Search results for Calcium

5588 hits were found for Calcium

# Family MCID Name MIFTS Score
1
NPH091 Nephrolithiasis, Calcium Oxalate 61 54.585
2
c CHN022 Chondrocalcinosis 2 40 40.554
3
FML307 Familial Calcium Pyrophosphate Deposition 38 38.932
4
P HYP069 Hyperparathyroidism 62 25.161
5
IMM066 Immunodeficiency 9 39 24.376
6
IMM065 Immunodeficiency 10 47 22.906
7
RCK004 Rickets 64 22.508
8
P OST002 Osteoporosis 76 22.294
9
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 20.711
10
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 20.711
11
P CHN059 Chondrocalcinosis 51 20.216
12
NPH009 Nephrolithiasis 54 18.088
13
c NRL036 Neurological Channelopathy of the Central Nervous System Due to a Genetic Calcium Channel Defect 2 17.804
14
c NRL030 Neurological Muscular Channelopathy Due to a Genetic Calcium Channel Defect 3 17.804
15
BNR002 Bone Resorption Disease 47 17.651
16
c SCN007 Secondary Hyperparathyroidism 50 16.572
17
c PRM005 Primary Hyperparathyroidism 59 15.620
18
c HYP595 Hypertension, Essential 84 15.524
19
URL001 Urolithiasis 45 14.641
20
P BND020 Bone Disease 60 14.455
21
P HYP024 Hypoparathyroidism 55 13.986
22
P KDN018 Kidney Disease 71 13.617
23
PRT037 Pertussis 49 13.239
24
HYP025 Hyperphosphatemia 47 13.187
25
c CHR684 Chronic Kidney Disease 73 12.995
26
c CHN021 Chondrocalcinosis 1 17 12.720
27
LPP008 Lipoprotein Quantitative Trait Locus 65 12.085
28
c BLD126 Bleeding Disorder, Platelet-Type, 18 39 11.993
29
ATH013 Atherosclerosis Susceptibility 63 11.243
30
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 11.232
31
ART140 Arteries, Anomalies of 52 11.113
32
P FML068 Familial Hypocalciuric Hypercalcemia 55 11.029
33
P CRN300 Coronary Heart Disease 1 73 10.808
34
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 10.264
35
END086 End Stage Renal Disease 54 10.253
36
P CLR023 Colorectal Cancer 100 10.251
37
ANG054 Angina Pectoris 65 10.182
38
c PRC016 Pre-Eclampsia 64 9.625
39
OST011 Osteomalacia 52 9.377
40
AML006 Amelogenesis Imperfecta Hypoplastic Type, Ig 25 9.350
41
ADN018 Adenoma 58 9.311
42
IDP073 Idiopathic Hypercalciuria 41 9.288
43
CMB055 Combined Immunodeficiency Due to Crac Channel Dysfunction 33 9.255
44
P NRB001 Neuroblastoma 66 9.211
45
KRT002 Keratomalacia 54 9.041
46
AGN016 Aging 53 8.688
47
NPH003 Nephrocalcinosis 49 8.677
48
DNT012 Dental Caries 53 8.664
49
CLC006 Calcinosis 47 8.603
50
RPD005 Rapidly Involuting Congenital Hemangioma 48 8.552
51
P PNC044 Pancreatitis 61 8.526
52
c ACT027 Acute Pancreatitis 60 8.484
53
ISC004 Ischemia 61 8.274
54
P HRT032 Heart Disease 84 8.257
55
LPD008 Lipid Metabolism Disorder 61 8.161
56
P HYP726 Hypercalcemia, Infantile, 1 58 7.898
57
P PRD008 Periodontitis 63 7.807
58
c HYP836 Hypercholesterolemia, Familial, 1 73 7.686
59
c TYP009 Type 2 Diabetes Mellitus 91 7.625
60
P MSC005 Muscular Dystrophy 66 7.603
61
48X005 48,xyyy 39 7.544
62
P VSC007 Vascular Disease 62 7.497
63
ALL029 Allergic Disease 61 7.396
64
PRT251 Proteinuria, Chronic Benign 58 7.376
65
OST159 Osteogenic Sarcoma 66 7.363
66
HLX001 Helix Syndrome 47 7.361
67
RNL011 Renal Osteodystrophy 48 7.262
68
HYP017 Hypophosphatemia 49 7.109
69
P DBT009 Diabetes Mellitus 67 7.026
70
P ECL001 Eclampsia 52 6.859
71
P HYP733 Hypercalciuria, Absorptive, 2 45 6.788
72
MTB004 Metabolic Acidosis 48 6.773
73
HYP005 Hypokalemia 55 6.758
74
INS001 Insulinoma 59 6.756
75
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 6.730
76
GT001 Gout 63 6.719
77
c ATR087 Atrial Standstill 1 74 6.663
78
P ALZ034 Alzheimer Disease 87 6.658
79
P SRC025 Sarcoidosis 1 70 6.609
80
P ADN016 Adenocarcinoma 63 6.505
81
CNG034 Congestive Heart Failure 69 6.496
82
HYP266 Hypoxia 56 6.429
83
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 6.393
84
c HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 49 6.360
85
GLM045 Glioma 62 6.349
86
c GLL024 Gallbladder Disease 1 53 6.331
87
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 6.294
88
P LTR001 Lateral Sclerosis 57 6.290
89
GLL048 Glial Tumor 51 6.290
90
c AMY091 Amyotrophic Lateral Sclerosis 1 87 6.274
91
P PRM002 Primary Hyperoxaluria 65 6.268
92
c ACT071 Acute Kidney Failure 60 6.268
93
P CRD119 Cardiac Arrest 68 6.230
94
P ART023 Arthropathy 59 6.229
95
P LKM002 Leukemia 65 6.193
96
THY029 Thyroid Carcinoma 55 6.183
97
CHL014 Cholera 62 6.176
98
P ART021 Arteriosclerosis 53 6.167
99
c MCR120 Microvascular Complications of Diabetes 7 47 6.116
100
P PRS040 Prostate Cancer 95 6.105
101
ANX004 Anoxia 40 6.084
102
LMB002 Lambert-Eaton Myasthenic Syndrome 51 6.079
103
MYL069 Myeloma, Multiple 76 6.064
104
P ATR011 Atrial Fibrillation 66 6.047
105
P LYM118 Lymphoma 66 6.036
106
CYS001 Cystic Fibrosis 77 6.035
107
c MCR113 Microvascular Complications of Diabetes 3 52 5.994
108
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.959
109
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 5.959
110
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.959
111
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 5.959
112
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.959
113
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 5.959
114
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 5.959
115
