Search results for Calcium

5473 hits were found for Calcium

# Family MCID Name MIFTS Score
1
NPH091 Nephrolithiasis, Calcium Oxalate 61 56.308
2
P HYP069 Hyperparathyroidism 62 50.644
3
c CHN022 Chondrocalcinosis 2 39 41.429
4
RCK004 Rickets 68 39.588
5
P OST002 Osteoporosis 76 39.200
6
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 37.636
7
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 37.636
8
BNR002 Bone Resorption Disease 47 35.469
9
NPH009 Nephrolithiasis 54 33.373
10
c SCN007 Secondary Hyperparathyroidism 51 32.910
11
FML307 Familial Calcium Pyrophosphate Deposition 38 32.843
12
c PRM005 Primary Hyperparathyroidism 59 31.623
13
c CHR684 Chronic Kidney Disease 69 27.548
14
URL001 Urolithiasis 46 27.008
15
P BND020 Bone Disease 59 26.705
16
c HYP595 Hypertension, Essential 85 26.052
17
P HYP024 Hypoparathyroidism 55 25.807
18
PRT037 Pertussis 65 25.472
19
P CHN059 Chondrocalcinosis 52 25.282
20
IMM066 Immunodeficiency 9 39 24.747
21
P KDN018 Kidney Disease 72 24.264
22
HYP025 Hyperphosphatemia 48 24.201
23
IMM065 Immunodeficiency 10 47 22.898
24
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 21.007
25
LPP008 Lipoprotein Quantitative Trait Locus 65 19.205
26
END086 End Stage Renal Disease 52 19.117
27
ATH013 Atherosclerosis Susceptibility 63 18.991
28
ADN018 Adenoma 59 18.692
29
OST011 Osteomalacia 52 18.364
30
ART140 Arteries, Anomalies of 53 18.068
31
ANG054 Angina Pectoris 66 17.740
32
c PRC016 Pre-Eclampsia 65 17.365
33
P CRN300 Coronary Heart Disease 1 73 17.190
34
P NRB001 Neuroblastoma 66 16.831
35
NPH003 Nephrocalcinosis 49 16.439
36
IDP073 Idiopathic Hypercalciuria 40 16.252
37
P FML068 Familial Hypocalciuric Hypercalcemia 55 15.479
38
CLC006 Calcinosis 47 15.052
39
RPD005 Rapidly Involuting Congenital Hemangioma 46 14.959
40
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 14.957
41
HYP017 Hypophosphatemia 49 14.346
42
c ACT027 Acute Pancreatitis 60 14.178
43
ISC004 Ischemia 61 14.083
44
MTB004 Metabolic Acidosis 48 13.864
45
HLX001 Helix Syndrome 48 13.830
46
RNL011 Renal Osteodystrophy 49 13.778
47
P MSC005 Muscular Dystrophy 67 13.776
48
P PNC044 Pancreatitis 61 13.714
49
P CLR023 Colorectal Cancer 100 13.666
50
PRT029 Parathyroid Adenoma 51 13.640
51
PRT251 Proteinuria, Chronic Benign 57 13.626
52
48X005 48,xyyy 39 13.489
53
LPD008 Lipid Metabolism Disorder 62 13.477
54
DNT012 Dental Caries 53 13.469
55
AGN016 Aging 54 13.408
56
P VSC007 Vascular Disease 63 13.248
57
P HRT032 Heart Disease 81 13.193
58
P PRD008 Periodontitis 64 13.077
59
c HYP836 Hypercholesterolemia, Familial, 1 73 13.072
60
c CHN021 Chondrocalcinosis 1 17 12.955
61
OST159 Osteogenic Sarcoma 66 12.826
62
P HYP726 Hypercalcemia, Infantile, 1 58 12.718
63
P ECL001 Eclampsia 52 12.620
64
c ATR087 Atrial Standstill 1 74 12.565
65
c GLL024 Gallbladder Disease 1 52 12.551
66
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 12.407
67
URM002 Uremia 47 12.362
68
c TYP009 Type 2 Diabetes Mellitus 92 12.305
69
HYP266 Hypoxia 57 12.284
70
c BLD126 Bleeding Disorder, Platelet-Type, 18 39 12.228
71
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 12.178
72
CHL014 Cholera 62 12.070
73
P LTR001 Lateral Sclerosis 58 11.947
74
ALL029 Allergic Disease 59 11.936
75
c AMY091 Amyotrophic Lateral Sclerosis 1 88 11.915
76
c ACT071 Acute Kidney Failure 60 11.818
77
P ALZ034 Alzheimer Disease 87 11.679
78
ANX004 Anoxia 40 11.642
79
HYP005 Hypokalemia 55 11.618
80
P SRC025 Sarcoidosis 1 71 11.609
81
INS001 Insulinoma 59 11.495
82
P DBT009 Diabetes Mellitus 67 11.426
83
P MLG056 Malignant Hyperthermia 66 11.411
84
GT001 Gout 64 11.382
85
CNG034 Congestive Heart Failure 69 11.362
86
THY029 Thyroid Carcinoma 51 11.321
87
P MYP004 Myopathy 67 11.297
88
c MCR120 Microvascular Complications of Diabetes 7 47 11.130
89
GLM045 Glioma 63 11.121
90
P CRD119 Cardiac Arrest 67 11.107
91
TTN003 Tetanus 65 11.013
92
c MCR113 Microvascular Complications of Diabetes 3 52 11.008
93
GLL048 Glial Tumor 52 11.001
94
P PLM037 Pulmonary Hypertension 72 10.918
95
c DLT002 Dilated Cardiomyopathy 78 10.826
96
P PHC003 Pheochromocytoma 69 10.816
97
ADR040 Adrenal Gland Pheochromocytoma 46 10.800
98
c MCR130 Microvascular Complications of Diabetes 6 41 10.795
99
c MCR133 Microvascular Complications of Diabetes 4 41 10.795
100
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 10.781
101
CYS001 Cystic Fibrosis 78 10.765
102
c MGR028 Migraine with or Without Aura 1 64 10.727
103
MYL069 Myeloma, Multiple 77 10.707
104
P HYP076 Hyperthyroidism 53 10.666
105
MSC157 Muscular Dystrophy, Duchenne Type 79 10.652
106
KRT002 Keratomalacia 55 10.543
107
47X002 47,xyy 48 10.514
108
CNS004 Constipation 56 10.439
109
P ART021 Arteriosclerosis 54 10.426
110
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 10.408
111
CLR108 Colorectal Adenoma 64 10.298
112
INT007 Intermediate Coronary Syndrome 54 10.232
113
P ATR011 Atrial Fibrillation 66 10.195
114
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 10.127
115
P HYP086 Hypothyroidism 69 10.112
116
P ART023 Arthropathy 61 10.073
117
IRN002 Iron Metabolism Disease 57 9.962
118
P PSD015 Pseudohypoparathyroidism 55 9.942
119
