Search results for pyrophosphate

1191 hits were found for pyrophosphate

# Family MCID Name MIFTS Score
1
FML307 Familial Calcium Pyrophosphate Deposition 38 45.808
2
c CHN022 Chondrocalcinosis 2 40 42.311
3
P CHN059 Chondrocalcinosis 51 25.293
4
c CHN021 Chondrocalcinosis 1 17 14.779
5
P ART023 Arthropathy 59 8.769
6
IRN002 Iron Metabolism Disease 56 8.636
7
GT001 Gout 63 6.843
8
P KDN018 Kidney Disease 71 6.360
9
c CHR684 Chronic Kidney Disease 73 6.089
10
END086 End Stage Renal Disease 54 6.049
11
P AMY004 Amyloidosis 69 4.976
12
DFC004 Deficiency Anemia 74 4.829
13
P HYP069 Hyperparathyroidism 62 4.766
14
c ACT075 Acute Myocardial Infarction 55 4.752
15
CRY024 Crystal Arthropathies 18 4.592
16
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 4.582
17
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.564
18
P ART022 Arthritis 70 4.412
19
BNR002 Bone Resorption Disease 47 4.244
20
ANK001 Ankylosis 50 4.017
21
OST012 Osteoarthritis 77 3.989
22
P BRB001 Beriberi 44 3.830
23
SYN007 Synovitis 54 3.824
24
PLC002 Plica Syndrome 35 3.824
25
P PSD087 Pseudoxanthoma Elasticum 66 3.557
26
P HYP035 Hypophosphatasia 61 3.496
27
HYP005 Hypokalemia 55 3.408
28
INT007 Intermediate Coronary Syndrome 53 3.268
29
ANG054 Angina Pectoris 65 2.981
30
SPT004 Septic Arthritis 58 2.933
31
P BND020 Bone Disease 60 2.911
32
IRN001 Iron Deficiency Anemia 58 2.811
33
c HMC039 Hemochromatosis, Type 1 73 2.768
34
CLC006 Calcinosis 47 2.722
35
c PRM005 Primary Hyperparathyroidism 59 2.623
36
c HYP292 Hypophosphatasia, Infantile 56 2.490
37
FRZ001 Frozen Shoulder 54 2.476
38
BRS064 Bursitis 51 2.476
39
OST017 Osteomyelitis 63 2.462
40
URL001 Urolithiasis 45 2.362
41
P RHM011 Rheumatoid Arthritis 81 2.247
42
CRT017 Cartilage Disease 52 2.231
43
c KNN009 Kenny-Caffey Syndrome, Type 1 35 2.177
44
c THM013 Thiamine Metabolism Dysfunction Syndrome 5 32 2.150
45
CHG001 Chagas Disease 65 2.129
46
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 2.102
47
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 2.102
48
P OST002 Osteoporosis 76 2.092
49
SYN031 Synovial Chondromatosis 42 2.075
50
OST003 Osteonecrosis 60 2.013
51
P HYP086 Hypothyroidism 68 1.986
52
HYP068 Hyperostosis 47 1.983
53
c HYP836 Hypercholesterolemia, Familial, 1 73 1.975
54
P PLY019 Polyneuropathy 52 1.958
55
MMM001 Mammary Paget's Disease 53 1.957
56
OST011 Osteomalacia 52 1.905
57
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.900
58
DSC004 Discitis 34 1.890
59
RCK004 Rickets 64 1.876
60
GTL001 Gitelman Syndrome 65 1.872
61
OLC001 Olecranon Bursitis 26 1.872
62
c HYP293 Hypophosphatasia, Adult 52 1.837
63
P CHN012 Chondrosarcoma 56 1.829
64
SPN027 Spinal Stenosis 58 1.792
65
HYP025 Hyperphosphatemia 47 1.782
66
HLX001 Helix Syndrome 47 1.775
67
TND005 Tendinitis 53 1.766
68
BCK006 Back Pain 43 1.736
69
HYP014 Hyperuricemia 51 1.735
70
URM002 Uremia 47 1.708
71
PRC013 Pericarditis 53 1.674
72
P CRN052 Craniometaphyseal Dysplasia, Autosomal Dominant 61 1.651
73
P MYC008 Myocarditis 59 1.637
74
ART035 Arterial Calcification of Infancy 58 1.615
75
P SPN052 Spondyloarthropathy 54 1.615
76
P TMP003 Temporal Arteritis 68 1.613
77
HYP596 Hypophosphatasia, Childhood 47 1.592
78
ENT004 Enthesopathy 51 1.588
79
RNL011 Renal Osteodystrophy 48 1.587
80
48X005 48,xyyy 39 1.579
81
AGN016 Aging 53 1.574
82
ADL002 Adult Syndrome 69 1.573
83
BRT054 Brittle Bone Disorder 74 1.566
84
c GLY060 Glycogen Storage Disease Ia 62 1.545
85
LSC001 Lesch-Nyhan Syndrome 62 1.544
86
OST159 Osteogenic Sarcoma 66 1.538
87
P SRC025 Sarcoidosis 1 70 1.535
88
SBN001 Subendocardial Myocardial Infarction 22 1.510
89
PRR001 Periarthritis 33 1.507
90
CFF002 Coffin-Lowry Syndrome 59 1.507
91
CRN264 Craniosynostosis with Fibular Aplasia 29 1.507
92
NPH009 Nephrolithiasis 54 1.500
93
TNS014 Tenosynovitis 45 1.493
94
c GLY017 Glycogen Storage Disease Ic 30 1.490
95
47X002 47,xyy 47 1.485
96
INF013 Inferior Myocardial Infarction 33 1.475
97
PSR001 Psoriatic Arthritis 61 1.475
98
P PLY041 Polymyositis 58 1.475
99
c TYP009 Type 2 Diabetes Mellitus 91 1.467
100
CRD137 Cardiogenic Shock 56 1.453
101
HYD003 Hydrarthrosis 33 1.439
102
INT182 Intermittent Hydrarthrosis 17 1.439
103
HMN044 Human Immunodeficiency Virus Type 1 76 1.432
104
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.429
105
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.429
106
ALL029 Allergic Disease 61 1.429
107
HYP066 Hyperglycemia 60 1.417
108
P MYS005 Myositis 55 1.417
109
RPD005 Rapidly Involuting Congenital Hemangioma 48 1.412
110
P NRB001 Neuroblastoma 66 1.412
111
P NRP001 Neuropathy 59 1.412
112
WRN002 Wernicke-Korsakoff Syndrome 49 1.410
113
c SCN007 Secondary Hyperparathyroidism 50 1.393
114
PLR008 Pleurisy 49 1.373
115
SPN051 Spondylitis 51 1.372
116
INF009 Inflammatory Spondylopathy 30 1.372
117
ADN024 Adenine Phosphoribosyltransferase Deficiency 53 1.369
118
P KLZ004 Kala-Azar 1 41 1.362
119
TRY001 Trypanosomiasis 50 1.362
120
LSH001 Leishmaniasis 63 1.362
121
P DBT009 Diabetes Mellitus 67 1.352
122
P HYP726 Hypercalcemia, Infantile, 1 58 1.310
123
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.304
124
HYP017 Hypophosphatemia 49 1.294
125
MYL069 Myeloma, Multiple 76 1.294
126
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.285
127