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.959
116
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.959
117
CLR108 Colorectal Adenoma 63 5.958
118
URM002 Uremia 47 5.955
119
IRN002 Iron Metabolism Disease 56 5.929
120
P ART022 Arthritis 70 5.919
121
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 5.911
122
PRT029 Parathyroid Adenoma 51 5.904
123
P BRS047 Breast Cancer 97 5.904
124
TTN003 Tetanus 64 5.901
125
P MLG056 Malignant Hyperthermia 65 5.884
126
CLN015 Colon Adenocarcinoma 64 5.866
127
P MYP004 Myopathy 67 5.850
128
P PLM037 Pulmonary Hypertension 69 5.793
129
c MGR028 Migraine with or Without Aura 1 63 5.786
130
c MCR133 Microvascular Complications of Diabetes 4 41 5.782
131
c MCR130 Microvascular Complications of Diabetes 6 41 5.782
132
MSC157 Muscular Dystrophy, Duchenne Type 78 5.773
133
OST012 Osteoarthritis 77 5.769
134
P PHC003 Pheochromocytoma 70 5.758
135
ADR040 Adrenal Gland Pheochromocytoma 45 5.745
136
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 5.743
137
47X002 47,xyy 47 5.691
138
HMN044 Human Immunodeficiency Virus Type 1 76 5.601
139
P MYC007 Myocardial Infarction 69 5.595
140
c DLT002 Dilated Cardiomyopathy 79 5.582
141
OST017 Osteomyelitis 63 5.525
142
P PSD015 Pseudohypoparathyroidism 54 5.495
143
INT007 Intermediate Coronary Syndrome 53 5.431
144
P SZR006 Seizure Disorder 69 5.431
145
P LKM062 Leukemia, Acute Lymphoblastic 69 5.405
146
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 5.363
147
LYM019 Lymphosarcoma 46 5.348
148
P RHM011 Rheumatoid Arthritis 81 5.331
149
CNS004 Constipation 56 5.327
150
c MCR115 Microvascular Complications of Diabetes 5 65 5.325
151
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 5.322
152
P EPL164 Epilepsy 70 5.309
153
P RCT021 Rectum Cancer 54 5.304
154
SPN186 Spinal Cord Injury 60 5.284
155
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 5.225
156
P PNC035 Pancreatic Cancer 87 5.220
157
P HYP086 Hypothyroidism 68 5.211
158
P HYP776 Hyperparathyroidism, Neonatal Severe 46 5.202
159
HRW001 Hair Whorl 35 5.185
160
c HYP794 Hyperoxaluria, Primary, Type I 63 5.181
161
P PLY014 Polycystic Kidney Disease 71 5.156
162
PRT010 Parathyroid Carcinoma 68 5.154
163
P HYP076 Hyperthyroidism 53 5.147
164
LVR012 Liver Cirrhosis 62 5.130
165
CRN030 Coronary Stenosis 50 5.092
166
MMM001 Mammary Paget's Disease 53 5.063
167
HYP056 Hypoglycemia 65 5.040
168
CLC001 Calciphylaxis 50 5.014
169
c ACT075 Acute Myocardial Infarction 55 4.979
170
P NRP001 Neuropathy 59 4.960
171
CRH001 Crohn's Disease 80 4.953
172
CRB039 Cerebrovascular Disease 65 4.927
173
PNG002 Pain Agnosia 51 4.918
174
P PSR002 Psoriasis 63 4.912
175
DWN001 Down Syndrome 70 4.910
176
P DRR001 Diarrhea 55 4.908
177
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 4.888
178
P INF032 Infertility 60 4.882
179
P HYP061 Hypertrophic Cardiomyopathy 68 4.832
180
P LNG032 Lung Cancer 98 4.822
181
P CRD246 Cardiovascular System Disease 55 4.791
182
CYT002 Cytokine Deficiency 43 4.783
183
P CHR345 Chronic Pain 50 4.768
184
P GST053 Gastric Cancer 82 4.736
185
P BPL003 Bipolar Disorder 56 4.727
186
HYP066 Hyperglycemia 60 4.719
187
P OVR042 Ovarian Cancer 88 4.713
188
c MJR022 Major Affective Disorder 8 37 4.707
189
c MJR024 Major Affective Disorder 9 40 4.707
190
IMM167 Immune Deficiency Disease 76 4.699
191
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 4.676
192
CRD132 Cardiac Conduction Defect 59 4.667
193
TRM010 Traumatic Brain Injury 50 4.656
194
P PRP019 Peripheral Nervous System Disease 57 4.583
195
PRP027 Peripheral Vascular Disease 71 4.554
196
HYP060 Hyperinsulinism 53 4.553
197
PLY150 Polykaryocytosis Inducer 29 4.529
198
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 4.521
199
P LCT002 Lactose Intolerance 51 4.519
200
ALC007 Alcohol Dependence 65 4.504
201
STR067 Stroke, Ischemic 79 4.496
202
P RNL007 Renal Tubular Acidosis 52 4.493
203
PST011 Pustulosis of Palm and Sole 52 4.463
204
PRT036 Peritonitis 65 4.447
205
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 4.444
206
c ATS007 Autism Spectrum Disorder 71 4.429
207
P URN019 Urinary Tract Infection 48 4.426
208
MNT002 Mental Depression 56 4.413
209
PPL052 Papillomatosis, Confluent and Reticulated 34 4.399
210
GLC003 Glucose Intolerance 53 4.377
211
GLB002 Glioblastoma 67 4.376
212
P GLM040 Glioma Susceptibility 1 70 4.369
213
BRN071 Brain Injury 50 4.363
214
RYN005 Raynaud Phenomenon 45 4.328
215
PRM020 Premenstrual Tension 39 4.326
216
CRD223 Cardiac Arrhythmia 63 4.316
217
ZLL002 Zollinger-Ellison Syndrome 55 4.303
218
ATR057 Atrioventricular Block 54 4.300
219
P INF037 Inflammatory Bowel Disease 53 4.283
220
PTT037 Pituitary Tumors 44 4.278
221
ACQ007 Acquired Immunodeficiency Syndrome 58 4.277
222
RNL114 Renal Cell Carcinoma, Nonpapillary 79 4.273
223
FTT001 Fatty Liver Disease 61 4.272
224
DNT006 Dental Pulp Necrosis 43 4.240
225
P BRT004 Bartter Disease 58 4.235
226
BNN003 Bone Inflammation Disease 47 4.231
227
P THL005 Thalassemia 56 4.223
228
DPR016 Depression 64 4.222
229
P GLM007 Glomerulonephritis 59 4.220
230
P BCL017 B-Cell Lymphoma 57 4.204
231
ESP021 Esophageal Cancer 84 4.195
232
c PLM164 Pulmonary Hypertension, Primary, 1 75 4.194
233
