Search results for Magnesium

2304 hits were found for Magnesium

# Family MCID Name MIFTS Score
1
IMM026 Immunodeficiency, X-Linked, with Magnesium Defect, Epstein-Barr Virus Infection, and Neoplasia 47 50.461
2
c HYP210 Hypomagnesemia 2, Renal 42 31.706
3
GTL001 Gitelman Syndrome 65 20.783
4
HYP550 Hypomagnesemia 1, Intestinal 45 20.761
5
MGN003 Magnesium, Elevated Red Cell 6 20.044
6
P HYP534 Hypomagnesemia 3, Renal 46 19.291
7
DSR028 Disorder of Magnesium Transport 3 19.256
8
c PRC016 Pre-Eclampsia 64 17.265
9
P ECL001 Eclampsia 52 16.558
10
PNG002 Pain Agnosia 51 10.796
11
HYP005 Hypokalemia 55 10.245
12
c SVR005 Severe Pre-Eclampsia 49 10.064
13
CRB037 Cerebral Palsy 66 9.334
14
P AST005 Asthma 75 8.903
15
c HYP595 Hypertension, Essential 84 8.464
16
c MGR028 Migraine with or Without Aura 1 63 8.194
17
c ACT249 Acute Asthma 40 7.722
18
c CHR684 Chronic Kidney Disease 73 7.527
19
c ACT075 Acute Myocardial Infarction 55 7.418
20
c TYP009 Type 2 Diabetes Mellitus 91 7.310
21
P KDN018 Kidney Disease 71 7.253
22
P DBT009 Diabetes Mellitus 67 6.706
23
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 6.682
24
CNS004 Constipation 56 6.658
25
P SZR006 Seizure Disorder 69 6.640
26
48X005 48,xyyy 39 6.620
27
P CRN300 Coronary Heart Disease 1 73 6.354
28
URL001 Urolithiasis 45 6.264
29
ALC007 Alcohol Dependence 65 6.262
30
BRN071 Brain Injury 50 6.161
31
LPP008 Lipoprotein Quantitative Trait Locus 65 6.113
32
TRM010 Traumatic Brain Injury 50 6.067
33
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 6.066
34
ART140 Arteries, Anomalies of 52 6.045
35
PLM129 Pulmonary Disease, Chronic Obstructive 74 6.011
36
PRM237 Primary Hypomagnesemia 44 5.928
37
P HRT032 Heart Disease 84 5.630
38
RCK004 Rickets 64 5.597
39
RPD005 Rapidly Involuting Congenital Hemangioma 48 5.590
40
P HYP069 Hyperparathyroidism 62 5.586
41
P HYP024 Hypoparathyroidism 55 5.513
42
END086 End Stage Renal Disease 54 5.478
43
P ATR011 Atrial Fibrillation 66 5.473
44
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.443
45
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 5.443
46
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.443
47
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 5.443
48
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.443
49
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 5.443
50
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 5.443
51
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.443
52
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.443
53
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 5.439
54
P HDC001 Headache 56 5.323
55
c EPS039 Episodic Pain Syndrome, Familial, 1 42 5.226
56
NPH009 Nephrolithiasis 54 5.215
57
SBC016 Subacute Delirium 42 5.213
58
BNR002 Bone Resorption Disease 47 5.189
59
ISC004 Ischemia 61 5.160
60
P ENC018 Encephalopathy 62 5.159
61
STR067 Stroke, Ischemic 79 5.059
62
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 5.035
63
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 5.035
64
GST092 Gastroesophageal Reflux 59 5.005
65
P OST002 Osteoporosis 76 5.003
66
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 5.002
67
LPD008 Lipid Metabolism Disorder 61 4.928
68
PRT251 Proteinuria, Chronic Benign 58 4.899
69
c PNS012 Paine Syndrome 60 4.888
70
P CLR023 Colorectal Cancer 100 4.853
71
P MYC007 Myocardial Infarction 69 4.759
72
P VSC007 Vascular Disease 62 4.743
73
HYP025 Hyperphosphatemia 47 4.721
74
P ALC033 Alcohol Use Disorder 67 4.675
75
P CHR345 Chronic Pain 50 4.636
76
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.634
77
IRN002 Iron Metabolism Disease 56 4.564
78
DFC004 Deficiency Anemia 74 4.562
79
c ACT071 Acute Kidney Failure 60 4.557
80
HYP266 Hypoxia 56 4.555
81
P DRR001 Diarrhea 55 4.515
82
P PLM037 Pulmonary Hypertension 69 4.448
83
CRB039 Cerebrovascular Disease 65 4.420
84
P PRC031 Preeclampsia/eclampsia 1 43 4.387
85
P BRS047 Breast Cancer 97 4.370
86
FBR047 Fibromyalgia 57 4.368
87
AGN016 Aging 53 4.346
88
P LVR013 Liver Disease 68 4.325
89
HYP066 Hyperglycemia 60 4.286
90
CNG034 Congestive Heart Failure 69 4.285
91
P BND020 Bone Disease 60 4.262
92
P NRP001 Neuropathy 59 4.244
93
NPH003 Nephrocalcinosis 49 4.236
94
LNG099 Lung Disease 62 4.232
95
NNL005 Non-Alcoholic Fatty Liver Disease 63 4.137
96
P SCK005 Sickle Cell Disease 56 4.132
97
PLC007 Placental Abruption 47 4.048
98
P ATT013 Attention Deficit-Hyperactivity Disorder 65 4.045
99
OST012 Osteoarthritis 77 4.019
100
LVR012 Liver Cirrhosis 62 4.002
101
P PNC044 Pancreatitis 61 3.963
102
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.955
103
GST033 Gestational Diabetes 60 3.914
104
CRD223 Cardiac Arrhythmia 63 3.900
105
c ACT027 Acute Pancreatitis 60 3.863
106
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 3.854
107
P RSP003 Respiratory Failure 73 3.843
108
KRT002 Keratomalacia 54 3.838
109
P ATS364 Autism 72 3.818
110
FTT001 Fatty Liver Disease 61 3.810
111
TTN003 Tetanus 64 3.797
112
P ART023 Arthropathy 59 3.743
113
c TYP008 Type 1 Diabetes Mellitus 77 3.707
114
P CRD119 Cardiac Arrest 68 3.704
115
HDN002 Head Injury 44 3.687
116
PRV004 Periventricular Leukomalacia 52 3.676
117