CRN030 Coronary Stenosis 50 9.897
120
P PRM002 Primary Hyperoxaluria 65 9.895
121
HYP056 Hypoglycemia 65 9.887
122
P HYP733 Hypercalciuria, Absorptive, 2 45 9.865
123
P SZR006 Seizure Disorder 70 9.856
124
LMB002 Lambert-Eaton Myasthenic Syndrome 52 9.813
125
PRT010 Parathyroid Carcinoma 68 9.726
126
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 21 9.688
127
OST012 Osteoarthritis 77 9.663
128
CRD132 Cardiac Conduction Defect 60 9.638
129
P MYC007 Myocardial Infarction 70 9.601
130
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 9.581
131
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 32 9.540
132
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 9.488
133
HRW001 Hair Whorl 35 9.482
134
CLC001 Calciphylaxis 51 9.466
135
P HYP061 Hypertrophic Cardiomyopathy 69 9.454
136
SPN186 Spinal Cord Injury 61 9.407
137
HYP066 Hyperglycemia 61 9.398
138
P PLY014 Polycystic Kidney Disease 69 9.377
139
c NRL030 Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect 3 9.357
140
c NRL036 Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect 2 9.357
141
P EPL164 Epilepsy 68 9.341
142
P BPL003 Bipolar Disorder 56 9.298
143
c MJR022 Major Affective Disorder 8 38 9.265
144
c MJR024 Major Affective Disorder 9 41 9.265
145
OST017 Osteomyelitis 63 9.196
146
P PRS040 Prostate Cancer 95 9.189
147
c ACT075 Acute Myocardial Infarction 56 9.111
148
MMM001 Mammary Paget's Disease 53 9.086
149
P ADN016 Adenocarcinoma 63 9.066
150
P ART022 Arthritis 71 9.003
151
P BRS047 Breast Cancer 98 8.970
152
HYP060 Hyperinsulinism 54 8.953
153
TRM010 Traumatic Brain Injury 51 8.872
154
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 8.865
155
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 8.865
156
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 8.865
157
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 8.865
158
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 8.865
159
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 8.865
160
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 8.865
161
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 8.865
162
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 8.865
163
P URN019 Urinary Tract Infection 49 8.857
164
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 8.852
165
P RNL007 Renal Tubular Acidosis 50 8.801
166
CYT002 Cytokine Deficiency 43 8.797
167
c MCR115 Microvascular Complications of Diabetes 5 65 8.770
168
INS024 Insulin-Like Growth Factor I 78 8.746
169
P CHR345 Chronic Pain 50 8.729
170
P RHM011 Rheumatoid Arthritis 82 8.722
171
PLY150 Polykaryocytosis Inducer 29 8.683
172
P LKM002 Leukemia 67 8.619
173
P PSR002 Psoriasis 63 8.619
174
P NRP001 Neuropathy 60 8.558
175
BRN071 Brain Injury 50 8.540
176
CRB039 Cerebrovascular Disease 66 8.459
177
HMN044 Human Immunodeficiency Virus Type 1 78 8.407
178
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 8.405
179
P DRR001 Diarrhea 55 8.378
180
BNN003 Bone Inflammation Disease 48 8.350
181
GTR002 Goiter 53 8.340
182
CRB004 Cerebral Artery Occlusion 45 8.314
183
PRP027 Peripheral Vascular Disease 71 8.293
184
P LCT002 Lactose Intolerance 52 8.226
185
P PRP019 Peripheral Nervous System Disease 58 8.176
186
PST011 Pustulosis of Palm and Sole 52 8.134
187
P MLT074 Multiple Endocrine Neoplasia 59 8.101
188
PPL052 Papillomatosis, Confluent and Reticulated 34 8.072
189
CRD223 Cardiac Arrhythmia 63 8.061
190
P INF037 Inflammatory Bowel Disease 53 8.034
191
P LKM062 Leukemia, Acute Lymphoblastic 69 8.010
192
LVR012 Liver Cirrhosis 63 7.973
193
P OVR082 Overgrowth Syndrome 49 7.963
194
P OVR042 Ovarian Cancer 88 7.950
195
STR067 Stroke, Ischemic 80 7.916
196
CRH001 Crohn's Disease 80 7.912
197
P LYM118 Lymphoma 67 7.902
198
PNG002 Pain Agnosia 51 7.900
199
ATR057 Atrioventricular Block 54 7.885
200
P GLM007 Glomerulonephritis 60 7.855
201
GLC086 Glucocorticoid-Induced Osteoporosis 43 7.844
202
P HNT016 Huntington Disease 73 7.842
203
P INF032 Infertility 57 7.803
204
TXC005 Toxic Shock Syndrome 62 7.799
205
P PNC035 Pancreatic Cancer 86 7.791
206
RYN005 Raynaud Phenomenon 45 7.773
207
RTR008 Root Resorption 44 7.724
208
c PLM164 Pulmonary Hypertension, Primary, 1 76 7.707
209
ALC007 Alcohol Dependence 66 7.701
210
P RCT021 Rectum Cancer 54 7.698
211
OST004 Osteitis Fibrosa 38 7.681
212
CLN015 Colon Adenocarcinoma 65 7.674
213
c ATS007 Autism Spectrum Disorder 72 7.653
214
FTT001 Fatty Liver Disease 62 7.645
215
PTT037 Pituitary Tumors 44 7.627
216
GLB002 Glioblastoma 67 7.604
217
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 7.600
218
STT001 Status Epilepticus 59 7.592
219
P HYP776 Hyperparathyroidism, Neonatal Severe 46 7.579
220
P TRM003 Tremor 48 7.560
221
GLC003 Glucose Intolerance 54 7.514
222
P GLM040 Glioma Susceptibility 1 71 7.510
223
IMM167 Immune Deficiency Disease 78 7.476
224
P CTR002 Cataract 60 7.465
225
c HYP794 Hyperoxaluria, Primary, Type I 63 7.460
226
PRT036 Peritonitis 65 7.408
227
P THL005 Thalassemia 56 7.336
228
P PRK039 Parkinsonism 55 7.307
229
OST003 Osteonecrosis 61 7.305
230
c TYP008 Type 1 Diabetes Mellitus 70 7.276
231
DWN001 Down Syndrome 70 7.255
232
P LNG032 Lung Cancer 98 7.239
