Search results for obesity OR diabetes

4545 hits were found for obesity OR diabetes

# Family MCID Name MIFTS Score
1
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 9.067
2
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 5.077
3
c DBT009 Diabetes Mellitus 67 4.650
4
P ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.234
5
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 3.478
6
MRB003 Morbid Obesity 62 3.036
7
GST033 Gestational Diabetes 63 2.963
8
c MCR115 Microvascular Complications of Diabetes 5 71 2.934
9
P MCR113 Microvascular Complications of Diabetes 3 58 2.714
10
P MCR120 Microvascular Complications of Diabetes 7 46 2.671
11
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 2.620
12
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 2.620
13
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 2.620
14
DBT087 Diabetes Insipidus, Neurohypophyseal 62 2.525
15
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 2.427
16
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 2.375
17
P MCR130 Microvascular Complications of Diabetes 6 43 2.339
18
P MCR133 Microvascular Complications of Diabetes 4 43 2.339
19
DBT084 Diabetes Mellitus, Ketosis-Prone 62 2.310
20
P MCR129 Microvascular Complications of Diabetes 1 66 2.133
21
DBT083 Diabetes Mellitus, Permanent Neonatal 61 1.979
22
DBT010 Diabetic Neuropathy 60 1.947
23
RNL051 Renal Cysts and Diabetes Syndrome 53 1.931
24
c DBT005 Diabetes Insipidus 55 1.871
25
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 39 1.763
26
c MTR004 Maturity-Onset Diabetes of the Young 61 1.744
27
LPT006 Leptin Receptor Deficiency 40 1.713
28
P MCR112 Microvascular Complications of Diabetes 2 42 1.703
29
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 51 1.635
30
OBS037 Obesity-Hypoventilation Syndrome 50 1.617
31
DBT090 Diabetes and Deafness, Maternally Inherited 41 1.594
32
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 1.557
33
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 36 1.529
34
OBS015 Obesity, Hyperphagia, and Developmental Delay 26 1.506
35
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 1.496
36
LPT014 Leptin Deficiency or Dysfunction 40 1.485
37
DBT008 Diabetic Angiopathy 48 1.453
38
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 25 1.429
39
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 44 1.415
40
MRB006 Morbid Obesity and Spermatogenic Failure 19 1.412
41
P BDY005 Body Mass Index Quantitative Trait Locus 9 29 1.411
42
P BDY006 Body Mass Index Quantitative Trait Locus 8 27 1.411
43
P BDY012 Body Mass Index Quantitative Trait Locus 7 27 1.411
44
P BDY015 Body Mass Index Quantitative Trait Locus 12 28 1.409
45
P BDY010 Body Mass Index Quantitative Trait Locus 4 27 1.409
46
MHM001 Mehmo Syndrome 33 1.408
47
P MTR026 Maturity-Onset Diabetes of the Young, Type 9 31 1.395
48
DBT002 Diabetic Autonomic Neuropathy 46 1.389
49
P MTR019 Maturity-Onset Diabetes of the Young, Type 2 52 1.381
50
P MTR023 Maturity-Onset Diabetes of the Young, Type 6 39 1.335
51
P MTR024 Maturity-Onset Diabetes of the Young, Type 7 39 1.334
52
P LPD015 Lipodystrophy, Familial Partial, Type 2 61 1.321
53
CHN016 Cohen Syndrome 54 1.315
54
P MTR020 Maturity-Onset Diabetes of the Young, Type 3 53 1.300
55
c WLF004 Wolfram Syndrome 60 1.275
56
MMS001 Momo Syndrome 30 1.242
57
DBT004 Diabetic Polyneuropathy 50 1.241
58
CNG376 Congenital Leptin Deficiency 26 1.239
59
RTN173 Retinal Dystrophy and Obesity 19 1.238
60
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 14 1.231
61
P MTR021 Maturity-Onset Diabetes of the Young, Type 4 38 1.227
62
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 1.211
63
P MTR044 Maturity-Onset Diabetes of the Young, Type 10 39 1.175
64
P DBT094 Diabetes Mellitus, Insulin-Dependent, 10 19 1.162
65
P DBT034 Diabetes Mellitus, Insulin-Dependent, 20 19 1.161
66
P DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 24 1.159
67
P TRN032 Transient Neonatal Diabetes Mellitus 44 1.149
68
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 28 1.136
69
c NNT009 Neonatal Diabetes Mellitus 48 1.135
70
DBT006 Diabetic Macular Edema 49 1.126
71
P DBT040 Diabetes Mellitus, Insulin-Dependent, 2 29 1.108
72
P MTR039 Maturity-Onset Diabetes of the Young, Type 11 21 1.106
73
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 26 1.105
74
PRP098 Proprotein Convertase 1/3 Deficiency 31 1.104
75
WDH003 Woodhouse-Sakati Syndrome 33 1.102
76
P DBT064 Diabetes Mellitus, Transient Neonatal, 1 31 1.082
77
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 73 1.070
78
CHP002 Chops Syndrome 32 1.067
79
P MTR075 Maturity-Onset Diabetes of the Young, Type 13 37 1.059
80
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 47 1.054
81
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 39 1.054
82
P MTR074 Maturity-Onset Diabetes of the Young, Type 14 30 1.052
83
P DBT098 Diabetes Mellitus, Transient Neonatal, 2 15 1.041
84
P DBT038 Diabetes Mellitus, Insulin-Dependent, 5 18 1.040
85
P DBT032 Diabetes Mellitus, Insulin-Dependent, 22 15 1.039
86
BRT037 Brittle Diabetes 25 1.023
87
DBT062 Diabetic Foot Ulcers 59 1.022
88
DBT007 Diabetic Cataract 38 1.002
89
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 56 0.986
90
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 28 0.982
91
P DBT044 Diabetes Mellitus, Transient Neonatal, 3 16 0.981
92
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.978
93
PNC104 Pancreatic and Cerebellar Agenesis 26 0.973
94
P DBT082 Diabetes Mellitus, Insulin-Dependent, 12 17 0.971
95
INS010 Insulin-Resistant Acanthosis Nigricans, Type a 16 0.971
96
P DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.947
97
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 20 0.904
98
P DBT054 Diabetes Mellitus, Insulin-Dependent, 24 27 0.903
99
HYP835 Hypothalamic Obesity 44 0.903
100
P DBT077 Diabetes Mellitus, Insulin-Dependent, 19 15 0.902
101
P DBT053 Diabetes Mellitus, Insulin-Dependent, 23 14 0.902
102
P DBT079 Diabetes Mellitus, Insulin-Dependent, 21 14 0.901
103
DBT060 Diabetes Mellitus, Insulin-Dependent, X-Linked 8 0.898
104
