Search results for obesity diabetes

3991 hits were found for obesity diabetes

# Family MCID Name MIFTS Score
1
P BDY004 Body Mass Index Quantitative Trait Locus 11 82 186.691
2
c TYP009 Type 2 Diabetes Mellitus 91 176.407
3
P DBT009 Diabetes Mellitus 67 158.042
4
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 149.743
5
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 149.603
6
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 149.600
7
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 148.937
8
c BDY019 Body Mass Index Quantitative Trait Locus 18 46 148.411
9
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 148.283
10
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 148.144
11
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 148.143
12
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 144.699
13
c TYP008 Type 1 Diabetes Mellitus 77 125.410
14
c MCR115 Microvascular Complications of Diabetes 5 65 104.458
15
GST033 Gestational Diabetes 60 102.060
16
c MCR113 Microvascular Complications of Diabetes 3 52 96.734
17
c MCR120 Microvascular Complications of Diabetes 7 47 95.489
18
LPT014 Leptin Deficiency or Dysfunction 77 92.351
19
c MCR133 Microvascular Complications of Diabetes 4 41 88.674
20
c MCR130 Microvascular Complications of Diabetes 6 41 88.673
21
P MCR129 Microvascular Complications of Diabetes 1 67 76.039
22
HYP066 Hyperglycemia 60 70.974
23
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 68.915
24
DBT084 Diabetes Mellitus, Ketosis-Prone 59 67.324
25
DBT010 Diabetic Neuropathy 54 66.729
26
c MCR112 Microvascular Complications of Diabetes 2 42 64.182
27
LPD008 Lipid Metabolism Disorder 61 61.046
28
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 57.549
29
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 57.247
30
HYP056 Hypoglycemia 65 55.675
31
P MTR004 Maturity-Onset Diabetes of the Young 66 54.896
32
P DBT005 Diabetes Insipidus 54 54.436
33
DBT087 Diabetes Insipidus, Neurohypophyseal 58 54.211
34
FTT001 Fatty Liver Disease 61 53.056
35
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 52.194
36
NNL005 Non-Alcoholic Fatty Liver Disease 63 51.836
37
GLC003 Glucose Intolerance 53 48.733
38
HYP060 Hyperinsulinism 53 47.459
39
DBT006 Diabetic Macular Edema 48 46.982
40
c TYP028 Type 1 Diabetes Mellitus 2 49 44.288
41
RNL051 Renal Cysts and Diabetes Syndrome 58 43.746
42
P NRP001 Neuropathy 59 43.329
43
P NNT058 Neonatal Diabetes 52 43.217
44
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 43.010
45
DBT090 Diabetes and Deafness, Maternally Inherited 44 42.463
46
DBT002 Diabetic Autonomic Neuropathy 40 40.685
47
LPT006 Leptin Receptor Deficiency 50 39.715
48
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 28 39.386
49
DBT004 Diabetic Polyneuropathy 50 39.130
50
OBS037 Obesity-Hypoventilation Syndrome 44 39.076
51
P VSC007 Vascular Disease 62 39.062
52
P PRM030 Permanent Neonatal Diabetes Mellitus 59 38.569
53
P KDN018 Kidney Disease 71 38.426
54
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 37.591
55
DBT008 Diabetic Angiopathy 47 37.372
56
P SLP006 Sleep Apnea 69 36.913
57
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 36.802
58
P CRN300 Coronary Heart Disease 1 73 36.780
59
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 36.725
60
c CHR684 Chronic Kidney Disease 73 36.341
61
P PRP019 Peripheral Nervous System Disease 57 35.605
62
c TRN032 Transient Neonatal Diabetes Mellitus 48 35.590
63
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 35.359
64
P LVR013 Liver Disease 68 35.145
65
PRT251 Proteinuria, Chronic Benign 58 34.829
66
c BLD140 Blood Group, I System 47 34.715
67
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 34.510
68
BCK003 Background Diabetic Retinopathy 46 34.127
69
END086 End Stage Renal Disease 54 34.118
70
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 33.842
71
P PLY011 Polycystic Ovary Syndrome 57 33.494
72
LPP008 Lipoprotein Quantitative Trait Locus 65 33.134
73
P HYP750 Hypertriglyceridemia, Familial 61 33.133
74
c DBT104 Diabetes Mellitus, Permanent Neonatal, 1 47 33.076
75
ATH013 Atherosclerosis Susceptibility 63 33.071
76
ART140 Arteries, Anomalies of 52 33.052
77
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 40 32.831
78
MNG006 Monogenic Diabetes 45 32.565
79
P HRT032 Heart Disease 84 32.354
80
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 32.259
81
MCL006 Macular Retinal Edema 56 31.628
82
c TYP053 Type 1 Diabetes Mellitus 20 42 31.403
83
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 44 31.367
84
c MTR023 Maturity-Onset Diabetes of the Young, Type 6 41 31.357
85
c HYP836 Hypercholesterolemia, Familial, 1 73 31.214
86
c MTR024 Maturity-Onset Diabetes of the Young, Type 7 41 31.160
87
MRB006 Morbid Obesity and Spermatogenic Failure 21 31.158
88
DBT007 Diabetic Cataract 36 31.027
89
BRT037 Brittle Diabetes 24 30.673
90
PRP027 Peripheral Vascular Disease 71 30.450
91
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 30.161
92
GNT167 Genetic Obesity 33 30.137
93
NNL006 Non-Alcoholic Steatohepatitis 54 29.886
94
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 29.760
95
