Search results for lox

934 hits were found for lox

# Family MCID Name MIFTS Score
1
c ART134 Aortic Aneurysm, Familial Thoracic 10 25 37.324
2
c ART118 Aortic Aneurysm, Familial Thoracic 9 29 30.952
3
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 65 26.305
4
P CLR023 Colorectal Cancer 100 24.783
5
P BRS047 Breast Cancer 98 22.647
6
P PNC035 Pancreatic Cancer 86 20.962
7
P PRS040 Prostate Cancer 95 19.358
8
P OVR042 Ovarian Cancer 88 18.427
9
P LNG032 Lung Cancer 98 17.620
10
ANR040 Aneurysm 61 17.171
11
ART016 Aortic Aneurysm 68 16.305
12
P HRT032 Heart Disease 81 14.447
13
CNN005 Connective Tissue Disease 67 14.441
14
P KRT007 Keratoconus 50 13.858
15
CLN015 Colon Adenocarcinoma 65 13.574
16
SKN016 Skin Disease 63 13.354
17
RNL114 Renal Cell Carcinoma, Nonpapillary 80 13.253
18
INT030 Intracranial Aneurysm 55 13.142
19
ART074 Aortic Dissection 53 12.924
20
MRF001 Marfan Syndrome 76 12.884
21
ORL004 Oral Submucous Fibrosis 56 12.706
22
c DLT002 Dilated Cardiomyopathy 78 12.225
23
P OST002 Osteoporosis 76 12.212
24
P CTS001 Cutis Laxa 65 12.212
25
WLS001 Wilson Disease 70 11.993
26
ART017 Aortic Disease 49 11.920
27
P PLV020 Pelvic Organ Prolapse 58 11.665
28
ATH013 Atherosclerosis Susceptibility 63 11.555
29
OCC006 Occipital Horn Syndrome 54 11.417
30
RTN017 Retinal Detachment 60 11.389
31
P EYD002 Eye Disease 57 11.346
32
c ART028 Aortic Aneurysm, Familial Thoracic 4 54 11.227
33
P ART021 Arteriosclerosis 54 11.120
34
MNK001 Menkes Disease 64 11.020
35
c AMY091 Amyotrophic Lateral Sclerosis 1 88 10.985
36
ANV001 Anovulation 47 10.945
37
BRN028 Brain Cancer 74 10.717
38
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 10.681
39
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 10.576
40
HYP266 Hypoxia 57 10.513
41
c HYP595 Hypertension, Essential 85 9.971
42
EXF001 Exfoliation Syndrome 56 9.886
43
CST001 Costello Syndrome 68 9.686
44
P SCL018 Scoliosis 57 9.686
45
PLM134 Pulmonary Fibrosis, Idiopathic 76 9.643
46
ING001 Inguinal Hernia 59 9.395
47
c ART115 Aortic Valve Disease 1 74 8.998
48
P HMC002 Homocystinuria 53 8.998
49
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 8.754
50
HRT036 Heritable Thoracic Aortic Disease 34 8.595
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 8.366
52
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 8.140
53
BRT054 Brittle Bone Disorder 74 7.578
54
c HYP836 Hypercholesterolemia, Familial, 1 73 7.350
55
c PRC016 Pre-Eclampsia 65 7.189
56
DSS008 Disease of Mental Health 74 6.924
57
ISC004 Ischemia 61 6.898
58
LPD008 Lipid Metabolism Disorder 62 6.872
59
P RTN008 Retinitis Pigmentosa 80 6.760
60
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 6.643
61
c RTN052 Retinitis Pigmentosa 23 37 6.362
62
KGM001 Kagami-Ogata Syndrome 53 6.362
63
BLD045 Bladder Diverticulum 39 6.362
64
c ALZ059 Alzheimer Disease 13 26 6.362
65
c EHL083 Ehlers-Danlos Syndrome, Spondylodysplastic Type, 3 47 6.362
66
c CRS017 Crisponi/cold-Induced Sweating Syndrome 2 44 6.362
67
KFM001 Kaufman Oculocerebrofacial Syndrome 55 6.362
68
P BRC015 Bruck Syndrome 48 6.362
69
PHC002 Phacogenic Glaucoma 25 6.362
70
HPT011 Hepatocellular Clear Cell Carcinoma 46 6.362
71
URT023 Ureteric Orifice Cancer 26 6.362
72
OST012 Osteoarthritis 77 6.042
73
c MCR115 Microvascular Complications of Diabetes 5 65 5.925
74
CRB004 Cerebral Artery Occlusion 45 5.890
75
P GST053 Gastric Cancer 83 5.865
76
P CRD246 Cardiovascular System Disease 56 5.827
77
P VSC007 Vascular Disease 63 5.826
78
KRT019 Keratitis, Hereditary 66 5.476
79
c PCH010 Pachyonychia Congenita 3 43 5.363
80
P PLM036 Pulmonary Fibrosis 66 5.157
81
P ICH004 Ichthyosis 56 4.971
82
P PLM037 Pulmonary Hypertension 72 4.950
83
P ADN016 Adenocarcinoma 63 4.933
84
P NRB001 Neuroblastoma 66 4.741
85
PRT036 Peritonitis 65 4.720
86
P MYC007 Myocardial Infarction 70 4.697
87
SQM006 Squamous Cell Carcinoma 60 4.654
88
PNC041 Pancreatic Ductal Adenocarcinoma 51 4.496
89
GLB002 Glioblastoma 67 4.474
90
ADN018 Adenoma 59 4.410
91
P FML011 Familial Adenomatous Polyposis 71 4.379
92
LPP008 Lipoprotein Quantitative Trait Locus 65 4.370
93
OST159 Osteogenic Sarcoma 66 4.359
94
P HPT023 Hepatocellular Carcinoma 96 4.256
95
ART140 Arteries, Anomalies of 53 4.239
96
FNG016 Fungal Keratitis 39 4.158
97
FTT001 Fatty Liver Disease 62 4.060
98
THY020 Thyroid Hyalinizing Trabecular Adenoma 20 4.023
99
ORL015 Oral Squamous Cell Carcinoma 43 3.947
100
c SML038 Small Cell Cancer of the Lung 69 3.925
101
P LNG064 Lung Cancer Susceptibility 3 70 3.901
102
HYP066 Hyperglycemia 61 3.893
103
P ART022 Arthritis 71 3.888
104
STR067 Stroke, Ischemic 80 3.834
105
c MCR130 Microvascular Complications of Diabetes 6 41 3.779
106
c MCR120 Microvascular Complications of Diabetes 7 47 3.779
107
c MCR113 Microvascular Complications of Diabetes 3 52 3.779
108
c MCR133 Microvascular Complications of Diabetes 4 41 3.779
109
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.756
110
ESP021 Esophageal Cancer 83 3.657
111
RTN020 Retinal Vascular Disease 46 3.599
112
CHL123 Chlamydia 58 3.556
113
CHL147 Chlamydia Pneumonia 47 3.528
114
HMC014 Homocysteinemia 52 3.462
115