TXC005 Toxic Shock Syndrome 61 4.190
234
P MLT020 Multiple Sclerosis 79 4.171
235
P PRK039 Parkinsonism 55 4.159
236
P HPT023 Hepatocellular Carcinoma 95 4.156
237
P MLT074 Multiple Endocrine Neoplasia 58 4.147
238
c SCL052 Scleroderma, Familial Progressive 60 4.146
239
OST003 Osteonecrosis 60 4.146
240
INS024 Insulin-Like Growth Factor I 77 4.144
241
RHB024 Rhabdomyosarcoma 2 65 4.133
242
IRR002 Irritable Bowel Syndrome 64 4.132
243
c ART101 Aortic Valve Disease 2 65 4.132
244
GLC086 Glucocorticoid-Induced Osteoporosis 43 4.130
245
c TYP008 Type 1 Diabetes Mellitus 77 4.125
246
MLG169 Malignant Astrocytoma 57 4.115
247
P ANR048 Aniridia 1 66 4.114
248
IDP085 Idiopathic Infantile Hypercalcemia 32 4.112
249
CRB004 Cerebral Artery Occlusion 45 4.109
250
P TXP001 Toxoplasmosis 59 4.103
251
P PGT001 Paget's Disease of Bone 60 4.100
252
STT001 Status Epilepticus 58 4.098
253
c HYP243 Hyperparathyroidism 1 48 4.090
254
P SYS005 Systemic Scleroderma 73 4.075
255
P PSD087 Pseudoxanthoma Elasticum 66 4.071
256
GTR002 Goiter 52 4.036
257
c CRN243 Carney Complex, Type 1 53 4.033
258
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.032
259
P OVR082 Overgrowth Syndrome 41 4.026
260
P PLY011 Polycystic Ovary Syndrome 57 4.023
261
P HRD086 Hereditary Hypophosphatemic Rickets 40 3.978
262
NTR005 Nutritional Deficiency Disease 60 3.966
263
LPT014 Leptin Deficiency or Dysfunction 77 3.957
264
c SYS001 Systemic Lupus Erythematosus 85 3.934
265
P NPH012 Nephrotic Syndrome 61 3.918
266
P HNT016 Huntington Disease 73 3.897
267
P TRN020 Turner Syndrome 67 3.891
268
P LNG028 Long Qt Syndrome 63 3.874
269
MYC005 Myocardial Stunning 45 3.867
270
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.867
271
P CTR002 Cataract 59 3.858
272
CRY024 Crystal Arthropathies 18 3.853
273
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 3.836
274
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 42 3.835
275
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 64 3.834
276
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 3.833
277
P ATS364 Autism 72 3.833
278
P LVR013 Liver Disease 68 3.820
279
HMS001 Hemosiderosis 48 3.807
280
P TRM003 Tremor 50 3.802
281
c HYP724 Hyperlipoproteinemia, Type Iii 66 3.799
282
RTR008 Root Resorption 44 3.778
283
ADL002 Adult Syndrome 69 3.777
284
HYP014 Hyperuricemia 51 3.766
285
P SCL018 Scoliosis 57 3.741
286
ACR007 Acromegaly 70 3.721
287
SKN016 Skin Disease 63 3.720
288
P PNM007 Pneumonia 64 3.710
289
P RRH023 Rare Hereditary Hemochromatosis 52 3.707
290
OST004 Osteitis Fibrosa 38 3.699
291
MCS002 Mucositis 55 3.677
292
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.662
293
SYN036 Syncope 44 3.611
294
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 3.602
295
P LPS004 Lupus Erythematosus 61 3.597
296
P HPT021 Hepatitis 68 3.580
297
THR024 Thrombosis 56 3.569
298
P MLN008 Melanoma 75 3.569
299
THY111 Thyroid Carcinoma, Familial Medullary 67 3.549
300
IMP005 Impotence 52 3.548
301
DFC004 Deficiency Anemia 74 3.543
302
BRT054 Brittle Bone Disorder 74 3.538
303
P DST107 Distal Renal Tubular Acidosis 48 3.533
304
P ENC018 Encephalopathy 62 3.510
305
c LKM061 Leukemia, Acute Myeloid 83 3.491
306
ATM095 Autoimmune Disease 61 3.488
307
P RSP003 Respiratory Failure 73 3.470
308
TND005 Tendinitis 53 3.466
309
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 3.458
310
P ALC033 Alcohol Use Disorder 67 3.456
311
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.442
312
P MLN007 Male Infertility 56 3.442
313
HMN014 Human Immunodeficiency Virus Infectious Disease 54 3.430
314
c BLD140 Blood Group, I System 47 3.430
315
WLL001 Williams-Beuren Syndrome 60 3.407
316
SQM006 Squamous Cell Carcinoma 59 3.406
317
P OST001 Osteopetrosis 70 3.389
318
c THR092 Thrombophilia Due to Thrombin Defect 74 3.387
319
GNG012 Gingival Overgrowth 49 3.370
320
P MSC003 Muscular Atrophy 52 3.367
321
PLP001 Pulpitis 48 3.366
322
P ESP024 Esophagitis 60 3.359
323
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.356
324
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 3.355
325
P PRD021 Periodic Paralysis 42 3.343
326
GST092 Gastroesophageal Reflux 59 3.340
327
c HYP753 Hypocalciuric Hypercalcemia, Familial, Type Ii 43 3.337
328
P DDN001 Duodenal Ulcer 52 3.334
329
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 42 3.330
330
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 3.321
331
LYM133 Lymphoma, Hodgkin, Classic 69 3.320
332
c HYP603 Hyperoxaluria, Primary, Type Iii 50 3.314
333
c FML021 Familial Hypercholesterolemia 71 3.311
334
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 3.302
335
P EPS003 Episodic Ataxia 59 3.300
336
PPT005 Peptic Ulcer Disease 58 3.298
337
P PRK057 Parkinson Disease, Late-Onset 79 3.291
338
STM007 Stomatitis 52 3.284
339
c LKM005 Leukemia, T-Cell, Chronic 33 3.278
340
BCT022 Bacterial Infectious Disease 55 3.267
341
PNC129 Pancreatic Adenocarcinoma 64 3.267
342
P DMN002 Dementia 65 3.261
343
SPN035 Spindle Cell Sarcoma 51 3.252
344
SRC014 Sarcoma 64 3.252
345
P FML023 Familial Hemiplegic Migraine 53 3.250
346
CLT003 Colitis 63 3.242
347
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.224
348
P RHN004 Rhinitis 56 3.217
349
c HPT003 Hepatitis a 63 3.214