DVL020 Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features 21 0.884
105
HYD021 Hydrocephalus Obesity Hypogonadism 17 0.884
106
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 16 0.882
107
CLB031 Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome 16 0.878
108
BCK003 Background Diabetic Retinopathy 38 0.878
109
MNG006 Monogenic Diabetes 41 0.862
110
MTC025 Mitochondrial Myopathy with Diabetes 23 0.830
111
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 21 0.826
112
P DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 14 0.822
113
OBS050 Obesity Due to Congenital Leptin Deficiency 23 0.800
114
P TYP038 Type 1 Diabetes Mellitus 15 23 0.799
115
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 13 0.786
116
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 48 0.766
117
SVR002 Severe Nonproliferative Diabetic Retinopathy 34 0.762
118
FBR065 Fibrocalculous Pancreatopathy 18 0.757
119
RHH001 Rohhad 27 0.752
120
P TYP035 Type 1 Diabetes Mellitus 11 28 0.752
121
P TYP031 Type 1 Diabetes Mellitus 5 25 0.751
122
P TYP033 Type 1 Diabetes Mellitus 7 26 0.750
124
P TYP028 Type 1 Diabetes Mellitus 2 24 0.747
125
GLC008 Glucose Metabolism Disease 54 0.746
126
P TYP036 Type 1 Diabetes Mellitus 12 23 0.745
127
P TYP027 Type 1 Diabetes Mellitus 10 24 0.743
128
ARD001 Aredyld 25 0.743
129
P TYP037 Type 1 Diabetes Mellitus 13 27 0.742
130
P TYP032 Type 1 Diabetes Mellitus 6 25 0.742
131
P TYP039 Type 1 Diabetes Mellitus 17 19 0.741
132
P TYP040 Type 1 Diabetes Mellitus 18 18 0.741
133
P DBT050 Diabetes Mellitus, Insulin-Dependent, 15 17 0.741
134
P TYP029 Type 1 Diabetes Mellitus 3 16 0.741
135
P TYP030 Type 1 Diabetes Mellitus 4 16 0.741
136
P TYP034 Type 1 Diabetes Mellitus 8 19 0.740
137
MSC133 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 17 0.740
138
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 16 0.740
139
P LPD033 Lipodystrophy, Congenital Generalized, Type 2 42 0.739
140
P DBT057 Diabetes Mellitus, Insulin-Dependent, 6 15 0.739
141
P DBT048 Diabetes Mellitus, Insulin-Dependent, 11 14 0.738
142
P DBT055 Diabetes Mellitus, Insulin-Dependent, 3 14 0.738
143
P DBT056 Diabetes Mellitus, Insulin-Dependent, 4 14 0.738
144
P DBT059 Diabetes Mellitus, Insulin-Dependent, 8 14 0.738
145
P DBT058 Diabetes Mellitus, Insulin-Dependent, 7 13 0.738
146
P DBT049 Diabetes Mellitus, Insulin-Dependent, 13 14 0.736
147
P DBT051 Diabetes Mellitus, Insulin-Dependent, 17 13 0.736
148
P DBT052 Diabetes Mellitus, Insulin-Dependent, 18 13 0.736
149
P DBT097 Diabetes Mellitus, Noninsulin-Dependent, 4 11 0.735
150
P DBT095 Diabetes Mellitus, Noninsulin-Dependent, 3 11 0.735
151
LYM029 Lymphedema-Distichiasis Syndrome 40 0.734
152
XLN122 X-Linked Intellectual Disability - Short Stature - Obesity 8 0.727
153
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 18 0.721
154
SHR107 Short Stature-Obesity Syndrome 17 0.721
155
PRL046 Prolactin Deficiency with Obesity and Enlarged Testes 10 0.721
156
AYZ001 Ayazi Syndrome 9 0.719
157
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 21 0.716
158
MN1002 Man1b1-Cdg 11 0.710
159
DBT018 Diabetic Mastopathy 20 0.685
160
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 44 0.662
161
P WLF013 Wolfram Syndrome 1 54 0.661
162
GST058 Gestational Diabetes Insipidus 16 0.656
163
P ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 52 0.654
164
c NRP001 Neuropathy 63 0.651
165
FNC009 Fanconi-Bickel Syndrome 54 0.649
166
P HMC039 Hemochromatosis, Type 1 74 0.647
167
TRP008 Tropical Calcific Pancreatitis 50 0.646
168
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 17 0.646
169
DBT089 Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification 18 0.642
170
BNG086 Bangstad Syndrome 21 0.639
171
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 29 0.638
172
c ACQ022 Acquired Generalized Lipodystrophy 54 0.605
173
P LPD032 Lipodystrophy, Congenital Generalized, Type 1 48 0.605
174
c KDN018 Kidney Disease 71 0.599
175
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.590
176
NTR005 Nutritional Deficiency Disease 60 0.584
177
INS034 Insulinomatosis and Diabetes Mellitus 25 0.581
178
DBT081 Diabetic Encephalopathy 28 0.571
179
HYP364 Hyperostosis Frontalis Interna 30 0.571
180
OVR063 Overnutrition 53 0.565
181
RNL024 Renal Glucosuria 54 0.546
182
DPS001 Dipsogenic Diabetes Insipidus 24 0.538
183
PRX085 Preaxial Hallucal Polydactyly 25 0.534
184
P CNG012 Congenital Generalized Lipodystrophy 52 0.532
185
P HRD156 Hereditary Central Diabetes Insipidus 17 0.530
186
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 17 0.529
187
P ACQ034 Acquired Central Diabetes Insipidus 16 0.529
188
RNL050 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia Due to Duplication of Mitochondrial Dna 7 0.529
189
ATH012 Atherosclerosis, Premature, with Deafness, Nephropathy, Diabetes Mellitus, Photomyoclonus, and Degenerative Neurologic Disease 19 0.527
190
LPT011 Lipoatrophy with Diabetes, Leukomelanodermic Papules, Liver Steatosis, and Hypertrophic Cardiomyopathy 17 0.527
191
MTC096 Mitchell-Riley Syndrome 23 0.526
192
PHT013 Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction 18 0.526
193
OBS060 Obesity Due to Sim1 Deficiency 12 0.524
194
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 12 0.524
195
FGN001 Feigenbaum Bergeron Richardson Syndrome 8 0.522
196
DBT003 Diabetic Peripheral Angiopathy 6 0.522
197
MDF004 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 14 0.522
198
ACH016 Achard Thiers Syndrome 7 0.520
199
YRF001 Yorifuji Okuno Syndrome 7 0.520
200
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 18 0.517
201
XLN211 X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome 17 0.517
202
INT298 Intellectual Disability-Obesity-Brain Malformations-Facial Dysmorphism Syndrome 16 0.517
203
OBS068 Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome 8 0.517
204
GLC003 Glucose Intolerance 59 0.512
205
CLR029 Clark-Baraitser Syndrome 23 0.508
206
P MNT236 Mental Retardation, Autosomal Dominant 39 22 0.508
207
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 22 0.508
208
FTT001 Fatty Liver Disease 66 0.504
209
