Search results for Simvastatin

1074 hits were found for Simvastatin

# Family MCID Name MIFTS Score
1
c HYP836 Hypercholesterolemia, Familial, 1 73 43.496
2
LPD008 Lipid Metabolism Disorder 62 25.512
3
P CRN300 Coronary Heart Disease 1 73 19.479
4
P MYP004 Myopathy 67 19.315
5
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 17.791
6
ATH013 Atherosclerosis Susceptibility 63 16.117
7
c TYP009 Type 2 Diabetes Mellitus 92 15.109
8
LPP008 Lipoprotein Quantitative Trait Locus 65 15.044
9
c FML021 Familial Hypercholesterolemia 72 14.446
10
ISC004 Ischemia 61 13.915
11
P HRT032 Heart Disease 81 13.774
12
ART140 Arteries, Anomalies of 53 13.051
13
P DBT009 Diabetes Mellitus 67 12.254
14
P VSC007 Vascular Disease 63 12.215
15
P HYP750 Hypertriglyceridemia, Familial 62 11.578
16
P PRD008 Periodontitis 64 10.228
17
P PLM037 Pulmonary Hypertension 72 10.031
18
FML035 Familial Hyperlipidemia 55 9.738
19
P KDN018 Kidney Disease 72 9.690
20
ANG054 Angina Pectoris 66 9.454
21
BRN071 Brain Injury 50 9.168
22
c CHR684 Chronic Kidney Disease 69 9.123
23
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 8.899
24
P MYC007 Myocardial Infarction 70 8.726
25
TRM010 Traumatic Brain Injury 51 8.571
26
c HYP272 Hypercholesterolemia, Familial, 3 45 8.496
27
PRP027 Peripheral Vascular Disease 71 8.449
28
CYT002 Cytokine Deficiency 43 8.281
29
P PLY011 Polycystic Ovary Syndrome 57 8.136
30
PRT013 Portal Hypertension 59 8.121
31
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 7.982
32
BNR002 Bone Resorption Disease 47 7.952
33
LVR012 Liver Cirrhosis 63 7.943
34
P CRD246 Cardiovascular System Disease 56 7.913
35
c PLM164 Pulmonary Hypertension, Primary, 1 76 7.874
36
FTT001 Fatty Liver Disease 62 7.868
37
48X005 48,xyyy 39 7.854
38
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 7.743
39
P MLT020 Multiple Sclerosis 79 7.714
40
P ALZ034 Alzheimer Disease 87 7.651
41
P PRS040 Prostate Cancer 95 7.455
42
c HYP595 Hypertension, Essential 85 7.436
43
CRB039 Cerebrovascular Disease 66 7.403
44
INT007 Intermediate Coronary Syndrome 54 7.381
45
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.315
46
c HYP724 Hyperlipoproteinemia, Type Iii 67 7.302
47
ANR040 Aneurysm 61 7.251
48
c ACT071 Acute Kidney Failure 60 7.206
49
P MYS005 Myositis 56 7.047
50
PLM129 Pulmonary Disease, Chronic Obstructive 74 7.042
51
c ACT027 Acute Pancreatitis 60 7.002
52
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 6.892
53
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 6.892
54
P LVR013 Liver Disease 69 6.872
55
PRT251 Proteinuria, Chronic Benign 57 6.865
56
P BRS047 Breast Cancer 98 6.822
57
P OST002 Osteoporosis 76 6.779
58
c MCR115 Microvascular Complications of Diabetes 5 65 6.761
59
P RHM011 Rheumatoid Arthritis 82 6.734
60
P CLR023 Colorectal Cancer 100 6.566
61
PRP080 Peripheral Artery Disease 54 6.426
62
CNG034 Congestive Heart Failure 69 6.403
63
HYP066 Hyperglycemia 61 6.396
64
c MCR130 Microvascular Complications of Diabetes 6 41 6.341
65
c MCR120 Microvascular Complications of Diabetes 7 47 6.341
66
c MCR113 Microvascular Complications of Diabetes 3 52 6.341
67
c MCR133 Microvascular Complications of Diabetes 4 41 6.341
68
P AST005 Asthma 76 6.246
69
c ACT075 Acute Myocardial Infarction 56 6.234
70
P LNG032 Lung Cancer 98 6.227
71
P PNC044 Pancreatitis 61 6.222
72
c SML038 Small Cell Cancer of the Lung 69 6.181
73
c PRD040 Periodontitis, Chronic 52 6.062
74
P HYP086 Hypothyroidism 69 6.031
75
END086 End Stage Renal Disease 52 6.018
76
RPD005 Rapidly Involuting Congenital Hemangioma 46 5.994
77
MYL069 Myeloma, Multiple 77 5.713
78
SPN186 Spinal Cord Injury 61 5.693
79
P BCL017 B-Cell Lymphoma 59 5.686
80
P NRB001 Neuroblastoma 66 5.598
81
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 5.552
82
STR067 Stroke, Ischemic 80 5.546
83
RLP002 Relapsing-Remitting Multiple Sclerosis 56 5.535
84
P ADN016 Adenocarcinoma 63 5.505
85
c BLD140 Blood Group, I System 46 5.482
86
RHB024 Rhabdomyosarcoma 2 67 5.477
87
HMZ003 Homozygous Familial Hypercholesterolemia 60 5.448
88
BRN004 Brain Edema 54 5.433
89
OST159 Osteogenic Sarcoma 66 5.423
90
CRB004 Cerebral Artery Occlusion 45 5.372
91
ART016 Aortic Aneurysm 68 5.369
92
P GST053 Gastric Cancer 83 5.154
93
P PNC035 Pancreatic Cancer 86 5.125
94
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 5.115
95
c ATR087 Atrial Standstill 1 74 5.041
96
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 5.031
97
c HNT011 Huntington Disease-Like 3 34 5.025
98
TXC005 Toxic Shock Syndrome 62 5.020
99
SMT004 Smith-Lemli-Opitz Syndrome 70 5.010
100
c OPT051 Opitz Gbbb Syndrome, Type I 46 5.010
101
P SCK005 Sickle Cell Disease 56 4.983
102
IMP005 Impotence 52 4.965
103
c HNT004 Huntington Disease-Like 2 52 4.957
104
P END044 Endometriosis 62 4.941
105
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 4.932
106
P ART022 Arthritis 71 4.918
107
P HPT023 Hepatocellular Carcinoma 96 4.914
108
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 4.907
109
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 4.907
110
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.894
111
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.894
