Search results for obesity OR diabetes

8081 hits were found for obesity OR 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
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 41 39.479
49
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 28 39.386
50
DBT004 Diabetic Polyneuropathy 50 39.130
51
OBS037 Obesity-Hypoventilation Syndrome 44 39.076
52
P VSC007 Vascular Disease 62 39.062
53
P PRM030 Permanent Neonatal Diabetes Mellitus 59 38.569
54
P KDN018 Kidney Disease 71 38.426
55
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 37.591
56
DBT008 Diabetic Angiopathy 47 37.372
57
P SLP006 Sleep Apnea 69 36.913
58
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 36.802
59
P CRN300 Coronary Heart Disease 1 73 36.780
60
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 36.725
61
c CHR684 Chronic Kidney Disease 73 36.341
62
P PRP019 Peripheral Nervous System Disease 57 35.605
63
c TRN032 Transient Neonatal Diabetes Mellitus 48 35.590
64
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 35.359
65
P LVR013 Liver Disease 68 35.145
66
PRT251 Proteinuria, Chronic Benign 58 34.829
67
c BLD140 Blood Group, I System 47 34.715
68
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 34.510
69
BCK003 Background Diabetic Retinopathy 46 34.127
70
END086 End Stage Renal Disease 54 34.118
71
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 33.842
72
P PLY011 Polycystic Ovary Syndrome 57 33.494
73
LPP008 Lipoprotein Quantitative Trait Locus 65 33.134
74
P HYP750 Hypertriglyceridemia, Familial 61 33.133
75
c DBT104 Diabetes Mellitus, Permanent Neonatal, 1 47 33.076
76
ATH013 Atherosclerosis Susceptibility 63 33.071
77
ART140 Arteries, Anomalies of 52 33.052
78
c TYP027 Type 1 Diabetes Mellitus 10 25 33.016
79
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 40 32.831
80
MNG006 Monogenic Diabetes 45 32.565
81
P HRT032 Heart Disease 84 32.354
82
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 32.259
83
c TYP036 Type 1 Diabetes Mellitus 12 30 31.744
84
MCL006 Macular Retinal Edema 56 31.628
85
c TYP053 Type 1 Diabetes Mellitus 20 42 31.403
86
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 44 31.367
87
c MTR023 Maturity-Onset Diabetes of the Young, Type 6 41 31.357
88
c HYP836 Hypercholesterolemia, Familial, 1 73 31.214
89
c MTR024 Maturity-Onset Diabetes of the Young, Type 7 41 31.160
90
MRB006 Morbid Obesity and Spermatogenic Failure 21 31.158
91
c TYP031 Type 1 Diabetes Mellitus 5 28 31.033
92
DBT007 Diabetic Cataract 36 31.027
93
BRT037 Brittle Diabetes 24 30.673
94
c MTR026 Maturity-Onset Diabetes of the Young, Type 9 36 30.643
95
PRP027 Peripheral Vascular Disease 71 30.450
96
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 30.161
97
GNT167 Genetic Obesity 33 30.137
98
NNL006 Non-Alcoholic Steatohepatitis 54 29.886
99
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 29.760
100
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 29.680
101
LTN029 Latent Autoimmune Diabetes in Adults 38 29.412
102
c TYP055 Type 1 Diabetes Mellitus 22 31 29.029
103
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 39 28.926
104
ETN001 Eating Disorder 59 28.851
105
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 54 28.687
106
P MCR384 Microcephaly, Epilepsy, and Diabetes Syndrome 1 41 28.440
107
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 42 28.196
108
c HYP595 Hypertension, Essential 84 27.960
109
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 39 27.900
110
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 49 27.854
111
RCK004 Rickets 64 27.722
112
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 40 27.652
113
CNG034 Congestive Heart Failure 69 27.605
114
HYP835 Hypothalamic Obesity 38 27.597
115
P WLF004 Wolfram Syndrome 61 27.343
116
c TYP030 Type 1 Diabetes Mellitus 4 20 27.324
117
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 27.291
118
SVR002 Severe Nonproliferative Diabetic Retinopathy 36 27.173
119
c TYP040 Type 1 Diabetes Mellitus 18 24 27.149
120
c TYP038 Type 1 Diabetes Mellitus 15 20 27.112
121
c TYP058 Type 2 Diabetes 5 25 27.102
122
c PRC016 Pre-Eclampsia 64 27.037
123
c TYP035 Type 1 Diabetes Mellitus 11 26 26.896
124
c TYP032 Type 1 Diabetes Mellitus 6 21 26.827
125
c MTR074 Maturity-Onset Diabetes of the Young, Type 14 33 26.793
126
c TYP037 Type 1 Diabetes Mellitus 13 20 26.765
127
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 24 26.726
128
c TYP033 Type 1 Diabetes Mellitus 7 21 26.701
129
c TYP052 Type 1 Diabetes Mellitus 19 19 26.581
130
c TYP029 Type 1 Diabetes Mellitus 3 24 26.542
131
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 29 26.515
132
c TYP034 Type 1 Diabetes Mellitus 8 22 26.473
133
c TYP039 Type 1 Diabetes Mellitus 17 23 26.424
134
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 55 26.409
135
P PRD008 Periodontitis 63 26.366
136
c DBT105 Diabetes Mellitus, Permanent Neonatal, 2 27 26.186
137
ATN004 Autonomic Neuropathy 42 26.113
138
WDH003 Woodhouse-Sakati Syndrome 41 26.042
139
TYP048 Type 1 Diabetes Mellitus, X-Linked 11 26.033
