Search results for Magnesium

2278 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 43.646
2
c HYP210 Hypomagnesemia 2, Renal 40 32.746
3
c PRC016 Pre-Eclampsia 65 29.567
4
P ECL001 Eclampsia 52 28.208
5
GTL001 Gitelman Syndrome 65 24.422
6
HYP550 Hypomagnesemia 1, Intestinal 45 21.913
7
P HYP534 Hypomagnesemia 3, Renal 46 21.761
8
HYP005 Hypokalemia 55 18.329
9
c SVR005 Severe Pre-Eclampsia 50 16.867
10
PNG002 Pain Agnosia 51 16.517
11
CRB037 Cerebral Palsy 67 15.889
12
c MGR028 Migraine with or Without Aura 1 64 14.284
13
c HYP595 Hypertension, Essential 85 13.882
14
c ACT075 Acute Myocardial Infarction 56 13.450
15
c ACT249 Acute Asthma 40 13.224
16
P AST005 Asthma 76 13.071
17
c CHR684 Chronic Kidney Disease 69 13.031
18
URL001 Urolithiasis 46 12.781
19
c TYP009 Type 2 Diabetes Mellitus 92 12.448
20
MGN003 Magnesium, Elevated Red Cell 6 12.105
21
P KDN018 Kidney Disease 72 11.777
22
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 11.273
23
CNS004 Constipation 56 11.263
24
P SZR006 Seizure Disorder 70 11.149
25
P DBT009 Diabetes Mellitus 67 10.967
26
NPH009 Nephrolithiasis 54 10.940
27
P HYP069 Hyperparathyroidism 62 10.934
28
48X005 48,xyyy 39 10.670
29
DSR028 Disorder of Magnesium Transport 3 10.608
30
P HYP024 Hypoparathyroidism 55 10.475
31
BRN071 Brain Injury 50 10.387
32
P CRN300 Coronary Heart Disease 1 73 10.244
33
TRM010 Traumatic Brain Injury 51 9.998
34
BNR002 Bone Resorption Disease 47 9.884
35
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 9.865
36
ALC007 Alcohol Dependence 66 9.842
37
RCK004 Rickets 68 9.796
38
P HDC001 Headache 57 9.443
39
ART140 Arteries, Anomalies of 53 9.349
40
LPP008 Lipoprotein Quantitative Trait Locus 65 9.250
41
RPD005 Rapidly Involuting Congenital Hemangioma 46 8.862
42
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 8.855
43
P ENC018 Encephalopathy 62 8.836
44
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 8.764
45
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 8.764
46
P OST002 Osteoporosis 76 8.715
47
PRT251 Proteinuria, Chronic Benign 57 8.700
48
P HRT032 Heart Disease 81 8.608
49
P ATR011 Atrial Fibrillation 66 8.588
50
NPH003 Nephrocalcinosis 49 8.502
51
PLM129 Pulmonary Disease, Chronic Obstructive 74 8.451
52
HYP025 Hyperphosphatemia 48 8.301
53
END086 End Stage Renal Disease 52 8.248
54
LPD008 Lipid Metabolism Disorder 62 8.215
55
PRM237 Primary Hypomagnesemia 44 8.143
56
SBC016 Subacute Delirium 43 8.064
57
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 7.950
58
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 7.950
59
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 7.950
60
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 7.950
61
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 7.950
62
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 7.950
63
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 7.950
64
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 7.950
65
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 7.950
66
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 7.950
67
STR067 Stroke, Ischemic 80 7.894
68
P DRR001 Diarrhea 55 7.778
69
c ACT071 Acute Kidney Failure 60 7.768
70
ISC004 Ischemia 61 7.722
71
P BND020 Bone Disease 59 7.649
72
P VSC007 Vascular Disease 63 7.613
73
IRN002 Iron Metabolism Disease 57 7.586
74
MTB004 Metabolic Acidosis 48 7.433
75
c TYP008 Type 1 Diabetes Mellitus 70 7.349
76
P CHR345 Chronic Pain 50 7.346
77
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 7.331
78
GST092 Gastroesophageal Reflux 61 7.290
79
P CRD119 Cardiac Arrest 67 7.245
80
DFC004 Deficiency Anemia 74 7.174
81
HYP066 Hyperglycemia 61 7.144
82
P RSP003 Respiratory Failure 74 7.092
83
CNG034 Congestive Heart Failure 69 7.092
84
HYP017 Hypophosphatemia 49 7.072
85
CRD223 Cardiac Arrhythmia 63 7.010
86
CRD132 Cardiac Conduction Defect 60 6.979
87
P PLM037 Pulmonary Hypertension 72 6.958
88
P MYC007 Myocardial Infarction 70 6.947
89
FBR047 Fibromyalgia 58 6.929
90
P NRP001 Neuropathy 60 6.905
91
HYP266 Hypoxia 57 6.815
92
GST033 Gestational Diabetes 61 6.793
93
P ALC033 Alcohol Use Disorder 61 6.771
94
PLC007 Placental Abruption 47 6.764
95
P ATT013 Attention Deficit-Hyperactivity Disorder 64 6.751
96
TTN003 Tetanus 65 6.744
97
NPH091 Nephrolithiasis, Calcium Oxalate 61 6.738
98
OCL069 Ocular Motor Apraxia 57 6.659
99
c SCN007 Secondary Hyperparathyroidism 51 6.649
100
P SCK005 Sickle Cell Disease 56 6.626
101
P CLR023 Colorectal Cancer 100 6.521
102
ATH013 Atherosclerosis Susceptibility 63 6.395
103
LVR012 Liver Cirrhosis 63 6.388
104
HLX001 Helix Syndrome 48 6.354
105
P LVR013 Liver Disease 69 6.341
106
AGN016 Aging 54 6.226
107
CRB039 Cerebrovascular Disease 66 6.162
108
P PRP019 Peripheral Nervous System Disease 58 6.148
109
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 6.145
110
HDN002 Head Injury 44 6.131
111
c ACT027 Acute Pancreatitis 60 6.120
112
MNT002 Mental Depression 57 6.073
113
OST012 Osteoarthritis 77 6.066
114
P ART023 Arthropathy 61 6.051
115
P HYP086 Hypothyroidism 69 5.991
116
NNL005 Non-Alcoholic Fatty Liver Disease 63 5.988
117
P ATS364 Autism 69 5.974
118
