Search results for sodium

5143 hits were found for sodium

# Family MCID Name MIFTS Score
1
DRR017 Diarrhea 3, Secretory Sodium, Congenital, with or Without Other Congenital Anomalies 35 43.039
2
c HYP595 Hypertension, Essential 85 34.703
3
DRR013 Diarrhea 8, Secretory Sodium, Congenital 35 30.205
4
CLT003 Colitis 63 27.906
5
MYT030 Myotonia, Potassium-Aggravated 46 21.141
6
MTB004 Metabolic Acidosis 48 20.068
7
SDM005 Sodium Serum Level Quantitative Trait Locus 1 10 19.998
8
HYP005 Hypokalemia 55 19.701
9
OVR093 Overhydrated Hereditary Stomatocytosis 41 19.696
10
P KDN018 Kidney Disease 72 19.593
11
c CHR684 Chronic Kidney Disease 69 19.301
12
c TYP009 Type 2 Diabetes Mellitus 92 17.868
13
HYP052 Hyperkalemic Periodic Paralysis 63 17.424
14
ULC004 Ulcerative Colitis 74 17.030
15
CNG034 Congestive Heart Failure 69 17.001
16
c ACT071 Acute Kidney Failure 60 16.709
17
P DBT009 Diabetes Mellitus 67 16.101
18
48X005 48,xyyy 39 15.676
19
CYS001 Cystic Fibrosis 78 15.417
20
OST012 Osteoarthritis 77 15.007
21
c MGR028 Migraine with or Without Aura 1 64 14.664
22
P SZR006 Seizure Disorder 70 14.583
23
PRT251 Proteinuria, Chronic Benign 57 14.543
25
P INF037 Inflammatory Bowel Disease 53 13.761
26
P EPL164 Epilepsy 68 13.702
27
P DRR001 Diarrhea 55 13.656
28
SDM004 Sodium-Potassium-Atpase Activity of Red Cell 7 13.623
29
P NRB001 Neuroblastoma 66 13.266
30
SDM006 Sodium Aurothiomalate Allergy 5 13.259
31
END086 End Stage Renal Disease 52 13.217
32
c MCR120 Microvascular Complications of Diabetes 7 47 13.214
33
P KLZ004 Kala-Azar 1 41 13.072
34
LSH001 Leishmaniasis 64 13.072
35
HYP066 Hyperglycemia 61 13.010
36
c MCR113 Microvascular Complications of Diabetes 3 52 12.906
37
ALL029 Allergic Disease 59 12.820
38
P OST002 Osteoporosis 76 12.769
39
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 12.764
40
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 12.764
41
HYP056 Hypoglycemia 65 12.761
42
c MCR130 Microvascular Complications of Diabetes 6 41 12.604
43
c MCR133 Microvascular Complications of Diabetes 4 41 12.604
44
LVR012 Liver Cirrhosis 63 12.534
45
P BRG001 Brugada Syndrome 69 12.402
46
NRD106 Neurodegeneration, Infantile-Onset, Biotin-Responsive 23 12.208
47
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 12.112
48
P NPH012 Nephrotic Syndrome 60 12.047
49
P HRT032 Heart Disease 81 12.004
50
c ACT027 Acute Pancreatitis 60 11.933
51
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 11.922
52
P HYP086 Hypothyroidism 69 11.815
53
P BPL003 Bipolar Disorder 56 11.809
54
c MJR022 Major Affective Disorder 8 38 11.790
55
c MJR024 Major Affective Disorder 9 41 11.790
56
P ENC018 Encephalopathy 62 11.777
57
P DBT005 Diabetes Insipidus 54 11.736
58
P PNC044 Pancreatitis 61 11.702
59
ISC004 Ischemia 61 11.440
60
RPD005 Rapidly Involuting Congenital Hemangioma 46 11.298
61
HRW001 Hair Whorl 35 11.281
62
CRH001 Crohn's Disease 80 11.264
63
DNT012 Dental Caries 53 11.254
64
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 11.174
65
PLM010 Pulmonary Edema 55 11.003
66
NPH009 Nephrolithiasis 54 10.970
67
P LNG028 Long Qt Syndrome 64 10.942
68
P RHN004 Rhinitis 57 10.932
69
P CTR002 Cataract 60 10.917
70
PNG002 Pain Agnosia 51 10.915
71
P CRD119 Cardiac Arrest 67 10.904
72
P HDC001 Headache 57 10.859
73
CNN003 Conn's Syndrome 79 10.838
74
SYN164 Syndromic Congenital Sodium Diarrhea 8 10.743
75
P NRC002 Narcolepsy 56 10.710
76
DBT084 Diabetes Mellitus, Ketosis-Prone 60 10.702
77
P PLM037 Pulmonary Hypertension 72 10.607
78
P URN019 Urinary Tract Infection 49 10.565
79
P PRD021 Periodic Paralysis 41 10.556
80
GLL048 Glial Tumor 52 10.507
81
OCL069 Ocular Motor Apraxia 57 10.506
82
PRT036 Peritonitis 65 10.482
83
GLM045 Glioma 63 10.471
84
c THR092 Thrombophilia Due to Thrombin Defect 74 10.339
85
P LVR013 Liver Disease 69 10.305
86
CNS004 Constipation 56 10.246
87
c HYP836 Hypercholesterolemia, Familial, 1 73 10.128
88
MYT011 Myotonia 39 10.029
89
P CNJ013 Conjunctivitis 66 10.004
90
CHL014 Cholera 62 9.952
91
HYP266 Hypoxia 57 9.951
92
c PNS012 Paine Syndrome 60 9.881
93
THY029 Thyroid Carcinoma 51 9.834
94
AGN016 Aging 54 9.812
95
c TYP008 Type 1 Diabetes Mellitus 70 9.793
96
c ACT068 Acute Cystitis 61 9.694
97
HYP060 Hyperinsulinism 54 9.554
98
CNT047 Contact Dermatitis 57 9.545
99
ALL003 Allergic Rhinitis 67 9.544
100
BNR002 Bone Resorption Disease 47 9.454
101
P CHR345 Chronic Pain 50 9.423
102
P PRD008 Periodontitis 64 9.294
103
CRD132 Cardiac Conduction Defect 60 9.289
104
BRN071 Brain Injury 50 9.282
105
P NRL027 Neurological Muscular Channelopathy Due to a Genetic Sodium Channel Defect 3 9.214
106
c NRL035 Neurological Channelopathy of the Central Nervous System Due to a Genetic Sodium Channel Defect 2 9.214
107
VSC003 Visceral Leishmaniasis 55 9.152
108
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 9.125
109
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 9.125
110
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 9.125
111
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 9.125
112
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 9.125
113
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 9.125
