Search results for Sulfasalazine

352 hits were found for Sulfasalazine

# Family MCID Name MIFTS Score
1
SLF018 Sulfasalazine Allergy 7 3.070
2
ULC004 Ulcerative Colitis 73 0.384
3
P INF037 Inflammatory Bowel Disease 56 0.357
4
P RHM011 Rheumatoid Arthritis 80 0.306
5
P ART022 Arthritis 70 0.296
6
CLT003 Colitis 62 0.291
7
SPN051 Spondylitis 52 0.264
8
INF009 Inflammatory Spondylopathy 32 0.264
9
CRH001 Crohn's Disease 74 0.262
10
c SPN225 Spondyloarthropathy 1 73 0.262
11
P EXN002 Exanthem 57 0.262
12
ALL026 Allergic Hypersensitivity Disease 64 0.218
13
P HYP098 Hypereosinophilic Syndrome 66 0.187
14
P DRR001 Diarrhea 57 0.173
15
PSR001 Psoriatic Arthritis 62 0.162
16
GRN017 Granulocytopenia 44 0.146
17
48X005 48,xyyy 39 0.146
18
c JVN010 Juvenile Rheumatoid Arthritis 67 0.141
19
P GLM045 Glioma 63 0.132
20
GLL048 Glial Tumor 45 0.132
21
P NTR004 Neutropenia 63 0.127
22
RHM027 Rheumatic Disease 56 0.127
23
P LPS004 Lupus Erythematosus 61 0.122
24
P URT039 Urticaria 58 0.122
25
GLB015 Glioblastoma Multiforme 75 0.117
26
P INF032 Infertility 57 0.117
27
P SPN052 Spondyloarthropathy 54 0.117
28
c RHB024 Rhabdomyosarcoma 2 65 0.112
29
RCT015 Reactive Arthritis 60 0.112
30
P ALP008 Alopecia 56 0.106
31
ENT004 Enthesopathy 48 0.106
32
P PSR002 Psoriasis 62 0.100
33
P MLN007 Male Infertility 56 0.100
34
PST011 Pustulosis of Palm and Sole 52 0.100
35
c MLG068 Malignant Glioma 45 0.093
36
BRN028 Brain Cancer 73 0.087
37
c INF071 Inflammatory Bowel Disease 1 68 0.087
38
P THR014 Thrombocytopenia 68 0.087
39
P ENC018 Encephalopathy 61 0.087
40
LNG099 Lung Disease 61 0.087
41
SYN007 Synovitis 55 0.087
42
P CHL066 Cholangitis 50 0.087
43
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.087
44
SPN119 Spondylarthropathy 44 0.087
45
c SYS001 Systemic Lupus Erythematosus 86 0.079
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.079
47
P GLM040 Glioma Susceptibility 1 81 0.079
48
DFC004 Deficiency Anemia 75 0.079
49
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.079
50
P PNM007 Pneumonia 68 0.079
51
ALC007 Alcohol Dependence 66 0.079
52
P CRN018 Coronary Artery Anomaly 63 0.079
53
P HML002 Hemolytic Anemia 62 0.079
54
DRM006 Dermatitis 61 0.079
55
c PNS012 Paine Syndrome 61 0.079
56
ATM095 Autoimmune Disease 61 0.079
57
P ALP009 Alopecia Areata 60 0.079
58
P SZR006 Seizure Disorder 58 0.079
59
VSL002 Visual Epilepsy 58 0.079
60
c CHL119 Cholangitis, Primary Sclerosing 57 0.079
61
P UVT001 Uveitis 57 0.079
62
P DRM007 Dermatitis Herpetiformis 54 0.079
63
P LCH002 Lichen Planus 54 0.079
64
ART140 Arteries, Anomalies of 53 0.079
65
CRH005 Crohn's Colitis 52 0.079
66
P SCL009 Sclerosing Cholangitis 47 0.079
67
MXD026 Mixed Glioma 45 0.079
68
BCK006 Back Pain 42 0.079
69
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.079
70
c DRM040 Dermatitis Herpetiformis, Familial 35 0.079
71
P BRS047 Breast Cancer 96 0.071
72
P MLT020 Multiple Sclerosis 72 0.071
73
P HPT021 Hepatitis 67 0.071
74
