Search results for obesity OR diabetes

3659 hits were found for obesity OR diabetes

# Family MCID Name MIFTS Score
1
BDY004 Body Mass Index Quantitative Trait Locus 11 68 7.971
2
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 5.153
3
P DBT009 Diabetes Mellitus 64 4.326
4
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 25 4.237
5
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 3.203
6
P MCR115 Microvascular Complications of Diabetes 5 71 2.629
7
MRB003 Morbid Obesity 60 2.565
8
GST033 Gestational Diabetes 60 2.451
9
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 2.440
10
DBT087 Diabetes Insipidus, Neurohypophyseal 60 2.418
11
c MCR113 Microvascular Complications of Diabetes 3 52 2.326
12
c MCR120 Microvascular Complications of Diabetes 7 37 2.324
13
c MCR129 Microvascular Complications of Diabetes 1 61 2.010
14
DBT084 Diabetes Mellitus, Ketosis-Prone 52 2.010
15
c MCR130 Microvascular Complications of Diabetes 6 40 1.992
16
c MCR133 Microvascular Complications of Diabetes 4 35 1.992
17
DBT083 Diabetes Mellitus, Permanent Neonatal 60 1.987
18
RNL051 Renal Cysts and Diabetes Syndrome 44 1.901
19
P MTR004 Maturity-Onset Diabetes of the Young 60 1.754
20
DBT010 Diabetic Neuropathy 59 1.740
21
LPT006 Leptin Receptor Deficiency 38 1.733
22
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 23 1.725
23
P DBT005 Diabetes Insipidus 54 1.703
24
c MCR112 Microvascular Complications of Diabetes 2 33 1.651
25
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 1.639
26
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 47 1.608
27
DBT090 Diabetes and Deafness, Maternally Inherited 40 1.595
28
LPT014 Leptin Deficiency or Dysfunction 37 1.536
29
OBS015 Obesity, Hyperphagia, and Developmental Delay 24 1.506
30
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 1.474
31
DBT008 Diabetic Angiopathy 47 1.450
32
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 34 1.446
33
BDY005 Body Mass Index Quantitative Trait Locus 9 27 1.440
34
BDY006 Body Mass Index Quantitative Trait Locus 8 23 1.440
35
BDY012 Body Mass Index Quantitative Trait Locus 7 23 1.440
36
BDY015 Body Mass Index Quantitative Trait Locus 12 25 1.438
37
BDY010 Body Mass Index Quantitative Trait Locus 4 25 1.438
38
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 25 1.429
39
MHM001 Mehmo Syndrome 28 1.420
40
OBS037 Obesity-Hypoventilation Syndrome 46 1.384
41
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 27 1.380
42
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 44 1.344
43
BDY019 Body Mass Index Quantitative Trait Locus 18 27 1.336
44
BDY017 Body Mass Index Quantitative Trait Locus 14 25 1.334
45
BDY020 Body Mass Index Quantitative Trait Locus 19 25 1.334
46
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 43 1.328
47
CHN016 Cohen Syndrome 47 1.324
48
MRB006 Morbid Obesity and Spermatogenic Failure 20 1.323
49
DBT004 Diabetic Polyneuropathy 51 1.295
50
c LPD015 Lipodystrophy, Familial Partial, Type 2 59 1.289
51
c MTR023 Maturity-Onset Diabetes of the Young, Type 6 26 1.276
52
c MTR024 Maturity-Onset Diabetes of the Young, Type 7 18 1.273
53
c MTR026 Maturity-Onset Diabetes of the Young, Type 9 18 1.273
54
MMS001 Momo Syndrome 30 1.243
55
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 41 1.243
56
RTN173 Retinal Dystrophy and Obesity 20 1.238
57
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 14 1.230
58
DBT002 Diabetic Autonomic Neuropathy 43 1.207
59
P WLF004 Wolfram Syndrome 61 1.199
60
CNG376 Congenital Leptin Deficiency 20 1.193
61
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 22 1.168
62
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 22 1.164
63
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 19 1.162
64
c DBT094 Diabetes Mellitus, Insulin-Dependent, 10 19 1.162
65
P NNT009 Neonatal Diabetes Mellitus 48 1.152
66
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 1.145
67
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 21 1.117
68
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 28 1.108
69
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 25 1.107
70
WDH003 Woodhouse-Sakati Syndrome 34 1.105
71
PRP098 Proprotein Convertase 1/3 Deficiency 29 1.103
72
BDY011 Body Mass Index Quantitative Trait Locus 10 24 1.083
73
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 1.051
74
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 29 1.049
75
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 29 1.042
76
c DBT098 Diabetes Mellitus, Transient Neonatal, 2 15 1.042
77
c DBT032 Diabetes Mellitus, Insulin-Dependent, 22 15 1.040
78
DBT007 Diabetic Cataract 32 1.035
79
BRT037 Brittle Diabetes 24 1.032
80
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 25 1.016
81
DBT062 Diabetic Foot Ulcers 59 0.995
82
DBT006 Diabetic Macular Edema 48 0.989
83
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 56 0.989
84
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 32 0.984
85
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 16 0.984
86
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 26 0.981
87
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 19 0.980
88
c MTR074 Maturity-Onset Diabetes of the Young, Type 14 18 0.978
89
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 44 0.975
90
PNC104 Pancreatic and Cerebellar Agenesis 26 0.974
91
INS010 Insulin-Resistant Acanthosis Nigricans, Type a 20 0.973
92
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 16 0.971
93
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 14 0.971
94
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.954
95
CHP002 Chops Syndrome 31 0.935
96
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 27 0.905
97
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 19 0.905
98
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 15 0.903
99
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 14 0.903
100
c DBT079 Diabetes Mellitus, Insulin-Dependent, 21 13 0.901
101
DBT060 Diabetes Mellitus, Insulin-Dependent, X-Linked 8 0.899
102
HYD021 Hydrocephalus Obesity Hypogonadism 15 0.884
103
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 16 0.882
104
CLB031 Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome 16 0.877
105
GLC008 Glucose Metabolism Disease 52 0.874
106
BCK003 Background Diabetic Retinopathy 36 0.871
