Search results for ADP

2213 hits were found for ADP

# Family MCID Name MIFTS Score
1
c BLD120 Bleeding Disorder, Platelet-Type, 8 35 26.121
2
CHL014 Cholera 62 12.091
3
PRT037 Pertussis 49 11.948
4
GLT038 Glutamyl Ribose-5-Phosphate Storage Disease 8 10.451
5
DPH001 Diphtheria 59 7.382
6
P OVR042 Ovarian Cancer 88 6.718
7
ISC004 Ischemia 61 5.576
8
GLM045 Glioma 62 4.909
9
GLL048 Glial Tumor 51 4.846
10
ART002 Arts Syndrome 66 4.771
11
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.762
12
LPP008 Lipoprotein Quantitative Trait Locus 65 4.420
13
GLB002 Glioblastoma 67 4.392
14
P PRS040 Prostate Cancer 95 4.251
15
P BRS047 Breast Cancer 97 4.185
16
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 4.146
17
P NRB001 Neuroblastoma 66 4.106
18
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 4.026
19
TLN003 Telangiectasis 51 3.962
20
P ATX030 Ataxia-Telangiectasia 80 3.954
21
P PNC035 Pancreatic Cancer 87 3.903
22
P THR014 Thrombocytopenia 66 3.628
23
ART140 Arteries, Anomalies of 52 3.615
24
P LKM002 Leukemia 65 3.556
25
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 3.511
26
HLX001 Helix Syndrome 47 3.470
27
OST159 Osteogenic Sarcoma 66 3.409
28
CRB004 Cerebral Artery Occlusion 45 3.327
29
c LKM061 Leukemia, Acute Myeloid 83 3.322
30
P GLM040 Glioma Susceptibility 1 70 3.303
31
P LNG032 Lung Cancer 98 3.212
32
SRC014 Sarcoma 64 3.193
33
SPN035 Spindle Cell Sarcoma 51 3.188
34
HYP266 Hypoxia 56 3.168
35
HYP066 Hyperglycemia 60 3.167
36
MLG169 Malignant Astrocytoma 57 3.165
37
P BCL017 B-Cell Lymphoma 57 3.151
38
P MYL006 Myeloid Leukemia 60 3.074
39
P CLR023 Colorectal Cancer 100 3.068
40
P MLN008 Melanoma 75 2.972
41
TRM010 Traumatic Brain Injury 50 2.905
42
OVR094 Ovarian Epithelial Cancer 39 2.898
43
48X005 48,xyyy 39 2.887
44
BRN071 Brain Injury 50 2.857
45
PRT036 Peritonitis 65 2.834
46
SVR001 Severe Acute Respiratory Syndrome 68 2.833
47
P MYC007 Myocardial Infarction 69 2.827
48
c SYS001 Systemic Lupus Erythematosus 85 2.802
49
HGH043 High Grade Glioma 46 2.795
50
DBT010 Diabetic Neuropathy 54 2.731
51
THR035 Thrombasthenia 48 2.691
52
P LKM071 Leukemia, Chronic Lymphocytic 74 2.669
53
47X002 47,xyy 47 2.663
54
ANX004 Anoxia 40 2.597
55
P ADN016 Adenocarcinoma 63 2.584
56
P VSC007 Vascular Disease 62 2.573
57
c ACT075 Acute Myocardial Infarction 55 2.573
58
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 2.565
59
c DLT002 Dilated Cardiomyopathy 79 2.564
60
MYL069 Myeloma, Multiple 76 2.520
61
P MYP004 Myopathy 67 2.510
62
TXC005 Toxic Shock Syndrome 61 2.505
63
P PNC044 Pancreatitis 61 2.483
64
P LNG064 Lung Cancer Susceptibility 3 69 2.473
65
P MDL005 Medulloblastoma 75 2.466
66
AGN016 Aging 53 2.436
67
RPD005 Rapidly Involuting Congenital Hemangioma 48 2.419
68
INS001 Insulinoma 59 2.410
69
P HRT032 Heart Disease 84 2.402
70
EWN003 Ewing Sarcoma 69 2.402
71
P LPS004 Lupus Erythematosus 61 2.389
72
THR024 Thrombosis 56 2.385
73
CLP006 Clopidogrel Resistance 44 2.309
74
ESP021 Esophageal Cancer 84 2.299
75
P CRN300 Coronary Heart Disease 1 73 2.273
76
c ACT027 Acute Pancreatitis 60 2.245
77
P GST053 Gastric Cancer 82 2.241
78
P NRP001 Neuropathy 59 2.226
79
END057 Endometrial Cancer 76 2.222
80
P LTR001 Lateral Sclerosis 57 2.205
81
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.197
82
ALL029 Allergic Disease 61 2.197
83
CYT002 Cytokine Deficiency 43 2.194
84
c MCR115 Microvascular Complications of Diabetes 5 65 2.192
85
CRB039 Cerebrovascular Disease 65 2.187
86
SQM006 Squamous Cell Carcinoma 59 2.159
87
P BRS044 Breast Adenocarcinoma 58 2.158
88
INT007 Intermediate Coronary Syndrome 53 2.150
89
MYL009 Myelodysplastic Syndrome 67 2.145
90
c ATR087 Atrial Standstill 1 74 2.134
91
P PRP029 Porphyria 60 2.124
92
XRD010 Xeroderma Pigmentosum, Variant Type 72 2.105
93
PRP027 Peripheral Vascular Disease 71 2.097
94
CRV035 Cervical Cancer 72 2.093
95
c SML038 Small Cell Cancer of the Lung 68 2.069
96
P PHC003 Pheochromocytoma 70 2.067
97
ADR040 Adrenal Gland Pheochromocytoma 45 2.067
98
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 2.038
99
ALL014 Allergic Encephalomyelitis 34 2.028
100
c OVR114 Ovarian Cancer 1 60 2.007
101
P HRP006 Herpes Simplex 65 2.002
102
WRN001 Werner Syndrome 69 1.998
103
P SPP010 Suppressor of Tumorigenicity 3 50 1.996
104
P NTR004 Neutropenia 62 1.987
105
P ATR011 Atrial Fibrillation 66 1.977
106
P PLM036 Pulmonary Fibrosis 65 1.974
107
c FNC027 Fanconi Anemia, Complementation Group a 80 1.963
108
PNC041 Pancreatic Ductal Adenocarcinoma 51 1.952
109
TRN015 Transient Cerebral Ischemia 62 1.935
110
SKN019 Skin Melanoma 70 1.928
111
P VNW001 Von Willebrand's Disease 64 1.923
112
STR067 Stroke, Ischemic 79 1.923
113
MDD018 Middle East Respiratory Syndrome 44 1.916
114
c HYP836 Hypercholesterolemia, Familial, 1 73 1.903
115
SPN186 Spinal Cord Injury 60 1.899
116
NNL005 Non-Alcoholic Fatty Liver Disease 63 1.896
117
RNL114 Renal Cell Carcinoma, Nonpapillary 79 1.894
118
P HPT023 Hepatocellular Carcinoma 95 1.891
119
SFT003 Soft Tissue Sarcoma 43 1.890
120
HMN044 Human Immunodeficiency Virus Type 1 76 1.873
121
P PLM037 Pulmonary Hypertension 69 1.873
123
ANG054 Angina Pectoris 65 1.842
124
P PRP019 Peripheral Nervous System Disease 57 1.842
125
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.841
126
c MCR133 Microvascular Complications of Diabetes 4 41 1.836
127
