Search results for obesity AND diabetes

1476 hits were found for obesity AND diabetes

# Family MCID Name MIFTS Score
1
P BDY004 Body Mass Index Quantitative Trait Locus 11 72 8.594
2
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.207
3
P DBT009 Diabetes Mellitus 67 1.642
4
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 1.208
5
c BDY020 Body Mass Index Quantitative Trait Locus 19 44 0.787
6
c BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.787
7
c BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.787
8
c BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.786
9
c BDY006 Body Mass Index Quantitative Trait Locus 8 41 0.786
10
c BDY012 Body Mass Index Quantitative Trait Locus 7 41 0.786
11
GLC008 Glucose Metabolism Disease 53 0.739
12
GST033 Gestational Diabetes 63 0.722
13
LPT014 Leptin Deficiency or Dysfunction 70 0.702
14
P NRP001 Neuropathy 63 0.645
15
P MCR115 Microvascular Complications of Diabetes 5 70 0.608
16
P KDN018 Kidney Disease 71 0.606
17
c BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.590
18
NTR005 Nutritional Deficiency Disease 59 0.581
19
c MCR113 Microvascular Complications of Diabetes 3 58 0.575
20
c MCR120 Microvascular Complications of Diabetes 7 46 0.575
21
c MCR133 Microvascular Complications of Diabetes 4 43 0.574
22
c MCR130 Microvascular Complications of Diabetes 6 43 0.574
23
OVR063 Overnutrition 53 0.562
24
GLC003 Glucose Intolerance 59 0.532
25
HYP056 Hypoglycemia 64 0.510
26
FTT001 Fatty Liver Disease 66 0.507
27
P LVR013 Liver Disease 76 0.496
28
HYP066 Hyperglycemia 64 0.492
29
HYP060 Hyperinsulinism 57 0.462
30
P NNL004 Nonalcoholic Fatty Liver Disease 56 0.454
31
DBT010 Diabetic Neuropathy 60 0.434
32
P DBT005 Diabetes Insipidus 55 0.426
33
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.414
34
P DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.393
35
LPD008 Lipid Metabolism Disorder 65 0.389
36
P HRT032 Heart Disease 76 0.385
37
P PLY011 Polycystic Ovary Syndrome 64 0.370
38
P SLP006 Sleep Apnea 70 0.349
39
P PRP019 Peripheral Nervous System Disease 66 0.346
40
ATM095 Autoimmune Disease 68 0.345
41
ETN001 Eating Disorder 65 0.341
42
ART140 Arteries, Anomalies of 66 0.336
43
c FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.335
44
P CRN018 Coronary Artery Anomaly 75 0.331
45
DPR016 Depression 72 0.327
46
P CRN300 Coronary Heart Disease 1 61 0.312
47
IMM136 Immune System Disease 57 0.310
48
c CHR089 Chronic Kidney Failure 73 0.303
49
VSC007 Vascular Disease 72 0.297
50
ISC004 Ischemia 67 0.297
51
P MYC007 Myocardial Infarction 78 0.291
52
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 61 0.289
54
ATN004 Autonomic Neuropathy 46 0.266
55
P PRD008 Periodontitis 66 0.265
56
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.265
57
DGS002 Degos 'en Cocarde' Erythrokeratoderma 25 0.265
58
AST005 Asthma 81 0.261
59
DBT002 Diabetic Autonomic Neuropathy 46 0.255
60
c HYP595 Hypertension, Essential 81 0.251
61
P BRS047 Breast Cancer 100 0.247
62
ISC006 Ischemic Heart Disease 72 0.244
63
NNL002 Nonalcoholic Steatohepatitis 54 0.244
64
ANX010 Anxiety 73 0.242
65
AGN016 Aging 63 0.242
66
P PLY019 Polyneuropathy 57 0.241
67
IMP005 Impotence 56 0.240
68
PRD007 Periodontal Disease 66 0.236
69
PLC008 Placenta Disease 59 0.231
70
RTN018 Retinal Disease 58 0.228
