Search results for Acetaminophen

1594 hits were found for Acetaminophen

# Family MCID Name MIFTS Score
1
ACT149 Acetaminophen Metabolism 37 34.336
2
PRC051 Paracetamol Poisoning 29 21.286
3
c ACT134 Acute Liver Failure 57 17.462
4
PNG002 Pain Agnosia 51 14.122
5
OST012 Osteoarthritis 77 10.155
6
P LVR013 Liver Disease 68 10.047
7
c EPS039 Episodic Pain Syndrome, Familial, 1 42 9.948
8
c PNS012 Paine Syndrome 60 9.809
9
BCK006 Back Pain 43 7.751
10
c MGR028 Migraine with or Without Aura 1 63 7.589
11
P HDC001 Headache 56 7.393
12
48X005 48,xyyy 39 7.264
13
P CHR345 Chronic Pain 50 6.285
14
P PTN014 Patent Ductus Arteriosus 1 59 6.073
15
P ALC033 Alcohol Use Disorder 67 5.961
16
ALC007 Alcohol Dependence 65 5.782
17
HPT004 Hepatic Coma 43 5.432
18
P AST005 Asthma 75 5.203
19
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 5.172
20
CNS004 Constipation 56 5.156
21
P ENC018 Encephalopathy 62 4.987
22
HPT019 Hepatic Encephalopathy 59 4.938
23
SBC016 Subacute Delirium 42 4.618
24
TNS005 Tonsillitis 57 4.575
25
ALL029 Allergic Disease 61 4.528
26
c ACT071 Acute Kidney Failure 60 4.482
27
AGN016 Aging 53 4.452
28
CMM005 Common Cold 55 4.357
29
OCL069 Ocular Motor Apraxia 57 4.347
30
MTB004 Metabolic Acidosis 48 4.297
31
P TRN020 Turner Syndrome 67 4.111
32
PLP001 Pulpitis 48 4.089
33
OST062 Osteoarthritis with Mild Chondrodysplasia 46 4.036
34
c HPT003 Hepatitis a 63 3.947
35
P EXN002 Exanthem 58 3.915
36
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.898
37
RHB024 Rhabdomyosarcoma 2 65 3.894
38
P HPT021 Hepatitis 68 3.864
39
P KDN018 Kidney Disease 71 3.795
40
FTT001 Fatty Liver Disease 61 3.715
41
ENT004 Enthesopathy 51 3.697
42
ADL002 Adult Syndrome 69 3.695
43
P ART022 Arthritis 70 3.587
44
P MTH007 Methemoglobinemia 46 3.530
45
ING001 Inguinal Hernia 59 3.525
46
FBR047 Fibromyalgia 57 3.519
47
P ANR048 Aniridia 1 66 3.500
48
c PRC016 Pre-Eclampsia 64 3.472
49
P NRP001 Neuropathy 59 3.450
50
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 3.437
51
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.437
52
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 3.437
53
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.437
54
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 3.437
55
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.437
56
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 3.437
57
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 3.437
58
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.437
59
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.437
60
DBT010 Diabetic Neuropathy 54 3.340
61
P URT039 Urticaria 57 3.324
62
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 39 3.240
63
P ATT013 Attention Deficit-Hyperactivity Disorder 65 3.195
64
DWN001 Down Syndrome 70 3.139
65
ILS001 Ileus 49 3.094
66
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 3.055
67
OPD001 Opioid Abuse 44 3.050
68
CRH001 Crohn's Disease 80 3.043
69
ANT039 Antisynthetase Syndrome 55 2.907
70
P VSC007 Vascular Disease 62 2.895
71
STR067 Stroke, Ischemic 79 2.895
72
P ECL001 Eclampsia 52 2.883
73
P CTR002 Cataract 59 2.865
74
P SCK005 Sickle Cell Disease 56 2.863
75
P LCT001 Lactic Acidosis 50 2.816
76
CYT002 Cytokine Deficiency 43 2.812
77
P THR014 Thrombocytopenia 66 2.805
78
SPN186 Spinal Cord Injury 60 2.792
79
P BCL017 B-Cell Lymphoma 57 2.761
80
CLF027 Cleft Palate, Isolated 64 2.757
81
SVR097 Severe Cutaneous Adverse Reaction 68 2.757
82
P SZR006 Seizure Disorder 69 2.746
83
LVR012 Liver Cirrhosis 62 2.695
84
P CLL015 Collagen Disease 47 2.673
85
ATX019 Ataxia with Vitamin E Deficiency 44 2.671
86
P RHN004 Rhinitis 56 2.629
87
P ATS364 Autism 72 2.617
88
CRB039 Cerebrovascular Disease 65 2.609
89
P MYC007 Myocardial Infarction 69 2.593
90
BLR008 Bilirubin Metabolic Disorder 57 2.529
91
P RHM011 Rheumatoid Arthritis 81 2.521
92
DYS073 Dysphagia 53 2.518
93
P SBS003 Substance Abuse 54 2.512
94
P SLP006 Sleep Apnea 69 2.512
95
c VRL010 Viral Hepatitis 52 2.503
96
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 41 2.498
97
RYS001 Reye Syndrome 49 2.474
98
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.458
99
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.450
100
P ANG015 Angioedema 56 2.438
101
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 2.433
102
P PNC044 Pancreatitis 61 2.431
103
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 2.404
104
HYP005 Hypokalemia 55 2.403
105
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.402
106
P MCR129 Microvascular Complications of Diabetes 1 67 2.401
107
CHL068 Cholestasis 61 2.397
108
P RSP003 Respiratory Failure 73 2.391
109
ACT003 Acute Kidney Tubular Necrosis 46 2.388
110
P FBR031 Febrile Seizures 52 2.374
111
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.364
112
EPT021 Epithelial Recurrent Erosion Dystrophy 45 2.357
113
PHR003 Pharyngitis 57 2.354
114
c ATS007 Autism Spectrum Disorder 71 2.350
115
OPT003 Opiate Dependence 49 2.347
117
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.326
118
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.326
119
CHC001 Chickenpox 56 2.305
120
ERY003 Erythema Multiforme 56 2.305
121
NNL006 Non-Alcoholic Steatohepatitis 54 2.301