c MCR113 Microvascular Complications of Diabetes 3 52 1.836
128
c MCR130 Microvascular Complications of Diabetes 6 41 1.836
129
c MCR120 Microvascular Complications of Diabetes 7 47 1.836
130
BNR002 Bone Resorption Disease 47 1.826
131
BRK010 Burkitt Lymphoma 65 1.826
132
P TMR010 Tumor Predisposition Syndrome 69 1.825
133
P GLN011 Glanzmann Thrombasthenia 1 66 1.824
134
CTN028 Cutaneous Telangiectasia and Cancer Syndrome, Familial 70 1.813
135
INH023 Inherited Cancer-Predisposing Syndrome 53 1.813
136
ASP030 Aspirin Resistance 41 1.809
137
P ALZ034 Alzheimer Disease 87 1.796
138
PRM329 Premature Aging 36 1.794
139
c HYP595 Hypertension, Essential 84 1.787
140
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 1.781
141
P PRS038 Personality Disorder 65 1.778
142
P CRD119 Cardiac Arrest 68 1.778
143
CYS001 Cystic Fibrosis 77 1.771
144
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.765
145
P RTN024 Retinoblastoma 72 1.749
146
BLD053 Blood Platelet Disease 51 1.741
147
STM007 Stomatitis 52 1.741
148
P BNG032 Benign Mesothelioma 53 1.732
149
TTN003 Tetanus 64 1.732
150
SVR004 Severe Combined Immunodeficiency 70 1.718
151
P RTN016 Retinal Degeneration 52 1.718
152
P LYM118 Lymphoma 66 1.716
153
P LVR013 Liver Disease 68 1.713
154
P ENC004 Encephalitis 61 1.713
155
c TYP009 Type 2 Diabetes Mellitus 91 1.699
156
FTT001 Fatty Liver Disease 61 1.694
157
PRS047 Prostatitis 57 1.672
158
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.661
159
PPL052 Papillomatosis, Confluent and Reticulated 34 1.655
160
c LKM005 Leukemia, T-Cell, Chronic 33 1.654
161
ATM095 Autoimmune Disease 61 1.646
162
ANT024 Anthrax Disease 57 1.645
163
c PCH010 Pachyonychia Congenita 3 43 1.643
164
ACT098 Acute Erythroid Leukemia 55 1.640
165
P PRK039 Parkinsonism 55 1.634
166
TRT001 Teratocarcinoma 41 1.634
167
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.624
168
P PRK057 Parkinson Disease, Late-Onset 79 1.615
169
P HNT016 Huntington Disease 73 1.614
170
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.608
171
ORL011 Oral Cancer 60 1.606
172
LNG099 Lung Disease 62 1.601
173
MTC005 Mitochondrial Metabolism Disease 44 1.597
174
c PRS130 Prostate Cancer, Hereditary, 8 32 1.593
175
c PRS136 Prostate Cancer, Hereditary, 6 33 1.593
176
ANT039 Antisynthetase Syndrome 55 1.593
177
GLS001 Gliosarcoma 63 1.590
178
c LKM063 Leukemia, Chronic Myeloid 70 1.588
179
P ESS003 Essential Thrombocythemia 68 1.583
180
P FML011 Familial Adenomatous Polyposis 70 1.582
181
c THY107 Thymoma, Familial 42 1.581
182
P THY023 Thymoma 64 1.581
183
c ACT071 Acute Kidney Failure 60 1.580
184
CHK001 Chikungunya 60 1.574
185
P PLY018 Polycythemia 56 1.567
186
CLT003 Colitis 63 1.562
187
ATH013 Atherosclerosis Susceptibility 63 1.561
188
THR004 Thrombocytosis 52 1.557
189
HYP056 Hypoglycemia 65 1.552
190
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 1.548
191
PNC129 Pancreatic Adenocarcinoma 64 1.547
192
P KDN018 Kidney Disease 71 1.545
193
P PRD008 Periodontitis 63 1.534
194
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 8 1.533
195
P MYC008 Myocarditis 59 1.529
196
PLY001 Polycythemia Vera 69 1.524
197
P CRD246 Cardiovascular System Disease 55 1.519
198
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.518
199
c HPT073 Hepatitis C Virus 70 1.518
200
P MTC133 Mitochondrial Myopathy 51 1.514
201
c CHR684 Chronic Kidney Disease 73 1.504
202
P BLD134 Bladder Cancer 79 1.502
203
DFC004 Deficiency Anemia 74 1.496
204
P NSP012 Nasopharyngeal Carcinoma 60 1.496
205
HYP060 Hyperinsulinism 53 1.493
206
LRY018 Laryngeal Squamous Cell Carcinoma 47 1.470
207
c SCL052 Scleroderma, Familial Progressive 60 1.466
208
P LKM062 Leukemia, Acute Lymphoblastic 69 1.456
209
P HYP076 Hyperthyroidism 53 1.455
210
PLR008 Pleurisy 49 1.454
211
P HDC001 Headache 56 1.450
212
P HYP086 Hypothyroidism 68 1.450
213
PPL022 Papilloma 53 1.448
214
SQM002 Squamous Cell Papilloma 45 1.448
215
c HPT001 Hepatitis C 61 1.448
216
P RTN008 Retinitis Pigmentosa 79 1.435
217
IMM167 Immune Deficiency Disease 76 1.434
218
P CCK001 Cockayne Syndrome 67 1.433
219
GST045 Gastroenteritis 58 1.425
220
VCC001 Vaccinia 49 1.423
221
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.418
222
ACT119 Acute Promyelocytic Leukemia 62 1.412
223
BRN004 Brain Edema 54 1.409
224
P HRM001 Hermansky-Pudlak Syndrome 65 1.407
225
P BRN019 Bernard-Soulier Syndrome 61 1.405
226
P SKN015 Skin Carcinoma 71 1.405
227
VNZ002 Venezuelan Equine Encephalitis 45 1.402
228
ORL015 Oral Squamous Cell Carcinoma 43 1.397
229
P PNM007 Pneumonia 64 1.396
230
P INF038 Influenza 68 1.384
231
ACT003 Acute Kidney Tubular Necrosis 46 1.383
232
P DBT009 Diabetes Mellitus 67 1.381
233
c HPT007 Hepatitis E 50 1.381
234
CLN015 Colon Adenocarcinoma 64 1.378
235
P ANR048 Aniridia 1 66 1.374
236
P MLN007 Male Infertility 56 1.366
237
NRR001 Neuroretinitis 42 1.354
238
RTN023 Retinitis 45 1.354
239
MLG079 Malignant Pleural Mesothelioma 42 1.353
240
AVD001 Avoidant Personality Disorder 49 1.348
241
DFF005 Diffuse Large B-Cell Lymphoma 55 1.344
242
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.341
243
c PRC016 Pre-Eclampsia 64 1.341
244
CRN017 Coronary Thrombosis 46 1.320
245
P RHB003 Rhabdomyosarcoma 66 1.319
246
P EXN002 Exanthem 58 1.310
247
P MTC069 Mitochondrial Disorders 57 1.304
248
BCT022 Bacterial Infectious Disease 55 1.302
249
c SPR009 Sporadic Breast Cancer 42 1.301
