Search results for ADP

2150 hits were found for ADP

# Family MCID Name MIFTS Score
1
c BLD120 Bleeding Disorder, Platelet-Type, 8 36 27.528
2
PRT037 Pertussis 65 26.403
3
CHL014 Cholera 62 24.263
4
DPH001 Diphtheria 59 14.881
5
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 12.469
6
P OVR042 Ovarian Cancer 88 12.129
7
GLT038 Glutamyl Ribose-5-Phosphate Storage Disease 8 10.864
8
ISC004 Ischemia 61 10.660
9
ART002 Arts Syndrome 66 9.462
10
GLM045 Glioma 63 9.069
11
LPP008 Lipoprotein Quantitative Trait Locus 65 8.958
12
GLL048 Glial Tumor 52 8.956
13
P THR014 Thrombocytopenia 66 8.595
14
P NRB001 Neuroblastoma 66 8.429
15
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 8.133
16
ART140 Arteries, Anomalies of 53 8.091
17
GLB002 Glioblastoma 67 7.886
18
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 7.877
19
TLN003 Telangiectasis 51 7.590
20
P BRS047 Breast Cancer 98 7.582
21
P ATX030 Ataxia-Telangiectasia 80 7.548
22
P BCL017 B-Cell Lymphoma 59 7.497
23
P PRS040 Prostate Cancer 95 7.494
24
HLX001 Helix Syndrome 48 7.446
25
P PNC035 Pancreatic Cancer 86 7.426
26
HYP266 Hypoxia 57 6.997
27
OST159 Osteogenic Sarcoma 66 6.760
28
HYP066 Hyperglycemia 61 6.646
29
ANX004 Anoxia 40 6.609
30
THR024 Thrombosis 56 6.571
31
P LKM002 Leukemia 67 6.514
32
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 6.457
33
CRB004 Cerebral Artery Occlusion 45 6.387
34
THR035 Thrombasthenia 48 6.380
35
P MYC007 Myocardial Infarction 70 6.367
36
48X005 48,xyyy 39 6.257
37
47X002 47,xyy 48 6.200
38
P VSC007 Vascular Disease 63 6.138
39
BRN071 Brain Injury 50 6.118
40
P LNG032 Lung Cancer 98 6.015
41
TRM010 Traumatic Brain Injury 51 5.972
42
P GLM040 Glioma Susceptibility 1 71 5.893
43
c LKM061 Leukemia, Acute Myeloid 83 5.883
44
P MYP004 Myopathy 67 5.850
45
INT007 Intermediate Coronary Syndrome 54 5.774
46
MLG169 Malignant Astrocytoma 57 5.744
47
RPD005 Rapidly Involuting Congenital Hemangioma 46 5.680
48
CLP006 Clopidogrel Resistance 44 5.665
49
P MLN008 Melanoma 76 5.655
50
PRP027 Peripheral Vascular Disease 71 5.570
51
MYL069 Myeloma, Multiple 77 5.537
52
c DLT002 Dilated Cardiomyopathy 78 5.534
53
OVR094 Ovarian Epithelial Cancer 39 5.512
54
c ACT075 Acute Myocardial Infarction 56 5.501
55
SVR001 Severe Acute Respiratory Syndrome 67 5.495
56
ASP030 Aspirin Resistance 40 5.477
57
DBT010 Diabetic Neuropathy 54 5.418
58
P MYL006 Myeloid Leukemia 61 5.405
59
c SYS001 Systemic Lupus Erythematosus 87 5.353
60
P CLR023 Colorectal Cancer 100 5.312
61
SRC014 Sarcoma 65 5.280
62
INS001 Insulinoma 59 5.272
63
SPN035 Spindle Cell Sarcoma 54 5.259
64
P LKM071 Leukemia, Chronic Lymphocytic 75 5.256
65
P VNW001 Von Willebrand's Disease 65 5.186
66
c HYP836 Hypercholesterolemia, Familial, 1 73 5.103
67
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 4.983
68
CRB039 Cerebrovascular Disease 66 4.952
69
P PHC003 Pheochromocytoma 69 4.937
70
ADR040 Adrenal Gland Pheochromocytoma 46 4.937
71
P PNC044 Pancreatitis 61 4.922
72
AGN016 Aging 54 4.893
73
c ATR087 Atrial Standstill 1 74 4.888
74
TRN015 Transient Cerebral Ischemia 63 4.881
75
ANG054 Angina Pectoris 66 4.844
76
P ADN016 Adenocarcinoma 63 4.830
77
TXC005 Toxic Shock Syndrome 62 4.811
78
P LNG064 Lung Cancer Susceptibility 3 70 4.806
79
P CRN300 Coronary Heart Disease 1 73 4.804
80
PRT036 Peritonitis 65 4.800
81
c ACT027 Acute Pancreatitis 60 4.721
82
P GST053 Gastric Cancer 83 4.649
83
c SML038 Small Cell Cancer of the Lung 69 4.624
84
P HRT032 Heart Disease 81 4.620
85
CRV035 Cervical Cancer 73 4.558
86
P NRP001 Neuropathy 60 4.514
87
c MCR115 Microvascular Complications of Diabetes 5 65 4.485
88
P RTN024 Retinoblastoma 73 4.485
89
P LPS004 Lupus Erythematosus 61 4.459
90
P LTR001 Lateral Sclerosis 58 4.447
91
CYT002 Cytokine Deficiency 43 4.435
92
STR067 Stroke, Ischemic 80 4.422
93
c PCH010 Pachyonychia Congenita 3 43 4.398
94
HGH043 High Grade Glioma 45 4.372
95
ALL029 Allergic Disease 59 4.360
96
P HPT023 Hepatocellular Carcinoma 96 4.342
97
SQM006 Squamous Cell Carcinoma 60 4.321
98
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.280
99
P HDC001 Headache 57 4.259
100
c HYP595 Hypertension, Essential 85 4.254
101
c TYP009 Type 2 Diabetes Mellitus 92 4.217
102
P SPP010 Suppressor of Tumorigenicity 3 51 4.198
103
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.183
104
P DBT009 Diabetes Mellitus 67 4.113
105
FTT001 Fatty Liver Disease 62 4.106
106
P PLM036 Pulmonary Fibrosis 66 4.091
107
P BRS044 Breast Adenocarcinoma 58 4.060
108
P NTR004 Neutropenia 63 4.059
109
SVR004 Severe Combined Immunodeficiency 72 4.058
110
END057 Endometrial Cancer 72 4.057
111
P PRP019 Peripheral Nervous System Disease 58 4.029
112
XRD010 Xeroderma Pigmentosum, Variant Type 73 4.024
113
HYP056 Hypoglycemia 65 4.018
114
P HRP006 Herpes Simplex 65 4.012
115
CYS001 Cystic Fibrosis 78 3.998
116
P ALZ034 Alzheimer Disease 87 3.989
117
P LKM062 Leukemia, Acute Lymphoblastic 69 3.983
118
ORL011 Oral Cancer 60 3.908
119
ALL014 Allergic Encephalomyelitis 34 3.901
120
ALC007 Alcohol Dependence 66 3.851
121
TTN003 Tetanus 65 3.839
122
P LYM118 Lymphoma 67 3.821
123
PPL052 Papillomatosis, Confluent and Reticulated 34 3.802
124
HYP060 Hyperinsulinism 54 3.794
125
P CRD119 Cardiac Arrest 67 3.792
126