71
PRD004 Prediabetes Syndrome 51 0.227
72
PRP027 Peripheral Vascular Disease 72 0.227
73
CNG034 Congestive Heart Failure 70 0.224
74
URN009 Urinary System Disease 59 0.224
75
DBT008 Diabetic Angiopathy 48 0.220
76
P MTR004 Maturity-Onset Diabetes of the Young 61 0.217
77
SPS003 Spastic Diplegia 55 0.216
78
P HYP750 Hypertriglyceridemia, Familial 58 0.214
79
MNT002 Mental Depression 65 0.212
80
P PNC044 Pancreatitis 62 0.211
81
DSS008 Disease of Mental Health 71 0.210
82
APN008 Apnea, Obstructive Sleep 68 0.210
83
OBS037 Obesity-Hypoventilation Syndrome 50 0.209
84
P ART022 Arthritis 77 0.209
85
P HPT021 Hepatitis 73 0.206
86
P CTR002 Cataract 59 0.205
87
P ART021 Arteriosclerosis 61 0.205
88
HYP835 Hypothalamic Obesity 43 0.205
89
c PRC016 Pre-Eclampsia 61 0.201
90
P HYP086 Hypothyroidism 66 0.201
91
HYP080 Hypogonadism 53 0.200
92
OST012 Osteoarthritis 80 0.200
93
P INF032 Infertility 60 0.198
94
END030 End Stage Renal Failure 60 0.198
95
HYP064 Hypogonadotropism 42 0.196
96
P PRD006 Prader-Willi Syndrome 61 0.195
97
INS024 Insulin-Like Growth Factor I 82 0.195
98
ACN002 Acanthosis Nigricans 64 0.195
99
THR024 Thrombosis 64 0.191
100
GST092 Gastroesophageal Reflux 66 0.191
101
P THY032 Thyroiditis 53 0.186
102
END057 Endometrial Cancer 68 0.186
103
FSH001 Fish-Eye Disease 50 0.185
104
GST037 Gastroparesis 57 0.184
105
HYP266 Hypoxia 63 0.182
106
DBT004 Diabetic Polyneuropathy 50 0.181
107
NRT004 Neuritis 58 0.178
108
P VSC018 Visceral Steatosis 37 0.178
109
c TRC078 Trichohepatoenteric Syndrome 2 35 0.176
110
ATH013 Atherosclerosis Susceptibility 60 0.174
112
c PRD040 Periodontitis, Chronic 59 0.172
113
P TRC086 Trichohepatoenteric Syndrome 1 60 0.171
114
P OST002 Osteoporosis 74 0.171
115
SLP005 Sleep Disorder 60 0.170
116
ANR007 Anorexia Nervosa 68 0.170
117
NRM005 Neuromuscular Disease 61 0.169
118
P ALZ034 Alzheimer Disease 87 0.167
119
P RTN016 Retinal Degeneration 56 0.166
120
c ATR087 Atrial Standstill 1 70 0.163
121
P CLR023 Colorectal Cancer 99 0.162
122
FTL021 Fetal Macrosomia 46 0.160
123
GST050 Gastrointestinal System Disease 67 0.160
124
P RHM011 Rheumatoid Arthritis 81 0.158
125
P LKM002 Leukemia 72 0.158
126
c ACT075 Acute Myocardial Infarction 57 0.158
127
c HPT001 Hepatitis C 69 0.157
128
P PNC035 Pancreatic Cancer 82 0.155
129
P NRV007 Nervous System Disease 71 0.155
130
P HPT023 Hepatocellular Carcinoma 96 0.153
131
P ADN016 Adenocarcinoma 70 0.153
132
P CLC063 Celiac Disease 1 71 0.153
133
SXL003 Sexual Disorder 53 0.153
134
LYM053 Lymphomatous Thyroiditis 27 0.152
135
P PRS040 Prostate Cancer 93 0.152
136
c ACT027 Acute Pancreatitis 59 0.152
137
P SCH015 Schizophrenia 73 0.150
138
DNT012 Dental Caries 52 0.150
139
P INF038 Influenza 75 0.150
140
PRP080 Peripheral Artery Disease 56 0.149
141
P MSC007 Muscle Hypertrophy 64 0.147
142
c PRS136 Prostate Cancer, Hereditary, 6 40 0.145
143
c PRS130 Prostate Cancer, Hereditary, 8 37 0.145
144
LVR012 Liver Cirrhosis 67 0.144
145
DMN002 Dementia 69 0.143
146
BRN106 Burns 59 0.143
147
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 62 0.141
148
P ECL001 Eclampsia 58 0.141
149
HYP014 Hyperuricemia 55 0.141
150
P RSP003 Respiratory Failure 72 0.140
151
P ATR011 Atrial Fibrillation 69 0.138
152
CRN036 Craniopharyngioma 66 0.138
153
CNN003 Conn's Syndrome 70 0.138
