Search results for sodium

5213 hits were found for sodium

# Family MCID Name MIFTS Score
1
DRR017 Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies 36 50.910
2
DRR013 Diarrhea 8, Secretory Sodium, Congenital 36 37.652
3
SDM005 Sodium Serum Level Quantitative Trait Locus 1 10 27.474
5
SDM006 Sodium Aurothiomalate Allergy 5 21.085
6
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 21.053
7
MYT030 Myotonia, Potassium-Aggravated 48 20.710
8
c HYP595 Hypertension, Essential 84 19.641
9
OVR093 Overhydrated Hereditary Stomatocytosis 41 19.097
10
SYN164 Syndromic Congenital Sodium Diarrhea 8 18.140
11
P NRL027 Neurological Muscular Channelopathy Due to a Genetic Sodium Channel Defect 3 17.037
12
c NRL035 Neurological Channelopathy of the Central Nervous System Due to a Genetic Sodium Channel Defect 2 17.037
13
CLT003 Colitis 63 16.570
14
HYP052 Hyperkalemic Periodic Paralysis 62 14.968
15
c CHR684 Chronic Kidney Disease 73 12.648
16
P KDN018 Kidney Disease 71 12.622
17
HYP005 Hypokalemia 55 12.103
18
NRD106 Neurodegeneration, Infantile-Onset, Biotin-Responsive 23 11.910
19
c TYP009 Type 2 Diabetes Mellitus 91 11.729
20
MTB004 Metabolic Acidosis 48 10.785
21
CNG034 Congestive Heart Failure 69 10.779
22
P DBT009 Diabetes Mellitus 67 10.432
23
OST012 Osteoarthritis 77 10.399
24
ULC004 Ulcerative Colitis 74 10.051
25
CYS001 Cystic Fibrosis 77 9.786
26
c ACT071 Acute Kidney Failure 60 9.387
27
48X005 48,xyyy 39 9.376
28
c MGR028 Migraine with or Without Aura 1 63 8.900
29
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 8.800
30
P SZR006 Seizure Disorder 69 8.743
31
END086 End Stage Renal Disease 54 8.742
32
P HRT032 Heart Disease 84 8.578
33
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 8.461
34
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 8.461
35
P OST002 Osteoporosis 76 8.457
36
CRH001 Crohn's Disease 80 8.227
37
ALL029 Allergic Disease 61 8.191
38
P EPL164 Epilepsy 70 7.991
39
P DRR001 Diarrhea 55 7.972
40
c PNS012 Paine Syndrome 60 7.903
41
P KLZ004 Kala-Azar 1 41 7.770
42
LSH001 Leishmaniasis 63 7.770
43
DNT012 Dental Caries 53 7.637
44
P NRB001 Neuroblastoma 66 7.522
45
c MCR120 Microvascular Complications of Diabetes 7 47 7.432
46
PRT251 Proteinuria, Chronic Benign 58 7.362
47
P INF037 Inflammatory Bowel Disease 53 7.362
48
P BPL003 Bipolar Disorder 56 7.361
49
c MJR022 Major Affective Disorder 8 37 7.345
50
c MJR024 Major Affective Disorder 9 40 7.345
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 7.192
52
HYP056 Hypoglycemia 65 7.158
53
ISC004 Ischemia 61 7.133
54
c MCR113 Microvascular Complications of Diabetes 3 52 7.125
55
P BRG001 Brugada Syndrome 69 7.016
56
c THR092 Thrombophilia Due to Thrombin Defect 74 6.997
57
P HYP086 Hypothyroidism 68 6.906
58
P RHN004 Rhinitis 56 6.904
59
HYP066 Hyperglycemia 60 6.882
60
AGN016 Aging 53 6.881
61
P PLM037 Pulmonary Hypertension 69 6.832
62
c MCR133 Microvascular Complications of Diabetes 4 41 6.824
63
c MCR130 Microvascular Complications of Diabetes 6 41 6.824
64
ADL002 Adult Syndrome 69 6.764
65
P URN019 Urinary Tract Infection 48 6.762
66
P HDC001 Headache 56 6.606
67
P CTR002 Cataract 59 6.548
68
PNG002 Pain Agnosia 51 6.543
69
P NRC002 Narcolepsy 55 6.532
70
GLL048 Glial Tumor 51 6.502
71
GLM045 Glioma 62 6.495
72
RPD005 Rapidly Involuting Congenital Hemangioma 48 6.479
73
c ACT068 Acute Cystitis 60 6.393
74
LVR012 Liver Cirrhosis 62 6.347
75
HRW001 Hair Whorl 35 6.313
76
P CRD119 Cardiac Arrest 68 6.308
77
DBT084 Diabetes Mellitus, Ketosis-Prone 59 6.307
78
P PRD021 Periodic Paralysis 42 6.249
79
PRT036 Peritonitis 65 6.243
80
c ACT027 Acute Pancreatitis 60 6.240
81
P PNC044 Pancreatitis 61 6.173
82
P CNJ013 Conjunctivitis 66 6.143
83
P LVR013 Liver Disease 68 6.130
84
PLM010 Pulmonary Edema 54 6.124
85
P ENC018 Encephalopathy 62 6.119
86
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 6.073
87
CNS004 Constipation 56 6.070
88
ALL003 Allergic Rhinitis 66 6.054
89
NPH009 Nephrolithiasis 54 6.007
90
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 5.999
91
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 5.990
92
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 5.990
93
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 5.990
94
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 5.990
95
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 5.990
96
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 5.990
97
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 5.990
98
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 5.990
99
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 5.990
100
P MYC007 Myocardial Infarction 69 5.987
101
THY029 Thyroid Carcinoma 55 5.962
102
P PRS040 Prostate Cancer 95 5.901
103
P LNG028 Long Qt Syndrome 63 5.900
104
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 5.868
106
KRT006 Keratoconjunctivitis 53 5.833
107
P NPH012 Nephrotic Syndrome 61 5.829
108
c HYP836 Hypercholesterolemia, Familial, 1 73 5.829
109
MYT011 Myotonia 37 5.791
110
P DBT005 Diabetes Insipidus 54 5.768
111
DRM006 Dermatitis 61 5.747
112
c TYP008 Type 1 Diabetes Mellitus 77 5.715
113
P ESP024 Esophagitis 60 5.713
114