107
MTC025 Mitochondrial Myopathy with Diabetes 20 0.829
108
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 19 0.825
109
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 13 0.823
110
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 13 0.823
111
OBS050 Obesity Due to Congenital Leptin Deficiency 23 0.810
112
c TYP038 Type 1 Diabetes Mellitus 15 22 0.803
113
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 10 0.793
114
FBR065 Fibrocalculous Pancreatopathy 18 0.780
115
MNG006 Monogenic Diabetes 37 0.775
116
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 47 0.770
117
SVR002 Severe Nonproliferative Diabetic Retinopathy 34 0.770
118
RHH001 Rohhad 27 0.754
119
c TYP031 Type 1 Diabetes Mellitus 5 23 0.753
120
c TYP035 Type 1 Diabetes Mellitus 11 26 0.752
121
c TYP037 Type 1 Diabetes Mellitus 13 26 0.750
122
c TYP028 Type 1 Diabetes Mellitus 2 23 0.750
123
c TYP033 Type 1 Diabetes Mellitus 7 25 0.749
124
c DBT013 Diabetes Mellitus, 6q24-Related Transient Neonatal 12 0.749
125
c TYP036 Type 1 Diabetes Mellitus 12 21 0.748
126
ARD001 Aredyld 25 0.746
127
c TYP032 Type 1 Diabetes Mellitus 6 24 0.746
128
c TYP027 Type 1 Diabetes Mellitus 10 20 0.746
129
c TYP039 Type 1 Diabetes Mellitus 17 19 0.745
130
c TYP029 Type 1 Diabetes Mellitus 3 16 0.743
131
c TYP030 Type 1 Diabetes Mellitus 4 14 0.743
132
c TYP040 Type 1 Diabetes Mellitus 18 18 0.742
133
c TYP034 Type 1 Diabetes Mellitus 8 13 0.742
134
MSC133 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 18 0.741
135
c DBT050 Diabetes Mellitus, Insulin-Dependent, 15 15 0.741
136
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 15 0.740
137
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 31 0.738
138
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 13 0.737
139
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 13 0.737
140
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 13 0.737
141
c DBT052 Diabetes Mellitus, Insulin-Dependent, 18 13 0.737
142
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 13 0.737
143
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 13 0.737
144
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 13 0.737
145
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 13 0.737
146
LYM029 Lymphedema-Distichiasis Syndrome 41 0.735
147
c DBT097 Diabetes Mellitus, Noninsulin-Dependent, 4 11 0.735
148
c DBT095 Diabetes Mellitus, Noninsulin-Dependent, 3 10 0.735
149
DVL020 Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features 14 0.723
150
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 18 0.720
151
SHR107 Short Stature-Obesity Syndrome 12 0.720
152
PRL046 Prolactin Deficiency with Obesity and Enlarged Testes 10 0.720
153
AYZ001 Ayazi Syndrome 9 0.720
154
XLN122 X-Linked Intellectual Disability - Short Stature - Obesity 4 0.720
155
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 20 0.717
156
MN1002 Man1b1-Cdg 11 0.710
157
DBT018 Diabetic Mastopathy 19 0.692
158
c WLF013 Wolfram Syndrome 1 51 0.659
159
GST058 Gestational Diabetes Insipidus 12 0.658
160
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 40 0.656
161
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 47 0.653
162
FNC009 Fanconi-Bickel Syndrome 53 0.648
163
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 17 0.648
164
TRP008 Tropical Calcific Pancreatitis 44 0.647
165
DBT089 Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification 18 0.643
166
BNG086 Bangstad Syndrome 21 0.641
167
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 29 0.640
168
c HMC039 Hemochromatosis, Type 1 70 0.621
169
OVR063 Overnutrition 53 0.614
170
c CNG012 Congenital Generalized Lipodystrophy 50 0.613
171
P ACQ022 Acquired Generalized Lipodystrophy 44 0.602
172
HYP364 Hyperostosis Frontalis Interna 28 0.569
173
DBT081 Diabetic Encephalopathy 27 0.568
174
P NRP001 Neuropathy 63 0.543
175
RNL024 Renal Glucosuria 49 0.533
176
DPS001 Dipsogenic Diabetes Insipidus 17 0.533
177
c HRD156 Hereditary Central Diabetes Insipidus 17 0.532
178
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 18 0.531
179
c ACQ034 Acquired Central Diabetes Insipidus 15 0.531
180
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 32 0.528
181
MTC096 Mitchell-Riley Syndrome 23 0.528
182
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 19 0.528
183
LPT011 Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy 17 0.528
184
RNL050 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna 5 0.528
185
PRX085 Preaxial Hallucal Polydactyly 23 0.526
186
PHT013 Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction 18 0.526
187
OBS060 Obesity Due to Sim1 Deficiency 12 0.524
188
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 12 0.524
189
FGN001 Feigenbaum Bergeron Richardson Syndrome 8 0.523
190
MDF004 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 14 0.522
191
DBT003 Diabetic Peripheral Angiopathy 9 0.521
192
ACH016 Achard Thiers Syndrome 7 0.521
193
YRF001 Yorifuji Okuno Syndrome 7 0.521
194
TYP041 Type I 56 0.520
195
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 18 0.516
196
XLN211 X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome 16 0.516
197
INT298 Intellectual Disability-Obesity-Brain Malformations-Facial Dysmorphism Syndrome 16 0.516
198
XLN208 X-Linked Intellectual Disability-Precocious Puberty-Obesity Syndrome 9 0.516
199
OBS068 Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome 8 0.516
200
CHR506 Choroideremia, Deafness, and Mental Retardation 24 0.513
201
CLR029 Clark-Baraitser Syndrome 23 0.509
202
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 22 0.509
203
c BMN004 Biemond Syndrome Ii 19 0.505
204
DPL003 Diploid-Triploid Mosaicism 15 0.505
205
AGN016 Aging 64 0.502
206
P KDN018 Kidney Disease 68 0.499
207
CMR005 Camera-Marugo-Cohen Syndrome 12 0.499
208
GLC036 Glucagonoma 51 0.467
209
HYP066 Hyperglycemia 63 0.442
210
HYP056 Hypoglycemia 62 0.426
211
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 21 0.418
212
END072 Endotheliitis 45 0.403
213
GLC003 Glucose Intolerance 56 0.396
214
HYP060 Hyperinsulinism 56 0.389
215
P SHR029 Short Syndrome 51 0.379
216
INS034 Insulinomatosis and Diabetes Mellitus 21 0.379
217
INT288 Intellectual Disability-Dysmorphism-Hypogonadism-Diabetes Mellitus Syndrome 8 0.379
218