P HPT021 Hepatitis 68 1.277
128
P HRP006 Herpes Simplex 65 1.275
129
P GLY013 Glycogen Storage Disease 59 1.265
130
P MYP004 Myopathy 67 1.265
131
c ATR087 Atrial Standstill 1 74 1.265
132
GLL008 Gilles De La Tourette Syndrome 64 1.241
133
P FML068 Familial Hypocalciuric Hypercalcemia 55 1.241
134
SFT003 Soft Tissue Sarcoma 43 1.241
135
P CRN037 Craniosynostosis 67 1.234
136
P PRP019 Peripheral Nervous System Disease 57 1.212
137
EXS001 Exostosis 49 1.212
138
P DRM010 Dermatomyositis 61 1.212
139
P INF032 Infertility 60 1.212
140
c ALM001 Al Amyloidosis 54 1.202
141
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 1.195
142
CLC004 Calcific Tendinitis 33 1.189
143
CRN030 Coronary Stenosis 50 1.184
144
RDC002 Radiculopathy 51 1.184
145
P SYS005 Systemic Scleroderma 73 1.176
146
ACR007 Acromegaly 70 1.164
147
P CRN300 Coronary Heart Disease 1 73 1.164
148
P DYS154 Dystonia 64 1.164
149
c SPN225 Spondyloarthropathy 1 70 1.151
150
c SCL052 Scleroderma, Familial Progressive 60 1.151
151
P CRP001 Carpal Tunnel Syndrome 65 1.151
152
P OPT006 Optic Nerve Disease 57 1.151
153
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 1.137
154
HRT012 Heart Valve Disease 53 1.137
155
CNG486 Congenital Disorders of N-Linked Glycosylation and Multiple Pathway 29 1.137
156
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.123
157
P MPL001 Maple Syrup Urine Disease 69 1.122
158
PHS004 Phosphoribosylpyrophosphate Synthetase Superactivity 48 1.122
159
P MCR010 Microcephaly 59 1.122
161
ANX004 Anoxia 40 1.103
162
NPH003 Nephrocalcinosis 49 1.093
163
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.091
164
HYP266 Hypoxia 56 1.091
165
P MYS003 Myasthenia Gravis 67 1.087
166
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.082
167
P MNC007 Monocytic Leukemia 48 1.074
168
P MSC005 Muscular Dystrophy 66 1.074
169
CNN005 Connective Tissue Disease 66 1.056
170
P HYP076 Hyperthyroidism 53 1.056
171
CYS001 Cystic Fibrosis 77 1.049
172
ALC007 Alcohol Dependence 65 1.049
173
c HPT073 Hepatitis C Virus 70 1.049
174
LFT001 Left Bundle Branch Hemiblock 47 1.037
175
NPH091 Nephrolithiasis, Calcium Oxalate 61 1.025
176
P SNS001 Sensorineural Hearing Loss 60 1.025
177
GLM045 Glioma 62 1.025
178
P ENC018 Encephalopathy 62 1.025
179
P HYP265 Hypotonia 42 1.025
180
GLL048 Glial Tumor 51 1.025
181
GNG013 Gingivitis 59 1.014
182
HRW001 Hair Whorl 35 1.012
183
VCC001 Vaccinia 49 1.012
184
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.999
185
HMP001 Hemopericardium 47 0.999
186
P HYP061 Hypertrophic Cardiomyopathy 68 0.999
187
P PGT001 Paget's Disease of Bone 60 0.997
188
MCR018 Microcytic Anemia 46 0.996
189
CYT002 Cytokine Deficiency 43 0.989
190
MYS001 Myositis Ossificans 44 0.989
191
MYC005 Myocardial Stunning 45 0.989
192
DSS032 Disease by Infectious Agent 55 0.985
193
BCT022 Bacterial Infectious Disease 55 0.985
194
P PRC012 Pericardial Effusion 50 0.985
195
SLP001 Sleeping Sickness 56 0.985
196
PRT037 Pertussis 49 0.972
197
P SCL018 Scoliosis 57 0.971
198
c HPT001 Hepatitis C 61 0.971
199
BNN003 Bone Inflammation Disease 47 0.971
200
P AVS003 Avascular Necrosis 41 0.971
201
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 63 0.955
202
c DLT002 Dilated Cardiomyopathy 79 0.955
203
c HYP794 Hyperoxaluria, Primary, Type I 63 0.953
204
P MYC084 Mycobacterium Tuberculosis 1 68 0.944
205
MCR257 Microcephaly, Amish Type 35 0.939
206
DNT012 Dental Caries 53 0.939
207
c ACT071 Acute Kidney Failure 60 0.939
208
c PCH010 Pachyonychia Congenita 3 43 0.935
209
P ATR011 Atrial Fibrillation 66 0.922
210
GTR002 Goiter 52 0.922
211
FTT001 Fatty Liver Disease 61 0.922
212
PRM329 Premature Aging 36 0.922
213
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.916
214
CLD014 Cole Disease 39 0.914
215
INF034 Infective Endocarditis 53 0.904
216
CHN010 Chondroma 43 0.904
217
P END033 Endocarditis 58 0.904
218
OST004 Osteitis Fibrosa 38 0.904
219
IRN004 Iron-Refractory Iron Deficiency Anemia 46 0.902
220
SPN119 Spondylarthropathy 37 0.899
221
MLR004 Malaria 77 0.885
222
c MCR115 Microvascular Complications of Diabetes 5 65 0.884
223
HMR002 Hemarthrosis 43 0.884
224
c HRD039 Hereditary Amyloidosis 45 0.884
226
P MCR129 Microvascular Complications of Diabetes 1 67 0.874
227
P LVR013 Liver Disease 68 0.867
228
PRT036 Peritonitis 65 0.867
229
ART002 Arts Syndrome 66 0.863
230
P CRD119 Cardiac Arrest 68 0.862
231
c SYS001 Systemic Lupus Erythematosus 85 0.862
232
TND004 Tendinopathy 45 0.862
233
c PRG106 Progressive Muscular Dystrophy 31 0.862
234
SPN020 Spondylosis 46 0.862
235
GNG003 Gingival Recession 50 0.862
236
P PRK001 Porokeratosis 54 0.862
237
P TRC031 Trichorhinophalangeal Syndrome 37 0.862
238
DYS073 Dysphagia 53 0.862
239
P LKM002 Leukemia 65 0.851
240
RCT015 Reactive Arthritis 60 0.839
241
ART140 Arteries, Anomalies of 52 0.837
242
LPP008 Lipoprotein Quantitative Trait Locus 65 0.837
243
P MLN007 Male Infertility 56 0.837
244
CNS002 Constrictive Pericarditis 39 0.837
245
P HYP098 Hypereosinophilic Syndrome 66 0.837
246
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.837
247
P BRT004 Bartter Disease 58 0.832
248
BNN005 Bunion 32 0.832
249
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 0.827
250
WLF014 Wolfram Syndrome, Mitochondrial Form 18 0.826
251