P BMN004 Biemond Syndrome Ii 19 0.504
210
DPL003 Diploid-Triploid Mosaicism 16 0.504
211
HYP056 Hypoglycemia 64 0.503
212
CMR005 Camera-Marugo-Cohen Syndrome 12 0.499
213
HYP066 Hyperglycemia 65 0.494
214
c SHR029 Short Syndrome 57 0.494
215
c LVR013 Liver Disease 77 0.493
216
GLC036 Glucagonoma 51 0.454
217
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.451
218
HYP060 Hyperinsulinism 57 0.434
219
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 21 0.410
220
c HRT032 Heart Disease 76 0.385
221
INT288 Intellectual Disability-Dysmorphism-Hypogonadism-Diabetes Mellitus Syndrome 8 0.377
222
LPT004 Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 3 0.375
223
WLF014 Wolfram Syndrome, Mitochondrial Form 15 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
MNT030 Mental Retardation Syndrome, Belgian Type 16 0.372
228
INT222 Intermediate Dend Syndrome 10 0.372
229
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 9 0.372
230
P DBT096 Diabetes Mellitus, Congenital Autoimmune 8 0.372
231
PRM187 Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome 7 0.372
232
XLN187 X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome 6 0.372
233
HYP790 Hypopituitarism, Congenital, with Central Diabetes Insipidus 3 0.372
234
DBT016 Diabetes Persistent Mullerian Ducts 2 0.372
235
PRM291 Premature Aging Syndrome, Okamoto Type 14 0.370
236
LPD008 Lipid Metabolism Disorder 65 0.366
237
c PLY011 Polycystic Ovary Syndrome 64 0.366
238
c PRP019 Peripheral Nervous System Disease 66 0.349
239
c SLP006 Sleep Apnea 70 0.348
240
ATM095 Autoimmune Disease 68 0.345
241
ETN001 Eating Disorder 65 0.342
242
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.339
243
ART140 Arteries, Anomalies of 67 0.336
244
c CRN018 Coronary Artery Anomaly 74 0.327
245
DPR016 Depression 73 0.325
246
c CRD246 Cardiovascular System Disease 57 0.317
247
c CRN300 Coronary Heart Disease 1 62 0.314
248
IMM136 Immune System Disease 57 0.311
249
P CHR089 Chronic Kidney Failure 73 0.300
250
VSC007 Vascular Disease 72 0.300
251
ISC004 Ischemia 67 0.295
252
c MYC007 Myocardial Infarction 78 0.288
254
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.270
255
ATN004 Autonomic Neuropathy 46 0.269
256
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.266
257
c PRD008 Periodontitis 66 0.264
258
AST005 Asthma 81 0.257
259
NNL002 Nonalcoholic Steatohepatitis 55 0.246
260
c PLY019 Polyneuropathy 58 0.244
261
ANX010 Anxiety 73 0.244
262
ISC006 Ischemic Heart Disease 72 0.244
263
c BRS047 Breast Cancer 100 0.244
264
AGN016 Aging 63 0.241
265
IMP005 Impotence 58 0.240
266
PRD007 Periodontal Disease 66 0.236
267
PLC008 Placenta Disease 59 0.230
268
RTN018 Retinal Disease 58 0.229
269
PRD004 Prediabetes Syndrome 51 0.229
270
URN009 Urinary System Disease 59 0.227
271
CNG034 Congestive Heart Failure 71 0.224
272
DSS008 Disease of Mental Health 70 0.219
273
SPS003 Spastic Diplegia 49 0.215
274
MNT002 Mental Depression 65 0.214
275
c PNC044 Pancreatitis 62 0.213
276
APN008 Apnea, Obstructive Sleep 68 0.209
277
c ART021 Arteriosclerosis 61 0.208
278
c ART022 Arthritis 78 0.207
279
c HPT021 Hepatitis 74 0.206
280
c CTR002 Cataract 58 0.202
281
c HYP086 Hypothyroidism 66 0.202
282
P PRC016 Pre-Eclampsia 61 0.201
283
HYP080 Hypogonadism 53 0.200
284
c INF032 Infertility 60 0.198
285
OST012 Osteoarthritis 81 0.197
286
INS024 Insulin-Like Growth Factor I 83 0.196
287
c PRD006 Prader-Willi Syndrome 62 0.196
288
ACN002 Acanthosis Nigricans 65 0.195
289
THR024 Thrombosis 64 0.193
290
END030 End Stage Renal Failure 60 0.192
291
GST092 Gastroesophageal Reflux 66 0.192
292
GST037 Gastroparesis 59 0.188
293
c THY032 Thyroiditis 54 0.187
294
END057 Endometrial Cancer 69 0.186
295
HYP266 Hypoxia 63 0.184
296
NRT004 Neuritis 58 0.179
297
c VSC018 Visceral Steatosis 38 0.179
298
FSH001 Fish-Eye Disease 51 0.175
299
P TRC078 Trichohepatoenteric Syndrome 2 35 0.175
301
SLP005 Sleep Disorder 60 0.172
302
c OST002 Osteoporosis 74 0.171
303
P PRD040 Periodontitis, Chronic 60 0.171
304
NRM005 Neuromuscular Disease 61 0.171
305
MCL006 Macular Retinal Edema 55 0.170
306
ATH013 Atherosclerosis Susceptibility 61 0.170
307
c TRC086 Trichohepatoenteric Syndrome 1 61 0.170
308
ANR007 Anorexia Nervosa 68 0.170
309
PRP027 Peripheral Vascular Disease 72 0.168
310
c RTN016 Retinal Degeneration 56 0.167
311
DST081 Distal Trisomy 11q 20 0.165
312
P HYP595 Hypertension, Essential 77 0.164
313
c ALZ034 Alzheimer Disease 88 0.164
314
GST050 Gastrointestinal System Disease 67 0.162
315
FTL021 Fetal Macrosomia 47 0.162
316
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.161
317
P ATR087 Atrial Standstill 1 69 0.160
318
P ACT075 Acute Myocardial Infarction 57 0.160
319
c NRV007 Nervous System Disease 72 0.158
320
c CLR023 Colorectal Cancer 99 0.158
321
c HYP750 Hypertriglyceridemia, Familial 58 0.158
322
c LKM002 Leukemia 72 0.158
323
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.157
324
P HPT001 Hepatitis C 69 0.157
325
c PNC035 Pancreatic Cancer 83 0.155
326
c CLC063 Celiac Disease 1 72 0.155
327
P ACT027 Acute Pancreatitis 59 0.155
328
SXL003 Sexual Disorder 53 0.154
329
c ADN016 Adenocarcinoma 71 0.153
330
DNT012 Dental Caries 52 0.152
331
c SCH015 Schizophrenia 73 0.151
332
HYP064 Hypogonadotropism 42 0.150
333
PRP080 Peripheral Artery Disease 56 0.150
334
c HPT023 Hepatocellular Carcinoma 97 0.149
335
c INF038 Influenza 75 0.148
336
c PRS040 Prostate Cancer 93 0.148
337
LVR012 Liver Cirrhosis 67 0.148
338
CYT017 Cytophagic Histiocytic Panniculitis 26 0.144
339
BRN106 Burns 59 0.142
340
DMN002 Dementia 69 0.142
341
c RHM011 Rheumatoid Arthritis 82 0.141
342
c ECL001 Eclampsia 59 0.141
343
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.141
344
CRN036 Craniopharyngioma 68 0.141
345
c HYP014 Hyperuricemia 56 0.140
346
P PRS136 Prostate Cancer, Hereditary, 6 40 0.140
347
P PRS130 Prostate Cancer, Hereditary, 8 37 0.140
348
c MSC007 Muscle Hypertrophy 64 0.140
349
c RSP003 Respiratory Failure 72 0.139
350
LMB062 Limb Ischemia 54 0.138
351
c PSR002 Psoriasis 67 0.137
352
c ART023 Arthropathy 68 0.136
353
P TYP024 Type Ii Mixed Cryoglobulinemia 40 0.136
