Search results for obesity OR diabetes

4293 hits were found for obesity OR diabetes

# Family MCID Name MIFTS Score
1
BDY004 Body Mass Index Quantitative Trait Locus 11 78 8.516
2
DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 4.743
3
DBT009 Diabetes Mellitus 67 4.392
4
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.249
5
DBT085 Diabetes Mellitus, Insulin-Dependent 72 3.321
6
MRB003 Morbid Obesity 61 2.692
7
MCR115 Microvascular Complications of Diabetes 5 70 2.674
8
GST033 Gestational Diabetes 62 2.651
9
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 2.434
10
DBT087 Diabetes Insipidus, Neurohypophyseal 62 2.413
11
c MCR113 Microvascular Complications of Diabetes 3 57 2.405
12
c MCR120 Microvascular Complications of Diabetes 7 44 2.404
13
c BDY019 Body Mass Index Quantitative Trait Locus 18 42 2.094
14
c BDY020 Body Mass Index Quantitative Trait Locus 19 41 2.093
15
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 2.093
16
DBT084 Diabetes Mellitus, Ketosis-Prone 60 2.075
17
c MCR130 Microvascular Complications of Diabetes 6 43 2.072
18
c MCR133 Microvascular Complications of Diabetes 4 43 2.072
19
c MCR129 Microvascular Complications of Diabetes 1 64 2.039
20
DBT083 Diabetes Mellitus, Permanent Neonatal 62 1.982
21
RNL051 Renal Cysts and Diabetes Syndrome 54 1.937
22
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 66 1.921
23
c BDY011 Body Mass Index Quantitative Trait Locus 10 40 1.846
24
MTR082 Maturity-Onset Diabetes of the Young, Type 8, with Exocrine Dysfunction 42 1.763
25
MTR004 Maturity-Onset Diabetes of the Young 60 1.757
26
DBT010 Diabetic Neuropathy 58 1.743
27
LPT006 Leptin Receptor Deficiency 43 1.722
28
DBT005 Diabetes Insipidus 52 1.694
29
c MCR112 Microvascular Complications of Diabetes 2 42 1.680
30
DBT090 Diabetes and Deafness, Maternally Inherited 45 1.596
31
OBS037 Obesity-Hypoventilation Syndrome 51 1.531
32
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 1.527
33
LPT014 Leptin Deficiency or Dysfunction 40 1.494
34
c DBT064 Diabetes Mellitus, Transient Neonatal, 1 47 1.470
35
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 45 1.446
36
OBS015 Obesity, Hyperphagia, and Developmental Delay 26 1.437
37
MNT318 Mental Retardation, Truncal Obesity, Retinal Dystrophy, and Micropenis Syndrome 26 1.436
38
c BDY005 Body Mass Index Quantitative Trait Locus 9 33 1.425
39
c BDY006 Body Mass Index Quantitative Trait Locus 8 31 1.425
40
c BDY012 Body Mass Index Quantitative Trait Locus 7 31 1.425
41
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 1.423
42
c BDY010 Body Mass Index Quantitative Trait Locus 4 31 1.423
43
MHM001 Mehmo Syndrome 31 1.417
44
DBT008 Diabetic Angiopathy 44 1.405
45
c MTR026 Maturity-Onset Diabetes of the Young, Type 9 33 1.399
46
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 1.387
47
WDH003 Woodhouse-Sakati Syndrome 52 1.365
48
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 46 1.348
49
c MTR023 Maturity-Onset Diabetes of the Young, Type 6 41 1.337
50
c MTR024 Maturity-Onset Diabetes of the Young, Type 7 42 1.335
51
MRB006 Morbid Obesity and Spermatogenic Failure 20 1.323
52
CHN016 Cohen Syndrome 54 1.316
53
c MTR020 Maturity-Onset Diabetes of the Young, Type 3 53 1.303
54
c LPD015 Lipodystrophy, Familial Partial, Type 2 56 1.254
55
DBT004 Diabetic Polyneuropathy 50 1.254
56
MMS001 Momo Syndrome 30 1.247
57
CNG376 Congenital Leptin Deficiency 29 1.246
58
RTN173 Retinal Dystrophy and Obesity 19 1.244
59
WLM019 Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation, and Obesity Syndrome 14 1.237
60
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 40 1.229
61
DBT002 Diabetic Autonomic Neuropathy 44 1.206
62
WLF004 Wolfram Syndrome 61 1.193
63
ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.182
64
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 41 1.180
65
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 1.178
66
c DBT094 Diabetes Mellitus, Insulin-Dependent, 10 20 1.163
67
c DBT034 Diabetes Mellitus, Insulin-Dependent, 20 19 1.162
68
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 1.160
69
NNT009 Neonatal Diabetes Mellitus 47 1.140
70
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 29 1.138
71
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 22 1.110
72
c DBT040 Diabetes Mellitus, Insulin-Dependent, 2 30 1.109
73
DBT022 Diabetes Mellitus, Neonatal, with Congenital Hypothyroidism 26 1.106
74
PRP098 Proprotein Convertase 1/3 Deficiency 29 1.099
75
c MTR075 Maturity-Onset Diabetes of the Young, Type 13 40 1.061
76
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 51 1.055
77
c MTR074 Maturity-Onset Diabetes of the Young, Type 14 34 1.054
78
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 39 1.051
79
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 77 1.050
80
c DBT098 Diabetes Mellitus, Transient Neonatal, 2 15 1.042
81
c DBT038 Diabetes Mellitus, Insulin-Dependent, 5 18 1.041
82
c DBT032 Diabetes Mellitus, Insulin-Dependent, 22 15 1.040
83
DBT062 Diabetic Foot Ulcers 57 1.027
84
BRT037 Brittle Diabetes 23 1.026
85
DBT006 Diabetic Macular Edema 50 1.024
86
DBT007 Diabetic Cataract 35 1.008
87
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.987
88
PNL019 Pineal Hyperplasia, Insulin-Resistant Diabetes Mellitus, and Somatic Abnormalities 56 0.987
89
DBT092 Diabetes Insipidus, Nephrogenic, X-Linked 37 0.983
90
c DBT044 Diabetes Mellitus, Transient Neonatal, 3 16 0.982
92
PNC104 Pancreatic and Cerebellar Agenesis 26 0.973
93
c DBT082 Diabetes Mellitus, Insulin-Dependent, 12 17 0.971
94
INS010 Insulin-Resistant Acanthosis Nigricans, Type a 24 0.969
95
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 14 0.950
96
CHP002 Chops Syndrome 33 0.933
97
FNC060 Fanconi Renotubular Syndrome 4 with Maturity-Onset Diabetes of the Young 20 0.905
98
c DBT054 Diabetes Mellitus, Insulin-Dependent, 24 28 0.904
99
c DBT077 Diabetes Mellitus, Insulin-Dependent, 19 15 0.902
100
c DBT053 Diabetes Mellitus, Insulin-Dependent, 23 14 0.902
101
c DBT079 Diabetes Mellitus, Insulin-Dependent, 21 14 0.901
102
DBT060 Diabetes Mellitus, Insulin-Dependent, X-Linked 8 0.899
103
DVL020 Developmental Delay, Intellectual Disability, Obesity, and Dysmorphic Features 21 0.888
104
HYD021 Hydrocephalus Obesity Hypogonadism 17 0.888
105