SVR097 Severe Cutaneous Adverse Reaction 67 0.071
75
P VSC011 Vasculitis 62 0.071
76
P PNC044 Pancreatitis 61 0.071
77
c ACT027 Acute Pancreatitis 59 0.071
78
BRN002 Bronchiolitis 59 0.071
79
ERY003 Erythema Multiforme 57 0.071
80
BRN012 Bronchiolitis Obliterans 56 0.071
81
P ANG015 Angioedema 54 0.071
82
IRD001 Iridocyclitis 50 0.071
83
ILT001 Ileitis 50 0.071
84
P ESN008 Eosinophilic Pneumonia 50 0.071
85
PRC003 Proctitis 47 0.071
86
DRG026 Drug Reaction with Eosinophilia and Systemic Symptoms 46 0.071
87
CLL021 Collagenous Colitis 42 0.071
88
ALL014 Allergic Encephalomyelitis 39 0.071
89
c ACT004 Acute Diarrhea 39 0.071
90
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.071
91
ERY066 Erythema Multiforme Major 28 0.071
92
P HPT023 Hepatocellular Carcinoma 100 0.061
93
P PNC035 Pancreatic Cancer 84 0.061
94
PFF001 Pfeiffer Syndrome 79 0.061
95
P MYC007 Myocardial Infarction 70 0.061
96
CNN005 Connective Tissue Disease 66 0.061
97
ATH013 Atherosclerosis Susceptibility 66 0.061
98
P CRN300 Coronary Heart Disease 1 63 0.061
99
SKN016 Skin Disease 63 0.061
100
P INT070 Intestinal Obstruction 58 0.061
101
P ALC033 Alcohol Use Disorder 58 0.061
102
CNS004 Constipation 57 0.061
103
P PRP019 Peripheral Nervous System Disease 57 0.061
104
P NRP001 Neuropathy 56 0.061
105
P MGL001 Megaloblastic Anemia 55 0.061
106
PNG002 Pain Agnosia 51 0.061
107
c ACT134 Acute Liver Failure 51 0.061
108
P CHR345 Chronic Pain 50 0.061
109
c RHM021 Rheumatoid Arthritis, Systemic Juvenile 48 0.061
110
INT067 Interstitial Nephritis 46 0.061
111
CYT002 Cytokine Deficiency 44 0.061
112
DSC009 Discoid Lupus Erythematosus 42 0.061
113
CYT018 Cytochrome P450 2d6 Variant 27 0.061
114
P PRS040 Prostate Cancer 97 0.050
115
ESP021 Esophageal Cancer 90 0.050
116
c HYP595 Hypertension, Essential 84 0.050
117
P GST053 Gastric Cancer 83 0.050
118
STR067 Stroke, Ischemic 80 0.050
119
P BLD134 Bladder Cancer 78 0.050
120
IMM167 Immune Deficiency Disease 78 0.050
121
ANX010 Anxiety 72 0.050
122
P NRB001 Neuroblastoma 71 0.050
123
P KDN018 Kidney Disease 70 0.050
124
CRB039 Cerebrovascular Disease 69 0.050
125
P LVR013 Liver Disease 68 0.050
126
P MYC084 Mycobacterium Tuberculosis 1 68 0.050
127
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.050
128
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.050
129
P MNN013 Meningitis 65 0.050
130
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.050
131
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.050
132
P ADN016 Adenocarcinoma 64 0.050
133
c PRC016 Pre-Eclampsia 63 0.050
134
DPR016 Depression 63 0.050
135
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.050
136
c SCL052 Scleroderma, Familial Progressive 62 0.050
137
P ART023 Arthropathy 62 0.050
138
BLL006 Bullous Pemphigoid 62 0.050
139
MDD011 Mood Disorder 62 0.050
140
P PRM006 Primary Biliary Cirrhosis 61 0.050
141
NTR005 Nutritional Deficiency Disease 61 0.050
142
ISC004 Ischemia 60 0.050
143
ETN001 Eating Disorder 59 0.050
