Search results for obesity AND diabetes

1269 hits were found for obesity AND diabetes

# Family MCID Name MIFTS Score
1
BDY004 Body Mass Index Quantitative Trait Locus 11 78 8.516
2
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.249
3
DBT009 Diabetes Mellitus 67 1.527
4
DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 1.082
5
GST033 Gestational Diabetes 62 0.588
6
OVR063 Overnutrition 48 0.587
7
MRB003 Morbid Obesity 61 0.574
8
NRP001 Neuropathy 62 0.561
9
KDN018 Kidney Disease 68 0.526
10
c BDY019 Body Mass Index Quantitative Trait Locus 18 42 0.501
11
c BDY020 Body Mass Index Quantitative Trait Locus 19 41 0.501
12
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.501
13
c BDY011 Body Mass Index Quantitative Trait Locus 10 40 0.500
14
MCR115 Microvascular Complications of Diabetes 5 70 0.498
15
GLC003 Glucose Intolerance 58 0.465
16
HYP056 Hypoglycemia 63 0.456
17
HYP066 Hyperglycemia 64 0.455
18
DBT085 Diabetes Mellitus, Insulin-Dependent 72 0.448
19
c MCR113 Microvascular Complications of Diabetes 3 57 0.444
20
c MCR120 Microvascular Complications of Diabetes 7 44 0.443
21
c MCR130 Microvascular Complications of Diabetes 6 43 0.443
22
c MCR133 Microvascular Complications of Diabetes 4 43 0.443
23
HYP060 Hyperinsulinism 55 0.421
24
LVR013 Liver Disease 75 0.412
25
FTT001 Fatty Liver Disease 66 0.410
26
DBT010 Diabetic Neuropathy 58 0.365
27
HRT032 Heart Disease 73 0.358
28
PLY011 Polycystic Ovary Syndrome 64 0.347
29
ATM095 Autoimmune Disease 65 0.343
30
DBT005 Diabetes Insipidus 52 0.341
31
c BDY007 Body Mass Index Quantitative Trait Locus 1 47 0.341
32
NNL004 Nonalcoholic Fatty Liver Disease 55 0.327
33
SLP006 Sleep Apnea 70 0.324
34
IMM136 Immune System Disease 49 0.323
35
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.322
36
PRP019 Peripheral Nervous System Disease 62 0.307
37
DPR016 Depression 73 0.305
38
ETN001 Eating Disorder 64 0.288
39
VSC007 Vascular Disease 68 0.283
40
LPD008 Lipid Metabolism Disorder 64 0.280
41
MYC007 Myocardial Infarction 77 0.275
42
ISC004 Ischemia 66 0.273
43
ART140 Arteries, Anomalies of 65 0.266
44
ATN004 Autonomic Neuropathy 46 0.254
45
NNL002 Nonalcoholic Steatohepatitis 53 0.253
46
CRN018 Coronary Artery Anomaly 75 0.246
47
DGS002 Degos \'en Cocarde\' Erythrokeratoderma 36 0.244
48
AST005 Asthma 82 0.242
49
ANX010 Anxiety 72 0.240
50
c CHR089 Chronic Kidney Failure 73 0.240
51
PLY019 Polyneuropathy 58 0.239
52
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.238
53
ISC006 Ischemic Heart Disease 67 0.237
54
PRD004 Prediabetes Syndrome 48 0.237
55
URN009 Urinary System Disease 49 0.237
56
RTN018 Retinal Disease 56 0.235
57
PRD008 Periodontitis 66 0.232
58
DBT008 Diabetic Angiopathy 44 0.229
59
AGN016 Aging 62 0.227
60
SPS003 Spastic Diplegia 54 0.224
61
OBS037 Obesity-Hypoventilation Syndrome 51 0.220
62
c CRN300 Coronary Heart Disease 1 59 0.219
63
MNT002 Mental Depression 62 0.217
64
BRS047 Breast Cancer 100 0.212
65
PRD007 Periodontal Disease 65 0.211
66
MTR004 Maturity-Onset Diabetes of the Young 60 0.209
67
APN008 Apnea, Obstructive Sleep 68 0.208
68
ART021 Arteriosclerosis 57 0.203
69
ACN002 Acanthosis Nigricans 66 0.203
70
CNG034 Congestive Heart Failure 68 0.201
71
INS024 Insulin-Like Growth Factor I 76 0.200
72
HYP080 Hypogonadism 52 0.196
73
INF032 Infertility 58 0.194
74
PNC044 Pancreatitis 63 0.191
75
ART022 Arthritis 77 0.189
76
DBT004 Diabetic Polyneuropathy 50 0.189
77
HPT021 Hepatitis 75 0.188
78
GST037 Gastroparesis 59 0.184
79
VSC018 Visceral Steatosis 29 0.184
80
IMP005 Impotence 57 0.184
81
PRD006 Prader-Willi Syndrome 63 0.184
82
PRP027 Peripheral Vascular Disease 71 0.182
83
THR024 Thrombosis 63 0.182
84
c TRC078 Trichohepatoenteric Syndrome 2 22 0.182
85
CTR002 Cataract 58 0.181
86
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 66 0.181
87
c PLY105 Polycystic Ovary Syndrome 1 45 0.180
88
SLP005 Sleep Disorder 57 0.178
89
NRM005 Neuromuscular Disease 58 0.178
90
c PRC016 Pre-Eclampsia 60 0.178
91
OST012 Osteoarthritis 81 0.176
92
GST092 Gastroesophageal Reflux 65 0.175
93
RTN016 Retinal Degeneration 53 0.174
94
TRC086 Trichohepatoenteric Syndrome 1 51 0.173
95
THY032 Thyroiditis 53 0.172
96
END030 End Stage Renal Failure 59 0.169
97
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.167
98
FTL021 Fetal Macrosomia 46 0.166
99
HYP266 Hypoxia 62 0.166
100
GST050 Gastrointestinal System Disease 63 0.165
101
DBT002 Diabetic Autonomic Neuropathy 44 0.165
102
ANR007 Anorexia Nervosa 68 0.164
103
OST002 Osteoporosis 74 0.162
104
NRV007 Nervous System Disease 69 0.155
105
HYP086 Hypothyroidism 63 0.153
106
c HYP595 Hypertension, Essential 78 0.152
107
ALZ034 Alzheimer Disease 86 0.148
108
SCH015 Schizophrenia 70 0.147
109
PRS040 Prostate Cancer 94 0.147
110
CLR023 Colorectal Cancer 99 0.145
111
NTR005 Nutritional Deficiency Disease 58 0.143
112
c HPT001 Hepatitis C 70 0.142
113
HYP014 Hyperuricemia 56 0.140
114
ADN016 Adenocarcinoma 70 0.140
115
DNT012 Dental Caries 51 0.139
116
END057 Endometrial Cancer 68 0.139
117
CRN036 Craniopharyngioma 66 0.138
118
INF038 Influenza 76 0.138
119
c PRD040 Periodontitis, Chronic 59 0.138
120
ECL001 Eclampsia 57 0.137
121
RSP003 Respiratory Failure 72 0.137
122
LMB062 Limb Ischemia 53 0.136
123
HYP043 Hyperandrogenism 50 0.135
124
c ACT075 Acute Myocardial Infarction 56 0.135
125
RHM011 Rheumatoid Arthritis 82 0.134
126
c ACT027 Acute Pancreatitis 61 0.134
127
OVR049 Ovarian Disease 58 0.132
128
BRN106 Burns 55 0.132
129
c PRC031 Preeclampsia/eclampsia 1 34 0.131
130
LNG099 Lung Disease 67 0.131
131
PNC035 Pancreatic Cancer 82 0.130
132
ANG054 Angina Pectoris 62 0.130
133
ENC018 Encephalopathy 62 0.130
134
DMN002 Dementia 68 0.130
135
PRP080 Peripheral Artery Disease 54 0.129
136
HYP064 Hypogonadotropism 39 0.129
137
ART023 Arthropathy 64 0.128
138
LVR012 Liver Cirrhosis 66 0.127
139
RTN020 Retinal Vascular Disease 54 0.126
140
MNG006 Monogenic Diabetes 39 0.126
141
LKM002 Leukemia 72 0.126
142
PSR002 Psoriasis 66 0.125
143
ART153 Arthrochalasia Ehlers-Danlos Syndrome 24 0.125