112
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.894
113
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 4.894
114
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 4.894
115
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.894
116
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 4.894
117
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.894
118
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.894
119
c ART101 Aortic Valve Disease 2 66 4.869
120
P ADL010 Adult Respiratory Distress Syndrome 71 4.837
121
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.833
122
GLL048 Glial Tumor 52 4.825
123
GLM045 Glioma 63 4.825
124
P HYP838 Hyperlipidemia, Familial Combined, 3 61 4.810
125
ANT039 Antisynthetase Syndrome 55 4.739
126
P PNM007 Pneumonia 67 4.720
127
HYP081 Hypolipoproteinemia 49 4.718
128
HYP266 Hypoxia 57 4.713
129
P RHB003 Rhabdomyosarcoma 66 4.680
130
c TYP008 Type 1 Diabetes Mellitus 70 4.642
131
MNT002 Mental Depression 57 4.495
132
DPR016 Depression 65 4.495
133
P MLN008 Melanoma 76 4.463
134
P ALP008 Alopecia 54 4.442
135
P NPH012 Nephrotic Syndrome 60 4.432
136
P SCH015 Schizophrenia 74 4.410
137
P PLM036 Pulmonary Fibrosis 66 4.402
138
NNL006 Non-Alcoholic Steatohepatitis 54 4.387
139
LMY002 Leiomyoma 51 4.356
140
LNG099 Lung Disease 62 4.341
141
LYM007 Lymphangioleiomyomatosis 68 4.319
142
c TBR025 Tuberous Sclerosis 1 84 4.319
143
P TBR001 Tuberous Sclerosis 69 4.319
144
PRT036 Peritonitis 65 4.303
145
TRN015 Transient Cerebral Ischemia 63 4.298
146
END072 Endotheliitis 36 4.242
147
GLC003 Glucose Intolerance 54 4.221
148
HMC014 Homocysteinemia 52 4.219
149
P ALP009 Alopecia Areata 59 4.193
150
ATM095 Autoimmune Disease 61 4.180
151
LMB062 Limb Ischemia 55 4.171
152
c SCN036 Secondary Progressive Multiple Sclerosis 55 4.156
153
SVR004 Severe Combined Immunodeficiency 72 4.145
154
P LNG064 Lung Cancer Susceptibility 3 70 4.095
155
BCT022 Bacterial Infectious Disease 56 4.092
156
CRN030 Coronary Stenosis 50 4.085
157
c PCH010 Pachyonychia Congenita 3 43 4.062
158
EPT021 Epithelial Recurrent Erosion Dystrophy 46 4.047
159
P PRK057 Parkinson Disease, Late-Onset 80 4.045
160
LMY014 Leiomyoma, Uterine 56 4.021
161
c GLL024 Gallbladder Disease 1 52 4.006
162
P MJR001 Major Depressive Disorder 68 4.004
163
ALL006 Allergic Asthma 56 3.983
164
P LKM071 Leukemia, Chronic Lymphocytic 75 3.954
165
P LPS004 Lupus Erythematosus 61 3.947
166
P ART021 Arteriosclerosis 54 3.913
167
P RTN024 Retinoblastoma 73 3.893
168
VRC005 Varicose Veins 60 3.892
169
P BND020 Bone Disease 59 3.869
170
P GLM007 Glomerulonephritis 60 3.869
171
P CHR345 Chronic Pain 50 3.857
172
P EXN002 Exanthem 58 3.811
173
P ATR011 Atrial Fibrillation 66 3.796
174
P RSP003 Respiratory Failure 74 3.788
175
CLT003 Colitis 63 3.781
176
P EPL164 Epilepsy 68 3.719
177
DWN001 Down Syndrome 70 3.692
178
P OPT009 Optic Neuritis 57 3.680
179
NRT004 Neuritis 53 3.680
180
c HPT001 Hepatitis C 62 3.655
181
P MCR129 Microvascular Complications of Diabetes 1 68 3.653
182
INT002 Intermittent Claudication 61 3.629
183
P ANR048 Aniridia 1 64 3.607
184
OST003 Osteonecrosis 61 3.563
185
P SZR006 Seizure Disorder 70 3.553
186
P PRP019 Peripheral Nervous System Disease 58 3.530
187
ADL002 Adult Syndrome 70 3.528
188
HYP043 Hyperandrogenism 48 3.497
189
P RTN018 Retinal Disease 53 3.487
190
P DMN002 Dementia 66 3.449
192
IMM167 Immune Deficiency Disease 78 3.418
193
ART004 Aortic Atherosclerosis 47 3.417
194
P OVR042 Ovarian Cancer 88 3.400
195
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.398
196
P DRM010 Dermatomyositis 61 3.398
197
PRT037 Pertussis 65 3.385
198
c SCL052 Scleroderma, Familial Progressive 61 3.378
199
c DLT002 Dilated Cardiomyopathy 78 3.373
200
DBT010 Diabetic Neuropathy 54 3.371
201
c SYS001 Systemic Lupus Erythematosus 87 3.342
202
P UVT001 Uveitis 57 3.303
203
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.230
204
HYP555 Hypertriglyceridemia, Transient Infantile 38 3.222
205
VSC002 Vascular Dementia 60 3.216
206
PRD004 Prediabetes Syndrome 52 3.213
207
GLM044 Glomerular Disease 35 3.201
208
CRD132 Cardiac Conduction Defect 60 3.201
209
P MSC005 Muscular Dystrophy 67 3.201
210
CRT013 Carotid Stenosis 51 3.198
211
CRT016 Carotid Artery Disease 52 3.187
212
OST012 Osteoarthritis 77 3.182
213
P RCT021 Rectum Cancer 54 3.166
214
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 3.164
215
P PLY019 Polyneuropathy 52 3.141
216
MSC157 Muscular Dystrophy, Duchenne Type 79 3.126
217
47X002 47,xyy 48 3.126
218
P ACN011 Acne 57 3.113
219
GLB002 Glioblastoma 67 3.108
220
P HPT021 Hepatitis 69 3.084
221
HYP060 Hyperinsulinism 54 3.066
222
c LKM061 Leukemia, Acute Myeloid 83 3.042
223
CHL065 Cholangiocarcinoma 58 3.042
224
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 3.042
225
INT079 Intrahepatic Cholangiocarcinoma 51 3.042
226
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.040
227
HYP056 Hypoglycemia 65 3.022
228
c HYP740 Hyperlipoproteinemia, Type V 53 3.001
229
c MCR112 Microvascular Complications of Diabetes 2 42 2.991
230
P INF038 Influenza 68 2.975
231
RTN003 Retinal Ischemia 49 2.968
232
