Search results for Lovastatin

215 hits were found for Lovastatin

# Family MCID Name MIFTS Score
1
LPD008 Lipid Metabolism Disorder 58 0.150
2
P FRG001 Fragile X Syndrome 69 0.139
3
P BRS047 Breast Cancer 100 0.133
4
P PRS040 Prostate Cancer 90 0.133
5
NRF026 Neurofibromatosis, Type Iv, of Riccardi 73 0.133
6
c NRF024 Neurofibromatosis, Type I 66 0.133
7
ART140 Arteries, Anomalies of 65 0.133
8
END072 Endotheliitis 45 0.133
9
P HYP607 Hypercholesterolemia, Familial 79 0.127
10
P HPT021 Hepatitis 76 0.127
11
P ART021 Arteriosclerosis 60 0.127
12
TYP041 Type I 56 0.127
13
P ATS366 Autism X-Linked 2 43 0.127
14
P HRT032 Heart Disease 74 0.121
15
VSC007 Vascular Disease 68 0.121
16
NRF007 Neurofibroma 65 0.121
17
P CHR084 Chromosomal Disease 40 0.121
18
P LKM002 Leukemia 72 0.114
19
ISC004 Ischemia 65 0.114
20
MLN008 Melanoma 62 0.114
21
NRT004 Neuritis 57 0.114
22
ANX010 Anxiety 72 0.106
23
P CRN018 Coronary Artery Anomaly 68 0.106
24
c CRN300 Coronary Heart Disease 1 64 0.106
25
ANP031 Anaplastic Thyroid Cancer 63 0.106
26
P NRP001 Neuropathy 63 0.106
27
P ENC018 Encephalopathy 62 0.106
28
NRV006 Nervous System Cancer 60 0.106
29
PRP019 Peripheral Nervous System Disease 60 0.106
30
PRS047 Prostatitis 60 0.106
31
NRM005 Neuromuscular Disease 60 0.106
32
PRP021 Peripheral Nervous System Neoplasm 53 0.106
33
XNT003 Xanthomatosis 53 0.106
34
ISC006 Ischemic Heart Disease 72 0.098
35
ADR007 Adrenoleukodystrophy 71 0.098
36
PRP027 Peripheral Vascular Disease 70 0.098
37
LNG099 Lung Disease 67 0.098
38
THY028 Thyroid Cancer 66 0.098
39
P DBT009 Diabetes Mellitus 64 0.098
40
CRB011 Cerebrotendinous Xanthomatosis 63 0.098
41
c CNT035 Central Nervous System Disease 63 0.098
42
INT002 Intermittent Claudication 61 0.098
43
EWN002 Ewing's Family of Tumors 56 0.098
44
P THY032 Thyroiditis 55 0.098
45
P GLM045 Glioma 54 0.098
46
ALL014 Allergic Encephalomyelitis 36 0.098
47
P OVR042 Ovarian Cancer 81 0.090
48
DPR016 Depression 72 0.090
49
P ATS364 Autism 70 0.090
50
SKN019 Skin Melanoma 69 0.090
51
P MYL006 Myeloid Leukemia 68 0.090
52
SKN016 Skin Disease 66 0.090
53
BRS051 Breast Disease 66 0.090
54
NRN004 Neuroendocrine Tumor 58 0.090
55
P HYP614 Hyperlipidemia, Familial Combined 56 0.090
56
c INS002 in Situ Carcinoma 56 0.090
57
PRP080 Peripheral Artery Disease 53 0.090
58
LRN003 Learning Disability 50 0.090
59
SKN027 Skin Conditions 48 0.090
60
PRS042 Prostate Disease 44 0.090
61
STR067 Stroke, Ischemic 82 0.080
62
c LKM061 Leukemia, Acute Myeloid 80 0.080
63
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.080
64
GLB002 Glioblastoma 72 0.080
65
P PNM007 Pneumonia 69 0.080
66
CRB039 Cerebrovascular Disease 67 0.080
67
RSP006 Respiratory System Disease 63 0.080
68
c OVR114 Ovarian Cancer 1 62 0.080
69
P EXN002 Exanthem 61 0.080
70
c HPT003 Hepatitis a 61 0.080
71
MNT002 Mental Depression 57 0.080
72
P BLD051 Blood Coagulation Disease 50 0.080
73
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.080
74
P RHM011 Rheumatoid Arthritis 80 0.070
75
P PRK057 Parkinson Disease, Late-Onset 76 0.070
76