ANR042 Aniridia - Ptosis - Intellectual Disability - Familial Obesity 16 0.886
106
CLB031 Coloboma-Obesity-Hypogenitalism-Mental Retardation Syndrome 16 0.882
107
BCK003 Background Diabetic Retinopathy 40 0.879
108
MTC025 Mitochondrial Myopathy with Diabetes 20 0.828
109
DBT020 Diabetes Mellitus, Insulin-Resistant, with Acanthosis Nigricans 20 0.826
110
c DBT033 Diabetes Mellitus, Noninsulin-Dependent, 2 15 0.823
111
OBS050 Obesity Due to Congenital Leptin Deficiency 18 0.804
112
c TYP038 Type 1 Diabetes Mellitus 15 24 0.801
113
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 13 0.793
114
EPP024 Epiphyseal Dysplasia, Multiple, with Early-Onset Diabetes Mellitus 49 0.768
115
FBR065 Fibrocalculous Pancreatopathy 18 0.767
116
SVR002 Severe Nonproliferative Diabetic Retinopathy 33 0.764
117
MNG006 Monogenic Diabetes 39 0.758
118
RHH001 Rohhad 24 0.758
119
c TYP035 Type 1 Diabetes Mellitus 11 29 0.753
120
c TYP031 Type 1 Diabetes Mellitus 5 25 0.752
121
c TYP033 Type 1 Diabetes Mellitus 7 27 0.751
122
c TYP037 Type 1 Diabetes Mellitus 13 29 0.748
123
c TYP028 Type 1 Diabetes Mellitus 2 26 0.747
124
c TYP036 Type 1 Diabetes Mellitus 12 25 0.746
125
c TYP032 Type 1 Diabetes Mellitus 6 28 0.745
126
ARD001 Aredyld 25 0.743
127
c TYP027 Type 1 Diabetes Mellitus 10 24 0.743
128
c TYP039 Type 1 Diabetes Mellitus 17 21 0.741
129
c TYP040 Type 1 Diabetes Mellitus 18 20 0.741
130
c TYP030 Type 1 Diabetes Mellitus 4 19 0.741
131
c TYP029 Type 1 Diabetes Mellitus 3 17 0.741
132
c DBT050 Diabetes Mellitus, Insulin-Dependent, 15 17 0.741
133
c TYP034 Type 1 Diabetes Mellitus 8 20 0.740
134
MSC133 Muscular Atrophy, Ataxia, Retinitis Pigmentosa, and Diabetes Mellitus 18 0.740
135
PNC050 Pancreatic Beta Cell Agenesis with Neonatal Diabetes Mellitus 16 0.740
136
c DBT057 Diabetes Mellitus, Insulin-Dependent, 6 15 0.739
137
c DBT048 Diabetes Mellitus, Insulin-Dependent, 11 14 0.738
138
c DBT055 Diabetes Mellitus, Insulin-Dependent, 3 14 0.738
139
c DBT056 Diabetes Mellitus, Insulin-Dependent, 4 14 0.738
140
c DBT059 Diabetes Mellitus, Insulin-Dependent, 8 14 0.738
141
c DBT058 Diabetes Mellitus, Insulin-Dependent, 7 13 0.738
142
c LPD033 Lipodystrophy, Congenital Generalized, Type 2 45 0.737
143
c DBT049 Diabetes Mellitus, Insulin-Dependent, 13 14 0.737
144
c DBT051 Diabetes Mellitus, Insulin-Dependent, 17 14 0.737
145
c DBT052 Diabetes Mellitus, Insulin-Dependent, 18 14 0.737
146
c DBT097 Diabetes Mellitus, Noninsulin-Dependent, 4 12 0.736
147
c DBT095 Diabetes Mellitus, Noninsulin-Dependent, 3 11 0.736
148
LYM029 Lymphedema-Distichiasis Syndrome 41 0.735
149
XLN122 X-Linked Intellectual Disability - Short Stature - Obesity 5 0.729
150
MNT259 Mental Retardation, Obesity, Mandibular Prognathism, and Eye and Skin Anomalies 18 0.725
151
SHR107 Short Stature-Obesity Syndrome 17 0.725
152
PRL046 Prolactin Deficiency with Obesity and Enlarged Testes 10 0.725
153
AYZ001 Ayazi Syndrome 9 0.722
154
CNZ007 Coenzyme Q10 Deficiency, Primary, 2 21 0.719
155
MN1002 Man1b1-Cdg 11 0.713
156
DBT018 Diabetic Mastopathy 20 0.688
157
c WLF013 Wolfram Syndrome 1 56 0.664
158
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 44 0.661
159
GST058 Gestational Diabetes Insipidus 16 0.657
160
c ATM092 Autoimmune Polyendocrine Syndrome, Type Ii 47 0.650
161
FNC009 Fanconi-Bickel Syndrome 55 0.649
162
ALN003 Alaninuria with Microcephaly, Dwarfism, Enamel Hypoplasia, and Diabetes Mellitus 18 0.647
163
TRP008 Tropical Calcific Pancreatitis 51 0.646
164
DBT089 Diabetes Insipidus, Nephrogenic, with Mental Retardation and Intracerebral Calcification 18 0.642
165
c HMC039 Hemochromatosis, Type 1 74 0.642
166
BNG086 Bangstad Syndrome 21 0.640
167
HRT039 Heart Defects, Congenital, and Other Congenital Anomalies 30 0.639
168
ACQ022 Acquired Generalized Lipodystrophy 53 0.610
169
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 50 0.608
170
OVR063 Overnutrition 48 0.587
171
HYP364 Hyperostosis Frontalis Interna 30 0.577
172
DBT081 Diabetic Encephalopathy 28 0.572
173
NRP001 Neuropathy 62 0.561
174
INS034 Insulinomatosis and Diabetes Mellitus 40 0.540
175
DPS001 Dipsogenic Diabetes Insipidus 24 0.539
176
RNL024 Renal Glucosuria 53 0.537
177
PRX085 Preaxial Hallucal Polydactyly 25 0.537
178
c CNG012 Congenital Generalized Lipodystrophy 48 0.532
179
c HRD156 Hereditary Central Diabetes Insipidus 18 0.531
180
c ACQ034 Acquired Central Diabetes Insipidus 18 0.530
181
RNL111 Renal Tubulopathy, Diabetes Mellitus, and Cerebellar Ataxia 18 0.530
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
OBS060 Obesity Due to Sim1 Deficiency 12 0.527
186
SVR045 Severe Early-Onset Obesity-Insulin Resistance Syndrome Due to Sh2b1 Deficiency 12 0.527
187
MTC096 Mitchell-Riley Syndrome 23 0.526
188
PHT013 Photomyoclonus, Diabetes Mellitus, Deafness, Nephropathy, and Cerebral Dysfunction 19 0.526
189
KDN018 Kidney Disease 68 0.526
190
MDF004 Midface Hypoplasia, Obesity, Developmental Delay, and Neonatal Hypotonia 14 0.525
191
FGN001 Feigenbaum Bergeron Richardson Syndrome 8 0.522
192
DBT003 Diabetic Peripheral Angiopathy 3 0.522
193
YRF001 Yorifuji Okuno Syndrome 7 0.520
194
INT226 Intellectual Disability-Seizures-Macrocephaly-Obesity Syndrome 18 0.520
195
XLN211 X-Linked Intellectual Disability-Hypogonadism-Ichthyosis-Obesity-Short Stature Syndrome 17 0.520
196
INT298 Intellectual Disability-Obesity-Brain Malformations-Facial Dysmorphism Syndrome 16 0.520
197
OBS068 Obesity-Colitis-Hypothyroidism-Cardiac Hypertrophy-Developmental Delay Syndrome 8 0.520
198
ACH016 Achard Thiers Syndrome 6 0.518
199
CHR506 Choroideremia, Deafness, and Mental Retardation 24 0.514
200
CLR029 Clark-Baraitser Syndrome 23 0.511
201
SHR102 Short Stature, Brachydactyly, Intellectual Developmental Disability, and Seizures 22 0.511
202
c BMN004 Biemond Syndrome Ii 19 0.506
203
DPL003 Diploid-Triploid Mosaicism 15 0.506
204
CMR005 Camera-Marugo-Cohen Syndrome 12 0.501
205
SHR029 Short Syndrome 59 0.501
206
GLC003 Glucose Intolerance 58 0.465
207
GLC036 Glucagonoma 51 0.459
208
HYP056 Hypoglycemia 63 0.456
209
HYP066 Hyperglycemia 64 0.455
210
HYP060 Hyperinsulinism 55 0.421
211
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 21 0.413
212
LVR013 Liver Disease 75 0.412
213
FTT001 Fatty Liver Disease 66 0.410
214
INT288 Intellectual Disability-Dysmorphism-Hypogonadism-Diabetes Mellitus Syndrome 8 0.378
