Search results for sp1

1166 hits were found for sp1

# Family MCID Name MIFTS Score
1
P CLR023 Colorectal Cancer 100 26.570
2
P BRS047 Breast Cancer 98 25.259
3
P LNG032 Lung Cancer 98 24.137
4
P GST053 Gastric Cancer 83 24.076
5
P PNC035 Pancreatic Cancer 86 22.706
6
P OVR042 Ovarian Cancer 88 21.574
7
P HPT023 Hepatocellular Carcinoma 96 21.086
8
HMN044 Human Immunodeficiency Virus Type 1 78 20.969
9
EMB004 Embryonal Carcinoma 56 19.837
10
P PRS040 Prostate Cancer 95 19.113
11
P HNT016 Huntington Disease 73 18.549
12
P OST002 Osteoporosis 76 17.207
13
P FBR017 Fibrosarcoma 56 16.868
14
IMM167 Immune Deficiency Disease 78 16.421
15
P KRT007 Keratoconus 50 16.310
16
TRT001 Teratocarcinoma 42 14.996
17
P SCH015 Schizophrenia 74 14.903
18
P MYC007 Myocardial Infarction 70 14.485
19
P AST005 Asthma 76 14.216
20
P BRS044 Breast Adenocarcinoma 58 13.722
21
P PHC003 Pheochromocytoma 69 13.594
22
P MCH002 Machado-Joseph Disease 62 12.870
23
P ALZ034 Alzheimer Disease 87 12.376
24
VNH007 Von Hippel-Lindau Syndrome 73 11.948
25
P HRD008 Hereditary Hemorrhagic Telangiectasia 65 11.903
26
c WLM013 Wilms Tumor 1 66 11.882
27
c ATS007 Autism Spectrum Disorder 72 10.691
28
WLS001 Wilson Disease 70 10.229
29
CRB011 Cerebrotendinous Xanthomatosis 65 10.073
30
P RTT002 Rett Syndrome 79 9.698
31
RPD005 Rapidly Involuting Congenital Hemangioma 46 9.068
32
P RTN024 Retinoblastoma 73 9.035
33
HYP266 Hypoxia 57 8.514
34
P OTS001 Otosclerosis 49 8.384
35
P NRB001 Neuroblastoma 66 8.163
36
P WLF004 Wolfram Syndrome 61 7.853
37
c RTN114 Retinitis Pigmentosa 58 41 7.696
38
GLM045 Glioma 63 7.687
39
GLL048 Glial Tumor 52 7.643
40
OST159 Osteogenic Sarcoma 66 7.069
41
SQM006 Squamous Cell Carcinoma 60 6.919
42
CHR074 Choriocarcinoma 46 6.898
43
P PLM158 Palmoplantar Keratoderma and Congenital Alopecia 1 42 6.858
44
c AML044 Amelogenesis Imperfecta, Type Ig 53 6.858
45
HRD005 Hard Palate Cancer 19 6.858
46
PRS004 Prostate Squamous Cell Carcinoma 32 6.858
47
P AML002 Amelogenesis Imperfecta 56 6.858
48
HLX001 Helix Syndrome 48 6.591
49
INS024 Insulin-Like Growth Factor I 78 6.451
50
GLB002 Glioblastoma 67 6.420
51
P HRP006 Herpes Simplex 65 5.988
52
P ADN016 Adenocarcinoma 63 5.856
53
P NSP012 Nasopharyngeal Carcinoma 61 5.772
54
c PRG020 Paragangliomas 3 39 5.529
55
ISC004 Ischemia 61 5.527
56
c LKM061 Leukemia, Acute Myeloid 83 5.370
57
P LKM002 Leukemia 67 5.332
58
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 5.330
59
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 5.330
60
P SPP010 Suppressor of Tumorigenicity 3 51 5.276
61
CRV035 Cervical Cancer 73 5.268
62
47X002 47,xyy 48 5.222
63
ACT098 Acute Erythroid Leukemia 55 5.105
64
P LNG064 Lung Cancer Susceptibility 3 70 5.030
65
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 4.994
66
c LKM005 Leukemia, T-Cell, Chronic 34 4.974
67
ORL015 Oral Squamous Cell Carcinoma 43 4.967
68
c SML038 Small Cell Cancer of the Lung 69 4.817
69
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 4.810
70
TLN003 Telangiectasis 51 4.754
71
P MYL006 Myeloid Leukemia 61 4.710
72
HYP066 Hyperglycemia 61 4.629
73
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.623
74
c HPT016 Hepatitis B 62 4.623
75
MYL069 Myeloma, Multiple 77 4.608
76
c PCH010 Pachyonychia Congenita 3 43 4.557
77
P BLD134 Bladder Cancer 79 4.557
78
c MCR115 Microvascular Complications of Diabetes 5 65 4.523
79
ORL011 Oral Cancer 60 4.410
80
SPN035 Spindle Cell Sarcoma 54 4.348
81
SRC014 Sarcoma 65 4.348
82
DWN001 Down Syndrome 70 4.294
83
P MLN008 Melanoma 76 4.256
84
CHC001 Chickenpox 57 4.111
85
RNL077 Renal Fibrosis 46 4.098
86
ATH013 Atherosclerosis Susceptibility 63 4.064
87
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.041
88
P BNG032 Benign Mesothelioma 53 4.018
89
c MCR130 Microvascular Complications of Diabetes 6 41 3.970
90
c MCR120 Microvascular Complications of Diabetes 7 47 3.970
91
c MCR113 Microvascular Complications of Diabetes 3 52 3.970
92
c MCR133 Microvascular Complications of Diabetes 4 41 3.970
93
c PRC016 Pre-Eclampsia 65 3.955
94
c HYD046 Hydatidiform Mole, Recurrent, 1 59 3.940
95
GST010 Gestational Trophoblastic Neoplasm 52 3.940
96
c HMN021 Human T-Cell Leukemia Virus Type 1 47 3.922
97
CYT002 Cytokine Deficiency 43 3.910
98
P ATX030 Ataxia-Telangiectasia 80 3.897
99
P LKM062 Leukemia, Acute Lymphoblastic 69 3.857
100
END057 Endometrial Cancer 72 3.853
101
ADR040 Adrenal Gland Pheochromocytoma 46 3.792
102
c HPT073 Hepatitis C Virus 71 3.751
103
MLG079 Malignant Pleural Mesothelioma 42 3.639
104
P SYS005 Systemic Scleroderma 74 3.604
105
KPS004 Kaposi Sarcoma 77 3.563
106
c SCL052 Scleroderma, Familial Progressive 61 3.557
107
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.530
108
ESP021 Esophageal Cancer 83 3.500
109
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.474
110
PNC129 Pancreatic Adenocarcinoma 65 3.472
111
GST040 Gastric Adenocarcinoma 67 3.391
112
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.383
113
OST012 Osteoarthritis 77 3.362
114
P KDN017 Kidney Cancer 61 3.353
115
CLN015 Colon Adenocarcinoma 65 3.322
116
P RHB003 Rhabdomyosarcoma 66 3.303
117
CHR178 Chromosomal Triplication 34 3.291
118
48X005 48,xyyy 39 3.237
119
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 3.234
120
P MSC005 Muscular Dystrophy 67 3.228
121