250
c MJR022 Major Affective Disorder 8 37 1.295
251
c MJR024 Major Affective Disorder 9 40 1.295
252
P BPL003 Bipolar Disorder 56 1.295
253
P FBR017 Fibrosarcoma 55 1.293
254
LYM143 Lymphoma, Non-Hodgkin, Familial 74 1.291
255
c TYP008 Type 1 Diabetes Mellitus 77 1.282
256
PLY150 Polykaryocytosis Inducer 29 1.281
257
GST040 Gastric Adenocarcinoma 66 1.277
258
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 1.275
259
P BNG030 Benign Ependymoma 51 1.273
260
CLL010 Cellular Ependymoma 58 1.273
261
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.270
262
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.270
263
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.270
264
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.270
265
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.270
266
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.270
267
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 1.270
268
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.270
269
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.270
270
P RHM011 Rheumatoid Arthritis 81 1.266
271
ARG004 Argyria 26 1.266
272
P LPS002 Liposarcoma 64 1.261
273
INS024 Insulin-Like Growth Factor I 77 1.256
274
P INF037 Inflammatory Bowel Disease 53 1.253
275
P ENC018 Encephalopathy 62 1.251
276
SKN016 Skin Disease 63 1.251
277
c BRN108 Branchiootic Syndrome 1 63 1.246
278
CHL123 Chlamydia 58 1.246
279
P MYC084 Mycobacterium Tuberculosis 1 68 1.243
280
URM002 Uremia 47 1.242
281
HMC014 Homocysteinemia 52 1.240
282
MXD026 Mixed Glioma 45 1.239
283
P LCT001 Lactic Acidosis 50 1.237
284
STR089 Storage Pool Platelet Disease 46 1.231
285
AND005 Androgen Insensitivity Syndrome, Mild 21 1.227
286
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 1.221
287
P MLN069 Melanoma, Uveal 59 1.215
288
P ADL010 Adult Respiratory Distress Syndrome 70 1.210
289
c THR090 Thrombocythemia 1 50 1.208
290
P HYP061 Hypertrophic Cardiomyopathy 68 1.207
291
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 1.195
292
c FNC042 Fanconi Anemia, Complementation Group D2 54 1.192
293
c THR092 Thrombophilia Due to Thrombin Defect 74 1.191
294
PLT033 Platelet Signal Processing Defect 9 1.190
295
P KDN017 Kidney Cancer 60 1.177
296
P DRR001 Diarrhea 55 1.175
297
P MSC005 Muscular Dystrophy 66 1.175
298
ART016 Aortic Aneurysm 68 1.174
299
c LRG001 Large Cell Carcinoma 48 1.174
300
P XRD029 Xeroderma Pigmentosum, Complementation Group a 55 1.173
301
P AST005 Asthma 75 1.173
302
P ANT006 Antiphospholipid Syndrome 55 1.167
303
P ART022 Arthritis 70 1.160
304
P ART021 Arteriosclerosis 53 1.159
305
RHB024 Rhabdomyosarcoma 2 65 1.158
306
P EPN001 Ependymoblastoma 44 1.158
307
IMP005 Impotence 52 1.154
308
P GST044 Gastritis 55 1.152
309
PLS011 Plasmacytoma 56 1.152
310
HPR003 Heparin-Induced Thrombocytopenia 47 1.152
311
P CTN015 Cutaneous T Cell Lymphoma 48 1.152
312
CLR109 Colorectal Adenocarcinoma 50 1.145
313
ANR040 Aneurysm 60 1.145
314
HYP114 Hypertensive Nephropathy 35 1.143
315
AZS001 Azoospermia 45 1.143
316
P SCK005 Sickle Cell Disease 56 1.136
317
CRH001 Crohn's Disease 80 1.134
318
P ADL017 Adult T-Cell Leukemia 53 1.125
319
OST012 Osteoarthritis 77 1.118
320
LYM133 Lymphoma, Hodgkin, Classic 69 1.116
321
c HPT016 Hepatitis B 62 1.105
322
P RCT021 Rectum Cancer 54 1.096
323
FLL027 Fallopian Tube Carcinoma 66 1.096
324
DWN001 Down Syndrome 70 1.084
325
c PNS012 Paine Syndrome 60 1.079
326
ADL002 Adult Syndrome 69 1.079
327
P MLG074 Malignant Mesenchymoma 40 1.079
328
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 1.079
329
LMB062 Limb Ischemia 55 1.079
330
BRN024 Bronchitis 67 1.079
331
P LMY004 Leiomyosarcoma 62 1.075
332
HMT002 Hematologic Cancer 61 1.075
333
PRT251 Proteinuria, Chronic Benign 58 1.074
334
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.071
335
KPS004 Kaposi Sarcoma 76 1.069
336
MTB004 Metabolic Acidosis 48 1.067
337
KRN002 Kearns-Sayre Syndrome 62 1.067
338
P HPT021 Hepatitis 68 1.060
339
P RTN018 Retinal Disease 53 1.060
340
ALL006 Allergic Asthma 55 1.060
341
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.057
342
CRT015 Carotid Artery Occlusion 45 1.054
343
c BRS111 Breast-Ovarian Cancer, Familial 2 53 1.050
344
PHS014 Phosphoglycerate Kinase 1 Deficiency 46 1.049
345
MNT001 Mantle Cell Lymphoma 65 1.047
346
P RHN004 Rhinitis 56 1.040
347
RTN003 Retinal Ischemia 48 1.040
348
P CTR002 Cataract 59 1.040
349
CHD001 Chediak-Higashi Syndrome 66 1.037
350
ATS010 Autosomal Recessive Disease 42 1.032
351
P HYP098 Hypereosinophilic Syndrome 66 1.032
352
LNG039 Lung Squamous Cell Carcinoma 57 1.027
353
BRN028 Brain Cancer 73 1.027
354
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 1.026
355
CRN030 Coronary Stenosis 50 1.025
356
LYM027 Lymphopenia 56 1.018
357
c CHR095 Chronic Progressive External Ophthalmoplegia 48 1.018
358
THY029 Thyroid Carcinoma 55 1.016
359
ADN018 Adenoma 58 1.010
360
MNN043 Meningioma, Familial 79 1.007
361
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.007
362
SCR001 Secretory Meningioma 40 1.007
363
INT395 Intracranial Meningioma 47 1.007
364
RHB001 Rhabdoid Cancer 68 1.007
365
CHL068 Cholestasis 61 1.003
366
OCL069 Ocular Motor Apraxia 57 1.000
367
ALL003 Allergic Rhinitis 66 0.996
368
HTC003 Hutchinson-Gilford Progeria Syndrome 65 0.996
369
P THR015 Thrombophilia 51 0.995
370
c MST023 Mesothelioma, Malignant 56 0.987
