Search results for fos

1926 hits were found for fos

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 19.214
2
P BRS047 Breast Cancer 97 18.470
3
c CNG012 Congenital Generalized Lipodystrophy 65 18.465
4
END057 Endometrial Cancer 76 16.767
5
OST159 Osteogenic Sarcoma 66 16.594
6
P PRS040 Prostate Cancer 95 16.322
7
P LNG032 Lung Cancer 98 15.742
8
P OVR042 Ovarian Cancer 88 15.520
9
PRT037 Pertussis 49 15.145
10
CHL014 Cholera 62 14.825
11
P PHC003 Pheochromocytoma 70 14.586
12
EMB004 Embryonal Carcinoma 55 14.267
13
P GST053 Gastric Cancer 82 14.106
14
P HPT023 Hepatocellular Carcinoma 95 14.017
15
P RHM011 Rheumatoid Arthritis 81 13.390
16
P SKN015 Skin Carcinoma 71 12.766
17
P ART022 Arthritis 70 12.665
18
P FBR017 Fibrosarcoma 55 12.500
19
P OST002 Osteoporosis 76 12.445
20
P NRB001 Neuroblastoma 66 11.657
21
P LVR013 Liver Disease 68 11.607
22
BNR002 Bone Resorption Disease 47 11.525
23
SRC014 Sarcoma 64 11.452
24
STT001 Status Epilepticus 58 11.362
25
CLN015 Colon Adenocarcinoma 64 11.342
26
MCR013 Microphthalmia 59 11.299
27
ESP021 Esophageal Cancer 84 11.292
28
FBR011 Fibrodysplasia Ossificans Progressiva 67 11.096
29
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 10.730
30
P ATT013 Attention Deficit-Hyperactivity Disorder 65 10.653
31
P BPL003 Bipolar Disorder 56 10.318
32
P VHW001 Vohwinkel Syndrome 50 10.296
33
P SCH015 Schizophrenia 74 10.073
34
OST006 Osteoblastoma 37 10.041
35
c MGR028 Migraine with or Without Aura 1 63 9.934
36
P LKM062 Leukemia, Acute Lymphoblastic 69 9.719
37
ACT119 Acute Promyelocytic Leukemia 62 9.644
38
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 9.584
39
c HYP595 Hypertension, Essential 84 9.570
40
P INF037 Inflammatory Bowel Disease 53 9.544
41
P PLY014 Polycystic Kidney Disease 71 9.514
42
IMM167 Immune Deficiency Disease 76 9.488
43
P BRS044 Breast Adenocarcinoma 58 9.396
44
OCL006 Ocular Hypertension 53 9.346
45
CFF002 Coffin-Lowry Syndrome 59 9.230
46
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 9.039
47
c DLT002 Dilated Cardiomyopathy 79 8.703
48
EST002 Estrogen-Receptor Negative Breast Cancer 45 8.582
49
GLC086 Glucocorticoid-Induced Osteoporosis 43 8.548
50
WTH001 Withdrawal Disorder 47 8.447
51
P CNR004 Cone-Rod Dystrophy 2 74 8.365
52
ADG002 Audiogenic Seizures 25 8.319
53
PNG002 Pain Agnosia 51 8.209
54
P OST001 Osteopetrosis 70 8.034
55
AMN003 Amnestic Disorder 53 8.018
56
MRP001 Morphine Dependence 41 7.849
57
MTN003 Motion Sickness 50 7.531
58
OPT003 Opiate Dependence 49 7.468
59
HST004 Histiocytoid Hemangioma 33 7.451
60
c LKM061 Leukemia, Acute Myeloid 83 7.051
61
P RTN008 Retinitis Pigmentosa 79 7.051
62
OST160 Osteoid Osteoma 37 7.049
63
P PRP019 Peripheral Nervous System Disease 57 7.032
64
TRG002 Trigeminal Neuralgia 61 6.976
65
P SLP005 Sleep Disorder 61 6.954
66
CRB090 Cerebral Hypoxia 42 6.877
67
P SZR006 Seizure Disorder 69 6.768
68
c PNS012 Paine Syndrome 60 6.662
69
FMR011 Fumarate Hydratase Deficiency 39 6.425
70
RTR001 Retrograde Amnesia 41 6.392
71
P CHL002 Childhood Absence Epilepsy 62 6.132
72
MYS001 Myositis Ossificans 44 6.098
73
CNT097 Central Hypoventilation Syndrome, Congenital 70 6.057
74
DSS008 Disease of Mental Health 74 6.057
75
SPC001 Space Motion Sickness 26 5.997
76
c CRD236 Cardiomyopathy, Familial Hypertrophic, 25 50 5.915
77
SPC003 Specific Developmental Disorder 32 5.915
78
KFM001 Kaufman Oculocerebrofacial Syndrome 55 5.915
79
HMT008 Hematuria, Benign Familial 54 5.915
80
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 48 5.915
81
c HYP840 Hypercholesterolemia, Familial, 4 48 5.915
82
c VNM003 Van Maldergem Syndrome 1 50 5.915
83
c AML044 Amelogenesis Imperfecta, Type Ig 54 5.915
85
SCH071 Schaaf-Yang Syndrome 53 5.915
86
c DVL050 Developmental and Epileptic Encephalopathy 24 37 5.915
87
KGM001 Kagami-Ogata Syndrome 54 5.915
88
c DMN018 Diamond-Blackfan Anemia 5 42 5.915
89
BNR001 Bone Remodeling Disease 29 5.915
90
P AML002 Amelogenesis Imperfecta 56 5.915
91
TTH005 Teeth Hard Tissue Disease 27 5.915
92
ANT019 Anterograde Amnesia 38 5.915
93
FMR002 Femoral Cancer 28 5.915
94
MLT013 Malt Worker's Lung 22 5.915
95
EXC001 Exocervical Carcinoma 21 5.915
96
P AGN002 Agnosia 53 5.915
97
PTL001 Patulous Eustachian Tube 36 5.915
98
VST003 Vestibular Nystagmus 25 5.915
99
VNC001 Von Economo's Disease 41 5.915
100
TRG003 Trigeminal Nerve Disease 38 5.915
101
OCC005 Occlusion Precerebral Artery 30 5.915
102
CYC003 Cyclotropia 22 5.915
103
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.670
104
ADR040 Adrenal Gland Pheochromocytoma 45 4.328
105
INS024 Insulin-Like Growth Factor I 77 3.554
106
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.505
107
PLY150 Polykaryocytosis Inducer 29 3.480
108
P BND020 Bone Disease 60 3.420
109
HYP266 Hypoxia 56 3.389
110
GLM045 Glioma 62 3.316
111
GLL048 Glial Tumor 51 3.304
112
CRB004 Cerebral Artery Occlusion 45 3.197
113
SQM006 Squamous Cell Carcinoma 59 3.148
114
RPD005 Rapidly Involuting Congenital Hemangioma 48 3.027
115
CYT002 Cytokine Deficiency 43 2.883
116
ISC004 Ischemia 61 2.834
117
PST028 Post-Traumatic Stress Disorder 58 2.808
118
48X005 48,xyyy 39 2.785
119
ANX010 Anxiety 70 2.759
