Search results for Pirfenidone

262 hits were found for Pirfenidone

# Family MCID Name MIFTS Score
1
P PLM036 Pulmonary Fibrosis 65 0.793
2
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.747
3
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.566
4
IDP011 Idiopathic Interstitial Pneumonia 59 0.351
5
LNG099 Lung Disease 60 0.338
6
ACT029 Acute Interstitial Pneumonia 49 0.332
8
INT066 Interstitial Lung Disease 60 0.271
9
P EXN002 Exanthem 57 0.171
10
P PNM007 Pneumonia 68 0.167
11
P RSP003 Respiratory Failure 74 0.158
12
P KDN018 Kidney Disease 72 0.153
13
c SCL052 Scleroderma, Familial Progressive 61 0.153
14
BRN002 Bronchiolitis 59 0.148
15
BRN012 Bronchiolitis Obliterans 55 0.148
16
RNL077 Renal Fibrosis 47 0.148
17
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.143
18
P SYS005 Systemic Scleroderma 68 0.138
19
ALL026 Allergic Hypersensitivity Disease 62 0.138
20
EXT034 Extrinsic Allergic Alveolitis 58 0.127
21
P NRF002 Neurofibromatosis 56 0.127
22
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.121
23
CNG034 Congestive Heart Failure 69 0.121
24
P PLM037 Pulmonary Hypertension 67 0.121
25
NRF007 Neurofibroma 64 0.121
26
P LNG032 Lung Cancer 98 0.115
27
ADR007 Adrenoleukodystrophy 75 0.115
28
c CHR684 Chronic Kidney Disease 70 0.115
29
LVR012 Liver Cirrhosis 62 0.115
30
CYT002 Cytokine Deficiency 42 0.115
31
DFF003 Diffuse Scleroderma 41 0.115
32
c NRF024 Neurofibromatosis, Type I 77 0.108
33
P HRT032 Heart Disease 75 0.108
34
P SRC025 Sarcoidosis 1 70 0.108
35
P HRM001 Hermansky-Pudlak Syndrome 64 0.108
36
PLX002 Plexiform Neurofibroma 44 0.108
37
P LVR013 Liver Disease 68 0.101
38
CNN005 Connective Tissue Disease 68 0.101
39
HYL004 Hyaline Fibromatosis Syndrome 67 0.101
40
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.101
41
P DRR001 Diarrhea 55 0.101
42
c MCR113 Microvascular Complications of Diabetes 3 52 0.101
43
c MCR120 Microvascular Complications of Diabetes 7 47 0.101
44
c MCR130 Microvascular Complications of Diabetes 6 41 0.101
45
c MCR133 Microvascular Complications of Diabetes 4 41 0.101
46
KLD004 Keloid Disorder 40 0.101
47
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.101
48
GST092 Gastroesophageal Reflux 67 0.094
49
c RHB024 Rhabdomyosarcoma 2 67 0.094
50
P DRM010 Dermatomyositis 61 0.094
51
P CRD246 Cardiovascular System Disease 57 0.094
52
CHL079 Children's Interstitial Lung Disease 26 0.094
53
P MYC007 Myocardial Infarction 70 0.086
54
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.086
55
P HPT021 Hepatitis 67 0.086
56
P MCR115 Microvascular Complications of Diabetes 5 66 0.086
57
c MCR129 Microvascular Complications of Diabetes 1 66 0.086
58
c SML038 Small Cell Cancer of the Lung 65 0.086
59
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.086
60
P OCL002 Oculocutaneous Albinism 60 0.086
61
ALB002 Albinism 46 0.086
62
c PRM038 Primary Agammaglobulinemia 44 0.086
63
ATX019 Ataxia with Vitamin E Deficiency 42 0.086
64
c MCR112 Microvascular Complications of Diabetes 2 41 0.086
65
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.086
66
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.086
67
P GRF003 Graft-Versus-Host Disease 72 0.077
68
DWN001 Down Syndrome 70 0.077
69
P MSC005 Muscular Dystrophy 66 0.077
70
P DBT009 Diabetes Mellitus 64 0.077
71
MSC007 Muscle Hypertrophy 64 0.077
72
c LCL006 Localized Scleroderma 62 0.077
73
c ACT071 Acute Kidney Failure 60 0.077
74
P FCL005 Focal Segmental Glomerulosclerosis 57 0.077
75
NNL006 Non-Alcoholic Steatohepatitis 54 0.077
76
c HRM005 Hermansky-Pudlak Syndrome 1 51 0.077
77
ATS010 Autosomal Recessive Disease 48 0.077
78
STR089 Storage Pool Platelet Disease 47 0.077
79
c SRC023 Sarcoidosis 2 43 0.077
80
SCN068 Secondary Interstitial Lung Disease in Childhood and Adulthood Associated with a Connective Tissue Disease 19 0.077
81
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.066
82
c HYP595 Hypertension, Essential 84 0.066
83
P PNC035 Pancreatic Cancer 84 0.066
