Search results for Efavirenz

160 hits were found for Efavirenz

# Family MCID Name MIFTS Score
1
EFV001 Efavirenz, Poor Metabolism of 13 6.639
2
ACQ007 Acquired Immunodeficiency Syndrome 65 0.947
3
HMN044 Human Immunodeficiency Virus Type 1 71 0.636
4
VRL011 Viral Infectious Disease 64 0.499
5
P HPT021 Hepatitis 75 0.312
6
c HPT003 Hepatitis a 63 0.302
7
IMM136 Immune System Disease 57 0.250
8
c VRL010 Viral Hepatitis 59 0.237
9
P LVR013 Liver Disease 76 0.223
10
c TRC078 Trichohepatoenteric Syndrome 2 34 0.199
11
OCL033 Oculocerebral Syndrome with Hypopigmentation 31 0.188
12
c HPT073 Hepatitis C Virus 73 0.176
13
c HPT001 Hepatitis C 73 0.176
14
SPS003 Spastic Diplegia 55 0.164
15
ANX010 Anxiety 72 0.158
16
P LPD010 Lipodystrophy 57 0.158
17
P EXN002 Exanthem 62 0.151
18
LPD008 Lipid Metabolism Disorder 59 0.151
19
MNT002 Mental Depression 60 0.144
20
MLR004 Malaria 86 0.137
21
SLP005 Sleep Disorder 59 0.137
22
c HPT016 Hepatitis B 68 0.129
23
P NRV007 Nervous System Disease 75 0.121
24
P KDN018 Kidney Disease 69 0.121
25
c CRD093 Cardiomyopathy, Dilated, 1a 58 0.121
26
PLM001 Pulmonary Tuberculosis 72 0.112
27
P MNN013 Meningitis 71 0.112
28
P PNC035 Pancreatic Cancer 89 0.102
29
P PRS040 Prostate Cancer 88 0.102
30
P MYL005 Myelofibrosis 75 0.102
31
KPS004 Kaposi Sarcoma 73 0.102
32
BRC012 Brucellosis 71 0.102
33
WRN001 Werner Syndrome 70 0.102
34
SRC014 Sarcoma 68 0.102
35
TTN003 Tetanus 65 0.102
36
AGN016 Aging 65 0.102
37
SFT003 Soft Tissue Sarcoma 58 0.102
38
IMM158 Immune Suppression 57 0.102
39
c MLG074 Malignant Mesenchymoma 51 0.102
40
HMN032 Human Herpesvirus 8 50 0.102
41
HPD002 Hepadnavirus Infection 14 0.102
42
P HRT032 Heart Disease 80 0.091
43
P OST002 Osteoporosis 75 0.091
44
c CHR089 Chronic Kidney Failure 72 0.091
45
P MYC084 Mycobacterium Tuberculosis 1 69 0.091
46
DPH001 Diphtheria 63 0.091
47
FTT001 Fatty Liver Disease 62 0.091
48
P HMP007 Hemophilia 61 0.091
49
P ENC018 Encephalopathy 58 0.091
50
TXC002 Toxic Encephalopathy 55 0.091
51
c MTR002 Mitral Valve Insufficiency 46 0.091
52
P VSC018 Visceral Steatosis 38 0.091
53
HRP008 Herpes Simiae 16 0.091
54
LVR012 Liver Cirrhosis 73 0.079
55
PSY004 Psychotic Disorder 72 0.079
56
P LYM118 Lymphoma 71 0.079
57
P ADN016 Adenocarcinoma 71 0.079
58
LYM143 Lymphoma, Non-Hodgkin, Familial 71 0.079
59
P PNM007 Pneumonia 70 0.079
60
DMN002 Dementia 68 0.079
61
P ALP009 Alopecia Areata 64 0.079
62
PNC033 Pancreas Adenocarcinoma 63 0.079
63
RGD003 Rigid Spine Muscular Dystrophy 1 59 0.079
64
PNC034 Pancreas Disease 59 0.079
65
LYM019 Lymphosarcoma 58 0.079
66
NPH009 Nephrolithiasis 57 0.079
67
P ALP008 Alopecia 56 0.079
68
PRS042 Prostate Disease 56 0.079
69
HYP060 Hyperinsulinism 56 0.079
70
P MYP006 Myopia 56 0.079
71
TBR011 Tuberculous Meningitis 54 0.079
72
CRY005 Cryptococcosis 54 0.079
73
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.079
74
GYN001 Gynecomastia 47 0.079
75
LYM024 Lymphatic System Disease 45 0.079
76
AST054 Australia Antigen 26 0.079
77
INF021 Infant Gynecomastia 25 0.079
78
PLS032 Plasmodium Falciparum Blood Infection Level 17 0.079
79
AST005 Asthma 83 0.064
80
ISC006 Ischemic Heart Disease 73 0.064
81
P CRN018 Coronary Artery Anomaly 69 0.064
82
LNG099 Lung Disease 67 0.064
83
DRM006 Dermatitis 67 0.064
84