P PNC044 Pancreatitis 64 0.376
219
WLF014 Wolfram Syndrome, Mitochondrial Form 15 0.375
220
LPT004 Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 3 0.375
221
FTT001 Fatty Liver Disease 60 0.374
222
MNT030 Mental Retardation Syndrome, Belgian Type 15 0.373
223
INT222 Intermediate Dend Syndrome 10 0.373
224
CRD024 Cardiomyopathy Diabetes Deafness 3 0.373
225
SHR028 Short Stature, Cranial Hyperostosis, Hepatomegaly and Diabetes 2 0.373
226
ECT013 Ectodermal Dysplasia Arthrogryposis Diabetes Mellitus 2 0.373
227
PRM291 Premature Aging Syndrome, Okamoto Type 14 0.371
228
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 9 0.371
229
c DBT096 Diabetes Mellitus, Congenital Autoimmune 8 0.371
230
PRM187 Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome 7 0.371
231
XLN187 X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome 6 0.371
232
HYP790 Hypopituitarism, Congenital, with Central Diabetes Insipidus 3 0.371
233
DBT016 Diabetes Persistent Mullerian Ducts 2 0.371
234
P HPT021 Hepatitis 76 0.369
235
ATM095 Autoimmune Disease 64 0.369
236
IMM136 Immune System Disease 56 0.363
237
P LVR013 Liver Disease 75 0.360
238
P HRT032 Heart Disease 74 0.357
239
DPR016 Depression 72 0.332
240
ART140 Arteries, Anomalies of 65 0.330
241
P PLY011 Polycystic Ovary Syndrome 63 0.327
242
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.323
243
P CRN018 Coronary Artery Anomaly 68 0.322
244
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.311
245
P SLP006 Sleep Apnea 66 0.303
246
c CRN300 Coronary Heart Disease 1 64 0.301
247
VSC007 Vascular Disease 68 0.289
248
P MYC007 Myocardial Infarction 79 0.284
249
c CHR089 Chronic Kidney Failure 72 0.278
250
ISC004 Ischemia 65 0.277
251
PRP019 Peripheral Nervous System Disease 60 0.277
252
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.275
253
ATN004 Autonomic Neuropathy 46 0.263
254
ANX010 Anxiety 72 0.259
255
RTN018 Retinal Disease 56 0.258
256
URN009 Urinary System Disease 55 0.258
257
APN008 Apnea, Obstructive Sleep 67 0.253
258
P PRD008 Periodontitis 66 0.253
259
PLC008 Placenta Disease 61 0.253
260
P THY032 Thyroiditis 55 0.251
261
ETN001 Eating Disorder 61 0.251
262
RTN023 Retinitis 50 0.250
263
PRD004 Prediabetes Syndrome 45 0.250
264
ISC006 Ischemic Heart Disease 72 0.249
265
P PLY019 Polyneuropathy 57 0.244
266
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.242
267
SPS003 Spastic Diplegia 54 0.242
268
AST005 Asthma 82 0.238
269
MNT002 Mental Depression 57 0.228
270
P BRS047 Breast Cancer 100 0.219
271
P ART021 Arteriosclerosis 60 0.219
272
LPD008 Lipid Metabolism Disorder 58 0.215
273
SLP005 Sleep Disorder 59 0.212
274
INS024 Insulin-Like Growth Factor I 82 0.210
275
NRT004 Neuritis 57 0.202
276
P INF032 Infertility 59 0.198
277
c TRC078 Trichohepatoenteric Syndrome 2 34 0.195
278
NRM005 Neuromuscular Disease 60 0.194
279
P VSC018 Visceral Steatosis 37 0.192
280
P HYP086 Hypothyroidism 64 0.189
281
PRD007 Periodontal Disease 64 0.189
282
CNG034 Congestive Heart Failure 72 0.188
283
P ART022 Arthritis 76 0.188
284
P RTN016 Retinal Degeneration 54 0.188
285
ACN002 Acanthosis Nigricans 60 0.186
286
HYP080 Hypogonadism 51 0.184
287
THR024 Thrombosis 61 0.182
288
FTL021 Fetal Macrosomia 46 0.180
289
P CTR002 Cataract 60 0.179
290
PRS047 Prostatitis 60 0.179
291
P PRD006 Prader-Willi Syndrome 61 0.179
292
c MCL042 Macular Degeneration, Age-Related, 1 84 0.178
293
GST037 Gastroparesis 56 0.176
294
CRB009 Cerebritis 41 0.174
295
OST012 Osteoarthritis 82 0.173
296
P NRV007 Nervous System Disease 73 0.173
297
GST050 Gastrointestinal System Disease 64 0.171
298
NNL002 Nonalcoholic Steatohepatitis 50 0.170
299
HYP266 Hypoxia 61 0.160
300
c PRC016 Pre-Eclampsia 59 0.159
301
NRN002 Neuronitis 41 0.158
302
PRP027 Peripheral Vascular Disease 70 0.157
303
P OST002 Osteoporosis 76 0.157
304
ATN005 Autonomic Dysfunction 50 0.156
305
HYP043 Hyperandrogenism 50 0.155
306
P PRS040 Prostate Cancer 90 0.154
307
P SCH015 Schizophrenia 69 0.153
308
GST092 Gastroesophageal Reflux 64 0.150
309
c HYP595 Hypertension, Essential 76 0.149
310
MCL006 Macular Retinal Edema 51 0.143
311
CRN036 Craniopharyngioma 64 0.142
312
P ALZ034 Alzheimer Disease 87 0.141
313
END030 End Stage Renal Failure 56 0.140
314
IMP005 Impotence 55 0.139
315
P CLR023 Colorectal Cancer 97 0.138
316
BRN106 Burns 56 0.137
317
ANG054 Angina Pectoris 66 0.135
318
c ACT075 Acute Myocardial Infarction 58 0.135
319
GND003 Gonadal Disease 46 0.135
320
c HPT001 Hepatitis C 71 0.134
321
P INF038 Influenza 76 0.134
322
c PRC031 Preeclampsia/eclampsia 1 39 0.133
323
P OVR049 Ovarian Disease 59 0.133
324
ANR040 Aneurysm 60 0.133
325
P TRC086 Trichohepatoenteric Syndrome 1 54 0.132
326
P ADN016 Adenocarcinoma 70 0.131
327
LNG099 Lung Disease 67 0.131
328
RSP006 Respiratory System Disease 63 0.130
329
P ART023 Arthropathy 67 0.128
330
P MYP006 Myopia 56 0.128
331
P LKM002 Leukemia 72 0.127
332
P PNC035 Pancreatic Cancer 79 0.126
333
P RSP003 Respiratory Failure 70 0.126
334
P ESP024 Esophagitis 63 0.125
335
P HYP014 Hyperuricemia 55 0.125
336
PRP080 Peripheral Artery Disease 53 0.124
337
DMN002 Dementia 68 0.123
338
c PLY105 Polycystic Ovary Syndrome 1 30 0.123
339
P ENC018 Encephalopathy 62 0.123
340
ANR007 Anorexia Nervosa 62 0.123
341
GNG011 Gingival Disease 49 0.123
342
MTH009 Mouth Disease 63 0.123
343
P ECL001 Eclampsia 57 0.123
344
P PSR002 Psoriasis 65 0.123
345
P RHM011 Rheumatoid Arthritis 80 0.121
346
DNT012 Dental Caries 51 0.120
347
P DRR001 Diarrhea 56 0.120
348
BND020 Bone Disease 62 0.120
349
END057 Endometrial Cancer 65 0.119
350
LMB062 Limb Ischemia 51 0.119
351
MDD011 Mood Disorder 63 0.118
352
BNF002 Bone Fracture 55 0.118
353
THY030 Thyroid Gland Disease 51 0.118
354
P PNM007 Pneumonia 69 0.116
355
c ACT027 Acute Pancreatitis 60 0.115
356
GNG013 Gingivitis 63 0.113
357
INS001 Insulinoma 65 0.113
358
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.112
359
CNN003 Conn's Syndrome 71 0.111
360
CRB039 Cerebrovascular Disease 67 0.110
361
P OVR046 Ovarian Cyst 50 0.110
362
SVR004 Severe Combined Immunodeficiency 69 0.109
363
P CLC063 Celiac Disease 1 71 0.109
364
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.109
365
P EXN002 Exanthem 61 0.108
366
CMB081 Combined Immunodeficiency, X-Linked 64 0.108
367
LVR012 Liver Cirrhosis 68 0.107