HGH043 High Grade Glioma 45 3.208
122
VCC001 Vaccinia 47 3.149
123
LNG099 Lung Disease 62 3.149
124
PTT037 Pituitary Tumors 44 3.146
125
ACT119 Acute Promyelocytic Leukemia 62 3.061
126
TNG009 Tongue Squamous Cell Carcinoma 43 3.025
127
c FTL067 Fetal Hemoglobin Quantitative Trait Locus 6 25 3.019
128
ECT026 Ectopic Pregnancy 48 3.019
129
P GLM040 Glioma Susceptibility 1 71 2.993
130
MSC157 Muscular Dystrophy, Duchenne Type 79 2.990
131
P HPT021 Hepatitis 69 2.985
132
THY029 Thyroid Carcinoma 51 2.951
133
INV018 Invasive Mole 23 2.939
134
c HYP595 Hypertension, Essential 85 2.916
135
AGN016 Aging 54 2.895
136
P ART022 Arthritis 71 2.861
137
P PLM036 Pulmonary Fibrosis 66 2.845
138
c HPT001 Hepatitis C 62 2.843
139
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 2.806
140
INS001 Insulinoma 59 2.791
141
VRL011 Viral Infectious Disease 61 2.780
142
EWN003 Ewing Sarcoma 70 2.747
143
c LKM063 Leukemia, Chronic Myeloid 71 2.730
144
BRK010 Burkitt Lymphoma 66 2.719
145
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.718
146
P VSC007 Vascular Disease 63 2.682
147
CHL065 Cholangiocarcinoma 58 2.676
148
INT079 Intrahepatic Cholangiocarcinoma 51 2.676
149
ACQ007 Acquired Immunodeficiency Syndrome 59 2.607
150
CHL068 Cholestasis 61 2.607
151
CYS001 Cystic Fibrosis 78 2.605
152
PRG009 Progressive Multifocal Leukoencephalopathy 58 2.605
153
P BCL017 B-Cell Lymphoma 59 2.571
154
URT010 Ureteral Obstruction 45 2.565
155
c PRG019 Paragangliomas 2 30 2.534
156
c ACT073 Acute Leukemia 58 2.525
157
DGN001 Degenerative Disc Disease 49 2.525
158
c HYP836 Hypercholesterolemia, Familial, 1 73 2.520
159
c MJR022 Major Affective Disorder 8 38 2.496
160
P LYM118 Lymphoma 67 2.496
161
c MJR024 Major Affective Disorder 9 41 2.496
162
P BPL003 Bipolar Disorder 56 2.496
163
P CRN024 Corneal Disease 44 2.484
164
P THL005 Thalassemia 56 2.441
165
c FTL070 Fetal Akinesia Deformation Sequence 2 36 2.441
166
SKN016 Skin Disease 63 2.418
167
P OVR082 Overgrowth Syndrome 49 2.398
168
P LNG028 Long Qt Syndrome 64 2.398
169
P TRT010 Teratoma 51 2.398
170
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.377
171
CLR030 Clear Cell Renal Cell Carcinoma 54 2.377
172
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.353
173
ATS010 Autosomal Recessive Disease 42 2.353
174
P SKN015 Skin Carcinoma 71 2.353
175
DMY004 Demyelinating Disease 50 2.353
176
HMN047 Human Cytomegalovirus Infection 57 2.341
177
HYP060 Hyperinsulinism 54 2.341
178
P ADL010 Adult Respiratory Distress Syndrome 71 2.336
179
CRB004 Cerebral Artery Occlusion 45 2.306
180
P BND020 Bone Disease 59 2.306
181
P ADL017 Adult T-Cell Leukemia 56 2.303
182
EPD052 Epidermolysis Bullosa Simplex Superficialis 17 2.293
183
PRT251 Proteinuria, Chronic Benign 57 2.293
184
P LMY004 Leiomyosarcoma 62 2.259
185
P CHN012 Chondrosarcoma 57 2.250
186
MCR004 Macroglobulinemia 49 2.250
187
TXC005 Toxic Shock Syndrome 62 2.250
188
PRT036 Peritonitis 65 2.225
189
LPP008 Lipoprotein Quantitative Trait Locus 65 2.213
190
P ECL001 Eclampsia 52 2.210
191
c TYP009 Type 2 Diabetes Mellitus 92 2.205
192
MDD018 Middle East Respiratory Syndrome 44 2.205
193
FTT001 Fatty Liver Disease 62 2.205
194
SMN007 Seminoma 42 2.205
195
c ACT027 Acute Pancreatitis 60 2.205
196
P PRN023 Prion Disease 60 2.205
197
P PNC044 Pancreatitis 61 2.205
198
P PRD008 Periodontitis 64 2.184
199
END041 Endometrial Adenocarcinoma 64 2.184
200
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.159
201
HYP457 Hypertrophic Scars 42 2.159
202
MMM001 Mammary Paget's Disease 53 2.159
203
P OVR106 Ovarian Clear Cell Carcinoma 44 2.159
204
P AGM001 Agammaglobulinemia 68 2.159
205
OVR094 Ovarian Epithelial Cancer 39 2.159
206
MLG169 Malignant Astrocytoma 57 2.143
207
NNL006 Non-Alcoholic Steatohepatitis 54 2.111
208
IRN002 Iron Metabolism Disease 57 2.111
209
c SVR005 Severe Pre-Eclampsia 50 2.100
210
SVR004 Severe Combined Immunodeficiency 72 2.089
211
BRT054 Brittle Bone Disorder 74 2.062
212
P CTR002 Cataract 60 2.062
213
P MNC007 Monocytic Leukemia 47 2.062
214
P PRK057 Parkinson Disease, Late-Onset 80 2.057
215
P PLY014 Polycystic Kidney Disease 69 2.057
216
c PRD040 Periodontitis, Chronic 52 2.057
217
BNR002 Bone Resorption Disease 47 2.050
218
ANN002 Anencephaly 57 2.012
219
BCT022 Bacterial Infectious Disease 56 2.012
220
END086 End Stage Renal Disease 52 2.012
221
TST014 Testicular Cancer 52 2.012
222
PLY100 Polyploidy 36 2.011
223
P CRD246 Cardiovascular System Disease 56 2.011
224
P END044 Endometriosis 62 1.992
225
P SJG008 Sjogren Syndrome 61 1.985
226
P RHM011 Rheumatoid Arthritis 82 1.966
227
MCP006 Mucoepidermoid Carcinoma 48 1.966
228
CNN005 Connective Tissue Disease 67 1.966
229
BRN028 Brain Cancer 74 1.966
230
PPL022 Papilloma 53 1.966
231
SQM002 Squamous Cell Papilloma 46 1.966
232
c FML021 Familial Hypercholesterolemia 72 1.966
233
P INF032 Infertility 57 1.958
234
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.958
235
P DRM053 Dermatitis, Atopic 65 1.949
236
SPN186 Spinal Cord Injury 61 1.918
237
HMC014 Homocysteinemia 52 1.918
238
P KDN018 Kidney Disease 72 1.918
239
c THY109 Thyroid Cancer, Nonmedullary, 1 55 1.902
240
P NPH012 Nephrotic Syndrome 60 1.902
241
P BNC003 Bone Cancer 58 1.902
242
STR067 Stroke, Ischemic 80 1.869
243
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.869
244
