Search results for pyrophosphate

1169 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
c CHN022 Chondrocalcinosis 2 39 44.246
2
FML307 Familial Calcium Pyrophosphate Deposition 38 40.408
3
P CHN059 Chondrocalcinosis 52 33.091
4
c CHN021 Chondrocalcinosis 1 17 15.053
5
P ART023 Arthropathy 61 14.675
6
GT001 Gout 64 12.241
7
IRN002 Iron Metabolism Disease 57 11.026
8
BNR002 Bone Resorption Disease 47 8.891
9
c CHR684 Chronic Kidney Disease 69 8.795
10
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 8.508
11
P KDN018 Kidney Disease 72 8.376
12
P AMY004 Amyloidosis 70 7.803
13
P HYP069 Hyperparathyroidism 62 7.794
14
c ACT075 Acute Myocardial Infarction 56 7.658
15
P BRB001 Beriberi 44 7.464
16
OST012 Osteoarthritis 77 7.294
17
ANK001 Ankylosis 51 7.209
18
END086 End Stage Renal Disease 52 7.072
19
PLC002 Plica Syndrome 35 6.908
20
SYN007 Synovitis 55 6.908
21
P ART022 Arthritis 71 6.864
22
P HYP035 Hypophosphatasia 62 6.845
23
CRY024 Crystal Arthropathies 18 6.814
24
DFC004 Deficiency Anemia 74 6.588
25
P BND020 Bone Disease 59 6.306
26
P PSD087 Pseudoxanthoma Elasticum 67 5.948
27
INT007 Intermediate Coronary Syndrome 54 5.509
28
ANG054 Angina Pectoris 66 5.221
29
SPT004 Septic Arthritis 58 5.208
30
c HMC039 Hemochromatosis, Type 1 73 4.842
31
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 4.577
32
CLC006 Calcinosis 47 4.566
33
IRN001 Iron Deficiency Anemia 58 4.430
34
MMM001 Mammary Paget's Disease 53 4.332
35
RCK004 Rickets 68 4.317
36
URL001 Urolithiasis 46 4.296
37
c PRM005 Primary Hyperparathyroidism 59 4.195
38
c KNN009 Kenny-Caffey Syndrome, Type 1 35 4.191
39
OST011 Osteomalacia 52 4.125
40
c HYP836 Hypercholesterolemia, Familial, 1 73 4.097
41
OST017 Osteomyelitis 63 4.059
42
OST003 Osteonecrosis 61 4.026
43
CHG001 Chagas Disease 66 3.972
44
HYP005 Hypokalemia 55 3.873
45
HYP014 Hyperuricemia 51 3.721
46
URM002 Uremia 47 3.641
47
HYP025 Hyperphosphatemia 48 3.631
48
ART035 Arterial Calcification of Infancy 58 3.608
49
FRZ001 Frozen Shoulder 55 3.607
50
BRS064 Bursitis 51 3.607
51
P HYP086 Hypothyroidism 69 3.607
52
HLX001 Helix Syndrome 48 3.602
53
P OST002 Osteoporosis 76 3.541
54
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 3.541
55
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 3.541
56
P RHM011 Rheumatoid Arthritis 82 3.521
57
HYP068 Hyperostosis 47 3.449
58
P PLY019 Polyneuropathy 52 3.312
59
OST159 Osteogenic Sarcoma 66 3.299
60
TND005 Tendinitis 54 3.285
61
HMN044 Human Immunodeficiency Virus Type 1 78 3.259
62
WRN002 Wernicke-Korsakoff Syndrome 50 3.170
63
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 60 3.169
64
ENT004 Enthesopathy 51 3.158
65
c HYP292 Hypophosphatasia, Infantile 55 3.150
66
PRR001 Periarthritis 34 3.144
67
48X005 48,xyyy 39 3.124
68
NPH009 Nephrolithiasis 54 3.111
69
SYN031 Synovial Chondromatosis 41 3.094
70
INF013 Inferior Myocardial Infarction 33 3.045
71
P SPN052 Spondyloarthropathy 55 3.025
72
SPN051 Spondylitis 51 3.015
73
INF009 Inflammatory Spondylopathy 30 3.015
74
LSC001 Lesch-Nyhan Syndrome 62 2.982
75
CRT017 Cartilage Disease 53 2.978
76
P SRC025 Sarcoidosis 1 71 2.945
77
ALL029 Allergic Disease 59 2.907
78
MYL069 Myeloma, Multiple 77 2.906
79
P CHN012 Chondrosarcoma 57 2.854
80
c HYP293 Hypophosphatasia, Adult 51 2.853
81
RNL011 Renal Osteodystrophy 49 2.849
82
P NRB001 Neuroblastoma 66 2.832
83
P NRP001 Neuropathy 60 2.832
84
RPD005 Rapidly Involuting Congenital Hemangioma 46 2.794
85
47X002 47,xyy 48 2.788
86
P MYC008 Myocarditis 59 2.766
87
BRT054 Brittle Bone Disorder 74 2.763
88
SPN027 Spinal Stenosis 59 2.763
89
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 2.743
90
c SCN007 Secondary Hyperparathyroidism 51 2.716
91
PSR001 Psoriatic Arthritis 62 2.705
92
P PLY041 Polymyositis 59 2.705
93
HYP017 Hypophosphatemia 49 2.704
94
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.696
95
DSC004 Discitis 34 2.689
96
P MYC084 Mycobacterium Tuberculosis 1 68 2.661
97
PLR008 Pleurisy 50 2.634
98
GNG013 Gingivitis 59 2.632
99
P HRP006 Herpes Simplex 65 2.627
100
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 2.627
101
OLC001 Olecranon Bursitis 25 2.621
102
CRD137 Cardiogenic Shock 56 2.616
103
PRC013 Pericarditis 53 2.597
104
TRY001 Trypanosomiasis 50 2.592
105
c SPN225 Spondyloarthropathy 1 70 2.589
106
P MYP004 Myopathy 67 2.588
107
P GLY013 Glycogen Storage Disease 60 2.588
108
P PGT001 Paget's Disease of Bone 61 2.566
109
P KLZ004 Kala-Azar 1 41 2.548
110
LSH001 Leishmaniasis 64 2.548
111
GTL001 Gitelman Syndrome 65 2.547
112
CYT002 Cytokine Deficiency 43 2.532
113
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.522
114
c PRG042 Progressive Familial Heart Block, Type Ia 66 2.475
115
HYP066 Hyperglycemia 61 2.473
116
TNS014 Tenosynovitis 46 2.471
117
BCK006 Back Pain 47 2.471
118
P CRN037 Craniosynostosis 68 2.463
119
PRT037 Pertussis 65 2.463
120
ANX004 Anoxia 40 2.395
121
P DRM010 Dermatomyositis 61 2.375
122
EXS001 Exostosis 49 2.375
123
P INF032 Infertility 57 2.375
124
P PRP019 Peripheral Nervous System Disease 58 2.375
125
c THM013 Thiamine Metabolism Dysfunction Syndrome 5 32 2.360
126
NPH003 Nephrocalcinosis 49 2.354
127
c PCH010 Pachyonychia Congenita 3 43 2.315
128
HTC003 Hutchinson-Gilford Progeria Syndrome 65 2.311