368
DDN006 Duodenitis 48 0.107
369
P ANR048 Aniridia 1 65 0.106
370
BLD137 Blood Group--Ahonen 17 0.106
371
BLM002 Bulimia Nervosa 58 0.105
372
P AMY004 Amyloidosis 68 0.104
373
c MTR002 Mitral Valve Insufficiency 46 0.104
374
P HYP083 Hypopituitarism 58 0.104
375
P ATR011 Atrial Fibrillation 68 0.104
376
PNM001 Pneumocystosis 55 0.104
377
JNT002 Joint Disorders 59 0.103
378
PRT036 Peritonitis 66 0.103
379
HYP064 Hypogonadotropism 40 0.103
380
RST023 Resting Heart Rate, Variation in 42 0.102
381
HPT082 Hepatic Adenomas, Familial 53 0.102
382
PTT009 Pituitary Gland Disease 56 0.102
383
HYP730 Hypogonadotropic Hypogonadism 56 0.101
384
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.100
385
P LYM118 Lymphoma 70 0.100
386
P EPL164 Epilepsy 69 0.100
387
SKN016 Skin Disease 66 0.100
388
MTB004 Metabolic Acidosis 48 0.099
389
P BRD002 Bardet-Biedl Syndrome 62 0.099
390
STM006 Stomach Disease 52 0.099
391
CYS001 Cystic Fibrosis 84 0.099
392
PSY004 Psychotic Disorder 71 0.098
393
c MYT020 Myotonic Dystrophy 2 56 0.098
394
P BPL003 Bipolar Disorder 59 0.098
395
c BRD013 Bardet-Biedl Syndrome 12 44 0.098
396
P MJR001 Major Depressive Disorder 65 0.098
397
ADN018 Adenoma 63 0.097
398
P HPT023 Hepatocellular Carcinoma 94 0.097
399
IRN002 Iron Metabolism Disease 55 0.096
400
P GLL020 Gallbladder Disease 64 0.096
401
GST053 Gastric Cancer 77 0.096
402
ALP046 Alport Syndrome, X-Linked 75 0.096
403
NRL016 Neural Tube Defects 78 0.095
404
P CLL015 Collagen Disease 52 0.095
405
GNR004 Generalized Anxiety Disorder 53 0.094
406
P TRM003 Tremor 54 0.094
407
GT001 Gout 57 0.094
408
c BRD014 Bardet-Biedl Syndrome 2 58 0.093
409
c BRD012 Bardet-Biedl Syndrome 11 45 0.093
410
c BRD011 Bardet-Biedl Syndrome 10 41 0.093
411
INT007 Intermediate Coronary Syndrome 52 0.093
412
c CHR579 Chiari Malformation Type Ii 45 0.093
413
RHM027 Rheumatic Disease 62 0.093
414
HDC001 Headache 59 0.092
415
ALR002 Al-Raqad Syndrome 31 0.092
416
c ART101 Aortic Valve Disease 2 73 0.092
417
GRW007 Growth Hormone Deficiency 51 0.092
418
ANV001 Anovulation 48 0.092
419
ENT004 Enthesopathy 46 0.091
420
ACT088 Acute Insulin Response 43 0.091
421
SKN027 Skin Conditions 48 0.091
422
P HYP069 Hyperparathyroidism 58 0.090
423
PNG002 Pain Agnosia 42 0.090
424
c PRD040 Periodontitis, Chronic 49 0.089
425
ANX004 Anoxia 49 0.089
426
P MLT020 Multiple Sclerosis 78 0.089
427
P LCT001 Lactic Acidosis 50 0.088
428
HYP085 Hypothalamic Disease 48 0.088
429
DWN001 Down Syndrome 69 0.087
430
BRN038 Bronchial Disease 56 0.087
431
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.087
432
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.086
433
SCH012 Schizoaffective Disorder 54 0.086
434
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.086
435
P DYS021 Dysautonomia 43 0.084
436
c THR092 Thrombophilia Due to Thrombin Defect 67 0.084
437
NPH009 Nephrolithiasis 55 0.084
438
CRD119 Cardiac Arrest 62 0.084
439
P CHR345 Chronic Pain 51 0.084
440
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.084
441
BRC012 Brucellosis 70 0.083
442
c HPT073 Hepatitis C Virus 72 0.083
443
ALS001 Alstrom Syndrome 54 0.083
444
URM002 Uremia 52 0.083
445
P HYP265 Hypotonia 40 0.082
446
IRN001 Iron Deficiency Anemia 55 0.082
447
PNC034 Pancreas Disease 57 0.082
448
ULC005 Ulcer of Lower Limbs 22 0.082
449
NCR002 Necrobiosis Lipoidica 38 0.082
450
ACQ007 Acquired Immunodeficiency Syndrome 63 0.081
451
SPN186 Spinal Cord Injury 68 0.081
452
P LYM026 Lymphoblastic Leukemia 64 0.081
453
P MYL005 Myelofibrosis 70 0.081
454
P PRC019 Precocious Puberty 52 0.081
455
c HPT003 Hepatitis a 61 0.080
456
PRS063 Paresthesia 37 0.079
457
P INT068 Intestinal Disease 64 0.079
458
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.079
459
THY028 Thyroid Cancer 66 0.079
460
P MSC003 Muscular Atrophy 54 0.078
461
P THR014 Thrombocytopenia 64 0.077
462
VRL011 Viral Infectious Disease 63 0.077
463
ATN002 Autonomic Nervous System Disease 51 0.077
464
INT075 Intracranial Hypertension 52 0.077
465
ACR007 Acromegaly 69 0.076
466
P CRV039 Cervicitis 49 0.076
467
P GLM007 Glomerulonephritis 61 0.076
468
BCK006 Back Pain 44 0.076
469
P TRN020 Turner Syndrome 68 0.076
470
SXL003 Sexual Disorder 44 0.076
471
P LYM025 Lymphedema 63 0.076
472
VTM002 Vitamin B12 Deficiency 47 0.075
473
JJN008 Jejunoileitis 41 0.075
474
SYS003 Systolic Heart Failure 46 0.075
475
P OVR042 Ovarian Cancer 81 0.074
476
P LNG032 Lung Cancer 98 0.074
477
c LKM062 Leukemia, Acute Lymphoblastic 69 0.074
478
P PSD015 Pseudohypoparathyroidism 50 0.074
479
c SYS001 Systemic Lupus Erythematosus 86 0.073
480
P MYP004 Myopathy 68 0.073
481
STR067 Stroke, Ischemic 82 0.072
482
BRS051 Breast Disease 66 0.072
483
PLM033 Pulmonary Embolism 62 0.072
484
CHL004 Cholelithiasis 50 0.072
485
CNS004 Constipation 56 0.072
486
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.072
487
PSR001 Psoriatic Arthritis 65 0.071
488
AMN001 Amenorrhea 55 0.071
489
P NRC002 Narcolepsy 63 0.070
490
FBR047 Fibromyalgia 57 0.070
491
LRN002 Laron Syndrome 62 0.070
492
ALX002 Alexithymia 42 0.070
493
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.070
494
CHR008 Choroiditis 46 0.070
495
P LPS004 Lupus Erythematosus 68 0.070
496
P HYP076 Hyperthyroidism 56 0.070
497
P RTN008 Retinitis Pigmentosa 81 0.070
498
c BLD140 Blood Group, I System 23 0.069
499
VGN023 Vaginitis 58 0.069
500
P CND004 Candidiasis 60 0.069
501
P CMR001 Camurati-Engelmann Disease 61 0.068
502
LYM027 Lymphopenia 55 0.068
503
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.068
504
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.068
505
CLT003 Colitis 62 0.068
506
DFC004 Deficiency Anemia 61 0.068
507
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 42 0.068
508
P HST010 Histiocytosis 59 0.068
509
P LPM005 Lipomatosis 50 0.067
510
INT303 Intracranial Hypertension, Idiopathic 50 0.067
511
MNN017 Mononeuropathy 43 0.067
512
P FCL005 Focal Segmental Glomerulosclerosis 59 0.067
513
P ATS364 Autism 70 0.067
514
c ACT071 Acute Kidney Failure 54 0.067
515
P KDN017 Kidney Cancer 58 0.067
516
P ADL010 Adult Respiratory Distress Syndrome 66 0.066
517
ART016 Aortic Aneurysm 69 0.066
518
EPD070 Epidermoid Cysts 47 0.066
519
P MYL006 Myeloid Leukemia 68 0.066
520
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.065
521