114
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 9.125
115
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 9.125
116
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 9.125
117
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 9.120
118
TRM010 Traumatic Brain Injury 51 9.108
119
STT001 Status Epilepticus 59 9.097
120
NNL005 Non-Alcoholic Fatty Liver Disease 63 9.053
121
TXC005 Toxic Shock Syndrome 62 9.038
122
P FBR031 Febrile Seizures 52 9.006
123
P VSC007 Vascular Disease 63 8.999
124
P MYC007 Myocardial Infarction 70 8.972
125
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 8.922
126
DRM006 Dermatitis 62 8.909
127
HLX001 Helix Syndrome 48 8.869
128
PRT037 Pertussis 65 8.836
130
P TRM003 Tremor 48 8.765
131
P NRP001 Neuropathy 60 8.709
132
DRV001 Dravet Syndrome 69 8.669
133
HPT004 Hepatic Coma 43 8.667
134
P GLM007 Glomerulonephritis 60 8.584
135
P CYS018 Cystitis 59 8.560
136
BRN004 Brain Edema 54 8.532
137
c PRC016 Pre-Eclampsia 65 8.528
138
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 8.497
139
ARG004 Argyria 26 8.483
140
HPT019 Hepatic Encephalopathy 59 8.472
141
P RNL015 Renal Hypertension 45 8.378
142
URL001 Urolithiasis 46 8.377
143
KRT006 Keratoconjunctivitis 53 8.371
144
P LCT001 Lactic Acidosis 51 8.365
145
DFC004 Deficiency Anemia 74 8.360
146
P CRN300 Coronary Heart Disease 1 73 8.343
147
GNG013 Gingivitis 59 8.297
148
HYP025 Hyperphosphatemia 48 8.203
149
P RNV001 Renovascular Hypertension 49 8.199
150
CTN007 Cutaneous Leishmaniasis 62 8.194
151
FTT001 Fatty Liver Disease 62 8.168
152
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 8.153
153
ADN018 Adenoma 59 8.147
154
GLB002 Glioblastoma 67 8.120
155
P EXN002 Exanthem 58 8.115
156
INP001 Inappropriate Adh Syndrome 48 8.108
157
IRN002 Iron Metabolism Disease 57 8.093
158
P PRS040 Prostate Cancer 95 8.092
159
CLC001 Calciphylaxis 51 8.080
160
LPD008 Lipid Metabolism Disorder 62 8.077
161
EXR010 Exercise-Induced Bronchoconstriction 34 8.062
162
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 8.058
163
P PSD003 Pseudohypoaldosteronism 44 8.037
164
P RSP003 Respiratory Failure 74 8.030
165
PRM057 Paramyotonia Congenita of Von Eulenburg 59 8.027
166
CHL068 Cholestasis 61 8.016
167
P ADL010 Adult Respiratory Distress Syndrome 71 8.012
168
GST092 Gastroesophageal Reflux 61 7.986
169
PLM033 Pulmonary Embolism 58 7.976
170
THR024 Thrombosis 56 7.964
171
P ESP024 Esophagitis 60 7.883
172
P PNM007 Pneumonia 67 7.868
173
P THR014 Thrombocytopenia 66 7.866
174
PRT013 Portal Hypertension 59 7.829
175
RCK004 Rickets 68 7.822
176
STR067 Stroke, Ischemic 80 7.822
177
P CLR023 Colorectal Cancer 100 7.820
178
c PLM164 Pulmonary Hypertension, Primary, 1 76 7.749
179
P EYD002 Eye Disease 57 7.746
180
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 7.741
181
ALL009 Allergic Conjunctivitis 51 7.692
182
P ATR011 Atrial Fibrillation 66 7.637
183
P GNR002 Generalized Epilepsy with Febrile Seizures Plus 60 7.631
184
STM007 Stomatitis 54 7.624
185
P MYP004 Myopathy 67 7.622
186
CYT002 Cytokine Deficiency 43 7.610
187
P PRP019 Peripheral Nervous System Disease 58 7.572
188
LNG099 Lung Disease 62 7.560
189
P AST005 Asthma 76 7.558
190
CNT025 Central Pontine Myelinolysis 43 7.530
191
ALC007 Alcohol Dependence 66 7.518
192
URM002 Uremia 47 7.513
193
P ADN016 Adenocarcinoma 63 7.509
194
c MCR115 Microvascular Complications of Diabetes 5 65 7.506
195
47X002 47,xyy 48 7.504
196
P PLY014 Polycystic Kidney Disease 69 7.490
197
ATH013 Atherosclerosis Susceptibility 63 7.480
198
NPH091 Nephrolithiasis, Calcium Oxalate 61 7.445
199
P MLT020 Multiple Sclerosis 79 7.441
200
P DRM053 Dermatitis, Atopic 65 7.440
201
SPN186 Spinal Cord Injury 61 7.435
202
c ACT075 Acute Myocardial Infarction 56 7.410
203
BCT022 Bacterial Infectious Disease 56 7.392
204
P RNL007 Renal Tubular Acidosis 50 7.367
205
P HPT021 Hepatitis 69 7.353
206
c ATR087 Atrial Standstill 1 74 7.307
207
P LDD007 Liddle Syndrome 1 57 7.296
208
c LNG048 Long Qt Syndrome 3 53 7.262
209
P BND020 Bone Disease 59 7.241
210
DBT010 Diabetic Neuropathy 54 7.241
211
ANX004 Anoxia 40 7.233
212
P ERY008 Erythromelalgia 50 7.220
213
P HYP069 Hyperparathyroidism 62 7.179
214
GST045 Gastroenteritis 58 7.169
215
CRB039 Cerebrovascular Disease 66 7.157
216
P HYP076 Hyperthyroidism 53 7.136
217
P LTR001 Lateral Sclerosis 58 7.114
218
c AMY091 Amyotrophic Lateral Sclerosis 1 88 7.100
219
VRC005 Varicose Veins 60 7.095
220
P INT143 Interstitial Cystitis 60 7.085
221
P LNG032 Lung Cancer 98 7.080
222
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 7.079
223
DRY001 Dry Eye Syndrome 50 7.069
224
CRD223 Cardiac Arrhythmia 63 7.045
225
HMN044 Human Immunodeficiency Virus Type 1 78 7.034
226
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 6.982
227
HYP017 Hypophosphatemia 49 6.965
228
HYP014 Hyperuricemia 51 6.948
229
P HPT023 Hepatocellular Carcinoma 96 6.934
230
CRB004 Cerebral Artery Occlusion 45 6.897
231
GT001 Gout 64 6.861
232
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 6.848
233
P SLP006 Sleep Apnea 69 6.830
234
INT075 Intracranial Hypertension 53 6.815
235