CRD132 Cardiac Conduction Defect 59 3.667
118
P HYP086 Hypothyroidism 68 3.664
119
MNT002 Mental Depression 56 3.643
120
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 44 3.640
121
P PLY011 Polycystic Ovary Syndrome 57 3.632
122
P ANR048 Aniridia 1 66 3.622
123
P HYP834 Hypomagnesemia, Seizures, and Mental Retardation 2 22 3.620
124
TXC005 Toxic Shock Syndrome 61 3.592
125
STT002 Status Asthmaticus 49 3.582
126
ATH013 Atherosclerosis Susceptibility 63 3.551
127
HLX001 Helix Syndrome 47 3.550
128
P TRN020 Turner Syndrome 67 3.536
129
BRN002 Bronchiolitis 57 3.520
130
SCK003 Sickle Cell Anemia 74 3.504
131
DPR016 Depression 64 3.498
132
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.490
133
P PRP019 Peripheral Nervous System Disease 57 3.482
134
P ESP024 Esophagitis 60 3.446
135
PLM010 Pulmonary Edema 54 3.414
136
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 3.380
137
CRH001 Crohn's Disease 80 3.348
138
ANT039 Antisynthetase Syndrome 55 3.314
139
c SCN007 Secondary Hyperparathyroidism 50 3.306
140
P LKM002 Leukemia 65 3.292
141
P PHC003 Pheochromocytoma 70 3.254
142
ADR040 Adrenal Gland Pheochromocytoma 45 3.254
143
MTB004 Metabolic Acidosis 48 3.248
144
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.221
145
SPN186 Spinal Cord Injury 60 3.211
146
P HYP750 Hypertriglyceridemia, Familial 61 3.196
147
c MCR115 Microvascular Complications of Diabetes 5 65 3.182
148
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.179
149
OCL069 Ocular Motor Apraxia 57 3.173
150
ANG054 Angina Pectoris 65 3.162
151
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.141
152
NPH091 Nephrolithiasis, Calcium Oxalate 61 3.137
153
HYP017 Hypophosphatemia 49 3.123
154
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 3.111
155
CLC006 Calcinosis 47 3.101
156
NNL006 Non-Alcoholic Steatohepatitis 54 3.061
157
c LKM061 Leukemia, Acute Myeloid 83 3.059
158
ADN018 Adenoma 58 3.033
159
P BRB001 Beriberi 44 3.032
160
HRN029 Hearing Loss, Noise-Induced 37 3.026
161
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 3.023
162
c MCR133 Microvascular Complications of Diabetes 4 41 3.021
163
c MCR113 Microvascular Complications of Diabetes 3 52 3.021
164
c MCR130 Microvascular Complications of Diabetes 6 41 3.021
165
c MCR120 Microvascular Complications of Diabetes 7 47 3.021
166
PRM020 Premenstrual Tension 39 3.020
167
P PSD087 Pseudoxanthoma Elasticum 66 3.008
168
RHB024 Rhabdomyosarcoma 2 65 2.978
169
ANR040 Aneurysm 60 2.965
170
PRT082 Preterm Premature Rupture of the Membranes 56 2.958
171
P EPL164 Epilepsy 70 2.938
172
ASP004 Asphyxia Neonatorum 50 2.932
173
c PRM005 Primary Hyperparathyroidism 59 2.930
174
WTH001 Withdrawal Disorder 47 2.915
175
CHL068 Cholestasis 61 2.887
176
c ATS007 Autism Spectrum Disorder 71 2.883
177
P ART021 Arteriosclerosis 53 2.855
178
P THL005 Thalassemia 56 2.849
179
HRW001 Hair Whorl 35 2.829
180
P THY032 Thyroiditis 56 2.819
181
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.816
182
c AMY091 Amyotrophic Lateral Sclerosis 1 87 2.801
183
P LTR001 Lateral Sclerosis 57 2.801
184
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 2.800
185
NTR005 Nutritional Deficiency Disease 60 2.796
186
ILS001 Ileus 49 2.779
187
ADG002 Audiogenic Seizures 25 2.753
188
P HYP076 Hyperthyroidism 53 2.749
189
CLT003 Colitis 63 2.715
190
P ORT004 Orthostatic Intolerance 61 2.691
191
P TRM003 Tremor 50 2.688
192
P OVR042 Ovarian Cancer 88 2.684
193
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 19 2.669
194
PRS047 Prostatitis 57 2.667
195
DWN001 Down Syndrome 70 2.666
196
P ART022 Arthritis 70 2.648
197
ULC004 Ulcerative Colitis 74 2.635
198
BNN005 Bunion 32 2.624
199
CRB009 Cerebritis 43 2.607
200
CHR005 Chorioamnionitis 50 2.590
201
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 2.581
202
c HYP836 Hypercholesterolemia, Familial, 1 73 2.559
203
HMN044 Human Immunodeficiency Virus Type 1 76 2.557
204
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 2.547
205
BRN024 Bronchitis 67 2.523
206
GST050 Gastrointestinal System Disease 55 2.511
207
P CRD246 Cardiovascular System Disease 55 2.506
208
P SCL018 Scoliosis 57 2.504
209
SDD001 Sudden Infant Death Syndrome 60 2.499
210
P HPT021 Hepatitis 68 2.485
211
PRT036 Peritonitis 65 2.468
212
ATX019 Ataxia with Vitamin E Deficiency 44 2.465
213
P PRK039 Parkinsonism 55 2.460
214
IMM167 Immune Deficiency Disease 76 2.444
215
THY030 Thyroid Gland Disease 50 2.416
216
OST159 Osteogenic Sarcoma 66 2.411
217
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.409
218
CHR066 Chronic Fatigue Syndrome 59 2.397
219
GLC003 Glucose Intolerance 53 2.392
220
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.391
221
P HYP265 Hypotonia 42 2.390
222
STM007 Stomatitis 52 2.385
223
P PRS038 Personality Disorder 65 2.372
224
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 2.369
225
ANX004 Anoxia 40 2.362
226
c BTT014 Beta-Thalassemia 72 2.357
227
HYP830 Hypomagnesemia, Seizures, and Mental Retardation 1 22 2.353
228
PST021 Postpartum Depression 50 2.352
229
BCK006 Back Pain 43 2.350
230
PLP001 Pulpitis 48 2.345
231
OST011 Osteomalacia 52 2.336
232
BRD001 Brody Myopathy 55 2.329
233
P CLS010 Cluster Headache 42 2.325