129
P TMP003 Temporal Arteritis 69 2.309
130
c GLY060 Glycogen Storage Disease Ia 63 2.290
131
CLC004 Calcific Tendinitis 33 2.281
132
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 2.277
133
AGN016 Aging 54 2.267
134
SBN001 Subendocardial Myocardial Infarction 22 2.258
135
MLR004 Malaria 80 2.237
136
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 2.201
137
P CRN300 Coronary Heart Disease 1 73 2.181
138
P DYS154 Dystonia 64 2.181
139
ALC007 Alcohol Dependence 66 2.177
140
CYS001 Cystic Fibrosis 78 2.177
141
c HPT073 Hepatitis C Virus 71 2.177
142
P MYS005 Myositis 56 2.164
143
c TYP009 Type 2 Diabetes Mellitus 92 2.139
144
DSS032 Disease by Infectious Agent 55 2.129
145
LFT001 Left Bundle Branch Hemiblock 47 2.129
146
P ENC018 Encephalopathy 62 2.129
147
P OPT006 Optic Nerve Disease 58 2.128
148
OST115 Osteonecrosis of the Jaw 41 2.121
149
c ATR087 Atrial Standstill 1 74 2.082
150
c HPT001 Hepatitis C 62 2.080
151
P SNS001 Sensorineural Hearing Loss 59 2.080
152
P HYP265 Hypotonia 42 2.080
153
HYP596 Hypophosphatasia, Childhood 46 2.077
154
c SCL052 Scleroderma, Familial Progressive 61 2.073
155
P CRP001 Carpal Tunnel Syndrome 66 2.073
156
HRT012 Heart Valve Disease 53 2.073
157
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 2.073
158
c GLY017 Glycogen Storage Disease Ic 30 2.053
159
NPH091 Nephrolithiasis, Calcium Oxalate 61 2.029
160
HRW001 Hair Whorl 35 2.029
161
GLL048 Glial Tumor 52 2.029
162
VCC001 Vaccinia 47 2.029
163
P SYS005 Systemic Scleroderma 74 2.029
164
GLM045 Glioma 63 2.029
165
ART002 Arts Syndrome 66 2.025
166
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 49 2.015
167
P MPL001 Maple Syrup Urine Disease 70 2.015
168
P MCR010 Microcephaly 60 2.015
169
CRN264 Craniosynostosis with Fibular Aplasia 29 1.998
170
CFF002 Coffin-Lowry Syndrome 60 1.998
171
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 1.997
172
CHL014 Cholera 62 1.984
173
P LKM002 Leukemia 67 1.978
174
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 1.976
175
HMP001 Hemopericardium 47 1.976
176
P HPT021 Hepatitis 69 1.954
178
c ALM001 Al Amyloidosis 54 1.949
179
RCT015 Reactive Arthritis 61 1.931
180
BCT022 Bacterial Infectious Disease 56 1.920
181
SLP001 Sleeping Sickness 56 1.920
182
P PRC012 Pericardial Effusion 50 1.920
183
c BRN108 Branchiootic Syndrome 1 62 1.912
184
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 1.890
185
HYP266 Hypoxia 57 1.890
186
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 1.882
187
CRN030 Coronary Stenosis 50 1.876
188
RDC002 Radiculopathy 52 1.876
189
P SCL018 Scoliosis 57 1.863
190
BNN003 Bone Inflammation Disease 48 1.863
191
MVL001 Mevalonic Aciduria 66 1.830
192
GLB002 Glioblastoma 67 1.830
193
P MSC005 Muscular Dystrophy 67 1.821
194
P MNC007 Monocytic Leukemia 47 1.821
195
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 64 1.802
196
P MYC007 Myocardial Infarction 70 1.802
197
c DLT002 Dilated Cardiomyopathy 78 1.802
198
ACR007 Acromegaly 70 1.796
199
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 1.777
200
P HYP061 Hypertrophic Cardiomyopathy 69 1.777
201
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 1.777
202
IMM167 Immune Deficiency Disease 78 1.759
203
P DBT009 Diabetes Mellitus 67 1.750
204
CNN005 Connective Tissue Disease 67 1.747
205
P HYP076 Hyperthyroidism 53 1.747
206
MCR257 Microcephaly, Amish Type 35 1.737
207
DNT012 Dental Caries 53 1.737
208
c ACT071 Acute Kidney Failure 60 1.737
209
HYD003 Hydrarthrosis 30 1.724
210
INT182 Intermittent Hydrarthrosis 17 1.724
211
ATS010 Autosomal Recessive Disease 42 1.718
212
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.702
213
PRM329 Premature Aging 36 1.669
214
FTT001 Fatty Liver Disease 62 1.669
215
GTR002 Goiter 53 1.669
216
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 1.664
217
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 41 1.664
218
MSC007 Muscle Hypertrophy 64 1.664
219
RNL114 Renal Cell Carcinoma, Nonpapillary 80 1.664
220
PST092 Posttransplant Acute Limbic Encephalitis 28 1.603
221
HMP009 Haemophilus Influenzae 41 1.603
222
INF034 Infective Endocarditis 54 1.595
223
P END033 Endocarditis 58 1.595
224
OST004 Osteitis Fibrosa 38 1.595
225
SPN119 Spondylarthropathy 38 1.590
226
P LVR013 Liver Disease 69 1.556
227
PRT036 Peritonitis 65 1.556
228
WRN003 Wernicke Encephalopathy 46 1.546
229
P AVS003 Avascular Necrosis 41 1.539
230
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 19 1.539
231
P PNC035 Pancreatic Cancer 86 1.539
232
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 1.539
233
P UVT001 Uveitis 57 1.539
234
DSS010 Dissociative Disorder 39 1.539
235
ACT058 Active Peptic Ulcer Disease 56 1.539
236
c JVN010 Juvenile Rheumatoid Arthritis 66 1.539
237
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 1.539
238
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 1.539
239
GLL008 Gilles De La Tourette Syndrome 65 1.525
240
P FML068 Familial Hypocalciuric Hypercalcemia 55 1.525
241
SFT003 Soft Tissue Sarcoma 57 1.525
243
c MCR115 Microvascular Complications of Diabetes 5 65 1.515
244
P ATR011 Atrial Fibrillation 66 1.515
245
P INF038 Influenza 68 1.515
246
CHN010 Chondroma 43 1.515
247
HMR002 Hemarthrosis 44 1.515
248
c HRD039 Hereditary Amyloidosis 45 1.515
