Search results for Colchicine

729 hits were found for Colchicine

# Family MCID Name MIFTS Score
1
CLC008 Colchicine Resistance 37 8.922
2
CLC053 Colchicine Poisoning 23 3.227
3
GT001 Gout 63 0.523
4
P FML018 Familial Mediterranean Fever 72 0.513
5
PRC013 Pericarditis 54 0.351
6
P AMY004 Amyloidosis 70 0.330
7
LVR012 Liver Cirrhosis 63 0.231
8
P MYP004 Myopathy 64 0.222
9
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.213
10
P ATR011 Atrial Fibrillation 66 0.197
11
P PRM006 Primary Biliary Cirrhosis 61 0.183
12
P MYC007 Myocardial Infarction 70 0.175
13
P DRR001 Diarrhea 57 0.169
14
P KDN018 Kidney Disease 70 0.167
15
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.165
16
P CRN018 Coronary Artery Anomaly 63 0.160
17
ISC004 Ischemia 60 0.160
18
P VSC011 Vasculitis 62 0.149
19
P TRN020 Turner Syndrome 65 0.144
20
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.144
21
PLY100 Polyploidy 40 0.144
22
48X005 48,xyyy 39 0.144
23
P ART022 Arthritis 70 0.142
24
c FML001 Familial Atrial Fibrillation 66 0.140
25
ATH013 Atherosclerosis Susceptibility 66 0.140
26
P PRC012 Pericardial Effusion 51 0.140
27
HMP001 Hemopericardium 46 0.140
28
P NPH012 Nephrotic Syndrome 63 0.137
29
CYT018 Cytochrome P450 2d6 Variant 27 0.137
30
P NTR004 Neutropenia 63 0.134
31
BRC012 Brucellosis 61 0.134
32
PNC001 Pancytopenia 54 0.134
33
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.132
34
P LVR013 Liver Disease 68 0.132
35
ART140 Arteries, Anomalies of 53 0.132
36
HYP014 Hyperuricemia 51 0.121
37
P CHN059 Chondrocalcinosis 51 0.121
38
CRD001 Cardiac Tamponade 46 0.118
39
CRB039 Cerebrovascular Disease 69 0.115
40
APH001 Aphthous Stomatitis 57 0.115
41
c ACT075 Acute Myocardial Infarction 56 0.115
42
c AMY009 Amyloidosis Aa 50 0.115
43
STM007 Stomatitis 49 0.115
44
STR067 Stroke, Ischemic 80 0.112
45
P CRN300 Coronary Heart Disease 1 63 0.112
46
PRP030 Purpura 55 0.112
47
P NRP001 Neuropathy 56 0.109
48
c CHR684 Chronic Kidney Disease 66 0.105
49
P HRT032 Heart Disease 75 0.102
50
PRT036 Peritonitis 65 0.102
51
IDP011 Idiopathic Interstitial Pneumonia 63 0.102
52
P PLM036 Pulmonary Fibrosis 61 0.102
53
END030 End Stage Renal Failure 58 0.102
54
CHL068 Cholestasis 60 0.099
55
P LYM031 Lymphocytic Leukemia 55 0.099
56
ALL026 Allergic Hypersensitivity Disease 64 0.095
57
P EPD016 Epidermolysis Bullosa 53 0.095
58
CNS002 Constrictive Pericarditis 40 0.095
59
P HPT023 Hepatocellular Carcinoma 100 0.091
60
P NRB001 Neuroblastoma 71 0.091
61
P SYS005 Systemic Scleroderma 70 0.091
62
P DBT009 Diabetes Mellitus 64 0.091
63
P CRD246 Cardiovascular System Disease 56 0.091
64
c PYR010 Peyronie's Disease 50 0.091
65
ATS010 Autosomal Recessive Disease 48 0.091
66
ATN014 Autoinflammation with Arthritis and Dyskeratosis 40 0.091
67
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.091
68
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.087
69
OST012 Osteoarthritis 78 0.087
70
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.087
71
CNG034 Congestive Heart Failure 70 0.087
72
P THR014 Thrombocytopenia 68 0.087
73
P PSR002 Psoriasis 62 0.087
74
PST011 Pustulosis of Palm and Sole 52 0.087
75
P CLR023 Colorectal Cancer 98 0.083
76
c HYP595 Hypertension, Essential 84 0.083
77
BHC003 Behcet Syndrome 70 0.083
78
P HPT021 Hepatitis 67 0.083
79
SKN016 Skin Disease 63 0.083
80
P MYC008 Myocarditis 59 0.083
81
c ACT071 Acute Kidney Failure 59 0.083
82
P EXN002 Exanthem 57 0.083
83
P ALP008 Alopecia 56 0.083
84
c MCR113 Microvascular Complications of Diabetes 3 52 0.083
85
c MCR120 Microvascular Complications of Diabetes 7 47 0.083
86
c MCR130 Microvascular Complications of Diabetes 6 41 0.083
87
c MCR133 Microvascular Complications of Diabetes 4 41 0.083
88
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.079
89
c ALM001 Al Amyloidosis 50 0.079
90
MTB004 Metabolic Acidosis 50 0.079
91
P VTR007 Vitreoretinopathy 46 0.079
92
STT009 Sutton Disease 2 30 0.079
93