144
BND020 Bone Disease 61 0.124
145
MDD011 Mood Disorder 62 0.121
146
SXL003 Sexual Disorder 49 0.121
147
CLC063 Celiac Disease 1 74 0.120
148
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 61 0.120
149
HYP730 Hypogonadotropic Hypogonadism 58 0.119
150
THR013 Thoracic Outlet Syndrome 55 0.117
151
WDH003 Woodhouse-Sakati Syndrome 52 0.117
152
HPT023 Hepatocellular Carcinoma 98 0.116
153
THY030 Thyroid Gland Disease 43 0.116
154
CRT049 Critical Limb Ischemia 54 0.116
155
c BDY005 Body Mass Index Quantitative Trait Locus 9 33 0.115
156
c BDY006 Body Mass Index Quantitative Trait Locus 8 31 0.115
157
c BDY012 Body Mass Index Quantitative Trait Locus 7 31 0.115
158
RSP006 Respiratory System Disease 56 0.114
159
ATR011 Atrial Fibrillation 69 0.114
160
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 0.114
161
c BDY010 Body Mass Index Quantitative Trait Locus 4 31 0.114
162
MTH009 Mouth Disease 61 0.114
163
JNT002 Joint Disorders 58 0.113
164
CRB039 Cerebrovascular Disease 67 0.113
165
DRR001 Diarrhea 57 0.113
166
HSH003 Hashimoto Thyroiditis 65 0.111
167
BLM002 Bulimia Nervosa 60 0.111
168
INS001 Insulinoma 64 0.111
169
ATH013 Atherosclerosis Susceptibility 66 0.110
170
ADN018 Adenoma 64 0.110
171
HYP083 Hypopituitarism 44 0.108
172
CNN003 Conn\'s Syndrome 73 0.108
173
BNF002 Bone Fracture 46 0.108
174
OVR046 Ovarian Cyst 53 0.106
175
PNM007 Pneumonia 71 0.106
176
ATX010 Ataxia Neuropathy Spectrum 32 0.105
177
SPN331 Spondyloocular Syndrome 42 0.105
178
HYP750 Hypertriglyceridemia, Familial 60 0.105
179
MLT020 Multiple Sclerosis 75 0.105
180
DBT007 Diabetic Cataract 35 0.104
181
RST023 Resting Heart Rate, Variation in 42 0.104
182
LYM053 Lymphomatous Thyroiditis 25 0.104
183
PTT009 Pituitary Gland Disease 55 0.104
184
FSH001 Fish-Eye Disease 50 0.104
185
ANR048 Aniridia 1 65 0.104
186
PSY004 Psychotic Disorder 72 0.104
187
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.103
188
ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.103
189
MJR001 Major Depressive Disorder 66 0.103
190
LYM118 Lymphoma 70 0.103
191
c HYP555 Hypertriglyceridemia, Transient Infantile 41 0.102
192
AMY004 Amyloidosis 68 0.102
193
c MTR002 Mitral Valve Insufficiency 48 0.102
194
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 46 0.101
195
ACT232 Acute Necrotizing Encephalopathy 33 0.101
196
BLD137 Blood Group--Ahonen 24 0.101
197
LPT014 Leptin Deficiency or Dysfunction 40 0.101
198
IRN002 Iron Metabolism Disease 60 0.101
199
c BRD013 Bardet-Biedl Syndrome 12 49 0.101
200
MTB004 Metabolic Acidosis 49 0.099
201
GT001 Gout 60 0.099
202
c BRD014 Bardet-Biedl Syndrome 2 61 0.098
203
EPL164 Epilepsy 73 0.098
204
HYP085 Hypothalamic Disease 47 0.098
205
PNM001 Pneumocystosis 53 0.098
206
VRL011 Viral Infectious Disease 72 0.097
207
BRD002 Bardet-Biedl Syndrome 64 0.097
208
c BRD012 Bardet-Biedl Syndrome 11 52 0.097
209
c BRD011 Bardet-Biedl Syndrome 10 45 0.097
210
CYS001 Cystic Fibrosis 83 0.097
211
ATT013 Attention Deficit-Hyperactivity Disorder 67 0.097
212
EXN002 Exanthem 56 0.097
213
NPH009 Nephrolithiasis 57 0.096
214
c SPN225 Spondyloarthropathy 1 75 0.096
215
SMT008 Smith-Magenis Syndrome 58 0.096
216
RTN023 Retinitis 48 0.095
217
GST053 Gastric Cancer 79 0.095
218
MSC007 Muscle Hypertrophy 64 0.095
219
BPL003 Bipolar Disorder 60 0.095
220
HYP069 Hyperparathyroidism 59 0.095
221
NRL016 Neural Tube Defects 79 0.095
222
LYM031 Lymphocytic Leukemia 61 0.095
223
GNG013 Gingivitis 62 0.094
224
DFC004 Deficiency Anemia 66 0.094
225
DWN001 Down Syndrome 72 0.093
226
GLL020 Gallbladder Disease 63 0.092
227
LKM062 Leukemia, Acute Lymphoblastic 68 0.092
228
RHM027 Rheumatic Disease 61 0.092
229
c MYT020 Myotonic Dystrophy 2 55 0.092
230
ATX030 Ataxia-Telangiectasia 84 0.092
231
PNG002 Pain Agnosia 39 0.091
232
ACT088 Acute Insulin Response 48 0.091
233
CLL015 Collagen Disease 46 0.091
234
GNR004 Generalized Anxiety Disorder 53 0.091
235
TRM003 Tremor 55 0.090
236
STM006 Stomach Disease 50 0.090
237
c CHR579 Chiari Malformation Type Ii 42 0.090
238
GRW007 Growth Hormone Deficiency 52 0.090
239
FRN020 Frontal Fibrosing Alopecia 31 0.090
240
AND002 Androgen Insensitivity Syndrome 65 0.090
241
AXN002 Axenfeld-Rieger Syndrome 56 0.089
242
ALR002 Al-Raqad Syndrome 41 0.089
243
LPT006 Leptin Receptor Deficiency 43 0.089
244
HDC001 Headache 61 0.089
245
ALP046 Alport Syndrome, X-Linked 74 0.088
246
SPN186 Spinal Cord Injury 65 0.088
247
BWN003 Bowenoid Papulosis 42 0.088
248
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.087
249
ART001 Arterial Tortuosity Syndrome 60 0.087
250
HLC007 Helicobacter Pylori Infection 65 0.087
251
THY028 Thyroid Cancer 71 0.087
252
c GLL024 Gallbladder Disease 1 51 0.087
253
SVR004 Severe Combined Immunodeficiency 69 0.087
254
HPT082 Hepatic Adenomas, Familial 51 0.087
255
ANG001 Angelman Syndrome 67 0.087
256
HNM002 Hinman Syndrome 32 0.087
257
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.087
258
SNS003 Sensory Peripheral Neuropathy 57 0.086
259
BRR014 Barrett Esophagus 70 0.086
260
ADP007 Adie Pupil 43 0.086
261
ANV001 Anovulation 49 0.085
262
SKN016 Skin Disease 64 0.085
263
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 68 0.085
264
INT007 Intermediate Coronary Syndrome 47 0.085
265
LCT001 Lactic Acidosis 52 0.085
266
CRP001 Carpal Tunnel Syndrome 71 0.085
267
BRN038 Bronchial Disease 55 0.084
268
ALC007 Alcohol Dependence 68 0.084
269
CRD119 Cardiac Arrest 64 0.084
270
MSC003 Muscular Atrophy 55 0.083
271
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.083
272
ACQ007 Acquired Immunodeficiency Syndrome 63 0.083
273
ART016 Aortic Aneurysm 70 0.083
274
PLC008 Placenta Disease 56 0.083
275
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 67 0.083
276
c HPT073 Hepatitis C Virus 67 0.083
277
THR100 Thrombocytopenic Purpura, Autoimmune 65 0.082
278
CRN030 Coronary Stenosis 51 0.082
279
INF037 Inflammatory Bowel Disease 54 0.082
280
PLM033 Pulmonary Embolism 63 0.081
281
LYM025 Lymphedema 55 0.081
282
