Search results for Interferon beta-1a

266 hits were found for Interferon beta-1a

# Family MCID Name MIFTS Score
1
P MLT020 Multiple Sclerosis 72 0.727
2
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.700
3
c HPT001 Hepatitis C 62 0.673
4
c HPT073 Hepatitis C Virus 72 0.508
5
P HPT021 Hepatitis 67 0.434
6
48X005 48,xyyy 39 0.379
7
c HPT016 Hepatitis B 59 0.370
8
ATM095 Autoimmune Disease 62 0.326
9
c HPT003 Hepatitis a 62 0.316
10
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.313
11
P NTR004 Neutropenia 63 0.272
12
P MLN008 Melanoma 69 0.269
13
P LKM002 Leukemia 68 0.258
14
VRL011 Viral Infectious Disease 61 0.257
15
P MYL006 Myeloid Leukemia 60 0.256
16
CYT002 Cytokine Deficiency 42 0.254
17
c LKM063 Leukemia, Chronic Myeloid 72 0.252
18
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.251
19
P HPT023 Hepatocellular Carcinoma 100 0.222
20
HMN044 Human Immunodeficiency Virus Type 1 71 0.221
21
P LPS004 Lupus Erythematosus 61 0.220
22
IMM167 Immune Deficiency Disease 78 0.218
23
HRY003 Hairy Cell Leukemia 55 0.217
24
KPS004 Kaposi Sarcoma 75 0.214
25
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.203
26
P LYM118 Lymphoma 68 0.199
27
MYL069 Myeloma, Multiple 85 0.190
28
ACQ007 Acquired Immunodeficiency Syndrome 60 0.186
29
P INF038 Influenza 68 0.185
30
DMY004 Demyelinating Disease 52 0.182
31
c SVR001 Severe Acute Respiratory Syndrome 62 0.179
32
c RHB024 Rhabdomyosarcoma 2 67 0.179
33
P THR014 Thrombocytopenia 67 0.179
34
P CLR023 Colorectal Cancer 99 0.177
35
P ENC004 Encephalitis 61 0.173
36
ALL014 Allergic Encephalomyelitis 38 0.173
37
P KDN017 Kidney Cancer 60 0.169
38
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.169
39
SKN019 Skin Melanoma 68 0.168
40
P DRR001 Diarrhea 55 0.162
41
P EXN002 Exanthem 57 0.160
42
DPR016 Depression 63 0.160
43
P THY032 Thyroiditis 52 0.159
44
MSL001 Measles 62 0.158
45
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.156
46
LYM027 Lymphopenia 58 0.155
47
c LKM005 Leukemia, T-Cell, Chronic 34 0.155
48
ULC004 Ulcerative Colitis 73 0.154
49
P VSC011 Vasculitis 62 0.153
50
CLT003 Colitis 62 0.152
51
P PSR002 Psoriasis 62 0.152
52
CVD001 Covid-19 44 0.151
53
NRT004 Neuritis 52 0.147
54
PST011 Pustulosis of Palm and Sole 52 0.146
55
CRH001 Crohn's Disease 74 0.146
56
P NRP001 Neuropathy 56 0.146
57
CRY004 Cryoglobulinemia 48 0.144
58
P GLM007 Glomerulonephritis 57 0.142
59
c HPT015 Hepatitis D 49 0.142
60
DRM006 Dermatitis 61 0.142
61
P ESS003 Essential Thrombocythemia 68 0.140
62
c PRM038 Primary Agammaglobulinemia 44 0.139
63
c PRM108 Primary Progressive Multiple Sclerosis 51 0.139
64
ATX019 Ataxia with Vitamin E Deficiency 42 0.138
65
P RSP003 Respiratory Failure 74 0.138
66
P OPT009 Optic Neuritis 57 0.137
67
LNG099 Lung Disease 60 0.137
68
P HYP098 Hypereosinophilic Syndrome 67 0.135
69
P RHM011 Rheumatoid Arthritis 80 0.134
70
MNT002 Mental Depression 58 0.134
71
PRP030 Purpura 54 0.132
72
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.131
73
MYC006 Mycosis Fungoides 66 0.131
74
LYM019 Lymphosarcoma 46 0.128
75
DWN001 Down Syndrome 70 0.128
76
CHC001 Chickenpox 60 0.126
77
END086 End Stage Renal Disease 51 0.126
78
AST005 Asthma 76 0.124
79
P KDN018 Kidney Disease 72 0.123
80
P PNM007 Pneumonia 68 0.123
81
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.122
82
47X002 47,xyy 49 0.122
83
DFC004 Deficiency Anemia 70 0.122
84
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.121
85
ADL002 Adult Syndrome 70 0.119
86
GLS018 Glass Syndrome 57 0.118
87
MLR004 Malaria 81 0.116
88
SPS019 Spastic Paraparesis 38 0.116
89
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 35 0.116
90
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.115
91
TRP002 Tropical Spastic Paraparesis 50 0.115
92
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.115
93
MYL057 Myelopathy, Htlv-1-Associated 39 0.114
94