MCS002 Mucositis 56 6.756
236
CYN003 Cyanide Poisoning 22 6.746
237
P ALZ034 Alzheimer Disease 87 6.720
238
P PHC003 Pheochromocytoma 69 6.671
239
ADR040 Adrenal Gland Pheochromocytoma 46 6.671
240
HPT014 Hepatorenal Syndrome 49 6.666
241
c DLT002 Dilated Cardiomyopathy 78 6.631
242
SYN036 Syncope 45 6.625
243
P ART022 Arthritis 71 6.623
244
KRT009 Keratosis 53 6.610
245
P GST053 Gastric Cancer 83 6.593
246
MCL006 Macular Retinal Edema 57 6.542
247
GST023 Gastric Ulcer 52 6.524
248
c HPT016 Hepatitis B 62 6.512
249
P ALC033 Alcohol Use Disorder 61 6.507
250
PLM129 Pulmonary Disease, Chronic Obstructive 74 6.505
251
P SCH015 Schizophrenia 74 6.490
252
ESP021 Esophageal Cancer 83 6.486
253
P ECL001 Eclampsia 52 6.484
254
LPP008 Lipoprotein Quantitative Trait Locus 65 6.467
255
P GST044 Gastritis 55 6.463
256
HGH043 High Grade Glioma 45 6.463
257
ACQ007 Acquired Immunodeficiency Syndrome 59 6.460
258
IRR003 Irritant Dermatitis 47 6.438
259
ANG054 Angina Pectoris 66 6.435
260
P HRP006 Herpes Simplex 65 6.426
261
P GLM040 Glioma Susceptibility 1 71 6.417
262
P FML187 Familial Hypertension 34 6.402
263
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 6.390
264
P THY032 Thyroiditis 57 6.354
265
OST159 Osteogenic Sarcoma 66 6.338
266
ART140 Arteries, Anomalies of 53 6.335
267
P MSC005 Muscular Dystrophy 67 6.313
268
P BRS047 Breast Cancer 98 6.313
269
MST005 Mastitis 53 6.299
270
PRS047 Prostatitis 58 6.286
271
IMP005 Impotence 52 6.262
272
P BRT004 Bartter Disease 58 6.224
273
P SCK005 Sickle Cell Disease 56 6.211
274
PRP027 Peripheral Vascular Disease 71 6.199
275
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 6.187
276
INT323 Intraocular Pressure Quantitative Trait Locus 64 6.178
277
ERL001 Early Myoclonic Encephalopathy 62 6.121
278
ATM095 Autoimmune Disease 61 6.115
279
KRT001 Keratoconjunctivitis Sicca 50 6.097
280
SKN016 Skin Disease 63 6.087
281
ADL002 Adult Syndrome 70 6.077
282
P LPS004 Lupus Erythematosus 61 6.076
283
P URT039 Urticaria 58 6.015
284
ACT003 Acute Kidney Tubular Necrosis 46 6.004
285
c SML038 Small Cell Cancer of the Lung 69 5.999
286
PRT058 Pure Autonomic Failure 58 5.990
287
DWN001 Down Syndrome 70 5.981
288
P LKM002 Leukemia 67 5.978
289
PRS045 Prostatic Hypertrophy 53 5.963
290
P NTR004 Neutropenia 63 5.961
291
P PRK039 Parkinsonism 55 5.949
292
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 60 5.933
293
ANT039 Antisynthetase Syndrome 55 5.933
294
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 5.929
295
P FNC004 Fanconi Syndrome 60 5.921
296
MYL069 Myeloma, Multiple 77 5.916
297
P PNC025 Panic Disorder 52 5.890
298
P MLG056 Malignant Hyperthermia 66 5.888
299
FCL014 Focal Epilepsy 53 5.881
300
ALL010 Allergic Contact Dermatitis 56 5.881
301
PPL052 Papillomatosis, Confluent and Reticulated 34 5.880
302
CLC006 Calcinosis 47 5.865
303
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 5.864
304
SBC016 Subacute Delirium 43 5.847
305
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 5.833
306
c SYS001 Systemic Lupus Erythematosus 87 5.820
307
GNT046 Genetic Epilepsy with Febrile Seizures Plus 29 5.800
308
NPH003 Nephrocalcinosis 49 5.779
309
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 5.756
310
PST092 Posttransplant Acute Limbic Encephalitis 28 5.724
311
SPN035 Spindle Cell Sarcoma 54 5.712
312
TTN003 Tetanus 65 5.697
313
P DDN001 Duodenal Ulcer 53 5.687
314
KRT019 Keratitis, Hereditary 66 5.673
315
c CHR711 Chronic Asthma 41 5.661
316
SPS057 Spasticity 42 5.647
317
SRC014 Sarcoma 65 5.645
318
PRS021 Prostatic Adenoma 43 5.633
319
NNL006 Non-Alcoholic Steatohepatitis 54 5.624
320
c EPS039 Episodic Pain Syndrome, Familial, 1 42 5.621
321
GTL001 Gitelman Syndrome 65 5.617
322
P RHM011 Rheumatoid Arthritis 82 5.598
323
c LKM061 Leukemia, Acute Myeloid 83 5.589
324
P MTH007 Methemoglobinemia 46 5.575
325
INS024 Insulin-Like Growth Factor I 78 5.563
326
P BCL017 B-Cell Lymphoma 59 5.557
327
APP015 Apparent Mineralocorticoid Excess 57 5.552
328
P HYP098 Hypereosinophilic Syndrome 66 5.550
329
P MLN008 Melanoma 76 5.524
330
FBR047 Fibromyalgia 58 5.513
331
P ANR048 Aniridia 1 64 5.512
332
GTR002 Goiter 53 5.475
333
P MJR007 Major Affective Disorder 1 42 5.466
334
RTN017 Retinal Detachment 60 5.452
335
PRX015 Paroxysmal Extreme Pain Disorder 56 5.452
336
P HYP750 Hypertriglyceridemia, Familial 62 5.440
337
PPT005 Peptic Ulcer Disease 58 5.436
338
P HYP120 Hypoaldosteronism 35 5.427
339
DYS073 Dysphagia 53 5.420
340
c GLL024 Gallbladder Disease 1 52 5.418
341
P BLD134 Bladder Cancer 79 5.413
342
P PNC035 Pancreatic Cancer 86 5.394
343
PRS129 Prostatic Hyperplasia, Benign 49 5.376
344
c HPT003 Hepatitis a 63 5.348
345
MDD011 Mood Disorder 62 5.326
346
P PYL005 Pyelonephritis 57 5.319
347
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 5.315
348
P CND004 Candidiasis 58 5.306
349
P MNN013 Meningitis 65 5.303
350
P MYL006 Myeloid Leukemia 61 5.296
351
RNL114 Renal Cell Carcinoma, Nonpapillary 80 5.287
352
KHN001 Kuhnt-Junius Degeneration 48 5.280
353
NRR001 Neuroretinitis 42 5.273
354
BCK006 Back Pain 47 5.257
355
RTN023 Retinitis 46 5.248
356
c BRN108 Branchiootic Syndrome 1 62 5.240
