Search results for Lovastatin

265 hits were found for Lovastatin

# Family MCID Name MIFTS Score
1
c HYP607 Hypercholesterolemia, Familial 82 0.205
2
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.167
3
NRF026 Neurofibromatosis, Type Iv, of Riccardi 76 0.150
4
P NRF024 Neurofibromatosis, Type I 69 0.145
5
LPD008 Lipid Metabolism Disorder 65 0.140
6
THY028 Thyroid Cancer 72 0.135
7
ANP031 Anaplastic Thyroid Cancer 65 0.135
8
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.135
9
c PRS040 Prostate Cancer 93 0.130
10
c FRG001 Fragile X Syndrome 70 0.130
11
ART140 Arteries, Anomalies of 67 0.130
12
c BRS047 Breast Cancer 100 0.124
13
ALL014 Allergic Encephalomyelitis 43 0.124
14
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.118
15
c ART021 Arteriosclerosis 61 0.118
16
c ATS366 Autism X-Linked 2 45 0.118
17
c HRT032 Heart Disease 76 0.112
18
VSC007 Vascular Disease 72 0.112
19
ISC004 Ischemia 67 0.112
20
NRF007 Neurofibroma 67 0.112
21
NRT004 Neuritis 58 0.112
22
c CHR084 Chromosomal Disease 40 0.112
23
c CRN018 Coronary Artery Anomaly 74 0.106
24
c PRP019 Peripheral Nervous System Disease 66 0.106
25
MLN008 Melanoma 64 0.106
26
c NRP001 Neuropathy 63 0.106
27
NRM005 Neuromuscular Disease 61 0.106
28
c NRV006 Nervous System Cancer 60 0.106
29
c PRP021 Peripheral Nervous System Neoplasm 51 0.106
30
c HPT021 Hepatitis 74 0.099
31
c LKM002 Leukemia 72 0.099
32
c ENC018 Encephalopathy 65 0.099
33
INT002 Intermittent Claudication 64 0.099
34
c CRN300 Coronary Heart Disease 1 62 0.099
35
c CRD246 Cardiovascular System Disease 57 0.099
36
c GLM045 Glioma 56 0.099
37
XNT003 Xanthomatosis 54 0.099
38
P PRS136 Prostate Cancer, Hereditary, 6 40 0.099
39
P PRS130 Prostate Cancer, Hereditary, 8 37 0.099
40
ISC006 Ischemic Heart Disease 72 0.092
41
ADR007 Adrenoleukodystrophy 72 0.092
42
PRP027 Peripheral Vascular Disease 72 0.092
43
LNG099 Lung Disease 70 0.092
44
c ATS364 Autism 68 0.092
45
c DBT009 Diabetes Mellitus 67 0.092
46
P CNT035 Central Nervous System Disease 65 0.092
47
CRB011 Cerebrotendinous Xanthomatosis 65 0.092
48
EWN002 Ewing's Family of Tumors 57 0.092
49
PRP080 Peripheral Artery Disease 56 0.092
50
c OVR042 Ovarian Cancer 83 0.084
51
c MDL005 Medulloblastoma 77 0.084
52
ANX010 Anxiety 73 0.084
53
DPR016 Depression 73 0.084
54
c ADN016 Adenocarcinoma 71 0.084
55
BRS051 Breast Disease 68 0.084
56
SKN019 Skin Melanoma 67 0.084
57
c MYP004 Myopathy 65 0.084
58
P INS002 in Situ Carcinoma 60 0.084
59
P MCR113 Microvascular Complications of Diabetes 3 58 0.084
60
c HYP614 Hyperlipidemia, Familial Combined 56 0.084
61
NRN004 Neuroendocrine Tumor 56 0.084
62
LRN003 Learning Disability 53 0.084
63
MLR006 Male Reproductive Organ Cancer 50 0.084
64
PRS042 Prostate Disease 47 0.084
65
P MCR120 Microvascular Complications of Diabetes 7 46 0.084
66
P MCR130 Microvascular Complications of Diabetes 6 43 0.084
67
