Search results for ACE

1209 hits were found for ACE

# Family MCID Name MIFTS Score
1
ANG049 Angioedema Induced by Ace Inhibitors 40 7.046
2
STH001 Saethre-Chotzen Syndrome 67 5.273
3
APR006 Apert Syndrome 70 5.252
4
FRB001 Farber Lipogranulomatosis 59 5.241
5
PFF001 Pfeiffer Syndrome 79 4.552
6
ACR008 Acrocallosal Syndrome 69 3.793
7
SPN289 Spondylometaepiphyseal Dysplasia, Short Limb-Hand Type 34 3.706
8
P RNL028 Renal Tubular Dysgenesis 51 3.164
9
c MCR113 Microvascular Complications of Diabetes 3 52 3.042
10
P HRT032 Heart Disease 75 2.785
11
ISC004 Ischemia 58 2.716
12
P ARC016 Auriculocondylar Syndrome 1 39 2.641
13
P KDN018 Kidney Disease 72 2.554
14
RNL078 Renal Dysplasia 50 2.514
15
P MYC007 Myocardial Infarction 70 2.511
16
P ANG015 Angioedema 57 2.482
17
CNG034 Congestive Heart Failure 69 2.407
18
LPP008 Lipoprotein Quantitative Trait Locus 62 2.326
19
c HYP595 Hypertension, Essential 84 2.322
20
P DBT009 Diabetes Mellitus 64 2.160
21
c CHR684 Chronic Kidney Disease 70 2.063
22
c ACT075 Acute Myocardial Infarction 57 2.063
23
END086 End Stage Renal Disease 51 2.061
24
HMR039 Hemorrhage, Intracerebral 57 2.032
25
c DLT002 Dilated Cardiomyopathy 79 2.022
26
STR067 Stroke, Ischemic 81 1.999
27
P CRD246 Cardiovascular System Disease 57 1.982
28
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 1.971
29
P VSC007 Vascular Disease 63 1.947
30
CRB039 Cerebrovascular Disease 67 1.924
31
P CRN300 Coronary Heart Disease 1 63 1.887
32
P ATR011 Atrial Fibrillation 66 1.879
33
P ALZ034 Alzheimer Disease 88 1.875
34
P RNV001 Renovascular Hypertension 48 1.852
35
P NPH012 Nephrotic Syndrome 60 1.798
36
PRP027 Peripheral Vascular Disease 71 1.793
37
P SRC025 Sarcoidosis 1 70 1.775
38
P PLM037 Pulmonary Hypertension 67 1.772
39
HYP005 Hypokalemia 55 1.767
40
P NRP001 Neuropathy 56 1.755
41
c HRD002 Hereditary Angioedema 60 1.749
42
c SYS001 Systemic Lupus Erythematosus 86 1.743
43
HYP006 Hypertensive Heart Disease 49 1.730
44
NPH010 Nephrosclerosis 50 1.723
45
P FCL005 Focal Segmental Glomerulosclerosis 57 1.716
46
P SYS005 Systemic Scleroderma 68 1.709
47
ANG054 Angina Pectoris 66 1.702
48
ANR004 Anuria 46 1.701
49
P HYP061 Hypertrophic Cardiomyopathy 70 1.693
50
DBT010 Diabetic Neuropathy 54 1.693
51
c MLG069 Malignant Hypertension 47 1.693
52
P PSR002 Psoriasis 62 1.655
53
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.655
54
ATH013 Atherosclerosis Susceptibility 65 1.654
55
CNN003 Conn's Syndrome 79 1.643
56
MLR004 Malaria 81 1.630
57
CHG001 Chagas Disease 66 1.630
58
CVD001 Covid-19 44 1.603
59
c DBT099 Diabetes Mellitus, Type I 65 1.576
60
P MCR115 Microvascular Complications of Diabetes 5 66 1.564
61
P GLM007 Glomerulonephritis 57 1.556
62
P CRD119 Cardiac Arrest 67 1.552
63
LPD008 Lipid Metabolism Disorder 62 1.547
64
c SVR001 Severe Acute Respiratory Syndrome 62 1.539
65
c PRC016 Pre-Eclampsia 63 1.525
66
P PNM007 Pneumonia 68 1.505
67
PLM010 Pulmonary Edema 54 1.495
68
PLM033 Pulmonary Embolism 59 1.489
69
ART016 Aortic Aneurysm 69 1.484
70
P DMN002 Dementia 66 1.484
71
P RNL015 Renal Hypertension 47 1.478
72
P PLY014 Polycystic Kidney Disease 62 1.466
73
LNG099 Lung Disease 60 1.466
74
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 1.454
75
P ART021 Arteriosclerosis 54 1.454
76
SYS003 Systolic Heart Failure 49 1.447
77
ART140 Arteries, Anomalies of 52 1.444
78
DFC004 Deficiency Anemia 70 1.440
79
P SLP006 Sleep Apnea 69 1.440
80
VSC002 Vascular Dementia 57 1.440
81
P RSP003 Respiratory Failure 74 1.433
82
SLC006 Silicosis 56 1.433
83
GLC003 Glucose Intolerance 54 1.433
84
CRT013 Carotid Stenosis 50 1.433
85
INT007 Intermediate Coronary Syndrome 55 1.430
86
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 1.426
87
ALC007 Alcohol Dependence 66 1.426
88
P MGR003 Migraine with Aura 52 1.426
89
CRN030 Coronary Stenosis 50 1.426
90
URM002 Uremia 49 1.426
91
ANX010 Anxiety 73 1.418
92
DST006 Diastolic Heart Failure 45 1.418
93
P MSC005 Muscular Dystrophy 66 1.410
94
PRP030 Purpura 54 1.410
95
PRP080 Peripheral Artery Disease 53 1.410
96
P ECL001 Eclampsia 50 1.410
97
P MJR001 Major Depressive Disorder 68 1.401
98
P GCH001 Gaucher's Disease 63 1.401
99
P MYC008 Myocarditis 59 1.401
100
PRT013 Portal Hypertension 59 1.401
101
P ATS364 Autism 70 1.392
102
P HYP086 Hypothyroidism 69 1.392
103
P ADL010 Adult Respiratory Distress Syndrome 65 1.392
104
P MMB011 Membranous Nephropathy 50 1.392
105
CRN020 Coronary Restenosis 39 1.392
106
MDD011 Mood Disorder 62 1.382
107
P SCL018 Scoliosis 60 1.382
108
P INF037 Inflammatory Bowel Disease 54 1.382
109
PLM012 Pulmonary Sarcoidosis 53 1.382
110
P CTR002 Cataract 60 1.372
111
ING001 Inguinal Hernia 60 1.372
112
CMP010 Complex Regional Pain Syndrome 58 1.372
113
INT030 Intracranial Aneurysm 56 1.372
114
P PLY019 Polyneuropathy 56 1.372
115
c FML035 Familial Hyperlipidemia 55 1.372
116
LMB062 Limb Ischemia 55 1.372
117
P PNC025 Panic Disorder 53 1.372
118
NRS005 Neurosarcoidosis 36 1.372
119
P SCH015 Schizophrenia 74 1.360
120
c FML021 Familial Hypercholesterolemia 66 1.360
121
P BPL003 Bipolar Disorder 56 1.360
122
OLG003 Oligohydramnios 51 1.360
123
INT067 Interstitial Nephritis 48 1.360
124
ART004 Aortic Atherosclerosis 47 1.360
125
P OST002 Osteoporosis 74 1.347
126
P PHC003 Pheochromocytoma 71 1.347
127
CNN005 Connective Tissue Disease 68 1.347
128
CRP001 Carpal Tunnel Syndrome 67 1.347
129
P HYD006 Hydrocephalus 66 1.347
130
INT002 Intermittent Claudication 61 1.347
131
P MTR012 Mitral Valve Disease 58 1.347
132
APH001 Aphthous Stomatitis 57 1.347
133
P PYL005 Pyelonephritis 56 1.347
134
PRP009 Peripartum Cardiomyopathy 55 1.347
135
PNC001 Pancytopenia 54 1.347
136
MYC087 Mycoplasma Pneumoniae Pneumonia 50 1.347
137
c ACT042 Acute Pyelonephritis 46 1.347
138
CRB008 Cerebral Atherosclerosis 44 1.347
139
ISC015 Ischemic Colitis 44 1.347
140
c ART115 Aortic Valve Disease 1 75 1.331
141
RHM001 Rheumatic Fever 60 1.331
142
