Search results for Efavirenz

183 hits were found for Efavirenz

# Family MCID Name MIFTS Score
1
EFV001 Efavirenz, Poor Metabolism of 13 7.232
2
ACQ007 Acquired Immunodeficiency Syndrome 63 0.903
3
HMN044 Human Immunodeficiency Virus Type 1 70 0.621
4
VRL011 Viral Infectious Disease 63 0.480
5
P HPT021 Hepatitis 76 0.304
6
c HPT003 Hepatitis a 61 0.295
7
IMM136 Immune System Disease 56 0.230
8
c VRL010 Viral Hepatitis 59 0.226
9
TYP041 Type I 56 0.217
10
P LVR013 Liver Disease 75 0.213
11
c TRC078 Trichohepatoenteric Syndrome 2 34 0.189
12
ANX010 Anxiety 72 0.179
13
P EXN002 Exanthem 61 0.179
14
SPS003 Spastic Diplegia 54 0.179
15
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.174
16
c HPT073 Hepatitis C Virus 72 0.168
17
c HPT001 Hepatitis C 71 0.168
18
DPR016 Depression 72 0.157
19
P NRV007 Nervous System Disease 73 0.151
20
LPD008 Lipid Metabolism Disorder 58 0.144
21
MNT002 Mental Depression 57 0.144
22
DNT012 Dental Caries 51 0.144
23
MLR004 Malaria 83 0.130
24
SLP005 Sleep Disorder 59 0.130
25
PLM001 Pulmonary Tuberculosis 71 0.123
26
c HPT016 Hepatitis B 67 0.123
27
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.115
28
PSY004 Psychotic Disorder 71 0.115
29
P KDN018 Kidney Disease 68 0.115
30
P MJR001 Major Depressive Disorder 65 0.115
31
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.115
32
P MNN013 Meningitis 70 0.106
33
DMN002 Dementia 68 0.106
34
P THR014 Thrombocytopenia 64 0.106
35
P MYP006 Myopia 56 0.106
36
P PRS040 Prostate Cancer 90 0.097
37
P PNC035 Pancreatic Cancer 79 0.097
38
KPS004 Kaposi Sarcoma 73 0.097
39
P MYL005 Myelofibrosis 70 0.097
40
BRC012 Brucellosis 70 0.097
41
P PNM007 Pneumonia 69 0.097
42
WRN001 Werner Syndrome 69 0.097
43
SRC014 Sarcoma 68 0.097
44
TTN003 Tetanus 64 0.097
45
AGN016 Aging 64 0.097
46
P ALP009 Alopecia Areata 63 0.097
47
SFT003 Soft Tissue Sarcoma 58 0.097
48
P ALP008 Alopecia 58 0.097
49
c MLG074 Malignant Mesenchymoma 54 0.097
50
HMN032 Human Herpesvirus 8 49 0.097
51
HPD002 Hepadnavirus Infection 25 0.097
52
P OST002 Osteoporosis 76 0.087
53
P HRT032 Heart Disease 74 0.087
54
c CHR089 Chronic Kidney Failure 72 0.087
55
MDD011 Mood Disorder 63 0.087
56
P ENC018 Encephalopathy 62 0.087
57
DPH001 Diphtheria 62 0.087
58
FTT001 Fatty Liver Disease 60 0.087
59
P HMP007 Hemophilia 60 0.087
60
P DRR001 Diarrhea 56 0.087
61
NPH009 Nephrolithiasis 55 0.087
62
TXC002 Toxic Encephalopathy 55 0.087
63
DRG003 Drug Dependence 51 0.087
64
c MTR002 Mitral Valve Insufficiency 46 0.087
65
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.087
66
P VSC018 Visceral Steatosis 37 0.087
67
HRP008 Herpes Simiae 16 0.087
68
P MYC007 Myocardial Infarction 79 0.075
69
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.075
70
P LYM118 Lymphoma 70 0.075
71
P ADN016 Adenocarcinoma 70 0.075
72
LVR012 Liver Cirrhosis 68 0.075
73
PNC033 Pancreas Adenocarcinoma 64 0.075
74
RGD003 Rigid Spine Muscular Dystrophy 1 62 0.075
75
THR024 Thrombosis 61 0.075
76
HDC001 Headache 59 0.075
77
PNC034 Pancreas Disease 57 0.075
78
HYP060 Hyperinsulinism 56 0.075
79
LYM019 Lymphosarcoma 55 0.075
80
PNM001 Pneumocystosis 55 0.075
81
P TRC086 Trichohepatoenteric Syndrome 1 54 0.075
82
LYM024 Lymphatic System Disease 54 0.075
83
TBR011 Tuberculous Meningitis 53 0.075
84
BRN071 Brain Injury 53 0.075
85
CRY005 Cryptococcosis 53 0.075
86
c ACT134 Acute Liver Failure 52 0.075
87
GYN001 Gynecomastia 46 0.075
88
PDT001 Pediatric Lymphoma 45 0.075
89
MTC005 Mitochondrial Metabolism Disease 44 0.075
90
PRS042 Prostate Disease 44 0.075
91
c ADL001 Adult Lymphoma 39 0.075
92
PRS123 Persistent Generalized Lymphadenopathy 38 0.075
93
c INF145 Infantile Liver Failure Syndrome 1 35 0.075
94
AST054 Australia Antigen 27 0.075