HLC007 Helicobacter Pylori Infection 67 1.869
246
ALL029 Allergic Disease 59 1.869
247
P GLM007 Glomerulonephritis 60 1.869
248
SPP011 Suppression of Tumorigenicity 12 61 1.844
249
HRW001 Hair Whorl 35 1.844
250
P AMY004 Amyloidosis 70 1.844
251
ULC004 Ulcerative Colitis 74 1.844
252
P GND004 Gonadal Dysgenesis 47 1.844
253
P END039 Endodermal Sinus Tumor 41 1.844
254
ATM095 Autoimmune Disease 61 1.838
255
P PRG092 Pregnancy Loss, Recurrent 1 41 1.818
256
TNG007 Tongue Carcinoma 52 1.818
257
OBS082 Obstructive Nephropathy 41 1.818
258
P MSC003 Muscular Atrophy 52 1.818
259
CHL014 Cholera 62 1.818
260
PTS001 Patau Syndrome 56 1.818
261
BRS051 Breast Disease 58 1.818
262
KLD004 Keloid Disorder 39 1.818
263
P DYS007 Dyskeratosis Congenita 67 1.799
264
P FRG001 Fragile X Syndrome 70 1.783
265
c THR092 Thrombophilia Due to Thrombin Defect 74 1.783
266
P CYS018 Cystitis 59 1.783
267
RCK004 Rickets 68 1.783
268
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.765
269
P DMN002 Dementia 66 1.765
270
AGM019 Agammaglobulinemia, X-Linked 72 1.719
271
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.719
272
SHG001 Shigellosis 63 1.719
273
END011 Endometriosis of Ovary 39 1.719
274
STM007 Stomatitis 54 1.719
275
TRP014 Triploidy 38 1.719
276
PLY150 Polykaryocytosis Inducer 29 1.709
277
c BTT014 Beta-Thalassemia 72 1.709
278
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.709
279
c PRX048 Peroxisome Biogenesis Disorder 10a 31 1.709
280
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.709
281
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.709
282
P HMN032 Human Herpesvirus 8 48 1.709
283
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 1.709
284
PLC005 Placental Insufficiency 56 1.709
285
OST003 Osteonecrosis 61 1.709
286
CNN003 Conn's Syndrome 79 1.709
287
P ICH004 Ichthyosis 56 1.709
288
P MYT002 Myotonic Dystrophy 51 1.709
289
P NRF002 Neurofibromatosis 57 1.709
290
c MST023 Mesothelioma, Malignant 56 1.678
291
P VTR007 Vitreoretinopathy 46 1.652
292
THY128 Thyroid Tumor 35 1.652
293
CRT072 Creutzfeldt-Jakob Disease 68 1.652
294
MYL009 Myelodysplastic Syndrome 67 1.652
295
MSC007 Muscle Hypertrophy 64 1.652
296
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 1.652
297
GLC003 Glucose Intolerance 54 1.652
298
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.652
299
P PSR002 Psoriasis 63 1.652
300
ART016 Aortic Aneurysm 68 1.652
301
NRM005 Neuromuscular Disease 63 1.652
302
SLC006 Silicosis 56 1.652
303
PRM236 Primary Biliary Cholangitis 60 1.652
304
EXS001 Exostosis 49 1.652
305
CNG034 Congestive Heart Failure 69 1.652
306
ANR040 Aneurysm 61 1.652
307
P MLT020 Multiple Sclerosis 79 1.651
308
P PLV020 Pelvic Organ Prolapse 58 1.651
309
DBT007 Diabetic Cataract 36 1.651
310
DRM006 Dermatitis 62 1.635
311
ECZ002 Eczema Herpeticum 45 1.591
312
HPT022 Hepatoblastoma 54 1.591
313
ADN018 Adenoma 59 1.591
314
ANX004 Anoxia 40 1.591
315
HMZ003 Homozygous Familial Hypercholesterolemia 60 1.591
316
c ATR087 Atrial Standstill 1 74 1.591
317
LYM157 Lymph Node Carcinoma 29 1.591
318
WRN001 Werner Syndrome 69 1.591
319
P EST001 Estrogen-Receptor Positive Breast Cancer 49 1.591
320
P RTN018 Retinal Disease 53 1.591
321
LPD008 Lipid Metabolism Disorder 62 1.591
322
c JVN010 Juvenile Rheumatoid Arthritis 66 1.591
323
ALC007 Alcohol Dependence 66 1.577
324
c LNG047 Long Qt Syndrome 2 59 1.577
325
P INT068 Intestinal Disease 53 1.577
326
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.526
327
P SPR120 Supranuclear Palsy, Progressive, 1 69 1.526
328
P MTR004 Maturity-Onset Diabetes of the Young 68 1.526
329
P EXN002 Exanthem 58 1.526
330
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.526
331
P PSD087 Pseudoxanthoma Elasticum 67 1.526
332
P MDL005 Medulloblastoma 75 1.526
333
MNN043 Meningioma, Familial 79 1.526
334
ARG004 Argyria 26 1.526
335
P BLD062 Bile Duct Cancer 67 1.526
336
P EPL164 Epilepsy 68 1.526
337
SCR001 Secretory Meningioma 40 1.526
338
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.526
339
LVR012 Liver Cirrhosis 63 1.526
340
SPN021 Spinal Meningioma 50 1.526
341
P INS002 in Situ Carcinoma 53 1.526
342
DYS164 Dyskeratosis Congenita, X-Linked 56 1.497
343
RTN017 Retinal Detachment 60 1.458
344
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 59 1.458
345
HMR023 Hemorrhagic Cystitis 43 1.458
346
c BRN108 Branchiootic Syndrome 1 62 1.458
347
SCK003 Sickle Cell Anemia 74 1.458
348
NRR001 Neuroretinitis 42 1.458
349
RTN023 Retinitis 46 1.458
350
P OLG002 Oligodendroglioma 66 1.458
351
P TRN020 Turner Syndrome 67 1.458
352
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.458
353
TST018 Testicular Yolk Sac Tumor 39 1.458
354
UND007 Undifferentiated Connective Tissue Disease 28 1.458
355
RYN005 Raynaud Phenomenon 45 1.458
356
PPL052 Papillomatosis, Confluent and Reticulated 34 1.453
357
OST017 Osteomyelitis 63 1.408
358
P GLL018 Gallbladder Cancer 53 1.408
359
P ATS364 Autism 69 1.404
360
PRT037 Pertussis 65 1.404
361
ART140 Arteries, Anomalies of 53 1.384
362
PHS025 Phosphatase, Acid, of Tissues 28 1.384
363
LYM012 Lymphoplasmacytic Lymphoma 50 1.384
364
WLD007 Waldenstroem's Macroglobulinemia 63 1.384
365
c RTN041 Retinitis Pigmentosa 11 42 1.384
366
LYM143 Lymphoma, Non-Hodgkin, Familial 75 1.384
367
c BNM010 Bone Marrow Failure Syndrome 1 37 1.384
369