c CRP023 Carpenter Syndrome 1 54 0.064
522
PST021 Postpartum Depression 53 0.064
523
DWR001 Dwarfism 45 0.064
524
PST055 Postural Hypotension 40 0.064
525
SCL022 Scleredema 28 0.064
526
CRN030 Coronary Stenosis 51 0.064
527
c ACT210 Acute Respiratory Distress Syndrome 61 0.064
528
ALC007 Alcohol Dependence 65 0.064
529
EXC002 Exocrine Pancreatic Insufficiency 43 0.064
530
ERY029 Erythermalgia, Primary 54 0.063
531
P VNS003 Venous Insufficiency 54 0.063
532
BRN071 Brain Injury 53 0.063
533
LNG108 Langerhans Cell Histiocytosis 63 0.063
534
PST053 Postherpetic Neuralgia 44 0.063
535
MLN008 Melanoma 62 0.063
536
c FML012 Familial Partial Lipodystrophy 52 0.063
537
ART008 Arteriosclerosis Obliterans 42 0.062
538
P MCR010 Microcephaly 57 0.062
539
DRM006 Dermatitis 66 0.062
540
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.061
541
c HPT016 Hepatitis B 67 0.061
542
P AST055 Asthma-Related Traits 1 30 0.061
543
P PRT078 Partial Lipodystrophy 46 0.061
544
CRP001 Carpal Tunnel Syndrome 66 0.061
545
P NPH012 Nephrotic Syndrome 59 0.061
546
P PLM037 Pulmonary Hypertension 75 0.061
547
APP008 Appendicitis 64 0.060
548
INT002 Intermittent Claudication 61 0.060
549
c VRL010 Viral Hepatitis 59 0.060
550
CLL003 Cellulitis 53 0.060
551
NWB001 Newborn Respiratory Distress Syndrome 52 0.060
552
MTC005 Mitochondrial Metabolism Disease 44 0.060
553
RSP007 Respiratory Distress Syndrome, Infant 34 0.060
554
P SCL057 Scoliosis, Isolated 1 40 0.060
555
P PLY006 Polydactyly 57 0.060
556
PSD088 Pseudobulbar Affect 37 0.060
557
BLD163 Blood Group, Dombrock System 22 0.059
558
P INF037 Inflammatory Bowel Disease 53 0.059
559
DMP001 Dumping Syndrome 44 0.059
560
P THR015 Thrombophilia 57 0.059
561
c CNT075 Central Precocious Puberty 51 0.059
562
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.059
563
WLL001 Williams-Beuren Syndrome 63 0.059
564
P HYP614 Hyperlipidemia, Familial Combined 56 0.059
565
CRT016 Carotid Artery Disease 57 0.059
566
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 41 0.058
567
c PTT057 Pituitary Adenoma 4, Acth-Secreting 45 0.058
568
PHR003 Pharyngitis 59 0.058
569
DYS073 Dysphagia 46 0.058
570
MNN028 Mononeuropathy of the Median Nerve, Mild 37 0.058
571
END038 Endocrine Pancreas Disease 36 0.058
572
WRN001 Werner Syndrome 69 0.058
573
LRN003 Learning Disability 50 0.057
574
CLC006 Calcinosis 51 0.057
575
HLC007 Helicobacter Pylori Infection 63 0.057
576
DRG003 Drug Dependence 51 0.057
577
P ACQ009 Acquired Metabolic Disease 32 0.057
578
P UTR058 Uterine Anomalies 59 0.057
579
ACR006 Aceruloplasminemia 73 0.056
580
P RNL007 Renal Tubular Acidosis 52 0.056
581
c BRD010 Bardet-Biedl Syndrome 1 54 0.056
582
SCN001 Secondary Hyperparathyroidism of Renal Origin 50 0.056
583
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.056
584
ELP001 Elephantiasis 38 0.056
585
P HYP061 Hypertrophic Cardiomyopathy 64 0.056
586
IRR002 Irritable Bowel Syndrome 62 0.056
587
HYD002 Hydronephrosis 48 0.056
588
CRN024 Corneal Disease 47 0.056
589
P PNC045 Pancreatic Agenesis 40 0.055
590
c LKM061 Leukemia, Acute Myeloid 80 0.055
591
P HYD006 Hydrocephalus 69 0.055
592
CLR108 Colorectal Adenoma 60 0.055
593
P ALP008 Alopecia 58 0.055
594
MDS022 Mediastinitis 40 0.055
595
P GST044 Gastritis 60 0.055
596
P MGL001 Megaloblastic Anemia 51 0.055
597
RCK004 Rickets 62 0.055
598
P DLT002 Dilated Cardiomyopathy 76 0.055
599
c PRM005 Primary Hyperparathyroidism 59 0.055
600
SLD003 Sialadenitis 49 0.055
601
SKN023 Skin Tag 42 0.055
602
SNS003 Sensory Peripheral Neuropathy 53 0.054
603
URN022 Urinary Tract Infections, Recurrent 29 0.054
604
P CRD132 Cardiac Conduction Defect 59 0.054
605
TRM010 Traumatic Brain Injury 55 0.054
606
SLP010 Slipped Capital Femoral Epiphysis 37 0.054
607
GSG001 Gas Gangrene 51 0.054
608
FSC004 Fasciitis 47 0.054
609
PSD014 Pseudopseudohypoparathyroidism 55 0.053
610
CRH001 Crohn's Disease 78 0.053
611
HYP020 Hyperprolactinemia 63 0.053
612
CRD223 Cardiac Arrhythmia 54 0.053
613
STT004 Steatorrhea 41 0.053
614
CLC001 Calciphylaxis 52 0.053
615
FXF002 Fox-Fordyce Disease 40 0.053
616
c MYT021 Myotonic Dystrophy 1 68 0.053
617
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.053
618
FCL044 Fecal Incontinence 38 0.052
619
CRT013 Carotid Stenosis 52 0.052
620
HMS001 Hemosiderosis 51 0.052
621
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 54 0.052
622
DST006 Diastolic Heart Failure 46 0.052
623
P MSC005 Muscular Dystrophy 66 0.051
624
P SZR006 Seizure Disorder 56 0.051
625
c SVR005 Severe Pre-Eclampsia 53 0.051
626
GYN001 Gynecomastia 46 0.051
627
P CHR084 Chromosomal Disease 40 0.051
628
ESP021 Esophageal Cancer 77 0.051
629
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.051
630
P CHL066 Cholangitis 52 0.050
631
P HLP001 Holoprosencephaly 66 0.050
632
NRR001 Neuroretinitis 46 0.050
633
c CNT035 Central Nervous System Disease 63 0.050
634
CLN019 Colonic Disease 54 0.050
635
P MSC033 Muscle Disorders 52 0.050
636
c LBR014 Leber Congenital Amaurosis 4 49 0.050
637
MSC004 Muscle Tissue Disease 39 0.050
638
GST007 Gastric Dilatation 33 0.050
639
P INT070 Intestinal Obstruction 56 0.050
640
MLN007 Male Infertility 53 0.050
641
RST001 Restless Legs Syndrome 52 0.050
642
P BLD134 Bladder Cancer 69 0.049
643
P ENC004 Encephalitis 65 0.049
644
VSC002 Vascular Dementia 58 0.049
645
P ALP009 Alopecia Areata 63 0.049
646
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 53 0.049
647
P RHN004 Rhinitis 61 0.048
648
PRP016 Paraplegia 53 0.048
649
FND002 Fundus Dystrophy 49 0.048
650
HRT012 Heart Valve Disease 44 0.048
651
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.048
652
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 53 0.048
653
P PHC003 Pheochromocytoma 73 0.048
654
P OPN001 Open-Angle Glaucoma 51 0.048
655
P SBS003 Substance Abuse 57 0.048
656
HPR003 Heparin-Induced Thrombocytopenia 48 0.048
657
HYP784 Hypogonadism, Male 41 0.048
658
EPD046 Epididymitis 36 0.048
659
ANG020 Angiosarcoma 56 0.048
660
HRN026 Hernia, Hiatus 43 0.048
661
DYS011 Dyskinesia of Esophagus 39 0.048
662
P HMP007 Hemophilia 60 0.048
663
BRB001 Beriberi 41 0.048
664
OST097 Osteoporotic Fracture 41 0.048
665
P PLY014 Polycystic Kidney Disease 60 0.047
666
HYP068 Hyperostosis 53 0.047
667
SPN051 Spondylitis 55 0.047
668
DYS014 Dyspepsia 54 0.047
669