P DBT009 Diabetes Mellitus 67 3.458
116
c SCN036 Secondary Progressive Multiple Sclerosis 55 3.442
117
P RHM011 Rheumatoid Arthritis 82 3.421
118
P MCR129 Microvascular Complications of Diabetes 1 68 3.382
119
c MCR112 Microvascular Complications of Diabetes 2 42 3.382
120
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 3.372
121
P BLD134 Bladder Cancer 79 3.352
122
BRN004 Brain Edema 54 3.352
123
GLL048 Glial Tumor 52 3.281
124
GLM045 Glioma 63 3.281
125
c SCL052 Scleroderma, Familial Progressive 61 3.254
126
P PLY011 Polycystic Ovary Syndrome 57 3.252
127
P MNC007 Monocytic Leukemia 47 3.244
128
ANG054 Angina Pectoris 66 3.231
129
SPP011 Suppression of Tumorigenicity 12 61 3.223
130
CLT003 Colitis 63 3.164
131
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.164
132
P RHN004 Rhinitis 57 3.163
133
CNG034 Congestive Heart Failure 69 3.158
134
P ECL001 Eclampsia 52 3.130
135
P CRN300 Coronary Heart Disease 1 73 3.126
136
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.103
137
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.103
138
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.103
139
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.103
140
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.103
141
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.103
142
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.103
143
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.103
144
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.103
145
HLX001 Helix Syndrome 48 3.103
146
THY029 Thyroid Carcinoma 51 3.097
147
P PRD008 Periodontitis 64 3.090
148
IMP005 Impotence 52 3.063
149
P NSP012 Nasopharyngeal Carcinoma 61 3.029
150
P RTN024 Retinoblastoma 73 3.010
151
DRM006 Dermatitis 62 3.010
152
PNC129 Pancreatic Adenocarcinoma 65 2.977
153
LNG099 Lung Disease 62 2.975
154
PRS045 Prostatic Hypertrophy 53 2.945
155
P ALZ034 Alzheimer Disease 87 2.912
156
c HPT016 Hepatitis B 62 2.886
157
P INF032 Infertility 57 2.879
158
BRN071 Brain Injury 50 2.879
159
PLY150 Polykaryocytosis Inducer 29 2.876
160
SVR004 Severe Combined Immunodeficiency 72 2.866
161
PRS129 Prostatic Hyperplasia, Benign 49 2.845
162
RNL077 Renal Fibrosis 46 2.845
163
PRS021 Prostatic Adenoma 43 2.845
164
THR024 Thrombosis 56 2.811
165
OVR094 Ovarian Epithelial Cancer 39 2.811
166
CLR108 Colorectal Adenoma 64 2.754
167
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.754
168
P MLN008 Melanoma 76 2.754
169
P DRM053 Dermatitis, Atopic 65 2.740
170
P SLP006 Sleep Apnea 69 2.740
171
48X005 48,xyyy 39 2.740
172
P HYP750 Hypertriglyceridemia, Familial 62 2.733
173
GT001 Gout 64 2.733
174
P LVR013 Liver Disease 69 2.725
175
P GLM040 Glioma Susceptibility 1 71 2.704
176
MLG169 Malignant Astrocytoma 57 2.704
177
P PLM034 Pulmonary Emphysema 58 2.700
178
P PSR002 Psoriasis 63 2.693
179
P INF037 Inflammatory Bowel Disease 53 2.668
180
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.637
181
P MSC005 Muscular Dystrophy 67 2.610
182
NNL006 Non-Alcoholic Steatohepatitis 54 2.606
183
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 2.593
184
END086 End Stage Renal Disease 52 2.593
185
CRV035 Cervical Cancer 73 2.592
186
ORL011 Oral Cancer 60 2.554
187
P LKM002 Leukemia 67 2.523
188
ALL003 Allergic Rhinitis 67 2.515
189
ULC004 Ulcerative Colitis 74 2.515
190
P BND020 Bone Disease 59 2.515
191
c LKM061 Leukemia, Acute Myeloid 83 2.482
192
PST011 Pustulosis of Palm and Sole 52 2.478
193
P MYC008 Myocarditis 59 2.474
194
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.433
195
c ATR087 Atrial Standstill 1 74 2.433
196
PRT251 Proteinuria, Chronic Benign 57 2.418
197
CYT002 Cytokine Deficiency 43 2.418
198
P BRS044 Breast Adenocarcinoma 58 2.392
199
BNR002 Bone Resorption Disease 47 2.385
200
MSC157 Muscular Dystrophy, Duchenne Type 79 2.384
201
P BCL017 B-Cell Lymphoma 59 2.349
202
INS001 Insulinoma 59 2.349
203
P CRC039 Coarctation of Aorta 46 2.336
204
P LKM062 Leukemia, Acute Lymphoblastic 69 2.317
205
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.305
206
BCT022 Bacterial Infectious Disease 56 2.305
207
VCC001 Vaccinia 47 2.305
208
P RTN016 Retinal Degeneration 52 2.305
209
MLG079 Malignant Pleural Mesothelioma 42 2.305
210
P BNG032 Benign Mesothelioma 53 2.305
211
AGN016 Aging 54 2.249
212
P PLY014 Polycystic Kidney Disease 69 2.243
213
DGN001 Degenerative Disc Disease 49 2.214
214
P NPH012 Nephrotic Syndrome 60 2.214
215
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.213
216
MYL005 Myelofibrosis 71 2.213
217
ALL006 Allergic Asthma 56 2.213
218
SCH014 Schistosomiasis 56 2.213
219
c LKM070 Leukemia, Acute Monocytic 56 2.179
220
P HNT016 Huntington Disease 73 2.179
221
P HPT021 Hepatitis 69 2.179
222
ACT200 Acute Monoblastic Leukemia 41 2.179
223
c CHR684 Chronic Kidney Disease 69 2.177
224
P SYS005 Systemic Scleroderma 74 2.177
225
ATM095 Autoimmune Disease 61 2.166
226
HLC007 Helicobacter Pylori Infection 67 2.166
227
LVR012 Liver Cirrhosis 63 2.166
228
LWF001 Low-Flow Priapism 16 2.117
229
PRP007 Priapism 47 2.117
230
CHL065 Cholangiocarcinoma 58 2.103
231
INT079 Intrahepatic Cholangiocarcinoma 51 2.103