354
c ENC018 Encephalopathy 65 0.135
355
ANG054 Angina Pectoris 70 0.132
356
c ATR011 Atrial Fibrillation 69 0.131
357
IRN002 Iron Metabolism Disease 60 0.130
358
BND020 Bone Disease 65 0.130
359
HYP043 Hyperandrogenism 50 0.128
360
RTN020 Retinal Vascular Disease 54 0.127
361
MDD011 Mood Disorder 65 0.126
362
P PRC031 Preeclampsia/eclampsia 1 41 0.125
363
c OVR049 Ovarian Disease 63 0.124
364
JNT002 Joint Disorders 64 0.124
365
c LYM118 Lymphoma 69 0.124
366
INS001 Insulinoma 66 0.123
367
GND003 Gonadal Disease 49 0.123
368
LNG099 Lung Disease 70 0.122
369
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.121
370
BLM002 Bulimia Nervosa 61 0.118
371
CRB039 Cerebrovascular Disease 70 0.118
372
P PLY105 Polycystic Ovary Syndrome 1 43 0.117
373
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.117
374
CYT002 Cytokine Deficiency 39 0.115
375
CRT049 Critical Limb Ischemia 52 0.115
376
ADN018 Adenoma 65 0.114
377
c MLT020 Multiple Sclerosis 76 0.114
378
ALL026 Allergic Hypersensitivity Disease 68 0.114
379
CLF033 Cleft Mitral Valve 22 0.114
380
HYP730 Hypogonadotropic Hypogonadism 58 0.114
381
THR013 Thoracic Outlet Syndrome 57 0.114
382
c MJR001 Major Depressive Disorder 67 0.113
383
LYM053 Lymphomatous Thyroiditis 27 0.113
384
c HYP083 Hypopituitarism 59 0.113
385
c DRR001 Diarrhea 58 0.113
386
THY030 Thyroid Gland Disease 51 0.113
387
HLC007 Helicobacter Pylori Infection 66 0.112
388
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.112
389
CNN003 Conn's Syndrome 73 0.111
390
c PNM007 Pneumonia 72 0.111
391
c BPL003 Bipolar Disorder 61 0.109
392
DST089 Distal Trisomy 3p 22 0.109
393
CYS001 Cystic Fibrosis 83 0.108
394
GT001 Gout 62 0.108
395
BRR014 Barrett Esophagus 71 0.108
396
MTH009 Mouth Disease 66 0.106
397
DFC004 Deficiency Anemia 65 0.106
398
c LYM031 Lymphocytic Leukemia 61 0.106
399
P GLL024 Gallbladder Disease 1 45 0.105
400
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.105
401
ACT088 Acute Insulin Response 50 0.105
402
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.105
403
c HYP069 Hyperparathyroidism 59 0.105
404
P ACT068 Acute Cystitis 56 0.105
405
DWN001 Down Syndrome 72 0.104
406
RST023 Resting Heart Rate, Variation in 44 0.104
407
c ATT013 Attention Deficit-Hyperactivity Disorder 67 0.103
408
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.103
409
c AMY004 Amyloidosis 69 0.103
410
RSP006 Respiratory System Disease 64 0.103
411
GST053 Gastric Cancer 78 0.103
412
ATX010 Ataxia Neuropathy Spectrum 39 0.102
413
c OVR046 Ovarian Cyst 52 0.102
414
c LKM062 Leukemia, Acute Lymphoblastic 70 0.102
415
BNF002 Bone Fracture 50 0.102
416
NRL016 Neural Tube Defects 79 0.102
417
P PNC128 Pain - Chronic 46 0.102
418
PLM033 Pulmonary Embolism 64 0.101
419
c ANR048 Aniridia 1 63 0.101
420
P THR092 Thrombophilia Due to Thrombin Defect 70 0.101
421
SPN331 Spondyloocular Syndrome 42 0.101
422
CRP001 Carpal Tunnel Syndrome 72 0.101
423
P BRD013 Bardet-Biedl Syndrome 12 49 0.100
424
DRL001 Dural Sinus Malformation 23 0.100
425
c EPL164 Epilepsy 73 0.100
426
PTT009 Pituitary Gland Disease 59 0.100
427
P MTR002 Mitral Valve Insufficiency 50 0.100
428
HRN028 Horns in Sheep 24 0.100
429
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.100
430
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.100
431
P BRD014 Bardet-Biedl Syndrome 2 61 0.099
432
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.099
433
c ACT232 Acute Necrotizing Encephalopathy 30 0.099
434
BLD137 Blood Group--Ahonen 21 0.099
435
c LCT001 Lactic Acidosis 53 0.099
436
MCR141 Mucormycosis 51 0.099
437
c BRD002 Bardet-Biedl Syndrome 65 0.098
438
HDC001 Headache 63 0.097
439
P BRD012 Bardet-Biedl Syndrome 11 52 0.097
440
P BRD011 Bardet-Biedl Syndrome 10 45 0.097
441
MTB004 Metabolic Acidosis 51 0.097
442
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.097
443
STM006 Stomach Disease 56 0.097
444
c ESP024 Esophagitis 62 0.097
445
SPN186 Spinal Cord Injury 66 0.097
446
c INF037 Inflammatory Bowel Disease 56 0.097
447
P ACT210 Acute Respiratory Distress Syndrome 66 0.097
448
c ATS364 Autism 68 0.096
449
P SPN225 Spondyloarthropathy 1 76 0.096
450
RTN023 Retinitis 48 0.096
451
ACR007 Acromegaly 71 0.095
452
c EXN002 Exanthem 62 0.095
453
NPH009 Nephrolithiasis 58 0.095
454
BWN003 Bowenoid Papulosis 43 0.095
455
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.095
456
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.094
457
DRM006 Dermatitis 69 0.094
458
THY028 Thyroid Cancer 72 0.093
459
c LYM025 Lymphedema 55 0.093
460
ATM052 Autoimmune Disease 1 41 0.093
461
ART016 Aortic Aneurysm 71 0.093
462
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.093
463
BRS090 Breast Reconstruction 44 0.093
464
PNM001 Pneumocystosis 58 0.093
465
PSY004 Psychotic Disorder 74 0.093
466
INT075 Intracranial Hypertension 58 0.092
467
GRW007 Growth Hormone Deficiency 53 0.092
468
PNG002 Pain Agnosia 54 0.092
469
c CRD119 Cardiac Arrest 66 0.092
470
c CRD132 Cardiac Conduction Defect 64 0.091
471
GNR004 Generalized Anxiety Disorder 55 0.091
472
SMT008 Smith-Magenis Syndrome 58 0.091
473
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.091
474
P HPT016 Hepatitis B 70 0.090
475
PRS129 Prostatic Hyperplasia, Benign 53 0.090
476
RHM027 Rheumatic Disease 65 0.090
477
GNG013 Gingivitis 63 0.090
478
P HPT073 Hepatitis C Virus 73 0.089
479
NTR027 Neutrophil Actin Dysfunction 32 0.089
480
c GLL020 Gallbladder Disease 64 0.089
481
c AXN002 Axenfeld-Rieger Syndrome 62 0.089
482
c ATX030 Ataxia-Telangiectasia 83 0.089
483
FBR047 Fibromyalgia 62 0.088
484
c LPS004 Lupus Erythematosus 69 0.088
485
P CHR579 Chiari Malformation Type Ii 49 0.088
486
c OVR042 Ovarian Cancer 83 0.088
487
c TRM003 Tremor 56 0.087
488
P MYT020 Myotonic Dystrophy 2 59 0.087
489
ALC007 Alcohol Dependence 70 0.087
490
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.087
491
c CLL015 Collagen Disease 52 0.087
492
AND002 Androgen Insensitivity Syndrome 62 0.087
494
P SYS001 Systemic Lupus Erythematosus 88 0.087
495
STR067 Stroke, Ischemic 84 0.086
496
c THR014 Thrombocytopenia 65 0.086
497
ALR002 Al-Raqad Syndrome 41 0.086