P ATT013 Attention Deficit-Hyperactivity Disorder 64 1.384
370
PLS011 Plasmacytoma 56 1.384
371
THR016 Thrombophlebitis 50 1.384
372
ERY003 Erythema Multiforme 56 1.384
373
P GRV001 Graves' Disease 55 1.384
374
RHM001 Rheumatic Fever 59 1.384
375
STT001 Status Epilepticus 59 1.384
376
ADN020 Adenosarcoma 42 1.384
377
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.384
378
P LKM071 Leukemia, Chronic Lymphocytic 75 1.352
379
P INF037 Inflammatory Bowel Disease 53 1.352
380
CLT003 Colitis 63 1.352
381
NRL016 Neural Tube Defects 81 1.352
382
P INF038 Influenza 68 1.352
383
P RSP003 Respiratory Failure 74 1.352
384
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 1.308
385
LYM133 Lymphoma, Hodgkin, Classic 74 1.304
386
P SMP003 Simpson-Golabi-Behmel Syndrome 49 1.304
387
MRF001 Marfan Syndrome 76 1.304
388
BNG091 Benign Chronic Pemphigus 57 1.304
389
TND004 Tendinopathy 45 1.304
390
TND005 Tendinitis 54 1.304
391
CRB138 Core Binding Factor Acute Myeloid Leukemia 45 1.304
392
ART074 Aortic Dissection 53 1.304
393
BTT017 Beta-Thalassemia Major 51 1.304
394
LKC009 Leukocyte Adhesion Deficiency, Type I 70 1.304
395
CHD004 Chudley-Mccullough Syndrome 48 1.304
396
c NML006 Nemaline Myopathy 5 41 1.304
397
P MCR129 Microvascular Complications of Diabetes 1 68 1.304
398
c XRD032 Xeroderma Pigmentosum, Complementation Group B 50 1.304
399
DRR014 Darier-White Disease 59 1.304
400
DCT002 Ductal Carcinoma in Situ 58 1.304
401
RNL078 Renal Dysplasia 46 1.304
402
P WRD001 Waardenburg's Syndrome 60 1.304
403
P TRM003 Tremor 48 1.304
404
MNG007 Manganese Poisoning 28 1.304
405
RHS001 Rh Isoimmunization 29 1.304
406
c MCR112 Microvascular Complications of Diabetes 2 42 1.304
407
c BSL007 Basal Cell Carcinoma 68 1.304
408
PRM013 Premature Menopause 58 1.304
409
SRS001 Serous Cystadenocarcinoma 52 1.304
410
P LPS002 Liposarcoma 64 1.304
411
MGC001 Megacolon 48 1.304
412
SFT003 Soft Tissue Sarcoma 57 1.304
413
BRN056 Bronchopulmonary Dysplasia 56 1.304
414
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.299
415
c SYS001 Systemic Lupus Erythematosus 87 1.244
416
P LPS004 Lupus Erythematosus 61 1.244
417
P CRN300 Coronary Heart Disease 1 73 1.216
418
AND002 Androgen Insensitivity Syndrome 63 1.216
419
AND020 Androgen Insensitivity, Partial 55 1.216
420
P MYC084 Mycobacterium Tuberculosis 1 68 1.216
421
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.216
422
THY121 Thyroid Gland Anaplastic Carcinoma 67 1.216
423
P ATR011 Atrial Fibrillation 66 1.216
424
P LYM033 Lymphoproliferative Syndrome 59 1.216
425
CRY035 Cryptorchidism, Unilateral or Bilateral 58 1.216
426
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.216
427
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.216
428
HYP114 Hypertensive Nephropathy 36 1.216
429
P SCL057 Scoliosis, Isolated 1 40 1.216
430
P SCL018 Scoliosis 57 1.216
431
HPT004 Hepatic Coma 43 1.216
432
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.216
433
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 43 1.216
434
P CNG001 Congenital Myasthenic Syndrome 68 1.216
435
TRP005 Trophoblastic Neoplasm 38 1.216
436
MCN008 Mucinous Cystadenocarcinoma 39 1.216
437
P MLN007 Male Infertility 56 1.216
438
HPT019 Hepatic Encephalopathy 59 1.216
439
CYS014 Cystadenocarcinoma 51 1.216
440
DDN003 Duodenum Adenocarcinoma 38 1.216
441
P CRN026 Corneal Edema 42 1.216
442
MTR010 Mature Teratoma 40 1.216
443
BRS099 Breast Ductal Carcinoma 61 1.216
444
P TCD001 Tic Disorder 49 1.216
445
IDP070 Idiopathic Scoliosis 42 1.216
446
SNL007 Senile Cataract 40 1.216
447
P PLM037 Pulmonary Hypertension 72 1.186
448
CMB007 Combined Immunodeficiency 57 1.186
449
P PLY011 Polycystic Ovary Syndrome 57 1.186
450
AZS001 Azoospermia 45 1.186
451
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.186
452
c ACT134 Acute Liver Failure 59 1.125
453
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.125
454
c ORF040 Orofaciodigital Syndrome Viii 50 1.125
455
CRD132 Cardiac Conduction Defect 60 1.125
456
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.125
457
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.125
458
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 1.125
459
LWG006 Low Grade Glioma 41 1.125
460
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.125
461
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 1.125
462
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.125
463
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 1.125
464
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 1.125
465
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.125
466
LMY002 Leiomyoma 51 1.125
467
P PRK039 Parkinsonism 55 1.125
468
TRM010 Traumatic Brain Injury 51 1.125
469
P GST044 Gastritis 55 1.125
470
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.125
471
MLR004 Malaria 80 1.115
472
MYX005 Myxoid Liposarcoma 65 1.115
473
c TYR012 Tyrosinemia, Type I 61 1.115
474
P HRS035 Hirschsprung Disease 1 66 1.115
475
c PHT009 Photoparoxysmal Response 2 12 1.115
476
c PHT011 Photoparoxysmal Response 3 12 1.115
477
LNG105 Lung Disease, Immunodeficiency, and Chromosome Breakage Syndrome 35 1.115
478
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.115
479
EMB006 Embryonal Testis Carcinoma 31 1.115
480
P TYR004 Tyrosinemia 50 1.115
481
HMG002 Hemoglobinuria 50 1.115
482