357
P LKM062 Leukemia, Acute Lymphoblastic 69 5.238
358
ATS010 Autosomal Recessive Disease 42 5.226
359
HDN002 Head Injury 44 5.225
360
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 5.209
361
P CRD246 Cardiovascular System Disease 56 5.205
362
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 5.199
363
THY030 Thyroid Gland Disease 50 5.189
364
P DYS154 Dystonia 64 5.188
365
SCK003 Sickle Cell Anemia 74 5.159
366
ENT011 Enterocolitis 55 5.149
367
c PRG042 Progressive Familial Heart Block, Type Ia 66 5.146
368
GLC003 Glucose Intolerance 54 5.123
369
RHB024 Rhabdomyosarcoma 2 67 5.113
370
P ACT008 Actinic Keratosis 54 5.112
371
P TMP001 Temporal Lobe Epilepsy 49 5.112
372
SVR001 Severe Acute Respiratory Syndrome 67 5.108
373
P ATS364 Autism 69 5.108
374
P DST107 Distal Renal Tubular Acidosis 48 5.101
375
BRN024 Bronchitis 67 5.099
376
DSS009 Disseminated Intravascular Coagulation 57 5.082
377
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 5.081
378
P UVT001 Uveitis 57 5.075
379
P MYC033 Myoclonus 47 5.072
380
P SLP005 Sleep Disorder 61 5.067
381
HPR003 Heparin-Induced Thrombocytopenia 47 5.045
382
URT010 Ureteral Obstruction 45 5.024
383
P GRV001 Graves' Disease 55 5.014
384
ALL014 Allergic Encephalomyelitis 34 4.987
385
MLG169 Malignant Astrocytoma 57 4.973
386
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 4.962
387
HMP009 Haemophilus Influenzae 41 4.961
388
ALL006 Allergic Asthma 56 4.942
389
IMM167 Immune Deficiency Disease 78 4.937
390
PPT001 Peptic Esophagitis 52 4.928
391
P TRN020 Turner Syndrome 67 4.921
392
SCR003 Secretory Diarrhea 35 4.885
393
KRT002 Keratomalacia 55 4.885
394
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 4.881
395
P OVR042 Ovarian Cancer 88 4.877
396
P AMY004 Amyloidosis 70 4.866
397
DSS032 Disease by Infectious Agent 55 4.865
398
P LYM118 Lymphoma 67 4.854
399
P SCK002 Sick Sinus Syndrome 55 4.854
400
P MSC003 Muscular Atrophy 52 4.838
401
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 4.811
402
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.790
403
ENT004 Enthesopathy 51 4.779
404
c FML191 Familial Long Qt Syndrome 55 4.779
405
IRR002 Irritable Bowel Syndrome 65 4.756
406
P THL005 Thalassemia 56 4.750
407
CLN015 Colon Adenocarcinoma 65 4.725
408
ACR007 Acromegaly 70 4.715
409
CVD001 Covid-19 57 4.710
410
P PRS038 Personality Disorder 65 4.660
411
URN010 Urinary Tract Obstruction 55 4.659
412
P RTN024 Retinoblastoma 73 4.651
413
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 4.644
414
OST017 Osteomyelitis 63 4.638
415
MNT002 Mental Depression 57 4.632
416
OTT002 Otitis Media 71 4.631
417
TRG002 Trigeminal Neuralgia 61 4.617
418
MLR004 Malaria 80 4.616
419
P ART021 Arteriosclerosis 54 4.615
420
P MCR129 Microvascular Complications of Diabetes 1 68 4.612
421
ILS001 Ileus 50 4.604
422
MYL009 Myelodysplastic Syndrome 67 4.601
423
ANX010 Anxiety 70 4.596
424
P HMN010 Hemangioma 62 4.575
425
IDP073 Idiopathic Hypercalciuria 40 4.567
426
SQM006 Squamous Cell Carcinoma 60 4.561
427
OST062 Osteoarthritis with Mild Chondrodysplasia 47 4.560
428
LYM019 Lymphosarcoma 46 4.555
429
PPL022 Papilloma 53 4.537
430
P DNT007 Dentin Sensitivity 34 4.536
431
ERY029 Erythermalgia, Primary 58 4.535
432
c ATS007 Autism Spectrum Disorder 72 4.530
433
AMN003 Amnestic Disorder 54 4.526
434
BRN002 Bronchiolitis 57 4.519
435
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 4.517
436
PST011 Pustulosis of Palm and Sole 52 4.506
437
PLM001 Pulmonary Tuberculosis 69 4.493
438
SDD001 Sudden Infant Death Syndrome 60 4.483
439
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 4.479
440
SCH014 Schistosomiasis 56 4.479
441
IDP033 Idiopathic Edema 41 4.466
442
P RTN016 Retinal Degeneration 52 4.454
443
P PSR002 Psoriasis 63 4.454
444
c MLG069 Malignant Hypertension 46 4.451
445
P SJG008 Sjogren Syndrome 61 4.451
446
INT007 Intermediate Coronary Syndrome 54 4.446
447
SQM002 Squamous Cell Papilloma 46 4.442
448
WTH001 Withdrawal Disorder 48 4.433
449
MSC157 Muscular Dystrophy, Duchenne Type 79 4.430
450
DPR016 Depression 65 4.426
451
TND005 Tendinitis 54 4.423
452
PLP001 Pulpitis 48 4.415
453
P ALP008 Alopecia 54 4.415
454
IRN001 Iron Deficiency Anemia 58 4.405
455
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 4.403
456
P PLM036 Pulmonary Fibrosis 66 4.395
457
P MYC008 Myocarditis 59 4.394
458
c ACT134 Acute Liver Failure 59 4.382
459
P HML002 Hemolytic Anemia 62 4.381
460
MSC007 Muscle Hypertrophy 64 4.380
461
c SCL052 Scleroderma, Familial Progressive 61 4.362
462
BRN056 Bronchopulmonary Dysplasia 56 4.350
463
P ACN011 Acne 57 4.350
464
ATR057 Atrioventricular Block 54 4.347
465
P INF032 Infertility 57 4.347
466
ENM002 Enamel Erosion 25 4.344
467
CRB086 Cerebral Aneurysms 40 4.312
468
OST011 Osteomalacia 52 4.307
469
TLN003 Telangiectasis 51 4.290
470
INT067 Interstitial Nephritis 46 4.288
471
HPT022 Hepatoblastoma 54 4.287
472
P BNG032 Benign Mesothelioma 53 4.287
473
P NRV007 Nervous System Disease 67 4.285
474
P ANP001 Anaplastic Large Cell Lymphoma 61 4.280
475
BLR008 Bilirubin Metabolic Disorder 57 4.272
476
DMY004 Demyelinating Disease 50 4.268