232
AML001 Amelanotic Melanoma 37 2.067
233
MYL031 Myeloproliferative Neoplasm 66 2.067
234
c TYP009 Type 2 Diabetes Mellitus 92 2.065
236
PLY100 Polyploidy 36 2.027
237
CLR030 Clear Cell Renal Cell Carcinoma 54 2.027
238
BRN056 Bronchopulmonary Dysplasia 56 2.027
239
P PNM007 Pneumonia 67 2.014
240
INT007 Intermediate Coronary Syndrome 54 2.003
241
P NRP001 Neuropathy 60 2.003
242
FML035 Familial Hyperlipidemia 55 2.003
243
P ENC018 Encephalopathy 62 2.003
244
P LTR001 Lateral Sclerosis 58 1.987
245
P TCD001 Tic Disorder 49 1.987
246
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.960
247
P AST005 Asthma 76 1.960
248
MLR004 Malaria 80 1.960
249
ANP005 Anaplastic Astrocytoma 57 1.960
250
PRV004 Periventricular Leukomalacia 52 1.947
251
SRC014 Sarcoma 65 1.947
252
BRN024 Bronchitis 67 1.947
253
P RCT021 Rectum Cancer 54 1.947
254
CRB090 Cerebral Hypoxia 42 1.938
255
P MYL006 Myeloid Leukemia 61 1.906
256
P END044 Endometriosis 62 1.906
257
c KRT029 Keratoconus 1 31 1.904
258
P SCK005 Sickle Cell Disease 56 1.904
259
ANX004 Anoxia 40 1.870
260
DBT010 Diabetic Neuropathy 54 1.870
261
LYM133 Lymphoma, Hodgkin, Classic 74 1.864
262
P INS002 in Situ Carcinoma 53 1.864
263
MLD018 Mild Cognitive Impairment 48 1.846
264
DSS032 Disease by Infectious Agent 55 1.846
265
P HRP006 Herpes Simplex 65 1.846
266
CHR074 Choriocarcinoma 46 1.846
267
c ATS007 Autism Spectrum Disorder 72 1.822
268
CRC021 Carcinosarcoma 64 1.822
269
SPN035 Spindle Cell Sarcoma 54 1.822
270
P THR014 Thrombocytopenia 66 1.797
271
EPD002 Epidermolytic Hyperkeratosis 56 1.784
272
P LYS001 Loeys-Dietz Syndrome 65 1.784
273
47X002 47,xyy 48 1.784
274
P GST044 Gastritis 55 1.784
275
GST040 Gastric Adenocarcinoma 67 1.784
276
P ESP024 Esophagitis 60 1.784
277
TRN018 Transitional Cell Carcinoma 56 1.784
278
INS024 Insulin-Like Growth Factor I 78 1.778
279
P MYC084 Mycobacterium Tuberculosis 1 68 1.778
280
ALL029 Allergic Disease 59 1.778
281
P PRD006 Prader-Willi Syndrome 61 1.733
282
INF034 Infective Endocarditis 54 1.720
283
P ESP035 Esophagitis, Eosinophilic, 1 58 1.720
284
GST033 Gestational Diabetes 61 1.720
285
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.719
286
P PRP019 Peripheral Nervous System Disease 58 1.651
287
P HYP076 Hyperthyroidism 53 1.651
288
PLG002 Plague 58 1.651
289
ACT098 Acute Erythroid Leukemia 55 1.639
290
EXS001 Exostosis 49 1.639
291
KRT009 Keratosis 53 1.639
292
TST014 Testicular Cancer 52 1.639
293
P ATS364 Autism 69 1.590
294
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 1.590
295
EWN003 Ewing Sarcoma 70 1.590
296
URT010 Ureteral Obstruction 45 1.590
297
CRY005 Cryptococcosis 60 1.590
298
P ESS003 Essential Thrombocythemia 69 1.590
299
P PNC044 Pancreatitis 61 1.590
300
ENT004 Enthesopathy 51 1.590
301
ADN027 Adenomyosis 57 1.579
302
P PHC003 Pheochromocytoma 69 1.579
303
HMN044 Human Immunodeficiency Virus Type 1 78 1.579
304
ADR040 Adrenal Gland Pheochromocytoma 46 1.579
305
CRH001 Crohn's Disease 80 1.579
306
P MMB011 Membranous Nephropathy 50 1.579
307
P KLZ004 Kala-Azar 1 41 1.539
308
c DPH024 Diaphragmatic Hernia, Congenital 64 1.539
309
CTN007 Cutaneous Leishmaniasis 62 1.539
310
CRN030 Coronary Stenosis 50 1.539
311
LSH001 Leishmaniasis 64 1.539
312
P SKN015 Skin Carcinoma 71 1.539
313
CRT013 Carotid Stenosis 51 1.539
314
c PRD040 Periodontitis, Chronic 52 1.501
315
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.501
316
LNG030 Lung Adenoma 37 1.501
317
ADT003 Auditory System Disease 49 1.501
318
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.501
319
DBT008 Diabetic Angiopathy 45 1.501
320
ART004 Aortic Atherosclerosis 47 1.501
321
P LRY044 Larynx Cancer 54 1.501
322
HPR003 Heparin-Induced Thrombocytopenia 47 1.501
323
P FML187 Familial Hypertension 34 1.501
324
BRS099 Breast Ductal Carcinoma 61 1.494
325
P MLN069 Melanoma, Uveal 61 1.487
326
c LKM063 Leukemia, Chronic Myeloid 71 1.487
328
P KDN018 Kidney Disease 72 1.487
329
PLR008 Pleurisy 50 1.487
330
PPL022 Papilloma 53 1.487
331
SKN013 Skin Benign Neoplasm 50 1.487
332
CNT047 Contact Dermatitis 57 1.487
333
TRD006 Tardive Dyskinesia 53 1.433
334
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.433
335
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.433
336
TRM010 Traumatic Brain Injury 51 1.433
337
c ACT027 Acute Pancreatitis 60 1.433
338
SQM002 Squamous Cell Papilloma 46 1.433
339
P KDN017 Kidney Cancer 61 1.433
340
P GLM007 Glomerulonephritis 60 1.433
341
DMY004 Demyelinating Disease 50 1.433
342
GST023 Gastric Ulcer 52 1.433
343
GLM044 Glomerular Disease 35 1.416
344
PPL052 Papillomatosis, Confluent and Reticulated 34 1.416
345
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 1.416
346
c ART101 Aortic Valve Disease 2 66 1.416
347
P MDL005 Medulloblastoma 75 1.416
348
P FBR017 Fibrosarcoma 56 1.416
349
P INF038 Influenza 68 1.416
350
PRP016 Paraplegia 52 1.416
351
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.377
352
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.377
353
GLC003 Glucose Intolerance 54 1.377
354
P UVT001 Uveitis 57 1.377
355
P SLP005 Sleep Disorder 61 1.377
356