371
GST033 Gestational Diabetes 60 0.987
372
ENT011 Enterocolitis 55 0.984
373
P BRD002 Bardet-Biedl Syndrome 66 0.984
374
GRM010 Germ Cells Tumors 33 0.983
375
P CNR004 Cone-Rod Dystrophy 2 74 0.982
376
ANP005 Anaplastic Astrocytoma 59 0.982
377
P ESP024 Esophagitis 60 0.982
378
PRP080 Peripheral Artery Disease 54 0.972
379
CHG001 Chagas Disease 65 0.972
380
CRB090 Cerebral Hypoxia 42 0.962
381
CRD137 Cardiogenic Shock 56 0.962
382
QBC001 Quebec Platelet Disorder 43 0.956
383
ALC007 Alcohol Dependence 65 0.956
384
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 0.953
385
P OLG002 Oligodendroglioma 66 0.949
386
ATY005 Atypical Teratoid Rhabdoid Tumor 69 0.949
387
P ECL001 Eclampsia 52 0.948
388
GLC003 Glucose Intolerance 53 0.948
389
P SRC025 Sarcoidosis 1 70 0.948
390
c LKM070 Leukemia, Acute Monocytic 56 0.948
391
P CNJ013 Conjunctivitis 66 0.948
392
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.936
393
DSS009 Disseminated Intravascular Coagulation 56 0.936
394
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 0.935
395
VRL011 Viral Infectious Disease 60 0.928
396
ANG020 Angiosarcoma 63 0.926
397
c TBR025 Tuberous Sclerosis 1 84 0.926
398
P CHR285 Chronic Myelomonocytic Leukemia 59 0.926
399
CNS004 Constipation 56 0.925
400
P NNT058 Neonatal Diabetes 52 0.925
401
HMP009 Haemophilus Influenzae 41 0.925
402
P DRM053 Dermatitis, Atopic 65 0.916
403
CWP001 Cowpox 44 0.916
404
PLM033 Pulmonary Embolism 58 0.911
405
DSS032 Disease by Infectious Agent 55 0.906
406
P UVT001 Uveitis 57 0.906
407
P PRN023 Prion Disease 60 0.906
408
P MNN013 Meningitis 65 0.906
409
CLS016 Clostridium Difficile Colitis 49 0.905
410
MYC006 Mycosis Fungoides 64 0.901
411
c WLF009 Wolfram Syndrome 2 43 0.900
412
c HRM009 Hermansky-Pudlak Syndrome 6 46 0.900
413
P MSC003 Muscular Atrophy 52 0.898
414
RTN020 Retinal Vascular Disease 45 0.895
415
RNL077 Renal Fibrosis 46 0.884
416
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 0.884
417
CNN005 Connective Tissue Disease 66 0.884
418
PLM010 Pulmonary Edema 54 0.884
419
IRN002 Iron Metabolism Disease 56 0.879
420
ACR013 Acrodysostosis 53 0.873
421
MSC157 Muscular Dystrophy, Duchenne Type 78 0.871
422
P GLM007 Glomerulonephritis 59 0.871
423
MNN042 Meningioma, Radiation-Induced 51 0.870
424
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.870
425
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.870
426
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.870
427
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.870
428
P PNB001 Pineoblastoma 49 0.870
429
CYS009 Cystadenoma 42 0.870
430
PNL014 Pineal Gland Cancer 40 0.870
431
P TRN020 Turner Syndrome 67 0.870
432
CNT033 Central Nervous System Cancer 47 0.870
433
CRN036 Craniopharyngioma 63 0.870
434
P NRV006 Nervous System Cancer 47 0.870
435
SPN021 Spinal Meningioma 43 0.870
436
SPN040 Spinal Cancer 44 0.870
437
P CHR573 Choroid Plexus Cancer 48 0.870
438
PNC056 Pineocytoma 44 0.870
439
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.870
440
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.869
441
LYM007 Lymphangioleiomyomatosis 68 0.861
442
P JBR020 Joubert Syndrome 1 74 0.861
443
DBT007 Diabetic Cataract 36 0.861
444
THY030 Thyroid Gland Disease 50 0.861
445
c BCT007 Bacterial Meningitis 55 0.861
446
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.861
447
CNG034 Congestive Heart Failure 69 0.857
448
GRY002 Gray Platelet Syndrome 57 0.850
449
P LPR021 Leprosy 3 71 0.849
450
c VRL010 Viral Hepatitis 52 0.849
451
SCB001 Scabies 49 0.849
452
HNS001 Hansen's Disease 32 0.849
453
P DBT005 Diabetes Insipidus 54 0.849
454
STT001 Status Epilepticus 58 0.842
455
c HRM017 Hermansky-Pudlak Syndrome 2 55 0.842
456
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 42 0.842
457
P ACN011 Acne 55 0.840
458
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.836
459
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.836
460
SCK003 Sickle Cell Anemia 74 0.835
461
P HMR003 Hemorrhagic Disease 59 0.835
462
P DMN002 Dementia 65 0.835
463
P SZR006 Seizure Disorder 69 0.835
464
c ACT073 Acute Leukemia 59 0.827
465
P SLM003 Salmonellosis 54 0.823
466
TYP007 Typhoid Fever 63 0.823
467
MST005 Mastitis 52 0.823
468
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.820
469
PNG002 Pain Agnosia 51 0.819
471
P KLZ004 Kala-Azar 1 41 0.819
472
LSH001 Leishmaniasis 63 0.819
473
P SLP006 Sleep Apnea 69 0.811
474
HMS001 Hemosiderosis 48 0.811
475
MST004 Mast Cell Neoplasm 41 0.811
476
EXT007 Extracutaneous Mastocytoma 38 0.811
477
P RRH023 Rare Hereditary Hemochromatosis 52 0.811
478
c BRS110 Breast-Ovarian Cancer, Familial 1 57 0.808
479
P PTS002 Ptosis 52 0.808
480
c ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.808
481
AFB002 Afibrinogenemia, Congenital 63 0.803
482
ADN001 Adenosine Deaminase Deficiency 59 0.803
483
P MNC007 Monocytic Leukemia 48 0.803
484
MYL005 Myelofibrosis 70 0.799
485
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.795
486
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.795
487
P OPT006 Optic Nerve Disease 57 0.795
488
P GRV001 Graves' Disease 54 0.795
489
SCH014 Schistosomiasis 56 0.795
490
P FRG001 Fragile X Syndrome 70 0.793
491
PRM013 Premature Menopause 57 0.793
492
VRC001 Varicocele 48 0.793
493
CHL065 Cholangiocarcinoma 57 0.792
494
INT079 Intrahepatic Cholangiocarcinoma 51 0.792
495