120
P RTN024 Retinoblastoma 72 2.757
121
P CHR345 Chronic Pain 50 2.660
122
P EPL164 Epilepsy 70 2.644
123
HLX001 Helix Syndrome 47 2.564
124
P GLM007 Glomerulonephritis 59 2.556
125
FBR012 Fabry Disease 71 2.508
126
TRT001 Teratocarcinoma 41 2.489
127
P ADN016 Adenocarcinoma 63 2.463
128
HYP056 Hypoglycemia 65 2.462
129
ACT084 Acute Stress Disorder 53 2.387
130
c LKM005 Leukemia, T-Cell, Chronic 33 2.365
131
P PRD008 Periodontitis 63 2.335
132
SPN186 Spinal Cord Injury 60 2.332
133
ALL029 Allergic Disease 61 2.330
134
PPL022 Papilloma 53 2.328
135
SQM002 Squamous Cell Papilloma 45 2.321
136
P END044 Endometriosis 62 2.274
137
LYM027 Lymphopenia 56 2.243
138
P HMN010 Hemangioma 61 2.242
139
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.191
140
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.191
141
P SLP006 Sleep Apnea 69 2.114
142
IRR002 Irritable Bowel Syndrome 64 2.108
143
P PNC035 Pancreatic Cancer 87 2.099
144
P TMP001 Temporal Lobe Epilepsy 49 2.087
145
P HDC001 Headache 56 2.078
146
P RTN016 Retinal Degeneration 52 2.066
147
CLT003 Colitis 63 2.046
148
MDD011 Mood Disorder 61 2.038
149
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.009
150
GST040 Gastric Adenocarcinoma 66 2.004
151
P HRP006 Herpes Simplex 65 1.984
152
P LKM002 Leukemia 65 1.979
153
P SPP010 Suppressor of Tumorigenicity 3 50 1.970
154
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.963
155
c MJR022 Major Affective Disorder 8 37 1.948
156
c MJR024 Major Affective Disorder 9 40 1.948
157
SKN016 Skin Disease 63 1.925
158
P LNG064 Lung Cancer Susceptibility 3 69 1.923
159
TRN015 Transient Cerebral Ischemia 62 1.919
160
P BLD134 Bladder Cancer 79 1.906
161
P HNT016 Huntington Disease 73 1.888
162
P TRM003 Tremor 50 1.888
163
P HYP086 Hypothyroidism 68 1.886
164
P BCL017 B-Cell Lymphoma 57 1.876
165
MYL009 Myelodysplastic Syndrome 67 1.866
166
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.866
167
CNS004 Constipation 56 1.847
168
P KDN018 Kidney Disease 71 1.846
169
P GLM040 Glioma Susceptibility 1 70 1.842
170
MNT002 Mental Depression 56 1.837
171
DPR016 Depression 64 1.825
172
ANX004 Anoxia 40 1.813
173
KRT009 Keratosis 52 1.807
174
OST012 Osteoarthritis 77 1.804
175
OCL052 Ocular Dominance 40 1.796
176
TRM010 Traumatic Brain Injury 50 1.792
177
CRV035 Cervical Cancer 72 1.790
178
P CYS018 Cystitis 58 1.788
179
P RHB003 Rhabdomyosarcoma 66 1.784
180
P MYC007 Myocardial Infarction 69 1.783
181
PRS047 Prostatitis 57 1.778
182
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.776
183
ILS001 Ileus 49 1.762
184
ADN018 Adenoma 58 1.748
185
ALC007 Alcohol Dependence 65 1.747
186
PTH003 Pathologic Nystagmus 52 1.745
187
MSC007 Muscle Hypertrophy 64 1.742
188
ORL015 Oral Squamous Cell Carcinoma 43 1.734
189
BRN071 Brain Injury 50 1.719
190
PRT036 Peritonitis 65 1.701
191
MLG169 Malignant Astrocytoma 57 1.688
192
P PNC025 Panic Disorder 52 1.667
193
NRR001 Neuroretinitis 42 1.664
194
RTN023 Retinitis 45 1.664
195
CRB039 Cerebrovascular Disease 65 1.654
196
CRH001 Crohn's Disease 80 1.652
197
HYP066 Hyperglycemia 60 1.649
198
IGG001 Iga Glomerulonephritis 50 1.646
199
ACT098 Acute Erythroid Leukemia 55 1.637
200
ORL011 Oral Cancer 60 1.633
201
P INF032 Infertility 60 1.627
202
LNG039 Lung Squamous Cell Carcinoma 57 1.617
203
TTN003 Tetanus 64 1.612
204
P BNG032 Benign Mesothelioma 53 1.604
205
THY029 Thyroid Carcinoma 55 1.592
206
c ATS007 Autism Spectrum Disorder 71 1.584
207
CRT015 Carotid Artery Occlusion 45 1.579
208
P HRT032 Heart Disease 84 1.576
209
P DYS154 Dystonia 64 1.567
210
FBR009 Fibrous Dysplasia 48 1.560
211
HDN002 Head Injury 44 1.553
212
P ENC018 Encephalopathy 62 1.536
213
P OVR082 Overgrowth Syndrome 41 1.536
214
LMY002 Leiomyoma 51 1.513
215
47X002 47,xyy 47 1.506
216
P LYM118 Lymphoma 66 1.482
217
P PLM036 Pulmonary Fibrosis 65 1.480
218
TXC005 Toxic Shock Syndrome 61 1.478
219
P MLN008 Melanoma 75 1.474
220
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.459
221
FCL014 Focal Epilepsy 53 1.458
222
P TMR010 Tumor Predisposition Syndrome 69 1.449
223
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.448
224
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.448
225
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.448
226
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.448
227
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.448
228
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.448
229
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.448
230
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.448
231
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.448
232
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.448
233
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.447
234
P GRV001 Graves' Disease 54 1.442
235
HMN044 Human Immunodeficiency Virus Type 1 76 1.435
236
P MYL006 Myeloid Leukemia 60 1.423
237
P PRK039 Parkinsonism 55 1.418
238
STR067 Stroke, Ischemic 79 1.412
239
P ADL017 Adult T-Cell Leukemia 53 1.412
240
P SBS003 Substance Abuse 54 1.412
241
BRK010 Burkitt Lymphoma 65 1.406
242
GLB002 Glioblastoma 67 1.396
243
P NRF002 Neurofibromatosis 60 1.393
244