215
LPT004 Lipoatrophy with Diabetes, Hepatic Steatosis, Cardiomyopathy, and Leukomelanodermic Papules 3 0.375
216
WLF014 Wolfram Syndrome, Mitochondrial Form 16 0.374
217
SHR028 Short Stature, Cranial Hyperostosis, Hepatomegaly and Diabetes 3 0.374
218
CRD024 Cardiomyopathy Diabetes Deafness 3 0.374
219
ECT013 Ectodermal Dysplasia Arthrogryposis Diabetes Mellitus 2 0.374
220
MNT030 Mental Retardation Syndrome, Belgian Type 16 0.372
221
INT222 Intermediate Dend Syndrome 10 0.372
222
INT279 Intrauterine Growth Restriction-Short Stature-Early Adult-Onset Diabetes Syndrome 9 0.372
223
c DBT096 Diabetes Mellitus, Congenital Autoimmune 8 0.372
224
PRM187 Primary Microcephaly-Mild Intellectual Disability-Young-Onset Diabetes Syndrome 7 0.372
225
XLN187 X-Linked Intellectual Disability-Limb Spasticity-Retinal Dystrophy-Diabetes Insipidus Syndrome 6 0.372
226
HYP790 Hypopituitarism, Congenital, with Central Diabetes Insipidus 3 0.372
227
DBT016 Diabetes Persistent Mullerian Ducts 2 0.372
228
PRM291 Premature Aging Syndrome, Okamoto Type 15 0.370
229
HRT032 Heart Disease 73 0.358
230
PLY011 Polycystic Ovary Syndrome 64 0.347
231
ATM095 Autoimmune Disease 65 0.343
232
c BDY007 Body Mass Index Quantitative Trait Locus 1 47 0.341
233
NNL004 Nonalcoholic Fatty Liver Disease 55 0.327
234
SLP006 Sleep Apnea 70 0.324
235
IMM136 Immune System Disease 49 0.323
236
PRP019 Peripheral Nervous System Disease 62 0.307
237
DPR016 Depression 73 0.305
238
ETN001 Eating Disorder 64 0.288
239
VSC007 Vascular Disease 68 0.283
240
LPD008 Lipid Metabolism Disorder 64 0.280
241
MYC007 Myocardial Infarction 77 0.275
242
ISC004 Ischemia 66 0.273
243
ART140 Arteries, Anomalies of 65 0.266
244
ATN004 Autonomic Neuropathy 46 0.254
245
NNL002 Nonalcoholic Steatohepatitis 53 0.253
246
CRN018 Coronary Artery Anomaly 75 0.246
247
DGS002 Degos \'en Cocarde\' Erythrokeratoderma 36 0.244
248
AST005 Asthma 82 0.242
249
ANX010 Anxiety 72 0.240
250
c CHR089 Chronic Kidney Failure 73 0.240
251
PLY019 Polyneuropathy 58 0.239
252
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.238
253
ISC006 Ischemic Heart Disease 67 0.237
254
PRD004 Prediabetes Syndrome 48 0.237
255
URN009 Urinary System Disease 49 0.237
256
RTN018 Retinal Disease 56 0.235
257
PRD008 Periodontitis 66 0.232
258
AGN016 Aging 62 0.227
259
SPS003 Spastic Diplegia 54 0.224
260
c CRN300 Coronary Heart Disease 1 59 0.219
261
MNT002 Mental Depression 62 0.217
262
BRS047 Breast Cancer 100 0.212
263
PRD007 Periodontal Disease 65 0.211
264
APN008 Apnea, Obstructive Sleep 68 0.208
265
ART021 Arteriosclerosis 57 0.203
266
ACN002 Acanthosis Nigricans 66 0.203
267
CNG034 Congestive Heart Failure 68 0.201
268
INS024 Insulin-Like Growth Factor I 76 0.200
269
HYP080 Hypogonadism 52 0.196
270
INF032 Infertility 58 0.194
271
PNC044 Pancreatitis 63 0.191
272
ART022 Arthritis 77 0.189
273
HPT021 Hepatitis 75 0.188
274
GST037 Gastroparesis 59 0.184
275
VSC018 Visceral Steatosis 29 0.184
276
IMP005 Impotence 57 0.184
277
PRD006 Prader-Willi Syndrome 63 0.184
278
PRP027 Peripheral Vascular Disease 71 0.182
279
THR024 Thrombosis 63 0.182
280
c TRC078 Trichohepatoenteric Syndrome 2 22 0.182
281
CTR002 Cataract 58 0.181
282
c PLY105 Polycystic Ovary Syndrome 1 45 0.180
283
SLP005 Sleep Disorder 57 0.178
284
NRM005 Neuromuscular Disease 58 0.178
285
c PRC016 Pre-Eclampsia 60 0.178
286
OST012 Osteoarthritis 81 0.176
287
GST092 Gastroesophageal Reflux 65 0.175
288
RTN016 Retinal Degeneration 53 0.174
289
TRC086 Trichohepatoenteric Syndrome 1 51 0.173
290
THY032 Thyroiditis 53 0.172
291
END030 End Stage Renal Failure 59 0.169
292
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.167
293
FTL021 Fetal Macrosomia 46 0.166
294
HYP266 Hypoxia 62 0.166
295
GST050 Gastrointestinal System Disease 63 0.165
296
ANR007 Anorexia Nervosa 68 0.164
297
OST002 Osteoporosis 74 0.162
298
MCL006 Macular Retinal Edema 52 0.160
299
NRV007 Nervous System Disease 69 0.155
300
HYP086 Hypothyroidism 63 0.153
301
c HYP595 Hypertension, Essential 78 0.152
302
ALZ034 Alzheimer Disease 86 0.148
303
SCH015 Schizophrenia 70 0.147
304
PRS040 Prostate Cancer 94 0.147
305
CLR023 Colorectal Cancer 99 0.145
306
NTR005 Nutritional Deficiency Disease 58 0.143
307
c HPT001 Hepatitis C 70 0.142
308
HYP014 Hyperuricemia 56 0.140
309
ADN016 Adenocarcinoma 70 0.140
310
DNT012 Dental Caries 51 0.139
311
END057 Endometrial Cancer 68 0.139
312
CRN036 Craniopharyngioma 66 0.138
313
INF038 Influenza 76 0.138
314
c PRD040 Periodontitis, Chronic 59 0.138
315
ECL001 Eclampsia 57 0.137
316
RSP003 Respiratory Failure 72 0.137
317
LMB062 Limb Ischemia 53 0.136
318
HYP043 Hyperandrogenism 50 0.135
319
c ACT075 Acute Myocardial Infarction 56 0.135
320
RHM011 Rheumatoid Arthritis 82 0.134
321
c ACT027 Acute Pancreatitis 61 0.134
322
OVR049 Ovarian Disease 58 0.132
323
BRN106 Burns 55 0.132
324
c PRC031 Preeclampsia/eclampsia 1 34 0.131
325
LNG099 Lung Disease 67 0.131
326
PNC035 Pancreatic Cancer 82 0.130
327
ANG054 Angina Pectoris 62 0.130
328
ENC018 Encephalopathy 62 0.130
329
DMN002 Dementia 68 0.130
330
PRP080 Peripheral Artery Disease 54 0.129
331
HYP064 Hypogonadotropism 39 0.129
332
ART023 Arthropathy 64 0.128
333
LVR012 Liver Cirrhosis 66 0.127
334
RTN020 Retinal Vascular Disease 54 0.126
335
LKM002 Leukemia 72 0.126
336
PSR002 Psoriasis 66 0.125
337
ART153 Arthrochalasia Ehlers-Danlos Syndrome 24 0.125
338
BND020 Bone Disease 61 0.124
339
MDD011 Mood Disorder 62 0.121
340
SXL003 Sexual Disorder 49 0.121
341
CLC063 Celiac Disease 1 74 0.120
342
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 61 0.120
343
HYP730 Hypogonadotropic Hypogonadism 58 0.119
344
THR013 Thoracic Outlet Syndrome 55 0.117
345
HPT023 Hepatocellular Carcinoma 98 0.116
346
THY030 Thyroid Gland Disease 43 0.116
347
CRT049 Critical Limb Ischemia 54 0.116
348
RSP006 Respiratory System Disease 56 0.114
349
ATR011 Atrial Fibrillation 69 0.114
350
MTH009 Mouth Disease 61 0.114
351
JNT002 Joint Disorders 58 0.113
352
CRB039 Cerebrovascular Disease 67 0.113
353
DRR001 Diarrhea 57 0.113
354
HSH003 Hashimoto Thyroiditis 65 0.111
355
BLM002 Bulimia Nervosa 60 0.111
356
INS001 Insulinoma 64 0.111
357
ATH013 Atherosclerosis Susceptibility 66 0.110
358
ADN018 Adenoma 64 0.110
359
HYP083 Hypopituitarism 44 0.108
360