P RRH023 Rare Hereditary Hemochromatosis 54 1.115
483
MTH009 Mouth Disease 57 1.115
484
P ART023 Arthropathy 61 1.115
485
P SNS001 Sensorineural Hearing Loss 59 1.115
486
HMS001 Hemosiderosis 48 1.115
487
c MLG084 Malignant Fibrous Histiocytoma 62 1.115
488
DSS009 Disseminated Intravascular Coagulation 57 1.115
489
P SCL048 Sclerosteosis 58 1.115
490
c 46X082 46,xy Sex Reversal 52 1.115
491
P ART005 Arteriovenous Malformation 65 1.115
492
HND002 Hand, Foot and Mouth Disease 50 1.115
493
PRR004 Preretinal Fibrosis 34 1.115
494
ALL014 Allergic Encephalomyelitis 34 1.115
495
PNM013 Pneumococcal Meningitis 43 1.061
496
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 1.061
497
MTB004 Metabolic Acidosis 48 1.061
498
P FML011 Familial Adenomatous Polyposis 71 1.061
499
P TTR001 Tetralogy of Fallot 69 1.061
500
SVR001 Severe Acute Respiratory Syndrome 67 1.061
501
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 1.061
502
P LTR001 Lateral Sclerosis 58 1.061
503
P MNN013 Meningitis 65 1.061
504
c PRS114 Prostate Cancer, Hereditary, 2 33 1.054
505
ADN011 Adenoid Cystic Carcinoma 68 1.039
506
c WLF013 Wolfram Syndrome 1 60 0.996
507
SMT004 Smith-Lemli-Opitz Syndrome 70 0.996
508
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.996
509
P APL001 Aplastic Anemia 73 0.996
510
DSR012 Disordered Steroidogenesis Due to Cytochrome P450 Oxidoreductase Deficiency 39 0.996
511
CRN264 Craniosynostosis with Fibular Aplasia 29 0.996
512
FCT007 Factor Vii Deficiency 64 0.996
513
IGR001 Ige Responsiveness, Atopic 59 0.996
514
CFF002 Coffin-Lowry Syndrome 60 0.996
515
P CRT085 Carotid Intimal Medial Thickness 2 22 0.996
516
P SLV026 Salivary Gland Carcinoma 58 0.996
517
CRV002 Cervix Uteri Carcinoma in Situ 47 0.996
518
PLM001 Pulmonary Tuberculosis 69 0.996
520
EPC002 Epicondylitis 44 0.996
521
P HYP024 Hypoparathyroidism 55 0.996
522
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.996
523
SPT004 Septic Arthritis 58 0.996
524
DNT008 Denture Stomatitis 35 0.996
525
GST023 Gastric Ulcer 52 0.996
526
CYT014 Cytochrome P450 Oxidoreductase Deficiency 34 0.996
527
CRV045 Cervical Intraepithelial Neoplasia 39 0.996
528
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.996
529
PRS129 Prostatic Hyperplasia, Benign 49 0.992
530
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.992
531
P ANP001 Anaplastic Large Cell Lymphoma 61 0.992
532
THR024 Thrombosis 56 0.992
533
P GLY112 Glycosylphosphatidylinositol Biosynthesis Defect 1 33 0.992
534
P FLL037 Follicular Lymphoma 74 0.992
535
P MYP006 Myopia 56 0.992
536
SCR011 Scrapie 39 0.992
537
PST092 Posttransplant Acute Limbic Encephalitis 28 0.992
538
PRS021 Prostatic Adenoma 43 0.992
539
PRS045 Prostatic Hypertrophy 53 0.992
540
ERL001 Early Myoclonic Encephalopathy 62 0.992
541
P HYP055 Hypoplastic Left Heart Syndrome 65 0.992
542
BRN071 Brain Injury 50 0.992
543
HYP642 Hypercoagulability Syndrome Due to Glycosylphosphatidylinositol Deficiency 24 0.992
544
SPS019 Spastic Paraparesis 38 0.919
545
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 0.919
546
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.919
547
c MCP045 Mucopolysaccharidosis, Type Iiic 59 0.919
548
P MLN069 Melanoma, Uveal 61 0.919
549
c PRG021 Paragangliomas 4 37 0.919
550
LMY014 Leiomyoma, Uterine 56 0.919
551
URM002 Uremia 47 0.919
552
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.919
553
P DBT009 Diabetes Mellitus 67 0.919
554
P DDN001 Duodenal Ulcer 53 0.919
555
P ECT006 Ectodermal Dysplasia 63 0.919
556
GST033 Gestational Diabetes 61 0.919
557
P HYD006 Hydrocephalus 61 0.919
558
P HYP040 Hypospadias 51 0.919
559
JPN002 Japanese Encephalitis 61 0.919
560
P EPD016 Epidermolysis Bullosa 53 0.919
561
c MCP001 Mucopolysaccharidosis Iii 69 0.919
562
PLC006 Placental Choriocarcinoma 38 0.919
563
PLC007 Placental Abruption 47 0.919
564
P ENC004 Encephalitis 61 0.919
565
SRF006 Surfactant Dysfunction 33 0.919
566
TTR011 Tetraploidy 43 0.840
567
TRT005 Teratoma with Malignant Transformation 16 0.840
568
FTL006 Fetal Alcohol Spectrum Disorder 43 0.840
569
P FTL001 Fetal Alcohol Syndrome 55 0.840
570
ULN003 Ulnar-Mammary Syndrome 56 0.840
571
XRD027 Xeroderma Pigmentosum Group E 39 0.840
572
FML008 Familial Retinoblastoma 50 0.840
573
BNM001 Bone Marrow Cancer 46 0.840
574
P ACN011 Acne 57 0.840
575
STR103 Streptococcus Pneumonia 47 0.840
576
PRT014 Protein S Deficiency 41 0.840
577
c MLG081 Malignant Teratoma 38 0.840
578
MSL001 Measles 61 0.840
579
c SPN296 Spinocerebellar Ataxia 17 47 0.839
580
ANX010 Anxiety 70 0.839
581
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.839
582
END062 Endometrial Hyperplasia 48 0.839
583
ILT001 Ileitis 48 0.839
584
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.839
585
c EPD076 Epidermolysis Bullosa Dystrophica, Autosomal Recessive 52 0.839
586
c OST124 Osteogenesis Imperfecta, Type V 43 0.839
587
ASB001 Asbestosis 47 0.839
588
P RCS002 Recessive Dystrophic Epidermolysis Bullosa 62 0.839
589
ASB003 Asbestos Intoxication 32 0.839
590
HDR004 Hidradenoma 37 0.839
591
P SYR003 Syringoma 38 0.839
592
PLY012 Polyhydramnios 46 0.839
593
MTC212 Mitchell Syndrome 26 0.839
594
XRP001 Xerophthalmia 41 0.839
595
c DLT002 Dilated Cardiomyopathy 78 0.839
596
MYM001 Myoma 54 0.839
597
ORC001 Orchitis 44 0.839
598
MCR013 Microphthalmia 60 0.839
599