84
P RHM011 Rheumatoid Arthritis 80 0.066
85
c ATR087 Atrial Standstill 1 75 0.066
86
CRH001 Crohn's Disease 74 0.066
87
c HPT073 Hepatitis C Virus 72 0.066
88
P HYP061 Hypertrophic Cardiomyopathy 70 0.066
89
ADL002 Adult Syndrome 70 0.066
90
P MYP004 Myopathy 70 0.066
91
P ASP006 Aspergillosis 69 0.066
92
P ART022 Arthritis 69 0.066
93
P INF038 Influenza 68 0.066
94
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.066
95
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.066
96
ANG054 Angina Pectoris 66 0.066
97
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.066
98
P ADL010 Adult Respiratory Distress Syndrome 65 0.066
99
P GLM045 Glioma 63 0.066
100
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.066
101
c HPT001 Hepatitis C 62 0.066
102
c HPT003 Hepatitis a 62 0.066
103
c SVR001 Severe Acute Respiratory Syndrome 62 0.066
104
P VSC011 Vasculitis 62 0.066
105
HYP066 Hyperglycemia 61 0.066
106
FTT001 Fatty Liver Disease 61 0.066
107
P NPH012 Nephrotic Syndrome 60 0.066
108
PNM010 Pneumothorax, Primary Spontaneous 60 0.066
109
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.066
110
c HPT016 Hepatitis B 59 0.066
111
P BRN022 Bronchiectasis 59 0.066
112
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.066
113
GLB001 Gilbert Syndrome 58 0.066
114
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.066
115
BLR008 Bilirubin Metabolic Disorder 57 0.066
116
PNM008 Pneumothorax 56 0.066
117
P NRP001 Neuropathy 56 0.066
118
INT007 Intermediate Coronary Syndrome 55 0.066
119
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.066
120
PLM012 Pulmonary Sarcoidosis 53 0.066
121
c HRM017 Hermansky-Pudlak Syndrome 2 53 0.066
122
LMY002 Leiomyoma 52 0.066
123
MCR088 Microscopic Polyangiitis 51 0.066
124
LNG031 Lung Benign Neoplasm 51 0.066
125
END086 End Stage Renal Disease 51 0.066
126
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.066
127
47X002 47,xyy 49 0.066
128
c INV001 Invasive Aspergillosis 49 0.066
129
c HRM008 Hermansky-Pudlak Syndrome 5 47 0.066
130
c INH020 Inherited Metabolic Disorder 47 0.066
131
c HRM007 Hermansky-Pudlak Syndrome 4 46 0.066
132
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.066
133
c DRR009 Diarrhea 6 46 0.066
134
GLL048 Glial Tumor 45 0.066
135
c HRM009 Hermansky-Pudlak Syndrome 6 45 0.066
136
c HRM006 Hermansky-Pudlak Syndrome 3 44 0.066
137
c HRM012 Hermansky-Pudlak Syndrome 9 43 0.066
138
P PHT010 Photoparoxysmal Response 1 42 0.066
139
ANC002 Anca-Associated Vasculitis 41 0.066
140
CRN322 Coronavirus Infectious Disease 40 0.066
141
P PRP021 Peripheral Nervous System Neoplasm 39 0.066
142
CVT001 Cavitary Optic Disc Anomalies 38 0.066
143
c HRM010 Hermansky-Pudlak Syndrome 7 37 0.066
144
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 36 0.066
145
c HRM011 Hermansky-Pudlak Syndrome 8 35 0.066
146
HML018 Homologous Wasting Disease 22 0.066
147
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.054
148
MSC157 Muscular Dystrophy, Duchenne Type 72 0.054
149
P MLT020 Multiple Sclerosis 72 0.054
150
P TRN020 Turner Syndrome 67 0.054
151
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.054
152
SKN016 Skin Disease 63 0.054
153
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.054
154
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.054
155
CLT003 Colitis 62 0.054
156
NTR005 Nutritional Deficiency Disease 62 0.054
157
P PNC044 Pancreatitis 61 0.054
158
P LPS004 Lupus Erythematosus 61 0.054
159
c ACT027 Acute Pancreatitis 60 0.054
160
P GLM007 Glomerulonephritis 57 0.054
161
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.054
162
c ACT134 Acute Liver Failure 56 0.054
163
LMY014 Leiomyoma, Uterine 56 0.054
164
SLC006 Silicosis 56 0.054
165
PLM010 Pulmonary Edema 54 0.054
166
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.054
167
P VTR007 Vitreoretinopathy 46 0.054
168
URT010 Ureteral Obstruction 45 0.054
169
MYF001 Myofibroma 45 0.054
170
CVD001 Covid-19 44 0.054
171
HYP457 Hypertrophic Scars 42 0.054