350
CHL068 Cholestasis 61 3.211
351
HYP789 Hypophosphatemic Rickets with Hypercalciuria, Hereditary 49 3.205
352
P THY032 Thyroiditis 56 3.202
353
ULC004 Ulcerative Colitis 74 3.200
354
P BRG001 Brugada Syndrome 69 3.180
355
P CNR004 Cone-Rod Dystrophy 2 74 3.177
356
THY125 Thyroid Gland Medullary Carcinoma 48 3.176
357
P PTT014 Pitt-Hopkins Syndrome 63 3.173
358
P HDC001 Headache 56 3.172
359
P DNT020 Dent Disease 1 63 3.170
360
P FML187 Familial Hypertension 34 3.168
361
GST030 Gastrinoma 45 3.148
362
c HYP602 Hyperoxaluria, Primary, Type Ii 51 3.145
363
CTS005 Catastrophic Antiphospholipid Syndrome 43 3.143
364
CRY008 Cryopyrin-Associated Periodic Syndrome 48 3.143
365
CHL065 Cholangiocarcinoma 57 3.139
366
INT079 Intrahepatic Cholangiocarcinoma 51 3.139
367
CNT105 Central Core Disease of Muscle 59 3.135
368
DSS032 Disease by Infectious Agent 55 3.130
369
TRN015 Transient Cerebral Ischemia 62 3.127
370
c PRD040 Periodontitis, Chronic 52 3.123
371
PLM010 Pulmonary Edema 54 3.121
372
P END044 Endometriosis 62 3.109
373
PRS047 Prostatitis 57 3.105
374
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 3.101
375
P HYP750 Hypertriglyceridemia, Familial 61 3.091
376
P MYL006 Myeloid Leukemia 60 3.089
377
LNG099 Lung Disease 62 3.086
378
c SPN309 Spinocerebellar Ataxia 6 58 3.078
379
P DRM010 Dermatomyositis 61 3.076
380
PLM001 Pulmonary Tuberculosis 69 3.071
381
c ART115 Aortic Valve Disease 1 72 3.061
382
P DRM053 Dermatitis, Atopic 65 3.058
383
INT323 Intraocular Pressure Quantitative Trait Locus 63 3.053
384
P ADL017 Adult T-Cell Leukemia 53 3.044
385
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 3.042
386
HYP080 Hypogonadism 49 3.042
387
c EPS035 Episodic Ataxia, Type 2 63 3.041
388
WTH001 Withdrawal Disorder 47 3.036
389
GTL001 Gitelman Syndrome 65 3.031
390
P BLD134 Bladder Cancer 79 3.029
391
CLN045 Colonic Benign Neoplasm 48 3.014
392
ART016 Aortic Aneurysm 68 3.008
393
P GRV001 Graves' Disease 54 3.004
394
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 3.004
395
c BRN108 Branchiootic Syndrome 1 63 3.002
396
P AST005 Asthma 75 2.998
397
c SML038 Small Cell Cancer of the Lung 68 2.987
398
P RNV001 Renovascular Hypertension 48 2.986
399
MDD011 Mood Disorder 61 2.982
400
BRD001 Brody Myopathy 55 2.978
401
LYM040 Lymphoblastic Lymphoma 53 2.978
402
P SCH015 Schizophrenia 74 2.968
403
c PNC108 Pancreatitis, Hereditary 68 2.959
404
P AMY004 Amyloidosis 69 2.943
405
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.942
406
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.942
407
PRT030 Parathyroid Gland Disease 44 2.939
408
THY030 Thyroid Gland Disease 50 2.932
409
c MLT156 Multiple Endocrine Neoplasia, Type I 71 2.923
410
LYM143 Lymphoma, Non-Hodgkin, Familial 74 2.922
411
c PSD108 Pseudohypoparathyroidism, Type Ia 64 2.920
412
P RTN018 Retinal Disease 53 2.914
413
ART002 Arts Syndrome 66 2.898
414
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 2.889
415
c GRV008 Graves Disease 1 54 2.886
416
P ENC004 Encephalitis 61 2.885
417
P VTM036 Vitamin D-Dependent Rickets 40 2.881
418
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 2.878
419
ANT039 Antisynthetase Syndrome 55 2.876
420
P LNG064 Lung Cancer Susceptibility 3 69 2.870
421
P CNG010 Congenital Stationary Night Blindness 56 2.866
422
ANK001 Ankylosis 50 2.864
423
c SVR005 Severe Pre-Eclampsia 49 2.862
424
P MYC084 Mycobacterium Tuberculosis 1 68 2.857
425
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.847
426
OVR029 Ovarian Hyperstimulation Syndrome 63 2.845
427
P CYS039 Cystic Kidney Disease 52 2.845
428
P HYP265 Hypotonia 42 2.841
429
P BSL038 Basal Ganglia Calcification, Idiopathic, 1 51 2.832
430
P CLC063 Celiac Disease 1 65 2.830
431
c JVN010 Juvenile Rheumatoid Arthritis 52 2.827
432
P ANP001 Anaplastic Large Cell Lymphoma 59 2.825
433
CHL004 Cholelithiasis 48 2.821
434
ANR007 Anorexia Nervosa 59 2.813
435
MYT011 Myotonia 37 2.810
436
DBT010 Diabetic Neuropathy 54 2.809
437
P MCR129 Microvascular Complications of Diabetes 1 67 2.801
438
P KDN017 Kidney Cancer 60 2.801
439
P MYT002 Myotonic Dystrophy 51 2.801
440
MRF001 Marfan Syndrome 76 2.796
441
P MJR001 Major Depressive Disorder 68 2.794
442
URN010 Urinary Tract Obstruction 55 2.791
443
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 2.789
444
CRN019 Coronary Artery Vasospasm 47 2.786
445
c ACT068 Acute Cystitis 60 2.784
446
CYS013 Cystinuria 66 2.781
447
NRL016 Neural Tube Defects 80 2.773
448
PRP080 Peripheral Artery Disease 54 2.758
449
P LCT001 Lactic Acidosis 50 2.753
450
BRR014 Barrett Esophagus 66 2.749
451
P TMP001 Temporal Lobe Epilepsy 49 2.731
452
DRM006 Dermatitis 61 2.728
453
P DYS154 Dystonia 64 2.728
454
ALL003 Allergic Rhinitis 66 2.715
455
DYS073 Dysphagia 53 2.712
457
PRP016 Paraplegia 52 2.705
458
P MYS003 Myasthenia Gravis 67 2.702
459
CNN003 Conn's Syndrome 77 2.696
460
OCL069 Ocular Motor Apraxia 57 2.689
461
P HRP006 Herpes Simplex 65 2.689
462
BLR008 Bilirubin Metabolic Disorder 57 2.687
463
PRS021 Prostatic Adenoma 43 2.681
464
MLR004 Malaria 77 2.677
465
c HYP272 Hypercholesterolemia, Familial, 3 46 2.676
466
P ALP008 Alopecia 53 2.669
467
IDP070 Idiopathic Scoliosis 41 2.665
468