249
P LCT001 Lactic Acidosis 51 1.500
250
P MYS003 Myasthenia Gravis 68 1.488
251
MYS001 Myositis Ossificans 44 1.478
252
MYC005 Myocardial Stunning 46 1.478
253
CRZ001 Crouzon Syndrome 65 1.471
254
GLC086 Glucocorticoid-Induced Osteoporosis 43 1.471
255
P PRS040 Prostate Cancer 95 1.471
256
HMS001 Hemosiderosis 48 1.471
257
P NMN002 Niemann-Pick Disease 60 1.471
258
P ALZ034 Alzheimer Disease 87 1.452
259
NRR001 Neuroretinitis 42 1.452
260
RTN023 Retinitis 46 1.452
261
c SYS001 Systemic Lupus Erythematosus 87 1.427
262
TND004 Tendinopathy 45 1.427
263
c PRG106 Progressive Muscular Dystrophy 32 1.427
264
P PRK001 Porokeratosis 55 1.427
265
P CRD119 Cardiac Arrest 67 1.427
266
GNG003 Gingival Recession 49 1.427
267
P TRC031 Trichorhinophalangeal Syndrome 38 1.427
268
DYS073 Dysphagia 53 1.427
269
SPN186 Spinal Cord Injury 61 1.397
270
P LKM071 Leukemia, Chronic Lymphocytic 75 1.397
271
LGH007 Leigh Syndrome 70 1.397
272
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 1.397
273
FBR011 Fibrodysplasia Ossificans Progressiva 67 1.397
274
P GST044 Gastritis 55 1.397
275
PGM001 Pigmented Villonodular Synovitis 55 1.397
276
MNN009 Meningoencephalitis 48 1.397
277
P SHR001 Short Bowel Syndrome 53 1.397
278
ISC004 Ischemia 61 1.397
279
VLL003 Villonodular Synovitis 41 1.397
280
P ART021 Arteriosclerosis 54 1.352
281
c HYP794 Hyperoxaluria, Primary, Type I 63 1.350
282
ART140 Arteries, Anomalies of 53 1.326
283
LPP008 Lipoprotein Quantitative Trait Locus 65 1.326
284
P HYP098 Hypereosinophilic Syndrome 66 1.326
285
P MLN007 Male Infertility 56 1.326
286
CNS002 Constrictive Pericarditis 40 1.326
287
c DNT047 Dentinogenesis Imperfecta Type 2 35 1.326
288
BNN005 Bunion 31 1.321
290
TNG002 Tangier Disease 64 1.317
291
PPL052 Papillomatosis, Confluent and Reticulated 34 1.317
292
c AMY091 Amyotrophic Lateral Sclerosis 1 88 1.317
293
BRK010 Burkitt Lymphoma 66 1.317
294
MYL009 Myelodysplastic Syndrome 67 1.317
295
P URN019 Urinary Tract Infection 49 1.317
296
PHN003 Phenylketonuria 76 1.317
297
MDD018 Middle East Respiratory Syndrome 44 1.317
298
P MLG056 Malignant Hyperthermia 66 1.317
299
ANT024 Anthrax Disease 58 1.317
300
PRP016 Paraplegia 52 1.317
301
P LTR001 Lateral Sclerosis 58 1.317
302
MGL001 Megaloblastic Anemia 58 1.317
303
CNG034 Congestive Heart Failure 69 1.317
304
CRB039 Cerebrovascular Disease 66 1.317
305
OCH001 Ochronosis 40 1.317
306
P BNC003 Bone Cancer 58 1.317
307
P TXP001 Toxoplasmosis 60 1.317
308
MCR018 Microcytic Anemia 47 1.276
309
P MCR129 Microvascular Complications of Diabetes 1 68 1.272
310
ATH013 Atherosclerosis Susceptibility 63 1.244
311
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.244
312
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.244
313
P PRD008 Periodontitis 64 1.244
314
CYT005 Cytomegalovirus Retinitis 50 1.244
315
P PLY011 Polycystic Ovary Syndrome 57 1.244
316
SPP011 Suppression of Tumorigenicity 12 61 1.229
317
SRC027 Sarcoma, Synovial 58 1.229
318
P EXN002 Exanthem 58 1.229
319
OPT071 Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive 18 1.229
320
SPN019 Spondylolisthesis 52 1.229
321
P LPS004 Lupus Erythematosus 61 1.229
322
VLK001 Volkmann Contracture 23 1.229
323
P RST002 Restrictive Cardiomyopathy 54 1.229
324
OST014 Osteopoikilosis 41 1.229
325
P HMN010 Hemangioma 62 1.229
326
EPD005 Epidural Abscess 31 1.229
327
CDQ001 Cauda Equina Syndrome 37 1.229
328
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.229
329
PRT029 Parathyroid Adenoma 51 1.229
330
OST016 Osteochondrosis 52 1.229
331
P OST001 Osteopetrosis 71 1.229
332
P HRD207 Hereditary Transthyretin Amyloidosis 25 1.229
333
c LKM005 Leukemia, T-Cell, Chronic 34 1.229
334
PYR016 Pyridoxine Deficiency 29 1.229
335
DWR001 Dwarfism 44 1.229
336
SPS057 Spasticity 42 1.207
337
STR067 Stroke, Ischemic 80 1.207
338
OCL069 Ocular Motor Apraxia 57 1.207
339
ART016 Aortic Aneurysm 68 1.207
340
c FTL070 Fetal Akinesia Deformation Sequence 2 36 1.207
341
TTN003 Tetanus 65 1.207
342
P HYP726 Hypercalcemia, Infantile, 1 58 1.202
343
P BRT004 Bartter Disease 58 1.202
344
CLD014 Cole Disease 38 1.194
345
P OVR082 Overgrowth Syndrome 49 1.186
346
P LKM062 Leukemia, Acute Lymphoblastic 69 1.186
347
P GST053 Gastric Cancer 83 1.186
348
CHC001 Chickenpox 57 1.186
349
P CHR071 Charcot-Marie-Tooth Disease 64 1.186
350
TTH006 Tooth Disease 51 1.186
351
LPD008 Lipid Metabolism Disorder 62 1.186
352
ALL014 Allergic Encephalomyelitis 34 1.186
353
c HPT003 Hepatitis a 63 1.168
354
NTR005 Nutritional Deficiency Disease 61 1.168
355
INS024 Insulin-Like Growth Factor I 78 1.128
356
MND023 Mend Syndrome 49 1.128
357
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.128
358
LMB062 Limb Ischemia 55 1.128
359
PRT251 Proteinuria, Chronic Benign 57 1.128
360
CLT003 Colitis 63 1.128
361
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.128
362
P ASP006 Aspergillosis 72 1.128
363
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 1.128
364
RBF001 Riboflavin Deficiency 49 1.128
365
FBR054 Fibroma 44 1.128
366
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 1.128
367
P ZLL001 Zellweger Syndrome 65 1.128
368
CTN007 Cutaneous Leishmaniasis 62 1.128
369
P BRS044 Breast Adenocarcinoma 58 1.128
370
EXT012 Extraskeletal Chondroma 17 1.128