P VSC007 Vascular Disease 62 5.705
115
DFC004 Deficiency Anemia 74 5.680
116
c EPS039 Episodic Pain Syndrome, Familial, 1 42 5.582
117
GST092 Gastroesophageal Reflux 59 5.574
118
P PRD008 Periodontitis 63 5.555
119
HYP266 Hypoxia 56 5.540
120
BRN071 Brain Injury 50 5.536
121
P CHR345 Chronic Pain 50 5.504
122
c PLM164 Pulmonary Hypertension, Primary, 1 75 5.497
123
CNT047 Contact Dermatitis 56 5.468
124
NNL005 Non-Alcoholic Fatty Liver Disease 63 5.455
125
VSC003 Visceral Leishmaniasis 54 5.446
126
IRN002 Iron Metabolism Disease 56 5.356
127
P AST005 Asthma 75 5.320
128
P NRP001 Neuropathy 59 5.319
129
TXC005 Toxic Shock Syndrome 61 5.280
130
GNG013 Gingivitis 59 5.260
131
THR024 Thrombosis 56 5.249
132
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 5.247
133
GLB002 Glioblastoma 67 5.222
134
CLC001 Calciphylaxis 50 5.211
135
DRY001 Dry Eye Syndrome 49 5.193
136
TRM010 Traumatic Brain Injury 50 5.185
137
BNR002 Bone Resorption Disease 47 5.164
138
P EYD002 Eye Disease 57 5.159
139
P ANR048 Aniridia 1 66 5.155
140
P CYS018 Cystitis 58 5.126
141
ALC007 Alcohol Dependence 65 5.106
142
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 5.101
143
P TRM003 Tremor 50 5.098
144
ANT039 Antisynthetase Syndrome 55 5.078
145
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.074
146
ATH013 Atherosclerosis Susceptibility 63 5.070
147
PRS047 Prostatitis 57 5.060
148
P ADN016 Adenocarcinoma 63 5.055
149
P CRN300 Coronary Heart Disease 1 73 5.052
150
CTN007 Cutaneous Leishmaniasis 61 4.993
151
c MCR115 Microvascular Complications of Diabetes 5 65 4.983
152
P CLR023 Colorectal Cancer 100 4.948
153
P TRN020 Turner Syndrome 67 4.946
154
P LNG032 Lung Cancer 98 4.922
155
STT001 Status Epilepticus 58 4.919
156
P PNM007 Pneumonia 64 4.907
157
FTT001 Fatty Liver Disease 61 4.906
158
DWN001 Down Syndrome 70 4.906
159
P ADL010 Adult Respiratory Distress Syndrome 70 4.899
160
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.864
161
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 60 4.848
162
LNG099 Lung Disease 62 4.842
163
STR067 Stroke, Ischemic 79 4.827
164
P RSP003 Respiratory Failure 73 4.808
165
CRD132 Cardiac Conduction Defect 59 4.798
166
c ACT075 Acute Myocardial Infarction 55 4.793
167
P GLM007 Glomerulonephritis 59 4.785
168
RCK004 Rickets 64 4.779
169
PLM033 Pulmonary Embolism 58 4.776
170
P LDD007 Liddle Syndrome 1 57 4.769
171
OCL069 Ocular Motor Apraxia 57 4.767
172
STM007 Stomatitis 52 4.725
173
CHL014 Cholera 62 4.719
174
EXR010 Exercise-Induced Bronchoconstriction 34 4.704
175
HYP060 Hyperinsulinism 53 4.694
176
RHB024 Rhabdomyosarcoma 2 65 4.690
177
KRT001 Keratoconjunctivitis Sicca 49 4.683
178
ALL009 Allergic Conjunctivitis 51 4.681
179
P HPT021 Hepatitis 68 4.680
180
OST062 Osteoarthritis with Mild Chondrodysplasia 46 4.671
181
CRB039 Cerebrovascular Disease 65 4.662
182
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 4.660
183
HMN044 Human Immunodeficiency Virus Type 1 76 4.658
184
P HPT023 Hepatocellular Carcinoma 95 4.654
185
P ERY008 Erythromelalgia 50 4.630
186
P THR014 Thrombocytopenia 66 4.629
187
P DRM053 Dermatitis, Atopic 65 4.629
188
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 4.621
189
P FBR031 Febrile Seizures 52 4.599
190
P BND020 Bone Disease 60 4.590
191
PRM057 Paramyotonia Congenita of Von Eulenburg 59 4.589
192
P ATR011 Atrial Fibrillation 66 4.588
193
HPT004 Hepatic Coma 43 4.562
194
P LCT001 Lactic Acidosis 50 4.555
195
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 4.537
196
P MLT020 Multiple Sclerosis 79 4.536
197
LPD008 Lipid Metabolism Disorder 61 4.533
198
P SCH015 Schizophrenia 74 4.529
199
BCT022 Bacterial Infectious Disease 55 4.518
200
MCL006 Macular Retinal Edema 56 4.517
201
HLX001 Helix Syndrome 47 4.517
202
MCS002 Mucositis 55 4.487
203
ADN018 Adenoma 58 4.482
204
P INT143 Interstitial Cystitis 59 4.480
205
P BRS047 Breast Cancer 97 4.461
206
c PRC016 Pre-Eclampsia 64 4.458
207
HPT019 Hepatic Encephalopathy 59 4.421
208
P EXN002 Exanthem 58 4.411
209
P ART022 Arthritis 70 4.406
210
P ALC033 Alcohol Use Disorder 67 4.406
211
P RNL015 Renal Hypertension 45 4.402
212
HGH043 High Grade Glioma 46 4.397
213
P PRP019 Peripheral Nervous System Disease 57 4.391
214
URL001 Urolithiasis 45 4.389
215
PLM129 Pulmonary Disease, Chronic Obstructive 74 4.387
216
KRT009 Keratosis 52 4.372
217
HYP025 Hyperphosphatemia 47 4.372
218
P RNL007 Renal Tubular Acidosis 52 4.359
219
ESP021 Esophageal Cancer 84 4.354
220
CYT002 Cytokine Deficiency 43 4.348
221
ACQ007 Acquired Immunodeficiency Syndrome 58 4.341
222
LPP008 Lipoprotein Quantitative Trait Locus 65 4.339
223
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 4.310
224
NPH091 Nephrolithiasis, Calcium Oxalate 61 4.305
225
CHL068 Cholestasis 61 4.294
226
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 4.293
227
P SLP006 Sleep Apnea 69 4.289
228
P LTR001 Lateral Sclerosis 57 4.280
229
P GLM040 Glioma Susceptibility 1 70 4.278
230
c AMY091 Amyotrophic Lateral Sclerosis 1 87 4.276
231
PRT037 Pertussis 49 4.275
232
DRV001 Dravet Syndrome 69 4.270
233
P PLY014 Polycystic Kidney Disease 71 4.269
234
P LKM002 Leukemia 65 4.268
235
c ATR087 Atrial Standstill 1 74 4.260