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 29.680
96
LTN029 Latent Autoimmune Diabetes in Adults 38 29.412
97
ETN001 Eating Disorder 59 28.851
98
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 54 28.687
99
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 28.440
100
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 42 28.196
101
c HYP595 Hypertension, Essential 84 27.960
102
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 39 27.900
103
RCK004 Rickets 64 27.722
104
CNG034 Congestive Heart Failure 69 27.605
105
HYP835 Hypothalamic Obesity 38 27.597
106
P WLF004 Wolfram Syndrome 61 27.343
107
c TYP030 Type 1 Diabetes Mellitus 4 20 27.324
108
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 27.291
109
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 27.173
110
c TYP040 Type 1 Diabetes Mellitus 18 24 27.149
111
c TYP058 Type 2 Diabetes 5 25 27.102
112
c PRC016 Pre-Eclampsia 64 27.037
113
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 29 26.515
114
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 55 26.409
115
P PRD008 Periodontitis 63 26.366
116
ATN004 Autonomic Neuropathy 42 26.113
117
TYP048 Type 1 Diabetes Mellitus, X-Linked 11 26.033
118
c TYP049 Type 2 Diabetes Mellitus 2 21 25.890
120
c LPD015 Lipodystrophy, Familial Partial, Type 2 61 25.283
121
MHM001 Mehmo Syndrome 47 25.177
122
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 25.163
123
ISC004 Ischemia 61 25.042
124
IMP005 Impotence 52 24.946
125
AGN016 Aging 53 24.565
126
PRP098 Proprotein Convertase 1/3 Deficiency 36 24.488
127
P PLY019 Polyneuropathy 52 24.321
128
CHN016 Cohen Syndrome 59 23.447
129
PRD004 Prediabetes Syndrome 52 23.353
130
DPR016 Depression 64 23.334
131
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 23.211
132
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 23.192
133
c WLF013 Wolfram Syndrome 1 60 23.053
134
ATM095 Autoimmune Disease 61 22.908
135
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 38 22.885
136
c TYP050 Type 2 Diabetes Mellitus 3 15 22.830
137
c ATR087 Atrial Standstill 1 74 22.812
138
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 28 22.658
139
c ABD015 Abdominal Obesity-Metabolic Syndrome 4 22 22.317
140
DBT081 Diabetic Encephalopathy 36 22.258
141
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 22.154
142
c TYP051 Type 2 Diabetes Mellitus 4 17 22.133
143
P MYC007 Myocardial Infarction 69 22.122
144
P HYP086 Hypothyroidism 68 21.875
145
CRB039 Cerebrovascular Disease 65 21.750
146
P CRD246 Cardiovascular System Disease 55 21.204
147
SYN116 Syndromic Obesity 27 20.169
148
c HMC039 Hemochromatosis, Type 1 73 20.106
149
P AST005 Asthma 75 20.096
150
P CTR002 Cataract 59 19.963
151
HYP080 Hypogonadism 49 19.856
152
P PNC044 Pancreatitis 61 19.638
153
MNT002 Mental Depression 56 19.304
154
CVD001 Covid-19 59 19.206
155
OST012 Osteoarthritis 77 19.040
156
NTR005 Nutritional Deficiency Disease 60 18.964
157
INS024 Insulin-Like Growth Factor I 77 18.870
158
SHR107 Short Stature-Obesity Syndrome 25 18.757
159
STR067 Stroke, Ischemic 79 18.372
160
P PRD006 Prader-Willi Syndrome 60 18.185
161
APN008 Apnea, Obstructive Sleep 66 18.054
162
CYT002 Cytokine Deficiency 43 18.050
163
RPD005 Rapidly Involuting Congenital Hemangioma 48 18.000
164
P ANR048 Aniridia 1 66 17.936
165
OCL069 Ocular Motor Apraxia 57 17.908
166
c ACT027 Acute Pancreatitis 60 17.774
167
HYP014 Hyperuricemia 51 17.461
168
DPS001 Dipsogenic Diabetes Insipidus 21 17.370
169
c CNG012 Congenital Generalized Lipodystrophy 65 17.360
170
P PNC035 Pancreatic Cancer 87 17.256
171
INS034 Insulinomatosis and Diabetes Mellitus 26 17.159
172
TRP008 Tropical Calcific Pancreatitis 46 17.107
173
GST092 Gastroesophageal Reflux 59 17.022
174
c ACT075 Acute Myocardial Infarction 55 17.020
175
P ATR011 Atrial Fibrillation 66 16.967
176
ATN005 Autonomic Dysfunction 45 16.834
177
PRP080 Peripheral Artery Disease 54 16.813
178
P OST002 Osteoporosis 76 16.811
179
P ART021 Arteriosclerosis 53 16.771
180
P URN019 Urinary Tract Infection 48 16.768
181
END057 Endometrial Cancer 76 16.691
182
P ECL001 Eclampsia 52 16.689
183
LVR012 Liver Cirrhosis 62 16.560
184
P INF032 Infertility 60 16.518
185
PLC008 Placenta Disease 48 16.325
186
ACN002 Acanthosis Nigricans 56 16.298
187
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 16.251
188
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 16.251
189
PLM129 Pulmonary Disease, Chronic Obstructive 74 16.155
190
ODN026 Odontochondrodysplasia 2 with Hearing Loss and Diabetes 12 16.145
191
P ALC033 Alcohol Use Disorder 67 16.107
192
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 56 16.074
193
P EYD002 Eye Disease 57 16.035
194
GST037 Gastroparesis 52 16.004
195
PRX085 Preaxial Hallucal Polydactyly 28 15.920
196
ANX010 Anxiety 70 15.851
197
OST017 Osteomyelitis 63 15.843
198
48X005 48,xyyy 39 15.704
199
ALC007 Alcohol Dependence 65 15.688
200
P THY032 Thyroiditis 56 15.643
201
P TRN020 Turner Syndrome 67 15.526
202
HYP266 Hypoxia 56 15.401
203
P CLC063 Celiac Disease 1 65 15.255
204
P HPT021 Hepatitis 68 15.203
205
P PRS038 Personality Disorder 65 15.193
206
47X002 47,xyy 47 15.169
207
RTN020 Retinal Vascular Disease 45 15.114
208