PLM010 Pulmonary Edema 55 5.969
119
P PNC044 Pancreatitis 61 5.969
120
DPR016 Depression 65 5.959
121
LNG099 Lung Disease 62 5.948
122
SPN186 Spinal Cord Injury 61 5.917
123
P PLY011 Polycystic Ovary Syndrome 57 5.827
124
c PRM005 Primary Hyperparathyroidism 59 5.826
125
P BRS047 Breast Cancer 98 5.816
126
STT002 Status Asthmaticus 49 5.799
127
PRV004 Periventricular Leukomalacia 52 5.767
128
FTT001 Fatty Liver Disease 62 5.750
129
PRM020 Premenstrual Tension 39 5.747
130
P TRM003 Tremor 48 5.716
131
TXC005 Toxic Shock Syndrome 62 5.642
132
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 5.598
133
HRW001 Hair Whorl 35 5.521
134
PRT082 Preterm Premature Rupture of the Membranes 57 5.473
135
P ORT004 Orthostatic Intolerance 63 5.469
136
CHR005 Chorioamnionitis 50 5.457
137
c AMY091 Amyotrophic Lateral Sclerosis 1 88 5.423
138
P LTR001 Lateral Sclerosis 58 5.423
139
P ART021 Arteriosclerosis 54 5.413
140
P HYP750 Hypertriglyceridemia, Familial 62 5.348
141
BRN002 Bronchiolitis 57 5.318
142
c MCR115 Microvascular Complications of Diabetes 5 65 5.312
143
CRH001 Crohn's Disease 80 5.297
144
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 5.290
145
P PHC003 Pheochromocytoma 69 5.290
146
ADR040 Adrenal Gland Pheochromocytoma 46 5.290
147
P EPL164 Epilepsy 68 5.180
148
c ATS007 Autism Spectrum Disorder 72 5.166
149
c PNS012 Paine Syndrome 60 5.107
150
HRN029 Hearing Loss, Noise-Induced 37 5.047
151
P HYP076 Hyperthyroidism 53 5.022
152
OST011 Osteomalacia 52 5.022
153
KRT002 Keratomalacia 55 4.928
154
WTH001 Withdrawal Disorder 48 4.909
155
CLC006 Calcinosis 47 4.905
156
ADG002 Audiogenic Seizures 25 4.895
157
ILS001 Ileus 50 4.881
158
P BRB001 Beriberi 44 4.841
159
c MCR130 Microvascular Complications of Diabetes 6 41 4.840
160
c MCR120 Microvascular Complications of Diabetes 7 47 4.840
161
c MCR113 Microvascular Complications of Diabetes 3 52 4.840
162
c MCR133 Microvascular Complications of Diabetes 4 41 4.840
163
47X002 47,xyy 48 4.828
164
SCK003 Sickle Cell Anemia 74 4.825
165
ANG054 Angina Pectoris 66 4.820
166
HYP060 Hyperinsulinism 54 4.784
167
P HYP265 Hypotonia 42 4.768
168
c HYP836 Hypercholesterolemia, Familial, 1 73 4.757
169
c EPS039 Episodic Pain Syndrome, Familial, 1 42 4.734
170
ADN018 Adenoma 59 4.729
171
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.720
172
P THL005 Thalassemia 56 4.651
173
ENT011 Enterocolitis 55 4.610
174
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.606
175
ASP004 Asphyxia Neonatorum 50 4.589
176
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 4.576
177
SDD001 Sudden Infant Death Syndrome 60 4.575
178
FML327 Familial Primary Hypomagnesemia with Hypercalciuria and Nephrocalcinosis 18 4.573
179
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.562
180
P ESP024 Esophagitis 60 4.559
181
GLC003 Glucose Intolerance 54 4.533
182
CHL068 Cholestasis 61 4.510
183
P LNG028 Long Qt Syndrome 64 4.498
184
HLL004 Hellp Syndrome 53 4.476
185
P LKM002 Leukemia 67 4.476
186
P SHR001 Short Bowel Syndrome 53 4.471
187
P PSD087 Pseudoxanthoma Elasticum 67 4.468
188
URM002 Uremia 47 4.465
189
OST159 Osteogenic Sarcoma 66 4.454
190
CHR066 Chronic Fatigue Syndrome 60 4.418
191
CLT003 Colitis 63 4.414
192
ANX004 Anoxia 40 4.410
193
P PRC031 Preeclampsia/eclampsia 1 43 4.397
194
PRN019 Perinatal Necrotizing Enterocolitis 60 4.380
195
P MJR001 Major Depressive Disorder 68 4.370
196
CYS001 Cystic Fibrosis 78 4.366
197
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 4.366
198
ULC004 Ulcerative Colitis 74 4.342
199
BRN004 Brain Edema 54 4.337
200
ATR057 Atrioventricular Block 54 4.275
201
NNL006 Non-Alcoholic Steatohepatitis 54 4.247
202
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 4.235
203
STT001 Status Epilepticus 59 4.227
204
P PRK039 Parkinsonism 55 4.214
205
CNN003 Conn's Syndrome 79 4.212
206
BRN024 Bronchitis 67 4.188
207
HMN044 Human Immunodeficiency Virus Type 1 78 4.178
208
RNL011 Renal Osteodystrophy 49 4.167
209
P HYP834 Hypomagnesemia, Seizures, and Mental Retardation 2 22 4.145
210
HYP827 Hypomagnesemia 5, Renal, with or Without Ocular Involvement 43 4.109
211
P OVR042 Ovarian Cancer 88 4.099
212
P THY032 Thyroiditis 57 4.091
213
P URN019 Urinary Tract Infection 49 4.075
214
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 4.054
215
IMM167 Immune Deficiency Disease 78 4.054
216
P MYP004 Myopathy 67 4.028
217
CRB004 Cerebral Artery Occlusion 45 4.023
218
SKN016 Skin Disease 63 4.004
219
c LKM061 Leukemia, Acute Myeloid 83 3.987
220
PRT036 Peritonitis 65 3.984
221
ATS010 Autosomal Recessive Disease 42 3.937
222
P DDN001 Duodenal Ulcer 53 3.930
223
BNN005 Bunion 31 3.921
224
P PRD008 Periodontitis 64 3.916
225
P HPT021 Hepatitis 69 3.910
226
LPT014 Leptin Deficiency or Dysfunction 78 3.902
227
P INF037 Inflammatory Bowel Disease 53 3.876
228
DWN001 Down Syndrome 70 3.873
229
ANX010 Anxiety 70 3.871
230
HYP014 Hyperuricemia 51 3.868
231
PRT037 Pertussis 65 3.856
232
HYP056 Hypoglycemia 65 3.842
233
IDP073 Idiopathic Hypercalciuria 40 3.821
234
P ALZ034 Alzheimer Disease 87 3.820
235
DBT084 Diabetes Mellitus, Ketosis-Prone 60 3.820
236
c GLL024 Gallbladder Disease 1 52 3.818