140
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 17 25.998
141
RTN173 Retinal Dystrophy and Obesity 22 25.961
142
c TYP056 Type 1 Diabetes Mellitus 23 32 25.900
143
c TYP049 Type 2 Diabetes Mellitus 2 21 25.890
145
c TYP057 Type 1 Diabetes Mellitus 24 25 25.534
146
c TYP054 Type 1 Diabetes Mellitus 21 33 25.317
147
c LPD015 Lipodystrophy, Familial Partial, Type 2 61 25.283
148
MHM001 Mehmo Syndrome 47 25.177
149
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 50 25.163
150
c DBT098 Diabetes Mellitus, Transient Neonatal, 2 20 25.092
151
ISC004 Ischemia 61 25.042
152
IMP005 Impotence 52 24.946
153
AGN016 Aging 53 24.565
154
c DBT106 Diabetes Mellitus, Permanent Neonatal, 3 24 24.513
155
PRP098 Proprotein Convertase 1/3 Deficiency 36 24.488
156
P PLY019 Polyneuropathy 52 24.321
157
c DBT107 Diabetes Mellitus, Permanent Neonatal, 4 29 24.285
158
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 25 23.527
159
CHN016 Cohen Syndrome 59 23.447
160
PRD004 Prediabetes Syndrome 52 23.353
161
DPR016 Depression 64 23.334
162
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 23.211
163
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 23.192
164
c WLF013 Wolfram Syndrome 1 60 23.053
165
ATM095 Autoimmune Disease 61 22.908
166
OBS067 Obesity Due to Melanocortin 4 Receptor Deficiency 38 22.885
167
c TYP050 Type 2 Diabetes Mellitus 3 15 22.830
168
c ATR087 Atrial Standstill 1 74 22.812
169
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 28 22.658
170
HYD021 Hydrocephalus Obesity Hypogonadism 19 22.596
171
c ABD015 Abdominal Obesity-Metabolic Syndrome 4 22 22.317
172
DBT081 Diabetic Encephalopathy 36 22.258
173
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 22.154
174
c TYP051 Type 2 Diabetes Mellitus 4 17 22.133
175
P MYC007 Myocardial Infarction 69 22.122
176
MTC025 Mitochondrial Myopathy with Diabetes 24 22.035
177
P HYP086 Hypothyroidism 68 21.875
178
CRB039 Cerebrovascular Disease 65 21.750
179
DBT018 Diabetic Mastopathy 18 21.518
180
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 48 21.333
181
P CRD246 Cardiovascular System Disease 55 21.204
182
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 19 21.143
183
CLB031 Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome 16 20.569
184
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 66 20.267
185
SYN116 Syndromic Obesity 27 20.169
186
MMS001 Momo Syndrome 28 20.168
187
c HMC039 Hemochromatosis, Type 1 73 20.106
188
P AST005 Asthma 75 20.096
189
c HRD156 Hereditary Central Diabetes Insipidus 24 19.999
190
P CTR002 Cataract 59 19.963
191
HYP080 Hypogonadism 49 19.856
192
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 17 19.785
193
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 15 19.736
194
P PNC044 Pancreatitis 61 19.638
195
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 48 19.627
196
MNT002 Mental Depression 56 19.304
197
MSC133 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 16 19.232
198
CVD001 Covid-19 59 19.206
199
OST012 Osteoarthritis 77 19.040
200
NTR005 Nutritional Deficiency Disease 60 18.964
201
OBS060 Obesity Due to Sim1 Deficiency 17 18.963
202
CHN077 Chung-Jansen Syndrome 30 18.934
203
INS024 Insulin-Like Growth Factor I 77 18.870
204
SHR107 Short Stature-Obesity Syndrome 25 18.757
205
GST058 Gestational Diabetes Insipidus 15 18.704
206
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 21 18.468
207
STR067 Stroke, Ischemic 79 18.372
208
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 18 18.278
209
P PRD006 Prader-Willi Syndrome 60 18.185
210
PRL046 Prolactin Deficiency with Obesity and Enlarged Testes 9 18.067
211
APN008 Apnea, Obstructive Sleep 66 18.054
212
CYT002 Cytokine Deficiency 43 18.050
213
RPD005 Rapidly Involuting Congenital Hemangioma 48 18.000
214
PNC104 Pancreatic and Cerebellar Agenesis 34 17.963
215
P ANR048 Aniridia 1 66 17.936
216
OCL069 Ocular Motor Apraxia 57 17.908
217
c ACT027 Acute Pancreatitis 60 17.774
218
INT298 Intellectual Disability-Obesity-Brain Malformations-Facial Dysmorphism Syndrome 17 17.687
219
HYP014 Hyperuricemia 51 17.461
220
DPS001 Dipsogenic Diabetes Insipidus 21 17.370
221
c CNG012 Congenital Generalized Lipodystrophy 65 17.360
222
P PNC035 Pancreatic Cancer 87 17.256
223
INS034 Insulinomatosis and Diabetes Mellitus 26 17.159
224
c ACQ034 Acquired Central Diabetes Insipidus 18 17.137
225
TRP008 Tropical Calcific Pancreatitis 46 17.107
226
GNT051 Genetic Non-Syndromic Obesity 3 17.038
227
GST092 Gastroesophageal Reflux 59 17.022
228
c ACT075 Acute Myocardial Infarction 55 17.020
229
P ATR011 Atrial Fibrillation 66 16.967
230
MCR385 Microcephaly, Epilepsy, and Diabetes Syndrome 2 15 16.925
231
ATN005 Autonomic Dysfunction 45 16.834
232
PRP080 Peripheral Artery Disease 54 16.813
233
P OST002 Osteoporosis 76 16.811
234
P ART021 Arteriosclerosis 53 16.771
235
P URN019 Urinary Tract Infection 48 16.768
236
CHP002 Chops Syndrome 47 16.765
237
END057 Endometrial Cancer 76 16.691
238
P ECL001 Eclampsia 52 16.689
239
LVR012 Liver Cirrhosis 62 16.560