P RTN018 Retinal Disease 53 15.017
209
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 52 14.982
211
OVR063 Overnutrition 42 14.860
212
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 14.834
213
P DMN002 Dementia 65 14.773
214
INS001 Insulinoma 59 14.677
215
P BRS047 Breast Cancer 97 14.645
216
HYP043 Hyperandrogenism 47 14.619
217
c THR092 Thrombophilia Due to Thrombin Defect 74 14.545
218
ANG054 Angina Pectoris 65 14.532
219
SVR001 Severe Acute Respiratory Syndrome 68 14.506
220
IRN002 Iron Metabolism Disease 56 14.502
221
LMB062 Limb Ischemia 55 14.480
222
PST011 Pustulosis of Palm and Sole 52 14.427
223
P PSR002 Psoriasis 63 14.408
224
P SLP005 Sleep Disorder 61 14.313
225
RHH001 Rohhad 27 14.253
226
ACT088 Acute Insulin Response 39 14.208
227
P SCH015 Schizophrenia 74 14.118
228
GT001 Gout 63 14.067
229
SVR004 Severe Combined Immunodeficiency 70 13.946
230
c GLL024 Gallbladder Disease 1 53 13.928
231
P MJR001 Major Depressive Disorder 68 13.898
232
c PRD040 Periodontitis, Chronic 52 13.878
233
SXL003 Sexual Disorder 49 13.840
234
CNS004 Constipation 56 13.814
235
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 13.791
236
DFC004 Deficiency Anemia 74 13.785
237
P RSP003 Respiratory Failure 73 13.679
238
DWN001 Down Syndrome 70 13.673
239
P ALZ034 Alzheimer Disease 87 13.536
240
P CLR023 Colorectal Cancer 100 13.480
241
c ACT071 Acute Kidney Failure 60 13.459
242
DSS008 Disease of Mental Health 74 13.446
243
RNL024 Renal Glucosuria 60 13.420
244
P ART022 Arthritis 70 13.413
245
FTL021 Fetal Macrosomia 40 13.364
246
CYS001 Cystic Fibrosis 77 13.110
247
c HPT001 Hepatitis C 61 13.057
248
PLM033 Pulmonary Embolism 58 12.880
249
c ACT068 Acute Cystitis 60 12.745
250
RTN017 Retinal Detachment 60 12.704
251
P HPT023 Hepatocellular Carcinoma 95 12.646
253
ANR007 Anorexia Nervosa 59 12.611
255
HYP005 Hypokalemia 55 12.466
256
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 52 12.378
257
ALL029 Allergic Disease 61 12.361
258
P MYC084 Mycobacterium Tuberculosis 1 68 12.359
259
P BPL003 Bipolar Disorder 56 12.272
260
CHR100 Chronic Ulcer of Skin 57 12.261
261
P RHM011 Rheumatoid Arthritis 81 12.248
262
P ACQ022 Acquired Generalized Lipodystrophy 45 12.237
263
P CHR345 Chronic Pain 50 12.227
264
RNL077 Renal Fibrosis 46 12.155
265
INT007 Intermediate Coronary Syndrome 53 12.127
266
CRH001 Crohn's Disease 80 12.046
267
MDD011 Mood Disorder 61 11.982
268
P HYP076 Hyperthyroidism 53 11.930
269
c MJR022 Major Affective Disorder 8 37 11.863
270
c MJR024 Major Affective Disorder 9 40 11.863
271
LNG099 Lung Disease 62 11.855
272
THR024 Thrombosis 56 11.829
273
KRT002 Keratomalacia 54 11.800
274
BNR002 Bone Resorption Disease 47 11.766
275
BCK006 Back Pain 43 11.758
276
CRN036 Craniopharyngioma 63 11.753
277
RST023 Resting Heart Rate, Variation in 40 11.740
278
P ATT013 Attention Deficit-Hyperactivity Disorder 65 11.699
279
P OVR082 Overgrowth Syndrome 41 11.686
280
P SHR029 Short Syndrome 59 11.660
281
BLM002 Bulimia Nervosa 56 11.638
282
ADN018 Adenoma 58 11.574
283
ACR007 Acromegaly 70 11.571
284
NRL016 Neural Tube Defects 80 11.559
285
DNT012 Dental Caries 53 11.558
286
P HYP069 Hyperparathyroidism 62 11.501
287
c BRN108 Branchiootic Syndrome 1 63 11.470
288
HSH003 Hashimoto Thyroiditis 60 11.457
289
MTB004 Metabolic Acidosis 48 11.338
290
P ART023 Arthropathy 59 11.314
291
P DRR001 Diarrhea 55 11.297
292
CRD132 Cardiac Conduction Defect 59 11.269
293
P GLM007 Glomerulonephritis 59 11.251
294
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 11.220
295
P LCT001 Lactic Acidosis 50 11.137
296
P BND020 Bone Disease 60 11.111
297
MLD018 Mild Cognitive Impairment 48 11.042
298
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 11.029
299
NRR001 Neuroretinitis 42 10.993
300
RTN023 Retinitis 45 10.967
301
CLL003 Cellulitis 53 10.953
302
P HYP730 Hypogonadotropic Hypogonadism 57 10.949
303
NPH009 Nephrolithiasis 54 10.917
304
ADL002 Adult Syndrome 69 10.831
305
FML035 Familial Hyperlipidemia 54 10.776
306
P PRS040 Prostate Cancer 95 10.710
307
P ENC018 Encephalopathy 62 10.668
308
PRT036 Peritonitis 65 10.649
309
P NPH012 Nephrotic Syndrome 61 10.634
310
P HYP083 Hypopituitarism 51 10.590
311
GNG013 Gingivitis 59 10.587
312
HMC014 Homocysteinemia 52 10.569
313
HYP364 Hyperostosis Frontalis Interna 29 10.537
314
PLM001 Pulmonary Tuberculosis 69 10.468
315
P ESP024 Esophagitis 60 10.459
316
PRT058 Pure Autonomic Failure 58 10.455
317
ANT039 Antisynthetase Syndrome 55 10.404
318
URM002 Uremia 47 10.372
319
P GST053 Gastric Cancer 82 10.370
320
SNS003 Sensory Peripheral Neuropathy 51 10.161
321
CRN030 Coronary Stenosis 50 10.126
322
DSS032 Disease by Infectious Agent 55 10.105
323
ALS001 Alstrom Syndrome 65 10.091
324
ANV001 Anovulation 46 10.073
325
c HPT016 Hepatitis B 62 9.975
326
P BRD002 Bardet-Biedl Syndrome 66 9.930
327
c VRL010 Viral Hepatitis 52 9.869
328
P ADL010 Adult Respiratory Distress Syndrome 70 9.856
329
P INF038 Influenza 68 9.824
330
P INF037 Inflammatory Bowel Disease 53 9.801
331
P PNM007 Pneumonia 64 9.773
332
HRW001 Hair Whorl 35 9.748
333
CHL004 Cholelithiasis 48 9.747
334
c MGR028 Migraine with or Without Aura 1 63 9.719
335