P ART022 Arthritis 76 0.070
77
P MDL005 Medulloblastoma 75 0.070
78
P NRV007 Nervous System Disease 73 0.070
79
HMN044 Human Immunodeficiency Virus Type 1 70 0.070
80
P ADN016 Adenocarcinoma 70 0.070
81
BRC012 Brucellosis 70 0.070
82
P KDN018 Kidney Disease 68 0.070
83
P MYP004 Myopathy 68 0.070
84
P ART023 Arthropathy 67 0.070
85
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.070
86
P PRD008 Periodontitis 66 0.070
87
PRD007 Periodontal Disease 64 0.070
88
ATM095 Autoimmune Disease 64 0.070
89
CNN005 Connective Tissue Disease 64 0.070
90
P PNC044 Pancreatitis 64 0.070
91
VRL011 Viral Infectious Disease 63 0.070
92
ACQ007 Acquired Immunodeficiency Syndrome 63 0.070
93
MTH009 Mouth Disease 63 0.070
94
BND020 Bone Disease 62 0.070
95
RHM027 Rheumatic Disease 62 0.070
96
MVM001 Movement Disease 60 0.070
97
JNT002 Joint Disorders 59 0.070
98
P NPH012 Nephrotic Syndrome 59 0.070
99
P OVR049 Ovarian Disease 59 0.070
100
SQM006 Squamous Cell Carcinoma 59 0.070
101
STS003 Sitosterolemia 58 0.070
102
IMM136 Immune System Disease 56 0.070
103
c BRS049 Breast Carcinoma in Situ 55 0.070
104
CHL061 Childhood Leukemia 55 0.070
105
P CLL015 Collagen Disease 52 0.070
106
P MSC033 Muscle Disorders 52 0.070
107
GNG011 Gingival Disease 49 0.070
108
c PRD040 Periodontitis, Chronic 49 0.070
109
ENT004 Enthesopathy 46 0.070
110
GND003 Gonadal Disease 46 0.070
111
BSL008 Basal Ganglia Disease 46 0.070
112
MMM006 Mammographic Density 43 0.070
113
MSC004 Muscle Tissue Disease 39 0.070
114
OVR094 Ovarian Epithelial Cancer 38 0.070
115
ACT118 Acute Non Lymphoblastic Leukemia 32 0.070
116
PRL016 Proliferative Type Fibrocystic Change of Breast 13 0.070
117
P LNG032 Lung Cancer 98 0.057
118
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.057
119
MYL069 Myeloma, Multiple 83 0.057
120
AST005 Asthma 82 0.057
121
P RTT002 Rett Syndrome 82 0.057
122
P NRB001 Neuroblastoma 72 0.057
123
c CHR089 Chronic Kidney Failure 72 0.057
124
PRT036 Peritonitis 66 0.057
125
P HYP086 Hypothyroidism 64 0.057
126
P THY102 Thyroid Cancer, Nonmedullary, 2 63 0.057
127
CRT016 Carotid Artery Disease 57 0.057
128
BRN038 Bronchial Disease 56 0.057
129
CNS004 Constipation 56 0.057
130
URN009 Urinary System Disease 55 0.057
131
c ACT071 Acute Kidney Failure 54 0.057
132
GLC008 Glucose Metabolism Disease 52 0.057
133
CRT013 Carotid Stenosis 52 0.057
134
SPC010 Speech and Communication Disorders 52 0.057
135
THY030 Thyroid Gland Disease 51 0.057
136
NPH010 Nephrosclerosis 47 0.057
137
P FML035 Familial Hyperlipidemia 47 0.057
138
NRN002 Neuronitis 41 0.057
139
CRB009 Cerebritis 41 0.057
140
P DYS005 Dyslexia 39 0.057
141
CHL050 Cholesterol Ester Storage Disease 37 0.057
142
RDN001 Reading Disorder 36 0.057
143
HYP114 Hypertensive Nephropathy 36 0.057
144
CRB087 Cerebral Arteriosclerosis 20 0.057
145
INT074 Intracranial Arteriosclerosis 15 0.057
146
P HPT023 Hepatocellular Carcinoma 94 0.040
147
P PNC035 Pancreatic Cancer 79 0.040
148
P MLT020 Multiple Sclerosis 78 0.040
149
P NNN008 Noonan Syndrome 1 77 0.040
150
BRN028 Brain Cancer 72 0.040
151