CNN003 Conn\'s Syndrome 73 0.108
361
BNF002 Bone Fracture 46 0.108
362
OVR046 Ovarian Cyst 53 0.106
363
PNM007 Pneumonia 71 0.106
364
ATX010 Ataxia Neuropathy Spectrum 32 0.105
365
SPN331 Spondyloocular Syndrome 42 0.105
366
HYP750 Hypertriglyceridemia, Familial 60 0.105
367
MLT020 Multiple Sclerosis 75 0.105
368
RST023 Resting Heart Rate, Variation in 42 0.104
369
LYM053 Lymphomatous Thyroiditis 25 0.104
370
PTT009 Pituitary Gland Disease 55 0.104
371
FSH001 Fish-Eye Disease 50 0.104
372
ANR048 Aniridia 1 65 0.104
373
PSY004 Psychotic Disorder 72 0.104
374
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.103
375
MJR001 Major Depressive Disorder 66 0.103
376
LYM118 Lymphoma 70 0.103
377
c HYP555 Hypertriglyceridemia, Transient Infantile 41 0.102
378
AMY004 Amyloidosis 68 0.102
379
c MTR002 Mitral Valve Insufficiency 48 0.102
380
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 46 0.101
381
ACT232 Acute Necrotizing Encephalopathy 33 0.101
382
BLD137 Blood Group--Ahonen 24 0.101
383
IRN002 Iron Metabolism Disease 60 0.101
384
c BRD013 Bardet-Biedl Syndrome 12 49 0.101
385
MTB004 Metabolic Acidosis 49 0.099
386
GT001 Gout 60 0.099
387
c BRD014 Bardet-Biedl Syndrome 2 61 0.098
388
EPL164 Epilepsy 73 0.098
389
HYP085 Hypothalamic Disease 47 0.098
390
PNM001 Pneumocystosis 53 0.098
391
VRL011 Viral Infectious Disease 72 0.097
392
BRD002 Bardet-Biedl Syndrome 64 0.097
393
c BRD012 Bardet-Biedl Syndrome 11 52 0.097
394
c BRD011 Bardet-Biedl Syndrome 10 45 0.097
395
CYS001 Cystic Fibrosis 83 0.097
396
ATT013 Attention Deficit-Hyperactivity Disorder 67 0.097
397
EXN002 Exanthem 56 0.097
398
NPH009 Nephrolithiasis 57 0.096
399
c SPN225 Spondyloarthropathy 1 75 0.096
400
SMT008 Smith-Magenis Syndrome 58 0.096
401
RTN023 Retinitis 48 0.095
402
GST053 Gastric Cancer 79 0.095
403
MSC007 Muscle Hypertrophy 64 0.095
404
BPL003 Bipolar Disorder 60 0.095
405
HYP069 Hyperparathyroidism 59 0.095
406
NRL016 Neural Tube Defects 79 0.095
407
LYM031 Lymphocytic Leukemia 61 0.095
408
GNG013 Gingivitis 62 0.094
409
DFC004 Deficiency Anemia 66 0.094
410
DWN001 Down Syndrome 72 0.093
411
GLL020 Gallbladder Disease 63 0.092
412
LKM062 Leukemia, Acute Lymphoblastic 68 0.092
413
RHM027 Rheumatic Disease 61 0.092
414
c MYT020 Myotonic Dystrophy 2 55 0.092
415
ATX030 Ataxia-Telangiectasia 84 0.092
416
PNG002 Pain Agnosia 39 0.091
417
ACT088 Acute Insulin Response 48 0.091
418
CLL015 Collagen Disease 46 0.091
419
GNR004 Generalized Anxiety Disorder 53 0.091
420
TRM003 Tremor 55 0.090
421
STM006 Stomach Disease 50 0.090
422
c CHR579 Chiari Malformation Type Ii 42 0.090
423
GRW007 Growth Hormone Deficiency 52 0.090
424
FRN020 Frontal Fibrosing Alopecia 31 0.090
425
AND002 Androgen Insensitivity Syndrome 65 0.090
426
AXN002 Axenfeld-Rieger Syndrome 56 0.089
427
ALR002 Al-Raqad Syndrome 41 0.089
428
HDC001 Headache 61 0.089
429
ALP046 Alport Syndrome, X-Linked 74 0.088
430
SPN186 Spinal Cord Injury 65 0.088
431
BWN003 Bowenoid Papulosis 42 0.088
432
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.087
433
ART001 Arterial Tortuosity Syndrome 60 0.087
434
HLC007 Helicobacter Pylori Infection 65 0.087
435
THY028 Thyroid Cancer 71 0.087
436
c GLL024 Gallbladder Disease 1 51 0.087
437
SVR004 Severe Combined Immunodeficiency 69 0.087
438
HPT082 Hepatic Adenomas, Familial 51 0.087
439
ANG001 Angelman Syndrome 67 0.087
440
HNM002 Hinman Syndrome 32 0.087
441
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.087
442
SNS003 Sensory Peripheral Neuropathy 57 0.086
443
BRR014 Barrett Esophagus 70 0.086
444
ADP007 Adie Pupil 43 0.086
445
ANV001 Anovulation 49 0.085
446
SKN016 Skin Disease 64 0.085
447
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 68 0.085
448
INT007 Intermediate Coronary Syndrome 47 0.085
449
LCT001 Lactic Acidosis 52 0.085
450
CRP001 Carpal Tunnel Syndrome 71 0.085
451
BRN038 Bronchial Disease 55 0.084
452
ALC007 Alcohol Dependence 68 0.084
453
CRD119 Cardiac Arrest 64 0.084
454
MSC003 Muscular Atrophy 55 0.083
455
ACQ007 Acquired Immunodeficiency Syndrome 63 0.083
456
ART016 Aortic Aneurysm 70 0.083
457
PLC008 Placenta Disease 56 0.083
458
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 67 0.083
459
c HPT073 Hepatitis C Virus 67 0.083
460
THR100 Thrombocytopenic Purpura, Autoimmune 65 0.082
461
CRN030 Coronary Stenosis 51 0.082
462
INF037 Inflammatory Bowel Disease 54 0.082
463
PLM033 Pulmonary Embolism 63 0.081
464
LYM025 Lymphedema 55 0.081
465
INT075 Intracranial Hypertension 57 0.081
466
SCH012 Schizoaffective Disorder 54 0.081
467
IRN001 Iron Deficiency Anemia 55 0.081
468
RNL114 Renal Cell Carcinoma, Nonpapillary 62 0.081
469
ALS001 Alstrom Syndrome 55 0.081
470
VTM002 Vitamin B12 Deficiency 48 0.080
471
URM002 Uremia 52 0.080
472
SKN027 Skin Conditions 46 0.080
473
THR014 Thrombocytopenia 64 0.080
474
ACR001 Aicardi-Goutieres Syndrome 61 0.080
475
c ACR116 Aicardi-Goutieres Syndrome 1 44 0.080
476
LPS004 Lupus Erythematosus 69 0.079
477
ESP024 Esophagitis 62 0.078
478
DYS021 Dysautonomia 45 0.078
479
KDN017 Kidney Cancer 59 0.078
480
LPM005 Lipomatosis 46 0.078
481
GLM007 Glomerulonephritis 60 0.078
482
c HPT016 Hepatitis B 70 0.078
483
ATS364 Autism 69 0.078
484
ACR007 Acromegaly 71 0.078
485
MCR141 Mucormycosis 49 0.078
486
MYC088 Mycobacterium Avium Complex Infections 33 0.078
487
AND005 Androgen Insensitivity Syndrome, Mild 22 0.078
488
MCL027 Macular Dystrophy, Dominant Cystoid 52 0.078
489
RTN008 Retinitis Pigmentosa 79 0.078
490
BCT022 Bacterial Infectious Disease 60 0.078
491
HYP050 Hyperinsulinemic Hypoglycemia 55 0.078
492
c AMY091 Amyotrophic Lateral Sclerosis 1 91 0.078
493
c SYS001 Systemic Lupus Erythematosus 88 0.077
494
HYP265 Hypotonia 41 0.077
495
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.077
496
BRC012 Brucellosis 66 0.077
497
JVN024 Juvenile Hereditary Hemochromatosis 42 0.077
498
HMN014 Human Immunodeficiency Virus Infectious Disease 60 0.076
499
CHL004 Cholelithiasis 50 0.076
500
CNS004 Constipation 57 0.076
501
CLT003 Colitis 64 0.076
502
INT068 Intestinal Disease 60 0.076
503
PRC019 Precocious Puberty 52 0.075
504
NRR001 Neuroretinitis 39 0.075
505
STR067 Stroke, Ischemic 85 0.075
506
DRM006 Dermatitis 68 0.075
507
GSG001 Gas Gangrene 45 0.075
508
OVR042 Ovarian Cancer 83 0.075
509
PSR001 Psoriatic Arthritis 67 0.075