c CNT035 Central Nervous System Disease 65 0.064
85
c PRC016 Pre-Eclampsia 65 0.064
86
ALC007 Alcohol Dependence 65 0.064
87
P NRP001 Neuropathy 63 0.064
88
RBS001 Rabies 63 0.064
89
DFC004 Deficiency Anemia 62 0.064
90
STT001 Status Epilepticus 60 0.064
91
PHR003 Pharyngitis 59 0.064
92
ALL026 Allergic Hypersensitivity Disease 59 0.064
93
c BCT007 Bacterial Meningitis 59 0.064
94
P CRN300 Coronary Heart Disease 1 57 0.064
95
P ECL001 Eclampsia 57 0.064
96
IRN001 Iron Deficiency Anemia 55 0.064
97
NRT004 Neuritis 55 0.064
98
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 54 0.064
99
MYL020 Myelomeningocele 54 0.064
100
PRP019 Peripheral Nervous System Disease 53 0.064
101
c ACT134 Acute Liver Failure 52 0.064
102
DRG003 Drug Dependence 51 0.064
103
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.064
104
PLC008 Placenta Disease 48 0.064
105
CRY014 Cryptococcal Meningitis 45 0.064
106
IRN002 Iron Metabolism Disease 45 0.064
107
ADS004 Aids Dementia Complex 42 0.064
108
P PRC031 Preeclampsia/eclampsia 1 41 0.064
109
P HYP265 Hypotonia 40 0.064
110
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 36 0.064
111
c INF145 Infantile Liver Failure Syndrome 1 33 0.064
112
ATX010 Ataxia Neuropathy Spectrum 29 0.064
113
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.064
114
P RHM011 Rheumatoid Arthritis 91 0.046
115
P MYC007 Myocardial Infarction 81 0.046
116
CRH001 Crohn's Disease 80 0.046
117
P ART022 Arthritis 77 0.046
118
ALP046 Alport Syndrome, X-Linked 74 0.046
119
P BCL006 B-Cell Lymphomas 70 0.046
120
P ANR048 Aniridia 1 68 0.046
121
P ATT013 Attention Deficit-Hyperactivity Disorder 67 0.046
122
ATM095 Autoimmune Disease 66 0.046
123
P ENC004 Encephalitis 66 0.046
124
P TXP001 Toxoplasmosis 65 0.046
125
SVR097 Severe Cutaneous Adverse Reaction 64 0.046
126
P MYS005 Myositis 63 0.046
127
RHM027 Rheumatic Disease 62 0.046
128
P PRP029 Porphyria 62 0.046
129
ANR040 Aneurysm 61 0.046
130
PRM042 Primary Effusion Lymphoma 61 0.046
131
P DRR001 Diarrhea 60 0.046
132
CCC001 Coccidioidomycosis 60 0.046
133
THR100 Thrombocytopenic Purpura, Autoimmune 57 0.046
134
BRN106 Burns 57 0.046
135
P BRN009 Burning Mouth Syndrome 56 0.046
136
HST011 Histoplasmosis 56 0.046
137
PNM001 Pneumocystosis 55 0.046
138
CPR004 Coproporphyria, Hereditary 54 0.046
139
c INF071 Inflammatory Bowel Disease 1 54 0.046
140
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.046
141
P CLL015 Collagen Disease 53 0.046
142
ILT001 Ileitis 52 0.046
143
OST011 Osteomalacia 52 0.046
144
HPT082 Hepatic Adenomas, Familial 52 0.046
145
CCC002 Coccidiosis 52 0.046
146
P LCT001 Lactic Acidosis 51 0.046
147
MTB004 Metabolic Acidosis 49 0.046
148
ASP007 Aspiration Pneumonia 49 0.046
149
P ENC008 Encephalocele 48 0.046
150
c ACT078 Acute Porphyria 48 0.046
151
c NNN010 Noonan Syndrome 3 42 0.046
152
ENT004 Enthesopathy 38 0.046
153
c CRN243 Carney Complex, Type 1 35 0.046
154
P RNG031 Ring Chromosome Y Syndrome 29 0.046
155
EXF003 Exfoliative Dermatitis 28 0.046
156
PHT004 Photoallergic Dermatitis 25 0.046
157
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 24 0.046
158
LYM126 Lymphoma Aids Related 21 0.046
159
ANR038 Anorexia Nervosa 1 21 0.046
160
BLD137 Blood Group--Ahonen 17 0.046
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