c MCR130 Microvascular Complications of Diabetes 6 41 3.773
127
c MCR120 Microvascular Complications of Diabetes 7 47 3.773
128
c MCR113 Microvascular Complications of Diabetes 3 52 3.773
129
c MCR133 Microvascular Complications of Diabetes 4 41 3.773
130
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 3.772
131
GLN010 Glanzmann Thrombasthenia 66 3.737
132
BNR002 Bone Resorption Disease 47 3.733
133
P BNG032 Benign Mesothelioma 53 3.711
134
HMN044 Human Immunodeficiency Virus Type 1 78 3.704
135
P PRP029 Porphyria 60 3.697
136
P ATR011 Atrial Fibrillation 66 3.677
137
BLD053 Blood Platelet Disease 51 3.673
138
MDD018 Middle East Respiratory Syndrome 44 3.666
139
EWN003 Ewing Sarcoma 70 3.654
140
P BLD134 Bladder Cancer 79 3.629
141
P MDL005 Medulloblastoma 75 3.619
142
WRN001 Werner Syndrome 69 3.612
143
P PLM037 Pulmonary Hypertension 72 3.598
144
c PRC016 Pre-Eclampsia 65 3.591
145
SPN186 Spinal Cord Injury 61 3.577
146
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.551
147
MYL009 Myelodysplastic Syndrome 67 3.537
148
P MTC133 Mitochondrial Myopathy 50 3.536
149
ESP021 Esophageal Cancer 83 3.513
150
c FNC027 Fanconi Anemia, Complementation Group a 81 3.507
151
P PRS038 Personality Disorder 65 3.498
152
ANT024 Anthrax Disease 58 3.490
153
c LKM063 Leukemia, Chronic Myeloid 71 3.482
154
c ACT071 Acute Kidney Failure 60 3.481
155
ATH013 Atherosclerosis Susceptibility 63 3.477
156
CRN017 Coronary Thrombosis 46 3.470
157
P ENC004 Encephalitis 61 3.468
158
P ESS003 Essential Thrombocythemia 69 3.462
159
ACT098 Acute Erythroid Leukemia 55 3.427
160
c CHR684 Chronic Kidney Disease 69 3.422
161
P SKN015 Skin Carcinoma 71 3.422
162
P RTN016 Retinal Degeneration 52 3.406
163
P PLY018 Polycythemia 56 3.400
164
STM007 Stomatitis 54 3.389
165
SKN019 Skin Melanoma 71 3.381
166
RNL114 Renal Cell Carcinoma, Nonpapillary 80 3.378
167
BRK010 Burkitt Lymphoma 66 3.363
168
P HNT016 Huntington Disease 73 3.362
169
P KDN018 Kidney Disease 72 3.358
170
THR004 Thrombocytosis 53 3.357
171
P BRN019 Bernard-Soulier Syndrome 61 3.351
172
P HYP086 Hypothyroidism 69 3.340
173
P PRD008 Periodontitis 64 3.315
174
P HYP076 Hyperthyroidism 53 3.299
175
MTC005 Mitochondrial Metabolism Disease 45 3.296
176
P MYC008 Myocarditis 59 3.293
177
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.287
178
ATM095 Autoimmune Disease 61 3.264
179
c HPT073 Hepatitis C Virus 71 3.250
180
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 3.249
181
INS024 Insulin-Like Growth Factor I 78 3.249
182
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 3.249
183
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 3.249
184
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 3.249
185
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 3.249
186
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 3.249
187
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 3.249
188
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 3.249
189
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 3.249
190
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 3.230
191
PLY001 Polycythemia Vera 69 3.226
192
ORL015 Oral Squamous Cell Carcinoma 43 3.202
193
P PRK039 Parkinsonism 55 3.191
194
TRT001 Teratocarcinoma 42 3.191
195
URM002 Uremia 47 3.191
196
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.185
197
CHK001 Chikungunya 60 3.180
198
PRM329 Premature Aging 36 3.177
199
VCC001 Vaccinia 47 3.171
200
DFC004 Deficiency Anemia 74 3.134
201
CLT003 Colitis 63 3.132
202
PLM134 Pulmonary Fibrosis, Idiopathic 76 3.127
203
P PRK057 Parkinson Disease, Late-Onset 80 3.116
204
P HRM001 Hermansky-Pudlak Syndrome 65 3.105
205
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 3.082
206
P LVR013 Liver Disease 69 3.072
207
P EXN002 Exanthem 58 3.057
208
c THY107 Thymoma, Familial 42 3.046
209
P THY023 Thymoma 64 3.046
210
c SCL052 Scleroderma, Familial Progressive 61 3.041
211
P MTC069 Mitochondrial Disorders 57 3.035
212
P HYP061 Hypertrophic Cardiomyopathy 69 3.029
213
P INF038 Influenza 68 3.013
214
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.996
215
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.995
216
PLR008 Pleurisy 50 2.992
217
P FBR017 Fibrosarcoma 56 2.991
218
IMM167 Immune Deficiency Disease 78 2.989
219
CLN015 Colon Adenocarcinoma 65 2.989
220
c THR092 Thrombophilia Due to Thrombin Defect 74 2.987
221
P DRR001 Diarrhea 55 2.987
222
P FML011 Familial Adenomatous Polyposis 71 2.984
223
P CRD246 Cardiovascular System Disease 56 2.981
224
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 2.975
225
P LCT001 Lactic Acidosis 51 2.975
226
c LKM005 Leukemia, T-Cell, Chronic 34 2.967
227
c TYP008 Type 1 Diabetes Mellitus 70 2.945
228
c HPT001 Hepatitis C 62 2.942
229
P MSC005 Muscular Dystrophy 67 2.922
230
PNC129 Pancreatic Adenocarcinoma 65 2.911
231
CHD001 Chediak-Higashi Syndrome 67 2.894
232
THY029 Thyroid Carcinoma 51 2.894
233
NRR001 Neuroretinitis 42 2.867
234
RTN023 Retinitis 46 2.867
235
AVD001 Avoidant Personality Disorder 49 2.867
236
SFT003 Soft Tissue Sarcoma 57 2.858
237
P ART021 Arteriosclerosis 54 2.855
238
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 2.853
239
P INF037 Inflammatory Bowel Disease 53 2.827
240