371
P PSD015 Pseudohypoparathyroidism 55 1.128
372
P GRV001 Graves' Disease 55 1.128
373
SPN020 Spondylosis 46 1.128
374
SPN029 Spondylolysis 39 1.128
375
c ACT027 Acute Pancreatitis 60 1.128
376
LYM017 Lyme Disease 62 1.128
377
P HYP024 Hypoparathyroidism 55 1.128
378
P KDN017 Kidney Cancer 61 1.128
379
QDR001 Quadriplegia 50 1.128
380
P DRR001 Diarrhea 55 1.128
381
HYP060 Hyperinsulinism 54 1.128
382
SBC016 Subacute Delirium 43 1.128
383
P PRG139 Progeroid Syndrome 27 1.125
384
P BRS047 Breast Cancer 98 1.125
385
ATR057 Atrioventricular Block 54 1.125
386
c LKM061 Leukemia, Acute Myeloid 83 1.125
387
P HNT016 Huntington Disease 73 1.125
388
ACQ007 Acquired Immunodeficiency Syndrome 59 1.125
389
P VSC007 Vascular Disease 63 1.125
390
P BNG032 Benign Mesothelioma 53 1.125
391
P CMP008 Compartment Syndrome 50 1.125
392
ADL002 Adult Syndrome 70 1.104
393
c ART115 Aortic Valve Disease 1 74 1.060
394
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 1.060
395
P OVR042 Ovarian Cancer 88 1.060
396
WTB001 Wet Beriberi 26 1.060
397
CRD003 Cardiac Sarcoidosis 44 1.060
398
P MLN008 Melanoma 76 1.060
399
GRD001 Giardiasis 46 1.060
400
GST045 Gastroenteritis 58 1.060
401
c RNG015 Ring Chromosome 2 22 1.060
402
ARG004 Argyria 26 1.052
403
c ACT076 Acute Myocarditis 47 1.052
404
c ACT134 Acute Liver Failure 59 1.009
405
ALK013 Alkaptonuria 59 1.009
406
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 1.009
407
WTH001 Withdrawal Disorder 48 1.009
408
EXT033 Extrapulmonary Tuberculosis 45 1.009
409
WLS001 Wilson Disease 70 1.009
411
DWN001 Down Syndrome 70 1.009
412
ATN021 Autoinflammatory Syndrome 32 1.009
413
CLC001 Calciphylaxis 51 1.009
414
MLR003 Melorheostosis 48 1.009
415
INT075 Intracranial Hypertension 53 1.009
416
PLM001 Pulmonary Tuberculosis 69 1.009
417
THR016 Thrombophlebitis 50 1.009
418
ALC010 Alcoholic Cardiomyopathy 42 1.009
419
P PYL005 Pyelonephritis 57 1.009
420
FNG004 Fungal Meningitis 46 1.009
421
c VRL005 Viral Pneumonia 53 1.009
422
NRV004 Nerve Compression Syndrome 44 1.009
423
GST050 Gastrointestinal System Disease 55 1.009
424
P GLM007 Glomerulonephritis 60 1.009
425
PLM010 Pulmonary Edema 55 1.009
426
RHM001 Rheumatic Fever 59 1.009
427
RCT020 Rectum Adenocarcinoma 48 1.009
428
ISL001 Islet Cell Tumor 56 1.009
429
GNT003 Genital Herpes 54 1.009
430
c HMN021 Human T-Cell Leukemia Virus Type 1 47 1.009
431
P FML018 Familial Mediterranean Fever 73 0.992
432
MTB004 Metabolic Acidosis 48 0.992
433
ACT098 Acute Erythroid Leukemia 55 0.992
434
HMN047 Human Cytomegalovirus Infection 57 0.992
435
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.992
436
THY029 Thyroid Carcinoma 51 0.992
437
P ALC033 Alcohol Use Disorder 61 0.992
438
P END044 Endometriosis 62 0.992
439
BRC012 Brucellosis 66 0.992
440
SVR004 Severe Combined Immunodeficiency 72 0.992
441
P PRM002 Primary Hyperoxaluria 65 0.992
442
RGH001 Right Bundle Branch Block 47 0.992
443
PTH003 Pathologic Nystagmus 52 0.992
444
P BLD134 Bladder Cancer 79 0.918
445
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.918
446
KRN002 Kearns-Sayre Syndrome 63 0.918
447
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.918
448
c DFN194 Deafness, X-Linked 1 35 0.918
449
P GLM040 Glioma Susceptibility 1 71 0.918
450
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 50 0.918
451
CRH001 Crohn's Disease 80 0.918
452
DGN001 Degenerative Disc Disease 49 0.918
453
CMB007 Combined Immunodeficiency 57 0.918
454
c PRC016 Pre-Eclampsia 65 0.918
455
c ACT068 Acute Cystitis 61 0.918
456
MLG169 Malignant Astrocytoma 57 0.918
457
SRC014 Sarcoma 65 0.918
458
LVR012 Liver Cirrhosis 63 0.918
459
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.918
460
STM007 Stomatitis 54 0.918
461
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.901
462
NRL025 Neural Tube Closure Defect 27 0.854
463
P SKL032 Skeletal Muscle Disease 25 0.854
464
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 0.854
465
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 0.854
466
HYP781 Hypoascorbemia 52 0.854
467
P SML001 Small Cell Carcinoma 52 0.854
468
c GLY004 Glycogen Storage Disease V 62 0.854
469
SPN392 Spondylosis, Cervical 30 0.854
470
ACT119 Acute Promyelocytic Leukemia 62 0.854
471
c GLC079 Glaucoma 1, Open Angle, P 23 0.854
472
ENT011 Enterocolitis 55 0.854
473
MYX004 Myxedema 43 0.854
474
INC002 Inclusion Body Myositis 57 0.854
475
c SYS048 Systemic Lupus Erythematosus 8 17 0.854
476
OBS082 Obstructive Nephropathy 41 0.854
477
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 0.854
478
ULN001 Ulnar Neuropathy 28 0.854
479
CHR074 Choriocarcinoma 46 0.854
480
CLC064 Calcifying Aponeurotic Fibroma 22 0.854
481
PRD026 Pre-Descemet Corneal Dystrophy 20 0.854
482
NRM005 Neuromuscular Disease 63 0.854
483
SMN007 Seminoma 42 0.854
484
INT071 Intestinal Perforation 49 0.854
485
P NRN021 Neuronal Ceroid Lipofuscinosis 65 0.854
486
LTR004 Lateral Myocardial Infarction 27 0.854
487
P PNC044 Pancreatitis 61 0.854
488
TNS001 Tenosynovial Giant Cell Tumor 40 0.854
489
CHN004 Chondroblastoma 41 0.854
490
HYP141 Hyperphenylalaninemia 42 0.854
491
HYP706 Hypermobile Ehlers-Danlos Syndrome 55 0.854
492
FSC004 Fasciitis 49 0.854
493
PLN007 Plantar Fasciitis 36 0.854
494
KDN013 Kidney Hypertrophy 34 0.854