KLD004 Keloid Disorder 39 1.377
357
LYM017 Lyme Disease 62 1.322
358
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 1.322
359
CRD132 Cardiac Conduction Defect 60 1.318
360
ACR008 Acrocallosal Syndrome 70 1.318
361
END057 Endometrial Cancer 72 1.318
362
c ICH049 Ichthyosis, Congenital, Autosomal Recessive 2 44 1.318
363
EPT021 Epithelial Recurrent Erosion Dystrophy 46 1.318
365
DCT002 Ductal Carcinoma in Situ 58 1.318
366
c ICH038 Ichthyosis, Congenital, Autosomal Recessive 3 32 1.318
367
P RRH023 Rare Hereditary Hemochromatosis 54 1.318
368
HMS001 Hemosiderosis 48 1.318
369
DPH001 Diphtheria 59 1.318
370
P EHL001 Ehlers-Danlos Syndrome 58 1.318
371
CHL068 Cholestasis 61 1.318
372
P TXP001 Toxoplasmosis 60 1.318
373
BCK006 Back Pain 47 1.318
374
ALL014 Allergic Encephalomyelitis 34 1.318
375
P ATR011 Atrial Fibrillation 66 1.257
376
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.257
377
PRM236 Primary Biliary Cholangitis 60 1.257
378
CRT015 Carotid Artery Occlusion 45 1.257
379
PRP027 Peripheral Vascular Disease 71 1.216
380
c BRN108 Branchiootic Syndrome 1 62 1.216
381
CVT001 Cavitary Optic Disc Anomalies 37 1.216
382
c ANR027 Aneurysm, Intracranial Berry, 1 21 1.216
383
AVN001 Avian Influenza 61 1.216
384
LYM040 Lymphoblastic Lymphoma 53 1.216
385
HYP080 Hypogonadism 50 1.216
386
SPN186 Spinal Cord Injury 61 1.192
387
GNT182 Genetic Nephrotic Syndrome 22 1.192
388
ANX010 Anxiety 70 1.192
389
P MLT020 Multiple Sclerosis 79 1.192
390
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.192
391
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.192
392
P SPP010 Suppressor of Tumorigenicity 3 51 1.192
393
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.192
394
MLD002 Mild Pre-Eclampsia 33 1.192
395
P MYP006 Myopia 56 1.192
396
HPT022 Hepatoblastoma 54 1.192
397
P PTT006 Pituitary Adenoma 55 1.192
398
CRB039 Cerebrovascular Disease 66 1.192
399
ENC005 Encephalomalacia 44 1.192
400
HYP014 Hyperuricemia 51 1.192
401
CRB037 Cerebral Palsy 67 1.192
402
c SVR005 Severe Pre-Eclampsia 50 1.192
403
ALC007 Alcohol Dependence 66 1.124
404
P PRK057 Parkinson Disease, Late-Onset 80 1.124
405
CHR100 Chronic Ulcer of Skin 57 1.124
406
DWN001 Down Syndrome 70 1.124
407
HRW001 Hair Whorl 35 1.124
408
PRT037 Pertussis 65 1.124
409
P GRV001 Graves' Disease 55 1.124
410
TXC005 Toxic Shock Syndrome 62 1.124
411
PRT013 Portal Hypertension 59 1.124
412
HYP006 Hypertensive Heart Disease 49 1.124
413
KLB003 Klebsiella Pneumonia 50 1.124
414
HYP060 Hyperinsulinism 54 1.124
415
SYS003 Systolic Heart Failure 49 1.124
416
P CHR345 Chronic Pain 50 1.124
417
PTT037 Pituitary Tumors 44 1.124
418
MTN003 Motion Sickness 51 1.089
419
c OST121 Osteogenesis Imperfecta, Type Iv 49 1.089
420
PRP080 Peripheral Artery Disease 54 1.089
421
P RHB003 Rhabdomyosarcoma 66 1.089
422
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 1.089
423
P AGG001 Aggressive Periodontitis 55 1.089
424
P MTR003 Mitral Valve Stenosis 53 1.089
425
ADR022 Adrenomyeloneuropathy 39 1.052
426
P SZR006 Seizure Disorder 70 1.052
427
ADR007 Adrenoleukodystrophy 73 1.052
428
c PNC108 Pancreatitis, Hereditary 69 1.052
429
CLF027 Cleft Palate, Isolated 64 1.052
430
BRK010 Burkitt Lymphoma 66 1.052
431
P ATX030 Ataxia-Telangiectasia 80 1.052
432
INV001 Invasive Aspergillosis 49 1.052
433
END062 Endometrial Hyperplasia 48 1.052
434
HYP025 Hyperphosphatemia 48 1.052
435
c ADM008 Adams-Oliver Syndrome 3 22 1.052
436
P ASP006 Aspergillosis 72 1.052
437
PLY001 Polycythemia Vera 69 1.052
438
P OPN001 Open-Angle Glaucoma 55 1.052
439
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.052
440
PRS042 Prostate Disease 42 1.052
441
P MYP004 Myopathy 67 1.052
442
ORB013 Orbital Disease 42 1.052
443
CLL010 Cellular Ependymoma 57 1.052
444
P PLY018 Polycythemia 56 1.052
445
P BNG030 Benign Ependymoma 51 1.052
446
TLN003 Telangiectasis 51 1.052
447
LYD001 Leydig Cell Tumor 45 1.052
448
P INT099 Intrahepatic Cholestasis of Pregnancy 62 1.052
449
MST005 Mastitis 53 1.052
450
TTN003 Tetanus 65 1.052
451
c ACT071 Acute Kidney Failure 60 1.052
452
CRN009 Corneal Ectasia 29 1.052
453
LCH001 Leech Infestation 38 1.052
454
NDL006 Nodular Prostate 23 1.052
455
CRB086 Cerebral Aneurysms 40 1.052
456
P VTR007 Vitreoretinopathy 46 0.974
457
c ACT134 Acute Liver Failure 59 0.974
458
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.974
459
c NPH049 Nephrotic Syndrome, Type 2 51 0.974
460
OTT002 Otitis Media 71 0.974
461
LMB062 Limb Ischemia 55 0.974
462
P ORT004 Orthostatic Intolerance 63 0.974
463
KWS002 Kawasaki Disease 65 0.974
464
c CHL119 Cholangitis, Primary Sclerosing 58 0.974
465
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.974
466
P PLY041 Polymyositis 59 0.974
467
c ACT075 Acute Myocardial Infarction 56 0.974
468
URM002 Uremia 47 0.974
469
SKN019 Skin Melanoma 71 0.974
470
P VSC011 Vasculitis 61 0.974
471
P CHL066 Cholangitis 52 0.974
472
P HYP098 Hypereosinophilic Syndrome 66 0.974
473
P CYS018 Cystitis 59 0.974
474
P DRM010 Dermatomyositis 61 0.974
475
ANG020 Angiosarcoma 64 0.974
476
PLC002 Plica Syndrome 35 0.974
477
P MLN007 Male Infertility 56 0.974
478