PTT037 Pituitary Tumors 44 1.393
245
P ALZ034 Alzheimer Disease 87 1.391
246
GST023 Gastric Ulcer 52 1.391
247
c PRG020 Paragangliomas 3 39 1.387
248
c LKM063 Leukemia, Chronic Myeloid 70 1.375
249
P ANT006 Antiphospholipid Syndrome 55 1.372
250
c TYP009 Type 2 Diabetes Mellitus 91 1.370
251
P PLY011 Polycystic Ovary Syndrome 57 1.365
252
c BRN108 Branchiootic Syndrome 1 63 1.361
253
P CHN012 Chondrosarcoma 56 1.361
254
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.354
255
P DRR001 Diarrhea 55 1.354
256
P MYS005 Myositis 55 1.348
257
GLC003 Glucose Intolerance 53 1.343
258
c HMN021 Human T-Cell Leukemia Virus Type 1 46 1.343
259
ATH013 Atherosclerosis Susceptibility 63 1.342
260
P LKM071 Leukemia, Chronic Lymphocytic 74 1.341
261
HPT019 Hepatic Encephalopathy 59 1.341
262
HPT004 Hepatic Coma 43 1.341
263
SFT003 Soft Tissue Sarcoma 43 1.341
264
TLN003 Telangiectasis 51 1.334
265
P PSR002 Psoriasis 63 1.319
266
P ALC033 Alcohol Use Disorder 67 1.315
267
PCD001 Pica Disease 38 1.312
268
P NSP012 Nasopharyngeal Carcinoma 60 1.309
269
PST011 Pustulosis of Palm and Sole 52 1.305
270
CHL068 Cholestasis 61 1.298
271
P HYP076 Hyperthyroidism 53 1.297
272
P NRP001 Neuropathy 59 1.297
273
P PRK057 Parkinson Disease, Late-Onset 79 1.282
274
c PRC016 Pre-Eclampsia 64 1.282
275
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.276
276
P MJR001 Major Depressive Disorder 68 1.266
277
P MSC005 Muscular Dystrophy 66 1.240
278
P MNC007 Monocytic Leukemia 48 1.233
279
c PCH010 Pachyonychia Congenita 3 43 1.229
280
OPD006 Opioid Addiction 48 1.219
281
P VTR007 Vitreoretinopathy 45 1.219
282
BCT022 Bacterial Infectious Disease 55 1.218
283
P BNG095 Benign Giant Cell Tumor 43 1.212
284
SPN035 Spindle Cell Sarcoma 51 1.207
285
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.201
286
P DRM053 Dermatitis, Atopic 65 1.201
287
c BSL007 Basal Cell Carcinoma 67 1.197
288
GTR002 Goiter 52 1.197
289
SDD001 Sudden Infant Death Syndrome 60 1.196
290
HYP457 Hypertrophic Scars 42 1.194
291
KLD004 Keloid Disorder 38 1.194
292
P HPT021 Hepatitis 68 1.190
293
PRT013 Portal Hypertension 59 1.190
294
PLP001 Pulpitis 48 1.190
295
MMM001 Mammary Paget's Disease 53 1.190
296
END040 Endogenous Depression 54 1.188
297
c MCR133 Microvascular Complications of Diabetes 4 41 1.184
298
c MCR113 Microvascular Complications of Diabetes 3 52 1.184
299
c MCR130 Microvascular Complications of Diabetes 6 41 1.184
300
c MCR120 Microvascular Complications of Diabetes 7 47 1.184
301
DBT010 Diabetic Neuropathy 54 1.182
302
P GST044 Gastritis 55 1.179
303
P PNM007 Pneumonia 64 1.173
304
ANG020 Angiosarcoma 63 1.159
305
P NRC002 Narcolepsy 55 1.155
306
P FTL001 Fetal Alcohol Syndrome 55 1.151
307
P OPT006 Optic Nerve Disease 57 1.151
308
P INS002 in Situ Carcinoma 52 1.151
309
P ADL010 Adult Respiratory Distress Syndrome 70 1.148
310
P KDN017 Kidney Cancer 60 1.143
311
c ACT073 Acute Leukemia 59 1.143
312
NRT001 Neurotic Disorder 56 1.139
313
P RSP003 Respiratory Failure 73 1.136
314
CRD132 Cardiac Conduction Defect 59 1.134
315
P LTR001 Lateral Sclerosis 57 1.134
316
MNN017 Mononeuropathy 41 1.126
317
INS001 Insulinoma 59 1.126
318
ANG054 Angina Pectoris 65 1.117
320
SVR004 Severe Combined Immunodeficiency 70 1.117
321
URM002 Uremia 47 1.108
322
HMN016 Hemangioendothelioma 35 1.108
323
P EPT020 Epithelioid Hemangioendothelioma 43 1.108
324
PNC129 Pancreatic Adenocarcinoma 64 1.098
325
ALL014 Allergic Encephalomyelitis 34 1.098
326
SPL018 Splenomegaly 47 1.098
327
P PLM037 Pulmonary Hypertension 69 1.098
328
c ACT071 Acute Kidney Failure 60 1.090
329
BRN024 Bronchitis 67 1.089
330
MTB004 Metabolic Acidosis 48 1.083
331
LPD008 Lipid Metabolism Disorder 61 1.083
332
RHB024 Rhabdomyosarcoma 2 65 1.072
333
AZS001 Azoospermia 45 1.069
334
ARG004 Argyria 26 1.069
335
P ART023 Arthropathy 59 1.069
336
CHR074 Choriocarcinoma 46 1.069
337
P VSC007 Vascular Disease 62 1.061
338
LVR012 Liver Cirrhosis 62 1.061
339
c ACT075 Acute Myocardial Infarction 55 1.061
340
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.061
341
CHL123 Chlamydia 58 1.059
342
c HPT073 Hepatitis C Virus 70 1.054
343
FTT001 Fatty Liver Disease 61 1.048
344
PCK003 Pick Disease of Brain 70 1.048
345
ADN011 Adenoid Cystic Carcinoma 68 1.047
346
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 1.047
347
HLC007 Helicobacter Pylori Infection 67 1.046
348
BRN004 Brain Edema 54 1.046
349
NWC001 Newcastle Disease 47 1.046
350
P HYP098 Hypereosinophilic Syndrome 66 1.046
351
ULC004 Ulcerative Colitis 74 1.046
352
P GRF003 Graft-Versus-Host Disease 71 1.046
353
P MDL005 Medulloblastoma 75 1.039
354
TBC004 Tobacco Addiction 63 1.039
355
LMY014 Leiomyoma, Uterine 55 1.039
356
PSY004 Psychotic Disorder 66 1.039
357
FBR047 Fibromyalgia 57 1.037
358
c HPT001 Hepatitis C 61 1.031
359
DRG003 Drug Dependence 46 1.031
360
PPL052 Papillomatosis, Confluent and Reticulated 34 1.030
361
CHL147 Chlamydia Pneumonia 47 1.025
363
KPS004 Kaposi Sarcoma 76 1.023
364
HYP020 Hyperprolactinemia 63 1.023
365
ILT001 Ileitis 49 1.015
366
P ATX030 Ataxia-Telangiectasia 80 1.015
367
END041 Endometrial Adenocarcinoma 63 1.015
368
ATN005 Autonomic Dysfunction 45 1.015