P MYS003 Myasthenia Gravis 67 0.786
496
SLP001 Sleeping Sickness 56 0.786
497
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 0.777
498
CRD132 Cardiac Conduction Defect 59 0.777
499
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.777
500
PHN003 Phenylketonuria 76 0.777
501
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.777
502
GST023 Gastric Ulcer 52 0.777
503
P MCR010 Microcephaly 59 0.777
504
P EYD002 Eye Disease 57 0.769
505
PRS045 Prostatic Hypertrophy 53 0.769
506
P INF032 Infertility 60 0.769
507
BRN132 Bernard-Soulier Syndrome, Type A2, Autosomal Dominant 23 0.763
508
c BLD133 Bleeding Disorder, Platelet-Type, 20 27 0.763
509
c THR125 Thrombocytopenia 7 22 0.763
510
MYL031 Myeloproliferative Neoplasm 66 0.761
511
P SNS001 Sensorineural Hearing Loss 60 0.759
512
GSG001 Gas Gangrene 52 0.759
513
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.759
514
CNT047 Contact Dermatitis 56 0.757
515
LKS001 Leukostasis 40 0.757
516
P MJR007 Major Affective Disorder 1 42 0.750
517
LGH007 Leigh Syndrome 70 0.750
518
P MLT020 Multiple Sclerosis 79 0.750
519
P DNG005 Dengue Virus 55 0.750
520
URT010 Ureteral Obstruction 44 0.750
521
PRS021 Prostatic Adenoma 43 0.750
522
P HYP265 Hypotonia 42 0.750
523
BCK006 Back Pain 43 0.742
524
PRS129 Prostatic Hyperplasia, Benign 48 0.740
525
P END044 Endometriosis 62 0.740
526
P ART018 Aortic Valve Insufficiency 52 0.740
527
PPT005 Peptic Ulcer Disease 58 0.740
528
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.740
529
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.737
530
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 0.736
531
P SJG008 Sjogren Syndrome 60 0.736
532
VTM033 Vitamin K Deficiency Bleeding 49 0.736
533
TTR011 Tetraploidy 43 0.736
534
INT358 Intestinal Polyposis Syndrome 26 0.736
535
PLT031 Platelet Membrane Fluidity 28 0.730
536
c RTN047 Retinitis Pigmentosa 18 45 0.730
537
P PRV002 Periventricular Nodular Heterotopia 52 0.730
538
HYP020 Hyperprolactinemia 63 0.730
539
MLD001 Melioidosis 67 0.730
540
PST011 Pustulosis of Palm and Sole 52 0.730
541
LWC001 Low Compliance Bladder 44 0.730
542
P HML001 Hemolytic-Uremic Syndrome 52 0.730
543
LYM019 Lymphosarcoma 46 0.728
544
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 0.720
545
NRD058 Neurodegeneration, Childhood-Onset, Stress-Induced, with Variable Ataxia and Seizures 27 0.720
546
P GRF003 Graft-Versus-Host Disease 71 0.720
547
c FML021 Familial Hypercholesterolemia 71 0.720
548
NRM005 Neuromuscular Disease 62 0.720
549
c ACT134 Acute Liver Failure 57 0.720
550
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.713
551
c FML001 Familial Atrial Fibrillation 65 0.713
552
KDN013 Kidney Hypertrophy 33 0.711
553
FRN006 Frontotemporal Dementia 68 0.709
554
TRY001 Trypanosomiasis 50 0.709
555
THY128 Thyroid Tumor 33 0.709
556
P RSP003 Respiratory Failure 73 0.709
557
P PSD015 Pseudohypoparathyroidism 54 0.709
558
c SVR005 Severe Pre-Eclampsia 49 0.709
559
P PSR002 Psoriasis 63 0.709
560
RNL065 Renal Cell Carcinoma, Papillary, 1 79 0.699
561
PCH007 Pouchitis 42 0.698
562
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.698
563
GLL008 Gilles De La Tourette Syndrome 64 0.698
564
BLM001 Bloom Syndrome 65 0.698
565
c ART101 Aortic Valve Disease 2 65 0.698
566
c OPT053 Optic Atrophy 1 62 0.698
567
EMB004 Embryonal Carcinoma 55 0.698
568
c MGR028 Migraine with or Without Aura 1 63 0.694
569
HRY003 Hairy Cell Leukemia 53 0.692
570
LPD008 Lipid Metabolism Disorder 61 0.690
571
P MCR129 Microvascular Complications of Diabetes 1 67 0.686
572
c MCR112 Microvascular Complications of Diabetes 2 42 0.686
573
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 0.686
574
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 0.686
575
EHR002 Ehrlichiosis 39 0.686
576
P MTC010 Mitochondrial Dna Depletion Syndrome 46 0.686
577
P RTN022 Retinal Vein Occlusion 54 0.686
578
P PLY011 Polycystic Ovary Syndrome 57 0.686
579
SNS003 Sensory Peripheral Neuropathy 51 0.686
580
P MLG056 Malignant Hyperthermia 65 0.686
581
DPR016 Depression 64 0.686
582
P CHN012 Chondrosarcoma 56 0.674
583
MNT002 Mental Depression 56 0.674
584
GLM044 Glomerular Disease 34 0.674
585
MST020 Mast Cell Activation Syndrome 27 0.674
586
PRP030 Purpura 54 0.671
587
SRC027 Sarcoma, Synovial 58 0.662
588
LNG095 Lung Abscess 50 0.661
589
c RTN032 Retinal Cone Dystrophy 1 24 0.661
590
TST044 Testicular Torsion 45 0.661
591
P MJR001 Major Depressive Disorder 68 0.661
592
P PLY019 Polyneuropathy 52 0.661
593
CRV040 Cervix Carcinoma 50 0.661
594
MCR013 Microphthalmia 59 0.661
595
MMM001 Mammary Paget's Disease 53 0.661
596
PLG002 Plague 58 0.661
597
PLY100 Polyploidy 36 0.661
598
CLP005 Ciliopathy 40 0.661
599
P TRM003 Tremor 50 0.661
600
P OVR082 Overgrowth Syndrome 41 0.661
601
HPT022 Hepatoblastoma 54 0.651
602
APR001 Apraxia 51 0.647
603
P NJM001 Nijmegen Breakage Syndrome 75 0.647
604
P LFT003 Left Ventricular Noncompaction 58 0.647
605
SLC006 Silicosis 55 0.647
606
P TBR001 Tuberous Sclerosis 69 0.647
607
FLL031 Follicular Adenoma 40 0.647
608
END041 Endometrial Adenocarcinoma 63 0.647
609
DMY004 Demyelinating Disease 50 0.647
610
CHL045 Choline Deficiency Disease 39 0.647
611
FML304 Familial Isolated Dilated Cardiomyopathy 50 0.647
612
TRN018 Transitional Cell Carcinoma 56 0.640
613
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.633
614