P NRM002 Normal Pressure Hydrocephalus 54 1.331
143
RHM028 Rheumatic Heart Disease 53 1.331
144
P RTN022 Retinal Vein Occlusion 53 1.331
145
CRT016 Carotid Artery Disease 52 1.331
146
GNG012 Gingival Overgrowth 51 1.331
147
HPT014 Hepatorenal Syndrome 50 1.331
148
TRY001 Trypanosomiasis 50 1.331
149
P OTS001 Otosclerosis 49 1.331
150
SPC010 Speech and Communication Disorders 47 1.331
151
P RTN014 Retinal Artery Occlusion 47 1.331
152
ALC010 Alcoholic Cardiomyopathy 42 1.331
153
RNL097 Renal Artery Disease 42 1.331
154
OBS082 Obstructive Nephropathy 42 1.331
155
HYP008 Hypertensive Retinopathy 39 1.331
156
GRN003 Granulomatous Dermatitis 35 1.331
157
IGG001 Iga Glomerulonephritis 48 1.238
158
P IGN003 Iga Nephropathy 1 49 1.187
159
c ACT068 Acute Cystitis 63 1.174
160
c HYP836 Hypercholesterolemia, Familial, 1 73 1.170
161
PLM129 Pulmonary Disease, Chronic Obstructive 73 1.136
162
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.136
163
c MGR028 Migraine with or Without Aura 1 67 1.120
164
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 1.115
165
c ATR087 Atrial Standstill 1 75 1.097
166
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 1.085
167
IMP005 Impotence 52 1.078
168
c MTR002 Mitral Valve Insufficiency 48 1.078
169
P EXN002 Exanthem 57 1.064
170
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.057
171
C1N001 C1 Inhibitor Deficiency 39 1.049
172
P PRP019 Peripheral Nervous System Disease 58 1.041
173
c VSC019 Vesicoureteral Reflux 1 57 1.032
174
MYC005 Myocardial Stunning 46 1.032
175
DSS008 Disease of Mental Health 58 1.023
176
PRT058 Pure Autonomic Failure 59 1.013
177
P ACT105 Acute Mountain Sickness 52 1.013
178
ASP007 Aspiration Pneumonia 48 1.013
179
IDP091 Idiopathic Nephrotic Syndrome 42 1.013
180
HYP114 Hypertensive Nephropathy 36 1.013
181
P ANT001 Anterolateral Myocardial Infarction 34 1.013
182
APN008 Apnea, Obstructive Sleep 64 1.003
183
PRC013 Pericarditis 54 1.003
184
P PRC012 Pericardial Effusion 51 1.003
185
GLM044 Glomerular Disease 37 1.003
186
P HRD209 Hereditary Angioedema with Normal C1inh 31 1.003
187
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.991
188
P OPT006 Optic Nerve Disease 60 0.991
189
P MTR003 Mitral Valve Stenosis 50 0.991
190
HYP540 Hypertension, Diastolic 40 0.991
191
P HYP055 Hypoplastic Left Heart Syndrome 63 0.978
192
P ORT004 Orthostatic Intolerance 62 0.978
193
URN010 Urinary Tract Obstruction 55 0.978
194
IRD001 Iridocyclitis 53 0.978
195
P ART018 Aortic Valve Insufficiency 49 0.978
196
CRN017 Coronary Thrombosis 47 0.978
197
CNS002 Constrictive Pericarditis 40 0.978
198
P HYP120 Hypoaldosteronism 36 0.978
199
ORT001 Orthostatic Proteinuria 25 0.978
200
BHC003 Behcet Syndrome 71 0.962
201
P TTR001 Tetralogy of Fallot 70 0.962
202
c ART101 Aortic Valve Disease 2 65 0.962
203
P PTN014 Patent Ductus Arteriosus 1 60 0.962
204
P SLP005 Sleep Disorder 59 0.962
205
P RST002 Restrictive Cardiomyopathy 56 0.962
206
ATR057 Atrioventricular Block 55 0.962
207
MCL006 Macular Retinal Edema 55 0.962
208
P CYS039 Cystic Kidney Disease 54 0.962
209
HRT012 Heart Valve Disease 53 0.962
210
THY030 Thyroid Gland Disease 52 0.962
211
LFT001 Left Bundle Branch Hemiblock 49 0.962
212
ART017 Aortic Disease 49 0.962
213
FBR032 Fibromuscular Dysplasia 48 0.962
214
INT010 Intracranial Embolism 48 0.962
215
SXL003 Sexual Disorder 47 0.962
216
PRD004 Prediabetes Syndrome 47 0.962
217
GNR003 Generalized Atherosclerosis 46 0.962
218
FCL012 Facial Paralysis 46 0.962
219
TRP008 Tropical Calcific Pancreatitis 46 0.962
220
c TRC022 Tricuspid Valve Insufficiency 45 0.962
221
CRD003 Cardiac Sarcoidosis 44 0.962
222
IDP033 Idiopathic Edema 44 0.962
223
DRG024 Drug Allergy 42 0.962
224
c PST041 Posterior Urethral Valves 41 0.962
225
BRY001 Berylliosis 40 0.962
226
GLC008 Glucose Metabolism Disease 40 0.962
227
c PLM022 Pulmonary Valve Insufficiency 39 0.962
228
SLN001 Silent Myocardial Infarction 34 0.962
229
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.962
230
INT084 Intrinsic Cardiomyopathy 28 0.962
231
OSS012 Osseous Heteroplasia, Progressive 61 0.941
232
PTN001 Patent Foramen Ovale 60 0.941
233
P ATR010 Atrial Heart Septal Defect 60 0.941
234
P SYP003 Syphilis 58 0.941
235
EYD002 Eye Disease 58 0.941
236
CHR177 Chromophobe Renal Cell Carcinoma 57 0.941
237
CCH002 Coach Syndrome 55 0.941
238
P ATN002 Autonomic Nervous System Disease 52 0.941
239
HYP074 Hypersensitivity Vasculitis 51 0.941
240
CHR078 Chorioretinitis 50 0.941
241
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.941
242
P PNV001 Panuveitis 50 0.941
243
PPL021 Papilledema 49 0.941
244
RYN001 Raynaud Disease 48 0.941
245
RGH001 Right Bundle Branch Block 48 0.941
246
URN009 Urinary System Disease 48 0.941
247
HYP596 Hypophosphatasia, Childhood 48 0.941
248
CRD001 Cardiac Tamponade 47 0.941
249
LMT001 Limited Scleroderma 47 0.941
250
RTN001 Retinal Vasculitis 47 0.941
251
c INH020 Inherited Metabolic Disorder 47 0.941
252
TST044 Testicular Torsion 47 0.941
253
c ACT076 Acute Myocarditis 46 0.941
254
HYP034 Hypertensive Encephalopathy 46 0.941
255
RTN020 Retinal Vascular Disease 46 0.941
256
BCK003 Background Diabetic Retinopathy 46 0.941
257
CHR008 Choroiditis 46 0.941
258
CRN019 Coronary Artery Vasospasm 46 0.941
259
c CNT015 Central Sleep Apnea 45 0.941
260
MLK003 Melkersson-Rosenthal Syndrome 45 0.941
261
ART035 Arterial Calcification of Infancy 45 0.941
262
ACT003 Acute Kidney Tubular Necrosis 45 0.941
263
THR099 Third-Degree Atrioventricular Block 45 0.941
264
ADR012 Adrenal Gland Disease 45 0.941
265
P TRC087 Tricuspid Valve Disease 44 0.941
266
IRT001 Iritis 44 0.941
267
OVR063 Overnutrition 44 0.941
268
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.941
269
c CHR096 Chronic Pulmonary Heart Disease 43 0.941
270
P CRN035 Cranial Nerve Palsy 42 0.941
271
P VND001 Vein Disease 42 0.941
272
NRR001 Neuroretinitis 42 0.941
273
URT031 Ureteral Disease 41 0.941
274
CTS002 Cat-Scratch Disease 41 0.941