234
P MJR001 Major Depressive Disorder 68 2.317
235
P DMN002 Dementia 65 2.316
236
c HYP445 Hypomagnesemia 6, Renal 23 2.315
237
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.303
238
SPS003 Spastic Diplegia 52 2.284
239
BRN004 Brain Edema 54 2.276
240
c FML001 Familial Atrial Fibrillation 65 2.275
241
P MYL006 Myeloid Leukemia 60 2.268
242
P INF037 Inflammatory Bowel Disease 53 2.266
243
DYS073 Dysphagia 53 2.263
244
GTR002 Goiter 52 2.258
245
47X002 47,xyy 47 2.241
246
HRT012 Heart Valve Disease 53 2.240
247
HYP060 Hyperinsulinism 53 2.238
248
ENT011 Enterocolitis 55 2.234
249
PLC009 Placenta Praevia 39 2.229
250
LPT014 Leptin Deficiency or Dysfunction 77 2.228
251
c HPT003 Hepatitis a 63 2.214
252
P LNG028 Long Qt Syndrome 63 2.210
253
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.209
254
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 2.202
255
MTH009 Mouth Disease 57 2.200
256
URM002 Uremia 47 2.198
257
P LCT001 Lactic Acidosis 50 2.181
258
SKN016 Skin Disease 63 2.172
259
CYT002 Cytokine Deficiency 43 2.164
260
P PRS040 Prostate Cancer 95 2.150
261
P TCD001 Tic Disorder 50 2.147
262
THY029 Thyroid Carcinoma 55 2.144
263
ANX010 Anxiety 70 2.144
264
PRN019 Perinatal Necrotizing Enterocolitis 60 2.137
265
ADL002 Adult Syndrome 69 2.133
266
P SHR001 Short Bowel Syndrome 53 2.123
267
P MCR129 Microvascular Complications of Diabetes 1 67 2.111
268
c MCR112 Microvascular Complications of Diabetes 2 42 2.111
269
PPL049 Papillon-Lefevre Syndrome 65 2.108
270
PPT005 Peptic Ulcer Disease 58 2.105
271
STT001 Status Epilepticus 58 2.099
272
CRB004 Cerebral Artery Occlusion 45 2.087
273
END040 Endogenous Depression 54 2.083
274
P ANP001 Anaplastic Large Cell Lymphoma 59 2.082
275
P LYM118 Lymphoma 66 2.075
276
BHR001 Behr Syndrome 51 2.075
277
P NRV007 Nervous System Disease 65 2.073
278
ATR057 Atrioventricular Block 54 2.070
279
CLN015 Colon Adenocarcinoma 64 2.063
280
P GST053 Gastric Cancer 82 2.054
281
P ALZ034 Alzheimer Disease 87 2.052
282
PRP080 Peripheral Artery Disease 54 2.042
283
P RST001 Restless Legs Syndrome 52 2.013
284
PPT001 Peptic Esophagitis 51 2.010
285
GLS018 Glass Syndrome 60 2.009
286
P GLM007 Glomerulonephritis 59 2.008
287
P MYP004 Myopathy 67 2.008
288
P GST044 Gastritis 55 2.004
289
RNL011 Renal Osteodystrophy 48 2.000
290
BRK010 Burkitt Lymphoma 65 2.000
291
c ATR087 Atrial Standstill 1 74 1.999
292
P INT143 Interstitial Cystitis 59 1.994
293
HLL004 Hellp Syndrome 53 1.993
294
WRN003 Wernicke Encephalopathy 45 1.990
295
DNT012 Dental Caries 53 1.990
296
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 1.985
297
c BLD140 Blood Group, I System 47 1.985
298
CYS001 Cystic Fibrosis 77 1.982
299
P MYC084 Mycobacterium Tuberculosis 1 68 1.979
300
CRV035 Cervical Cancer 72 1.973
301
P CNR004 Cone-Rod Dystrophy 2 74 1.971
302
MCS002 Mucositis 55 1.969
303
P CTR002 Cataract 59 1.965
304
WRN002 Wernicke-Korsakoff Syndrome 49 1.962
305
CRB086 Cerebral Aneurysms 40 1.962
306
RYN005 Raynaud Phenomenon 45 1.956
307
VSL002 Visual Epilepsy 39 1.949
308
HND002 Hand, Foot and Mouth Disease 50 1.946
309
P PRD008 Periodontitis 63 1.937
310
HPT004 Hepatic Coma 43 1.935
311
P PNC035 Pancreatic Cancer 87 1.934
312
P HYP733 Hypercalciuria, Absorptive, 2 45 1.916
313
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 1.914
314
DBT084 Diabetes Mellitus, Ketosis-Prone 59 1.913
315
c DLT002 Dilated Cardiomyopathy 79 1.907
316
P DDN001 Duodenal Ulcer 52 1.896
317
P HYD006 Hydrocephalus 62 1.880
318
AND005 Androgen Insensitivity Syndrome, Mild 21 1.879
319
ESP021 Esophageal Cancer 84 1.875
320
P MGR003 Migraine with Aura 51 1.868
321
SPR126 Superior Semicircular Canal Dehiscence 41 1.860
322
c HMG029 Hemoglobin Se Disease 41 1.860
323
HMN047 Human Cytomegalovirus Infection 59 1.855
324
HYP056 Hypoglycemia 65 1.854
325
P SLP005 Sleep Disorder 61 1.852
326
NRT001 Neurotic Disorder 56 1.851
327
LYM027 Lymphopenia 56 1.847
328
HYP014 Hyperuricemia 51 1.847
329
MYM001 Myoma 54 1.840
330
CRN019 Coronary Artery Vasospasm 47 1.840
331
c MJR022 Major Affective Disorder 8 37 1.830
332
c MJR024 Major Affective Disorder 9 40 1.830
333
P BPL003 Bipolar Disorder 56 1.830
334
P ADL010 Adult Respiratory Distress Syndrome 70 1.828
335
MDD011 Mood Disorder 61 1.824
336
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 1.823
337
INT007 Intermediate Coronary Syndrome 53 1.818
338
HYP781 Hypoascorbemia 52 1.816
339
GST023 Gastric Ulcer 52 1.813
340
P CNJ013 Conjunctivitis 66 1.806
341
PRP027 Peripheral Vascular Disease 71 1.803
342
PPL052 Papillomatosis, Confluent and Reticulated 34 1.803
343
P HYP098 Hypereosinophilic Syndrome 66 1.801
344
P NTR004 Neutropenia 62 1.794
345
P PRV006 Pervasive Developmental Disorder 52 1.794
346
BCT022 Bacterial Infectious Disease 55 1.792
347
P SCH015 Schizophrenia 74 1.789
348
DBT010 Diabetic Neuropathy 54 1.788
349
CRD137 Cardiogenic Shock 56 1.786
350
P OVR082 Overgrowth Syndrome 41 1.786
351
THR024 Thrombosis 56 1.784
352
P PTN014 Patent Ductus Arteriosus 1 59 1.776
353
ATN005 Autonomic Dysfunction 45 1.770
354
SPS057 Spasticity 43 1.764
355
P PYL005 Pyelonephritis 56 1.764
356
PRP030 Purpura 54 1.760
357
P FNG006 Feingold Syndrome 1 61 1.760