233
MLG169 Malignant Astrocytoma 57 7.227
234
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 7.217
235
NNL005 Non-Alcoholic Fatty Liver Disease 63 7.189
236
ATM095 Autoimmune Disease 61 7.182
237
P BCL017 B-Cell Lymphoma 59 7.163
238
c SYS001 Systemic Lupus Erythematosus 87 7.150
239
SKN016 Skin Disease 63 7.128
240
c SCL052 Scleroderma, Familial Progressive 61 7.126
241
ZLL002 Zollinger-Ellison Syndrome 55 7.119
242
THY111 Thyroid Carcinoma, Familial Medullary 67 7.113
243
MNT002 Mental Depression 57 7.094
244
LPT014 Leptin Deficiency or Dysfunction 78 7.082
245
HYP014 Hyperuricemia 51 7.072
246
IRR002 Irritable Bowel Syndrome 65 7.053
247
MYC005 Myocardial Stunning 46 6.977
248
HMS001 Hemosiderosis 48 6.973
249
P NPH012 Nephrotic Syndrome 60 6.967
250
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 46 6.924
251
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 6.891
252
RNL114 Renal Cell Carcinoma, Nonpapillary 80 6.872
253
P SYS005 Systemic Scleroderma 74 6.867
254
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 6.863
255
P ENC018 Encephalopathy 62 6.862
256
DPR016 Depression 65 6.860
257
P LPS004 Lupus Erythematosus 61 6.831
258
P RRH023 Rare Hereditary Hemochromatosis 54 6.809
259
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 6.779
260
P LNG028 Long Qt Syndrome 64 6.749
261
IMP005 Impotence 52 6.746
262
THY125 Thyroid Gland Medullary Carcinoma 48 6.723
263
P GST053 Gastric Cancer 83 6.720
264
P PGT001 Paget's Disease of Bone 61 6.702
265
CNN003 Conn's Syndrome 79 6.697
266
HYP080 Hypogonadism 50 6.655
267
PRM020 Premenstrual Tension 39 6.650
268
P MLT020 Multiple Sclerosis 79 6.639
269
c ART101 Aortic Valve Disease 2 66 6.637
270
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 6.626
271
P BRT004 Bartter Disease 58 6.611
272
DFC004 Deficiency Anemia 74 6.610
273
TND005 Tendinitis 54 6.603
274
DNT006 Dental Pulp Necrosis 43 6.596
275
LYM019 Lymphosarcoma 46 6.577
276
P PLY011 Polycystic Ovary Syndrome 57 6.569
277
P GRV001 Graves' Disease 55 6.557
278
PPT005 Peptic Ulcer Disease 58 6.555
279
P ATS364 Autism 69 6.541
280
P HRD086 Hereditary Hypophosphatemic Rickets 40 6.538
281
P LVR013 Liver Disease 69 6.508
282
SYN036 Syncope 45 6.448
283
P FML187 Familial Hypertension 34 6.429
284
P RSP003 Respiratory Failure 74 6.425
285
P DST107 Distal Renal Tubular Acidosis 48 6.419
286
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 6.399
287
ESP021 Esophageal Cancer 83 6.357
288
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 6.348
289
GNG012 Gingival Overgrowth 49 6.347
290
ACR007 Acromegaly 70 6.339
291
P CLC063 Celiac Disease 1 66 6.337
292
P MSC003 Muscular Atrophy 52 6.331
293
P DRM053 Dermatitis, Atopic 65 6.319
294
c BRN108 Branchiootic Syndrome 1 62 6.314
295
P CRD246 Cardiovascular System Disease 56 6.298
296
P ALC033 Alcohol Use Disorder 61 6.286
297
P SCL018 Scoliosis 57 6.277
298
P PSD087 Pseudoxanthoma Elasticum 67 6.267
299
P MLN007 Male Infertility 56 6.220
300
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 6.197
301
ACQ007 Acquired Immunodeficiency Syndrome 59 6.196
302
BRT054 Brittle Bone Disorder 74 6.153
303
P HPT023 Hepatocellular Carcinoma 96 6.132
304
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 6.129
305
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 6.118
306
PLM129 Pulmonary Disease, Chronic Obstructive 74 6.117
307
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 6.107
308
CHL068 Cholestasis 61 6.097
309
P FML023 Familial Hemiplegic Migraine 53 6.061
310
BCT022 Bacterial Infectious Disease 56 6.038
311
P HDC001 Headache 57 5.984
312
P PRD021 Periodic Paralysis 41 5.980
313
c GRV008 Graves Disease 1 54 5.958
314
MDD011 Mood Disorder 62 5.948
315
SQM006 Squamous Cell Carcinoma 60 5.911
316
P MLN008 Melanoma 76 5.884
317
P SCH015 Schizophrenia 74 5.883
318
LNG099 Lung Disease 62 5.874
319
GST092 Gastroesophageal Reflux 61 5.872
320
ART016 Aortic Aneurysm 68 5.872
321
c HYP243 Hyperparathyroidism 1 47 5.867
322
TRN015 Transient Cerebral Ischemia 63 5.856
323
P AMY004 Amyloidosis 70 5.844
324
P DDN001 Duodenal Ulcer 53 5.838
325
P RHN004 Rhinitis 57 5.826
326
PLM010 Pulmonary Edema 55 5.824
327
P PRK057 Parkinson Disease, Late-Onset 80 5.819
328
c MLT156 Multiple Endocrine Neoplasia, Type I 72 5.806
329
P EPS003 Episodic Ataxia 59 5.801
330
P THY032 Thyroiditis 57 5.790
331
P TXP001 Toxoplasmosis 60 5.754
332
c LKM005 Leukemia, T-Cell, Chronic 34 5.738
333
P OST001 Osteopetrosis 71 5.715
334
INT323 Intraocular Pressure Quantitative Trait Locus 64 5.708
335
c ART115 Aortic Valve Disease 1 74 5.699
336
c ACT068 Acute Cystitis 61 5.686
337
P DMN002 Dementia 66 5.649
338
OCL069 Ocular Motor Apraxia 57 5.633
339
ULC004 Ulcerative Colitis 74 5.617
340
P BLD134 Bladder Cancer 79 5.585
341
c SVR005 Severe Pre-Eclampsia 50 5.570
342
CHL004 Cholelithiasis 49 5.568
343
GST030 Gastrinoma 45 5.523
344
PLP001 Pulpitis 48 5.517
345
CRY024 Crystal Arthropathies 18 5.486
346
WTH001 Withdrawal Disorder 48 5.460
347
ANR007 Anorexia Nervosa 60 5.444
348
CRN019 Coronary Artery Vasospasm 47 5.427
349
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 5.409
350