369
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 18 1.015
370
P CLS010 Cluster Headache 42 1.013
371
OCL069 Ocular Motor Apraxia 57 1.013
372
ETN001 Eating Disorder 59 1.013
373
PRT251 Proteinuria, Chronic Benign 58 1.006
374
CNG034 Congestive Heart Failure 69 1.005
375
c THY107 Thymoma, Familial 42 0.998
376
P THY023 Thymoma 64 0.998
377
PPT005 Peptic Ulcer Disease 58 0.998
378
SBC016 Subacute Delirium 42 0.998
379
GST050 Gastrointestinal System Disease 55 0.998
380
P EYD002 Eye Disease 57 0.989
381
P EPT012 Epithelioid Sarcoma 41 0.989
382
DWN001 Down Syndrome 70 0.981
383
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.981
384
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.981
385
c HPT016 Hepatitis B 62 0.981
386
BCK006 Back Pain 43 0.981
387
INT029 Interleukin-7 Receptor Alpha Deficiency 27 0.972
388
FND002 Fundus Dystrophy 54 0.972
389
c INH030 Inherited Retinal Disorder 28 0.972
390
HMC014 Homocysteinemia 52 0.962
391
c CNG006 Congenital Hypothyroidism 63 0.962
392
IFP003 Ifap Syndrome 2 41 0.962
393
HGH043 High Grade Glioma 46 0.962
394
WLL004 Wallerian Degeneration 38 0.962
395
c WLM013 Wilms Tumor 1 65 0.953
396
ALC006 Alcoholic Hepatitis 61 0.952
397
c SML038 Small Cell Cancer of the Lung 68 0.952
398
P MYP006 Myopia 55 0.946
399
P PTT006 Pituitary Adenoma 55 0.943
400
SLP001 Sleeping Sickness 56 0.943
401
P DBT005 Diabetes Insipidus 54 0.943
402
TRY001 Trypanosomiasis 50 0.933
403
HYP080 Hypogonadism 49 0.933
404
CDQ001 Cauda Equina Syndrome 37 0.933
405
NRL016 Neural Tube Defects 80 0.925
406
ART140 Arteries, Anomalies of 52 0.923
407
LPP008 Lipoprotein Quantitative Trait Locus 65 0.923
408
HRY003 Hairy Cell Leukemia 53 0.923
409
VSC006 Vascular Cancer 46 0.923
410
BWN006 Bowen's Disease 32 0.923
411
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.919
412
P LPS004 Lupus Erythematosus 61 0.912
413
TMM013 Tmem70 Defect 17 0.912
414
PPL002 Papillary Carcinoma 46 0.912
415
BRS099 Breast Ductal Carcinoma 61 0.912
416
BRN028 Brain Cancer 73 0.912
417
CCN002 Cocaine Abuse 49 0.912
418
BLD173 Bladder Small Cell Carcinoma 44 0.905
419
ADN089 Adenosquamous Lung Carcinoma 51 0.905
420
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.901
421
SQM013 Squamous Cell Carcinoma, Head and Neck 75 0.901
422
GT001 Gout 63 0.901
423
P PRC019 Precocious Puberty 48 0.901
424
PRS045 Prostatic Hypertrophy 53 0.898
425
URT010 Ureteral Obstruction 44 0.889
426
DGN001 Degenerative Disc Disease 48 0.889
427
c ACT134 Acute Liver Failure 57 0.889
428
c ATR087 Atrial Standstill 1 74 0.884
429
P BNC003 Bone Cancer 58 0.884
430
P RHN004 Rhinitis 56 0.884
431
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.877
432
c MLG084 Malignant Fibrous Histiocytoma 62 0.877
433
c SYS001 Systemic Lupus Erythematosus 85 0.876
434
HRW001 Hair Whorl 35 0.876
435
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.876
436
P NTR004 Neutropenia 62 0.876
437
P THR014 Thrombocytopenia 66 0.866
438
CRN264 Craniosynostosis with Fibular Aplasia 29 0.864
439
FBR019 Fibromatosis 44 0.864
440
PRS021 Prostatic Adenoma 43 0.861
441
FSC004 Fasciitis 49 0.861
442
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.856
443
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.853
444
P FML023 Familial Hemiplegic Migraine 53 0.851
445
SKN013 Skin Benign Neoplasm 49 0.851
446
ATM095 Autoimmune Disease 61 0.850
447
c SCL052 Scleroderma, Familial Progressive 60 0.846
448
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.846
449
P SCL018 Scoliosis 57 0.845
450
P ART005 Arteriovenous Malformation 64 0.845
451
P HYP750 Hypertriglyceridemia, Familial 61 0.843
452
RTN017 Retinal Detachment 60 0.837
453
PRS129 Prostatic Hyperplasia, Benign 48 0.837
454
JXT003 Juxtacortical Osteosarcoma 30 0.837
455
CCN001 Cocaine Dependence 47 0.837
456
AVN001 Avian Influenza 61 0.822
457
P NMN002 Niemann-Pick Disease 60 0.822
458
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.822
459
P CRN300 Coronary Heart Disease 1 73 0.821
460
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.821
461
SPN392 Spondylosis, Cervical 30 0.821
462
SPN020 Spondylosis 46 0.821
463
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.812
464
P LRY044 Larynx Cancer 53 0.812
465
ART016 Aortic Aneurysm 68 0.812
466
P LNG021 Lung Occult Small Cell Carcinoma 20 0.809
467
LNG019 Lung Combined Type Small Cell Carcinoma 34 0.809
468
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.809
469
TRD006 Tardive Dyskinesia 53 0.806
470
MSN004 Mesenchymal Cell Neoplasm 42 0.806
471
CHR178 Chromosomal Triplication 33 0.806
472
SPP011 Suppression of Tumorigenicity 12 61 0.803
473
MNN043 Meningioma, Familial 79 0.803
474
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.803
475
SCR001 Secretory Meningioma 40 0.803
476
INT395 Intracranial Meningioma 47 0.803
477
P MYC008 Myocarditis 59 0.803
478
GLM044 Glomerular Disease 34 0.803
479
NRT004 Neuritis 53 0.794
480
DFC004 Deficiency Anemia 74 0.785
481
P MJR007 Major Affective Disorder 1 42 0.785
482
VCC001 Vaccinia 49 0.785
483
ERL001 Early Myoclonic Encephalopathy 62 0.775
484
LYS002 Lysosomal Storage Disease 51 0.775
485
P HYD006 Hydrocephalus 62 0.775