122
P SKN015 Skin Carcinoma 71 2.293
123
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 2.290
124
HYP056 Hypoglycemia 65 2.284
125
ALL003 Allergic Rhinitis 66 2.277
126
c ACT027 Acute Pancreatitis 60 2.277
127
GLB001 Gilbert Syndrome 53 2.275
128
47X002 47,xyy 47 2.271
129
P CRP001 Carpal Tunnel Syndrome 65 2.257
130
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 2.250
131
c SPN225 Spondyloarthropathy 1 70 2.242
132
SPN051 Spondylitis 51 2.242
133
INF009 Inflammatory Spondylopathy 30 2.242
134
DBT002 Diabetic Autonomic Neuropathy 40 2.216
135
P LPS004 Lupus Erythematosus 61 2.214
136
c HYP595 Hypertension, Essential 84 2.200
137
P ACT105 Acute Mountain Sickness 52 2.196
138
BRN024 Bronchitis 67 2.189
139
P OVR042 Ovarian Cancer 88 2.188
140
DRG002 Drug-Induced Hepatitis 42 2.187
141
P HRT032 Heart Disease 84 2.165
142
ART140 Arteries, Anomalies of 52 2.157
143
LPP008 Lipoprotein Quantitative Trait Locus 65 2.157
144
P PRS038 Personality Disorder 65 2.157
145
ABD010 Abdominal Wall Defect 37 2.151
146
ALC006 Alcoholic Hepatitis 61 2.117
147
P PRP019 Peripheral Nervous System Disease 57 2.097
148
PRT037 Pertussis 49 2.086
149
PRP030 Purpura 54 2.083
150
ERY066 Erythema Multiforme Major 29 2.080
151
P LNG032 Lung Cancer 98 2.074
152
P MLT020 Multiple Sclerosis 79 2.068
153
INT067 Interstitial Nephritis 46 2.061
154
P LYM118 Lymphoma 66 2.047
155
c MCL013 Mucolipidosis Iv 64 2.046
156
ENT001 Enterocele 42 2.046
157
IFP003 Ifap Syndrome 2 41 2.043
158
SPN027 Spinal Stenosis 58 2.041
159
P MLN008 Melanoma 75 2.039
160
P ADL010 Adult Respiratory Distress Syndrome 70 2.038
161
ANR040 Aneurysm 60 2.036
162
P SCL018 Scoliosis 57 2.033
163
P CNR004 Cone-Rod Dystrophy 2 74 2.031
164
SKN016 Skin Disease 63 2.025
165
P PRD008 Periodontitis 63 2.019
166
MSC007 Muscle Hypertrophy 64 2.012
167
c LKM063 Leukemia, Chronic Myeloid 70 2.012
168
CMP010 Complex Regional Pain Syndrome 59 2.011
169
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.999
170
c SVR005 Severe Pre-Eclampsia 49 1.997
171
P HML002 Hemolytic Anemia 62 1.995
172
AND005 Androgen Insensitivity Syndrome, Mild 21 1.995
173
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.992
174
IDP070 Idiopathic Scoliosis 41 1.991
175
CRY035 Cryptorchidism, Unilateral or Bilateral 57 1.986
176
HYP266 Hypoxia 56 1.975
177
DPH001 Diphtheria 59 1.965
178
SKN019 Skin Melanoma 70 1.963
179
TTN003 Tetanus 64 1.959
180
BRN056 Bronchopulmonary Dysplasia 57 1.949
181
PYL006 Pyloric Stenosis 48 1.936
182
RFL001 Reflex Sympathetic Dystrophy 51 1.935
183
TRM010 Traumatic Brain Injury 50 1.927
184
TXC005 Toxic Shock Syndrome 61 1.919
185
END057 Endometrial Cancer 76 1.900
186
P PLV020 Pelvic Organ Prolapse 57 1.899
187
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 1.896
188
BRD004 Borderline Personality Disorder 53 1.890
189
DRM006 Dermatitis 61 1.869
190
MCS002 Mucositis 55 1.868
191
MYF002 Myofascial Pain Syndrome 46 1.865
192
c ACT075 Acute Myocardial Infarction 55 1.864
193
DFC004 Deficiency Anemia 74 1.845
194
ANG049 Angioedema Induced by Ace Inhibitors 38 1.833
195
FXD003 Fixed Drug Eruption 34 1.823
196
NTR005 Nutritional Deficiency Disease 60 1.811
197
c INF145 Infantile Liver Failure Syndrome 1 44 1.811
198
P HYP086 Hypothyroidism 68 1.811
199
P CRD119 Cardiac Arrest 68 1.809
200
OTT002 Otitis Media 70 1.792
201
P KDN017 Kidney Cancer 60 1.792
202
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.785
203
P VSC011 Vasculitis 61 1.784
204
INT075 Intracranial Hypertension 52 1.777
205
HYP066 Hyperglycemia 60 1.766
206
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.763
207
AVD001 Avoidant Personality Disorder 49 1.760
208
IGR001 Ige Responsiveness, Atopic 58 1.753
209
c PRM038 Primary Agammaglobulinemia 47 1.748
210
P DBT009 Diabetes Mellitus 67 1.747
211
MNN028 Mononeuropathy of the Median Nerve, Mild 47 1.740
212
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.740
213
DQR001 De Quervain Disease 26 1.740
214
LPT014 Leptin Deficiency or Dysfunction 77 1.738
215
HPT022 Hepatoblastoma 54 1.725
216
P LKM002 Leukemia 65 1.718
217
MYL069 Myeloma, Multiple 76 1.711
218
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.706
219
LYM133 Lymphoma, Hodgkin, Classic 69 1.706
220
P HYP265 Hypotonia 42 1.699
221
CHL079 Children's Interstitial Lung Disease 25 1.699
222
HPT085 Hepatitis, Fulminant Viral 33 1.685
223
c ATM011 Autoimmune Hepatitis 62 1.684
224
P CRN300 Coronary Heart Disease 1 73 1.676
225
P LKM062 Leukemia, Acute Lymphoblastic 69 1.666
226
SCK003 Sickle Cell Anemia 74 1.640
227
P GST044 Gastritis 55 1.635
228
DSS009 Disseminated Intravascular Coagulation 56 1.632
229
P GLM007 Glomerulonephritis 59 1.630
230
STM007 Stomatitis 52 1.620
231
RDC002 Radiculopathy 51 1.614
232
CHN016 Cohen Syndrome 59 1.607
233
LPT006 Leptin Receptor Deficiency 50 1.607
234
P PRC031 Preeclampsia/eclampsia 1 43 1.578
235
END086 End Stage Renal Disease 54 1.574
236
c TYP009 Type 2 Diabetes Mellitus 91 1.572
237
MNT002 Mental Depression 56 1.564
238
OPD006 Opioid Addiction 48 1.548
239
ISC004 Ischemia 61 1.547
240
END041 Endometrial Adenocarcinoma 63 1.547
241
P NRB001 Neuroblastoma 66 1.541
242
SPN019 Spondylolisthesis 51 1.537