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 9.713
336
PNG002 Pain Agnosia 51 9.713
337
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 9.711
338
c HYP724 Hyperlipoproteinemia, Type Iii 66 9.646
339
ANR040 Aneurysm 60 9.629
340
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 9.618
341
c HPT073 Hepatitis C Virus 70 9.594
342
ACH016 Achard Thiers Syndrome 9 9.587
343
P CRP001 Carpal Tunnel Syndrome 65 9.540
344
INT323 Intraocular Pressure Quantitative Trait Locus 63 9.506
345
c HPT003 Hepatitis a 63 9.429
346
TXC005 Toxic Shock Syndrome 61 9.366
347
P PYL005 Pyelonephritis 56 9.321
348
HLC007 Helicobacter Pylori Infection 67 9.202
349
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 9.199
350
P CRD119 Cardiac Arrest 68 9.183
351
c HNT004 Huntington Disease-Like 2 51 9.183
352
P GST044 Gastritis 55 9.126
353
INT002 Intermittent Claudication 61 9.114
354
RNL114 Renal Cell Carcinoma, Nonpapillary 79 9.088
355
P ADN016 Adenocarcinoma 63 9.083
356
P PLM037 Pulmonary Hypertension 69 9.081
357
GLC008 Glucose Metabolism Disease 40 9.044
358
BLR008 Bilirubin Metabolic Disorder 57 9.013
359
MSC007 Muscle Hypertrophy 64 9.000
360
ART016 Aortic Aneurysm 68 8.997
361
P LKM062 Leukemia, Acute Lymphoblastic 69 8.990
362
IMM167 Immune Deficiency Disease 76 8.975
363
HMS001 Hemosiderosis 48 8.959
364
MCR141 Mucormycosis 59 8.957
365
SKN016 Skin Disease 63 8.946
366
CHL067 Cholecystitis 59 8.919
367
P MSC003 Muscular Atrophy 52 8.914
368
BCT022 Bacterial Infectious Disease 55 8.907
369
P RRH023 Rare Hereditary Hemochromatosis 52 8.894
370
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 8.892
371
P MYP004 Myopathy 67 8.892
372
c ATS007 Autism Spectrum Disorder 71 8.888
373
P BLD134 Bladder Cancer 79 8.846
374
P RCT021 Rectum Cancer 54 8.844
375
NPH091 Nephrolithiasis, Calcium Oxalate 61 8.807
376
P KDN017 Kidney Cancer 60 8.806
377
RHB024 Rhabdomyosarcoma 2 65 8.785
378
P FCL005 Focal Segmental Glomerulosclerosis 57 8.767
379
c PNS012 Paine Syndrome 60 8.764
380
P SBS003 Substance Abuse 54 8.758
381
ACQ007 Acquired Immunodeficiency Syndrome 58 8.758
382
P CND004 Candidiasis 57 8.755
383
TRN015 Transient Cerebral Ischemia 62 8.733
384
AMN001 Amenorrhea 53 8.730
385
HMN044 Human Immunodeficiency Virus Type 1 76 8.711
386
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 8.704
387
P AMY004 Amyloidosis 69 8.612
388
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 8.444
389
P RHN004 Rhinitis 56 8.423
390
GRW007 Growth Hormone Deficiency 47 8.405
391
SPN186 Spinal Cord Injury 60 8.371
392
P NRV007 Nervous System Disease 65 8.369
393
CNN003 Conn's Syndrome 77 8.349
394
P GLL020 Gallbladder Disease 57 8.324
395
CRT013 Carotid Stenosis 51 8.276
396
VSC002 Vascular Dementia 59 8.215
397
PST028 Post-Traumatic Stress Disorder 58 8.211
398
PRS021 Prostatic Adenoma 43 8.182
399
ULC004 Ulcerative Colitis 74 8.163
400
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 8.135
401
APP008 Appendicitis 62 8.131
402
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 8.067
403
PRS045 Prostatic Hypertrophy 53 8.066
404
P ATS364 Autism 72 8.060
405
DYS073 Dysphagia 53 8.015
406
THY029 Thyroid Carcinoma 55 8.009
407
c BRD010 Bardet-Biedl Syndrome 1 64 7.973
408
PRS129 Prostatic Hyperplasia, Benign 48 7.954
409
IGR001 Ige Responsiveness, Atopic 58 7.949
410
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.943
411
HRN026 Hernia, Hiatus 46 7.928
412
P MLN007 Male Infertility 56 7.924
413
P OPT006 Optic Nerve Disease 57 7.892
414
FSC004 Fasciitis 49 7.886
415
P GRV001 Graves' Disease 54 7.880
416
P BCL017 B-Cell Lymphoma 57 7.876
417
c SCN007 Secondary Hyperparathyroidism 50 7.871
418
PSY004 Psychotic Disorder 66 7.856
419
DRM006 Dermatitis 61 7.802
420
P HDC001 Headache 56 7.799
421
THY030 Thyroid Gland Disease 50 7.796
422
END072 Endotheliitis 36 7.787
423
P LKM002 Leukemia 65 7.776
424
P RTN022 Retinal Vein Occlusion 54 7.769
425
c SYS001 Systemic Lupus Erythematosus 85 7.709
426
ART002 Arts Syndrome 66 7.708
427
PPT005 Peptic Ulcer Disease 58 7.690
428
P EPL164 Epilepsy 70 7.688
429
MCL027 Macular Dystrophy, Dominant Cystoid 51 7.681
430
VTM002 Vitamin B12 Deficiency 48 7.672
431
PLM010 Pulmonary Edema 54 7.645
432
HST010 Histiocytosis 49 7.635
433
LYM027 Lymphopenia 56 7.635
434
ALL003 Allergic Rhinitis 66 7.625
435
P LPS004 Lupus Erythematosus 61 7.616
436
P SRC025 Sarcoidosis 1 70 7.608
437
IGG001 Iga Glomerulonephritis 50 7.605
438
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 19 7.591
439
ESP021 Esophageal Cancer 84 7.586
440
MNC019 Monocarboxylate Transporter 1 Deficiency 46 7.570
441
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 7.565
442
PLY105 Polycystic Ovary Syndrome 1 39 7.517
443
BRN071 Brain Injury 50 7.498
444
P MLT020 Multiple Sclerosis 79 7.496
445
LRN002 Laron Syndrome 62 7.474
446
FBR047 Fibromyalgia 57 7.429
447
KRN002 Kearns-Sayre Syndrome 62 7.422
448
P SZR006 Seizure Disorder 69 7.408
449
P LNG032 Lung Cancer 98 7.388
450
CRD137 Cardiogenic Shock 56 7.387
451
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 7.373
452
P RTN008 Retinitis Pigmentosa 79 7.355
453
PSR001 Psoriatic Arthritis 61 7.330
454
