Search results for Telbivudine

111 hits were found for Telbivudine

# Family MCID Name MIFTS Score
1
c HPT016 Hepatitis B 59 0.821
2
P HPT021 Hepatitis 67 0.642
3
c HPT003 Hepatitis a 62 0.522
4
HRP008 Herpes Simiae 25 0.401
5
LVR012 Liver Cirrhosis 62 0.341
6
48X005 48,xyyy 39 0.252
7
P MYP004 Myopathy 70 0.224
8
P LVR013 Liver Disease 68 0.218
9
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.192
10
VRL011 Viral Infectious Disease 61 0.185
11
P HPT023 Hepatocellular Carcinoma 100 0.170
12
c VRL010 Viral Hepatitis 52 0.163
13
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.145
14
P LCT001 Lactic Acidosis 51 0.145
15
c CHR684 Chronic Kidney Disease 70 0.136
16
ADL002 Adult Syndrome 70 0.136
17
P MYS005 Myositis 56 0.136
18
CHL079 Children's Interstitial Lung Disease 26 0.136
19
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.126
20
P KDN018 Kidney Disease 72 0.115
21
DWN001 Down Syndrome 70 0.115
22
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.115
23
c RHB024 Rhabdomyosarcoma 2 67 0.115
24
c MCL013 Mucolipidosis Iv 66 0.115
25
P GLM007 Glomerulonephritis 57 0.115
26
CMR002 Coumarin Resistance 56 0.115
27
c INF145 Infantile Liver Failure Syndrome 1 50 0.115
28
P NRP001 Neuropathy 56 0.103
29
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.089
30
INC002 Inclusion Body Myositis 58 0.089
31
P PRP019 Peripheral Nervous System Disease 58 0.089
32
HYP005 Hypokalemia 55 0.089
33
HPT014 Hepatorenal Syndrome 50 0.089
34
PLC008 Placenta Disease 50 0.089
35
P OVR096 Overlap Myositis 27 0.089
36
c HYP595 Hypertension, Essential 84 0.073
37
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.073
38
RCK004 Rickets 68 0.073
39
BLR008 Bilirubin Metabolic Disorder 57 0.073
40
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.073
41
ESP002 Esophageal Varix 51 0.073
42
END086 End Stage Renal Disease 51 0.073
43
P MTC133 Mitochondrial Myopathy 49 0.073
44
47X002 47,xyy 49 0.073
45
c PRM038 Primary Agammaglobulinemia 44 0.073
46
TRP009 Triple X Syndrome 42 0.073
47
P CLR023 Colorectal Cancer 99 0.051
48
P LNG032 Lung Cancer 98 0.051
49
P BRS047 Breast Cancer 97 0.051
50
ESP021 Esophageal Cancer 90 0.051
51
P CNR004 Cone-Rod Dystrophy 2 73 0.051
52
c HPT073 Hepatitis C Virus 72 0.051
53
HMN044 Human Immunodeficiency Virus Type 1 71 0.051
54
MYL005 Myelofibrosis 70 0.051
55
LYM133 Lymphoma, Hodgkin, Classic 69 0.051
56
P LYM118 Lymphoma 68 0.051
57
P MYC084 Mycobacterium Tuberculosis 1 68 0.051
58
P LKM002 Leukemia 68 0.051
59
P ESS003 Essential Thrombocythemia 68 0.051
60
MYL031 Myeloproliferative Neoplasm 66 0.051
61
c SML038 Small Cell Cancer of the Lung 65 0.051
62
PRT036 Peritonitis 64 0.051
63
NRM005 Neuromuscular Disease 64 0.051
64
HMT002 Hematologic Cancer 62 0.051
65
P VSC011 Vasculitis 62 0.051
66
TXC005 Toxic Shock Syndrome 62 0.051
67
P ENC018 Encephalopathy 61 0.051
68
P HMN010 Hemangioma 61 0.051
69
HPT019 Hepatic Encephalopathy 60 0.051
70
CRD223 Cardiac Arrhythmia 60 0.051
71
VRC005 Varicose Veins 60 0.051
72
P MYC008 Myocarditis 59 0.051
73
PRT013 Portal Hypertension 59 0.051
74
MTC097 Mitochondrial Complex Iv Deficiency 59 0.051
75
c ACT073 Acute Leukemia 58 0.051
76
P BCL017 B-Cell Lymphoma 58 0.051
77
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.051
78
P PLY041 Polymyositis 57 0.051
79
THR024 Thrombosis 57 0.051
80
P PLY019 Polyneuropathy 56 0.051
81
DFF005 Diffuse Large B-Cell Lymphoma 55 0.051
82
CLF004 Cleft Lip/palate 54 0.051
83
CLF001 Cleft Lip 53 0.051
84
NRT004 Neuritis 52 0.051
85
P RCT021 Rectum Cancer 52 0.051
86
THR004 Thrombocytosis 51 0.051
87
LNG031 Lung Benign Neoplasm 51 0.051
88
P MMB011 Membranous Nephropathy 50 0.051
89
PRT018 Portal Vein Thrombosis 50 0.051
90
ECT026 Ectopic Pregnancy 50 0.051
91
MTB004 Metabolic Acidosis 50 0.051
92
BLR001 Biliary Atresia 50 0.051
93
DYS073 Dysphagia 50 0.051
94
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.051
95
c THR090 Thrombocythemia 1 49 0.051
96
CRY004 Cryoglobulinemia 48 0.051
97
RNL077 Renal Fibrosis 47 0.051
98
RTC005 Reticulosarcoma 47 0.051
99
LYM019 Lymphosarcoma 46 0.051
100
URT010 Ureteral Obstruction 45 0.051
101
HPT004 Hepatic Coma 45 0.051
102
ACT003 Acute Kidney Tubular Necrosis 45 0.051
103
ANK020 Ankyloglossia with or Without Tooth Anomalies 44 0.051
104
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.051
105
NSP002 Nasopharyngitis 43 0.051
106
CYT002 Cytokine Deficiency 42 0.051
107
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 41 0.051
108
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.051
109
P AXN001 Axonal Neuropathy 36 0.051
110
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.051
111
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.051
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