243
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.536
244
P OST002 Osteoporosis 76 1.536
245
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.536
246
DPR016 Depression 64 1.534
247
HMT002 Hematologic Cancer 61 1.532
248
P SNS001 Sensorineural Hearing Loss 60 1.522
249
CYT018 Cytochrome P450 2d6 Variant 26 1.519
250
HRP004 Herpes Zoster 60 1.515
251
LYM019 Lymphosarcoma 46 1.514
252
SPR126 Superior Semicircular Canal Dehiscence 41 1.509
253
c HMG029 Hemoglobin Se Disease 41 1.509
254
P DMN002 Dementia 65 1.508
255
P NRV007 Nervous System Disease 65 1.506
256
c EXD008 Exudative Vitreoretinopathy 1 71 1.500
257
BRN004 Brain Edema 54 1.498
258
VGN023 Vaginitis 56 1.497
259
ACQ007 Acquired Immunodeficiency Syndrome 58 1.487
260
AMD002 Amed Syndrome, Digenic 36 1.485
261
c ACT073 Acute Leukemia 59 1.483
262
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.471
263
P MYL006 Myeloid Leukemia 60 1.471
264
ESP021 Esophageal Cancer 84 1.466
265
CYN002 Cyanosis, Transient Neonatal 43 1.465
266
PLS009 Plasma Cell Neoplasm 64 1.449
267
ENT011 Enterocolitis 55 1.438
268
GST009 Gastroschisis 53 1.437
269
AGG012 Aggressive Nk-Cell Leukemia 47 1.433
270
UMB002 Umbilical Hernia 46 1.432
271
c BCT007 Bacterial Meningitis 55 1.431
272
GST037 Gastroparesis 52 1.429
273
HMS001 Hemosiderosis 48 1.428
274
URM002 Uremia 47 1.424
275
P VNT002 Ventricular Septal Defect 58 1.416
276
PRN019 Perinatal Necrotizing Enterocolitis 60 1.411
277
c CHR684 Chronic Kidney Disease 73 1.411
278
P CRG003 Crigler-Najjar Syndrome, Type I 64 1.410
279
CHL067 Cholecystitis 59 1.407
280
CHL004 Cholelithiasis 48 1.407
281
NSP002 Nasopharyngitis 45 1.405
282
GLM045 Glioma 62 1.405
283
GLL048 Glial Tumor 51 1.405
284
HMR039 Hemorrhage, Intracerebral 57 1.404
285
NPH009 Nephrolithiasis 54 1.404
286
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.403
287
APN008 Apnea, Obstructive Sleep 66 1.403
288
GLS018 Glass Syndrome 60 1.403
289
TRN015 Transient Cerebral Ischemia 62 1.398
290
MSL001 Measles 61 1.394
291
OVR094 Ovarian Epithelial Cancer 39 1.394
292
P RRH023 Rare Hereditary Hemochromatosis 52 1.394
293
P ALZ034 Alzheimer Disease 87 1.393
294
c LKM061 Leukemia, Acute Myeloid 83 1.388
295
MLR004 Malaria 77 1.387
296
c CHR708 Chronic Urticaria 42 1.385
297
BCT022 Bacterial Infectious Disease 55 1.383
298
P HYP750 Hypertriglyceridemia, Familial 61 1.380
299
GST023 Gastric Ulcer 52 1.376
300
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.376
301
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.376
302
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.373
303
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.373
304
PTT037 Pituitary Tumors 44 1.373
305
P HMP007 Hemophilia 52 1.366
306
P HPT023 Hepatocellular Carcinoma 95 1.362
307
P INF032 Infertility 60 1.362
308
GST050 Gastrointestinal System Disease 55 1.356
309
PPT005 Peptic Ulcer Disease 58 1.346
310
APP008 Appendicitis 62 1.344
311
PST011 Pustulosis of Palm and Sole 52 1.340
312
P PSR002 Psoriasis 63 1.340
313
APH001 Aphthous Stomatitis 57 1.340
315
P CNJ013 Conjunctivitis 66 1.323
316
GLT007 Glutathione Synthetase Deficiency 48 1.317
317
P BLD134 Bladder Cancer 79 1.314
318
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 42 1.311
319
c BLD140 Blood Group, I System 47 1.311
320
c CHR064 Chronic Monocytic Leukemia 35 1.311
321
GT001 Gout 63 1.310
322
c SYS001 Systemic Lupus Erythematosus 85 1.301
323
CYS001 Cystic Fibrosis 77 1.298
324
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 1.298
325
GLB002 Glioblastoma 67 1.298
326
P STR020 Strabismus 56 1.298
327
MCH006 Mechanical Strabismus 40 1.298
328
ACT058 Active Peptic Ulcer Disease 55 1.293
329
P NTR004 Neutropenia 62 1.289
330
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.283
331
IMM167 Immune Deficiency Disease 76 1.280
332
DRG003 Drug Dependence 46 1.273
333
P DDN001 Duodenal Ulcer 52 1.272
334
c HPT007 Hepatitis E 50 1.272
335
STM006 Stomach Disease 47 1.266
336
DVR002 Diverticulitis 46 1.265
337
P DRM053 Dermatitis, Atopic 65 1.263
338
c HPT001 Hepatitis C 61 1.260
339
P MNN013 Meningitis 65 1.260
340
P PRK057 Parkinson Disease, Late-Onset 79 1.248
341
SVR004 Severe Combined Immunodeficiency 70 1.247
342
P CLR023 Colorectal Cancer 100 1.235
343
P CRV039 Cervicitis 52 1.233
344
P SLP005 Sleep Disorder 61 1.232
345
ANX010 Anxiety 70 1.228
346
PRT251 Proteinuria, Chronic Benign 58 1.225
347
P BRS047 Breast Cancer 97 1.219
348
MYF001 Myofibroma 42 1.219
349
LMY002 Leiomyoma 51 1.219
350
HLL004 Hellp Syndrome 53 1.219
351
GST092 Gastroesophageal Reflux 59 1.213
352
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.202
353
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.202
354
P NJM001 Nijmegen Breakage Syndrome 75 1.202
355
SPN354 Spinal Arachnoiditis 35 1.202
356
P OCY003 Oocyte Maturation Defect 1 46 1.202
357
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.202
358
ARC002 Arachnoiditis 49 1.202
359
CRT013 Carotid Stenosis 51 1.202
360
BRS051 Breast Disease 58 1.202
361
PRP017 Periapical Periodontitis 47 1.202
362
ACT055 Actinomycosis 54 1.202
363
GST039 Gastroduodenitis 37 1.202
364
CTS005 Catastrophic Antiphospholipid Syndrome 43 1.202