358
TXC002 Toxic Encephalopathy 51 1.760
359
ALL029 Allergic Disease 61 1.757
360
c HPT016 Hepatitis B 62 1.753
361
P NPH012 Nephrotic Syndrome 61 1.745
362
MYF002 Myofascial Pain Syndrome 46 1.739
363
PRT037 Pertussis 49 1.728
364
IDP070 Idiopathic Scoliosis 41 1.724
365
IDP073 Idiopathic Hypercalciuria 41 1.719
366
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 1.719
367
P THR005 Thrombotic Thrombocytopenic Purpura 64 1.710
368
CRB089 Cerebral Beriberi 19 1.710
369
MLT131 Multifocal Atrial Tachycardia 18 1.708
370
ANR007 Anorexia Nervosa 59 1.706
371
P EXN002 Exanthem 58 1.700
372
HPT019 Hepatic Encephalopathy 59 1.690
373
MYC005 Myocardial Stunning 45 1.688
374
P OPT006 Optic Nerve Disease 57 1.679
375
c BRN108 Branchiootic Syndrome 1 63 1.672
376
AMD002 Amed Syndrome, Digenic 36 1.667
377
P INF032 Infertility 60 1.667
378
P RCT021 Rectum Cancer 54 1.658
379
PHR003 Pharyngitis 57 1.657
380
MLD002 Mild Pre-Eclampsia 33 1.647
381
DSS032 Disease by Infectious Agent 55 1.643
382
IFP003 Ifap Syndrome 2 41 1.641
383
P CHN059 Chondrocalcinosis 51 1.630
384
PRP016 Paraplegia 52 1.630
385
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 1.625
386
P MYS003 Myasthenia Gravis 67 1.625
387
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 14 1.622
388
P URN019 Urinary Tract Infection 48 1.607
389
P NRB001 Neuroblastoma 66 1.607
390
DRM006 Dermatitis 61 1.601
391
c GLL024 Gallbladder Disease 1 53 1.600
392
MNN043 Meningioma, Familial 79 1.599
393
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.599
394
SCR001 Secretory Meningioma 40 1.599
395
INT395 Intracranial Meningioma 47 1.599
396
DYS011 Dyskinesia of Esophagus 41 1.599
397
BLR008 Bilirubin Metabolic Disorder 57 1.595
398
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 1.581
399
ATS010 Autosomal Recessive Disease 42 1.562
400
c HPT073 Hepatitis C Virus 70 1.546
401
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.543
402
P LNG032 Lung Cancer 98 1.538
403
P HML002 Hemolytic Anemia 62 1.536
404
P LPR021 Leprosy 3 71 1.526
405
HNS001 Hansen's Disease 32 1.526
406
PRT038 Protein-Energy Malnutrition 53 1.518
407
P CRV039 Cervicitis 52 1.517
408
CVD001 Covid-19 59 1.516
409
ING001 Inguinal Hernia 59 1.516
410
PLY105 Polycystic Ovary Syndrome 1 39 1.512
411
P MYP006 Myopia 55 1.508
412
ACQ007 Acquired Immunodeficiency Syndrome 58 1.507
413
c ACT068 Acute Cystitis 60 1.501
414
P RHM011 Rheumatoid Arthritis 81 1.500
415
CRB090 Cerebral Hypoxia 42 1.500
416
VGN023 Vaginitis 56 1.495
417
P INT070 Intestinal Obstruction 57 1.495
418
SCR035 Sacral Agenesis with Vertebral Anomalies 38 1.495
419
THY122 Thyroid Gland Cancer 59 1.495
420
P MLG056 Malignant Hyperthermia 65 1.491
422
c EXD008 Exudative Vitreoretinopathy 1 71 1.484
423
HMS001 Hemosiderosis 48 1.477
424
PST053 Postherpetic Neuralgia 39 1.475
425
P FBR031 Febrile Seizures 52 1.472
426
P RRH023 Rare Hereditary Hemochromatosis 52 1.472
427
c PLM164 Pulmonary Hypertension, Primary, 1 75 1.467
428
ANT018 Anthracosis 50 1.465
429
P PNM006 Pneumoconiosis 55 1.458
430
P DRM053 Dermatitis, Atopic 65 1.454
431
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 1.451
432
P GRV001 Graves' Disease 54 1.451
433
CHL014 Cholera 62 1.448
434
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 32 1.447
435
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.443
436
PTH003 Pathologic Nystagmus 52 1.442
437
P MGR001 Migraine Without Aura 48 1.430
438
ETN001 Eating Disorder 59 1.416
439
P BNG032 Benign Mesothelioma 53 1.416
440
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.416
441
SPN369 Spinal Disease 43 1.416
442
RDN001 Reading Disorder 40 1.416
443
BLR001 Biliary Atresia 55 1.414
444
OST003 Osteonecrosis 60 1.414
445
P PLY019 Polyneuropathy 52 1.405
446
c GRV008 Graves Disease 1 54 1.403
447
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 1.403
448
URN010 Urinary Tract Obstruction 55 1.402
449
NRM005 Neuromuscular Disease 62 1.396
450
ENT001 Enterocele 42 1.383
451
SYN036 Syncope 44 1.381
452
P VSC018 Visceral Steatosis 32 1.380
453
SNL007 Senile Cataract 40 1.372
454
GST045 Gastroenteritis 58 1.372
455
P RNL007 Renal Tubular Acidosis 52 1.370
456
P HYP061 Hypertrophic Cardiomyopathy 68 1.368
457
CLR108 Colorectal Adenoma 63 1.361
458
P THR014 Thrombocytopenia 66 1.354
459
P LKM062 Leukemia, Acute Lymphoblastic 69 1.349
460
P MYC033 Myoclonus 46 1.346
461
P MLN007 Male Infertility 56 1.338
462
PRS030 Persistent Fetal Circulation Syndrome 46 1.336
463
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.335
464
CHR073 Choreatic Disease 53 1.335
465
P INT068 Intestinal Disease 53 1.334
466
P FML187 Familial Hypertension 34 1.328
467
CLN019 Colonic Disease 47 1.323
468
PLM001 Pulmonary Tuberculosis 69 1.315
469
P RHN004 Rhinitis 56 1.314
470
MTH071 Methane Production 24 1.311
471
c HYP302 Hypomagnesemia 4, Renal 36 1.305
472
P HRD086 Hereditary Hypophosphatemic Rickets 40 1.300
473
BNG091 Benign Chronic Pemphigus 56 1.299
474
P SNS001 Sensorineural Hearing Loss 60 1.293
475
TST014 Testicular Cancer 51 1.290
476
P CLC063 Celiac Disease 1 65 1.287
477
P PTS002 Ptosis 52 1.286
478
c SPN225 Spondyloarthropathy 1 70 1.269
479