P HYP750 Hypertriglyceridemia, Familial 62 5.403
351
P ALP008 Alopecia 54 5.401
352
P BRG001 Brugada Syndrome 69 5.385
353
CLT003 Colitis 63 5.379
354
c FML021 Familial Hypercholesterolemia 72 5.360
355
P HYP265 Hypotonia 42 5.356
356
P TMP001 Temporal Lobe Epilepsy 49 5.345
357
CYS013 Cystinuria 66 5.334
358
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 5.333
359
c LKM061 Leukemia, Acute Myeloid 83 5.331
360
MCS002 Mucositis 56 5.318
361
DSS032 Disease by Infectious Agent 55 5.306
362
P HPT021 Hepatitis 69 5.306
363
AMN001 Amenorrhea 54 5.300
364
CNT105 Central Core Disease of Muscle 59 5.297
365
P LCT001 Lactic Acidosis 51 5.278
366
P RNV001 Renovascular Hypertension 49 5.277
367
ANR040 Aneurysm 61 5.269
368
P MJR001 Major Depressive Disorder 68 5.257
369
WLL001 Williams-Beuren Syndrome 61 5.257
370
STM007 Stomatitis 54 5.257
371
P DYS154 Dystonia 64 5.248
372
P MYS003 Myasthenia Gravis 68 5.242
373
P END044 Endometriosis 62 5.240
374
P MYC008 Myocarditis 59 5.230
375
DYS073 Dysphagia 53 5.226
376
P DRM010 Dermatomyositis 61 5.220
377
IDP085 Idiopathic Infantile Hypercalcemia 32 5.220
378
DBT010 Diabetic Neuropathy 54 5.214
379
CRD137 Cardiogenic Shock 56 5.210
380
c EPS035 Episodic Ataxia, Type 2 63 5.204
381
P ESP024 Esophagitis 60 5.182
382
P SKN015 Skin Carcinoma 71 5.174
383
P RTN016 Retinal Degeneration 52 5.146
384
c PRD040 Periodontitis, Chronic 52 5.135
385
P MYT002 Myotonic Dystrophy 51 5.117
386
P LNG064 Lung Cancer Susceptibility 3 70 5.107
387
ANK001 Ankylosis 51 5.107
388
MRF001 Marfan Syndrome 76 5.104
389
BLR008 Bilirubin Metabolic Disorder 57 5.096
391
c THR092 Thrombophilia Due to Thrombin Defect 74 5.081
392
THR024 Thrombosis 56 5.076
393
SPN035 Spindle Cell Sarcoma 54 5.069
394
SRC014 Sarcoma 65 5.069
395
P ADL017 Adult T-Cell Leukemia 56 5.068
396
P AST005 Asthma 76 5.049
397
ALL003 Allergic Rhinitis 67 5.033
398
P MYL006 Myeloid Leukemia 61 5.030
399
THY030 Thyroid Gland Disease 50 5.017
400
HYP057 Hypervitaminosis D 37 5.017
401
ALL014 Allergic Encephalomyelitis 34 5.014
402
DRM006 Dermatitis 62 5.008
403
P THR014 Thrombocytopenia 66 4.991
404
PRP016 Paraplegia 52 4.980
405
P PNM007 Pneumonia 67 4.965
406
SPN051 Spondylitis 51 4.962
407
P HRP006 Herpes Simplex 65 4.960
408
VSC002 Vascular Dementia 60 4.958
409
P ENC004 Encephalitis 61 4.927
410
P EXN002 Exanthem 58 4.904
411
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 4.902
412
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 4.892
413
GTL001 Gitelman Syndrome 65 4.879
414
PLM001 Pulmonary Tuberculosis 69 4.875
415
RST023 Resting Heart Rate, Variation in 40 4.873
416
P CYS039 Cystic Kidney Disease 53 4.870
417
P TRC031 Trichorhinophalangeal Syndrome 38 4.862
418
PLC002 Plica Syndrome 35 4.845
419
SYN007 Synovitis 55 4.845
420
LYM133 Lymphoma, Hodgkin, Classic 74 4.831
421
P TRN020 Turner Syndrome 67 4.830
422
HYP020 Hyperprolactinemia 63 4.829
423
c SPN309 Spinocerebellar Ataxia 6 58 4.827
424
PRP080 Peripheral Artery Disease 54 4.815
425
CNN005 Connective Tissue Disease 67 4.806
426
P SCK005 Sickle Cell Disease 56 4.803
427
P GST044 Gastritis 55 4.801
428
P PYL005 Pyelonephritis 57 4.800
429
P MTR014 Motor Neuron Disease 65 4.795
430
CHL065 Cholangiocarcinoma 58 4.789
431
INT079 Intrahepatic Cholangiocarcinoma 51 4.789
432
NTR005 Nutritional Deficiency Disease 61 4.758
433
c SPN225 Spondyloarthropathy 1 70 4.756
434
P HYP035 Hypophosphatasia 62 4.749
435
END057 Endometrial Cancer 72 4.736
436
BRN004 Brain Edema 54 4.736
437
BCK006 Back Pain 47 4.735
438
HDN002 Head Injury 44 4.734
439
PRS021 Prostatic Adenoma 43 4.731
440
c JVN010 Juvenile Rheumatoid Arthritis 66 4.730
441
NRR001 Neuroretinitis 42 4.717
442
RTN023 Retinitis 46 4.708
443
P RTN018 Retinal Disease 53 4.704
444
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 4.703
445
SVR004 Severe Combined Immunodeficiency 72 4.696
446
URN010 Urinary Tract Obstruction 55 4.686
447
MLR004 Malaria 80 4.684
448
NRM005 Neuromuscular Disease 63 4.682
449
MYT011 Myotonia 39 4.669
450
BSL009 Basal Ganglia Calcification 45 4.668
451
CLC004 Calcific Tendinitis 33 4.666
452
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 4.664
453
PNC129 Pancreatic Adenocarcinoma 65 4.655
454
HYD002 Hydronephrosis 58 4.654
455
P ACN011 Acne 57 4.646
456
RHB024 Rhabdomyosarcoma 2 67 4.638
457
MSC007 Muscle Hypertrophy 64 4.638
458
P RTN024 Retinoblastoma 73 4.637
459
PST092 Posttransplant Acute Limbic Encephalitis 28 4.625
460
P SLP006 Sleep Apnea 69 4.622
461
ENM002 Enamel Erosion 25 4.620
462
PRS129 Prostatic Hyperplasia, Benign 49 4.616
463
P RNL015 Renal Hypertension 45 4.612
464
CMM004 Common Variable Immunodeficiency 72 4.612
465
c SML038 Small Cell Cancer of the Lung 69 4.608
466
P LKM071 Leukemia, Chronic Lymphocytic 75 4.585
467
P DNT020 Dent Disease 1 63 4.580
468
P ANR048 Aniridia 1 64 4.577
469
P CNG010 Congenital Stationary Night Blindness 56 4.570
470
CRB037 Cerebral Palsy 67 4.570
471
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.564
472
HRT012 Heart Valve Disease 53 4.556
473
ANX010 Anxiety 70 4.550
474
CRT013 Carotid Stenosis 51 4.548
475
INT067 Interstitial Nephritis 46 4.547
476
