Search results for Quercetin

930 hits were found for Quercetin

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 46 10.842
2
HYP066 Hyperglycemia 61 10.628
3
ISC004 Ischemia 61 10.490
4
c PCH010 Pachyonychia Congenita 3 43 9.837
5
P PRS040 Prostate Cancer 95 8.926
6
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 8.707
7
NNL005 Non-Alcoholic Fatty Liver Disease 63 8.381
8
HYP266 Hypoxia 57 7.949
9
FTT001 Fatty Liver Disease 62 7.879
10
CYT002 Cytokine Deficiency 43 7.761
11
LPD008 Lipid Metabolism Disorder 62 7.619
12
GLL048 Glial Tumor 52 7.516
13
GLM045 Glioma 63 7.516
14
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 7.397
15
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 7.397
16
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 7.397
17
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 7.397
18
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 7.397
19
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 7.397
20
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 7.397
21
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 7.397
22
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 7.397
23
ATH013 Atherosclerosis Susceptibility 63 7.299
24
P PNC035 Pancreatic Cancer 86 7.057
25
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 7.038
26
P BCL017 B-Cell Lymphoma 59 6.924
27
GLB002 Glioblastoma 67 6.729
28
P ADN016 Adenocarcinoma 63 6.681
29
P NRB001 Neuroblastoma 66 6.669
30
P OVR042 Ovarian Cancer 88 6.535
31
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 6.453
32
P PLM036 Pulmonary Fibrosis 66 6.418
33
P ALZ034 Alzheimer Disease 87 6.347
34
P BRS047 Breast Cancer 98 6.317
35
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 6.171
36
P MLN008 Melanoma 76 6.140
37
P ART022 Arthritis 71 6.048
38
48X005 48,xyyy 39 6.048
39
PLM129 Pulmonary Disease, Chronic Obstructive 74 6.004
40
PRS047 Prostatitis 58 5.971
41
HYP014 Hyperuricemia 51 5.877
42
BRN071 Brain Injury 50 5.837
43
CRB004 Cerebral Artery Occlusion 45 5.799
44
P HPT023 Hepatocellular Carcinoma 96 5.791
45
P SKN015 Skin Carcinoma 71 5.739
46
BNR002 Bone Resorption Disease 47 5.738
47
c MCR130 Microvascular Complications of Diabetes 6 41 5.707
48
c MCR120 Microvascular Complications of Diabetes 7 47 5.707
49
c MCR113 Microvascular Complications of Diabetes 3 52 5.707
50
c MCR133 Microvascular Complications of Diabetes 4 41 5.707
51
AGN016 Aging 54 5.675
52
SVR001 Severe Acute Respiratory Syndrome 67 5.624
53
P GST053 Gastric Cancer 83 5.619
54
BRN024 Bronchitis 67 5.580
55
ORL011 Oral Cancer 60 5.532
56
ALL003 Allergic Rhinitis 67 5.491
57
P RHM011 Rheumatoid Arthritis 82 5.455
58
P RHN004 Rhinitis 57 5.348
59
P LNG032 Lung Cancer 98 5.320
60
P LKM002 Leukemia 67 5.315
61
c TYP009 Type 2 Diabetes Mellitus 92 5.309
62
OST159 Osteogenic Sarcoma 66 5.306
63
CRV035 Cervical Cancer 73 5.243
65
P CRN300 Coronary Heart Disease 1 73 5.208
66
P BLD134 Bladder Cancer 79 5.173
67
CLN015 Colon Adenocarcinoma 65 5.151
68
SPN186 Spinal Cord Injury 61 5.142
69
P PLY011 Polycystic Ovary Syndrome 57 5.133
70
LNG099 Lung Disease 62 5.125
71
SKN016 Skin Disease 63 5.080
72
GT001 Gout 64 5.067
73
P KLZ004 Kala-Azar 1 41 4.971
74
LSH001 Leishmaniasis 64 4.971
75
P INF037 Inflammatory Bowel Disease 53 4.948
76
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.901
77
SQM006 Squamous Cell Carcinoma 60 4.893
78
CLT003 Colitis 63 4.858
79
P PRD008 Periodontitis 64 4.779
80
P DBT009 Diabetes Mellitus 67 4.768
81
PLM134 Pulmonary Fibrosis, Idiopathic 76 4.741
82
P BRS044 Breast Adenocarcinoma 58 4.736
83
HMS001 Hemosiderosis 48 4.677
84
TRM010 Traumatic Brain Injury 51 4.669
85
P CLR023 Colorectal Cancer 100 4.621
86
P MSC005 Muscular Dystrophy 67 4.613
87
MSC157 Muscular Dystrophy, Duchenne Type 79 4.544
88
PRT251 Proteinuria, Chronic Benign 57 4.543
89
GST023 Gastric Ulcer 52 4.512
90
P CTR002 Cataract 60 4.471
91
c HPT001 Hepatitis C 62 4.459
92
P KDN018 Kidney Disease 72 4.451
93
P RRH023 Rare Hereditary Hemochromatosis 54 4.399
94
P INF038 Influenza 68 4.385
95
OST012 Osteoarthritis 77 4.358
96
P LNG064 Lung Cancer Susceptibility 3 70 4.343
97
c HYP836 Hypercholesterolemia, Familial, 1 73 4.339
98
P MYL006 Myeloid Leukemia 61 4.313
99
P LVR013 Liver Disease 69 4.313
100
DFC004 Deficiency Anemia 74 4.296
101
c LKM061 Leukemia, Acute Myeloid 83 4.261
102
RNL077 Renal Fibrosis 46 4.174
103
c MCR115 Microvascular Complications of Diabetes 5 65 4.128
104
BCT022 Bacterial Infectious Disease 56 4.128
105
c PLM164 Pulmonary Hypertension, Primary, 1 76 4.126
106
c LKM063 Leukemia, Chronic Myeloid 71 4.126
107
P INF032 Infertility 57 4.126
108
SPP011 Suppression of Tumorigenicity 12 61 4.114
109
BRN004 Brain Edema 54 4.094
110
NNL006 Non-Alcoholic Steatohepatitis 54 4.071
111
P LKM071 Leukemia, Chronic Lymphocytic 75 4.069
112
ATM095 Autoimmune Disease 61 4.069
113
P VSC007 Vascular Disease 63 4.040
114
P PHC003 Pheochromocytoma 69 3.998
115
ADR040 Adrenal Gland Pheochromocytoma 46 3.998