477
P LKM071 Leukemia, Chronic Lymphocytic 75 4.268
478
PLC002 Plica Syndrome 35 4.264
479
MSL001 Measles 61 4.261
480
SYN007 Synovitis 55 4.252
481
NTR005 Nutritional Deficiency Disease 61 4.249
482
P HYP024 Hypoparathyroidism 55 4.247
483
RLP002 Relapsing-Remitting Multiple Sclerosis 56 4.245
484
URC002 Urea Cycle Disorder 51 4.244
485
P PRD017 Periodic Paralyses 24 4.242
486
SVR004 Severe Combined Immunodeficiency 72 4.223
487
IGR001 Ige Responsiveness, Atopic 59 4.218
488
P SNS001 Sensorineural Hearing Loss 59 4.199
489
RNL077 Renal Fibrosis 46 4.191
490
EXT039 Extrapontine Myelinolysis 18 4.169
491
P MYC084 Mycobacterium Tuberculosis 1 68 4.166
492
c ACT004 Acute Diarrhea 40 4.163
493
P INT070 Intestinal Obstruction 57 4.159
494
P HYP265 Hypotonia 42 4.158
495
P ART023 Arthropathy 61 4.147
496
P INT068 Intestinal Disease 53 4.146
497
P MYT002 Myotonic Dystrophy 51 4.140
498
P SHR001 Short Bowel Syndrome 53 4.132
499
PSY004 Psychotic Disorder 66 4.129
500
P ATT013 Attention Deficit-Hyperactivity Disorder 64 4.128
501
P MGR001 Migraine Without Aura 49 4.121
502
P ENC004 Encephalitis 61 4.118
503
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 4.111
504
ANR040 Aneurysm 61 4.107
505
CYN002 Cyanosis, Transient Neonatal 43 4.105
506
DBT006 Diabetic Macular Edema 48 4.102
507
P LNG064 Lung Cancer Susceptibility 3 70 4.102
508
CHL123 Chlamydia 58 4.102
509
BRR014 Barrett Esophagus 66 4.100
510
DYS015 Dysentery 50 4.092
511
PRP080 Peripheral Artery Disease 54 4.091
512
CHR074 Choriocarcinoma 46 4.091
513
VCC001 Vaccinia 47 4.088
514
c PRM108 Primary Progressive Multiple Sclerosis 51 4.081
515
FDL002 Food Allergy 47 4.080
516
PRS063 Paresthesia 39 4.076
517
INT002 Intermittent Claudication 61 4.074
518
c MCR112 Microvascular Complications of Diabetes 2 42 4.071
519
ART016 Aortic Aneurysm 68 4.070
520
P PRK057 Parkinson Disease, Late-Onset 80 4.067
521
CHL065 Cholangiocarcinoma 58 4.066
522
INT079 Intrahepatic Cholangiocarcinoma 51 4.066
523
P RTN018 Retinal Disease 53 4.061
524
SCH012 Schizoaffective Disorder 50 4.060
525
P VSC011 Vasculitis 61 4.056
526
P PLY019 Polyneuropathy 52 4.049
527
IGG001 Iga Glomerulonephritis 50 4.043
528
c SCN007 Secondary Hyperparathyroidism 51 4.040
529
MMM001 Mammary Paget's Disease 53 4.035
530
MTH071 Methane Production 25 4.026
531
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 4.018
532
P HNT016 Huntington Disease 73 4.008
533
PRP030 Purpura 54 4.005
534
P HYP083 Hypopituitarism 52 4.002
535
LMB062 Limb Ischemia 55 3.999
536
MTH009 Mouth Disease 57 3.998
537
c PRM005 Primary Hyperparathyroidism 59 3.993
538
DPH001 Diphtheria 59 3.983
539
P HYP061 Hypertrophic Cardiomyopathy 69 3.978
540
c BPL002 Bipolar I Disorder 47 3.977
541
c THY109 Thyroid Cancer, Nonmedullary, 1 55 3.976
542
VRN004 Vernal Keratoconjunctivitis 47 3.975
543
P OVR082 Overgrowth Syndrome 49 3.972
544
GST050 Gastrointestinal System Disease 55 3.967
545
ETN001 Eating Disorder 59 3.966
546
c PCH010 Pachyonychia Congenita 3 43 3.954
547
P MYT023 Myotonia Congenita 55 3.953
548
KPS004 Kaposi Sarcoma 77 3.948
549
c GRV008 Graves Disease 1 54 3.945
550
P MTR014 Motor Neuron Disease 65 3.930
551
P HYD006 Hydrocephalus 61 3.930
552
NWB001 Newborn Respiratory Distress Syndrome 56 3.905
553
P PTN014 Patent Ductus Arteriosus 1 59 3.902
554
P END033 Endocarditis 58 3.898
555
P HRD086 Hereditary Hypophosphatemic Rickets 40 3.898
556
P MVM001 Movement Disease 61 3.894
557
P CRN026 Corneal Edema 42 3.892
558
TND004 Tendinopathy 45 3.892
559
ALD013 Aldosterone-Producing Adenoma 36 3.882
560
c BLD140 Blood Group, I System 46 3.882
561
c ACT073 Acute Leukemia 58 3.882
562
P EPL140 Epilepsy, Idiopathic Generalized 62 3.881
563
CHD004 Chudley-Mccullough Syndrome 48 3.881
564
RTR008 Root Resorption 44 3.877
565
ANR004 Anuria 44 3.864
566
NRL016 Neural Tube Defects 81 3.864
567
END057 Endometrial Cancer 72 3.859
568
RTC003 Root Caries 32 3.858
569
HMP005 Hemiplegia 54 3.856
570
PTT037 Pituitary Tumors 44 3.855
571
AND005 Androgen Insensitivity Syndrome, Mild 21 3.851
572
P OPN001 Open-Angle Glaucoma 55 3.848
574
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 3.826
575
c MYC068 Myoclonic Epilepsy of Infancy 34 3.825
576
ACT119 Acute Promyelocytic Leukemia 62 3.818
577
APN008 Apnea, Obstructive Sleep 67 3.816
578
PLL012 Pollen Allergy 45 3.797
579
P SYS005 Systemic Scleroderma 74 3.797
580
HLC007 Helicobacter Pylori Infection 67 3.796
581
P SKN015 Skin Carcinoma 71 3.792
582
P INF038 Influenza 68 3.787
583
DNT006 Dental Pulp Necrosis 43 3.786
584
CRD137 Cardiogenic Shock 56 3.782
585
CYS013 Cystinuria 66 3.780
586
P END047 Endophthalmitis 53 3.778
587
WST001 West Syndrome 59 3.772
588
P GRF003 Graft-Versus-Host Disease 71 3.772
589
HNS001 Hansen's Disease 32 3.768
590
P LPR021 Leprosy 3 71 3.752
591
ACT098 Acute Erythroid Leukemia 55 3.739
592
SCH036 Scheie Syndrome 73 3.734
593
c CNG006 Congenital Hypothyroidism 63 3.719
594
c HPT001 Hepatitis C 62 3.713
595
KRT008 Keratopathy 46 3.693
596
P CHL066 Cholangitis 52 3.688
597
SCR011 Scrapie 39 3.668
598
CHL067 Cholecystitis 60 3.667
599
THR016 Thrombophlebitis 50 3.666
600