P ALZ034 Alzheimer Disease 88 0.075
94
P RHM011 Rheumatoid Arthritis 80 0.075
95
P RSP003 Respiratory Failure 74 0.075
96
DWN001 Down Syndrome 70 0.075
97
P CRD119 Cardiac Arrest 67 0.075
98
CNN005 Connective Tissue Disease 66 0.075
99
P MCR115 Microvascular Complications of Diabetes 5 66 0.075
100
c MCR129 Microvascular Complications of Diabetes 1 66 0.075
101
P VSC007 Vascular Disease 63 0.075
102
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.075
103
P ART023 Arthropathy 62 0.075
104
CNS004 Constipation 57 0.075
105
ATX019 Ataxia with Vitamin E Deficiency 48 0.075
106
c MCR112 Microvascular Complications of Diabetes 2 41 0.075
107
CHR178 Chromosomal Triplication 35 0.075
108
P HYP086 Hypothyroidism 68 0.070
109
c HPT001 Hepatitis C 63 0.070
110
c HPT003 Hepatitis a 63 0.070
111
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.070
112
TRN015 Transient Cerebral Ischemia 62 0.070
113
P HYP750 Hypertriglyceridemia, Familial 61 0.070
114
PHR003 Pharyngitis 56 0.070
115
RHM027 Rheumatic Disease 56 0.070
116
PYD002 Pyoderma 51 0.070
117
AZS001 Azoospermia 50 0.070
118
EPD006 Epidermolysis Bullosa Acquisita 49 0.070
119
BNR002 Bone Resorption Disease 48 0.070
120
ENT004 Enthesopathy 48 0.070
121
CRD137 Cardiogenic Shock 48 0.070
122
c PCH010 Pachyonychia Congenita 3 43 0.070
123
MYT011 Myotonia 35 0.070
124
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.070
125
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.065
126
c SPN225 Spondyloarthropathy 1 73 0.065
127
c HYP836 Hypercholesterolemia, Familial, 1 72 0.065
128
P SRC025 Sarcoidosis 1 70 0.065
129
ADL002 Adult Syndrome 69 0.065
130
P LKM002 Leukemia 66 0.065
131
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.065
132
P ADL010 Adult Respiratory Distress Syndrome 63 0.065
133
LPD008 Lipid Metabolism Disorder 62 0.065
134
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.065
135
GST045 Gastroenteritis 59 0.065
136
SCH014 Schistosomiasis 56 0.065
137
P PLY019 Polyneuropathy 56 0.065
138
SYN007 Synovitis 55 0.065
139
GSG001 Gas Gangrene 50 0.065
140
RNL077 Renal Fibrosis 47 0.065
141
BCK006 Back Pain 42 0.065
142
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.065
143
c CHR682 Chronic Bilirubin Encephalopathy 38 0.065
144
P AXN001 Axonal Neuropathy 36 0.065
145
CHL079 Children's Interstitial Lung Disease 27 0.065
146
P PRS040 Prostate Cancer 97 0.059
147
CYS001 Cystic Fibrosis 80 0.059
148
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.059
149
PRP027 Peripheral Vascular Disease 71 0.059
150
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.059
151
ATM095 Autoimmune Disease 61 0.059
152
PRT013 Portal Hypertension 60 0.059
153
CRD223 Cardiac Arrhythmia 60 0.059
154
RTN017 Retinal Detachment 60 0.059
155
P FBR017 Fibrosarcoma 56 0.059
156
GST050 Gastrointestinal System Disease 56 0.059
157
PYD001 Pyoderma Gangrenosum 54 0.059
158
HNC001 Henoch-Schoenlein Purpura 54 0.059
159
RLP001 Relapsing Polychondritis 54 0.059
160
P LTR001 Lateral Sclerosis 53 0.059
161
GLS018 Glass Syndrome 53 0.059
162
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.059
163
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.059
164
ILS001 Ileus 51 0.059
165
P LCT001 Lactic Acidosis 51 0.059
166
HDR003 Hidradenitis 49 0.059
167
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.059
168
TTR011 Tetraploidy 47 0.059
169
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.059
170
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.059
171
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.059
172
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.059
173
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.059
174
PRL008 Paralytic Ileus 44 0.059
175
CYT002 Cytokine Deficiency 44 0.059
176
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.059
177
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.059
178
c PRM038 Primary Agammaglobulinemia 43 0.059
179
ART006 Arthus Reaction 42 0.059