PLM129 Pulmonary Disease, Chronic Obstructive 74 2.815
241
c MGR028 Migraine with or Without Aura 1 64 2.814
242
BRN004 Brain Edema 54 2.810
243
c BRN108 Branchiootic Syndrome 1 62 2.802
244
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.794
245
VNZ002 Venezuelan Equine Encephalitis 46 2.782
246
LPD008 Lipid Metabolism Disorder 62 2.778
247
HMC014 Homocysteinemia 52 2.778
248
CHL123 Chlamydia 58 2.778
249
ACT119 Acute Promyelocytic Leukemia 62 2.775
250
P SCK005 Sickle Cell Disease 56 2.763
251
GST040 Gastric Adenocarcinoma 67 2.761
252
P RHM011 Rheumatoid Arthritis 82 2.754
253
OCL069 Ocular Motor Apraxia 57 2.746
254
P NSP012 Nasopharyngeal Carcinoma 61 2.740
255
P RTN008 Retinitis Pigmentosa 80 2.737
256
PRP030 Purpura 54 2.704
257
c HPT007 Hepatitis E 51 2.697
258
OST012 Osteoarthritis 77 2.692
259
BCT022 Bacterial Infectious Disease 56 2.682
260
P HPT021 Hepatitis 69 2.682
261
PRT251 Proteinuria, Chronic Benign 57 2.667
262
c MJR022 Major Affective Disorder 8 38 2.654
263
c MJR024 Major Affective Disorder 9 41 2.654
264
P BPL003 Bipolar Disorder 56 2.654
265
STR089 Storage Pool Platelet Disease 47 2.647
266
P CCK001 Cockayne Syndrome 68 2.636
267
PRP080 Peripheral Artery Disease 54 2.633
268
CHG001 Chagas Disease 66 2.633
269
P MLN007 Male Infertility 56 2.608
270
GST045 Gastroenteritis 58 2.604
271
PLY150 Polykaryocytosis Inducer 29 2.597
272
P ART022 Arthritis 71 2.597
273
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.595
274
P ENC018 Encephalopathy 62 2.571
275
ADN018 Adenoma 59 2.568
276
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.563
277
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.563
278
P ECL001 Eclampsia 52 2.539
279
ARG004 Argyria 26 2.537
280
ART016 Aortic Aneurysm 68 2.511
281
ANR040 Aneurysm 61 2.511
282
DFF005 Diffuse Large B-Cell Lymphoma 54 2.501
283
PPL022 Papilloma 53 2.493
284
SQM002 Squamous Cell Papilloma 46 2.493
285
DSS009 Disseminated Intravascular Coagulation 57 2.491
286
GLS001 Gliosarcoma 64 2.490
287
MTB004 Metabolic Acidosis 48 2.487
288
KRN002 Kearns-Sayre Syndrome 63 2.487
289
P ANT006 Antiphospholipid Syndrome 55 2.483
290
SKN016 Skin Disease 63 2.476
291
LNG099 Lung Disease 62 2.476
292
GLC003 Glucose Intolerance 54 2.441
294
IRN002 Iron Metabolism Disease 57 2.436
295
CRT015 Carotid Artery Occlusion 45 2.433
296
ACT003 Acute Kidney Tubular Necrosis 46 2.432
297
END086 End Stage Renal Disease 52 2.427
298
P GST044 Gastritis 55 2.423
299
PLS011 Plasmacytoma 56 2.423
300
HPR003 Heparin-Induced Thrombocytopenia 47 2.423
301
MNT001 Mantle Cell Lymphoma 67 2.405
302
P RHB003 Rhabdomyosarcoma 66 2.398
303
PLM033 Pulmonary Embolism 58 2.390
304
c SPR009 Sporadic Breast Cancer 42 2.377
305
P CTR002 Cataract 60 2.376
306
CRT004 Carotid Artery Thrombosis 39 2.363
307
P KDN017 Kidney Cancer 61 2.358
308
ATS010 Autosomal Recessive Disease 42 2.347
309
P HYP098 Hypereosinophilic Syndrome 66 2.347
310
P MSC003 Muscular Atrophy 52 2.338
311
MLG079 Malignant Pleural Mesothelioma 42 2.325
312
CRN030 Coronary Stenosis 50 2.318
313
CLS016 Clostridium Difficile Colitis 49 2.311
314
c CHR095 Chronic Progressive External Ophthalmoplegia 49 2.288
315
LYM027 Lymphopenia 56 2.288
316
LYM143 Lymphoma, Non-Hodgkin, Familial 75 2.287
317
P CTN015 Cutaneous T Cell Lymphoma 48 2.257
318
CNG034 Congestive Heart Failure 69 2.256
319
AMN017 Aminolevulinic Acid Dehydratase Deficiency Porphyria 8 2.252
320
c HPT016 Hepatitis B 62 2.232
321
MSC157 Muscular Dystrophy, Duchenne Type 79 2.228
322
P GLM007 Glomerulonephritis 60 2.228
323
CHL068 Cholestasis 61 2.227
324
DWN001 Down Syndrome 70 2.204
325
c FNC042 Fanconi Anemia, Complementation Group D2 54 2.203
326
c ACT073 Acute Leukemia 58 2.201
327
P MYC084 Mycobacterium Tuberculosis 1 68 2.198
328
P THR015 Thrombophilia 51 2.195
329
CRH001 Crohn's Disease 80 2.185
330
P XRD029 Xeroderma Pigmentosum, Complementation Group a 56 2.165
331
P PNM007 Pneumonia 67 2.165
332
c MST023 Mesothelioma, Malignant 56 2.163
333
GST033 Gestational Diabetes 61 2.163
334
P ADL017 Adult T-Cell Leukemia 56 2.148
335
GRY002 Gray Platelet Syndrome 58 2.142
336
P DMN002 Dementia 66 2.142
337
P AST005 Asthma 76 2.126
338
LMB062 Limb Ischemia 55 2.126
339
BRN024 Bronchitis 67 2.126
340
P ADL010 Adult Respiratory Distress Syndrome 71 2.126
341
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.116
342
MYL005 Myelofibrosis 71 2.116
343
STT001 Status Epilepticus 59 2.112
344
LYM133 Lymphoma, Hodgkin, Classic 74 2.110
345
KPS004 Kaposi Sarcoma 77 2.089
346
CHL065 Cholangiocarcinoma 58 2.087
347
INT079 Intrahepatic Cholangiocarcinoma 51 2.087
348
IMP005 Impotence 52 2.085
349
P SZR006 Seizure Disorder 70 2.081
350
SCK003 Sickle Cell Anemia 74 2.081
351
P HMR003 Hemorrhagic Disease 59 2.081
352
LVR012 Liver Cirrhosis 63 2.065
353
CRD137 Cardiogenic Shock 56 2.062
354
CRB090 Cerebral Hypoxia 42 2.062
355
P CMP072 Camptodactyly Syndrome, Guadalajara, Type I 31 2.056
356
ALL006 Allergic Asthma 56 2.051
357
P RTN018 Retinal Disease 53 2.051
358
HYP114 Hypertensive Nephropathy 36 2.044
359
AZS001 Azoospermia 45 2.044
360
P RCT021 Rectum Cancer 54 2.031
361
c ATS025 Autosomal Dominant Progressive External Ophthalmoplegia 45 2.027
362
P KLZ004 Kala-Azar 1 41 2.019
363
LSH001 Leishmaniasis 64 2.019
364