c HNT011 Huntington Disease-Like 3 33 7.310
455
IRN001 Iron Deficiency Anemia 58 7.304
456
CLT003 Colitis 63 7.266
457
IRR002 Irritable Bowel Syndrome 64 7.265
458
P SNS001 Sensorineural Hearing Loss 60 7.242
459
URL001 Urolithiasis 45 7.219
460
P VSC011 Vasculitis 61 7.205
461
c EPS039 Episodic Pain Syndrome, Familial, 1 42 7.192
462
NVS001 Neovascular Glaucoma 52 7.186
463
BRN024 Bronchitis 67 7.106
464
P HYP061 Hypertrophic Cardiomyopathy 68 7.059
465
SCH012 Schizoaffective Disorder 49 7.045
466
c DLT002 Dilated Cardiomyopathy 79 7.026
467
P MLN008 Melanoma 75 7.012
468
END040 Endogenous Depression 54 6.997
469
INT075 Intracranial Hypertension 52 6.973
470
P HYP050 Hyperinsulinemic Hypoglycemia 56 6.964
471
P ACN011 Acne 55 6.959
472
ATS010 Autosomal Recessive Disease 42 6.950
473
CMB007 Combined Immunodeficiency 56 6.949
474
P OPN001 Open-Angle Glaucoma 55 6.944
475
NCR002 Necrobiosis Lipoidica 38 6.930
476
BCT004 Bacteriuria 48 6.917
477
CRD223 Cardiac Arrhythmia 63 6.914
478
CHL068 Cholestasis 61 6.912
479
HYP020 Hyperprolactinemia 63 6.900
480
P UVT001 Uveitis 57 6.891
481
CRB004 Cerebral Artery Occlusion 45 6.867
482
MYL069 Myeloma, Multiple 76 6.847
483
PTT009 Pituitary Gland Disease 52 6.841
484
P RTN016 Retinal Degeneration 52 6.826
485
LNG108 Langerhans Cell Histiocytosis 57 6.810
486
BRR014 Barrett Esophagus 66 6.807
487
P LYM118 Lymphoma 66 6.806
488
PRS063 Paresthesia 39 6.805
489
P MYP006 Myopia 55 6.787
490
P THR014 Thrombocytopenia 66 6.784
491
P HYP265 Hypotonia 42 6.754
492
GLM044 Glomerular Disease 34 6.728
493
c PNC106 Pancreatic Agenesis 1 51 6.727
494
DMP001 Dumping Syndrome 43 6.702
495
P PTT006 Pituitary Adenoma 55 6.685
496
HYP081 Hypolipoproteinemia 49 6.670
497
P ALP008 Alopecia 53 6.660
498
AND005 Androgen Insensitivity Syndrome, Mild 21 6.648
499
P OVR042 Ovarian Cancer 88 6.640
500
SYS003 Systolic Heart Failure 49 6.635
501
P OVR049 Ovarian Disease 50 6.611
502
P CNR004 Cone-Rod Dystrophy 2 74 6.608
503
P PHC003 Pheochromocytoma 70 6.591
504
NRT001 Neurotic Disorder 56 6.585
505
c FML021 Familial Hypercholesterolemia 71 6.574
506
RTN004 Retinal Microaneurysm 32 6.562
507
PNC041 Pancreatic Ductal Adenocarcinoma 51 6.559
508
P DRM053 Dermatitis, Atopic 65 6.551
509
NCR007 Necrotizing Fasciitis 48 6.535
510
VRC005 Varicose Veins 59 6.528
511
PST021 Postpartum Depression 50 6.520
512
P THR015 Thrombophilia 51 6.502
513
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 6.489
514
P HYD006 Hydrocephalus 62 6.479
515
LWC001 Low Compliance Bladder 44 6.469
516
P PRK057 Parkinson Disease, Late-Onset 79 6.464
517
GTR002 Goiter 52 6.443
518
CLR108 Colorectal Adenoma 63 6.430
519
P RNL015 Renal Hypertension 45 6.397
520
P CNJ013 Conjunctivitis 66 6.396
521
DST006 Diastolic Heart Failure 45 6.359
522
MCL003 Macular Holes 44 6.341
523
CRT016 Carotid Artery Disease 52 6.338
524
DCB001 Decubitus Ulcer 61 6.337
525
P EXN002 Exanthem 58 6.328
526
ALX002 Alexithymia 36 6.323
527
P PRC019 Precocious Puberty 48 6.279
528
c HRD202 Hereditary Lymphedema I 54 6.270
529
TRM010 Traumatic Brain Injury 50 6.241
530
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 6.235
531
P MYC008 Myocarditis 59 6.191
532
EXC002 Exocrine Pancreatic Insufficiency 42 6.183
533
P VNS003 Venous Insufficiency 54 6.183
534
PLY012 Polyhydramnios 46 6.153
535
PRT037 Pertussis 49 6.152
536
ART008 Arteriosclerosis Obliterans 40 6.121
537
P PLY014 Polycystic Kidney Disease 71 6.113
538
P PLY018 Polycythemia 56 6.112
539
NPH010 Nephrosclerosis 50 6.097
540
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 6.096
541
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 6.096
542
P HYP098 Hypereosinophilic Syndrome 66 6.093
543
HYD002 Hydronephrosis 58 6.084
544
ATX019 Ataxia with Vitamin E Deficiency 44 6.064
545
STF001 Stiff-Person Syndrome 57 6.061
546
CHL079 Children's Interstitial Lung Disease 25 6.047
547
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 6.034
548
c FNC043 Fanconi Anemia, Complementation Group E 62 6.026
549
GST023 Gastric Ulcer 52 6.015
550
PNC034 Pancreas Disease 49 5.997
551
ILS001 Ileus 49 5.991
552
CRV035 Cervical Cancer 72 5.982
553
SPN051 Spondylitis 51 5.964
554
c BRD014 Bardet-Biedl Syndrome 2 53 5.909
555
P LPM005 Lipomatosis 47 5.873
556
INT303 Intracranial Hypertension, Idiopathic 56 5.871
557
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 5.864
558
MNN017 Mononeuropathy 41 5.863
559
P FML012 Familial Partial Lipodystrophy 54 5.854
560
P THL005 Thalassemia 56 5.822
561
P MMB011 Membranous Nephropathy 50 5.818
562
LYM133 Lymphoma, Hodgkin, Classic 69 5.817
563
P END033 Endocarditis 58 5.814
564
P CYS018 Cystitis 58 5.781
565
KRT009 Keratosis 52 5.774
566
GST050 Gastrointestinal System Disease 55 5.757
567
GSG001 Gas Gangrene 52 5.748
568
DDN006 Duodenitis 49 5.746
569
CRB037 Cerebral Palsy 66 5.743
570
LRN003 Learning Disability 49 5.721
571
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 5.707
572
KDN013 Kidney Hypertrophy 33 5.701
573
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 5.692
574
CRT084 Creatinine Clearance Quantitative Trait Locus 25 5.684
575
ADR040 Adrenal Gland Pheochromocytoma 45 5.673
576
PRP030 Purpura 54 5.663
577