116
P LKM062 Leukemia, Acute Lymphoblastic 69 3.900
117
HYP781 Hypoascorbemia 52 3.897
118
CVD001 Covid-19 57 3.872
119
P NSP012 Nasopharyngeal Carcinoma 61 3.872
120
P SPP010 Suppressor of Tumorigenicity 3 51 3.810
121
P HNT016 Huntington Disease 73 3.779
122
KLD004 Keloid Disorder 39 3.753
123
ADN018 Adenoma 59 3.747
124
P CYS018 Cystitis 59 3.727
125
ORL015 Oral Squamous Cell Carcinoma 43 3.717
126
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.685
127
DBT010 Diabetic Neuropathy 54 3.685
128
ART140 Arteries, Anomalies of 53 3.685
129
LPP008 Lipoprotein Quantitative Trait Locus 65 3.685
130
c ACT068 Acute Cystitis 61 3.658
131
HYP060 Hyperinsulinism 54 3.629
132
STM007 Stomatitis 54 3.600
133
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.597
134
P OST002 Osteoporosis 76 3.597
135
c CHR684 Chronic Kidney Disease 69 3.594
136
IMP005 Impotence 52 3.583
137
P DRM053 Dermatitis, Atopic 65 3.565
138
DRM006 Dermatitis 62 3.565
139
P NRP001 Neuropathy 60 3.565
140
P ESP024 Esophagitis 60 3.543
141
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.502
142
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.502
143
c ACT073 Acute Leukemia 58 3.502
144
P LCH002 Lichen Planus 54 3.484
145
ORL013 Oral Lichen Planus 46 3.484
146
SVR004 Severe Combined Immunodeficiency 72 3.484
147
ANX010 Anxiety 70 3.465
148
GLC003 Glucose Intolerance 54 3.431
149
ENT004 Enthesopathy 51 3.411
150
P CRD246 Cardiovascular System Disease 56 3.401
151
P EPL164 Epilepsy 68 3.396
152
c ACT071 Acute Kidney Failure 60 3.396
153
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 3.361
154
MCS002 Mucositis 56 3.357
155
P GST044 Gastritis 55 3.352
156
ANG054 Angina Pectoris 66 3.336
157
P HYP086 Hypothyroidism 69 3.336
158
CRT015 Carotid Artery Occlusion 45 3.332
159
c ACT027 Acute Pancreatitis 60 3.325
160
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.301
161
P LYM118 Lymphoma 67 3.266
162
GST092 Gastroesophageal Reflux 61 3.238
163
47X002 47,xyy 48 3.231
164
c SML038 Small Cell Cancer of the Lung 69 3.230
165
P END044 Endometriosis 62 3.230
166
P GLM040 Glioma Susceptibility 1 71 3.194
167
MLG169 Malignant Astrocytoma 57 3.194
168
P SZR006 Seizure Disorder 70 3.161
169
c HPT073 Hepatitis C Virus 71 3.161
170
P ENC018 Encephalopathy 62 3.161
171
P PNC044 Pancreatitis 61 3.137
172
HGH043 High Grade Glioma 45 3.125
173
GST040 Gastric Adenocarcinoma 67 3.112
174
P DRR001 Diarrhea 55 3.112
175
P PLM037 Pulmonary Hypertension 72 3.089
176
P PRK039 Parkinsonism 55 3.089
177
P FBR017 Fibrosarcoma 56 3.089
178
P PRP019 Peripheral Nervous System Disease 58 3.089
179
c PRC016 Pre-Eclampsia 65 3.070
180
c FNC027 Fanconi Anemia, Complementation Group a 81 3.026
181
P FML011 Familial Adenomatous Polyposis 71 3.014
182
P URN019 Urinary Tract Infection 49 3.014
183
P CNJ013 Conjunctivitis 66 3.014
184
URT010 Ureteral Obstruction 45 3.003
185
P AST005 Asthma 76 2.980
186
ALL006 Allergic Asthma 56 2.976
187
P ART021 Arteriosclerosis 54 2.970
188
P NRV007 Nervous System Disease 67 2.957
189
P SRC025 Sarcoidosis 1 71 2.936
190
P ANP001 Anaplastic Large Cell Lymphoma 61 2.936
191
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.933
192
CYS001 Cystic Fibrosis 78 2.928
193
NRL016 Neural Tube Defects 81 2.895
194
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.881
195
NPH009 Nephrolithiasis 54 2.881
196
ANX004 Anoxia 40 2.857
197
ULC004 Ulcerative Colitis 74 2.857
198
P HRP006 Herpes Simplex 65 2.828
199
TRD006 Tardive Dyskinesia 53 2.816
200
CRB039 Cerebrovascular Disease 66 2.792
201
P MYC084 Mycobacterium Tuberculosis 1 68 2.791
202
HLC007 Helicobacter Pylori Infection 67 2.778
203
P MSC003 Muscular Atrophy 52 2.773
204
END086 End Stage Renal Disease 52 2.773
205
P RTN018 Retinal Disease 53 2.773
206
P RTN024 Retinoblastoma 73 2.745
207
ART016 Aortic Aneurysm 68 2.738
208
P BND020 Bone Disease 59 2.738
209
ANR040 Aneurysm 61 2.738
210
ALL014 Allergic Encephalomyelitis 34 2.738
211
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.730
212
HYP346 Hypotrichosis and Recurrent Skin Vesicles 29 2.730
213
P LTR001 Lateral Sclerosis 58 2.730
214
P AMY004 Amyloidosis 70 2.699
215
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.696
216
P RNV001 Renovascular Hypertension 49 2.696
217
PPL022 Papilloma 53 2.696
218
CHL014 Cholera 62 2.696
219
CHL068 Cholestasis 61 2.696
220
P HRT032 Heart Disease 81 2.677
221
P HYP750 Hypertriglyceridemia, Familial 62 2.654
222
DBT081 Diabetic Encephalopathy 36 2.654
223
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 2.654
224
P EYD002 Eye Disease 57 2.654
225
IRN002 Iron Metabolism Disease 57 2.654
226
RCK004 Rickets 68 2.638
227
CHD004 Chudley-Mccullough Syndrome 48 2.637
228
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.611
229
HRW001 Hair Whorl 35 2.611
230
HPT009 Hepatopulmonary Syndrome 48 2.611
231
MDD011 Mood Disorder 62 2.611
232
DYS015 Dysentery 50 2.607
233
CNS004 Constipation 56 2.596
234
