Search results for Tenofovir disoproxil

200 hits were found for Tenofovir disoproxil

# Family MCID Name MIFTS Score
1
HMN044 Human Immunodeficiency Virus Type 1 71 1.009
2
c HPT016 Hepatitis B 59 1.007
3
48X005 48,xyyy 39 0.929
4
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.902
5
P HPT021 Hepatitis 67 0.881
6
c HPT003 Hepatitis a 62 0.710
7
IMM167 Immune Deficiency Disease 78 0.676
8
ACQ007 Acquired Immunodeficiency Syndrome 60 0.641
9
HRP008 Herpes Simiae 25 0.600
10
LVR012 Liver Cirrhosis 62 0.425
11
CHL079 Children's Interstitial Lung Disease 26 0.409
12
P LVR013 Liver Disease 68 0.388
13
c RHB024 Rhabdomyosarcoma 2 67 0.376
14
P HPT023 Hepatocellular Carcinoma 100 0.361
15
CMR002 Coumarin Resistance 56 0.328
16
P FNC004 Fanconi Syndrome 50 0.323
17
P FNC034 Fanconi Renotubular Syndrome 2 40 0.323
18
P KDN018 Kidney Disease 72 0.291
19
VRL011 Viral Infectious Disease 61 0.273
20
c HPT001 Hepatitis C 62 0.273
21
c HPT073 Hepatitis C Virus 72 0.249
22
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.245
23
HYP017 Hypophosphatemia 50 0.240
24
RCK004 Rickets 68 0.239
25
c CHR684 Chronic Kidney Disease 70 0.236
26
ATX019 Ataxia with Vitamin E Deficiency 42 0.233
27
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.225
28
P CRD246 Cardiovascular System Disease 57 0.221
29
ADL002 Adult Syndrome 70 0.218
30
c VRL010 Viral Hepatitis 52 0.212
31
49X006 49, Xxxxy Syndrome 41 0.207
32
c ACT071 Acute Kidney Failure 60 0.206
33
P MYC084 Mycobacterium Tuberculosis 1 68 0.203
34
c PRM038 Primary Agammaglobulinemia 44 0.200
35
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.198
36
DWN001 Down Syndrome 70 0.195
37
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.190
38
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.186
39
c INF145 Infantile Liver Failure Syndrome 1 50 0.185
40
P HRP006 Herpes Simplex 65 0.182
41
BNR002 Bone Resorption Disease 48 0.180
42
P OST002 Osteoporosis 74 0.176
43
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.176
44
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.176
45
LPD008 Lipid Metabolism Disorder 62 0.175
46
NTR005 Nutritional Deficiency Disease 62 0.171
47
P EXN002 Exanthem 57 0.170
48
P BND020 Bone Disease 59 0.169
49
OST011 Osteomalacia 52 0.166
50
P NRP001 Neuropathy 56 0.163
51
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.162
52
c HPT015 Hepatitis D 49 0.160
53
P CNR004 Cone-Rod Dystrophy 2 73 0.157
54
P LCT001 Lactic Acidosis 51 0.155
55
HYP005 Hypokalemia 55 0.153
56
P PRP019 Peripheral Nervous System Disease 58 0.151
57
ANX010 Anxiety 73 0.148
58
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.148
59
P DRR001 Diarrhea 55 0.147
60
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.144
61
DPR016 Depression 63 0.134
62
MNT002 Mental Depression 58 0.134
63
c MCL013 Mucolipidosis Iv 66 0.133
64
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.131
65
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.131
66
CVD001 Covid-19 44 0.123
67
NSP002 Nasopharyngitis 43 0.123
68
c HYP836 Hypercholesterolemia, Familial, 1 73 0.123
69
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.123
70
P TRN020 Turner Syndrome 67 0.123
71
P SLP005 Sleep Disorder 59 0.122
72
KPS004 Kaposi Sarcoma 75 0.119
73
SRC014 Sarcoma 65 0.119
74
c SVR001 Severe Acute Respiratory Syndrome 62 0.119
75
SFT003 Soft Tissue Sarcoma 56 0.119
76
SPN035 Spindle Cell Sarcoma 53 0.119
77
P MLG074 Malignant Mesenchymoma 40 0.119
78
P LYM118 Lymphoma 68 0.119
79
LYM019 Lymphosarcoma 46 0.119
80
MLR004 Malaria 81 0.115
81
P HRT032 Heart Disease 75 0.111
82
LYM133 Lymphoma, Hodgkin, Classic 69 0.111
83
ART002 Arts Syndrome 64 0.111
84
TXC002 Toxic Encephalopathy 53 0.111
85
CRN322 Coronavirus Infectious Disease 40 0.110
86
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.108
87
47X002 47,xyy 49 0.107
88
P HMN032 Human Herpesvirus 8 47 0.107
89
END086 End Stage Renal Disease 51 0.106
90
P PRM006 Primary Biliary Cirrhosis 62 0.102
91
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.102
92
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.102
93
STR067 Stroke, Ischemic 81 0.102
94
CRB039 Cerebrovascular Disease 67 0.102
95
ANG049 Angioedema Induced by Ace Inhibitors 40 0.102
96
P HYP069 Hyperparathyroidism 63 0.101
97
AGN016 Aging 56 0.101
98
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.101
99
P MYC007 Myocardial Infarction 70 0.097
100
ALL026 Allergic Hypersensitivity Disease 62 0.097
101
HYP081 Hypolipoproteinemia 51 0.097
102
CYT018 Cytochrome P450 2d6 Variant 27 0.097
103
TRP009 Triple X Syndrome 42 0.097