NRL016 Neural Tube Defects 81 4.547
477
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 42 4.539
478
P KDN017 Kidney Cancer 61 4.538
479
GST033 Gestational Diabetes 61 4.517
480
INF009 Inflammatory Spondylopathy 30 4.502
481
HMN014 Human Immunodeficiency Virus Infectious Disease 54 4.491
482
c PSD108 Pseudohypoparathyroidism, Type Ia 65 4.478
483
PRT030 Parathyroid Gland Disease 45 4.470
484
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 4.460
485
P OPN001 Open-Angle Glaucoma 55 4.458
486
P MYC084 Mycobacterium Tuberculosis 1 68 4.456
487
c HPT003 Hepatitis a 63 4.453
488
SCK003 Sickle Cell Anemia 74 4.443
489
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.442
490
P SHR001 Short Bowel Syndrome 53 4.441
491
c PRG042 Progressive Familial Heart Block, Type Ia 66 4.434
492
CRT015 Carotid Artery Occlusion 45 4.432
493
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 4.427
494
PRS045 Prostatic Hypertrophy 53 4.427
495
ATS010 Autosomal Recessive Disease 42 4.396
496
GNG013 Gingivitis 59 4.373
497
P MYS005 Myositis 56 4.368
499
c PCH010 Pachyonychia Congenita 3 43 4.349
500
ALL006 Allergic Asthma 56 4.348
501
MST005 Mastitis 53 4.348
502
P NGH001 Night Blindness 52 4.348
503
P VSC011 Vasculitis 61 4.344
504
IDP070 Idiopathic Scoliosis 42 4.326
505
BRN024 Bronchitis 67 4.323
506
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 4.323
507
HMC014 Homocysteinemia 52 4.321
508
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 4.320
509
c HMC039 Hemochromatosis, Type 1 73 4.302
510
c HYP603 Hyperoxaluria, Primary, Type Iii 50 4.297
511
LYM143 Lymphoma, Non-Hodgkin, Familial 75 4.290
512
c HPT016 Hepatitis B 62 4.281
513
c HYP602 Hyperoxaluria, Primary, Type Ii 49 4.279
514
c LKM063 Leukemia, Chronic Myeloid 71 4.278
515
PLM033 Pulmonary Embolism 58 4.259
516
PRP030 Purpura 54 4.258
517
PRS047 Prostatitis 58 4.245
518
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 4.238
519
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 4.238
520
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 4.230
521
DGR001 Digeorge Syndrome 62 4.221
522
PTH003 Pathologic Nystagmus 52 4.218
523
P TMT001 Timothy Syndrome 55 4.215
524
MLG086 Malignant Hyperthermia Susceptibility 39 4.205
525
c BTT014 Beta-Thalassemia 72 4.204
526
PRT058 Pure Autonomic Failure 58 4.181
527
c THY109 Thyroid Cancer, Nonmedullary, 1 55 4.156
528
ETN001 Eating Disorder 59 4.154
529
c PNC108 Pancreatitis, Hereditary 69 4.143
530
P SNS001 Sensorineural Hearing Loss 59 4.130
531
ACT098 Acute Erythroid Leukemia 55 4.126
532
BNG018 Benign Paroxysmal Positional Nystagmus 41 4.121
533
P NTR004 Neutropenia 63 4.118
534
SPS057 Spasticity 42 4.117
535
ACT003 Acute Kidney Tubular Necrosis 46 4.117
536
P ADL010 Adult Respiratory Distress Syndrome 71 4.112
537
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 4.105
538
PRM236 Primary Biliary Cholangitis 60 4.091
539
CHL067 Cholecystitis 60 4.089
540
PLM017 Pulmonary Alveolar Microlithiasis 47 4.083
541
ENT004 Enthesopathy 51 4.080
542
P PLY019 Polyneuropathy 52 4.069
543
P PMP001 Pemphigus 55 4.065
544
P HYP098 Hypereosinophilic Syndrome 66 4.049
545
P DBT005 Diabetes Insipidus 54 4.048
546
c ACT073 Acute Leukemia 58 4.039
547
P PTT014 Pitt-Hopkins Syndrome 64 4.035
548
PRT013 Portal Hypertension 59 4.007
549
BRK010 Burkitt Lymphoma 66 4.004
550
SBC016 Subacute Delirium 43 4.001
551
ADL002 Adult Syndrome 70 3.992
552
P MCR129 Microvascular Complications of Diabetes 1 68 3.991
553
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 53 3.990
554
P HMP007 Hemophilia 52 3.989
555
c CRN243 Carney Complex, Type 1 53 3.981
556
P CRB059 Cerebellar Degeneration 36 3.979
557
MTR002 Mitral Valve Insufficiency 52 3.978
558
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.961
559
P ANP001 Anaplastic Large Cell Lymphoma 61 3.960
560
ART002 Arts Syndrome 66 3.952
561
P FCL005 Focal Segmental Glomerulosclerosis 57 3.950
562
P GRF003 Graft-Versus-Host Disease 71 3.949
563
DNT001 Dental Fluorosis 43 3.945
564
PRS063 Paresthesia 39 3.945
565
NPH010 Nephrosclerosis 50 3.944
566
P FBR017 Fibrosarcoma 56 3.944
567
ENM001 Enamel Caries 27 3.940
568
P CNR004 Cone-Rod Dystrophy 2 74 3.938
569
LWC001 Low Compliance Bladder 45 3.921
570
P ATT013 Attention Deficit-Hyperactivity Disorder 64 3.901
571
c THY107 Thymoma, Familial 42 3.899
572
P THY023 Thymoma 64 3.899
573
URT010 Ureteral Obstruction 45 3.896
574
MLK006 Milk Allergy 47 3.888
575
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 3.872
576
MDL009 Medullary Sponge Kidney 39 3.868
577
P MTR003 Mitral Valve Stenosis 53 3.856
578
P VNS003 Venous Insufficiency 55 3.852
579
DST006 Diastolic Heart Failure 45 3.851
580
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 3.850
581
SCH014 Schistosomiasis 56 3.850
582
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 41 3.848
583
IRN001 Iron Deficiency Anemia 58 3.847
584
ENT011 Enterocolitis 55 3.846
585
PRN039 Paraneoplastic Syndromes 37 3.838
586
VTM033 Vitamin K Deficiency Bleeding 48 3.830
587
AMN006 Aminoaciduria 37 3.824
588
OVR029 Ovarian Hyperstimulation Syndrome 63 3.818
589
SYS003 Systolic Heart Failure 49 3.817
590