CHL152 Childhood Acute Lymphocytic Leukemia 50 2.665
469
c VTM027 Vitamin D-Dependent Rickets, Type 2a 54 2.660
470
CMM004 Common Variable Immunodeficiency 71 2.654
471
PRS129 Prostatic Hyperplasia, Benign 48 2.653
472
P ACN011 Acne 55 2.650
473
c LKM063 Leukemia, Chronic Myeloid 70 2.645
474
VSC002 Vascular Dementia 59 2.641
475
SPN051 Spondylitis 51 2.631
476
ANX010 Anxiety 70 2.628
477
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 2.626
478
RST023 Resting Heart Rate, Variation in 40 2.623
479
P LKM071 Leukemia, Chronic Lymphocytic 74 2.621
480
HYP831 Hyperparathyroidism, Transient Neonatal 25 2.615
481
P RNL015 Renal Hypertension 45 2.609
482
HYP020 Hyperprolactinemia 63 2.606
483
HYD002 Hydronephrosis 58 2.601
484
c PNS012 Paine Syndrome 60 2.599
485
P PYL005 Pyelonephritis 56 2.590
486
P SLP006 Sleep Apnea 69 2.590
487
c ACT073 Acute Leukemia 59 2.586
488
CLC004 Calcific Tendinitis 33 2.584
489
CRD137 Cardiogenic Shock 56 2.583
490
c SPN225 Spondyloarthropathy 1 70 2.580
491
c MCR112 Microvascular Complications of Diabetes 2 42 2.577
492
SYN007 Synovitis 54 2.577
493
PLC002 Plica Syndrome 35 2.577
494
HRT012 Heart Valve Disease 53 2.574
495
GNG013 Gingivitis 59 2.570
496
P MYS005 Myositis 55 2.568
497
CVD001 Covid-19 59 2.564
498
PLM017 Pulmonary Alveolar Microlithiasis 48 2.556
499
P THR014 Thrombocytopenia 66 2.555
500
P OPN001 Open-Angle Glaucoma 55 2.554
501
P SCK005 Sickle Cell Disease 56 2.554
502
P RTN016 Retinal Degeneration 52 2.553
503
PNC041 Pancreatic Ductal Adenocarcinoma 51 2.551
505
SCK003 Sickle Cell Anemia 74 2.544
506
P TRC031 Trichorhinophalangeal Syndrome 37 2.542
507
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 2.540
508
AMN001 Amenorrhea 53 2.536
509
P HYP035 Hypophosphatasia 61 2.535
510
P FML362 Familial Isolated Hypoparathyroidism 49 2.533
511
BNG018 Benign Paroxysmal Positional Nystagmus 40 2.533
512
P MYC008 Myocarditis 59 2.529
513
P CNJ013 Conjunctivitis 66 2.527
514
P EXN002 Exanthem 58 2.522
515
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.518
516
ANR040 Aneurysm 60 2.514
517
KLD004 Keloid Disorder 38 2.504
518
ETN001 Eating Disorder 59 2.494
519
P SKN015 Skin Carcinoma 71 2.488
520
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.486
521
END057 Endometrial Cancer 76 2.481
522
MSC007 Muscle Hypertrophy 64 2.479
523
P MTR014 Motor Neuron Disease 65 2.479
524
c HMC039 Hemochromatosis, Type 1 73 2.472
525
HYP057 Hypervitaminosis D 37 2.472
526
PRP030 Purpura 54 2.464
527
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.451
528
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.451
529
P NRV007 Nervous System Disease 65 2.448
530
CRB037 Cerebral Palsy 66 2.447
531
ENM002 Enamel Erosion 25 2.443
532
NRR001 Neuroretinitis 42 2.442
533
RTN023 Retinitis 45 2.440
534
CLR109 Colorectal Adenocarcinoma 50 2.439
535
c PRG042 Progressive Familial Heart Block, Type Ia 65 2.439
536
PST092 Posttransplant Acute Limbic Encephalitis 29 2.435
537
ALL014 Allergic Encephalomyelitis 34 2.435
538
BCK006 Back Pain 43 2.434
539
SVR004 Severe Combined Immunodeficiency 70 2.431
540
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 2.427
541
P SHR001 Short Bowel Syndrome 53 2.423
542
P NTR004 Neutropenia 62 2.417
543
P MYP087 Myopathy, Tubular Aggregate, 1 49 2.416
544
c HPT016 Hepatitis B 62 2.410
545
P NGH001 Night Blindness 52 2.405
546
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 2.404
547
BRN024 Bronchitis 67 2.402
548
P GST044 Gastritis 55 2.398
549
CNN005 Connective Tissue Disease 66 2.397
550
STR081 Stormorken Syndrome 56 2.389
551
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 2.382
552
P GRF003 Graft-Versus-Host Disease 71 2.374
553
HDN002 Head Injury 44 2.374
554
PNM001 Pneumocystosis 60 2.371
555
NRM005 Neuromuscular Disease 62 2.363
556
RYN001 Raynaud Disease 49 2.362
557
P SCL057 Scoliosis, Isolated 1 40 2.352
558
BRN004 Brain Edema 54 2.350
559
c BTT014 Beta-Thalassemia 72 2.349
560
c PRS130 Prostate Cancer, Hereditary, 8 32 2.346
561
c PRS136 Prostate Cancer, Hereditary, 6 33 2.346
562
P RTN024 Retinoblastoma 72 2.339
563
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 2.337
564
CRT013 Carotid Stenosis 51 2.336
565
INT067 Interstitial Nephritis 46 2.334
566
PRT013 Portal Hypertension 59 2.330
567
P HMP007 Hemophilia 52 2.322
568
END040 Endogenous Depression 54 2.315
569
P PRS038 Personality Disorder 65 2.313
570
GST040 Gastric Adenocarcinoma 66 2.308
571
PRP017 Periapical Periodontitis 47 2.299
572
ENT004 Enthesopathy 51 2.296
573
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 2.291
574
PPL001 Papillary Adenoma 44 2.291
575
MLG086 Malignant Hyperthermia Susceptibility 40 2.290
576
ENM001 Enamel Caries 28 2.280
577
DNT001 Dental Fluorosis 43 2.269
578
c CHR688 Chronic Acquired Demyelinating Polyneuropathy 16 2.268
579
P BNC003 Bone Cancer 58 2.267
580
c ATM068 Autoimmune Hypoparathyroidism 31 2.267
581
SFT003 Soft Tissue Sarcoma 43 2.265
582
PRS045 Prostatic Hypertrophy 53 2.260
583
ATX019 Ataxia with Vitamin E Deficiency 44 2.244
584
CHR074 Choriocarcinoma 46 2.243
585
LNG031 Lung Benign Neoplasm 51 2.238
586
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 2.234
587
BRK010 Burkitt Lymphoma 65 2.224
588