LKS001 Leukostasis 40 5.654
578
P MYL006 Myeloid Leukemia 60 5.626
579
ERY029 Erythermalgia, Primary 57 5.620
580
c GRV008 Graves Disease 1 54 5.608
581
ALL006 Allergic Asthma 55 5.594
582
P MNN013 Meningitis 65 5.570
583
P HYP838 Hyperlipidemia, Familial Combined, 3 61 5.522
584
c SPN225 Spondyloarthropathy 1 70 5.521
585
FRN014 Fournier Gangrene 26 5.512
586
KRT008 Keratopathy 46 5.498
587
RDC002 Radiculopathy 51 5.498
588
DWR001 Dwarfism 44 5.480
589
c PRM005 Primary Hyperparathyroidism 59 5.469
590
RTN003 Retinal Ischemia 48 5.462
591
PRT013 Portal Hypertension 59 5.461
592
OTT002 Otitis Media 70 5.460
593
P ATX030 Ataxia-Telangiectasia 80 5.456
594
c GLC092 Glaucoma, Primary Open Angle 60 5.450
595
GST045 Gastroenteritis 58 5.447
596
P PSD015 Pseudohypoparathyroidism 54 5.436
597
c PNC108 Pancreatitis, Hereditary 68 5.429
598
P NRC002 Narcolepsy 55 5.424
599
P MSC005 Muscular Dystrophy 66 5.420
600
RDN001 Reading Disorder 40 5.406
601
TTN003 Tetanus 64 5.399
602
HRT012 Heart Valve Disease 53 5.383
603
HYP780 Hypoadrenocorticism, Familial 61 5.362
604
PRM329 Premature Aging 36 5.354
605
HLX001 Helix Syndrome 47 5.352
606
IDP033 Idiopathic Edema 41 5.346
607
P GRF003 Graft-Versus-Host Disease 71 5.340
608
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 5.320
609
SYN036 Syncope 44 5.319
610
TND005 Tendinitis 53 5.316
611
MDS022 Mediastinitis 47 5.315
612
PNC129 Pancreatic Adenocarcinoma 64 5.314
613
P END044 Endometriosis 62 5.313
614
PRP016 Paraplegia 52 5.313
615
P ASP006 Aspergillosis 71 5.300
616
P SCK005 Sickle Cell Disease 56 5.298
617
c PSD108 Pseudohypoparathyroidism, Type Ia 64 5.296
618
ASP026 Asplenia, Isolated Congenital 43 5.286
619
P BRB001 Beriberi 44 5.285
620
RFR003 Refractive Error 41 5.273
621
PTT037 Pituitary Tumors 44 5.273
622
WRN001 Werner Syndrome 69 5.272
623
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 5.267
624
PPT001 Peptic Esophagitis 51 5.265
625
c AMY091 Amyotrophic Lateral Sclerosis 1 87 5.250
626
CRY036 Cryptogenic Cirrhosis 36 5.244
627
GNR004 Generalized Anxiety Disorder 54 5.226
628
P PLY006 Polydactyly 58 5.214
629
END062 Endometrial Hyperplasia 47 5.211
630
P RST001 Restless Legs Syndrome 52 5.210
631
HYP784 Hypogonadism, Male 43 5.207
632
P ENC004 Encephalitis 61 5.205
633
CHL014 Cholera 62 5.198
634
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 5.194
635
DYS009 Dysthymic Disorder 51 5.192
636
c LKM061 Leukemia, Acute Myeloid 83 5.181
637
P NTR004 Neutropenia 62 5.173
638
HDN002 Head Injury 44 5.167
639
c SVR005 Severe Pre-Eclampsia 49 5.161
640
P SCL018 Scoliosis 57 5.157
641
CHL123 Chlamydia 58 5.143
642
OCL006 Ocular Hypertension 53 5.136
643
P MMP001 Mumps 56 5.133
644
P FNG006 Feingold Syndrome 1 61 5.132
645
P PTS002 Ptosis 52 5.127
646
P LTR001 Lateral Sclerosis 57 5.120
647
SCL002 Scleredema Adultorum 45 5.118
648
P MCR010 Microcephaly 59 5.107
649
ENT004 Enthesopathy 51 5.104
650
SKN023 Skin Tag 44 5.097
651
BLL003 Bell's Palsy 48 5.089
652
P NRB001 Neuroblastoma 66 5.078
653
VGN023 Vaginitis 56 5.077
654
c BRD011 Bardet-Biedl Syndrome 10 49 5.056
655
P PLM036 Pulmonary Fibrosis 65 5.052
656
P CMP008 Compartment Syndrome 49 5.051
657
BRN004 Brain Edema 54 5.050
658
c SML038 Small Cell Cancer of the Lung 68 5.037
659
P CHL066 Cholangitis 51 5.009
660
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 5.001
661
c PLM164 Pulmonary Hypertension, Primary, 1 75 4.992
662
FRZ001 Frozen Shoulder 54 4.987
663
MNN043 Meningioma, Familial 79 4.984
664
HDR002 Hidradenitis Suppurativa 54 4.970
665
c ATM011 Autoimmune Hepatitis 62 4.955
666
PPL021 Papilledema 49 4.944
667
P GLY013 Glycogen Storage Disease 59 4.941
668
CNT016 Central Retinal Vein Occlusion 53 4.941
669
c HYP272 Hypercholesterolemia, Familial, 3 46 4.929
670
HMN047 Human Cytomegalovirus Infection 59 4.928
671
HYP006 Hypertensive Heart Disease 48 4.926
672
P DDN001 Duodenal Ulcer 52 4.925
673
TBC004 Tobacco Addiction 63 4.917
674
EMP001 Empty Sella Syndrome 41 4.912
675
P MYS003 Myasthenia Gravis 67 4.905
676
P TRM003 Tremor 50 4.897
677
P SYS005 Systemic Scleroderma 73 4.895
678
ASP030 Aspirin Resistance 41 4.884
679
P PNC045 Pancreatic Agenesis 42 4.875
680
P DYS021 Dysautonomia 38 4.872
681
SPN027 Spinal Stenosis 58 4.840
682
NRG002 Neurogenic Bladder 54 4.835
683
INF009 Inflammatory Spondylopathy 30 4.832
684
LYM143 Lymphoma, Non-Hodgkin, Familial 74 4.827
685
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 4.811
686
ACT084 Acute Stress Disorder 53 4.810
687
c OPT053 Optic Atrophy 1 62 4.806
688
CHL147 Chlamydia Pneumonia 47 4.805
689
DPH001 Diphtheria 59 4.781
690
P SKN015 Skin Carcinoma 71 4.778
691
P HYP768 Hyperlipoproteinemia, Type I 67 4.769
692
P INT070 Intestinal Obstruction 57 4.764
693
ART074 Aortic Dissection 53 4.763
694
HYP458 Hyper Ige Syndrome 60 4.762
695
GLC036 Glucagonoma 45 4.745
696
URN010 Urinary Tract Obstruction 55 4.736
697
SBC016 Subacute Delirium 42 4.731
698
P PNC025 Panic Disorder 52 4.727
699
SQM006 Squamous Cell Carcinoma 59 4.718
700
ART004 Aortic Atherosclerosis 46 4.718
701
PRS047 Prostatitis 57 4.712
702
HYP114 Hypertensive Nephropathy 35 4.704
703
TLN003 Telangiectasis 51 4.703
704