ATN005 Autonomic Dysfunction 46 3.644
601
c INH020 Inherited Metabolic Disorder 48 3.639
602
c BTT014 Beta-Thalassemia 72 3.636
603
HRP004 Herpes Zoster 61 3.625
604
c PRG043 Progressive Familial Heart Block, Type Ib 54 3.621
605
RGH001 Right Bundle Branch Block 47 3.621
606
P MYP006 Myopia 56 3.619
607
P BRN022 Bronchiectasis 60 3.618
608
P RTN022 Retinal Vein Occlusion 54 3.618
609
TNS005 Tonsillitis 57 3.613
610
PMP014 Pemphigoid 51 3.597
611
MCC002 Mucocutaneous Leishmaniasis 47 3.596
612
THR004 Thrombocytosis 53 3.594
613
PNS018 Pain Sensitivity Quantitative Trait Locus 1 23 3.592
614
CCC002 Coccidiosis 50 3.592
615
BRN028 Brain Cancer 74 3.588
616
P MDL005 Medulloblastoma 75 3.580
617
P GLL022 Guillain-Barre Syndrome 60 3.579
618
LYM143 Lymphoma, Non-Hodgkin, Familial 75 3.574
619
P NSP012 Nasopharyngeal Carcinoma 61 3.573
620
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 3.571
621
EPC002 Epicondylitis 44 3.566
622
PRR019 Perioral Myoclonia with Absences 27 3.552
623
INS001 Insulinoma 59 3.549
624
P DMN002 Dementia 66 3.543
625
NND001 Nondystrophic Myotonia 20 3.537
626
CRT084 Creatinine Clearance Quantitative Trait Locus 25 3.533
627
HRT012 Heart Valve Disease 53 3.522
628
P DRM010 Dermatomyositis 61 3.517
629
SFT003 Soft Tissue Sarcoma 57 3.507
630
PTH003 Pathologic Nystagmus 52 3.503
631
HYD002 Hydronephrosis 58 3.502
632
RSP019 Respiratory Distress Syndrome in Premature Infants 52 3.496
633
PLY150 Polykaryocytosis Inducer 29 3.494
634
P OBS001 Obstructive Jaundice 48 3.487
635
CNN005 Connective Tissue Disease 67 3.486
636
P BRS044 Breast Adenocarcinoma 58 3.473
637
c BRG005 Brugada Syndrome 1 54 3.472
638
GST040 Gastric Adenocarcinoma 67 3.470
639
GLC086 Glucocorticoid-Induced Osteoporosis 43 3.467
640
ORL015 Oral Squamous Cell Carcinoma 43 3.457
641
HMN047 Human Cytomegalovirus Infection 57 3.456
642
LPT014 Leptin Deficiency or Dysfunction 78 3.437
643
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 3.436
644
c DRR009 Diarrhea 6 45 3.427
645
PRN019 Perinatal Necrotizing Enterocolitis 60 3.427
646
ORL005 Oral Candidiasis 56 3.417
647
P SYP003 Syphilis 59 3.408
648
P PTT006 Pituitary Adenoma 55 3.396
649
CMM005 Common Cold 56 3.396
650
P ART005 Arteriovenous Malformation 65 3.395
651
RNL024 Renal Glucosuria 60 3.383
652
LNG031 Lung Benign Neoplasm 51 3.377
653
NRM004 Neuroma 49 3.377
654
SQM013 Squamous Cell Carcinoma, Head and Neck 73 3.368
655
c CRN243 Carney Complex, Type 1 53 3.361
656
CHR100 Chronic Ulcer of Skin 57 3.357
657
SPL018 Splenomegaly 49 3.353
658
SYS003 Systolic Heart Failure 49 3.350
659
c PRM093 Premature Ovarian Failure 7 48 3.347
660
P KDN017 Kidney Cancer 61 3.344
661
BLL006 Bullous Pemphigoid 61 3.343
662
P HYP733 Hypercalciuria, Absorptive, 2 45 3.341
663
RSC001 Rosacea 55 3.333
664
TRN018 Transitional Cell Carcinoma 56 3.322
665
CLL003 Cellulitis 53 3.318
666
CRB037 Cerebral Palsy 67 3.310
667
P PRP029 Porphyria 60 3.310
668
PNM008 Pneumothorax 54 3.301
669
BRK010 Burkitt Lymphoma 66 3.297
670
P SRC025 Sarcoidosis 1 71 3.289
671
ESP002 Esophageal Varix 51 3.287
672
CHG001 Chagas Disease 66 3.282
673
P END044 Endometriosis 62 3.272
674
APP008 Appendicitis 62 3.268
675
HMC014 Homocysteinemia 52 3.266
676
CRV035 Cervical Cancer 73 3.264
677
TRN015 Transient Cerebral Ischemia 63 3.252
678
PLY012 Polyhydramnios 46 3.245
679
SPN051 Spondylitis 51 3.236
680
INF009 Inflammatory Spondylopathy 30 3.236
681
P FBR017 Fibrosarcoma 56 3.235
682
LTH043 Lithium Transport 17 3.226
683
MCN017 Meconium Ileus 53 3.220
684
c SPN225 Spondyloarthropathy 1 70 3.220
685
P OTS001 Otosclerosis 49 3.217
686
SPT004 Septic Arthritis 58 3.196
687
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 3.190
688
NRT004 Neuritis 53 3.178
689
BNN003 Bone Inflammation Disease 48 3.178
690
FNG017 Fungal Infectious Disease 54 3.174
691
CYT005 Cytomegalovirus Retinitis 50 3.171
692
c VRL010 Viral Hepatitis 53 3.170
693
ORL011 Oral Cancer 60 3.167
694
BRC012 Brucellosis 66 3.157
695
c PRS136 Prostate Cancer, Hereditary, 6 33 3.151
696
c PRS130 Prostate Cancer, Hereditary, 8 32 3.151
697
P PLY011 Polycystic Ovary Syndrome 57 3.149
698
MST021 Meester-Loeys Syndrome 42 3.148
699
KWS002 Kawasaki Disease 65 3.144
700
PHR003 Pharyngitis 58 3.142
701
GRN017 Granulocytopenia 42 3.135
702
CRT015 Carotid Artery Occlusion 45 3.129
703
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 39 3.125
704
CHR073 Choreatic Disease 54 3.125
705
FSC004 Fasciitis 49 3.123
706
P RHB003 Rhabdomyosarcoma 66 3.123
707
NPH010 Nephrosclerosis 50 3.119
708
YLL002 Yellow Fever 61 3.116
709
P MST009 Mastocytosis 64 3.116
710
P MGR003 Migraine with Aura 52 3.115
711
OSM001 Osmotic Diarrhea 28 3.115
712
CHL004 Cholelithiasis 49 3.112
713
PRM236 Primary Biliary Cholangitis 60 3.107
714
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 3.104
715
CRH005 Crohn's Colitis 53 3.103
716
THY121 Thyroid Gland Anaplastic Carcinoma 67 3.103
717
P SPN046 Spinal Muscular Atrophy 63 3.099
718
P ERL057 Early Infantile Epileptic Encephalopathy 60 3.099
719
LYM133 Lymphoma, Hodgkin, Classic 74 3.097
720
c HPT015 Hepatitis D 49 3.093
721
HMS001 Hemosiderosis 48 3.092