240
P INF032 Infertility 60 16.518
241
PLC008 Placenta Disease 48 16.325
242
ACN002 Acanthosis Nigricans 56 16.298
243
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 16.251
244
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 16.251
245
PLM129 Pulmonary Disease, Chronic Obstructive 74 16.155
246
ODN026 Odontochondrodysplasia 2 with Hearing Loss and Diabetes 12 16.145
247
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 10 16.133
248
P ALC033 Alcohol Use Disorder 67 16.107
249
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 56 16.074
250
MDF004 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 13 16.044
251
P EYD002 Eye Disease 57 16.035
252
GST037 Gastroparesis 52 16.004
253
PRX085 Preaxial Hallucal Polydactyly 28 15.920
254
ANX010 Anxiety 70 15.851
255
OST017 Osteomyelitis 63 15.843
256
PHT013 Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction 16 15.711
257
48X005 48,xyyy 39 15.704
258
ALC007 Alcohol Dependence 65 15.688
259
P HRD221 Hereditary Nephrogenic Diabetes Insipidus 18 15.666
260
P THY032 Thyroiditis 56 15.643
261
P TRN020 Turner Syndrome 67 15.526
262
DBT089 Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification 13 15.499
263
OBS083 Obesity Due to Congenital Leptin Resistance 3 15.484
264
HYP266 Hypoxia 56 15.401
265
P CLC063 Celiac Disease 1 65 15.255
266
XLN211 X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome 15 15.224
267
P HPT021 Hepatitis 68 15.203
268
P PRS038 Personality Disorder 65 15.193
269
47X002 47,xyy 47 15.169
270
RNL050 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna 6 15.150
271
RTN020 Retinal Vascular Disease 45 15.114
272
P RTN018 Retinal Disease 53 15.017
273
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 52 14.982
274
HYP790 Hypopituitarism, Congenital, with Central Diabetes Insipidus 5 14.968
275
XLN122 X-Linked Intellectual Disability - Short Stature - Obesity 2 14.954
277
OVR063 Overnutrition 42 14.860
278
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 15 14.858
279
OBS068 Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome 8 14.858
280
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 34 14.837
281
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 14.834
282
P DMN002 Dementia 65 14.773
283
INS001 Insulinoma 59 14.677
284
P BRS047 Breast Cancer 97 14.645
285
HYP043 Hyperandrogenism 47 14.619
286
c RRD012 Rare Diabetes Mellitus Type 1 5 14.611
287
c RRD013 Rare Diabetes Mellitus Type 2 5 14.611
288
OVR124 Overgrowth/obesity Syndrome 3 14.575
289
c THR092 Thrombophilia Due to Thrombin Defect 74 14.545
290
ANG054 Angina Pectoris 65 14.532
291
SVR001 Severe Acute Respiratory Syndrome 68 14.506
292
IRN002 Iron Metabolism Disease 56 14.502
293
LMB062 Limb Ischemia 55 14.480
294
PST011 Pustulosis of Palm and Sole 52 14.427
295
P PSR002 Psoriasis 63 14.408
296
P SLP005 Sleep Disorder 61 14.313
297
RHH001 Rohhad 27 14.253
298
GNT071 Genetic Overgrowth/obesity Syndrome 2 14.208
300
ACT088 Acute Insulin Response 39 14.208
301
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 45 14.170
302
P SCH015 Schizophrenia 74 14.118
303
GT001 Gout 63 14.067
304
ARD001 Aredyld 22 13.966
305
SVR004 Severe Combined Immunodeficiency 70 13.946
306
c GLL024 Gallbladder Disease 1 53 13.928
307
P MJR001 Major Depressive Disorder 68 13.898
308
c PRD040 Periodontitis, Chronic 52 13.878
309
SXL003 Sexual Disorder 49 13.840
310
CNS004 Constipation 56 13.814
311
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 13.791
312
DFC004 Deficiency Anemia 74 13.785
313
P RSP003 Respiratory Failure 73 13.679
314
DWN001 Down Syndrome 70 13.673
315
P ALZ034 Alzheimer Disease 87 13.536
316
P CLR023 Colorectal Cancer 100 13.480
317
FNC009 Fanconi-Bickel Syndrome 53 13.471
318
c ACT071 Acute Kidney Failure 60 13.459
319
DSS008 Disease of Mental Health 74 13.446
320
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 12 13.437
321
RNL024 Renal Glucosuria 60 13.420
322
P ART022 Arthritis 70 13.413
323
FTL021 Fetal Macrosomia 40 13.364
324
PRM187 Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome 21 13.294
325
NPH116 Nephrogenic Diabetes Insipidus-Intracranial Calcification-Facial Dysmorphism Syndrome 11 13.254
326
CYS001 Cystic Fibrosis 77 13.110
327
LYM029 Lymphedema-Distichiasis Syndrome 52 13.097
328
c HPT001 Hepatitis C 61 13.057
329
INT288 Intellectual Disability-Dysmorphism-Hypogonadism-Diabetes Mellitus Syndrome 13 13.033
330
PLM033 Pulmonary Embolism 58 12.880
331
XLN187 X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome 13 12.760
332
c ACT068 Acute Cystitis 60 12.745
333
RTN017 Retinal Detachment 60 12.704
334
P HPT023 Hepatocellular Carcinoma 95 12.646
336
ANR007 Anorexia Nervosa 59 12.611
337
c RRD067 Rare Diabetes Mellitus 7 12.528
339
HYP005 Hypokalemia 55 12.466
340
c DBT096 Diabetes Mellitus, Congenital Autoimmune 7 12.411
341
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 52 12.378
342
ALL029 Allergic Disease 61 12.361
343
P MYC084 Mycobacterium Tuberculosis 1 68 12.359
344
P BPL003 Bipolar Disorder 56 12.272
345