510
MLN008 Melanoma 63 0.075
511
PRS063 Paresthesia 39 0.075
512
WRN001 Werner Syndrome 70 0.075
513
MNN028 Mononeuropathy of the Median Nerve, Mild 45 0.075
514
FBR047 Fibromyalgia 61 0.075
515
CLR108 Colorectal Adenoma 61 0.075
516
ATN002 Autonomic Nervous System Disease 49 0.074
517
PLM037 Pulmonary Hypertension 77 0.074
518
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.074
519
ULC005 Ulcer of Lower Limbs 14 0.074
520
HRN028 Horns in Sheep 22 0.074
521
NRC002 Narcolepsy 59 0.074
522
ALX002 Alexithymia 41 0.073
523
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 47 0.073
524
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 44 0.073
525
BCT004 Bacteriuria 48 0.073
526
NCR002 Necrobiosis Lipoidica 34 0.073
527
TRN020 Turner Syndrome 69 0.073
528
c HPT003 Hepatitis a 67 0.073
529
PNC034 Pancreas Disease 56 0.073
530
NRL018 Neural Tube Defects, Folate-Sensitive 53 0.073
531
MYP004 Myopathy 63 0.073
532
LNG108 Langerhans Cell Histiocytosis 63 0.072
533
HYP076 Hyperthyroidism 56 0.072
534
c ACT071 Acute Kidney Failure 51 0.072
535
LNG032 Lung Cancer 99 0.071
536
SYS003 Systolic Heart Failure 46 0.071
537
LRN002 Laron Syndrome 64 0.071
538
BRS090 Breast Reconstruction 43 0.071
539
AMN001 Amenorrhea 56 0.070
540
ATM052 Autoimmune Disease 1 46 0.070
541
HST010 Histiocytosis 61 0.070
542
DSS008 Disease of Mental Health 65 0.070
543
MYL005 Myelofibrosis 69 0.070
544
c ACT210 Acute Respiratory Distress Syndrome 62 0.070
545
OST097 Osteoporotic Fracture 44 0.070
546
ASP030 Aspirin Resistance 47 0.069
547
HRN026 Hernia, Hiatus 48 0.069
548
c ART138 Aortic Aneurysm, Familial Abdominal, 1 65 0.069
549
CLL003 Cellulitis 59 0.069
550
SKN023 Skin Tag 39 0.069
551
c BRD010 Bardet-Biedl Syndrome 1 59 0.069
552
CRD132 Cardiac Conduction Defect 62 0.069
553
c ACT068 Acute Cystitis 56 0.069
554
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.069
556
c THR092 Thrombophilia Due to Thrombin Defect 69 0.068
557
INT303 Intracranial Hypertension, Idiopathic 50 0.068
558
BRS051 Breast Disease 63 0.068
559
PSD015 Pseudohypoparathyroidism 50 0.068
560
STS002 Situs Inversus 49 0.067
561
CND004 Candidiasis 60 0.067
562
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.067
563
IRR002 Irritable Bowel Syndrome 50 0.066
564
LYM027 Lymphopenia 57 0.066
565
ALC004 Alcohol Abuse 69 0.066
566
GLC008 Glucose Metabolism Disease 48 0.066
567
RST001 Restless Legs Syndrome 54 0.066
568
SZR006 Seizure Disorder 58 0.065
569
FCL005 Focal Segmental Glomerulosclerosis 60 0.065
570
RNL007 Renal Tubular Acidosis 52 0.065
571
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.065
572
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 54 0.065
573
HPR003 Heparin-Induced Thrombocytopenia 49 0.065
574
PRS129 Prostatic Hyperplasia, Benign 51 0.065
575
MYL069 Myeloma, Multiple 85 0.065
576
MYL006 Myeloid Leukemia 67 0.065
577
ADL010 Adult Respiratory Distress Syndrome 62 0.065
578
GST044 Gastritis 60 0.065
579
DYS073 Dysphagia 51 0.064
580
RCK004 Rickets 65 0.064
581
CRT013 Carotid Stenosis 53 0.064
582
c BLD140 Blood Group, I System 30 0.064
583
CRH001 Crohn\'s Disease 77 0.064
584
DMP001 Dumping Syndrome 47 0.064
585
BRN071 Brain Injury 54 0.063
586
BRB001 Beriberi 45 0.063
587
DYS011 Dyskinesia of Esophagus 38 0.063
588
LRN003 Learning Disability 52 0.063
589
SCN001 Secondary Hyperparathyroidism of Renal Origin 52 0.063
590
MLN007 Male Infertility 52 0.063
591
APP008 Appendicitis 65 0.063
592
PST021 Postpartum Depression 55 0.063
593
CMR001 Camurati-Engelmann Disease 56 0.062
594
SGM006 Segmental Odontomaxillary Dysplasia 21 0.062
595
FSC004 Fasciitis 49 0.062
596
MNN017 Mononeuropathy 40 0.062
597
CHL123 Chlamydia 66 0.061
598
PMP004 Pemphigus Foliaceus 46 0.061
599
SLD003 Sialadenitis 49 0.061
600
CRT016 Carotid Artery Disease 57 0.061
601
WRN003 Wernicke Encephalopathy 48 0.061
602
c VRL010 Viral Hepatitis 60 0.061
603
NTR027 Neutrophil Actin Dysfunction 31 0.061
604
ESP021 Esophageal Cancer 83 0.061
605
c PTT057 Pituitary Adenoma 4, Acth-Secreting 53 0.061
606
PRT036 Peritonitis 66 0.061
607
VNS003 Venous Insufficiency 54 0.060
608
c PNC128 Pain - Chronic 46 0.060
609
c ATS007 Autism Spectrum Disorder 64 0.060
610
INT002 Intermittent Claudication 63 0.060
611
OBS082 Obstructive Nephropathy 51 0.060
612
FML012 Familial Partial Lipodystrophy 52 0.060
613
c LRG017 Large Intestine Cancer 59 0.060
614
GLY013 Glycogen Storage Disease 60 0.059
615
DYS014 Dyspepsia 52 0.059
616
DWR001 Dwarfism 45 0.059
617
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.059
618
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 32 0.059
619
TTR001 Tetralogy of Fallot 71 0.059
620
EPD070 Epidermoid Cysts 43 0.059
621
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.059
622
PRP030 Purpura 61 0.059
623
PNC033 Pancreas Adenocarcinoma 66 0.058
624
EXC002 Exocrine Pancreatic Insufficiency 40 0.058
625
PST055 Postural Hypotension 38 0.058
626
PLY006 Polydactyly 59 0.058
627
GYN001 Gynecomastia 47 0.058
628
HYP061 Hypertrophic Cardiomyopathy 58 0.058
629
BNR002 Bone Resorption Disease 53 0.058
630
SNS001 Sensorineural Hearing Loss 58 0.058
631
END038 Endocrine Pancreas Disease 38 0.058
632
ALL003 Allergic Rhinitis 70 0.057
633
SLP010 Slipped Capital Femoral Epiphysis 37 0.057
634
RHN004 Rhinitis 62 0.057
635
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 52 0.057
636
SCL022 Scleredema 31 0.057
637
DLT002 Dilated Cardiomyopathy 74 0.057
638
SPN051 Spondylitis 54 0.057
639
SRC014 Sarcoma 70 0.057
640
OPN001 Open-Angle Glaucoma 53 0.057
641
NWB001 Newborn Respiratory Distress Syndrome 55 0.057
642
RSP007 Respiratory Distress Syndrome, Infant 35 0.057
643
NPH012 Nephrotic Syndrome 59 0.057
644
PLY014 Polycystic Kidney Disease 63 0.056
645
c LKM061 Leukemia, Acute Myeloid 83 0.056
646
HYP724 Hyperlipoproteinemia, Type Iii 62 0.056
647
MCR010 Microcephaly 55 0.056
648
ADM013 Adamantinoma of Long Bones 48 0.056
649
PST053 Postherpetic Neuralgia 45 0.056
650
PNC045 Pancreatic Agenesis 40 0.056
651
CRD223 Cardiac Arrhythmia 55 0.056
652
HYD002 Hydronephrosis 49 0.056
653
FRL002 Froelich Syndrome 14 0.056
654
VSC002 Vascular Dementia 55 0.055
655
FNG006 Feingold Syndrome 1 48 0.055
656
BLD163 Blood Group, Dombrock System 26 0.055
657
ART008 Arteriosclerosis Obliterans 42 0.055
658