INT002 Intermittent Claudication 61 2.015
365
FLL027 Fallopian Tube Carcinoma 67 1.989
366
P SLP006 Sleep Apnea 69 1.987
368
EXT007 Extracutaneous Mastocytoma 38 1.987
369
P RRH023 Rare Hereditary Hemochromatosis 54 1.987
370
MST004 Mast Cell Neoplasm 42 1.987
371
HMS001 Hemosiderosis 48 1.987
372
P MLN069 Melanoma, Uveal 61 1.980
373
RTN003 Retinal Ischemia 49 1.971
374
P RHN004 Rhinitis 57 1.971
375
MYL031 Myeloproliferative Neoplasm 66 1.964
376
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 52 1.954
377
AFB002 Afibrinogenemia, Congenital 64 1.954
378
ADN001 Adenosine Deaminase Deficiency 59 1.954
379
P MNC007 Monocytic Leukemia 47 1.954
380
P LPS002 Liposarcoma 64 1.949
381
HMT002 Hematologic Cancer 61 1.945
382
P LMY004 Leiomyosarcoma 62 1.945
383
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.920
384
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.920
385
P OPT006 Optic Nerve Disease 58 1.920
386
P GRV001 Graves' Disease 55 1.920
387
SCH014 Schistosomiasis 56 1.920
388
P RSP003 Respiratory Failure 74 1.920
389
P NNT058 Neonatal Diabetes 52 1.916
390
P INF032 Infertility 57 1.916
391
PRS047 Prostatitis 58 1.913
392
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 1.899
393
P MYS003 Myasthenia Gravis 68 1.886
394
SLP001 Sleeping Sickness 56 1.886
395
P HML002 Hemolytic Anemia 62 1.885
396
P DRM053 Dermatitis, Atopic 65 1.877
397
CNS004 Constipation 56 1.877
398
HMP009 Haemophilus Influenzae 41 1.877
399
CLL010 Cellular Ependymoma 57 1.861
400
P BNG030 Benign Ependymoma 51 1.861
401
P ACN011 Acne 57 1.854
402
CRD132 Cardiac Conduction Defect 60 1.851
403
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.851
404
PHN003 Phenylketonuria 76 1.851
405
PNG002 Pain Agnosia 51 1.851
406
P MCR010 Microcephaly 60 1.851
407
GST023 Gastric Ulcer 52 1.851
408
CVD001 Covid-19 57 1.836
409
DSS032 Disease by Infectious Agent 55 1.836
410
CWP001 Cowpox 45 1.836
411
P UVT001 Uveitis 57 1.836
412
P PRN023 Prion Disease 60 1.836
413
P MNN013 Meningitis 65 1.836
414
c LRG001 Large Cell Carcinoma 48 1.816
415
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 1.815
416
PRS045 Prostatic Hypertrophy 53 1.815
417
P EYD002 Eye Disease 57 1.815
418
P HRD200 Hereditary Breast Ovarian Cancer Syndrome 67 1.804
419
RTN020 Retinal Vascular Disease 46 1.794
420
ALL003 Allergic Rhinitis 67 1.794
421
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.794
422
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 47 1.793
423
P MLT020 Multiple Sclerosis 79 1.778
424
GSG001 Gas Gangrene 52 1.778
425
P SNS001 Sensorineural Hearing Loss 59 1.778
426
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.778
427
P HYP750 Hypertriglyceridemia, Familial 62 1.774
428
P NPH012 Nephrotic Syndrome 60 1.774
429
BRN028 Brain Cancer 74 1.752
430
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 1.751
431
RNL077 Renal Fibrosis 46 1.751
432
CNN005 Connective Tissue Disease 67 1.751
433
ENT011 Enterocolitis 55 1.745
434
P BRD002 Bardet-Biedl Syndrome 66 1.745
435
LGH007 Leigh Syndrome 70 1.740
436
P MJR007 Major Affective Disorder 1 42 1.740
437
URT010 Ureteral Obstruction 45 1.740
438
P DNG005 Dengue Virus 56 1.740
439
PRS021 Prostatic Adenoma 43 1.740
440
P HYP265 Hypotonia 42 1.740
441
c PNS012 Paine Syndrome 60 1.715
442
c BRS111 Breast-Ovarian Cancer, Familial 2 53 1.706
443
ACR013 Acrodysostosis 51 1.706
444
PRS129 Prostatic Hyperplasia, Benign 49 1.700
445
CLR109 Colorectal Adenocarcinoma 50 1.700
446
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.700
447
P ART018 Aortic Valve Insufficiency 52 1.700
448
PPT005 Peptic Ulcer Disease 58 1.700
449
P END044 Endometriosis 62 1.700
450
LNG039 Lung Squamous Cell Carcinoma 57 1.698
451
c OVR114 Ovarian Cancer 1 59 1.693
452
c ATS007 Autism Spectrum Disorder 72 1.686
453
NNL006 Non-Alcoholic Steatohepatitis 54 1.686
454
IRN001 Iron Deficiency Anemia 58 1.686
455
HRY003 Hairy Cell Leukemia 61 1.685
456
c RTN047 Retinitis Pigmentosa 18 46 1.660
457
P PRV002 Periventricular Nodular Heterotopia 52 1.660
458
PLT031 Platelet Membrane Fluidity 28 1.660
459
HYP020 Hyperprolactinemia 63 1.660
460
P HML001 Hemolytic-Uremic Syndrome 52 1.660
461
PST011 Pustulosis of Palm and Sole 52 1.660
462
LWC001 Low Compliance Bladder 45 1.660
463
c BCT007 Bacterial Meningitis 55 1.659
464
LYM007 Lymphangioleiomyomatosis 68 1.659
465
THY030 Thyroid Gland Disease 50 1.659
466
DBT007 Diabetic Cataract 36 1.659
467
c HMN021 Human T-Cell Leukemia Virus Type 1 47 1.659
468
CMB007 Combined Immunodeficiency 57 1.656
469
P ALC033 Alcohol Use Disorder 61 1.625
470
HDN002 Head Injury 44 1.625
471
c ACT134 Acute Liver Failure 59 1.618
472
NRD058 Neurodegeneration, Childhood-Onset, Stress-Induced, with Variable Ataxia and Seizures 27 1.618
473
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.618
474
MLD001 Melioidosis 67 1.618
475
P GRF003 Graft-Versus-Host Disease 71 1.618
476
c FML021 Familial Hypercholesterolemia 72 1.618
477
LYM019 Lymphosarcoma 46 1.611
478
P DBT005 Diabetes Insipidus 54 1.610
479
P LPR021 Leprosy 3 71 1.610
480
P JBR020 Joubert Syndrome 1 74 1.610
481
c VRL010 Viral Hepatitis 53 1.610
482
SCB001 Scabies 50 1.610
483
HNS001 Hansen's Disease 32 1.610
484
c PRS136 Prostate Cancer, Hereditary, 6 33 1.594