INT075 Intracranial Hypertension 57 0.081
283
SCH012 Schizoaffective Disorder 54 0.081
284
IRN001 Iron Deficiency Anemia 55 0.081
285
RNL114 Renal Cell Carcinoma, Nonpapillary 62 0.081
286
ALS001 Alstrom Syndrome 55 0.081
287
VTM002 Vitamin B12 Deficiency 48 0.080
288
URM002 Uremia 52 0.080
289
SKN027 Skin Conditions 46 0.080
290
THR014 Thrombocytopenia 64 0.080
291
ACR001 Aicardi-Goutieres Syndrome 61 0.080
292
c ACR116 Aicardi-Goutieres Syndrome 1 44 0.080
293
LPS004 Lupus Erythematosus 69 0.079
294
ESP024 Esophagitis 62 0.078
295
DYS021 Dysautonomia 45 0.078
296
KDN017 Kidney Cancer 59 0.078
297
LPM005 Lipomatosis 46 0.078
298
GLM007 Glomerulonephritis 60 0.078
299
c HPT016 Hepatitis B 70 0.078
300
ATS364 Autism 69 0.078
301
ACR007 Acromegaly 71 0.078
302
MCR141 Mucormycosis 49 0.078
303
MYC088 Mycobacterium Avium Complex Infections 33 0.078
304
AND005 Androgen Insensitivity Syndrome, Mild 22 0.078
305
RTN008 Retinitis Pigmentosa 79 0.078
306
BCT022 Bacterial Infectious Disease 60 0.078
307
HYP050 Hyperinsulinemic Hypoglycemia 55 0.078
308
c AMY091 Amyotrophic Lateral Sclerosis 1 91 0.078
309
CNG376 Congenital Leptin Deficiency 29 0.077
310
c SYS001 Systemic Lupus Erythematosus 88 0.077
311
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 45 0.077
312
HYP265 Hypotonia 41 0.077
313
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.077
314
BRC012 Brucellosis 66 0.077
315
JVN024 Juvenile Hereditary Hemochromatosis 42 0.077
316
HMN014 Human Immunodeficiency Virus Infectious Disease 60 0.076
317
CHL004 Cholelithiasis 50 0.076
318
CNS004 Constipation 57 0.076
319
CLT003 Colitis 64 0.076
320
INT068 Intestinal Disease 60 0.076
321
PRC019 Precocious Puberty 52 0.075
322
NRR001 Neuroretinitis 39 0.075
323
STR067 Stroke, Ischemic 85 0.075
324
DRM006 Dermatitis 68 0.075
325
GSG001 Gas Gangrene 45 0.075
326
OVR042 Ovarian Cancer 83 0.075
327
PSR001 Psoriatic Arthritis 67 0.075
328
MLN008 Melanoma 63 0.075
329
PRS063 Paresthesia 39 0.075
330
WRN001 Werner Syndrome 70 0.075
331
MNN028 Mononeuropathy of the Median Nerve, Mild 45 0.075
332
FBR047 Fibromyalgia 61 0.075
333
CLR108 Colorectal Adenoma 61 0.075
334
ATN002 Autonomic Nervous System Disease 49 0.074
335
RNL051 Renal Cysts and Diabetes Syndrome 54 0.074
336
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 53 0.074
337
PLM037 Pulmonary Hypertension 77 0.074
338
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.074
339
FBR065 Fibrocalculous Pancreatopathy 18 0.074
340
HRN028 Horns in Sheep 22 0.074
341
NRC002 Narcolepsy 59 0.074
342
ALX002 Alexithymia 41 0.073
343
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 47 0.073
344
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 44 0.073
345
BCT004 Bacteriuria 48 0.073
346
NCR002 Necrobiosis Lipoidica 34 0.073
347
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 37 0.073
348
TRN020 Turner Syndrome 69 0.073
349
c HPT003 Hepatitis a 67 0.073
350
PNC034 Pancreas Disease 56 0.073
351
NRL018 Neural Tube Defects, Folate-Sensitive 53 0.073
352
MYP004 Myopathy 63 0.073
353
LNG108 Langerhans Cell Histiocytosis 63 0.072
354
HYP076 Hyperthyroidism 56 0.072
355
c ACT071 Acute Kidney Failure 51 0.072
356
SHR029 Short Syndrome 59 0.071
357
LNG032 Lung Cancer 99 0.071
358
SYS003 Systolic Heart Failure 46 0.071
359
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.071
360
LRN002 Laron Syndrome 64 0.071
361
BRS090 Breast Reconstruction 43 0.071
362
AMN001 Amenorrhea 56 0.070
363
ATM052 Autoimmune Disease 1 46 0.070
364
HST010 Histiocytosis 61 0.070
365
DSS008 Disease of Mental Health 65 0.070
366
MYL005 Myelofibrosis 69 0.070
367
c ACT210 Acute Respiratory Distress Syndrome 62 0.070
368
OST097 Osteoporotic Fracture 44 0.070
369
ASP030 Aspirin Resistance 47 0.069
370
HRN026 Hernia, Hiatus 48 0.069
371
c ART138 Aortic Aneurysm, Familial Abdominal, 1 65 0.069
372
CLL003 Cellulitis 59 0.069
373
SKN023 Skin Tag 39 0.069
374
c BRD010 Bardet-Biedl Syndrome 1 59 0.069
375
CRD132 Cardiac Conduction Defect 62 0.069
376
c ACT068 Acute Cystitis 56 0.069
377
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.069
379
c HMC039 Hemochromatosis, Type 1 74 0.068
380
c THR092 Thrombophilia Due to Thrombin Defect 69 0.068
381
INT303 Intracranial Hypertension, Idiopathic 50 0.068
382
BRS051 Breast Disease 63 0.068
383
PSD015 Pseudohypoparathyroidism 50 0.068
384
STS002 Situs Inversus 49 0.067
385
CND004 Candidiasis 60 0.067
386
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.067
387
IRR002 Irritable Bowel Syndrome 50 0.066
388
LYM027 Lymphopenia 57 0.066
389
ALC004 Alcohol Abuse 69 0.066
390
GLC008 Glucose Metabolism Disease 48 0.066
391
RST001 Restless Legs Syndrome 54 0.066
392
SZR006 Seizure Disorder 58 0.065
393
FCL005 Focal Segmental Glomerulosclerosis 60 0.065
394
RNL007 Renal Tubular Acidosis 52 0.065
395
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.065
396
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 54 0.065
397
HPR003 Heparin-Induced Thrombocytopenia 49 0.065
398
PRS129 Prostatic Hyperplasia, Benign 51 0.065
399
MYL069 Myeloma, Multiple 85 0.065
400
MYL006 Myeloid Leukemia 67 0.065
401
ADL010 Adult Respiratory Distress Syndrome 62 0.065
402
GST044 Gastritis 60 0.065
403
DYS073 Dysphagia 51 0.064
404
RCK004 Rickets 65 0.064
405
CRT013 Carotid Stenosis 53 0.064
406
c BLD140 Blood Group, I System 30 0.064
407
CRH001 Crohn\'s Disease 77 0.064
408
DMP001 Dumping Syndrome 47 0.064
409
MRB006 Morbid Obesity and Spermatogenic Failure 20 0.064
410
BRN071 Brain Injury 54 0.063
411
BRB001 Beriberi 45 0.063
412
DYS011 Dyskinesia of Esophagus 38 0.063
413
MHM001 Mehmo Syndrome 31 0.063
414
LRN003 Learning Disability 52 0.063
415
SCN001 Secondary Hyperparathyroidism of Renal Origin 52 0.063
416
MLN007 Male Infertility 52 0.063
417
APP008 Appendicitis 65 0.063
418
PST021 Postpartum Depression 55 0.063
419
CMR001 Camurati-Engelmann Disease 56 0.062
420
SGM006 Segmental Odontomaxillary Dysplasia 21 0.062
421
FSC004 Fasciitis 49 0.062
422
MNN017 Mononeuropathy 40 0.062
423