CHR100 Chronic Ulcer of Skin 57 12.261
346
P RHM011 Rheumatoid Arthritis 81 12.248
347
P ACQ022 Acquired Generalized Lipodystrophy 45 12.237
348
P CHR345 Chronic Pain 50 12.227
349
RNL077 Renal Fibrosis 46 12.155
350
DBT016 Diabetes Persistent Mullerian Ducts 1 12.145
351
OTH013 Other Rare Diabetes Mellitus 3 12.145
352
CRD024 Cardiomyopathy Diabetes Deafness 2 12.145
353
ECT013 Ectodermal Dysplasia Arthrogryposis Diabetes Mellitus 1 12.145
354
RRG011 Rare Genetic Diabetes Mellitus 2 12.145
355
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 8 12.145
356
LPT004 Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 2 12.145
357
INT007 Intermediate Coronary Syndrome 53 12.127
358
CRH001 Crohn's Disease 80 12.046
359
MDD011 Mood Disorder 61 11.982
360
BNG086 Bangstad Syndrome 19 11.949
361
P HYP076 Hyperthyroidism 53 11.930
362
c MJR022 Major Affective Disorder 8 37 11.863
363
c MJR024 Major Affective Disorder 9 40 11.863
364
LNG099 Lung Disease 62 11.855
365
THR024 Thrombosis 56 11.829
366
KRT002 Keratomalacia 54 11.800
367
BNR002 Bone Resorption Disease 47 11.766
368
BCK006 Back Pain 43 11.758
369
CRN036 Craniopharyngioma 63 11.753
370
RST023 Resting Heart Rate, Variation in 40 11.740
371
P ATT013 Attention Deficit-Hyperactivity Disorder 65 11.699
372
P OVR082 Overgrowth Syndrome 41 11.686
373
P SHR029 Short Syndrome 59 11.660
374
BLM002 Bulimia Nervosa 56 11.638
375
ADN018 Adenoma 58 11.574
376
ACR007 Acromegaly 70 11.571
377
NRL016 Neural Tube Defects 80 11.559
378
DNT012 Dental Caries 53 11.558
379
P HYP069 Hyperparathyroidism 62 11.501
380
c BRN108 Branchiootic Syndrome 1 63 11.470
381
HSH003 Hashimoto Thyroiditis 60 11.457
382
MTB004 Metabolic Acidosis 48 11.338
383
P ART023 Arthropathy 59 11.314
384
P DRR001 Diarrhea 55 11.297
385
MTC096 Mitchell-Riley Syndrome 31 11.272
386
CRD132 Cardiac Conduction Defect 59 11.269
387
P GLM007 Glomerulonephritis 59 11.251
388
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 11.220
389
c MNT236 Mental Retardation, Autosomal Dominant 39 25 11.194
390
P LCT001 Lactic Acidosis 50 11.137
391
P BND020 Bone Disease 60 11.111
392
MLD018 Mild Cognitive Impairment 48 11.042
393
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 11.029
394
NRR001 Neuroretinitis 42 10.993
395
RTN023 Retinitis 45 10.967
396
CLL003 Cellulitis 53 10.953
397
P HYP730 Hypogonadotropic Hypogonadism 57 10.950
398
MN1002 Man1b1-Cdg 22 10.924
399
NPH009 Nephrolithiasis 54 10.917
400
AYZ001 Ayazi Syndrome 9 10.891
401
ADL002 Adult Syndrome 69 10.831
402
FML035 Familial Hyperlipidemia 54 10.776
403
P PRS040 Prostate Cancer 95 10.710
404
P ENC018 Encephalopathy 62 10.668
405
PRT036 Peritonitis 65 10.649
406
P NPH012 Nephrotic Syndrome 61 10.634
407
P HYP083 Hypopituitarism 51 10.590
408
GNG013 Gingivitis 59 10.587
409
HMC014 Homocysteinemia 52 10.569
410
HYP364 Hyperostosis Frontalis Interna 29 10.537
411
PLM001 Pulmonary Tuberculosis 69 10.468
412
P ESP024 Esophagitis 60 10.459
413
PRT058 Pure Autonomic Failure 58 10.455
414
ANT039 Antisynthetase Syndrome 55 10.404
415
URM002 Uremia 47 10.372
416
P GST053 Gastric Cancer 82 10.370
417
SNS003 Sensory Peripheral Neuropathy 51 10.161
418
CRN030 Coronary Stenosis 50 10.126
419
DSS032 Disease by Infectious Agent 55 10.105
420
ALS001 Alstrom Syndrome 65 10.091
421
ANV001 Anovulation 46 10.073
422
c HPT016 Hepatitis B 62 9.975
423
P BRD002 Bardet-Biedl Syndrome 66 9.930
424
c VRL010 Viral Hepatitis 52 9.869
425
P ADL010 Adult Respiratory Distress Syndrome 70 9.856
426
P INF038 Influenza 68 9.824
427
P INF037 Inflammatory Bowel Disease 53 9.801
428
WLF014 Wolfram Syndrome, Mitochondrial Form 18 9.791
429
P PNM007 Pneumonia 64 9.773
430
HRW001 Hair Whorl 35 9.748
431
CHL004 Cholelithiasis 48 9.747
432
c MGR028 Migraine with or Without Aura 1 63 9.719
433
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 9.713
434
PNG002 Pain Agnosia 51 9.713
435
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 9.711
436
c HYP724 Hyperlipoproteinemia, Type Iii 66 9.646
437
ANR040 Aneurysm 60 9.629
438
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 9.618
439
c HPT073 Hepatitis C Virus 70 9.594
440
ACH016 Achard Thiers Syndrome 9 9.587
441
P CRP001 Carpal Tunnel Syndrome 65 9.540
442
INT323 Intraocular Pressure Quantitative Trait Locus 63 9.506
443
c HPT003 Hepatitis a 63 9.429
444
TXC005 Toxic Shock Syndrome 61 9.366
445
P PYL005 Pyelonephritis 56 9.321
446
HLC007 Helicobacter Pylori Infection 67 9.202
447
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 9.199
448
P CRD119 Cardiac Arrest 68 9.183
449
c HNT004 Huntington Disease-Like 2 51 9.183
450
P GST044 Gastritis 55 9.126
451
INT002 Intermittent Claudication 61 9.114
452
RNL114 Renal Cell Carcinoma, Nonpapillary 79 9.088
453
P ADN016 Adenocarcinoma 63 9.083
454
P PLM037 Pulmonary Hypertension 69 9.081
455
GLC008 Glucose Metabolism Disease 40 9.044
456
BLR008 Bilirubin Metabolic Disorder 57 9.013
457
MSC007 Muscle Hypertrophy 64 9.000
458
ART016 Aortic Aneurysm 68 8.997
459
P LKM062 Leukemia, Acute Lymphoblastic 69 8.990
460