365
SWL001 Swallowing Disorders 37 1.202
366
CRY008 Cryopyrin-Associated Periodic Syndrome 48 1.202
367
P MYP006 Myopia 55 1.201
368
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.201
369
BRN071 Brain Injury 50 1.200
370
SPN020 Spondylosis 46 1.190
371
c SML038 Small Cell Cancer of the Lung 68 1.188
372
PST092 Posttransplant Acute Limbic Encephalitis 29 1.175
373
GST019 Gastrointestinal Stromal Tumor 78 1.161
374
P MMP001 Mumps 56 1.161
375
P RBL001 Rubella 58 1.161
376
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.161
377
ADN027 Adenomyosis 59 1.151
378
OST159 Osteogenic Sarcoma 66 1.149
379
P GRF003 Graft-Versus-Host Disease 71 1.143
380
PNC001 Pancytopenia 52 1.137
381
ALC005 Alcoholic Pancreatitis 38 1.133
382
c MJR022 Major Affective Disorder 8 37 1.132
383
c MJR024 Major Affective Disorder 9 40 1.132
384
P BPL003 Bipolar Disorder 56 1.132
385
KRT009 Keratosis 52 1.125
386
c DMN005 Diamond-Blackfan Anemia 2 28 1.124
387
P GST053 Gastric Cancer 82 1.120
388
PLM033 Pulmonary Embolism 58 1.120
389
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.111
390
c AMY091 Amyotrophic Lateral Sclerosis 1 87 1.109
391
P LTR001 Lateral Sclerosis 57 1.109
392
PRT013 Portal Hypertension 59 1.109
393
DNG003 Dengue Disease 65 1.109
394
P KHL003 Kohlschutter-Tonz Syndrome 57 1.105
395
P AGN002 Agnosia 53 1.105
396
PLY068 Polysubstance Abuse 41 1.100
397
DSS008 Disease of Mental Health 74 1.100
398
CNG034 Congestive Heart Failure 69 1.097
399
P HYP098 Hypereosinophilic Syndrome 66 1.089
400
P ADN016 Adenocarcinoma 63 1.084
401
HPT014 Hepatorenal Syndrome 49 1.080
402
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.075
403
PLM010 Pulmonary Edema 54 1.068
404
PLC007 Placental Abruption 47 1.068
405
VSC002 Vascular Dementia 59 1.063
406
HMP009 Haemophilus Influenzae 41 1.059
407
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.059
408
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 1.059
409
P INT260 Intracranial Berry Aneurysm 40 1.059
410
P DPY001 Dupuytren Contracture 39 1.059
411
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.059
412
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.059
413
c PNC106 Pancreatic Agenesis 1 51 1.059
414
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.059
415
LMY014 Leiomyoma, Uterine 55 1.059
416
c FNC043 Fanconi Anemia, Complementation Group E 62 1.059
417
SKN013 Skin Benign Neoplasm 49 1.059
418
P ANT006 Antiphospholipid Syndrome 55 1.059
419
PNC034 Pancreas Disease 49 1.059
420
CRB009 Cerebritis 43 1.059
421
NWB001 Newborn Respiratory Distress Syndrome 56 1.059
422
INT053 Intracranial Vasospasm 37 1.059
423
LNG031 Lung Benign Neoplasm 51 1.059
424
RSP007 Respiratory Distress Syndrome, Infant 41 1.059
425
P HYP040 Hypospadias 51 1.059
426
VRC005 Varicose Veins 59 1.057
427
c HMP029 Hemophilia a 69 1.057
428
P PRK039 Parkinsonism 55 1.057
429
MST005 Mastitis 52 1.057
430
CMB007 Combined Immunodeficiency 56 1.053
431
BNR002 Bone Resorption Disease 47 1.049
432
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.043
433
P LKM071 Leukemia, Chronic Lymphocytic 74 1.043
434
URL001 Urolithiasis 45 1.043
435
PRP027 Peripheral Vascular Disease 71 1.043
436
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.038
437
P MYC008 Myocarditis 59 1.038
438
c TYP008 Type 1 Diabetes Mellitus 77 1.035
439
P PLM037 Pulmonary Hypertension 69 1.028
440
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.016
441
CLL003 Cellulitis 53 1.016
442
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.016
443
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.012
444
MCN017 Meconium Ileus 52 1.012
445
P RCT021 Rectum Cancer 54 1.012
446
CLN045 Colonic Benign Neoplasm 48 1.012
447
DVR001 Diverticulitis of Colon 24 1.012
448
AST052 Asthma, Nasal Polyps, and Aspirin Intolerance 42 1.012
449
CHR005 Chorioamnionitis 50 1.012
450
P MTR014 Motor Neuron Disease 65 1.012
451
P HML001 Hemolytic-Uremic Syndrome 52 1.012
452
PRT036 Peritonitis 65 1.012
453
5XP001 5-Oxoprolinase Deficiency 30 1.004
454
P CND004 Candidiasis 57 1.004
455
CRB004 Cerebral Artery Occlusion 45 1.004
456
P ESN008 Eosinophilic Pneumonia 50 1.004
457
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.995
458
HGH043 High Grade Glioma 46 0.995
459
DMP001 Dumping Syndrome 43 0.995
460
BRN002 Bronchiolitis 57 0.992
461
PLM031 Poliomyelitis 62 0.992
462
DDN004 Duodenogastric Reflux 31 0.992
463
SPL018 Splenomegaly 47 0.992
464
LYM040 Lymphoblastic Lymphoma 53 0.983
465
ATH013 Atherosclerosis Susceptibility 63 0.977
466
P GLM040 Glioma Susceptibility 1 70 0.977
467
PNM013 Pneumococcal Meningitis 43 0.977
468
TND005 Tendinitis 53 0.976
469
CMR002 Coumarin Resistance 59 0.970
470
CRD005 Cardia Cancer 37 0.970
471
HYP017 Hypophosphatemia 49 0.966
472
ORL005 Oral Candidiasis 55 0.966
473
LNG099 Lung Disease 62 0.966
474
CRT017 Cartilage Disease 52 0.957
475
PRM236 Primary Biliary Cholangitis 62 0.953
476
INS024 Insulin-Like Growth Factor I 77 0.951
477
c GLL024 Gallbladder Disease 1 53 0.950
478
c HPT016 Hepatitis B 62 0.945
479
P HMR005 Hemorrhoid 49 0.945
480
P THY032 Thyroiditis 56 0.941
481
SYN007 Synovitis 54 0.938
482
PLC002 Plica Syndrome 35 0.938
483