P PLM036 Pulmonary Fibrosis 66 3.804
591
P ART018 Aortic Valve Insufficiency 52 3.792
592
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 3.791
593
THR035 Thrombasthenia 48 3.787
594
P SCL057 Scoliosis, Isolated 1 40 3.786
595
ETH012 Ethylene Glycol Poisoning 29 3.781
596
CLR109 Colorectal Adenocarcinoma 50 3.778
597
AMN003 Amnestic Disorder 54 3.777
598
P RTN008 Retinitis Pigmentosa 80 3.769
599
c MCR112 Microvascular Complications of Diabetes 2 42 3.766
600
c HYP724 Hyperlipoproteinemia, Type Iii 67 3.765
601
P FRG001 Fragile X Syndrome 70 3.763
602
P FNC004 Fanconi Syndrome 60 3.758
603
P CND004 Candidiasis 58 3.757
604
BRD001 Brody Myopathy 55 3.726
605
PRR001 Periarthritis 34 3.722
606
P INT068 Intestinal Disease 53 3.720
607
CVD001 Covid-19 57 3.719
608
WLL004 Wallerian Degeneration 38 3.718
609
CHG001 Chagas Disease 66 3.709
610
ATN005 Autonomic Dysfunction 46 3.699
611
CHL152 Childhood Acute Lymphocytic Leukemia 50 3.695
612
P NRF002 Neurofibromatosis 57 3.692
613
P SML001 Small Cell Carcinoma 52 3.690
614
SNS003 Sensory Peripheral Neuropathy 52 3.690
615
LMB062 Limb Ischemia 55 3.689
616
IGG001 Iga Glomerulonephritis 50 3.677
617
P KLZ004 Kala-Azar 1 41 3.667
618
LSH001 Leishmaniasis 64 3.667
619
CHR074 Choriocarcinoma 46 3.666
620
GLM044 Glomerular Disease 35 3.665
621
P MLT008 Multinodular Goiter 42 3.660
622
SXL003 Sexual Disorder 49 3.652
623
OST115 Osteonecrosis of the Jaw 41 3.649
624
TRD006 Tardive Dyskinesia 53 3.642
625
P BNC003 Bone Cancer 58 3.637
626
CHR431 Chronic Venous Insufficiency 48 3.636
627
FBR047 Fibromyalgia 58 3.629
628
HLL004 Hellp Syndrome 53 3.628
629
GRW007 Growth Hormone Deficiency 46 3.627
630
P MGR003 Migraine with Aura 52 3.627
631
P EYD002 Eye Disease 57 3.626
632
P CHL002 Childhood Absence Epilepsy 63 3.620
633
P HML002 Hemolytic Anemia 62 3.607
634
CRB090 Cerebral Hypoxia 42 3.598
635
P CNJ013 Conjunctivitis 66 3.591
636
P MVM001 Movement Disease 61 3.590
637
GST040 Gastric Adenocarcinoma 67 3.590
638
P PRN023 Prion Disease 60 3.586
639
HYP006 Hypertensive Heart Disease 49 3.585
640
P PTT006 Pituitary Adenoma 55 3.580
641
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 3.579
642
P ASP006 Aspergillosis 72 3.575
643
INT075 Intracranial Hypertension 53 3.573
644
P CYS018 Cystitis 59 3.566
645
SPT004 Septic Arthritis 58 3.559
646
GST050 Gastrointestinal System Disease 55 3.555
647
HPT004 Hepatic Coma 43 3.552
648
HGH043 High Grade Glioma 45 3.547
649
P LMB006 Limb-Girdle Muscular Dystrophy 52 3.545
650
KRT008 Keratopathy 46 3.542
651
BRR014 Barrett Esophagus 66 3.538
652
P CHL066 Cholangitis 52 3.537
653
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.536
654
EXR010 Exercise-Induced Bronchoconstriction 34 3.535
655
P NRV007 Nervous System Disease 67 3.533
656
RYN001 Raynaud Disease 50 3.525
657
DSS009 Disseminated Intravascular Coagulation 57 3.505
658
TND004 Tendinopathy 45 3.502
659
MNN043 Meningioma, Familial 79 3.500
660
GST045 Gastroenteritis 58 3.498
661
FDL002 Food Allergy 47 3.493
662
SVR001 Severe Acute Respiratory Syndrome 67 3.485
663
P SCK002 Sick Sinus Syndrome 55 3.481
664
ANT024 Anthrax Disease 58 3.476
665
SCR001 Secretory Meningioma 40 3.475
666
LYM002 Lymphoplasmacyte-Rich Meningioma 35 3.475
667
SPN021 Spinal Meningioma 50 3.475
668
PLG002 Plague 58 3.475
669
HYP068 Hyperostosis 47 3.474
670
ARG004 Argyria 26 3.472
671
c HPT073 Hepatitis C Virus 71 3.468
672
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 3.461
673
ACH005 Achalasia 55 3.459
674
LYM040 Lymphoblastic Lymphoma 53 3.458
675
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 3.457
676
HPT019 Hepatic Encephalopathy 59 3.457
677
P OPT006 Optic Nerve Disease 58 3.454
678
ILS001 Ileus 50 3.447
679
P HYP050 Hyperinsulinemic Hypoglycemia 57 3.441
680
c BLD140 Blood Group, I System 46 3.439
681
PNC041 Pancreatic Ductal Adenocarcinoma 51 3.432
682
EMB004 Embryonal Carcinoma 56 3.425
683
KLD004 Keloid Disorder 39 3.425
684
RTC003 Root Caries 32 3.424
685
BNG091 Benign Chronic Pemphigus 57 3.418
686
GST023 Gastric Ulcer 52 3.413
687
DRR014 Darier-White Disease 59 3.407
688
INT066 Interstitial Lung Disease 60 3.405
689
P RTT002 Rett Syndrome 79 3.405
690
P URT039 Urticaria 58 3.405
691
c ATM068 Autoimmune Hypoparathyroidism 30 3.402
692
c MLG069 Malignant Hypertension 46 3.393
693
DGN001 Degenerative Disc Disease 49 3.392
694
ISL001 Islet Cell Tumor 56 3.390
695
P SPR041 Spermatogenic Failure 6 47 3.388
696
OVR094 Ovarian Epithelial Cancer 39 3.387
697
VRC005 Varicose Veins 60 3.383
698
P MYP087 Myopathy, Tubular Aggregate, 1 49 3.374
699
P GCH001 Gaucher's Disease 70 3.367
700
CNT047 Contact Dermatitis 57 3.361
701
NRN004 Neuroendocrine Tumor 59 3.359
702
P INF038 Influenza 68 3.356
703
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 3.351
704
PSR001 Psoriatic Arthritis 62 3.345
705
CHR100 Chronic Ulcer of Skin 57 3.344
706
TRN018 Transitional Cell Carcinoma 56 3.339
707
DPH001 Diphtheria 59 3.338
708
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 3.338
709
P FML362 Familial Isolated Hypoparathyroidism 48 3.336
710
MST004 Mast Cell Neoplasm 42 3.331
711
MLD018 Mild Cognitive Impairment 48 3.326
712