485
c PRS130 Prostate Cancer, Hereditary, 8 32 1.594
486
THR100 Thrombocytopenic Purpura, Autoimmune 61 1.593
487
PHS014 Phosphoglycerate Kinase 1 Deficiency 45 1.583
488
GRM010 Germ Cells Tumors 33 1.577
489
THY128 Thyroid Tumor 35 1.575
490
FRN006 Frontotemporal Dementia 68 1.575
491
P PSR002 Psoriasis 63 1.575
492
P PSD015 Pseudohypoparathyroidism 55 1.575
493
NRM005 Neuromuscular Disease 63 1.575
494
TRY001 Trypanosomiasis 50 1.575
495
c SVR005 Severe Pre-Eclampsia 50 1.575
496
HRW001 Hair Whorl 35 1.561
497
INT078 Intracranial Thrombosis 50 1.561
498
RHB024 Rhabdomyosarcoma 2 67 1.558
499
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 1.558
500
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 1.558
501
QBC001 Quebec Platelet Disorder 44 1.542
502
c OPT053 Optic Atrophy 1 62 1.530
503
GLL008 Gilles De La Tourette Syndrome 65 1.530
504
c ART101 Aortic Valve Disease 2 66 1.530
505
EMB004 Embryonal Carcinoma 56 1.530
506
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.528
507
PLT033 Platelet Signal Processing Defect 9 1.528
508
HPT022 Hepatoblastoma 54 1.520
509
VRL011 Viral Infectious Disease 61 1.518
510
P SLM003 Salmonellosis 54 1.503
511
TYP007 Typhoid Fever 64 1.503
512
P THL005 Thalassemia 56 1.495
513
c ACQ017 Acquired Von Willebrand Syndrome 48 1.495
514
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.495
515
SPL018 Splenomegaly 49 1.495
516
RYN005 Raynaud Phenomenon 45 1.495
517
P MCR129 Microvascular Complications of Diabetes 1 68 1.483
518
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 51 1.483
519
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 53 1.483
520
P MLG056 Malignant Hyperthermia 66 1.483
521
c MCR112 Microvascular Complications of Diabetes 2 42 1.483
522
SNS003 Sensory Peripheral Neuropathy 52 1.483
523
P MTC010 Mitochondrial Dna Depletion Syndrome 47 1.483
524
P PLY011 Polycystic Ovary Syndrome 57 1.483
525
EHR002 Ehrlichiosis 39 1.483
526
PLM010 Pulmonary Edema 55 1.483
527
P RTN022 Retinal Vein Occlusion 54 1.483
528
TRN018 Transitional Cell Carcinoma 56 1.475
529
P ATS364 Autism 69 1.460
530
P WSK001 Wiskott-Aldrich Syndrome 72 1.460
531
P HMP007 Hemophilia 52 1.460
532
BCK006 Back Pain 47 1.458
533
c THR090 Thrombocythemia 1 50 1.451
534
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 1.445
535
P PTS002 Ptosis 52 1.445
536
c LKM070 Leukemia, Acute Monocytic 56 1.434
537
P SRC025 Sarcoidosis 1 71 1.434
538
P CNJ013 Conjunctivitis 66 1.434
539
GLM044 Glomerular Disease 35 1.433
540
P CHN012 Chondrosarcoma 57 1.433
541
BLM001 Bloom Syndrome 65 1.433
542
MNT002 Mental Depression 57 1.433
543
MST020 Mast Cell Activation Syndrome 28 1.433
544
ANT039 Antisynthetase Syndrome 55 1.431
545
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.428
546
MLR004 Malaria 80 1.425
547
P MYT002 Myotonic Dystrophy 51 1.425
548
MNN043 Meningioma, Familial 79 1.424
549
RHB001 Rhabdoid Cancer 68 1.424
550
SCR001 Secretory Meningioma 40 1.424
551
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.424
552
SPN021 Spinal Meningioma 50 1.424
553
P EPN001 Ependymoblastoma 44 1.399
554
GT001 Gout 64 1.389
555
MYC005 Myocardial Stunning 46 1.389
556
P FRG001 Fragile X Syndrome 70 1.382
557
VRC001 Varicocele 48 1.382
558
CLP005 Ciliopathy 41 1.382
559
PLY100 Polyploidy 36 1.382
560
LNG095 Lung Abscess 51 1.382
561
P MJR001 Major Depressive Disorder 68 1.382
562
c RTN032 Retinal Cone Dystrophy 1 24 1.382
563
TST044 Testicular Torsion 45 1.382
564
P TRM003 Tremor 48 1.382
565
CRV040 Cervix Carcinoma 50 1.382
566
MCR013 Microphthalmia 60 1.382
567
MMM001 Mammary Paget's Disease 53 1.382
568
PLG002 Plague 58 1.382
569
P PLY019 Polyneuropathy 52 1.382
570
DPR016 Depression 65 1.382
571
CLR030 Clear Cell Renal Cell Carcinoma 54 1.378
572
P ANR048 Aniridia 1 64 1.374
573
P DDN001 Duodenal Ulcer 53 1.352
574
PTT037 Pituitary Tumors 44 1.352
575
c TBR025 Tuberous Sclerosis 1 84 1.348
576
P CHR285 Chronic Myelomonocytic Leukemia 60 1.348
577
ANG020 Angiosarcoma 64 1.348
578
SRC027 Sarcoma, Synovial 58 1.347
579
APR001 Apraxia 52 1.327
580
P NJM001 Nijmegen Breakage Syndrome 76 1.327
581
FLL031 Follicular Adenoma 40 1.327
582
CHL045 Choline Deficiency Disease 39 1.327
583
SLC006 Silicosis 56 1.327
584
END041 Endometrial Adenocarcinoma 64 1.327
585
P TBR001 Tuberous Sclerosis 69 1.327
586
DMY004 Demyelinating Disease 50 1.327
587
ANP005 Anaplastic Astrocytoma 57 1.323
588
PRM013 Premature Menopause 58 1.314
589
FCT001 Factor Viii Deficiency 60 1.314
590
c GRV008 Graves Disease 1 54 1.314
591
PRP083 Porphyria, Acute Intermittent 65 1.314
592
c HMP029 Hemophilia a 68 1.314
593
PLT015 Platelet Aggregation, Spontaneous 34 1.314
594
PST092 Posttransplant Acute Limbic Encephalitis 28 1.314
595
P LYN001 Lynch Syndrome 76 1.314
596
CRT013 Carotid Stenosis 51 1.314
597
INT030 Intracranial Aneurysm 55 1.314
598
STC016 Sticky Platelet Syndrome 23 1.314
599
c WLF009 Wolfram Syndrome 2 43 1.314
600
c HRM009 Hermansky-Pudlak Syndrome 6 45 1.314
601
PCH007 Pouchitis 42 1.282
602
VLK001 Volkmann Contracture 23 1.275
603
c ATM102 Autoimmune Cardiomyopathy 29 1.275
604
ALB002 Albinism 47 1.275
605
P CHR345 Chronic Pain 50 1.275
606
PST053 Postherpetic Neuralgia 40 1.275
607
NRN004 Neuroendocrine Tumor 59 1.272
608