237
P DMN002 Dementia 66 3.813
238
ANR007 Anorexia Nervosa 60 3.794
239
PST021 Postpartum Depression 50 3.792
240
GTR002 Goiter 53 3.791
241
DNT012 Dental Caries 53 3.791
242
P LCT001 Lactic Acidosis 51 3.786
243
P SCL018 Scoliosis 57 3.780
244
PRS047 Prostatitis 58 3.778
245
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 3.765
246
HPT004 Hepatic Coma 43 3.736
247
P ART022 Arthritis 71 3.684
248
c ACT068 Acute Cystitis 61 3.676
249
CRD137 Cardiogenic Shock 56 3.658
250
P CHN059 Chondrocalcinosis 52 3.655
251
P MGR003 Migraine with Aura 52 3.637
252
c BTT014 Beta-Thalassemia 72 3.633
253
PPT005 Peptic Ulcer Disease 58 3.631
254
P ANR048 Aniridia 1 64 3.628
255
P GST044 Gastritis 55 3.625
256
ANR040 Aneurysm 61 3.610
257
DYS073 Dysphagia 53 3.602
258
MDD011 Mood Disorder 62 3.599
259
P MYC084 Mycobacterium Tuberculosis 1 68 3.595
260
c MJR022 Major Affective Disorder 8 38 3.584
261
c MJR024 Major Affective Disorder 9 41 3.584
262
P BPL003 Bipolar Disorder 56 3.584
263
P ANP001 Anaplastic Large Cell Lymphoma 61 3.559
264
PPL052 Papillomatosis, Confluent and Reticulated 34 3.557
265
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 3.554
266
P SLP005 Sleep Disorder 61 3.552
267
NTR005 Nutritional Deficiency Disease 61 3.548
268
ESP021 Esophageal Cancer 83 3.548
269
CYT002 Cytokine Deficiency 43 3.543
270
P TRN020 Turner Syndrome 67 3.542
271
P EXN002 Exanthem 58 3.532
272
GST023 Gastric Ulcer 52 3.520
273
RYN005 Raynaud Phenomenon 45 3.501
274
STM007 Stomatitis 54 3.495
275
HPT019 Hepatic Encephalopathy 59 3.491
276
GST050 Gastrointestinal System Disease 55 3.488
277
c DLT002 Dilated Cardiomyopathy 78 3.457
278
P ADL010 Adult Respiratory Distress Syndrome 71 3.448
279
P PTN014 Patent Ductus Arteriosus 1 59 3.448
280
BCK006 Back Pain 47 3.444
281
P MYS003 Myasthenia Gravis 68 3.441
282
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 3.441
283
INT007 Intermediate Coronary Syndrome 54 3.440
284
P HYD006 Hydrocephalus 61 3.430
285
ATN005 Autonomic Dysfunction 46 3.426
286
P HYP733 Hypercalciuria, Absorptive, 2 45 3.410
287
P GLM007 Glomerulonephritis 60 3.408
288
PLC009 Placenta Praevia 38 3.390
289
P PNC035 Pancreatic Cancer 86 3.380
290
P HYP098 Hypereosinophilic Syndrome 66 3.370
291
P NTR004 Neutropenia 63 3.364
292
P RCT021 Rectum Cancer 54 3.363
293
MLT131 Multifocal Atrial Tachycardia 17 3.363
294
P CRD246 Cardiovascular System Disease 56 3.361
295
CRN019 Coronary Artery Vasospasm 47 3.354
296
THY030 Thyroid Gland Disease 50 3.348
297
P CTR002 Cataract 60 3.329
298
HMS001 Hemosiderosis 48 3.323
299
ANT039 Antisynthetase Syndrome 55 3.320
300
MLD002 Mild Pre-Eclampsia 33 3.319
301
BCT022 Bacterial Infectious Disease 56 3.306
302
P RRH023 Rare Hereditary Hemochromatosis 54 3.303
303
P RST001 Restless Legs Syndrome 52 3.288
304
P OVR082 Overgrowth Syndrome 49 3.281
305
PRP016 Paraplegia 52 3.251
306
BRK010 Burkitt Lymphoma 66 3.250
307
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.227
308
c ATR087 Atrial Standstill 1 74 3.222
309
P PYL005 Pyelonephritis 57 3.222
310
P PRS040 Prostate Cancer 95 3.200
311
LYM027 Lymphopenia 56 3.198
312
HRT012 Heart Valve Disease 53 3.187
313
DRM006 Dermatitis 62 3.181
314
SYN036 Syncope 45 3.171
315
P NRB001 Neuroblastoma 66 3.157
316
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.147
317
P NPH012 Nephrotic Syndrome 60 3.144
318
PLP001 Pulpitis 48 3.132
319
P RNL007 Renal Tubular Acidosis 50 3.129
320
P MYL006 Myeloid Leukemia 61 3.120
321
BLR008 Bilirubin Metabolic Disorder 57 3.109
322
c EXD008 Exudative Vitreoretinopathy 1 71 3.105
323
END040 Endogenous Depression 55 3.088
324
DBT010 Diabetic Neuropathy 54 3.061
325
P PRS038 Personality Disorder 65 3.044
326
P MCR129 Microvascular Complications of Diabetes 1 68 3.028
327
c MCR112 Microvascular Complications of Diabetes 2 42 3.028
328
URN010 Urinary Tract Obstruction 55 3.022
329
WRN003 Wernicke Encephalopathy 46 3.022
330
PRT038 Protein-Energy Malnutrition 53 3.013
331
ETN001 Eating Disorder 59 3.002
332
NRM005 Neuromuscular Disease 63 2.999
333
P DRM053 Dermatitis, Atopic 65 2.987
334
ALL029 Allergic Disease 59 2.986
335
CHL014 Cholera 62 2.962
336
P LKM062 Leukemia, Acute Lymphoblastic 69 2.954
337
P SCH015 Schizophrenia 74 2.940
338
PTH003 Pathologic Nystagmus 52 2.938
339
MTH071 Methane Production 25 2.931
340
PRP080 Peripheral Artery Disease 54 2.929
341
GT001 Gout 64 2.918
342
MYC005 Myocardial Stunning 46 2.917
343
RHB024 Rhabdomyosarcoma 2 67 2.917
344
MTH009 Mouth Disease 57 2.912
345
P LYM118 Lymphoma 67 2.911
346
WRN002 Wernicke-Korsakoff Syndrome 50 2.909
347
CRB086 Cerebral Aneurysms 40 2.909
348
P GST053 Gastric Cancer 83 2.908
349
INT323 Intraocular Pressure Quantitative Trait Locus 64 2.901
350
c BRN108 Branchiootic Syndrome 1 62 2.901
351
DSS032 Disease by Infectious Agent 55 2.899
352
P MGR001 Migraine Without Aura 49 2.887
354
P INF032 Infertility 57 2.885
355
GST045 Gastroenteritis 58 2.880
356
SQM013 Squamous Cell Carcinoma, Head and Neck 73 2.879
357
SPS057 Spasticity 42 2.875
358
P HML002 Hemolytic Anemia 62 2.874
359
MLC004 Mulchandani-Bhoj-Conlin Syndrome 51 2.854
360