154
JNT002 Joint Disorders 64 0.138
155
P ART023 Arthropathy 68 0.137
156
LMB062 Limb Ischemia 54 0.137
157
ANG054 Angina Pectoris 69 0.135
158
P PSR002 Psoriasis 67 0.135
159
P ENC018 Encephalopathy 65 0.135
160
RTN020 Retinal Vascular Disease 54 0.131
161
IRN002 Iron Metabolism Disease 60 0.129
162
HYP043 Hyperandrogenism 50 0.128
163
BND020 Bone Disease 64 0.127
164
c PRC031 Preeclampsia/eclampsia 1 41 0.125
165
P LYM118 Lymphoma 69 0.125
166
MDD011 Mood Disorder 65 0.125
167
BRR014 Barrett Esophagus 70 0.125
168
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 44 0.124
169
P OVR049 Ovarian Disease 63 0.123
170
LNG099 Lung Disease 70 0.122
171
GND003 Gonadal Disease 49 0.121
172
CYS009 Cystadenoma 41 0.121
173
MNG006 Monogenic Diabetes 40 0.121
174
INS001 Insulinoma 64 0.121
175
BLM002 Bulimia Nervosa 61 0.121
176
THR013 Thoracic Outlet Syndrome 56 0.119
177
STR067 Stroke, Ischemic 82 0.119
178
CYT002 Cytokine Deficiency 39 0.119
179
ALL026 Allergic Hypersensitivity Disease 68 0.118
180
P MJR001 Major Depressive Disorder 67 0.118
181
P JVN024 Juvenile Hereditary Hemochromatosis 44 0.117
182
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.117
183
CRB039 Cerebrovascular Disease 70 0.117
184
ADN018 Adenoma 64 0.115
185
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.115
186
c PLY105 Polycystic Ovary Syndrome 1 42 0.115
187
c BDY021 Body Mass Index Quantitative Trait Locus 20 30 0.114
188
P MLT020 Multiple Sclerosis 75 0.114
189
c BDY005 Body Mass Index Quantitative Trait Locus 9 35 0.113
190
CRT049 Critical Limb Ischemia 53 0.113
191
CYS001 Cystic Fibrosis 82 0.112
192
P HYP083 Hypopituitarism 58 0.112
193
BWN003 Bowenoid Papulosis 42 0.112
194
THY030 Thyroid Gland Disease 50 0.111
195
P DRR001 Diarrhea 58 0.111
196
c GLL024 Gallbladder Disease 1 45 0.111
197
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 34 0.111
198
HYP730 Hypogonadotropic Hypogonadism 58 0.111
199
c BDY010 Body Mass Index Quantitative Trait Locus 4 32 0.111
200
P PNM007 Pneumonia 72 0.110
201
BLD165 Blood Group, Colton System 34 0.110
202
c BDY015 Body Mass Index Quantitative Trait Locus 12 32 0.110
203
HLC007 Helicobacter Pylori Infection 65 0.109
204
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.109
205
P BPL003 Bipolar Disorder 61 0.109
206
MCR141 Mucormycosis 51 0.109
207
DFC004 Deficiency Anemia 66 0.108
208
GT001 Gout 62 0.107
209
MTH009 Mouth Disease 64 0.106
210
c BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.106
211
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.106
212
SPN331 Spondyloocular Syndrome 41 0.106
213
NTR027 Neutrophil Actin Dysfunction 32 0.106
214
GST053 Gastric Cancer 78 0.105
215
DWN001 Down Syndrome 71 0.105
216
DBT087 Diabetes Insipidus, Neurohypophyseal 61 0.105
217
RST023 Resting Heart Rate, Variation in 44 0.105
218
P LYM031 Lymphocytic Leukemia 61 0.104
219
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.104
220
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.104
221
c ACT068 Acute Cystitis 56 0.103
222
NRL016 Neural Tube Defects 79 0.103
223
P AMY004 Amyloidosis 64 0.102
224
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.102
225
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 47 0.102
226
P ANR048 Aniridia 1 64 0.101
227
P HYP069 Hyperparathyroidism 59 0.101
228