P OVR082 Overgrowth Syndrome 49 1.269
609
MTC146 Mitochondrial Complex I Deficiency, Nuclear Type 1 61 1.269
610
P OST002 Osteoporosis 76 1.269
611
c EXD008 Exudative Vitreoretinopathy 1 71 1.269
612
P ZNC008 Zinc Finger Protein 1 23 1.269
613
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.269
614
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.269
615
P PLY014 Polycystic Kidney Disease 69 1.269
616
P CYS018 Cystitis 59 1.269
617
MTH009 Mouth Disease 57 1.269
618
P GLL022 Guillain-Barre Syndrome 60 1.269
619
P HMN010 Hemangioma 62 1.269
620
BLR008 Bilirubin Metabolic Disorder 57 1.269
621
PPL002 Papillary Carcinoma 46 1.269
622
MST005 Mastitis 53 1.269
623
DXR001 Doxorubicin Induced Cardiomyopathy 32 1.269
624
MYC006 Mycosis Fungoides 65 1.247
625
P MLG074 Malignant Mesenchymoma 40 1.240
626
MXD026 Mixed Glioma 45 1.240
627
CNT047 Contact Dermatitis 57 1.239
628
LKS001 Leukostasis 41 1.239
629
P EPL164 Epilepsy 68 1.234
630
SBC011 Sebaceous Adenocarcinoma 43 1.234
631
RCK004 Rickets 68 1.234
632
AND005 Androgen Insensitivity Syndrome, Mild 21 1.224
633
P PRG013 Paraganglioma 57 1.214
634
CRC021 Carcinosarcoma 64 1.214
635
PLC002 Plica Syndrome 35 1.214
636
P GLL018 Gallbladder Cancer 53 1.214
637
SYN007 Synovitis 55 1.214
638
RCR030 Recurrent Idiopathic Neuroretinitis 11 1.206
639
P RTT002 Rett Syndrome 79 1.206
640
c BRD015 Bardet-Biedl Syndrome 3 48 1.206
641
MSC007 Muscle Hypertrophy 64 1.206
642
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 1.206
643
P PLY041 Polymyositis 59 1.206
644
P ATR005 Atrophic Gastritis 50 1.206
645
P DRM010 Dermatomyositis 61 1.206
646
BRN014 Bronchopneumonia 53 1.206
647
DNT012 Dental Caries 53 1.206
648
P PST095 Post-Thrombotic Syndrome 51 1.206
649
SKN020 Skin Papilloma 40 1.206
650
MXD005 Mixed Connective Tissue Disease 57 1.206
651
P TXP001 Toxoplasmosis 60 1.206
652
IQS001 Iqsec2 18 1.206
653
P ANP001 Anaplastic Large Cell Lymphoma 61 1.192
654
INF034 Infective Endocarditis 54 1.192
655
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 1.192
656
PLC005 Placental Insufficiency 56 1.192
657
PRP016 Paraplegia 52 1.192
658
HYP014 Hyperuricemia 51 1.192
659
P CNR004 Cone-Rod Dystrophy 2 74 1.191
660
P OLG002 Oligodendroglioma 66 1.191
661
ATY005 Atypical Teratoid Rhabdoid Tumor 69 1.191
662
INT358 Intestinal Polyposis Syndrome 25 1.154
663
TTR011 Tetraploidy 43 1.154
664
P SJG008 Sjogren Syndrome 61 1.154
665
c MCR247 Microcephaly 1, Primary, Autosomal Recessive 42 1.154
666
VTM033 Vitamin K Deficiency Bleeding 48 1.154
667
SPP011 Suppression of Tumorigenicity 12 61 1.151
669
HYP005 Hypokalemia 55 1.151
670
THR123 Thrombotic Microangiopathy 40 1.149
671
VRG001 Variegate Porphyria 56 1.149
672
DBT084 Diabetes Mellitus, Ketosis-Prone 60 1.149
673
CPR004 Coproporphyria, Hereditary 57 1.149
674
CHR066 Chronic Fatigue Syndrome 60 1.149
675
HMG002 Hemoglobinuria 50 1.149
676
P RNV001 Renovascular Hypertension 49 1.149
677
P SYS005 Systemic Scleroderma 74 1.149
678
c BSL007 Basal Cell Carcinoma 68 1.149
679
MDD011 Mood Disorder 62 1.149
680
NWC001 Newcastle Disease 47 1.149
681
PTH003 Pathologic Nystagmus 52 1.149
682
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 1.138
683
LSC001 Lesch-Nyhan Syndrome 62 1.138
684
P SPR119 Spermatogenic Failure, X-Linked, 1 36 1.138
685
MTC029 Mitochondrial Complex V Deficiency, Nuclear Type 1 40 1.138
686
PRV020 Periventricular Heterotopia with Microcephaly, Autosomal Recessive 26 1.138
687
P STR022 Stargardt Disease 61 1.138
688
c SCN036 Secondary Progressive Multiple Sclerosis 55 1.138
689
P FNC044 Fanconi Anemia, Complementation Group C 56 1.138
690
c XRD030 Xeroderma Pigmentosum, Complementation Group C 55 1.138
691
P PLV020 Pelvic Organ Prolapse 58 1.138
692
c DFN196 Deafness, Autosomal Dominant 22 43 1.138
693
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 1.138
694
c RTN210 Retinitis Pigmentosa 50 37 1.138
695
CHR072 Chordoma 57 1.138
696
c FML347 Familial Adenomatous Polyposis 2 55 1.138
697
c FML299 Familial Adenomatous Polyposis 3 27 1.138
698
c FML339 Familial Adenomatous Polyposis 4 30 1.138
699
P OVR106 Ovarian Clear Cell Carcinoma 44 1.138
700
ASB001 Asbestosis 47 1.138
701
STN011 Sting-Associated Vasculopathy with Onset in Infancy 45 1.138
702
AVN001 Avian Influenza 61 1.138
703
SCR011 Scrapie 39 1.138
704
P RBL001 Rubella 58 1.138
705
ASB003 Asbestos Intoxication 32 1.138
706
LRY018 Laryngeal Squamous Cell Carcinoma 44 1.138
707
CRY003 Cryptosporidiosis 56 1.138
708
ATN004 Autonomic Neuropathy 42 1.138
709
ADR008 Adrenal Adenoma 55 1.138
710
P INT068 Intestinal Disease 53 1.138
711
HND002 Hand, Foot and Mouth Disease 50 1.138
712
ACT200 Acute Monoblastic Leukemia 41 1.138
713
c DFN024 Deafness, Autosomal Dominant Nonsyndromic Sensorineural 22 14 1.138
714
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 72 1.115
715
c HNT011 Huntington Disease-Like 3 34 1.104
716
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.104
717
P OPN001 Open-Angle Glaucoma 55 1.104
718
HRP004 Herpes Zoster 61 1.104
719
P FML187 Familial Hypertension 34 1.104
720
FCT007 Factor Vii Deficiency 64 1.083
721
c TBR026 Tuberous Sclerosis 2 71 1.083
722
P FLL037 Follicular Lymphoma 74 1.083
723