MVL001 Mevalonic Aciduria 65 0.814
252
GLB002 Glioblastoma 67 0.814
253
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.807
254
OCL069 Ocular Motor Apraxia 57 0.807
255
STR067 Stroke, Ischemic 79 0.807
256
ART016 Aortic Aneurysm 68 0.807
257
TTN003 Tetanus 64 0.807
258
P LPS004 Lupus Erythematosus 61 0.807
259
PRS063 Paresthesia 39 0.807
260
SPS057 Spasticity 43 0.807
261
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 0.801
262
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 0.801
263
c CHR408 Charcot-Marie-Tooth Disease, X-Linked Recessive, 5 43 0.773
264
PYR012 Pyruvate Dehydrogenase E1-Beta Deficiency 40 0.773
265
MSC007 Muscle Hypertrophy 64 0.773
266
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.773
267
NTR005 Nutritional Deficiency Disease 60 0.770
268
c HPT003 Hepatitis a 63 0.770
269
c ACT076 Acute Myocarditis 46 0.769
270
ARG004 Argyria 26 0.769
271
c JVN010 Juvenile Rheumatoid Arthritis 52 0.758
272
HMP009 Haemophilus Influenzae 41 0.758
273
PST092 Posttransplant Acute Limbic Encephalitis 29 0.758
274
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.742
275
c BLD140 Blood Group, I System 47 0.742
276
P PNC035 Pancreatic Cancer 87 0.742
277
SPN209 Spondyloepiphyseal Dysplasia with Congenital Joint Dislocations 66 0.742
278
DSS010 Dissociative Disorder 39 0.742
279
CNG034 Congestive Heart Failure 69 0.742
280
P UVT001 Uveitis 57 0.742
281
CHR121 Charcot-Marie-Tooth Neuropathy X Type 5 17 0.742
282
ACT058 Active Peptic Ulcer Disease 55 0.742
283
DFN002 Dfnx1 Nonsyndromic Hearing Loss and Deafness 8 0.742
284
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 18 0.742
285
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.725
286
P PRS040 Prostate Cancer 95 0.725
287
CRZ001 Crouzon Syndrome 64 0.725
288
PCK003 Pick Disease of Brain 70 0.725
289
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 0.725
290
P MYC007 Myocardial Infarction 69 0.725
291
HMS001 Hemosiderosis 48 0.725
292
P NMN002 Niemann-Pick Disease 60 0.725
293
FBR011 Fibrodysplasia Ossificans Progressiva 67 0.706
294
LGH007 Leigh Syndrome 70 0.706
295
P LKM071 Leukemia, Chronic Lymphocytic 74 0.706
296
VLL003 Villonodular Synovitis 41 0.706
297
P SHR001 Short Bowel Syndrome 53 0.706
298
MGL001 Megaloblastic Anemia 59 0.706
299
PGM001 Pigmented Villonodular Synovitis 55 0.706
300
P GST044 Gastritis 55 0.706
301
MNN009 Meningoencephalitis 47 0.706
302
SPN186 Spinal Cord Injury 60 0.706
303
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.694
304
MYL009 Myelodysplastic Syndrome 67 0.686
305
TNG002 Tangier Disease 63 0.686
306
PPL052 Papillomatosis, Confluent and Reticulated 34 0.686
308
PHN003 Phenylketonuria 76 0.686
309
c AMY091 Amyotrophic Lateral Sclerosis 1 87 0.686
310
BRK010 Burkitt Lymphoma 65 0.686
311
P HMN010 Hemangioma 61 0.686
312
P BNC003 Bone Cancer 58 0.686
313
ISC004 Ischemia 61 0.686
314
PRP016 Paraplegia 52 0.686
315
P LTR001 Lateral Sclerosis 57 0.686
316
MDD018 Middle East Respiratory Syndrome 44 0.686
317
P URN019 Urinary Tract Infection 48 0.686
318
OCH001 Ochronosis 40 0.686
319
CRB039 Cerebrovascular Disease 65 0.686
320
ANT024 Anthrax Disease 57 0.686
321
P MLG056 Malignant Hyperthermia 65 0.686
322
P TXP001 Toxoplasmosis 59 0.686
323
DWR001 Dwarfism 44 0.686
324
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.675
325
OST062 Osteoarthritis with Mild Chondrodysplasia 46 0.670
326
ENC044 Enchondromatosis, Multiple, Ollier Type 57 0.670
327
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.670
328
PPL049 Papillon-Lefevre Syndrome 65 0.670
329
c PNS012 Paine Syndrome 60 0.670
330
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.670
331
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.670
332
P VND007 Van Der Woude Syndrome 1 60 0.670
333
SPN041 Spinal Cord Disease 54 0.670
334
FBR054 Fibroma 44 0.664
335
SPP011 Suppression of Tumorigenicity 12 61 0.664
336
SRC027 Sarcoma, Synovial 58 0.664
337
P PLM037 Pulmonary Hypertension 69 0.664
338
P EXN002 Exanthem 58 0.664
339
SPN019 Spondylolisthesis 51 0.664
340
OPT071 Optic Atrophy, Hearing Loss, and Peripheral Neuropathy, Autosomal Recessive 18 0.664
341
EPD005 Epidural Abscess 31 0.664
342
P OST001 Osteopetrosis 70 0.664
343
VLK001 Volkmann Contracture 23 0.664
344
FBR047 Fibromyalgia 57 0.664
345
LYM017 Lyme Disease 63 0.664
346
P RST002 Restrictive Cardiomyopathy 54 0.664
347
EXT012 Extraskeletal Chondroma 19 0.664
348
CDQ001 Cauda Equina Syndrome 37 0.664
349
OST014 Osteopoikilosis 41 0.664
350
PRT029 Parathyroid Adenoma 51 0.664
351
OST016 Osteochondrosis 52 0.664
352
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.664
353
c LKM005 Leukemia, T-Cell, Chronic 33 0.664
354
P HRD207 Hereditary Transthyretin Amyloidosis 26 0.664
355
PYR016 Pyridoxine Deficiency 29 0.664
356
CLT003 Colitis 63 0.639
357
PRT251 Proteinuria, Chronic Benign 58 0.639
358
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.639
359
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.639
360
INS024 Insulin-Like Growth Factor I 77 0.639
361
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 0.639
362
MND023 Mend Syndrome 49 0.639
363
RBF001 Riboflavin Deficiency 49 0.639
364
P ASP006 Aspergillosis 71 0.639
365
LMB062 Limb Ischemia 55 0.639
366
c VRL005 Viral Pneumonia 52 0.639