c RNG019 Ring Chromosome 3 19 2.593
235
ALL009 Allergic Conjunctivitis 51 2.590
236
c HYP595 Hypertension, Essential 85 2.570
237
DNT012 Dental Caries 53 2.569
238
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 2.566
239
DBT007 Diabetic Cataract 36 2.566
240
INS001 Insulinoma 59 2.555
241
P KRT007 Keratoconus 50 2.545
242
MST005 Mastitis 53 2.545
243
c ATS007 Autism Spectrum Disorder 72 2.536
244
MTH071 Methane Production 25 2.531
245
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 37 2.521
246
LNG015 Lingual-Facial-Buccal Dyskinesia 47 2.521
247
ALL029 Allergic Disease 59 2.512
248
IRR002 Irritable Bowel Syndrome 65 2.512
249
P ATX030 Ataxia-Telangiectasia 80 2.496
250
TLN003 Telangiectasis 51 2.496
251
PRS021 Prostatic Adenoma 43 2.492
252
ESP021 Esophageal Cancer 83 2.474
253
P MLN007 Male Infertility 56 2.474
254
TRN015 Transient Cerebral Ischemia 63 2.474
255
P ACN011 Acne 57 2.469
256
PRT036 Peritonitis 65 2.452
257
ACT119 Acute Promyelocytic Leukemia 62 2.426
258
INS024 Insulin-Like Growth Factor I 78 2.425
259
CHL065 Cholangiocarcinoma 58 2.425
260
P DNG005 Dengue Virus 56 2.425
261
INT079 Intrahepatic Cholangiocarcinoma 51 2.425
263
P ECL001 Eclampsia 52 2.420
264
PRS045 Prostatic Hypertrophy 53 2.412
265
P EST001 Estrogen-Receptor Positive Breast Cancer 49 2.379
266
VSC003 Visceral Leishmaniasis 55 2.379
267
PPT005 Peptic Ulcer Disease 58 2.379
268
DPR016 Depression 65 2.377
269
P HMR005 Hemorrhoid 49 2.370
270
P BNG032 Benign Mesothelioma 53 2.338
271
P FLL037 Follicular Lymphoma 74 2.336
272
OVR094 Ovarian Epithelial Cancer 39 2.333
273
PST092 Posttransplant Acute Limbic Encephalitis 28 2.328
274
P RSP003 Respiratory Failure 74 2.328
275
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 2.285
276
GLC086 Glucocorticoid-Induced Osteoporosis 43 2.285
277
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.285
278
MYL069 Myeloma, Multiple 77 2.285
279
TXC005 Toxic Shock Syndrome 62 2.285
280
P ADL010 Adult Respiratory Distress Syndrome 71 2.285
281
KRT002 Keratomalacia 55 2.274
282
PRS129 Prostatic Hyperplasia, Benign 49 2.240
283
c HPT003 Hepatitis a 63 2.237
284
END057 Endometrial Cancer 72 2.235
285
P PRK057 Parkinson Disease, Late-Onset 80 2.235
286
TRT001 Teratocarcinoma 42 2.235
287
c HPT016 Hepatitis B 62 2.235
288
P MYC008 Myocarditis 59 2.218
289
PLR008 Pleurisy 50 2.195
290
CTN007 Cutaneous Leishmaniasis 62 2.184
291
P RTN016 Retinal Degeneration 52 2.184
292
CRV040 Cervix Carcinoma 50 2.184
293
SQM002 Squamous Cell Papilloma 46 2.184
294
P HYP076 Hyperthyroidism 53 2.184
295
AMN003 Amnestic Disorder 54 2.184
296
P ATS364 Autism 69 2.173
297
c MST023 Mesothelioma, Malignant 56 2.162
298
P TRM003 Tremor 48 2.162
299
P LRY044 Larynx Cancer 54 2.160
300
MTH009 Mouth Disease 57 2.148
301
ADN027 Adenomyosis 57 2.132
302
P SLP005 Sleep Disorder 61 2.132
303
STR067 Stroke, Ischemic 80 2.108
304
HLX001 Helix Syndrome 48 2.100
305
CHG001 Chagas Disease 66 2.100
306
HND002 Hand, Foot and Mouth Disease 50 2.100
307
BRK010 Burkitt Lymphoma 66 2.077
308
c ATM022 Autoimmune Myocarditis 36 2.077
309
P ALP008 Alopecia 54 2.077
310
c DLT002 Dilated Cardiomyopathy 78 2.077
311
ART004 Aortic Atherosclerosis 47 2.077
312
PLM010 Pulmonary Edema 55 2.077
313
VSC002 Vascular Dementia 60 2.077
314
P TCD001 Tic Disorder 49 2.051
315
c OPT053 Optic Atrophy 1 62 2.041
316
THR024 Thrombosis 56 2.041
317
NTR005 Nutritional Deficiency Disease 61 2.039
318
CLR108 Colorectal Adenoma 64 2.020
319
P MDL005 Medulloblastoma 75 2.020
320
P MYC007 Myocardial Infarction 70 2.020
321
PRM329 Premature Aging 36 2.020
322
INT253 Intestinal Benign Neoplasm 46 2.020
323
P MNC007 Monocytic Leukemia 47 2.020
324
BRN028 Brain Cancer 74 2.020
325
SKN020 Skin Papilloma 40 2.020
326
KLB003 Klebsiella Pneumonia 50 2.020
327
P VNS003 Venous Insufficiency 55 2.014
328
P MYP004 Myopathy 67 2.000
329
P INT070 Intestinal Obstruction 57 2.000
330
c SCN007 Secondary Hyperparathyroidism 51 2.000
331
P HYP069 Hyperparathyroidism 62 2.000
332
CHL123 Chlamydia 58 2.000
333
URM002 Uremia 47 1.975
334
P CND004 Candidiasis 58 1.975
335
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.964
336
CYS036 Cystinosis, Nephropathic 51 1.964
337
P FNC004 Fanconi Syndrome 60 1.964
338
P THL005 Thalassemia 56 1.961
339
ARG004 Argyria 26 1.961
340
SLP001 Sleeping Sickness 56 1.961
341
PPT001 Peptic Esophagitis 52 1.961
342
CHR431 Chronic Venous Insufficiency 48 1.961
343
CHL147 Chlamydia Pneumonia 47 1.947
344
MST020 Mast Cell Activation Syndrome 28 1.947
345
CND006 Candida Glabrata 30 1.947
346
PRT058 Pure Autonomic Failure 58 1.947
347
P PLY019 Polyneuropathy 52 1.911
348
TST044 Testicular Torsion 45 1.907
349
SCK003 Sickle Cell Anemia 74 1.906
350
RST023 Resting Heart Rate, Variation in 40 1.899
351
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.899
352
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.899
353
DGN001 Degenerative Disc Disease 49 1.899
354
BCK006 Back Pain 47 1.899