180
WLL004 Wallerian Degeneration 39 0.059
181
IDP041 Idiopathic Recurrent Pericarditis 30 0.059
182
c LKM071 Leukemia, Chronic Lymphocytic 79 0.053
183
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.053
184
ULC004 Ulcerative Colitis 73 0.053
185
c HPT073 Hepatitis C Virus 70 0.053
186
P LYM118 Lymphoma 68 0.053
187
OST159 Osteogenic Sarcoma 66 0.053
188
ANG054 Angina Pectoris 66 0.053
189
CHG001 Chagas Disease 66 0.053
190
SRC014 Sarcoma 65 0.053
191
P MNN013 Meningitis 65 0.053
192
P MTR014 Motor Neuron Disease 64 0.053
193
CLT003 Colitis 62 0.053
194
P PRP029 Porphyria 62 0.053
195
ALC006 Alcoholic Hepatitis 61 0.053
196
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.053
197
P DRM010 Dermatomyositis 61 0.053
198
INT002 Intermittent Claudication 61 0.053
199
FTT001 Fatty Liver Disease 61 0.053
200
HYP066 Hyperglycemia 61 0.053
201
P ENC018 Encephalopathy 61 0.053
202
LNG099 Lung Disease 61 0.053
203
P PNC044 Pancreatitis 61 0.053
204
P URT039 Urticaria 58 0.053
205
P INF032 Infertility 57 0.053
206
DSS009 Disseminated Intravascular Coagulation 57 0.053
207
P PRP019 Peripheral Nervous System Disease 57 0.053
208
THR024 Thrombosis 56 0.053
209
P INF037 Inflammatory Bowel Disease 56 0.053
210
c SVR001 Severe Acute Respiratory Syndrome 55 0.053
211
CHL014 Cholera 55 0.053
212
INT007 Intermediate Coronary Syndrome 55 0.053
213
DBT010 Diabetic Neuropathy 55 0.053
214
KRT009 Keratosis 53 0.053
215
PRP080 Peripheral Artery Disease 53 0.053
216
SPN051 Spondylitis 52 0.053
217
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.053
218
PNG002 Pain Agnosia 51 0.053
219
SPN035 Spindle Cell Sarcoma 51 0.053
220
PNN001 Panniculitis 49 0.053
221
CRY004 Cryoglobulinemia 49 0.053
222
ERY004 Erysipelas 48 0.053
223
GRN017 Granulocytopenia 44 0.053
224
SBC012 Subcorneal Pustular Dermatosis 44 0.053
225
c HYP272 Hypercholesterolemia, Familial, 3 43 0.053
226
CRV030 Cervical Adenitis 38 0.053
227
ATN021 Autoinflammatory Syndrome 33 0.053
228
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.053
229
INF009 Inflammatory Spondylopathy 32 0.053
230
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.053
231
P BRS047 Breast Cancer 96 0.046
232
MYL069 Myeloma, Multiple 85 0.046
233
c DLT002 Dilated Cardiomyopathy 79 0.046
234
IMM167 Immune Deficiency Disease 78 0.046
235
AST005 Asthma 77 0.046
236
P NRF023 Neurofibromatosis, Type Ii 76 0.046
237
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.046
238
c ART115 Aortic Valve Disease 1 75 0.046
239
DFC004 Deficiency Anemia 75 0.046
240
P APL001 Aplastic Anemia 74 0.046
241
c ATR087 Atrial Standstill 1 74 0.046
242
CRH001 Crohn's Disease 74 0.046
243
P MLT020 Multiple Sclerosis 72 0.046
244
P LKM062 Leukemia, Acute Lymphoblastic 68 0.046
245
P LPR021 Leprosy 3 67 0.046
246
HYP056 Hypoglycemia 66 0.046
247
MYC006 Mycosis Fungoides 66 0.046
248
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.046
249
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.046
250
CLN015 Colon Adenocarcinoma 63 0.046
251
TXC005 Toxic Shock Syndrome 61 0.046
252
DRM006 Dermatitis 61 0.046
253
P ENC004 Encephalitis 61 0.046
254
c PNS012 Paine Syndrome 61 0.046
255
ACQ007 Acquired Immunodeficiency Syndrome 60 0.046
256
ORL011 Oral Cancer 60 0.046
257
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.046
258
P CYS018 Cystitis 59 0.046
259
c HPT016 Hepatitis B 59 0.046
260
BRN002 Bronchiolitis 59 0.046
261
c CHL119 Cholangitis, Primary Sclerosing 57 0.046
262
P PLY041 Polymyositis 57 0.046
263
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.046
264
P DRM007 Dermatitis Herpetiformis 54 0.046
265
CRT017 Cartilage Disease 54 0.046
266
HDR002 Hidradenitis Suppurativa 53 0.046
267
MMM001 Mammary Paget's Disease 53 0.046
268
TND005 Tendinitis 52 0.046
269
P ACT008 Actinic Keratosis 52 0.046
270
HYP088 Hyper-Igd Syndrome 52 0.046
271
MSC190 Muscular Disease 51 0.046
272
THR016 Thrombophlebitis 51 0.046
273