ALL014 Allergic Encephalomyelitis 34 4.701
705
ASP004 Asphyxia Neonatorum 50 4.699
706
INT067 Interstitial Nephritis 46 4.697
707
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 4.690
708
c JVN010 Juvenile Rheumatoid Arthritis 52 4.689
709
P HLP001 Holoprosencephaly 68 4.686
710
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 27 4.685
711
NRT004 Neuritis 53 4.684
712
CNT097 Central Hypoventilation Syndrome, Congenital 70 4.670
713
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 4.668
714
NRM005 Neuromuscular Disease 62 4.665
715
HNS001 Hansen's Disease 32 4.665
716
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 4.653
717
HYP068 Hyperostosis 47 4.642
718
P PLV020 Pelvic Organ Prolapse 57 4.638
719
PLC005 Placental Insufficiency 55 4.631
720
HYP017 Hypophosphatemia 49 4.627
721
TND004 Tendinopathy 45 4.626
722
INF034 Infective Endocarditis 53 4.622
723
P VTR007 Vitreoretinopathy 45 4.620
724
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 4.614
725
P LPR021 Leprosy 3 71 4.604
726
c PRG042 Progressive Familial Heart Block, Type Ia 65 4.601
727
DVR002 Diverticulitis 46 4.584
728
c CNT075 Central Precocious Puberty 53 4.565
729
CHR005 Chorioamnionitis 50 4.559
730
HYP555 Hypertriglyceridemia, Transient Infantile 39 4.538
731
P GLC113 Galactosemia I 65 4.531
732
c ART101 Aortic Valve Disease 2 65 4.523
733
P HML002 Hemolytic Anemia 62 4.520
734
HRT011 Heart Septal Defect 49 4.507
735
P HYP024 Hypoparathyroidism 55 4.506
736
NNT012 Neonatal Jaundice 53 4.498
737
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 4.485
738
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 4.473
739
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 4.470
740
PST092 Posttransplant Acute Limbic Encephalitis 29 4.469
741
NRG003 Neurogenic Arthropathy 42 4.459
742
c ACT073 Acute Leukemia 59 4.455
743
PRM236 Primary Biliary Cholangitis 62 4.452
744
ACR006 Aceruloplasminemia 63 4.446
745
P RNL007 Renal Tubular Acidosis 52 4.441
746
SCH071 Schaaf-Yang Syndrome 53 4.439
747
CHR431 Chronic Venous Insufficiency 48 4.428
748
P GLL022 Guillain-Barre Syndrome 59 4.426
749
c BRD013 Bardet-Biedl Syndrome 12 44 4.423
750
SLD003 Sialadenitis 47 4.419
751
ART010 Arteriolosclerosis 37 4.419
752
P MTC069 Mitochondrial Disorders 57 4.417
753
P DMY001 Demyelinating Polyneuropathy 41 4.415
754
HDR003 Hidradenitis 49 4.411
755
TNS014 Tenosynovitis 45 4.410
756
DSS009 Disseminated Intravascular Coagulation 56 4.410
757
P HMP007 Hemophilia 52 4.408
758
HYP008 Hypertensive Retinopathy 39 4.403
759
PHY002 Physical Disorder 40 4.403
760
SYN007 Synovitis 54 4.399
761
CHL065 Cholangiocarcinoma 57 4.396
762
SMT008 Smith-Magenis Syndrome 53 4.393
763
c CHL119 Cholangitis, Primary Sclerosing 57 4.388
764
PRT038 Protein-Energy Malnutrition 53 4.380
765
P LNG064 Lung Cancer Susceptibility 3 69 4.375
766
MTR002 Mitral Valve Insufficiency 51 4.364
767
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 4.362
768
P FRD001 Friedreich Ataxia 62 4.343
769
HYP110 Hyperproinsulinemia 37 4.342
770
P SJG008 Sjogren Syndrome 60 4.339
771
P PRK039 Parkinsonism 55 4.338
772
SPT006 Septooptic Dysplasia 62 4.332
773
P RBL001 Rubella 58 4.329
774
WLL001 Williams-Beuren Syndrome 60 4.324
775
P GLL018 Gallbladder Cancer 59 4.324
776
c ACT042 Acute Pyelonephritis 45 4.317
777
HPT019 Hepatic Encephalopathy 59 4.315
778
MLD001 Melioidosis 67 4.311
779
HYP781 Hypoascorbemia 52 4.309
780
PLC002 Plica Syndrome 35 4.299
781
LPM012 Lipomatosis, Multiple 59 4.299
782
ACT055 Actinomycosis 54 4.296
783
P CRT085 Carotid Intimal Medial Thickness 2 22 4.293
784
UMB002 Umbilical Hernia 46 4.292
785
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 4.288
786
SLN001 Silent Myocardial Infarction 33 4.288
787
EXP004 Exophthalmos 50 4.281
788
c BRD018 Bardet-Biedl Syndrome 6 50 4.278
789
SNL007 Senile Cataract 40 4.272
790
MYL009 Myelodysplastic Syndrome 67 4.271
791
c SCN036 Secondary Progressive Multiple Sclerosis 55 4.265
792
GLB002 Glioblastoma 67 4.264
793
GRM004 Germinoma 40 4.263
794
PSD014 Pseudopseudohypoparathyroidism 54 4.261
795
MSL001 Measles 61 4.261
796
PLC007 Placental Abruption 47 4.258
797
HPT004 Hepatic Coma 43 4.258
798
P HYP120 Hypoaldosteronism 33 4.254
799
P HRP006 Herpes Simplex 65 4.251
800
OST011 Osteomalacia 52 4.251
801
NSP002 Nasopharyngitis 45 4.241
802
P ANT006 Antiphospholipid Syndrome 55 4.233
803
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 4.232
804
CHR073 Choreatic Disease 53 4.232
805
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.211
806
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 4.197
807
CHL152 Childhood Acute Lymphocytic Leukemia 50 4.181
808
c BTT014 Beta-Thalassemia 72 4.176
809
PRC013 Pericarditis 53 4.169
810
P RTN024 Retinoblastoma 72 4.159
811
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 4.158
812
INT395 Intracranial Meningioma 47 4.157
813
HYP026 Hypoglycemic Coma 37 4.156
814
INT079 Intrahepatic Cholangiocarcinoma 51 4.154
815
c BRD016 Bardet-Biedl Syndrome 4 44 4.148
816
P MYT002 Myotonic Dystrophy 51 4.147
817
P GND004 Gonadal Dysgenesis 46 4.139
818
DGN001 Degenerative Disc Disease 48 4.138
819
P TTR001 Tetralogy of Fallot 69 4.135
820