IMM167 Immune Deficiency Disease 76 8.975
461
HMS001 Hemosiderosis 48 8.959
462
MCR141 Mucormycosis 59 8.957
463
SKN016 Skin Disease 63 8.946
464
CHL067 Cholecystitis 59 8.919
465
P MSC003 Muscular Atrophy 52 8.914
466
BCT022 Bacterial Infectious Disease 55 8.907
467
P RRH023 Rare Hereditary Hemochromatosis 52 8.894
468
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 8.892
469
P MYP004 Myopathy 67 8.892
470
c ATS007 Autism Spectrum Disorder 71 8.888
471
P BLD134 Bladder Cancer 79 8.846
472
P RCT021 Rectum Cancer 54 8.844
473
NPH091 Nephrolithiasis, Calcium Oxalate 61 8.807
474
P KDN017 Kidney Cancer 60 8.806
475
RHB024 Rhabdomyosarcoma 2 65 8.785
476
P FCL005 Focal Segmental Glomerulosclerosis 57 8.767
477
c PNS012 Paine Syndrome 60 8.764
478
P SBS003 Substance Abuse 54 8.758
479
ACQ007 Acquired Immunodeficiency Syndrome 58 8.758
480
P CND004 Candidiasis 57 8.755
481
TRN015 Transient Cerebral Ischemia 62 8.733
482
AMN001 Amenorrhea 53 8.730
483
HMN044 Human Immunodeficiency Virus Type 1 76 8.711
484
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 8.704
485
P AMY004 Amyloidosis 69 8.612
486
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 8.444
487
P RHN004 Rhinitis 56 8.423
488
GRW007 Growth Hormone Deficiency 47 8.405
489
SPN186 Spinal Cord Injury 60 8.371
490
P NRV007 Nervous System Disease 65 8.369
491
CNN003 Conn's Syndrome 77 8.349
492
P GLL020 Gallbladder Disease 57 8.324
493
CRT013 Carotid Stenosis 51 8.276
494
VSC002 Vascular Dementia 59 8.215
495
PST028 Post-Traumatic Stress Disorder 58 8.211
496
PRS021 Prostatic Adenoma 43 8.182
497
ULC004 Ulcerative Colitis 74 8.163
498
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 8.135
499
APP008 Appendicitis 62 8.131
500
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 8.066
501
PRS045 Prostatic Hypertrophy 53 8.066
502
P ATS364 Autism 72 8.060
503
DYS073 Dysphagia 53 8.015
504
THY029 Thyroid Carcinoma 55 8.009
505
c BRD010 Bardet-Biedl Syndrome 1 64 7.973
506
PRS129 Prostatic Hyperplasia, Benign 48 7.954
507
IGR001 Ige Responsiveness, Atopic 58 7.949
508
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.943
509
HRN026 Hernia, Hiatus 46 7.928
510
P MLN007 Male Infertility 56 7.924
511
P OPT006 Optic Nerve Disease 57 7.892
512
FSC004 Fasciitis 49 7.886
513
P GRV001 Graves' Disease 54 7.880
514
P BCL017 B-Cell Lymphoma 57 7.876
515
c SCN007 Secondary Hyperparathyroidism 50 7.871
516
PSY004 Psychotic Disorder 66 7.856
517
DRM006 Dermatitis 61 7.802
518
P HDC001 Headache 56 7.799
519
THY030 Thyroid Gland Disease 50 7.796
520
END072 Endotheliitis 36 7.787
521
P LKM002 Leukemia 65 7.776
522
P RTN022 Retinal Vein Occlusion 54 7.769
523
SHR124 Short Stature, Brachydactyly, Impaired Intellectual Development, and Seizures 27 7.749
524
c SYS001 Systemic Lupus Erythematosus 85 7.709
525
ART002 Arts Syndrome 66 7.708
526
PPT005 Peptic Ulcer Disease 58 7.690
527
P EPL164 Epilepsy 70 7.688
528
MCL027 Macular Dystrophy, Dominant Cystoid 51 7.681
529
VTM002 Vitamin B12 Deficiency 48 7.672
530
PLM010 Pulmonary Edema 54 7.645
531
HST010 Histiocytosis 49 7.635
532
LYM027 Lymphopenia 56 7.635
533
ALL003 Allergic Rhinitis 66 7.625
534
P LPS004 Lupus Erythematosus 61 7.616
535
P SRC025 Sarcoidosis 1 70 7.608
536
IGG001 Iga Glomerulonephritis 50 7.605
537
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 19 7.591
538
ESP021 Esophageal Cancer 84 7.586
539
MNC019 Monocarboxylate Transporter 1 Deficiency 46 7.570
540
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 7.565
541
PLY105 Polycystic Ovary Syndrome 1 39 7.517
542
BRN071 Brain Injury 50 7.498
543
P MLT020 Multiple Sclerosis 79 7.496
544
LRN002 Laron Syndrome 62 7.474
545
FBR047 Fibromyalgia 57 7.429
546
KRN002 Kearns-Sayre Syndrome 62 7.422
547
P SZR006 Seizure Disorder 69 7.408
548
P LNG032 Lung Cancer 98 7.388
549
CRD137 Cardiogenic Shock 56 7.387
550
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 51 7.373
551
P RTN008 Retinitis Pigmentosa 79 7.355
552
PSR001 Psoriatic Arthritis 61 7.330
553
c HNT011 Huntington Disease-Like 3 33 7.310
554
IRN001 Iron Deficiency Anemia 58 7.304
555
CLT003 Colitis 63 7.266
556
IRR002 Irritable Bowel Syndrome 64 7.265
557
MNT030 Mental Retardation Syndrome, Belgian Type 16 7.244
558
P SNS001 Sensorineural Hearing Loss 60 7.242
559
URL001 Urolithiasis 45 7.219
560
P VSC011 Vasculitis 61 7.205
561
c EPS039 Episodic Pain Syndrome, Familial, 1 42 7.192
562
NVS001 Neovascular Glaucoma 52 7.186
563
BRN024 Bronchitis 67 7.106
564
P HYP061 Hypertrophic Cardiomyopathy 68 7.059
565
SCH012 Schizoaffective Disorder 49 7.045
566
INT222 Intermediate Dend Syndrome 9 7.044
567
c DLT002 Dilated Cardiomyopathy 79 7.026
568
P MLN008 Melanoma 75 7.012
569
END040 Endogenous Depression 54 6.997
570
INT075 Intracranial Hypertension 52 6.973
571
P HYP050 Hyperinsulinemic Hypoglycemia 56 6.964
572
P ACN011 Acne 55 6.959
573
ATS010 Autosomal Recessive Disease 42 6.950
574
CMB007 Combined Immunodeficiency 56 6.949
575
P OPN001 Open-Angle Glaucoma 55 6.944
576
NCR002 Necrobiosis Lipoidica 38 6.930
577