486
P FML187 Familial Hypertension 34 0.775
487
PRM329 Premature Aging 36 0.775
488
P CRD246 Cardiovascular System Disease 55 0.774
489
OST032 Osteofibrous Dysplasia 52 0.769
490
DMP001 Dumping Syndrome 43 0.769
491
P MTC069 Mitochondrial Disorders 57 0.769
492
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.766
493
c TYP008 Type 1 Diabetes Mellitus 77 0.766
494
CMP010 Complex Regional Pain Syndrome 59 0.766
495
GST045 Gastroenteritis 58 0.766
496
HPT022 Hepatoblastoma 54 0.766
497
P FBR031 Febrile Seizures 52 0.766
498
c JVN010 Juvenile Rheumatoid Arthritis 52 0.760
499
FBR054 Fibroma 44 0.756
500
P FRG001 Fragile X Syndrome 70 0.756
501
CLR108 Colorectal Adenoma 63 0.756
502
P CTR002 Cataract 59 0.756
503
LNG099 Lung Disease 62 0.756
504
P THY032 Thyroiditis 56 0.756
505
P IGN003 Iga Nephropathy 1 39 0.748
506
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.747
507
ADL002 Adult Syndrome 69 0.747
508
FLL027 Fallopian Tube Carcinoma 66 0.747
509
P ACN011 Acne 55 0.745
510
P RNL015 Renal Hypertension 45 0.745
511
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.745
512
PSD016 Pseudosarcomatous Fibromatosis 37 0.745
513
P ATR005 Atrophic Gastritis 50 0.745
514
VSC002 Vascular Dementia 59 0.745
515
ANR040 Aneurysm 60 0.745
516
PST092 Posttransplant Acute Limbic Encephalitis 29 0.745
517
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.745
518
APN008 Apnea, Obstructive Sleep 66 0.745
519
PLS011 Plasmacytoma 56 0.734
520
RDC002 Radiculopathy 51 0.734
521
RTN003 Retinal Ischemia 48 0.734
522
MSL001 Measles 61 0.734
523
PPL021 Papilledema 49 0.729
524
CVD001 Covid-19 59 0.729
525
P NRV007 Nervous System Disease 65 0.729
526
c NRF024 Neurofibromatosis, Type I 76 0.723
527
MCC012 Mccune-Albright Syndrome 69 0.723
528
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.723
529
P KLZ004 Kala-Azar 1 41 0.723
530
c CHR087 Chronic Cystitis 37 0.723
531
P BRB001 Beriberi 44 0.723
532
PLM001 Pulmonary Tuberculosis 69 0.723
533
LSH001 Leishmaniasis 63 0.723
534
PST021 Postpartum Depression 50 0.723
535
ANR009 Aneurysmal Bone Cysts 43 0.712
536
VRC005 Varicose Veins 59 0.712
537
HSH003 Hashimoto Thyroiditis 60 0.712
538
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.712
539
CRT004 Carotid Artery Thrombosis 39 0.712
540
NRM004 Neuroma 49 0.712
541
BNG036 Bone Giant Cell Tumor 48 0.712
542
P HYP040 Hypospadias 51 0.712
543
P UVT001 Uveitis 57 0.712
544
PRL005 Proliferative Fasciitis 22 0.712
545
P VSC018 Visceral Steatosis 32 0.712
546
P AMY004 Amyloidosis 69 0.712
547
c JVN061 Juvenile Arthritis 56 0.711
548
MYL057 Myelopathy, Htlv-1-Associated 39 0.700
549
DPH001 Diphtheria 59 0.700
550
RTR008 Root Resorption 44 0.700
551
P END033 Endocarditis 58 0.700
552
ANG016 Angiokeratoma 37 0.700
553
SNS003 Sensory Peripheral Neuropathy 51 0.700
554
TRP002 Tropical Spastic Paraparesis 48 0.700
555
HYP043 Hyperandrogenism 47 0.700
556
P RTN018 Retinal Disease 53 0.700
557
P FBR003 Fibrous Histiocytoma 43 0.700
558
LRN003 Learning Disability 49 0.700
559
CRV002 Cervix Uteri Carcinoma in Situ 48 0.700
560
c CNG216 Congenital Hydrocephalus 50 0.700
561
CRV045 Cervical Intraepithelial Neoplasia 38 0.700
562
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 37 0.700
563
PLY100 Polyploidy 36 0.700
564
SPS019 Spastic Paraparesis 38 0.700
565
CRH005 Crohn's Colitis 53 0.692
566
c THR092 Thrombophilia Due to Thrombin Defect 74 0.687
567
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.687
568
CYN002 Cyanosis, Transient Neonatal 43 0.687
569
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.687
570
c MST023 Mesothelioma, Malignant 56 0.687
571
DNT012 Dental Caries 53 0.687
572
CHL067 Cholecystitis 59 0.687
573
BRX001 Bruxism 50 0.687
574
ANH002 Anhidrosis 45 0.687
575
SCR011 Scrapie 39 0.687
576
BRR012 Berardinelli-Seip Congenital Lipodystrophy 26 0.687
577
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.687
578
c HMP012 Hemophagocytic Lymphohistiocytosis, Familial, 2 47 0.674
579
RCT015 Reactive Arthritis 60 0.674
580
c VRL010 Viral Hepatitis 52 0.674
581
SKN020 Skin Papilloma 40 0.674
582
P TRT010 Teratoma 50 0.674
583
MLG014 Malignant Fibrous Histiocytoma of Bone 32 0.674
584
FML008 Familial Retinoblastoma 49 0.674
585
SYN005 Synostosis 43 0.674
586
CNN003 Conn's Syndrome 77 0.674
587
RKT003 Rokitansky-Aschoff Sinuses of the Gallbladder 13 0.674
588
IDP070 Idiopathic Scoliosis 41 0.670
589
ART141 Arteriovenous Malformations of the Brain 58 0.670
590
MSC157 Muscular Dystrophy, Duchenne Type 78 0.670
591
WST001 West Syndrome 64 0.660
592
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 56 0.660
593
LYM133 Lymphoma, Hodgkin, Classic 69 0.660
594
c PTT061 Pituitary Adenoma 3, Multiple Types 32 0.660
595
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.660
596
c EXS021 Exostoses, Multiple, Type Iii 19 0.660
597
CHR003 Cherubism 57 0.660
598
KRT008 Keratopathy 46 0.660
599
CHN004 Chondroblastoma 41 0.660
600
SXC001 Sex Cord-Gonadal Stromal Tumor 47 0.660
601
CRB037 Cerebral Palsy 66 0.660
602
P HYP730 Hypogonadotropic Hypogonadism 57 0.660
603
P BNG030 Benign Ependymoma 51 0.660
604
MST004 Mast Cell Neoplasm 41 0.660