HYP614 Hyperlipidemia, Familial Combined 54 0.055
659
DXT002 Dextrocardia with Situs Inversus 43 0.055
660
CYS009 Cystadenoma 42 0.055
661
GTR002 Goiter 53 0.055
662
MSC033 Muscle Disorders 50 0.055
663
PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 65 0.055
664
SBS003 Substance Abuse 59 0.055
665
KRT002 Keratomalacia 56 0.055
666
c SVR005 Severe Pre-Eclampsia 56 0.055
667
c LBR014 Leber Congenital Amaurosis 4 63 0.055
668
c CNT035 Central Nervous System Disease 62 0.055
669
ALP008 Alopecia 55 0.055
670
THR015 Thrombophilia 55 0.054
671
WLL001 Williams-Beuren Syndrome 63 0.054
672
STF001 Stiff-Person Syndrome 65 0.054
673
ERY029 Erythermalgia, Primary 56 0.054
674
CRB037 Cerebral Palsy 71 0.053
675
FCL044 Fecal Incontinence 36 0.053
676
HYP784 Hypogonadism, Male 42 0.053
677
c MYT021 Myotonic Dystrophy 1 70 0.053
678
HMT018 Hematopoietic Stem Cell Transplantation 58 0.053
679
CLC001 Calciphylaxis 53 0.053
680
TRM010 Traumatic Brain Injury 56 0.053
681
CRN024 Corneal Disease 44 0.053
682
END072 Endotheliitis 40 0.053
683
HYP110 Hyperproinsulinemia 37 0.053
684
HYD006 Hydrocephalus 66 0.053
685
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 52 0.053
686
c PRM005 Primary Hyperparathyroidism 60 0.053
687
EXP004 Exophthalmos 51 0.053
688
TND004 Tendinopathy 44 0.053
689
FXF002 Fox-Fordyce Disease 30 0.053
690
c CNT075 Central Precocious Puberty 53 0.053
691
PRS021 Prostatic Adenoma 49 0.053
692
BLD134 Bladder Cancer 70 0.052
693
GLL008 Gilles De La Tourette Syndrome 68 0.052
694
c PTT056 Pituitary Adenoma 1, Multiple Types 52 0.052
695
RPD005 Rapidly Involuting Congenital Hemangioma 20 0.052
696
CHL065 Cholangiocarcinoma 64 0.052
697
CLC006 Calcinosis 48 0.052
698
ACT105 Acute Mountain Sickness 56 0.052
699
ALP009 Alopecia Areata 64 0.052
700
c ACT074 Acute Lymphocytic Leukemia 63 0.052
701
HYP068 Hyperostosis 50 0.052
702
MYC084 Mycobacterium Tuberculosis 1 74 0.052
703
ACR006 Aceruloplasminemia 70 0.052
704
CRV035 Cervical Cancer 76 0.052
705
FND002 Fundus Dystrophy 50 0.052
706
c MGR028 Migraine with or Without Aura 1 69 0.052
707
HMN044 Human Immunodeficiency Virus Type 1 74 0.051
708
MGL001 Megaloblastic Anemia 54 0.051
709
URN022 Urinary Tract Infections, Recurrent 28 0.051
710
ACH005 Achalasia 53 0.051
711
DVR002 Diverticulitis 46 0.051
712
ELP001 Elephantiasis 37 0.051
713
CHR084 Chromosomal Disease 34 0.051
714
DRM053 Dermatitis, Atopic 71 0.051
715
NTR004 Neutropenia 60 0.051
716
DRG003 Drug Dependence 50 0.051
717
DST006 Diastolic Heart Failure 46 0.051
718
GNG011 Gingival Disease 46 0.051
719
ACQ009 Acquired Metabolic Disease 34 0.051
720
DGN001 Degenerative Disc Disease 52 0.051
721
PHC003 Pheochromocytoma 72 0.051
722
HYP607 Hypercholesterolemia, Familial 81 0.051
723
ERY003 Erythema Multiforme 58 0.051
724
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 53 0.051
725
MYL009 Myelodysplastic Syndrome 70 0.051
726
PPT005 Peptic Ulcer Disease 62 0.051
727
SQM006 Squamous Cell Carcinoma 59 0.051
728
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.050
729
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.050
730
HMS001 Hemosiderosis 52 0.050
731
BLD165 Blood Group, Colton System 27 0.050
732
PTS002 Ptosis 52 0.050
733
SYN007 Synovitis 61 0.049
734
PST011 Pustulosis of Palm and Sole 49 0.049
735
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.049
736
HMC014 Homocysteinemia 54 0.049
737
c FCL025 Focal Segmental Glomerulosclerosis 1 55 0.049
738
PPT001 Peptic Esophagitis 45 0.049
739
c SML038 Small Cell Cancer of the Lung 72 0.049
740
IGG001 Iga Glomerulonephritis 58 0.049
741
ART002 Arts Syndrome 54 0.049
742
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.049
743
STT004 Steatorrhea 40 0.049
744
PRP016 Paraplegia 54 0.049
745
c HMP029 Hemophilia a 70 0.049
746
VRC005 Varicose Veins 65 0.049
747
SJG008 Sjogren Syndrome 59 0.049
748
c LPD040 Lipodystrophy, Familial Partial, Type 1 44 0.049
749
IDP033 Idiopathic Edema 43 0.049
750
TTR016 Tetra-Amelia Syndrome 38 0.049
751
PSD014 Pseudopseudohypoparathyroidism 51 0.049
752
ANL018 Analbuminemia 48 0.049
753
VSC011 Vasculitis 66 0.049
754
PLM010 Pulmonary Edema 58 0.049
755
CHL066 Cholangitis 51 0.049
756
CHL147 Chlamydia Pneumonia 41 0.049
757
OST017 Osteomyelitis 64 0.048
758
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.048
759
MSC005 Muscular Dystrophy 66 0.048
760
HYP020 Hyperprolactinemia 64 0.048
761
PST028 Post-Traumatic Stress Disorder 62 0.048
762
CLN019 Colonic Disease 57 0.048
763
ALL006 Allergic Asthma 61 0.048
764
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 57 0.048
765
ENC004 Encephalitis 66 0.048
766
HLP001 Holoprosencephaly 66 0.048
767
MYP006 Myopia 58 0.048
768
ULC004 Ulcerative Colitis 80 0.048
769
SPN027 Spinal Stenosis 61 0.048
770
MSC190 Muscular Disease 51 0.048
771
CMP008 Compartment Syndrome 48 0.048
772
MSC004 Muscle Tissue Disease 27 0.048
773
TTH006 Tooth Disease 49 0.048
774
PNS012 Paine Syndrome 62 0.047
775
DSR011 Disorganization, Mouse, Homolog of 23 0.047
776
GLN010 Glanzmann Thrombasthenia 68 0.047
777
BLL003 Bell\'s Palsy 52 0.047
778
c PLM164 Pulmonary Hypertension, Primary, 1 74 0.047
779
PLV020 Pelvic Organ Prolapse 63 0.047
780
HRT012 Heart Valve Disease 54 0.047
781
HDR002 Hidradenitis Suppurativa 56 0.047
782
HDR003 Hidradenitis 47 0.047
783
CYT008 Cytomegalovirus Infection 60 0.046
784
c EPS039 Episodic Pain Syndrome, Familial, 1 31 0.046
785
c ART101 Aortic Valve Disease 2 65 0.046
786
FML035 Familial Hyperlipidemia 51 0.046
787
ACH004 Achondroplasia 68 0.046
788
PRT018 Portal Vein Thrombosis 50 0.046
789
CNN005 Connective Tissue Disease 64 0.045
790
CRB085 Cerebral Hemorrhage 45 0.045
791
c ATR087 Atrial Standstill 1 67 0.045
792
DCB001 Decubitus Ulcer 45 0.045
793
BCL006 B-Cell Lymphomas 65 0.045
794
CHL068 Cholestasis 60 0.045
795
TND005 Tendinitis 44 0.045
796
c AMY009 Amyloidosis Aa 56 0.045
797
SFT003 Soft Tissue Sarcoma 56 0.045
798
CHR005 Chorioamnionitis 54 0.045
799
INT070 Intestinal Obstruction 53 0.045
800
PNN001 Panniculitis 47 0.045
801
BRN024 Bronchitis 67 0.045
802
MNC006 Monoclonal Gammopathy of Uncertain Significance 53 0.045
803
c CHR431 Chronic Venous Insufficiency 48 0.045
804
CRY036 Cryptogenic Cirrhosis 38 0.045
805
HYP017 Hypophosphatemia 48 0.045
806
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 43 0.045