P SCH015 Schizophrenia 74 0.935
484
P RTN024 Retinoblastoma 72 0.935
485
P INT143 Interstitial Cystitis 59 0.935
486
P CHR342 Chiari Malformation 41 0.925
487
P PHC003 Pheochromocytoma 70 0.923
488
ADR040 Adrenal Gland Pheochromocytoma 45 0.923
489
ATN004 Autonomic Neuropathy 42 0.923
490
TND004 Tendinopathy 45 0.921
491
INT146 Intervertebral Disc Disease 61 0.920
492
P SRC025 Sarcoidosis 1 70 0.912
493
HMN044 Human Immunodeficiency Virus Type 1 76 0.912
494
P INF038 Influenza 68 0.912
495
CRV035 Cervical Cancer 72 0.911
496
P FCL005 Focal Segmental Glomerulosclerosis 57 0.911
497
P MSC003 Muscular Atrophy 52 0.911
498
PRS063 Paresthesia 39 0.911
499
GRN017 Granulocytopenia 42 0.910
500
c BRN108 Branchiootic Syndrome 1 63 0.907
501
ULC004 Ulcerative Colitis 74 0.907
502
BHR001 Behr Syndrome 51 0.903
503
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.903
504
AMN003 Amnestic Disorder 53 0.903
505
DRG024 Drug Allergy 40 0.900
506
PST021 Postpartum Depression 50 0.900
507
CHL013 Cholecystolithiasis 37 0.896
508
HML018 Homologous Wasting Disease 21 0.891
509
PSR001 Psoriatic Arthritis 61 0.891
510
PFF001 Pfeiffer Syndrome 77 0.891
511
c HMC039 Hemochromatosis, Type 1 73 0.891
512
THR004 Thrombocytosis 52 0.891
513
CNT047 Contact Dermatitis 56 0.891
514
CVD001 Covid-19 59 0.891
515
HMG002 Hemoglobinuria 50 0.891
516
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.891
517
P PNC035 Pancreatic Cancer 87 0.881
518
LYM027 Lymphopenia 56 0.881
519
P EPL164 Epilepsy 70 0.874
520
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.874
521
HDR003 Hidradenitis 49 0.872
522
HLT002 Halothane Hepatitis 32 0.861
523
P MGR003 Migraine with Aura 51 0.860
524
P END033 Endocarditis 58 0.853
525
ALL010 Allergic Contact Dermatitis 55 0.853
526
P THL005 Thalassemia 56 0.853
527
ACR008 Acrocallosal Syndrome 69 0.853
528
P HYP069 Hyperparathyroidism 62 0.849
529
ATR009 Atrophy of Testis 22 0.849
530
P SPN046 Spinal Muscular Atrophy 62 0.843
531
INT002 Intermittent Claudication 61 0.843
532
CRD132 Cardiac Conduction Defect 59 0.838
533
INF034 Infective Endocarditis 53 0.831
534
ANT078 Antipyrine Metabolism 24 0.831
535
P PRP034 Purpura Fulminans 41 0.831
536
SBS004 Substance Dependence 46 0.827
537
CLF001 Cleft Lip 54 0.827
538
P TRM003 Tremor 50 0.827
539
ADN018 Adenoma 58 0.823
540
ZKF001 Zika Fever 51 0.821
541
BLL003 Bell's Palsy 48 0.821
542
PTH003 Pathologic Nystagmus 52 0.815
543
CHL123 Chlamydia 58 0.806
544
GST045 Gastroenteritis 58 0.803
545
PRT058 Pure Autonomic Failure 58 0.799
546
P CLS010 Cluster Headache 42 0.790
547
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.781
548
CHP002 Chops Syndrome 47 0.781
549
PRP080 Peripheral Artery Disease 54 0.781
550
END040 Endogenous Depression 54 0.781
551
PHM001 Phimosis 37 0.781
552
NRT001 Neurotic Disorder 56 0.781
553
PRP013 Paraphimosis 29 0.781
554
SPP003 Suppurative Periapical Periodontitis 38 0.781
555
VSL002 Visual Epilepsy 39 0.781
556
BLN010 Balanitis 37 0.781
557
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.781
558
HDG004 Hodgkin's Granuloma 22 0.781
559
RTC005 Reticulosarcoma 47 0.781
560
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.781
561
HDG006 Hodgkin's Paragranuloma 22 0.781
562
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.781
563
CHR682 Chronic Bilirubin Encephalopathy 37 0.781
564
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.781
565
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.777
566
ANS023 Anus, Imperforate 56 0.777
567
ANR004 Anuria 44 0.777
568
P MYP004 Myopathy 67 0.777
569
KDN001 Kidney Cortex Necrosis 31 0.777
570
LWC001 Low Compliance Bladder 44 0.777
571
MYL009 Myelodysplastic Syndrome 67 0.769
572
c ANM038 Anemia, Autoimmune Hemolytic 63 0.769
573
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.769
574
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.769
575
P GLY013 Glycogen Storage Disease 59 0.769
576
ART016 Aortic Aneurysm 68 0.769
577
DNB001 Danubian Endemic Familial Nephropathy 42 0.769
578
TRD006 Tardive Dyskinesia 53 0.769
579
GST013 Gastrojejunal Ulcer 41 0.769
580
ESP018 Esophageal Candidiasis 47 0.769
581
NNT008 Neonatal Abstinence Syndrome 41 0.769
582
c CHR579 Chiari Malformation Type Ii 44 0.765
583
HYP781 Hypoascorbemia 52 0.765
584
ACL001 Acalculous Cholecystitis 34 0.765
585
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.765
586
INF039 Infratentorial Cancer 39 0.765
587
KRT002 Keratomalacia 54 0.765
588
FCT001 Factor Viii Deficiency 61 0.763
589
P SPP010 Suppressor of Tumorigenicity 3 50 0.763
590
LYM021 Lymphadenitis 55 0.763
591
RTR008 Root Resorption 44 0.763
592
P CHR012 Chronic Granulomatous Disease 69 0.763
593
P BRS044 Breast Adenocarcinoma 58 0.763
594
PRC013 Pericarditis 53 0.763
595
DGN001 Degenerative Disc Disease 48 0.760
596
ANN002 Anencephaly 57 0.749
597
c CHR711 Chronic Asthma 41 0.749
598
SVR001 Severe Acute Respiratory Syndrome 68 0.749
599
PLM035 Pulmonary Eosinophilia 49 0.749
600
GRM010 Germ Cells Tumors 33 0.738
601
TRN021 Transaldolase Deficiency 43 0.734
602
STT001 Status Epilepticus 58 0.734
603
PLR007 Pleural Empyema 50 0.734
604
P HYP009 Hypertrophic Pyloric Stenosis 41 0.734
605
CHR066 Chronic Fatigue Syndrome 59 0.734