367
HYP060 Hyperinsulinism 53 0.639
368
SPN029 Spondylolysis 39 0.639
369
TNS001 Tenosynovial Giant Cell Tumor 42 0.639
370
P DRR001 Diarrhea 55 0.639
371
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.639
372
P KDN017 Kidney Cancer 60 0.639
373
P PSD015 Pseudohypoparathyroidism 54 0.639
374
P BRS044 Breast Adenocarcinoma 58 0.639
375
c ACT027 Acute Pancreatitis 60 0.639
376
P GRV001 Graves' Disease 54 0.639
377
QDR001 Quadriplegia 49 0.639
378
P HYP024 Hypoparathyroidism 55 0.639
379
P ZLL001 Zellweger Syndrome 65 0.639
380
P INF038 Influenza 68 0.639
381
SBC016 Subacute Delirium 42 0.639
382
CTN007 Cutaneous Leishmaniasis 61 0.639
383
c INF145 Infantile Liver Failure Syndrome 1 44 0.638
384
AND005 Androgen Insensitivity Syndrome, Mild 21 0.638
385
WTH001 Withdrawal Disorder 47 0.610
386
DWN001 Down Syndrome 70 0.610
387
ALK013 Alkaptonuria 58 0.610
388
WLS001 Wilson Disease 70 0.610
389
EXT033 Extrapulmonary Tuberculosis 45 0.610
391
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.610
392
RCT020 Rectum Adenocarcinoma 48 0.610
393
CHN004 Chondroblastoma 41 0.610
394
P PYL005 Pyelonephritis 56 0.610
395
NRV004 Nerve Compression Syndrome 48 0.610
396
MLR003 Melorheostosis 48 0.610
397
FNG004 Fungal Meningitis 46 0.610
398
ISL001 Islet Cell Tumor 55 0.610
399
P GLM007 Glomerulonephritis 59 0.610
400
PLM001 Pulmonary Tuberculosis 69 0.610
401
CLC001 Calciphylaxis 50 0.610
402
THR016 Thrombophlebitis 50 0.610
403
PLM010 Pulmonary Edema 54 0.610
404
RHM001 Rheumatic Fever 59 0.610
405
ALC010 Alcoholic Cardiomyopathy 42 0.610
406
PLM033 Pulmonary Embolism 58 0.610
407
GNT003 Genital Herpes 54 0.610
408
GST050 Gastrointestinal System Disease 55 0.610
409
ANR040 Aneurysm 60 0.610
410
INT075 Intracranial Hypertension 52 0.610
411
ATN021 Autoinflammatory Syndrome 30 0.610
412
c HMN021 Human T-Cell Leukemia Virus Type 1 46 0.610
413
c ACT134 Acute Liver Failure 57 0.610
414
ACT119 Acute Promyelocytic Leukemia 62 0.571
415
c GLC079 Glaucoma 1, Open Angle, P 23 0.571
416
MYX004 Myxedema 43 0.571
417
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.571
418
P SML001 Small Cell Carcinoma 52 0.571
419
ENT011 Enterocolitis 55 0.571
420
HYP781 Hypoascorbemia 52 0.571
421
SPN392 Spondylosis, Cervical 30 0.571
422
INC002 Inclusion Body Myositis 56 0.571
423
c GLY004 Glycogen Storage Disease V 62 0.571
424
c SYS048 Systemic Lupus Erythematosus 8 17 0.571
425
OBS082 Obstructive Nephropathy 41 0.571
426
MLD018 Mild Cognitive Impairment 48 0.571
427
INT071 Intestinal Perforation 49 0.571
428
SMN007 Seminoma 42 0.571
429
HMP005 Hemiplegia 53 0.571
430
NRM005 Neuromuscular Disease 62 0.571
431
ULN001 Ulnar Neuropathy 28 0.571
432
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.571
433
CHR074 Choriocarcinoma 46 0.571
434
LTR004 Lateral Myocardial Infarction 29 0.571
435
HYP141 Hyperphenylalaninemia 42 0.571
436
FSC004 Fasciitis 49 0.571
437
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 0.571
438
PLN007 Plantar Fasciitis 37 0.571
439
KDN013 Kidney Hypertrophy 33 0.571
440
PRN019 Perinatal Necrotizing Enterocolitis 60 0.571
441
IDP085 Idiopathic Infantile Hypercalcemia 32 0.571
442
CLC064 Calcifying Aponeurotic Fibroma 25 0.571
443
CRD016 Cardiac Rupture 34 0.571
444
HYP706 Hypermobile Ehlers-Danlos Syndrome 54 0.571
445
P SKL032 Skeletal Muscle Disease 25 0.571
446
PRD026 Pre-Descemet Corneal Dystrophy 20 0.571
447
HMP018 Hemophilic Arthropathy 33 0.571
448
FTD001 Foot Drop 36 0.571
449
NRL025 Neural Tube Closure Defect 27 0.571
450
OST115 Osteonecrosis of the Jaw 40 0.528
451
CHL014 Cholera 62 0.494
452
P OST135 Osteogenesis Imperfecta, Type I 60 0.477
453
PRC052 Pericardial Effusion, Chronic 19 0.477
454
HMN004 Hemangioma of Liver 34 0.477
455
P LMY004 Leiomyosarcoma 62 0.477
456
BRX001 Bruxism 50 0.477
457
TTH007 Tooth Erosion 30 0.477
458
PYM001 Pyomyositis 42 0.477
459
c BRN108 Branchiootic Syndrome 1 63 0.476
460
ATS010 Autosomal Recessive Disease 42 0.428
461
IMM167 Immune Deficiency Disease 76 0.407
462
WRN003 Wernicke Encephalopathy 45 0.385
463
P LCT001 Lactic Acidosis 50 0.374
464
NRR001 Neuroretinitis 42 0.362
465
RTN023 Retinitis 45 0.362
466
P ART021 Arteriosclerosis 53 0.337
467
ATH013 Atherosclerosis Susceptibility 63 0.310
468
P GST053 Gastric Cancer 82 0.310
469
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.310
470
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.310
471
CYT005 Cytomegalovirus Retinitis 50 0.310
472
P PLY011 Polycystic Ovary Syndrome 57 0.310
473
P PRD008 Periodontitis 63 0.310
474
P ALZ034 Alzheimer Disease 87 0.295
475
P LKM062 Leukemia, Acute Lymphoblastic 69 0.295
476
TTH006 Tooth Disease 51 0.295
477
LPD008 Lipid Metabolism Disorder 61 0.295
478
P CHR071 Charcot-Marie-Tooth Disease 64 0.295
479
CHC001 Chickenpox 56 0.295
480
ALL014 Allergic Encephalomyelitis 34 0.295
481
P OVR082 Overgrowth Syndrome 41 0.295
482
ATR057 Atrioventricular Block 54 0.280
483
c LKM061 Leukemia, Acute Myeloid 83 0.280
484
P HNT016 Huntington Disease 73 0.280
485
P BNG032 Benign Mesothelioma 53 0.280
486
ACQ007 Acquired Immunodeficiency Syndrome 58 0.280
487
P CMP008 Compartment Syndrome 49 0.280
488
P PRG139 Progeroid Syndrome 30 0.280
489
c ART115 Aortic Valve Disease 1 72 0.264
490