807
CLR030 Clear Cell Renal Cell Carcinoma 49 0.044
808
ASP006 Aspergillosis 66 0.044
809
CHR071 Charcot-Marie-Tooth Disease 62 0.044
810
SDD008 Sudden Sensorineural Hearing Loss 46 0.044
811
TRC026 Tracheal Disease 32 0.044
812
NRB001 Neuroblastoma 73 0.044
813
PRT013 Portal Hypertension 60 0.044
814
BLD044 Bladder Disease 51 0.044
815
EMP001 Empty Sella Syndrome 46 0.044
816
ANG020 Angiosarcoma 58 0.044
817
HRP004 Herpes Zoster 61 0.044
818
FRN014 Fournier Gangrene 40 0.044
819
PLY018 Polycythemia 60 0.044
820
c INF145 Infantile Liver Failure Syndrome 1 57 0.044
821
GST007 Gastric Dilatation 31 0.044
822
MYS003 Myasthenia Gravis 74 0.043
823
c ACT073 Acute Leukemia 61 0.043
824
END046 Endometritis 51 0.043
825
MLR004 Malaria 85 0.043
826
APL001 Aplastic Anemia 74 0.043
827
HMP007 Hemophilia 61 0.043
828
RDC002 Radiculopathy 53 0.043
829
TXP001 Toxoplasmosis 65 0.043
830
CMP010 Complex Regional Pain Syndrome 62 0.043
831
NPH010 Nephrosclerosis 45 0.043
832
SNL007 Senile Cataract 40 0.043
833
SHH001 Sheehan Syndrome 51 0.042
834
c HNT004 Huntington Disease-Like 2 41 0.042
835
ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 55 0.042
836
MCR011 Microinvasive Gastric Cancer 46 0.042
837
RCT017 Rectal Disease 40 0.042
838
PRT058 Pure Autonomic Failure 61 0.042
839
CHL067 Cholecystitis 58 0.042
840
OCL069 Ocular Motor Apraxia 55 0.042
841
CHR008 Choroiditis 42 0.042
842
END041 Endometrial Adenocarcinoma 60 0.042
843
LRN001 Laurence-Moon Syndrome 40 0.042
844
END044 Endometriosis 65 0.042
845
c CNG006 Congenital Hypothyroidism 63 0.042
846
INT146 Intervertebral Disc Disease 62 0.042
847
BCK002 Beckwith-Wiedemann Syndrome 59 0.042
848
LYM019 Lymphosarcoma 56 0.042
849
PRT038 Protein-Energy Malnutrition 52 0.042
850
VSL002 Visual Epilepsy 35 0.042
851
LYM133 Lymphoma, Hodgkin, Classic 75 0.042
852
GST019 Gastrointestinal Stromal Tumor 74 0.042
853
OTT002 Otitis Media 68 0.042
854
DGR001 Digeorge Syndrome 62 0.042
855
ISL003 Isolated Growth Hormone Deficiency 51 0.042
856
INT051 Intussusception 50 0.042
857
HYP263 Hypersomnia 44 0.042
858
BNC003 Bone Cancer 58 0.041
859
MMP001 Mumps 59 0.041
860
PLY112 Polyarteritis Nodosa, Childhood-Onset 49 0.041
861
OPT070 Optic Nerve Hypoplasia, Bilateral 49 0.041
862
GLC022 Glucose/galactose Malabsorption 44 0.041
863
MTR007 Motor Peripheral Neuropathy 38 0.041
864
RTN017 Retinal Detachment 59 0.041
865
PNC041 Pancreatic Ductal Adenocarcinoma 53 0.041
866
AYM001 Ayme-Gripp Syndrome 40 0.041
867
RTN024 Retinoblastoma 72 0.040
868
ANT006 Antiphospholipid Syndrome 60 0.040
869
OST011 Osteomalacia 52 0.040
870
PPL021 Papilledema 48 0.040
871
PRK057 Parkinson Disease, Late-Onset 76 0.040
872
TMP003 Temporal Arteritis 69 0.040
873
CNR004 Cone-Rod Dystrophy 2 63 0.040
874
END033 Endocarditis 60 0.040
875
c GLC092 Glaucoma, Primary Open Angle 58 0.040
876
ICH020 Ichthyosis Prematurity Syndrome 45 0.040
877
ART004 Aortic Atherosclerosis 45 0.040
878
MNC002 Munchausen by Proxy 34 0.040
879
SRC025 Sarcoidosis 1 76 0.040
880
c LKM063 Leukemia, Chronic Myeloid 74 0.040
881
SCK003 Sickle Cell Anemia 72 0.040
882
SNS014 Sinusitis 63 0.040
883
CHK001 Chikungunya 61 0.040
884
GLM045 Glioma 55 0.040
885
PTT006 Pituitary Adenoma 53 0.040
886
OCC006 Occipital Horn Syndrome 52 0.040
887
HYP077 Hypertrichosis 49 0.040
888
SYN036 Syncope 47 0.040
889
MDS022 Mediastinitis 41 0.040
890
SPN041 Spinal Cord Disease 52 0.039
891
PRS042 Prostate Disease 42 0.039
892
TQP001 Taqi Polymorphism 30 0.039
893
GST023 Gastric Ulcer 57 0.039
894
ALB001 Albright\'s Hereditary Osteodystrophy 53 0.039
895
c BPL002 Bipolar I Disorder 50 0.039
896
c BRD015 Bardet-Biedl Syndrome 3 43 0.039
897
HPT067 Hepatocellular Adenoma 42 0.039
898
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.039
899
DDN001 Duodenal Ulcer 53 0.039
900
GLC096 Galactorrhea 47 0.039
901
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 45 0.039
902
IMM001 Immune-Complex Glomerulonephritis 42 0.039
903
c MYS011 Myasthenia Gravis Congenital 36 0.039
904
KBK002 Kabuki Syndrome 1 66 0.039
905
GST045 Gastroenteritis 62 0.039
906
CRH005 Crohn\'s Colitis 61 0.039
907
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.039
908
ICH004 Ichthyosis 56 0.039
909
ACT010 Acth-Secreting Pituitary Adenoma 52 0.039
910
ART031 Aortic Coarctation 49 0.039
911
SCH003 Schizophreniform Disorder 43 0.039
912
ALL014 Allergic Encephalomyelitis 42 0.039
913
DDN009 Duodenal Obstruction 34 0.039
914
c HYP602 Hyperoxaluria, Primary, Type Ii 33 0.039
915
CMP096 Complete Generalized Lipodystrophy 25 0.039
916
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.038
917
PHR003 Pharyngitis 57 0.038
918
KWS001 Kwashiorkor 45 0.038
919
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 42 0.038
920
c BRD018 Bardet-Biedl Syndrome 6 41 0.038
921
c PLM022 Pulmonary Valve Insufficiency 37 0.038
922
SPN046 Spinal Muscular Atrophy 66 0.038
923
c ATM011 Autoimmune Hepatitis 61 0.038
924
c MLG069 Malignant Hypertension 50 0.038
925
RTN014 Retinal Artery Occlusion 48 0.038
926
THR005 Thrombotic Thrombocytopenic Purpura 64 0.038
927
TBC004 Tobacco Addiction 64 0.038
928
c HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.038
929
MLT074 Multiple Endocrine Neoplasia 57 0.038
930
MYX004 Myxedema 45 0.038
931
CDQ001 Cauda Equina Syndrome 44 0.038
932
SPR007 Superior Mesenteric Artery Syndrome 42 0.038
933
ACT055 Actinomycosis 40 0.038
934
c MLG042 Malignant Otitis Externa 29 0.038
935
HYP098 Hypereosinophilic Syndrome 65 0.037
936
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 55 0.037
937
KRT006 Keratoconjunctivitis 54 0.037
938
BRN080 Brain Ischemia 41 0.037
939
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 36 0.037
940
PHN003 Phenylketonuria 73 0.037
941
CLR109 Colorectal Adenocarcinoma 54 0.037
942
PRV006 Pervasive Developmental Disorder 53 0.037
943
KRT007 Keratoconus 49 0.037
944
CRN074 Coronary Artery Aneurysm 47 0.037
945
IDP041 Idiopathic Recurrent Pericarditis 33 0.037
946
MRL001 Meralgia Paresthetica 27 0.037
947
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 62 0.037
948
NGH001 Night Blindness 49 0.036
949
c BRD016 Bardet-Biedl Syndrome 4 47 0.036
950
GST040 Gastric Adenocarcinoma 65 0.036
951
RCT018 Rectal Neoplasm 59 0.036
952
ARM001 Aromatase Deficiency 52 0.036
953