605
CLL010 Cellular Ependymoma 58 0.660
606
EXT007 Extracutaneous Mastocytoma 38 0.660
607
CHL122 Cholesteatoma of Middle Ear 51 0.660
608
IRD001 Iridocyclitis 54 0.660
609
CHN053 Chondromyxoid Fibroma 40 0.660
610
DYS073 Dysphagia 53 0.660
611
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.650
612
AGN016 Aging 53 0.650
613
INF034 Infective Endocarditis 53 0.645
614
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.645
615
P MLT020 Multiple Sclerosis 79 0.645
616
P PRV002 Periventricular Nodular Heterotopia 52 0.645
617
P LPR021 Leprosy 3 71 0.645
618
c SCH080 Schizophrenia 3 27 0.645
619
CHL065 Cholangiocarcinoma 57 0.645
620
AML029 Ameloblastoma 46 0.645
621
P MGR003 Migraine with Aura 51 0.645
622
P INT068 Intestinal Disease 53 0.645
623
THY030 Thyroid Gland Disease 50 0.645
624
INT079 Intrahepatic Cholangiocarcinoma 51 0.645
625
FNC002 Functional Diarrhea 39 0.645
626
CYS005 Cysticercosis 60 0.645
627
CMP006 Complex Partial Epilepsy 36 0.645
628
CLR005 Clear Cell Chondrosarcoma 38 0.645
629
PRS029 Periosteal Osteogenic Sarcoma 31 0.645
630
P LCT001 Lactic Acidosis 50 0.645
631
LNG031 Lung Benign Neoplasm 51 0.645
632
TLN002 Telangiectatic Osteogenic Sarcoma 32 0.645
633
HNS001 Hansen's Disease 32 0.645
634
MYC005 Myocardial Stunning 45 0.645
635
P RRT020 Rare Tumor 39 0.645
636
P MYC033 Myoclonus 46 0.645
637
VGN023 Vaginitis 56 0.644
638
c HYP836 Hypercholesterolemia, Familial, 1 73 0.639
639
PSR001 Psoriatic Arthritis 61 0.629
640
FTL006 Fetal Alcohol Spectrum Disorder 43 0.629
641
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.629
642
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.629
643
P MLN069 Melanoma, Uveal 59 0.629
644
c PNC108 Pancreatitis, Hereditary 68 0.629
645
HST010 Histiocytosis 49 0.629
646
EXS001 Exostosis 49 0.629
647
SKN018 Skin Hemangioma 29 0.629
648
c MLG069 Malignant Hypertension 46 0.629
649
P SBR004 Seborrheic Dermatitis 44 0.629
650
KRT063 Keratocystic Odontogenic Tumor 40 0.629
651
c CHR684 Chronic Kidney Disease 73 0.612
652
P APL001 Aplastic Anemia 72 0.611
653
ING001 Inguinal Hernia 59 0.611
654
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.611
656
P ASP006 Aspergillosis 71 0.611
657
P KRT005 Keratoacanthoma 47 0.611
658
RFL002 Reflex Epilepsy 40 0.611
659
NRN004 Neuroendocrine Tumor 55 0.611
660
P ECL001 Eclampsia 52 0.611
661
FRZ001 Frozen Shoulder 54 0.611
662
FBR002 Fibrosarcoma of Bone 47 0.611
663
BRS064 Bursitis 51 0.611
664
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 42 0.611
665
P PRN023 Prion Disease 60 0.611
666
SKN019 Skin Melanoma 70 0.611
667
P INF038 Influenza 68 0.611
668
CHC001 Chickenpox 56 0.611
669
c INF071 Inflammatory Bowel Disease 1 65 0.610
670
ART002 Arts Syndrome 66 0.610
671
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.610
672
P CRV039 Cervicitis 52 0.610
673
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.610
674
FDL002 Food Allergy 47 0.607
675
P URN019 Urinary Tract Infection 48 0.601
676
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.592
677
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 0.592
678
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.592
679
THY111 Thyroid Carcinoma, Familial Medullary 67 0.592
680
CRT072 Creutzfeldt-Jakob Disease 67 0.592
681
OPD001 Opioid Abuse 44 0.592
682
MRG003 Marginal Zone B-Cell Lymphoma 52 0.592
683
THR004 Thrombocytosis 52 0.592
684
P LMY004 Leiomyosarcoma 62 0.592
685
CRV038 Cervical Squamous Cell Carcinoma 56 0.592
686
CLR030 Clear Cell Renal Cell Carcinoma 53 0.592
687
SCH012 Schizoaffective Disorder 49 0.592
688
HRT012 Heart Valve Disease 53 0.592
689
THY125 Thyroid Gland Medullary Carcinoma 48 0.592
690
ANV001 Anovulation 46 0.592
691
TNS005 Tonsillitis 57 0.592
692
c LCL006 Localized Scleroderma 64 0.592
693
P CHL066 Cholangitis 51 0.592
694
NRF007 Neurofibroma 63 0.592
695
SHK001 Shaken Baby Syndrome 21 0.592
696
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.592
697
HYP060 Hyperinsulinism 53 0.573
698
c ACT027 Acute Pancreatitis 60 0.573
699
CNG064 Congenital Chloride Diarrhea 34 0.570
700
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.570
701
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.570
702
TNG009 Tongue Squamous Cell Carcinoma 43 0.570
703
VNH007 Von Hippel-Lindau Syndrome 72 0.570
704
LPM012 Lipomatosis, Multiple 59 0.570
705
PRR015 Preauricular Fistulae, Congenital 20 0.570
706
MYX004 Myxedema 43 0.570
707
CHR100 Chronic Ulcer of Skin 57 0.570
708
YST001 Yeast Factor 6 0.570
709
WRN001 Werner Syndrome 69 0.570
710
c ART101 Aortic Valve Disease 2 65 0.570
711
CD4008 Cd4/cd8 T-Cell Ratio 19 0.570
712
PLM005 Pleomorphic Lipoma 39 0.570
713
MGC001 Megacolon 48 0.570
714
c ACT249 Acute Asthma 40 0.570
715
CRB026 Cerebellar Astrocytoma 32 0.570
716
GNG004 Ganglioglioma 53 0.570
717
P EMB005 Embryonal Rhabdomyosarcoma 53 0.570
718
NDL024 Nodal Marginal Zone Lymphoma 36 0.570
719
LRY018 Laryngeal Squamous Cell Carcinoma 47 0.570
720
PRM236 Primary Biliary Cholangitis 62 0.570
721
TNG007 Tongue Carcinoma 55 0.570
722
TRN012 Transient Global Amnesia 38 0.570
723
CHL004 Cholelithiasis 48 0.570
724
TST003 Testicular Leukemia 24 0.570