236
BRN004 Brain Edema 54 4.236
237
CLC006 Calcinosis 47 4.228
238
P MYP004 Myopathy 67 4.217
239
P GST053 Gastric Cancer 82 4.210
240
ART140 Arteries, Anomalies of 52 4.190
241
P ALZ034 Alzheimer Disease 87 4.147
242
DBT010 Diabetic Neuropathy 54 4.129
243
c SML038 Small Cell Cancer of the Lung 68 4.119
244
KRT002 Keratomalacia 54 4.115
245
MYL069 Myeloma, Multiple 76 4.112
246
GST023 Gastric Ulcer 52 4.109
247
VRC005 Varicose Veins 59 4.079
248
P MJR007 Major Affective Disorder 1 42 4.065
249
c LKM061 Leukemia, Acute Myeloid 83 4.063
250
CNT025 Central Pontine Myelinolysis 42 4.035
251
P LPS004 Lupus Erythematosus 61 4.027
252
P THY032 Thyroiditis 56 4.018
253
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 59 4.016
254
c LNG048 Long Qt Syndrome 3 52 3.965
255
c BLD140 Blood Group, I System 47 3.962
256
P PSD003 Pseudohypoaldosteronism 45 3.956
257
SPN186 Spinal Cord Injury 60 3.935
258
ARG004 Argyria 26 3.917
259
c SYS001 Systemic Lupus Erythematosus 85 3.906
260
P SCK005 Sickle Cell Disease 56 3.903
261
P MYL006 Myeloid Leukemia 60 3.902
262
HYP014 Hyperuricemia 51 3.896
263
PRP027 Peripheral Vascular Disease 71 3.894
264
c HPT003 Hepatitis a 63 3.892
265
SPN035 Spindle Cell Sarcoma 51 3.890
266
INT075 Intracranial Hypertension 52 3.888
267
INP001 Inappropriate Adh Syndrome 48 3.887
268
ANG054 Angina Pectoris 65 3.859
269
INT323 Intraocular Pressure Quantitative Trait Locus 63 3.854
270
SRC014 Sarcoma 64 3.849
271
AND005 Androgen Insensitivity Syndrome, Mild 21 3.839
272
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 3.837
273
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 3.832
274
P BRT004 Bartter Disease 58 3.826
275
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 3.805
276
KHN001 Kuhnt-Junius Degeneration 48 3.803
277
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 3.796
278
THY030 Thyroid Gland Disease 50 3.778
279
CRD223 Cardiac Arrhythmia 63 3.755
280
P CRD246 Cardiovascular System Disease 55 3.754
281
CVD001 Covid-19 59 3.750
282
GT001 Gout 63 3.744
283
ATM095 Autoimmune Disease 61 3.744
284
P RNV001 Renovascular Hypertension 48 3.739
285
OST159 Osteogenic Sarcoma 66 3.731
286
SCH036 Scheie Syndrome 73 3.729
287
URM002 Uremia 47 3.727
288
P DDN001 Duodenal Ulcer 52 3.723
289
P MSC005 Muscular Dystrophy 66 3.703
290
P DNT007 Dentin Sensitivity 35 3.694
291
CRB004 Cerebral Artery Occlusion 45 3.682
292
P MLN008 Melanoma 75 3.668
293
PRT013 Portal Hypertension 59 3.663
294
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.660
295
HYP017 Hypophosphatemia 49 3.660
296
ANX004 Anoxia 40 3.658
297
P ACT008 Actinic Keratosis 53 3.656
298
NNL006 Non-Alcoholic Steatohepatitis 54 3.644
299
NRR001 Neuroretinitis 42 3.644
300
P SJG008 Sjogren Syndrome 60 3.639
301
P HYP069 Hyperparathyroidism 62 3.638
302
RTN023 Retinitis 45 3.638
303
PRX015 Paroxysmal Extreme Pain Disorder 56 3.636
304
FBR047 Fibromyalgia 57 3.633
305
c DLT002 Dilated Cardiomyopathy 79 3.631
306
NTR005 Nutritional Deficiency Disease 60 3.615
307
c HPT016 Hepatitis B 62 3.613
308
P GST044 Gastritis 55 3.595
309
PPT001 Peptic Esophagitis 51 3.584
310
P PRK039 Parkinsonism 55 3.572
311
SKN016 Skin Disease 63 3.568
312
P RHM011 Rheumatoid Arthritis 81 3.563
313
LYM019 Lymphosarcoma 46 3.555
314
GST045 Gastroenteritis 58 3.553
315
c CHR711 Chronic Asthma 41 3.546
316
GTL001 Gitelman Syndrome 65 3.545
317
P NTR004 Neutropenia 62 3.537
318
CYN003 Cyanide Poisoning 22 3.537
319
P LYM118 Lymphoma 66 3.526
320
P ECL001 Eclampsia 52 3.525
321
IRR003 Irritant Dermatitis 47 3.518
322
P HRP006 Herpes Simplex 65 3.501
323
BCK006 Back Pain 43 3.499
324
P ATS364 Autism 72 3.495
325
P PNC035 Pancreatic Cancer 87 3.494
326
P MCR129 Microvascular Complications of Diabetes 1 67 3.479
327
P HYP076 Hyperthyroidism 53 3.477
328
c PRM108 Primary Progressive Multiple Sclerosis 51 3.463
329
P FNC004 Fanconi Syndrome 60 3.459
330
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.435
331
47X002 47,xyy 47 3.431
332
P PHC003 Pheochromocytoma 70 3.400
333
ADR040 Adrenal Gland Pheochromocytoma 45 3.400
334
P PNC025 Panic Disorder 52 3.393
335
P PRS038 Personality Disorder 65 3.385
336
c BRG005 Brugada Syndrome 1 56 3.378
337
c CRN243 Carney Complex, Type 1 53 3.376
338
MYL009 Myelodysplastic Syndrome 67 3.365
339
SPS057 Spasticity 43 3.362
340
SCK003 Sickle Cell Anemia 74 3.335
341
APP015 Apparent Mineralocorticoid Excess 57 3.302
342
MST005 Mastitis 52 3.274
343
ALL010 Allergic Contact Dermatitis 55 3.269
344
FCL014 Focal Epilepsy 53 3.239
345
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 3.231
346
SVR001 Severe Acute Respiratory Syndrome 68 3.204
347
MDD011 Mood Disorder 61 3.182
348
ERL001 Early Myoclonic Encephalopathy 62 3.163
349
RTN017 Retinal Detachment 60 3.162
350
P BCL017 B-Cell Lymphoma 57 3.160
351
P CND004 Candidiasis 57 3.149
352
c PRS130 Prostate Cancer, Hereditary, 8 32 3.147
353
c PRS136 Prostate Cancer, Hereditary, 6 33 3.147
354
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 3.146
355
P OVR042 Ovarian Cancer 88 3.146
356
P UVT001 Uveitis 57 3.144
357
P MTH007 Methemoglobinemia 46 3.116
358
TND005 Tendinitis 53 3.115
359
PPT005 Peptic Ulcer Disease 58 3.105
