Search results for Peginterferon alfa-2b

272 hits were found for Peginterferon alfa-2b

# Family MCID Name MIFTS Score
1
c HPT001 Hepatitis C 63 0.956
2
P HPT021 Hepatitis 67 0.911
3
c HPT003 Hepatitis a 63 0.796
4
c HPT073 Hepatitis C Virus 70 0.718
5
48X005 48,xyyy 39 0.712
6
c HPT016 Hepatitis B 59 0.529
7
LVR012 Liver Cirrhosis 63 0.365
8
P NTR004 Neutropenia 63 0.304
9
P LVR013 Liver Disease 68 0.276
10
MLN008 Melanoma 69 0.273
11
HRP008 Herpes Simiae 25 0.261
12
SKN019 Skin Melanoma 67 0.257
13
VRL011 Viral Infectious Disease 61 0.253
14
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.246
15
c RHB024 Rhabdomyosarcoma 2 65 0.239
16
P HPT023 Hepatocellular Carcinoma 100 0.226
17
IMM167 Immune Deficiency Disease 78 0.203
18
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.201
19
HMN044 Human Immunodeficiency Virus Type 1 71 0.197
20
DFC004 Deficiency Anemia 75 0.193
21
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.191
22
c VRL010 Viral Hepatitis 51 0.191
23
P LKM002 Leukemia 66 0.175
24
c LKM063 Leukemia, Chronic Myeloid 71 0.169
25
c HPT015 Hepatitis D 49 0.166
26
P THR014 Thrombocytopenia 68 0.162
27
c INF145 Infantile Liver Failure Syndrome 1 50 0.158
28
P MLT020 Multiple Sclerosis 72 0.150
29
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.148
30
P KDN017 Kidney Cancer 61 0.148
31
P EXN002 Exanthem 57 0.146
32
c PRM038 Primary Agammaglobulinemia 43 0.143
33
ACQ007 Acquired Immunodeficiency Syndrome 60 0.142
34
END030 End Stage Renal Failure 58 0.142
35
MYL069 Myeloma, Multiple 85 0.136
36
P HML002 Hemolytic Anemia 62 0.136
37
DWN001 Down Syndrome 70 0.136
38
P ALP008 Alopecia 56 0.135
39
P TRN020 Turner Syndrome 65 0.133
40
CMR002 Coumarin Resistance 56 0.131
41
P KDN018 Kidney Disease 70 0.128
42
P MYL006 Myeloid Leukemia 60 0.127
43
CYT002 Cytokine Deficiency 44 0.125
44
KPS004 Kaposi Sarcoma 75 0.124
45
P MLN066 Melanoma, Cutaneous Malignant 1 70 0.124
46
HRY003 Hairy Cell Leukemia 55 0.123
47
ADL002 Adult Syndrome 69 0.123
48
PRT013 Portal Hypertension 60 0.117
49
CRY004 Cryoglobulinemia 49 0.116
50
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.110
51
P HYP086 Hypothyroidism 68 0.109
52
MYC006 Mycosis Fungoides 66 0.108
53
P LYM118 Lymphoma 68 0.107
54
47X002 47,xyy 49 0.106
55
BRN028 Brain Cancer 73 0.104
56
P ESS003 Essential Thrombocythemia 67 0.104
57
P HMP007 Hemophilia 51 0.104
58
LYM019 Lymphosarcoma 47 0.103
59
c CHR684 Chronic Kidney Disease 66 0.102
60
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.100
61
P HMN010 Hemangioma 61 0.099
62
PLS009 Plasma Cell Neoplasm 51 0.099
63
ATM095 Autoimmune Disease 61 0.099
64
P THL005 Thalassemia 60 0.099
65
P HMN032 Human Herpesvirus 8 46 0.095
66
P FLL037 Follicular Lymphoma 66 0.093
67
NRF007 Neurofibroma 64 0.093
68
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.093
69
P DRR001 Diarrhea 57 0.093
70
c THR090 Thrombocythemia 1 49 0.093
71
P OVR042 Ovarian Cancer 89 0.092
72
SKN013 Skin Benign Neoplasm 49 0.092
73