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.839
600
CHR076 Choriocarcinoma of the Testis 33 0.839
601
MXD005 Mixed Connective Tissue Disease 57 0.839
602
KRT001 Keratoconjunctivitis Sicca 50 0.839
603
GRM010 Germ Cells Tumors 33 0.839
604
HYP056 Hypoglycemia 65 0.839
605
P MTC069 Mitochondrial Disorders 57 0.839
606
P SCK005 Sickle Cell Disease 56 0.839
607
ANT039 Antisynthetase Syndrome 55 0.828
608
PRR019 Perioral Myoclonia with Absences 27 0.750
609
ATH010 Athyreosis 34 0.750
610
FBR012 Fabry Disease 70 0.750
611
ART002 Arts Syndrome 66 0.750
612
HYD038 Hydrops Fetalis, Nonimmune 59 0.750
613
P BRG001 Brugada Syndrome 69 0.750
614
c CNG006 Congenital Hypothyroidism 63 0.750
615
KRT019 Keratitis, Hereditary 66 0.750
616
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.750
617
P MJR001 Major Depressive Disorder 68 0.750
618
c LNG109 Lung Cancer Susceptibility 1 26 0.750
619
c HYD064 Hydrocephalus, Congenital, 1 51 0.750
620
P SRC025 Sarcoidosis 1 71 0.750
621
MYL057 Myelopathy, Htlv-1-Associated 38 0.750
622
DSS032 Disease by Infectious Agent 55 0.750
623
CLR109 Colorectal Adenocarcinoma 50 0.750
624
AML029 Ameloblastoma 47 0.750
625
P HML001 Hemolytic-Uremic Syndrome 52 0.750
626
ACT250 Acute Megakaryocytic Leukemia 60 0.750
627
P MYP004 Myopathy 67 0.750
628
BLP005 Blepharitis 50 0.750
629
NNT008 Neonatal Abstinence Syndrome 40 0.750
630
SYN036 Syncope 45 0.750
631
MNT002 Mental Depression 57 0.750
632
CRV038 Cervical Squamous Cell Carcinoma 58 0.750
633
c VRL007 Viral Encephalitis 50 0.750
634
EXT034 Extrinsic Allergic Alveolitis 57 0.750
635
SWN001 Swine Influenza 46 0.750
636
P UVT001 Uveitis 57 0.750
637
CRT013 Carotid Stenosis 51 0.750
638
P HYP086 Hypothyroidism 69 0.750
639
P CRN037 Craniosynostosis 68 0.750
640
P CRD119 Cardiac Arrest 67 0.750
641
ING001 Inguinal Hernia 59 0.750
642
KRT002 Keratomalacia 55 0.750
643
GST029 Gastric Cardia Adenocarcinoma 29 0.750
644
P CNJ013 Conjunctivitis 66 0.750
645
P SLP005 Sleep Disorder 61 0.750
646
P MLT074 Multiple Endocrine Neoplasia 59 0.750
647
TRP002 Tropical Spastic Paraparesis 49 0.750
648
P HRD011 Hereditary Spherocytosis 64 0.750
649
P DRR001 Diarrhea 55 0.750
650
HYP080 Hypogonadism 50 0.750
651
P RCT021 Rectum Cancer 54 0.750
652
P MYC008 Myocarditis 59 0.750
653
HRP004 Herpes Zoster 61 0.750
654
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 38 0.750
655
DPR016 Depression 65 0.750
657
c HMC039 Hemochromatosis, Type 1 73 0.650
658
STR077 Streptococcal Toxic-Shock Syndrome 35 0.650
659
ACT186 Acute Megakaryoblastic Leukemia in Down Syndrome 15 0.650
660
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.650
661
c PLN017 Peeling Skin Syndrome 1 39 0.650
662
P TST021 Testicular Germ Cell Tumor 61 0.650
663
SQM013 Squamous Cell Carcinoma, Head and Neck 73 0.650
664
SRC027 Sarcoma, Synovial 58 0.650
665
TNG002 Tangier Disease 64 0.650
666
APL002 Aplasia of Lacrimal and Salivary Glands 56 0.650
667
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.650
668
P ZNC008 Zinc Finger Protein 1 23 0.650
669
c MGR028 Migraine with or Without Aura 1 64 0.650
670
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 53 0.650
672
FCT032 Factor Xiii, a Subunit, Deficiency of 27 0.650
673
ASP038 Aspirin-Induced Respiratory Disease 16 0.650
674
PTZ001 Peutz-Jeghers Syndrome 70 0.650
675
c SPN293 Spinocerebellar Ataxia 12 45 0.650
676
c THR048 Thrombocytopenia 4 28 0.650
677
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.650
678
ACH004 Achondroplasia 66 0.650
679
P ANG001 Angelman Syndrome 65 0.650
680
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.650
681
ACT165 Acute Megakaryoblastic Leukemia Without Down Syndrome 15 0.650
682
AVN001 Avian Influenza 61 0.650
683
P THR014 Thrombocytopenia 66 0.650
684
P PTT006 Pituitary Adenoma 55 0.650
685
P LVR013 Liver Disease 69 0.650
686
c VRL010 Viral Hepatitis 53 0.650
687
P MST009 Mastocytosis 64 0.650
688
HRT012 Heart Valve Disease 53 0.650
689
ADR005 Adrenal Carcinoma 62 0.650
690
P PNC025 Panic Disorder 52 0.650
691
P RTN016 Retinal Degeneration 52 0.650
692
CLR003 Clear Cell Adenocarcinoma 50 0.650
693
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.650
694
P DNG005 Dengue Virus 56 0.650
695
P HYP061 Hypertrophic Cardiomyopathy 69 0.650
696
OLG003 Oligohydramnios 51 0.650
697
CNS004 Constipation 56 0.650
698
DNT012 Dental Caries 53 0.650
699
LYD001 Leydig Cell Tumor 45 0.650
700
P HYP069 Hyperparathyroidism 62 0.650
701
RTN020 Retinal Vascular Disease 46 0.650
702
FCT005 Factor Xiii Deficiency 55 0.650
703
THR004 Thrombocytosis 53 0.650
704
P TBR001 Tuberous Sclerosis 69 0.650
705
MST005 Mastitis 53 0.650
706
P CHN059 Chondrocalcinosis 52 0.650
707
BRN024 Bronchitis 67 0.650
708
P RHN004 Rhinitis 57 0.650
709
TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.650
710
PLC008 Placenta Disease 49 0.650
711
c SPR009 Sporadic Breast Cancer 42 0.650
712
c ACT071 Acute Kidney Failure 60 0.650
713
LYS002 Lysosomal Storage Disease 51 0.650
714
ANS011 Anus Cancer 57 0.650
715
P PRP029 Porphyria 60 0.650
716
P OST001 Osteopetrosis 71 0.650
717
NRN004 Neuroendocrine Tumor 59 0.650
718
P ENC018 Encephalopathy 62 0.650
719
c ICH014 Ichthyosis Lamellar 1 32 0.650
720
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.650
721
P KRB001 Krabbe Disease 69 0.530
722
SKL017 Skeletal Dysplasias 41 0.530