P OVR042 Ovarian Cancer 88 0.264
491
OSS014 Ossification of the Posterior Longitudinal Ligament of Spine 48 0.264
492
WTB001 Wet Beriberi 27 0.264
493
P VSC007 Vascular Disease 62 0.264
494
CRD003 Cardiac Sarcoidosis 44 0.264
495
GST045 Gastroenteritis 58 0.264
496
P END044 Endometriosis 62 0.264
497
GRD001 Giardiasis 46 0.264
498
P MLN008 Melanoma 75 0.264
499
c RNG015 Ring Chromosome 2 22 0.264
500
MTB004 Metabolic Acidosis 48 0.247
501
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.247
502
P FML018 Familial Mediterranean Fever 73 0.247
503
HMN047 Human Cytomegalovirus Infection 59 0.247
504
P PRM002 Primary Hyperoxaluria 65 0.247
505
P ALC033 Alcohol Use Disorder 67 0.247
506
SVR004 Severe Combined Immunodeficiency 70 0.247
507
ACT098 Acute Erythroid Leukemia 55 0.247
508
BRC012 Brucellosis 66 0.247
509
RGH001 Right Bundle Branch Block 47 0.247
510
PTH003 Pathologic Nystagmus 52 0.247
511
P BLD134 Bladder Cancer 79 0.229
512
c DFN194 Deafness, X-Linked 1 35 0.229
513
P GLM040 Glioma Susceptibility 1 70 0.229
514
KRN002 Kearns-Sayre Syndrome 62 0.229
515
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 51 0.229
516
CMB007 Combined Immunodeficiency 56 0.229
517
MLG169 Malignant Astrocytoma 57 0.229
518
LVR012 Liver Cirrhosis 62 0.229
519
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.229
520
NNL005 Non-Alcoholic Fatty Liver Disease 63 0.229
521
c ACT068 Acute Cystitis 60 0.229
522
c PRC016 Pre-Eclampsia 64 0.229
523
SRC014 Sarcoma 64 0.229
524
DGN001 Degenerative Disc Disease 48 0.229
525
STM007 Stomatitis 52 0.229
526
CRH001 Crohn's Disease 80 0.229
527
THY029 Thyroid Carcinoma 55 0.229
528
P THM010 Thiamine Metabolism Dysfunction Syndrome 2 49 0.209
529
c CNG196 Congenital Disorder of Glycosylation, Type Ic 40 0.209
530
c MCR133 Microvascular Complications of Diabetes 4 41 0.209
531
c MCR113 Microvascular Complications of Diabetes 3 52 0.209
532
c MCR130 Microvascular Complications of Diabetes 6 41 0.209
533
c MCR120 Microvascular Complications of Diabetes 7 47 0.209
534
P SPP010 Suppressor of Tumorigenicity 3 50 0.209
535
P DNG005 Dengue Virus 55 0.209
536
INT051 Intussusception 53 0.209
537
FBR009 Fibrous Dysplasia 48 0.209
538
P PRK039 Parkinsonism 55 0.209
539
c ANK022 Ankylosing Spondylitis 2 9 0.209
540
CLN015 Colon Adenocarcinoma 64 0.209
541
P GCH001 Gaucher's Disease 69 0.209
542
P TCD001 Tic Disorder 50 0.209
543
P FBR017 Fibrosarcoma 55 0.209
544
MTH009 Mouth Disease 57 0.209
545
P SYP003 Syphilis 59 0.209
546
SPN035 Spindle Cell Sarcoma 51 0.209
547
VRC001 Varicocele 48 0.209
548
P VSC011 Vasculitis 61 0.209
549
P NRF002 Neurofibromatosis 60 0.209
550
ULC004 Ulcerative Colitis 74 0.209
551
P NNS072 Nonsyndromic Hearing Loss 42 0.209
552
P RRH023 Rare Hereditary Hemochromatosis 52 0.209
553
ALG024 Alg6-Congenital Disorder of Glycosylation 21 0.209
554
GLY081 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency 48 0.209
555
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.187
556
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 0.187
557
BSL009 Basal Ganglia Calcification 45 0.187
558
c SML038 Small Cell Cancer of the Lung 68 0.187
559
SCH076 Schnyder Corneal Dystrophy 48 0.187
560
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 0.187
561
P CLR023 Colorectal Cancer 100 0.187
562
SCK003 Sickle Cell Anemia 74 0.187
563
PRP027 Peripheral Vascular Disease 71 0.187
564
c HYP369 Hypophosphatemic Rickets, Autosomal Recessive, 2 29 0.187
565
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.187
566
P LNG032 Lung Cancer 98 0.187
567
CYS013 Cystinuria 66 0.187
568
LGG001 Legg-Calve-Perthes Disease 59 0.187
569
MYL005 Myelofibrosis 70 0.187
570
c NMN015 Niemann-Pick Disease, Type C1 68 0.187
571
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.187
572
P PHC003 Pheochromocytoma 70 0.187
573
ORT008 Orotic Aciduria 56 0.187
574
MCS002 Mucositis 55 0.187
575
ADR040 Adrenal Gland Pheochromocytoma 45 0.187
576
CLR109 Colorectal Adenocarcinoma 50 0.187
577
c CHR571 Charcot-Marie-Tooth Disease Type 5 23 0.187
578
CLL003 Cellulitis 53 0.187
579
c FML021 Familial Hypercholesterolemia 71 0.187
580
P ANT006 Antiphospholipid Syndrome 55 0.187
581
P CRN025 Corneal Dystrophy 49 0.187
582
c HPT016 Hepatitis B 62 0.187
583
MSC072 Muscle Cancer 48 0.187
584
HYP043 Hyperandrogenism 47 0.187
585
c ACT073 Acute Leukemia 59 0.187
586
P NTR004 Neutropenia 62 0.187
587
TXC005 Toxic Shock Syndrome 61 0.187
588
BRN028 Brain Cancer 73 0.187
589
c INH020 Inherited Metabolic Disorder 47 0.187
590
PYR009 Pyridoxine Deficiency Anemia 35 0.187
591
CHR066 Chronic Fatigue Syndrome 59 0.187
592
NRF007 Neurofibroma 63 0.187
593
P EPS003 Episodic Ataxia 59 0.187
594
VSC002 Vascular Dementia 59 0.187
595
CND006 Candida Glabrata 29 0.187
596
PTT037 Pituitary Tumors 44 0.187
597
P SZR006 Seizure Disorder 69 0.187
598
P DBT005 Diabetes Insipidus 54 0.187
599
ATN005 Autonomic Dysfunction 45 0.187
600
c XLN110 X-Linked Charcot-Marie-Tooth Disease 33 0.187
601
HYP056 Hypoglycemia 65 0.187
602
MNG007 Manganese Poisoning 28 0.187
603
CRB089 Cerebral Beriberi 19 0.187
604
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 0.187
605
P SCL048 Sclerosteosis 58 0.162
606
P LYM118 Lymphoma 66 0.162
607
P INF037 Inflammatory Bowel Disease 53 0.162
608