NPH010 Nephrosclerosis 47 0.047
670
SNL007 Senile Cataract 40 0.047
671
HYP110 Hyperproinsulinemia 39 0.047
672
CRT049 Critical Limb Ischemia 57 0.046
673
BRN024 Bronchitis 66 0.046
674
SYN007 Synovitis 60 0.046
675
P PLY018 Polycythemia 58 0.046
676
P ACT105 Acute Mountain Sickness 57 0.046
677
P BLD051 Blood Coagulation Disease 50 0.046
678
INT051 Intussusception 49 0.046
679
IDP033 Idiopathic Edema 42 0.046
680
GST045 Gastroenteritis 64 0.046
681
P SNS014 Sinusitis 62 0.046
682
c CNG006 Congenital Hypothyroidism 60 0.046
683
P PRT013 Portal Hypertension 59 0.046
684
P BCK002 Beckwith-Wiedemann Syndrome 57 0.046
685
PLM010 Pulmonary Edema 56 0.046
686
TTH006 Tooth Disease 53 0.046
687
PRP030 Purpura 61 0.046
688
DCB001 Decubitus Ulcer 45 0.046
689
BLD165 Blood Group, Colton System 23 0.046
690
P GLY013 Glycogen Storage Disease 61 0.046
691
CYT008 Cytomegalovirus Infection 56 0.046
692
SHH001 Sheehan Syndrome 50 0.046
693
P OPT070 Optic Nerve Hypoplasia, Bilateral 43 0.046
694
ADP007 Adie Pupil 41 0.046
695
GLC022 Glucose/galactose Malabsorption 41 0.046
696
LPD012 Lipoid Congenital Adrenal Hyperplasia 69 0.046
697
c ATS007 Autism Spectrum Disorder 61 0.046
698
PRT018 Portal Vein Thrombosis 50 0.046
699
CRB037 Cerebral Palsy 71 0.045
700
OTT002 Otitis Media 66 0.045
701
ADR013 Adrenal Gland Hyperfunction 54 0.045
702
GTR002 Goiter 52 0.045
703
WRN003 Wernicke Encephalopathy 45 0.045
704
CNN005 Connective Tissue Disease 64 0.045
705
CYS039 Cystic Kidney Disease 51 0.045
706
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.045
707
c SML038 Small Cell Cancer of the Lung 68 0.045
708
VSC011 Vasculitis 65 0.045
709
CHL123 Chlamydia 64 0.045
710
BLD044 Bladder Disease 55 0.045
711
HYP077 Hypertrichosis 50 0.045
712
TBC004 Tobacco Addiction 60 0.044
713
CHR005 Chorioamnionitis 51 0.044
714
ULC004 Ulcerative Colitis 72 0.044
715
P ALC004 Alcohol Abuse 63 0.044
716
PRT038 Protein-Energy Malnutrition 51 0.044
717
EMP001 Empty Sella Syndrome 42 0.044
718
SPS057 Spasticity 41 0.044
719
IGG001 Iga Glomerulonephritis 55 0.044
720
ART004 Aortic Atherosclerosis 47 0.044
721
P FNG006 Feingold Syndrome 1 45 0.044
722
MYL069 Myeloma, Multiple 83 0.043
723
P MMP001 Mumps 61 0.043
724
CHL068 Cholestasis 60 0.043
725
MCS002 Mucositis 60 0.043
726
P PTS002 Ptosis 53 0.043
727
IMM001 Immune-Complex Glomerulonephritis 38 0.043
728
BRR014 Barrett Esophagus 63 0.043
729
ALL006 Allergic Asthma 59 0.043
730
PST028 Post-Traumatic Stress Disorder 58 0.043
731
PRS042 Prostate Disease 44 0.043
732
LRN001 Laurence-Moon Syndrome 44 0.043
733
TRC026 Tracheal Disease 35 0.043
734
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.043
735
PPL021 Papilledema 49 0.043
736
TND004 Tendinopathy 46 0.043
737
RCT017 Rectal Disease 39 0.043
738
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.043
739
P HYP607 Hypercholesterolemia, Familial 79 0.043
740
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.043
741
BLL003 Bell's Palsy 49 0.043
742
BNC003 Bone Cancer 59 0.042
743
c BPL002 Bipolar I Disorder 49 0.042
744
PST095 Post-Thrombotic Syndrome 52 0.042
745
P END046 Endometritis 50 0.042
746
KWS001 Kwashiorkor 42 0.042
747
c BRD018 Bardet-Biedl Syndrome 6 39 0.042
748
TQP001 Taqi Polymorphism 33 0.042
749
P MRL001 Meralgia Paresthetica 27 0.042
750
MYL009 Myelodysplastic Syndrome 70 0.042
751
SNS001 Sensorineural Hearing Loss 56 0.042
752
c CHR431 Chronic Venous Insufficiency 47 0.042
753
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 44 0.042
754
MYX004 Myxedema 43 0.042
755
SPR007 Superior Mesenteric Artery Syndrome 42 0.042
756
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 40 0.042
757
OST017 Osteomyelitis 63 0.041
758
MLR004 Malaria 83 0.041
759
c HMP029 Hemophilia a 68 0.041
760
P DRM053 Dermatitis, Atopic 67 0.041
761
PRV006 Pervasive Developmental Disorder 55 0.041
762
CLR109 Colorectal Adenocarcinoma 53 0.041
763
OST011 Osteomalacia 52 0.041
764
P CNJ013 Conjunctivitis 63 0.040
765
PRT058 Pure Autonomic Failure 59 0.040
766
KRT006 Keratoconjunctivitis 55 0.040
767
P BCL006 B-Cell Lymphomas 65 0.040
768
PPT005 Peptic Ulcer Disease 61 0.040
769
P NTR004 Neutropenia 60 0.040
770
P HMN010 Hemangioma 60 0.040
771
P MLT074 Multiple Endocrine Neoplasia 55 0.040
772
EXP004 Exophthalmos 51 0.040
773
PLC007 Placental Abruption 50 0.040
774
c MLG042 Malignant Otitis Externa 27 0.040
775
RTN017 Retinal Detachment 58 0.040
776
P CRV035 Cervical Cancer 69 0.040
777
END041 Endometrial Adenocarcinoma 60 0.040
778
ARM001 Aromatase Deficiency 52 0.040
779
ACH004 Achondroplasia 66 0.039
780
ISL003 Isolated Growth Hormone Deficiency 55 0.039
781
DSS008 Disease of Mental Health 52 0.039
782
ACH005 Achalasia 51 0.039
783
P NGH001 Night Blindness 51 0.039
784
CLR030 Clear Cell Renal Cell Carcinoma 49 0.039
785
HPT067 Hepatocellular Adenoma 43 0.039
786
c BRD015 Bardet-Biedl Syndrome 3 40 0.039
787
P NRB001 Neuroblastoma 72 0.039
788
SCK003 Sickle Cell Anemia 72 0.039
789
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.039
790
c MLG069 Malignant Hypertension 48 0.039
791
c PTT056 Pituitary Adenoma 1, Multiple Types 44 0.039
792
c PLM022 Pulmonary Valve Insufficiency 37 0.039
793
SMT008 Smith-Magenis Syndrome 53 0.038
794
HYP081 Hypolipoproteinemia 48 0.038
795
PRS129 Prostatic Hyperplasia, Benign 48 0.038
796
ART031 Aortic Coarctation 47 0.038
797
MCR011 Microinvasive Gastric Cancer 46 0.038
798
NNT019 Neonatal Hypothyroidism 39 0.038
799
48X003 48,xxyy Syndrome 34 0.038
800
IDP041 Idiopathic Recurrent Pericarditis 31 0.038
801
CHG001 Chagas Disease 71 0.038
802
P MYS005 Myositis 63 0.038
803
P SLV001 Silver-Russell Syndrome 56 0.038
804
LYM019 Lymphosarcoma 55 0.038
805
PNN001 Panniculitis 49 0.038
806
P CMP008 Compartment Syndrome 47 0.038
807
c HYP057 Hypervitaminosis D 41 0.038
808
P TMP003 Temporal Arteritis 66 0.037
809
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 52 0.037
810
SYN036 Syncope 47 0.037
811
P RTN014 Retinal Artery Occlusion 46 0.037
812
P CRB088 Cerebral Atrophy 39 0.037
813
ATX010 Ataxia Neuropathy Spectrum 35 0.037
814
GGN002 Gigantism 35 0.037
815
P ANT006 Antiphospholipid Syndrome 59 0.036
816
P HYP724 Hyperlipoproteinemia, Type Iii 58 0.036
817
HDR002 Hidradenitis Suppurativa 54 0.036
818
RDC002 Radiculopathy 53 0.036
819
P DDN001 Duodenal Ulcer 52 0.036