360
SYN036 Syncope 44 3.103
361
IMP005 Impotence 52 3.098
362
P BLD134 Bladder Cancer 79 3.096
363
c BRN108 Branchiootic Syndrome 1 63 3.092
364
SBC016 Subacute Delirium 42 3.085
365
ENT004 Enthesopathy 51 3.078
366
PRT058 Pure Autonomic Failure 58 3.070
367
ATX019 Ataxia with Vitamin E Deficiency 44 3.064
368
DBT006 Diabetic Macular Edema 48 3.057
369
PSY004 Psychotic Disorder 66 3.055
370
P HYP098 Hypereosinophilic Syndrome 66 3.052
371
PST092 Posttransplant Acute Limbic Encephalitis 29 3.049
372
P MLG056 Malignant Hyperthermia 65 3.043
373
P URT039 Urticaria 57 3.039
374
P LKM062 Leukemia, Acute Lymphoblastic 69 3.038
375
SQM006 Squamous Cell Carcinoma 59 3.035
376
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.035
377
EPT021 Epithelial Recurrent Erosion Dystrophy 45 3.026
378
GTR002 Goiter 52 3.024
379
ANX010 Anxiety 70 3.019
380
KRT019 Keratitis, Hereditary 66 3.009
381
TTN003 Tetanus 64 2.997
382
P DYS154 Dystonia 64 2.994
383
c GLL024 Gallbladder Disease 1 53 2.990
384
P SLP005 Sleep Disorder 61 2.988
385
GLS018 Glass Syndrome 60 2.987
386
c MCR112 Microvascular Complications of Diabetes 2 42 2.982
387
DYS073 Dysphagia 53 2.981
388
PRS045 Prostatic Hypertrophy 53 2.967
389
MNT002 Mental Depression 56 2.963
390
PLM001 Pulmonary Tuberculosis 69 2.959
391
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.959
392
IRN001 Iron Deficiency Anemia 58 2.957
393
PST011 Pustulosis of Palm and Sole 52 2.949
394
GNT046 Genetic Epilepsy with Febrile Seizures Plus 30 2.949
395
c DRR009 Diarrhea 6 46 2.937
396
P BNG032 Benign Mesothelioma 53 2.936
397
P PSR002 Psoriasis 63 2.936
398
LNG031 Lung Benign Neoplasm 51 2.934
399
P HYP750 Hypertriglyceridemia, Familial 61 2.934
400
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 2.934
401
ERY029 Erythermalgia, Primary 57 2.931
402
NPH003 Nephrocalcinosis 49 2.930
403
P FML187 Familial Hypertension 34 2.920
404
PLP001 Pulpitis 48 2.908
405
SFT003 Soft Tissue Sarcoma 43 2.904
406
URC002 Urea Cycle Disorder 51 2.901
407
P THL005 Thalassemia 56 2.893
408
NWB001 Newborn Respiratory Distress Syndrome 56 2.891
409
P MNN013 Meningitis 65 2.881
410
IMM167 Immune Deficiency Disease 76 2.873
411
APN008 Apnea, Obstructive Sleep 66 2.865
412
ENT011 Enterocolitis 55 2.859
413
P SCK002 Sick Sinus Syndrome 55 2.857
414
P PYL005 Pyelonephritis 56 2.852
415
INT002 Intermittent Claudication 61 2.852
416
P LKM071 Leukemia, Chronic Lymphocytic 74 2.849
417
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 2.849
418
ATS010 Autosomal Recessive Disease 42 2.849
419
MSC007 Muscle Hypertrophy 64 2.847
420
MLG169 Malignant Astrocytoma 57 2.844
421
P HMN010 Hemangioma 61 2.838
422
BRN028 Brain Cancer 73 2.838
423
c ATS007 Autism Spectrum Disorder 71 2.837
424
TND004 Tendinopathy 45 2.836
425
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 2.831
426
PPL052 Papillomatosis, Confluent and Reticulated 34 2.830
427
CLN015 Colon Adenocarcinoma 64 2.827
428
SCR003 Secretory Diarrhea 35 2.824
429
PRS021 Prostatic Adenoma 43 2.824
430
P MTR014 Motor Neuron Disease 65 2.814
431
P NRV007 Nervous System Disease 65 2.813
432
P AMY004 Amyloidosis 69 2.812
433
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.807
434
ACT003 Acute Kidney Tubular Necrosis 46 2.802
435
MLR004 Malaria 77 2.798
436
ALL006 Allergic Asthma 55 2.794
437
P MSC003 Muscular Atrophy 52 2.791
438
IDP033 Idiopathic Edema 41 2.786
439
P PLM036 Pulmonary Fibrosis 65 2.784
440
P DST107 Distal Renal Tubular Acidosis 48 2.781
441
c MJR006 Major Affective Disorder 5 32 2.778
442
c MJR003 Major Affective Disorder 6 32 2.778
443
GLC003 Glucose Intolerance 53 2.777
444
DPR016 Depression 64 2.776
445
P PRD017 Periodic Paralyses 24 2.750
446
P GRV001 Graves' Disease 54 2.750
447
c PRG042 Progressive Familial Heart Block, Type Ia 65 2.742
448
BRN024 Bronchitis 67 2.740
449
PRP080 Peripheral Artery Disease 54 2.740
450
P PRK057 Parkinson Disease, Late-Onset 79 2.736
451
ANR040 Aneurysm 60 2.729
452
HPT014 Hepatorenal Syndrome 49 2.724
453
OST017 Osteomyelitis 63 2.716
454
HPR003 Heparin-Induced Thrombocytopenia 47 2.713
455
BRN002 Bronchiolitis 57 2.702
456
P HYP120 Hypoaldosteronism 33 2.701
457
P ATT013 Attention Deficit-Hyperactivity Disorder 65 2.701
458
DSS032 Disease by Infectious Agent 55 2.698
459
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 2.696
460
c MJR008 Major Affective Disorder 2 34 2.695
461
c MJR023 Major Affective Disorder 7 33 2.695
462
c MJR004 Major Affective Disorder 4 28 2.695
463
WTH001 Withdrawal Disorder 47 2.688
464
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.686
465
SCH014 Schistosomiasis 56 2.686
466
P RTN018 Retinal Disease 53 2.683
467
P ACN011 Acne 55 2.672
468
c INH020 Inherited Metabolic Disorder 47 2.672
469
CNN003 Conn's Syndrome 77 2.658
470
BRN056 Bronchopulmonary Dysplasia 57 2.656
471
TRG002 Trigeminal Neuralgia 61 2.656
472
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 2.655
473
DSS009 Disseminated Intravascular Coagulation 56 2.655
474
ENM002 Enamel Erosion 25 2.653
475
END057 Endometrial Cancer 76 2.650
476
HPT022 Hepatoblastoma 54 2.644
477
ACR007 Acromegaly 70 2.643
478
c SCL052 Scleroderma, Familial Progressive 60 2.638