725
DYS015 Dysentery 49 0.570
726
CHR176 Chromophil Renal Cell Carcinoma 23 0.570
727
TXC020 Toxic Oil Syndrome 33 0.570
728
LKP003 Leukoplakia 39 0.570
729
MRK002 Marek Disease 22 0.570
730
SPT007 Spitz Nevus 34 0.570
731
P PNC044 Pancreatitis 61 0.567
732
DCT002 Ductal Carcinoma in Situ 58 0.544
733
P HMN038 Human Coronavirus Sensitivity 30 0.544
734
c DYS191 Dystonia 1, Torsion, Autosomal Dominant 47 0.544
735
c ERY062 Erythrokeratodermia Variabilis Et Progressiva 5 25 0.544
736
P ZNC008 Zinc Finger Protein 1 22 0.544
737
c NMN015 Niemann-Pick Disease, Type C1 68 0.544
738
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 0.544
739
P ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 57 0.544
740
P FTL002 Fatal Familial Insomnia 50 0.544
741
PRL017 Prolymphocytic Leukemia 47 0.544
742
PNM008 Pneumothorax 54 0.544
743
P CRV031 Cervical Adenocarcinoma 48 0.544
744
LYD001 Leydig Cell Tumor 45 0.544
745
P SYP003 Syphilis 59 0.544
746
CRC021 Carcinosarcoma 62 0.544
747
P NGH001 Night Blindness 52 0.544
748
P BCL005 B Cell Prolymphocytic Leukemia 39 0.544
749
CRC006 Carcinoid Syndrome 55 0.544
750
SYN036 Syncope 44 0.544
751
PST047 Post-Traumatic Epilepsy 20 0.544
752
VNT036 Ventilator-Induced Diaphragmatic Dysfunction 15 0.544
753
INH023 Inherited Cancer-Predisposing Syndrome 53 0.544
754
P ATS364 Autism 72 0.530
755
MTH071 Methane Production 24 0.530
756
P FNG006 Feingold Syndrome 1 61 0.528
757
P SCL057 Scoliosis, Isolated 1 40 0.528
758
ACR041 Acromelic Frontonasal Dysostosis 53 0.528
759
c PRS130 Prostate Cancer, Hereditary, 8 32 0.528
760
MYL005 Myelofibrosis 70 0.528
761
P OCY003 Oocyte Maturation Defect 1 46 0.528
762
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 0.528
763
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.528
764
CNG510 Congenital Lipomatous Overgrowth, Vascular Malformations, and Epidermal Nevi 63 0.528
765
c PRS136 Prostate Cancer, Hereditary, 6 33 0.528
766
OPT010 Optic Papillitis 38 0.528
767
FML035 Familial Hyperlipidemia 54 0.528
768
PRR004 Preretinal Fibrosis 35 0.528
769
PRC003 Proctitis 49 0.528
770
MCL006 Macular Retinal Edema 56 0.528
771
NTR005 Nutritional Deficiency Disease 60 0.528
772
P END046 Endometritis 46 0.528
773
ATX019 Ataxia with Vitamin E Deficiency 44 0.528
774
PRM126 Primary Peritoneal Carcinoma 61 0.528
775
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.524
776
OBS002 Obsessive-Compulsive Disorder 67 0.524
777
HRT011 Heart Septal Defect 49 0.518
778
ENT011 Enterocolitis 55 0.511
779
MYL069 Myeloma, Multiple 76 0.511
780
NNL006 Non-Alcoholic Steatohepatitis 54 0.511
781
SPL004 Splenic Marginal Zone Lymphoma 50 0.510
782
PFF001 Pfeiffer Syndrome 77 0.510
783
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 0.510
784
PNM010 Pneumothorax, Primary Spontaneous 58 0.510
785
c OTP006 Otopalatodigital Syndrome, Type I 59 0.510
786
TRN074 Turnpenny-Fry Syndrome 33 0.510
787
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.510
788
CHR593 Chromosome 16p13.3 Deletion Syndrome, Proximal 68 0.510
789
P CRN037 Craniosynostosis 67 0.510
790
INT020 Intravenous Leiomyomatosis 35 0.510
791
LMY003 Leiomyomatosis 43 0.510
792
P MLT074 Multiple Endocrine Neoplasia 58 0.510
793
MMB001 Membranoproliferative Glomerulonephritis 56 0.510
794
LFT001 Left Bundle Branch Hemiblock 47 0.510
795
AMB001 Amebiasis 56 0.510
796
P PRG139 Progeroid Syndrome 30 0.510
797
WHP002 Whiplash 35 0.510
798
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.510
799
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.498
800
PRN019 Perinatal Necrotizing Enterocolitis 60 0.491
801
P ATR011 Atrial Fibrillation 66 0.484
802
P ART021 Arteriosclerosis 53 0.484
803
P ATR010 Atrial Heart Septal Defect 58 0.477
804
END086 End Stage Renal Disease 54 0.477
805
MCS002 Mucositis 55 0.470
806
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.463
807
P DBT009 Diabetes Mellitus 67 0.463
808
P HYP263 Hypersomnia 40 0.456
809
c MCR115 Microvascular Complications of Diabetes 5 65 0.448
810
P SNS001 Sensorineural Hearing Loss 60 0.448
811
P SHR001 Short Bowel Syndrome 53 0.448
812
SNG003 Single Ventricular Heart 30 0.433
813
AST054 Australia Antigen 25 0.428
814
VRL003 Variola Major 43 0.428
816
P PRK101 Parkinsonism-Dystonia, Infantile, 1 40 0.428
817
c PRG106 Progressive Muscular Dystrophy 31 0.428
818
MLT006 Multidrug-Resistant Tuberculosis 47 0.428
819
SBC014 Subclavian Steal Syndrome 30 0.428
820
RHM001 Rheumatic Fever 59 0.428
821
MCR019 Microglandular Adenosis 44 0.428
822
PNC016 Pancreatic Cholera 32 0.428
823
PTY002 Pityriasis Versicolor 38 0.428
824
OST016 Osteochondrosis 52 0.428
825
SML019 Smallpox 55 0.428
826
MLR002 Miliary Tuberculosis 47 0.428
827
BCR002 Bicornuate Uterus 24 0.428
828
GNG003 Gingival Recession 50 0.425
829
P MVM001 Movement Disease 61 0.417
830
PLM010 Pulmonary Edema 54 0.417
831
c HNT011 Huntington Disease-Like 3 33 0.409
832
c HNT004 Huntington Disease-Like 2 51 0.409
833
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.409
834
P CRD119 Cardiac Arrest 68 0.401
835
CRD223 Cardiac Arrhythmia 63 0.401
836
ANR007 Anorexia Nervosa 59 0.401
837
HMN047 Human Cytomegalovirus Infection 59 0.401