MCR359 Macrothrombocytopenia and Granulocyte Inclusions with or Without Nephritis or Sensorineural Hearing Loss 44 1.080
724
c HRM017 Hermansky-Pudlak Syndrome 2 55 1.080
725
ADL002 Adult Syndrome 70 1.080
726
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 1.080
727
MCK005 Mckusick-Kaufman Syndrome 61 1.063
728
OCL015 Oculomotor Apraxia 39 1.063
729
RHM028 Rheumatic Heart Disease 56 1.063
730
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 1.063
731
KRT019 Keratitis, Hereditary 66 1.063
732
P PLY006 Polydactyly 59 1.063
733
WST005 West Nile Virus 57 1.063
734
P TYR004 Tyrosinemia 50 1.063
735
NRN046 Neuronal Tumor 19 1.063
736
HRT012 Heart Valve Disease 53 1.063
737
MNC006 Monoclonal Gammopathy of Uncertain Significance 47 1.063
738
ASP003 Aseptic Meningitis 50 1.063
739
DSS010 Dissociative Disorder 39 1.063
740
HYP043 Hyperandrogenism 48 1.063
741
LYS002 Lysosomal Storage Disease 51 1.063
742
DBT002 Diabetic Autonomic Neuropathy 41 1.063
743
ART006 Arthus Reaction 40 1.063
744
DBT004 Diabetic Polyneuropathy 50 1.063
745
FSC004 Fasciitis 49 1.063
746
c CHR417 Chronic Graft Versus Host Disease 55 1.063
747
P OCL002 Oculocutaneous Albinism 59 1.057
748
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.057
749
CHR003 Cherubism 57 1.057
750
LPT014 Leptin Deficiency or Dysfunction 78 1.057
751
HMM004 Hamamy Syndrome 39 1.057
752
c GLC092 Glaucoma, Primary Open Angle 62 1.057
753
CHR074 Choriocarcinoma 46 1.057
754
DYS015 Dysentery 50 1.057
755
ANT011 Antisocial Personality Disorder 47 1.057
756
MRP001 Morphine Dependence 42 1.057
757
P HYP050 Hyperinsulinemic Hypoglycemia 57 1.057
758
LCH001 Leech Infestation 38 1.057
759
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.057
760
KDN013 Kidney Hypertrophy 34 1.053
761
CHL028 Childhood Type Dermatomyositis 59 1.021
762
P CRV031 Cervical Adenocarcinoma 48 1.008
763
TST014 Testicular Cancer 52 1.008
764
P LRY044 Larynx Cancer 54 1.008
765
P BNC003 Bone Cancer 58 1.008
766
RST023 Resting Heart Rate, Variation in 40 1.008
767
RTN017 Retinal Detachment 60 1.008
768
CYN002 Cyanosis, Transient Neonatal 43 1.008
769
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.008
770
SCT005 Scott Syndrome 50 1.008
771
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 1.008
772
DCT002 Ductal Carcinoma in Situ 58 1.008
773
VLL006 Villous Adenoma 41 1.008
774
MTC004 Mitochondrial Encephalomyopathy 42 1.008
775
P HYD006 Hydrocephalus 61 1.008
776
P BND020 Bone Disease 59 1.008
777
c HMG003 Hemoglobin E Disease 42 1.008
778
P AXN001 Axonal Neuropathy 35 1.008
779
P OBS001 Obstructive Jaundice 48 1.008
780
PLR005 Pleuropneumonia 33 1.008
781
P INS002 in Situ Carcinoma 53 1.008
782
c RNG015 Ring Chromosome 2 22 1.008
783
c HMC039 Hemochromatosis, Type 1 73 0.978
784
P PRM011 Primary Ciliary Dyskinesia 69 0.978
785
END062 Endometrial Hyperplasia 48 0.978
786
c MTC059 Mitochondrial Dna Depletion Syndrome 5 48 0.978
787
HRN029 Hearing Loss, Noise-Induced 37 0.978
788
STS002 Situs Inversus 45 0.978
789
CRV002 Cervix Uteri Carcinoma in Situ 47 0.978
790
YLL002 Yellow Fever 61 0.978
791
SHW001 Shwartzman Phenomenon 36 0.978
792
ALL010 Allergic Contact Dermatitis 56 0.978
793
MCR141 Mucormycosis 59 0.978
794
P CRN024 Corneal Disease 44 0.978
795
PCD001 Pica Disease 38 0.978
796
HYP072 Hypersensitivity Reaction Type Iii Disease 39 0.978
797
INP001 Inappropriate Adh Syndrome 48 0.978
798
P MTR014 Motor Neuron Disease 65 0.978
799
BRS051 Breast Disease 58 0.978
800
ENT004 Enthesopathy 51 0.978
801
NCR007 Necrotizing Fasciitis 49 0.978
802
c JVN010 Juvenile Rheumatoid Arthritis 66 0.978
803
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 0.978
804
MYC013 Mycobacterium Abscessus 42 0.978
805
CRV045 Cervical Intraepithelial Neoplasia 39 0.978
806
NNT024 Neonatal Stroke 33 0.978
807
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 0.956
808
P HRD217 Hereditary Optic Neuropathy 36 0.956
809
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 0.956
810
P MYS005 Myositis 56 0.956
811
BLS001 Blau Syndrome 68 0.956
812
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.956
813
P PRP003 Porphyria Cutanea Tarda 66 0.956
814
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 0.956
815
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.956
816
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.956
817
PLT016 Platelet Adenylate Cyclase Activity 16 0.956
819
INT075 Intracranial Hypertension 53 0.956
820
P CHL066 Cholangitis 52 0.956
821
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.956
822
ACT078 Acute Porphyria 49 0.956
823
DBT008 Diabetic Angiopathy 45 0.956
824
QLT001 Qualitative Platelet Defect 29 0.956
825
P PYL005 Pyelonephritis 57 0.956
826
BRD004 Borderline Personality Disorder 53 0.956
827
P END033 Endocarditis 58 0.956
828
P SHR001 Short Bowel Syndrome 53 0.956
829
HMR002 Hemarthrosis 44 0.956
830
HYP026 Hypoglycemic Coma 37 0.956
831
P ACT105 Acute Mountain Sickness 52 0.956
832
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.923
833
BRR014 Barrett Esophagus 66 0.923
834
c WLM013 Wilms Tumor 1 66 0.923
835
GST019 Gastrointestinal Stromal Tumor 78 0.923
836
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.923
837
MCR004 Macroglobulinemia 49 0.923
838
P BCL004 B-Cell Non-Hodgkin Lymphoma 42 0.923
839