479
MSC157 Muscular Dystrophy, Duchenne Type 78 2.627
480
TLN003 Telangiectasis 51 2.624
481
PRS129 Prostatic Hyperplasia, Benign 48 2.623
482
CRB086 Cerebral Aneurysms 40 2.621
483
c FML191 Familial Long Qt Syndrome 54 2.618
484
c HPT001 Hepatitis C 61 2.610
485
P INF032 Infertility 60 2.602
486
P ANP001 Anaplastic Large Cell Lymphoma 59 2.593
487
IRR002 Irritable Bowel Syndrome 64 2.592
488
MMM001 Mammary Paget's Disease 53 2.591
489
AMN003 Amnestic Disorder 53 2.588
490
P ALP008 Alopecia 53 2.587
491
INS024 Insulin-Like Growth Factor I 77 2.585
492
EPC002 Epicondylitis 43 2.583
493
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 2.582
494
P ART021 Arteriosclerosis 53 2.580
495
INT007 Intermediate Coronary Syndrome 53 2.577
496
P MYC033 Myoclonus 46 2.563
497
CHL065 Cholangiocarcinoma 57 2.563
498
INT079 Intrahepatic Cholangiocarcinoma 51 2.563
499
IGG001 Iga Glomerulonephritis 50 2.560
500
LYM143 Lymphoma, Non-Hodgkin, Familial 74 2.559
501
SQM013 Squamous Cell Carcinoma, Head and Neck 75 2.559
502
IFP003 Ifap Syndrome 2 41 2.553
503
HMP005 Hemiplegia 53 2.552
504
P HYP024 Hypoparathyroidism 55 2.548
505
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 2.541
506
P RTN016 Retinal Degeneration 52 2.540
507
P TMP001 Temporal Lobe Epilepsy 49 2.536
508
P HRD086 Hereditary Hypophosphatemic Rickets 40 2.532
509
P INF038 Influenza 68 2.526
510
ETN001 Eating Disorder 59 2.525
511
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.525
512
P SYS005 Systemic Scleroderma 73 2.525
513
P MYC084 Mycobacterium Tuberculosis 1 68 2.523
514
OTT002 Otitis Media 70 2.517
515
KPS004 Kaposi Sarcoma 76 2.516
517
P MGR001 Migraine Without Aura 48 2.506
518
LMB062 Limb Ischemia 55 2.503
519
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 2.499
520
P MDL005 Medulloblastoma 75 2.493
521
MSL001 Measles 61 2.490
522
P HYP061 Hypertrophic Cardiomyopathy 68 2.486
523
ALL014 Allergic Encephalomyelitis 34 2.486
524
BRR014 Barrett Esophagus 66 2.485
525
RSP019 Respiratory Distress Syndrome in Premature Infants 52 2.482
526
PLC002 Plica Syndrome 35 2.478
527
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 2.476
528
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 2.476
529
SYN007 Synovitis 54 2.476
530
P DRM010 Dermatomyositis 61 2.473
531
HDN002 Head Injury 44 2.463
532
P ART023 Arthropathy 59 2.460
533
SDD001 Sudden Infant Death Syndrome 60 2.458
534
RLP002 Relapsing-Remitting Multiple Sclerosis 56 2.457
535
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 2.457
536
P RTN022 Retinal Vein Occlusion 54 2.456
537
SCH012 Schizoaffective Disorder 49 2.445
538
TNS005 Tonsillitis 57 2.443
539
ACT113 Acute Myeloblastic Leukemia with Maturation 46 2.434
540
c BPL002 Bipolar I Disorder 47 2.430
541
MCL027 Macular Dystrophy, Dominant Cystoid 51 2.429
542
HNS001 Hansen's Disease 32 2.424
543
P LPR021 Leprosy 3 71 2.420
544
P GRF003 Graft-Versus-Host Disease 71 2.418
545
P NJM001 Nijmegen Breakage Syndrome 75 2.414
546
DNT006 Dental Pulp Necrosis 43 2.409
547
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.407
548
CHL067 Cholecystitis 59 2.399
549
c ACT073 Acute Leukemia 59 2.386
550
PPL022 Papilloma 53 2.386
551
P INT068 Intestinal Disease 53 2.384
552
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 2.378
553
RTC003 Root Caries 33 2.361
554
GLC086 Glucocorticoid-Induced Osteoporosis 43 2.353
555
BLR008 Bilirubin Metabolic Disorder 57 2.353
556
HRT015 Heritable Pulmonary Arterial Hypertension 46 2.342
557
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 2.341
558
HRP004 Herpes Zoster 60 2.340
559
ART016 Aortic Aneurysm 68 2.340
560
P ERL057 Early Infantile Epileptic Encephalopathy 61 2.336
561
ILS001 Ileus 49 2.336
562
DMY004 Demyelinating Disease 50 2.331
563
P MYC008 Myocarditis 59 2.330
564
c BTT014 Beta-Thalassemia 72 2.329
565
CMM005 Common Cold 55 2.328
566
IDP073 Idiopathic Hypercalciuria 41 2.323
567
SQM002 Squamous Cell Papilloma 45 2.321
568
GST050 Gastrointestinal System Disease 55 2.320
569
P RTN024 Retinoblastoma 72 2.315
570
P KDN017 Kidney Cancer 60 2.310
571
URN010 Urinary Tract Obstruction 55 2.304
572
P INT070 Intestinal Obstruction 57 2.303
573
P HNT016 Huntington Disease 73 2.301
574
HMN047 Human Cytomegalovirus Infection 59 2.286
575
P HYP733 Hypercalciuria, Absorptive, 2 45 2.285
576
VGN023 Vaginitis 56 2.283
577
c THY109 Thyroid Cancer, Nonmedullary, 1 55 2.276
578
c ART101 Aortic Valve Disease 2 65 2.274
579
FNG017 Fungal Infectious Disease 54 2.274
580
c DNT047 Dentinogenesis Imperfecta Type 2 35 2.260
581
MCC002 Mucocutaneous Leishmaniasis 47 2.253
582
HRT012 Heart Valve Disease 53 2.251
583
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 2.249
584
EXT039 Extrapontine Myelinolysis 18 2.247
585
CHD004 Chudley-Mccullough Syndrome 47 2.246
586
P BRN022 Bronchiectasis 59 2.241
587
INT067 Interstitial Nephritis 46 2.237
588
HYP781 Hypoascorbemia 52 2.237
589
CYS013 Cystinuria 66 2.234
590
VSL002 Visual Epilepsy 39 2.234
591
MTH009 Mouth Disease 57 2.228
592
CNN005 Connective Tissue Disease 66 2.227
593
PRP030 Purpura 54 2.226
594
c CHR064 Chronic Monocytic Leukemia 35 2.223
595
SKN019 Skin Melanoma 70 2.220