P CRB048 Cerebral Cavernous Malformations 63 2.962
233
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 2.950
234
THR024 Thrombosis 56 2.944
236
P PRK039 Parkinsonism 55 2.934
237
c MJR022 Major Affective Disorder 8 38 2.894
238
c MJR024 Major Affective Disorder 9 41 2.894
239
P BPL003 Bipolar Disorder 56 2.894
240
CHG001 Chagas Disease 66 2.883
241
P CNJ013 Conjunctivitis 66 2.870
242
PLM134 Pulmonary Fibrosis, Idiopathic 76 2.853
243
P CRD119 Cardiac Arrest 67 2.853
244
c HPT003 Hepatitis a 63 2.851
245
URM002 Uremia 47 2.833
246
CHL068 Cholestasis 61 2.833
247
P MYG005 Myoglobinuria 40 2.813
248
PRP030 Purpura 54 2.790
249
MSC007 Muscle Hypertrophy 64 2.775
250
TND005 Tendinitis 54 2.772
251
ALL014 Allergic Encephalomyelitis 34 2.772
252
GNG013 Gingivitis 59 2.756
253
P PRL003 Proliferative Glomerulonephritis 43 2.751
254
PRM236 Primary Biliary Cholangitis 60 2.748
255
LYM012 Lymphoplasmacytic Lymphoma 50 2.745
256
WLD007 Waldenstroem's Macroglobulinemia 63 2.745
257
ALL029 Allergic Disease 59 2.738
258
P NTR004 Neutropenia 63 2.736
259
CVR010 Cavernous Malformation 30 2.714
260
P PSR002 Psoriasis 63 2.701
261
PST011 Pustulosis of Palm and Sole 52 2.701
262
SCR011 Scrapie 39 2.696
263
P NRP001 Neuropathy 60 2.696
264
P FBR017 Fibrosarcoma 56 2.696
265
c PRC016 Pre-Eclampsia 65 2.696
266
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.687
267
P BLD134 Bladder Cancer 79 2.677
268
P EST001 Estrogen-Receptor Positive Breast Cancer 49 2.677
269
ACQ007 Acquired Immunodeficiency Syndrome 59 2.676
270
P PRN023 Prion Disease 60 2.676
271
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.655
272
P HNT016 Huntington Disease 73 2.655
273
P LTR001 Lateral Sclerosis 58 2.655
274
PRS021 Prostatic Adenoma 43 2.655
275
RTN020 Retinal Vascular Disease 46 2.655
276
PRS045 Prostatic Hypertrophy 53 2.655
277
MSN001 Mesangial Proliferative Glomerulonephritis 44 2.637
278
P PLM034 Pulmonary Emphysema 58 2.623
279
P NSP012 Nasopharyngeal Carcinoma 61 2.613
280
DGN001 Degenerative Disc Disease 49 2.613
281
P NRF002 Neurofibromatosis 57 2.613
282
SVR001 Severe Acute Respiratory Syndrome 67 2.605
283
KLD004 Keloid Disorder 39 2.598
284
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 2.595
285
MLD018 Mild Cognitive Impairment 48 2.592
286
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.588
287
TND004 Tendinopathy 45 2.571
288
c HPT073 Hepatitis C Virus 71 2.571
289
P CLC063 Celiac Disease 1 66 2.544
290
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 2.533
291
MCS002 Mucositis 56 2.527
292
ESP002 Esophageal Varix 51 2.527
293
XNT003 Xanthomatosis 49 2.527
294
CMB007 Combined Immunodeficiency 57 2.527
295
CLB022 Coloboma, Ocular, Autosomal Recessive 28 2.517
296
SCH003 Schizophreniform Disorder 55 2.505
297
P TRN020 Turner Syndrome 67 2.504
298
HRT012 Heart Valve Disease 53 2.483
299
P CHN012 Chondrosarcoma 57 2.482
300
OCL069 Ocular Motor Apraxia 57 2.482
301
RNL114 Renal Cell Carcinoma, Nonpapillary 80 2.482
302
SBC016 Subacute Delirium 43 2.482
303
ESP021 Esophageal Cancer 83 2.475
304
ALP097 Alopecia Universalis Congenita 57 2.457
305
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 2.446
306
ENT004 Enthesopathy 51 2.443
307
P MYC008 Myocarditis 59 2.436
308
c ACT134 Acute Liver Failure 59 2.432
309
P KDN017 Kidney Cancer 61 2.432
310
c HPT016 Hepatitis B 62 2.423
311
AGN016 Aging 54 2.405
312
LPD009 Lipid Storage Disease 45 2.395
313
DBT004 Diabetic Polyneuropathy 50 2.394
314
CRB011 Cerebrotendinous Xanthomatosis 65 2.388
315
PLP001 Pulpitis 48 2.386
316
P CTR002 Cataract 60 2.354
317
P PRP029 Porphyria 60 2.354
318
ALP048 Alopecia Totalis 31 2.354
319
P HYP040 Hypospadias 51 2.349
320
RCT020 Rectum Adenocarcinoma 48 2.349
321
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 2.344
322
RNL077 Renal Fibrosis 46 2.300
323
CHL147 Chlamydia Pneumonia 47 2.300
324
CHL123 Chlamydia 58 2.300
325
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.289
326
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 2.268
327
P ALC033 Alcohol Use Disorder 61 2.252
328
c THY107 Thymoma, Familial 42 2.250
329
c MST023 Mesothelioma, Malignant 56 2.250
330
P MYL006 Myeloid Leukemia 61 2.250
331
HLX001 Helix Syndrome 48 2.250
332
P THY023 Thymoma 64 2.250
333
P BNG032 Benign Mesothelioma 53 2.250
334
GST023 Gastric Ulcer 52 2.250
335
P PLY014 Polycystic Kidney Disease 69 2.201
336
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 2.201
337
P BLD062 Bile Duct Cancer 67 2.201
338
ANX010 Anxiety 70 2.183
339
P PLY041 Polymyositis 59 2.183
340
FBR047 Fibromyalgia 58 2.183
341
SQM006 Squamous Cell Carcinoma 60 2.183
342
P SLP005 Sleep Disorder 61 2.170
343
MVL001 Mevalonic Aciduria 66 2.163
344
P THY032 Thyroiditis 57 2.163
345
CNG184 Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects 56 2.162
346
P FNG006 Feingold Syndrome 1 62 2.154
347
PRS129 Prostatic Hyperplasia, Benign 49 2.151
348
ALL003 Allergic Rhinitis 67 2.151
349
P RNV001 Renovascular Hypertension 49 2.151
350
SKN016 Skin Disease 63 2.151
351
BRN012 Bronchiolitis Obliterans 56 2.151
352
P RHN004 Rhinitis 57 2.151
353
BRN002 Bronchiolitis 57 2.151
354
c MGR028 Migraine with or Without Aura 1 64 2.133