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.162
609
PFF001 Pfeiffer Syndrome 77 0.162
610
P ATS364 Autism 72 0.162
611
c MTC056 Mitochondrial Dna Depletion Syndrome 4a 62 0.162
612
PRN011 Pernicious Anemia 52 0.162
613
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.162
614
PLY150 Polykaryocytosis Inducer 29 0.162
615
c PLM163 Palmoplantar Keratoderma, Punctate Type Ii 28 0.162
616
c GCH013 Gaucher Disease, Type Iiic 39 0.162
617
URT049 Urate Oxidase, Pseudogene 24 0.162
618
P HYP750 Hypertriglyceridemia, Familial 61 0.162
619
KTL001 Keutel Syndrome 41 0.162
620
ANG004 Angioid Streaks 39 0.162
621
c CNG194 Congenital Disorder of Glycosylation, Type Ig 49 0.162
622
LGN006 Legionnaire Disease 52 0.162
623
c SHR068 Short-Rib Thoracic Dysplasia 5 with or Without Polydactyly 48 0.162
624
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.162
625
CHL065 Cholangiocarcinoma 57 0.162
626
ATM095 Autoimmune Disease 61 0.162
627
c CRN278 Craniosynostosis 1 55 0.162
628
c OST122 Osteogenesis Imperfecta, Type Iii 57 0.162
629
CRV035 Cervical Cancer 72 0.162
630
P ADL017 Adult T-Cell Leukemia 53 0.162
631
P RSP003 Respiratory Failure 73 0.162
632
DPH001 Diphtheria 59 0.162
633
P FLL037 Follicular Lymphoma 66 0.162
634
MYL001 Myelitis 49 0.162
635
SQM006 Squamous Cell Carcinoma 59 0.162
636
KRT009 Keratosis 52 0.162
637
ADN018 Adenoma 58 0.162
638
P PNM007 Pneumonia 64 0.162
639
ALC011 Alcoholic Neuropathy 35 0.162
640
ART074 Aortic Dissection 53 0.162
641
P ESP024 Esophagitis 60 0.162
642
P ADN016 Adenocarcinoma 63 0.162
643
AVN001 Avian Influenza 61 0.162
644
THY030 Thyroid Gland Disease 50 0.162
645
ERD001 Erdheim-Chester Disease 53 0.162
646
ART006 Arthus Reaction 40 0.162
647
P RHB003 Rhabdomyosarcoma 66 0.162
648
PLS011 Plasmacytoma 56 0.162
649
URM001 Uremic Neuropathy 20 0.162
650
INT079 Intrahepatic Cholangiocarcinoma 51 0.162
651
GLC003 Glucose Intolerance 53 0.162
652
KRT002 Keratomalacia 54 0.162
653
P GLL022 Guillain-Barre Syndrome 59 0.162
654
CRT013 Carotid Stenosis 51 0.162
655
SCH014 Schistosomiasis 56 0.162
656
NRG003 Neurogenic Arthropathy 42 0.162
657
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 0.162
658
P MYL006 Myeloid Leukemia 60 0.162
659
BSL008 Basal Ganglia Disease 41 0.162
660
P BCL017 B-Cell Lymphoma 57 0.162
661
FND002 Fundus Dystrophy 54 0.162
662
DBT010 Diabetic Neuropathy 54 0.162
663
ETN001 Eating Disorder 59 0.162
664
PNC060 Punctate Porokeratosis 28 0.162
665
PRM243 Primary Bone Cancer 22 0.162
666
P ACT008 Actinic Keratosis 53 0.162
667
DHY008 Dihydroxyadeninuria 24 0.162
668
c INH030 Inherited Retinal Disorder 28 0.162
670
P SNG014 Singleton-Merten Syndrome 36 0.162
671
HMZ003 Homozygous Familial Hypercholesterolemia 60 0.162
672
FML091 Familial Tumoral Calcinosis 45 0.162
673
P TRM003 Tremor 50 0.162
674
P CHR345 Chronic Pain 50 0.162
675
c ATS007 Autism Spectrum Disorder 71 0.132
676
c MJR022 Major Affective Disorder 8 37 0.132
677
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.132
678
RNL077 Renal Fibrosis 46 0.132
679
ANR009 Aneurysmal Bone Cysts 43 0.132
680
FRS012 First-Degree Atrioventricular Block 39 0.132
681
BHC003 Behcet Syndrome 70 0.132
682
c CRD186 Ceroid Lipofuscinosis, Neuronal, 3 62 0.132
683
CLB022 Coloboma, Ocular, Autosomal Recessive 29 0.132
684
P MDL005 Medulloblastoma 75 0.132
685
OSS012 Osseous Heteroplasia, Progressive 61 0.132
686
CRD132 Cardiac Conduction Defect 59 0.132
687
CHR619 Chromosome 2q35 Duplication Syndrome 64 0.132
688
RTC012 Reticuloendotheliosis, X-Linked 35 0.132
689
RHB024 Rhabdomyosarcoma 2 65 0.132
690
ADR007 Adrenoleukodystrophy 73 0.132
691
P MLT020 Multiple Sclerosis 79 0.132
692
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.132
693
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.132
694
HMC014 Homocysteinemia 52 0.132
695
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.132
696
P NSP012 Nasopharyngeal Carcinoma 60 0.132
697
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.132
698
P USH001 Usher Syndrome 63 0.132
699
CNZ001 Coenzyme Q10 Deficiency Disease 41 0.132
700
VTM002 Vitamin B12 Deficiency 48 0.132
701
c MCR312 Microphthalmia, Syndromic 10 39 0.132
702
c MJR024 Major Affective Disorder 9 40 0.132
703
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.132
704
c MCR112 Microvascular Complications of Diabetes 2 42 0.132
705
MYP035 Myopathy, Distal, with Anterior Tibial Onset 33 0.132
706
ANR007 Anorexia Nervosa 59 0.132
707
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.132
708
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.132
709
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.132
710
ANG020 Angiosarcoma 63 0.132
711
KPS004 Kaposi Sarcoma 76 0.132
712
PPL054 Popliteal Cyst 22 0.132
713
RTN187 Retinitis Pigmentosa-Deafness Syndrome 48 0.132
714
c GLL024 Gallbladder Disease 1 53 0.132
715
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.132
716
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.132
717
c MYC058 Myocardial Infarction 2 23 0.132
718
LPT014 Leptin Deficiency or Dysfunction 77 0.132
719
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 0.132
720
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 0.132
721
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.132
722