c LPD015 Lipodystrophy, Familial Partial, Type 2 56 0.062
424
CHL123 Chlamydia 66 0.061
425
PMP004 Pemphigus Foliaceus 46 0.061
426
SLD003 Sialadenitis 49 0.061
427
CRT016 Carotid Artery Disease 57 0.061
428
WRN003 Wernicke Encephalopathy 48 0.061
429
PRP098 Proprotein Convertase 1/3 Deficiency 29 0.061
430
c VRL010 Viral Hepatitis 60 0.061
431
NTR027 Neutrophil Actin Dysfunction 31 0.061
432
ESP021 Esophageal Cancer 83 0.061
433
c PTT057 Pituitary Adenoma 4, Acth-Secreting 53 0.061
434
PRT036 Peritonitis 66 0.061
435
VNS003 Venous Insufficiency 54 0.060
436
c PNC128 Pain - Chronic 46 0.060
437
CHN016 Cohen Syndrome 54 0.060
438
c ATS007 Autism Spectrum Disorder 64 0.060
439
INT002 Intermittent Claudication 63 0.060
440
OBS082 Obstructive Nephropathy 51 0.060
441
FML012 Familial Partial Lipodystrophy 52 0.060
442
c LRG017 Large Intestine Cancer 59 0.060
443
GLY013 Glycogen Storage Disease 60 0.059
444
DYS014 Dyspepsia 52 0.059
445
DWR001 Dwarfism 45 0.059
446
ACT103 Acute Lymphoblastic Leukemia, Childhood 53 0.059
447
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 32 0.059
448
TTR001 Tetralogy of Fallot 71 0.059
449
EPD070 Epidermoid Cysts 43 0.059
450
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.059
451
PRP030 Purpura 61 0.059
452
PNC033 Pancreas Adenocarcinoma 66 0.058
453
EXC002 Exocrine Pancreatic Insufficiency 40 0.058
454
PST055 Postural Hypotension 38 0.058
455
PLY006 Polydactyly 59 0.058
456
GYN001 Gynecomastia 47 0.058
457
HYP061 Hypertrophic Cardiomyopathy 58 0.058
458
BNR002 Bone Resorption Disease 53 0.058
459
SNS001 Sensorineural Hearing Loss 58 0.058
460
END038 Endocrine Pancreas Disease 38 0.058
461
ALL003 Allergic Rhinitis 70 0.057
462
SLP010 Slipped Capital Femoral Epiphysis 37 0.057
463
RHN004 Rhinitis 62 0.057
464
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 52 0.057
465
SCL022 Scleredema 31 0.057
466
DLT002 Dilated Cardiomyopathy 74 0.057
467
SPN051 Spondylitis 54 0.057
468
OBS050 Obesity Due to Congenital Leptin Deficiency 18 0.057
469
SRC014 Sarcoma 70 0.057
470
OPN001 Open-Angle Glaucoma 53 0.057
471
NWB001 Newborn Respiratory Distress Syndrome 55 0.057
472
RSP007 Respiratory Distress Syndrome, Infant 35 0.057
473
NPH012 Nephrotic Syndrome 59 0.057
474
PLY014 Polycystic Kidney Disease 63 0.056
475
c LKM061 Leukemia, Acute Myeloid 83 0.056
476
HYP724 Hyperlipoproteinemia, Type Iii 62 0.056
477
MCR010 Microcephaly 55 0.056
478
ADM013 Adamantinoma of Long Bones 48 0.056
479
PST053 Postherpetic Neuralgia 45 0.056
480
PNC045 Pancreatic Agenesis 40 0.056
481
CRD223 Cardiac Arrhythmia 55 0.056
482
HYD002 Hydronephrosis 49 0.056
483
FRL002 Froelich Syndrome 14 0.056
484
VSC002 Vascular Dementia 55 0.055
485
FNG006 Feingold Syndrome 1 48 0.055
486
BLD163 Blood Group, Dombrock System 26 0.055
487
ART008 Arteriosclerosis Obliterans 42 0.055
488
HYP614 Hyperlipidemia, Familial Combined 54 0.055
489
DXT002 Dextrocardia with Situs Inversus 43 0.055
490
CYS009 Cystadenoma 42 0.055
491
GTR002 Goiter 53 0.055
492
MSC033 Muscle Disorders 50 0.055
493
PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 65 0.055
494
SBS003 Substance Abuse 59 0.055
495
KRT002 Keratomalacia 56 0.055
496
c SVR005 Severe Pre-Eclampsia 56 0.055
497
c MTR026 Maturity-Onset Diabetes of the Young, Type 9 33 0.055
498
c LBR014 Leber Congenital Amaurosis 4 63 0.055
499
c CNT035 Central Nervous System Disease 62 0.055
500
ALP008 Alopecia 55 0.055
501
THR015 Thrombophilia 55 0.054
502
WLL001 Williams-Beuren Syndrome 63 0.054
503
STF001 Stiff-Person Syndrome 65 0.054
504
ERY029 Erythermalgia, Primary 56 0.054
505
CRB037 Cerebral Palsy 71 0.053
506
FCL044 Fecal Incontinence 36 0.053
507
HYP784 Hypogonadism, Male 42 0.053
508
c MYT021 Myotonic Dystrophy 1 70 0.053
509
HMT018 Hematopoietic Stem Cell Transplantation 58 0.053
510
c MTR044 Maturity-Onset Diabetes of the Young, Type 10 41 0.053
511
CLC001 Calciphylaxis 53 0.053
512
TRM010 Traumatic Brain Injury 56 0.053
513
CRN024 Corneal Disease 44 0.053
514
END072 Endotheliitis 40 0.053
515
HYP110 Hyperproinsulinemia 37 0.053
516
HYD006 Hydrocephalus 66 0.053
517
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 52 0.053
518
c PRM005 Primary Hyperparathyroidism 60 0.053
519
EXP004 Exophthalmos 51 0.053
520
TND004 Tendinopathy 44 0.053
521
FXF002 Fox-Fordyce Disease 30 0.053
522
c CNT075 Central Precocious Puberty 53 0.053
523
PRS021 Prostatic Adenoma 49 0.053
524
BLD134 Bladder Cancer 70 0.052
525
GLL008 Gilles De La Tourette Syndrome 68 0.052
526
c PTT056 Pituitary Adenoma 1, Multiple Types 52 0.052
527
RPD005 Rapidly Involuting Congenital Hemangioma 20 0.052
528
CHL065 Cholangiocarcinoma 64 0.052
529
CLC006 Calcinosis 48 0.052
530
ACT105 Acute Mountain Sickness 56 0.052
531
ALP009 Alopecia Areata 64 0.052
532
c ACT074 Acute Lymphocytic Leukemia 63 0.052
533
ACQ022 Acquired Generalized Lipodystrophy 53 0.052
534
HYP068 Hyperostosis 50 0.052
535
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 77 0.052
536
MYC084 Mycobacterium Tuberculosis 1 74 0.052
537
ACR006 Aceruloplasminemia 70 0.052
538
CRV035 Cervical Cancer 76 0.052
539
FND002 Fundus Dystrophy 50 0.052
540
c MGR028 Migraine with or Without Aura 1 69 0.052
541
HMN044 Human Immunodeficiency Virus Type 1 74 0.051
542
MGL001 Megaloblastic Anemia 54 0.051
543
URN022 Urinary Tract Infections, Recurrent 28 0.051
544
ACH005 Achalasia 53 0.051
545
DVR002 Diverticulitis 46 0.051
546
ELP001 Elephantiasis 37 0.051
547
CHR084 Chromosomal Disease 34 0.051
548
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 13 0.051
549
DRM053 Dermatitis, Atopic 71 0.051
550
NTR004 Neutropenia 60 0.051
551
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 50 0.051
552
DRG003 Drug Dependence 50 0.051
553
DST006 Diastolic Heart Failure 46 0.051
554
GNG011 Gingival Disease 46 0.051
555
ACQ009 Acquired Metabolic Disease 34 0.051
556
DGN001 Degenerative Disc Disease 52 0.051
557
PHC003 Pheochromocytoma 72 0.051
558
HYP607 Hypercholesterolemia, Familial 81 0.051
559
ERY003 Erythema Multiforme 58 0.051
560