END041 Endometrial Adenocarcinoma 64 0.974
479
P SCL009 Sclerosing Cholangitis 48 0.974
480
P MCR010 Microcephaly 60 0.974
481
MTR002 Mitral Valve Insufficiency 52 0.974
482
P MTR012 Mitral Valve Disease 57 0.974
483
P CNJ013 Conjunctivitis 66 0.974
484
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.974
485
PLC008 Placenta Disease 49 0.974
486
P CYS039 Cystic Kidney Disease 53 0.974
487
SYN007 Synovitis 55 0.974
488
ART006 Arthus Reaction 40 0.974
489
P LMY004 Leiomyosarcoma 62 0.974
490
HYP056 Hypoglycemia 65 0.974
491
LTH004 Lathyrism 15 0.974
492
c LKM005 Leukemia, T-Cell, Chronic 34 0.974
493
NDL013 Nodular Regenerative Hyperplasia 46 0.974
494
CHK001 Chikungunya 60 0.925
495
TST044 Testicular Torsion 45 0.925
496
CRN235 Corneal Dystrophy, Groenouw Type I 37 0.925
497
P CRN024 Corneal Disease 44 0.925
498
LRY004 Laryngotracheitis 33 0.925
499
NWC001 Newcastle Disease 47 0.925
500
ASP030 Aspirin Resistance 40 0.889
501
CYS001 Cystic Fibrosis 78 0.889
502
c MJR022 Major Affective Disorder 8 38 0.889
503
WTH001 Withdrawal Disorder 48 0.889
504
KRN002 Kearns-Sayre Syndrome 63 0.889
506
c MJR024 Major Affective Disorder 9 41 0.889
507
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.889
508
PRT082 Preterm Premature Rupture of the Membranes 57 0.889
509
MYL069 Myeloma, Multiple 77 0.889
510
TBC004 Tobacco Addiction 63 0.889
511
CRN270 Coronary Artery Dissection, Spontaneous 32 0.889
512
SLF015 Self-Improving Collodion Baby 33 0.889
513
P AMY004 Amyloidosis 70 0.889
514
P MSC003 Muscular Atrophy 52 0.889
515
BRR002 Barrett's Adenocarcinoma 37 0.889
516
PRP002 Periapical Granuloma 38 0.889
517
P SBR004 Seborrheic Dermatitis 44 0.889
518
P ANT006 Antiphospholipid Syndrome 55 0.889
519
P BPL003 Bipolar Disorder 56 0.889
520
HST010 Histiocytosis 49 0.889
521
P ACN011 Acne 57 0.889
522
BRN014 Bronchopneumonia 53 0.889
523
TRN015 Transient Cerebral Ischemia 63 0.889
524
P HMN010 Hemangioma 62 0.889
525
P HYP069 Hyperparathyroidism 62 0.889
526
P DDN001 Duodenal Ulcer 53 0.889
527
IRR003 Irritant Dermatitis 47 0.889
528
VGN017 Vaginal Cancer 59 0.889
529
ALL009 Allergic Conjunctivitis 51 0.889
530
STT001 Status Epilepticus 59 0.889
531
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.889
532
c RNG015 Ring Chromosome 2 22 0.889
533
HMR014 Hemorrhagic Shock and Encephalopathy Syndrome 19 0.889
534
c HMC039 Hemochromatosis, Type 1 73 0.795
535
P THL005 Thalassemia 56 0.795
536
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.795
537
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.795
538
AND002 Androgen Insensitivity Syndrome 63 0.795
539
c EXD008 Exudative Vitreoretinopathy 1 71 0.795
540
MNR012 Meniere Disease 56 0.795
541
P MGL010 Megalencephalic Leukoencephalopathy with Subcortical Cysts 2a 40 0.795
542
c ADM007 Adams-Oliver Syndrome 2 33 0.795
543
HLT001 Holt-Oram Syndrome 66 0.795
544
c PSR033 Psoriasis 12 26 0.795
545
P MJR001 Major Depressive Disorder 68 0.795
546
c GLC092 Glaucoma, Primary Open Angle 62 0.795
547
TRC020 Tracheitis 43 0.795
548
P DYS154 Dystonia 64 0.795
549
PRS047 Prostatitis 58 0.795
550
SHW001 Shwartzman Phenomenon 36 0.795
551
MNT002 Mental Depression 57 0.795
552
PPT005 Peptic Ulcer Disease 58 0.795
553
P OLM003 Olmsted Syndrome 1 32 0.795
554
P MTL007 Mutilating Palmoplantar Keratoderma with Periorificial Keratotic Plaques 49 0.795
555
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.795
556
BRN012 Bronchiolitis Obliterans 56 0.795
557
c BSL007 Basal Cell Carcinoma 68 0.795
558
P CRD119 Cardiac Arrest 67 0.795
559
MCR013 Microphthalmia 60 0.795
560
MCL006 Macular Retinal Edema 57 0.795
561
MTN002 Mite Infestation 35 0.795
562
PLM029 Palmoplantar Keratosis 48 0.795
563
BRN002 Bronchiolitis 57 0.795
564
PLM010 Pulmonary Edema 55 0.795
565
RNL011 Renal Osteodystrophy 49 0.795
566
P NRF002 Neurofibromatosis 57 0.795
567
P ENC004 Encephalitis 61 0.795
568
NSS002 Neisseria Meningitidis Infection 47 0.795
569
DPR016 Depression 65 0.795
570
ETN001 Eating Disorder 59 0.795
571
c PNS012 Paine Syndrome 60 0.747
572
c FML346 Familial Adenomatous Polyposis 1 65 0.747
573
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.747
574
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.747
575
P TRN020 Turner Syndrome 67 0.747
576
INT358 Intestinal Polyposis Syndrome 25 0.688
577
DRV001 Dravet Syndrome 69 0.688
578
ANR007 Anorexia Nervosa 60 0.688
579
P TMP003 Temporal Arteritis 69 0.688
580
TND004 Tendinopathy 45 0.688
581
HRT040 Hirata Disease 38 0.688
582
TND005 Tendinitis 54 0.688
583
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.688
584
HMN047 Human Cytomegalovirus Infection 57 0.688
585
c PRG020 Paragangliomas 3 39 0.688
586
AST006 Astigmatism 47 0.688
587
c HPT073 Hepatitis C Virus 71 0.688
588
P SCL057 Scoliosis, Isolated 1 40 0.688
589
c TBR025 Tuberous Sclerosis 1 84 0.688
590
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.688
591
CLR109 Colorectal Adenocarcinoma 50 0.688
592
OBS082 Obstructive Nephropathy 41 0.688
593
ACT250 Acute Megakaryocytic Leukemia 60 0.688
594
CRN036 Craniopharyngioma 64 0.688
595
FDL002 Food Allergy 47 0.688
596
P EPL164 Epilepsy 68 0.688