495
FTD001 Foot Drop 35 0.854
496
PRS063 Paresthesia 39 0.854
497
ANR040 Aneurysm 61 0.854
498
CRD016 Cardiac Rupture 34 0.854
499
HMP018 Hemophilic Arthropathy 34 0.854
500
PRN019 Perinatal Necrotizing Enterocolitis 60 0.854
501
ALG024 Alg6-Congenital Disorder of Glycosylation 21 0.838
502
P THM010 Thiamine Metabolism Dysfunction Syndrome 2 50 0.838
503
c CNG196 Congenital Disorder of Glycosylation, Type Ic 38 0.838
504
P CLR023 Colorectal Cancer 100 0.838
505
c MCR130 Microvascular Complications of Diabetes 6 41 0.838
506
c ANK022 Ankylosing Spondylitis 2 9 0.838
507
c MCR120 Microvascular Complications of Diabetes 7 47 0.838
508
P SPP010 Suppressor of Tumorigenicity 3 51 0.838
509
INT051 Intussusception 52 0.838
510
P PRK039 Parkinsonism 55 0.838
511
P VSC011 Vasculitis 61 0.838
512
ULC004 Ulcerative Colitis 74 0.838
513
P MYL006 Myeloid Leukemia 61 0.838
514
P RRH023 Rare Hereditary Hemochromatosis 54 0.838
515
P FBR017 Fibrosarcoma 56 0.838
516
MTH009 Mouth Disease 57 0.838
517
P SYP003 Syphilis 59 0.838
518
SPN035 Spindle Cell Sarcoma 54 0.838
519
c MCR113 Microvascular Complications of Diabetes 3 52 0.838
520
c MCR133 Microvascular Complications of Diabetes 4 41 0.838
521
P DNG005 Dengue Virus 56 0.838
522
VRC001 Varicocele 48 0.838
523
P GCH001 Gaucher's Disease 70 0.838
524
CLN015 Colon Adenocarcinoma 65 0.838
525
P TCD001 Tic Disorder 49 0.838
526
P NRF002 Neurofibromatosis 57 0.838
527
HYP056 Hypoglycemia 65 0.838
528
P NNS072 Nonsyndromic Hearing Loss 40 0.838
529
WLF014 Wolfram Syndrome, Mitochondrial Form 17 0.824
530
P DBT005 Diabetes Insipidus 54 0.750
531
P SZR006 Seizure Disorder 70 0.750
532
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.750
533
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.750
534
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.750
535
P PHC003 Pheochromocytoma 69 0.750
536
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.750
537
PRP027 Peripheral Vascular Disease 71 0.750
538
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 0.750
539
LGG001 Legg-Calve-Perthes Disease 60 0.750
540
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.750
541
SCK003 Sickle Cell Anemia 74 0.750
542
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.750
543
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.750
544
c HYP369 Hypophosphatemic Rickets, Autosomal Recessive, 2 30 0.750
545
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.750
546
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.750
547
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.750
548
CYS013 Cystinuria 66 0.750
549
MYL005 Myelofibrosis 71 0.750
550
ORT008 Orotic Aciduria 57 0.750
551
c NMN015 Niemann-Pick Disease, Type C1 68 0.750
552
c SML038 Small Cell Cancer of the Lung 69 0.750
553
SCH076 Schnyder Corneal Dystrophy 47 0.750
554
BSL009 Basal Ganglia Calcification 45 0.750
555
CLR109 Colorectal Adenocarcinoma 50 0.750
556
ADR040 Adrenal Gland Pheochromocytoma 46 0.750
557
FBR009 Fibrous Dysplasia 48 0.750
558
c ACT073 Acute Leukemia 58 0.750
559
CHR066 Chronic Fatigue Syndrome 60 0.750
560
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.750
561
MNG007 Manganese Poisoning 28 0.750
562
P ANT006 Antiphospholipid Syndrome 55 0.750
563
CLL003 Cellulitis 53 0.750
564
MSC072 Muscle Cancer 48 0.750
565
PYR009 Pyridoxine Deficiency Anemia 35 0.750
566
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.750
567
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.750
568
BRN028 Brain Cancer 74 0.750
569
P NTR004 Neutropenia 63 0.750
570
TXC005 Toxic Shock Syndrome 62 0.750
571
c CHR571 Charcot-Marie-Tooth Disease Type 5 23 0.750
572
MCS002 Mucositis 56 0.750
573
HYP043 Hyperandrogenism 48 0.750
574
c INH020 Inherited Metabolic Disorder 48 0.750
575
P CRN025 Corneal Dystrophy 49 0.750
576
c FML021 Familial Hypercholesterolemia 72 0.750
577
VSC002 Vascular Dementia 60 0.750
578
NRF007 Neurofibroma 64 0.750
579
P EPS003 Episodic Ataxia 59 0.750
580
c XLN110 X-Linked Charcot-Marie-Tooth Disease 31 0.750
581
CRB089 Cerebral Beriberi 19 0.750
582
PTT037 Pituitary Tumors 44 0.750
583
ATN005 Autonomic Dysfunction 46 0.750
584
CND006 Candida Glabrata 30 0.750
585
c BLD140 Blood Group, I System 46 0.741
586
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 0.741
587
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.693
588
INT323 Intraocular Pressure Quantitative Trait Locus 64 0.677
589
c PNS012 Paine Syndrome 60 0.672
590
P VND007 Van Der Woude Syndrome 1 60 0.672
591
ENC044 Enchondromatosis, Multiple, Ollier Type 56 0.672
592
PPL049 Papillon-Lefevre Syndrome 66 0.672
593
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.672
594
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.672
595
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 0.672
596
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.672
597
SPN041 Spinal Cord Disease 55 0.672
598
P ATS364 Autism 69 0.649
599
P LNG032 Lung Cancer 98 0.649
600
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 47 0.649
601
P SNG014 Singleton-Merten Syndrome 36 0.649
602
SKL017 Skeletal Dysplasias 41 0.649
603
c INH030 Inherited Retinal Disorder 28 0.649
604
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.649
605