HYP074 Hypersensitivity Vasculitis 51 0.046
274
HYP081 Hypolipoproteinemia 50 0.046
275
HYP781 Hypoascorbemia 50 0.046
276
P CHL066 Cholangitis 50 0.046
277
P PLG001 Pelger-Huet Anomaly 50 0.046
278
P CHR345 Chronic Pain 50 0.046
279
P OVR082 Overgrowth Syndrome 50 0.046
280
WLL006 Wells Syndrome 50 0.046
281
NTR046 Neutrophil Migration 50 0.046
282
CLC006 Calcinosis 48 0.046
283
BNN003 Bone Inflammation Disease 48 0.046
284
P SCL009 Sclerosing Cholangitis 47 0.046
285
TND004 Tendinopathy 44 0.046
286
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.046
287
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.046
288
ANX004 Anoxia 42 0.046
289
GST020 Gastric Antral Vascular Ectasia 41 0.046
290
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.046
291
LNR006 Linear Iga Disease 40 0.046
292
RTR011 Retroperitoneal Fibrosis 40 0.046
293
ULC007 Ulcerative Stomatitis 39 0.046
294
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.046
295
FML307 Familial Calcium Pyrophosphate Deposition 38 0.046
296
P PST059 Pustular Psoriasis 38 0.046
297
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.046
298
c DRM040 Dermatitis Herpetiformis, Familial 35 0.046
299
HNS001 Hansen's Disease 34 0.046
300
NND010 Nondisjunction 34 0.046
301
c PRS136 Prostate Cancer, Hereditary, 6 33 0.046
302
c PRS130 Prostate Cancer, Hereditary, 8 32 0.046
303
PLY150 Polykaryocytosis Inducer 31 0.046
304
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.046
305
SNG003 Single Ventricular Heart 30 0.046
306
c MYC058 Myocardial Infarction 2 28 0.046
307
TBL029 Tubulin, Beta 28 0.046
308
c RNG015 Ring Chromosome 2 26 0.046
309
c FML344 Familial Mediterranean Fever, Autosomal Dominant 25 0.046
310
P OVR042 Ovarian Cancer 89 0.037
311
P PNC035 Pancreatic Cancer 84 0.037
312
P GST053 Gastric Cancer 83 0.037
313
MLR004 Malaria 80 0.037
314
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.037
315
GLB015 Glioblastoma Multiforme 75 0.037
316
P PHC003 Pheochromocytoma 71 0.037
317
HMN044 Human Immunodeficiency Virus Type 1 71 0.037
318
RCK004 Rickets 69 0.037
319
LYM133 Lymphoma, Hodgkin, Classic 69 0.037
320
P MYC084 Mycobacterium Tuberculosis 1 68 0.037
321
P CLC063 Celiac Disease 1 68 0.037
322
P PNM007 Pneumonia 68 0.037
323
P DMN002 Dementia 67 0.037
324
P PRP003 Porphyria Cutanea Tarda 67 0.037
325
P ANG001 Angelman Syndrome 67 0.037
326
P SKN015 Skin Carcinoma 67 0.037
327
FCT007 Factor Vii Deficiency 66 0.037
328
CHD001 Chediak-Higashi Syndrome 66 0.037
329
P HYP098 Hypereosinophilic Syndrome 66 0.037
330
P NRV007 Nervous System Disease 66 0.037
331
c RHB024 Rhabdomyosarcoma 2 65 0.037
332
PRT037 Pertussis 65 0.037
333
P EPD009 Epidermolysis Bullosa Dystrophica 64 0.037
334
MVL001 Mevalonic Aciduria 64 0.037
335
TTN003 Tetanus 64 0.037
336
P GLM045 Glioma 63 0.037
337
P ANR048 Aniridia 1 63 0.037
338
c ACT068 Acute Cystitis 63 0.037
339
ACT119 Acute Promyelocytic Leukemia 63 0.037
340
ANR007 Anorexia Nervosa 63 0.037
341
c SCL052 Scleroderma, Familial Progressive 62 0.037
342
P PRD008 Periodontitis 62 0.037
343
P HML002 Hemolytic Anemia 62 0.037
344
c LCL006 Localized Scleroderma 62 0.037
345
BLL006 Bullous Pemphigoid 62 0.037
346
PSR001 Psoriatic Arthritis 62 0.037
347
P HMN010 Hemangioma 61 0.037
348
P CTR002 Cataract 60 0.037
349
VRC005 Varicose Veins 60 0.037
350
ACN002 Acanthosis Nigricans 60 0.037
351
P TXP001 Toxoplasmosis 60 0.037
352
P PGT001 Paget's Disease of Bone 60 0.037
353
P HRD011 Hereditary Spherocytosis 60 0.037
354
c ACT027 Acute Pancreatitis 59 0.037
355
P TRC086 Trichohepatoenteric Syndrome 1 59 0.037
356
P PLY017 Polyarteritis Nodosa 58 0.037
357
ADN018 Adenoma 58 0.037
358
P SZR006 Seizure Disorder 58 0.037
359
EYD002 Eye Disease 58 0.037
360
c ACT073 Acute Leukemia 58 0.037
361
RBS001 Rabies 58 0.037
362
VSL002 Visual Epilepsy 58 0.037
363
ADL030 Adult-Onset Still's Disease 58 0.037
364
EMB004 Embryonal Carcinoma 57 0.037
365
P HDC001 Headache 57 0.037