P MCR133 Microvascular Complications of Diabetes 4 43 0.084
68
STR067 Stroke, Ischemic 84 0.075
69
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.075
70
GLB002 Glioblastoma 75 0.075
71
c PNM007 Pneumonia 72 0.075
72
c KDN018 Kidney Disease 71 0.075
73
CRB039 Cerebrovascular Disease 70 0.075
74
SKN016 Skin Disease 68 0.075
75
c MYL006 Myeloid Leukemia 68 0.075
76
P HPT003 Hepatitis a 66 0.075
77
P OVR114 Ovarian Cancer 1 66 0.075
78
MNT002 Mental Depression 65 0.075
79
RSP006 Respiratory System Disease 64 0.075
80
c EXN002 Exanthem 62 0.075
81
c NPH012 Nephrotic Syndrome 59 0.075
82
CNS004 Constipation 58 0.075
83
END035 Endocrine Gland Cancer 57 0.075
84
c BLD051 Blood Coagulation Disease 51 0.075
85
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.075
86
P LKM061 Leukemia, Acute Myeloid 83 0.065
87
c RHM011 Rheumatoid Arthritis 82 0.065
88
AST005 Asthma 81 0.065
89
c ART022 Arthritis 78 0.065
90
c PRK057 Parkinson Disease, Late-Onset 77 0.065
91
HMN044 Human Immunodeficiency Virus Type 1 75 0.065
92
c NRB001 Neuroblastoma 73 0.065
93
c NRV007 Nervous System Disease 72 0.065
94
BRC012 Brucellosis 71 0.065
95
VRL011 Viral Infectious Disease 69 0.065
96
c ART023 Arthropathy 68 0.065
97
ATM095 Autoimmune Disease 68 0.065
98
ALL026 Allergic Hypersensitivity Disease 68 0.065
99
CNN005 Connective Tissue Disease 67 0.065
100
c ATT013 Attention Deficit-Hyperactivity Disorder 67 0.065
101
MVM001 Movement Disease 67 0.065
102
c PRD008 Periodontitis 66 0.065
103
PRD007 Periodontal Disease 66 0.065
104
MTH009 Mouth Disease 66 0.065
105
ACQ007 Acquired Immunodeficiency Syndrome 66 0.065
106
RHM027 Rheumatic Disease 65 0.065
107
BND020 Bone Disease 65 0.065
108
IRR002 Irritable Bowel Syndrome 64 0.065
109
JNT002 Joint Disorders 64 0.065
110
c OVR049 Ovarian Disease 63 0.065
111
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.065
112
P PRD040 Periodontitis, Chronic 60 0.065
113
c HYP750 Hypertriglyceridemia, Familial 58 0.065
114
STS003 Sitosterolemia 58 0.065
115
IMM136 Immune System Disease 57 0.065
116
P BRS049 Breast Carcinoma in Situ 56 0.065
117
c MSC033 Muscle Disorders 56 0.065
118
MSC190 Muscular Disease 55 0.065
119
BNR002 Bone Resorption Disease 54 0.065
120
P INH020 Inherited Metabolic Disorder 54 0.065
121
c CLL015 Collagen Disease 52 0.065
122
SKN027 Skin Conditions 51 0.065
123
BSL008 Basal Ganglia Disease 49 0.065
124
GND003 Gonadal Disease 49 0.065
125
MMM006 Mammographic Density 47 0.065
126
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 0.065
127
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.065
128
STR015 Stereotypic Movement Disorder 42 0.065
129
OVR094 Ovarian Epithelial Cancer 41 0.065
130
MSC004 Muscle Tissue Disease 39 0.065
131
ACT118 Acute Non Lymphoblastic Leukemia 33 0.065
132
PRL016 Proliferative Type Fibrocystic Change of Breast 16 0.065
133
c LNG032 Lung Cancer 99 0.053
134