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 53 0.051
561
MYL009 Myelodysplastic Syndrome 70 0.051
562
PPT005 Peptic Ulcer Disease 62 0.051
563
SQM006 Squamous Cell Carcinoma 59 0.051
564
GLC036 Glucagonoma 51 0.051
565
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.050
566
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.050
567
HMS001 Hemosiderosis 52 0.050
568
BLD165 Blood Group, Colton System 27 0.050
569
PTS002 Ptosis 52 0.050
570
SYN007 Synovitis 61 0.049
571
PST011 Pustulosis of Palm and Sole 49 0.049
572
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.049
573
HMC014 Homocysteinemia 54 0.049
574
c FCL025 Focal Segmental Glomerulosclerosis 1 55 0.049
575
PPT001 Peptic Esophagitis 45 0.049
576
c SML038 Small Cell Cancer of the Lung 72 0.049
577
IGG001 Iga Glomerulonephritis 58 0.049
578
ART002 Arts Syndrome 54 0.049
579
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 44 0.049
580
STT004 Steatorrhea 40 0.049
581
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 22 0.049
582
PRP016 Paraplegia 54 0.049
583
c HMP029 Hemophilia a 70 0.049
584
VRC005 Varicose Veins 65 0.049
585
SJG008 Sjogren Syndrome 59 0.049
586
c LPD040 Lipodystrophy, Familial Partial, Type 1 44 0.049
587
IDP033 Idiopathic Edema 43 0.049
588
TTR016 Tetra-Amelia Syndrome 38 0.049
589
PSD014 Pseudopseudohypoparathyroidism 51 0.049
590
ANL018 Analbuminemia 48 0.049
591
VSC011 Vasculitis 66 0.049
592
PLM010 Pulmonary Edema 58 0.049
593
CHL066 Cholangitis 51 0.049
594
CHL147 Chlamydia Pneumonia 41 0.049
595
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.048
596
MSC005 Muscular Dystrophy 66 0.048
597
HYP020 Hyperprolactinemia 64 0.048
598
PST028 Post-Traumatic Stress Disorder 62 0.048
599
CLN019 Colonic Disease 57 0.048
600
ALL006 Allergic Asthma 61 0.048
601
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 57 0.048
602
ENC004 Encephalitis 66 0.048
603
HLP001 Holoprosencephaly 66 0.048
604
MYP006 Myopia 58 0.048
605
ULC004 Ulcerative Colitis 80 0.048
606
SPN027 Spinal Stenosis 61 0.048
607
MSC190 Muscular Disease 51 0.048
608
CMP008 Compartment Syndrome 48 0.048
609
MSC004 Muscle Tissue Disease 27 0.048
610
TTH006 Tooth Disease 49 0.048
611
PNS012 Paine Syndrome 62 0.047
612
DSR011 Disorganization, Mouse, Homolog of 23 0.047
613
GLN010 Glanzmann Thrombasthenia 68 0.047
614
BLL003 Bell\'s Palsy 52 0.047
615
c PLM164 Pulmonary Hypertension, Primary, 1 74 0.047
616
PLV020 Pelvic Organ Prolapse 63 0.047
617
HRT012 Heart Valve Disease 54 0.047
618
HDR002 Hidradenitis Suppurativa 56 0.047
619
HDR003 Hidradenitis 47 0.047
620
CYT008 Cytomegalovirus Infection 60 0.046
621
c EPS039 Episodic Pain Syndrome, Familial, 1 31 0.046
622
c ART101 Aortic Valve Disease 2 65 0.046
623
FML035 Familial Hyperlipidemia 51 0.046
624
ACH004 Achondroplasia 68 0.046
625
PRT018 Portal Vein Thrombosis 50 0.046
626
CNN005 Connective Tissue Disease 64 0.045
627
CRB085 Cerebral Hemorrhage 45 0.045
628
c ATR087 Atrial Standstill 1 67 0.045
629
DCB001 Decubitus Ulcer 45 0.045
630
BCL006 B-Cell Lymphomas 65 0.045
631
CHL068 Cholestasis 60 0.045
632
TND005 Tendinitis 44 0.045
633
c AMY009 Amyloidosis Aa 56 0.045
634
SFT003 Soft Tissue Sarcoma 56 0.045
635
CHR005 Chorioamnionitis 54 0.045
636
INT070 Intestinal Obstruction 53 0.045
637
PNN001 Panniculitis 47 0.045
638
BRN024 Bronchitis 67 0.045
639
MNC006 Monoclonal Gammopathy of Uncertain Significance 53 0.045
640
c CHR431 Chronic Venous Insufficiency 48 0.045
641
CRY036 Cryptogenic Cirrhosis 38 0.045
642
HYP017 Hypophosphatemia 48 0.045
643
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 43 0.045
644
CLR030 Clear Cell Renal Cell Carcinoma 49 0.044
645
ASP006 Aspergillosis 66 0.044
646
CHR071 Charcot-Marie-Tooth Disease 62 0.044
647
SDD008 Sudden Sensorineural Hearing Loss 46 0.044
648
TRC026 Tracheal Disease 32 0.044
649
HYP364 Hyperostosis Frontalis Interna 30 0.044
650
NRB001 Neuroblastoma 73 0.044
651
PRT013 Portal Hypertension 60 0.044
652
BLD044 Bladder Disease 51 0.044
653
EMP001 Empty Sella Syndrome 46 0.044
654
ANG020 Angiosarcoma 58 0.044
655
CHP002 Chops Syndrome 33 0.044
656
HRP004 Herpes Zoster 61 0.044
657
FRN014 Fournier Gangrene 40 0.044
658
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.044
659
PLY018 Polycythemia 60 0.044
660
c INF145 Infantile Liver Failure Syndrome 1 57 0.044
661
GST007 Gastric Dilatation 31 0.044
662
MYS003 Myasthenia Gravis 74 0.043
663
c ACT073 Acute Leukemia 61 0.043
664
END046 Endometritis 51 0.043
665
MLR004 Malaria 85 0.043
666
APL001 Aplastic Anemia 74 0.043
667
HMP007 Hemophilia 61 0.043
668
RDC002 Radiculopathy 53 0.043
669
TXP001 Toxoplasmosis 65 0.043
670
CMP010 Complex Regional Pain Syndrome 62 0.043
671
NPH010 Nephrosclerosis 45 0.043
672
SNL007 Senile Cataract 40 0.043
673
c TYP038 Type 1 Diabetes Mellitus 15 24 0.043
674
SHH001 Sheehan Syndrome 51 0.042
675
c HNT004 Huntington Disease-Like 2 41 0.042
676
ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 55 0.042
677
MCR011 Microinvasive Gastric Cancer 46 0.042
678
RCT017 Rectal Disease 40 0.042
679
PRT058 Pure Autonomic Failure 61 0.042
680
CHL067 Cholecystitis 58 0.042
681
OCL069 Ocular Motor Apraxia 55 0.042
682
CHR008 Choroiditis 42 0.042
683
END041 Endometrial Adenocarcinoma 60 0.042
684
LRN001 Laurence-Moon Syndrome 40 0.042
685
END044 Endometriosis 65 0.042
686
c CNG006 Congenital Hypothyroidism 63 0.042
687
INT146 Intervertebral Disc Disease 62 0.042
688
BCK002 Beckwith-Wiedemann Syndrome 59 0.042
689
LYM019 Lymphosarcoma 56 0.042
690
PRT038 Protein-Energy Malnutrition 52 0.042
691
VSL002 Visual Epilepsy 35 0.042
692
LYM133 Lymphoma, Hodgkin, Classic 75 0.042
693
GST019 Gastrointestinal Stromal Tumor 74 0.042
694
OTT002 Otitis Media 68 0.042
695
DGR001 Digeorge Syndrome 62 0.042
696
ISL003 Isolated Growth Hormone Deficiency 51 0.042
697
INT051 Intussusception 50 0.042
698
HYP263 Hypersomnia 44 0.042
699
BNC003 Bone Cancer 58 0.041
700
MMP001 Mumps 59 0.041
701
PLY112 Polyarteritis Nodosa, Childhood-Onset 49 0.041
702