355
c DWL002 Dowling-Degos Disease 1 58 1.892
356
PST011 Pustulosis of Palm and Sole 52 1.892
357
TST014 Testicular Cancer 52 1.892
358
c CNT035 Central Nervous System Disease 54 1.892
359
KRT019 Keratitis, Hereditary 66 1.836
360
P PSR002 Psoriasis 63 1.836
361
CHR074 Choriocarcinoma 46 1.836
362
PNC129 Pancreatic Adenocarcinoma 65 1.836
363
P INT143 Interstitial Cystitis 60 1.836
364
THY030 Thyroid Gland Disease 50 1.836
365
DCB001 Decubitus Ulcer 62 1.836
366
PTT037 Pituitary Tumors 44 1.836
367
DXR001 Doxorubicin Induced Cardiomyopathy 32 1.836
368
c EXD008 Exudative Vitreoretinopathy 1 71 1.834
369
GST050 Gastrointestinal System Disease 55 1.834
370
CNT047 Contact Dermatitis 57 1.834
371
P CHR345 Chronic Pain 50 1.834
372
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 1.833
373
PLM001 Pulmonary Tuberculosis 69 1.833
374
CMB007 Combined Immunodeficiency 57 1.833
375
P HPT021 Hepatitis 69 1.792
376
DMY004 Demyelinating Disease 50 1.777
377
P ENC004 Encephalitis 61 1.777
378
CHR100 Chronic Ulcer of Skin 57 1.765
379
MLR004 Malaria 80 1.765
380
MNN043 Meningioma, Familial 79 1.765
381
OBS082 Obstructive Nephropathy 41 1.765
382
SCR001 Secretory Meningioma 40 1.765
383
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.765
384
MCR013 Microphthalmia 60 1.765
385
ANP005 Anaplastic Astrocytoma 57 1.765
386
P KDN017 Kidney Cancer 61 1.765
387
BRN002 Bronchiolitis 57 1.765
388
SPN021 Spinal Meningioma 50 1.765
389
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 1.743
390
GLM044 Glomerular Disease 35 1.715
391
c SYS001 Systemic Lupus Erythematosus 87 1.715
392
ALC007 Alcohol Dependence 66 1.715
393
HMN044 Human Immunodeficiency Virus Type 1 78 1.715
394
PRP027 Peripheral Vascular Disease 71 1.715
395
PLL012 Pollen Allergy 45 1.715
396
EST002 Estrogen-Receptor Negative Breast Cancer 45 1.715
397
MDD018 Middle East Respiratory Syndrome 44 1.715
398
P ALP009 Alopecia Areata 59 1.715
399
P HYP098 Hypereosinophilic Syndrome 66 1.715
400
PNT038 Peanut Allergy 46 1.715
401
TRY001 Trypanosomiasis 50 1.715
402
SNS003 Sensory Peripheral Neuropathy 52 1.715
403
P INT068 Intestinal Disease 53 1.715
404
P LPS002 Liposarcoma 64 1.715
405
P RCT021 Rectum Cancer 54 1.715
406
HMP009 Haemophilus Influenzae 41 1.715
408
STT001 Status Epilepticus 59 1.692
409
c MJR022 Major Affective Disorder 8 38 1.649
410
c MJR024 Major Affective Disorder 9 41 1.649
411
P BPL003 Bipolar Disorder 56 1.649
412
c ACT004 Acute Diarrhea 40 1.649
413
SCR003 Secretory Diarrhea 35 1.649
414
CLN044 Colon Adenoma 44 1.649
415
CLN019 Colonic Disease 47 1.649
416
GST052 Gestational Choriocarcinoma 35 1.649
417
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.649
418
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.613
419
P SCK005 Sickle Cell Disease 56 1.599
420
c ACT134 Acute Liver Failure 59 1.581
421
c RTN047 Retinitis Pigmentosa 18 46 1.581
423
P PLY014 Polycystic Kidney Disease 69 1.581
424
ILT001 Ileitis 48 1.581
425
P FTL001 Fetal Alcohol Syndrome 55 1.581
426
LMY014 Leiomyoma, Uterine 56 1.581
427
c PRG020 Paragangliomas 3 39 1.581
428
c HNT011 Huntington Disease-Like 3 34 1.581
429
c HYD064 Hydrocephalus, Congenital, 1 51 1.581
430
LMY002 Leiomyoma 51 1.581
431
ACT003 Acute Kidney Tubular Necrosis 46 1.581
432
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.581
433
LRN003 Learning Disability 49 1.581
434
CRD005 Cardia Cancer 38 1.581
435
ALC006 Alcoholic Hepatitis 61 1.581
436
END041 Endometrial Adenocarcinoma 64 1.581
437
KRT009 Keratosis 53 1.581
438
P RNL015 Renal Hypertension 45 1.581
439
P HYD006 Hydrocephalus 61 1.581
440
P CYS039 Cystic Kidney Disease 53 1.581
441
SPN035 Spindle Cell Sarcoma 54 1.527
442
SRC014 Sarcoma 65 1.527
443
TTN003 Tetanus 65 1.527
444
P INS002 in Situ Carcinoma 53 1.527
445
GLS018 Glass Syndrome 61 1.523
446
RHB024 Rhabdomyosarcoma 2 67 1.523
447
c HYP724 Hyperlipoproteinemia, Type Iii 67 1.523
448
P THR015 Thrombophilia 51 1.523
449
AND005 Androgen Insensitivity Syndrome, Mild 21 1.523
450
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.523
451
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.507
452
P VTR007 Vitreoretinopathy 46 1.507
453
P RTT002 Rett Syndrome 79 1.507
454
CLF027 Cleft Palate, Isolated 64 1.507
455
P MLT020 Multiple Sclerosis 79 1.507
456
c BTT014 Beta-Thalassemia 72 1.507
457
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.507
458
ART074 Aortic Dissection 53 1.507
459
P OMP004 Omphalocele 48 1.507
460
LPT014 Leptin Deficiency or Dysfunction 78 1.507
461
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.507
462
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.507
463
INT051 Intussusception 52 1.507
465
RNL078 Renal Dysplasia 46 1.507
466
ADN011 Adenoid Cystic Carcinoma 68 1.507
467
CRH001 Crohn's Disease 80 1.507
468
P LPS004 Lupus Erythematosus 61 1.507
469
P PLM034 Pulmonary Emphysema 58 1.507
470
FDL002 Food Allergy 47 1.507
471
TRC005 Tracheal Stenosis 43 1.507
472
P CRN024 Corneal Disease 44 1.507