606
ANX004 Anoxia 40 0.734
607
CHR178 Chromosomal Triplication 33 0.734
608
CRH005 Crohn's Colitis 53 0.731
609
MNT001 Mantle Cell Lymphoma 65 0.731
610
HND002 Hand, Foot and Mouth Disease 50 0.731
611
HRY003 Hairy Cell Leukemia 53 0.731
612
SYS004 Systemic Mastocytosis 62 0.731
613
SMT001 Somatization Disorder 49 0.731
614
THY030 Thyroid Gland Disease 50 0.731
615
P SYS005 Systemic Scleroderma 73 0.731
616
MTH009 Mouth Disease 57 0.731
617
GTR002 Goiter 52 0.731
618
PTL002 Patellofemoral Pain Syndrome 34 0.731
619
P MST009 Mastocytosis 64 0.731
620
KWS002 Kawasaki Disease 65 0.718
621
PLL012 Pollen Allergy 44 0.718
622
P BNC003 Bone Cancer 58 0.718
623
AMN001 Amenorrhea 53 0.718
624
MYC005 Myocardial Stunning 45 0.718
625
ADG002 Audiogenic Seizures 25 0.718
626
P ATR001 Atrioventricular Septal Defect 54 0.714
627
SCH036 Scheie Syndrome 73 0.714
628
CLT003 Colitis 63 0.701
629
ISC015 Ischemic Colitis 43 0.701
630
P CLC063 Celiac Disease 1 65 0.701
631
AST006 Astigmatism 46 0.701
632
ANR007 Anorexia Nervosa 59 0.701
633
HYP865 Hypogonadotropic Hypogonadism 25 with Anosmia 23 0.701
634
BDD001 Budd-Chiari Syndrome 62 0.701
635
P CYS018 Cystitis 58 0.701
636
HMP001 Hemopericardium 47 0.701
637
P PRC012 Pericardial Effusion 50 0.701
638
GLC003 Glucose Intolerance 53 0.701
639
BRN028 Brain Cancer 73 0.701
640
CHR074 Choriocarcinoma 46 0.701
641
CRN088 Craniorachischisis 35 0.701
642
P ENC008 Encephalocele 46 0.701
643
CLF056 Cleft Lip with or Without Cleft Palate 43 0.701
644
P ALP008 Alopecia 53 0.701
645
MCR103 Microtia 40 0.701
646
FNT004 Fainting 29 0.701
647
PST053 Postherpetic Neuralgia 39 0.686
648
OBN001 Ouabain Resistance 15 0.683
649
DRV001 Dravet Syndrome 69 0.683
650
HYP025 Hyperphosphatemia 47 0.683
652
HLX001 Helix Syndrome 47 0.683
653
P MYM013 Moyamoya Disease 1 59 0.683
654
P DNG005 Dengue Virus 55 0.683
655
P NPH012 Nephrotic Syndrome 61 0.683
656
HYP060 Hyperinsulinism 53 0.683
657
MLG169 Malignant Astrocytoma 57 0.683
658
NRM004 Neuroma 49 0.683
659
PLR008 Pleurisy 49 0.683
660
DYS015 Dysentery 49 0.683
661
ALL006 Allergic Asthma 55 0.683
662
P HYP076 Hyperthyroidism 53 0.683
663
P INF037 Inflammatory Bowel Disease 53 0.677
664
HPT067 Hepatocellular Adenoma 42 0.676
665
CRD229 Cardiomyopathy, Dilated, with Hypergonadotropic Hypogonadism 49 0.676
666
HYP766 Hyperbilirubinemia, Transient Familial Neonatal 43 0.676
667
c HYP731 Hyperaldosteronism, Familial, Type I 59 0.676
668
BLR030 Bilirubin, Serum Level of, Quantitative Trait Locus 1 32 0.676
669
P THP004 Thiopurines, Poor Metabolism of, 1 41 0.676
670
CRG004 Crigler-Najjar Syndrome, Type Ii 46 0.676
671
LWC002 Lowe Oculocerebrorenal Syndrome 68 0.676
672
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.676
673
CND001 Conidiobolomycosis 26 0.676
674
CHL159 Childhood-Onset Asthma 30 0.676
675
OTL001 Outlet Dysfunction Constipation 26 0.676
676
P KRN004 Kernicterus 47 0.676
677
MXD010 Mixed Epithelial Stromal Tumour 26 0.676
678
MLT001 Multiple Chemical Sensitivity 38 0.676
679
c PLY008 Polyneuropathy Due to Drug 20 0.676
680
HYP049 Hypertrophy of Tongue Papillae 24 0.676
681
ANG012 Angiodysplasia of Intestine 24 0.676
682
PRC008 Pericholangitis 27 0.676
683
INH003 Inhibited Female Orgasm 29 0.676
684
FML031 Female Stress Incontinence 39 0.676
685
CLP006 Clopidogrel Resistance 44 0.676
686
TXC020 Toxic Oil Syndrome 33 0.676
687
CTR172 Citrullinemia, Classic 64 0.663
688
PPL052 Papillomatosis, Confluent and Reticulated 34 0.663
689
NRL016 Neural Tube Defects 80 0.663
690
c DWL002 Dowling-Degos Disease 1 58 0.663
691
c HPT073 Hepatitis C Virus 70 0.663
692
c HMP004 Hemophilia B 68 0.663
693
c THR071 Thrombocytopenia 1 48 0.663
694
VCC001 Vaccinia 49 0.663
695
TRN018 Transitional Cell Carcinoma 56 0.663
696
CHR001 Churg-Strauss Syndrome 61 0.663
697
ADJ001 Adjustment Disorder 46 0.663
698
P ACN011 Acne 55 0.663
699
TXC010 Toxic Myocarditis 23 0.663
700
INT007 Intermediate Coronary Syndrome 53 0.663
701
SCN067 Scn1a Seizure Disorders 13 0.663
702
c ACQ014 Acquired Hemophilia 45 0.663
703
ALL012 Allergic Angiitis 24 0.663
704
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.663
705
PGM010 Pigmented Purpuric Eruption 24 0.642
706
GRS011 Gerstmann-Straussler Disease 56 0.642
707
c RTN047 Retinitis Pigmentosa 18 45 0.642
708
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.642
709
RBF001 Riboflavin Deficiency 49 0.642
710
EXT006 Extrahepatic Cholestasis 41 0.642
711
CLN015 Colon Adenocarcinoma 64 0.642
712
c BSL007 Basal Cell Carcinoma 67 0.642
713
HYP014 Hyperuricemia 51 0.642
714
ASP008 Aspiration Pneumonitis 43 0.642
715
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.642
716
BLD052 Blood Group Incompatibility 31 0.642
717
c PSR028 Psoriasis 7 42 0.638
718
ANL022 Anal Fistula 47 0.638
719
P GLL020 Gallbladder Disease 57 0.638
720
ADN067 Adenoid Hypertrophy 38 0.638
721
ADN002 Adenoiditis 36 0.638
722
c PSR023 Psoriasis 1 52 0.638
723
CSY001 C Syndrome 61 0.638
724
NRF026 Neurofibromatosis, Type Iv, of Riccardi 24 0.638
725
c NRF024 Neurofibromatosis, Type I 76 0.638
726
c SCL052 Scleroderma, Familial Progressive 60 0.638
727
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 0.638
728