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.114
95
P HMN010 Hemangioma 61 0.114
96
P DRM010 Dermatomyositis 61 0.113
97
c ATM011 Autoimmune Hepatitis 63 0.112
98
P TRN020 Turner Syndrome 67 0.111
99
c HMN021 Human T-Cell Leukemia Virus Type 1 47 0.110
100
P NPH012 Nephrotic Syndrome 60 0.110
101
MYL009 Myelodysplastic Syndrome 70 0.109
102
c INF071 Inflammatory Bowel Disease 1 67 0.109
103
P VSC007 Vascular Disease 63 0.108
104
P HMN032 Human Herpesvirus 8 47 0.107
105
PRG009 Progressive Multifocal Leukoencephalopathy 59 0.106
106
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.105
107
RCK004 Rickets 68 0.105
108
P OPT006 Optic Nerve Disease 60 0.104
109
P PRP019 Peripheral Nervous System Disease 58 0.104
110
P TXP001 Toxoplasmosis 60 0.104
111
P MMP001 Mumps 58 0.104
112
TXC005 Toxic Shock Syndrome 62 0.103
113
THR123 Thrombotic Microangiopathy 36 0.102
114
HRP004 Herpes Zoster 60 0.102
116
c BSL007 Basal Cell Carcinoma 68 0.099
117
BRN002 Bronchiolitis 59 0.099
118
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.099
119
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.099
120
P ALZ034 Alzheimer Disease 88 0.098
121
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.097
122
PDT025 Pediatric Multiple Sclerosis 36 0.097
123
P PLY019 Polyneuropathy 56 0.096
124
P PLY020 Polyradiculoneuropathy 48 0.096
125
BRC012 Brucellosis 64 0.095
126
P GLL022 Guillain-Barre Syndrome 59 0.095
127
MCL006 Macular Retinal Edema 55 0.095
128
P APL001 Aplastic Anemia 74 0.094
129
P PLY041 Polymyositis 57 0.094
130
CMM005 Common Cold 57 0.093
131
MDD018 Middle East Respiratory Syndrome 43 0.093
132
SCH014 Schistosomiasis 57 0.092
133
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.091
134
c MLT093 Multiple Sclerosis 2 23 0.091
135
P CTN003 Cutaneous Lupus Erythematosus 53 0.091
136
P MJR001 Major Depressive Disorder 68 0.090
137
P URT039 Urticaria 58 0.090
138
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.089
139
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.088
140
c ACT071 Acute Kidney Failure 60 0.088
142
c ATR087 Atrial Standstill 1 75 0.087
143
PLS009 Plasma Cell Neoplasm 51 0.087
144
CNG034 Congestive Heart Failure 69 0.086
145
c MNN043 Meningioma, Familial 74 0.086
146
P ADL010 Adult Respiratory Distress Syndrome 65 0.086
147
MNN042 Meningioma, Radiation-Induced 62 0.086
148
CRH005 Crohn's Colitis 53 0.086
149
SPN021 Spinal Meningioma 50 0.086
150
BRN071 Brain Injury 49 0.086
151
SCR001 Secretory Meningioma 41 0.086
152
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.086
153
SZR001 Sezary's Disease 60 0.086
154
P RBL001 Rubella 59 0.085
155
P DMN002 Dementia 66 0.084
156
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.084
158
P HMP007 Hemophilia 51 0.083
159
P CNR004 Cone-Rod Dystrophy 2 73 0.083
160
MNN009 Meningoencephalitis 49 0.082
161
STR067 Stroke, Ischemic 81 0.082
162
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.081
163
CRB039 Cerebrovascular Disease 67 0.081
164
SPN041 Spinal Cord Disease 56 0.081
165
ART016 Aortic Aneurysm 69 0.079
166
ANX010 Anxiety 73 0.079
167
TRP009 Triple X Syndrome 42 0.079
168
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.078
169
BRN028 Brain Cancer 74 0.078
170
P HDC001 Headache 57 0.078
171
ANR040 Aneurysm 59 0.078
172
MRG013 Mirage Syndrome 43 0.078
173
c ACT027 Acute Pancreatitis 60 0.077
174
PNN001 Panniculitis 51 0.077
175
MYC088 Mycobacterium Avium Complex Infections 29 0.077
176
KRT013 Keratolytic Winter Erythema 46 0.077
177
P HML001 Hemolytic-Uremic Syndrome 53 0.077
178
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.076
179
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.076
180
P PNC044 Pancreatitis 61 0.076
181
IRN002 Iron Metabolism Disease 57 0.076
182
P LTR001 Lateral Sclerosis 54 0.076
183
P NRV007 Nervous System Disease 66 0.075
184
SKN013 Skin Benign Neoplasm 51 0.075