820
HYP006 Hypertensive Heart Disease 50 0.036
821
CRB025 Carbohydrate Metabolic Disorder 50 0.036
822
P MTC069 Mitochondrial Disorders 49 0.036
823
HDR003 Hidradenitis 46 0.036
824
c ADL001 Adult Lymphoma 39 0.036
825
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.036
826
ALL003 Allergic Rhinitis 67 0.036
827
ALB001 Albright's Hereditary Osteodystrophy 52 0.036
828
SPN041 Spinal Cord Disease 51 0.036
829
c BRD044 Bardet-Biedl Syndrome 17 45 0.036
830
c BRD016 Bardet-Biedl Syndrome 4 42 0.036
831
c BRD048 Bardet-Biedl Syndrome 18 42 0.036
832
c BRD033 Bardet-Biedl Syndrome 13 41 0.036
833
c BRD020 Bardet-Biedl Syndrome 8 40 0.036
834
c BRD032 Bardet-Biedl Syndrome 14 40 0.036
835
LPM010 Lipomatosis, Multiple Symmetric 39 0.036
836
c BRD017 Bardet-Biedl Syndrome 5 37 0.036
837
c BRD045 Bardet-Biedl Syndrome 19 34 0.036
838
c BRD047 Bardet-Biedl Syndrome 16 33 0.036
839
c BRD019 Bardet-Biedl Syndrome 7 28 0.036
840
c BRD050 Bardet-Biedl Syndrome 21 25 0.036
841
c BRD021 Bardet-Biedl Syndrome 9 23 0.036
842
c BRD051 Bardet-Biedl Syndrome 20 22 0.036
843
CRB089 Cerebral Beriberi 20 0.036
844
P MYS003 Myasthenia Gravis 72 0.036
845
P CHR071 Charcot-Marie-Tooth Disease 65 0.036
846
VRC005 Varicose Veins 64 0.036
847
c ATM011 Autoimmune Hepatitis 62 0.036
848
HRP004 Herpes Zoster 60 0.036
849
SPN027 Spinal Stenosis 59 0.036
850
MST005 Mastitis 55 0.036
851
P PRC012 Pericardial Effusion 53 0.036
852
ISL001 Islet Cell Tumor 53 0.036
853
PTT037 Pituitary Tumors 48 0.036
854
HMC014 Homocysteinemia 48 0.036
855
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.036
856
PHN003 Phenylketonuria 73 0.036
857
TNG002 Tangier Disease 64 0.036
858
DGN001 Degenerative Disc Disease 53 0.036
859
CLN015 Colon Adenocarcinoma 53 0.036
860
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.036
861
P CRN074 Coronary Artery Aneurysm 46 0.036
862
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 46 0.036
863
SCH003 Schizophreniform Disorder 43 0.036
864
TCL003 T Cell Deficiency 42 0.036
865
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 26 0.036
866
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 59 0.034
867
P WSK001 Wiskott-Aldrich Syndrome 77 0.034
868
P SRC025 Sarcoidosis 1 66 0.034
869
P INT001 Intrahepatic Cholestasis 60 0.034
870
STT001 Status Epilepticus 60 0.034
871
P MSC007 Muscle Hypertrophy 58 0.034
872
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.034
873
P GLM045 Glioma 54 0.034
874
OCL006 Ocular Hypertension 53 0.034
875
QDR001 Quadriplegia 52 0.034
876
P THR117 Three M Syndrome 1 51 0.034
877
PRS045 Prostatic Hypertrophy 49 0.034
878
OCC006 Occipital Horn Syndrome 49 0.034
879
HDN002 Head Injury 47 0.034
880
GLC096 Galactorrhea 45 0.034
881
BRN080 Brain Ischemia 44 0.034
882
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 41 0.034
883
c CNT028 Central Retinal Artery Occlusion 40 0.034
884
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.034
885
OVR093 Overhydrated Hereditary Stomatocytosis 34 0.034
886
PRN007 Perinephritis 34 0.034
887
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 32 0.034
888
ART010 Arteriolosclerosis 28 0.034
889
c CRT085 Carotid Intimal Medial Thickness 2 22 0.034
890
MTH081 Mthfr Gene Variant 15 0.034
891
P PRK057 Parkinson Disease, Late-Onset 76 0.034
892
APL001 Aplastic Anemia 73 0.034
893
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.034
894
SKN019 Skin Melanoma 69 0.034
895
CHR066 Chronic Fatigue Syndrome 66 0.034
896
MVM001 Movement Disease 60 0.034
897
P LRY019 Laryngitis 56 0.034
898
P SHR001 Short Bowel Syndrome 51 0.034
899
ECT093 Ectopic Cushing Syndrome 50 0.034
900
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 46 0.034
901
ANL022 Anal Fistula 44 0.034
902
ACD008 Acid-Labile Subunit Deficiency 43 0.034
903
ACT055 Actinomycosis 43 0.034
904
CDQ001 Cauda Equina Syndrome 40 0.034
905
ALC005 Alcoholic Pancreatitis 38 0.034
906
TMP012 Temple Syndrome 34 0.034
907
CGN007 Cognitive Function 1, Social 30 0.034
908
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 23 0.034
909
P GRF003 Graft-Versus-Host Disease 71 0.032
910
P ASP006 Aspergillosis 65 0.032
911
CHL065 Cholangiocarcinoma 63 0.032
912
P MLG056 Malignant Hyperthermia 59 0.032
913
TXC002 Toxic Encephalopathy 55 0.032
914
HPT009 Hepatopulmonary Syndrome 53 0.032
915
P SCL009 Sclerosing Cholangitis 53 0.032
916
DST005 Diastrophic Dysplasia 52 0.032
917
P TRT010 Teratoma 52 0.032
918
TLN003 Telangiectasis 51 0.032
919
P BRT004 Bartter Disease 51 0.032
920
LYM009 Lymphocytic Choriomeningitis 50 0.032
921
PRT029 Parathyroid Adenoma 49 0.032
922
PRM003 Premature Ejaculation 47 0.032
923
CRB004 Cerebral Artery Occlusion 46 0.032
924
SDD008 Sudden Sensorineural Hearing Loss 45 0.032
925
PHC013 Phaeochromocytoma 43 0.032
926
MTR007 Motor Peripheral Neuropathy 40 0.032
927
NTR007 Neutral Lipid Storage Disease with Myopathy 36 0.032
928
P DCR003 Dacryoadenitis 33 0.032
929
SVN002 Sveinsson Chorioretinal Atrophy 29 0.032
930
c LPD040 Lipodystrophy, Familial Partial, Type 1 27 0.032
931
P ANG001 Angelman Syndrome 61 0.032
932
ISL014 Isolated Growth Hormone Deficiency, Type Ia 57 0.032
933
ILT001 Ileitis 56 0.032
934
MYL020 Myelomeningocele 53 0.032
935
GNT050 Genitourinary Tract Anomalies 40 0.032
936
PDT040 Pediatric Hypertension 29 0.032
937
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 28 0.032
938
NRG005 Neurogenic Hypertension 28 0.032
939
c PGM021 Pigmented Nodular Adrenocortical Disease, Primary, 1 26 0.032
940
c PGM011 Pigmented Nodular Adrenocortical Disease, Primary, 2 25 0.032
941
LYM133 Lymphoma, Hodgkin, Classic 71 0.031
942
P SPN052 Spondyloarthropathy 60 0.031
943
P PRG013 Paraganglioma 56 0.031
944
CHL061 Childhood Leukemia 55 0.031
945
BLR006 Biliary Tract Disease 54 0.031
946
P THY054 Thyrotoxic Periodic Paralysis 53 0.031
947
GLL018 Gallbladder Cancer 51 0.031
948
P CRB185 Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 49 0.031
949
P KRT007 Keratoconus 48 0.031
950
FML026 Familial Lipoprotein Lipase Deficiency 46 0.031
951
P ENC008 Encephalocele 46 0.031
952
NNT049 Nontuberculous Mycobacterial Lung Disease 45 0.031
953
TTH032 Tooth Size 44 0.031
954
NTR005 Nutritional Deficiency Disease 43 0.031
955
SPN369 Spinal Disease 42 0.031
956
CHL013 Cholecystolithiasis 40 0.031
957