c CHR064 Chronic Monocytic Leukemia 34 0.092
74
LYM133 Lymphoma, Hodgkin, Classic 69 0.090
75
FCT007 Factor Vii Deficiency 66 0.090
76
SPL018 Splenomegaly 48 0.090
77
CLS052 Classic Hairy Cell Leukemia 27 0.090
78
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.090
79
LYM027 Lymphopenia 57 0.090
80
WGN007 Wagner Vitreoretinopathy 38 0.090
81
WGN003 Wagner Syndrome 35 0.090
82
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.089
83
ANX010 Anxiety 72 0.089
84
DPR016 Depression 63 0.089
85
MNT002 Mental Depression 57 0.089
86
MYL009 Myelodysplastic Syndrome 70 0.087
87
PLY001 Polycythemia Vera 69 0.087
88
P VSC011 Vasculitis 62 0.087
89
SZR001 Sezary's Disease 60 0.087
90
P PLY018 Polycythemia 55 0.087
91
P HYP098 Hypereosinophilic Syndrome 66 0.087
92
PLX002 Plexiform Neurofibroma 45 0.087
93
c CHR682 Chronic Bilirubin Encephalopathy 38 0.087
94
PRP030 Purpura 55 0.085
95
CLR030 Clear Cell Renal Cell Carcinoma 53 0.085
96
P CTN015 Cutaneous T Cell Lymphoma 49 0.085
97
c HYP595 Hypertension, Essential 84 0.085
98
P ENC018 Encephalopathy 61 0.085
99
ATX019 Ataxia with Vitamin E Deficiency 48 0.085
100
c HMP029 Hemophilia a 65 0.085
101
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.085
102
FTT001 Fatty Liver Disease 61 0.085
103
FCT001 Factor Viii Deficiency 55 0.085
104
P GRF003 Graft-Versus-Host Disease 71 0.081
105
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.081
106
c ACT027 Acute Pancreatitis 59 0.081
107
49X006 49, Xxxxy Syndrome 41 0.080
108
CHL079 Children's Interstitial Lung Disease 27 0.080
109
P CLR023 Colorectal Cancer 98 0.080
111
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.080
112
P GLM045 Glioma 63 0.080
113
c ADL017 Adult T-Cell Leukemia 57 0.080
114
GLL048 Glial Tumor 45 0.080
115
c MLG068 Malignant Glioma 45 0.080
116
c OVR114 Ovarian Cancer 1 38 0.080
117
c DWL002 Dowling-Degos Disease 1 58 0.079
118
P THY032 Thyroiditis 53 0.079
119
P MLN069 Melanoma, Uveal 58 0.075
120
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.075
121
c ALP101 Alpha-Thalassemia 62 0.075
122
IRN002 Iron Metabolism Disease 57 0.075
123
P GLM040 Glioma Susceptibility 1 81 0.073
124
CHL065 Cholangiocarcinoma 67 0.073
125
P SKN015 Skin Carcinoma 67 0.073
126
FLL027 Fallopian Tube Carcinoma 67 0.073
127
DRM006 Dermatitis 61 0.073
128
P PNC044 Pancreatitis 61 0.073
129
SQM006 Squamous Cell Carcinoma 60 0.073
130
P LCH002 Lichen Planus 54 0.073
131
THR004 Thrombocytosis 51 0.073
132
INT079 Intrahepatic Cholangiocarcinoma 50 0.073
133
MXD026 Mixed Glioma 45 0.073
134
PRT035 Peritoneum Cancer 44 0.073
135
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.073
136
OVR094 Ovarian Epithelial Cancer 38 0.073
137
ILM001 Ileum Cancer 26 0.073
138
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.073
139
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.073
140
HMT002 Hematologic Cancer 62 0.073
141
SRC014 Sarcoma 65 0.070
142
P BCL017 B-Cell Lymphoma 58 0.070
143
SPN035 Spindle Cell Sarcoma 51 0.070
144