596
CYT005 Cytomegalovirus Retinitis 50 2.215
597
NND001 Nondystrophic Myotonia 20 2.208
598
MCN017 Meconium Ileus 52 2.202
599
c MLG069 Malignant Hypertension 46 2.196
600
P MYT002 Myotonic Dystrophy 51 2.192
601
P PLY019 Polyneuropathy 52 2.189
602
HLC007 Helicobacter Pylori Infection 67 2.188
603
DST006 Diastolic Heart Failure 45 2.187
604
URT010 Ureteral Obstruction 44 2.186
605
ORL005 Oral Candidiasis 55 2.186
606
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 46 2.185
607
THR004 Thrombocytosis 52 2.185
608
SVR004 Severe Combined Immunodeficiency 70 2.178
609
c CNG006 Congenital Hypothyroidism 63 2.178
610
c HYP724 Hyperlipoproteinemia, Type Iii 66 2.175
611
P EPL140 Epilepsy, Idiopathic Generalized 60 2.173
612
P CRV039 Cervicitis 52 2.172
613
P SNS001 Sensorineural Hearing Loss 60 2.170
614
DYS015 Dysentery 49 2.165
615
FDL002 Food Allergy 47 2.158
616
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 2.156
617
CHR074 Choriocarcinoma 46 2.155
618
P SKN015 Skin Carcinoma 71 2.152
619
TRN018 Transitional Cell Carcinoma 56 2.152
620
c HYP272 Hypercholesterolemia, Familial, 3 46 2.149
621
APP008 Appendicitis 62 2.148
622
P MVM001 Movement Disease 61 2.144
623
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 2.139
624
MXD026 Mixed Glioma 45 2.134
625
OST011 Osteomalacia 52 2.132
626
LYM133 Lymphoma, Hodgkin, Classic 69 2.131
627
NRM004 Neuroma 49 2.130
628
DPH001 Diphtheria 59 2.127
629
c FML001 Familial Atrial Fibrillation 65 2.127
630
P SYP003 Syphilis 59 2.125
631
BNN003 Bone Inflammation Disease 47 2.120
632
P END033 Endocarditis 58 2.119
633
P MYT023 Myotonia Congenita 55 2.119
634
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 2.116
635
PHR003 Pharyngitis 57 2.114
636
HYP458 Hyper Ige Syndrome 60 2.112
637
P LNG064 Lung Cancer Susceptibility 3 69 2.112
638
P HML002 Hemolytic Anemia 62 2.105
639
P MYP006 Myopia 55 2.104
640
CRB009 Cerebritis 43 2.099
641
P HYP265 Hypotonia 42 2.094
642
IGR001 Ige Responsiveness, Atopic 58 2.090
643
THR016 Thrombophlebitis 50 2.084
644
HYP267 Hyperchlorhidrosis, Isolated 24 2.083
645
END072 Endotheliitis 36 2.082
646
PLL012 Pollen Allergy 44 2.080
647
SPP011 Suppression of Tumorigenicity 12 61 2.074
648
P END044 Endometriosis 62 2.073
649
FRZ001 Frozen Shoulder 54 2.071
650
P CRN026 Corneal Edema 42 2.070
651
PRS063 Paresthesia 39 2.060
652
END040 Endogenous Depression 54 2.059
653
c SCN007 Secondary Hyperparathyroidism 50 2.058
654
P PRP029 Porphyria 60 2.057
655
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 2.055
656
HMP009 Haemophilus Influenzae 41 2.053
657
NRL016 Neural Tube Defects 80 2.053
658
RNL077 Renal Fibrosis 46 2.053
659
c PCH010 Pachyonychia Congenita 3 43 2.051
660
ATR057 Atrioventricular Block 54 2.049
661
P END047 Endophthalmitis 53 2.043
662
P MGR003 Migraine with Aura 51 2.041
663
CYN002 Cyanosis, Transient Neonatal 43 2.039
664
ACT119 Acute Promyelocytic Leukemia 62 2.038
665
PLS009 Plasma Cell Neoplasm 64 2.032
666
c FML021 Familial Hypercholesterolemia 71 2.032
667
THY121 Thyroid Gland Anaplastic Carcinoma 66 2.030
668
VRN004 Vernal Keratoconjunctivitis 47 2.029
669
c ACT134 Acute Liver Failure 57 2.026
670
CHR066 Chronic Fatigue Syndrome 59 2.023
671
P SHR001 Short Bowel Syndrome 53 2.017
672
AGG012 Aggressive Nk-Cell Leukemia 47 2.013
673
P CLS010 Cluster Headache 42 2.013
674
P OPN001 Open-Angle Glaucoma 55 2.003
675
RSC001 Rosacea 55 2.002
676
APH001 Aphthous Stomatitis 57 1.999
677
P SPN046 Spinal Muscular Atrophy 62 1.998
678
AYM001 Ayme-Gripp Syndrome 57 1.996
679
WST001 West Syndrome 64 1.996
680
KRT008 Keratopathy 46 1.994
681
P GLL022 Guillain-Barre Syndrome 59 1.994
682
P DVL113 Developmental and Epileptic Encephalopathy 46 1.991
683
P CRP001 Carpal Tunnel Syndrome 65 1.986
684
P ALT001 Alternating Hemiplegia of Childhood 56 1.986
685
CRV035 Cervical Cancer 72 1.980
686
CHL123 Chlamydia 58 1.977
687
SYS003 Systolic Heart Failure 49 1.977
688
P HYP263 Hypersomnia 40 1.970
689
P VSC011 Vasculitis 61 1.970
690
LWC002 Lowe Oculocerebrorenal Syndrome 68 1.965
691
MTH071 Methane Production 24 1.965
692
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 1.956
693
P ART005 Arteriovenous Malformation 64 1.956
694
VCC001 Vaccinia 49 1.953
695
FSC004 Fasciitis 49 1.952
696
c HRD202 Hereditary Lymphedema I 54 1.950
697
c PRM005 Primary Hyperparathyroidism 59 1.948
698
c GRV008 Graves Disease 1 54 1.945
699
OHT001 Ohtahara Syndrome 39 1.935
700
P CHL066 Cholangitis 51 1.929
701
P NSP012 Nasopharyngeal Carcinoma 60 1.929
702
NRT001 Neurotic Disorder 56 1.927
703
IRD001 Iridocyclitis 54 1.919
704
c PRM093 Premature Ovarian Failure 7 47 1.918
705
c MST023 Mesothelioma, Malignant 56 1.918
706
ACT058 Active Peptic Ulcer Disease 55 1.914
707
TRN015 Transient Cerebral Ischemia 62 1.914
708
OSM001 Osmotic Diarrhea 27 1.913
709
LPT014 Leptin Deficiency or Dysfunction 77 1.912
710
SPT004 Septic Arthritis 58 1.906
711
CRT017 Cartilage Disease 52 1.905
712
RTR008 Root Resorption 44 1.901
713
PRR019 Perioral Myoclonia with Absences 26 1.899
714
GST040 Gastric Adenocarcinoma 66 1.894
715
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.891
716