838
PTN001 Patent Foramen Ovale 61 0.401
839
c ACT068 Acute Cystitis 60 0.401
840
RNL077 Renal Fibrosis 46 0.392
841
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.392
842
DSS032 Disease by Infectious Agent 55 0.392
843
BLR008 Bilirubin Metabolic Disorder 57 0.392
844
P EXN002 Exanthem 58 0.384
845
SYN007 Synovitis 54 0.384
846
MLK006 Milk Allergy 47 0.384
847
PLC002 Plica Syndrome 35 0.384
848
P HYP055 Hypoplastic Left Heart Syndrome 65 0.384
849
P MNN013 Meningitis 65 0.384
850
c NRB010 Neuroblastoma 1 59 0.380
851
GST092 Gastroesophageal Reflux 59 0.375
852
P NPH012 Nephrotic Syndrome 61 0.375
853
P INT143 Interstitial Cystitis 59 0.375
854
LWC001 Low Compliance Bladder 44 0.375
855
SPP007 Suppression Amblyopia 38 0.366
856
P RCT021 Rectum Cancer 54 0.366
857
AMB002 Amblyopia 49 0.366
858
P MSC003 Muscular Atrophy 52 0.366
859
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.357
860
ALL003 Allergic Rhinitis 66 0.347
861
P AST005 Asthma 75 0.347
862
c TRN038 Transposition of the Great Arteries, Dextro-Looped 1 39 0.347
863
P TBR001 Tuberous Sclerosis 69 0.347
865
ATR057 Atrioventricular Block 54 0.337
866
IRN002 Iron Metabolism Disease 56 0.337
867
CHG001 Chagas Disease 65 0.337
868
CPL003 Capillary Leak Syndrome 54 0.337
869
TND004 Tendinopathy 45 0.327
870
TND005 Tendinitis 53 0.327
871
P MYC084 Mycobacterium Tuberculosis 1 68 0.327
872
P CYS039 Cystic Kidney Disease 52 0.327
873
IMP005 Impotence 52 0.327
874
TRC022 Tricuspid Valve Insufficiency 46 0.327
875
P THL005 Thalassemia 56 0.327
876
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.317
877
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 0.317
878
HND015 Hand Skill, Relative 29 0.317
879
BRN056 Bronchopulmonary Dysplasia 57 0.317
880
P SCK005 Sickle Cell Disease 56 0.317
881
INT276 Interatrial Communication 52 0.317
882
c TBR025 Tuberous Sclerosis 1 84 0.306
883
P SLM003 Salmonellosis 54 0.306
884
CLR109 Colorectal Adenocarcinoma 50 0.306
885
FML063 Familial Glucocorticoid Deficiency 58 0.306
886
GST037 Gastroparesis 52 0.306
887
P DMN002 Dementia 65 0.306
888
CNG284 Congenital Pseudoarthrosis of the Tibia 18 0.306
889
BNG077 Benign Idiopathic Neonatal Seizures 23 0.306
890
DWR001 Dwarfism 44 0.306
891
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.295
892
TLR001 Tularemia 56 0.295
893
HMS001 Hemosiderosis 48 0.295
894
P MYP004 Myopathy 67 0.295
895
PLN007 Plantar Fasciitis 37 0.295
896
c BCT007 Bacterial Meningitis 55 0.295
897
CLF027 Cleft Palate, Isolated 64 0.283
898
CMB007 Combined Immunodeficiency 56 0.283
899
OST003 Osteonecrosis 60 0.283
900
OST017 Osteomyelitis 63 0.283
901
RBS001 Rabies 57 0.283
902
P HYP069 Hyperparathyroidism 62 0.283
903
DRM006 Dermatitis 61 0.283
904
NPH010 Nephrosclerosis 50 0.283
905
BCT004 Bacteriuria 48 0.283
906
PRT058 Pure Autonomic Failure 58 0.283
907
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 18 0.283
908
PRS063 Paresthesia 39 0.283
909
SXL003 Sexual Disorder 49 0.271
910
GLC012 Galactosialidosis 55 0.271
911
FCS002 Fucosidosis 61 0.271
912
ASP002 Aspartylglucosaminuria 57 0.271
913
ENC038 Encephalopathy, Progressive, with or Without Lipodystrophy 40 0.271
914
MLD018 Mild Cognitive Impairment 48 0.271
915
LMB062 Limb Ischemia 55 0.271
916
P VNT002 Ventricular Septal Defect 58 0.271
917
IRN001 Iron Deficiency Anemia 58 0.271
918
P MTR003 Mitral Valve Stenosis 53 0.271
919
GLY031 Glycoproteinosis 49 0.271
920
MST005 Mastitis 52 0.271
921
ACQ007 Acquired Immunodeficiency Syndrome 58 0.271
922
STM007 Stomatitis 52 0.271
924
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.259
925
CYS001 Cystic Fibrosis 77 0.259
926
P EPL198 Epilepsy, Myoclonic Juvenile 61 0.259
927
P RTT002 Rett Syndrome 79 0.259
928
CRB204 Cerebellar, Ocular, Craniofacial, and Genital Syndrome 27 0.259
929
c OPT053 Optic Atrophy 1 62 0.259
930
P MMP001 Mumps 56 0.259
931
THR024 Thrombosis 56 0.259
932
c ATM011 Autoimmune Hepatitis 62 0.259
933
PRP030 Purpura 54 0.259
934
TRN018 Transitional Cell Carcinoma 56 0.259
935
P DYS005 Dyslexia 40 0.259
936
OVR063 Overnutrition 42 0.259
937
DBT002 Diabetic Autonomic Neuropathy 40 0.259
938
ATN004 Autonomic Neuropathy 42 0.259
939
ALL006 Allergic Asthma 55 0.259
940
P ALP008 Alopecia 53 0.259
941
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.259
942
CHR463 Chronic Actinic Dermatitis 37 0.259
943
BLM002 Bulimia Nervosa 56 0.246
944
APH002 Aphasia 55 0.246
945
P CLC063 Celiac Disease 1 65 0.246
946
OTT002 Otitis Media 70 0.246
947
LPT014 Leptin Deficiency or Dysfunction 77 0.246
948
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.246
949
P EPL140 Epilepsy, Idiopathic Generalized 60 0.246
950
ANK001 Ankylosis 50 0.246
951
c GM2006 Gm2 Gangliosidosis 46 0.246
952
P HYP061 Hypertrophic Cardiomyopathy 68 0.246
953
FLR002 Filariasis 55 0.246
954
PTL002 Patellofemoral Pain Syndrome 34 0.246
955
P PRS038 Personality Disorder 65 0.246
956
PLR008 Pleurisy 49 0.246
957
P OPT009 Optic Neuritis 57 0.246
958
FLR001 Filarial Elephantiasis 59 0.246
959
c INH020 Inherited Metabolic Disorder 47 0.246
960
EXP004 Exophthalmos 50 0.246
961
P RRH023 Rare Hereditary Hemochromatosis 52 0.246