366
P UVT001 Uveitis 57 0.037
367
APH002 Aphasia 57 0.037
368
P GLM007 Glomerulonephritis 57 0.037
369
P PYL005 Pyelonephritis 56 0.037
370
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.037
371
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.037
372
ATR057 Atrioventricular Block 55 0.037
373
ORL004 Oral Submucous Fibrosis 55 0.037
374
P PMP001 Pemphigus 55 0.037
375
CLL003 Cellulitis 54 0.037
376
AMN003 Amnestic Disorder 54 0.037
377
P JNC001 Junctional Epidermolysis Bullosa 54 0.037
378
P PRM018 Primary Hypertrophic Osteoarthropathy 54 0.037
379
c CNT035 Central Nervous System Disease 54 0.037
380
RCS002 Recessive Dystrophic Epidermolysis Bullosa 53 0.037
381
P ART018 Aortic Valve Insufficiency 53 0.037
382
THR013 Thoracic Outlet Syndrome 53 0.037
383
DMY004 Demyelinating Disease 52 0.037
384
IMP005 Impotence 52 0.037
386
PLS009 Plasma Cell Neoplasm 51 0.037
387
c VRL010 Viral Hepatitis 51 0.037
388
ESP002 Esophageal Varix 51 0.037
389
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.037
390
c INF145 Infantile Liver Failure Syndrome 1 50 0.037
391
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.037
392
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.037
393
HYP017 Hypophosphatemia 49 0.037
394
c PSR021 Psoriasis 14, Pustular 49 0.037
395
VTM002 Vitamin B12 Deficiency 48 0.037
396
IGG001 Iga Glomerulonephritis 48 0.037
397
SPL018 Splenomegaly 48 0.037
398
PST062 Pustulosis Palmaris Et Plantaris 47 0.037
399
VSC058 Vasculitis, Autoinflammation, Immunodeficiency, and Hematologic Defects Syndrome 47 0.037
400
TST044 Testicular Torsion 47 0.037
401
c MTR002 Mitral Valve Insufficiency 47 0.037
402
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.037
403
LYM019 Lymphosarcoma 47 0.037
404
ADR040 Adrenal Gland Pheochromocytoma 46 0.037
405
URT010 Ureteral Obstruction 46 0.037
406
FLL008 Folliculitis 46 0.037
407
GLL048 Glial Tumor 45 0.037
408
SCL002 Scleredema Adultorum 45 0.037
409
PTT037 Pituitary Tumors 44 0.037
410
RFR003 Refractive Error 44 0.037
411
FBR019 Fibromatosis 44 0.037
412
P MYG005 Myoglobinuria 43 0.037
413
ERY017 Erythema Elevatum Diutinum 41 0.037
414
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.037
415
P TRC031 Trichorhinophalangeal Syndrome 40 0.037
416
ALL014 Allergic Encephalomyelitis 39 0.037
417
ATX010 Ataxia Neuropathy Spectrum 38 0.037
418
P HRD214 Hereditary Periodic Fever Syndrome 34 0.037
419
ACT064 Acute Necrotizing Encephalitis 32 0.037
420
LCH014 Lichen Amyloidosis 31 0.037
421
c BLD140 Blood Group, I System 30 0.037
422
DFF012 Differentiating Neuroblastoma 29 0.037
423
PST092 Posttransplant Acute Limbic Encephalitis 29 0.037
424
c SYS066 Systemic Polyarteritis Nodosa 27 0.037
425
P CRY006 Cryofibrinogenemia 26 0.037
426
PRQ002 Paraquat Poisoning 25 0.037
427
MLL006 Mollaret Meningitis 23 0.037
428
BLD137 Blood Group--Ahonen 19 0.037
429
OBN001 Ouabain Resistance 18 0.037
430
PRT231 Partial Duplication of Chromosome 4 8 0.037
431
P LNG032 Lung Cancer 97 0.026
432
c SYS001 Systemic Lupus Erythematosus 86 0.026
433
P ATX030 Ataxia-Telangiectasia 83 0.026
434
P GLM040 Glioma Susceptibility 1 81 0.026
435
P LNG064 Lung Cancer Susceptibility 3 77 0.026
436
CRV035 Cervical Cancer 76 0.026
437
SVR004 Severe Combined Immunodeficiency 73 0.026
438
c THR092 Thrombophilia Due to Thrombin Defect 73 0.026
439
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.026
440
P HNT016 Huntington Disease 71 0.026
441
OTT002 Otitis Media 71 0.026
442
P OST001 Osteopetrosis 71 0.026
443
MLT157 Multiple System Atrophy 1 70 0.026
444
P TBR001 Tuberous Sclerosis 70 0.026
445
PLM001 Pulmonary Tuberculosis 70 0.026
446
c MGR028 Migraine with or Without Aura 1 69 0.026
447
CRT072 Creutzfeldt-Jakob Disease 69 0.026
448
MLN008 Melanoma 69 0.026
449
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.026
450
c BSL007 Basal Cell Carcinoma 68 0.026
451
P INF038 Influenza 68 0.026
452
BRK010 Burkitt Lymphoma 67 0.026