473
RTN020 Retinal Vascular Disease 46 1.507
474
c ATM011 Autoimmune Hepatitis 63 1.507
475
P BRS053 Breast Fibroadenoma 49 1.507
476
ATN004 Autonomic Neuropathy 42 1.507
477
PLP001 Pulpitis 48 1.507
478
ART017 Aortic Disease 49 1.507
479
AMN001 Amenorrhea 54 1.507
480
OLG001 Oligospermia 45 1.507
481
P PTS002 Ptosis 52 1.507
482
P HYP121 Hypoalphalipoproteinemia 43 1.507
483
ACT114 Acute Myeloblastic Leukemia Without Maturation 26 1.507
484
EXN003 Exencephaly 30 1.507
485
DSS032 Disease by Infectious Agent 55 1.502
486
URL001 Urolithiasis 46 1.447
487
PLY100 Polyploidy 36 1.428
488
DFF005 Diffuse Large B-Cell Lymphoma 54 1.428
489
BTT017 Beta-Thalassemia Major 51 1.428
490
IMM167 Immune Deficiency Disease 78 1.428
491
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.428
492
CVT001 Cavitary Optic Disc Anomalies 37 1.428
493
P RHB003 Rhabdomyosarcoma 66 1.428
494
CRC021 Carcinosarcoma 64 1.428
495
P UNP013 Uniparental Disomy of Chromosome 1 22 1.428
496
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.428
497
PGM003 Pigmentation Disease 45 1.428
498
VLV032 Vulva Cancer 60 1.428
499
URT001 Urethritis 53 1.428
500
IRN001 Iron Deficiency Anemia 58 1.428
501
JPN002 Japanese Encephalitis 61 1.428
502
DSS009 Disseminated Intravascular Coagulation 57 1.428
503
P TRC031 Trichorhinophalangeal Syndrome 38 1.428
504
KDN013 Kidney Hypertrophy 34 1.428
505
P FBR031 Febrile Seizures 52 1.428
506
HVY002 Heavy Metal Poisoning 22 1.428
507
GNT019 Giant Cell Myocarditis 29 1.428
508
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 1.390
509
GST045 Gastroenteritis 58 1.390
510
P SMP003 Simpson-Golabi-Behmel Syndrome 49 1.343
511
STR077 Streptococcal Toxic-Shock Syndrome 35 1.343
512
c LKM070 Leukemia, Acute Monocytic 56 1.343
513
WRN001 Werner Syndrome 69 1.343
514
THY029 Thyroid Carcinoma 51 1.343
515
c ACT075 Acute Myocardial Infarction 56 1.343
516
OCL006 Ocular Hypertension 53 1.343
517
CHC001 Chickenpox 57 1.343
518
P MVM001 Movement Disease 61 1.343
519
c VRL010 Viral Hepatitis 53 1.343
520
P PLY018 Polycythemia 56 1.343
521
P SML016 Small Intestine Cancer 48 1.343
522
CRY005 Cryptococcosis 60 1.343
523
THR004 Thrombocytosis 53 1.343
524
IRR003 Irritant Dermatitis 47 1.343
525
LVR012 Liver Cirrhosis 63 1.343
526
ALC011 Alcoholic Neuropathy 34 1.343
527
ACT200 Acute Monoblastic Leukemia 41 1.343
528
P RTN008 Retinitis Pigmentosa 80 1.331
529
CLR109 Colorectal Adenocarcinoma 50 1.331
530
NRR001 Neuroretinitis 42 1.331
531
AVN001 Avian Influenza 61 1.331
532
RTN023 Retinitis 46 1.331
533
P SYP003 Syphilis 59 1.331
534
VLV011 Vulvovaginal Candidiasis 49 1.325
535
P ACT105 Acute Mountain Sickness 52 1.306
536
HMC014 Homocysteinemia 52 1.248
537
OTT002 Otitis Media 71 1.248
538
MYL009 Myelodysplastic Syndrome 67 1.248
539
P SLM003 Salmonellosis 54 1.248
540
c PRD040 Periodontitis, Chronic 52 1.248
541
TNG007 Tongue Carcinoma 52 1.248
542
PRT037 Pertussis 65 1.248
543
EXT007 Extracutaneous Mastocytoma 38 1.248
544
MCC002 Mucocutaneous Leishmaniasis 47 1.248
545
MST004 Mast Cell Neoplasm 42 1.248
546
P ART023 Arthropathy 61 1.248
547
CLL014 Cll/sll 45 1.248
548
CMM005 Common Cold 56 1.248
549
P UVT001 Uveitis 57 1.248
550
LWC001 Low Compliance Bladder 45 1.248
551
TRN018 Transitional Cell Carcinoma 56 1.248
552
PRM013 Premature Menopause 58 1.248
553
P TRT010 Teratoma 51 1.248
554
ANG005 Anogenital Venereal Wart 56 1.248
555
P BNC003 Bone Cancer 58 1.248
556
APH001 Aphthous Stomatitis 58 1.248
557
SNL007 Senile Cataract 40 1.248
558
APC006 Apc-Associated Polyposis Conditions 21 1.248
559
STT009 Sutton Disease 2 29 1.248
560
P ORL007 Oral Cavity Cancer 51 1.248
561
END072 Endotheliitis 36 1.209
562
c BLD140 Blood Group, I System 46 1.209
563
c PRS136 Prostate Cancer, Hereditary, 6 33 1.209
564
c PRS130 Prostate Cancer, Hereditary, 8 32 1.209
565
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 1.209
566
ACT098 Acute Erythroid Leukemia 55 1.204
567
P PNM007 Pneumonia 67 1.204
568
PRP083 Porphyria, Acute Intermittent 65 1.197
569
ENT011 Enterocolitis 55 1.197
570
P TYR004 Tyrosinemia 50 1.197
571
MNG007 Manganese Poisoning 28 1.197
572
PLC002 Plica Syndrome 35 1.197
573
SYN007 Synovitis 55 1.197
574
P PRP029 Porphyria 60 1.197
575
ACT228 Acute Radiation Syndrome 30 1.140
576
HRN029 Hearing Loss, Noise-Induced 37 1.140
577
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 1.140
578
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.140
579
ACQ007 Acquired Immunodeficiency Syndrome 59 1.140
580
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.140
581
BCT004 Bacteriuria 47 1.140
582
MNN017 Mononeuropathy 41 1.140
583
P AGG001 Aggressive Periodontitis 55 1.140
584
P FML187 Familial Hypertension 34 1.140
585
BRN056 Bronchopulmonary Dysplasia 56 1.140
586
HYP457 Hypertrophic Scars 42 1.135
587
FNG017 Fungal Infectious Disease 54 1.135
588
HYP056 Hypoglycemia 65 1.135
589
c PNS012 Paine Syndrome 60 1.064
590
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.064