CLN015 Colon Adenocarcinoma 65 2.849
361
c HPT073 Hepatitis C Virus 71 2.841
362
P CLC063 Celiac Disease 1 66 2.837
363
CVD001 Covid-19 57 2.832
364
P FBR031 Febrile Seizures 52 2.831
365
P THR014 Thrombocytopenia 66 2.830
366
THY029 Thyroid Carcinoma 51 2.826
367
SPS003 Spastic Diplegia 53 2.817
368
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 2.814
369
ANT018 Anthracosis 51 2.803
370
c HPT003 Hepatitis a 63 2.796
371
CRV035 Cervical Cancer 73 2.794
372
c GRV008 Graves Disease 1 54 2.782
373
MCS002 Mucositis 56 2.779
374
P PNM006 Pneumoconiosis 55 2.775
375
P INT068 Intestinal Disease 53 2.753
376
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 2.747
377
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 2.742
378
P CNR004 Cone-Rod Dystrophy 2 74 2.739
379
THR024 Thrombosis 56 2.729
380
CRB090 Cerebral Hypoxia 42 2.729
381
P FML187 Familial Hypertension 34 2.727
382
PRP027 Peripheral Vascular Disease 71 2.721
383
P GRV001 Graves' Disease 55 2.718
384
P TCD001 Tic Disorder 49 2.717
385
INT075 Intracranial Hypertension 53 2.710
386
P MYP006 Myopia 56 2.690
387
P RHN004 Rhinitis 57 2.673
388
ADL002 Adult Syndrome 70 2.671
389
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 2.662
390
P HYP061 Hypertrophic Cardiomyopathy 69 2.642
391
P LPR021 Leprosy 3 71 2.635
392
HNS001 Hansen's Disease 32 2.635
393
P HRD086 Hereditary Hypophosphatemic Rickets 40 2.617
394
CRB009 Cerebritis 43 2.613
395
CLR108 Colorectal Adenoma 64 2.612
396
P MTR014 Motor Neuron Disease 65 2.610
397
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 2.610
398
ING001 Inguinal Hernia 59 2.601
399
OST003 Osteonecrosis 61 2.596
400
P SNS001 Sensorineural Hearing Loss 59 2.588
401
P PLY019 Polyneuropathy 52 2.587
402
PRP030 Purpura 54 2.581
403
P INT143 Interstitial Cystitis 60 2.576
404
P PTS002 Ptosis 52 2.559
405
PST053 Postherpetic Neuralgia 40 2.559
406
c HPT016 Hepatitis B 62 2.552
407
P MYC033 Myoclonus 47 2.552
408
c HYP445 Hypomagnesemia 6, Renal 23 2.548
409
P OPT006 Optic Nerve Disease 58 2.533
410
P MLN007 Male Infertility 56 2.520
411
P PRD021 Periodic Paralysis 41 2.505
412
BRN056 Bronchopulmonary Dysplasia 56 2.505
413
ACT003 Acute Kidney Tubular Necrosis 46 2.497
414
PRS063 Paresthesia 39 2.497
415
P MLG056 Malignant Hyperthermia 66 2.494
416
P RHM011 Rheumatoid Arthritis 82 2.489
417
HMN047 Human Cytomegalovirus Infection 57 2.483
418
HND002 Hand, Foot and Mouth Disease 50 2.477
419
ATX019 Ataxia with Vitamin E Deficiency 44 2.469
420
PRM003 Premature Ejaculation 44 2.468
421
SNS003 Sensory Peripheral Neuropathy 52 2.468
422
TST014 Testicular Cancer 52 2.464
423
IGR001 Ige Responsiveness, Atopic 59 2.439
424
INT067 Interstitial Nephritis 46 2.438
425
IDP070 Idiopathic Scoliosis 42 2.435
426
NRT001 Neurotic Disorder 56 2.432
427
SNL007 Senile Cataract 40 2.430
428
PPT001 Peptic Esophagitis 52 2.423
429
HYP034 Hypertensive Encephalopathy 43 2.422
430
PST092 Posttransplant Acute Limbic Encephalitis 28 2.422
431
c HYP724 Hyperlipoproteinemia, Type Iii 67 2.414
432
P NRV007 Nervous System Disease 67 2.410
433
c CHR711 Chronic Asthma 41 2.394
434
NRL016 Neural Tube Defects 81 2.394
435
P THR005 Thrombotic Thrombocytopenic Purpura 64 2.381
436
CRB089 Cerebral Beriberi 19 2.381
437
ALL003 Allergic Rhinitis 67 2.374
438
c PRD040 Periodontitis, Chronic 52 2.365
439
P BNG032 Benign Mesothelioma 53 2.363
440
DSS009 Disseminated Intravascular Coagulation 57 2.355
441
P STR092 Striatal Degeneration, Autosomal Dominant 2 47 2.354
442
HYP830 Hypomagnesemia, Seizures, and Mental Retardation 1 20 2.350
443
c HPT001 Hepatitis C 62 2.348
444
OBS002 Obsessive-Compulsive Disorder 68 2.347
445
HLC007 Helicobacter Pylori Infection 67 2.347
446
OLG003 Oligohydramnios 51 2.341
447
P CNJ013 Conjunctivitis 66 2.336
448
P ACT105 Acute Mountain Sickness 52 2.335
449
BRD001 Brody Myopathy 55 2.334
450
P PRV006 Pervasive Developmental Disorder 52 2.325
451
INF118 Inflammatory Myopathy with Abundant Macrophages 27 2.315
452
P CLS010 Cluster Headache 42 2.307
453
CRN017 Coronary Thrombosis 46 2.305
454
IRN001 Iron Deficiency Anemia 58 2.302
455
P BLD134 Bladder Cancer 79 2.300
456
c HPT015 Hepatitis D 49 2.300
457
ACQ007 Acquired Immunodeficiency Syndrome 59 2.291
458
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 2.281
459
CHR073 Choreatic Disease 54 2.281
460
MYM001 Myoma 54 2.279
461
c FML001 Familial Atrial Fibrillation 65 2.279
462
P GRF003 Graft-Versus-Host Disease 71 2.275
463
DNT001 Dental Fluorosis 43 2.271
464
c PLM164 Pulmonary Hypertension, Primary, 1 76 2.251
465
c SPN225 Spondyloarthropathy 1 70 2.244
466
c VRL010 Viral Hepatitis 53 2.244
467
SPN051 Spondylitis 51 2.244
468
INF009 Inflammatory Spondylopathy 30 2.244
469
P INT070 Intestinal Obstruction 57 2.243
470
HYP781 Hypoascorbemia 52 2.226
471
P LNG032 Lung Cancer 98 2.226
472
ACR008 Acrocallosal Syndrome 70 2.226
473
MYL020 Myelomeningocele 51 2.215
474
P PSD015 Pseudohypoparathyroidism 55 2.213
475
P OPN001 Open-Angle Glaucoma 55 2.212
476
PLM001 Pulmonary Tuberculosis 69 2.200
477
GNR004 Generalized Anxiety Disorder 55 2.188
478
P BRT004 Bartter Disease 58 2.182
479