498
ACQ007 Acquired Immunodeficiency Syndrome 66 0.086
499
c MSC003 Muscular Atrophy 56 0.086
500
CLT003 Colitis 65 0.086
501
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.085
502
c ANG001 Angelman Syndrome 65 0.085
503
FRN020 Frontal Fibrosing Alopecia 32 0.085
504
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.085
505
INT007 Intermediate Coronary Syndrome 50 0.085
506
URM002 Uremia 53 0.085
507
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.085
508
CLL003 Cellulitis 61 0.085
509
c GLM007 Glomerulonephritis 62 0.084
510
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.084
511
ART001 Arterial Tortuosity Syndrome 59 0.084
512
P ALP106 Alport Syndrome 1, X-Linked 49 0.084
513
PRS021 Prostatic Adenoma 55 0.084
514
MLN008 Melanoma 64 0.084
515
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 63 0.084
516
c PLM037 Pulmonary Hypertension 77 0.083
517
PRT058 Pure Autonomic Failure 66 0.083
518
SKN016 Skin Disease 68 0.083
519
HPT082 Hepatic Adenomas, Familial 49 0.083
520
SVR004 Severe Combined Immunodeficiency 70 0.083
521
IRN001 Iron Deficiency Anemia 54 0.083
522
HNM002 Hinman Syndrome 29 0.083
523
PSR001 Psoriatic Arthritis 68 0.082
524
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.082
525
c PRC019 Precocious Puberty 52 0.082
526
OCL069 Ocular Motor Apraxia 51 0.082
527
ADP007 Adie Pupil 43 0.082
528
APP008 Appendicitis 66 0.082
529
c HST010 Histiocytosis 63 0.081
530
BCT004 Bacteriuria 52 0.081
531
ANV001 Anovulation 49 0.081
532
ALX002 Alexithymia 43 0.080
533
P AMY091 Amyotrophic Lateral Sclerosis 1 90 0.080
534
P ATS007 Autism Spectrum Disorder 68 0.080
535
c INT068 Intestinal Disease 62 0.080
536
c RTN008 Retinitis Pigmentosa 79 0.080
537
BCT022 Bacterial Infectious Disease 63 0.080
538
c PYL005 Pyelonephritis 57 0.080
539
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.080
540
CLB026 Colobomatous Microphthalmia 40 0.080
541
BRN038 Bronchial Disease 58 0.080
542
c MYC084 Mycobacterium Tuberculosis 1 68 0.079
543
LNG108 Langerhans Cell Histiocytosis 63 0.079
544
P MGR028 Migraine with or Without Aura 1 69 0.079
545
CRN030 Coronary Stenosis 52 0.079
546
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.079
547
ALS001 Alstrom Syndrome 55 0.079
548
c KDN017 Kidney Cancer 59 0.078
549
BRC012 Brucellosis 71 0.078
550
NRR001 Neuroretinitis 48 0.078
551
PST011 Pustulosis of Palm and Sole 50 0.078
552
c LNG032 Lung Cancer 99 0.078
553
c ACR001 Aicardi-Goutieres Syndrome 63 0.078
554
c HYP076 Hyperthyroidism 56 0.078
555
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.078
556
c PRS038 Personality Disorder 68 0.077
557
c ALC004 Alcohol Abuse 69 0.077
558
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 23 0.077
559
SCH012 Schizoaffective Disorder 54 0.077
560
MYC088 Mycobacterium Avium Complex Infections 34 0.077
561
AND005 Androgen Insensitivity Syndrome, Mild 19 0.077
562
CHL004 Cholelithiasis 52 0.077
563
c HYP050 Hyperinsulinemic Hypoglycemia 55 0.077
564
P ACR116 Aicardi-Goutieres Syndrome 1 48 0.077
565
VTM002 Vitamin B12 Deficiency 48 0.077
566
END040 Endogenous Depression 59 0.076
567
CNS004 Constipation 58 0.076
568
c NRC002 Narcolepsy 59 0.075
569
SKN027 Skin Conditions 51 0.075
570
DWR001 Dwarfism 48 0.075
571
c MYP004 Myopathy 65 0.075
572
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.075
573
AMN001 Amenorrhea 56 0.075
574
P SCN007 Secondary Hyperparathyroidism 56 0.075
575
c RCT021 Rectum Cancer 58 0.075
576
c LPM005 Lipomatosis 53 0.074
577
P HPT003 Hepatitis a 66 0.074
578
FSC004 Fasciitis 50 0.074
579
c DYS021 Dysautonomia 49 0.074
580
CRH001 Crohn's Disease 79 0.074
581
RFR010 Refractory Anemia 41 0.074
582
c DRM053 Dermatitis, Atopic 73 0.074
583
c TRN020 Turner Syndrome 72 0.074
584
c GST044 Gastritis 61 0.074
585
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.074
586
PLY112 Polyarteritis Nodosa, Childhood-Onset 51 0.074
587
IGG001 Iga Glomerulonephritis 58 0.073
588
c HYP265 Hypotonia 43 0.073
589
WRN001 Werner Syndrome 74 0.073
590
VRL011 Viral Infectious Disease 69 0.073
591
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.073
592
c TTR001 Tetralogy of Fallot 71 0.073
593
GSG001 Gas Gangrene 48 0.073
594
PNC034 Pancreas Disease 60 0.072
595
ULC005 Ulcer of Lower Limbs 24 0.072
596
ATN002 Autonomic Nervous System Disease 54 0.072
597
BRN071 Brain Injury 54 0.071
598
CHR100 Chronic Ulcer of Skin 53 0.071
599
P ACT071 Acute Kidney Failure 54 0.071
600
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.071
601
INT002 Intermittent Claudication 64 0.071
602
c NPH012 Nephrotic Syndrome 59 0.071
603
NCR002 Necrobiosis Lipoidica 39 0.070
604
CLR108 Colorectal Adenoma 64 0.070
605
HPR003 Heparin-Induced Thrombocytopenia 49 0.069
606
PRS063 Paresthesia 45 0.069
607
ADL002 Adult Syndrome 55 0.069
608
SKN023 Skin Tag 43 0.069
609
c CND004 Candidiasis 63 0.068
610
DYS073 Dysphagia 53 0.068
611
c FCL005 Focal Segmental Glomerulosclerosis 60 0.068
612
P BRD010 Bardet-Biedl Syndrome 1 58 0.068
613
GST049 Gastrointestinal System Cancer 62 0.068
614
GST071 Gastrointestinal Carcinoma 46 0.068
615
c BLD134 Bladder Cancer 71 0.068
616
c RST001 Restless Legs Syndrome 60 0.068
617
ASP030 Aspirin Resistance 46 0.068
618
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.068
619
PHK010 Phakomatosis Spilorosea 18 0.068
620
P ACT074 Acute Lymphocytic Leukemia 62 0.068
621
SYS003 Systolic Heart Failure 46 0.068
622
PNC033 Pancreas Adenocarcinoma 67 0.068
623
LRN002 Laron Syndrome 63 0.067
624
INT303 Intracranial Hypertension, Idiopathic 53 0.067
625
MYL005 Myelofibrosis 70 0.067
626
BNR002 Bone Resorption Disease 54 0.067
627
c SBS003 Substance Abuse 61 0.067
628
PRT036 Peritonitis 67 0.067
629
MYL069 Myeloma, Multiple 85 0.066
630
PLM010 Pulmonary Edema 60 0.066
631
c MYL006 Myeloid Leukemia 68 0.066
632
c MLN007 Male Infertility 52 0.066
633
BRS051 Breast Disease 68 0.066
634
c SZR006 Seizure Disorder 61 0.066
635
HRN026 Hernia, Hiatus 49 0.066
636
c PHC003 Pheochromocytoma 73 0.066
637
CRT013 Carotid Stenosis 52 0.066
638
c PSD015 Pseudohypoparathyroidism 51 0.066
639
OST097 Osteoporotic Fracture 36 0.065