275
DBT002 Diabetic Autonomic Neuropathy 41 0.941
276
DFF003 Diffuse Scleroderma 41 0.941
277
SKN006 Skin Sarcoidosis 41 0.941
278
CRN322 Coronavirus Infectious Disease 40 0.941
279
c HYP072 Hypersensitivity Reaction Type Iii Disease 40 0.941
280
PYL004 Pyelitis 40 0.941
281
MNR003 Mineral Metabolism Disease 39 0.941
282
CHL070 Cholesterol Embolism 39 0.941
283
ANG016 Angiokeratoma 38 0.941
284
PTT002 Potter's Syndrome 38 0.941
285
FRS012 First-Degree Atrioventricular Block 38 0.941
286
OPT010 Optic Papillitis 38 0.941
287
c CHR098 Chronic Pyelonephritis 38 0.941
288
c CRD087 Cardiomyopathy, Familial Hypertrophic, 10 37 0.941
289
KNZ001 Kanzaki Disease 37 0.941
290
SVR002 Severe Nonproliferative Diabetic Retinopathy 37 0.941
291
CGH001 Cough Variant Asthma 37 0.941
292
P SCL013 Scleral Disease 36 0.941
293
FCH002 Fuchs' Heterochromic Uveitis 35 0.941
294
UVL010 Uveal Disease 35 0.941
295
TLS001 Tolosa-Hunt Syndrome 35 0.941
296
FCL011 Facial Nerve Disease 35 0.941
297
PYR009 Pyridoxine Deficiency Anemia 34 0.941
298
MCR334 Microcolon 34 0.941
299
PLM180 Pulmonary Artery Disease 33 0.941
300
c SBC035 Subacute Cutaneous Lupus Erythematosus 32 0.941
301
KDN013 Kidney Hypertrophy 32 0.941
302
HRT008 Heart Conduction Disease 32 0.941
303
MRK002 Marek Disease 32 0.941
304
RNL001 Renal Artery Obstruction 31 0.941
305
OCL051 Ocular Tuberculosis 31 0.941
306
GRN006 Granulomatous Angiitis 30 0.941
307
c PST008 Posterior Scleritis 30 0.941
308
SKN018 Skin Hemangioma 29 0.941
309
P PRC050 Pericardium Disease 29 0.941
310
KDN006 Kidney Papillary Necrosis 28 0.941
311
VSC004 Vasculogenic Impotence 28 0.941
312
INT379 Integumentary System Disease 28 0.941
313
UVP001 Uveoparotid Fever 28 0.941
314
ANG014 Angiokeratoma of Fordyce 27 0.941
315
P FML284 Familial Vesicoureteral Reflux 27 0.941
316
MDR006 Moderate and Severe Traumatic Brain Injury 27 0.941
317
CRD217 Cardiac Tuberculosis 26 0.941
318
P ACQ009 Acquired Metabolic Disease 26 0.941
319
TXC010 Toxic Myocarditis 26 0.941
320
EXT035 Extrinsic Cardiomyopathy 25 0.941
321
MBT001 Mobitz Type Ii Atrioventricular Block 25 0.941
322
c MLT009 Multiple Cranial Nerve Palsy 25 0.941
323
c ACT052 Acute Anterolateral Myocardial Infarction 24 0.941
324
c PNM004 Pneumoconiosis Due to Talc 24 0.941
325
HPT066 Hepatoportal Sclerosis 23 0.941
326
END074 Endocardium Disease 22 0.941
327
ACT041 Acute Diffuse Nephritis 22 0.941
328
LNG018 Lingual Goiter 22 0.941
329
GRN036 Granulomatous Myositis 22 0.941
330
BRW005 Brawny Scleritis 21 0.941
331
MDS011 Mediastinum Teratoma 21 0.941
332
CNJ011 Conjunctival Deposit 19 0.941
333
PNC007 Pancreas Lymphoma 18 0.941
334
c ACT030 Acute Dacryoadenitis 18 0.941
335
KLN003 Kaolin Pneumoconiosis 16 0.941
336
HST003 Histoplasmosis Pericarditis 14 0.941
337
HST005 Histoplasmosis Meningitis 14 0.941
338
CCT004 Cicatricial Lagophthalmos 13 0.941
339
MSN011 Mesangioproliferative Glomerulopathy 12 0.941
340
c MCR120 Microvascular Complications of Diabetes 7 47 0.410
341
c MCR130 Microvascular Complications of Diabetes 6 41 0.410
342
c MCR133 Microvascular Complications of Diabetes 4 41 0.410
343
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.288
344
P BRS047 Breast Cancer 97 0.250
345
EST005 Esotropia 42 0.164
346
MNC001 Monocular Esotropia 30 0.164
347
c ACT071 Acute Kidney Failure 60 0.160
348
DWN001 Down Syndrome 70 0.152
349
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.148
350
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.144
351
HYP056 Hypoglycemia 66 0.132
352
c RHB024 Rhabdomyosarcoma 2 67 0.130
353
48X005 48,xyyy 39 0.130
354
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.123
355
P NTR004 Neutropenia 63 0.123
356
CRD137 Cardiogenic Shock 47 0.123
357
P DRR001 Diarrhea 55 0.120
358
c THR092 Thrombophilia Due to Thrombin Defect 73 0.117
359
P TRN020 Turner Syndrome 67 0.117
360
P CMP008 Compartment Syndrome 49 0.117
361
DPR016 Depression 63 0.115
362
TXC005 Toxic Shock Syndrome 62 0.115
363
c MCR129 Microvascular Complications of Diabetes 1 66 0.109
364
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.109
365
THR024 Thrombosis 57 0.109
366
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.109
367
c MCR112 Microvascular Complications of Diabetes 2 41 0.109
368
MSC007 Muscle Hypertrophy 64 0.106
369
MNT002 Mental Depression 58 0.106
370
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.106
371
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.106
372
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.106
373
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.106
374
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.106
375
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.106
376
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.106
377
HYP066 Hyperglycemia 61 0.103
378
CRD132 Cardiac Conduction Defect 58 0.103
379
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.103
380
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.103
381
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.103
382
ACC003 Accommodative Esotropia 26 0.103
383
P LKM002 Leukemia 68 0.100
384
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.100
385
RNL077 Renal Fibrosis 47 0.100
386
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.097
387
CHL014 Cholera 59 0.097
388
P MYP006 Myopia 55 0.097
389
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.097
390
P CLR023 Colorectal Cancer 99 0.094
391
P LNG032 Lung Cancer 98 0.094
392
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.094
393
c FML001 Familial Atrial Fibrillation 65 0.094
394
P ADN016 Adenocarcinoma 64 0.094
395
RFR003 Refractive Error 43 0.094
396
P STR020 Strabismus 55 0.090
397
MCH006 Mechanical Strabismus 42 0.090
398
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.090
399
ADL002 Adult Syndrome 70 0.087
400
P LPS004 Lupus Erythematosus 61 0.087
401
c PRM038 Primary Agammaglobulinemia 44 0.087
402