144
P MYC008 Myocarditis 59 0.050
145
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.050
146
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.050
147
EXT034 Extrinsic Allergic Alveolitis 58 0.050
148
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.050
149
MNT002 Mental Depression 57 0.050
150
PHR003 Pharyngitis 56 0.050
151
P PMP001 Pemphigus 55 0.050
152
PYD001 Pyoderma Gangrenosum 54 0.050
153
OCL020 Ocular Cicatricial Pemphigoid 54 0.050
154
PNM001 Pneumocystosis 54 0.050
155
PNC001 Pancytopenia 54 0.050
156
PRC013 Pericarditis 54 0.050
157
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.050
158
GST037 Gastroparesis 53 0.050
159
DMY004 Demyelinating Disease 52 0.050
160
OCL069 Ocular Motor Apraxia 51 0.050
161
PYD002 Pyoderma 51 0.050
162
THR004 Thrombocytosis 51 0.050
163
ASP003 Aseptic Meningitis 51 0.050
164
ENT011 Enterocolitis 50 0.050
165
P AST007 Astrocytoma 50 0.050
166
P OVR082 Overgrowth Syndrome 50 0.050
167
CCT002 Cicatricial Pemphigoid 50 0.050
168
STM007 Stomatitis 49 0.050
169
47X002 47,xyy 49 0.050
170
DMP001 Dumping Syndrome 44 0.050
171
OBS082 Obstructive Nephropathy 43 0.050
172
DRG024 Drug Allergy 43 0.050
173
c PRM038 Primary Agammaglobulinemia 43 0.050
174
ILC002 Ileocolitis 43 0.050
175
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.050
176
CRD005 Cardia Cancer 40 0.050
177
PCH007 Pouchitis 39 0.050
178
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.050
180
GRN009 Granulomatous Hepatitis 31 0.050
181
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.050
182
ACT133 Acetylation, Slow 23 0.050
183
MSC026 Muscular Dystrophy White Matter Spongiosis 16 0.050
184
P CLR023 Colorectal Cancer 98 0.035
185
OST012 Osteoarthritis 78 0.035
186
P LNG064 Lung Cancer Susceptibility 3 77 0.035
187
P NRF023 Neurofibromatosis, Type Ii 76 0.035
188
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.035
189
P APL001 Aplastic Anemia 74 0.035
190
ADR007 Adrenoleukodystrophy 74 0.035
191
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.035
192
P OST002 Osteoporosis 73 0.035
193
P GRF003 Graft-Versus-Host Disease 71 0.035
194
P PHC003 Pheochromocytoma 71 0.035
195
P CNR004 Cone-Rod Dystrophy 2 71 0.035
196
PRP027 Peripheral Vascular Disease 71 0.035
197
OTT002 Otitis Media 71 0.035
198
P SRC025 Sarcoidosis 1 70 0.035
199
DWN001 Down Syndrome 70 0.035
200
P SYS005 Systemic Scleroderma 70 0.035
201
P HLP001 Holoprosencephaly 68 0.035
202
P CLC063 Celiac Disease 1 68 0.035
203
AND002 Androgen Insensitivity Syndrome 66 0.035
204
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.035
205
P ASP006 Aspergillosis 66 0.035
206
c SML038 Small Cell Cancer of the Lung 65 0.035
207
GST092 Gastroesophageal Reflux 65 0.035
208
P MYP004 Myopathy 64 0.035
209
OST017 Osteomyelitis 64 0.035
210
TTN003 Tetanus 64 0.035
211
IRR002 Irritable Bowel Syndrome 63 0.035
212
P VSC007 Vascular Disease 63 0.035
213
IDP011 Idiopathic Interstitial Pneumonia 63 0.035
214