640
CYS009 Cystadenoma 41 0.065
641
DYS014 Dyspepsia 56 0.065
642
c ADL010 Adult Respiratory Distress Syndrome 64 0.065
643
OBS082 Obstructive Nephropathy 52 0.065
644
GTR002 Goiter 54 0.065
645
HMT018 Hematopoietic Stem Cell Transplantation 59 0.065
646
PPT005 Peptic Ulcer Disease 64 0.065
647
TRN015 Transient Cerebral Ischemia 59 0.064
648
CHL123 Chlamydia 66 0.064
649
c SLL003 Salla Disease 53 0.064
650
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.064
651
STS002 Situs Inversus 50 0.064
652
c MMP001 Mumps 61 0.064
653
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.064
654
SRC014 Sarcoma 70 0.064
655
c SJG008 Sjogren Syndrome 60 0.064
656
PST021 Postpartum Depression 55 0.064
657
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.064
658
c OPN001 Open-Angle Glaucoma 53 0.063
659
c GLY013 Glycogen Storage Disease 62 0.063
660
PLM017 Pulmonary Alveolar Microlithiasis 52 0.063
661
c RHN004 Rhinitis 63 0.063
662
c CMR001 Camurati-Engelmann Disease 62 0.063
663
LYM027 Lymphopenia 57 0.063
664
CRT016 Carotid Artery Disease 58 0.062
665
P VRL010 Viral Hepatitis 60 0.062
666
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.062
667
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.062
668
PRP030 Purpura 62 0.062
669
c SCL057 Scoliosis, Isolated 1 46 0.062
670
LYM133 Lymphoma, Hodgkin, Classic 73 0.062
671
c SNS001 Sensorineural Hearing Loss 60 0.062
672
IRR002 Irritable Bowel Syndrome 64 0.061
673
RCK004 Rickets 66 0.061
674
P LKM060 Leukemia, Acute Lymphoblastic 3 52 0.061
675
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 55 0.061
676
P LRG017 Large Intestine Cancer 63 0.061
677
c PLY018 Polycythemia 60 0.061
678
c DLT002 Dilated Cardiomyopathy 74 0.061
679
HMC014 Homocysteinemia 52 0.061
680
P CRP023 Carpenter Syndrome 1 59 0.061
681
DMP001 Dumping Syndrome 46 0.061
682
P BLD140 Blood Group, I System 26 0.061
683
NCR007 Necrotizing Fasciitis 51 0.060
684
PMP004 Pemphigus Foliaceus 47 0.060
685
c NRF023 Neurofibromatosis, Type Ii 76 0.060
686
P PTT057 Pituitary Adenoma 4, Acth-Secreting 55 0.060
687
HYP081 Hypolipoproteinemia 49 0.060
688
BRB001 Beriberi 43 0.060
689
ERY029 Erythermalgia, Primary 58 0.060
690
P LKM061 Leukemia, Acute Myeloid 83 0.060
691
HMN044 Human Immunodeficiency Virus Type 1 75 0.060
692
OPT006 Optic Nerve Disease 60 0.060
693
LRN003 Learning Disability 53 0.060
694
ACH005 Achalasia 54 0.060
695
DVR002 Diverticulitis 46 0.060
696
DYS011 Dyskinesia of Esophagus 42 0.060
697
ESP021 Esophageal Cancer 84 0.060
698
P PRM005 Primary Hyperparathyroidism 60 0.060
699
P PNC106 Pancreatic Agenesis 1 52 0.059
700
SLD003 Sialadenitis 49 0.059
701
c PRK057 Parkinson Disease, Late-Onset 77 0.059
702
c HYP061 Hypertrophic Cardiomyopathy 59 0.059
703
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 0.059
704
LPD012 Lipoid Congenital Adrenal Hyperplasia 72 0.059
705
SPN051 Spondylitis 55 0.059
706
c RNL007 Renal Tubular Acidosis 51 0.059
707
UND005 Undifferentiated Pleomorphic Sarcoma 51 0.059
708
EPD070 Epidermoid Cysts 50 0.058
709
WRN003 Wernicke Encephalopathy 49 0.058
710
c PLY014 Polycystic Kidney Disease 63 0.058
711
ERY003 Erythema Multiforme 63 0.058
712
HYD002 Hydronephrosis 52 0.058
713
ALL003 Allergic Rhinitis 69 0.058
714
HSH003 Hashimoto Thyroiditis 67 0.058
715
NWB001 Newborn Respiratory Distress Syndrome 61 0.058
716
c CMP008 Compartment Syndrome 52 0.058
717
P LBR014 Leber Congenital Amaurosis 4 55 0.058
718
c FML012 Familial Partial Lipodystrophy 52 0.058
719
c VNS003 Venous Insufficiency 54 0.058
720
OST017 Osteomyelitis 65 0.057
721
FRL002 Froelich Syndrome 20 0.057
722
CRV035 Cervical Cancer 76 0.057
723
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.057
724
FCL044 Fecal Incontinence 38 0.057
725
CHL065 Cholangiocarcinoma 65 0.057
726
c MSC033 Muscle Disorders 56 0.057
727
P PTT056 Pituitary Adenoma 1, Multiple Types 51 0.057
728
c HYD006 Hydrocephalus 66 0.057
729
BLD163 Blood Group, Dombrock System 23 0.057
730
ULC004 Ulcerative Colitis 80 0.057
731
c PLY006 Polydactyly 58 0.056
732
c VSC011 Vasculitis 67 0.056
733
END062 Endometrial Hyperplasia 51 0.056
734
c ALP008 Alopecia 56 0.056
735
P CRD065 Cardiomyopathy, Familial Hypertrophic, 2 45 0.056
736
INT051 Intussusception 51 0.056
737
CRB037 Cerebral Palsy 71 0.056
738
MTC005 Mitochondrial Metabolism Disease 46 0.056
739
RSP007 Respiratory Distress Syndrome, Infant 38 0.056
740
c END033 Endocarditis 60 0.055
741
P GRV008 Graves Disease 1 57 0.055
742
c MCR010 Microcephaly 59 0.055
743
GST045 Gastroenteritis 65 0.055
744
GYN001 Gynecomastia 47 0.055
745
P MJR004 Major Affective Disorder 4 40 0.055
746
EXC002 Exocrine Pancreatic Insufficiency 42 0.055
747
c PNS012 Paine Syndrome 63 0.055
748
P CHR682 Chronic Bilirubin Encephalopathy 22 0.055
749
P FCL025 Focal Segmental Glomerulosclerosis 1 52 0.055
750
SLP010 Slipped Capital Femoral Epiphysis 38 0.055
751
SCL022 Scleredema 31 0.055
752
P CNT075 Central Precocious Puberty 52 0.054
753
c BCL006 B-Cell Lymphomas 66 0.054
754
TRM010 Traumatic Brain Injury 56 0.054
755
END038 Endocrine Pancreas Disease 36 0.054
756
ACR006 Aceruloplasminemia 72 0.054
757
FRZ001 Frozen Shoulder 53 0.054
758
CRD223 Cardiac Arrhythmia 56 0.054
759
HMS001 Hemosiderosis 52 0.054
760
WLL001 Williams-Beuren Syndrome 64 0.053
761
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.053
762
MYL009 Myelodysplastic Syndrome 71 0.053
763
c PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 70 0.053
764
ART002 Arts Syndrome 56 0.053
765
CHL147 Chlamydia Pneumonia 42 0.053
766
c SRC025 Sarcoidosis 1 76 0.053
767
P CNT035 Central Nervous System Disease 65 0.053
768
c THR015 Thrombophilia 56 0.053
769
PST053 Postherpetic Neuralgia 45 0.053
770
ART008 Arteriosclerosis Obliterans 42 0.053
771
c PNC045 Pancreatic Agenesis 40 0.053
772
c ENC004 Encephalitis 66 0.053
773
c FNG006 Feingold Syndrome 1 47 0.053
774
HYP085 Hypothalamic Disease 46 0.053
775
OTT002 Otitis Media 68 0.053
776
PRP016 Paraplegia 55 0.053
777
VRC005 Varicose Veins 67 0.053
778
HYP068 Hyperostosis 52 0.053
779
DST006 Diastolic Heart Failure 46 0.053
780