PST095 Post-Thrombotic Syndrome 51 0.036
954
WSK001 Wiskott-Aldrich Syndrome 76 0.036
955
MYS005 Myositis 64 0.036
956
SLV001 Silver-Russell Syndrome 55 0.036
957
GLC009 Glucosephosphate Dehydrogenase Deficiency 51 0.036
958
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 46 0.036
959
NRV004 Nerve Compression Syndrome 31 0.036
960
CCC001 Coccidioidomycosis 60 0.036
961
STT001 Status Epilepticus 60 0.036
962
FNC043 Fanconi Anemia, Complementation Group E 54 0.036
963
ART017 Aortic Disease 54 0.036
964
ISL001 Islet Cell Tumor 50 0.036
965
QDR001 Quadriplegia 50 0.036
966
PTT037 Pituitary Tumors 47 0.036
967
MTH081 Mthfr Gene Variant 27 0.036
968
NRF023 Neurofibromatosis, Type Ii 75 0.035
969
BRN056 Bronchopulmonary Dysplasia 60 0.035
970
PLM034 Pulmonary Emphysema 56 0.035
971
c INF071 Inflammatory Bowel Disease 1 53 0.035
972
SPN035 Spindle Cell Sarcoma 50 0.035
973
CLP006 Clopidogrel Resistance 45 0.035
974
HYP081 Hypolipoproteinemia 43 0.035
975
NNT019 Neonatal Hypothyroidism 41 0.035
976
TMP012 Temple Syndrome 35 0.035
977
48X003 48,xxyy Syndrome 33 0.035
978
FNC027 Fanconi Anemia, Complementation Group a 82 0.035
979
KPS004 Kaposi Sarcoma 76 0.035
980
HRP006 Herpes Simplex 70 0.035
981
OST003 Osteonecrosis 66 0.035
982
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 63 0.035
983
MYC008 Myocarditis 59 0.035
984
ACR008 Acrocallosal Syndrome 58 0.035
985
VGN023 Vaginitis 57 0.035
986
DSS009 Disseminated Intravascular Coagulation 56 0.035
987
TLN003 Telangiectasis 54 0.035
988
ALC009 Alcoholic Liver Cirrhosis 53 0.035
989
c CRD093 Cardiomyopathy, Dilated, 1a 49 0.035
990
CRB004 Cerebral Artery Occlusion 45 0.035
991
ARC016 Auriculocondylar Syndrome 1 41 0.035
992
OVR093 Overhydrated Hereditary Stomatocytosis 39 0.035
993
CRB088 Cerebral Atrophy 38 0.035
994
GGN002 Gigantism 37 0.035
995
CHT005 Chitotriosidase Deficiency 28 0.035
996
c CRT085 Carotid Intimal Medial Thickness 2 25 0.035
997
CHG001 Chagas Disease 72 0.035
998
GRF003 Graft-Versus-Host Disease 72 0.035
999
ORT004 Orthostatic Intolerance 68 0.035
1000
URT039 Urticaria 61 0.035
1001
URN010 Urinary Tract Obstruction 57 0.035
1002
FML026 Familial Lipoprotein Lipase Deficiency 53 0.035
1003
PYD002 Pyoderma 52 0.035
1004
PLC007 Placental Abruption 51 0.035
1005
ACD008 Acid-Labile Subunit Deficiency 51 0.035
1006
CRD137 Cardiogenic Shock 51 0.035
1007
HYP006 Hypertensive Heart Disease 50 0.035
1008
c HYP057 Hypervitaminosis D 40 0.035
1009
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 26 0.035
1010
MDL005 Medulloblastoma 75 0.033
1011
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 65 0.033
1012
FTL001 Fetal Alcohol Syndrome 63 0.033
1013
HYP190 Hypoalphalipoproteinemia, Primary 60 0.033
1014
OCL013 Oculodentodigital Dysplasia 60 0.033
1015
c BLD124 Bleeding Disorder, Platelet-Type, 11 59 0.033
1016
MLK003 Melkersson-Rosenthal Syndrome 58 0.033
1017
MST005 Mastitis 57 0.033
1018
PLV003 Pelvic Inflammatory Disease 55 0.033
1019
OCL006 Ocular Hypertension 55 0.033
1020
c GLY005 Glycogen Storage Disease Vi 49 0.033
1021
c HYP768 Hyperlipoproteinemia, Type I 44 0.033
1022
DDN006 Duodenitis 43 0.033
1023
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.033
1024
MYS004 Myiasis 34 0.033
1025
c HNT011 Huntington Disease-Like 3 33 0.033
1026
SBC016 Subacute Delirium 32 0.033
1027
SCL018 Scoliosis 58 0.033
1028
c BRD044 Bardet-Biedl Syndrome 17 48 0.033
1029
c BRD033 Bardet-Biedl Syndrome 13 44 0.033
1030
c BRD020 Bardet-Biedl Syndrome 8 44 0.033
1031
c BRD048 Bardet-Biedl Syndrome 18 43 0.033
1032
LPM010 Lipomatosis, Multiple Symmetric 43 0.033
1033
c BRD017 Bardet-Biedl Syndrome 5 40 0.033
1034
PLN026 Pilonidal Sinus 40 0.033
1035
c BRD032 Bardet-Biedl Syndrome 14 39 0.033
1036
c BRD045 Bardet-Biedl Syndrome 19 36 0.033
1037
c BRD047 Bardet-Biedl Syndrome 16 35 0.033
1038
c BRD019 Bardet-Biedl Syndrome 7 30 0.033
1039
c BRD050 Bardet-Biedl Syndrome 21 26 0.033
1040
c BRD021 Bardet-Biedl Syndrome 9 26 0.033
1041
c BRD051 Bardet-Biedl Syndrome 20 24 0.033
1042
CRB089 Cerebral Beriberi 21 0.033
1043
RNL077 Renal Fibrosis 50 0.033
1044
CHR066 Chronic Fatigue Syndrome 67 0.033
1045
IGR001 Ige Responsiveness, Atopic 62 0.033
1046
c ACT135 Acute Graft Versus Host Disease 57 0.033
1047
GLL018 Gallbladder Cancer 55 0.033
1048
INT079 Intrahepatic Cholangiocarcinoma 54 0.033
1049
BLR006 Biliary Tract Disease 51 0.033
1050
ATS010 Autosomal Recessive Disease 47 0.033
1051
SPN021 Spinal Meningioma 41 0.033
1052
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 35 0.033
1053
INF021 Infant Gynecomastia 27 0.033
1054
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 23 0.033
1055
BRN028 Brain Cancer 74 0.033
1056
TNG002 Tangier Disease 64 0.033
1057
CLN015 Colon Adenocarcinoma 57 0.033
1058
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.033
1059
TCL003 T Cell Deficiency 44 0.033
1060
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 32 0.033
1061
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 28 0.033
1062
APR006 Apert Syndrome 69 0.032
1063
c WLM013 Wilms Tumor 1 65 0.032
1064
TRG002 Trigeminal Neuralgia 60 0.032
1065
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 59 0.032
1066
NRN004 Neuroendocrine Tumor 56 0.032
1067
WHM001 Whim Syndrome 54 0.032
1068
ATR057 Atrioventricular Block 53 0.032
1069
PRC012 Pericardial Effusion 53 0.032
1070
HPT009 Hepatopulmonary Syndrome 52 0.032
1071
PRS045 Prostatic Hypertrophy 48 0.032
1072
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.032
1073
c CNG216 Congenital Hydrocephalus 47 0.032
1074
GLC011 Galactose Epimerase Deficiency 45 0.032
1075
OST115 Osteonecrosis of the Jaw 44 0.032
1076
BRN026 Branch Retinal Artery Occlusion 42 0.032
1077
TRD008 Triiodothyronine Receptor Auxiliary Protein 25 0.032
1078
LYM017 Lyme Disease 71 0.031
1079
MSC157 Muscular Dystrophy, Duchenne Type 66 0.031
1080
OVR029 Ovarian Hyperstimulation Syndrome 65 0.031
1081
CRC006 Carcinoid Syndrome 61 0.031
1082
LPS002 Liposarcoma 60 0.031
1083
PRG013 Paraganglioma 58 0.031
1084
HMR003 Hemorrhagic Disease 56 0.031
1085
CYS039 Cystic Kidney Disease 54 0.031
1086
SHR001 Short Bowel Syndrome 53 0.031
1087
ECT093 Ectopic Cushing Syndrome 52 0.031
1089
PRP009 Peripartum Cardiomyopathy 50 0.031
1090
ANL022 Anal Fistula 48 0.031
1091
MMM006 Mammographic Density 47 0.031
1092
PHY002