c HPT023 Hepatocellular Carcinoma 97 0.053
135
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.053
136
MYL069 Myeloma, Multiple 85 0.053
137
c RTT002 Rett Syndrome 83 0.053
138
c NNN008 Noonan Syndrome 1 79 0.053
139
c MLT020 Multiple Sclerosis 76 0.053
140
PSY004 Psychotic Disorder 74 0.053
141
P CHR089 Chronic Kidney Failure 73 0.053
142
ANG054 Angina Pectoris 70 0.053
143
P ATS007 Autism Spectrum Disorder 68 0.053
144
c HYP086 Hypothyroidism 66 0.053
145
c THY102 Thyroid Cancer, Nonmedullary, 2 64 0.053
146
c PNC044 Pancreatitis 62 0.053
147
STT001 Status Epilepticus 61 0.053
148
SQM006 Squamous Cell Carcinoma 59 0.053
149
URN009 Urinary System Disease 59 0.053
150
BRN038 Bronchial Disease 58 0.053
151
c CTR002 Cataract 58 0.053
152
CRT016 Carotid Artery Disease 58 0.053
153
c ICH004 Ichthyosis 57 0.053
154
PRV006 Pervasive Developmental Disorder 56 0.053
155
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 55 0.053
156
P ACT071 Acute Kidney Failure 54 0.053
157
GLC008 Glucose Metabolism Disease 54 0.053
158
CRT013 Carotid Stenosis 52 0.053
159
SPC010 Speech and Communication Disorders 51 0.053
160
THY030 Thyroid Gland Disease 51 0.053
161
c FML035 Familial Hyperlipidemia 50 0.053
162
HMZ003 Homozygous Familial Hypercholesterolemia 49 0.053
163
P MLG068 Malignant Glioma 47 0.053
164
NPH010 Nephrosclerosis 46 0.053
165
CRB008 Cerebral Atherosclerosis 44 0.053
166
P OPT050 Opitz Gbbb Syndrome, Type Ii 44 0.053
167
c DYS005 Dyslexia 42 0.053
168
RDN001 Reading Disorder 39 0.053
169
HYP114 Hypertensive Nephropathy 37 0.053
170
CHL050 Cholesterol Ester Storage Disease 37 0.053
171
MTH071 Methane Production 27 0.053
172
P PSD047 Pseudo-Turner Syndrome 25 0.053
173
CRB087 Cerebral Arteriosclerosis 21 0.053
174
P XLN229 X-Linked Chondrodysplasia Punctata 2 21 0.053
175
INT074 Intracranial Arteriosclerosis 16 0.053
176
c PNC035 Pancreatic Cancer 83 0.037
177
SQM013 Squamous Cell Carcinoma, Head and Neck 82 0.037
178
GST053 Gastric Cancer 78 0.037
179
c LVR013 Liver Disease 77 0.037
180
c OST002 Osteoporosis 74 0.037
181
BRN028 Brain Cancer 74 0.037
182
c EPL164 Epilepsy 73 0.037
183
c PHC003 Pheochromocytoma 73 0.037
184
c GRF003 Graft-Versus-Host Disease 72 0.037
185
c PLM036 Pulmonary Fibrosis 70 0.037
186
P HPT001 Hepatitis C 69 0.037
187
SMT004 Smith-Lemli-Opitz Syndrome 69 0.037
188
P NMN015 Niemann-Pick Disease, Type C1 68 0.037
189
GST050 Gastrointestinal System Disease 67 0.037
190
PNC033 Pancreas Adenocarcinoma 67 0.037
191
OST159 Osteogenic Sarcoma 67 0.037
192
c HYP098 Hypereosinophilic Syndrome 67 0.037
193
c MJR001 Major Depressive Disorder 67 0.037
194
FTT001 Fatty Liver Disease 66 0.037
195
c DRM010 Dermatomyositis 66 0.037
196
c NSP012 Nasopharyngeal Carcinoma 66 0.037
197
GST040 Gastric Adenocarcinoma 66 0.037
198
c END044 Endometriosis 65 0.037
199
c HLP001 Holoprosencephaly 65 0.037
200