BCT004 Bacteriuria 48 6.917
578
CRD223 Cardiac Arrhythmia 63 6.914
579
CHL068 Cholestasis 61 6.912
580
HYP020 Hyperprolactinemia 63 6.900
581
P UVT001 Uveitis 57 6.891
582
PRM291 Premature Aging Syndrome, Okamoto Type 12 6.885
583
CRB004 Cerebral Artery Occlusion 45 6.867
584
MYL069 Myeloma, Multiple 76 6.847
585
PTT009 Pituitary Gland Disease 52 6.841
586
P RTN016 Retinal Degeneration 52 6.826
587
LNG108 Langerhans Cell Histiocytosis 57 6.810
588
BRR014 Barrett Esophagus 66 6.807
589
P LYM118 Lymphoma 66 6.806
590
PRS063 Paresthesia 39 6.805
591
P MYP006 Myopia 55 6.787
592
P THR014 Thrombocytopenia 66 6.784
593
P HYP265 Hypotonia 42 6.754
594
GLM044 Glomerular Disease 34 6.728
595
c PNC106 Pancreatic Agenesis 1 51 6.727
596
DMP001 Dumping Syndrome 43 6.702
597
P PTT006 Pituitary Adenoma 55 6.685
598
HYP081 Hypolipoproteinemia 49 6.670
599
P ALP008 Alopecia 53 6.660
600
AND005 Androgen Insensitivity Syndrome, Mild 21 6.648
601
P OVR042 Ovarian Cancer 88 6.640
602
SYS003 Systolic Heart Failure 49 6.635
603
P OVR049 Ovarian Disease 50 6.611
604
P CNR004 Cone-Rod Dystrophy 2 74 6.608
605
P PHC003 Pheochromocytoma 70 6.591
606
NRT001 Neurotic Disorder 56 6.585
607
c FML021 Familial Hypercholesterolemia 71 6.574
608
RTN004 Retinal Microaneurysm 32 6.562
609
PNC041 Pancreatic Ductal Adenocarcinoma 51 6.559
610
P DRM053 Dermatitis, Atopic 65 6.551
611
NCR007 Necrotizing Fasciitis 48 6.535
612
VRC005 Varicose Veins 59 6.528
613
PST021 Postpartum Depression 50 6.520
614
P THR015 Thrombophilia 51 6.502
615
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 6.489
616
P HYD006 Hydrocephalus 62 6.479
617
LWC001 Low Compliance Bladder 44 6.469
618
P PRK057 Parkinson Disease, Late-Onset 79 6.464
619
GTR002 Goiter 52 6.443
620
CLR108 Colorectal Adenoma 63 6.430
621
P RNL015 Renal Hypertension 45 6.397
622
P CNJ013 Conjunctivitis 66 6.396
623
DST006 Diastolic Heart Failure 45 6.359
624
MCL003 Macular Holes 44 6.341
625
CRT016 Carotid Artery Disease 52 6.338
626
DCB001 Decubitus Ulcer 61 6.337
627
P EXN002 Exanthem 58 6.328
628
ALX002 Alexithymia 36 6.323
629
P PRC019 Precocious Puberty 48 6.279
630
c HRD202 Hereditary Lymphedema I 54 6.270
631
TRM010 Traumatic Brain Injury 50 6.241
632
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 6.235
633
P MYC008 Myocarditis 59 6.191
634
EXC002 Exocrine Pancreatic Insufficiency 42 6.183
635
P VNS003 Venous Insufficiency 54 6.183
636
PLY012 Polyhydramnios 46 6.153
637
PRT037 Pertussis 49 6.152
638
ART008 Arteriosclerosis Obliterans 40 6.121
639
P PLY014 Polycystic Kidney Disease 71 6.113
640
P PLY018 Polycythemia 56 6.112
641
NPH010 Nephrosclerosis 50 6.097
642
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 6.096
643
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 6.096
644
P HYP098 Hypereosinophilic Syndrome 66 6.093
645
HYD002 Hydronephrosis 58 6.084
646
ATX019 Ataxia with Vitamin E Deficiency 44 6.064
647
STF001 Stiff-Person Syndrome 57 6.061
648
CHL079 Children's Interstitial Lung Disease 25 6.047
649
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 6.034
650
c FNC043 Fanconi Anemia, Complementation Group E 62 6.026
651
GST023 Gastric Ulcer 52 6.015
652
PNC034 Pancreas Disease 49 5.997
653
ILS001 Ileus 49 5.991
654
CRV035 Cervical Cancer 72 5.982
655
SPN051 Spondylitis 51 5.964
656
c BRD014 Bardet-Biedl Syndrome 2 53 5.909
657
P LPM005 Lipomatosis 47 5.873
658
INT303 Intracranial Hypertension, Idiopathic 56 5.871
659
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 5.864
660
MNN017 Mononeuropathy 41 5.863
661
P FML012 Familial Partial Lipodystrophy 54 5.854
662
P THL005 Thalassemia 56 5.822
663
P MMB011 Membranous Nephropathy 50 5.818
664
LYM133 Lymphoma, Hodgkin, Classic 69 5.817
665
P END033 Endocarditis 58 5.814
666
P CYS018 Cystitis 58 5.781
667
KRT009 Keratosis 52 5.774
668
GST050 Gastrointestinal System Disease 55 5.757
669
GSG001 Gas Gangrene 52 5.748
670
DDN006 Duodenitis 49 5.746
671
CRB037 Cerebral Palsy 66 5.743
672
LRN003 Learning Disability 49 5.721
673
PTT046 Pituitary Hormone Deficiency, Combined, 2 62 5.707
674
KDN013 Kidney Hypertrophy 33 5.701
675
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 38 5.692
676
CRT084 Creatinine Clearance Quantitative Trait Locus 25 5.684
677
P END047 Endophthalmitis 53 5.680
678
ADR040 Adrenal Gland Pheochromocytoma 45 5.673
679
PRP030 Purpura 54 5.663
680
LKS001 Leukostasis 40 5.654
681
P MYL006 Myeloid Leukemia 60 5.626
682
ERY029 Erythermalgia, Primary 57 5.620
683
c GRV008 Graves Disease 1 54 5.608
684
ALL006 Allergic Asthma 55 5.594
685
P MNN013 Meningitis 65 5.570
686
P HYP838 Hyperlipidemia, Familial Combined, 3 61 5.522
687
c SPN225 Spondyloarthropathy 1 70 5.521
688
FRN014 Fournier Gangrene 26 5.512
689
KRT008 Keratopathy 46 5.498
690
RDC002 Radiculopathy 51 5.498
691
DWR001 Dwarfism 44 5.480
692
c PRM005 Primary Hyperparathyroidism 59 5.469
693
RTN003 Retinal Ischemia 48 5.462
694
PRT013 Portal Hypertension 59 5.461
695
OTT002 Otitis Media 70 5.460
696
P ATX030 Ataxia-Telangiectasia 80 5.456
697
c GLC092 Glaucoma, Primary Open Angle 60 5.450