172
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.054
173
48X005 48,xyyy 39 0.054
174
TRC005 Tracheal Stenosis 38 0.054
175
PRQ002 Paraquat Poisoning 26 0.054
176
P HPT023 Hepatocellular Carcinoma 100 0.038
177
P BRS047 Breast Cancer 97 0.038
178
c SYS001 Systemic Lupus Erythematosus 86 0.038
179
CYS001 Cystic Fibrosis 81 0.038
180
c NRF023 Neurofibromatosis, Type Ii 80 0.038
181
P LNG064 Lung Cancer Susceptibility 3 78 0.038
182
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.038
183
SVR004 Severe Combined Immunodeficiency 73 0.038
184
c HYP836 Hypercholesterolemia, Familial, 1 73 0.038
185
P FML011 Familial Adenomatous Polyposis 72 0.038
186
MYL005 Myelofibrosis 70 0.038
187
PLM001 Pulmonary Tuberculosis 69 0.038
188
ART016 Aortic Aneurysm 69 0.038
189
P MYC084 Mycobacterium Tuberculosis 1 68 0.038
190
c BSL007 Basal Cell Carcinoma 68 0.038
191
BRN024 Bronchitis 68 0.038
192
P HYP098 Hypereosinophilic Syndrome 67 0.038
193
SRC014 Sarcoma 65 0.038
194
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.038
195
PRT036 Peritonitis 64 0.038
196
P ADN016 Adenocarcinoma 64 0.038
197
P NTR004 Neutropenia 63 0.038
198
P VSC007 Vascular Disease 63 0.038
199
c MLG084 Malignant Fibrous Histiocytoma 63 0.038
200
c GLC092 Glaucoma, Primary Open Angle 62 0.038
201
c FNC043 Fanconi Anemia, Complementation Group E 62 0.038
202
TXC005 Toxic Shock Syndrome 62 0.038
203
DRM006 Dermatitis 61 0.038
204
HPT019 Hepatic Encephalopathy 60 0.038
205
CHC001 Chickenpox 60 0.038
206
P CTR002 Cataract 60 0.038
207
ISC004 Ischemia 58 0.038
208
P BCL017 B-Cell Lymphoma 58 0.038
209
P ALC033 Alcohol Use Disorder 58 0.038
210
CNT047 Contact Dermatitis 58 0.038
211
c CHR417 Chronic Graft Versus Host Disease 57 0.038
212
c CHL119 Cholangitis, Primary Sclerosing 57 0.038
213
c MST023 Mesothelioma, Malignant 57 0.038
214
HYP266 Hypoxia 57 0.038
215
P ADL017 Adult T-Cell Leukemia 56 0.038
216
SFT003 Soft Tissue Sarcoma 56 0.038
217
PRS047 Prostatitis 56 0.038
218
P STR020 Strabismus 55 0.038
219
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.038
220
GLC003 Glucose Intolerance 54 0.038
221
P INF037 Inflammatory Bowel Disease 54 0.038
222
CRY001 Cryptogenic Organizing Pneumonia 53 0.038
223
SPN035 Spindle Cell Sarcoma 53 0.038
224
IMP005 Impotence 52 0.038
225
THR004 Thrombocytosis 51 0.038
226
c PRM108 Primary Progressive Multiple Sclerosis 51 0.038
227
P CHL066 Cholangitis 51 0.038
228
PLR008 Pleurisy 50 0.038
229
P ESN008 Eosinophilic Pneumonia 50 0.038
230
c HRD202 Hereditary Lymphedema I 50 0.038
231
MTB004 Metabolic Acidosis 50 0.038
232
P OPN001 Open-Angle Glaucoma 49 0.038
233
c BCT013 Bacterial Pneumonia 48 0.038
234
P SCL009 Sclerosing Cholangitis 48 0.038
235
SPL018 Splenomegaly 48 0.038
236
DRG013 Drug-Induced Lupus Erythematosus 48 0.038
237
PRP007 Priapism 47 0.038
238
P CLL015 Collagen Disease 47 0.038
239
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.038
240
CHR074 Choriocarcinoma 47 0.038
241
KRT013 Keratolytic Winter Erythema 46 0.038
242
P BNG032 Benign Mesothelioma 46 0.038
243
c MLG068 Malignant Glioma 46 0.038
244
HPT004 Hepatic Coma 45 0.038
245
NNS002 Nonspecific Interstitial Pneumonia 45 0.038
246
c PCH010 Pachyonychia Congenita 3 44 0.038
247
P FBR003 Fibrous Histiocytoma 44 0.038
248
MTR010 Mature Teratoma 44 0.038
249
SMN007 Seminoma 43 0.038
250
NSP002 Nasopharyngitis 43 0.038
251
MCH006 Mechanical Strabismus 42 0.038
252
P CYS017 Cystic Teratoma 41 0.038
253
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
254
PNB004 Panbronchiolitis, Diffuse 37 0.038
255
c BNG093 Benign Teratoma 37 0.038
256
c LKM005 Leukemia, T-Cell, Chronic 34 0.038
257
DFF031 Diffuse Alveolar Hemorrhage 30 0.038
258
c PLM044 Pulmonary Fibrosis, Familial 27 0.038
259
EXF003 Exfoliative Dermatitis 27 0.038
260
PLR025 Pleuroparenchymal Fibroelastosis 22 0.038
261
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.038
262
LWF001 Low-Flow Priapism 19 0.038
Content
Loading form....