722
P ANG015 Angioedema 56 3.091
723
INF034 Infective Endocarditis 54 3.091
724
DFF036 Differentiated Thyroid Carcinoma 51 3.090
725
EMB004 Embryonal Carcinoma 56 3.090
726
P HYP263 Hypersomnia 41 3.085
727
ATN004 Autonomic Neuropathy 42 3.084
728
c FML021 Familial Hypercholesterolemia 72 3.074
729
P CLS010 Cluster Headache 42 3.071
730
ATX019 Ataxia with Vitamin E Deficiency 44 3.068
731
HRT011 Heart Septal Defect 49 3.067
732
PRP016 Paraplegia 52 3.065
733
GLM044 Glomerular Disease 35 3.055
734
LYM027 Lymphopenia 56 3.055
735
FRZ001 Frozen Shoulder 55 3.053
736
NRL004 Neuroleptic Malignant Syndrome 52 3.052
737
P ORT004 Orthostatic Intolerance 63 3.052
738
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 3.051
739
SNT005 Sinoatrial Node Disease 47 3.050
740
DMP001 Dumping Syndrome 43 3.048
741
HMR023 Hemorrhagic Cystitis 43 3.042
742
ERY003 Erythema Multiforme 56 3.034
743
OST003 Osteonecrosis 61 3.034
744
DST006 Diastolic Heart Failure 45 3.034
745
EPT021 Epithelial Recurrent Erosion Dystrophy 46 3.030
746
c MJR006 Major Affective Disorder 5 32 3.030
747
c MJR003 Major Affective Disorder 6 32 3.030
748
c DWL002 Dowling-Degos Disease 1 58 3.029
749
c LNG047 Long Qt Syndrome 2 59 3.023
750
P MJR001 Major Depressive Disorder 68 3.016
751
ENM001 Enamel Caries 27 3.014
752
P SBS003 Substance Abuse 54 3.009
753
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 3.001
754
P VNS003 Venous Insufficiency 55 2.996
755
P PMP001 Pemphigus 55 2.995
756
c HYP731 Hyperaldosteronism, Familial, Type I 58 2.989
757
MCL027 Macular Dystrophy, Dominant Cystoid 51 2.988
758
MNN043 Meningioma, Familial 79 2.987
759
SCR001 Secretory Meningioma 40 2.987
760
LYM002 Lymphoplasmacyte-Rich Meningioma 35 2.987
761
SPN021 Spinal Meningioma 50 2.987
762
P GCH001 Gaucher's Disease 70 2.983
763
P CRP001 Carpal Tunnel Syndrome 66 2.983
764
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 2.981
765
MYC005 Myocardial Stunning 46 2.976
766
SPP011 Suppression of Tumorigenicity 12 61 2.974
767
NWC001 Newcastle Disease 47 2.972
768
GLS018 Glass Syndrome 61 2.955
769
P FML023 Familial Hemiplegic Migraine 53 2.950
770
P SLM003 Salmonellosis 54 2.945
771
END040 Endogenous Depression 55 2.941
772
RYN005 Raynaud Phenomenon 45 2.941
773
P BLD124 Bleeding Disorder, Platelet-Type, 11 67 2.938
774
P FCL005 Focal Segmental Glomerulosclerosis 57 2.937
775
SCN067 Scn1a Seizure Disorders 12 2.936
776
P SPP010 Suppressor of Tumorigenicity 3 51 2.931
777
PST028 Post-Traumatic Stress Disorder 59 2.930
778
APH001 Aphthous Stomatitis 58 2.916
779
c ACT249 Acute Asthma 40 2.914
780
P ACT105 Acute Mountain Sickness 52 2.910
781
CLR109 Colorectal Adenocarcinoma 50 2.908
782
c SVR005 Severe Pre-Eclampsia 50 2.900
783
c PRD040 Periodontitis, Chronic 52 2.899
784
EXT007 Extracutaneous Mastocytoma 38 2.896
785
MST004 Mast Cell Neoplasm 42 2.896
786
P RRH023 Rare Hereditary Hemochromatosis 54 2.896
787
P BRT053 Bartter Syndrome, Type 4a, Neonatal, with Sensorineural Deafness 45 2.894
788
CTR172 Citrullinemia, Classic 65 2.885
789
PRT018 Portal Vein Thrombosis 50 2.882
790
SKN019 Skin Melanoma 71 2.881
791
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 2.874
792
P EPL198 Epilepsy, Myoclonic Juvenile 61 2.871
793
c HPT073 Hepatitis C Virus 71 2.870
794
HSH003 Hashimoto Thyroiditis 60 2.870
795
VGN023 Vaginitis 56 2.870
796
PLM031 Poliomyelitis 63 2.869
797
c GLC092 Glaucoma, Primary Open Angle 62 2.861
798
IRD001 Iridocyclitis 53 2.852
799
CHR066 Chronic Fatigue Syndrome 60 2.851
800
CRN030 Coronary Stenosis 50 2.848
801
HYP264 Hypertonia 36 2.848
802
PLM017 Pulmonary Alveolar Microlithiasis 47 2.848
803
HYP781 Hypoascorbemia 52 2.846
804
CLR108 Colorectal Adenoma 64 2.842
805
P PLY018 Polycythemia 56 2.841
806
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.840
807
RST023 Resting Heart Rate, Variation in 40 2.838
808
ART074 Aortic Dissection 53 2.836
809
NSP002 Nasopharyngitis 45 2.829
810
c CNT035 Central Nervous System Disease 54 2.823
811
ACT058 Active Peptic Ulcer Disease 56 2.813
812
P RCT021 Rectum Cancer 54 2.806
813
NRM009 Normokalemic Periodic Paralysis 28 2.803
814
OCL006 Ocular Hypertension 53 2.802
815
ANT024 Anthrax Disease 58 2.800
816
P ASP006 Aspergillosis 72 2.794
817
TRD006 Tardive Dyskinesia 53 2.789
818
P TXP001 Toxoplasmosis 60 2.789
819
P MLN007 Male Infertility 56 2.777
820
GLC022 Glucose/galactose Malabsorption 44 2.775
821
ANR007 Anorexia Nervosa 60 2.774
822
P STR020 Strabismus 56 2.768
823
MCH006 Mechanical Strabismus 40 2.768
824
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 2.764
825
P PTS002 Ptosis 52 2.761
826
OVR029 Ovarian Hyperstimulation Syndrome 63 2.759
827
P MMB011 Membranous Nephropathy 50 2.758
828
LNN001 Lennox-Gastaut Syndrome 61 2.756
829
P SCL018 Scoliosis 57 2.756
830
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 2.755
831
P INS002 in Situ Carcinoma 53 2.753
832
c BCT013 Bacterial Pneumonia 48 2.751
833
DNT001 Dental Fluorosis 43 2.748
834
P SBR004 Seborrheic Dermatitis 44 2.745
835
OCC016 Occupational Asthma 33 2.745
836
P HRD011 Hereditary Spherocytosis 64 2.745
837
P MYS005 Myositis 56 2.744