END021 Endomyocardial Fibrosis 56 2.179
480
SPL018 Splenomegaly 49 2.179
481
APH002 Aphasia 56 2.168
482
P MSC005 Muscular Dystrophy 67 2.162
483
PHN003 Phenylketonuria 76 2.152
484
P HYP726 Hypercalcemia, Infantile, 1 58 2.152
485
HYP786 Hypokalemic Alkalosis, Familial, with Specific Renal Tubulopathy 14 2.150
486
AMN001 Amenorrhea 54 2.146
487
INS024 Insulin-Like Growth Factor I 78 2.140
488
P DST107 Distal Renal Tubular Acidosis 48 2.121
489
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 2.115
490
PPL049 Papillon-Lefevre Syndrome 66 2.113
491
DYS015 Dysentery 50 2.112
492
P FML068 Familial Hypocalciuric Hypercalcemia 55 2.111
493
CHL067 Cholecystitis 60 2.108
494
P ANG001 Angelman Syndrome 65 2.089
495
ORL015 Oral Squamous Cell Carcinoma 43 2.089
496
OST017 Osteomyelitis 63 2.083
497
INT071 Intestinal Perforation 49 2.083
498
KWS001 Kwashiorkor 45 2.081
499
IRT001 Iritis 45 2.081
500
BHR001 Behr Syndrome 51 2.079
501
c GLC092 Glaucoma, Primary Open Angle 62 2.077
502
c FML191 Familial Long Qt Syndrome 55 2.077
503
MYF002 Myofascial Pain Syndrome 46 2.077
504
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.066
505
c ACT134 Acute Liver Failure 59 2.056
506
VTM002 Vitamin B12 Deficiency 48 2.056
507
VCC001 Vaccinia 47 2.053
508
P PNM007 Pneumonia 67 2.042
509
BNN003 Bone Inflammation Disease 48 2.042
510
DRG003 Drug Dependence 46 2.042
511
P MLT020 Multiple Sclerosis 79 2.040
512
MLR004 Malaria 80 2.023
513
SQM006 Squamous Cell Carcinoma 60 2.023
514
AMN006 Aminoaciduria 37 2.023
515
P END046 Endometritis 46 2.023
516
GLS018 Glass Syndrome 61 2.012
517
PRM329 Premature Aging 36 2.005
518
P ALP008 Alopecia 54 1.992
519
CMP010 Complex Regional Pain Syndrome 60 1.992
520
IRR002 Irritable Bowel Syndrome 65 1.989
521
c BLD140 Blood Group, I System 46 1.989
522
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 1.989
523
GLB002 Glioblastoma 67 1.981
524
CYN002 Cyanosis, Transient Neonatal 43 1.961
525
HND015 Hand Skill, Relative 30 1.961
526
c HMC039 Hemochromatosis, Type 1 73 1.955
527
P DYS154 Dystonia 64 1.954
528
VSL002 Visual Epilepsy 39 1.952
529
WLF001 Wolff-Parkinson-White Syndrome 65 1.951
530
ANR004 Anuria 44 1.951
531
ART016 Aortic Aneurysm 68 1.951
532
IMP005 Impotence 52 1.949
533
MNN043 Meningioma, Familial 79 1.935
534
DYS011 Dyskinesia of Esophagus 40 1.935
535
SCR001 Secretory Meningioma 40 1.935
536
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.935
537
SPN021 Spinal Meningioma 50 1.935
538
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.929
539
OVR094 Ovarian Epithelial Cancer 39 1.929
540
BNG091 Benign Chronic Pemphigus 57 1.925
541
OSM001 Osmotic Diarrhea 28 1.924
542
P PRK057 Parkinson Disease, Late-Onset 80 1.923
543
P CYS018 Cystitis 59 1.919
544
PRS064 Persistent Vegetative State 33 1.919
545
CYS013 Cystinuria 66 1.916
546
BRT054 Brittle Bone Disorder 74 1.908
547
HMC014 Homocysteinemia 52 1.908
548
P END044 Endometriosis 62 1.908
549
BLR001 Biliary Atresia 55 1.889
550
RHM028 Rheumatic Heart Disease 56 1.888
551
P ACN011 Acne 57 1.888
552
PRL008 Paralytic Ileus 45 1.888
553
PRN009 Paranoid Schizophrenia 49 1.888
554
PRT029 Parathyroid Adenoma 51 1.882
555
ORL011 Oral Cancer 60 1.882
556
AND005 Androgen Insensitivity Syndrome, Mild 21 1.881
557
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 1.865
558
SPR126 Superior Semicircular Canal Dehiscence 41 1.864
559
c HMG029 Hemoglobin Se Disease 40 1.864
560
MST005 Mastitis 53 1.863
561
QDR001 Quadriplegia 50 1.863
562
c HNT004 Huntington Disease-Like 2 52 1.863
563
c SYS001 Systemic Lupus Erythematosus 87 1.862
564
MSL001 Measles 61 1.847
565
JLL001 Jalili Syndrome 45 1.845
566
c HYP302 Hypomagnesemia 4, Renal 36 1.833
567
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 1.829
568
ATM095 Autoimmune Disease 61 1.829
569
P PRM002 Primary Hyperoxaluria 65 1.829
570
PYR016 Pyridoxine Deficiency 29 1.817
571
P LPS004 Lupus Erythematosus 61 1.816
572
WST001 West Syndrome 59 1.806
573
ASP007 Aspiration Pneumonia 49 1.806
574
P KRT007 Keratoconus 50 1.804
575
PRS045 Prostatic Hypertrophy 53 1.804
576
VSC002 Vascular Dementia 60 1.804
577
CHL004 Cholelithiasis 49 1.795
578
PLC008 Placenta Disease 49 1.795
579
c BRT042 Bartter Syndrome, Type 3 46 1.790
580
PLM031 Poliomyelitis 63 1.784
581
LMB062 Limb Ischemia 55 1.768
582
PLC002 Plica Syndrome 35 1.768
583
SYN007 Synovitis 55 1.768
584
MRS001 Marasmus 42 1.766
585
P EYD002 Eye Disease 57 1.766
586
MMM001 Mammary Paget's Disease 53 1.766
587
P FNG006 Feingold Syndrome 1 62 1.763
588
TXC002 Toxic Encephalopathy 52 1.763
589
MSC157 Muscular Dystrophy, Duchenne Type 79 1.760
590
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 1.760
591
P MNN013 Meningitis 65 1.754
592
VGN023 Vaginitis 56 1.735
593
P CRC039 Coarctation of Aorta 46 1.734
594
INT030 Intracranial Aneurysm 55 1.734
595
SCR035 Sacral Agenesis with Vertebral Anomalies 38 1.733
596
THY122 Thyroid Gland Cancer 59 1.733
597
P VSC011 Vasculitis 61 1.726
598
c BCT007 Bacterial Meningitis 55 1.724
599
ART035 Arterial Calcification of Infancy 58 1.724
600
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 1.724
601