597
c VRL010 Viral Hepatitis 53 0.688
598
P ART023 Arthropathy 61 0.688
599
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.688
600
CRN017 Coronary Thrombosis 46 0.688
601
CRV040 Cervix Carcinoma 50 0.688
602
THR004 Thrombocytosis 53 0.688
603
HGH043 High Grade Glioma 45 0.688
604
P TBR001 Tuberous Sclerosis 69 0.688
605
P RSP003 Respiratory Failure 74 0.688
606
P PSD003 Pseudohypoaldosteronism 44 0.688
607
OST004 Osteitis Fibrosa 38 0.688
608
BNN003 Bone Inflammation Disease 48 0.688
609
MDD003 Middle Cerebral Artery Infarction 37 0.688
610
PLR005 Pleuropneumonia 33 0.688
611
IDP070 Idiopathic Scoliosis 42 0.688
612
IRR001 Irregular Astigmatism 32 0.688
613
ACT017 Acute Chest Syndrome 50 0.688
615
P ACT105 Acute Mountain Sickness 52 0.688
616
DST006 Diastolic Heart Failure 45 0.688
617
P HMP007 Hemophilia 52 0.688
618
ATN005 Autonomic Dysfunction 46 0.688
619
CHR178 Chromosomal Triplication 34 0.688
620
c TYP008 Type 1 Diabetes Mellitus 70 0.562
621
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.562
622
P PRM011 Primary Ciliary Dyskinesia 69 0.562
623
P OVR082 Overgrowth Syndrome 49 0.562
624
P RTT002 Rett Syndrome 79 0.562
625
ASP026 Asplenia, Isolated Congenital 43 0.562
626
P FRG001 Fragile X Syndrome 70 0.562
627
c SPR086 Spermatogenic Failure 3 46 0.562
628
c ALP101 Alpha-Thalassemia 62 0.562
629
P MTR004 Maturity-Onset Diabetes of the Young 68 0.562
630
P SCH015 Schizophrenia 74 0.562
631
c SYS001 Systemic Lupus Erythematosus 87 0.562
632
c ADM005 Adams-Oliver Syndrome 1 39 0.562
633
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.562
634
ARG007 Argininemia 58 0.562
635
c ICH047 Ichthyosis, Congenital, Autosomal Recessive 1 53 0.562
636
c ICH069 Ichthyosis, Congenital, Autosomal Recessive 4b 52 0.562
637
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.562
638
HYP457 Hypertrophic Scars 42 0.562
639
PLM101 Pulmonary Hypertension, Chronic Thromboembolic, Without Deep Vein Thrombosis 37 0.562
640
MSC007 Muscle Hypertrophy 64 0.562
641
P SLM003 Salmonellosis 54 0.562
642
SXL003 Sexual Disorder 49 0.562
643
P LYM118 Lymphoma 67 0.562
644
CRH005 Crohn's Colitis 53 0.562
645
ANT003 Antley-Bixler Syndrome 49 0.562
646
c ATM022 Autoimmune Myocarditis 36 0.562
647
P CHN012 Chondrosarcoma 57 0.562
648
LTN004 Late-Onset Retinal Degeneration 60 0.562
649
c HNT011 Huntington Disease-Like 3 34 0.562
650
ACR011 Acromesomelic Dysplasia, Maroteaux Type 44 0.562
651
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.562
652
c BRS111 Breast-Ovarian Cancer, Familial 2 53 0.562
653
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.562
654
BRL010 Buruli Ulcer 45 0.562
655
ART001 Arterial Tortuosity Syndrome 65 0.562
656
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 0.562
657
c PNC106 Pancreatic Agenesis 1 51 0.562
658
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 60 0.562
659
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 0.562
660
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.562
661
INT051 Intussusception 52 0.562
662
c NRF024 Neurofibromatosis, Type I 72 0.562
663
c SPN294 Spinocerebellar Ataxia 1 53 0.562
664
ACT149 Acetaminophen Metabolism 35 0.562
665
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.562
666
MNN043 Meningioma, Familial 79 0.562
667
P LKD001 Leukodystrophy 59 0.562
668
P LCT002 Lactose Intolerance 52 0.562
670
LMY002 Leiomyoma 51 0.562
671
TNG007 Tongue Carcinoma 52 0.562
672
HPT004 Hepatic Coma 43 0.562
673
PRC002 Paracoccidioidomycosis 54 0.562
674
P PRK039 Parkinsonism 55 0.562
675
P LPS004 Lupus Erythematosus 61 0.562
676
P LCH002 Lichen Planus 54 0.562
677
YLL002 Yellow Fever 61 0.562
678
P ALP008 Alopecia 54 0.562
679
P RNV001 Renovascular Hypertension 49 0.562
680
SVR001 Severe Acute Respiratory Syndrome 67 0.562
681
P OPT006 Optic Nerve Disease 58 0.562
682
LNG031 Lung Benign Neoplasm 51 0.562
683
P RST002 Restrictive Cardiomyopathy 54 0.562
684
OVR063 Overnutrition 42 0.562
685
MYF001 Myofibroma 42 0.562
686
SCR001 Secretory Meningioma 40 0.562
687
LYM002 Lymphoplasmacyte-Rich Meningioma 35 0.562
688
SCB001 Scabies 50 0.562
689
TRC123 Trichohepatoneurodevelopmental Syndrome 28 0.562
690
MCR011 Microinvasive Gastric Cancer 41 0.562
691
c ACT068 Acute Cystitis 61 0.562
692
NRX001 Neuroaxonal Dystrophy 38 0.562
693
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.562
694
MYM001 Myoma 54 0.562
695
HPT019 Hepatic Encephalopathy 59 0.562
696
c MLG084 Malignant Fibrous Histiocytoma 62 0.562
697
PPL002 Papillary Carcinoma 46 0.562
698
P GLY013 Glycogen Storage Disease 60 0.562
699
P CRN026 Corneal Edema 42 0.562
700
HYP043 Hyperandrogenism 48 0.562
701
P NNT058 Neonatal Diabetes 52 0.562
702
P RTN018 Retinal Disease 53 0.562
703
P CRN025 Corneal Dystrophy 49 0.562
704
PNC034 Pancreas Disease 50 0.562
705
c FML021 Familial Hypercholesterolemia 72 0.562
706
P SCK002 Sick Sinus Syndrome 55 0.562
707
PHR002 Pharyngoconjunctival Fever 32 0.562
708
PRM024 Primary Angle-Closure Glaucoma 39 0.562
709
SPN021 Spinal Meningioma 50 0.562
710
CHL122 Cholesteatoma of Middle Ear 51 0.562
711
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.562