591
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.064
592
PRT038 Protein-Energy Malnutrition 53 1.031
593
P BRN022 Bronchiectasis 60 1.031
594
NRT004 Neuritis 53 1.027
595
CNG034 Congestive Heart Failure 69 1.027
596
c AMY088 Amyotrophic Lateral Sclerosis 3 31 1.013
597
P CLC063 Celiac Disease 1 66 1.013
598
AND014 Androgenic Alopecia 47 1.013
599
P CRP001 Carpal Tunnel Syndrome 66 1.013
600
THY065 Thyroid Carcinoma, Papillary, with Papillary Renal Neoplasia 23 1.013
601
ZKF001 Zika Fever 52 1.013
602
P SPN046 Spinal Muscular Atrophy 63 1.013
603
TST015 Testicular Disease 42 1.013
604
DPH001 Diphtheria 59 1.013
605
P END033 Endocarditis 58 1.013
606
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.993
607
c MSM022 Mismatch Repair Cancer Syndrome 1 70 0.993
608
FLL041 Follicular Lymphoma 1 45 0.993
609
SCL046 Scalp-Ear-Nipple Syndrome 49 0.993
610
c HYP525 Hypotrichosis 2 36 0.993
611
ADL002 Adult Syndrome 70 0.993
612
ACT029 Acute Interstitial Pneumonia 59 0.993
613
IDP011 Idiopathic Interstitial Pneumonia 59 0.993
614
LYM019 Lymphosarcoma 46 0.993
615
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.989
616
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.989
617
c SRC023 Sarcoidosis 2 44 0.989
618
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.989
619
AMD002 Amed Syndrome, Digenic 37 0.989
620
49X006 49, Xxxxy Syndrome 40 0.989
621
CHL079 Children's Interstitial Lung Disease 26 0.989
622
c ATR087 Atrial Standstill 1 74 0.983
623
HMR023 Hemorrhagic Cystitis 43 0.983
624
P PRG002 Progesterone-Receptor Positive Breast Cancer 32 0.983
625
ACT149 Acetaminophen Metabolism 35 0.983
626
PLM031 Poliomyelitis 63 0.983
627
RYN005 Raynaud Phenomenon 45 0.983
628
PRN035 Perniosis 27 0.983
629
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.898
630
MSC007 Muscle Hypertrophy 64 0.898
631
SYS004 Systemic Mastocytosis 63 0.898
632
P MST009 Mastocytosis 64 0.898
633
P GRV001 Graves' Disease 55 0.898
634
c TYP008 Type 1 Diabetes Mellitus 70 0.847
635
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.847
636
NND010 Nondisjunction 34 0.847
637
FTL006 Fetal Alcohol Spectrum Disorder 43 0.847
638
KWS002 Kawasaki Disease 65 0.847
639
P CRC039 Coarctation of Aorta 46 0.847
640
ASP008 Aspiration Pneumonitis 42 0.847
641
P HMC002 Homocystinuria 53 0.847
642
P VSC011 Vasculitis 61 0.847
643
MLG079 Malignant Pleural Mesothelioma 42 0.847
644
P HYP061 Hypertrophic Cardiomyopathy 69 0.847
645
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.847
646
CRT004 Carotid Artery Thrombosis 39 0.847
647
CRB090 Cerebral Hypoxia 42 0.847
648
PRN019 Perinatal Necrotizing Enterocolitis 60 0.847
649
P OVR082 Overgrowth Syndrome 49 0.803
650
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.803
651
OST024 Osteoporosis-Pseudoglioma Syndrome 60 0.803
652
KPS004 Kaposi Sarcoma 77 0.803
653
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.803
654
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 0.803
655
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.803
656
HYP005 Hypokalemia 55 0.803
657
AML001 Amelanotic Melanoma 37 0.803
658
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.803
659
P DMN002 Dementia 66 0.803
660
DNG002 Dengue Hemorrhagic Fever 60 0.803
661
P DDN001 Duodenal Ulcer 53 0.803
662
SCH014 Schistosomiasis 56 0.803
663
GRD001 Giardiasis 46 0.803
664
PLC008 Placenta Disease 49 0.803
665
EMB004 Embryonal Carcinoma 56 0.803
666
c RNG021 Ring Chromosome 5 20 0.803
667
c RNG023 Ring Chromosome 7 43 0.803
668
PRN029 Parainfluenza Virus Type 3 32 0.803
669
c BCT007 Bacterial Meningitis 55 0.695
670
MLG164 Malignant Epithelial Tumor of Ovary 24 0.695
671
c INH030 Inherited Retinal Disorder 28 0.695
672
ATS010 Autosomal Recessive Disease 42 0.695
673
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.695
674
CHK001 Chikungunya 60 0.695
675
c CHR711 Chronic Asthma 41 0.695
676
GLC106 Glucocorticoid Resistance, Generalized 48 0.695
677
P ASP006 Aspergillosis 72 0.695
678
SKN019 Skin Melanoma 71 0.695
679
GSG001 Gas Gangrene 52 0.695
680
CHR066 Chronic Fatigue Syndrome 60 0.695
681
FND002 Fundus Dystrophy 55 0.695
682
P ALC033 Alcohol Use Disorder 61 0.695
683
P OPT006 Optic Nerve Disease 58 0.695
684
CLR030 Clear Cell Renal Cell Carcinoma 54 0.695
685
CHL061 Childhood Leukemia 47 0.695
686
DNG003 Dengue Disease 65 0.695
687
GST033 Gestational Diabetes 61 0.695
688
P PRN023 Prion Disease 60 0.695
689
ALC005 Alcoholic Pancreatitis 38 0.695
690
GNG013 Gingivitis 59 0.695
691
PRN014 Paronychia 50 0.695
692
ADS004 Aids Dementia Complex 40 0.695
693
P NRF002 Neurofibromatosis 57 0.695
694
LKP003 Leukoplakia 39 0.695
695
c RNG015 Ring Chromosome 2 22 0.695
696
c HMC039 Hemochromatosis, Type 1 73 0.568
697
MTC005 Mitochondrial Metabolism Disease 45 0.568
698
c SCL052 Scleroderma, Familial Progressive 61 0.568
699
P LPR021 Leprosy 3 71 0.568
700
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.568
701