698
GST045 Gastroenteritis 58 5.447
699
P PSD015 Pseudohypoparathyroidism 54 5.436
700
c PNC108 Pancreatitis, Hereditary 68 5.429
701
P NRC002 Narcolepsy 55 5.424
702
P MSC005 Muscular Dystrophy 66 5.420
703
RDN001 Reading Disorder 40 5.406
704
TTN003 Tetanus 64 5.399
705
HRT012 Heart Valve Disease 53 5.383
706
HYP780 Hypoadrenocorticism, Familial 61 5.362
707
PRM329 Premature Aging 36 5.354
708
HLX001 Helix Syndrome 47 5.352
709
IDP033 Idiopathic Edema 41 5.346
710
P GRF003 Graft-Versus-Host Disease 71 5.340
711
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 5.320
712
SYN036 Syncope 44 5.319
713
TND005 Tendinitis 53 5.316
714
MDS022 Mediastinitis 47 5.315
715
PNC129 Pancreatic Adenocarcinoma 64 5.314
716
P END044 Endometriosis 62 5.313
717
PRP016 Paraplegia 52 5.313
718
P ASP006 Aspergillosis 71 5.300
719
P SCK005 Sickle Cell Disease 56 5.298
720
c PSD108 Pseudohypoparathyroidism, Type Ia 64 5.296
721
ASP026 Asplenia, Isolated Congenital 43 5.286
722
P BRB001 Beriberi 44 5.285
723
RFR003 Refractive Error 41 5.273
724
PTT037 Pituitary Tumors 44 5.273
725
WRN001 Werner Syndrome 69 5.272
726
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 5.267
727
PPT001 Peptic Esophagitis 51 5.265
728
VTR003 Vitreous Detachment 41 5.253
729
c AMY091 Amyotrophic Lateral Sclerosis 1 87 5.250
730
CRY036 Cryptogenic Cirrhosis 36 5.244
731
GNR004 Generalized Anxiety Disorder 54 5.226
732
P PLY006 Polydactyly 58 5.214
733
END062 Endometrial Hyperplasia 47 5.211
734
P RST001 Restless Legs Syndrome 52 5.210
735
HYP784 Hypogonadism, Male 43 5.207
736
P ENC004 Encephalitis 61 5.205
737
CHL014 Cholera 62 5.198
738
ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 5.194
739
DYS009 Dysthymic Disorder 51 5.192
740
c LKM061 Leukemia, Acute Myeloid 83 5.181
741
P NTR004 Neutropenia 62 5.173
742
HDN002 Head Injury 44 5.167
743
c SVR005 Severe Pre-Eclampsia 49 5.161
744
P SCL018 Scoliosis 57 5.157
745
CHL123 Chlamydia 58 5.143
746
OCL006 Ocular Hypertension 53 5.136
747
P MMP001 Mumps 56 5.133
748
P FNG006 Feingold Syndrome 1 61 5.132
749
P PTS002 Ptosis 52 5.127
750
P LTR001 Lateral Sclerosis 57 5.120
751
SCL002 Scleredema Adultorum 45 5.118
752
P MCR010 Microcephaly 59 5.107
753
ENT004 Enthesopathy 51 5.104
754
SKN023 Skin Tag 44 5.097
755
BLL003 Bell's Palsy 48 5.089
756
P NRB001 Neuroblastoma 66 5.078
757
VGN023 Vaginitis 56 5.077
758
c BRD011 Bardet-Biedl Syndrome 10 49 5.056
759
P PLM036 Pulmonary Fibrosis 65 5.052
760
P CMP008 Compartment Syndrome 49 5.051
761
BRN004 Brain Edema 54 5.050
762
c SML038 Small Cell Cancer of the Lung 68 5.037
763
P CHL066 Cholangitis 51 5.009
764
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 5.001
765
c PLM164 Pulmonary Hypertension, Primary, 1 75 4.992
766
FRZ001 Frozen Shoulder 54 4.987
767
MNN043 Meningioma, Familial 79 4.984
768
HDR002 Hidradenitis Suppurativa 54 4.970
769
c ATM011 Autoimmune Hepatitis 62 4.955
770
PPL021 Papilledema 49 4.944
771
P GLY013 Glycogen Storage Disease 59 4.941
772
CNT016 Central Retinal Vein Occlusion 53 4.941
773
c HYP272 Hypercholesterolemia, Familial, 3 46 4.929
774
HMN047 Human Cytomegalovirus Infection 59 4.928
775
HYP006 Hypertensive Heart Disease 48 4.926
776
P DDN001 Duodenal Ulcer 52 4.925
777
TBC004 Tobacco Addiction 63 4.917
778
EMP001 Empty Sella Syndrome 41 4.912
779
P MYS003 Myasthenia Gravis 67 4.905
780
P TRM003 Tremor 50 4.897
781
P SYS005 Systemic Scleroderma 73 4.895
782
ASP030 Aspirin Resistance 41 4.884
783
P PNC045 Pancreatic Agenesis 42 4.875
784
P DYS021 Dysautonomia 38 4.872
785
SPN027 Spinal Stenosis 58 4.840
786
NRG002 Neurogenic Bladder 54 4.835
787
INF009 Inflammatory Spondylopathy 30 4.832
788
LYM143 Lymphoma, Non-Hodgkin, Familial 74 4.827
789
NRD100 Neurodevelopmental, Jaw, Eye, and Digital Syndrome 50 4.811
790
ACT084 Acute Stress Disorder 53 4.810
791
c OPT053 Optic Atrophy 1 62 4.806
792
CHL147 Chlamydia Pneumonia 47 4.805
793
DPH001 Diphtheria 59 4.781
794
P SKN015 Skin Carcinoma 71 4.778
795
P HYP768 Hyperlipoproteinemia, Type I 67 4.769
796
P INT070 Intestinal Obstruction 57 4.764
797
ART074 Aortic Dissection 53 4.763
798
HYP458 Hyper Ige Syndrome 60 4.762
799
GLC036 Glucagonoma 45 4.745
800
URN010 Urinary Tract Obstruction 55 4.736
801
SBC016 Subacute Delirium 42 4.731
802
P PNC025 Panic Disorder 52 4.727
803
SQM006 Squamous Cell Carcinoma 59 4.718
804
ART004 Aortic Atherosclerosis 46 4.718
805
PRS047 Prostatitis 57 4.712
806
HYP114 Hypertensive Nephropathy 35 4.704
807
TLN003 Telangiectasis 51 4.703
808
ALL014 Allergic Encephalomyelitis 34 4.701
809
ASP004 Asphyxia Neonatorum 50 4.699
810
INT067 Interstitial Nephritis 46 4.697
811
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 62 4.690
812
c JVN010 Juvenile Rheumatoid Arthritis 52 4.689
813
P HLP001 Holoprosencephaly 68 4.686
814
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 27 4.685
815
NRT004 Neuritis 53 4.684
816
CNT097 Central Hypoventilation Syndrome, Congenital 70 4.670
817
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 56 4.668
818