712
P BRN022 Bronchiectasis 60 0.562
713
DCB001 Decubitus Ulcer 62 0.562
714
SFT003 Soft Tissue Sarcoma 57 0.562
715
SPL018 Splenomegaly 49 0.562
716
P HYP265 Hypotonia 42 0.562
717
CHR466 Chronic Thromboembolic Pulmonary Hypertension 48 0.562
718
CNG092 Congenital Extrahepatic Portosystemic Shunt 24 0.562
719
AMR003 Amaurosis Fugax 33 0.562
720
AMN006 Aminoaciduria 37 0.562
721
ORL013 Oral Lichen Planus 46 0.562
722
WLL004 Wallerian Degeneration 38 0.527
723
SYN106 Syndromic Craniosynostosis 32 0.397
724
CLP005 Ciliopathy 41 0.397
725
SNG003 Single Ventricular Heart 30 0.397
726
P RRT020 Rare Tumor 39 0.397
727
THY128 Thyroid Tumor 35 0.397
728
RTC012 Reticuloendotheliosis, X-Linked 35 0.397
729
P MYM013 Moyamoya Disease 1 59 0.397
730
P ATS366 Autism X-Linked 2 41 0.397
731
MLT135 Multiple Sulfatase Deficiency 53 0.397
732
c THY107 Thymoma, Familial 42 0.397
733
c NGH025 Night Blindness, Congenital Stationary, Type 2a 44 0.397
734
c ICH051 Ichthyosis, Congenital, Autosomal Recessive 11 42 0.397
735
c DRM040 Dermatitis Herpetiformis, Familial 35 0.397
736
c ICH040 Ichthyosis, Congenital, Autosomal Recessive 4a 41 0.397
737
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.397
738
c RBN018 Robinow Syndrome, Autosomal Dominant 1 50 0.397
739
P LFR001 Li-Fraumeni Syndrome 73 0.397
740
P ALG028 Alagille Syndrome 1 73 0.397
741
CNT099 Contractural Arachnodactyly, Congenital 54 0.397
742
P SPR041 Spermatogenic Failure 6 47 0.397
743
FCT001 Factor Viii Deficiency 60 0.397
744
FBR032 Fibromuscular Dysplasia 48 0.397
745
VNH007 Von Hippel-Lindau Syndrome 73 0.397
746
c MGR028 Migraine with or Without Aura 1 64 0.397
747
OCL008 Oculopharyngeal Muscular Dystrophy 53 0.397
748
P CRN038 Carney Complex Variant 64 0.397
749
MTB004 Metabolic Acidosis 48 0.397
750
P RST001 Restless Legs Syndrome 52 0.397
751
HYP001 Hypochromic Microcytic Anemia 37 0.397
752
MRG003 Marginal Zone B-Cell Lymphoma 52 0.397
753
SPL004 Splenic Marginal Zone Lymphoma 50 0.397
754
LYM012 Lymphoplasmacytic Lymphoma 50 0.397
755
DFF005 Diffuse Large B-Cell Lymphoma 54 0.397
756
c ICH044 Ichthyosis, Congenital, Autosomal Recessive 8 26 0.397
757
BRR014 Barrett Esophagus 66 0.397
758
BCT021 Bacterial Sepsis 43 0.397
759
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.397
760
c CHR711 Chronic Asthma 41 0.397
761
P CRB045 Cerebellar Hypoplasia 40 0.397
762
WLD007 Waldenstroem's Macroglobulinemia 63 0.397
763
INT029 Interleukin-7 Receptor Alpha Deficiency 28 0.397
764
c CNG006 Congenital Hypothyroidism 63 0.397
765
P CNG010 Congenital Stationary Night Blindness 56 0.397
766
TNS007 Taeniasis 46 0.397
767
P SML001 Small Cell Carcinoma 52 0.397
768
APP015 Apparent Mineralocorticoid Excess 57 0.397
769
CYS045 Cystinosis, Adult Nonnephropathic 32 0.397
770
KPS004 Kaposi Sarcoma 77 0.397
771
GRY002 Gray Platelet Syndrome 58 0.397
772
P PLY006 Polydactyly 59 0.397
773
c NPH031 Nephronophthisis 3 46 0.397
774
c ICH050 Ichthyosis, Congenital, Autosomal Recessive 5 31 0.397
775
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.397
776
c ICH045 Ichthyosis, Congenital, Autosomal Recessive 7 32 0.397
777
c ICH048 Ichthyosis, Congenital, Autosomal Recessive 9 30 0.397
778
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.397
779
CHP002 Chops Syndrome 47 0.397
780
c ICH042 Ichthyosis, Congenital, Autosomal Recessive 6 32 0.397
781
PLM156 Palmoplantar Carcinoma, Multiple Self-Healing 35 0.397
782
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.397
783
ACT119 Acute Promyelocytic Leukemia 62 0.397
784
HRN029 Hearing Loss, Noise-Induced 37 0.397
785
RHB024 Rhabdomyosarcoma 2 67 0.397
786
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 36 0.397
787
c HMP029 Hemophilia a 68 0.397
788
c HYP581 Hypotrichosis 6 40 0.397
789
c LYS019 Loeys-Dietz Syndrome 1 58 0.397
790
c LFR007 Li-Fraumeni Syndrome 2 46 0.397
791
c CTS038 Cutis Laxa, Autosomal Recessive, Type Iia 47 0.397
792
GLY058 Glycogen Storage Disease 0, Liver 34 0.397
793
c WLM013 Wilms Tumor 1 66 0.397
794
P MLT065 Multicentric Osteolysis, Nodulosis, and Arthropathy 41 0.397
795
LRN002 Laron Syndrome 63 0.397
796
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.397
797
P CNG499 Congenital Anomalies of Kidney and Urinary Tract 2 52 0.397
798
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.397
799
HYP186 Hypertrophic Neuropathy of Dejerine-Sottas 51 0.397
800
P CLD001 Cleidocranial Dysplasia 64 0.397
801
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.397
802
APR006 Apert Syndrome 70 0.397
803
P ANR048 Aniridia 1 64 0.397
804
MMM006 Mammographic Density 39 0.397
805
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 0.397
806
c ICH039 Ichthyosis, Congenital, Autosomal Recessive 10 27 0.397
807
SZR028 Seizures, Scoliosis, and Macrocephaly/microcephaly Syndrome 36 0.397
808
PNG002 Pain Agnosia 51 0.397
809
TNG009 Tongue Squamous Cell Carcinoma 43 0.397
810
NRR001 Neuroretinitis 42 0.397
811
P PNM006 Pneumoconiosis 55 0.397
812
P PRS062 Persistent Hyperplastic Primary Vitreous 48 0.397
813
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.397
814