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 55 0.101
229
P OVR046 Ovarian Cyst 52 0.101
230
DBT007 Diabetic Cataract 38 0.101
231
c HMC039 Hemochromatosis, Type 1 74 0.101
232
ATX010 Ataxia Neuropathy Spectrum 39 0.101
233
P LKM062 Leukemia, Acute Lymphoblastic 68 0.101
234
PTT009 Pituitary Gland Disease 59 0.101
235
c THR092 Thrombophilia Due to Thrombin Defect 69 0.101
236
P EPL164 Epilepsy 72 0.101
237
c PNC128 Pain - Chronic 49 0.100
238
BNF002 Bone Fracture 48 0.100
239
CRP001 Carpal Tunnel Syndrome 71 0.099
240
c MTR002 Mitral Valve Insufficiency 50 0.099
241
HRN028 Horns in Sheep 24 0.099
242
MTB004 Metabolic Acidosis 50 0.099
243
ACT088 Acute Insulin Response 50 0.099
244
PLM033 Pulmonary Embolism 64 0.099
245
c BRD013 Bardet-Biedl Syndrome 12 48 0.099
246
SPN186 Spinal Cord Injury 66 0.099
247
RSP006 Respiratory System Disease 64 0.098
248
P LCT001 Lactic Acidosis 52 0.098
249
HDC001 Headache 62 0.098
250
c ACT210 Acute Respiratory Distress Syndrome 66 0.098
251
c BRD014 Bardet-Biedl Syndrome 2 60 0.098
252
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.097
253
P ACT232 Acute Necrotizing Encephalopathy 30 0.097
254
RPD005 Rapidly Involuting Congenital Hemangioma 25 0.097
255
BLD137 Blood Group--Ahonen 24 0.097
256
P BRD002 Bardet-Biedl Syndrome 63 0.097
257
c SPN225 Spondyloarthropathy 1 75 0.097
258
P INF037 Inflammatory Bowel Disease 56 0.097
259
STM006 Stomach Disease 55 0.096
260
c BRD012 Bardet-Biedl Syndrome 11 51 0.096
261
c BRD011 Bardet-Biedl Syndrome 10 44 0.096
262
SMT008 Smith-Magenis Syndrome 57 0.096
263
P ESP024 Esophagitis 60 0.096
264
ALC007 Alcohol Dependence 69 0.096
265
P ATS364 Autism 67 0.096
266
NPH009 Nephrolithiasis 58 0.095
267
ACR007 Acromegaly 70 0.095
268
P EXN002 Exanthem 62 0.095
269
c LPD015 Lipodystrophy, Familial Partial, Type 2 60 0.094
270
PSY004 Psychotic Disorder 74 0.094
271
PNG002 Pain Agnosia 54 0.094
272
ART016 Aortic Aneurysm 71 0.093
273
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.093
274
RTN023 Retinitis 48 0.093
275
DRM006 Dermatitis 69 0.093
276
ATM052 Autoimmune Disease 1 40 0.092
277
P CRD119 Cardiac Arrest 66 0.092
278
THY028 Thyroid Cancer 72 0.092
279
INT075 Intracranial Hypertension 57 0.092
280
PNM001 Pneumocystosis 58 0.091
281
LPT006 Leptin Receptor Deficiency 41 0.091
282
RHM027 Rheumatic Disease 65 0.091
283
P LYM025 Lymphedema 54 0.091
284
P AXN002 Axenfeld-Rieger Syndrome 57 0.091
285
ALS001 Alstrom Syndrome 57 0.091
286
GRW007 Growth Hormone Deficiency 49 0.091
287
FRN020 Frontal Fibrosing Alopecia 33 0.091
288
BRS090 Breast Reconstruction 34 0.090
289
P CRD132 Cardiac Conduction Defect 63 0.090
290
c SYS001 Systemic Lupus Erythematosus 88 0.090
292
c HPT016 Hepatitis B 70 0.090
293
GNR004 Generalized Anxiety Disorder 54 0.090
294
OCL069 Ocular Motor Apraxia 49 0.090
295
GNG013 Gingivitis 63 0.089
296
AND002 Androgen Insensitivity Syndrome 61 0.089
297
c HPT073 Hepatitis C Virus 72 0.089
298
P ATX030 Ataxia-Telangiectasia 82 0.089
299
PRS021 Prostatic Adenoma 55 0.089
300
PRS129 Prostatic Hyperplasia, Benign 53 0.089
301
ALR002 Al-Raqad Syndrome 40 0.089
302
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.089
303
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.089
304
P ANG001 Angelman Syndrome 64 0.089
305