453
CHL065 Cholangiocarcinoma 67 0.026
454
ALL003 Allergic Rhinitis 67 0.026
455
CRP001 Carpal Tunnel Syndrome 67 0.026
456
ABT001 Abetalipoproteinemia 67 0.026
457
P NSP012 Nasopharyngeal Carcinoma 67 0.026
458
ALC007 Alcohol Dependence 66 0.026
459
AND002 Androgen Insensitivity Syndrome 66 0.026
460
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.026
461
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.026
462
ART001 Arterial Tortuosity Syndrome 66 0.026
463
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.026
464
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.026
465
P HYD006 Hydrocephalus 65 0.026
466
P CNJ013 Conjunctivitis 65 0.026
467
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.026
468
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.026
469
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.026
470
P HRP006 Herpes Simplex 65 0.026
471
CNC002 Cinca Syndrome 65 0.026
472
BRR014 Barrett Esophagus 64 0.026
473
OST017 Osteomyelitis 64 0.026
474
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.026
475
P ADN016 Adenocarcinoma 64 0.026
477
DPR016 Depression 63 0.026
478
MCK007 Muckle-Wells Syndrome 63 0.026
479
TYP007 Typhoid Fever 63 0.026
480
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.026
481
P END044 Endometriosis 62 0.026
482
c PRG047 Progressive Familial Intrahepatic Cholestasis 62 0.026
483
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.026
484
BDD001 Budd-Chiari Syndrome 62 0.026
485
TKY002 Takayasu Arteritis 61 0.026
486
CRC021 Carcinosarcoma 61 0.026
487
P INT143 Interstitial Cystitis 61 0.026
488
c HRD002 Hereditary Angioedema 61 0.026
489
P LPS004 Lupus Erythematosus 61 0.026
490
P KDN017 Kidney Cancer 61 0.026
491
RHM001 Rheumatic Fever 61 0.026
492
HPT019 Hepatic Encephalopathy 60 0.026
493
P MYL006 Myeloid Leukemia 60 0.026
494
DPH001 Diphtheria 60 0.026
495
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.026
496
SQM006 Squamous Cell Carcinoma 60 0.026
497
P ALP009 Alopecia Areata 60 0.026
498
STF001 Stiff-Person Syndrome 60 0.026
499
PNM010 Pneumothorax, Primary Spontaneous 60 0.026
500
HRP004 Herpes Zoster 60 0.026
501
CHC001 Chickenpox 60 0.026
502
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.026
503
P GLL022 Guillain-Barre Syndrome 59 0.026
504
THY029 Thyroid Carcinoma 59 0.026
505
MXD005 Mixed Connective Tissue Disease 59 0.026
506
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.026
507
SPP011 Suppression of Tumorigenicity 12 59 0.026
508
HYD002 Hydronephrosis 59 0.026
509
P PLY014 Polycystic Kidney Disease 59 0.026
510
FBR047 Fibromyalgia 59 0.026
511
DBN001 Dubin-Johnson Syndrome 59 0.026
512
P RBL001 Rubella 58 0.026
513
P INT070 Intestinal Obstruction 58 0.026
514
PPT005 Peptic Ulcer Disease 58 0.026
515
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.026
516
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.026
517
P ALC033 Alcohol Use Disorder 58 0.026
518
P AXN002 Axenfeld-Rieger Syndrome 58 0.026
519
P MCR010 Microcephaly 58 0.026
520
P BCL017 B-Cell Lymphoma 58 0.026
521
P OPT006 Optic Nerve Disease 57 0.026
522
CST005 Castleman Disease 57 0.026
523
P CND004 Candidiasis 57 0.026
524
ARS001 Aarskog-Scott Syndrome 57 0.026
525
AMY082 Amyloidosis, Familial Visceral 57 0.026
526
BLM002 Bulimia Nervosa 57 0.026
527
P RHN004 Rhinitis 57 0.026
528
BLR008 Bilirubin Metabolic Disorder 57 0.026
529
PLY023 Polycystic Liver Disease 57 0.026
530
BRN056 Bronchopulmonary Dysplasia 57 0.026
531
TNS005 Tonsillitis 57 0.026
532
PLM031 Poliomyelitis 57 0.026
533
P SJG008 Sjogren Syndrome 56 0.026
534
PRS047 Prostatitis 56 0.026
535
P STR020 Strabismus 56 0.026
536
ERY051 Erythroleukemia, Familial 56 0.026
537
HYP266 Hypoxia 56 0.026
538
CMR002 Coumarin Resistance 56 0.026
539
PNM008 Pneumothorax 56 0.026
540
c INT072 Intestinal Pseudo-Obstruction 56 0.026
541
P PLY011 Polycystic Ovary Syndrome 56 0.026
542
SLC006 Silicosis 56 0.026
543