ART102 Arterial Calcification, Generalized, of Infancy, 2 25 0.132
723
c SPS101 Spastic Paraplegia 56, Autosomal Recessive 43 0.132
724
MLD001 Melioidosis 67 0.132
725
c BTT014 Beta-Thalassemia 72 0.132
726
c SPN294 Spinocerebellar Ataxia 1 53 0.132
727
P HPT023 Hepatocellular Carcinoma 95 0.132
728
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.132
729
RFL001 Reflex Sympathetic Dystrophy 51 0.132
730
P LNG064 Lung Cancer Susceptibility 3 69 0.132
731
DFF005 Diffuse Large B-Cell Lymphoma 55 0.132
732
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.132
733
HMN048 Human Papillomavirus Infectious Disease 45 0.132
734
CHL123 Chlamydia 58 0.132
735
PRX005 Peroxisomal Biogenesis Disorder 35 0.132
736
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.132
737
P NPH012 Nephrotic Syndrome 61 0.132
738
ANT018 Anthracosis 50 0.132
739
P PNM006 Pneumoconiosis 55 0.132
740
INT067 Interstitial Nephritis 46 0.132
741
P RNV001 Renovascular Hypertension 48 0.132
742
OST015 Osteochondrodysplasia 60 0.132
743
PHR003 Pharyngitis 57 0.132
744
HYP080 Hypogonadism 49 0.132
745
c HRD010 Hereditary Spastic Paraplegia 65 0.132
746
PPL022 Papilloma 53 0.132
747
HST010 Histiocytosis 49 0.132
748
RTN020 Retinal Vascular Disease 45 0.132
749
IMP005 Impotence 52 0.132
750
CHL068 Cholestasis 61 0.132
751
OPS001 Opisthorchiasis 41 0.132
752
PNM008 Pneumothorax 54 0.132
753
DST103 Distal Muscular Dystrophy with Anterior Tibial Onset 29 0.132
754
URT010 Ureteral Obstruction 44 0.132
755
P BPL003 Bipolar Disorder 56 0.132
756
FCL012 Facial Paralysis 49 0.132
757
RTC003 Root Caries 33 0.132
758
P HRT032 Heart Disease 84 0.132
759
HYP006 Hypertensive Heart Disease 48 0.132
760
MTR002 Mitral Valve Insufficiency 51 0.132
761
P DFF019 Diffuse Gastric Cancer 50 0.132
762
P EPL164 Epilepsy 70 0.132
763
c VRL010 Viral Hepatitis 52 0.132
764
SKN006 Skin Sarcoidosis 42 0.132
765
SQM002 Squamous Cell Papilloma 45 0.132
766
TYP007 Typhoid Fever 63 0.132
767
P RHN004 Rhinitis 56 0.132
768
MYF001 Myofibroma 42 0.132
769
PST011 Pustulosis of Palm and Sole 52 0.132
770
P ANG015 Angioedema 56 0.132
771
TRT001 Teratocarcinoma 41 0.132
772
ALC006 Alcoholic Hepatitis 61 0.132
773
ATN004 Autonomic Neuropathy 42 0.132
774
PRT013 Portal Hypertension 59 0.132
775
RSP002 Respiratory Syncytial Virus Infectious Disease 51 0.132
776
HYP021 Hypercementosis 28 0.132
777
P RNL015 Renal Hypertension 45 0.132
778
LMY002 Leiomyoma 51 0.132
779
CMM005 Common Cold 55 0.132
780
CYS010 Cystinosis 61 0.132
781
CRY003 Cryptosporidiosis 55 0.132
782
ALG001 Algoneurodystrophy 37 0.132
783
BCT004 Bacteriuria 48 0.132
784
OLV001 Olivopontocerebellar Atrophy 50 0.132
785
ACT003 Acute Kidney Tubular Necrosis 46 0.132
786
P CRD246 Cardiovascular System Disease 55 0.132
787
DYS015 Dysentery 49 0.132
788
c PST005 Posterior Uveitis 54 0.132
789
P MLT007 Multiple Epiphyseal Dysplasia 56 0.132
790
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 0.132
791
P RTN018 Retinal Disease 53 0.132
793
ADR022 Adrenomyeloneuropathy 38 0.132
794
P PSR002 Psoriasis 63 0.132
795
VSC003 Visceral Leishmaniasis 54 0.132
796
P RTN016 Retinal Degeneration 52 0.132
797
SYS003 Systolic Heart Failure 49 0.132
798
P MTC069 Mitochondrial Disorders 57 0.132
799
P SCK005 Sickle Cell Disease 56 0.132
800
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.132
801
GRN017 Granulocytopenia 42 0.132
802
P THL005 Thalassemia 56 0.132
803
c RNG019 Ring Chromosome 3 19 0.132
804
CRL001 Cerulean Cataract 26 0.132
805
OVR094 Ovarian Epithelial Cancer 39 0.132
806
DST006 Diastolic Heart Failure 45 0.132
807
MTC015 Mitochondrial Dna-Associated Leigh Syndrome and Narp 24 0.132
808
NCL011 Nuclear Gene-Encoded Leigh Syndrome Spectrum 21 0.132
809
PHS018 Phosphorylase Kinase Deficiency 37 0.132
810
c AMY009 Amyloidosis Aa 47 0.132
811
WLD005 Wild Type Attr Amyloidosis 29 0.132
812
XLN174 X-Linked Non-Syndromic Sensorineural Deafness Type Dfn 20 0.132
813
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 38 0.132
814
GLY111 Glycogen Storage Disease Due to Glucose-6-Phosphatase Deficiency Type Ib 36 0.132
815
SPL018 Splenomegaly 47 0.132
816
P DYS021 Dysautonomia 38 0.132
817
HDN002 Head Injury 44 0.132
818
CLS052 Classic Hairy Cell Leukemia 25 0.132
819
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 0.132
820
OST006 Osteoblastoma 37 0.093
821
CNN010 Connective Tissue Benign Neoplasm 44 0.093
822
IDP070 Idiopathic Scoliosis 41 0.093
823
ORL019 Oral Hairy Leukoplakia 39 0.093
824
c SHR067 Short-Rib Thoracic Dysplasia 2 with or Without Polydactyly 43 0.093
825
SQL002 Squalene Synthase Deficiency 27 0.093
826
ALL003 Allergic Rhinitis 66 0.093
827
TRC062 Tricuspid Atresia 54 0.093
828
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.093
829
CZC002 Czech Dysplasia 30 0.093
830
P APL001 Aplastic Anemia 72 0.093
831
c ALP101 Alpha-Thalassemia 62 0.093
832
PRP001 Propionic Acidemia 65 0.093
833
CRS005 Crest Syndrome 36 0.093
834
P XNT004 Xanthinuria 38 0.093
835
P WRB001 Warburg Micro Syndrome 41 0.093
836
ORL015 Oral Squamous Cell Carcinoma 43 0.093
837
DCT002 Ductal Carcinoma in Situ 58 0.093
838
c ATS204 Autosomal Recessive Non-Syndromic Intellectual Disability 47 0.093
839
DNG001 Dengue Shock Syndrome 40 0.093
840
ERY003 Erythema Multiforme 56 0.093