c CHR579 Chiari Malformation Type Ii 49 0.088
306
INT007 Intermediate Coronary Syndrome 50 0.088
307
c MYT020 Myotonic Dystrophy 2 58 0.087
308
P OVR042 Ovarian Cancer 83 0.087
309
P CLL015 Collagen Disease 52 0.087
310
P THR014 Thrombocytopenia 64 0.087
311
FBR047 Fibromyalgia 66 0.087
312
P MSC003 Muscular Atrophy 56 0.086
313
CLT003 Colitis 65 0.086
314
P TRM003 Tremor 55 0.086
315
MLN008 Melanoma 63 0.086
316
HMC014 Homocysteinemia 53 0.086
317
P GLL020 Gallbladder Disease 62 0.086
318
ACQ007 Acquired Immunodeficiency Syndrome 66 0.086
319
P LNG032 Lung Cancer 99 0.085
320
c ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.085
321
P LPS004 Lupus Erythematosus 69 0.085
322
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.085
323
ART001 Arterial Tortuosity Syndrome 59 0.085
324
c ALP106 Alport Syndrome 1, X-Linked 53 0.085
325
P PLM037 Pulmonary Hypertension 77 0.085
326
c MGR028 Migraine with or Without Aura 1 69 0.084
327
CLL003 Cellulitis 60 0.084
328
P MYC084 Mycobacterium Tuberculosis 1 67 0.083
329
CRN030 Coronary Stenosis 52 0.083
330
THR100 Thrombocytopenic Purpura, Autoimmune 67 0.083
331
SVR004 Severe Combined Immunodeficiency 65 0.083
332
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 62 0.083
333
P SJG008 Sjogren Syndrome 60 0.082
334
HPT082 Hepatic Adenomas, Familial 50 0.082
335
PSR001 Psoriatic Arthritis 68 0.082
336
PRT058 Pure Autonomic Failure 65 0.082
337
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 62 0.082
338
IRN001 Iron Deficiency Anemia 55 0.082
339
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.081
340
NNC002 Nance-Horan Syndrome 48 0.081
341
URM002 Uremia 53 0.081
342
P HST010 Histiocytosis 60 0.081
343
P PRC019 Precocious Puberty 52 0.081
344
BCT004 Bacteriuria 51 0.081
345
PST011 Pustulosis of Palm and Sole 50 0.081
346
BCT022 Bacterial Infectious Disease 62 0.080
347
ATN002 Autonomic Nervous System Disease 56 0.080
348
P GLM007 Glomerulonephritis 61 0.080
349
c ATS007 Autism Spectrum Disorder 67 0.080
350
ANV001 Anovulation 49 0.080
351
P RTN008 Retinitis Pigmentosa 80 0.080
352
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 53 0.079
353
APP008 Appendicitis 66 0.079
354
P INT068 Intestinal Disease 62 0.079
355
CNG376 Congenital Leptin Deficiency 26 0.079
356
HNM002 Hinman Syndrome 31 0.079
357
BRN038 Bronchial Disease 58 0.079
358
ALX002 Alexithymia 43 0.078
359
P KDN017 Kidney Cancer 59 0.078
360
SKN016 Skin Disease 68 0.078
361
ADP007 Adie Pupil 42 0.078
362
P PRS038 Personality Disorder 67 0.078
363
END040 Endogenous Depression 59 0.078
364
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.078
365
P ACR001 Aicardi-Goutieres Syndrome 65 0.077
366
P HYP076 Hyperthyroidism 55 0.077
367
MYC088 Mycobacterium Avium Complex Infections 33 0.077
368
AND005 Androgen Insensitivity Syndrome, Mild 21 0.077
369
P ALC004 Alcohol Abuse 68 0.077
370
SCH012 Schizoaffective Disorder 54 0.077
371
c AMY091 Amyotrophic Lateral Sclerosis 1 90 0.077
372
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 54 0.077
373
IGR001 Ige Responsiveness, Atopic 59 0.077
374
c ACR116 Aicardi-Goutieres Syndrome 1 50 0.076
375
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 36 0.076
376
BRC012 Brucellosis 70 0.076
377
c ACT074 Acute Lymphocytic Leukemia 63 0.075
378
P NRC002 Narcolepsy 59 0.075
379