SPN051 Spondylitis 51 1.269
480
c VRL010 Viral Hepatitis 52 1.269
481
INF009 Inflammatory Spondylopathy 30 1.269
482
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.264
483
INT067 Interstitial Nephritis 46 1.264
484
c MCL013 Mucolipidosis Iv 64 1.261
485
c OVR114 Ovarian Cancer 1 60 1.261
486
P CRC039 Coarctation of Aorta 46 1.259
487
INT030 Intracranial Aneurysm 55 1.259
488
BRN028 Brain Cancer 73 1.259
489
BLR028 Biliary Atresia, Extrahepatic 36 1.257
490
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 1.257
491
P ALG028 Alagille Syndrome 1 73 1.257
492
PPL001 Papillary Adenoma 44 1.257
493
P PRK057 Parkinson Disease, Late-Onset 79 1.254
494
P NJM001 Nijmegen Breakage Syndrome 75 1.244
495
ACT011 Acute Contagious Conjunctivitis 41 1.244
496
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 1.243
497
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.243
498
GT001 Gout 63 1.241
499
ALL003 Allergic Rhinitis 66 1.240
500
OLG003 Oligohydramnios 50 1.231
501
KWS001 Kwashiorkor 44 1.228
502
IRT001 Iritis 45 1.228
503
ACR008 Acrocallosal Syndrome 69 1.223
504
VRL011 Viral Infectious Disease 60 1.222
505
GNR004 Generalized Anxiety Disorder 54 1.213
506
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.213
507
c MST023 Mesothelioma, Malignant 56 1.213
508
P TRC031 Trichorhinophalangeal Syndrome 37 1.213
509
PLM031 Poliomyelitis 62 1.204
510
ACT003 Acute Kidney Tubular Necrosis 46 1.202
511
PRS063 Paresthesia 39 1.202
512
PRM003 Premature Ejaculation 44 1.195
513
SNS003 Sensory Peripheral Neuropathy 51 1.195
514
IGR001 Ige Responsiveness, Atopic 58 1.188
515
P MSC005 Muscular Dystrophy 66 1.187
516
TCL003 T Cell Deficiency 44 1.185
517
INT075 Intracranial Hypertension 52 1.178
518
c HPT001 Hepatitis C 61 1.173
519
OST017 Osteomyelitis 63 1.167
520
INT071 Intestinal Perforation 49 1.167
521
P END044 Endometriosis 62 1.167
522
P MLT020 Multiple Sclerosis 79 1.167
523
OBS002 Obsessive-Compulsive Disorder 67 1.165
524
HLC007 Helicobacter Pylori Infection 67 1.165
525
P ENC004 Encephalitis 61 1.157
526
INF118 Inflammatory Myopathy with Abundant Macrophages 27 1.157
527
P MTR014 Motor Neuron Disease 65 1.153
528
CHL079 Children's Interstitial Lung Disease 25 1.151
529
MYL020 Myelomeningocele 51 1.149
530
P PNM007 Pneumonia 64 1.149
531
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.148
532
ALC009 Alcoholic Liver Cirrhosis 54 1.138
533
P DYS154 Dystonia 64 1.135
534
BRR014 Barrett Esophagus 66 1.127
535
BRN056 Bronchopulmonary Dysplasia 57 1.127
536
P PRD021 Periodic Paralysis 42 1.127
537
BRT054 Brittle Bone Disorder 74 1.123
538
FRZ001 Frozen Shoulder 54 1.121
539
BRS064 Bursitis 51 1.121
540
HYP034 Hypertensive Encephalopathy 43 1.106
541
PST092 Posttransplant Acute Limbic Encephalitis 29 1.106
542
CHL067 Cholecystitis 59 1.105
543
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.105
544
MNN042 Meningioma, Radiation-Induced 51 1.102
545
c INF071 Inflammatory Bowel Disease 1 65 1.102
546
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 1.102
547
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 1.102
548
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 57 1.102
549
P AGN002 Agnosia 53 1.102
550
INT053 Intracranial Vasospasm 37 1.102
551
SPN021 Spinal Meningioma 43 1.102
552
SPN027 Spinal Stenosis 58 1.102
553
OCL006 Ocular Hypertension 53 1.102
554
CYT004 Cytomegalic Inclusion Disease 31 1.102
555
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 27 1.102
556
TMP019 Temporomandibular Joint Anomaly 28 1.102
557
NRL016 Neural Tube Defects 80 1.099
558
c CHR711 Chronic Asthma 41 1.099
559
P SYS005 Systemic Scleroderma 73 1.097
560
c PRD040 Periodontitis, Chronic 52 1.092
561
P MNN013 Meningitis 65 1.085
562
P ACT105 Acute Mountain Sickness 52 1.084
563
CRN017 Coronary Thrombosis 46 1.077
564
CMP010 Complex Regional Pain Syndrome 59 1.076
565
P GRF003 Graft-Versus-Host Disease 71 1.069
566
WLF001 Wolff-Parkinson-White Syndrome 63 1.066
567
ANR004 Anuria 44 1.066
568
ART016 Aortic Aneurysm 68 1.066
569
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 1.063
570
PRM345 Primary Hypomagnesemia with Refractory Seizures and Intellectual Disability 9 1.061
571
HMC014 Homocysteinemia 52 1.055
572
P OPN001 Open-Angle Glaucoma 55 1.053
573
PRM236 Primary Biliary Cholangitis 62 1.050
574
P CHL066 Cholangitis 51 1.050
575
LYM019 Lymphosarcoma 46 1.046
576
END021 Endomyocardial Fibrosis 56 1.045
577
SPL018 Splenomegaly 47 1.045
578
c HNT004 Huntington Disease-Like 2 51 1.044
579
c SYS001 Systemic Lupus Erythematosus 85 1.042
580
OSM001 Osmotic Diarrhea 27 1.040
581
AMN001 Amenorrhea 53 1.037
582
MCN017 Meconium Ileus 52 1.036
583
IMP005 Impotence 52 1.034
584
HYP555 Hypertriglyceridemia, Transient Infantile 39 1.032
585
PYR016 Pyridoxine Deficiency 29 1.032
586
P LPS004 Lupus Erythematosus 61 1.030
587
OST062 Osteoarthritis with Mild Chondrodysplasia 46 1.029
588
DYS015 Dysentery 49 1.028
589
LMB062 Limb Ischemia 55 1.020
590
SYN007 Synovitis 54 1.020
591
PLC002 Plica Syndrome 35 1.020
592
CRT015 Carotid Artery Occlusion 45 1.020
593
c GLC092 Glaucoma, Primary Open Angle 60 1.020
594
c FML191 Familial Long Qt Syndrome 54 1.020
595