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.224
589
P DNT007 Dentin Sensitivity 35 2.221
590
PRT058 Pure Autonomic Failure 58 2.219
591
P SNS001 Sensorineural Hearing Loss 60 2.216
592
P INT068 Intestinal Disease 53 2.213
593
P ADL010 Adult Respiratory Distress Syndrome 70 2.209
594
DGN001 Degenerative Disc Disease 48 2.204
595
P TMT001 Timothy Syndrome 55 2.203
596
SCT005 Scott Syndrome 51 2.184
597
GLS018 Glass Syndrome 60 2.183
598
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.183
599
c PCH010 Pachyonychia Congenita 3 43 2.182
600
P CRB059 Cerebellar Degeneration 36 2.179
601
CRT015 Carotid Artery Occlusion 45 2.177
602
c INF071 Inflammatory Bowel Disease 1 65 2.173
603
MST005 Mastitis 52 2.173
604
BSL009 Basal Ganglia Calcification 45 2.171
605
INF009 Inflammatory Spondylopathy 30 2.171
606
c OST164 Osteoporosis, Juvenile 55 2.169
607
SBC016 Subacute Delirium 42 2.167
608
ISL001 Islet Cell Tumor 55 2.166
609
SYS003 Systolic Heart Failure 49 2.160
610
P VNS003 Venous Insufficiency 54 2.158
611
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.158
612
HGH043 High Grade Glioma 46 2.147
613
P HYP098 Hypereosinophilic Syndrome 66 2.142
614
SPS057 Spasticity 43 2.138
615
P GLL018 Gallbladder Cancer 59 2.136
616
RNL065 Renal Cell Carcinoma, Papillary, 1 79 2.136
617
PRM013 Premature Menopause 57 2.136
618
ALL006 Allergic Asthma 55 2.133
619
c EPS039 Episodic Pain Syndrome, Familial, 1 42 2.131
620
P CHL002 Childhood Absence Epilepsy 62 2.127
621
HLL004 Hellp Syndrome 53 2.126
622
HYP741 Hyperparathyroidism 2 with Jaw Tumors 51 2.125
623
ACT098 Acute Erythroid Leukemia 55 2.124
624
PRN039 Paraneoplastic Syndromes 37 2.122
625
LWC001 Low Compliance Bladder 44 2.122
626
IGG001 Iga Glomerulonephritis 50 2.119
627
DRR014 Darier-White Disease 58 2.117
628
AMN006 Aminoaciduria 37 2.114
629
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 2.109
630
DGR001 Digeorge Syndrome 62 2.109
631
MYL031 Myeloproliferative Neoplasm 66 2.107
632
c SRC023 Sarcoidosis 2 44 2.103
633
MLK006 Milk Allergy 47 2.103
634
BCK003 Background Diabetic Retinopathy 46 2.101
635
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.099
636
SCH014 Schistosomiasis 56 2.099
637
PLM033 Pulmonary Embolism 58 2.099
638
P SPR041 Spermatogenic Failure 6 47 2.095
639
PSR001 Psoriatic Arthritis 61 2.095
640
HMC014 Homocysteinemia 52 2.093
641
c CHL119 Cholangitis, Primary Sclerosing 57 2.088
642
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 70 2.084
643
P DBT005 Diabetes Insipidus 54 2.083
644
P TTR001 Tetralogy of Fallot 69 2.082
645
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.082
646
c INH020 Inherited Metabolic Disorder 47 2.077
647
CHR431 Chronic Venous Insufficiency 48 2.077
648
PTH003 Pathologic Nystagmus 52 2.076
649
P VSC011 Vasculitis 61 2.073
650
P PLY019 Polyneuropathy 52 2.070
651
ETH012 Ethylene Glycol Poisoning 29 2.067
652
URT010 Ureteral Obstruction 44 2.065
653
AND005 Androgen Insensitivity Syndrome, Mild 21 2.065
654
DST006 Diastolic Heart Failure 45 2.060
655
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 46 2.056
656
P FCL005 Focal Segmental Glomerulosclerosis 57 2.056
657
TRD006 Tardive Dyskinesia 53 2.055
658
INT075 Intracranial Hypertension 52 2.054
659
ACT003 Acute Kidney Tubular Necrosis 46 2.051
660
P PMP001 Pemphigus 54 2.051
661
MDL009 Medullary Sponge Kidney 40 2.050
662
P RTT002 Rett Syndrome 79 2.050
663
GST033 Gestational Diabetes 60 2.047
664
PHS001 Phosphorus Metabolism Disease 40 2.042
665
P INF038 Influenza 68 2.042
666
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 2.041
667
SPT004 Septic Arthritis 58 2.039
668
P INT143 Interstitial Cystitis 59 2.038
669
EWN003 Ewing Sarcoma 69 2.036
670
FRZ001 Frozen Shoulder 54 2.036
671
NPH010 Nephrosclerosis 50 2.033
672
P MGR003 Migraine with Aura 51 2.030
673
BNM001 Bone Marrow Cancer 45 2.028
674
P FNC004 Fanconi Syndrome 60 2.023
675
EXR010 Exercise-Induced Bronchoconstriction 34 2.022
676
ENT011 Enterocolitis 55 2.020
677
P GCH001 Gaucher's Disease 69 2.019
678
P SJG008 Sjogren Syndrome 60 2.016
679
P MYP006 Myopia 55 2.016
680
BRS064 Bursitis 51 2.009
681
P FBR017 Fibrosarcoma 55 2.006
682
c THY107 Thymoma, Familial 42 2.003
683
P THY023 Thymoma 64 2.003
684
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 2.002
685
SVR001 Severe Acute Respiratory Syndrome 68 1.999
686
MYL009 Myelodysplastic Syndrome 67 1.992
687
AMN003 Amnestic Disorder 53 1.991
688
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 44 1.991
689
VTM033 Vitamin K Deficiency Bleeding 49 1.991
690
c PRM108 Primary Progressive Multiple Sclerosis 51 1.988
691
GST050 Gastrointestinal System Disease 55 1.984
692
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 1.983
693
PRR001 Periarthritis 33 1.983
694
LMB062 Limb Ischemia 55 1.979
695
FCL014 Focal Epilepsy 53 1.978
696
TXC002 Toxic Encephalopathy 51 1.978
697
SXL003 Sexual Disorder 49 1.977
698
P PTT006 Pituitary Adenoma 55 1.975
699
ATN005 Autonomic Dysfunction 45 1.972
700
TBC004 Tobacco Addiction 63 1.969
701
GNG003 Gingival Recession 50 1.964
702
DFF005 Diffuse Large B-Cell Lymphoma 55 1.959
703
c FML001 Familial Atrial Fibrillation 65 1.956
704
P CNT004 Centronuclear Myopathy 56 1.955