723
GRW007 Growth Hormone Deficiency 46 0.530
724
ADR022 Adrenomyeloneuropathy 39 0.530
725
MLG164 Malignant Epithelial Tumor of Ovary 24 0.530
726
c NRF023 Neurofibromatosis, Type Ii 71 0.530
727
FRN006 Frontotemporal Dementia 68 0.530
728
P MYM013 Moyamoya Disease 1 59 0.530
729
P MYS003 Myasthenia Gravis 68 0.530
730
ADR007 Adrenoleukodystrophy 73 0.530
731
P WSK001 Wiskott-Aldrich Syndrome 72 0.530
732
P MYR002 Mayer-Rokitansky-Kuster-Hauser Syndrome 60 0.530
733
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.530
734
P RTN008 Retinitis Pigmentosa 80 0.530
735
ALL003 Allergic Rhinitis 67 0.530
736
c DFN117 Deafness, Autosomal Dominant 15 38 0.530
737
P LFR001 Li-Fraumeni Syndrome 73 0.530
738
P TRC072 Treacher Collins Syndrome 1 62 0.530
739
c MYT021 Myotonic Dystrophy 1 68 0.530
740
BLD141 Blood Group--Kell System 20 0.530
741
P THN009 Thanatophoric Dysplasia, Type I 63 0.530
742
MCC012 Mccune-Albright Syndrome 70 0.530
743
c FNC027 Fanconi Anemia, Complementation Group a 81 0.530
744
GRN037 Granulomatosis with Polyangiitis 64 0.530
745
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.530
746
ADR016 Adrenal Cortical Carcinoma 62 0.530
747
P GST047 Gastrointestinal Neuroendocrine Tumor 36 0.530
748
DFF005 Diffuse Large B-Cell Lymphoma 54 0.530
749
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 53 0.530
750
c CRD150 Cardiomyopathy, Familial Hypertrophic, 18 26 0.530
751
DFC004 Deficiency Anemia 74 0.530
752
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 0.530
753
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.530
754
P SML001 Small Cell Carcinoma 52 0.530
755
CLR108 Colorectal Adenoma 64 0.530
756
BTT018 Beta-Thalassemia Intermedia 31 0.530
757
KRN002 Kearns-Sayre Syndrome 63 0.530
758
CRP032 Corpus Callosum, Agenesis of 49 0.530
759
CST001 Costello Syndrome 68 0.530
760
P FRD001 Friedreich Ataxia 61 0.530
761
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.530
762
OST024 Osteoporosis-Pseudoglioma Syndrome 60 0.530
763
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.530
764
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.530
765
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.530
766
c INF093 Inflammatory Bowel Disease 14 35 0.530
767
SCR035 Sacral Agenesis with Vertebral Anomalies 38 0.530
768
IMM066 Immunodeficiency 9 39 0.530
769
c TBR026 Tuberous Sclerosis 2 71 0.530
770
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.530
771
c SYS040 Systemic Lupus Erythematosus 10 22 0.530
772
MSS001 Masa Syndrome 60 0.530
774
ADR054 Adrenocortical Carcinoma, Hereditary 47 0.530
775
c LFR007 Li-Fraumeni Syndrome 2 46 0.530
776
ENT011 Enterocolitis 55 0.530
777
GYR004 Gyrate Atrophy of Choroid and Retina 58 0.530
778
P IMR002 Imerslund-Grasbeck Syndrome 1 42 0.530
779
PRP082 Porphyria, Congenital Erythropoietic 56 0.530
780
c TRC092 Trichorhinophalangeal Syndrome, Type I 54 0.530
781
TBC004 Tobacco Addiction 63 0.530
782
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.530
783
HYP351 Hypertrichosis Universalis Congenita, Ambras Type 35 0.530
784
P HYP750 Hypertriglyceridemia, Familial 62 0.530
785
IMM165 Immunoglobulin Switch Sequences 14 0.530
786
P CRC039 Coarctation of Aorta 46 0.530
787
THY111 Thyroid Carcinoma, Familial Medullary 67 0.530
788
c SPN294 Spinocerebellar Ataxia 1 53 0.530
789
STT041 Stuttering 52 0.530
790
P LKD001 Leukodystrophy 59 0.530
791
CRH001 Crohn's Disease 80 0.530
792
P ZLL001 Zellweger Syndrome 65 0.530
793
c ACT075 Acute Myocardial Infarction 56 0.530
794
BRN004 Brain Edema 54 0.530
795
OVR012 Ovarian Serous Cystadenocarcinoma 55 0.530
796
P HYP077 Hypertrichosis 46 0.530
797
DYS017 Dysgerminoma of Ovary 37 0.530
798
P DYS154 Dystonia 64 0.530
799
CRC021 Carcinosarcoma 64 0.530
800
SKN019 Skin Melanoma 71 0.530
801
P HMC002 Homocystinuria 53 0.530
802
OCL006 Ocular Hypertension 53 0.530
803
PRP007 Priapism 47 0.530
804
GSG001 Gas Gangrene 52 0.530
805
ALL006 Allergic Asthma 56 0.530
806
P ATR005 Atrophic Gastritis 50 0.530
807
P MVM001 Movement Disease 61 0.530
808
TST020 Testis Seminoma 28 0.530
809
HYD048 Hydrocephalus with Stenosis of the Aqueduct of Sylvius 38 0.530
810
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 32 0.530
811
ADR004 Adrenal Cortical Adenocarcinoma 38 0.530
812
IGG001 Iga Glomerulonephritis 50 0.530
813
DYS018 Dysostosis 44 0.530
814
GRM004 Germinoma 44 0.530
815
LNG031 Lung Benign Neoplasm 51 0.530
816
THL004 Theileriasis 31 0.530
817
THY125 Thyroid Gland Medullary Carcinoma 48 0.530
818
THY123 Thyroid Gland Follicular Carcinoma 55 0.530
819
P CNT037 Central Nervous System Germinoma 32 0.530
820
DYS101 Dysgerminoma 44 0.530
821
PRP016 Paraplegia 52 0.530
822
HMT002 Hematologic Cancer 61 0.530
823
P CCK001 Cockayne Syndrome 68 0.530
824
ACC008 Accelerated Tumor Formation 20 0.530
825
DNG001 Dengue Shock Syndrome 40 0.530
826
RTN003 Retinal Ischemia 49 0.530
827
VRC001 Varicocele 48 0.530
828
GTR002 Goiter 53 0.530
829
P HMN010 Hemangioma 62 0.530
830
CLN044 Colon Adenoma 44 0.530
831
c HPT015 Hepatitis D 49 0.530
832
ISL003 Isolated Growth Hormone Deficiency 57 0.530
833
P MCR010 Microcephaly 60 0.530
834
HYP006 Hypertensive Heart Disease 49 0.530
835
ADR008 Adrenal Adenoma 55 0.530
836
P CYS039 Cystic Kidney Disease 53 0.530
837
NWC001 Newcastle Disease 47 0.530
838