PPL022 Papilloma 53 3.322
713
GSG001 Gas Gangrene 52 3.320
714
ORL015 Oral Squamous Cell Carcinoma 43 3.320
715
P TRT010 Teratoma 51 3.318
716
TBC004 Tobacco Addiction 63 3.318
717
END040 Endogenous Depression 55 3.316
718
P INS002 in Situ Carcinoma 53 3.316
719
c INH020 Inherited Metabolic Disorder 48 3.312
720
FRZ001 Frozen Shoulder 55 3.306
721
P INT143 Interstitial Cystitis 60 3.304
722
BRS051 Breast Disease 58 3.292
723
DMY004 Demyelinating Disease 50 3.292
724
P MYP006 Myopia 56 3.274
725
PMP014 Pemphigoid 51 3.274
726
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 3.273
727
VLK001 Volkmann Contracture 23 3.267
728
P END033 Endocarditis 58 3.266
729
P FML011 Familial Adenomatous Polyposis 71 3.264
730
P RHB003 Rhabdomyosarcoma 66 3.262
731
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 3.261
732
c DWL002 Dowling-Degos Disease 1 58 3.259
733
EXT007 Extracutaneous Mastocytoma 38 3.253
734
FCL014 Focal Epilepsy 53 3.247
735
RNL077 Renal Fibrosis 46 3.246
736
OTT002 Otitis Media 71 3.239
737
P BRS044 Breast Adenocarcinoma 58 3.230
738
c PRG043 Progressive Familial Heart Block, Type Ib 54 3.229
739
ORL011 Oral Cancer 60 3.226
740
SQM002 Squamous Cell Papilloma 46 3.225
741
SPL018 Splenomegaly 49 3.225
742
HYP540 Hypertension, Diastolic 37 3.222
743
QDR001 Quadriplegia 50 3.214
744
SCT005 Scott Syndrome 50 3.200
745
BRS064 Bursitis 51 3.195
746
P GLY013 Glycogen Storage Disease 60 3.194
747
VCC001 Vaccinia 47 3.190
748
c VSC019 Vesicoureteral Reflux 1 57 3.174
749
P UVT001 Uveitis 57 3.170
750
c HPT001 Hepatitis C 62 3.169
751
CRV035 Cervical Cancer 73 3.168
752
c PNS012 Paine Syndrome 60 3.168
753
CMB007 Combined Immunodeficiency 57 3.166
754
P TTR001 Tetralogy of Fallot 69 3.165
755
CTS005 Catastrophic Antiphospholipid Syndrome 43 3.153
756
CRY008 Cryopyrin-Associated Periodic Syndrome 48 3.153
757
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 3.137
758
P MJR007 Major Affective Disorder 1 42 3.133
759
P SMK004 Smoking As a Quantitative Trait Locus 3 44 3.128
760
P SLP005 Sleep Disorder 61 3.127
761
P AVS003 Avascular Necrosis 41 3.126
762
P HYD006 Hydrocephalus 61 3.123
763
OST016 Osteochondrosis 52 3.113
764
P MDL005 Medulloblastoma 75 3.112
765
HLC007 Helicobacter Pylori Infection 67 3.109
766
PMP006 Pemphigus Vulgaris, Familial 58 3.094
767
HYP741 Hyperparathyroidism 2 with Jaw Tumors 51 3.092
768
DFF005 Diffuse Large B-Cell Lymphoma 54 3.090
769
P MTR012 Mitral Valve Disease 57 3.089
770
P LPR021 Leprosy 3 71 3.088
771
HNS001 Hansen's Disease 32 3.088
772
c MGR032 Migraine, Familial Hemiplegic, 1 54 3.085
773
RTN020 Retinal Vascular Disease 46 3.084
774
BTT017 Beta-Thalassemia Major 51 3.076
775
P CRC039 Coarctation of Aorta 46 3.074
776
ART074 Aortic Dissection 53 3.070
777
BRN056 Bronchopulmonary Dysplasia 56 3.068
778
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 3.064
779
CHL028 Childhood Type Dermatomyositis 59 3.050
780
PRP017 Periapical Periodontitis 46 3.049
781
NDL007 Nodular Goiter 48 3.041
782
c ESS001 Essential Tremor 57 3.032
783
P GLL018 Gallbladder Cancer 53 3.028
784
c CHL119 Cholangitis, Primary Sclerosing 58 3.026
785
CLN045 Colonic Benign Neoplasm 48 3.022
786
TLN003 Telangiectasis 51 3.018
787
ALD013 Aldosterone-Producing Adenoma 36 3.017
788
PHN003 Phenylketonuria 76 3.013
789
CRB086 Cerebral Aneurysms 40 3.012
790
GNG003 Gingival Recession 49 3.010
791
P MNC007 Monocytic Leukemia 47 3.007
792
KRT009 Keratosis 53 3.005
793
CHL123 Chlamydia 58 3.004
794
c GLC092 Glaucoma, Primary Open Angle 62 2.999
795
PRN019 Perinatal Necrotizing Enterocolitis 60 2.993
796
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 2.991
797
P SBS003 Substance Abuse 54 2.988
798
RLP002 Relapsing-Remitting Multiple Sclerosis 56 2.980
799
P CHR012 Chronic Granulomatous Disease 69 2.979
800
MYL009 Myelodysplastic Syndrome 67 2.977
801
P HMR005 Hemorrhoid 49 2.975
802
P PLY018 Polycythemia 56 2.972
803
CCN002 Cocaine Abuse 49 2.968
804
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 2.964
805
DYS015 Dysentery 50 2.964
806
MTH071 Methane Production 25 2.958
807
STR081 Stormorken Syndrome 55 2.956
808
PRM013 Premature Menopause 58 2.950
809
OCL006 Ocular Hypertension 53 2.945
810
c HMP004 Hemophilia B 68 2.944
811
SPN027 Spinal Stenosis 59 2.943
812
P SJG008 Sjogren Syndrome 61 2.939
813
PSD014 Pseudopseudohypoparathyroidism 54 2.939
814
c BSL007 Basal Cell Carcinoma 68 2.936
815
P PRS038 Personality Disorder 65 2.934
816
FBR009 Fibrous Dysplasia 48 2.933
817
BCK003 Background Diabetic Retinopathy 47 2.925
818
P MYC033 Myoclonus 47 2.924
819
ATN004 Autonomic Neuropathy 42 2.923
820
DRG003 Drug Dependence 46 2.921
821
PRN032 Paraneoplastic Cerebellar Degeneration 25 2.905
822
P BNG032 Benign Mesothelioma 53 2.902
823
PRT038 Protein-Energy Malnutrition 53 2.899
824
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.895
825
c JVN025 Juvenile Primary Osteoporosis 21 2.894
826
CRN288 Corneal Dystrophy, Band-Shaped 36 2.894
827
c CHR098 Chronic Pyelonephritis 34 2.893
828
P ANG015 Angioedema 56 2.893
829
INT030 Intracranial Aneurysm 55 2.890
830
HVY002 Heavy Metal Poisoning 22 2.881
831