FXF002 Fox-Fordyce Disease 41 0.053
781
c MGL001 Megaloblastic Anemia 52 0.052
782
DXT002 Dextrocardia with Situs Inversus 39 0.052
783
STF001 Stiff-Person Syndrome 64 0.052
784
P HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 62 0.052
785
KRT002 Keratomalacia 51 0.052
786
P INF145 Infantile Liver Failure Syndrome 1 48 0.052
787
VSC002 Vascular Dementia 58 0.052
788
c MSC005 Muscular Dystrophy 66 0.052
789
TBC004 Tobacco Addiction 64 0.052
790
HYP784 Hypogonadism, Male 43 0.052
791
MNS002 Mini Stroke 25 0.052
792
CLC006 Calcinosis 53 0.052
793
c CHL066 Cholangitis 52 0.052
794
c ALP009 Alopecia Areata 68 0.051
795
TND004 Tendinopathy 47 0.051
796
DCB001 Decubitus Ulcer 47 0.051
797
HYP110 Hyperproinsulinemia 41 0.051
798
c UTR058 Uterine Anomalies 60 0.051
799
HDR002 Hidradenitis Suppurativa 57 0.051
800
HDR003 Hidradenitis 49 0.051
801
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.051
802
P SML038 Small Cell Cancer of the Lung 69 0.051
803
P ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.051
804
CRN024 Corneal Disease 45 0.051
805
SPN027 Spinal Stenosis 62 0.051
806
c NTR004 Neutropenia 61 0.051
807
CHL068 Cholestasis 60 0.051
808
c HYP614 Hyperlipidemia, Familial Combined 56 0.050
809
EXP004 Exophthalmos 52 0.050
810
P MYT021 Myotonic Dystrophy 1 72 0.050
812
P JVN010 Juvenile Rheumatoid Arthritis 72 0.050
813
END072 Endotheliitis 39 0.050
814
c PTS002 Ptosis 55 0.050
815
CLC001 Calciphylaxis 53 0.050
816
c HYP607 Hypercholesterolemia, Familial 82 0.050
817
HYP026 Hypoglycemic Coma 44 0.050
818
c ACT105 Acute Mountain Sickness 58 0.050
819
PNN001 Panniculitis 52 0.050
820
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.050
821
IDP033 Idiopathic Edema 42 0.050
822
c INT070 Intestinal Obstruction 55 0.049
823
FND002 Fundus Dystrophy 51 0.049
824
ALL014 Allergic Encephalomyelitis 43 0.049
825
c ASP006 Aspergillosis 67 0.049
826
c MYS003 Myasthenia Gravis 74 0.049
827
CYT008 Cytomegalovirus Infection 61 0.049
828
SQM006 Squamous Cell Carcinoma 59 0.049
829
c PTT006 Pituitary Adenoma 54 0.049
830
URN022 Urinary Tract Infections, Recurrent 34 0.049
831
c CHR084 Chromosomal Disease 40 0.049
832
ELP001 Elephantiasis 38 0.049
833
P HMP029 Hemophilia a 70 0.049
834
P ART101 Aortic Valve Disease 2 68 0.049
835
DRG003 Drug Dependence 51 0.049
836
GNG011 Gingival Disease 49 0.049
837
c ACQ009 Acquired Metabolic Disease 32 0.049
838
c FML035 Familial Hyperlipidemia 50 0.048
839
P EPS039 Episodic Pain Syndrome, Familial, 1 27 0.048
840
MCR011 Microinvasive Gastric Cancer 47 0.048
841
P ACT073 Acute Leukemia 62 0.048
842
P SVR005 Severe Pre-Eclampsia 55 0.048
843
c DDN001 Duodenal Ulcer 52 0.048
844
c ART084 Arteriovenous Fistula 50 0.048
845
CLS049 Classic Phenylketonuria 38 0.048
846
c MYP006 Myopia 62 0.048
847
CHL067 Cholecystitis 59 0.048
848
BLL003 Bell's Palsy 53 0.048
849
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 43 0.048
850
BLD165 Blood Group, Colton System 23 0.048
851
SWL001 Swallowing Disorders 36 0.048
852
BRN024 Bronchitis 70 0.047
853
HYP020 Hyperprolactinemia 64 0.047
854
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 46 0.047
855
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.047
856
PSD088 Pseudobulbar Affect 39 0.047
857
P GLC092 Glaucoma, Primary Open Angle 58 0.047
858
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 43 0.047
859
STT004 Steatorrhea 43 0.047
860
MLR004 Malaria 85 0.047
861
P LPD040 Lipodystrophy, Familial Partial, Type 1 43 0.047
862
HRT012 Heart Valve Disease 57 0.046
863
PSD014 Pseudopseudohypoparathyroidism 56 0.046
864
PRT018 Portal Vein Thrombosis 51 0.046
865
SPN021 Spinal Meningioma 50 0.046
866
CLR030 Clear Cell Renal Cell Carcinoma 49 0.046
867
INT079 Intrahepatic Cholangiocarcinoma 55 0.046
868
TTH006 Tooth Disease 54 0.046
869
P MYS011 Myasthenia Gravis Congenital 33 0.046
870
CHL014 Cholera 61 0.046
871
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.046
872
c SKN015 Skin Carcinoma 65 0.046
873
CLN019 Colonic Disease 62 0.046
874
c HLP001 Holoprosencephaly 65 0.046
875
NNT012 Neonatal Jaundice 52 0.046
876
SNL007 Senile Cataract 40 0.046
877
ALL006 Allergic Asthma 61 0.046
878
SFT003 Soft Tissue Sarcoma 60 0.046
879
c END044 Endometriosis 65 0.045
880
P CNG006 Congenital Hypothyroidism 64 0.045
881
PST028 Post-Traumatic Stress Disorder 63 0.045
882
c HMP007 Hemophilia 62 0.045
883
P HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 57 0.045
884
CNN005 Connective Tissue Disease 67 0.045
885
RDC002 Radiculopathy 54 0.045
886
DSR011 Disorganization, Mouse, Homolog of 23 0.045
887
GLN010 Glanzmann Thrombasthenia 69 0.045
888
GLL008 Gilles De La Tourette Syndrome 69 0.045
889
HYP030 Hypoactive Sexual Desire Disorder 44 0.045
890
P PRM038 Primary Agammaglobulinemia 39 0.045
891
c SCL018 Scoliosis 59 0.045
892
c PLV020 Pelvic Organ Prolapse 64 0.045
893
SPN041 Spinal Cord Disease 55 0.045
894
c ANL018 Analbuminemia 48 0.045
895
LRN001 Laurence-Moon Syndrome 46 0.045
896
OVR094 Ovarian Epithelial Cancer 41 0.045
897
CRD220 Cardiac Valvular Defect, Developmental 36 0.045
898
SYN007 Synovitis 61 0.044
899
CRH005 Crohn's Colitis 61 0.044
900
SPN035 Spindle Cell Sarcoma 52 0.044
901
P HNT004 Huntington Disease-Like 2 48 0.044
902
c CHR071 Charcot-Marie-Tooth Disease 65 0.044
903
HMR039 Hemorrhage, Intracerebral 62 0.044
904
HRP004 Herpes Zoster 63 0.044
905
CRB009 Cerebritis 39 0.044
906
ACH004 Achondroplasia 69 0.044
907
ALB001 Albright's Hereditary Osteodystrophy 55 0.044
908
P PSD108 Pseudohypoparathyroidism, Type Ia 57 0.044
909
c OCY003 Oocyte Maturation Defect 1 42 0.044
910
HYP017 Hypophosphatemia 48 0.043
911
FRN014 Fournier Gangrene 42 0.043
912
c MYC008 Myocarditis 59 0.043
913
CRB085 Cerebral Hemorrhage 46 0.043
914
SDD008 Sudden Sensorineural Hearing Loss 46 0.043
915
c NRB001 Neuroblastoma 73 0.043
916
IGR001 Ige Responsiveness, Atopic 59 0.043
917
c GLM045 Glioma 56 0.043
918
c KRT007 Keratoconus 50 0.043
919
SYN036 Syncope 49 0.043
920
PTL001 Patulous Eustachian Tube 31 0.043
921
RTN017 Retinal Detachment 62 0.043
922
INT253 Intestinal Benign Neoplasm 57 0.043
923