95
PLS032 Plasmodium Falciparum Blood Infection Level 17 0.075
96
AST005 Asthma 82 0.061
97
ISC006 Ischemic Heart Disease 72 0.061
98
CHG001 Chagas Disease 71 0.061
99
P CRN018 Coronary Artery Anomaly 68 0.061
100
LNG099 Lung Disease 67 0.061
101
DRM006 Dermatitis 66 0.061
102
ALC007 Alcohol Dependence 65 0.061
103
c CRN300 Coronary Heart Disease 1 64 0.061
104
GST045 Gastroenteritis 64 0.061
105
c CNT035 Central Nervous System Disease 63 0.061
106
HYP066 Hyperglycemia 63 0.061
107
P NRP001 Neuropathy 63 0.061
108
RBS001 Rabies 62 0.061
109
HYP056 Hypoglycemia 62 0.061
110
PLC008 Placenta Disease 61 0.061
111
DFC004 Deficiency Anemia 61 0.061
112
PRP019 Peripheral Nervous System Disease 60 0.061
113
STT001 Status Epilepticus 60 0.061
114
PHR003 Pharyngitis 59 0.061
115
c PRC016 Pre-Eclampsia 59 0.061
116
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.061
117
c BCT007 Bacterial Meningitis 58 0.061
118
NRT004 Neuritis 57 0.061
119
P ECL001 Eclampsia 57 0.061
120
IRN002 Iron Metabolism Disease 55 0.061
121
IRN001 Iron Deficiency Anemia 55 0.061
122
MYL020 Myelomeningocele 53 0.061
123
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.061
124
HYP005 Hypokalemia 53 0.061
125
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.061
126
CRY014 Cryptococcal Meningitis 45 0.061
127
MCR020 Microsporidiosis 43 0.061
128
ADS004 Aids Dementia Complex 41 0.061
129
P HYP265 Hypotonia 40 0.061
130
c PRC031 Preeclampsia/eclampsia 1 39 0.061
131
PSD088 Pseudobulbar Affect 37 0.061
132
ATX010 Ataxia Neuropathy Spectrum 35 0.061
133
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.061
134
P RHM011 Rheumatoid Arthritis 80 0.043
135
CRH001 Crohn's Disease 78 0.043
136
P ART022 Arthritis 76 0.043
137
ALP046 Alport Syndrome, X-Linked 75 0.043
138
c ART101 Aortic Valve Disease 2 73 0.043
139
LSH001 Leishmaniasis 70 0.043
140
SVR097 Severe Cutaneous Adverse Reaction 68 0.043
141
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.043
142
P ANR048 Aniridia 1 65 0.043
143
P ASP006 Aspergillosis 65 0.043
144
P BCL006 B-Cell Lymphomas 65 0.043
145
P ENC004 Encephalitis 65 0.043
146
P TXP001 Toxoplasmosis 64 0.043
147
ATM095 Autoimmune Disease 64 0.043
148
P MYS005 Myositis 63 0.043
149
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.043
150
P PRP029 Porphyria 62 0.043
151
RHM027 Rheumatic Disease 62 0.043
152
P NTR004 Neutropenia 60 0.043
153
ANR040 Aneurysm 60 0.043
154
CCC001 Coccidioidomycosis 59 0.043
155
PRM042 Primary Effusion Lymphoma 58 0.043
156
BRN106 Burns 56 0.043
157
ILT001 Ileitis 56 0.043
158
END030 End Stage Renal Failure 56 0.043
159
CPR004 Coproporphyria, Hereditary 56 0.043
160
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.043
161
HST011 Histoplasmosis 54 0.043
162
c INF071 Inflammatory Bowel Disease 1 53 0.043
163
P BRN009 Burning Mouth Syndrome 53 0.043
164
HPT082 Hepatic Adenomas, Familial 53 0.043
165
P CLL015 Collagen Disease 52 0.043
166
OST011 Osteomalacia 52 0.043
167
CCC002 Coccidiosis 52 0.043
168
P LCT001 Lactic Acidosis 50 0.043
169
c NNN010 Noonan Syndrome 3 49 0.043
170
MTB004 Metabolic Acidosis 48 0.043
171
ASP007 Aspiration Pneumonia 47 0.043
172
c ACT078 Acute Porphyria 47 0.043
173
ENT004 Enthesopathy 46 0.043
174
P ENC008 Encephalocele 46 0.043
175
NCR004 Nocardiosis 44 0.043
176
GRN017 Granulocytopenia 43 0.043
177
CRR001 Carrion's Disease 40 0.043
178
BRT043 Bartonellosis 37 0.043
179
PHT004 Photoallergic Dermatitis 33 0.043
180
EXF003 Exfoliative Dermatitis 29 0.043
181
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 27 0.043
182
LYM126 Lymphoma Aids Related 22 0.043
183
BLD137 Blood Group--Ahonen 17 0.043
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