PPL052 Papillomatosis, Confluent and Reticulated 34 0.568
702
c MGR028 Migraine with or Without Aura 1 64 0.568
703
BRG013 Buerger Disease 57 0.568
704
INV001 Invasive Aspergillosis 49 0.568
705
P STR022 Stargardt Disease 61 0.568
706
BCT021 Bacterial Sepsis 43 0.568
707
P MCL001 Mucolipidosis 49 0.568
708
SXL003 Sexual Disorder 49 0.568
709
STL007 Steel Syndrome 42 0.568
710
TTT001 Tatton-Brown-Rahman Syndrome 46 0.568
711
P MJR001 Major Depressive Disorder 68 0.568
712
c HNT004 Huntington Disease-Like 2 52 0.568
713
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.568
714
HPT004 Hepatic Coma 43 0.568
715
TRC020 Tracheitis 43 0.568
716
LCN001 Lice Infestation 41 0.568
717
VLK001 Volkmann Contracture 23 0.568
718
CRN030 Coronary Stenosis 50 0.568
719
P ATR005 Atrophic Gastritis 50 0.568
720
HPT022 Hepatoblastoma 54 0.568
721
TRC003 Trichomoniasis 53 0.568
722
CHL067 Cholecystitis 60 0.568
723
VCC001 Vaccinia 47 0.568
724
MNT002 Mental Depression 57 0.568
725
c SBC007 Subacute Thyroiditis 43 0.568
726
P THY032 Thyroiditis 57 0.568
727
FBR047 Fibromyalgia 58 0.568
728
GRN004 Granulomatous Amebic Encephalitis 30 0.568
729
TCK001 Tick-Borne Encephalitis 59 0.568
730
CHL004 Cholelithiasis 49 0.568
731
TNS005 Tonsillitis 57 0.568
732
P OTS001 Otosclerosis 49 0.568
733
VRC001 Varicocele 48 0.568
734
ASP003 Aseptic Meningitis 50 0.568
735
CGH001 Cough Variant Asthma 34 0.568
736
HPT019 Hepatic Encephalopathy 59 0.568
737
RTC003 Root Caries 32 0.568
738
CRN027 Corneal Neovascularization 47 0.568
739
GLS001 Gliosarcoma 64 0.568
740
STM006 Stomach Disease 47 0.568
741
SPT004 Septic Arthritis 58 0.568
742
BRS051 Breast Disease 58 0.568
743
NWC001 Newcastle Disease 47 0.568
744
HRP001 Herpangina 43 0.568
745
PLM033 Pulmonary Embolism 58 0.568
746
ACN019 Acanthamoeba Keratitis 30 0.568
747
HNS001 Hansen's Disease 32 0.568
748
PRS063 Paresthesia 39 0.568
749
BLR013 Biliary Tract Cancer 43 0.568
750
CHR178 Chromosomal Triplication 34 0.568
751
DSS012 Disseminated Infection with Mycobacterium Avium Complex 19 0.568
752
MSL001 Measles 61 0.568
753
c CLC046 Celiac Disease 5 21 0.459
754
c THR092 Thrombophilia Due to Thrombin Defect 74 0.459
755
BWN001 Bowen-Conradi Syndrome 53 0.459
756
P PRV006 Pervasive Developmental Disorder 52 0.459
757
CHL159 Childhood-Onset Asthma 30 0.459
758
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.459
759
P PRC031 Preeclampsia/eclampsia 1 43 0.459
760
P ANR048 Aniridia 1 64 0.459
761
SPR126 Superior Semicircular Canal Dehiscence 41 0.459
762
ANT039 Antisynthetase Syndrome 55 0.459
763
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.459
764
P OPT009 Optic Neuritis 57 0.459
765
PLM012 Pulmonary Sarcoidosis 53 0.459
766
INT066 Interstitial Lung Disease 60 0.459
767
ACT011 Acute Contagious Conjunctivitis 42 0.459
768
DST006 Diastolic Heart Failure 45 0.459
769
c HMG029 Hemoglobin Se Disease 40 0.459
770
P SCH015 Schizophrenia 74 0.445
771
P PRG139 Progeroid Syndrome 27 0.401
772
P HRD217 Hereditary Optic Neuropathy 36 0.401
773
STN013 Stenotrophomonas Maltophilia Infection 26 0.401
774
P HRD084 Hereditary Cerebral Amyloid Angiopathy 30 0.401
775
THY128 Thyroid Tumor 35 0.401
776
c STC015 Stickler Syndrome, Type I 51 0.401
777
P MCH002 Machado-Joseph Disease 62 0.401
778
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.401
779
AMN014 Aminopterin Syndrome Sine Aminopterin 32 0.401
780
c GLL024 Gallbladder Disease 1 52 0.401
781
P MYS003 Myasthenia Gravis 68 0.401
782
FRG010 Fragile X Tremor/ataxia Syndrome 44 0.401
783
MND023 Mend Syndrome 49 0.401
784
P FRG001 Fragile X Syndrome 70 0.401
785
CRD132 Cardiac Conduction Defect 60 0.401
786
RTN017 Retinal Detachment 60 0.401
787
OBS002 Obsessive-Compulsive Disorder 68 0.401
788
c PRT059 Parietal Foramina 1 32 0.401
789
PHS027 Phosphoglycoprotein 1 15 0.401
790
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.401
791
c PGT007 Paget Disease of Bone 3 38 0.401
792
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.401
793
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.401
794
ADR016 Adrenal Cortical Carcinoma 62 0.401
795
FDB001 Foodborne Botulism 55 0.401
796
PRP080 Peripheral Artery Disease 54 0.401
797
P SLP006 Sleep Apnea 69 0.401
798
MNT001 Mantle Cell Lymphoma 67 0.401
799
LMB062 Limb Ischemia 55 0.401
800
CYN002 Cyanosis, Transient Neonatal 43 0.401
801
INF034 Infective Endocarditis 54 0.401
802
ISC015 Ischemic Colitis 43 0.401
803
CMP034 Complete Androgen Insensitivity Syndrome 55 0.401
804
HMN047 Human Cytomegalovirus Infection 57 0.401
805
APH002 Aphasia 56 0.401
806
LNG095 Lung Abscess 51 0.401
807
P LYM033 Lymphoproliferative Syndrome 59 0.401
808
FSR001 Fusariosis 45 0.401
809
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.401
810
EXR010 Exercise-Induced Bronchoconstriction 34 0.401
811
KRN002 Kearns-Sayre Syndrome 63 0.401
812
c FBR075 Febrile Seizures, Familial, 2 32 0.401
813
P FNC044 Fanconi Anemia, Complementation Group C 56 0.401
814