RNL051 Renal Cysts and Diabetes Syndrome 53 0.075
380
LNG108 Langerhans Cell Histiocytosis 63 0.075
381
DWR001 Dwarfism 47 0.075
382
P MYP004 Myopathy 64 0.075
383
NRR001 Neuroretinitis 47 0.075
384
CHL004 Cholelithiasis 51 0.074
385
SKN027 Skin Conditions 51 0.074
386
VTM002 Vitamin B12 Deficiency 48 0.074
387
P DYS021 Dysautonomia 45 0.074
388
AMN001 Amenorrhea 55 0.074
389
FSC004 Fasciitis 50 0.074
390
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 72 0.074
391
P DRM053 Dermatitis, Atopic 71 0.074
392
P RCT021 Rectum Cancer 58 0.074
393
P LPM005 Lipomatosis 53 0.073
394
LRY021 Laryngeal Adductor Paralysis 26 0.073
395
VRL011 Viral Infectious Disease 68 0.073
396
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.073
397
INT002 Intermittent Claudication 64 0.073
398
LWC002 Lowe Oculocerebrorenal Syndrome 66 0.073
399
P TRN020 Turner Syndrome 71 0.073
400
WRN001 Werner Syndrome 73 0.073
401
c HPT003 Hepatitis a 66 0.073
402
CRH001 Crohn's Disease 79 0.073
403
IGG001 Iga Glomerulonephritis 58 0.073
404
CNS004 Constipation 58 0.073
405
HSH003 Hashimoto Thyroiditis 67 0.072
406
c SCN007 Secondary Hyperparathyroidism 55 0.072
407
P HYP265 Hypotonia 43 0.072
408
P WLF004 Wolfram Syndrome 60 0.072
409
GSG001 Gas Gangrene 47 0.072
410
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 38 0.072
411
PNC034 Pancreas Disease 59 0.071
412
ADL002 Adult Syndrome 55 0.071
413
HPR003 Heparin-Induced Thrombocytopenia 53 0.071
414
P TTR001 Tetralogy of Fallot 70 0.071
415
BRN071 Brain Injury 55 0.071
416
CHR100 Chronic Ulcer of Skin 53 0.071
417
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 46 0.070
418
P SLL003 Salla Disease 52 0.070
419
FBR065 Fibrocalculous Pancreatopathy 18 0.070
420
P GST044 Gastritis 60 0.070
421
P BLD134 Bladder Cancer 70 0.070
422
P RST001 Restless Legs Syndrome 59 0.070
423
NCR002 Necrobiosis Lipoidica 39 0.070
424
P NPH012 Nephrotic Syndrome 63 0.070
425
IRR002 Irritable Bowel Syndrome 64 0.070
426
P RHN004 Rhinitis 64 0.070
427
PRS063 Paresthesia 45 0.069
428
CLR108 Colorectal Adenoma 64 0.069
429
LRN002 Laron Syndrome 62 0.069
430
c BRD010 Bardet-Biedl Syndrome 1 59 0.068
431
BNR002 Bone Resorption Disease 54 0.068
432
c ACT071 Acute Kidney Failure 54 0.068
433
P CND004 Candidiasis 63 0.068
434
P SBS003 Substance Abuse 60 0.068
435
SYS003 Systolic Heart Failure 46 0.068
436
PRP098 Proprotein Convertase 1/3 Deficiency 32 0.068
437
P FCL005 Focal Segmental Glomerulosclerosis 60 0.067
438
GST049 Gastrointestinal System Cancer 62 0.067
439
GST071 Gastrointestinal Carcinoma 45 0.067
440
ASP030 Aspirin Resistance 47 0.067
441
MYL005 Myelofibrosis 69 0.067
442
OBS082 Obstructive Nephropathy 52 0.067
443
P NRF023 Neurofibromatosis, Type Ii 75 0.067
444
BRS051 Breast Disease 66 0.067
445
P MYL006 Myeloid Leukemia 67 0.067
446
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.067
447
DYS073 Dysphagia 48 0.066
448
PRT036 Peritonitis 66 0.066
449
OST097 Osteoporotic Fracture 36 0.066
450
PLM010 Pulmonary Edema 59 0.065
451
P ADL010 Adult Respiratory Distress Syndrome 64 0.065
452
P MLN007 Male Infertility 52 0.065
453
INT303 Intracranial Hypertension, Idiopathic 52 0.065
454
HRN026 Hernia, Hiatus 49 0.065
455
CRT013 Carotid Stenosis 53 0.065
456
P SHR029 Short Syndrome 57 0.065
457
MYL069 Myeloma, Multiple 85 0.065
458