355
PLY105 Polycystic Ovary Syndrome 1 39 2.132
356
GT001 Gout 64 2.127
357
CVD001 Covid-19 57 2.109
358
WTH001 Withdrawal Disorder 48 2.099
359
c DPH024 Diaphragmatic Hernia, Congenital 64 2.099
360
P SKN015 Skin Carcinoma 71 2.099
361
P HYD006 Hydrocephalus 61 2.099
362
P THR015 Thrombophilia 51 2.099
363
P PRP003 Porphyria Cutanea Tarda 66 2.069
364
P VSC011 Vasculitis 61 2.069
365
AND005 Androgen Insensitivity Syndrome, Mild 21 2.069
366
HMN044 Human Immunodeficiency Virus Type 1 78 2.063
367
c BCT007 Bacterial Meningitis 55 2.045
368
P FML018 Familial Mediterranean Fever 73 2.045
369
P GLM040 Glioma Susceptibility 1 71 2.045
370
PRP016 Paraplegia 52 2.045
371
MLG169 Malignant Astrocytoma 57 2.045
372
STT001 Status Epilepticus 59 2.045
373
STM007 Stomatitis 54 2.045
374
c SYS043 Systemic Lupus Erythematosus 1 38 2.028
375
P END047 Endophthalmitis 53 2.021
376
MYC005 Myocardial Stunning 46 2.021
377
P HYP098 Hypereosinophilic Syndrome 66 2.007
378
P MNC007 Monocytic Leukemia 47 2.007
379
P CMP008 Compartment Syndrome 50 1.992
380
P INF032 Infertility 57 1.989
381
DSS032 Disease by Infectious Agent 55 1.989
382
ADN011 Adenoid Cystic Carcinoma 68 1.989
383
P CYS018 Cystitis 59 1.989
384
P ART023 Arthropathy 61 1.989
385
HGH043 High Grade Glioma 45 1.989
386
GNR004 Generalized Anxiety Disorder 55 1.989
387
CNS004 Constipation 56 1.971
388
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.961
389
HPT022 Hepatoblastoma 54 1.952
390
CRH001 Crohn's Disease 80 1.945
391
P THR014 Thrombocytopenia 66 1.943
392
HDN002 Head Injury 44 1.943
393
INS024 Insulin-Like Growth Factor I 78 1.930
394
P OVR049 Ovarian Disease 52 1.930
395
P TXP001 Toxoplasmosis 60 1.930
396
BRR014 Barrett Esophagus 66 1.919
397
P BRS044 Breast Adenocarcinoma 58 1.919
398
P MMB011 Membranous Nephropathy 50 1.919
399
DMY004 Demyelinating Disease 50 1.919
400
CRB086 Cerebral Aneurysms 40 1.919
401
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.914
402
INT030 Intracranial Aneurysm 55 1.914
403
c HYP839 Hyperlipidemia, Familial Combined, 1 30 1.879
404
LNG031 Lung Benign Neoplasm 51 1.877
405
CRN020 Coronary Restenosis 39 1.875
406
GSG001 Gas Gangrene 52 1.875
407
P DBT005 Diabetes Insipidus 54 1.869
408
BRK010 Burkitt Lymphoma 66 1.869
409
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.869
410
P MSC003 Muscular Atrophy 52 1.869
411
P OBS001 Obstructive Jaundice 48 1.869
412
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.865
413
c CRB191 Cerebral Cavernous Malformations 2 45 1.865
414
TST044 Testicular Torsion 45 1.865
415
P MLG056 Malignant Hyperthermia 66 1.865
416
P GLL018 Gallbladder Cancer 53 1.865
417
DRM006 Dermatitis 62 1.841
418
DBT002 Diabetic Autonomic Neuropathy 41 1.833
419
P PHC003 Pheochromocytoma 69 1.809
420
ADR040 Adrenal Gland Pheochromocytoma 46 1.809
421
c ATM011 Autoimmune Hepatitis 63 1.809
422
P ENC018 Encephalopathy 62 1.809
423
PTT037 Pituitary Tumors 44 1.809
424
ATN005 Autonomic Dysfunction 46 1.809
425
P LKM002 Leukemia 67 1.808
426
END057 Endometrial Cancer 72 1.805
427
INT323 Intraocular Pressure Quantitative Trait Locus 64 1.805
428
HYP088 Hyper-Igd Syndrome 51 1.805
429
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.805
430
P HMC002 Homocystinuria 53 1.805
431
ULC004 Ulcerative Colitis 74 1.805
432
HMP001 Hemopericardium 47 1.805
433
P PRC012 Pericardial Effusion 50 1.805
434
PLM010 Pulmonary Edema 55 1.805
435
CND006 Candida Glabrata 30 1.805
436
ASP030 Aspirin Resistance 40 1.803
437
c LKM070 Leukemia, Acute Monocytic 56 1.803
438
ACT200 Acute Monoblastic Leukemia 41 1.803
439
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.781
440
DFC004 Deficiency Anemia 74 1.770
441
CNT047 Contact Dermatitis 57 1.757
442
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.750
443
NSP002 Nasopharyngitis 45 1.750
444
SCH014 Schistosomiasis 56 1.750
445
MCL006 Macular Retinal Edema 57 1.750
446
PLM033 Pulmonary Embolism 58 1.750
447
OVR094 Ovarian Epithelial Cancer 39 1.750
448
IDP022 Idiopathic Spinal Cord Herniation 17 1.750
449
P ATS364 Autism 69 1.737
450
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.737
451
P DRR001 Diarrhea 55 1.737
452
MYF001 Myofibroma 42 1.720
453
PSY004 Psychotic Disorder 66 1.712
454
CYS001 Cystic Fibrosis 78 1.705
455
PLS009 Plasma Cell Neoplasm 64 1.690
456
STR077 Streptococcal Toxic-Shock Syndrome 35 1.689
457
ALC007 Alcohol Dependence 66 1.689
458
GST092 Gastroesophageal Reflux 61 1.689
459
THY029 Thyroid Carcinoma 51 1.689
460
ADG002 Audiogenic Seizures 25 1.689
461
INS001 Insulinoma 59 1.689
462
P ECL001 Eclampsia 52 1.689
463
HYP014 Hyperuricemia 51 1.689
464
AMR003 Amaurosis Fugax 33 1.689
465
CHR178 Chromosomal Triplication 34 1.689
466
P INS002 in Situ Carcinoma 53 1.682
467
SCH012 Schizoaffective Disorder 50 1.681
468
SCK003 Sickle Cell Anemia 74 1.674
469
SPR126 Superior Semicircular Canal Dehiscence 41 1.674
470
c HMG029 Hemoglobin Se Disease 40 1.674
471
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 1.664
472
CHR100 Chronic Ulcer of Skin 57 1.664
473
INF013 Inferior Myocardial Infarction 33 1.664
474
SYS003 Systolic Heart Failure 49 1.664
475
NNC012 Non-Classic Congenital Adrenal Hyperplasia Due to 21-Hydroxylase Deficiency 17 1.664
476
c HMC039 Hemochromatosis, Type 1 73 1.625
477
P FML011 Familial Adenomatous Polyposis 71 1.625
478
ATR057 Atrioventricular Block 54 1.625
479
P ASP006 Aspergillosis 72 1.625
480
P ART018 Aortic Valve Insufficiency 52 1.625
481
P LCH002 Lichen Planus 54 1.625
482
P HYP061 Hypertrophic Cardiomyopathy 69 1.625
483
P URT039 Urticaria 58 1.625
484
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.625
485
P HRD022 Hordeolum 28 1.625
486
SPN027 Spinal Stenosis 59 1.625
487
ANC002 Anca-Associated Vasculitis 44 1.625
488
PNC129 Pancreatic Adenocarcinoma 65 1.587
489
P PLY018 Polycythemia 56 1.587
490
CHL056 Cheilitis 46 1.587
491
HMG005 Hemoglobinopathy 56 1.587
492
c PNS012 Paine Syndrome 60 1.560
493
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.560
494
CD4008 Cd4/cd8 T-Cell Ratio 19 1.557
495
P KLZ004 Kala-Azar 1 41 1.557
496
LPM012 Lipomatosis, Multiple 60 1.557
497
P MDL005 Medulloblastoma 75 1.557
498
HPT004 Hepatic Coma 43 1.557
499
CMP010 Complex Regional Pain Syndrome 60 1.557
500
LSH001 Leishmaniasis 64 1.557
501
PLM005 Pleomorphic Lipoma 40 1.557
502
ANG020 Angiosarcoma 64 1.557
503
ERY003 Erythema Multiforme 56 1.557
504
HPT019 Hepatic Encephalopathy 59 1.557
505
P TMP001 Temporal Lobe Epilepsy 49 1.557
506
P BNC003 Bone Cancer 58 1.557
507
P HYP121 Hypoalphalipoproteinemia 43 1.557
508
BCK006 Back Pain 47 1.557
509
PRM243 Primary Bone Cancer 22 1.557
510
END040 Endogenous Depression 55 1.548
511
NRT001 Neurotic Disorder 56 1.548
512
ACT011 Acute Contagious Conjunctivitis 42 1.548
513
CLF027 Cleft Palate, Isolated 64 1.517
514
P SRC025 Sarcoidosis 1 71 1.517
515
MCR004 Macroglobulinemia 49 1.517
516
ILS001 Ileus 50 1.502
517
P ANG015 Angioedema 56 1.502
518
GST037 Gastroparesis 52 1.502
519
INC002 Inclusion Body Myositis 57 1.487
520
CRV035 Cervical Cancer 73 1.484
521
P ATX030 Ataxia-Telangiectasia 80 1.484
522
CNZ001 Coenzyme Q10 Deficiency Disease 41 1.484
523
ATS010 Autosomal Recessive Disease 42 1.484
524
PYR010 Peyronie's Disease 50 1.484
525
HSH003 Hashimoto Thyroiditis 60 1.484
526
CTN007 Cutaneous Leishmaniasis 62 1.484
527
ADR005 Adrenal Carcinoma 62 1.484
528
BNG036 Bone Giant Cell Tumor 49 1.484
529
TRC005 Tracheal Stenosis 43 1.484
530
TLN003 Telangiectasis 51 1.484
531
P RNL015 Renal Hypertension 45 1.484
532
c VRL005 Viral Pneumonia 53 1.484
533
BRN024 Bronchitis 67 1.484
534
P TST026 Testicular Germ Cell Cancer 44 1.484
535
GRM005 Germ Cell Cancer 46 1.484
536
MRP001 Morphine Dependence 42 1.484
537
AMN001 Amenorrhea 54 1.484
538
AZS001 Azoospermia 45 1.484
539
P ICH004 Ichthyosis 56 1.484
540
PRT035 Peritoneum Cancer 45 1.484
541
c JVN010 Juvenile Rheumatoid Arthritis 66 1.484
542
BRN056 Bronchopulmonary Dysplasia 56 1.484
543
P VTR007 Vitreoretinopathy 46 1.484
544
RTN017 Retinal Detachment 60 1.484
545
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.484
546
PRS047 Prostatitis 58 1.481
547
CRB009 Cerebritis 43 1.481
548
RTR008 Root Resorption 44 1.448
549
ADR022 Adrenomyeloneuropathy 39 1.440
550
ADR007 Adrenoleukodystrophy 73 1.440
552
P VNB005 Van Buchem Disease 58 1.434
553
P OPT048 Opitz-Gbbb Syndrome 49 1.434
554
CYT018 Cytochrome P450 2d6 Variant 26 1.434
555
HRW001 Hair Whorl 35 1.408
556
NRM005 Neuromuscular Disease 63 1.408
557
ANX004 Anoxia 40 1.406
558
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 1.406
559
P MYS003 Myasthenia Gravis 68 1.406
560
P FRG001 Fragile X Syndrome 70 1.406
561
c NPH049 Nephrotic Syndrome, Type 2 51 1.406
562
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.406
563
SVR097 Severe Cutaneous Adverse Reaction 69 1.406
564
c NPH055 Nephrotic Syndrome, Type 1 52 1.406
565
CHR619 Chromosome 2q35 Duplication Syndrome 64 1.406
566
ERY066 Erythema Multiforme Major 29 1.406
567
LRN003 Learning Disability 49 1.406
568
P MVM001 Movement Disease 61 1.406
569
P GST044 Gastritis 55 1.406
570
KRT009 Keratosis 53 1.406
571
P AGG001 Aggressive Periodontitis 55 1.406
572
AMN003 Amnestic Disorder 54 1.406
573
WLL004 Wallerian Degeneration 38 1.406
574
LCH013 Lichen Planus Pemphigoides 33 1.406
575
c HRM017 Hermansky-Pudlak Syndrome 2 55 1.374
576
OST017 Osteomyelitis 63 1.374
577
ADN018 Adenoma 59 1.361
578
PNM013 Pneumococcal Meningitis 43 1.322
579
P MYC084 Mycobacterium Tuberculosis 1 68 1.322
580
c OPT053 Optic Atrophy 1 62 1.322
581
PLY150 Polykaryocytosis Inducer 29 1.322
582
BCT021 Bacterial Sepsis 43 1.322
583
GLC086 Glucocorticoid-Induced Osteoporosis 43 1.322
584
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.322
585
CRD137 Cardiogenic Shock 56 1.322
586
ATN021 Autoinflammatory Syndrome 32 1.322
587
BRR002 Barrett's Adenocarcinoma 37 1.322
588
CLL010 Cellular Ependymoma 57 1.322
589
c HRD002 Hereditary Angioedema 62 1.322
590
P BNG030 Benign Ependymoma 51 1.322
591
P GRF003 Graft-Versus-Host Disease 71 1.322
592
PLC002 Plica Syndrome 35 1.322
593
P GRV001 Graves' Disease 55 1.322
594
P PST095 Post-Thrombotic Syndrome 51 1.322
595
HMP005 Hemiplegia 54 1.322
596
c INF023 Inflammatory Breast Carcinoma 49 1.322
597
FLL008 Folliculitis 46 1.322
598
SYN007 Synovitis 55 1.322
599
P MNN013 Meningitis 65 1.322
600
DYS073 Dysphagia 53 1.322
601
P AMY004 Amyloidosis 70 1.302
602
URT010 Ureteral Obstruction 45 1.302
603
GST045 Gastroenteritis 58 1.302
604
LYS002 Lysosomal Storage Disease 51 1.302
605
CHR081 Choroideremia 58 1.285
606
RCK004 Rickets 68 1.270
607
P INT260 Intracranial Berry Aneurysm 40 1.270
608
VSC053 Visceral Steatosis, Congenital 34 1.270
609
c MJR006 Major Affective Disorder 5 32 1.270
610
c MJR023 Major Affective Disorder 7 33 1.270
611
c MJR004 Major Affective Disorder 4 28 1.270
612
c MJR003 Major Affective Disorder 6 32 1.270
613
c MJR008 Major Affective Disorder 2 34 1.270
614
P MJR007 Major Affective Disorder 1 42 1.270
615
DSS008 Disease of Mental Health 74 1.270
616
INT053 Intracranial Vasospasm 36 1.270
617
c THR092 Thrombophilia Due to Thrombin Defect 74 1.254
618
KRT002 Keratomalacia 55 1.246
619
P AVS003 Avascular Necrosis 41 1.228
620
CRD223 Cardiac Arrhythmia 63 1.228
621
c LKM063 Leukemia, Chronic Myeloid 71 1.228
622
P APL001 Aplastic Anemia 73 1.228
623
HMR023 Hemorrhagic Cystitis 43 1.228
624
ILT001 Ileitis 48 1.228
625
HYP025 Hyperphosphatemia 48 1.228
626
DDN011 Duodenal Atresia 48 1.228
627
ACT119 Acute Promyelocytic Leukemia 62 1.228
628
c AVS006 Avascular Necrosis of Femoral Head, Primary, 1 42 1.228
629
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.228
630
P ANG001 Angelman Syndrome 65 1.228
631
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.228
632
LNG091 Lung Mucoepidermoid Carcinoma 32 1.228
633
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.228
634
c PST005 Posterior Uveitis 54 1.228
635
MCP006 Mucoepidermoid Carcinoma 48 1.228
636
CLF001 Cleft Lip 53 1.228
637
CHR074 Choriocarcinoma 46 1.228
638
HMG002 Hemoglobinuria 50 1.228
639
P LCT001 Lactic Acidosis 51 1.228
641
ALV001 Alveolar Periostitis 34 1.228
642
BRC012 Brucellosis 66 1.228
643
PHR003 Pharyngitis 58 1.228
644
BRS051 Breast Disease 58 1.228
645
ANK001 Ankylosis 51 1.228
646
IRN002 Iron Metabolism Disease 57 1.228
647
SKN023 Skin Tag 41 1.228
648
c ACT135 Acute Graft Versus Host Disease 51 1.228
649
HML018 Homologous Wasting Disease 21 1.228
650
DFC001 Defective Apolipoprotein B-100 24 1.228
651
ORL015 Oral Squamous Cell Carcinoma 43 1.190
652
P OVR106 Ovarian Clear Cell Carcinoma 44 1.190
653
LYS012 Lysosomal Acid Lipase Deficiency 65 1.176
654
c PCH015 Pachyonychia Congenita 1 60 1.158
655
NRR001 Neuroretinitis 42 1.152
656
RTN023 Retinitis 46 1.152
657
c PRS136 Prostate Cancer, Hereditary, 6 33 1.139
658
c PRS130 Prostate Cancer, Hereditary, 8 32 1.139
659
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.122
660
ATM100 Autoimmune Optic Neuritis 28 1.122
661
LPT014 Leptin Deficiency or Dysfunction 78 1.122
662
c VSC019 Vesicoureteral Reflux 1 57 1.122
664
DFF010 Diffuse Alopecia Areata 25 1.122
665
P PNM006 Pneumoconiosis 55 1.122
666
MDD018 Middle East Respiratory Syndrome 44 1.122
667
CHL070 Cholesterol Embolism 39 1.122
668
P ESN008 Eosinophilic Pneumonia 50 1.122
669
CHL004 Cholelithiasis 49 1.122
670
ANT018 Anthracosis 51 1.122
671
GTR002 Goiter 53 1.122
672
TST015 Testicular Disease 42 1.122
673
THR004 Thrombocytosis 53 1.122
674
MTR002 Mitral Valve Insufficiency 52 1.122
675
TTN003 Tetanus 65 1.122
676
MDD011 Mood Disorder 62 1.122
677
c ART115 Aortic Valve Disease 1 74 1.121
678
MYT011 Myotonia 39 1.121
679
LYM133 Lymphoma, Hodgkin, Classic 74 1.121
680
c LKM056 Leukemia, Chronic Lymphocytic 2 48 1.121
681
AND020 Androgen Insensitivity, Partial 55 1.121
682
c PNC108 Pancreatitis, Hereditary 69 1.121
683
P CNR004 Cone-Rod Dystrophy 2 74 1.121
684
CRN239 Carnitine Deficiency, Systemic Primary 61 1.121
685
P LYM118 Lymphoma 67 1.121
686
RHM028 Rheumatic Heart Disease 56 1.121
687
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 1.121
688
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 1.121
689
EWN003 Ewing Sarcoma 70 1.121
690
HMR039 Hemorrhage, Intracerebral 57 1.121
691
c TBR026 Tuberous Sclerosis 2 71 1.121
692
c CHL119 Cholangitis, Primary Sclerosing 58 1.121
693
CNT061 Conotruncal Heart Malformations 66 1.121
694
SCH038 Schopf-Schulz-Passarge Syndrome 51 1.121
695
c BRT038 Baraitser-Winter Syndrome 1 41 1.121
696
c WLM013 Wilms Tumor 1 66 1.121
697
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.121
698
HYP748 Hypertelorism 46 1.121
699
IMM162 Immunoglobulin E Concentration, Serum 28 1.121
700
CMR002 Coumarin Resistance 59 1.121
701
P NNN008 Noonan Syndrome 1 77 1.121
702
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 1.121
703
c INF145 Infantile Liver Failure Syndrome 1 43 1.121
704
GST071 Gastrointestinal Carcinoma 46 1.121
705
INT253 Intestinal Benign Neoplasm 46 1.121
706
FML008 Familial Retinoblastoma 50 1.121
707
NTR005 Nutritional Deficiency Disease 61 1.121
708
P MLG074 Malignant Mesenchymoma 40 1.121
709
HDG004 Hodgkin's Granuloma 23 1.121
710
P CHL066 Cholangitis 52 1.121
711
TXC002 Toxic Encephalopathy 52 1.121
712
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 1.121
713
RHB001 Rhabdoid Cancer 68 1.121
714
CLR017 Clear Cell Sarcoma 44 1.121
715
SPN035 Spindle Cell Sarcoma 54 1.121
716
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 1.121
717
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 1.121
718
CMM005 Common Cold 56 1.121
719
BRN028 Brain Cancer 74 1.121
720
P ESP024 Esophagitis 60 1.121
721
P SCL009 Sclerosing Cholangitis 48 1.121
722
SRC014 Sarcoma 65 1.121
723
THY030 Thyroid Gland Disease 50 1.121
724
P EYD002 Eye Disease 57 1.121
725
GST049 Gastrointestinal System Cancer 49 1.121
726
c PSD047 Pseudo-Turner Syndrome 52 1.121
727
SFT003 Soft Tissue Sarcoma 57 1.121
728
LYM019 Lymphosarcoma 46 1.121
729
HDG006 Hodgkin's Paragranuloma 21 1.121
730
c EHL080 Ehlers-Danlos Syndrome, Musculocontractural Type, 1 52 1.085
731
ADR016 Adrenal Cortical Carcinoma 62 1.049
732
ADR054 Adrenocortical Carcinoma, Hereditary 47 1.049
733
P STS003 Sitosterolemia 53 1.049
734
ADR004 Adrenal Cortical Adenocarcinoma 38 1.049
735
P END033 Endocarditis 58 1.049
736
ESN015 Eosinophilic Fasciitis 47 1.012
737
FSC004 Fasciitis 49 1.012
738
P THL005 Thalassemia 56 0.996
739
MRL006 Meralgia Paraesthetica, Familial 27 0.996
740
P MLT008 Multinodular Goiter 42 0.996
741
c BTT014 Beta-Thalassemia 72 0.996
742
P CTN015 Cutaneous T Cell Lymphoma 48 0.996
743
P RPP006 Rippling Muscle Disease 2 44 0.996
744
ODN022 Odontoid Hypoplasia 17 0.996
745
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.996
746
P ERY008 Erythromelalgia 50 0.996
747
FLL031 Follicular Adenoma 40 0.996
748
INT010 Intracranial Embolism 48 0.996
749
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.996
750
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.996
751
HRY003 Hairy Cell Leukemia 61 0.996
752
FRZ001 Frozen Shoulder 55 0.996
753
BRS064 Bursitis 51 0.996
754
DSS009 Disseminated Intravascular Coagulation 57 0.996
755
P PTS002 Ptosis 52 0.996
756
INF057 Inflammatory Linear Verrucous Epidermal Nevus 33 0.996
757
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.971
758
c ATM022 Autoimmune Myocarditis 36 0.971
759
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 0.971
760
P HYP076 Hyperthyroidism 53 0.971
761
PRT082 Preterm Premature Rupture of the Membranes 57 0.887
762
P CRC039 Coarctation of Aorta 46 0.887
763
P HYP083 Hypopituitarism 52 0.887
764
P EMB005 Embryonal Rhabdomyosarcoma 53 0.887
765
P GLL022 Guillain-Barre Syndrome 60 0.887
766
CRT004 Carotid Artery Thrombosis 39 0.887
767
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.887
768
HMP009 Haemophilus Influenzae 41 0.887
769
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.874
770
HYP781 Hypoascorbemia 52 0.874
771
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.874
772
c SBC035 Subacute Cutaneous Lupus Erythematosus 34 0.832
773
ACT167 Acute Generalized Exanthematous Pustulosis 38 0.832
774
MLR004 Malaria 80 0.832
775
TND006 Tendinosis 41 0.832
776
P MTC003 Metachromatic Leukodystrophy 71 0.832
777
PLY001 Polycythemia Vera 69 0.832
778
P LKD001 Leukodystrophy 59 0.832
779
TNG007 Tongue Carcinoma 52 0.832
780
OBS082 Obstructive Nephropathy 41 0.832
781
INT075 Intracranial Hypertension 53 0.832
782
P CTN003 Cutaneous Lupus Erythematosus 52 0.832
783
PLR008 Pleurisy 50 0.832
784
P BRN022 Bronchiectasis 60 0.832
785
c RNG021 Ring Chromosome 5 20 0.832
786
XNT009 Xanthoma Disseminatum 34 0.832
787
LTH002 Lathosterolosis 38 0.793
788
P PTY003 Pityriasis Rubra Pilaris 57 0.793
789
HYP457 Hypertrophic Scars 42 0.793
790
P ERY036 Erythema Nodosum 49 0.793
791
P DFF019 Diffuse Gastric Cancer 50 0.793
792
c CRB094 Cerebral Cavernous Malformations 3 41 0.793
793
NRM001 Neuromyelitis Optica 61 0.793
794
P PMP001 Pemphigus 55 0.793
795
PST092 Posttransplant Acute Limbic Encephalitis 28 0.793
796
c VRL010 Viral Hepatitis 53 0.793
797
EMB004 Embryonal Carcinoma 56 0.793
798
MSL001 Measles 61 0.793
799
HLC007 Helicobacter Pylori Infection 67 0.762
800
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.762
801
ANG049 Angioedema Induced by Ace Inhibitors 40 0.761
802
CHN019 Chand Syndrome 32 0.761
803
SCH036 Scheie Syndrome 73 0.761
804
VGN023 Vaginitis 56 0.761
805
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.756
806
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 0.756
807
NWB001 Newborn Respiratory Distress Syndrome 56 0.756
808
IND017 Indolent Plasma Cell Myeloma 39 0.756
809
RSP007 Respiratory Distress Syndrome, Infant 40 0.756
810
c OVR114 Ovarian Cancer 1 59 0.725
811
c FML001 Familial Atrial Fibrillation 65 0.725
812
BRD001 Brody Myopathy 55 0.725
813
ACR041 Acromelic Frontonasal Dysostosis 53 0.725
814
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.725
815
APR006 Apert Syndrome 70 0.725
816
CVR006 Cavernous Hemangioma 51 0.725
817
P HMN010 Hemangioma 62 0.725
818
P CPL006 Capillary Hemangioma 53 0.725
819
c CRN172 Coronary Heart Disease 3 15 0.687
820
CRT045 Creatine Phosphokinase, Elevated Serum 39 0.687
821
P URN019 Urinary Tract Infection 49 0.687
822
CHR710 Chronic Spontaneous Urticaria 45 0.687
823
c PRG020 Paragangliomas 3 39 0.687
824
VTR016 Vater/vacterl Association 49 0.687
825
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 0.687
826
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 0.687
827
PNG002 Pain Agnosia 51 0.687
828
BLD051 Blood Coagulation Disease 53 0.687
829
P TRM003 Tremor 48 0.687