OPT070 Optic Nerve Hypoplasia, Bilateral 49 0.041
703
GLC022 Glucose/galactose Malabsorption 44 0.041
704
MTR007 Motor Peripheral Neuropathy 38 0.041
705
PNC041 Pancreatic Ductal Adenocarcinoma 53 0.041
706
AYM001 Ayme-Gripp Syndrome 40 0.041
707
RTN024 Retinoblastoma 72 0.040
708
ANT006 Antiphospholipid Syndrome 60 0.040
709
OST011 Osteomalacia 52 0.040
710
PPL021 Papilledema 48 0.040
711
PRK057 Parkinson Disease, Late-Onset 76 0.040
712
TMP003 Temporal Arteritis 69 0.040
713
CNR004 Cone-Rod Dystrophy 2 63 0.040
714
END033 Endocarditis 60 0.040
715
c GLC092 Glaucoma, Primary Open Angle 58 0.040
716
ICH020 Ichthyosis Prematurity Syndrome 45 0.040
717
ART004 Aortic Atherosclerosis 45 0.040
718
MNC002 Munchausen by Proxy 34 0.040
719
SRC025 Sarcoidosis 1 76 0.040
720
c LKM063 Leukemia, Chronic Myeloid 74 0.040
721
SCK003 Sickle Cell Anemia 72 0.040
722
SNS014 Sinusitis 63 0.040
723
CHK001 Chikungunya 61 0.040
724
GLM045 Glioma 55 0.040
725
PTT006 Pituitary Adenoma 53 0.040
726
OCC006 Occipital Horn Syndrome 52 0.040
727
HYP077 Hypertrichosis 49 0.040
728
SYN036 Syncope 47 0.040
729
MDS022 Mediastinitis 41 0.040
730
SPN041 Spinal Cord Disease 52 0.039
731
PRS042 Prostate Disease 42 0.039
732
TQP001 Taqi Polymorphism 30 0.039
733
GST023 Gastric Ulcer 57 0.039
734
ALB001 Albright\'s Hereditary Osteodystrophy 53 0.039
735
c BPL002 Bipolar I Disorder 50 0.039
736
c BRD015 Bardet-Biedl Syndrome 3 43 0.039
737
HPT067 Hepatocellular Adenoma 42 0.039
738
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 54 0.039
739
DDN001 Duodenal Ulcer 53 0.039
740
GLC096 Galactorrhea 47 0.039
741
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 45 0.039
742
IMM001 Immune-Complex Glomerulonephritis 42 0.039
743
c MYS011 Myasthenia Gravis Congenital 36 0.039
744
KBK002 Kabuki Syndrome 1 66 0.039
745
GST045 Gastroenteritis 62 0.039
746
CRH005 Crohn\'s Colitis 61 0.039
747
c THY109 Thyroid Cancer, Nonmedullary, 1 58 0.039
748
ICH004 Ichthyosis 56 0.039
749
ACT010 Acth-Secreting Pituitary Adenoma 52 0.039
750
ART031 Aortic Coarctation 49 0.039
751
SCH003 Schizophreniform Disorder 43 0.039
752
ALL014 Allergic Encephalomyelitis 42 0.039
753
DDN009 Duodenal Obstruction 34 0.039
754
c HYP602 Hyperoxaluria, Primary, Type Ii 33 0.039
755
CMP096 Complete Generalized Lipodystrophy 25 0.039
756
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.038
757
PHR003 Pharyngitis 57 0.038
758
KWS001 Kwashiorkor 45 0.038
759
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 42 0.038
760
c BRD018 Bardet-Biedl Syndrome 6 41 0.038
761
SPN046 Spinal Muscular Atrophy 66 0.038
762
c ATM011 Autoimmune Hepatitis 61 0.038
763
c MLG069 Malignant Hypertension 50 0.038
764
RTN014 Retinal Artery Occlusion 48 0.038
765
THR005 Thrombotic Thrombocytopenic Purpura 64 0.038
766
TBC004 Tobacco Addiction 64 0.038
767
c HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.038
768
MLT074 Multiple Endocrine Neoplasia 57 0.038
769
MYX004 Myxedema 45 0.038
770
CDQ001 Cauda Equina Syndrome 44 0.038
771
SPR007 Superior Mesenteric Artery Syndrome 42 0.038
772
ACT055 Actinomycosis 40 0.038
773
c MLG042 Malignant Otitis Externa 29 0.038
774
HYP098 Hypereosinophilic Syndrome 65 0.037
775
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 55 0.037
776
KRT006 Keratoconjunctivitis 54 0.037
777
BRN080 Brain Ischemia 41 0.037
778
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 36 0.037
779
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 14 0.037
780
PHN003 Phenylketonuria 73 0.037
781
CLR109 Colorectal Adenocarcinoma 54 0.037
782
PRV006 Pervasive Developmental Disorder 53 0.037
783
KRT007 Keratoconus 49 0.037
784
CRN074 Coronary Artery Aneurysm 47 0.037
785
IDP041 Idiopathic Recurrent Pericarditis 33 0.037
786
MRL001 Meralgia Paresthetica 27 0.037
787
NGH001 Night Blindness 49 0.036
788
c BRD016 Bardet-Biedl Syndrome 4 47 0.036
789
GST040 Gastric Adenocarcinoma 65 0.036
790
RCT018 Rectal Neoplasm 59 0.036
791
ARM001 Aromatase Deficiency 52 0.036
792
PST095 Post-Thrombotic Syndrome 51 0.036
793
WSK001 Wiskott-Aldrich Syndrome 76 0.036
794
MYS005 Myositis 64 0.036
795
SLV001 Silver-Russell Syndrome 55 0.036
796
GLC009 Glucosephosphate Dehydrogenase Deficiency 51 0.036
797
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 46 0.036
798
NRV004 Nerve Compression Syndrome 31 0.036
799
CCC001 Coccidioidomycosis 60 0.036
800
STT001 Status Epilepticus 60 0.036
801
FNC043 Fanconi Anemia, Complementation Group E 54 0.036
802
ART017 Aortic Disease 54 0.036
803
ISL001 Islet Cell Tumor 50 0.036
804
QDR001 Quadriplegia 50 0.036
805
PTT037 Pituitary Tumors 47 0.036
806
MTH081 Mthfr Gene Variant 27 0.036
807
NRF023 Neurofibromatosis, Type Ii 75 0.035
808
BRN056 Bronchopulmonary Dysplasia 60 0.035
809
PLM034 Pulmonary Emphysema 56 0.035
810
c INF071 Inflammatory Bowel Disease 1 53 0.035
811
SPN035 Spindle Cell Sarcoma 50 0.035
812
CLP006 Clopidogrel Resistance 45 0.035
813
HYP081 Hypolipoproteinemia 43 0.035
814
NNT019 Neonatal Hypothyroidism 41 0.035
815
TMP012 Temple Syndrome 35 0.035
816
48X003 48,xxyy Syndrome 33 0.035
817
FNC027 Fanconi Anemia, Complementation Group a 82 0.035
818
KPS004 Kaposi Sarcoma 76 0.035
819
HRP006 Herpes Simplex 70 0.035
820
OST003 Osteonecrosis 66 0.035
821
VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 63 0.035
822
MYC008 Myocarditis 59 0.035
823
ACR008 Acrocallosal Syndrome 58 0.035
824
VGN023 Vaginitis 57 0.035
825
DSS009 Disseminated Intravascular Coagulation 56 0.035
826
TLN003 Telangiectasis 54 0.035
827
ALC009 Alcoholic Liver Cirrhosis 53 0.035
828
c CRD093 Cardiomyopathy, Dilated, 1a 49 0.035
829
CRB004 Cerebral Artery Occlusion 45 0.035
830
ARC016 Auriculocondylar Syndrome 1 41 0.035
831
OVR093 Overhydrated Hereditary Stomatocytosis 39 0.035
832
CRB088 Cerebral Atrophy 38 0.035
833
GGN002 Gigantism 37 0.035
834
CHT005 Chitotriosidase Deficiency 28 0.035
835
c CRT085 Carotid Intimal Medial Thickness 2 25 0.035
836
CHG001 Chagas Disease 72 0.035
837
GRF003 Graft-Versus-Host Disease 72 0.035
838
ORT004 Orthostatic Intolerance 68 0.035