838
DNG003 Dengue Disease 65 2.743
839
ACT113 Acute Myeloblastic Leukemia with Maturation 46 2.743
840
c FML001 Familial Atrial Fibrillation 65 2.739
841
P VNW001 Von Willebrand's Disease 65 2.734
842
c LNG044 Long Qt Syndrome 1 66 2.732
843
CHK001 Chikungunya 60 2.730
844
FRN014 Fournier Gangrene 26 2.727
845
MNR012 Meniere Disease 56 2.723
846
DRG024 Drug Allergy 40 2.715
848
c ART101 Aortic Valve Disease 2 66 2.710
849
INT030 Intracranial Aneurysm 55 2.707
850
CHC001 Chickenpox 57 2.701
851
CRN036 Craniopharyngioma 64 2.700
852
P OLG002 Oligodendroglioma 66 2.699
853
c MJR023 Major Affective Disorder 7 33 2.699
854
c MJR004 Major Affective Disorder 4 28 2.699
855
c MJR008 Major Affective Disorder 2 34 2.699
856
BRT054 Brittle Bone Disorder 74 2.693
858
RHM001 Rheumatic Fever 59 2.686
859
c ESS001 Essential Tremor 57 2.686
860
P NJM001 Nijmegen Breakage Syndrome 76 2.668
861
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 2.667
862
P ATX030 Ataxia-Telangiectasia 80 2.665
863
CNG064 Congenital Chloride Diarrhea 34 2.660
864
PRT038 Protein-Energy Malnutrition 53 2.660
865
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 46 2.659
866
P ALT001 Alternating Hemiplegia of Childhood 57 2.658
867
BCT004 Bacteriuria 47 2.658
868
P EPD016 Epidermolysis Bullosa 53 2.658
869
c LKM005 Leukemia, T-Cell, Chronic 34 2.657
870
GST033 Gestational Diabetes 61 2.657
871
NRT001 Neurotic Disorder 56 2.655
872
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 2.654
873
P MRC003 Mercury Poisoning 49 2.652
874
QDR001 Quadriplegia 50 2.650
875
OLG003 Oligohydramnios 51 2.650
876
BRD004 Borderline Personality Disorder 53 2.649
877
LWC001 Low Compliance Bladder 45 2.647
878
OVR094 Ovarian Epithelial Cancer 39 2.643
879
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 45 2.641
880
P MYG005 Myoglobinuria 40 2.640
881
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 2.637
882
PLS011 Plasmacytoma 56 2.619
883
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 36 2.616
884
c SCN036 Secondary Progressive Multiple Sclerosis 55 2.610
885
CRN027 Corneal Neovascularization 47 2.606
886
LPT001 Leptospirosis 66 2.606
887
c LKM063 Leukemia, Chronic Myeloid 71 2.604
888
c GNR039 Generalized Epilepsy with Febrile Seizures Plus, Type 2 47 2.601
889
P PGT001 Paget's Disease of Bone 61 2.597
890
RTN020 Retinal Vascular Disease 46 2.594
891
c MST023 Mesothelioma, Malignant 56 2.594
892
FML159 Familial Periodic Paralyses 16 2.594
893
BRS064 Bursitis 51 2.590
894
MCR004 Macroglobulinemia 49 2.583
895
P BLD062 Bile Duct Cancer 67 2.579
896
c HYP724 Hyperlipoproteinemia, Type Iii 67 2.571
897
P THY054 Thyrotoxic Periodic Paralysis 50 2.565
898
ALC009 Alcoholic Liver Cirrhosis 54 2.562
899
P FML011 Familial Adenomatous Polyposis 71 2.562
900
NPH013 Nephrogenic Syndrome of Inappropriate Antidiuresis 37 2.559
901
MYX004 Myxedema 43 2.558
902
OBS002 Obsessive-Compulsive Disorder 68 2.557
903
HYP114 Hypertensive Nephropathy 36 2.556
904
P BNC003 Bone Cancer 58 2.550
905
HYP020 Hyperprolactinemia 63 2.549
906
ADR008 Adrenal Adenoma 55 2.539
907
WLL004 Wallerian Degeneration 38 2.538
908
c BCT007 Bacterial Meningitis 55 2.536
909
TBR011 Tuberculous Meningitis 48 2.536
910
P THR015 Thrombophilia 51 2.533
911
SNL007 Senile Cataract 40 2.531
912
BRN014 Bronchopneumonia 53 2.529
913
GLY010 Glycine Encephalopathy 57 2.527
914
P HML001 Hemolytic-Uremic Syndrome 52 2.522
915
HRT015 Heritable Pulmonary Arterial Hypertension 46 2.522
916
HMG005 Hemoglobinopathy 56 2.518
917
EXN003 Exencephaly 30 2.511
918
ORN008 Ornithine Transcarbamylase Deficiency, Hyperammonemia Due to 62 2.510
919
PRP007 Priapism 47 2.505
920
CYS010 Cystinosis 62 2.501
921
HYP540 Hypertension, Diastolic 37 2.500
922
DBT002 Diabetic Autonomic Neuropathy 41 2.497
923
PRC013 Pericarditis 53 2.496
924
P MTR012 Mitral Valve Disease 57 2.496
925
AMN006 Aminoaciduria 37 2.491
926
GRW007 Growth Hormone Deficiency 46 2.484
927
APH002 Aphasia 56 2.480
928
P CRV039 Cervicitis 52 2.479
929
LST001 Listeriosis 59 2.479
930
PRR001 Periarthritis 34 2.479
931
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 2.479
932
c CHR064 Chronic Monocytic Leukemia 36 2.474
933
INT066 Interstitial Lung Disease 60 2.471
934
DVR002 Diverticulitis 46 2.469
935
MYT003 Myotonic Disease 36 2.469
936
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 2.462
937
CCN002 Cocaine Abuse 49 2.456
938
P SCL009 Sclerosing Cholangitis 48 2.456
939
MLD018 Mild Cognitive Impairment 48 2.455
940
P DNG005 Dengue Virus 56 2.449
941
NRM005 Neuromuscular Disease 63 2.447
942
P MYS003 Myasthenia Gravis 68 2.439
943
VSC002 Vascular Dementia 60 2.436
944
P RTN008 Retinitis Pigmentosa 80 2.434
945
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 2.431
946
SNS003 Sensory Peripheral Neuropathy 52 2.431
947
P RNL115 Renal Tubular Acidosis, Proximal 32 2.428
948
P MTR003 Mitral Valve Stenosis 53 2.428
949
SYS004 Systemic Mastocytosis 63 2.427
950
c PSD092 Pseudohypoaldosteronism, Type Iie 48 2.420
951
CRT072 Creutzfeldt-Jakob Disease 68 2.419
952
ADR016 Adrenal Cortical Carcinoma 62 2.418
953
P CRC039 Coarctation of Aorta 46 2.418
954