185
P DMY001 Demyelinating Polyneuropathy 43 0.075
186
KHL003 Kohlschutter-Tonz Syndrome 65 0.075
187
NWB001 Newborn Respiratory Distress Syndrome 58 0.075
188
P SZR006 Seizure Disorder 56 0.074
189
c THR090 Thrombocythemia 1 49 0.074
190
VSL002 Visual Epilepsy 59 0.073
191
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.073
192
HPT004 Hepatic Coma 45 0.072
193
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.071
194
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.071
195
RSP007 Respiratory Distress Syndrome, Infant 30 0.071
196
P HRT032 Heart Disease 75 0.071
197
c DRR009 Diarrhea 6 46 0.071
198
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.070
199
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.069
200
BRN012 Bronchiolitis Obliterans 55 0.069
201
SBC016 Subacute Delirium 44 0.069
202
49X006 49, Xxxxy Syndrome 41 0.069
203
CLS052 Classic Hairy Cell Leukemia 27 0.069
204
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.068
205
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
206
ATR057 Atrioventricular Block 55 0.067
207
c DWL002 Dowling-Degos Disease 1 58 0.066
208
MYL001 Myelitis 51 0.066
209
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.066
210
c SBC007 Subacute Thyroiditis 45 0.066
211
P TRN034 Transverse Myelitis 45 0.066
212
ERY003 Erythema Multiforme 58 0.065
213
ATM052 Autoimmune Disease 1 37 0.065
214
P FML018 Familial Mediterranean Fever 73 0.064
215
OCL069 Ocular Motor Apraxia 51 0.063
216
SPS057 Spasticity 45 0.062
217
ENC065 Encephalitis/encephalopathy, Mild, with Reversible Myelin Vacuolization 33 0.062
218
c MLT124 Multiple Sclerosis 5 21 0.060
219
c HMP029 Hemophilia a 67 0.059
220
c ACR116 Aicardi-Goutieres Syndrome 1 52 0.059
221
CHR043 Chronic Inflammatory Demyelinating Polyneuritis 23 0.058
222
c ACQ054 Acquired Peripheral Neuropathy 13 0.058
223
CLL003 Cellulitis 54 0.057
224
PRS063 Paresthesia 41 0.057
225
c CHR682 Chronic Bilirubin Encephalopathy 39 0.057
226
ILM001 Ileum Cancer 27 0.057
227
c MGR028 Migraine with or Without Aura 1 67 0.056
228
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.056
229
IMM136 Immune System Disease 45 0.056
230
HLN001 Halo Nevi 27 0.056
231
SVR097 Severe Cutaneous Adverse Reaction 69 0.054
232
FSC004 Fasciitis 50 0.054
233
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.054
234
KRT001 Keratoconjunctivitis Sicca 49 0.053
235
SYN036 Syncope 45 0.053
236
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.053
237
ERY066 Erythema Multiforme Major 30 0.053
238
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 0.053
239
P SYP003 Syphilis 58 0.051
240
RSP006 Respiratory System Disease 50 0.051
241
LPT014 Leptin Deficiency or Dysfunction 74 0.049
242
P SLP006 Sleep Apnea 69 0.049
243
CRD223 Cardiac Arrhythmia 60 0.049
244
HRW001 Hair Whorl 36 0.049
245
P HYD006 Hydrocephalus 66 0.047
246
c PNS012 Paine Syndrome 61 0.047
247
ACT049 Acute Disseminated Encephalomyelitis 51 0.047
248
c ACQ014 Acquired Hemophilia 45 0.047
249
CRB027 Cerebellar Disease 44 0.047
250
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.047
251
RST023 Resting Heart Rate, Variation in 41 0.047
252
SCL025 Scleromyxedema 32 0.047
253
PHR003 Pharyngitis 57 0.044
254
P AVS003 Avascular Necrosis 42 0.044
255
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.044
256
THR099 Third-Degree Atrioventricular Block 45 0.041
257
NSP002 Nasopharyngitis 43 0.041
258
XRP001 Xerophthalmia 41 0.041
259
SSC001 Susac Syndrome 32 0.041
260
c MLT095 Multiple Sclerosis 4 19 0.041
261
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.037
262
NRG002 Neurogenic Bladder 55 0.037
263
LFT001 Left Bundle Branch Hemiblock 49 0.037
264
MLT075 Multifocal Motor Neuropathy 46 0.037
265
c ACQ042 Acquired Hemophilia a 37 0.037
266
PDP001 Pedophilia 30 0.037
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