P TCL004 T-Cell Leukemia 47 0.070
145
MYL031 Myeloproliferative Neoplasm 65 0.070
146
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.070
147
VRC005 Varicose Veins 60 0.070
148
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.070
149
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.070
151
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.066
152
GLB015 Glioblastoma Multiforme 75 0.066
153
c BTT014 Beta-Thalassemia 72 0.066
154
c NRF024 Neurofibromatosis, Type I 71 0.066
155
P CNR004 Cone-Rod Dystrophy 2 71 0.066
156
CRN036 Craniopharyngioma 65 0.066
157
CHR066 Chronic Fatigue Syndrome 61 0.066
158
c ACT073 Acute Leukemia 58 0.066
159
P HYP076 Hyperthyroidism 55 0.066
160
c PRM012 Primary Polycythemia 52 0.066
161
P AST007 Astrocytoma 50 0.066
162
CYS009 Cystadenoma 43 0.066
163
P PNC035 Pancreatic Cancer 84 0.064
164
c LKM071 Leukemia, Chronic Lymphocytic 79 0.064
165
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.064
166
OCL022 Ocular Melanoma 53 0.064
167
MRG003 Marginal Zone B-Cell Lymphoma 53 0.064
168
SPL004 Splenic Marginal Zone Lymphoma 51 0.064
169
c FLL041 Follicular Lymphoma 1 49 0.064
170
c HMN021 Human T-Cell Leukemia Virus Type 1 48 0.064
171
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.064
172
GST019 Gastrointestinal Stromal Tumor 76 0.063
173
P SRC025 Sarcoidosis 1 70 0.063
174
P PNM007 Pneumonia 68 0.063
175
MYL005 Myelofibrosis 67 0.063
176
P ALC033 Alcohol Use Disorder 58 0.063
177
BLR008 Bilirubin Metabolic Disorder 57 0.063
178
P GLM007 Glomerulonephritis 57 0.063
179
THR024 Thrombosis 56 0.063
180
GST050 Gastrointestinal System Disease 56 0.063
181
P SBS003 Substance Abuse 54 0.063
182
END040 Endogenous Depression 54 0.063
183
NRT001 Neurotic Disorder 52 0.063
184
PRG017 Paraganglioma and Gastric Stromal Sarcoma 52 0.063
185
P SCK005 Sickle Cell Disease 50 0.063
186
P LNG032 Lung Cancer 97 0.056
187
c SYS001 Systemic Lupus Erythematosus 86 0.056
188
OST159 Osteogenic Sarcoma 66 0.056
189
P LPS004 Lupus Erythematosus 61 0.056
190
P OPT006 Optic Nerve Disease 57 0.056
191
c CHR417 Chronic Graft Versus Host Disease 56 0.056
192
CRC006 Carcinoid Syndrome 55 0.056
193
P BRN035 Brain Stem Glioma 51 0.056
194
c ACT135 Acute Graft Versus Host Disease 51 0.056
195
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.056
196
OPT003 Opiate Dependence 50 0.056
197
GST049 Gastrointestinal System Cancer 49 0.056
198
CRC014 Carcinoid Tumors, Intestinal 48 0.056
199
OPD006 Opioid Addiction 48 0.056
200
SRT004 Serotonin Syndrome 46 0.056
201
GST071 Gastrointestinal Carcinoma 45 0.056
202
OPD001 Opioid Abuse 45 0.056
203
INT253 Intestinal Benign Neoplasm 44 0.056
204
DFF037 Diffuse Intrinsic Pontine Glioma 42 0.056
205
SML008 Small Intestine Lymphoma 35 0.056
206
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.056
207
MLG164 Malignant Epithelial Tumor of Ovary 26 0.056
208
HML018 Homologous Wasting Disease 22 0.056
209
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.056
210