P MYS005 Myositis 56 0.026
544
BRN012 Bronchiolitis Obliterans 56 0.026
545
P GST044 Gastritis 55 0.026
546
FCT003 Factor X Deficiency 55 0.026
547
P MYT023 Myotonia Congenita 55 0.026
548
c FML035 Familial Hyperlipidemia 55 0.026
549
MCS002 Mucositis 55 0.026
550
MCL006 Macular Retinal Edema 55 0.026
551
P ALP106 Alport Syndrome 1, X-Linked 55 0.026
552
PLV003 Pelvic Inflammatory Disease 55 0.026
553
CPL003 Capillary Leak Syndrome 55 0.026
554
P HYP076 Hyperthyroidism 55 0.026
555
P MYP006 Myopia 55 0.026
556
P DBT005 Diabetes Insipidus 55 0.026
557
PLM010 Pulmonary Edema 55 0.026
558
BLP046 Blepharophimosis, Ptosis, and Epicanthus Inversus 55 0.026
559
P FNG006 Feingold Syndrome 1 55 0.026
560
PRN019 Perinatal Necrotizing Enterocolitis 54 0.026
561
OCL020 Ocular Cicatricial Pemphigoid 54 0.026
562
HYP458 Hyper Ige Syndrome 54 0.026
563
GNT003 Genital Herpes 54 0.026
564
P LCH002 Lichen Planus 54 0.026
565
FRY006 Fryns Microphthalmia Syndrome 54 0.026
566
P ART021 Arteriosclerosis 54 0.026
567
P ANG015 Angioedema 54 0.026
568
GLC003 Glucose Intolerance 54 0.026
569
P SPN052 Spondyloarthropathy 54 0.026
570
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.026
571
CHK001 Chikungunya 53 0.026
572
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.026
573
FRZ001 Frozen Shoulder 53 0.026
574
c ACT020 Acute T Cell Leukemia 53 0.026
575
P TRM003 Tremor 53 0.026
576
P LCT002 Lactose Intolerance 53 0.026
577
GST023 Gastric Ulcer 53 0.026
578
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.026
579
TXC002 Toxic Encephalopathy 52 0.026
580
RYS001 Reye Syndrome 51 0.026
581
OCL069 Ocular Motor Apraxia 51 0.026
582
TLN003 Telangiectasis 51 0.026
583
THR004 Thrombocytosis 51 0.026
584
CRY001 Cryptogenic Organizing Pneumonia 51 0.026
585
PLR008 Pleurisy 51 0.026
586
c ACT134 Acute Liver Failure 51 0.026
587
ENT011 Enterocolitis 50 0.026
588
HPT014 Hepatorenal Syndrome 50 0.026
589
IRD001 Iridocyclitis 50 0.026
590
BRN014 Bronchopneumonia 50 0.026
591
P AST007 Astrocytoma 50 0.026
592
INT079 Intrahepatic Cholangiocarcinoma 50 0.026
593
VLV047 Volvulus of Midgut 50 0.026
594
P DDN001 Duodenal Ulcer 50 0.026
595
LPR001 Lepromatous Leprosy 50 0.026
596
ILT001 Ileitis 50 0.026
597
CRV040 Cervix Carcinoma 50 0.026
598
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.026
599
SYS003 Systolic Heart Failure 50 0.026
600
P KRT007 Keratoconus 49 0.026
601
P INT099 Intrahepatic Cholestasis of Pregnancy 49 0.026
602
P IGN003 Iga Nephropathy 1 49 0.026
603
PLC008 Placenta Disease 49 0.026
604
47X002 47,xyy 49 0.026
605
NXS001 Naxos Disease 49 0.026
606
VCC001 Vaccinia 49 0.026
607
P AMY084 Amyloidosis, Finnish Type 49 0.026
608
URM002 Uremia 49 0.026
609
URT001 Urethritis 48 0.026
610
MCR020 Microsporidiosis 48 0.026
611
P OBS001 Obstructive Jaundice 48 0.026
612
LPD009 Lipid Storage Disease 48 0.026
613
P RNL015 Renal Hypertension 48 0.026
614
ACT098 Acute Erythroid Leukemia 48 0.026
615
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.026
616
ART004 Aortic Atherosclerosis 48 0.026
617
IRR003 Irritant Dermatitis 47 0.026
618
P CRN028 Corneal Ulcer 47 0.026
619
BRS064 Bursitis 47 0.026
620
INT017 Intestinal Schistosomiasis 47 0.026
621
HYP082 Hypopharynx Cancer 47 0.026
622
CHR074 Choriocarcinoma 46 0.026
623
P PLY020 Polyradiculoneuropathy 46 0.026
624
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.026
625
ASB001 Asbestosis 46 0.026
626
CTS011 Cutis Marmorata Telangiectatica Congenita 46 0.026
627
CNT025 Central Pontine Myelinolysis 45 0.026
628
CYN002 Cyanosis, Transient Neonatal 45 0.026
629
ACT003 Acute Kidney Tubular Necrosis 45 0.026
630
GRN007 Granuloma Annulare 45 0.026
631
THR099 Third-Degree Atrioventricular Block 45 0.026
632
GRD001 Giardiasis 45 0.026
633
c HRD039 Hereditary Amyloidosis 45 0.026
634
OLG001 Oligospermia 45 0.026
635
CRB004 Cerebral Artery Occlusion 44 0.026
636
c ACT042 Acute Pyelonephritis 44 0.026
637