LVR012 Liver Cirrhosis 63 0.035
215
P ADL010 Adult Respiratory Distress Syndrome 63 0.035
216
P NPH012 Nephrotic Syndrome 63 0.035
217
c LCL006 Localized Scleroderma 62 0.035
218
ALC006 Alcoholic Hepatitis 61 0.035
219
P PLM036 Pulmonary Fibrosis 61 0.035
220
TXC005 Toxic Shock Syndrome 61 0.035
221
HYP066 Hyperglycemia 61 0.035
222
P LYM033 Lymphoproliferative Syndrome 60 0.035
223
CHL068 Cholestasis 60 0.035
224
HPT019 Hepatic Encephalopathy 60 0.035
225
ORL011 Oral Cancer 60 0.035
226
THY029 Thyroid Carcinoma 59 0.035
227
STT001 Status Epilepticus 59 0.035
228
GST045 Gastroenteritis 59 0.035
229
GRD007 Grade Iii Astrocytoma 59 0.035
230
P PLV020 Pelvic Organ Prolapse 59 0.035
231
P BRS044 Breast Adenocarcinoma 59 0.035
232
ADN018 Adenoma 58 0.035
233
CHL067 Cholecystitis 58 0.035
234
P AXN002 Axenfeld-Rieger Syndrome 58 0.035
235
ADL030 Adult-Onset Still's Disease 58 0.035
236
PMP006 Pemphigus Vulgaris, Familial 58 0.035
237
LYM027 Lymphopenia 57 0.035
238
DSS009 Disseminated Intravascular Coagulation 57 0.035
239
BLR008 Bilirubin Metabolic Disorder 57 0.035
240
P HDC001 Headache 57 0.035
241
P PLY041 Polymyositis 57 0.035
242
P GLM007 Glomerulonephritis 57 0.035
243
c CHR417 Chronic Graft Versus Host Disease 56 0.035
244
P PYL005 Pyelonephritis 56 0.035
245
THR024 Thrombosis 56 0.035
246
ALP097 Alopecia Universalis Congenita 56 0.035
247
c ACT075 Acute Myocardial Infarction 56 0.035
248
P OPT009 Optic Neuritis 56 0.035
249
BCT022 Bacterial Infectious Disease 56 0.035
250
ANG005 Anogenital Venereal Wart 56 0.035
251
CMR002 Coumarin Resistance 56 0.035
252
BRN004 Brain Edema 55 0.035
253
MCL006 Macular Retinal Edema 55 0.035
254
LMB062 Limb Ischemia 55 0.035
255
SHG001 Shigellosis 55 0.035
256
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.035
257
P MYP006 Myopia 55 0.035
258
DBT010 Diabetic Neuropathy 55 0.035
259
P ANT006 Antiphospholipid Syndrome 54 0.035
260
CLL003 Cellulitis 54 0.035
261
AMN003 Amnestic Disorder 54 0.035
262
CRT017 Cartilage Disease 54 0.035
263
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.035
264
HDR002 Hidradenitis Suppurativa 53 0.035
265
NRT004 Neuritis 53 0.035
266
PRP080 Peripheral Artery Disease 53 0.035
267
IMP005 Impotence 52 0.035
268
HYP088 Hyper-Igd Syndrome 52 0.035
269
P MSC003 Muscular Atrophy 52 0.035
270
c PSR017 Psoriasis 2 52 0.035
272
P LRY019 Laryngitis 51 0.035
273
MYL001 Myelitis 51 0.035
274
CRY001 Cryptogenic Organizing Pneumonia 51 0.035
275
P LCT001 Lactic Acidosis 51 0.035
276
PLR008 Pleurisy 51 0.035
277
P CHN059 Chondrocalcinosis 51 0.035
278
RTN003 Retinal Ischemia 50 0.035
279
LGN006 Legionnaire Disease 50 0.035
280
P MMB011 Membranous Nephropathy 50 0.035
281
DYS073 Dysphagia 50 0.035
282
FSC004 Fasciitis 50 0.035
283
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.035
284
WLL006 Wells Syndrome 50 0.035
285
BRN071 Brain Injury 49 0.035
286
c PSR023 Psoriasis 1 49 0.035
287
HDR003 Hidradenitis 49 0.035
288