c ANG001 Angelman Syndrome 65 0.037
201
MDD011 Mood Disorder 65 0.037
202
c HML002 Hemolytic Anemia 65 0.037
203
CHL065 Cholangiocarcinoma 65 0.037
204
GLB015 Glioblastoma Multiforme 64 0.037
205
c GLL022 Guillain-Barre Syndrome 64 0.037
206
c GLM040 Glioma Susceptibility 1 64 0.037
207
c DNG005 Dengue Virus 64 0.037
208
DPH001 Diphtheria 63 0.037
209
P MST023 Mesothelioma, Malignant 63 0.037
210
QFV001 Q Fever 63 0.037
211
c PLY014 Polycystic Kidney Disease 63 0.037
212
CLN019 Colonic Disease 62 0.037
213
SCH014 Schistosomiasis 62 0.037
214
c INT068 Intestinal Disease 62 0.037
215
c GLM007 Glomerulonephritis 62 0.037
216
c FBR017 Fibrosarcoma 61 0.037
217
GRD007 Grade Iii Astrocytoma 61 0.037
218
ALL006 Allergic Asthma 61 0.037
219
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.037
220
CHL068 Cholestasis 60 0.037
221
ORL011 Oral Cancer 60 0.037
222
MLG077 Malignant Peripheral Nerve Sheath Tumor 60 0.037
223
EMB004 Embryonal Carcinoma 60 0.037
224
c CHL002 Childhood Absence Epilepsy 59 0.037
225
PTT009 Pituitary Gland Disease 59 0.037
226
PLG002 Plague 59 0.037
227
IMP005 Impotence 58 0.037
228
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.037
229
RTN018 Retinal Disease 58 0.037
230
c DRR001 Diarrhea 58 0.037
231
HYP060 Hyperinsulinism 57 0.037
232
CLN015 Colon Adenocarcinoma 57 0.037
233
c ACT008 Actinic Keratosis 55 0.037
234
INT079 Intrahepatic Cholangiocarcinoma 55 0.037
235
c DBT005 Diabetes Insipidus 55 0.037
236
NNL002 Nonalcoholic Steatohepatitis 55 0.037
237
KRT009 Keratosis 55 0.037
238
PNG002 Pain Agnosia 54 0.037
239
GNG012 Gingival Overgrowth 53 0.037
240
P ACT134 Acute Liver Failure 53 0.037
241
URM002 Uremia 53 0.037
242
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 52 0.037
243
MCP006 Mucoepidermoid Carcinoma 52 0.037
244
c AST007 Astrocytoma 51 0.037
245
INT007 Intermediate Coronary Syndrome 50 0.037
246
c NMN002 Niemann-Pick Disease 50 0.037
247
SPS003 Spastic Diplegia 49 0.037
248
ADR040 Adrenal Gland Pheochromocytoma 48 0.037
249
P OPT051 Opitz Gbbb Syndrome, Type I 48 0.037
250
ICH002 Ichthyosis Bullosa of Siemens 47 0.037
251
P GLL024 Gallbladder Disease 1 45 0.037
252
SYN058 Synucleinopathy 44 0.037
253
NRF003 Neurofibrosarcoma 43 0.037
254
c CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 43 0.037
255
TRT001 Teratocarcinoma 41 0.037
256
CRN020 Coronary Restenosis 39 0.037
257
BLT003 Blue Toe Syndrome 37 0.037
258
STR018 Steroid Inherited Metabolic Disorder 35 0.037
259
DFC001 Defective Apolipoprotein B-100 32 0.037
260
EXF003 Exfoliative Dermatitis 30 0.037
261
P HYP805 Hypercholesterolemia, Autosomal Dominant, 3 29 0.037
262
FNC005 Functional Colonic Disease 29 0.037
263
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.037
264
SLN001 Silent Myocardial Infarction 24 0.037
265
LNG091 Lung Mucoepidermoid Carcinoma 24 0.037
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