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.013
596
BNN003 Bone Inflammation Disease 47 1.011
597
DRG003 Drug Dependence 46 1.011
598
P HMN010 Hemangioma 61 1.007
599
P MVM001 Movement Disease 61 1.007
600
c BRT042 Bartter Syndrome, Type 3 47 1.007
601
PRM329 Premature Aging 36 1.002
602
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 55 1.000
603
ENT004 Enthesopathy 51 0.999
604
DSS009 Disseminated Intravascular Coagulation 56 0.997
605
PRT013 Portal Hypertension 59 0.994
606
P MJR007 Major Affective Disorder 1 42 0.992
607
c HPT015 Hepatitis D 49 0.990
608
DNT001 Dental Fluorosis 43 0.983
609
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 0.983
610
OVR094 Ovarian Epithelial Cancer 39 0.983
611
TRG002 Trigeminal Neuralgia 61 0.980
612
P VSC011 Vasculitis 61 0.978
613
RHM028 Rheumatic Heart Disease 55 0.973
614
P ACN011 Acne 55 0.973
615
P PLM036 Pulmonary Fibrosis 65 0.973
616
PRN009 Paranoid Schizophrenia 49 0.973
617
PRL008 Paralytic Ileus 44 0.973
618
P PNC025 Panic Disorder 52 0.965
619
MSL001 Measles 61 0.962
620
P PSD015 Pseudohypoparathyroidism 54 0.962
621
P DST107 Distal Renal Tubular Acidosis 48 0.954
622
P ADN016 Adenocarcinoma 63 0.952
623
DBT004 Diabetic Polyneuropathy 50 0.952
624
PRS045 Prostatic Hypertrophy 53 0.952
625
P KRT007 Keratoconus 49 0.952
626
VSC002 Vascular Dementia 59 0.952
627
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.947
628
P MYS005 Myositis 55 0.947
629
DGT004 Digitalis Poisoning 13 0.947
630
PHN003 Phenylketonuria 76 0.946
631
P HYP726 Hypercalcemia, Infantile, 1 58 0.946
632
MSC157 Muscular Dystrophy, Duchenne Type 78 0.941
633
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.941
634
P GLM040 Glioma Susceptibility 1 70 0.937
635
ORL015 Oral Squamous Cell Carcinoma 43 0.931
636
P ANG001 Angelman Syndrome 64 0.931
637
P RNV001 Renovascular Hypertension 48 0.929
638
VTM002 Vitamin B12 Deficiency 48 0.923
639
c ACT134 Acute Liver Failure 57 0.923
640
ZLL002 Zollinger-Ellison Syndrome 55 0.917
641
RBR002 Roberts-Sc Phocomelia Syndrome 63 0.917
642
c DRR009 Diarrhea 6 46 0.917
644
c CHR098 Chronic Pyelonephritis 34 0.917
645
ALL006 Allergic Asthma 55 0.917
646
SQM006 Squamous Cell Carcinoma 59 0.914
647
AMN006 Aminoaciduria 37 0.914
648
c ALP101 Alpha-Thalassemia 62 0.913
649
P BLR024 Biliary Cirrhosis, Primary, 1 27 0.913
650
BRX001 Bruxism 50 0.908
651
IRR002 Irritable Bowel Syndrome 64 0.906
652
PSY004 Psychotic Disorder 66 0.903
653
c HMC039 Hemochromatosis, Type 1 73 0.897
654
GST030 Gastrinoma 45 0.896
655
EXS001 Exostosis 49 0.891
656
P FML068 Familial Hypocalciuric Hypercalcemia 55 0.889
657
PRS064 Persistent Vegetative State 33 0.888
658
P CYS018 Cystitis 58 0.888
659
c ART115 Aortic Valve Disease 1 72 0.887
660
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.887
661
NWB001 Newborn Respiratory Distress Syndrome 56 0.887
662
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.886
663
CRN270 Coronary Artery Dissection, Spontaneous 33 0.883
664
PRT029 Parathyroid Adenoma 51 0.879
665
ORL011 Oral Cancer 60 0.879
666
c CNG411 Congenital Disorder of Glycosylation, Type in 66 0.878
667
DYS016 Dysgammaglobulinemia 33 0.878
668
c PRC045 Preeclampsia/eclampsia 5 24 0.876
669
LPR001 Lepromatous Leprosy 49 0.876
670
P TXP001 Toxoplasmosis 59 0.876
671
MYT011 Myotonia 37 0.876
672
JLL001 Jalili Syndrome 45 0.870
673
MLR020 Malaria, Mild 28 0.870
674
MDN008 Median Arcuate Ligament Syndrome 37 0.870
675
HYP458 Hyper Ige Syndrome 60 0.870
676
RYN001 Raynaud Disease 49 0.866
677
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.866
678
IRN001 Iron Deficiency Anemia 58 0.864
679
SWL001 Swallowing Disorders 37 0.864
680
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 23 0.861
681
PRT112 Portal Hypertension, Noncirrhotic 29 0.861
682
MGB001 Megabladder, Congenital 24 0.861
683
INS001 Insulinoma 59 0.861
684
ASP007 Aspiration Pneumonia 49 0.860
685
WST001 West Syndrome 64 0.860
686
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 42 0.857
687
c HYP794 Hyperoxaluria, Primary, Type I 63 0.857
688
P LYM033 Lymphoproliferative Syndrome 59 0.857
689
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 22 0.855
690
P EYD002 Eye Disease 57 0.850
691
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.850
692
MRS001 Marasmus 41 0.850
693
MMM001 Mammary Paget's Disease 53 0.850
694
INT002 Intermittent Claudication 61 0.844
695
RTN003 Retinal Ischemia 48 0.844
696
HMG002 Hemoglobinuria 50 0.844
697
ACT088 Acute Insulin Response 39 0.840
698
ART035 Arterial Calcification of Infancy 58 0.840
699
c BCT007 Bacterial Meningitis 55 0.840
700
CMB007 Combined Immunodeficiency 56 0.832
701
MYL069 Myeloma, Multiple 76 0.831
702
APH002 Aphasia 55 0.830
703
PRS021 Prostatic Adenoma 43 0.829
704
P BCL017 B-Cell Lymphoma 57 0.829
705
P MYC008 Myocarditis 59 0.829
706
THR035 Thrombasthenia 48 0.829
707
PPL022 Papilloma 53 0.825
708
INS024 Insulin-Like Growth Factor I 77 0.823
709
TBC004 Tobacco Addiction 63 0.818
710
P ADV001 Advanced Sleep Phase Syndrome 41 0.818
711
DLY008 Delayed Sleep Phase Disorder 44 0.818
712
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.818
713
MDD018 Middle East Respiratory Syndrome 44 0.818
714