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.035
289
P OBS001 Obstructive Jaundice 48 0.035
290
CRD137 Cardiogenic Shock 48 0.035
291
PLM035 Pulmonary Eosinophilia 48 0.035
292
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.035
293
ESN015 Eosinophilic Fasciitis 47 0.035
294
RDT013 Radiation Proctitis 47 0.035
295
TST044 Testicular Torsion 47 0.035
296
RNL077 Renal Fibrosis 47 0.035
297
CRD001 Cardiac Tamponade 46 0.035
298
RYN005 Raynaud Phenomenon 46 0.035
299
CLS016 Clostridium Difficile Colitis 46 0.035
300
MGC001 Megacolon 46 0.035
301
SPN020 Spondylosis 46 0.035
302
ADR040 Adrenal Gland Pheochromocytoma 46 0.035
303
URT010 Ureteral Obstruction 46 0.035
304
MCR191 Microscopic Colitis 46 0.035
305
P MTH007 Methemoglobinemia 46 0.035
306
P TRN034 Transverse Myelitis 46 0.035
307
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.035
308
IMM003 Immunoglobulin Alpha Deficiency 45 0.035
309
ORL013 Oral Lichen Planus 45 0.035
310
CRB004 Cerebral Artery Occlusion 44 0.035
311
c RTN047 Retinitis Pigmentosa 18 44 0.035
312
c PCH010 Pachyonychia Congenita 3 43 0.035
313
HPT004 Hepatic Coma 43 0.035
314
ORL015 Oral Squamous Cell Carcinoma 43 0.035
315
P AVS003 Avascular Necrosis 42 0.035
316
DFF003 Diffuse Scleroderma 42 0.035
317
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.035
318
ERY017 Erythema Elevatum Diutinum 41 0.035
319
PSR016 Psoriatic Juvenile Idiopathic Arthritis 40 0.035
320
LNR006 Linear Iga Disease 40 0.035
321
ACR005 Acrodermatitis 40 0.035
322
ADP007 Adie Pupil 39 0.035
323
TXC001 Toxic Megacolon 39 0.035
324
c PSR028 Psoriasis 7 39 0.035
325
c THR111 Thrombocytopenia 3 38 0.035
326
c PSR032 Psoriasis 11 38 0.035
327
c PSR018 Psoriasis 13 38 0.035
328
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.035
329
P PLY187 Polyarticular Juvenile Idiopathic Arthritis 37 0.035
330
PRS037 Periostitis 37 0.035
331
HPT082 Hepatic Adenomas, Familial 37 0.035
332
ACL001 Acalculous Cholecystitis 35 0.035
333
FXD003 Fixed Drug Eruption 35 0.035
334
ALR002 Al-Raqad Syndrome 34 0.035
335
c PLY065 Polyarticular Onset Juvenile Idiopathic Arthritis 34 0.035
336
P HRD214 Hereditary Periodic Fever Syndrome 34 0.035
337
c INF088 Inflammatory Bowel Disease 5 34 0.035
338
MTH086 Methotrexate Toxicity 33 0.035
339
c PRS136 Prostate Cancer, Hereditary, 6 33 0.035
340
c PRS130 Prostate Cancer, Hereditary, 8 32 0.035
341
GST090 Gastroduodenal Crohn's Disease 31 0.035
342
UND007 Undifferentiated Connective Tissue Disease 30 0.035
343
HNM002 Hinman Syndrome 29 0.035
344
BLD041 Bladder Calculus 28 0.035
345
EXF003 Exfoliative Dermatitis 27 0.035
346
SPC030 Specific Language Disorder 26 0.035
347
TXC010 Toxic Myocarditis 25 0.035
348
c JVN047 Juvenile Spondyloarthropathy 24 0.035
349
ULC008 Ulcerative Proctitis 23 0.035
350
SLF017 Sulfamethoxazole Allergy 21 0.035
351
DRG017 Drug-Induced Vasculitis 17 0.035
352
NCT004 N Acetyltransferase Deficiency 15 0.035
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