PFF001 Pfeiffer Syndrome 77 0.649
606
ANG004 Angioid Streaks 40 0.649
607
c CNG194 Congenital Disorder of Glycosylation, Type Ig 47 0.649
608
CRV035 Cervical Cancer 73 0.649
609
c PLM164 Pulmonary Hypertension, Primary, 1 76 0.649
610
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.649
611
PRN011 Pernicious Anemia 53 0.649
612
PLY150 Polykaryocytosis Inducer 29 0.649
613
c CRN278 Craniosynostosis 1 55 0.649
614
ATM095 Autoimmune Disease 61 0.649
615
P PLM037 Pulmonary Hypertension 72 0.649
616
P ADL017 Adult T-Cell Leukemia 56 0.649
617
P INF037 Inflammatory Bowel Disease 53 0.649
618
ART074 Aortic Dissection 53 0.649
619
P LYM118 Lymphoma 67 0.649
620
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 29 0.649
621
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.649
622
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.649
623
LGN006 Legionnaire Disease 52 0.649
624
c GCH013 Gaucher Disease, Type Iiic 38 0.649
625
KTL001 Keutel Syndrome 41 0.649
626
P OST122 Osteogenesis Imperfecta, Type Iii 57 0.649
627
URT049 Urate Oxidase, Pseudogene 24 0.649
628
P HYP750 Hypertriglyceridemia, Familial 62 0.649
629
CHL065 Cholangiocarcinoma 58 0.649
630
P FLL037 Follicular Lymphoma 74 0.649
631
GLC003 Glucose Intolerance 54 0.649
633
c SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 47 0.649
634
XLN244 X-Linked Sensorineural Deafness 15 0.649
635
P BCL017 B-Cell Lymphoma 59 0.649
636
URM001 Uremic Neuropathy 19 0.649
637
AVN001 Avian Influenza 61 0.649
638
P RHB003 Rhabdomyosarcoma 66 0.649
639
P ACT008 Actinic Keratosis 54 0.649
640
BSL008 Basal Ganglia Disease 41 0.649
641
FND002 Fundus Dystrophy 55 0.649
642
P TRM003 Tremor 48 0.649
643
DBT010 Diabetic Neuropathy 54 0.649
644
PLS011 Plasmacytoma 56 0.649
645
FBR047 Fibromyalgia 58 0.649
646
MYL001 Myelitis 50 0.649
647
ERD001 Erdheim-Chester Disease 53 0.649
648
P ESP024 Esophagitis 60 0.649
649
P GLL022 Guillain-Barre Syndrome 60 0.649
650
CRT013 Carotid Stenosis 51 0.649
651
KRT009 Keratosis 53 0.649
652
P ADN016 Adenocarcinoma 63 0.649
653
SCH014 Schistosomiasis 56 0.649
654
DPH001 Diphtheria 59 0.649
655
P HRT032 Heart Disease 81 0.649
656
P RSP003 Respiratory Failure 74 0.649
657
KRT002 Keratomalacia 55 0.649
658
INT079 Intrahepatic Cholangiocarcinoma 51 0.649
659
THY030 Thyroid Gland Disease 50 0.649
660
P PNM007 Pneumonia 67 0.649
661
P SCL048 Sclerosteosis 58 0.649
662
ALC011 Alcoholic Neuropathy 34 0.649
663
ART006 Arthus Reaction 40 0.649
664
NRG003 Neurogenic Arthropathy 42 0.649
665
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.649
666
P CHR345 Chronic Pain 50 0.649
667
FML091 Familial Tumoral Calcinosis 43 0.649
668
PNC060 Punctate Porokeratosis 28 0.649
669
DHY008 Dihydroxyadeninuria 24 0.649
670
PRM243 Primary Bone Cancer 22 0.649
671
ETN001 Eating Disorder 59 0.649
672
c INF145 Infantile Liver Failure Syndrome 1 43 0.637
673
AND005 Androgen Insensitivity Syndrome, Mild 21 0.637
674
ADR022 Adrenomyeloneuropathy 39 0.530
675
XLN174 X-Linked Non-Syndromic Sensorineural Deafness Type Dfn 20 0.530
676
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 36 0.530
677
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 29 0.530
678
P THL005 Thalassemia 56 0.530
679
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.530
680
P NSP012 Nasopharyngeal Carcinoma 61 0.530
681
RTC012 Reticuloendotheliosis, X-Linked 35 0.530
682
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.530
683
c GLL024 Gallbladder Disease 1 52 0.530
684
ADR007 Adrenoleukodystrophy 73 0.530
685
CRD132 Cardiac Conduction Defect 60 0.530
686
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 63 0.530
687
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.530
688
ANR007 Anorexia Nervosa 60 0.530
689
HMC014 Homocysteinemia 52 0.530
690
P MLT020 Multiple Sclerosis 79 0.530
691
BHC003 Behcet Syndrome 71 0.530
692
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 0.530
693
FRS012 First-Degree Atrioventricular Block 39 0.530
694
CNZ001 Coenzyme Q10 Deficiency Disease 41 0.530
695
VTM002 Vitamin B12 Deficiency 48 0.530
696
c MJR022 Major Affective Disorder 8 38 0.530
697
c BTT014 Beta-Thalassemia 72 0.530
698
DFF005 Diffuse Large B-Cell Lymphoma 54 0.530
699
PRX005 Peroxisomal Biogenesis Disorder 33 0.530
700
THY121 Thyroid Gland Anaplastic Carcinoma 67 0.530
701
c ATS007 Autism Spectrum Disorder 72 0.530
702
P USH001 Usher Syndrome 64 0.530
703
P DFF019 Diffuse Gastric Cancer 50 0.530
704
KPS004 Kaposi Sarcoma 77 0.530
705
PPL054 Popliteal Cyst 22 0.530
706
RFL001 Reflex Sympathetic Dystrophy 51 0.530
707
LPT014 Leptin Deficiency or Dysfunction 78 0.530
708
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 0.530
709
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.530
710
c MCR312 Microphthalmia, Syndromic 10 40 0.530
711
c MJR024 Major Affective Disorder 9 41 0.530
712
RHB024 Rhabdomyosarcoma 2 67 0.530
713
c MYC058 Myocardial Infarction 2 24 0.530
714
CLB022 Coloboma, Ocular, Autosomal Recessive 28 0.530
715
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.530
716
P MDL005 Medulloblastoma 75 0.530
717
c SPN294 Spinocerebellar Ataxia 1 53 0.530
718
OSS012 Osseous Heteroplasia, Progressive 61 0.530
719
P HPT023 Hepatocellular Carcinoma 96 0.530
720