ACT088 Acute Insulin Response 39 1.724
602
P PLM036 Pulmonary Fibrosis 66 1.724
603
P SYS005 Systemic Scleroderma 74 1.723
604
P DBT005 Diabetes Insipidus 54 1.722
605
P KLZ004 Kala-Azar 1 41 1.722
606
LSH001 Leishmaniasis 64 1.722
607
PLM033 Pulmonary Embolism 58 1.722
608
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 1.722
609
ALC009 Alcoholic Liver Cirrhosis 54 1.717
610
P MVM001 Movement Disease 61 1.717
611
P HMN010 Hemangioma 62 1.717
612
P ENC004 Encephalitis 61 1.717
613
P RNV001 Renovascular Hypertension 49 1.713
614
VRL011 Viral Infectious Disease 61 1.694
615
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 1.685
616
P SBS003 Substance Abuse 54 1.685
617
EXC002 Exocrine Pancreatic Insufficiency 42 1.685
618
PRS021 Prostatic Adenoma 43 1.682
619
P MYC008 Myocarditis 59 1.682
620
THR035 Thrombasthenia 48 1.682
621
HMN014 Human Immunodeficiency Virus Infectious Disease 54 1.681
622
P PNC025 Panic Disorder 52 1.674
623
AMD002 Amed Syndrome, Digenic 37 1.670
624
ALL006 Allergic Asthma 56 1.665
625
c CHR098 Chronic Pyelonephritis 34 1.665
626
P MJR007 Major Affective Disorder 1 42 1.662
627
PHR003 Pharyngitis 58 1.660
628
FRZ001 Frozen Shoulder 55 1.650
629
BRS064 Bursitis 51 1.650
630
PRQ002 Paraquat Poisoning 28 1.637
631
P ADV001 Advanced Sleep Phase Syndrome 41 1.637
632
DLY008 Delayed Sleep Phase Disorder 44 1.637
633
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.637
634
TBC004 Tobacco Addiction 63 1.637
635
MDD018 Middle East Respiratory Syndrome 44 1.637
636
PLC005 Placental Insufficiency 56 1.637
637
GST040 Gastric Adenocarcinoma 67 1.637
638
HYD002 Hydronephrosis 58 1.637
639
PRT058 Pure Autonomic Failure 58 1.637
640
P TMP001 Temporal Lobe Epilepsy 49 1.637
641
P ADN016 Adenocarcinoma 63 1.620
642
DBT004 Diabetic Polyneuropathy 50 1.620
643
PLY150 Polykaryocytosis Inducer 29 1.606
644
P SLP006 Sleep Apnea 69 1.606
645
BCT004 Bacteriuria 47 1.606
646
CHL123 Chlamydia 58 1.606
647
LPT001 Leptospirosis 66 1.606
648
TRG002 Trigeminal Neuralgia 61 1.605
649
PRT013 Portal Hypertension 59 1.605
650
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 1.591
651
P FRD001 Friedreich Ataxia 61 1.591
653
P PGT001 Paget's Disease of Bone 61 1.591
654
PRS030 Persistent Fetal Circulation Syndrome 49 1.574
655
MCN017 Meconium Ileus 53 1.565
656
CRH005 Crohn's Colitis 53 1.565
657
SVR001 Severe Acute Respiratory Syndrome 67 1.565
658
CLL003 Cellulitis 53 1.565
659
P INF038 Influenza 68 1.565
660
ALC005 Alcoholic Pancreatitis 38 1.565
661
ORL004 Oral Submucous Fibrosis 56 1.565
662
P GLM040 Glioma Susceptibility 1 71 1.563
663
EXS001 Exostosis 49 1.560
664
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.558
665
c MST023 Mesothelioma, Malignant 56 1.549
666
NRN005 Neuronal Ceroid-Lipofuscinoses 61 1.549
667
BRN028 Brain Cancer 74 1.549
668
P TRC031 Trichorhinophalangeal Syndrome 38 1.549
669
PRS129 Prostatic Hyperplasia, Benign 49 1.542
670
OTT002 Otitis Media 71 1.542
671
THR099 Third-Degree Atrioventricular Block 42 1.542
672
TND005 Tendinitis 54 1.542
673
c ACT042 Acute Pyelonephritis 45 1.542
674
TRC005 Tracheal Stenosis 43 1.542
675
P VNS003 Venous Insufficiency 55 1.542
676
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 1.542
677
CCN002 Cocaine Abuse 49 1.542
678
P PRP029 Porphyria 60 1.542
679
MYL069 Myeloma, Multiple 77 1.540
680
HYP540 Hypertension, Diastolic 37 1.522
681
CHR103 Charge Syndrome 66 1.522
682
CLB010 Coloboma of Macula 53 1.522
683
P PSR002 Psoriasis 63 1.522
684
PST011 Pustulosis of Palm and Sole 52 1.522
685
SLL001 Sialolithiasis 36 1.522
686
P CRV039 Cervicitis 52 1.520
687
LYM019 Lymphosarcoma 46 1.519
688
PLY105 Polycystic Ovary Syndrome 1 39 1.515
689
c PRC045 Preeclampsia/eclampsia 5 25 1.502
690
LPR001 Lepromatous Leprosy 49 1.502
691
P TXP001 Toxoplasmosis 60 1.502
692
MYT011 Myotonia 39 1.502
693
CRT015 Carotid Artery Occlusion 45 1.493
694
THR123 Thrombotic Microangiopathy 40 1.491
695
SPS007 Spastic Cerebral Palsy 46 1.491
696
BTT017 Beta-Thalassemia Major 51 1.491
697
c HNT011 Huntington Disease-Like 3 34 1.491
698
URD002 Uridine 5-Prime Monophosphate Hydrolase Deficiency, Hemolytic Anemia Due to 26 1.491
699
PYR041 Pyruvate Kinase Deficiency of Red Cells 57 1.491
700
RNL077 Renal Fibrosis 46 1.491
701
c ACT073 Acute Leukemia 58 1.491
702
P MTC133 Mitochondrial Myopathy 50 1.491
703
SPN035 Spindle Cell Sarcoma 54 1.491
704
SRC014 Sarcoma 65 1.491
705
GRD001 Giardiasis 46 1.491
706
NWC001 Newcastle Disease 47 1.491
707
BCK003 Background Diabetic Retinopathy 47 1.491
708
c PRG042 Progressive Familial Heart Block, Type Ia 66 1.477
709
P PLY014 Polycystic Kidney Disease 69 1.477
710
c VSC019 Vesicoureteral Reflux 1 57 1.477
711
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 1.477
712
VSC003 Visceral Leishmaniasis 55 1.477
713
P ERY008 Erythromelalgia 50 1.477
714
P ALP009 Alopecia Areata 59 1.477
715
BRN009 Burning Mouth Syndrome 51 1.477
716
TNS005 Tonsillitis 57 1.477
717
ATN004 Autonomic Neuropathy 42 1.477
718
DST006 Diastolic Heart Failure 45 1.477
719
DGT004 Digitalis Poisoning 13 1.476
720
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.476
721