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.087
403
AST005 Asthma 76 0.083
404
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.083
405
ANR040 Aneurysm 59 0.083
406
c ACT073 Acute Leukemia 58 0.083
407
HLX001 Helix Syndrome 47 0.083
408
EXT022 Exotropia 41 0.083
409
ALT003 Alternating Exotropia 34 0.083
410
P PRS040 Prostate Cancer 97 0.079
411
OST012 Osteoarthritis 78 0.079
412
c SML038 Small Cell Cancer of the Lung 65 0.079
413
P PLM036 Pulmonary Fibrosis 65 0.079
414
PRT037 Pertussis 65 0.079
415
TRN015 Transient Cerebral Ischemia 63 0.079
416
c ACT027 Acute Pancreatitis 60 0.079
417
CNS004 Constipation 58 0.079
418
P HDC001 Headache 57 0.079
419
47X002 47,xyy 49 0.079
420
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.079
421
CYT002 Cytokine Deficiency 42 0.079
422
LVR012 Liver Cirrhosis 62 0.075
423
c SCL052 Scleroderma, Familial Progressive 61 0.075
424
P END033 Endocarditis 57 0.075
425
ATX019 Ataxia with Vitamin E Deficiency 42 0.075
426
LPT014 Leptin Deficiency or Dysfunction 74 0.071
427
P GLM045 Glioma 63 0.071
428
ATM095 Autoimmune Disease 62 0.071
429
P PNC044 Pancreatitis 61 0.071
430
APP008 Appendicitis 61 0.071
431
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.071
432
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.071
433
CHL067 Cholecystitis 57 0.071
434
P RHN004 Rhinitis 57 0.071
435
P RCT021 Rectum Cancer 52 0.071
436
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.071
437
CHL079 Children's Interstitial Lung Disease 26 0.071
438
NRL016 Neural Tube Defects 82 0.066
439
CRH001 Crohn's Disease 74 0.066
440
P MYP004 Myopathy 70 0.066
441
P LYM118 Lymphoma 68 0.066
442
P ALP004 Alport Syndrome 68 0.066
443
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.066
444
ALL026 Allergic Hypersensitivity Disease 62 0.066
445
P ENC004 Encephalitis 61 0.066
446
PST028 Post-Traumatic Stress Disorder 58 0.066
447
P ALC033 Alcohol Use Disorder 58 0.066
448
HYP060 Hyperinsulinism 54 0.066
449
AMB002 Amblyopia 49 0.066
450
P MGR001 Migraine Without Aura 49 0.066
451
ACT084 Acute Stress Disorder 47 0.066
452
GLL048 Glial Tumor 45 0.066
453
SBC016 Subacute Delirium 44 0.066
454
SPP007 Suppression Amblyopia 39 0.066
455
P LVR013 Liver Disease 68 0.061
456
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.061
457
P END044 Endometriosis 63 0.061
458
CLT003 Colitis 62 0.061
459
c FNC043 Fanconi Anemia, Complementation Group E 62 0.061
460
CHC001 Chickenpox 60 0.061
461
ADN018 Adenoma 59 0.061
462
P SZR006 Seizure Disorder 56 0.061
463
P HYP076 Hyperthyroidism 55 0.061
464
PNG002 Pain Agnosia 51 0.061
465
P SCK005 Sickle Cell Disease 50 0.061
466
URT010 Ureteral Obstruction 45 0.061
467
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.061
468
P FML187 Familial Hypertension 37 0.061
469
MYL069 Myeloma, Multiple 85 0.056
470
SCK003 Sickle Cell Anemia 74 0.056
471
ULC004 Ulcerative Colitis 73 0.056
472
MSC157 Muscular Dystrophy, Duchenne Type 72 0.056
473
P FRN006 Frontotemporal Dementia 68 0.056
474
c ATS007 Autism Spectrum Disorder 67 0.056
475
PRT036 Peritonitis 64 0.056
476
NTR005 Nutritional Deficiency Disease 62 0.056
477
CRD223 Cardiac Arrhythmia 60 0.056
478
VSL002 Visual Epilepsy 59 0.056
479
P BCL017 B-Cell Lymphoma 58 0.056
480
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.056
481
P UVT001 Uveitis 57 0.056
482
CYT008 Cytomegalovirus Infection 57 0.056
483
JPN002 Japanese Encephalitis 57 0.056
484
P PLY011 Polycystic Ovary Syndrome 56 0.056
485
P SBS003 Substance Abuse 55 0.056
486
ILS001 Ileus 51 0.056
487
ACT017 Acute Chest Syndrome 51 0.056
488
HYP081 Hypolipoproteinemia 51 0.056
489
DYS073 Dysphagia 50 0.056
490
c INF023 Inflammatory Breast Carcinoma 50 0.056
491
c DRR009 Diarrhea 6 46 0.056
492
SYN036 Syncope 45 0.056
493
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.056
494
PPL052 Papillomatosis, Confluent and Reticulated 33 0.056
495
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.056
496
CYT004 Cytomegalic Inclusion Disease 31 0.056
497
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.050
498
c LKM061 Leukemia, Acute Myeloid 84 0.050
499
P PNC035 Pancreatic Cancer 84 0.050
500
CYS001 Cystic Fibrosis 81 0.050
501
P BLD134 Bladder Cancer 79 0.050
502
GLB015 Glioblastoma Multiforme 75 0.050
503
ACR007 Acromegaly 71 0.050
504
PLY001 Polycythemia Vera 69 0.050
505
PLM001 Pulmonary Tuberculosis 69 0.050
506
c BSL007 Basal Cell Carcinoma 68 0.050
507
P INF038 Influenza 68 0.050
508
P HRP006 Herpes Simplex 65 0.050
509
c BRN108 Branchiootic Syndrome 1 62 0.050
510
P HYP750 Hypertriglyceridemia, Familial 62 0.050
511
GST033 Gestational Diabetes 61 0.050
512
VRC005 Varicose Veins 60 0.050
513
P THL005 Thalassemia 60 0.050
514
THY029 Thyroid Carcinoma 59 0.050
515
IGR001 Ige Responsiveness, Atopic 59 0.050
516
CHL123 Chlamydia 59 0.050
517
GST045 Gastroenteritis 59 0.050
518
P URT039 Urticaria 58 0.050
519
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.050
520
NWB001 Newborn Respiratory Distress Syndrome 58 0.050
521
P PLY018 Polycythemia 56 0.050
522
BCT022 Bacterial Infectious Disease 56 0.050
523
HMG005 Hemoglobinopathy 56 0.050
524
BRN004 Brain Edema 56 0.050
525
AGN016 Aging 56 0.050
526
NRN004 Neuroendocrine Tumor 55 0.050
527
P ALP008 Alopecia 54 0.050
528
PRS045 Prostatic Hypertrophy 53 0.050
529
INT075 Intracranial Hypertension 53 0.050
530
OCL069 Ocular Motor Apraxia 51 0.050
531
TRM010 Traumatic Brain Injury 51 0.050
532
P THR015 Thrombophilia 51 0.050
533
PLC008 Placenta Disease 50 0.050
534
MTB004 Metabolic Acidosis 50 0.050
535
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.050
536
PRS129 Prostatic Hyperplasia, Benign 49 0.050
537
BRN071 Brain Injury 49 0.050
538
HMP001 Hemopericardium 48 0.050
539
LYM019 Lymphosarcoma 46 0.050
540
CRB004 Cerebral Artery Occlusion 45 0.050
541
P CHR345 Chronic Pain 44 0.050
542
RST023 Resting Heart Rate, Variation in 41 0.050
543
BRK012 Broken Heart Syndrome 35 0.050
544
c CHR064 Chronic Monocytic Leukemia 33 0.050
545
NNS011 Nonseminomatous Germ Cell Tumor 33 0.050
546
c PRG003 Progesterone-Receptor Negative Breast Cancer 33 0.050
548
P GST053 Gastric Cancer 83 0.043
549
P RHM011 Rheumatoid Arthritis 80 0.043
550
c NRF023 Neurofibromatosis, Type Ii 80 0.043
551
INS024 Insulin-Like Growth Factor I 79 0.043
552
CRV035 Cervical Cancer 76 0.043
553
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.043
554
c SPN225 Spondyloarthropathy 1 73 0.043
555
FBR012 Fabry Disease 72 0.043
556
MYL009 Myelodysplastic Syndrome 70 0.043
557
P MLN008 Melanoma 69 0.043
558
P ART022 Arthritis 69 0.043
559
LYM133 Lymphoma, Hodgkin, Classic 69 0.043
560
P ESS003 Essential Thrombocythemia 68 0.043
561
P THR014 Thrombocytopenia 67 0.043
562
ALL003 Allergic Rhinitis 67 0.043
563
P SKN015 Skin Carcinoma 66 0.043
564
P MNN013 Meningitis 66 0.043
565
KHL003 Kohlschutter-Tonz Syndrome 65 0.043
566
P PRD008 Periodontitis 64 0.043
567
HYP020 Hyperprolactinemia 64 0.043
568
P HYP069 Hyperparathyroidism 63 0.043
569
c HPT003 Hepatitis a 62 0.043
570
P VSC011 Vasculitis 62 0.043
571
FTT001 Fatty Liver Disease 61 0.043
572
RTN017 Retinal Detachment 61 0.043
573
P MYL006 Myeloid Leukemia 60 0.043
574
SPN186 Spinal Cord Injury 60 0.043
575
P VNT002 Ventricular Septal Defect 60 0.043
576
P SNS001 Sensorineural Hearing Loss 60 0.043
577
P GLY013 Glycogen Storage Disease 60 0.043
578
P HRD011 Hereditary Spherocytosis 60 0.043
579
P BRS044 Breast Adenocarcinoma 59 0.043
580
INC002 Inclusion Body Myositis 58 0.043
581
BRN056 Bronchopulmonary Dysplasia 57 0.043
582
DSS009 Disseminated Intravascular Coagulation 57 0.043
583
P FTL001 Fetal Alcohol Syndrome 57 0.043
584
HYP266 Hypoxia 57 0.043
585
HMT008 Hematuria, Benign Familial 56 0.043
586
ERY051 Erythroleukemia, Familial 56 0.043
587
ACT058 Active Peptic Ulcer Disease 55 0.043
588
HNC001 Henoch-Schoenlein Purpura 55 0.043
589
GNT003 Genital Herpes 54 0.043
590
P PMP001 Pemphigus 54 0.043
591
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.043
592
AMN001 Amenorrhea 54 0.043
593
P LTR001 Lateral Sclerosis 54 0.043
594
INF034 Infective Endocarditis 53 0.043
595
PRP016 Paraplegia 52 0.043
596
ACR041 Acromelic Frontonasal Dysostosis 52 0.043
597
THR004 Thrombocytosis 51 0.043
598
PRS021 Prostatic Adenoma 51 0.043
599
FDL002 Food Allergy 51 0.043
600
CLR109 Colorectal Adenocarcinoma 51 0.043
601
THR016 Thrombophlebitis 51 0.043
602
PLR007 Pleural Empyema 50 0.043
603
P MYS079 Miyoshi Muscular Dystrophy 50 0.043
604
HRT011 Heart Septal Defect 50 0.043
605
TBL009 Tibial Muscular Dystrophy 50 0.043
606
ATS010 Autosomal Recessive Disease 48 0.043
607
SPL018 Splenomegaly 48 0.043
608
CHL147 Chlamydia Pneumonia 48 0.043
609
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.043
610
ATN005 Autonomic Dysfunction 46 0.043
611
NNK001 Nonaka Myopathy 46 0.043
612
GRN017 Granulocytopenia 44 0.043
613
c HYP272 Hypercholesterolemia, Familial, 3 44 0.043
614
DVR002 Diverticulitis 43 0.043
615
BCK006 Back Pain 42 0.043
616
49X006 49, Xxxxy Syndrome 41 0.043
617
ARC008 Auriculo-Condylar Syndrome 41 0.043
618
RDN001 Reading Disorder 40 0.043
619
SPR126 Superior Semicircular Canal Dehiscence 40 0.043
620
c HMG029 Hemoglobin Se Disease 39 0.043
621
PRS025 Presbyopia 38 0.043
622
FRS019 Farsightedness 38 0.043
623
HRW001 Hair Whorl 36 0.043
624
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.043
625
RTR010 Retroperitoneal Sarcoma 34 0.043
626
c MYC058 Myocardial Infarction 2 34 0.043
627
CMP040 Complement Component 4, Partial Deficiency of 33 0.043
628
c PRS136 Prostate Cancer, Hereditary, 6 33 0.043
629
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.043
630
c PRS130 Prostate Cancer, Hereditary, 8 32 0.043
631
SNG003 Single Ventricular Heart 30 0.043
632
MYP120 Myopathy, Distal, with Rimmed Vacuoles 28 0.043
633
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 26 0.043
634
P HPT023 Hepatocellular Carcinoma 100 0.035
635
ESP021 Esophageal Cancer 90 0.035
636
P OVR042 Ovarian Cancer 88 0.035
637
IMM167 Immune Deficiency Disease 78 0.035
638
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.035
639
MRF001 Marfan Syndrome 77 0.035
640
BRN028 Brain Cancer 74 0.035
641
END057 Endometrial Cancer 74 0.035
642
SVR004 Severe Combined Immunodeficiency 73 0.035
643
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.035
644
P NRB001 Neuroblastoma 72 0.035
645
P GRF003 Graft-Versus-Host Disease 72 0.035
646
HMN044 Human Immunodeficiency Virus Type 1 71 0.035
647
c EXD008 Exudative Vitreoretinopathy 1 71 0.035
648
P AMY004 Amyloidosis 70 0.035
649
c GLY008 Glycogen Storage Disease Ii 70 0.035
650
MYL005 Myelofibrosis 70 0.035
651
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.035
652
P LPR021 Leprosy 3 69 0.035
653
MNT001 Mantle Cell Lymphoma 69 0.035
654
SKN019 Skin Melanoma 68 0.035
655
BRN024 Bronchitis 68 0.035
656
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.035
657
SRC014 Sarcoma 65 0.035
658
P VNW001 Von Willebrand's Disease 65 0.035
659
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.035
660
BRR014 Barrett Esophagus 65 0.035
661
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.035
662
P PRS038 Personality Disorder 65 0.035
663
GT001 Gout 64 0.035
664
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.035
665
BRC012 Brucellosis 64 0.035
666
ART002 Arts Syndrome 64 0.035
667
SKN016 Skin Disease 63 0.035
668
ACT119 Acute Promyelocytic Leukemia 63 0.035
669
P MVM001 Movement Disease 63 0.035
670
c ALP101 Alpha-Thalassemia 62 0.035
671
P ART023 Arthropathy 62 0.035
672
P PRM006 Primary Biliary Cirrhosis 62 0.035
673
MSL001 Measles 62 0.035
675
OST003 Osteonecrosis 61 0.035
676
c PNS012 Paine Syndrome 61 0.035
677
VRL011 Viral Infectious Disease 61 0.035
678
HRP004 Herpes Zoster 60 0.035
679
ACQ007 Acquired Immunodeficiency Syndrome 60 0.035
680
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.035
681
ORL011 Oral Cancer 60 0.035
682
P RBL001 Rubella 59 0.035
683
c HPT016 Hepatitis B 59 0.035
684
HLC007 Helicobacter Pylori Infection 59 0.035
685
FBR047 Fibromyalgia 58 0.035
686
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.035
687
CNT047 Contact Dermatitis 58 0.035
688
P MMP001 Mumps 58 0.035
689
P INF032 Infertility 57 0.035
690
P PLV020 Pelvic Organ Prolapse 57 0.035
691
P PRV006 Pervasive Developmental Disorder 57 0.035
692
APH002 Aphasia 57 0.035
693
PNM008 Pneumothorax 56 0.035
694
P FBR017 Fibrosarcoma 56 0.035
695
P MLT074 Multiple Endocrine Neoplasia 56 0.035
696
GNR004 Generalized Anxiety Disorder 56 0.035
697
ANS011 Anus Cancer 56 0.035
698
P HYP024 Hypoparathyroidism 56 0.035
699
P GST044 Gastritis 56 0.035
700
P MLN007 Male Infertility 55 0.035
701
P GRV001 Graves' Disease 55 0.035
702
P PTT006 Pituitary Adenoma 55 0.035
703
END040 Endogenous Depression 55 0.035
704
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.035
705
TND005 Tendinitis 54 0.035
706
P TRM003 Tremor 54 0.035
707
CLL003 Cellulitis 54 0.035
708
P INS002 in Situ Carcinoma 53 0.035
709
P MNC007 Monocytic Leukemia 53 0.035
710
P HML001 Hemolytic-Uremic Syndrome 53 0.035
711
MTN003 Motion Sickness 53 0.035
712
CLF001 Cleft Lip 53 0.035
713
HMC014 Homocysteinemia 53 0.035
714
SPN035 Spindle Cell Sarcoma 53 0.035
715
DNT012 Dental Caries 53 0.035
716
c GLL024 Gallbladder Disease 1 53 0.035
717
P INT068 Intestinal Disease 53 0.035
718
P RTN018 Retinal Disease 53 0.035
719
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.035
720
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.035
721
P LRY019 Laryngitis 52 0.035
722
PST011 Pustulosis of Palm and Sole 52 0.035
723
P MSC003 Muscular Atrophy 52 0.035
724
FML037 Female Breast Cancer 52 0.035
725
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.035
726
P TRT010 Teratoma 52 0.035
727
SPN051 Spondylitis 51 0.035
729
MYL020 Myelomeningocele 51 0.035
730
LNG031 Lung Benign Neoplasm 51 0.035
731
ESP002 Esophageal Varix 51 0.035
732
P AST007 Astrocytoma 51 0.035
733
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.035
734
c SVR005 Severe Pre-Eclampsia 50 0.035
735
DBT004 Diabetic Polyneuropathy 49 0.035
736
BLL004 Bullous Keratopathy 49 0.035
737
PCT003 Pectus Excavatum 49 0.035
738
c BPL002 Bipolar I Disorder 49 0.035
739
VCC001 Vaccinia 49 0.035
740
KRT008 Keratopathy 47 0.035
741
AST006 Astigmatism 47 0.035
742
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.035
743
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.035
744
P CRC039 Coarctation of Aorta 47 0.035
745
MCR037 Macroglossia 45 0.035
746
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.035
747
TND004 Tendinopathy 43 0.035
748
ANG002 Angiostrongyliasis 43 0.035
749
ANC001 Ancylostomiasis 43 0.035
750
TRP009 Triple X Syndrome 42 0.035
751
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.035
752
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.035
753
IDP070 Idiopathic Scoliosis 42 0.035
754
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.035
755
c MJR024 Major Affective Disorder 9 41 0.035
756
P SCL057 Scoliosis, Isolated 1 41 0.035
757
ADN067 Adenoid Hypertrophy 39 0.035
758
c ACQ012 Acquired Angioedema 38 0.035
759
c MJR022 Major Affective Disorder 8 38 0.035
760
SWL001 Swallowing Disorders 38 0.035
761
CRD016 Cardiac Rupture 37 0.035
762
SYS071 Systemic Autoimmune Disease 37 0.035
763
SCR003 Secretory Diarrhea 37 0.035
765
ANS004 Anisometropia 35 0.035
766
HNS001 Hansen's Disease 34 0.035
767
c LKM005 Leukemia, T-Cell, Chronic 34 0.035
768
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.035
770
TQP001 Taqi Polymorphism 32 0.035
771
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.035
772
INF009 Inflammatory Spondylopathy 31 0.035
773
NRG001 Neurogenic Bowel 31 0.035
774
FNT004 Fainting 30 0.035
775
SBD001 Subdural Empyema 28 0.035
776
KLB004 Klebsiella Infection 27 0.035
777
ADG002 Audiogenic Seizures 25 0.035
778
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 19 0.035
779
P LKM071 Leukemia, Chronic Lymphocytic 79 0.025
780
P LNG064 Lung Cancer Susceptibility 3 78 0.025
781
P PRK057 Parkinson Disease, Late-Onset 78 0.025
782
KPS004 Kaposi Sarcoma 75 0.025
783
P APL001 Aplastic Anemia 74 0.025
784
c BTT014 Beta-Thalassemia 74 0.025
785
P CNR004 Cone-Rod Dystrophy 2 73 0.025
786
P FML018 Familial Mediterranean Fever 73 0.025
787
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.025
788
P RTN024 Retinoblastoma 73 0.025
789
c HPT073 Hepatitis C Virus 72 0.025
790
OTT002 Otitis Media 72 0.025
791
P EPL164 Epilepsy 71 0.025
792
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.025
793
GST040 Gastric Adenocarcinoma 70 0.025
794
c GCH015 Gaucher Disease, Type I 70 0.025
795
PTZ001 Peutz-Jeghers Syndrome 70 0.025
796
P ASP006 Aspergillosis 69 0.025
797
WRN001 Werner Syndrome 69 0.025
798
P OCL013 Oculodentodigital Dysplasia 69 0.025
799
P ANG001 Angelman Syndrome 69 0.025
800
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.025
801
P MYC084 Mycobacterium Tuberculosis 1 68 0.025
802
CHL065 Cholangiocarcinoma 68 0.025
803
P HML033 Hemolytic Uremic Syndrome, Atypical 1 68 0.025
804
RCK004 Rickets 68 0.025
805
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.025
806
c INF071 Inflammatory Bowel Disease 1 67 0.025
807
FCT007 Factor Vii Deficiency 67 0.025
808
BRK010 Burkitt Lymphoma 67 0.025
809
P FLL037 Follicular Lymphoma 67 0.025
810
PSY004 Psychotic Disorder 67 0.025
811
P HYP098 Hypereosinophilic Syndrome 67 0.025
812
MYC006 Mycosis Fungoides 66 0.025
813
LPT001 Leptospirosis 66 0.025
814
P CLC063 Celiac Disease 1 66 0.025
815
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.025
816
CHD001 Chediak-Higashi Syndrome 66 0.025
817
P NSP012 Nasopharyngeal Carcinoma 66 0.025
818
ACH004 Achondroplasia 66 0.025
819
MYL031 Myeloproliferative Neoplasm 66 0.025
820
c MCL013 Mucolipidosis Iv 66 0.025
821
TTN003 Tetanus 65 0.025
822
P HRS035 Hirschsprung Disease 1 65 0.025
823
P CNJ013 Conjunctivitis 65 0.025
824
c WLM013 Wilms Tumor 1 65 0.025
825
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.025
826
CLN015 Colon Adenocarcinoma 65 0.025
827
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.025
828
P HRM001 Hermansky-Pudlak Syndrome 64 0.025
829
NRF007 Neurofibroma 64 0.025
830
P CMP005 Campomelic Dysplasia 64 0.025
831
CLF027 Cleft Palate, Isolated 64 0.025
832
TBC004 Tobacco Addiction 64 0.025
833
c CNG006 Congenital Hypothyroidism 64 0.025
834
LYM017 Lyme Disease 64 0.025
835
OST017 Osteomyelitis 64 0.025
836
KRN002 Kearns-Sayre Syndrome 63 0.025
837
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.025
838
P RNL100 Renal Hypodysplasia/aplasia 1 63 0.025
839
CYS013 Cystinuria 63 0.025
840
P ANR048 Aniridia 1 63 0.025
841
MSC152 Muscular Dystrophy, Becker Type 63 0.025
842
INT146 Intervertebral Disc Disease 63 0.025
843
c GLY060 Glycogen Storage Disease Ia 63 0.025
844
ANR007 Anorexia Nervosa 63 0.025
845
c ATM011 Autoimmune Hepatitis 63 0.025
846
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.025
847
RTN209 Retinoschisis 1, X-Linked, Juvenile 62 0.025
848
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.025
849
P ESP024 Esophagitis 62 0.025
850
P TRC086 Trichohepatoenteric Syndrome 1 62 0.025
851
CHL068 Cholestasis 61 0.025
852
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.025
853
PSR001 Psoriatic Arthritis 61 0.025
854
DRM006 Dermatitis 61 0.025
855
WST001 West Syndrome 61 0.025
856
P ENC018 Encephalopathy 61 0.025
857
YLL002 Yellow Fever 61 0.025
858
CHR066 Chronic Fatigue Syndrome 61 0.025
859
c WLM018 Wilms Tumor 5 61 0.025
860
RCT015 Reactive Arthritis 61 0.025
861
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.025
862
DCB001 Decubitus Ulcer 61 0.025
863
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.025
864
NTH001 Netherton Syndrome 60 0.025
865
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.025
866
P KDN017 Kidney Cancer 60 0.025
867
PNM010 Pneumothorax, Primary Spontaneous 60 0.025
868
SZR001 Sezary's Disease 60 0.025
869
TRG002 Trigeminal Neuralgia 60 0.025
870
P TXP001 Toxoplasmosis 60 0.025
871
HPT019 Hepatic Encephalopathy 60 0.025
872
ACN002 Acanthosis Nigricans 60 0.025
873
c ORF037 Orofaciodigital Syndrome I 60 0.025
874
P ALP009 Alopecia Areata 60 0.025
875
SQM006 Squamous Cell Carcinoma 60 0.025
876
HYD002 Hydronephrosis 60 0.025
877
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.025
878
P MCR010 Microcephaly 59 0.025
879
IDP011 Idiopathic Interstitial Pneumonia 59 0.025
880
PNM001 Pneumocystosis 59 0.025
881
PRN019 Perinatal Necrotizing Enterocolitis 59 0.025
882
CYS010 Cystinosis 59 0.025
883
P NPH005 Nephronophthisis 59 0.025
884
PPT005 Peptic Ulcer Disease 59 0.025
885
P ANP001 Anaplastic Large Cell Lymphoma 58 0.025
886
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.025
887
RBS001 Rabies 58 0.025
888
CHR072 Chordoma 58 0.025
889
c PTT056 Pituitary Adenoma 1, Multiple Types 58 0.025
890
SPT004 Septic Arthritis 58 0.025
891
c PRM005 Primary Hyperparathyroidism 58 0.025
892
BRS051 Breast Disease 58 0.025
893
ERY003 Erythema Multiforme 58 0.025
894
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.025
895
P CND004 Candidiasis 58 0.025
896
EXT034 Extrinsic Allergic Alveolitis 58 0.025
897
MXD005 Mixed Connective Tissue Disease 58 0.025
898
ACR056 Acrodermatitis Enteropathica, Zinc-Deficiency Type 57 0.025
899
PMP006 Pemphigus Vulgaris, Familial 57 0.025
900
GLS018 Glass Syndrome 57 0.025
901
P OPT009 Optic Neuritis 57 0.025
902
THY122 Thyroid Gland Cancer 57 0.025
903
TNS005 Tonsillitis 57 0.025
904
c ANG068 Angioedema, Hereditary, Type I 57 0.025
905
c LKM070 Leukemia, Acute Monocytic 57 0.025
906
c BSL024 Basal Cell Carcinoma 1 56 0.025
907
P ADL017 Adult T-Cell Leukemia 56 0.025
908
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.025
909
TCK001 Tick-Borne Encephalitis 56 0.025
910
ALL006 Allergic Asthma 56 0.025
911
EXF001 Exfoliation Syndrome 56 0.025
912
LMY014 Leiomyoma, Uterine 56 0.025
913
SFT003 Soft Tissue Sarcoma 56 0.025
914
PRS047 Prostatitis 56 0.025
915
ISL001 Islet Cell Tumor 56 0.025
916
SML019 Smallpox 56 0.025
917
P PNM006 Pneumoconiosis 56 0.025
918
c GLY005 Glycogen Storage Disease Vi 56 0.025
919
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.025
920
FLR001 Filarial Elephantiasis 55 0.025
921
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.025
922
P ATR001 Atrioventricular Septal Defect 55 0.025
923
NRG002 Neurogenic Bladder 55 0.025
924
c BCT007 Bacterial Meningitis 55 0.025
925
DFF005 Diffuse Large B-Cell Lymphoma 55 0.025
926
NPH009 Nephrolithiasis 55 0.025
927
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.025
928
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.025
929
ALP077 Alpha-Methylacetoacetic Aciduria 55 0.025
930
FLR002 Filariasis 55 0.025
931
P VNS003 Venous Insufficiency 55 0.025
932
P DBT005 Diabetes Insipidus 55 0.025
933
SYN007 Synovitis 54 0.025
934
P SPN052 Spondyloarthropathy 54 0.025
935
GLS001 Gliosarcoma 54 0.025
936
AMN003 Amnestic Disorder 54 0.025
937
THR013 Thoracic Outlet Syndrome 54 0.025
938
LYM040 Lymphoblastic Lymphoma 54 0.025
939
PPL022 Papilloma 54 0.025
940
NNL006 Non-Alcoholic Steatohepatitis 54 0.025
941
CLR030 Clear Cell Renal Cell Carcinoma 53 0.025
942
GST009 Gastroschisis 53 0.025
943
P LCH002 Lichen Planus 53 0.025
944
CRH005 Crohn's Colitis 53 0.025
945
P RNL017 Renal Oncocytoma 53 0.025
946
P RTN016 Retinal Degeneration 53 0.025
947
OCL006 Ocular Hypertension 53 0.025
948
BRD004 Borderline Personality Disorder 53 0.025
949
P SHR001 Short Bowel Syndrome 53 0.025
950
FNG017 Fungal Infectious Disease 53 0.025
951
GTR002 Goiter 53 0.025
952
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.025
953
GSG001 Gas Gangrene 53 0.025
954
P ACT008 Actinic Keratosis 53 0.025
955
NRT001 Neurotic Disorder 53 0.025
956
GST023 Gastric Ulcer 53 0.025
957