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.530
721
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.530
722
MLD001 Melioidosis 67 0.530
723
RNL077 Renal Fibrosis 46 0.530
724
c ATS307 Autosomal Recessive Cerebellar Ataxia 39 0.530
725
P PNM006 Pneumoconiosis 55 0.530
726
INT067 Interstitial Nephritis 46 0.530
727
CLS052 Classic Hairy Cell Leukemia 25 0.530
728
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.530
729
ART102 Arterial Calcification, Generalized, of Infancy, 2 25 0.530
730
c PST005 Posterior Uveitis 54 0.530
731
LMY002 Leiomyoma 51 0.530
732
ACT003 Acute Kidney Tubular Necrosis 46 0.530
733
URT010 Ureteral Obstruction 45 0.530
734
VSC003 Visceral Leishmaniasis 55 0.530
735
P PSR002 Psoriasis 63 0.530
736
WLD005 Wild Type Attr Amyloidosis 29 0.530
737
P RNV001 Renovascular Hypertension 49 0.530
738
P EPL164 Epilepsy 68 0.530
739
c VRL010 Viral Hepatitis 53 0.530
740
TRT001 Teratocarcinoma 42 0.530
741
P BPL003 Bipolar Disorder 56 0.530
742
HST010 Histiocytosis 49 0.530
743
P OLV001 Olivopontocerebellar Atrophy 51 0.530
744
PNM008 Pneumothorax 54 0.530
745
P RTN016 Retinal Degeneration 52 0.530
746
MYF001 Myofibroma 42 0.530
747
PST011 Pustulosis of Palm and Sole 52 0.530
748
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 39 0.530
749
CMM005 Common Cold 56 0.530
750
P LNG064 Lung Cancer Susceptibility 3 70 0.530
751
c MCR112 Microvascular Complications of Diabetes 2 42 0.530
752
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.530
753
ANG020 Angiosarcoma 64 0.530
754
ANT018 Anthracosis 51 0.530
755
P MLT007 Multiple Epiphyseal Dysplasia 56 0.530
756
RSP002 Respiratory Syncytial Virus Infectious Disease 52 0.530
757
DYS015 Dysentery 50 0.530
758
ALC006 Alcoholic Hepatitis 61 0.530
759
PPL022 Papilloma 53 0.530
760
SQM002 Squamous Cell Papilloma 46 0.530
761
ALG001 Algoneurodystrophy 38 0.530
762
RTC003 Root Caries 32 0.530
763
IMP005 Impotence 52 0.530
764
CRY003 Cryptosporidiosis 56 0.530
765
RTN020 Retinal Vascular Disease 46 0.530
766
P NPH012 Nephrotic Syndrome 60 0.530
767
c HRD010 Hereditary Spastic Paraplegia 66 0.530
768
P ANG015 Angioedema 56 0.530
769
SKN006 Skin Sarcoidosis 42 0.530
770
FCL012 Facial Paralysis 49 0.530
771
BCT004 Bacteriuria 47 0.530
772
ATN004 Autonomic Neuropathy 42 0.530
773
P RNL015 Renal Hypertension 45 0.530
774
PRT013 Portal Hypertension 59 0.530
775
CHL123 Chlamydia 58 0.530
776
MTR002 Mitral Valve Insufficiency 52 0.530
777
HYP006 Hypertensive Heart Disease 49 0.530
778
CYS010 Cystinosis 62 0.530
779
P RHN004 Rhinitis 57 0.530
780
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.530
781
P RTN018 Retinal Disease 53 0.530
782
PHR003 Pharyngitis 58 0.530
783
TYP007 Typhoid Fever 64 0.530
784
HMN048 Human Papillomavirus Infectious Disease 46 0.530
785
CHL068 Cholestasis 61 0.530
786
OPS001 Opisthorchiasis 41 0.530
787
HYP021 Hypercementosis 28 0.530
788
P CRD246 Cardiovascular System Disease 56 0.530
789
c HPT016 Hepatitis B 62 0.530
790
HYP080 Hypogonadism 50 0.530
791
SQM006 Squamous Cell Carcinoma 60 0.530
792
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 17 0.530
793
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.530
794
PHS018 Phosphorylase Kinase Deficiency 39 0.530
795
GRN017 Granulocytopenia 42 0.530
796
SYS003 Systolic Heart Failure 49 0.530
797
DST006 Diastolic Heart Failure 45 0.530
799
c RNG019 Ring Chromosome 3 19 0.530
800
SPL018 Splenomegaly 49 0.530
801
HDN002 Head Injury 44 0.530
802
P MTC069 Mitochondrial Disorders 57 0.530
803
P SCK005 Sickle Cell Disease 56 0.530
804
P DYS021 Dysautonomia 38 0.530
805
c AMY009 Amyloidosis Aa 47 0.530
806
CRL001 Cerulean Cataract 26 0.530
807
OVR094 Ovarian Epithelial Cancer 39 0.530
808
ERY069 Erythrokeratoderma ''en Cocardes'' 27 0.530
809
PYM001 Pyomyositis 42 0.479
810
c OST135 Osteogenesis Imperfecta, Type I 53 0.479
811
PRC052 Pericardial Effusion, Chronic 19 0.479
812
HMN004 Hemangioma of Liver 35 0.479
813
BRX001 Bruxism 51 0.479
814
TTH007 Tooth Erosion 29 0.479
815
P LMY004 Leiomyosarcoma 62 0.479
816
c WLF013 Wolfram Syndrome 1 60 0.375
817
LYM133 Lymphoma, Hodgkin, Classic 74 0.375
818
SLP010 Slipped Capital Femoral Epiphysis 38 0.375
819
IDP069 Idiopathic Avascular Necrosis 23 0.375
820
VNZ002 Venezuelan Equine Encephalitis 46 0.375
821
ETH012 Ethylene Glycol Poisoning 29 0.375
822
BNG077 Benign Idiopathic Neonatal Seizures 23 0.375
823
CHN053 Chondromyxoid Fibroma 39 0.375
824
NRM021 Neurometabolic Disorder Due to Serine Deficiency 15 0.375
825
THY128 Thyroid Tumor 35 0.375
826
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.375
827
FRN006 Frontotemporal Dementia 68 0.375
828
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.375
829
SMT004 Smith-Lemli-Opitz Syndrome 70 0.375
830
c OPT051 Opitz Gbbb Syndrome, Type I 46 0.375
831
SDD001 Sudden Infant Death Syndrome 60 0.375
832
BDY003 Body Length, Mouse, Human Homolog 4 0.375
833
P LPR021 Leprosy 3 71 0.375
834
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 0.375
835
P RTN008 Retinitis Pigmentosa 80 0.375
836
LYM007 Lymphangioleiomyomatosis 68 0.375
837
ALL003 Allergic Rhinitis 67 0.375
838
P AST005 Asthma 76 0.375
839
c WRB002 Warburg Micro Syndrome 1 51 0.375
840
P NRP066 Neuropathy, Hereditary Motor and Sensory, Type Via, with Optic Atrophy 42 0.375