OLG001 Oligospermia 45 0.530
839
HMN048 Human Papillomavirus Infectious Disease 46 0.530
840
P EHL001 Ehlers-Danlos Syndrome 58 0.530
841
CHR073 Choreatic Disease 54 0.530
842
BRN031 Brain Germinoma 31 0.530
843
NRF007 Neurofibroma 64 0.530
844
SPL018 Splenomegaly 49 0.530
846
CYT019 Cytogenetically Normal Acute Myeloid Leukemia 30 0.530
847
CRC006 Carcinoid Syndrome 55 0.530
848
P GNG009 Gangliosidosis 44 0.530
849
PRN019 Perinatal Necrotizing Enterocolitis 60 0.530
850
SML031 Small Cell Carcinoma of the Bladder 46 0.523
851
IRN008 Iron Overload in Africa 51 0.523
852
c CHL136 Cholestasis, Progressive Familial Intrahepatic, 2 57 0.523
853
HPT079 Hepatoid Adenocarcinoma 39 0.523
854
c PRS097 Prostate Cancer, Hereditary, 1 39 0.523
855
RJS001 Ruijs-Aalfs Syndrome 47 0.523
856
c PRS070 Prostate Cancer, Hereditary, 12 22 0.523
857
c PRS071 Prostate Cancer, Hereditary, 13 25 0.523
858
c PRS117 Prostate Cancer, Hereditary, 11 24 0.523
859
GST103 Gastric Cancer, Hereditary Diffuse 68 0.523
860
PDT042 Pediatric Hepatocellular Carcinoma 49 0.523
861
c PRG047 Progressive Familial Intrahepatic Cholestasis 64 0.523
862
ADL096 Adult Hepatocellular Carcinoma 60 0.523
863
FBR086 Fibrolamellar Carcinoma 59 0.523
864
HPT011 Hepatocellular Clear Cell Carcinoma 46 0.523
865
PRS015 Prostate Signet Ring Cell Adenocarcinoma 25 0.523
866
PTY007 Pityriasis Rotunda 26 0.523
867
c TYP008 Type 1 Diabetes Mellitus 70 0.375
868
c GLC111 Galactosemia Ii 50 0.375
869
VLV044 Vulvar Intraepithelial Neoplasia 43 0.375
870
PRT086 Partial Hydatidiform Mole 23 0.375
871
CLR137 Clear Cell Adenocarcinoma of the Ovary 31 0.375
872
ERY002 Erythema Infectiosum 35 0.375
873
ACT248 Acute Monoblastic/monocytic Leukemia 26 0.375
874
CYN003 Cyanide Poisoning 22 0.375
875
c JVN038 Juvenile Myasthenia Gravis 30 0.375
876
c SPS023 Spastic Paraplegia 13 21 0.375
877
P SCH017 Schindler Disease 37 0.375
878
PFF001 Pfeiffer Syndrome 77 0.375
879
P ALP061 Alopecia, Androgenetic, 1 49 0.375
880
c ART115 Aortic Valve Disease 1 74 0.375
881
HRL003 Hurler Syndrome 66 0.375
882
RTC012 Reticuloendotheliosis, X-Linked 35 0.375
883
3HY007 3-Hydroxy-3-Methylglutaryl-Coa Lyase Deficiency 51 0.375
884
c MCP047 Mucopolysaccharidosis, Type Iva 62 0.375
885
VSD002 Vas Deferens, Congenital Bilateral Aplasia of 49 0.375
886
c THY107 Thymoma, Familial 42 0.375
887
MCL009 Mcleod Syndrome 46 0.375
888
SJG002 Sjogren-Larsson Syndrome 54 0.375
889
SDD001 Sudden Infant Death Syndrome 60 0.375
890
P LPR021 Leprosy 3 71 0.375
891
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 59 0.375
892
P RTH006 Rothmund-Thomson Syndrome, Type 2 67 0.375
893
SND001 Sandhoff Disease 66 0.375
894
c PRX045 Peroxisome Biogenesis Disorder 1b 62 0.375
895
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.375
896
c TLN011 Telangiectasia, Hereditary Hemorrhagic, Type 2 45 0.375
897
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 0.375
898
BDD001 Budd-Chiari Syndrome 62 0.375
899
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.375
900
XNT003 Xanthomatosis 49 0.375
901
INT146 Intervertebral Disc Disease 63 0.375
902
OVR029 Ovarian Hyperstimulation Syndrome 63 0.375
903
P KLZ004 Kala-Azar 1 41 0.375
904
c LKM070 Leukemia, Acute Monocytic 56 0.375
905
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.375
906
OBS002 Obsessive-Compulsive Disorder 68 0.375
907
PRL019 Prolidase Deficiency 50 0.375
908
PHS027 Phosphoglycoprotein 1 15 0.375
909
CLF027 Cleft Palate, Isolated 64 0.375
910
P CNR004 Cone-Rod Dystrophy 2 74 0.375
911
c EXD008 Exudative Vitreoretinopathy 1 71 0.375
912
BLD144 Blood Group System, Landsteiner-Wiener 13 0.375
913
c EPP017 Epiphyseal Dysplasia, Multiple, 1 46 0.375
914
VLV047 Volvulus of Midgut 52 0.375
915
c OTS005 Otosclerosis 1 25 0.375
916
OTT002 Otitis Media 71 0.375
917
c PGT007 Paget Disease of Bone 3 38 0.375
918
ASP002 Aspartylglucosaminuria 58 0.375
919
P VNB005 Van Buchem Disease 58 0.375
920
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.375
921
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.375
922
ANG054 Angina Pectoris 66 0.375
923
P OCL002 Oculocutaneous Albinism 59 0.375
924
P SLP006 Sleep Apnea 69 0.375
925
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.375
926
BTN004 Biotin Deficiency 45 0.375
927
ATR057 Atrioventricular Block 54 0.375
928
PRX005 Peroxisomal Biogenesis Disorder 33 0.375
929
HYP458 Hyper Ige Syndrome 60 0.375
930
CHL158 Childhood Acute Megakaryoblastic Leukemia 24 0.375
931
NSL029 Nasal Type Extranodal Nk/t-Cell Lymphoma 40 0.375
932
DGN006 Digenic Disease 24 0.375
933
CHL155 Childhood Spinal Muscular Atrophy 30 0.375
934
RSP021 Respiratory Allergy 41 0.375
935
CRH005 Crohn's Colitis 53 0.375
936
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.375
937
MLD018 Mild Cognitive Impairment 48 0.375
938
TQP001 Taqi Polymorphism 29 0.375
939
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 0.375
940
FRB001 Farber Lipogranulomatosis 58 0.375
941
P BRN019 Bernard-Soulier Syndrome 61 0.375
942
c GLY011 Glycogen Storage Disease Vii 54 0.375
943
P TYS001 Tay-Sachs Disease 69 0.375
944
c OST164 Osteoporosis, Juvenile 54 0.375
945
ODN023 Odontochondrodysplasia 67 0.375
946
CNT105 Central Core Disease of Muscle 59 0.375
947
VRG001 Variegate Porphyria 56 0.375
948
c SPH013 Spherocytosis, Type 1 42 0.375
949