PLN005 Palindromic Rheumatism 44 0.026
638
FBR054 Fibroma 44 0.026
639
PMP004 Pemphigus Foliaceus 43 0.026
640
HPT004 Hepatic Coma 43 0.026
641
c SPH013 Spherocytosis, Type 1 43 0.026
642
RTC009 Reticulum Cell Sarcoma 43 0.026
643
ORL015 Oral Squamous Cell Carcinoma 43 0.026
644
URT037 Urethral Stricture 43 0.026
645
PRS063 Paresthesia 43 0.026
646
MYF002 Myofascial Pain Syndrome 42 0.026
647
MCR103 Microtia 42 0.026
648
TRP014 Triploidy 42 0.026
649
P FML355 Familial Intrahepatic Cholestasis 41 0.026
650
ISC020 Ischiocoxopodopatellar Syndrome with or Without Pulmonary Arterial Hypertension 41 0.026
651
OCL052 Ocular Dominance 41 0.026
652
ACT088 Acute Insulin Response 41 0.026
653
P DMY001 Demyelinating Polyneuropathy 41 0.026
654
EXT006 Extrahepatic Cholestasis 40 0.026
655
MYP153 Myopathy, Myofibrillar, 9, with Early Respiratory Failure 40 0.026
656
c CNG027 Congenital Hemolytic Anemia 40 0.026
657
UTR043 Uterine Sarcoma 40 0.026
658
P BLL007 Bullous Skin Disease 40 0.026
659
c ACT004 Acute Diarrhea 39 0.026
660
ESN002 Eosinophilia-Myalgia Syndrome 39 0.026
661
LKP003 Leukoplakia 39 0.026
662
MCH006 Mechanical Strabismus 39 0.026
663
ADP007 Adie Pupil 39 0.026
664
SKN006 Skin Sarcoidosis 39 0.026
666
ORN001 Ornithosis 39 0.026
667
HMF008 Hemifacial Atrophy, Progressive 39 0.026
668
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.026
669
P STR001 Striatonigral Degeneration 38 0.026
670
NCR002 Necrobiosis Lipoidica 38 0.026
671
CTN033 Cutaneous Candidiasis 38 0.026
672
CHL073 Cholestasis-Lymphedema Syndrome 38 0.026
673
FBR089 Fibrosclerosis, Multifocal 38 0.026
674
CHL070 Cholesterol Embolism 37 0.026
675
PRS037 Periostitis 37 0.026
676
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.026
677
HPT082 Hepatic Adenomas, Familial 37 0.026
678
SHW001 Shwartzman Phenomenon 36 0.026
679
P PYR039 Peyronie Disease 36 0.026
680
SVN002 Sveinsson Chorioretinal Atrophy 36 0.026
681
SCN049 Second-Degree Atrioventricular Block 36 0.026
682
c CHR098 Chronic Pyelonephritis 35 0.026
683
ACR062 Acroosteolysis 35 0.026
684
FXD003 Fixed Drug Eruption 35 0.026
685
ALR002 Al-Raqad Syndrome 34 0.026
686
ART010 Arteriolosclerosis 34 0.026
687
DRS001 Dressler's Syndrome 34 0.026
688
GGN002 Gigantism 34 0.026
690
HLT002 Halothane Hepatitis 33 0.026
691
BWN006 Bowen's Disease 32 0.026
692
HYD003 Hydrarthrosis 32 0.026
693
HPT085 Hepatitis, Fulminant Viral 32 0.026
694
WTR001 Waterhouse-Friderichsen Syndrome 32 0.026
695
RRS014 Rare Surgical Neurologic Disease 32 0.026
696
MNG003 Mungan Syndrome 32 0.026
697
CHL040 Cholangiolocellular Carcinoma 32 0.026
698
PRR001 Periarthritis 31 0.026
699
CLF051 Cleft Larynx, Posterior 31 0.026
700
ALP048 Alopecia Totalis 31 0.026
701
EXN003 Exencephaly 31 0.026
702
ERY069 Erythrokeratoderma ''en Cocardes'' 30 0.026
704
MYC088 Mycobacterium Avium Complex Infections 29 0.026
705
HNM002 Hinman Syndrome 29 0.026
706
RHM013 Rheumatoid Nodulosis 29 0.026
707
c DRR018 Diarrhea 9 29 0.026
708
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.026
709
LRY026 Laryngeal Cleft 28 0.026
710
TMP002 Temporal Lobe Neoplasm 28 0.026
711
ARG004 Argyria 28 0.026
712
MST020 Mast Cell Activation Syndrome 27 0.026
713
IGP001 Iga Pemphigus 26 0.026
714
ASB003 Asbestos Intoxication 26 0.026
715
DFF010 Diffuse Alopecia Areata 25 0.026
716
ERY023 Erythroplakia 24 0.026
717
GNT018 Gianotti Crosti Syndrome 24 0.026
719
BLD165 Blood Group, Colton System 23 0.026
720
AND005 Androgen Insensitivity Syndrome, Mild 22 0.026
721
MCL047 Macular Amyloidosis 21 0.026
722
LCH008 Lichen Planus Pigmentosus 21 0.026
723
PRM290 Premature Centromere Division 21 0.026
724
URM001 Uremic Neuropathy 21 0.026
725
INT182 Intermittent Hydrarthrosis 18 0.026
726
INT062 Interstitial Myocarditis 18 0.026
727
P PRM145 Primary Anetoderma 18 0.026
728
PRQ001 Paraquat Lung 16 0.026
729
OBS524 Obsolete: Benign Exophthalmos Syndrome 15 0.026
Content
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