P MYS005 Myositis 56 1.476
722
BRR014 Barrett Esophagus 66 1.461
723
P CHL066 Cholangitis 52 1.461
724
PRM236 Primary Biliary Cholangitis 60 1.461
725
c HYP365 Hyperphenylalaninemia, Bh4-Deficient, D 31 1.445
726
OST151 Osteoporosis and Oculocutaneous Hypopigmentation Syndrome 22 1.440
727
PRT112 Portal Hypertension, Noncirrhotic 30 1.440
728
MGB001 Megabladder, Congenital 23 1.440
729
INS001 Insulinoma 59 1.440
730
SDD008 Sudden Sensorineural Hearing Loss 41 1.437
731
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 1.437
732
P FBR025 Fibrochondrogenesis 55 1.437
733
P AMY004 Amyloidosis 70 1.437
734
P BCL017 B-Cell Lymphoma 59 1.437
735
AVD001 Avoidant Personality Disorder 49 1.437
736
P GLY013 Glycogen Storage Disease 60 1.437
737
P URT039 Urticaria 58 1.437
738
PSY004 Psychotic Disorder 66 1.433
739
P FML023 Familial Hemiplegic Migraine 53 1.431
740
HSH003 Hashimoto Thyroiditis 60 1.431
741
URT010 Ureteral Obstruction 45 1.431
742
ANL017 Anal Squamous Cell Carcinoma 44 1.431
743
P ANT006 Antiphospholipid Syndrome 55 1.431
744
APP008 Appendicitis 62 1.431
745
P KDN017 Kidney Cancer 61 1.431
746
OST004 Osteitis Fibrosa 38 1.431
747
CTR027 Cataract-Glaucoma 22 1.431
748
TCL003 T Cell Deficiency 44 1.421
749
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 1.418
750
SPN369 Spinal Disease 44 1.418
751
RDN001 Reading Disorder 40 1.418
752
ENT004 Enthesopathy 51 1.409
753
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 58 1.405
754
ZLL002 Zollinger-Ellison Syndrome 55 1.391
755
c SCL052 Scleroderma, Familial Progressive 61 1.388
756
ENT001 Enterocele 42 1.386
757
P VSC018 Visceral Steatosis 32 1.383
758
PLY100 Polyploidy 36 1.382
759
P NSP012 Nasopharyngeal Carcinoma 61 1.382
760
PSR001 Psoriatic Arthritis 62 1.382
761
VLV047 Volvulus of Midgut 52 1.382
762
KRN002 Kearns-Sayre Syndrome 63 1.382
763
CLR109 Colorectal Adenocarcinoma 50 1.382
764
ARG004 Argyria 26 1.382
765
BRN014 Bronchopneumonia 53 1.382
766
P HMR003 Hemorrhagic Disease 59 1.382
767
MTR002 Mitral Valve Insufficiency 52 1.382
768
P SCK002 Sick Sinus Syndrome 55 1.382
769
CHT001 Chaotic Atrial Tachycardia 10 1.382
770
VRS002 Virus-Associated Trichodysplasia Spinulosa 30 1.379
771
BTT018 Beta-Thalassemia Intermedia 31 1.379
772
CHR074 Choriocarcinoma 46 1.379
773
P PTT006 Pituitary Adenoma 55 1.379
774
CNT047 Contact Dermatitis 57 1.379
775
CHR028 Chronic Wasting Disease 33 1.379
776
P OST028 Osteochondroma 45 1.379
777
HMG002 Hemoglobinuria 50 1.373
778
INT002 Intermittent Claudication 61 1.373
779
RTN003 Retinal Ischemia 49 1.373
780
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 1.373
781
c ART115 Aortic Valve Disease 1 74 1.359
782
RSP019 Respiratory Distress Syndrome in Premature Infants 52 1.359
783
NWB001 Newborn Respiratory Distress Syndrome 56 1.359
784
c CNG411 Congenital Disorder of Glycosylation, Type in 67 1.350
785
DYS016 Dysgammaglobulinemia 33 1.350
786
P AML002 Amelogenesis Imperfecta 56 1.336
787
P MTR004 Maturity-Onset Diabetes of the Young 68 1.331
788
MTN003 Motion Sickness 51 1.331
789
P BRN019 Bernard-Soulier Syndrome 61 1.331
790
VRC005 Varicose Veins 60 1.331
791
P HNT016 Huntington Disease 73 1.331
792
HYP082 Hypopharynx Cancer 47 1.331
793
P MTR012 Mitral Valve Disease 57 1.331
794
MRP001 Morphine Dependence 42 1.331
795
HYP264 Hypertonia 36 1.331
796
RVR002 Reversible Cerebral Vasoconstriction Syndrome 28 1.331
797
BRX001 Bruxism 51 1.318
798
CRC021 Carcinosarcoma 64 1.317
799
IDP091 Idiopathic Nephrotic Syndrome 47 1.317
800
P FBR017 Fibrosarcoma 56 1.317
801
P OTS001 Otosclerosis 49 1.317
802
RTN020 Retinal Vascular Disease 46 1.317
803
DBT007 Diabetic Cataract 36 1.317
804
KRT008 Keratopathy 46 1.317
805
HYP057 Hypervitaminosis D 37 1.317
806
GST030 Gastrinoma 45 1.306
807
PNM008 Pneumothorax 54 1.299
808
PLY012 Polyhydramnios 46 1.299
809
P FNC004 Fanconi Syndrome 60 1.299
810
PPL022 Papilloma 53 1.299
811
ISC015 Ischemic Colitis 43 1.277
812
P GLC113 Galactosemia I 66 1.277
813
c GLY008 Glycogen Storage Disease Ii 72 1.277
814
c SML038 Small Cell Cancer of the Lung 69 1.277
815
CNT025 Central Pontine Myelinolysis 43 1.277
816
P DRM010 Dermatomyositis 61 1.277
817
ADT003 Auditory System Disease 49 1.277
818
P NMN002 Niemann-Pick Disease 60 1.277
819
P RNL015 Renal Hypertension 45 1.277
820
P PRN023 Prion Disease 60 1.277
821
P DYS005 Dyslexia 41 1.277
822
MNN017 Mononeuropathy 41 1.277
823
CHL028 Childhood Type Dermatomyositis 59 1.277
824
c ACT135 Acute Graft Versus Host Disease 51 1.277
825
LTH004 Lathyrism 15 1.277
826
FNT004 Fainting 29 1.277
827
P DYS021 Dysautonomia 38 1.277
828
LKP003 Leukoplakia 39 1.277
829
HVY002 Heavy Metal Poisoning 22 1.277
830
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 1.275
831
RYN001 Raynaud Disease 50 1.275
832
SWL001 Swallowing Disorders 38 1.274
833
P LYM033 Lymphoproliferative Syndrome 59 1.266
834
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.265
835
c MCL013 Mucolipidosis Iv 65 1.263
836
c OVR114 Ovarian Cancer 1 59 1.263
837
P ALG028 Alagille Syndrome 1 73 1.259
838
BLR028 Biliary Atresia, Extrahepatic 36 1.259
839
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 1.259