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.401
815
KLD003 Keloid Formation 34 0.401
816
IGR001 Ige Responsiveness, Atopic 59 0.401
817
c BRN108 Branchiootic Syndrome 1 62 0.401
818
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.401
819
P MCR129 Microvascular Complications of Diabetes 1 68 0.401
820
LYM143 Lymphoma, Non-Hodgkin, Familial 75 0.401
821
PRD041 Periodic Fever, Menstrual Cycle-Dependent 24 0.401
822
CHR515 Chronic Atrial and Intestinal Dysrhythmia 43 0.401
823
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.401
824
c CHL119 Cholangitis, Primary Sclerosing 58 0.401
825
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.401
826
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.401
827
BRL010 Buruli Ulcer 45 0.401
829
SNL009 Senile Plaque Formation 29 0.401
830
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.401
831
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.401
832
HYP784 Hypogonadism, Male 43 0.401
833
c ART112 Arthrogryposis, Distal, Type 10 34 0.401
834
TBC004 Tobacco Addiction 63 0.401
835
URT049 Urate Oxidase, Pseudogene 24 0.401
836
c FBR073 Febrile Seizures, Familial, 1 40 0.401
838
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.401
839
PNG002 Pain Agnosia 51 0.401
840
HPT067 Hepatocellular Adenoma 43 0.401
841
FRG008 Fragile X-Associated Tremor/ataxia Syndrome 44 0.401
842
P LCT002 Lactose Intolerance 52 0.401
844
TRC013 Trichostrongylosis 21 0.401
845
c CHR095 Chronic Progressive External Ophthalmoplegia 49 0.401
846
DRM011 Dermatophytosis 52 0.401
847
P RBL001 Rubella 58 0.401
848
MTC004 Mitochondrial Encephalomyopathy 42 0.401
849
EXP004 Exophthalmos 51 0.401
850
AMB001 Amebiasis 57 0.401
851
P CHL066 Cholangitis 52 0.401
852
SML019 Smallpox 55 0.401
853
P PRD021 Periodic Paralysis 41 0.401
854
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 39 0.401
855
PRD003 Periodontosis 25 0.401
856
ADR004 Adrenal Cortical Adenocarcinoma 38 0.401
857
IGG001 Iga Glomerulonephritis 50 0.401
858
ALL010 Allergic Contact Dermatitis 56 0.401
859
CNT033 Central Nervous System Cancer 47 0.401
860
P LCT001 Lactic Acidosis 51 0.401
861
P CRV031 Cervical Adenocarcinoma 48 0.401
862
P LYN001 Lynch Syndrome 76 0.401
863
PYD002 Pyoderma 50 0.401
864
GLC008 Glucose Metabolism Disease 40 0.401
865
OVR059 Ovary Adenocarcinoma 49 0.401
866
OVR063 Overnutrition 42 0.401
867
APP008 Appendicitis 62 0.401
868
ANT024 Anthrax Disease 58 0.401
869
BRN009 Burning Mouth Syndrome 51 0.401
870
P NGH001 Night Blindness 52 0.401
871
NSP002 Nasopharyngitis 45 0.401
872
c MCR112 Microvascular Complications of Diabetes 2 42 0.401
873
DNG001 Dengue Shock Syndrome 40 0.401
874
P MGR003 Migraine with Aura 52 0.401
875
DRY001 Dry Eye Syndrome 50 0.401
876
OST003 Osteonecrosis 61 0.401
877
P NTR004 Neutropenia 63 0.401
878
RTN003 Retinal Ischemia 49 0.401
879
CRN017 Coronary Thrombosis 46 0.401
880
PCD001 Pica Disease 38 0.401
881
OPP002 Opportunistic Mycosis 39 0.401
882
SKN005 Skin Atrophy 41 0.401
883
ADT003 Auditory System Disease 49 0.401
884
P DMN001 Diamond-Blackfan Anemia 71 0.401
885
c BSL007 Basal Cell Carcinoma 68 0.401
886
P SCL009 Sclerosing Cholangitis 48 0.401
887
ORC001 Orchitis 44 0.401
888
RTR008 Root Resorption 44 0.401
889
P HMR003 Hemorrhagic Disease 59 0.401
890
HPT014 Hepatorenal Syndrome 49 0.401
891
P MCR010 Microcephaly 60 0.401
892
RBS001 Rabies 58 0.401
893
MCR018 Microcytic Anemia 47 0.401
894
HYP006 Hypertensive Heart Disease 49 0.401
895
FCH001 Fuchs' Endothelial Dystrophy 50 0.401
896
c VRL005 Viral Pneumonia 53 0.401
897
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.401
898
PRM020 Premenstrual Tension 39 0.401
899
PRP030 Purpura 54 0.401
900
CRB025 Carbohydrate Metabolic Disorder 40 0.401
901
P NRV006 Nervous System Cancer 48 0.401
902
ERL001 Early Myoclonic Encephalopathy 62 0.401
903
P CRN025 Corneal Dystrophy 49 0.401
904
P DYS007 Dyskeratosis Congenita 67 0.401
905
PLG002 Plague 58 0.401
906
P GLM007 Glomerulonephritis 60 0.401
907
NRL002 Neurilemmomatosis 52 0.401
908
ORL005 Oral Candidiasis 56 0.401
909
ERY004 Erysipelas 47 0.401
910
DNT008 Denture Stomatitis 35 0.401
911
GST037 Gastroparesis 52 0.401
912
DBT002 Diabetic Autonomic Neuropathy 41 0.401
913
P URT039 Urticaria 58 0.401
914
RHM001 Rheumatic Fever 59 0.401
915
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.401
916
ANK001 Ankylosis 51 0.401
917
HYP080 Hypogonadism 50 0.401
918
P LMY004 Leiomyosarcoma 62 0.401
919
ALB002 Albinism 47 0.401
920
c ALM001 Al Amyloidosis 54 0.401
921
GNT003 Genital Herpes 54 0.401
922
HRP004 Herpes Zoster 61 0.401
923
CCN001 Cocaine Dependence 48 0.401
924
c LKM005 Leukemia, T-Cell, Chronic 34 0.401
925
PRR013 Prurigo Nodularis 37 0.401
926
HDN002 Head Injury 44 0.401
927
P MTC069 Mitochondrial Disorders 57 0.401
928
MYT011 Myotonia 39 0.401
929
CTR027 Cataract-Glaucoma 22 0.401
930
P INH011 Inherited Bone Marrow Failure Syndromes 32 0.401
Content
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