TXC002 Toxic Encephalopathy 53 0.025
958
c FML008 Familial Retinoblastoma 53 0.025
959
LYS002 Lysosomal Storage Disease 52 0.025
960
NRT004 Neuritis 52 0.025
961
P CHN059 Chondrocalcinosis 52 0.025
962
MRG003 Marginal Zone B-Cell Lymphoma 52 0.025
963
DYS015 Dysentery 52 0.025
964
P THY032 Thyroiditis 52 0.025
965
HYP014 Hyperuricemia 52 0.025
966
APR001 Apraxia 52 0.025
967
ACT200 Acute Monoblastic Leukemia 52 0.025
968
ART074 Aortic Dissection 52 0.025
969
HYP088 Hyper-Igd Syndrome 52 0.025
970
P OVR049 Ovarian Disease 52 0.025
971
c ACT135 Acute Graft Versus Host Disease 52 0.025
972
LMY002 Leiomyoma 52 0.025
973
LYM004 Lymphoid Interstitial Pneumonia 51 0.025
974
P SPP010 Suppressor of Tumorigenicity 3 51 0.025
975
c HRM005 Hermansky-Pudlak Syndrome 1 51 0.025
976
KRT009 Keratosis 51 0.025
977
MYL001 Myelitis 51 0.025
978
PLS009 Plasma Cell Neoplasm 51 0.025
979
ANK001 Ankylosis 51 0.025
980
ENT011 Enterocolitis 51 0.025
981
CYS014 Cystadenocarcinoma 51 0.025
982
INT079 Intrahepatic Cholangiocarcinoma 51 0.025
983
SPN019 Spondylolisthesis 51 0.025
984
SPL004 Splenic Marginal Zone Lymphoma 51 0.025
985
BLL003 Bell's Palsy 51 0.025
986
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.025
987
ASP003 Aseptic Meningitis 51 0.025
988
c SCN007 Secondary Hyperparathyroidism 51 0.025
989
SKN013 Skin Benign Neoplasm 51 0.025
990
c NPH019 Nephronophthisis 1 50 0.025
991
PTT041 Pituitary Stalk Interruption Syndrome 50 0.025
992
P FNC004 Fanconi Syndrome 50 0.025
993
RDC002 Radiculopathy 50 0.025
994
ALL009 Allergic Conjunctivitis 50 0.025
995
LPD016 Lipoid Proteinosis of Urbach and Wiethe 50 0.025
996
HRT031 Hartnup Disorder 50 0.025
997
P ESN008 Eosinophilic Pneumonia 50 0.025
998
AZS001 Azoospermia 50 0.025
999
STM007 Stomatitis 50 0.025
1000
c HRD202 Hereditary Lymphedema I 50 0.025
1001
NPH018 Nephrogenic Systemic Fibrosis 50 0.025
1002
PRT018 Portal Vein Thrombosis 50 0.025
1003
P AGG001 Aggressive Periodontitis 50 0.025
1004
NTR046 Neutrophil Migration 50 0.025
1005
HMG002 Hemoglobinuria 50 0.025
1006
OPT003 Opiate Dependence 50 0.025
1007
P ATR005 Atrophic Gastritis 50 0.025
1008
ISL003 Isolated Growth Hormone Deficiency 49 0.025
1009
ONC007 Oncocytoma 49 0.025
1010
c ACQ017 Acquired Von Willebrand Syndrome 49 0.025
1011
c CHR431 Chronic Venous Insufficiency 49 0.025
1012
VLV047 Volvulus of Midgut 49 0.025
1013
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 49 0.025
1014
END021 Endomyocardial Fibrosis 49 0.025
1015
CCN002 Cocaine Abuse 49 0.025
1016
c FLL041 Follicular Lymphoma 1 49 0.025
1017
CHL004 Cholelithiasis 49 0.025
1018
CHN065 Choanal Atresia, Posterior 49 0.025
1019
ACT029 Acute Interstitial Pneumonia 49 0.025
1020
P CTN015 Cutaneous T Cell Lymphoma 49 0.025
1021
c INV001 Invasive Aspergillosis 49 0.025
1022
CKT002 Cakut 48 0.025
1023
BNR002 Bone Resorption Disease 48 0.025
1024
HYP043 Hyperandrogenism 48 0.025
1025
INT054 Intraocular Lymphoma 48 0.025
1026
c DSB006 Desbuquois Dysplasia 1 48 0.025
1027
CLC006 Calcinosis 48 0.025
1028
CLS016 Clostridium Difficile Colitis 48 0.025
1029
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.025
1030
DGN001 Degenerative Disc Disease 48 0.025
1031
BNN003 Bone Inflammation Disease 48 0.025
1032
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.025
1033
RCT020 Rectum Adenocarcinoma 48 0.025
1034
ANT018 Anthracosis 48 0.025
1035
HRN026 Hernia, Hiatus 47 0.025
1036
GRM005 Germ Cell Cancer 47 0.025
1037
SMN008 Semantic Dementia 47 0.025
1038
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.025
1039
ASB001 Asbestosis 47 0.025
1040
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.025
1041
P PRR002 Pure Red-Cell Aplasia 47 0.025
1042
P CLL015 Collagen Disease 47 0.025
1043
ANT011 Antisocial Personality Disorder 47 0.025
1044
RTC005 Reticulosarcoma 47 0.025
1045
KHN001 Kuhnt-Junius Degeneration 47 0.025
1046
ZKF001 Zika Fever 47 0.025
1047
PLS025 Plasmablastic Lymphoma 47 0.025
1048
PLC003 Placental Site Trophoblastic Tumor 47 0.025
1049
NSS002 Neisseria Meningitidis Infection 47 0.025
1050
P PRC019 Precocious Puberty 46 0.025
1051
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.025
1052
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.025
1053
ALB002 Albinism 46 0.025
1054
EXS001 Exostosis 46 0.025
1055
KRT013 Keratolytic Winter Erythema 46 0.025
1056
UMB002 Umbilical Hernia 46 0.025
1057
CHD004 Chudley-Mccullough Syndrome 46 0.025
1058
ADR040 Adrenal Gland Pheochromocytoma 46 0.025
1059
GRW007 Growth Hormone Deficiency 46 0.025
1060
3MC003 3mc Syndrome 46 0.025
1061
SQM002 Squamous Cell Papilloma 46 0.025
1062
c MLG068 Malignant Glioma 46 0.025
1063
P TRN034 Transverse Myelitis 45 0.025
1064
c CRD233 Cardiomyopathy, Dilated, 1b 45 0.025
1065
IMN001 Iminoglycinuria 45 0.025
1066
CYN002 Cyanosis, Transient Neonatal 45 0.025
1067
INT253 Intestinal Benign Neoplasm 45 0.025
1068
ORL013 Oral Lichen Planus 45 0.025
1069
HPT004 Hepatic Coma 45 0.025
1070
P CMM008 Communicating Hydrocephalus 45 0.025
1071
LYD001 Leydig Cell Tumor 45 0.025
1072
CHR466 Chronic Thromboembolic Pulmonary Hypertension 45 0.025
1073
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.025
1074
P END084 Endocrine System Disease 45 0.025
1075
ATN004 Autonomic Neuropathy 45 0.025
1076
AGR002 Agoraphobia 45 0.025
1077
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.025
1078
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.025
1079
CYS009 Cystadenoma 44 0.025
1080
ART012 Aortitis 44 0.025
1081
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.025
1082
c PCH010 Pachyonychia Congenita 3 44 0.025
1083
PPL001 Papillary Adenoma 44 0.025
1084
SPN119 Spondylarthropathy 44 0.025
1085
c SPR086 Spermatogenic Failure 3 44 0.025
1086
P RPD001 Rapidly Progressive Glomerulonephritis 44 0.025
1087
MND023 Mend Syndrome 43 0.025
1088
SMN007 Seminoma 43 0.025
1089
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.025
1090
SPC005 Speech Disorder 43 0.025
1091