104
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.094
105
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.094
106
P HYP750 Hypertriglyceridemia, Familial 62 0.093
107
CHL123 Chlamydia 59 0.093
108
c FML035 Familial Hyperlipidemia 55 0.093
109
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.093
110
AMN001 Amenorrhea 54 0.093
111
LPT014 Leptin Deficiency or Dysfunction 74 0.087
112
DFC004 Deficiency Anemia 70 0.087
113
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.085
114
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.085
115
P CRN300 Coronary Heart Disease 1 63 0.085
116
LPP008 Lipoprotein Quantitative Trait Locus 62 0.085
117
P PNC044 Pancreatitis 61 0.085
118
c ACT134 Acute Liver Failure 56 0.085
119
GNT003 Genital Herpes 54 0.085
120
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.085
121
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.085
122
OST012 Osteoarthritis 78 0.081
123
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.081
124
DSS008 Disease of Mental Health 58 0.081
125
P HDC001 Headache 57 0.081
126
HYP266 Hypoxia 57 0.081
127
BCT022 Bacterial Infectious Disease 56 0.081
128
PTS001 Patau Syndrome 55 0.081
129
HMF006 Hemifacial Microsomia 55 0.081
130
ACR041 Acromelic Frontonasal Dysostosis 52 0.081
131
PNG002 Pain Agnosia 51 0.081
132
P CHL066 Cholangitis 51 0.081
133
c ORF040 Orofaciodigital Syndrome Viii 50 0.081
134
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.081
135
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.081
136
IMM136 Immune System Disease 45 0.081
137
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.081
138
c CHR682 Chronic Bilirubin Encephalopathy 39 0.081
139
CHR178 Chromosomal Triplication 35 0.081
140
CRN051 Craniofacial Microsomia 28 0.081
141
c DRR021 Diarrhea 11, Malabsorptive, Congenital 25 0.081
142
HMS005 Homosexuality 1 23 0.081
143
P LKM071 Leukemia, Chronic Lymphocytic 79 0.080
144
P LKM002 Leukemia 68 0.080
145
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.080
146
HPT019 Hepatic Encephalopathy 60 0.080
147
ART140 Arteries, Anomalies of 52 0.080
148
HPT004 Hepatic Coma 45 0.080
149
c HYP595 Hypertension, Essential 84 0.075
150
PRP027 Peripheral Vascular Disease 71 0.075
151
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.075
152
P ENC018 Encephalopathy 61 0.075
153
P SYP003 Syphilis 58 0.075
154
P RNL007 Renal Tubular Acidosis 51 0.075
155
c ATR087 Atrial Standstill 1 75 0.069
156
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.069
157
P VSC007 Vascular Disease 63 0.069
158
c FNC043 Fanconi Anemia, Complementation Group E 62 0.069
159
VRC005 Varicose Veins 60 0.069
160
IRN002 Iron Metabolism Disease 57 0.069
161
HMR039 Hemorrhage, Intracerebral 57 0.069
162
P SBS003 Substance Abuse 55 0.069
163
HRT012 Heart Valve Disease 53 0.069
164
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.069
165
CLL014 Cll/sll 45 0.069
166
IMM064 Immunodeficiency, Common Variable, 10 44 0.069
167
c HYP272 Hypercholesterolemia, Familial, 3 44 0.069
168
CRD017 Cardiac Valvular Dysplasia, X-Linked 40 0.069
169
c FNC026 Fanconi Renotubular Syndrome 1 39 0.069
170
MCL069 Macular Dystrophy, Retinal, 1, North Carolina Type 39 0.069
171
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.069
172
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.069
173
HPT085 Hepatitis, Fulminant Viral 32 0.069
174
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.062
175
BRN024 Bronchitis 68 0.062
176
P DMN002 Dementia 66 0.062
177
KHL003 Kohlschutter-Tonz Syndrome 65 0.062
178
TTN003 Tetanus 65 0.062
179
LYM017 Lyme Disease 64 0.062
180
DPH001 Diphtheria 60 0.062
181
P HYP726 Hypercalcemia, Infantile, 1 58 0.062
182
HPT022 Hepatoblastoma 56 0.062
183
P ALP008 Alopecia 54 0.062
184
BCT002 Bacterial Vaginosis 53 0.062
185
PLC008 Placenta Disease 50 0.062
186
DYS073 Dysphagia 50 0.062
187
P DST107 Distal Renal Tubular Acidosis 42 0.062
188
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.062
189
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.062
190
CNN003 Conn's Syndrome 79 0.052
191
P PHC003 Pheochromocytoma 71 0.052
192
c WLM018 Wilms Tumor 5 61 0.052
193
P BPL003 Bipolar Disorder 56 0.052
194
P TRM003 Tremor 54 0.052
195
ADR040 Adrenal Gland Pheochromocytoma 46 0.052
196
VGN019 Vaginal Discharge 46 0.052
197
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.052
198
P CLS010 Cluster Headache 42 0.052
199
c MJR024 Major Affective Disorder 9 41 0.052
200
c MJR022 Major Affective Disorder 8 38 0.052
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