c THR092 Thrombophilia Due to Thrombin Defect 73 0.056
211
SCK003 Sickle Cell Anemia 72 0.056
212
P OLG002 Oligodendroglioma 67 0.056
213
P PRP003 Porphyria Cutanea Tarda 67 0.056
214
P LPR021 Leprosy 3 67 0.056
215
ALL026 Allergic Hypersensitivity Disease 64 0.056
216
P PRP029 Porphyria 62 0.056
217
GRD007 Grade Iii Astrocytoma 59 0.056
218
SKN022 Skin Squamous Cell Carcinoma 56 0.056
219
HMG005 Hemoglobinopathy 55 0.056
220
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.056
221
NNL006 Non-Alcoholic Steatohepatitis 51 0.056
222
BNM001 Bone Marrow Cancer 43 0.056
223
ANP009 Anaplastic Oligodendroglioma 43 0.056
224
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.056
225
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.056
226
c LPR022 Leprosy 2 37 0.056
227
OLG006 Oligoastrocytoma 35 0.056
228
HNS001 Hansen's Disease 34 0.056
229
P SCK034 Sickle Beta Thalassemia 29 0.056
230
STR067 Stroke, Ischemic 80 0.047
231
VNH007 Von Hippel-Lindau Syndrome 73 0.047
232
P MYC007 Myocardial Infarction 70 0.047
233
CRB039 Cerebrovascular Disease 69 0.047
234
P MYC084 Mycobacterium Tuberculosis 1 68 0.047
235
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.047
236
c SML038 Small Cell Cancer of the Lung 65 0.047
237
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.047
238
IDP011 Idiopathic Interstitial Pneumonia 63 0.047
239
P HRD008 Hereditary Hemorrhagic Telangiectasia 62 0.047
240
c FNC043 Fanconi Anemia, Complementation Group E 62 0.047
241
P PLM036 Pulmonary Fibrosis 61 0.047
242
LNG099 Lung Disease 61 0.047
243
INT066 Interstitial Lung Disease 59 0.047
244
END081 Endosteal Hyperostosis, Autosomal Dominant 59 0.047
245
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.047
246
IRN001 Iron Deficiency Anemia 58 0.047
247
P SZR006 Seizure Disorder 58 0.047
248
VSL002 Visual Epilepsy 58 0.047
249
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.047
250
SPN041 Spinal Cord Disease 56 0.047
251
HYP266 Hypoxia 56 0.047
252
c GRV008 Graves Disease 1 55 0.047
253
c TLN006 Telangiectasia, Hereditary Hemorrhagic, Type 1 54 0.047
254
LYM040 Lymphoblastic Lymphoma 54 0.047
255
P CNT005 Central Nervous System Lymphoma 53 0.047
256
GLS018 Glass Syndrome 53 0.047
257
TLN003 Telangiectasis 51 0.047
258
HPT014 Hepatorenal Syndrome 50 0.047
259
HYL004 Hyaline Fibromatosis Syndrome 50 0.047
260
P PRR002 Pure Red-Cell Aplasia 48 0.047
261
c BCT013 Bacterial Pneumonia 47 0.047
262
MRG013 Mirage Syndrome 44 0.047
263
RDC006 Red Cell Aplasia 42 0.047
264
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.047
265
c PST022 Posterior Uveal Melanoma 41 0.047
266
RDN001 Reading Disorder 40 0.047
267
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.047
268
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.047
269
ATM052 Autoimmune Disease 1 37 0.047
270
RTN179 Retinal Arteries, Tortuosity of 36 0.047
271
LCL004 Localized Osteosarcoma 27 0.047
272
JVN026 Jeavons Syndrome 24 0.047
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