NRM005 Neuromuscular Disease 62 4.665
819
HNS001 Hansen's Disease 32 4.665
820
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 47 4.653
821
HYP068 Hyperostosis 47 4.642
822
P PLV020 Pelvic Organ Prolapse 57 4.638
823
PLC005 Placental Insufficiency 55 4.631
824
HYP017 Hypophosphatemia 49 4.627
825
TND004 Tendinopathy 45 4.626
826
RBS002 Rubeosis Iridis 32 4.625
827
INF034 Infective Endocarditis 53 4.622
828
P VTR007 Vitreoretinopathy 45 4.620
829
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 4.614
830
P LPR021 Leprosy 3 71 4.604
831
c PRG042 Progressive Familial Heart Block, Type Ia 65 4.601
832
DVR002 Diverticulitis 46 4.584
833
c CNT075 Central Precocious Puberty 53 4.565
834
CHR005 Chorioamnionitis 50 4.559
835
HYP555 Hypertriglyceridemia, Transient Infantile 39 4.538
836
P GLC113 Galactosemia I 65 4.531
837
c ART101 Aortic Valve Disease 2 65 4.523
838
P HML002 Hemolytic Anemia 62 4.520
839
HRT011 Heart Septal Defect 49 4.507
840
P HYP024 Hypoparathyroidism 55 4.506
841
NNT012 Neonatal Jaundice 53 4.498
842
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 4.485
843
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 52 4.473
844
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 50 4.470
845
PST092 Posttransplant Acute Limbic Encephalitis 29 4.469
846
NRG003 Neurogenic Arthropathy 42 4.459
847
c ACT073 Acute Leukemia 59 4.455
848
PRM236 Primary Biliary Cholangitis 62 4.452
849
ACR006 Aceruloplasminemia 63 4.446
850
P RNL007 Renal Tubular Acidosis 52 4.441
851
SCH071 Schaaf-Yang Syndrome 53 4.439
852
CHR431 Chronic Venous Insufficiency 48 4.428
853
P GLL022 Guillain-Barre Syndrome 59 4.426
854
c BRD013 Bardet-Biedl Syndrome 12 44 4.423
855
SLD003 Sialadenitis 47 4.419
856
ART010 Arteriolosclerosis 37 4.419
857
P MTC069 Mitochondrial Disorders 57 4.417
858
P DMY001 Demyelinating Polyneuropathy 41 4.415
859
HDR003 Hidradenitis 49 4.411
860
TNS014 Tenosynovitis 45 4.410
861
DSS009 Disseminated Intravascular Coagulation 56 4.410
862
P HMP007 Hemophilia 52 4.408
863
HYP008 Hypertensive Retinopathy 39 4.403
864
PHY002 Physical Disorder 40 4.403
865
SYN007 Synovitis 54 4.399
866
CHL065 Cholangiocarcinoma 57 4.396
867
SMT008 Smith-Magenis Syndrome 53 4.393
868
c CHL119 Cholangitis, Primary Sclerosing 57 4.388
869
PRT038 Protein-Energy Malnutrition 53 4.380
870
P LNG064 Lung Cancer Susceptibility 3 69 4.375
871
MTR002 Mitral Valve Insufficiency 51 4.364
872
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 50 4.362
873
P FRD001 Friedreich Ataxia 62 4.343
874
HYP110 Hyperproinsulinemia 37 4.342
875
P SJG008 Sjogren Syndrome 60 4.339
876
P PRK039 Parkinsonism 55 4.338
877
SPT006 Septooptic Dysplasia 62 4.332
878
P RBL001 Rubella 58 4.329
879
WLL001 Williams-Beuren Syndrome 60 4.324
880
P GLL018 Gallbladder Cancer 59 4.324
881
c ACT042 Acute Pyelonephritis 45 4.317
882
HPT019 Hepatic Encephalopathy 59 4.315
883
MLD001 Melioidosis 67 4.311
884
HYP781 Hypoascorbemia 52 4.309
885
PLC002 Plica Syndrome 35 4.299
886
LPM012 Lipomatosis, Multiple 59 4.299
887
ACT055 Actinomycosis 54 4.296
888
P CRT085 Carotid Intimal Medial Thickness 2 22 4.293
889
UMB002 Umbilical Hernia 46 4.292
890
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 4.288
891
SLN001 Silent Myocardial Infarction 33 4.288
892
EXP004 Exophthalmos 50 4.281
893
c BRD018 Bardet-Biedl Syndrome 6 50 4.278
894
SNL007 Senile Cataract 40 4.272
895
MYL009 Myelodysplastic Syndrome 67 4.271
896
c SCN036 Secondary Progressive Multiple Sclerosis 55 4.265
897
GLB002 Glioblastoma 67 4.264
898
GRM004 Germinoma 40 4.263
899
PSD014 Pseudopseudohypoparathyroidism 54 4.261
900
MSL001 Measles 61 4.261
901
PLC007 Placental Abruption 47 4.258
902
HPT004 Hepatic Coma 43 4.258
903
P HYP120 Hypoaldosteronism 33 4.254
904
P HRP006 Herpes Simplex 65 4.251
905
OST011 Osteomalacia 52 4.251
906
NSP002 Nasopharyngitis 45 4.241
907
P ANT006 Antiphospholipid Syndrome 55 4.233
908
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 4.232
909
CHR073 Choreatic Disease 53 4.232
910
c DNT047 Dentinogenesis Imperfecta Type 2 35 4.211
911
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 4.197
912
CHL152 Childhood Acute Lymphocytic Leukemia 50 4.181
913
c BTT014 Beta-Thalassemia 72 4.176
914
PRC013 Pericarditis 53 4.169
915
P RTN024 Retinoblastoma 72 4.159
916
c ATS347 Autosomal Dominant Polycystic Kidney Disease 64 4.158
917
INT395 Intracranial Meningioma 47 4.157
918
HYP026 Hypoglycemic Coma 37 4.156
919
INT079 Intrahepatic Cholangiocarcinoma 51 4.154
920
c BRD016 Bardet-Biedl Syndrome 4 44 4.148
921
P MYT002 Myotonic Dystrophy 51 4.147
922
P GND004 Gonadal Dysgenesis 46 4.139
923
DGN001 Degenerative Disc Disease 48 4.138
924
P TTR001 Tetralogy of Fallot 69 4.135
925
KHN001 Kuhnt-Junius Degeneration 48 4.132
926
P GLM040 Glioma Susceptibility 1 70 4.120
927
FND002 Fundus Dystrophy 54 4.115
928
VRL011 Viral Infectious Disease 60 4.109
929
c WLM013 Wilms Tumor 1 65 4.102
930
SCK003 Sickle Cell Anemia 74 4.097
931
HRP004 Herpes Zoster 60 4.088
932
AVD001 Avoidant Personality Disorder 49 4.086
933