c GLY008 Glycogen Storage Disease Ii 72 0.638
729
c INF071 Inflammatory Bowel Disease 1 65 0.638
730
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 53 0.638
731
c PSR017 Psoriasis 2 53 0.638
732
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 0.638
733
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.638
734
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.638
735
c PSR018 Psoriasis 13 40 0.638
736
P MMB011 Membranous Nephropathy 50 0.638
737
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.638
738
c SPN330 Spondylocostal Dysostosis 5 55 0.638
739
MST024 Mastocytosis, Cutaneous 66 0.638
740
PMP006 Pemphigus Vulgaris, Familial 57 0.638
741
c PSR032 Psoriasis 11 47 0.638
742
HYL004 Hyaline Fibromatosis Syndrome 67 0.638
743
PRT010 Parathyroid Carcinoma 68 0.638
744
DFF005 Diffuse Large B-Cell Lymphoma 55 0.638
745
PRT030 Parathyroid Gland Disease 44 0.638
746
ANS012 Anus Disease 49 0.638
747
ACR007 Acromegaly 70 0.638
748
THY122 Thyroid Gland Cancer 59 0.638
749
URT037 Urethral Stricture 42 0.638
750
DFF003 Diffuse Scleroderma 41 0.638
751
PLX002 Plexiform Neurofibroma 44 0.638
752
PTT009 Pituitary Gland Disease 52 0.638
753
LYM017 Lyme Disease 63 0.638
754
P PTT006 Pituitary Adenoma 55 0.638
755
PPL001 Papillary Adenoma 44 0.638
756
IMM136 Immune System Disease 46 0.638
757
DNT006 Dental Pulp Necrosis 43 0.638
758
HRP001 Herpangina 45 0.638
759
PLR005 Pleuropneumonia 33 0.638
760
P NRF002 Neurofibromatosis 60 0.638
761
P PMP001 Pemphigus 54 0.638
762
P MST002 Mast-Cell Leukemia 50 0.638
763
HMC030 Homocystinuria Caused by Cystathionine Beta-Synthase Deficiency 36 0.638
764
P HMC002 Homocystinuria 52 0.638
765
IND017 Indolent Plasma Cell Myeloma 41 0.638
766
NRF007 Neurofibroma 63 0.638
767
PDT045 Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcus Infections 24 0.638
768
c HRD173 Hereditary Late-Onset Parkinson Disease 50 0.638
769
c CHR417 Chronic Graft Versus Host Disease 55 0.638
770
WRM004 Warm Antibody Hemolytic Anemia 19 0.638
771
THY029 Thyroid Carcinoma 55 0.638
772
RNL077 Renal Fibrosis 46 0.617
773
P CTR177 Citrullinemia, Type Ii, Adult-Onset 56 0.617
774
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.617
775
P HNT016 Huntington Disease 73 0.617
776
RNL013 Renal Adenoma 30 0.617
777
P ACT046 Acute Apical Periodontitis 25 0.617
778
DRS001 Dressler's Syndrome 32 0.617
779
P GLL022 Guillain-Barre Syndrome 59 0.617
780
CLL014 Cll/sll 45 0.617
781
RRC029 Rare Cause of Hypertension 13 0.617
782
TRC123 Trichohepatoneurodevelopmental Syndrome 27 0.587
783
ARY002 Aryl Hydrocarbon Hydroxylase Inducibility 24 0.587
784
NTR042 Neutrophilic Dermatosis, Acute Febrile 56 0.587
785
ORN001 Ornithosis 39 0.587
786
PRV004 Periventricular Leukomalacia 52 0.587
787
PRM013 Premature Menopause 57 0.587
788
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.587
789
PRP005 Parapsoriasis 38 0.587
790
RHM036 Rheumatoid Arthritis Interstitial Lung Disease 31 0.587
791
c VRL008 Viral Exanthem 30 0.587
792
P DBT005 Diabetes Insipidus 54 0.587
793
ACQ039 Acquired Purpura Fulminans 16 0.587
794
P ESP024 Esophagitis 60 0.571
795
c JVN010 Juvenile Rheumatoid Arthritis 52 0.571
796
SPS057 Spasticity 43 0.571
797
P CRN037 Craniosynostosis 67 0.555
798
P ART023 Arthropathy 59 0.555
799
P PNM007 Pneumonia 64 0.551
800
P BCK002 Beckwith-Wiedemann Syndrome 61 0.549
801
EWN003 Ewing Sarcoma 69 0.549
802
c RTN090 Retinitis Pigmentosa 55 39 0.549
803
ADR049 Adrenal Hypoplasia, Congenital 52 0.549
804
c 46X049 46,xy Sex Reversal 2 51 0.549
805
c PCH010 Pachyonychia Congenita 3 43 0.549
806
c INF088 Inflammatory Bowel Disease 5 29 0.549
807
HPT046 Hepatic Veno-Occlusive Disease 54 0.549
808
P GCH001 Gaucher's Disease 69 0.549
809
INT066 Interstitial Lung Disease 60 0.549
810
EMB004 Embryonal Carcinoma 55 0.549
811
TST014 Testicular Cancer 51 0.549
812
PLC008 Placenta Disease 48 0.549
813
PLY012 Polyhydramnios 46 0.549
814
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.549
815
ETH012 Ethylene Glycol Poisoning 29 0.549
816
P DRR001 Diarrhea 55 0.539
817
CRB037 Cerebral Palsy 66 0.520
818
ETN001 Eating Disorder 59 0.520
819
P HRP006 Herpes Simplex 65 0.520
820
P OVR082 Overgrowth Syndrome 41 0.520
821
P PRS040 Prostate Cancer 95 0.508
822
GNG013 Gingivitis 59 0.508
823
c SYS043 Systemic Lupus Erythematosus 1 38 0.487
824
P APL001 Aplastic Anemia 72 0.479
825
c THR092 Thrombophilia Due to Thrombin Defect 74 0.479
826
P MYC084 Mycobacterium Tuberculosis 1 68 0.479
828
PST028 Post-Traumatic Stress Disorder 58 0.479
829
c CNT035 Central Nervous System Disease 53 0.479
830
PLS007 Plasmodium Falciparum Malaria 52 0.479
831
ACT084 Acute Stress Disorder 53 0.479
832
FSC004 Fasciitis 49 0.479
833
ALV005 Alveolar Soft Part Sarcoma 61 0.475
834
SNL009 Senile Plaque Formation 28 0.457
835
P BRB001 Beriberi 44 0.457
836
MTR001 Mature Cataract 27 0.457
837
GRM005 Germ Cell Cancer 46 0.457
838
P TST026 Testicular Germ Cell Cancer 42 0.457
839
HYP074 Hypersensitivity Vasculitis 53 0.457
840
P MRC003 Mercury Poisoning 48 0.457
841
CRD137 Cardiogenic Shock 56 0.457
842
THR024 Thrombosis 56 0.454
843
CLR030 Clear Cell Renal Cell Carcinoma 53 0.454
844
P CRD246 Cardiovascular System Disease 55 0.454