PLC005 Placental Insufficiency 55 0.818
715
HYD002 Hydronephrosis 58 0.818
716
GST040 Gastric Adenocarcinoma 66 0.818
717
PRT058 Pure Autonomic Failure 58 0.818
718
PRQ002 Paraquat Poisoning 28 0.818
719
RFR010 Refractory Anemia 49 0.808
720
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.806
722
VLV047 Volvulus of Midgut 55 0.806
723
P FRD001 Friedreich Ataxia 62 0.806
724
P PGT001 Paget's Disease of Bone 60 0.806
725
SPN035 Spindle Cell Sarcoma 51 0.806
726
SRC014 Sarcoma 64 0.806
727
OST016 Osteochondrosis 52 0.806
728
CMR002 Coumarin Resistance 59 0.806
729
TNS007 Taeniasis 46 0.804
730
P SPP010 Suppressor of Tumorigenicity 3 50 0.804
731
ANK001 Ankylosis 50 0.804
732
P PMP001 Pemphigus 54 0.804
733
VCC001 Vaccinia 49 0.802
734
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.797
735
P END046 Endometritis 46 0.794
736
P ALP008 Alopecia 53 0.794
737
THR099 Third-Degree Atrioventricular Block 42 0.794
738
OTT002 Otitis Media 70 0.794
739
TND005 Tendinitis 53 0.794
740
PRS129 Prostatic Hyperplasia, Benign 48 0.794
741
P VNS003 Venous Insufficiency 54 0.794
742
c ACT042 Acute Pyelonephritis 45 0.794
743
TRC005 Tracheal Stenosis 43 0.794
744
P PRP029 Porphyria 60 0.794
745
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.794
746
CCN002 Cocaine Abuse 49 0.794
747
c HNT011 Huntington Disease-Like 3 33 0.781
748
RNL077 Renal Fibrosis 46 0.781
749
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 26 0.781
750
PYR041 Pyruvate Kinase Deficiency of Red Cells 56 0.781
751
SPS007 Spastic Cerebral Palsy 45 0.781
752
BTT017 Beta-Thalassemia Major 54 0.781
753
NWC001 Newcastle Disease 47 0.781
754
c ACT073 Acute Leukemia 59 0.781
755
GRD001 Giardiasis 46 0.781
756
BCK003 Background Diabetic Retinopathy 46 0.781
757
P MTC133 Mitochondrial Myopathy 51 0.781
758
THR123 Thrombotic Microangiopathy 40 0.781
759
HND015 Hand Skill, Relative 29 0.779
760
CYN002 Cyanosis, Transient Neonatal 43 0.779
761
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.768
762
P FBR025 Fibrochondrogenesis 55 0.768
763
P GLY013 Glycogen Storage Disease 59 0.768
764
AVD001 Avoidant Personality Disorder 49 0.768
765
P URT039 Urticaria 57 0.768
766
P AMY004 Amyloidosis 69 0.768
767
SDD008 Sudden Sensorineural Hearing Loss 41 0.768
768
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 55 0.758
769
QDR001 Quadriplegia 49 0.755
770
MST005 Mastitis 52 0.755
771
CNT047 Contact Dermatitis 56 0.754
772
P PTT006 Pituitary Adenoma 55 0.754
773
CRN030 Coronary Stenosis 50 0.754
774
BTT018 Beta-Thalassemia Intermedia 31 0.754
775
CHR074 Choriocarcinoma 46 0.754
776
CHR028 Chronic Wasting Disease 33 0.754
777
P OST009 Osteochondritis Dissecans 61 0.754
778
P OST028 Osteochondroma 44 0.754
779
IDP069 Idiopathic Avascular Necrosis 23 0.754
780
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 0.754
781
c KNN009 Kenny-Caffey Syndrome, Type 1 35 0.750
782
c CRN108 Cranioectodermal Dysplasia 1 48 0.750
783
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.750
784
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.746
785
ATM095 Autoimmune Disease 61 0.746
786
P PRM002 Primary Hyperoxaluria 65 0.746
787
PLC008 Placenta Disease 48 0.746
788
ISL027 Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 5 0.743
789
DSR036 Disorder of Mineral Absorption and Transport 5 0.743
790
GNT180 Genetic Primary Hypomagnesemia with Normocalciuria 3 0.743
791
KRT008 Keratopathy 46 0.738
792
P FBR017 Fibrosarcoma 55 0.738
793
RTN020 Retinal Vascular Disease 45 0.738
794
P OTS001 Otosclerosis 49 0.738
795
DBT007 Diabetic Cataract 36 0.738
796
CRC021 Carcinosarcoma 62 0.738
797
HYP057 Hypervitaminosis D 37 0.738
798
IDP091 Idiopathic Nephrotic Syndrome 49 0.738
799
P BLD134 Bladder Cancer 79 0.737
800
CHL004 Cholelithiasis 48 0.737
801
PLM033 Pulmonary Embolism 58 0.737
802
SCN001 Secondary Hyperparathyroidism of Renal Origin 24 0.729
803
P TRC086 Trichohepatoenteric Syndrome 1 59 0.727
804
LPT006 Leptin Receptor Deficiency 50 0.727
805
c RST012 Restless Legs Syndrome 1 33 0.727
807
P KHL003 Kohlschutter-Tonz Syndrome 57 0.727
808
c THY107 Thymoma, Familial 42 0.721
809
P THY023 Thymoma 64 0.721
810
TYP007 Typhoid Fever 63 0.721
811
AVN001 Avian Influenza 61 0.721
812
ERY069 Erythrokeratoderma ''en Cocardes'' 26 0.721
813
MDL009 Medullary Sponge Kidney 40 0.721
814
CRN011 Coronin-1a Deficiency 19 0.721
815
CD4003 Cd40 Ligand Deficiency 53 0.721
816
IMM122 Immunodeficiency 41 with Lymphoproliferation and Autoimmunity 53 0.721
817
c GRN062 Granulomatous Disease, Chronic, Autosomal Recessive, 1 46 0.721
818
LYM114 Lymphoproliferative Syndrome, X-Linked, 2 51 0.721
819
IMM105 Immunodeficiency with Hyper-Igm, Type 3 49 0.721
820
IMM120 Immunodeficiency 40 43 0.721
821
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 58 0.721
822
IMM070 Immunodeficiency 13 41 0.721
823
c LYM107 Lymphoproliferative Syndrome 2 50 0.721
824
c LYM106 Lymphoproliferative Syndrome 1 45 0.721
825
ADP007 Adie Pupil 40 0.721
826
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 35 0.721
827
SLC007 Selective Immunoglobulin Deficiency Disease 23 0.721
828
HNM002 Hinman Syndrome 29 0.721
829
P KLZ004 Kala-Azar 1 41 0.719
830
LSH001 Leishmaniasis 63 0.719