839
URT039 Urticaria 61 0.035
840
URN010 Urinary Tract Obstruction 57 0.035
841
FML026 Familial Lipoprotein Lipase Deficiency 53 0.035
842
PYD002 Pyoderma 52 0.035
843
PLC007 Placental Abruption 51 0.035
844
ACD008 Acid-Labile Subunit Deficiency 51 0.035
845
CRD137 Cardiogenic Shock 51 0.035
846
HYP006 Hypertensive Heart Disease 50 0.035
847
c HYP057 Hypervitaminosis D 40 0.035
848
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 26 0.035
849
MDL005 Medulloblastoma 75 0.033
850
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 65 0.033
851
FTL001 Fetal Alcohol Syndrome 63 0.033
852
HYP190 Hypoalphalipoproteinemia, Primary 60 0.033
853
OCL013 Oculodentodigital Dysplasia 60 0.033
854
c BLD124 Bleeding Disorder, Platelet-Type, 11 59 0.033
855
MLK003 Melkersson-Rosenthal Syndrome 58 0.033
856
MST005 Mastitis 57 0.033
857
PLV003 Pelvic Inflammatory Disease 55 0.033
858
OCL006 Ocular Hypertension 55 0.033
859
c GLY005 Glycogen Storage Disease Vi 49 0.033
860
c HYP768 Hyperlipoproteinemia, Type I 44 0.033
861
DDN006 Duodenitis 43 0.033
862
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 42 0.033
863
MYS004 Myiasis 34 0.033
864
c HNT011 Huntington Disease-Like 3 33 0.033
865
SBC016 Subacute Delirium 32 0.033
866
SCL018 Scoliosis 58 0.033
867
c BRD044 Bardet-Biedl Syndrome 17 48 0.033
868
c BRD033 Bardet-Biedl Syndrome 13 44 0.033
869
c BRD020 Bardet-Biedl Syndrome 8 44 0.033
870
c BRD048 Bardet-Biedl Syndrome 18 43 0.033
871
LPM010 Lipomatosis, Multiple Symmetric 43 0.033
872
c BRD017 Bardet-Biedl Syndrome 5 40 0.033
873
PLN026 Pilonidal Sinus 40 0.033
874
c BRD032 Bardet-Biedl Syndrome 14 39 0.033
875
c BRD045 Bardet-Biedl Syndrome 19 36 0.033
876
c BRD047 Bardet-Biedl Syndrome 16 35 0.033
877
c BRD019 Bardet-Biedl Syndrome 7 30 0.033
878
c BRD050 Bardet-Biedl Syndrome 21 26 0.033
879
c BRD021 Bardet-Biedl Syndrome 9 26 0.033
880
c BRD051 Bardet-Biedl Syndrome 20 24 0.033
881
CRB089 Cerebral Beriberi 21 0.033
882
CHR066 Chronic Fatigue Syndrome 67 0.033
883
IGR001 Ige Responsiveness, Atopic 62 0.033
884
c ACT135 Acute Graft Versus Host Disease 57 0.033
885
GLL018 Gallbladder Cancer 55 0.033
886
INT079 Intrahepatic Cholangiocarcinoma 54 0.033
887
BLR006 Biliary Tract Disease 51 0.033
888
ATS010 Autosomal Recessive Disease 47 0.033
889
SPN021 Spinal Meningioma 41 0.033
890
CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 35 0.033
891
INF021 Infant Gynecomastia 27 0.033
892
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 23 0.033
893
BRN028 Brain Cancer 74 0.033
894
TNG002 Tangier Disease 64 0.033
895
CLN015 Colon Adenocarcinoma 57 0.033
896
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 47 0.033
897
TCL003 T Cell Deficiency 44 0.033
898
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 32 0.033
899
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 28 0.033
900
APR006 Apert Syndrome 69 0.032
901
c WLM013 Wilms Tumor 1 65 0.032
902
TRG002 Trigeminal Neuralgia 60 0.032
903
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 59 0.032
904
NRN004 Neuroendocrine Tumor 56 0.032
905
WHM001 Whim Syndrome 54 0.032
906
ATR057 Atrioventricular Block 53 0.032
907
PRC012 Pericardial Effusion 53 0.032
908
HPT009 Hepatopulmonary Syndrome 52 0.032
909
PRS045 Prostatic Hypertrophy 48 0.032
910
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.032
911
c CNG216 Congenital Hydrocephalus 47 0.032
912
GLC011 Galactose Epimerase Deficiency 45 0.032
913
OST115 Osteonecrosis of the Jaw 44 0.032
914
BRN026 Branch Retinal Artery Occlusion 42 0.032
915
TRD008 Triiodothyronine Receptor Auxiliary Protein 25 0.032
916
LYM017 Lyme Disease 71 0.031
917
MSC157 Muscular Dystrophy, Duchenne Type 66 0.031
918
OVR029 Ovarian Hyperstimulation Syndrome 65 0.031
919
CRC006 Carcinoid Syndrome 61 0.031
920
LPS002 Liposarcoma 60 0.031
921
PRG013 Paraganglioma 58 0.031
922
HMR003 Hemorrhagic Disease 56 0.031
923
CYS039 Cystic Kidney Disease 54 0.031
924
SHR001 Short Bowel Syndrome 53 0.031
925
ECT093 Ectopic Cushing Syndrome 52 0.031
927
PRP009 Peripartum Cardiomyopathy 50 0.031
928
ANL022 Anal Fistula 48 0.031
929
MMM006 Mammographic Density 47 0.031
930
PHY002 Physical Disorder 47 0.031
931
NNT049 Nontuberculous Mycobacterial Lung Disease 45 0.031
932
SCL057 Scoliosis, Isolated 1 42 0.031
933
PTT003 Pituitary-Dependent Cushing\'s Disease 39 0.031
934
ALC005 Alcoholic Pancreatitis 38 0.031
935
PRM056 Primrose Syndrome 35 0.031
936
PST035 Postgastrectomy Syndrome 34 0.031
937
SPT019 Septo-Optic Dysplasia Spectrum 34 0.031
938
c PRS080 Prostate Cancer, Hereditary, 7 28 0.031
939
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 24 0.031
940
CHR189 Chromosome 12p Deletion 12 0.031
941
LSH001 Leishmaniasis 71 0.031
942
c OVR114 Ovarian Cancer 1 62 0.031
943
EPL140 Epilepsy, Idiopathic Generalized 62 0.031
944
HMN010 Hemangioma 60 0.031
945
DMY004 Demyelinating Disease 57 0.031
946
ARS001 Aarskog-Scott Syndrome 56 0.031
947
DST005 Diastrophic Dysplasia 53 0.031
948
TRT010 Teratoma 53 0.031
949
c PSR017 Psoriasis 2 52 0.031
950
NRT001 Neurotic Disorder 51 0.031
951
MTC069 Mitochondrial Disorders 49 0.031
952
HDN002 Head Injury 48 0.031
953
PRM003 Premature Ejaculation 47 0.031
954
DNG001 Dengue Shock Syndrome 47 0.031
955
c PSR028 Psoriasis 7 46 0.031
956
c PSR032 Psoriasis 11 46 0.031
957
c PSR018 Psoriasis 13 45 0.031
958
c CNT028 Central Retinal Artery Occlusion 41 0.031
959
PNC008 Pancreatic Endocrine Carcinoma 38 0.031
960
DCR003 Dacryoadenitis 36 0.031
961
FCT008 Factitious Disorder 34 0.031
962
ART010 Arteriolosclerosis 31 0.031
963
SVN002 Sveinsson Chorioretinal Atrophy 31 0.031
964
c LPD036 Lipodystrophy, Familial Partial, Type 6 26 0.031
965
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.030
966
BRN049 Brain Tumor, Childhood 30 0.030
967
LPD026 Lipedema 30 0.030
968
PDT040 Pediatric Hypertension 30 0.030
969
GNT050 Genitourinary Tract Anomalies 29 0.030
970
c PGM011 Pigmented Nodular Adrenocortical Disease, Primary, 2 26 0.030
971