c MYC068 Myoclonic Epilepsy of Infancy 35 1.888
717
c GNR039 Generalized Epilepsy with Febrile Seizures Plus, Type 2 49 1.884
718
BRS064 Bursitis 51 1.883
719
SPN051 Spondylitis 51 1.882
720
INF009 Inflammatory Spondylopathy 30 1.882
721
c PST005 Posterior Uveitis 54 1.881
722
PMP014 Pemphigoid 48 1.881
723
P SRC025 Sarcoidosis 1 70 1.880
724
c SPN225 Spondyloarthropathy 1 70 1.878
725
P MLG074 Malignant Mesenchymoma 40 1.878
726
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 1.875
727
P PTN014 Patent Ductus Arteriosus 1 59 1.874
728
P DMN002 Dementia 65 1.873
729
NRM009 Normokalemic Periodic Paralysis 28 1.871
730
FML159 Familial Periodic Paralyses 16 1.865
731
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 1.860
732
c FNC043 Fanconi Anemia, Complementation Group E 62 1.859
733
RNL024 Renal Glucosuria 60 1.857
734
CCC002 Coccidiosis 50 1.857
735
c ACT004 Acute Diarrhea 40 1.854
736
P BLD062 Bile Duct Cancer 69 1.851
737
P OTS001 Otosclerosis 49 1.841
738
c ESS001 Essential Tremor 56 1.840
739
P OVR082 Overgrowth Syndrome 41 1.838
740
P OLG002 Oligodendroglioma 66 1.835
741
SCR011 Scrapie 39 1.834
742
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.823
743
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 57 1.819
744
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.818
745
CHR073 Choreatic Disease 53 1.818
746
GLC022 Glucose/galactose Malabsorption 45 1.818
747
BLL006 Bullous Pemphigoid 61 1.817
748
CRB037 Cerebral Palsy 66 1.816
750
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 1.815
751
CSY001 C Syndrome 61 1.814
752
DBT002 Diabetic Autonomic Neuropathy 40 1.813
753
ANR004 Anuria 44 1.811
754
CHR100 Chronic Ulcer of Skin 57 1.808
755
P ENC004 Encephalitis 61 1.807
756
GRN017 Granulocytopenia 42 1.804
758
RHM001 Rheumatic Fever 59 1.803
759
ACT011 Acute Contagious Conjunctivitis 41 1.800
760
c BCT013 Bacterial Pneumonia 47 1.800
761
MYF002 Myofascial Pain Syndrome 46 1.797
762
EMB004 Embryonal Carcinoma 55 1.795
763
INT066 Interstitial Lung Disease 60 1.787
764
P HYP083 Hypopituitarism 51 1.787
765
PNM008 Pneumothorax 54 1.784
766
P MYS005 Myositis 55 1.784
767
P ORT004 Orthostatic Intolerance 61 1.781
768
NRT004 Neuritis 53 1.780
769
BRT054 Brittle Bone Disorder 74 1.777
770
P PLY011 Polycystic Ovary Syndrome 57 1.776
771
P VNS003 Venous Insufficiency 54 1.776
772
PRR001 Periarthritis 33 1.772
773
DRG024 Drug Allergy 40 1.772
774
P RHB003 Rhabdomyosarcoma 66 1.763
775
P PRV006 Pervasive Developmental Disorder 52 1.762
776
CRD137 Cardiogenic Shock 56 1.760
777
PTH003 Pathologic Nystagmus 52 1.757
778
P SBS003 Substance Abuse 54 1.751
779
APP009 Appendix Adenocarcinoma 47 1.748
780
P HYD006 Hydrocephalus 62 1.748
781
PTT037 Pituitary Tumors 44 1.745
782
P BNC003 Bone Cancer 58 1.741
783
DVR002 Diverticulitis 46 1.741
784
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 1.738
785
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 1.736
786
PST028 Post-Traumatic Stress Disorder 58 1.735
787
P PGT001 Paget's Disease of Bone 60 1.732
788
CLR108 Colorectal Adenoma 63 1.730
789
DNG003 Dengue Disease 65 1.730
790
P MST009 Mastocytosis 64 1.729
791
YLL002 Yellow Fever 61 1.729
792
ACT098 Acute Erythroid Leukemia 55 1.719
793
P OBS001 Obstructive Jaundice 49 1.717
794
SCH003 Schizophreniform Disorder 54 1.717
795
ATN005 Autonomic Dysfunction 45 1.716
796
KWS002 Kawasaki Disease 65 1.715
797
HRT011 Heart Septal Defect 49 1.714
798
P BRS044 Breast Adenocarcinoma 58 1.712
799
PLM017 Pulmonary Alveolar Microlithiasis 48 1.707
800
CLL003 Cellulitis 53 1.707
801
CRH005 Crohn's Colitis 53 1.706
802
THY122 Thyroid Gland Cancer 59 1.701
803
PLM031 Poliomyelitis 62 1.699
804
P CHR285 Chronic Myelomonocytic Leukemia 59 1.696
805
ENM001 Enamel Caries 28 1.695
806
BRK010 Burkitt Lymphoma 65 1.693
807
BCT004 Bacteriuria 48 1.692
808
CHL004 Cholelithiasis 48 1.692
809
SPS016 Spasmodic Dysphonia 32 1.689
810
c MYT029 Myotonia Congenita, Autosomal Recessive 41 1.687
811
DSS008 Disease of Mental Health 74 1.687
812
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 42 1.687
813
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 1.685
814
ORL015 Oral Squamous Cell Carcinoma 43 1.684
815
IDP011 Idiopathic Interstitial Pneumonia 59 1.684
816
ALD013 Aldosterone-Producing Adenoma 36 1.684
817
INF034 Infective Endocarditis 53 1.682
818
CNG064 Congenital Chloride Diarrhea 34 1.681
819
c LNG044 Long Qt Syndrome 1 66 1.681
820
P RCT021 Rectum Cancer 54 1.678
821
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 1.675
822
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.674
823
P PMP001 Pemphigus 54 1.673
824
MLG079 Malignant Pleural Mesothelioma 42 1.670
825
INS001 Insulinoma 59 1.669
826
HMT002 Hematologic Cancer 61 1.668
827
c SZR007 Seizures, Benign Familial Infantile, 3 45 1.665
828
CND002 Conduct Disorder 50 1.656
829
DCB001 Decubitus Ulcer 61 1.656
830
c PRM038 Primary Agammaglobulinemia 47 1.656
831
PLY150 Polykaryocytosis Inducer 29 1.656
832
PLS011 Plasmacytoma 56 1.654
833
c PRD040 Periodontitis, Chronic 52 1.653
834
ESN005 Eosinophilic Gastroenteritis 55 1.652
835
TXC002 Toxic Encephalopathy 51 1.650
836
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 1.649