KHN001 Kuhnt-Junius Degeneration 48 4.132
821
P GLM040 Glioma Susceptibility 1 70 4.120
822
FND002 Fundus Dystrophy 54 4.115
823
VRL011 Viral Infectious Disease 60 4.109
824
c WLM013 Wilms Tumor 1 65 4.102
825
SCK003 Sickle Cell Anemia 74 4.097
826
HRP004 Herpes Zoster 60 4.088
827
AVD001 Avoidant Personality Disorder 49 4.086
828
GYN001 Gynecomastia 48 4.083
829
P END046 Endometritis 46 4.073
830
CHR178 Chromosomal Triplication 33 4.066
831
END041 Endometrial Adenocarcinoma 63 4.059
832
P CYS039 Cystic Kidney Disease 52 4.054
833
c INH030 Inherited Retinal Disorder 28 4.053
834
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 62 4.036
835
HYP025 Hyperphosphatemia 47 4.028
836
MTC005 Mitochondrial Metabolism Disease 44 4.021
837
P PLY188 Polyendocrinopathy 29 4.019
838
INF021 Infant Gynecomastia 30 4.013
839
QDR001 Quadriplegia 49 4.010
840
LYM009 Lymphocytic Choriomeningitis 46 4.008
841
ORL005 Oral Candidiasis 55 4.005
842
CMP010 Complex Regional Pain Syndrome 59 3.989
843
FNG017 Fungal Infectious Disease 54 3.988
844
ALC006 Alcoholic Hepatitis 61 3.980
845
OLG003 Oligohydramnios 50 3.979
846
P FML187 Familial Hypertension 34 3.978
847
ASP007 Aspiration Pneumonia 49 3.978
848
TST015 Testicular Disease 42 3.976
849
HMG005 Hemoglobinopathy 55 3.974
850
ATR057 Atrioventricular Block 54 3.974
851
CHC001 Chickenpox 56 3.968
852
ENT011 Enterocolitis 55 3.959
853
HMP005 Hemiplegia 53 3.957
854
P MJR007 Major Affective Disorder 1 42 3.956
855
c THY109 Thyroid Cancer, Nonmedullary, 1 55 3.955
856
FML037 Female Breast Cancer 51 3.952
857
SCR001 Secretory Meningioma 40 3.936
858
CMM005 Common Cold 55 3.931
859
P HMC002 Homocystinuria 52 3.929
860
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 3.927
861
ANX004 Anoxia 40 3.924
862
c PSR017 Psoriasis 2 53 3.921
863
ING001 Inguinal Hernia 59 3.919
864
P PRP029 Porphyria 60 3.916
865
CLC006 Calcinosis 47 3.912
866
P TMP003 Temporal Arteritis 68 3.912
867
GNR003 Generalized Atherosclerosis 42 3.909
868
SCR020 Sacral Defect with Anterior Meningocele 59 3.904
869
SPN020 Spondylosis 46 3.904
870
THR016 Thrombophlebitis 50 3.891
871
SLW005 Slowed Nerve Conduction Velocity, Autosomal Dominant 35 3.888
872
P RNL100 Renal Hypodysplasia/aplasia 1 63 3.888
873
P NJM001 Nijmegen Breakage Syndrome 75 3.884
874
P TRT010 Teratoma 50 3.881
875
SPN019 Spondylolisthesis 51 3.877
876
INT051 Intussusception 53 3.876
877
c ACT134 Acute Liver Failure 57 3.875
878
P URT039 Urticaria 57 3.870
879
P TXP001 Toxoplasmosis 59 3.869
880
P LRY019 Laryngitis 53 3.866
881
P MVM001 Movement Disease 61 3.857
882
BRS051 Breast Disease 58 3.856
883
TMP012 Temple Syndrome 38 3.855
884
WLM014 Wilms Tumor, Aniridia, Genitourinary Anomalies, and Mental Retardation Syndrome 53 3.855
885
c WLF009 Wolfram Syndrome 2 43 3.845
886
P ACT010 Acth-Secreting Pituitary Adenoma 60 3.843
887
SPN035 Spindle Cell Sarcoma 51 3.839
888
SRC014 Sarcoma 64 3.839
889
OBS002 Obsessive-Compulsive Disorder 67 3.835
890
c CHR098 Chronic Pyelonephritis 34 3.833
891
CNN005 Connective Tissue Disease 66 3.830
892
P ATR005 Atrophic Gastritis 50 3.821
893
GLM045 Glioma 62 3.817
894
P SYP003 Syphilis 59 3.813
895
OST062 Osteoarthritis with Mild Chondrodysplasia 46 3.810
896
PNM008 Pneumothorax 54 3.807
897
PRP009 Peripartum Cardiomyopathy 54 3.806
898
c DWL002 Dowling-Degos Disease 1 58 3.804
899
P HYP263 Hypersomnia 40 3.798
900
c LKM063 Leukemia, Chronic Myeloid 70 3.793
901
OVR094 Ovarian Epithelial Cancer 39 3.793
902
PPL022 Papilloma 53 3.793
903
GRN007 Granuloma Annulare 43 3.792
904
OST003 Osteonecrosis 60 3.781
905
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 3.777
906
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 48 3.776
907
CLF001 Cleft Lip 54 3.773
908
P VNT002 Ventricular Septal Defect 58 3.773
909
GLL048 Glial Tumor 51 3.770
910
PNN001 Panniculitis 52 3.768
911
MGL001 Megaloblastic Anemia 59 3.768
912
P ATN002 Autonomic Nervous System Disease 51 3.751
913
DRM011 Dermatophytosis 52 3.748
914
DFF005 Diffuse Large B-Cell Lymphoma 55 3.744
915
P SHR001 Short Bowel Syndrome 53 3.744
916
PHN003 Phenylketonuria 76 3.740
917
BNN003 Bone Inflammation Disease 47 3.735
918
WRN003 Wernicke Encephalopathy 45 3.733
919
SPN362 Spondylometaphyseal Dysplasia, Sedaghatian Type 42 3.731
920
CRY035 Cryptorchidism, Unilateral or Bilateral 57 3.728
921
PTT004 Pituitary Apoplexy 46 3.727
922
P CRB088 Cerebral Atrophy 32 3.720
923
CNT015 Central Sleep Apnea 46 3.720
924
LYM002 Lymphoplasmacyte-Rich Meningioma 35 3.715
925
BLL006 Bullous Pemphigoid 61 3.710
926
ACH005 Achalasia 54 3.709
927
CLR030 Clear Cell Renal Cell Carcinoma 53 3.699
928
ACT003 Acute Kidney Tubular Necrosis 46 3.696
929
FST010 Fasting Hypoglycemia 33 3.691
930
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 3.691
931
MTC023 Mitochondrial Encephalomyopathy Lactic Acidosis and Stroke-Like Episodes 44 3.689
932
FCL012 Facial Paralysis 49 3.688
933
c BRD012 Bardet-Biedl Syndrome 11 52 3.685
934
BLD044 Bladder Disease 48 3.684
935
BRN002 Bronchiolitis 57 3.682
936
CLP005 Ciliopathy 40 3.681
937
MYX004 Myxedema 43 3.668
938
PLR007 Pleural Empyema 50 3.664
939
c THY107 Thymoma, Familial 42 3.657
940
P THY023 Thymoma