 39 0.065
149
c PRC031 Preeclampsia/eclampsia 1 39 0.065
150
c TRC078 Trichohepatoenteric Syndrome 2 34 0.065
151
P RFR008 Refractory Anemia with Excess Blasts 33 0.065
152
ARG006 Aregenerative Anemia 25 0.065
153
BRN097 Brainstem Auditory Evoked Responses 25 0.065
154
MNS002 Mini Stroke 23 0.065
155
P PRS040 Prostate Cancer 90 0.053
156
INS024 Insulin-Like Growth Factor I 82 0.053
157
STR067 Stroke, Ischemic 82 0.053
158
c HYP595 Hypertension, Essential 76 0.053
159
P INF038 Influenza 76 0.053
160
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.053
161
HMN044 Human Immunodeficiency Virus Type 1 70 0.053
162
P PLM036 Pulmonary Fibrosis 69 0.053
163
P AMY004 Amyloidosis 68 0.053
164
LNG099 Lung Disease 67 0.053
165
SKN016 Skin Disease 66 0.053
166
P PRP003 Porphyria Cutanea Tarda 66 0.053
167
c CHR417 Chronic Graft Versus Host Disease 64 0.053
168
P PNC044 Pancreatitis 64 0.053
169
CRB011 Cerebrotendinous Xanthomatosis 63 0.053
170
c CNT035 Central Nervous System Disease 63 0.053
171
P MYS005 Myositis 63 0.053
172
HSH003 Hashimoto Thyroiditis 63 0.053
173
P NRP001 Neuropathy 63 0.053
174
P PRP029 Porphyria 62 0.053
175
P HRM001 Hermansky-Pudlak Syndrome 62 0.053
176
c ACT073 Acute Leukemia 60 0.053
177
CHL068 Cholestasis 60 0.053
178
ERY003 Erythema Multiforme 60 0.053
179
PRP019 Peripheral Nervous System Disease 60 0.053
180
P HMR003 Hemorrhagic Disease 60 0.053
181
c PCH015 Pachyonychia Congenita 1 59 0.053
182
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.053
183
P OCL002 Oculocutaneous Albinism 58 0.053
184
NRT004 Neuritis 57 0.053
185
CRT016 Carotid Artery Disease 57 0.053
186
BLD053 Blood Platelet Disease 55 0.053
187
XNT003 Xanthomatosis 53 0.053
188
P MSC033 Muscle Disorders 52 0.053
189
CYS039 Cystic Kidney Disease 51 0.053
190
P BLD051 Blood Coagulation Disease 50 0.053
191
IDP024 Idiopathic Inflammatory Myopathy 49 0.053
192
SKN027 Skin Conditions 48 0.053
193
HDN002 Head Injury 47 0.053
194
NPH010 Nephrosclerosis 47 0.053
195
AMN002 Amino Acid Metabolic Disorder 47 0.053
196
P FML035 Familial Hyperlipidemia 47 0.053
197
c PCH012 Pachyonychia Congenita 2 47 0.053
198
ALB002 Albinism 46 0.053
199
STR089 Storage Pool Platelet Disease 46 0.053
200
PGM003 Pigmentation Disease 45 0.053
201
P HYP750 Hypertriglyceridemia, Familial 44 0.053
202
BRN080 Brain Ischemia 44 0.053
203
PRS042 Prostate Disease 44 0.053
204
c INH004 Inherited Blood Coagulation Disease 41 0.053
205
MSC004 Muscle Tissue Disease 39 0.053
206
c HNT004 Huntington Disease-Like 2 39 0.053
207
HYP114 Hypertensive Nephropathy 36 0.053
208
c HYP555 Hypertriglyceridemia, Transient Infantile 31 0.053
209
c HNT011 Huntington Disease-Like 3 30 0.053
210
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 28 0.053
211
DLT018 Dilution, Pigmentary 26 0.053
212
HYP213 Hypomelanotic Disorder 25 0.053
213
AMN012 Aminoacidopathies 24 0.053
214
LYM053 Lymphomatous Thyroiditis 19 0.053
215
c HYP163 Hyperlipidemia Type 3 18 0.053
216
HML018 Homologous Wasting Disease 18 0.053
217
INB001 Inborn Amino Acid Metabolism Disorder 16 0.053
218
P PLM037 Pulmonary Hypertension 75 0.037
219
P NRV007 Nervous System Disease 73 0.037
220
c HPT073 Hepatitis C Virus 72 0.037
221
c HPT001 Hepatitis C 71 0.037
222
KWS002 Kawasaki Disease 70 0.037
223
PRT036 Peritonitis 66 0.037
224
MXD005 Mixed Connective Tissue Disease 65 0.037
225
P END044 Endometriosis 64 0.037
226
P DRM010 Dermatomyositis 64 0.037
227
OST003 Osteonecrosis 63 0.037
228
PRP030 Purpura 61 0.037
229
HYP266 Hypoxia 61 0.037
230
P NTR004 Neutropenia 60 0.037
231
P CND004 Candidiasis 60 0.037
232
BRN012 Bronchiolitis Obliterans 60 0.037
233
NRM005 Neuromuscular Disease 60 0.037
234
P FCL005 Focal Segmental Glomerulosclerosis 59 0.037
235
P INF032 Infertility 59 0.037
236
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.037
237
ING001 Inguinal Hernia 59 0.037
238
P HST010 Histiocytosis 59 0.037
239
BRN002 Bronchiolitis 59 0.037
240
P THR015 Thrombophilia 57 0.037
241
IMP005 Impotence 55 0.037
242
TRM010 Traumatic Brain Injury 55 0.037
243
LYM024 Lymphatic System Disease 54 0.037
244
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.037
245
P GLM045 Glioma 54 0.037
246
BRN071 Brain Injury 53 0.037
247
HLL004 Hellp Syndrome 52 0.037
248
MYC005 Myocardial Stunning 47 0.037
249
CRB004 Cerebral Artery Occlusion 46 0.037
250
P PRP034 Purpura Fulminans 45 0.037
251
ASP030 Aspirin Resistance 43 0.037
252
PNG002 Pain Agnosia 42 0.037
253
NRN002 Neuronitis 41 0.037
254
CRB086 Cerebral Aneurysms 41 0.037
255
MYT011 Myotonia 41 0.037
256
SCR011 Scrapie 40 0.037
257
CRT004 Carotid Artery Thrombosis 38 0.037
258
DFC001 Defective Apolipoprotein B-100 31 0.037
259
BLN006 Blind Loop Syndrome 29 0.037
260
VSC009 Vascular Skin Disease 20 0.037
261
IND009 Indeterminate Cell Histiocytosis 19 0.037
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