PRM056 Primrose Syndrome 34 0.031
958
c GLL024 Gallbladder Disease 1 30 0.031
959
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 26 0.031
960
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.031
961
CHR189 Chromosome 12p Deletion 24 0.031
962
ACR119 Acrodysostosis 2 with or Without Hormone Resistance 23 0.031
963
HYP531 Hypogonadotropic Hypogonadism 4 with or Without Anosmia 23 0.031
964
c CSH006 Cushing Syndrome Due to Macronodular Adrenal Hyperplasia 23 0.031
965
48X002 48,xxxy Syndrome 21 0.031
966
MSC089 Mosaic Monosomy X 21 0.031
967
c TRN055 Turner Syndrome Due to Structural X Chromosome Anomalies 21 0.031
968
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.031
969
HYP686 Hypogonadism, Male, with Mental Retardation and Skeletal Anomalies 19 0.031
970
BCT004 Bacteriuria 47 0.031
971
P END044 Endometriosis 64 0.030
972
OVR029 Ovarian Hyperstimulation Syndrome 64 0.030
973
P SPN046 Spinal Muscular Atrophy 63 0.030
974
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 60 0.030
975
P MYC008 Myocarditis 58 0.030
976
FLR002 Filariasis 57 0.030
977
TRG002 Trigeminal Neuralgia 57 0.030
978
c ACT135 Acute Graft Versus Host Disease 56 0.030
979
PYD001 Pyoderma Gangrenosum 55 0.030
980
KRT009 Keratosis 53 0.030
981
PYD002 Pyoderma 51 0.030
982
P FML035 Familial Hyperlipidemia 47 0.030
983
CRN031 Cranial Nerve Disease 45 0.030
984
PDT001 Pediatric Lymphoma 45 0.030
985
PND004 Pandas 42 0.030
986
SCT001 Sciatic Neuropathy 42 0.030
987
TND005 Tendinitis 41 0.030
988
HMP001 Hemopericardium 41 0.030
989
RNL021 Renal Tubular Transport Disease 38 0.030
990
c MYS011 Myasthenia Gravis Congenital 30 0.030
991
c LPD036 Lipodystrophy, Familial Partial, Type 6 25 0.030
992
c ATM089 Autoimmune Neuropathy 22 0.030
993
PNC065 Pinched Nerve 16 0.030
994
P PYL005 Pyelonephritis 56 0.028
995
P RTT002 Rett Syndrome 82 0.028
996
P FRG001 Fragile X Syndrome 69 0.028
997
PNC033 Pancreas Adenocarcinoma 64 0.028
998
c PNS012 Paine Syndrome 62 0.028
999
URT039 Urticaria 60 0.028
1000
P HYP040 Hypospadias 59 0.028
1001
PLC005 Placental Insufficiency 58 0.028
1002
TRP002 Tropical Spastic Paraparesis 57 0.028
1003
DMY004 Demyelinating Disease 57 0.028
1004
P EPL140 Epilepsy, Idiopathic Generalized 57 0.028
1005
APP015 Apparent Mineralocorticoid Excess 54 0.028
1006
P PTT006 Pituitary Adenoma 52 0.028
1007
MGR028 Migraine with or Without Aura 1 49 0.028
1008
MNN009 Meningoencephalitis 49 0.028
1009
RNL011 Renal Osteodystrophy 49 0.028
1010
c CHR037 Chronic Eosinophilic Pneumonia 48 0.028
1011
c HYP740 Hyperlipoproteinemia, Type V 48 0.028
1012
ASP007 Aspiration Pneumonia 47 0.028
1013
HYP457 Hypertrophic Scars 47 0.028
1014
NSP002 Nasopharyngitis 46 0.028
1015
P HYP750 Hypertriglyceridemia, Familial 44 0.028
1016
LCH009 Lichen Sclerosus 44 0.028
1017
IDP064 Idiopathic Neutropenia 44 0.028
1018
LPD014 Lipodermatosclerosis 42 0.028
1019
DYS009 Dysthymic Disorder 41 0.028
1020
c WLM011 Wilms Tumor 6 38 0.028
1021
47X003 47, Xxy 37 0.028
1022
VSC008 Vascular Hemostatic Disease 36 0.028
1023
ALL014 Allergic Encephalomyelitis 36 0.028
1024
NRV004 Nerve Compression Syndrome 35 0.028
1025
c HNT011 Huntington Disease-Like 3 30 0.028
1026
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.028
1027
P TTR001 Tetralogy of Fallot 69 0.028
1028
c HMP004 Hemophilia B 67 0.028
1029
P CRN015 Cornelia De Lange Syndrome 64 0.028
1030
P KBK002 Kabuki Syndrome 1 63 0.028
1031
P KLL001 Kallmann Syndrome 63 0.028
1032
LYM021 Lymphadenitis 61 0.028
1033
c ACT073 Acute Leukemia 60 0.028
1034
P HMR003 Hemorrhagic Disease 60 0.028
1035
CHK001 Chikungunya 59 0.028
1036
P STS008 Sotos Syndrome 1 56 0.028
1037
P SCL018 Scoliosis 55 0.028
1038
P ICH004 Ichthyosis 54 0.028
1039
c INF071 Inflammatory Bowel Disease 1 53 0.028
1040
c CNT015 Central Sleep Apnea 49 0.028
1041
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.028
1042
CLN044 Colon Adenoma 42 0.028
1043
RMN001 Rumination Disorder 41 0.028
1044
PST035 Postgastrectomy Syndrome 36 0.028
1045
ALG027 Al-Gazali-Bakalinova Syndrome 30 0.028
1046
LPD026 Lipedema 29 0.028
1047
c NRC017 Narcolepsy 7 18 0.028
1048
NVS001 Neovascular Glaucoma 48 0.027
1049
ATM052 Autoimmune Disease 1 34 0.027
1050
P GRV001 Graves' Disease 61 0.027
1051
c LKM063 Leukemia, Chronic Myeloid 70 0.026
1052
MSC157 Muscular Dystrophy, Duchenne Type 68 0.026
1053
P MCL013 Mucolipidosis Iv 67 0.026
1054
P LNG028 Long Qt Syndrome 65 0.026
1055
SCH014 Schistosomiasis 62 0.026
1056
CRC006 Carcinoid Syndrome 60 0.026
1057
TNS005 Tonsillitis 60 0.026
1058
P LPS002 Liposarcoma 59 0.026
1059
P MNC007 Monocytic Leukemia 57 0.026
1060
CMP010 Complex Regional Pain Syndrome 57 0.026
1061
c FML116 Familial Cold Autoinflammatory Syndrome 1 57 0.026
1062
c VSC019 Vesicoureteral Reflux 1 57 0.026
1063
LYM040 Lymphoblastic Lymphoma 57 0.026
1064
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.026
1065
DFF005 Diffuse Large B-Cell Lymphoma 56 0.026
1066
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.026
1067
EXT034 Extrinsic Allergic Alveolitis 56 0.026
1068
P PNC025 Panic Disorder 55 0.026
1069
FCL014 Focal Epilepsy 55 0.026
1070
c CWD006 Cowden Syndrome 1 55 0.026
1071
TCD001 Tic Disorder 54 0.026
1072
ABL002 Ablepharon-Macrostomia Syndrome 54 0.026
1073
LYM024 Lymphatic System Disease 54 0.026
1074
OST016 Osteochondrosis 54 0.026
1075
P FML052 Familial Cold Autoinflammatory Syndrome 53 0.026
1076
c AMY009 Amyloidosis Aa 53 0.026
1077
P CPL006 Capillary Hemangioma 53 0.026
1078
WLF002 Wolf-Hirschhorn Syndrome 52 0.026
1079
SPC010 Speech and Communication Disorders 52 0.026
1080
MNC006 Monoclonal Gammopathy of Uncertain Significance 51 0.026
1081
PRN021 Paranasal Sinus Disease 50 0.026
1082
P BRC006 Brachydactyly 50 0.026
1083
CYC008 Cyclic Vomiting Syndrome 49 0.026
1084
ALL001 Allan-Herndon-Dudley Syndrome 49 0.026
1085
KLD001 Keloids 49 0.026
1086
SKL017 Skeletal Dysplasias 48 0.026
1087
P SDR002 Siderosis 47 0.026
1088
AMN002 Amino Acid Metabolic Disorder 47 0.026
1089
GLC106 Glucocorticoid Resistance, Generalized 46 0.026
1090
IMP006 Impulse Control Disorder 43 0.026
1091
TRN007 Transsexualism 43 0.026
1092
ASP004 Asphyxia Neonatorum 43 0.026
1093
PTT003 Pituitary-Dependent Cushing's Disease 42 0.026
1094
SWN001 Swine Influenza 42 0.026
1095
CRB008 Cerebral Atherosclerosis