705
LWC002 Lowe Oculocerebrorenal Syndrome 68 1.954
706
P OPT006 Optic Nerve Disease 57 1.954
707
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 44 1.947
708
P FRG001 Fragile X Syndrome 70 1.945
709
PLS009 Plasma Cell Neoplasm 64 1.942
710
VRC005 Varicose Veins 59 1.941
711
CHL067 Cholecystitis 59 1.941
712
P ART018 Aortic Valve Insufficiency 52 1.933
713
MNN043 Meningioma, Familial 79 1.932
714
PRT018 Portal Vein Thrombosis 50 1.927
715
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.926
716
SCR001 Secretory Meningioma 40 1.926
717
INT395 Intracranial Meningioma 47 1.926
718
P HMR005 Hemorrhoid 49 1.919
719
P KLZ004 Kala-Azar 1 41 1.914
720
LSH001 Leishmaniasis 63 1.914
721
HPT004 Hepatic Coma 43 1.905
722
CHG001 Chagas Disease 65 1.905
723
INT066 Interstitial Lung Disease 60 1.905
724
P RHB003 Rhabdomyosarcoma 66 1.903
725
PLG002 Plague 58 1.901
726
NRN004 Neuroendocrine Tumor 55 1.897
727
DNT010 Dentin Caries 32 1.896
728
OST015 Osteochondrodysplasia 60 1.896
729
TND004 Tendinopathy 45 1.895
730
P ASP006 Aspergillosis 71 1.893
731
SPN027 Spinal Stenosis 58 1.893
732
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.893
733
c XNT010 Xanthinuria, Type I 52 1.892
734
P MDL005 Medulloblastoma 75 1.882
735
CRB090 Cerebral Hypoxia 42 1.881
736
BNG091 Benign Chronic Pemphigus 56 1.877
737
P TRT010 Teratoma 50 1.876
738
SMT003 Somatostatinoma 52 1.871
739
CNT047 Contact Dermatitis 56 1.869
740
CRT017 Cartilage Disease 52 1.868
741
P NJM001 Nijmegen Breakage Syndrome 75 1.865
742
IRN001 Iron Deficiency Anemia 58 1.863
743
c MLG069 Malignant Hypertension 46 1.863
744
MTR002 Mitral Valve Insufficiency 51 1.861
745
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.861
746
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.859
747
P MTR003 Mitral Valve Stenosis 53 1.858
748
DSS009 Disseminated Intravascular Coagulation 56 1.856
749
FDL002 Food Allergy 47 1.856
750
ATS010 Autosomal Recessive Disease 42 1.855
751
c FML347 Familial Adenomatous Polyposis 2 56 1.853
752
P EYD002 Eye Disease 57 1.852
753
c HYP210 Hypomagnesemia 2, Renal 42 1.852
754
GRW007 Growth Hormone Deficiency 47 1.851
755
HYP068 Hyperostosis 47 1.846
756
MSC152 Muscular Dystrophy, Becker Type 69 1.844
757
THR035 Thrombasthenia 48 1.843
758
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 65 1.840
759
BRN028 Brain Cancer 73 1.837
760
CHR100 Chronic Ulcer of Skin 57 1.837
761
GLC036 Glucagonoma 45 1.837
762
5XP001 5-Oxoprolinase Deficiency 30 1.835
763
P PRC031 Preeclampsia/eclampsia 1 43 1.834
764
P HML002 Hemolytic Anemia 62 1.831
765
P CHL066 Cholangitis 51 1.828
766
P NRF002 Neurofibromatosis 60 1.828
767
PRM236 Primary Biliary Cholangitis 62 1.825
768
c DWL002 Dowling-Degos Disease 1 58 1.824
769
PST021 Postpartum Depression 50 1.822
770
BRS051 Breast Disease 58 1.820
771
TRN018 Transitional Cell Carcinoma 56 1.813
772
c JVN025 Juvenile Primary Osteoporosis 21 1.813
773
HPT019 Hepatic Encephalopathy 59 1.811
774
P RTN008 Retinitis Pigmentosa 79 1.810
775
URT014 Ureterolithiasis 42 1.810
776
OVR094 Ovarian Epithelial Cancer 39 1.810
777
c HPT073 Hepatitis C Virus 70 1.808
778
DPH001 Diphtheria 59 1.799
779
P PLM036 Pulmonary Fibrosis 65 1.797
780
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.794
781
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 1.793
782
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.791
783
c JVN061 Juvenile Arthritis 56 1.788
784
CHR682 Chronic Bilirubin Encephalopathy 37 1.786
785
PMP014 Pemphigoid 48 1.783
786
P URT039 Urticaria 57 1.782
787
OST016 Osteochondrosis 52 1.776
788
P GLY013 Glycogen Storage Disease 59 1.774
789
c MCL013 Mucolipidosis Iv 64 1.771
790
NPH078 Nephrolithiasis, Uric Acid 39 1.771
791
CRV035 Cervical Cancer 72 1.769
792
P EPL140 Epilepsy, Idiopathic Generalized 60 1.769
793
HYP006 Hypertensive Heart Disease 48 1.762
794
BSL043 Basal Ganglia Calcification, Idiopathic, Childhood-Onset 19 1.761
795
FBR047 Fibromyalgia 57 1.758
796
CCN002 Cocaine Abuse 49 1.758
797
P SML001 Small Cell Carcinoma 52 1.756
798
SNS003 Sensory Peripheral Neuropathy 51 1.756
799
DMY004 Demyelinating Disease 50 1.756
800
ILS001 Ileus 49 1.755
801
P PLY018 Polycythemia 56 1.750
802
HYP052 Hyperkalemic Periodic Paralysis 62 1.750
803
PLM031 Poliomyelitis 62 1.749
804
RTC003 Root Caries 33 1.749
805
KRT008 Keratopathy 46 1.749
806
ACR041 Acromelic Frontonasal Dysostosis 53 1.749
807
P LMB006 Limb-Girdle Muscular Dystrophy 52 1.748
808
P CND004 Candidiasis 57 1.742
809
GST045 Gastroenteritis 58 1.741
810
P HYP050 Hyperinsulinemic Hypoglycemia 56 1.738
811
PSD014 Pseudopseudohypoparathyroidism 54 1.738
812
VLK001 Volkmann Contracture 23 1.737
813
HYP550 Hypomagnesemia 1, Intestinal 45 1.736
814
ANT024 Anthrax Disease 57 1.732
815
WLL004 Wallerian Degeneration 38 1.732
816
P AVS003 Avascular Necrosis 41 1.730
817
P INS002 in Situ Carcinoma 52 1.730
818
P PRN023 Prion Disease 60 1.728
819
ACT011 Acute Contagious Conjunctivitis 41 1.727
820
c PRM038 Primary Agammaglobulinemia 47 1.724
821
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.723
822
c DRR009 Diarrhea 6 46 1.717
823
OST115 Osteonecrosis of the Jaw 40 1.715
824
RTN020 Retinal Vascular Disease 45 1.715