845
P SJG008 Sjogren Syndrome 60 0.425
846
P FLL037 Follicular Lymphoma 66 0.425
847
P BNG032 Benign Mesothelioma 53 0.425
848
PLM001 Pulmonary Tuberculosis 69 0.425
849
P HYD006 Hydrocephalus 62 0.425
850
ALG001 Algoneurodystrophy 37 0.425
851
MMM001 Mammary Paget's Disease 53 0.425
852
CCN002 Cocaine Abuse 49 0.425
853
c PRS130 Prostate Cancer, Hereditary, 8 32 0.415
854
OST022 Osteopathia Striata with Cranial Sclerosis 54 0.415
855
P OCL013 Oculodentodigital Dysplasia 66 0.415
856
c PRS136 Prostate Cancer, Hereditary, 6 33 0.415
857
ACT011 Acute Contagious Conjunctivitis 41 0.415
858
HYP458 Hyper Ige Syndrome 60 0.415
859
PRS047 Prostatitis 57 0.415
860
GGN004 Gigantomastia 26 0.415
861
P URN019 Urinary Tract Infection 48 0.392
862
P ATR011 Atrial Fibrillation 66 0.386
863
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.386
864
P MTR004 Maturity-Onset Diabetes of the Young 66 0.386
865
P MJR007 Major Affective Disorder 1 42 0.386
866
P HML033 Hemolytic Uremic Syndrome, Atypical 1 67 0.386
867
P HRS035 Hirschsprung Disease 1 66 0.386
868
MRF001 Marfan Syndrome 76 0.386
869
c MST023 Mesothelioma, Malignant 56 0.386
870
P CTS001 Cutis Laxa 64 0.386
871
HMG005 Hemoglobinopathy 55 0.386
872
SPN035 Spindle Cell Sarcoma 51 0.386
873
P NRM002 Normal Pressure Hydrocephalus 49 0.386
874
PSY004 Psychotic Disorder 66 0.386
875
P RHB003 Rhabdomyosarcoma 66 0.386
876
FML008 Familial Retinoblastoma 49 0.386
877
P HYP024 Hypoparathyroidism 55 0.386
878
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.386
879
URT014 Ureterolithiasis 42 0.386
880
SRC014 Sarcoma 64 0.386
881
OST016 Osteochondrosis 52 0.386
882
SPT004 Septic Arthritis 58 0.386
883
PLN007 Plantar Fasciitis 37 0.386
884
P BLR006 Biliary Tract Disease 46 0.386
885
c ACT135 Acute Graft Versus Host Disease 51 0.386
886
NSS002 Neisseria Meningitidis Infection 46 0.386
887
P AVS003 Avascular Necrosis 41 0.386
888
BNN005 Bunion 32 0.386
889
TMP019 Temporomandibular Joint Anomaly 28 0.386
890
SRT004 Serotonin Syndrome 54 0.381
891
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.358
892
ANG066 Angel-Shaped Phalangoepiphyseal Dysplasia 30 0.345
893
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 48 0.345
894
CHR100 Chronic Ulcer of Skin 57 0.341
895
SCR015 Scarlet Fever 38 0.341
896
P SCL057 Scoliosis, Isolated 1 40 0.334
897
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.320
898
PRS045 Prostatic Hypertrophy 53 0.307
899
c INH020 Inherited Metabolic Disorder 47 0.307
900
C1N001 C1 Inhibitor Deficiency 43 0.294
901
PRT082 Preterm Premature Rupture of the Membranes 56 0.294
902
YSY001 Yao Syndrome 34 0.294
903
SPL004 Splenic Marginal Zone Lymphoma 50 0.294
904
PRP001 Propionic Acidemia 65 0.294
905
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.294
906
VLC001 Velocardiofacial Syndrome 57 0.294
907
P FNG006 Feingold Syndrome 1 61 0.294
908
PGT003 Paget Disease, Extramammary 48 0.294
909
RYN001 Raynaud Disease 49 0.294
910
PPL049 Papillon-Lefevre Syndrome 65 0.294
911
GLL008 Gilles De La Tourette Syndrome 64 0.294
912
BKS003 Beukes Hip Dysplasia 46 0.294
913
MRD002 Marden-Walker Syndrome 56 0.294
914
c SPN395 Spinal Muscular Atrophy, Type Ii 55 0.294
915
DGR001 Digeorge Syndrome 62 0.294
916
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.294
917
AND020 Androgen Insensitivity, Partial 54 0.294
918
c MJR008 Major Affective Disorder 2 34 0.294
919
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 57 0.294
920
ACR041 Acromelic Frontonasal Dysostosis 53 0.294
921
c FCL025 Focal Segmental Glomerulosclerosis 1 49 0.294
922
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 0.294
923
ALN001 Aland Island Eye Disease 55 0.294
924
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.294
925
c JVN061 Juvenile Arthritis 56 0.294
926
P RST001 Restless Legs Syndrome 52 0.294
927
c MJR006 Major Affective Disorder 5 32 0.294
928
c MJR023 Major Affective Disorder 7 33 0.294
929
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.294
930
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 36 0.294
931
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.294
932
FLL041 Follicular Lymphoma 1 44 0.294
933
c CTS033 Cutis Laxa, Autosomal Recessive, Type Ic 50 0.294
934
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 0.294
935
c XNT010 Xanthinuria, Type I 52 0.294
936
P CHN012 Chondrosarcoma 56 0.294
937
AND017 Anodontia of Permanent Dentition 26 0.294
938
P LRY029 Laryngomalacia 47 0.294
939
MYL005 Myelofibrosis 70 0.294
940
INT303 Intracranial Hypertension, Idiopathic 56 0.294
941
c MCL062 Mucolipidosis Ii Alpha/beta 69 0.294
942
c HRS036 Hirschsprung Disease 2 36 0.294
943
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 0.294
944
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.294
945
c OVR114 Ovarian Cancer 1 60 0.294
946
c FBR072 Febrile Seizures, Familial, 11 41 0.294
947
STL007 Steel Syndrome 42 0.294
948
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.294
949
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.294
950
c DRR009 Diarrhea 6 46 0.294
951
HYD065 Hydrocephalus, Congenital, 2, with or Without Brain or Eye Anomalies 34 0.294
952
IMM064 Immunodeficiency, Common Varia