MSC152 Muscular Dystrophy, Becker Type 69 2.880
832
P NSP012 Nasopharyngeal Carcinoma 61 2.880
833
P EPL140 Epilepsy, Idiopathic Generalized 62 2.879
834
P LTH003 Lethal Congenital Contracture Syndrome 41 2.878
835
SNT005 Sinoatrial Node Disease 47 2.874
836
NPH078 Nephrolithiasis, Uric Acid 39 2.869
837
ASP004 Asphyxia Neonatorum 50 2.869
838
PLC007 Placental Abruption 47 2.868
839
LMY002 Leiomyoma 51 2.868
840
P CHN012 Chondrosarcoma 57 2.866
841
ANT039 Antisynthetase Syndrome 55 2.862
842
CRC021 Carcinosarcoma 64 2.861
843
PST053 Postherpetic Neuralgia 40 2.860
844
SFT003 Soft Tissue Sarcoma 57 2.856
845
BRN028 Brain Cancer 74 2.852
846
RGH001 Right Bundle Branch Block 47 2.847
847
P GLL022 Guillain-Barre Syndrome 60 2.837
848
PNM001 Pneumocystosis 61 2.829
849
NNL006 Non-Alcoholic Steatohepatitis 54 2.828
850
PRM329 Premature Aging 36 2.827
851
URM005 Uremic Pruritus 45 2.826
852
P TMP003 Temporal Arteritis 69 2.823
853
ERL001 Early Myoclonic Encephalopathy 62 2.822
854
ASP026 Asplenia, Isolated Congenital 43 2.814
855
RTN003 Retinal Ischemia 49 2.810
856
GLC036 Glucagonoma 46 2.806
857
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 2.805
858
PST028 Post-Traumatic Stress Disorder 59 2.803
859
LFT001 Left Bundle Branch Hemiblock 47 2.801
860
c VRL010 Viral Hepatitis 53 2.798
861
INT002 Intermittent Claudication 61 2.797
862
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.797
863
CHR178 Chromosomal Triplication 34 2.796
864
P PTS002 Ptosis 52 2.785
865
FRN006 Frontotemporal Dementia 68 2.782
866
TRT001 Teratocarcinoma 42 2.782
867
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.781
868
P SPP010 Suppressor of Tumorigenicity 3 51 2.779
869
HRN029 Hearing Loss, Noise-Induced 37 2.778
870
ANR004 Anuria 44 2.777
871
MST020 Mast Cell Activation Syndrome 28 2.774
872
KRT019 Keratitis, Hereditary 66 2.772
873
GLN010 Glanzmann Thrombasthenia 66 2.768
874
EWN003 Ewing Sarcoma 70 2.765
875
URT014 Ureterolithiasis 43 2.763
876
c OST164 Osteoporosis, Juvenile 54 2.762
877
PST021 Postpartum Depression 50 2.761
878
MMM006 Mammographic Density 39 2.754
879
ACT119 Acute Promyelocytic Leukemia 62 2.750
880
P WLF004 Wolfram Syndrome 61 2.744
881
P CNT004 Centronuclear Myopathy 57 2.740
882
DMP001 Dumping Syndrome 43 2.733
883
HMP005 Hemiplegia 54 2.726
884
P ANT006 Antiphospholipid Syndrome 55 2.717
885
ONC003 Oncogenic Osteomalacia 42 2.716
886
P PNC025 Panic Disorder 52 2.708
887
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 2.706
888
P CLS010 Cluster Headache 42 2.705
889
P SCL048 Sclerosteosis 58 2.704
890
HYP052 Hyperkalemic Periodic Paralysis 63 2.699
891
DFF036 Differentiated Thyroid Carcinoma 51 2.691
892
BLL006 Bullous Pemphigoid 61 2.689
893
P SCL009 Sclerosing Cholangitis 48 2.686
894
c HYP272 Hypercholesterolemia, Familial, 3 45 2.683
895
MYL005 Myelofibrosis 71 2.678
896
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.677
897
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 49 2.675
898
PLM031 Poliomyelitis 63 2.673
899
VSC003 Visceral Leishmaniasis 55 2.672
900
c PSD066 Pseudohypoparathyroidism, Type Ib 52 2.663
901
PHS001 Phosphorus Metabolism Disease 38 2.662
902
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.660
903
SMT003 Somatostatinoma 52 2.658
904
P TBR001 Tuberous Sclerosis 69 2.656
905
CRT016 Carotid Artery Disease 52 2.656
906
P MNN013 Meningitis 65 2.654
907
P LCH002 Lichen Planus 54 2.652
908
VTM002 Vitamin B12 Deficiency 48 2.649
909
AZS001 Azoospermia 45 2.649
910
PLR008 Pleurisy 50 2.649
911
P MLT007 Multiple Epiphyseal Dysplasia 56 2.649
912
BCT004 Bacteriuria 47 2.647
913
c ACT134 Acute Liver Failure 59 2.647
914
P DNT007 Dentin Sensitivity 34 2.646
915
P NMN002 Niemann-Pick Disease 60 2.628
916
c ACT249 Acute Asthma 40 2.626
917
SCR011 Scrapie 39 2.621
918
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 64 2.615
919
P BRB001 Beriberi 44 2.609
920
PCD001 Pica Disease 38 2.606
921
P CMP008 Compartment Syndrome 50 2.602
922
NWC001 Newcastle Disease 47 2.600
923
DNT010 Dentin Caries 31 2.600
924
c CTR132 Cataract 3, Multiple Types 42 2.598
925
c BPL002 Bipolar I Disorder 47 2.598
926
LWC002 Lowe Oculocerebrorenal Syndrome 68 2.595
927
KWS002 Kawasaki Disease 65 2.595
928
MYL031 Myeloproliferative Neoplasm 66 2.595
929
THR004 Thrombocytosis 53 2.592
930
ODN023 Odontochondrodysplasia 67 2.591
931
MSL001 Measles 61 2.583
932
P CRP001 Carpal Tunnel Syndrome 66 2.583
933
P GLL020 Gallbladder Disease 56 2.583
934
XLN012 X-Linked Congenital Stationary Night Blindness 28 2.579
935
c BCT007 Bacterial Meningitis 55 2.578
936
P PLY041 Polymyositis 59 2.577
937
DCT002 Ductal Carcinoma in Situ 58 2.576
938
PLS009 Plasma Cell Neoplasm 64 2.571
939
P ICH004 Ichthyosis 56 2.569
940
SLL001 Sialolithiasis 36 2.567
941
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.562
942
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.562
943
CHR073 Choreatic Disease 54 2.562
944
c MCL013 Mucolipidosis Iv 65 2.558
945
CMP034 Complete Androgen Insensitivity Syndrome 55 2.556
946
ART004 Aortic Atherosclerosis 47 2.555
947
HSH003 Hashimoto Thyroiditis 60 2.552
948
CRT084 Creatinine Clearance Quantitative Trait Locus 25 2.547