c PGM021 Pigmented Nodular Adrenocortical Disease, Primary, 1 25 0.030
972
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.029
973
FRG001 Fragile X Syndrome 70 0.029
974
c LPM012 Lipomatosis, Multiple 64 0.029
975
PLL001 Pallister-Hall Syndrome 64 0.029
976
MLG056 Malignant Hyperthermia 62 0.029
977
KRT009 Keratosis 54 0.029
978
SCL009 Sclerosing Cholangitis 54 0.029
979
FML037 Female Breast Cancer 53 0.029
980
HYP458 Hyper Ige Syndrome 52 0.029
981
THR117 Three M Syndrome 1 52 0.029
982
PRT029 Parathyroid Adenoma 51 0.029
983
RNL011 Renal Osteodystrophy 49 0.029
984
STT007 Steatocystoma Multiplex 46 0.029
985
LYM009 Lymphocytic Choriomeningitis 46 0.029
986
c HYP349 Hyperinsulinemic Hypoglycemia, Familial, 7 38 0.029
987
NTR007 Neutral Lipid Storage Disease with Myopathy 36 0.029
988
CRN031 Cranial Nerve Disease 36 0.029
989
STR103 Streptococcus Pneumonia 33 0.029
990
PTL001 Patulous Eustachian Tube 32 0.029
991
MLN070 Melanoma-Astrocytoma Syndrome 32 0.029
993
SKN019 Skin Melanoma 63 0.029
994
LYM021 Lymphadenitis 62 0.029
995
ING001 Inguinal Hernia 61 0.029
996
PRT082 Preterm Premature Rupture of the Membranes 57 0.029
997
BLR008 Bilirubin Metabolic Disorder 55 0.029
998
PPL022 Papilloma 55 0.029
999
HRN001 Horner\'s Syndrome 48 0.029
1000
VND001 Vein Disease 47 0.029
1001
SPN369 Spinal Disease 42 0.029
1002
AND014 Androgenic Alopecia 41 0.029
1003
TTH032 Tooth Size 40 0.029
1004
PLN007 Plantar Fasciitis 33 0.029
1005
DDN004 Duodenogastric Reflux 31 0.029
1006
c HYP531 Hypogonadotropic Hypogonadism 4 with or Without Anosmia 25 0.029
1007
c ACR119 Acrodysostosis 2 with or Without Hormone Resistance 24 0.029
1008
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.029
1009
c CSH006 Cushing Syndrome Due to Macronodular Adrenal Hyperplasia 24 0.029
1010
48X002 48,xxxy Syndrome 24 0.029
1011
ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 23 0.029
1012
MSC089 Mosaic Monosomy X 21 0.029
1013
c TRN055 Turner Syndrome Due to Structural X Chromosome Anomalies 21 0.029
1014
HYP686 Hypogonadism, Male, with Mental Retardation and Skeletal Anomalies 20 0.029
1015
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.029
1016
AGM001 Agammaglobulinemia 71 0.027
1017
c CWD006 Cowden Syndrome 1 71 0.027
1018
DNG005 Dengue Virus 64 0.027
1019
CMM005 Common Cold 63 0.027
1020
CFF002 Coffin-Lowry Syndrome 61 0.027
1021
RSC001 Rosacea 60 0.027
1022
MCS002 Mucositis 59 0.027
1023
c FML116 Familial Cold Autoinflammatory Syndrome 1 59 0.027
1024
FLR002 Filariasis 58 0.027
1025
PYD001 Pyoderma Gangrenosum 57 0.027
1026
MCK005 Mckusick-Kaufman Syndrome 54 0.027
1027
PTT014 Pitt-Hopkins Syndrome 54 0.027
1028
LRY019 Laryngitis 54 0.027
1029
WLF002 Wolf-Hirschhorn Syndrome 53 0.027
1030
SCB001 Scabies 51 0.027
1031
PRM020 Premenstrual Tension 51 0.027
1032
c ATM017 Autoimmune Disease of the Nervous System 49 0.027
1033
MNN009 Meningoencephalitis 49 0.027
1034
c WLM011 Wilms Tumor 6 48 0.027
1035
ISC015 Ischemic Colitis 48 0.027
1036
c PSR023 Psoriasis 1 47 0.027
1037
CHC001 Chickenpox 47 0.027
1038
ASP007 Aspiration Pneumonia 46 0.027
1039
ENT001 Enterocele 45 0.027
1040
LCH009 Lichen Sclerosus 44 0.027
1041
CRV039 Cervicitis 44 0.027
1042
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 41 0.027
1043
SCT001 Sciatic Neuropathy 39 0.027
1044
THY039 Thyrotropin-Releasing Hormone Deficiency 37 0.027
1045
ANS004 Anisometropia 33 0.027
1046
PLM005 Pleomorphic Lipoma 33 0.027
1047
CHN040 Choanal Atresia and Lymphedema 28 0.027
1048
XP2001 Xp22.3 Microdeletion Syndrome 25 0.027
1049
c ATM089 Autoimmune Neuropathy 25 0.027
1050
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 21 0.027
1051
PNC065 Pinched Nerve 5 0.027
1052
c HMP004 Hemophilia B 66 0.026
1053
KLL001 Kallmann Syndrome 64 0.026
1054
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 63 0.026
1055
RBS001 Rabies 62 0.026
1056
CRN015 Cornelia De Lange Syndrome 62 0.026
1057
BRN002 Bronchiolitis 62 0.026
1058
c INS002 in Situ Carcinoma 59 0.026
1059
PTN001 Patent Foramen Ovale 58 0.026
1060
SPN052 Spondyloarthropathy 56 0.026
1061
STS008 Sotos Syndrome 1 56 0.026
1062
FCT001 Factor Viii Deficiency 55 0.026
1063
PHL006 Phelan-Mcdermid Syndrome 54 0.026
1064
MYL020 Myelomeningocele 54 0.026
1065
MNN042 Meningioma, Radiation-Induced 52 0.026
1066
THY054 Thyrotoxic Periodic Paralysis 52 0.026
1067
c CNT015 Central Sleep Apnea 47 0.026
1068
PLL008 Pallister-Killian Syndrome 46 0.026
1069
CRV045 Cervical Intraepithelial Neoplasia 45 0.026
1070
BSL008 Basal Ganglia Disease 43 0.026
1071
ESP025 Esophagus Adenocarcinoma 42 0.026
1072
ANS012 Anus Disease 42 0.026
1073
TRC005 Tracheal Stenosis 40 0.026
1074
RMN001 Rumination Disorder 36 0.026
1075
ALG027 Al-Gazali-Bakalinova Syndrome 36 0.026
1076
HYD003 Hydrarthrosis 34 0.026
1077
CHL013 Cholecystolithiasis 34 0.026
1078
CRN033 Cranial Nerve Malignant Neoplasm 32 0.026
1079
OPT076 Optic Perineuritis 21 0.026
1080
CLL020 Collagenopathy Type 2 Alpha 1 20 0.026
1081
c NRC017 Narcolepsy 7 18 0.026
1082
RTT002 Rett Syndrome 84 0.026
1083
c MNN043 Meningioma, Familial 70 0.026
1084
OBS002 Obsessive-Compulsive Disorder 69 0.026
1085
DYS154 Dystonia 65 0.026
1086
PTT048 Pituitary Adenoma, Prolactin-Secreting 62 0.026
1087
VSC003 Visceral Leishmaniasis 59 0.026
1088
PLC005 Placental Insufficiency 59 0.026
1089
EXT034 Extrinsic Allergic Alveolitis 58 0.026
1090
HYP040 Hypospadias 58 0.026
1091
DFF005 Diffuse Large B-Cell Lymphoma 56 0.026
1092
CLF001 Cleft Lip 56 0.026
1093
TCD001 Tic Disorder 55 0.026
1094
TRP002 Tropical Spastic Paraparesis 55 0.026
1095
CLF004 Cleft Lip/palate 55 0.026
1096
FLR001 Filarial Elephantiasis 55 0.026
1097
FCL014 Focal Epilepsy 54 0.026
1098
FRY006 Fryns Microphthalmia Syndrome 53 0.026
1099
TXC002 Toxic Encephalopathy 53 0.026
1100
PRM002 Primary Hyperoxaluria 53 0.026
1101
c VRL007 Viral Encephalitis 53 0.026
1102
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 52 0.026
1103
CMR002 Coumarin Resistance 51 0.026
1104
CLB010 Coloboma of Macula 51 0.026
1105
AST007 Astrocytoma 49 0.026
1106