837
DFF036 Differentiated Thyroid Carcinoma 51 1.648
838
PRM236 Primary Biliary Cholangitis 62 1.643
839
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.641
840
STT009 Sutton Disease 2 30 1.640
841
MST021 Meester-Loeys Syndrome 37 1.639
842
P PLY018 Polycythemia 56 1.638
843
MCR004 Macroglobulinemia 48 1.634
844
CYS014 Cystadenocarcinoma 51 1.633
845
c PSD112 Pseudohypoaldosteronism, Type I, Autosomal Dominant 50 1.629
846
PLS007 Plasmodium Falciparum Malaria 52 1.624
847
RMS001 Rem Sleep Behavior Disorder 47 1.623
848
MNN043 Meningioma, Familial 79 1.622
849
LYM002 Lymphoplasmacyte-Rich Meningioma 35 1.622
850
SCR001 Secretory Meningioma 40 1.622
851
INT395 Intracranial Meningioma 47 1.622
852
NSP002 Nasopharyngitis 45 1.621
853
HMR023 Hemorrhagic Cystitis 43 1.621
854
LTH043 Lithium Transport 17 1.621
855
RST023 Resting Heart Rate, Variation in 40 1.619
856
ERY003 Erythema Multiforme 56 1.614
857
CLN019 Colonic Disease 47 1.613
858
SNT005 Sinoatrial Node Disease 48 1.612
859
PRP016 Paraplegia 52 1.612
860
INT030 Intracranial Aneurysm 55 1.607
861
ART074 Aortic Dissection 53 1.607
862
OST003 Osteonecrosis 60 1.607
863
DMP001 Dumping Syndrome 43 1.607
864
PRN019 Perinatal Necrotizing Enterocolitis 60 1.605
865
HMC014 Homocysteinemia 52 1.605
866
P SBR004 Seborrheic Dermatitis 44 1.603
867
CLC004 Calcific Tendinitis 33 1.601
868
IMM162 Immunoglobulin E Concentration, Serum 28 1.600
869
c PSD092 Pseudohypoaldosteronism, Type Iie 48 1.596
870
c ART115 Aortic Valve Disease 1 72 1.596
871
P MJR001 Major Depressive Disorder 68 1.596
872
MNR012 Meniere Disease 55 1.595
873
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 1.595
874
P SLM003 Salmonellosis 54 1.592
875
c HPT073 Hepatitis C Virus 70 1.591
876
P PTT006 Pituitary Adenoma 55 1.590
877
P FLL037 Follicular Lymphoma 66 1.589
878
P TCD001 Tic Disorder 50 1.589
879
P GLL018 Gallbladder Cancer 59 1.588
880
c HPT015 Hepatitis D 49 1.588
881
SPL004 Splenic Marginal Zone Lymphoma 50 1.586
882
GLY010 Glycine Encephalopathy 57 1.584
883
CHG001 Chagas Disease 65 1.584
884
NRL005 Neurilemmoma 60 1.583
885
P ATX030 Ataxia-Telangiectasia 80 1.583
886
c VRL010 Viral Hepatitis 52 1.581
887
BRC012 Brucellosis 66 1.575
888
ESP002 Esophageal Varix 51 1.571
889
MYC005 Myocardial Stunning 45 1.566
890
c SVR005 Severe Pre-Eclampsia 49 1.558
891
P INS002 in Situ Carcinoma 52 1.558
892
P STR020 Strabismus 56 1.558
893
MCH006 Mechanical Strabismus 40 1.558
894
FRN014 Fournier Gangrene 26 1.558
895
ANT024 Anthrax Disease 57 1.554
896
c SZR020 Seizures, Benign Familial Infantile, 5 29 1.554
897
c DYS056 Dystonia 12 63 1.552
898
P GLY013 Glycogen Storage Disease 59 1.549
899
END021 Endomyocardial Fibrosis 56 1.549
900
P MTR012 Mitral Valve Disease 57 1.547
901
AMD002 Amed Syndrome, Digenic 36 1.545
902
TRD006 Tardive Dyskinesia 53 1.543
903
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 49 1.543
904
RSP007 Respiratory Distress Syndrome, Infant 41 1.543
905
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 1.542
906
HMS001 Hemosiderosis 48 1.540
907
ADR016 Adrenal Cortical Carcinoma 61 1.540
908
GST071 Gastrointestinal Carcinoma 46 1.539
909
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 1.537
910
P THR015 Thrombophilia 51 1.536
911
OBS002 Obsessive-Compulsive Disorder 67 1.530
912
SCC011 Succinyl-Coa:3-Oxoacid-Coa Transferase Deficiency 34 1.527
913
CLR109 Colorectal Adenocarcinoma 50 1.524
914
P ALP009 Alopecia Areata 59 1.524
915
c BNG023 Benign Familial Infantile Epilepsy 57 1.524
916
c LNG053 Long Qt Syndrome 9 43 1.522
917
c SYS043 Systemic Lupus Erythematosus 1 38 1.522
918
ING001 Inguinal Hernia 59 1.520
919
P TXP001 Toxoplasmosis 59 1.519
920
HYP081 Hypolipoproteinemia 49 1.518
921
GNG003 Gingival Recession 50 1.516
922
SPL018 Splenomegaly 47 1.515
923
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 1.514
924
CHL028 Childhood Type Dermatomyositis 58 1.510
925
ACR041 Acromelic Frontonasal Dysostosis 53 1.508
926
c HYP731 Hyperaldosteronism, Familial, Type I 59 1.508
927
BRD004 Borderline Personality Disorder 53 1.507
928
ORL011 Oral Cancer 60 1.506
929
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.504
930
RGH001 Right Bundle Branch Block 47 1.504
931
RYN005 Raynaud Phenomenon 45 1.499
932
c PSR017 Psoriasis 2 53 1.499
933
CRT015 Carotid Artery Occlusion 45 1.496
934
c INF071 Inflammatory Bowel Disease 1 65 1.495
935
CRN030 Coronary Stenosis 50 1.495
936
HYP264 Hypertonia 35 1.495
937
GST049 Gastrointestinal System Cancer 49 1.490
938
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 39 1.490
939
CRC021 Carcinosarcoma 62 1.487
940
P ANG015 Angioedema 56 1.487
941
c DVL039 Developmental and Epileptic Encephalopathy 11 41 1.485
942
c ACT249 Acute Asthma 40 1.484
943
OCL006 Ocular Hypertension 53 1.483
944
SCN067 Scn1a Seizure Disorders 13 1.483
945
P MRC003 Mercury Poisoning 48 1.483
946
ACS001 Acoustic Neuroma 55 1.482
947
P BCT020 Bacteremia 2 43 1.481
948
SRS001 Serous Cystadenocarcinoma 51 1.481
949
NRL004 Neuroleptic Malignant Syndrome 52 1.481
950
MYL031 Myeloproliferative Neoplasm 66 1.479
951
RDC002 Radiculopathy 51 1.477
952
URM005 Uremic Pruritus 46 1.475