PRM126 Primary Peritoneal Carcinoma 62 0.923
840
NRN001 Neuroendocrine Carcinoma 47 0.923
841
RCT020 Rectum Adenocarcinoma 48 0.923
842
BLR013 Biliary Tract Cancer 43 0.923
843
RFR010 Refractory Anemia 49 0.901
844
MTB016 Metabolic Myopathy 30 0.901
845
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.901
846
ANX010 Anxiety 70 0.901
847
EPD015 Epidemic Typhus 44 0.901
848
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.901
849
HYP025 Hyperphosphatemia 48 0.901
850
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.901
851
c BLD154 Bleeding Disorder, Platelet-Type, 12 28 0.901
852
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.901
853
THY111 Thyroid Carcinoma, Familial Medullary 67 0.901
854
APN008 Apnea, Obstructive Sleep 67 0.901
855
P SCL018 Scoliosis 57 0.901
856
LMY002 Leiomyoma 51 0.901
857
ULC004 Ulcerative Colitis 74 0.901
858
END040 Endogenous Depression 55 0.901
859
MND031 Mandibuloacral Dysplasia Progeroid Syndrome 33 0.901
860
PRM236 Primary Biliary Cholangitis 60 0.901
861
PSY004 Psychotic Disorder 66 0.901
862
RYS001 Reye Syndrome 49 0.901
863
P GCH001 Gaucher's Disease 70 0.901
864
P RHZ001 Rhizomelic Chondrodysplasia Punctata 57 0.901
865
PRT013 Portal Hypertension 59 0.901
866
P TMP001 Temporal Lobe Epilepsy 49 0.901
867
LST001 Listeriosis 59 0.901
868
AMN003 Amnestic Disorder 54 0.901
869
SYS003 Systolic Heart Failure 49 0.901
870
CLD007 Cold Agglutinin Disease 42 0.901
871
PNM013 Pneumococcal Meningitis 43 0.876
872
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 0.876
873
c MTC060 Mitochondrial Dna Depletion Syndrome 9 50 0.876
874
SHR097 Short Tarsus with Absence of Lower Eyelashes 25 0.876
875
P LFR001 Li-Fraumeni Syndrome 73 0.876
876
CHL131 Chlorpropamide-Alcohol Flushing 21 0.876
877
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 58 0.876
878
c ACT249 Acute Asthma 40 0.876
879
c CHR627 Charcot-Marie-Tooth Disease, Demyelinating, Type 1a 56 0.876
880
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 0.876
881
BLD163 Blood Group, Dombrock System 16 0.876
882
NST002 Nestor-Guillermo Progeria Syndrome 35 0.876
883
c LFR007 Li-Fraumeni Syndrome 2 46 0.876
884
c PNC106 Pancreatic Agenesis 1 51 0.876
885
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 0.876
886
P KBK002 Kabuki Syndrome 1 65 0.876
887
c PRK085 Parkinson Disease 1, Autosomal Dominant 49 0.876
888
P HLP001 Holoprosencephaly 69 0.876
889
BRN018 Borna Disease 36 0.876
890
AMB001 Amebiasis 57 0.876
891
SYS071 Systemic Autoimmune Disease 35 0.876
892
CHL018 Childhood Medulloblastoma 48 0.876
893
MRK001 Merkel Cell Carcinoma 64 0.876
894
MLG077 Malignant Peripheral Nerve Sheath Tumor 54 0.876
895
SMN007 Seminoma 42 0.876
896
c JBR047 Joubert Syndrome 35 23 0.876
897
c ESS001 Essential Tremor 57 0.876
898
PNC034 Pancreas Disease 50 0.876
899
P OST001 Osteopetrosis 71 0.876
900
CHR073 Choreatic Disease 54 0.876
901
APH001 Aphthous Stomatitis 58 0.876
902
ISL099 Isolated Methylmalonic Acidemia 36 0.876
903
PRN019 Perinatal Necrotizing Enterocolitis 60 0.876
904
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.872
905
MNN042 Meningioma, Radiation-Induced 51 0.872
906
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.872
907
P RHB008 Rhabdoid Tumor Predisposition Syndrome 1 53 0.872
908
CRN036 Craniopharyngioma 64 0.872
909
P TRN020 Turner Syndrome 67 0.872
910
P PNB001 Pineoblastoma 49 0.872
911
CNT033 Central Nervous System Cancer 47 0.872
912
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.872
913
LYM040 Lymphoblastic Lymphoma 53 0.872
914
PNL014 Pineal Gland Cancer 40 0.872
915
SPN040 Spinal Cancer 45 0.872
916
P NRV006 Nervous System Cancer 48 0.872
917
CYS009 Cystadenoma 43 0.872
918
P CHR573 Choroid Plexus Cancer 48 0.872
919
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.872
920
PNC056 Pineocytoma 44 0.872
921
c WLF013 Wolfram Syndrome 1 60 0.843
922
GRW007 Growth Hormone Deficiency 46 0.843
923
LSS003 Lassa Fever 49 0.843
924
ADR022 Adrenomyeloneuropathy 39 0.843
925
P MYM013 Moyamoya Disease 1 59 0.843
926
ADR007 Adrenoleukodystrophy 73 0.843
927
ANR007 Anorexia Nervosa 60 0.843
928
P PRG130 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 1 54 0.843
929
ARG007 Argininemia 58 0.843
930
P APL001 Aplastic Anemia 73 0.843
931
c BTT014 Beta-Thalassemia 72 0.843
932
c RHZ004 Rhizomelic Chondrodysplasia Punctata, Type 3 42 0.843
933
HLC007 Helicobacter Pylori Infection 67 0.843
934
IGR001 Ige Responsiveness, Atopic 59 0.843
935
KWS002 Kawasaki Disease 65 0.843
936
LGN006 Legionnaire Disease 52 0.843
937
c PRG038 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 2 49 0.843
938
SNG007 Sengers Syndrome 45 0.843
939
P GLC113 Galactosemia I 66 0.843
940
TRG002 Trigeminal Neuralgia 61 0.843
941
PRP082 Porphyria, Congenital Erythropoietic 56 0.843
942
c PRG040 Progressive External Ophthalmoplegia with Mitochondrial Dna Deletions, Autosomal Dominant 4 53 0.843
943
HPT004 Hepatic Coma 43 0.843
944
P DYS154 Dystonia 64 0.843
945
P VSC011 Vasculitis 61 0.843
946
CHC001 Chickenpox 57 0.843
947
ACY011 Acyl-Coa Dehydrogenase Deficiency 30 0.843
948
THY125 Thyroid Gland Medullary Carcinoma 48 0.843
949
ACQ007 Acquired Immunodeficiency Syndrome 59 0.843
950
OVR063 Overnutrition 42 0.843
951
ILS001 Ileus