P STR022 Stargardt Disease 61 0.633
615
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 59 0.633
616
c EXD008 Exudative Vitreoretinopathy 1 71 0.633
617
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.633
618
P ZNC008 Zinc Finger Protein 1 22 0.633
619
P PLY014 Polycystic Kidney Disease 71 0.633
620
P CYS018 Cystitis 58 0.633
621
PPL002 Papillary Carcinoma 46 0.633
622
BLR008 Bilirubin Metabolic Disorder 57 0.633
623
P HMN010 Hemangioma 61 0.633
624
MTH009 Mouth Disease 57 0.633
625
MLT006 Multidrug-Resistant Tuberculosis 47 0.633
626
P GLL022 Guillain-Barre Syndrome 59 0.633
627
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.633
628
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.628
629
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.617
630
P RTT002 Rett Syndrome 79 0.617
631
c CRD097 Cardiomyopathy, Dilated, 1d 47 0.617
632
MSC007 Muscle Hypertrophy 64 0.617
633
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.617
634
c BRD015 Bardet-Biedl Syndrome 3 49 0.617
635
c FML347 Familial Adenomatous Polyposis 2 56 0.617
636
c CRD098 Cardiomyopathy, Familial Restrictive, 3 35 0.617
637
P PLY041 Polymyositis 58 0.617
638
DNT012 Dental Caries 53 0.617
639
BRN014 Bronchopneumonia 52 0.617
640
P PST095 Post-Thrombotic Syndrome 51 0.617
641
SKN020 Skin Papilloma 40 0.617
642
P DRM010 Dermatomyositis 61 0.617
643
MXD005 Mixed Connective Tissue Disease 57 0.617
644
P ATR005 Atrophic Gastritis 50 0.617
645
P TXP001 Toxoplasmosis 59 0.617
646
IQS001 Iqsec2 19 0.617
647
RCR030 Recurrent Idiopathic Neuroretinitis 11 0.617
648
FML293 Familial Isolated Restrictive Cardiomyopathy 42 0.617
649
CLR030 Clear Cell Renal Cell Carcinoma 53 0.616
650
END086 End Stage Renal Disease 54 0.608
651
CHL028 Childhood Type Dermatomyositis 58 0.608
652
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 0.601
653
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.601
654
INC018 Inclusion Body Myopathy with Paget Disease of Bone and Frontotemporal Dementia 51 0.601
655
CHR072 Chordoma 56 0.601
656
P INC029 Inclusion Body Myopathy with Early-Onset Paget Disease with or Without Frontotemporal Dementia 1 38 0.601
657
P PLV020 Pelvic Organ Prolapse 57 0.601
658
LSC001 Lesch-Nyhan Syndrome 62 0.601
659
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 0.601
660
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.601
661
c FML299 Familial Adenomatous Polyposis 3 28 0.601
662
c RTN210 Retinitis Pigmentosa 50 37 0.601
663
c FML339 Familial Adenomatous Polyposis 4 31 0.601
664
P SPR119 Spermatogenic Failure, X-Linked, 1 36 0.601
665
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.601
666
c FRN060 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 6 28 0.601
667
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 64 0.601
668
P FNC044 Fanconi Anemia, Complementation Group C 56 0.601
669
c DFN196 Deafness, Autosomal Dominant 22 43 0.601
670
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 26 0.601
671
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.601
672
ASB001 Asbestosis 47 0.601
673
HND002 Hand, Foot and Mouth Disease 50 0.601
674
P OVR106 Ovarian Clear Cell Carcinoma 42 0.601
675
P INT068 Intestinal Disease 53 0.601
676
AVN001 Avian Influenza 61 0.601
677
ATN004 Autonomic Neuropathy 42 0.601
678
CRY003 Cryptosporidiosis 55 0.601
679
SCR011 Scrapie 39 0.601
680
ADR008 Adrenal Adenoma 55 0.601
681
P RBL001 Rubella 58 0.601
682
ACT200 Acute Monoblastic Leukemia 40 0.601
683
c DFN024 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 22 14 0.601
684
ASB003 Asbestos Intoxication 32 0.601
685
NRN004 Neuroendocrine Tumor 55 0.590
686
CRT004 Carotid Artery Thrombosis 39 0.587
687
P NNS032 Non-Syndromic X-Linked Intellectual Disability 46 0.582
688
MCK005 Mckusick-Kaufman Syndrome 61 0.582
689
P PLY006 Polydactyly 58 0.582
690
KRT019 Keratitis, Hereditary 66 0.582
691
P LFR001 Li-Fraumeni Syndrome 73 0.582
692
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.582
693
WST005 West Nile Virus 55 0.582
694
DSS010 Dissociative Disorder 39 0.582
695
RHM028 Rheumatic Heart Disease 55 0.582
696
HRT012 Heart Valve Disease 53 0.582
697
ART006 Arthus Reaction 40 0.582
698
LYS002 Lysosomal Storage Disease 51 0.582
699
ASP003 Aseptic Meningitis 50 0.582
700
DBT002 Diabetic Autonomic Neuropathy 40 0.582
701
HYP043 Hyperandrogenism 47 0.582
702
DBT004 Diabetic Polyneuropathy 50 0.582
703
P TYR004 Tyrosinemia 49 0.582
704
FSC004 Fasciitis 49 0.582
705
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 0.582
706
NRN046 Neuronal Tumor 19 0.582
707
OCL015 Oculomotor Apraxia 39 0.582
708
c CHR417 Chronic Graft Versus Host Disease 55 0.582
709
c NRB010 Neuroblastoma 1 59 0.576
710
P PRG013 Paraganglioma 57 0.575
711
P GLL018 Gallbladder Cancer 59 0.575
712
SYN007 Synovitis 54 0.575
713
CRC021 Carcinosarcoma 62 0.575
714
PLC002 Plica Syndrome 35 0.575
715
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.575
716
c MTC059 Mitochondrial Dna Depletion Syndrome 5 49 0.561
717
c HMC039 Hemochromatosis, Type 1 73 0.561
718
HRN029 Hearing Loss, Noise-Induced 37 0.561
719
P CRN024 Corneal Disease 43 0.561
720
INP001 Inappropriate Adh Syndrome 48 0.561
721
P MTR014 Motor Neuron Disease 65 0.561
722
ENT004 Enthesopathy 51 0.561
723
HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.561
724
SHW001 Shwartzman Phenomenon 36 0.561
725
ALL010 Allergic Contact Dermatitis 55 0.561