841
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.093
842
ACH004 Achondroplasia 65 0.093
843
APR006 Apert Syndrome 69 0.093
844
c LNG044 Long Qt Syndrome 1 66 0.093
845
c WLM013 Wilms Tumor 1 65 0.093
846
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 63 0.093
847
MRT007 Martsolf Syndrome 48 0.093
848
DST008 Diastematomyelia 31 0.093
849
VRC005 Varicose Veins 59 0.093
850
CLC017 Calcification of Joints and Arteries 45 0.093
851
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 0.093
852
CHD001 Chediak-Higashi Syndrome 66 0.093
853
CTR172 Citrullinemia, Classic 64 0.093
854
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.093
855
c NRF024 Neurofibromatosis, Type I 76 0.093
856
P NNN008 Noonan Syndrome 1 76 0.093
857
PHS025 Phosphatase, Acid, of Tissues 28 0.093
858
CLB010 Coloboma of Macula 53 0.093
859
SCH072 Scheuermann Disease 41 0.093
860
P SCL057 Scoliosis, Isolated 1 40 0.093
861
P RTN024 Retinoblastoma 72 0.093
862
c GLY007 Glycogen Storage Disease Iv 58 0.093
863
LYM133 Lymphoma, Hodgkin, Classic 69 0.093
864
PHS027 Phosphoglycoprotein 1 14 0.093
865
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 0.093
866
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.093
867
P URC014 Uric Acid Concentration, Serum, Quantitative Trait Locus 1 20 0.093
868
DHY010 Dihydrolipoamide Dehydrogenase Deficiency 48 0.093
869
MLY008 Molybdenum Cofactor Deficiency, Complementation Group a 47 0.093
870
SCH068 Schwartz-Jampel Syndrome, Type 1 52 0.093
871
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 56 0.093
872
STR089 Storage Pool Platelet Disease 46 0.093
873
c SYN060 Syndactyly, Type Iii 40 0.093
874
c GLY016 Glycogen Storage Disease Ib 41 0.093
875
c GLY008 Glycogen Storage Disease Ii 72 0.093
876
c PSD108 Pseudohypoparathyroidism, Type Ia 64 0.093
877
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.093
878
PYR037 Pyruvate Carboxylase Deficiency 45 0.093
879
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.093
880
CRP035 Corpus Callosum, Partial Agenesis of, X-Linked 37 0.093
881
P BRS047 Breast Cancer 97 0.093
882
PRS131 Prostate Cancer/brain Cancer Susceptibility 23 0.093
883
c HYP602 Hyperoxaluria, Primary, Type Ii 51 0.093
884
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 36 0.093
885
EPL050 Epilepsy, Partial, with Pericentral Spikes 26 0.093
886
CHR100 Chronic Ulcer of Skin 57 0.093
887
VRL003 Variola Major 43 0.093
888
c XLN004 X-Linked Nonsyndromic Deafness 28 0.093
889
P BRC006 Brachydactyly 52 0.093
890
SRN001 Serine Deficiency 24 0.093
891
P THP004 Thiopurines, Poor Metabolism of, 1 41 0.093
892
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 0.093
893
SHR103 Short Stature, Developmental Delay, and Congenital Heart Defects 29 0.093
894
SDD009 Sudden Cardiac Failure, Infantile 24 0.093
895
SDD010 Sudden Cardiac Failure, Alcohol-Induced 14 0.093
896
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.093
897
LYM007 Lymphangioleiomyomatosis 68 0.093
898
c DFN374 Deafness, Autosomal Recessive 100 28 0.093
899
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 0.093
900
c ACT004 Acute Diarrhea 40 0.093
901
PNT001 Pontiac Fever 28 0.093
902
FDB001 Foodborne Botulism 55 0.093
903
P LSS002 Lissencephaly 52 0.093
904
HYP001 Hypochromic Microcytic Anemia 36 0.093
905
PLY001 Polycythemia Vera 69 0.093
906
CHR081 Choroideremia 58 0.093
907
WLF001 Wolff-Parkinson-White Syndrome 63 0.093
908
CRN240 Craniometaphyseal Dysplasia, Autosomal Recessive 29 0.093
909
c DFN097 Deafness, Autosomal Recessive 1a 49 0.093
910
P CRB048 Cerebral Cavernous Malformations 63 0.093
911
c PLY136 Polydactyly, Preaxial I 32 0.093
912
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.093
913
LMY014 Leiomyoma, Uterine 55 0.093
914
P LPR021 Leprosy 3 71 0.093
915
P RTN008 Retinitis Pigmentosa 79 0.093
916
SMT004 Smith-Lemli-Opitz Syndrome 69 0.093
917
SDD001 Sudden Infant Death Syndrome 60 0.093
918
BDY003 Body Length, Mouse, Human Homolog 4 0.093
919
c EPL200 Epilepsy, Childhood Absence 1 30 0.093
920
FRN006 Frontotemporal Dementia 68 0.093
921
P STR020 Strabismus 56 0.093
922
P AST005 Asthma 75 0.093
923
c LKM055 Leukemia, Acute Lymphoblastic 2 18 0.093
924
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.093
925
c THM014 Thiamine Metabolism Dysfunction Syndrome 4 27 0.093
926
MNN043 Meningioma, Familial 79 0.093
927
P GRF003 Graft-Versus-Host Disease 71 0.093
929
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.093
930
c LKM063 Leukemia, Chronic Myeloid 70 0.093
931
MYP071 Myopathy Due to Myoadenylate Deaminase Deficiency 44 0.093
932
P TMR010 Tumor Predisposition Syndrome 69 0.093
933
RSS025 Ras-Associated Autoimmune Leukoproliferative Disorder 52 0.093
934
KWS002 Kawasaki Disease 65 0.093
935
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.093
936
INS015 Inosine Triphosphatase Deficiency 22 0.093
937
AMY082 Amyloidosis, Familial Visceral 53 0.093
938
MTP025 Metaphyseal Chondrodysplasia, Schmid Type 54 0.093
939
P OCL013 Oculodentodigital Dysplasia 66 0.093
940
P PRK057 Parkinson Disease, Late-Onset 79 0.093
941
c HYP595 Hypertension, Essential 84 0.093
942
ESP021 Esophageal Cancer 84 0.093
943
c MST023 Mesothelioma, Malignant 56 0.093
944
NLP001 Nail-Patella Syndrome 63 0.093
945