831
P DBT005 Diabetes Insipidus 54 0.719
832
ERY051 Erythroleukemia, Familial 37 0.718
833
P TST021 Testicular Germ Cell Tumor 61 0.718
834
c LKM070 Leukemia, Acute Monocytic 56 0.718
835
KRT013 Keratolytic Winter Erythema 45 0.718
836
c FNC043 Fanconi Anemia, Complementation Group E 62 0.718
837
c CHR064 Chronic Monocytic Leukemia 35 0.718
838
ACT250 Acute Megakaryocytic Leukemia 63 0.718
839
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.710
840
EXC002 Exocrine Pancreatic Insufficiency 42 0.710
841
P SBS003 Substance Abuse 54 0.710
842
GLL008 Gilles De La Tourette Syndrome 64 0.703
843
MGC001 Megacolon 48 0.703
844
MCR017 Macrocytic Anemia 44 0.703
845
CMP034 Complete Androgen Insensitivity Syndrome 55 0.703
846
MTS001 Mutism 44 0.700
847
BCT004 Bacteriuria 48 0.700
848
P SLP006 Sleep Apnea 69 0.690
849
PLY150 Polykaryocytosis Inducer 29 0.690
850
CHL123 Chlamydia 58 0.690
851
LPT001 Leptospirosis 65 0.690
852
SVR001 Severe Acute Respiratory Syndrome 68 0.690
853
MNS015 Monosodium Glutamate Sensitivity 18 0.682
854
c CHR418 Chronic Leukemia 48 0.682
855
CCC002 Coccidiosis 50 0.682
856
EXT034 Extrinsic Allergic Alveolitis 56 0.682
857
MLR004 Malaria 77 0.680
858
CRH005 Crohn's Colitis 53 0.680
859
CLL003 Cellulitis 53 0.680
860
PST011 Pustulosis of Palm and Sole 52 0.680
861
ALC005 Alcoholic Pancreatitis 38 0.680
862
ORL004 Oral Submucous Fibrosis 56 0.680
863
P PSR002 Psoriasis 63 0.680
864
HYP540 Hypertension, Diastolic 38 0.669
865
CLB010 Coloboma of Macula 53 0.669
866
CHR103 Charge Syndrome 65 0.669
867
c PRG042 Progressive Familial Heart Block, Type Ia 65 0.669
868
SLL001 Sialolithiasis 36 0.669
869
P MYT023 Myotonia Congenita 55 0.668
870
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.658
871
c VSC019 Vesicoureteral Reflux 1 56 0.658
872
P PLY014 Polycystic Kidney Disease 71 0.658
873
BRN009 Burning Mouth Syndrome 51 0.658
874
ATN004 Autonomic Neuropathy 42 0.658
875
TNS005 Tonsillitis 57 0.658
876
P ERY008 Erythromelalgia 50 0.658
877
VSC003 Visceral Leishmaniasis 54 0.658
878
P INF038 Influenza 68 0.658
879
DST006 Diastolic Heart Failure 45 0.658
880
P ALP009 Alopecia Areata 59 0.658
881
c AMY088 Amyotrophic Lateral Sclerosis 3 33 0.657
882
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.657
883
c AMY094 Amyotrophic Lateral Sclerosis 5, Juvenile 31 0.657
884
CHP002 Chops Syndrome 47 0.657
885
P LRY044 Larynx Cancer 53 0.657
886
ENM002 Enamel Erosion 25 0.657
887
P BNC003 Bone Cancer 58 0.657
888
MSN001 Mesangial Proliferative Glomerulonephritis 44 0.657
889
MYS001 Myositis Ossificans 44 0.657
890
P HMC002 Homocystinuria 52 0.657
891
CSY001 C Syndrome 61 0.649
892
P FML023 Familial Hemiplegic Migraine 53 0.647
893
HSH003 Hashimoto Thyroiditis 60 0.647
894
URT010 Ureteral Obstruction 44 0.647
895
ANL017 Anal Squamous Cell Carcinoma 44 0.647
896
P ANT006 Antiphospholipid Syndrome 55 0.647
897
P KDN017 Kidney Cancer 60 0.647
898
OST004 Osteitis Fibrosa 38 0.647
899
APP008 Appendicitis 62 0.647
900
CTR027 Cataract-Glaucoma 21 0.647
901
PSR001 Psoriatic Arthritis 61 0.634
902
VRC005 Varicose Veins 59 0.634
903
P NSP012 Nasopharyngeal Carcinoma 60 0.634
904
KRN002 Kearns-Sayre Syndrome 62 0.634
905
CLR109 Colorectal Adenocarcinoma 50 0.634
906
P HMR003 Hemorrhagic Disease 59 0.634
907
P SCK002 Sick Sinus Syndrome 55 0.634
908
BRN014 Bronchopneumonia 52 0.634
909
MTR002 Mitral Valve Insufficiency 51 0.634
910
CHT001 Chaotic Atrial Tachycardia 10 0.634
911
PLY100 Polyploidy 36 0.634
912
ARG004 Argyria 26 0.634
913
LSC001 Lesch-Nyhan Syndrome 62 0.624
914
PYR010 Peyronie's Disease 50 0.624
915
BLC012 Bile Acid Malabsorption, Primary 45 0.624
916
ACL001 Acalculous Cholecystitis 34 0.624
917
CNN005 Connective Tissue Disease 66 0.624
918
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.624
919
UTR020 Uterine Inversion 27 0.624
920
P HMR005 Hemorrhoid 49 0.622
921
P MTR004 Maturity-Onset Diabetes of the Young 66 0.622
922
P BRN019 Bernard-Soulier Syndrome 61 0.622
923
P HNT016 Huntington Disease 73 0.622
924
MTN003 Motion Sickness 50 0.622
925
MRP001 Morphine Dependence 41 0.622
926
P MTR012 Mitral Valve Disease 57 0.622
927
HYP082 Hypopharynx Cancer 47 0.622
928
RVR002 Reversible Cerebral Vasoconstriction Syndrome 32 0.622
929
HYP264 Hypertonia 35 0.622
930
ISC015 Ischemic Colitis 43 0.608
931
c SML038 Small Cell Cancer of the Lung 68 0.608
932
P GLC113 Galactosemia I 65 0.608
933
c GLY008 Glycogen Storage Disease Ii 72 0.608
934
PCK003 Pick Disease of Brain 70 0.608
935
MLD018 Mild Cognitive Impairment 48 0.608
936
ADT003 Auditory System Disease 48 0.608
937
MNN017 Mononeuropathy 41 0.608
938
P DYS005 Dyslexia 40 0.608
939
P RNL015 Renal Hypertension 45 0.608
940
P NMN002 Niemann-Pick Disease 60 0.608
941
CHL028 Childhood Type Dermatomyositis 58 0.608
942
P DRM010 Dermatomyositis 61 0.608
943
P PRN023 Prion Disease 60 0.608
944
CNT025 Central Pontine Myelinolysis 42 0.608
945
c ACT135 Acute Graft Versus Host Disease 51 0.608
946
HVY002 Heavy Metal Poisoning 22 0.608
947
LTH004 Lathyrism 15 0.608
948
LKP003 Leukoplakia 39 0.608
949
FNT004 Fainting 29 0.608
950
P DYS021 Dysautonomia 38 0.608
951
c SCL052 Scleroderma, Familial Progressive 60