CHR005 Chorioamnionitis 53 0.043
924
c RTN024 Retinoblastoma 73 0.043
925
MNC006 Monoclonal Gammopathy of Uncertain Significance 54 0.043
926
P CHR431 Chronic Venous Insufficiency 50 0.043
927
BRC010 Brachial Plexus Lesion 46 0.043
928
CRY036 Cryptogenic Cirrhosis 38 0.043
929
GST007 Gastric Dilatation 32 0.043
930
CMP010 Complex Regional Pain Syndrome 64 0.043
931
CHR073 Choreatic Disease 50 0.043
932
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 49 0.043
933
P FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.043
934
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.043
935
SCK003 Sickle Cell Anemia 75 0.042
936
c SNS014 Sinusitis 64 0.042
937
TND005 Tendinitis 45 0.042
938
BRK012 Broken Heart Syndrome 39 0.042
939
c PRT013 Portal Hypertension 61 0.042
940
LYM019 Lymphosarcoma 59 0.042
941
BLD044 Bladder Disease 57 0.042
942
MSC190 Muscular Disease 55 0.042
943
BLR008 Bilirubin Metabolic Disorder 53 0.042
944
ADR040 Adrenal Gland Pheochromocytoma 48 0.042
945
EMP001 Empty Sella Syndrome 43 0.042
946
MSC004 Muscle Tissue Disease 39 0.042
947
P MNN043 Meningioma, Familial 63 0.042
948
TRC026 Tracheal Disease 37 0.042
949
c HRP006 Herpes Simplex 71 0.042
950
c HML002 Hemolytic Anemia 65 0.042
951
DSS009 Disseminated Intravascular Coagulation 58 0.042
952
c ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 53 0.042
953
NPH010 Nephrosclerosis 46 0.042
954
c BNC003 Bone Cancer 61 0.042
955
ANG020 Angiosarcoma 59 0.042
956
AML029 Ameloblastoma 53 0.042
957
P LPM012 Lipomatosis, Multiple 66 0.042
958
c ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 54 0.042
959
KWS001 Kwashiorkor 46 0.042
960
P LKM063 Leukemia, Chronic Myeloid 74 0.041
961
c ANT006 Antiphospholipid Syndrome 60 0.041
962
SHH001 Sheehan Syndrome 51 0.041
963
DGR001 Digeorge Syndrome 62 0.041
964
P AMY009 Amyloidosis Aa 56 0.041
965
ISL003 Isolated Growth Hormone Deficiency 53 0.041
966
c END046 Endometritis 53 0.041
967
c HYP263 Hypersomnia 45 0.041
968
SCR011 Scrapie 42 0.041
969
CHR008 Choroiditis 44 0.041
970
APL001 Aplastic Anemia 75 0.041
971
c BCK002 Beckwith-Wiedemann Syndrome 59 0.041
972
VSL002 Visual Epilepsy 33 0.041
973
PYD002 Pyoderma 53 0.040
974
GLC022 Glucose/galactose Malabsorption 44 0.040
975
c TXP001 Toxoplasmosis 65 0.040
976
P CNR004 Cone-Rod Dystrophy 2 63 0.040
977
PHN003 Phenylketonuria 75 0.040
978
NNT019 Neonatal Hypothyroidism 42 0.040
979
RCT017 Rectal Disease 42 0.040
980
PLM005 Pleomorphic Lipoma 39 0.040
981
END041 Endometrial Adenocarcinoma 60 0.040
982
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.040
983
PRS042 Prostate Disease 47 0.040
984
SCR001 Secretory Meningioma 40 0.040
985
INT146 Intervertebral Disc Disease 65 0.040
986
PRT038 Protein-Energy Malnutrition 53 0.040
987
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.040
988
GST019 Gastrointestinal Stromal Tumor 74 0.039
989
GST040 Gastric Adenocarcinoma 66 0.039
990
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.039
991
PPT001 Peptic Esophagitis 45 0.039
992
KPS004 Kaposi Sarcoma 77 0.039
993
c THR005 Thrombotic Thrombocytopenic Purpura 65 0.039
994
c SLV001 Silver-Russell Syndrome 58 0.039
995
HDN002 Head Injury 52 0.039
996
ISL001 Islet Cell Tumor 51 0.039
997
OCC006 Occipital Horn Syndrome 50 0.039
998
HYP077 Hypertrichosis 49 0.039
999
c OPT070 Optic Nerve Hypoplasia, Bilateral 49 0.039
1000
MTR007 Motor Peripheral Neuropathy 41 0.039
1001
P CRT085 Carotid Intimal Medial Thickness 2 25 0.039
1002
c LTR001 Lateral Sclerosis 60 0.039
1003
INF034 Infective Endocarditis 57 0.039
1004
PRS047 Prostatitis 57 0.039
1005
ICH020 Ichthyosis Prematurity Syndrome 45 0.039
1006
AYM001 Ayme-Gripp Syndrome 39 0.039
1007
CLR109 Colorectal Adenocarcinoma 54 0.038
1008
c BLD051 Blood Coagulation Disease 51 0.038
1009
INT052 Intestinal Volvulus 43 0.038
1010
c TMP003 Temporal Arteritis 68 0.038
1011
c HYP098 Hypereosinophilic Syndrome 67 0.038
1012
P ATM011 Autoimmune Hepatitis 66 0.038
1013
ART004 Aortic Atherosclerosis 45 0.038
1014
MNC002 Munchausen by Proxy 32 0.038
1015
c GRF003 Graft-Versus-Host Disease 72 0.038
1016
c KBK002 Kabuki Syndrome 1 67 0.038
1017
c ICH004 Ichthyosis 57 0.038
1018
c ACT010 Acth-Secreting Pituitary Adenoma 52 0.038
1019
OST011 Osteomalacia 52 0.038
1020
PPL021 Papilledema 49 0.038
1021
NRT001 Neurotic Disorder 48 0.038
1022
c MYS005 Myositis 62 0.038
1023
CHK001 Chikungunya 61 0.038
1024
ACT055 Actinomycosis 45 0.038
1025
MYX004 Myxedema 44 0.038
1026
P CRD093 Cardiomyopathy, Dilated, 1a 41 0.038
1027
MDS022 Mediastinitis 41 0.038
1028
IMM001 Immune-Complex Glomerulonephritis 38 0.038
1029
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 35 0.037
1030
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.037
1031
P PLM022 Pulmonary Valve Insufficiency 44 0.037
1032
BRN028 Brain Cancer 74 0.037
1033
P VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.037
1034
PLL001 Pallister-Hall Syndrome 63 0.037
1035
URT039 Urticaria 60 0.037
1036
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.037
1037
P CNG216 Congenital Hydrocephalus 56 0.037
1038
CHN055 Chanarin-Dorfman Syndrome 56 0.037
1039
c MYT002 Myotonic Dystrophy 52 0.037
1040
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.037
1041
GLC096 Galactorrhea 47 0.037
1042
P HYP768 Hyperlipoproteinemia, Type I 42 0.037
1043
P HNT011 Huntington Disease-Like 3 40 0.037
1044
NTR007 Neutral Lipid Storage Disease with Myopathy 38 0.037
1045
P BPL002 Bipolar I Disorder 50 0.037
1046
P BRD016 Bardet-Biedl Syndrome 4 46 0.037
1047
HPT067 Hepatocellular Adenoma 45 0.037
1048
DDN027 Duodenum Disease 43 0.037
1049
P BRD015 Bardet-Biedl Syndrome 3 41 0.037
1050
BRN056 Bronchopulmonary Dysplasia 61 0.037
1051
P THY109 Thyroid Cancer, Nonmedullary, 1 60 0.037
1052
P HYP602 Hyperoxaluria, Primary, Type Ii 38 0.037
1053
XP2001 Xp22.3 Microdeletion Syndrome 26 0.037
1054
CMP096 Complete Generalized Lipodystrophy 23 0.037
1055
CRN167 Caronte 19 0.037
1056
CNT097 Central Hypoventilation Syndrome, Congenital 67 0.037
1057
ING001 Inguinal Hernia 61 0.037
1058
c PLM034 Pulmonary Emphysema 59 0.037
1059
PHR003 Pharyngitis 58 0.037