830
P ANT006 Antiphospholipid Syndrome 55 0.687
831
P CND004 Candidiasis 58 0.687
832
MLT006 Multidrug-Resistant Tuberculosis 47 0.687
833
ANV001 Anovulation 47 0.687
834
HYP005 Hypokalemia 55 0.687
835
SBC019 Subcutaneous Mycosis 35 0.687
836
CRB008 Cerebral Atherosclerosis 46 0.687
837
NRG002 Neurogenic Bladder 55 0.687
838
NRL004 Neuroleptic Malignant Syndrome 52 0.687
839
SPR010 Sporotrichosis 46 0.687
840
ORL005 Oral Candidiasis 56 0.687
841
VCT001 Vacterl Association 47 0.687
842
CHR463 Chronic Actinic Dermatitis 36 0.615
843
P OVR082 Overgrowth Syndrome 49 0.561
844
RST023 Resting Heart Rate, Variation in 40 0.561
845
P MYM013 Moyamoya Disease 1 59 0.561
846
MND023 Mend Syndrome 49 0.561
847
MST021 Meester-Loeys Syndrome 42 0.561
848
CRT072 Creutzfeldt-Jakob Disease 68 0.561
849
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.561
850
MTR088 Mature T-Cell and Nk-Cell Lymphoma 42 0.561
851
c XLN229 X-Linked Chondrodysplasia Punctata 2 46 0.561
852
INF034 Infective Endocarditis 54 0.561
853
CMP034 Complete Androgen Insensitivity Syndrome 55 0.561
854
P SLM003 Salmonellosis 54 0.561
855
CLS016 Clostridium Difficile Colitis 49 0.561
856
KRT019 Keratitis, Hereditary 66 0.561
857
LGG001 Legg-Calve-Perthes Disease 60 0.561
858
c MYT020 Myotonic Dystrophy 2 57 0.561
859
P LKM062 Leukemia, Acute Lymphoblastic 69 0.561
860
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.561
861
HYP236 Hyperbilirubinemia, Rotor Type 44 0.561
862
SPR004 Supravalvular Aortic Stenosis 57 0.561
863
c SZR022 Seizures, Benign Familial Neonatal, 1 43 0.561
864
c NRF024 Neurofibromatosis, Type I 72 0.561
865
DCT002 Ductal Carcinoma in Situ 58 0.561
866
CHR431 Chronic Venous Insufficiency 48 0.561
867
c HRD026 Hereditary Ataxia 47 0.561
868
INT067 Interstitial Nephritis 46 0.561
869
PMP014 Pemphigoid 51 0.561
870
GYN001 Gynecomastia 47 0.561
871
P OPN001 Open-Angle Glaucoma 55 0.561
872
AVN001 Avian Influenza 61 0.561
873
P RBL001 Rubella 58 0.561
874
DBT006 Diabetic Macular Edema 48 0.561
875
MSC193 Muscular Lipidosis 22 0.561
876
SYN036 Syncope 45 0.561
877
P SYS005 Systemic Scleroderma 74 0.561
878
MTS001 Mutism 44 0.561
879
LNG039 Lung Squamous Cell Carcinoma 57 0.561
880
ANT024 Anthrax Disease 58 0.561
881
BLL006 Bullous Pemphigoid 61 0.561
882
P VNS003 Venous Insufficiency 55 0.561
883
P MMP001 Mumps 57 0.561
884
P DNG005 Dengue Virus 56 0.561
885
P FCL005 Focal Segmental Glomerulosclerosis 57 0.561
886
P HYP069 Hyperparathyroidism 62 0.561
887
MYL031 Myeloproliferative Neoplasm 66 0.561
888
P MCR010 Microcephaly 60 0.561
889
INF021 Infant Gynecomastia 30 0.561
890
MNN009 Meningoencephalitis 48 0.561
891
P AXN001 Axonal Neuropathy 35 0.561
892
PLC008 Placenta Disease 49 0.561
893
c SPR009 Sporadic Breast Cancer 42 0.561
894
BCT002 Bacterial Vaginosis 53 0.561
895
GNG012 Gingival Overgrowth 49 0.561
896
P MTR014 Motor Neuron Disease 65 0.561
897
PLR005 Pleuropneumonia 33 0.561
898
P ART005 Arteriovenous Malformation 65 0.561
899
HYP080 Hypogonadism 50 0.561
900
PST028 Post-Traumatic Stress Disorder 59 0.561
901
P MYT002 Myotonic Dystrophy 51 0.561
902
MST020 Mast Cell Activation Syndrome 28 0.561
903
CLP006 Clopidogrel Resistance 44 0.561
904
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.509
905
GLC008 Glucose Metabolism Disease 40 0.509
906
OST115 Osteonecrosis of the Jaw 41 0.435
907
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.435
908
P DPY001 Dupuytren Contracture 39 0.435
909
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.435
910
PRT019 Protein-Losing Enteropathy 45 0.435
911
P MTC133 Mitochondrial Myopathy 50 0.435
912
P PRK001 Porokeratosis 55 0.435
913
MNN017 Mononeuropathy 41 0.435
914
LST001 Listeriosis 59 0.435
915
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 0.435
916
LYS003 Lysinuric Protein Intolerance 57 0.397
917
CRN309 Cranial Neuralgia 21 0.397
918
SRT004 Serotonin Syndrome 54 0.397
919
SPS057 Spasticity 42 0.397
920
c DWL002 Dowling-Degos Disease 1 58 0.397
921
MSC152 Muscular Dystrophy, Becker Type 69 0.397
922
MYC006 Mycosis Fungoides 65 0.397
923
TNG002 Tangier Disease 64 0.397
924
P RTN008 Retinitis Pigmentosa 80 0.397
925
PSR001 Psoriatic Arthritis 62 0.397
926
P SPR120 Supranuclear Palsy, Progressive, 1 69 0.397
927
P DRM053 Dermatitis, Atopic 65 0.397
928
BRT054 Brittle Bone Disorder 74 0.397
929
c SPN225 Spondyloarthropathy 1 70 0.397
930
OTT002 Otitis Media 71 0.397
931
P ADL017 Adult T-Cell Leukemia 56 0.397
932
MTB004 Metabolic Acidosis 48 0.397
933
FRS012 First-Degree Atrioventricular Block 39 0.397
934
THR099 Third-Degree Atrioventricular Block 42 0.397
935
c PRM108 Primary Progressive Multiple Sclerosis 51 0.397
936
c NLD006 Nail Disorder, Nonsyndromic Congenital, 9 35 0.397
937
DFF005 Diffuse Large B-Cell Lymphoma 54 0.397
938
CYN002 Cyanosis, Transient Neonatal 43 0.397
939
c ATM024 Autoimmune Pancreatitis 52 0.397
940
MCR191 Microscopic Colitis 46 0.397
941
C1N001 C1 Inhibitor Deficiency 43 0.397
942
SXL003 Sexual Disorder 49 0.397
943
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.397
944
c GRV008 Graves Disease 1 54 0.397
945
c HNT010 Huntington Disease-Like 1 55 0.397
946