726
END062 Endometrial Hyperplasia 47 0.561
727
PCD001 Pica Disease 38 0.561
728
BRS051 Breast Disease 58 0.561
729
c JVN010 Juvenile Rheumatoid Arthritis 52 0.561
730
YLL002 Yellow Fever 61 0.561
731
CRV002 Cervix Uteri Carcinoma in Situ 48 0.561
732
MCR141 Mucormycosis 59 0.561
733
MYC013 Mycobacterium Abscessus 42 0.561
734
P PRM011 Primary Ciliary Dyskinesia 68 0.561
735
STS002 Situs Inversus 44 0.561
736
NNT024 Neonatal Stroke 31 0.561
737
NCR007 Necrotizing Fasciitis 48 0.561
738
CRV045 Cervical Intraepithelial Neoplasia 38 0.561
739
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.561
740
SPP011 Suppression of Tumorigenicity 12 61 0.560
741
HYP005 Hypokalemia 55 0.560
743
c TBR026 Tuberous Sclerosis 2 71 0.543
744
FCT007 Factor Vii Deficiency 64 0.543
745
P FLL037 Follicular Lymphoma 66 0.543
746
PNC001 Pancytopenia 52 0.543
747
INT066 Interstitial Lung Disease 60 0.543
748
NSP002 Nasopharyngitis 45 0.543
749
c JBR047 Joubert Syndrome 35 23 0.536
750
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 60 0.536
751
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 66 0.536
752
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 57 0.536
753
c RTN090 Retinitis Pigmentosa 55 39 0.536
754
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 0.536
755
c PNC106 Pancreatic Agenesis 1 51 0.536
756
P KBK002 Kabuki Syndrome 1 66 0.536
757
c MTC060 Mitochondrial Dna Depletion Syndrome 9 51 0.536
758
c LFR007 Li-Fraumeni Syndrome 2 45 0.536
759
NST002 Nestor-Guillermo Progeria Syndrome 35 0.536
760
CHL131 Chlorpropamide-Alcohol Flushing 21 0.536
761
c PRK085 Parkinson Disease 1, Autosomal Dominant 50 0.536
762
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.536
763
c ACT249 Acute Asthma 40 0.536
764
P OST001 Osteopetrosis 70 0.536
765
BLD163 Blood Group, Dombrock System 16 0.536
766
SMN007 Seminoma 42 0.536
767
PNC034 Pancreas Disease 49 0.536
768
c ESS001 Essential Tremor 56 0.536
769
MRK001 Merkel Cell Carcinoma 64 0.536
770
CHL018 Childhood Medulloblastoma 48 0.536
771
P HLP001 Holoprosencephaly 68 0.536
772
CHR073 Choreatic Disease 53 0.536
773
MLG077 Malignant Peripheral Nerve Sheath Tumor 53 0.536
774
BRN018 Borna Disease 36 0.536
775
ISL099 Isolated Methylmalonic Acidemia 35 0.536
776
APH001 Aphthous Stomatitis 57 0.536
777
AMB001 Amebiasis 56 0.536
778
PRN019 Perinatal Necrotizing Enterocolitis 60 0.536
779
SYS071 Systemic Autoimmune Disease 35 0.536
780
PNM013 Pneumococcal Meningitis 43 0.536
781
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.536
782
LVR012 Liver Cirrhosis 62 0.531
783
P LRY044 Larynx Cancer 53 0.524
784
P BNC003 Bone Cancer 58 0.524
785
P CRV031 Cervical Adenocarcinoma 48 0.524
786
TST014 Testicular Cancer 51 0.524
787
MYX005 Myxoid Liposarcoma 65 0.504
788
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 34 0.504
789
CLL004 Cellular Myxoid Liposarcoma 30 0.504
790
MXD006 Mixed Liposarcoma 30 0.504
791
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 35 0.504
792
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.503
793
c WLM013 Wilms Tumor 1 65 0.503
794
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.503
795
GST019 Gastrointestinal Stromal Tumor 78 0.503
796
BRR014 Barrett Esophagus 66 0.503
797
RCT020 Rectum Adenocarcinoma 48 0.503
798
NRN001 Neuroendocrine Carcinoma 47 0.503
799
MCR004 Macroglobulinemia 48 0.503
800
BLR013 Biliary Tract Cancer 43 0.503
801
PRM126 Primary Peritoneal Carcinoma 61 0.503
802
P BCL004 B-Cell Non-Hodgkin Lymphoma 41 0.503
803
P RNL059 Renal-Hepatic-Pancreatic Dysplasia 34 0.503
804
HPT067 Hepatocellular Adenoma 42 0.503
805
STR033 Storm Syndrome 28 0.503
806
c OST126 Osteopetrosis, Autosomal Recessive 1 51 0.503
807
MTG002 Mutagen Sensitivity 34 0.503
809
c FNC048 Fanconi Anemia, Complementation Group O 51 0.503
810
TNP004 Tn Polyagglutination Syndrome 42 0.503
811
ASC009 Ascites, Chylous 31 0.503
812
c WLL036 Weill-Marchesani Syndrome 1 42 0.503
813
PRD041 Periodic Fever, Menstrual Cycle-Dependent 23 0.503
814
MNR012 Meniere Disease 55 0.503
815
MYL057 Myelopathy, Htlv-1-Associated 39 0.503
816
c CCK007 Cockayne Syndrome B 56 0.503
817
CHN056 Chondrosarcoma, Extraskeletal Myxoid 42 0.503
818
OBS082 Obstructive Nephropathy 41 0.503
819
HMN002 Human Granulocytic Anaplasmosis 31 0.503
820
STR077 Streptococcal Toxic-Shock Syndrome 34 0.503
821
BRN012 Bronchiolitis Obliterans 56 0.503
822
P EXT030 Extraosseous Chondrosarcoma 31 0.503
823
P MVM001 Movement Disease 61 0.503
824
BRN002 Bronchiolitis 57 0.503
825
ADR005 Adrenal Carcinoma 58 0.503
826
TST015 Testicular Disease 42 0.503
827
TRP002 Tropical Spastic Paraparesis 48 0.503
828
CRN027 Corneal Neovascularization 47 0.503
829
P MYX008 Myxoid Chondrosarcoma 28 0.503
830
LRN003 Learning Disability 49 0.503
831
UND007 Undifferentiated Connective Tissue Disease 29 0.503
832
c ATS282 Autosomal Recessive Malignant Osteopetrosis 45 0.503
833
HTL001 Htlv-1 Associated Myelopathy/tropical Spastic Paraparesis 37 0.503
834
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.503
835
ACT228 Acute Radiation Syndrome 30 0.503
836
SPS019 Spastic Paraparesis 38 0.503
837
CHR603 Chronic Enteropathy Associated with Slco2a1 Gene 25 0.503
838
INT002 Intermittent Claudication 61 0.500
839
EST002 Estrogen-Receptor Negative Breast Cancer 45 0.478
840
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 0.478