P NRD007 Neurodegeneration with Brain Iron Accumulation 52 0.397
815
c PSD093 Pseudohypoaldosteronism, Type Iid 32 0.397
816
MDD018 Middle East Respiratory Syndrome 44 0.397
817
c ACT073 Acute Leukemia 58 0.397
818
MDD015 Mid-Dermal Elastolysis 24 0.397
819
MCR004 Macroglobulinemia 49 0.397
820
PLM014 Pleomorphic Adenoma 51 0.397
821
P HYP087 Hypotrichosis 42 0.397
822
EXT007 Extracutaneous Mastocytoma 38 0.397
823
P EMB005 Embryonal Rhabdomyosarcoma 53 0.397
824
RTN023 Retinitis 46 0.397
825
P KLL001 Kallmann Syndrome 65 0.397
826
P TYR004 Tyrosinemia 50 0.397
827
IRD001 Iridocyclitis 53 0.397
828
RMS001 Rem Sleep Behavior Disorder 47 0.397
829
CHC001 Chickenpox 57 0.397
830
P HML002 Hemolytic Anemia 62 0.397
831
HMG002 Hemoglobinuria 50 0.397
832
PST092 Posttransplant Acute Limbic Encephalitis 28 0.397
833
P TRM003 Tremor 48 0.397
834
EPS023 Epstein-Barr Virus-Associated Gastric Carcinoma 37 0.397
835
SYN036 Syncope 45 0.397
836
c PRG106 Progressive Muscular Dystrophy 32 0.397
837
MST004 Mast Cell Neoplasm 42 0.397
838
P KRT005 Keratoacanthoma 47 0.397
839
SKN022 Skin Squamous Cell Carcinoma 54 0.397
840
P LPM005 Lipomatosis 47 0.397
841
P OLG002 Oligodendroglioma 66 0.397
842
P BRD002 Bardet-Biedl Syndrome 66 0.397
843
CHL067 Cholecystitis 60 0.397
844
P CHR012 Chronic Granulomatous Disease 69 0.397
845
BNG006 Benign Familial Neonatal Epilepsy 55 0.397
846
P CND004 Candidiasis 58 0.397
847
P LCT001 Lactic Acidosis 51 0.397
848
P CRV031 Cervical Adenocarcinoma 48 0.397
849
BLR004 Biliary Dyskinesia 37 0.397
850
RHB001 Rhabdoid Cancer 68 0.397
851
OVR059 Ovary Adenocarcinoma 49 0.397
852
LNG039 Lung Squamous Cell Carcinoma 57 0.397
853
P PSD015 Pseudohypoparathyroidism 55 0.397
854
P ESN008 Eosinophilic Pneumonia 50 0.397
855
ACQ007 Acquired Immunodeficiency Syndrome 59 0.397
856
HYP005 Hypokalemia 55 0.397
857
P BNG002 Benign Meningioma 36 0.397
858
NPH009 Nephrolithiasis 54 0.397
859
ADN009 Adenosquamous Carcinoma 48 0.397
860
P NGH001 Night Blindness 52 0.397
861
P DRM007 Dermatitis Herpetiformis 54 0.397
862
CMB007 Combined Immunodeficiency 57 0.397
863
P CTN003 Cutaneous Lupus Erythematosus 52 0.397
864
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.397
865
PLV003 Pelvic Inflammatory Disease 55 0.397
866
CYS005 Cysticercosis 60 0.397
867
ANT018 Anthracosis 51 0.397
868
RTN003 Retinal Ischemia 49 0.397
869
P HYP061 Hypertrophic Cardiomyopathy 69 0.397
870
c SCN007 Secondary Hyperparathyroidism 51 0.397
871
ALC006 Alcoholic Hepatitis 61 0.397
872
ACR007 Acromegaly 70 0.397
873
P HYP035 Hypophosphatasia 62 0.397
874
P NPH005 Nephronophthisis 56 0.397
875
TST015 Testicular Disease 42 0.397
876
P HYP086 Hypothyroidism 69 0.397
877
P CRN037 Craniosynostosis 68 0.397
878
P RNL015 Renal Hypertension 45 0.397
879
P MTH007 Methemoglobinemia 46 0.397
880
P STC001 Stickler Syndrome 60 0.397
881
PLC009 Placenta Praevia 38 0.397
882
PRM013 Premature Menopause 58 0.397
883
JPN002 Japanese Encephalitis 61 0.397
884
QFV001 Q Fever 62 0.397
885
P FNC004 Fanconi Syndrome 60 0.397
886
CYS010 Cystinosis 62 0.397
887
P INT068 Intestinal Disease 53 0.397
888
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.397
889
STM006 Stomach Disease 47 0.397
890
GST050 Gastrointestinal System Disease 55 0.397
891
OST016 Osteochondrosis 52 0.397
892
SPT004 Septic Arthritis 58 0.397
893
P TRT010 Teratoma 51 0.397
894
EMB004 Embryonal Carcinoma 56 0.397
895
BCT002 Bacterial Vaginosis 53 0.397
896
GNG013 Gingivitis 59 0.397
897
INT066 Interstitial Lung Disease 60 0.397
898
P MLT074 Multiple Endocrine Neoplasia 59 0.397
899
PRC003 Proctitis 49 0.397
900
P THY023 Thymoma 64 0.397
901
MDD011 Mood Disorder 62 0.397
902
PHR003 Pharyngitis 58 0.397
903
P MTR014 Motor Neuron Disease 65 0.397
904
CRT016 Carotid Artery Disease 52 0.397
905
P PLY019 Polyneuropathy 52 0.397
906
P SCL048 Sclerosteosis 58 0.397
907
EXC002 Exocrine Pancreatic Insufficiency 42 0.397
908
CNG021 Congenital Toxoplasmosis 55 0.397
909
PLS007 Plasmodium Falciparum Malaria 52 0.397
910
P ADL010 Adult Respiratory Distress Syndrome 71 0.397
911
AMN003 Amnestic Disorder 54 0.397
912
DBT004 Diabetic Polyneuropathy 50 0.397
913
LKS001 Leukostasis 41 0.397
914
IRN002 Iron Metabolism Disease 57 0.397
915
P BNC003 Bone Cancer 58 0.397
916
NRN004 Neuroendocrine Tumor 59 0.397
917
PLM035 Pulmonary Eosinophilia 49 0.397
918
XLN012 X-Linked Congenital Stationary Night Blindness 28 0.397
919
c CLD019 Cleidocranial Dysplasia Spectrum Disorder 20 0.397
920
NRF007 Neurofibroma 64 0.397
921
STM007 Stomatitis 54 0.397
922
MST020 Mast Cell Activation Syndrome 28 0.397
923
UTR043 Uterine Sarcoma 40 0.397
924
c GLY023 Glycogen Storage Disease Type 0 27 0.397
925
DYS073 Dysphagia 53 0.397
926
P BRT047 Brittle Cornea Syndrome 42 0.397
927
CRD016 Cardiac Rupture 34 0.397
928
HMP009 Haemophilus Influenzae 41 0.397
929
P MRC003 Mercury Poisoning 49 0.397
930
DHY008 Dihydroxyadeninuria 24 0.397
931
FML168 Familial Isolated Pituitary Adenoma 32 0.397
932
HVY002 Heavy Metal Poisoning 22 0.397
933
DWR001 Dwarfism 44 0.397
934
PRT058 Pure Autonomic Failure 58 0.397
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