840
PPL001 Papillary Adenoma 44 1.259
841
c THY107 Thymoma, Familial 42 1.250
842
AVN001 Avian Influenza 61 1.250
843
P THY023 Thymoma 64 1.250
844
ERY069 Erythrokeratoderma ''en Cocardes'' 27 1.250
845
MDL009 Medullary Sponge Kidney 39 1.250
846
P NJM001 Nijmegen Breakage Syndrome 76 1.246
847
CLN019 Colonic Disease 47 1.246
848
ACT011 Acute Contagious Conjunctivitis 42 1.246
849
P GLL018 Gallbladder Cancer 53 1.234
850
BSL009 Basal Ganglia Calcification 45 1.220
851
CRT012 Cortical Blindness 42 1.220
852
SCR039 Scorpion Envenomation 41 1.219
853
c CTR132 Cataract 3, Multiple Types 42 1.219
854
MRF001 Marfan Syndrome 76 1.219
855
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 1.219
856
SXL003 Sexual Disorder 49 1.219
857
MLD018 Mild Cognitive Impairment 48 1.219
858
HTC003 Hutchinson-Gilford Progeria Syndrome 65 1.219
859
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 1.219
860
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.219
861
c PRK058 Parkinson Disease 16 18 1.219
862
PRP083 Porphyria, Acute Intermittent 65 1.219
863
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 1.219
864
P STR020 Strabismus 56 1.219
865
c SZR022 Seizures, Benign Familial Neonatal, 1 43 1.219
866
MCH006 Mechanical Strabismus 40 1.219
867
INT011 Interstitial Emphysema 33 1.219
868
TRY001 Trypanosomiasis 50 1.219
869
c ACT004 Acute Diarrhea 40 1.219
870
CHG001 Chagas Disease 66 1.219
871
PCD001 Pica Disease 38 1.219
872
ACR007 Acromegaly 70 1.219
873
NNT012 Neonatal Jaundice 53 1.219
874
MLG169 Malignant Astrocytoma 57 1.219
875
OST016 Osteochondrosis 52 1.219
876
GNG013 Gingivitis 59 1.219
877
OPD001 Opioid Abuse 44 1.219
878
RGH001 Right Bundle Branch Block 47 1.219
879
TLR001 Tularemia 56 1.219
880
END028 Endemic Goiter 41 1.219
881
DWR001 Dwarfism 44 1.219
882
IDP022 Idiopathic Spinal Cord Herniation 17 1.219
883
CRN270 Coronary Artery Dissection, Spontaneous 32 1.218
884
TNS007 Taeniasis 46 1.214
885
P SPP010 Suppressor of Tumorigenicity 3 51 1.214
886
P PMP001 Pemphigus 55 1.214
887
ANK001 Ankylosis 51 1.214
888
c HYP608 Hypocalciuric Hypercalcemia, Familial, Type Iii 42 1.191
889
c HYP794 Hyperoxaluria, Primary, Type I 63 1.191
890
FML315 Familial Primary Hypomagnesemia with Normocalciuria and Normocalcemia 22 1.188
891
P MSC003 Muscular Atrophy 52 1.178
892
P LRY019 Laryngitis 53 1.177
893
GLL008 Gilles De La Tourette Syndrome 65 1.176
894
CMP034 Complete Androgen Insensitivity Syndrome 55 1.176
895
TYP007 Typhoid Fever 64 1.176
896
MGC001 Megacolon 48 1.176
897
MCR017 Macrocytic Anemia 44 1.176
898
CMB007 Combined Immunodeficiency 57 1.166
899
HTT002 Hutterite Cerebroosteonephrodysplasia Syndrome 25 1.158
900
PNM013 Pneumococcal Meningitis 43 1.158
901
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 1.158
903
PRT010 Parathyroid Carcinoma 68 1.158
904
DYS017 Dysgerminoma of Ovary 37 1.158
905
CRN030 Coronary Stenosis 50 1.158
906
PRD002 Periodic Limb Movement Disorder 34 1.158
907
MLT006 Multidrug-Resistant Tuberculosis 47 1.158
908
GLC008 Glucose Metabolism Disease 40 1.158
909
DYS101 Dysgerminoma 44 1.158
910
ANT024 Anthrax Disease 58 1.158
911
GST007 Gastric Dilatation 30 1.158
912
c PLM128 Pulmonary Hypertension, Primary, 2 28 1.158
913
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.158
914
NRG002 Neurogenic Bladder 55 1.158
915
P FCL005 Focal Segmental Glomerulosclerosis 57 1.158
916
TRN015 Transient Cerebral Ischemia 63 1.158
917
FCL014 Focal Epilepsy 53 1.158
918
SCH014 Schistosomiasis 56 1.158
919
P MCR010 Microcephaly 60 1.158
920
ADJ001 Adjustment Disorder 47 1.158
921
PLG002 Plague 58 1.158
922
OLG001 Oligospermia 45 1.158
923
DNT008 Denture Stomatitis 35 1.158
924
ESN002 Eosinophilia-Myalgia Syndrome 40 1.158
925
HRP004 Herpes Zoster 61 1.158
926
MYC019 Mycobacterium Marinum 29 1.158
927
CHL079 Children's Interstitial Lung Disease 26 1.153
928
P HRP006 Herpes Simplex 65 1.136
929
HRT011 Heart Septal Defect 49 1.136
930
GLM045 Glioma 63 1.136
931
PNC129 Pancreatic Adenocarcinoma 65 1.115
932
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 64 1.106
933
c THR124 Thrombotic Thrombocytopenic Purpura, Hereditary 53 1.104
934
MNN042 Meningioma, Radiation-Induced 51 1.104
935
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 57 1.104
936
c INF071 Inflammatory Bowel Disease 1 65 1.104
937
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.104
938
OCL006 Ocular Hypertension 53 1.104
939
TMP019 Temporomandibular Joint Anomaly 28 1.104
940
P AGN002 Agnosia 54 1.104
941
INT053 Intracranial Vasospasm 36 1.104
942
SPN027 Spinal Stenosis 59 1.104
943
c THR044 Thrombotic Thrombocytopenic Purpura, Acquired 26 1.104
944
CYT004 Cytomegalic Inclusion Disease 31 1.104
945
MNS015 Monosodium Glutamate Sensitivity 18 1.091
946
c CHR418 Chronic Leukemia 48 1.091
947
EXT034 Extrinsic Allergic Alveolitis 57 1.091
948
CCC002 Coccidiosis 50 1.091
949
XRD010 Xeroderma Pigmentosum, Variant Type 73 1.091
950
P SRC025 Sarcoidosis 1 71 1.091
951
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 1.091
952
GLL048 Glial Tumor 52 1.091
953
TRP020 Tropical Endomyocardial Fibrosis 36 1.090
954
LPD012