825
HVY002 Heavy Metal Poisoning 22 1.712
826
ART074 Aortic Dissection 53 1.712
827
PPL022 Papilloma 53 1.710
828
NDL007 Nodular Goiter 48 1.708
829
P SCK002 Sick Sinus Syndrome 55 1.707
830
GST049 Gastrointestinal System Cancer 49 1.706
831
DYS015 Dysentery 49 1.706
832
MLD018 Mild Cognitive Impairment 48 1.705
833
DDN006 Duodenitis 49 1.702
834
c HPT001 Hepatitis C 61 1.702
835
P BRS044 Breast Adenocarcinoma 58 1.700
836
SPL018 Splenomegaly 47 1.699
837
ACH005 Achalasia 54 1.699
838
c FNC043 Fanconi Anemia, Complementation Group E 62 1.698
839
CRB086 Cerebral Aneurysms 40 1.698
840
P HYP534 Hypomagnesemia 3, Renal 46 1.697
841
CHL028 Childhood Type Dermatomyositis 58 1.694
842
ENP001 Enophthalmos 40 1.693
843
EMB004 Embryonal Carcinoma 55 1.690
844
CMB007 Combined Immunodeficiency 56 1.690
845
SQM002 Squamous Cell Papilloma 45 1.686
846
DRG003 Drug Dependence 46 1.675
847
P CRC039 Coarctation of Aorta 46 1.674
848
P LTH003 Lethal Congenital Contracture Syndrome 40 1.671
849
MNT001 Mantle Cell Lymphoma 65 1.671
850
c ESS001 Essential Tremor 56 1.671
851
P LCH002 Lichen Planus 54 1.669
852
P END033 Endocarditis 58 1.669
853
VTM029 Vitamin D Hydroxylation-Deficient Rickets, Type 1b 28 1.668
854
P CYS018 Cystitis 58 1.665
855
P MNN013 Meningitis 65 1.665
856
c MGR032 Migraine, Familial Hemiplegic, 1 54 1.664
857
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 1.661
858
GLM044 Glomerular Disease 34 1.659
859
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 1.658
860
P BLD062 Bile Duct Cancer 69 1.657
861
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.657
862
HYP540 Hypertension, Diastolic 38 1.656
863
PRN032 Paraneoplastic Cerebellar Degeneration 25 1.647
864
P PRV006 Pervasive Developmental Disorder 52 1.644
865
MMM006 Mammographic Density 39 1.644
866
MST020 Mast Cell Activation Syndrome 27 1.643
867
OCL006 Ocular Hypertension 53 1.642
868
ARG004 Argyria 26 1.640
869
FML035 Familial Hyperlipidemia 54 1.638
870
PRS063 Paresthesia 39 1.638
871
P BNG032 Benign Mesothelioma 53 1.637
872
P SLP005 Sleep Disorder 61 1.637
873
MTH071 Methane Production 24 1.633
874
c HMP004 Hemophilia B 68 1.630
875
P MVM001 Movement Disease 61 1.629
876
P ANG015 Angioedema 56 1.628
877
NRT001 Neurotic Disorder 56 1.627
878
ASP004 Asphyxia Neonatorum 50 1.623
879
P UVT001 Uveitis 57 1.619
880
RNL077 Renal Fibrosis 46 1.618
881
P SCL009 Sclerosing Cholangitis 46 1.617
882
c CHR098 Chronic Pyelonephritis 34 1.614
883
ERL001 Early Myoclonic Encephalopathy 62 1.612
884
TCL027 T-Cell Acute Lymphoblastic Leukemia 52 1.611
885
LFT001 Left Bundle Branch Hemiblock 47 1.611
886
P CHN012 Chondrosarcoma 56 1.609
887
P LPR021 Leprosy 3 71 1.607
888
HNS001 Hansen's Disease 32 1.607
889
CRH005 Crohn's Colitis 53 1.605
890
MST004 Mast Cell Neoplasm 41 1.605
891
LMY002 Leiomyoma 51 1.604
892
P MJR007 Major Affective Disorder 1 42 1.604
893
CRB009 Cerebritis 43 1.602
894
P CHR012 Chronic Granulomatous Disease 69 1.600
895
c ACT004 Acute Diarrhea 40 1.598
896
c VSC019 Vesicoureteral Reflux 1 56 1.597
897
ORL011 Oral Cancer 60 1.595
898
CHP002 Chops Syndrome 47 1.595
899
NNL006 Non-Alcoholic Steatohepatitis 54 1.594
900
AZS001 Azoospermia 45 1.593
901
INT030 Intracranial Aneurysm 55 1.591
902
CMP010 Complex Regional Pain Syndrome 59 1.590
903
HLC007 Helicobacter Pylori Infection 67 1.590
904
CRT016 Carotid Artery Disease 52 1.589
905
PRD004 Prediabetes Syndrome 52 1.588
906
VCC001 Vaccinia 49 1.586
907
P MLT008 Multinodular Goiter 41 1.583
908
P CLS010 Cluster Headache 42 1.583
909
OTT002 Otitis Media 70 1.582
910
P SBS003 Substance Abuse 54 1.581
911
PRM237 Primary Hypomagnesemia 44 1.581
912
PST053 Postherpetic Neuralgia 39 1.580
913
GSG001 Gas Gangrene 52 1.577
914
SKN019 Skin Melanoma 70 1.576
915
PLY105 Polycystic Ovary Syndrome 1 39 1.575
916
EPT021 Epithelial Recurrent Erosion Dystrophy 45 1.572
917
ASP026 Asplenia, Isolated Congenital 43 1.569
918
PRN019 Perinatal Necrotizing Enterocolitis 60 1.562
919
P LYN001 Lynch Syndrome 76 1.560
920
SPN369 Spinal Disease 43 1.558
921
RDC002 Radiculopathy 51 1.557
922
FBR009 Fibrous Dysplasia 48 1.557
923
GST023 Gastric Ulcer 52 1.557
924
P MNC007 Monocytic Leukemia 48 1.556
925
c BPL002 Bipolar I Disorder 47 1.556
926
c BSL049 Basal Ganglia Calcification, Idiopathic, 8, Autosomal Recessive 23 1.555
927
P FML011 Familial Adenomatous Polyposis 70 1.555
928
PLR008 Pleurisy 49 1.553
929
P MLT007 Multiple Epiphyseal Dysplasia 56 1.553
930
EXT007 Extracutaneous Mastocytoma 38 1.552
931
OST062 Osteoarthritis with Mild Chondrodysplasia 46 1.551
932
PMP006 Pemphigus Vulgaris, Familial 57 1.546
933
BRN056 Bronchopulmonary Dysplasia 57 1.543
934
c ACT135 Acute Graft Versus Host Disease 51 1.539
935
HST010 Histiocytosis 49 1.539
936
GST071 Gastrointestinal Carcinoma 46 1.535
937
CYS014 Cystadenocarcinoma 51 1.535
938
c AML044 Amelogenesis Imperfecta, Type Ig 54 1.531
939
TLN003 Telangiectasis 51 1.530
940
BLL006 Bullous Pemphigoid 61 1.528
941
P GLL022 Guillain-Barre Syndrome 59 1.527
942
RTC005 Reticulosarcoma 47 1.525
943
GST019 Gastrointestinal Stromal Tumor 78 1.525
944
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.524
945
MYL005 Myelofibrosis 70 1.518
946
OBS082