PSY004 Psychotic Disorder 71 0.040
152
c HPT001 Hepatitis C 71 0.040
153
SMT004 Smith-Lemli-Opitz Syndrome 68 0.040
154
c NMN015 Niemann-Pick Disease, Type C1 68 0.040
155
ANG054 Angina Pectoris 66 0.040
156
P HLP001 Holoprosencephaly 66 0.040
157
P MJR001 Major Depressive Disorder 65 0.040
158
AGN016 Aging 64 0.040
159
MDD011 Mood Disorder 63 0.040
160
GNG013 Gingivitis 63 0.040
161
CHL065 Cholangiocarcinoma 63 0.040
162
P GLM007 Glomerulonephritis 61 0.040
163
P ANG001 Angelman Syndrome 61 0.040
164
CNG008 Congenital Ichthyosiform Erythroderma 60 0.040
165
P PLY014 Polycystic Kidney Disease 60 0.040
166
MLG077 Malignant Peripheral Nerve Sheath Tumor 60 0.040
167
GRD007 Grade Iii Astrocytoma 60 0.040
168
P NMN002 Niemann-Pick Disease 60 0.040
169
GLB015 Glioblastoma Multiforme 60 0.040
170
STT001 Status Epilepticus 60 0.040
171
ORL011 Oral Cancer 59 0.040
172
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.040
173
P HYP724 Hyperlipoproteinemia, Type Iii 58 0.040
174
HYP060 Hyperinsulinism 56 0.040
175
PTT009 Pituitary Gland Disease 56 0.040
176
PLG002 Plague 56 0.040
177
RTN018 Retinal Disease 56 0.040
178
P ACT008 Actinic Keratosis 54 0.040
179
P ICH004 Ichthyosis 54 0.040
180
SPS003 Spastic Diplegia 54 0.040
181
HMZ003 Homozygous Familial Hypercholesterolemia 54 0.040
182
P DBT005 Diabetes Insipidus 54 0.040
183
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 53 0.040
184
KRT009 Keratosis 53 0.040
185
CLN015 Colon Adenocarcinoma 53 0.040
186
c MCR113 Microvascular Complications of Diabetes 3 52 0.040
187
INT079 Intrahepatic Cholangiocarcinoma 52 0.040
188
P GLM040 Glioma Susceptibility 1 52 0.040
189
INT007 Intermediate Coronary Syndrome 52 0.040
190
MCP006 Mucoepidermoid Carcinoma 51 0.040
191
P AST007 Astrocytoma 51 0.040
192
RTN023 Retinitis 50 0.040
193
GNG012 Gingival Overgrowth 50 0.040
194
NNL002 Nonalcoholic Steatohepatitis 50 0.040
195
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 49 0.040
196
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.040
197
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.040
198
P HYP750 Hypertriglyceridemia, Familial 44 0.040
199
NRF003 Neurofibrosarcoma 44 0.040
200
PNG002 Pain Agnosia 42 0.040
201
c OPT050 Opitz Gbbb Syndrome, Type Ii 41 0.040
202
c CHN074 Chondrodysplasia Punctata 2, X-Linked Dominant 41 0.040
203
TRT001 Teratocarcinoma 40 0.040
204
c MCR130 Microvascular Complications of Diabetes 6 40 0.040
205
CRN020 Coronary Restenosis 39 0.040
206
c MLG068 Malignant Glioma 38 0.040
207
BLT003 Blue Toe Syndrome 37 0.040
208
c MCR120 Microvascular Complications of Diabetes 7 37 0.040
209
c MCR133 Microvascular Complications of Diabetes 4 35 0.040
210
DFC001 Defective Apolipoprotein B-100 31 0.040
211
c HYP555 Hypertriglyceridemia, Transient Infantile 31 0.040
212
EXF003 Exfoliative Dermatitis 29 0.040
213
c HYP805 Hypercholesterolemia, Autosomal Dominant, 3 28 0.040
214
c CHN018 Chondrodysplasia Punctata 2, X-Linked 25 0.040
215
LNG091 Lung Mucoepidermoid Carcinoma 24 0.040
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