841
c ALP101 Alpha-Thalassemia 62 0.375
842
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 55 0.375
843
P OCL013 Oculodentodigital Dysplasia 67 0.375
844
PHS025 Phosphatase, Acid, of Tissues 28 0.375
845
PHS027 Phosphoglycoprotein 1 15 0.375
846
c TBL031 Tubulointerstitial Kidney Disease, Autosomal Dominant, 1 47 0.375
847
c PSD108 Pseudohypoparathyroidism, Type Ia 65 0.375
848
P SYN060 Syndactyly, Type Iii 41 0.375
849
c MST023 Mesothelioma, Malignant 56 0.375
850
P PRK057 Parkinson Disease, Late-Onset 80 0.375
851
c PLY136 Polydactyly, Preaxial I 32 0.375
852
MRT007 Martsolf Syndrome 48 0.375
853
c GLY007 Glycogen Storage Disease Iv 58 0.375
854
c LKM063 Leukemia, Chronic Myeloid 71 0.375
855
P APL001 Aplastic Anemia 73 0.375
856
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 0.375
857
CHR100 Chronic Ulcer of Skin 57 0.375
858
FDB001 Foodborne Botulism 55 0.375
859
P LSS002 Lissencephaly 50 0.375
860
SRN001 Serine Deficiency 24 0.375
861
P ANP001 Anaplastic Large Cell Lymphoma 61 0.375
862
PRP080 Peripheral Artery Disease 54 0.375
863
HYP001 Hypochromic Microcytic Anemia 37 0.375
864
c SHR067 Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly 44 0.375
865
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 36 0.375
866
INS015 Inosine Triphosphatase Deficiency 22 0.375
867
VRL003 Variola Major 43 0.375
868
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.375
869
P TMR010 Tumor Predisposition Syndrome 67 0.375
870
INV001 Invasive Aspergillosis 49 0.375
871
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.375
872
P PRM293 Primary Mediastinal B-Cell Lymphoma 43 0.375
873
NPH113 Nephroma 37 0.375
874
THL010 Thalassemia Minor 32 0.375
875
P PLY014 Polycystic Kidney Disease 69 0.375
876
OST006 Osteoblastoma 38 0.375
877
CRS005 Crest Syndrome 36 0.375
878
ORL019 Oral Hairy Leukoplakia 39 0.375
879
THM026 Thiamine Deficiency Disease 24 0.375
880
P CRB045 Cerebellar Hypoplasia 40 0.375
881
P PRP034 Purpura Fulminans 41 0.375
882
c ERL056 Early-Onset Parkinson's Disease 40 0.375
883
THR024 Thrombosis 56 0.375
884
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.375
885
P XNT004 Xanthinuria 37 0.375
886
P WRB001 Warburg Micro Syndrome 41 0.375
887
c XLN004 X-Linked Nonsyndromic Deafness 28 0.375
888
P BRC006 Brachydactyly 51 0.375
889
SPN405 Spondyloepiphyseal Dysplasia Tarda, X-Linked 47 0.375
890
c EPL200 Epilepsy, Childhood Absence 1 32 0.375
891
GNY003 Guanylate Cyclase 2e, Pseudogene 12 0.375
892
CLC017 Calcification of Joints and Arteries 44 0.375
893
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 0.375
894
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.375
895
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.375
896
DST008 Diastematomyelia 31 0.375
897
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 0.375
898
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.375
899
c HYP602 Hyperoxaluria, Primary, Type Ii 49 0.375
900
P CRB048 Cerebral Cavernous Malformations 63 0.375
901
P URC014 Uric Acid Concentration, Serum, Quantitative Trait Locus 1 20 0.375
902
P SPN301 Spinocerebellar Ataxia 2 59 0.375
903
LMY014 Leiomyoma, Uterine 56 0.375
904
ANR009 Aneurysmal Bone Cysts 43 0.375
905
TRC062 Tricuspid Atresia 55 0.375
906
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 0.375
907
PRP001 Propionic Acidemia 65 0.375
908
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.375
909
c PSR025 Psoriasis 4 29 0.375
910
c LKM055 Leukemia, Acute Lymphoblastic 2 18 0.375
911
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 28 0.375
912
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 43 0.375
913
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.375
914
SDD010 Sudden Cardiac Failure, Alcohol-Induced 14 0.375
915
SQL002 Squalene Synthase Deficiency 28 0.375
916
SHR103 Short Stature, Developmental Delay, and Congenital Heart Defects 29 0.375
917
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.375
918
CHR081 Choroideremia 58 0.375
919
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 38 0.375
920
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 0.375
921
BRL010 Buruli Ulcer 45 0.375
922
P THP004 Thiopurines, Poor Metabolism of, 1 42 0.375
923
c CNG206 Congenital Disorder of Glycosylation, Type Ie 51 0.375
924
CZC002 Czech Dysplasia 30 0.375
925
CHD001 Chediak-Higashi Syndrome 67 0.375
926
CTR172 Citrullinemia, Classic 65 0.375
927
c GLY016 Glycogen Storage Disease Ib 40 0.375
928
VRC005 Varicose Veins 60 0.375
929
c WLM013 Wilms Tumor 1 66 0.375
930
SCH068 Schwartz-Jampel Syndrome, Type 1 52 0.375
931
PLY001 Polycythemia Vera 69 0.375
932
STR089 Storage Pool Platelet Disease 47 0.375
933
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.375
934
WLF001 Wolff-Parkinson-White Syndrome 65 0.375
935
P RTN024 Retinoblastoma 73 0.375
936
SCH072 Scheuermann Disease 42 0.375
937
P SCL057 Scoliosis, Isolated 1 40 0.375
938
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 57 0.375
939
PYR037 Pyruvate Carboxylase Deficiency 45 0.375
940
P STR020 Strabismus 56 0.375
941
c LNG044 Long Qt Syndrome 1 66 0.375
942
c HYP595 Hypertension, Essential 85 0.375
943
CLB010 Coloboma of Macula 53 0.375
944
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy