Search results for obesity OR diabetes

4609 hits were found for obesity OR diabetes

# Family MCID Name MIFTS Score
1
P BDY004 Body Mass Index Quantitative Trait Locus 11 72 8.594
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 5.105
3
P DBT009 Diabetes Mellitus 67 4.674
4
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.207
5
LPT014 Leptin Deficiency or Dysfunction 70 3.393
6
P DBT085 Diabetes Mellitus, Insulin-Dependent 73 3.250
7
GST033 Gestational Diabetes 63 2.968
8
P MCR115 Microvascular Complications of Diabetes 5 70 2.939
9
c MCR113 Microvascular Complications of Diabetes 3 58 2.717
10
c MCR120 Microvascular Complications of Diabetes 7 46 2.674
11
c BDY020 Body Mass Index Quantitative Trait Locus 19 44 2.652
12
c BDY019 Body Mass Index Quantitative Trait Locus 18 43 2.651
13
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 2.651
14
c BDY006 Body Mass Index Quantitative Trait Locus 8 41 2.651
15
c BDY012 Body Mass Index Quantitative Trait Locus 7 41 2.651
16
DBT087 Diabetes Insipidus, Neurohypophyseal 61 2.539
17
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 2.435
18
c BDY011 Body Mass Index Quantitative Trait Locus 10 41 2.408
19
c MCR133 Microvascular Complications of Diabetes 4 43 2.340
20
c MCR130 Microvascular Complications of Diabetes 6 43 2.340
21
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.309
22
c MCR129 Microvascular Complications of Diabetes 1 66 2.140
23
RNL051 Renal Cysts and Diabetes Syndrome 53 1.947
24
DBT010 Diabetic Neuropathy 60 1.946
25
DBT083 Diabetes Mellitus, Permanent Neonatal 60 1.922
26
P DBT005 Diabetes Insipidus 55 1.868
27
P MTR004 Maturity-Onset Diabetes of the Young 61 1.825
28
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 40 1.768
29
c MCR112 Microvascular Complications of Diabetes 2 42 1.708
30
LPT006 Leptin Receptor Deficiency 41 1.707
31
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 53 1.640
32
DBT090 Diabetes and Deafness, Maternally Inherited 42 1.606
33
OBS037 Obesity-Hypoventilation Syndrome 50 1.600
34
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 61 1.543
35
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 36 1.516
36
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 1.479
37
DBT008 Diabetic Angiopathy 48 1.455
38
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 26 1.415
39
c BDY005 Body Mass Index Quantitative Trait Locus 9 35 1.408
40
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 46 1.404
41
c BDY010 Body Mass Index Quantitative Trait Locus 4 32 1.402
42
OBS015 Obesity, Hyperphagia, and Developmental Delay 28 1.401
43
MRB006 Morbid Obesity and Spermatogenic Failure 19 1.401
44
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 1.401
45
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 54 1.398
46
MHM001 Mehmo Syndrome 35 1.394
47
DBT002 Diabetic Autonomic Neuropathy 46 1.390
48
c MTR023 Maturity-Onset Diabetes of the Young, Type 6 40 1.341
49
c MTR024 Maturity-Onset Diabetes of the Young, Type 7 42 1.339
50
c MTR026 Maturity-Onset Diabetes of the Young, Type 9 32 1.335
51
c LPD015 Lipodystrophy, Familial Partial, Type 2 60 1.324
52
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 54 1.314
53
CHN016 Cohen Syndrome 53 1.305
54
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 41 1.304
55
P WLF004 Wolfram Syndrome 60 1.280
56
DBT004 Diabetic Polyneuropathy 50 1.241
57
CNG376 Congenital Leptin Deficiency 26 1.236
58
MMS001 Momo Syndrome 29 1.230
59
RTN173 Retinal Dystrophy and Obesity 18 1.226
60
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 14 1.221
61
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 1.218
62
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 38 1.191
63
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 22 1.171
64
c DBT094 Diabetes Mellitus, Insulin-Dependent, 10 21 1.169
65
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 25 1.168
66
c TRN032 Transient Neonatal Diabetes Mellitus 44 1.153
67
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 1.147
68
P NNT009 Neonatal Diabetes Mellitus 47 1.138
69
DBT006 Diabetic Macular Edema 49 1.129
70
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 31 1.123
71
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 24 1.111
72
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 28 1.111
73
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 22 1.110
74
WDH003 Woodhouse-Sakati Syndrome 32 1.108
75
PRP098 Proprotein Convertase 1/3 Deficiency 32 1.099
76
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 72 1.098
77
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 39 1.064
78
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 38 1.060
79
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 48 1.060
80
CHP002 Chops Syndrome 38 1.057
81
c MTR074 Maturity-Onset Diabetes of the Young, Type 14 32 1.056
82
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 23 1.053
83
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 21 1.048
84
c DBT098 Diabetes Mellitus, Transient Neonatal, 2 15 1.046
85
c DBT032 Diabetes Mellitus, Insulin-Dependent, 22 15 1.043
86
BRT037 Brittle Diabetes 24 1.030
87
DBT062 Diabetic Foot Ulcers 58 1.026
88
DBT007 Diabetic Cataract 38 1.005
89
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 21 0.996
90
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 55 0.990
91
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 19 0.990
92
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 28 0.986
93
INS010 Insulin-Resistant Acanthosis Nigricans, Type a 20 0.981
94
PNC104 Pancreatic and Cerebellar Agenesis 27 0.977
95
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.968
96
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 14 0.952
97
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 21 0.907
98
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 27 0.907
99
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 15 0.905
100
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 14 0.905
101
c DBT079 Diabetes Mellitus, Insulin-Dependent, 21 14 0.904
102
DBT060 Diabetes Mellitus, Insulin-Dependent, X-Linked 8 0.902
103
HYP835 Hypothalamic Obesity 43 0.892
104
BCK003 Background Diabetic Retinopathy 38 0.888
105
DVL020 Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features 21 0.875
106
HYD021 Hydrocephalus Obesity Hypogonadism 16 0.875
107
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 15 0.873
108
CLB031 Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome 15 0.869
109
MNG006 Monogenic Diabetes 40 0.864
110
MTC025 Mitochondrial Myopathy with Diabetes 25 0.837
111
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 21 0.829
112
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 18 0.829
113
OBS050 Obesity Due to Congenital Leptin Deficiency 18 0.792
114
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 16 0.778
115
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 48 0.769
116
SVR002 Severe Nonproliferative Diabetic Retinopathy 34 0.767
117
FBR065 Fibrocalculous Pancreatopathy 18 0.762
118
c TYP031 Type 1 Diabetes Mellitus 5 26 0.756
119
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 19 0.755
120
c TYP035 Type 1 Diabetes Mellitus 11 29 0.754
121
c TYP033 Type 1 Diabetes Mellitus 7 27 0.754
122
c TYP028 Type 1 Diabetes Mellitus 2 26 0.750
124
c TYP036 Type 1 Diabetes Mellitus 12 24 0.749
125
c TYP038 Type 1 Diabetes Mellitus 15 23 0.748
126
c TYP029 Type 1 Diabetes Mellitus 3 17 0.747
127
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 17 0.747
128
c TYP030 Type 1 Diabetes Mellitus 4 16 0.747
129
c TYP037 Type 1 Diabetes Mellitus 13 28 0.746
130
c TYP027 Type 1 Diabetes Mellitus 10 24 0.746
131
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 16 0.746
132
c TYP032 Type 1 Diabetes Mellitus 6 25 0.745
133
ARD001 Aredyld 24 0.745
134
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 18 0.745
135
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 17 0.745
136
c TYP034 Type 1 Diabetes Mellitus 8 15 0.745
137
RHH001 Rohhad 28 0.745
138
c TYP039 Type 1 Diabetes Mellitus 17 21 0.743
139
c TYP040 Type 1 Diabetes Mellitus 18 18 0.743
140
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 17 0.743
141
c DBT050 Diabetes Mellitus, Insulin-Dependent, 15 15 0.743
142
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 43 0.742
143
MSC133 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 16 0.742
144
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 14 0.742
145
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 15 0.741
146
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 14 0.740
147
c DBT052 Diabetes Mellitus, Insulin-Dependent, 18 14 0.740
148
GLC008 Glucose Metabolism Disease 53 0.739
149
c DBT097 Diabetes Mellitus, Noninsulin-Dependent, 4 11 0.738
150
c DBT095 Diabetes Mellitus, Noninsulin-Dependent, 3 11 0.738
151
LYM029 Lymphedema-Distichiasis Syndrome 39 0.737
152
XLN122 X-Linked Intellectual Disability - Short Stature - Obesity 8 0.720
153
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 17 0.714
154
SHR107 Short Stature-Obesity Syndrome 16 0.714
155
PRL046 Prolactin Deficiency with Obesity and Enlarged Testes 9 0.714
156
AYZ001 Ayazi Syndrome 9 0.712
157
c BDY021 Body Mass Index Quantitative Trait Locus 20 30 0.710
158
c HMC039 Hemochromatosis, Type 1 74 0.710
159
GNT051 Genetic Non-Syndromic Obesity 4 0.709
160
MN1002 Man1b1-Cdg 10 0.703
161
DBT018 Diabetic Mastopathy 19 0.687
162
c WLF013 Wolfram Syndrome 1 55 0.677
163
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 43 0.666
164
GST058 Gestational Diabetes Insipidus 15 0.658
165
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 52 0.656
166
FNC009 Fanconi-Bickel Syndrome 53 0.652
167
TRP008 Tropical Calcific Pancreatitis 50 0.648
168
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 16 0.648
169
P NRP001 Neuropathy 63 0.645
170
DBT089 Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification 17 0.644
171
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 30 0.643
172
BNG086 Bangstad Syndrome 20 0.642
173
P KDN018 Kidney Disease 71 0.606
174
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 50 0.600
175
P ACQ022 Acquired Generalized Lipodystrophy 51 0.594
176
c BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.590
177
INS034 Insulinomatosis and Diabetes Mellitus 24 0.582
178
NTR005 Nutritional Deficiency Disease 59 0.581
179
PRX085 Preaxial Hallucal Polydactyly 27 0.580
180
DBT081 Diabetic Encephalopathy 29 0.573
181
HYP364 Hyperostosis Frontalis Interna 29 0.565
182
OVR063 Overnutrition 53 0.562
183
RNL024 Renal Glucosuria 54 0.548
184
DPS001 Dipsogenic Diabetes Insipidus 24 0.541
185
c CNG012 Congenital Generalized Lipodystrophy 52 0.534
186
GLC003 Glucose Intolerance 59 0.532
187
MTC096 Mitchell-Riley Syndrome 23 0.532
188
c HRD156 Hereditary Central Diabetes Insipidus 16 0.532
189
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 16 0.531
190
c ACQ034 Acquired Central Diabetes Insipidus 15 0.531
191
RNL050 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna 7 0.531
192
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 18 0.529
193
LPT011 Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy 16 0.529
194
PHT013 Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction 17 0.528
195
YRF001 Yorifuji Okuno Syndrome 9 0.525
196
FGN001 Feigenbaum Bergeron Richardson Syndrome 8 0.523
197
DBT003 Diabetic Peripheral Angiopathy 6 0.523
198
ACH016 Achard Thiers Syndrome 6 0.522
199
OBS060 Obesity Due to Sim1 Deficiency 11 0.519
200
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 11 0.519
201
MDF004 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 13 0.516
202
OBS083 Obesity Due to Congenital Leptin Resistance 4 0.514
203
c MNT236 Mental Retardation, Autosomal Dominant 39 26 0.512
204
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 17 0.512
205
XLN211 X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome 16 0.512
206
INT298 Intellectual Disability-Obesity-Brain Malformations-Facial Dysmorphism Syndrome 15 0.512
207
OBS068 Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome 7 0.512
208
HYP056 Hypoglycemia 64 0.510
209
FTT001 Fatty Liver Disease 66 0.507
210
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 23 0.503
211
CLR029 Clark-Baraitser Syndrome 22 0.503
212
c BMN004 Biemond Syndrome Ii 18 0.499
213
DPL003 Diploid-Triploid Mosaicism 15 0.499
214
P LVR013 Liver Disease 76 0.496
215
CMR005 Camera-Marugo-Cohen Syndrome 12 0.494
216
HYP066 Hyperglycemia 64 0.492
217
P SHR029 Short Syndrome 57 0.489
218
HYP060 Hyperinsulinism 57 0.462
219
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.454
220
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 20 0.411
221
LPD008 Lipid Metabolism Disorder 65 0.389
222
P HRT032 Heart Disease 76 0.385
223
INT288 Intellectual Disability-Dysmorphism-Hypogonadism-Diabetes Mellitus Syndrome 11 0.379
224
LPT004 Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 3 0.376
225
MNT030 Mental Retardation Syndrome, Belgian Type 17 0.375
226
WLF014 Wolfram Syndrome, Mitochondrial Form 15 0.375
227
CRD024 Cardiomyopathy Diabetes Deafness 2 0.375
228
ECT013 Ectodermal Dysplasia Arthrogryposis Diabetes Mellitus 1 0.375
229
INT222 Intermediate Dend Syndrome 10 0.373
230
c DBT096 Diabetes Mellitus, Congenital Autoimmune 8 0.373
231
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 8 0.373
232
PRM187 Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome 7 0.373
233
XLN187 X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome 6 0.373
234
HYP790 Hypopituitarism, Congenital, with Central Diabetes Insipidus 3 0.373
235
DBT016 Diabetes Persistent Mullerian Ducts 1 0.373
236
PRM291 Premature Aging Syndrome, Okamoto Type 13 0.371
237
P PLY011 Polycystic Ovary Syndrome 64 0.370
238
P SLP006 Sleep Apnea 70 0.349
239
P PRP019 Peripheral Nervous System Disease 66 0.346
240
ATM095 Autoimmune Disease 68 0.345
241
ETN001 Eating Disorder 65 0.341
242
ART140 Arteries, Anomalies of 66 0.336
243
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.335
244
P CRN018 Coronary Artery Anomaly 75 0.331
245
DPR016 Depression 72 0.327
246
P CRN300 Coronary Heart Disease 1 61 0.312
247
IMM136 Immune System Disease 57 0.310
248
c CHR089 Chronic Kidney Failure 73 0.303
249
VSC007 Vascular Disease 72 0.297
250
ISC004 Ischemia 67 0.297
251
P MYC007 Myocardial Infarction 78 0.291
253
ATN004 Autonomic Neuropathy 46 0.266
254
P PRD008 Periodontitis 66 0.265
255
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.265
256
DGS002 Degos 'en Cocarde' Erythrokeratoderma 25 0.265
257
AST005 Asthma 81 0.261
258
c HYP595 Hypertension, Essential 81 0.251
259
P BRS047 Breast Cancer 100 0.247
260
ISC006 Ischemic Heart Disease 72 0.244
261
NNL002 Nonalcoholic Steatohepatitis 54 0.244
262
ANX010 Anxiety 73 0.242
263
AGN016 Aging 63 0.242
264
P PLY019 Polyneuropathy 57 0.241
265
IMP005 Impotence 56 0.240
266
PRD007 Periodontal Disease 66 0.236
267
PLC008 Placenta Disease 59 0.231
268
RTN018 Retinal Disease 58 0.228
269
PRD004 Prediabetes Syndrome 51 0.227
270
PRP027 Peripheral Vascular Disease 72 0.227
271
CNG034 Congestive Heart Failure 70 0.224
272
URN009 Urinary System Disease 59 0.224
273
SPS003 Spastic Diplegia 55 0.216
274
P HYP750 Hypertriglyceridemia, Familial 58 0.214
275
MNT002 Mental Depression 65 0.212
276
P PNC044 Pancreatitis 62 0.211
277
DSS008 Disease of Mental Health 71 0.210
278
APN008 Apnea, Obstructive Sleep 68 0.210
279
P ART022 Arthritis 77 0.209
280
P HPT021 Hepatitis 73 0.206
281
P CTR002 Cataract 59 0.205
282
P ART021 Arteriosclerosis 61 0.205
283
c PRC016 Pre-Eclampsia 61 0.201
284
P HYP086 Hypothyroidism 66 0.201
285
HYP080 Hypogonadism 53 0.200
286
OST012 Osteoarthritis 80 0.200
287
P INF032 Infertility 60 0.198
288
END030 End Stage Renal Failure 60 0.198
289
HYP064 Hypogonadotropism 42 0.196
290
P PRD006 Prader-Willi Syndrome 61 0.195
291
INS024 Insulin-Like Growth Factor I 82 0.195
292
ACN002 Acanthosis Nigricans 64 0.195
293
THR024 Thrombosis 64 0.191
294
GST092 Gastroesophageal Reflux 66 0.191
295
P THY032 Thyroiditis 53 0.186
296
END057 Endometrial Cancer 68 0.186
297
FSH001 Fish-Eye Disease 50 0.185
298
GST037 Gastroparesis 57 0.184
299
HYP266 Hypoxia 63 0.182
300
NRT004 Neuritis 58 0.178
301
P VSC018 Visceral Steatosis 37 0.178
302
c TRC078 Trichohepatoenteric Syndrome 2 35 0.176
303
ATH013 Atherosclerosis Susceptibility 60 0.174
305
c PRD040 Periodontitis, Chronic 59 0.172
306
P TRC086 Trichohepatoenteric Syndrome 1 60 0.171
307
P OST002 Osteoporosis 74 0.171
308
MCL006 Macular Retinal Edema 53 0.170
309
SLP005 Sleep Disorder 60 0.170
310
ANR007 Anorexia Nervosa 68 0.170
311
NRM005 Neuromuscular Disease 61 0.169
312
P ALZ034 Alzheimer Disease 87 0.167
313
P RTN016 Retinal Degeneration 56 0.166
314
c ATR087 Atrial Standstill 1 70 0.163
315
P CLR023 Colorectal Cancer 99 0.162
316
FTL021 Fetal Macrosomia 46 0.160
317
GST050 Gastrointestinal System Disease 67 0.160
318
P RHM011 Rheumatoid Arthritis 81 0.158
319
P LKM002 Leukemia 72 0.158
320
c ACT075 Acute Myocardial Infarction 57 0.158
321
c HPT001 Hepatitis C 69 0.157
322
P PNC035 Pancreatic Cancer 82 0.155
323
P NRV007 Nervous System Disease 71 0.155
324
P HPT023 Hepatocellular Carcinoma 96 0.153
325
P ADN016 Adenocarcinoma 70 0.153
326
P CLC063 Celiac Disease 1 71 0.153
327
SXL003 Sexual Disorder 53 0.153
328
LYM053 Lymphomatous Thyroiditis 27 0.152
329
P PRS040 Prostate Cancer 93 0.152
330
c ACT027 Acute Pancreatitis 59 0.152
331
P SCH015 Schizophrenia 73 0.150
332
DNT012 Dental Caries 52 0.150
333
P INF038 Influenza 75 0.150
334
PRP080 Peripheral Artery Disease 56 0.149
335
P MSC007 Muscle Hypertrophy 64 0.147
336
c PRS136 Prostate Cancer, Hereditary, 6 40 0.145
337
c PRS130 Prostate Cancer, Hereditary, 8 37 0.145
338
LVR012 Liver Cirrhosis 67 0.144
339
DMN002 Dementia 69 0.143
340
BRN106 Burns 59 0.143
341
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.141
342
P ECL001 Eclampsia 58 0.141
343
HYP014 Hyperuricemia 55 0.141
344
P RSP003 Respiratory Failure 72 0.140
345
P ATR011 Atrial Fibrillation 69 0.138
346
CRN036 Craniopharyngioma 66 0.138
347
CNN003 Conn's Syndrome 70 0.138
348
JNT002 Joint Disorders 64 0.138
349
P ART023 Arthropathy 68 0.137
350
LMB062 Limb Ischemia 54 0.137
351
ANG054 Angina Pectoris 69 0.135
352
P PSR002 Psoriasis 67 0.135
353
P ENC018 Encephalopathy 65 0.135
354
RTN020 Retinal Vascular Disease 54 0.131
355
IRN002 Iron Metabolism Disease 60 0.129
356
HYP043 Hyperandrogenism 50 0.128
357
BND020 Bone Disease 64 0.127
358
c PRC031 Preeclampsia/eclampsia 1 41 0.125
359
P LYM118 Lymphoma 69 0.125
360
MDD011 Mood Disorder 65 0.125
361
BRR014 Barrett Esophagus 70 0.125
362
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.124
363
P OVR049 Ovarian Disease 63 0.123
364
LNG099 Lung Disease 70 0.122
365
GND003 Gonadal Disease 49 0.121
366
CYS009 Cystadenoma 41 0.121
367
INS001 Insulinoma 64 0.121
368
BLM002 Bulimia Nervosa 61 0.121
369
THR013 Thoracic Outlet Syndrome 56 0.119
370
STR067 Stroke, Ischemic 82 0.119
371
CYT002 Cytokine Deficiency 39 0.119
372
ALL026 Allergic Hypersensitivity Disease 68 0.118
373
P MJR001 Major Depressive Disorder 67 0.118
374
P JVN024 Juvenile Hereditary Hemochromatosis 44 0.117
375
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.117
376
CRB039 Cerebrovascular Disease 70 0.117
377
ADN018 Adenoma 64 0.115
378
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.115
379
c PLY105 Polycystic Ovary Syndrome 1 42 0.115
380
P MLT020 Multiple Sclerosis 75 0.114
381
CRT049 Critical Limb Ischemia 53 0.113
382
CYS001 Cystic Fibrosis 82 0.112
383
P HYP083 Hypopituitarism 58 0.112
384
BWN003 Bowenoid Papulosis 42 0.112
385
THY030 Thyroid Gland Disease 50 0.111
386
P DRR001 Diarrhea 58 0.111
387
c GLL024 Gallbladder Disease 1 45 0.111
388
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 34 0.111
389
HYP730 Hypogonadotropic Hypogonadism 58 0.111
390
P PNM007 Pneumonia 72 0.110
391
BLD165 Blood Group, Colton System 34 0.110
392
HLC007 Helicobacter Pylori Infection 65 0.109
393
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.109
394
P BPL003 Bipolar Disorder 61 0.109
395
MCR141 Mucormycosis 51 0.109
396
DFC004 Deficiency Anemia 66 0.108
397
GT001 Gout 62 0.107
398
MTH009 Mouth Disease 64 0.106
399
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.106
400
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.106
401
SPN331 Spondyloocular Syndrome 41 0.106
402
NTR027 Neutrophil Actin Dysfunction 32 0.106
403
GST053 Gastric Cancer 78 0.105
404
DWN001 Down Syndrome 71 0.105
405
RST023 Resting Heart Rate, Variation in 44 0.105
406
P LYM031 Lymphocytic Leukemia 61 0.104
407
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.104
408
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.104
409
c ACT068 Acute Cystitis 56 0.103
410
NRL016 Neural Tube Defects 79 0.103
411
P AMY004 Amyloidosis 64 0.102
412
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.102
413
P ANR048 Aniridia 1 64 0.101
414
P HYP069 Hyperparathyroidism 59 0.101
415
P OVR046 Ovarian Cyst 52 0.101
416
ATX010 Ataxia Neuropathy Spectrum 39 0.101
417
P LKM062 Leukemia, Acute Lymphoblastic 68 0.101
418
PTT009 Pituitary Gland Disease 59 0.101
419
c THR092 Thrombophilia Due to Thrombin Defect 69 0.101
420
P EPL164 Epilepsy 72 0.101
421
c PNC128 Pain - Chronic 49 0.100
422
BNF002 Bone Fracture 48 0.100
423
CRP001 Carpal Tunnel Syndrome 71 0.099
424
c MTR002 Mitral Valve Insufficiency 50 0.099
425
HRN028 Horns in Sheep 24 0.099
426
MTB004 Metabolic Acidosis 50 0.099
427
ACT088 Acute Insulin Response 50 0.099
428
PLM033 Pulmonary Embolism 64 0.099
429
c BRD013 Bardet-Biedl Syndrome 12 48 0.099
430
SPN186 Spinal Cord Injury 66 0.099
431
RSP006 Respiratory System Disease 64 0.098
432
P LCT001 Lactic Acidosis 52 0.098
433
HDC001 Headache 62 0.098
434
c ACT210 Acute Respiratory Distress Syndrome 66 0.098
435
c BRD014 Bardet-Biedl Syndrome 2 60 0.098
436
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.097
437
P ACT232 Acute Necrotizing Encephalopathy 30 0.097
438
RPD005 Rapidly Involuting Congenital Hemangioma 25 0.097
439
BLD137 Blood Group--Ahonen 24 0.097
440
P BRD002 Bardet-Biedl Syndrome 63 0.097
441
c SPN225 Spondyloarthropathy 1 75 0.097
442
P INF037 Inflammatory Bowel Disease 56 0.097
443
STM006 Stomach Disease 55 0.096
444
c BRD012 Bardet-Biedl Syndrome 11 51 0.096
445
c BRD011 Bardet-Biedl Syndrome 10 44 0.096
446
SMT008 Smith-Magenis Syndrome 57 0.096
447
P ESP024 Esophagitis 60 0.096
448
ALC007 Alcohol Dependence 69 0.096
449
P ATS364 Autism 67 0.096
450
NPH009 Nephrolithiasis 58 0.095
451
ACR007 Acromegaly 70 0.095
452
P EXN002 Exanthem 62 0.095
453
PSY004 Psychotic Disorder 74 0.094
454
PNG002 Pain Agnosia 54 0.094
455
ART016 Aortic Aneurysm 71 0.093
456
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.093
457
RTN023 Retinitis 48 0.093
458
DRM006 Dermatitis 69 0.093
459
ATM052 Autoimmune Disease 1 40 0.092
460
P CRD119 Cardiac Arrest 66 0.092
461
THY028 Thyroid Cancer 72 0.092
462
INT075 Intracranial Hypertension 57 0.092
463
PNM001 Pneumocystosis 58 0.091
464
RHM027 Rheumatic Disease 65 0.091
465
P LYM025 Lymphedema 54 0.091
466
P AXN002 Axenfeld-Rieger Syndrome 57 0.091
467
ALS001 Alstrom Syndrome 57 0.091
468
GRW007 Growth Hormone Deficiency 49 0.091
469
FRN020 Frontal Fibrosing Alopecia 33 0.091
470
BRS090 Breast Reconstruction 34 0.090
471
P CRD132 Cardiac Conduction Defect 63 0.090
472
c SYS001 Systemic Lupus Erythematosus 88 0.090
474
c HPT016 Hepatitis B 70 0.090
475
GNR004 Generalized Anxiety Disorder 54 0.090
476
OCL069 Ocular Motor Apraxia 49 0.090
477
GNG013 Gingivitis 63 0.089
478
AND002 Androgen Insensitivity Syndrome 61 0.089
479
c HPT073 Hepatitis C Virus 72 0.089
480
P ATX030 Ataxia-Telangiectasia 82 0.089
481
PRS021 Prostatic Adenoma 55 0.089
482
PRS129 Prostatic Hyperplasia, Benign 53 0.089
483
ALR002 Al-Raqad Syndrome 40 0.089
484
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.089
485
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.089
486
P ANG001 Angelman Syndrome 64 0.089
487
c CHR579 Chiari Malformation Type Ii 49 0.088
488
INT007 Intermediate Coronary Syndrome 50 0.088
489
c MYT020 Myotonic Dystrophy 2 58 0.087
490
P OVR042 Ovarian Cancer 83 0.087
491
P CLL015 Collagen Disease 52 0.087
492
P THR014 Thrombocytopenia 64 0.087
493
FBR047 Fibromyalgia 66 0.087
494
P MSC003 Muscular Atrophy 56 0.086
495
CLT003 Colitis 65 0.086
496
P TRM003 Tremor 55 0.086
497
MLN008 Melanoma 63 0.086
498
HMC014 Homocysteinemia 53 0.086
499
P GLL020 Gallbladder Disease 62 0.086
500
ACQ007 Acquired Immunodeficiency Syndrome 66 0.086
501
P LNG032 Lung Cancer 99 0.085
502
c ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.085
503
P LPS004 Lupus Erythematosus 69 0.085
504
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.085
505
ART001 Arterial Tortuosity Syndrome 59 0.085
506
c ALP106 Alport Syndrome 1, X-Linked 53 0.085
507
P PLM037 Pulmonary Hypertension 77 0.085
508
c MGR028 Migraine with or Without Aura 1 69 0.084
509
CLL003 Cellulitis 60 0.084
510
P MYC084 Mycobacterium Tuberculosis 1 67 0.083
511
CRN030 Coronary Stenosis 52 0.083
512
THR100 Thrombocytopenic Purpura, Autoimmune 67 0.083
513
SVR004 Severe Combined Immunodeficiency 65 0.083
514
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 62 0.083
515
P SJG008 Sjogren Syndrome 60 0.082
516
HPT082 Hepatic Adenomas, Familial 50 0.082
517
PSR001 Psoriatic Arthritis 68 0.082
518
PRT058 Pure Autonomic Failure 65 0.082
519
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 62 0.082
520
IRN001 Iron Deficiency Anemia 55 0.082
521
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.081
522
NNC002 Nance-Horan Syndrome 48 0.081
523
URM002 Uremia 53 0.081
524
P HST010 Histiocytosis 60 0.081
525
P PRC019 Precocious Puberty 52 0.081
526
BCT004 Bacteriuria 51 0.081
527
PST011 Pustulosis of Palm and Sole 50 0.081
528
BCT022 Bacterial Infectious Disease 62 0.080
529
ATN002 Autonomic Nervous System Disease 56 0.080
530
P GLM007 Glomerulonephritis 61 0.080
531
c ATS007 Autism Spectrum Disorder 67 0.080
532
ANV001 Anovulation 49 0.080
533
P RTN008 Retinitis Pigmentosa 80 0.080
534
APP008 Appendicitis 66 0.079
535
P INT068 Intestinal Disease 62 0.079
536
HNM002 Hinman Syndrome 31 0.079
537
BRN038 Bronchial Disease 58 0.079
538
ALX002 Alexithymia 43 0.078
539
P KDN017 Kidney Cancer 59 0.078
540
SKN016 Skin Disease 68 0.078
541
ADP007 Adie Pupil 42 0.078
542
P PRS038 Personality Disorder 67 0.078
543
END040 Endogenous Depression 59 0.078
544
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.078
545
P ACR001 Aicardi-Goutieres Syndrome 65 0.077
546
P HYP076 Hyperthyroidism 55 0.077
547
MYC088 Mycobacterium Avium Complex Infections 33 0.077
548
AND005 Androgen Insensitivity Syndrome, Mild 21 0.077
549
P ALC004 Alcohol Abuse 68 0.077
550
SCH012 Schizoaffective Disorder 54 0.077
551
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.077
552
IGR001 Ige Responsiveness, Atopic 59 0.077
553
c ACR116 Aicardi-Goutieres Syndrome 1 50 0.076
554
BRC012 Brucellosis 70 0.076
555
c ACT074 Acute Lymphocytic Leukemia 63 0.075
556
P NRC002 Narcolepsy 59 0.075
557
LNG108 Langerhans Cell Histiocytosis 63 0.075
558
DWR001 Dwarfism 47 0.075
559
P MYP004 Myopathy 64 0.075
560
NRR001 Neuroretinitis 47 0.075
561
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.075
562
CHL004 Cholelithiasis 51 0.074
563
SKN027 Skin Conditions 51 0.074
564
VTM002 Vitamin B12 Deficiency 48 0.074
565
P DYS021 Dysautonomia 45 0.074
566
AMN001 Amenorrhea 55 0.074
567
FSC004 Fasciitis 50 0.074
568
P DRM053 Dermatitis, Atopic 71 0.074
569
P RCT021 Rectum Cancer 58 0.074
570
P LPM005 Lipomatosis 53 0.073
571
LRY021 Laryngeal Adductor Paralysis 26 0.073
572
VRL011 Viral Infectious Disease 68 0.073
573
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.073
574
INT002 Intermittent Claudication 64 0.073
575
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.073
576
P TRN020 Turner Syndrome 71 0.073
577
WRN001 Werner Syndrome 73 0.073
578
c HPT003 Hepatitis a 66 0.073
579
CRH001 Crohn's Disease 79 0.073
580
IGG001 Iga Glomerulonephritis 58 0.073
581
CNS004 Constipation 58 0.073
582
HSH003 Hashimoto Thyroiditis 67 0.072
583
c SCN007 Secondary Hyperparathyroidism 55 0.072
584
P HYP265 Hypotonia 43 0.072
585
GSG001 Gas Gangrene 47 0.072
586
MCC013 Mucocutaneous Ulceration, Chronic 45 0.072
587
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.072
588
ULC005 Ulcer of Lower Limbs 25 0.072
589
PNC034 Pancreas Disease 59 0.071
590
ADL002 Adult Syndrome 55 0.071
591
HPR003 Heparin-Induced Thrombocytopenia 53 0.071
592
P TTR001 Tetralogy of Fallot 70 0.071
593
BRN071 Brain Injury 55 0.071
594
CHR100 Chronic Ulcer of Skin 53 0.071
595
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 0.070
596
P SLL003 Salla Disease 52 0.070
597
P GST044 Gastritis 60 0.070
598
P BLD134 Bladder Cancer 70 0.070
599
P RST001 Restless Legs Syndrome 59 0.070
600
NCR002 Necrobiosis Lipoidica 39 0.070
601
P NPH012 Nephrotic Syndrome 63 0.070
602
IRR002 Irritable Bowel Syndrome 64 0.070
603
P RHN004 Rhinitis 64 0.070
604
PRS063 Paresthesia 45 0.069
605
CLR108 Colorectal Adenoma 64 0.069
606
LRN002 Laron Syndrome 62 0.069
607
c BRD010 Bardet-Biedl Syndrome 1 59 0.068
608
BNR002 Bone Resorption Disease 54 0.068
609
c ACT071 Acute Kidney Failure 54 0.068
610
P CND004 Candidiasis 63 0.068
611
P SBS003 Substance Abuse 60 0.068
612
SYS003 Systolic Heart Failure 46 0.068
613
P FCL005 Focal Segmental Glomerulosclerosis 60 0.067
614
GST049 Gastrointestinal System Cancer 62 0.067
615
GST071 Gastrointestinal Carcinoma 45 0.067
616
ASP030 Aspirin Resistance 47 0.067
617
MYL005 Myelofibrosis 69 0.067
618
OBS082 Obstructive Nephropathy 52 0.067
619
P NRF023 Neurofibromatosis, Type Ii 75 0.067
620
BRS051 Breast Disease 66 0.067
621
P MYL006 Myeloid Leukemia 67 0.067
622
DYS073 Dysphagia 48 0.066
623
PRT036 Peritonitis 66 0.066
624
OST097 Osteoporotic Fracture 36 0.066
625
PLM010 Pulmonary Edema 59 0.065
626
P ADL010 Adult Respiratory Distress Syndrome 64 0.065
627
P MLN007 Male Infertility 52 0.065
628
INT303 Intracranial Hypertension, Idiopathic 52 0.065
629
HRN026 Hernia, Hiatus 49 0.065
630
CRT013 Carotid Stenosis 53 0.065
631
MYL069 Myeloma, Multiple 85 0.065
632
SRC014 Sarcoma 70 0.065
633
GTR002 Goiter 54 0.065
634
DYS014 Dyspepsia 56 0.064
635
PLM017 Pulmonary Alveolar Microlithiasis 52 0.064
636
P SZR006 Seizure Disorder 61 0.064
637
PNC033 Pancreas Adenocarcinoma 67 0.064
638
TRN015 Transient Cerebral Ischemia 59 0.064
639
HMT018 Hematopoietic Stem Cell Transplantation 59 0.064
640
PPT005 Peptic Ulcer Disease 63 0.064
641
PST021 Postpartum Depression 56 0.064
642
P PHC003 Pheochromocytoma 72 0.064
643
CHL123 Chlamydia 66 0.063
644
LYM027 Lymphopenia 57 0.063
645
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.063
646
P DLT002 Dilated Cardiomyopathy 75 0.063
647
P OPN001 Open-Angle Glaucoma 53 0.063
648
HYP005 Hypokalemia 55 0.063
649
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.063
650
P PSD015 Pseudohypoparathyroidism 51 0.063
651
DVR002 Diverticulitis 46 0.063
652
c BLD140 Blood Group, I System 29 0.063
653
LYM133 Lymphoma, Hodgkin, Classic 72 0.063
654
P CMR001 Camurati-Engelmann Disease 61 0.062
655
c VRL010 Viral Hepatitis 60 0.062
656
ALL003 Allergic Rhinitis 70 0.062
657
c APL023 Aplasia Cutis Congenita, Nonsyndromic 40 0.062
658
PMP004 Pemphigus Foliaceus 46 0.062
659
ESP021 Esophageal Cancer 82 0.062
660
P GLY013 Glycogen Storage Disease 61 0.062
661
STS002 Situs Inversus 49 0.062
662
SLD003 Sialadenitis 48 0.062
663
CRT016 Carotid Artery Disease 58 0.062
664
P SNS001 Sensorineural Hearing Loss 60 0.061
665
P MSC033 Muscle Disorders 57 0.061
666
P MNN013 Meningitis 69 0.061
667
c GRV008 Graves Disease 1 57 0.061
668
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.061
669
WRN003 Wernicke Encephalopathy 49 0.061
670
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.060
671
NCR007 Necrotizing Fasciitis 51 0.060
672
c LRG017 Large Intestine Cancer 63 0.060
673
P PLY018 Polycythemia 60 0.060
674
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 54 0.060
675
P HYP061 Hypertrophic Cardiomyopathy 59 0.060
676
c CRP023 Carpenter Syndrome 1 58 0.060
677
P SCL057 Scoliosis, Isolated 1 45 0.060
678
PRP030 Purpura 60 0.060
679
c PTT057 Pituitary Adenoma 4, Acth-Secreting 54 0.060
680
CHL147 Chlamydia Pneumonia 42 0.059
681
OPT006 Optic Nerve Disease 60 0.059
682
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.059
683
LRN003 Learning Disability 53 0.059
684
DYS011 Dyskinesia of Esophagus 42 0.059
685
ERY029 Erythermalgia, Primary 57 0.059
686
HYP081 Hypolipoproteinemia 49 0.059
687
P THL005 Thalassemia 65 0.059
688
c PNC106 Pancreatic Agenesis 1 51 0.059
689
EPD070 Epidermoid Cysts 48 0.059
690
c LKM061 Leukemia, Acute Myeloid 81 0.059
691
P MMP001 Mumps 61 0.058
692
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.058
693
SPN051 Spondylitis 55 0.058
694
NWB001 Newborn Respiratory Distress Syndrome 59 0.058
695
RSP007 Respiratory Distress Syndrome, Infant 37 0.058
696
DMP001 Dumping Syndrome 46 0.058
697
ACH005 Achalasia 53 0.057
698
HMN044 Human Immunodeficiency Virus Type 1 75 0.057
699
P PLY014 Polycystic Kidney Disease 62 0.057
700
HYD002 Hydronephrosis 52 0.057
701
P PRK057 Parkinson Disease, Late-Onset 76 0.057
702
RCK004 Rickets 66 0.057
703
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 0.057
704
P CMP008 Compartment Syndrome 52 0.057
705
c LBR014 Leber Congenital Amaurosis 4 54 0.057
706
P BRB001 Beriberi 46 0.057
707
OST017 Osteomyelitis 64 0.057
708
CLR030 Clear Cell Renal Cell Carcinoma 49 0.057
709
P SRC025 Sarcoidosis 1 76 0.057
710
P VNS003 Venous Insufficiency 54 0.057
711
CHR073 Choreatic Disease 50 0.057
712
FRL002 Froelich Syndrome 20 0.057
713
CHL065 Cholangiocarcinoma 64 0.056
714
c PTT056 Pituitary Adenoma 1, Multiple Types 53 0.056
715
BRN041 Bornholm Eye Disease 45 0.056
716
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.056
717
P MJR007 Major Affective Disorder 1 45 0.056
718
FCL044 Fecal Incontinence 38 0.056
719
P ALP008 Alopecia 56 0.056
720
P HYD006 Hydrocephalus 67 0.056
721
c BST008 Bestrophinopathy, Autosomal Recessive 33 0.056
722
OVR094 Ovarian Epithelial Cancer 41 0.056
723
END062 Endometrial Hyperplasia 51 0.056
724
P HYP098 Hypereosinophilic Syndrome 67 0.055
725
P END033 Endocarditis 60 0.055
726
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.055
727
ACR006 Aceruloplasminemia 73 0.055
728
FRZ001 Frozen Shoulder 53 0.055
729
P CHL066 Cholangitis 51 0.055
730
MTC005 Mitochondrial Metabolism Disease 47 0.055
731
SKN023 Skin Tag 40 0.055
732
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.055
733
P RNL007 Renal Tubular Acidosis 51 0.055
734
P PNS012 Paine Syndrome 60 0.055
735
P MCR010 Microcephaly 55 0.055
736
P FML012 Familial Partial Lipodystrophy 52 0.055
737
EXC002 Exocrine Pancreatic Insufficiency 41 0.055
738
CRV035 Cervical Cancer 76 0.055
739
GST045 Gastroenteritis 65 0.055
740
GYN001 Gynecomastia 47 0.055
741
INF021 Infant Gynecomastia 28 0.055
742
EXP004 Exophthalmos 53 0.054
743
ADR040 Adrenal Gland Pheochromocytoma 49 0.054
744
HYP110 Hyperproinsulinemia 41 0.054
745
CRD223 Cardiac Arrhythmia 55 0.054
746
HMS001 Hemosiderosis 52 0.054
747
SCL022 Scleredema 31 0.054
748
c FCL025 Focal Segmental Glomerulosclerosis 1 51 0.054
749
SLP010 Slipped Capital Femoral Epiphysis 37 0.054
750
P PLY006 Polydactyly 57 0.054
751
ERY003 Erythema Multiforme 62 0.054
752
TRM010 Traumatic Brain Injury 56 0.054
753
ULC004 Ulcerative Colitis 80 0.053
754
c CNT035 Central Nervous System Disease 65 0.053
755
c PRM005 Primary Hyperparathyroidism 60 0.053
756
CRB037 Cerebral Palsy 71 0.053
757
FRN014 Fournier Gangrene 41 0.053
758
INT051 Intussusception 53 0.053
759
HYP784 Hypogonadism, Male 42 0.053
760
c CHR682 Chronic Bilirubin Encephalopathy 33 0.053
761
BLD163 Blood Group, Dombrock System 27 0.053
762
PST053 Postherpetic Neuralgia 45 0.053
763
WLL001 Williams-Beuren Syndrome 63 0.053
764
HDR002 Hidradenitis Suppurativa 57 0.053
765
P HYP724 Hyperlipoproteinemia, Type Iii 63 0.053
766
P PTS002 Ptosis 55 0.053
767
P PTT006 Pituitary Adenoma 54 0.053
768
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 69 0.053
769
ART002 Arts Syndrome 55 0.053
770
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 62 0.052
771
ART008 Arteriosclerosis Obliterans 42 0.052
772
P PNC045 Pancreatic Agenesis 39 0.052
773
c JVN010 Juvenile Rheumatoid Arthritis 70 0.052
774
P ENC004 Encephalitis 66 0.052
775
P FNG006 Feingold Syndrome 1 46 0.052
776
HYP085 Hypothalamic Disease 46 0.052
777
OTT002 Otitis Media 69 0.052
778
VRC005 Varicose Veins 66 0.052
779
DST006 Diastolic Heart Failure 46 0.052
780
FXF002 Fox-Fordyce Disease 40 0.052
781
P VSC011 Vasculitis 66 0.052
782
CLC006 Calcinosis 53 0.052
783
P MYS003 Myasthenia Gravis 73 0.052
784
MYL009 Myelodysplastic Syndrome 70 0.052
785
TND005 Tendinitis 45 0.052
786
c MYT021 Myotonic Dystrophy 1 71 0.052
788
MNS002 Mini Stroke 25 0.052
789
VSC002 Vascular Dementia 57 0.052
790
CRN024 Corneal Disease 45 0.052
791
c INF145 Infantile Liver Failure Syndrome 1 47 0.051
792
P MSC005 Muscular Dystrophy 66 0.051
793
c CNT075 Central Precocious Puberty 52 0.051
794
HYP068 Hyperostosis 51 0.051
795
TND004 Tendinopathy 47 0.051
796
P UTR058 Uterine Anomalies 60 0.051
797
P HYP607 Hypercholesterolemia, Familial 81 0.050
798
c BTT014 Beta-Thalassemia 72 0.050
799
TBC004 Tobacco Addiction 64 0.050
800
c ACT073 Acute Leukemia 62 0.050
801
c SVR005 Severe Pre-Eclampsia 55 0.050
802
HDR003 Hidradenitis 52 0.050
803
PNN001 Panniculitis 49 0.050
804
P THR015 Thrombophilia 56 0.050
805
END038 Endocrine Pancreas Disease 39 0.050
806
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.050
807
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.050
808
DCB001 Decubitus Ulcer 47 0.050
809
c PLM164 Pulmonary Hypertension, Primary, 1 70 0.050
810
PRP016 Paraplegia 54 0.050
811
P CHR084 Chromosomal Disease 42 0.050
812
SPN027 Spinal Stenosis 61 0.050
813
P NTR004 Neutropenia 60 0.050
814
CHL068 Cholestasis 60 0.050
815
P HYP614 Hyperlipidemia, Familial Combined 55 0.050
816
CRD137 Cardiogenic Shock 42 0.050
817
DXT002 Dextrocardia with Situs Inversus 39 0.050
818
HYP026 Hypoglycemic Coma 42 0.050
819
c SML038 Small Cell Cancer of the Lung 68 0.049
820
HMR039 Hemorrhage, Intracerebral 62 0.049
821
SQM006 Squamous Cell Carcinoma 58 0.049
822
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.049
823
CLC001 Calciphylaxis 52 0.049
824
STF001 Stiff-Person Syndrome 64 0.049
825
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.049
826
P ACT105 Acute Mountain Sickness 57 0.049
827
KRT002 Keratomalacia 51 0.049
828
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.049
829
GNG011 Gingival Disease 49 0.049
830
HRT012 Heart Valve Disease 58 0.049
831
P INT070 Intestinal Obstruction 55 0.049
832
FND002 Fundus Dystrophy 51 0.049
833
ALL014 Allergic Encephalomyelitis 43 0.049
834
P ASP006 Aspergillosis 66 0.049
835
c EPS039 Episodic Pain Syndrome, Familial, 1 31 0.049
836
CYT008 Cytomegalovirus Infection 62 0.048
837
P MGL001 Megaloblastic Anemia 51 0.048
838
URN022 Urinary Tract Infections, Recurrent 34 0.048
839
MLR004 Malaria 84 0.048
840
DRG003 Drug Dependence 51 0.048
841
SYN036 Syncope 49 0.048
842
XP2001 Xp22.3 Microdeletion Syndrome 22 0.048
843
BLL003 Bell's Palsy 53 0.048
844
MCR011 Microinvasive Gastric Cancer 47 0.048
845
KPS004 Kaposi Sarcoma 77 0.048
846
INT079 Intrahepatic Cholangiocarcinoma 55 0.048
847
RDC002 Radiculopathy 55 0.048
848
P ART084 Arteriovenous Fistula 48 0.048
849
ALL006 Allergic Asthma 61 0.047
850
P MYP006 Myopia 59 0.047
851
CHL067 Cholecystitis 58 0.047
852
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 44 0.047
853
c HNT004 Huntington Disease-Like 2 47 0.047
854
SWL001 Swallowing Disorders 36 0.047
855
EPP010 Epiphysiolysis of the Hip 26 0.047
856
c HYP768 Hyperlipoproteinemia, Type I 47 0.047
857
P RTN024 Retinoblastoma 72 0.047
858
P SKN015 Skin Carcinoma 65 0.047
859
HYP020 Hyperprolactinemia 63 0.047
860
SPN035 Spindle Cell Sarcoma 53 0.047
861
NVS015 Nevus Comedonicus 42 0.047
862
c GLC092 Glaucoma, Primary Open Angle 57 0.047
863
c CNG124 Congenital Rubella 48 0.047
864
PSD088 Pseudobulbar Affect 39 0.047
865
STT004 Steatorrhea 43 0.046
866
ELP001 Elephantiasis 38 0.046
867
P HMP007 Hemophilia 62 0.046
868
HLX001 Helix Syndrome 40 0.046
869
P HLP001 Holoprosencephaly 65 0.046
870
SNL007 Senile Cataract 40 0.046
871
PSD014 Pseudopseudohypoparathyroidism 55 0.046
872
SPN021 Spinal Meningioma 50 0.046
873
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 32 0.046
874
c HMP029 Hemophilia a 70 0.046
875
P SNS014 Sinusitis 65 0.046
876
TTH006 Tooth Disease 54 0.046
877
IDP033 Idiopathic Edema 41 0.046
878
c MYS011 Myasthenia Gravis Congenital 33 0.046
879
CNN005 Connective Tissue Disease 67 0.046
880
CHL014 Cholera 60 0.046
881
GLC036 Glucagonoma 50 0.046
882
CLN019 Colonic Disease 62 0.045
883
KRN002 Kearns-Sayre Syndrome 63 0.045
884
NNT012 Neonatal Jaundice 52 0.045
885
c PRM038 Primary Agammaglobulinemia 41 0.045
886
PRT018 Portal Vein Thrombosis 50 0.045
887
P END044 Endometriosis 65 0.045
888
c CNG006 Congenital Hypothyroidism 59 0.045
889
c CNG216 Congenital Hydrocephalus 57 0.045
890
P DDN001 Duodenal Ulcer 51 0.045
891
P ALP009 Alopecia Areata 66 0.045
892
c ART101 Aortic Valve Disease 2 63 0.045
893
P ANT006 Antiphospholipid Syndrome 60 0.045
894
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 56 0.045
895
P KRT007 Keratoconus 50 0.045
896
P ACQ009 Acquired Metabolic Disease 35 0.045
897
DSR011 Disorganization, Mouse, Homolog of 22 0.045
898
HRP004 Herpes Zoster 63 0.044
899
HYP030 Hypoactive Sexual Desire Disorder 44 0.044
900
END072 Endotheliitis 39 0.044
901
P SCL018 Scoliosis 58 0.044
902
c MNN043 Meningioma, Familial 63 0.044
903
P PLV020 Pelvic Organ Prolapse 62 0.044
904
SPN041 Spinal Cord Disease 54 0.044
905
PPT001 Peptic Esophagitis 45 0.044
906
c BRD018 Bardet-Biedl Syndrome 6 44 0.044
907
CRD220 Cardiac Valvular Defect, Developmental 36 0.044
908
PHN003 Phenylketonuria 74 0.044
909
SYN007 Synovitis 59 0.044
910
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.044
911
PTL001 Patulous Eustachian Tube 31 0.044
912
P TMP003 Temporal Arteritis 69 0.044
913
P CHR071 Charcot-Marie-Tooth Disease 65 0.044
914
SDD008 Sudden Sensorineural Hearing Loss 45 0.044
915
CRB085 Cerebral Hemorrhage 42 0.044
916
BRN024 Bronchitis 70 0.044
917
c LPM012 Lipomatosis, Multiple 65 0.044
918
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 63 0.044
919
CRB009 Cerebritis 39 0.044
920
ACH004 Achondroplasia 68 0.043
921
PPL022 Papilloma 58 0.043
922
P OCY003 Oocyte Maturation Defect 1 42 0.043
923
RTN017 Retinal Detachment 61 0.043
924
P RNL015 Renal Hypertension 49 0.043
925
HYP017 Hypophosphatemia 49 0.043
926
SCK003 Sickle Cell Anemia 74 0.043
927
P MYC008 Myocarditis 59 0.043
928
P GLM045 Glioma 55 0.043
929
c LPD040 Lipodystrophy, Familial Partial, Type 1 43 0.043
930
SFT003 Soft Tissue Sarcoma 59 0.042
931
INT253 Intestinal Benign Neoplasm 57 0.042
932
CHR005 Chorioamnionitis 53 0.042
933
CRH005 Crohn's Colitis 61 0.042
934
MNC006 Monoclonal Gammopathy of Uncertain Significance 53 0.042
935
c CHR431 Chronic Venous Insufficiency 50 0.042
936
BRC010 Brachial Plexus Lesion 47 0.042
937
PLM005 Pleomorphic Lipoma 40 0.042
938
CRY036 Cryptogenic Cirrhosis 38 0.042
939
P HML002 Hemolytic Anemia 64 0.042
940
CMP010 Complex Regional Pain Syndrome 63 0.042
941
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 42 0.042
942
CDQ001 Cauda Equina Syndrome 40 0.042
943
HPT067 Hepatocellular Adenoma 44 0.042
944
SCR001 Secretory Meningioma 41 0.042
945
PST028 Post-Traumatic Stress Disorder 63 0.042
946
P PRT013 Portal Hypertension 61 0.042
947
BLD044 Bladder Disease 57 0.042
948
BLR008 Bilirubin Metabolic Disorder 54 0.042
949
MSC190 Muscular Disease 53 0.042
950
EMP001 Empty Sella Syndrome 43 0.042
951
MSC004 Muscle Tissue Disease 39 0.042
952
LRN001 Laurence-Moon Syndrome 46 0.042
953
TRC026 Tracheal Disease 36 0.042
954
P HRP006 Herpes Simplex 71 0.041
955
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 64 0.041
956
DSS009 Disseminated Intravascular Coagulation 58 0.041
957
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 52 0.041
958
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 46 0.041
959
NPH010 Nephrosclerosis 45 0.041
960
P BNC003 Bone Cancer 62 0.041
961
c PSD108 Pseudohypoparathyroidism, Type Ia 56 0.041
962
AML029 Ameloblastoma 53 0.041
963
c BRD016 Bardet-Biedl Syndrome 4 47 0.041
964
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 53 0.041
965
P ACT010 Acth-Secreting Pituitary Adenoma 52 0.041
966
KWS001 Kwashiorkor 46 0.041
967
c LKM063 Leukemia, Chronic Myeloid 73 0.041
968
P NSP012 Nasopharyngeal Carcinoma 65 0.041
969
PYD002 Pyoderma 52 0.041
970
SHH001 Sheehan Syndrome 50 0.041
971
GLC022 Glucose/galactose Malabsorption 44 0.041
972
DGR001 Digeorge Syndrome 61 0.041
973
ISL003 Isolated Growth Hormone Deficiency 52 0.041
974
P END046 Endometritis 52 0.041
975
ALB001 Albright's Hereditary Osteodystrophy 51 0.041
976
P HYP263 Hypersomnia 45 0.041
977
SCR011 Scrapie 43 0.041
978
INT146 Intervertebral Disc Disease 64 0.040
979
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.040
980
P BCK002 Beckwith-Wiedemann Syndrome 58 0.040
981
P TXP001 Toxoplasmosis 66 0.040
982
P LTR001 Lateral Sclerosis 60 0.040
983
TBR011 Tuberculous Meningitis 55 0.040
984
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.040
985
BRN056 Bronchopulmonary Dysplasia 60 0.040
986
RCT017 Rectal Disease 43 0.040
987
END041 Endometrial Adenocarcinoma 60 0.039
988
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.039
989
PRS042 Prostate Disease 47 0.039
990
PRT038 Protein-Energy Malnutrition 53 0.039
991
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.039
992
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.039
993
VSL002 Visual Epilepsy 37 0.039
994
GST007 Gastric Dilatation 32 0.039
995
BLD164 Blood Group, Gerbich System 31 0.039
996
GST019 Gastrointestinal Stromal Tumor 73 0.039
997
ANG020 Angiosarcoma 59 0.039
998
P THR005 Thrombotic Thrombocytopenic Purpura 62 0.039
999
P SLV001 Silver-Russell Syndrome 57 0.039
1000
HDN002 Head Injury 52 0.039
1001
ISL001 Islet Cell Tumor 51 0.039
1002
HYP077 Hypertrichosis 49 0.039
1003
P OPT070 Optic Nerve Hypoplasia, Bilateral 48 0.039
1004
MTR007 Motor Peripheral Neuropathy 41 0.039
1005
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.039
1006
c CRT085 Carotid Intimal Medial Thickness 2 26 0.039
1007
P GLL022 Guillain-Barre Syndrome 66 0.039
1008
PRS047 Prostatitis 56 0.039
1009
INF034 Infective Endocarditis 56 0.039
1010
MTC097 Mitochondrial Complex Iv Deficiency 56 0.039
1011
GST040 Gastric Adenocarcinoma 66 0.038
1012
c AMY009 Amyloidosis Aa 55 0.038
1013
P BLD051 Blood Coagulation Disease 52 0.038
1014
INT052 Intestinal Volvulus 43 0.038
1015
c ATM011 Autoimmune Hepatitis 67 0.038
1016
ART004 Aortic Atherosclerosis 45 0.038
1017
ICH020 Ichthyosis Prematurity Syndrome 45 0.038
1018
BRK012 Broken Heart Syndrome 39 0.038
1019
MNC002 Munchausen by Proxy 32 0.038
1020
NRN002 Neuronitis 32 0.038
1021
P GRF003 Graft-Versus-Host Disease 71 0.038
1022
c INF071 Inflammatory Bowel Disease 1 60 0.038
1023
OST011 Osteomalacia 52 0.038
1024
ESN002 Eosinophilia-Myalgia Syndrome 50 0.038
1025
PPL021 Papilledema 48 0.038
1026
NRT001 Neurotic Disorder 47 0.038
1027
P MYS005 Myositis 61 0.038
1028
CHK001 Chikungunya 61 0.038
1029
MST005 Mastitis 57 0.038
1030
ATR057 Atrioventricular Block 54 0.038
1031
OCC006 Occipital Horn Syndrome 51 0.038
1032
c CRD093 Cardiomyopathy, Dilated, 1a 44 0.038
1033
MYX004 Myxedema 43 0.038
1034
MDS022 Mediastinitis 41 0.038
1035
c HNT011 Huntington Disease-Like 3 40 0.038
1036
c PLM022 Pulmonary Valve Insufficiency 39 0.037
1037
P SPN046 Spinal Muscular Atrophy 66 0.037
1038
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 56 0.037
1039
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 53 0.037
1040
HNT002 Hantavirus Pulmonary Syndrome 52 0.037
1041
BRN080 Brain Ischemia 43 0.037
1042
HNS001 Hansen's Disease 36 0.037
1043
BRN028 Brain Cancer 72 0.037
1044
CHR178 Chromosomal Triplication 41 0.037
1045
URT039 Urticaria 60 0.037
1046
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 58 0.037
1047
URN010 Urinary Tract Obstruction 58 0.037
1048
P MYT002 Myotonic Dystrophy 52 0.037
1049
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 49 0.037
1050
GLC096 Galactorrhea 47 0.037
1051
NTR007 Neutral Lipid Storage Disease with Myopathy 37 0.037
1052
DFN039 Deafness-Infertility Syndrome 34 0.037
1053
c BPL002 Bipolar I Disorder 49 0.037
1054
c BRD015 Bardet-Biedl Syndrome 3 43 0.037
1055
DDN027 Duodenum Disease 43 0.037
1056
TQP001 Taqi Polymorphism 35 0.037
1057
APL001 Aplastic Anemia 74 0.036
1058
CHR066 Chronic Fatigue Syndrome 68 0.036
1059
c THY109 Thyroid Cancer, Nonmedullary, 1 59 0.036
1060
P ICH004 Ichthyosis 57