841
PRL017 Prolymphocytic Leukemia 47 0.478
842
P OVR010 Ovarian Brenner Tumor 39 0.478
843
OVR105 Ovarian Serous Carcinoma 37 0.478
844
P BLD062 Bile Duct Cancer 69 0.478
845
c CNT035 Central Nervous System Disease 53 0.478
846
CYS014 Cystadenocarcinoma 51 0.478
847
P FNC004 Fanconi Syndrome 60 0.478
848
RTC005 Reticulosarcoma 47 0.478
849
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.478
850
P NRV007 Nervous System Disease 65 0.478
851
ACT250 Acute Megakaryocytic Leukemia 63 0.478
852
MLG164 Malignant Epithelial Tumor of Ovary 24 0.478
853
P HML002 Hemolytic Anemia 62 0.468
854
EPT021 Epithelial Recurrent Erosion Dystrophy 45 0.445
855
P SML001 Small Cell Carcinoma 52 0.445
856
DYS179 Dyssegmental Dysplasia, Rolland-Desbuquois Type 25 0.445
857
CYS036 Cystinosis, Nephropathic 51 0.445
858
HRD029 Hereditary Leiomyomatosis and Renal Cell Cancer 56 0.445
859
WLD007 Waldenstroem's Macroglobulinemia 59 0.445
860
LYM012 Lymphoplasmacytic Lymphoma 50 0.445
861
SRS001 Serous Cystadenocarcinoma 51 0.445
862
SKN013 Skin Benign Neoplasm 49 0.445
863
GST071 Gastrointestinal Carcinoma 46 0.445
864
MYL075 Myelodysplastic/myeloproliferative Neoplasm 51 0.445
865
BRN015 Bronchiolo-Alveolar Adenocarcinoma 55 0.445
866
INT020 Intravenous Leiomyomatosis 35 0.445
867
LMY003 Leiomyomatosis 43 0.445
868
c INF023 Inflammatory Breast Carcinoma 48 0.445
869
P OVR049 Ovarian Disease 50 0.445
870
P DMN001 Diamond-Blackfan Anemia 73 0.445
871
GRM005 Germ Cell Cancer 46 0.445
872
ADN009 Adenosquamous Carcinoma 49 0.445
873
FNG017 Fungal Infectious Disease 54 0.445
874
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 56 0.445
875
HNT002 Hantavirus Pulmonary Syndrome 55 0.445
876
P PRT096 Peritoneal Mesothelioma 49 0.445
877
P TST026 Testicular Germ Cell Cancer 42 0.445
878
OVR044 Ovarian Carcinosarcoma 47 0.445
879
UTR024 Uterine Carcinosarcoma 58 0.445
880
LNG031 Lung Benign Neoplasm 51 0.445
881
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.445
882
SZR001 Sezary's Disease 60 0.445
883
HRD031 Hereditary Paraganglioma-Pheochromocytoma Syndromes 61 0.445
884
FHT001 Fh Tumor Predisposition Syndrome 27 0.445
885
P HYP750 Hypertriglyceridemia, Familial 61 0.441
886
P NPH012 Nephrotic Syndrome 61 0.441
887
c RTN152 Retinitis Pigmentosa 66 34 0.424
888
RTN216 Retinitis Pigmentosa 82 with or Without Situs Inversus 21 0.424
889
CRT072 Creutzfeldt-Jakob Disease 67 0.424
890
GST103 Gastric Cancer, Hereditary Diffuse 68 0.424
891
c CLR068 Ciliary Dyskinesia, Primary, 5 24 0.424
892
OCC001 Occupational Dermatitis 27 0.424
893
FLL013 Follicular Dendritic Cell Sarcoma 44 0.424
894
HPT014 Hepatorenal Syndrome 49 0.424
895
P DFF019 Diffuse Gastric Cancer 50 0.424
896
HGH041 High-Grade Astrocytoma 36 0.424
897
c ATS007 Autism Spectrum Disorder 71 0.419
898
NNL006 Non-Alcoholic Steatohepatitis 54 0.419
899
IRN001 Iron Deficiency Anemia 58 0.419
900
CMB007 Combined Immunodeficiency 56 0.411
901
P ALC033 Alcohol Use Disorder 67 0.403
902
HDN002 Head Injury 44 0.403
903
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.396
904
HRW001 Hair Whorl 35 0.388
905
INT078 Intracranial Thrombosis 50 0.388
906
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.379
907
c ACQ017 Acquired Von Willebrand Syndrome 48 0.371
908
P THR005 Thrombotic Thrombocytopenic Purpura 64 0.371
909
P THL005 Thalassemia 56 0.371
910
RYN005 Raynaud Phenomenon 45 0.371
911
SPL018 Splenomegaly 47 0.371
912
LNG108 Langerhans Cell Histiocytosis 57 0.366
913
P TRC086 Trichohepatoenteric Syndrome 1 59 0.366
914
P FNG006 Feingold Syndrome 1 61 0.366
915
ERY051 Erythroleukemia, Familial 37 0.366
916
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.366
917
ACR041 Acromelic Frontonasal Dysostosis 53 0.366
918
ATH001 Athabaskan Brainstem Dysgenesis Syndrome 52 0.366
919
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.366
920
ALN001 Aland Island Eye Disease 55 0.366
921
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.366
922
PRG017 Paraganglioma and Gastric Stromal Sarcoma 63 0.366
923
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.366
924
FLL041 Follicular Lymphoma 1 44 0.366
925
KPR003 Keipert Syndrome 43 0.366
926
URT051 Ureter, Cancer of 46 0.366
927
PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.366
928
BRT001 Bart-Pumphrey Syndrome 49 0.366
929
HYP134 Hypoparathyroidism-Retardation-Dysmorphism Syndrome 54 0.366
930
LTT002 Letterer-Siwe Disease 33 0.366
931
SLT014 Salt and Pepper Developmental Regression Syndrome 43 0.366
932
JVN004 Juvenile Myelomonocytic Leukemia 66 0.366
933
c LKM060 Leukemia, Acute Lymphoblastic 3 49 0.366
934
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.366
935
c INF145 Infantile Liver Failure Syndrome 1 44 0.366
936
c PRS080 Prostate Cancer, Hereditary, 7 21 0.366
937
P OCL013 Oculodentodigital Dysplasia 66 0.366
938
IMM162 Immunoglobulin E Concentration, Serum 28 0.366
939
CMR002 Coumarin Resistance 59 0.366
940
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 57 0.366
941
c PRG018 Paragangliomas 1 59 0.366
942
GLS018 Glass Syndrome 60 0.366
943
LYM040 Lymphoblastic Lymphoma 53 0.366
944
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 31 0.366
945
ATY042 Atypical Chronic Myeloid Leukemia 50 0.366
946
VLL003 Villonodular Synovitis 41 0.366
947
ACT011 Acute Contagious Conjunctivitis 41 0.366
948
GST105 Gastroesophageal Adenocarcinoma