SRC014 Sarcoma 70 0.065
459
GTR002 Goiter 54 0.065
460
DYS014 Dyspepsia 56 0.064
461
PLM017 Pulmonary Alveolar Microlithiasis 52 0.064
462
P SZR006 Seizure Disorder 61 0.064
463
PNC033 Pancreas Adenocarcinoma 67 0.064
464
TRN015 Transient Cerebral Ischemia 59 0.064
465
HMT018 Hematopoietic Stem Cell Transplantation 59 0.064
466
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 46 0.064
467
PPT005 Peptic Ulcer Disease 63 0.064
468
PST021 Postpartum Depression 56 0.064
469
P PHC003 Pheochromocytoma 72 0.064
470
CHL123 Chlamydia 66 0.063
471
LYM027 Lymphopenia 57 0.063
472
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.063
473
P DLT002 Dilated Cardiomyopathy 75 0.063
474
P OPN001 Open-Angle Glaucoma 53 0.063
475
HYP005 Hypokalemia 55 0.063
476
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.063
477
P PSD015 Pseudohypoparathyroidism 51 0.063
478
DVR002 Diverticulitis 46 0.063
479
c BLD140 Blood Group, I System 29 0.063
480
LYM133 Lymphoma, Hodgkin, Classic 72 0.063
481
OBS015 Obesity, Hyperphagia, and Developmental Delay 28 0.062
482
MRB006 Morbid Obesity and Spermatogenic Failure 19 0.062
483
P CMR001 Camurati-Engelmann Disease 61 0.062
484
c VRL010 Viral Hepatitis 60 0.062
485
ALL003 Allergic Rhinitis 70 0.062
486
c APL023 Aplasia Cutis Congenita, Nonsyndromic 40 0.062
487
PMP004 Pemphigus Foliaceus 46 0.062
488
ESP021 Esophageal Cancer 82 0.062
489
P GLY013 Glycogen Storage Disease 61 0.062
490
CHN016 Cohen Syndrome 53 0.062
491
STS002 Situs Inversus 49 0.062
492
SLD003 Sialadenitis 48 0.062
493
CRT016 Carotid Artery Disease 58 0.062
494
P SNS001 Sensorineural Hearing Loss 60 0.061
495
P MSC033 Muscle Disorders 57 0.061
496
P MNN013 Meningitis 69 0.061
497
c GRV008 Graves Disease 1 57 0.061
498
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 50 0.061
499
WRN003 Wernicke Encephalopathy 49 0.061
500
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.060
501
NCR007 Necrotizing Fasciitis 51 0.060
502
c LRG017 Large Intestine Cancer 63 0.060
503
P PLY018 Polycythemia 60 0.060
504
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 54 0.060
505
P HYP061 Hypertrophic Cardiomyopathy 59 0.060
506
c CRP023 Carpenter Syndrome 1 58 0.060
507
P SCL057 Scoliosis, Isolated 1 45 0.060
508
PRP030 Purpura 60 0.060
509
c PTT057 Pituitary Adenoma 4, Acth-Secreting 54 0.060
510
CHL147 Chlamydia Pneumonia 42 0.059
511
OPT006 Optic Nerve Disease 60 0.059
512
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.059
513
LRN003 Learning Disability 53 0.059
514
DYS011 Dyskinesia of Esophagus 42 0.059
515
MHM001 Mehmo Syndrome 35 0.059
516
ERY029 Erythermalgia, Primary 57 0.059
517
HYP081 Hypolipoproteinemia 49 0.059
518
P THL005 Thalassemia 65 0.059
519
c PNC106 Pancreatic Agenesis 1 51 0.059
520
EPD070 Epidermoid Cysts 48 0.059
521
c LKM061 Leukemia, Acute Myeloid 81 0.059
522
P MMP001 Mumps 61 0.058
523
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.058
524
SPN051 Spondylitis 55 0.058
525
NWB001 Newborn Respiratory Distress Syndrome 59 0.058
526
RSP007 Respiratory Distress Syndrome, Infant 37 0.058
527
DMP001 Dumping Syndrome 46 0.058
528
ACH005 Achalasia 53 0.057
529
HMN044 Human Immunodeficiency Virus Type 1 75 0.057
530
P PLY014 Polycystic Kidney Disease 62 0.057
531
HYD002 Hydronephrosis 52 0.057
532
P PRK057 Parkinson Disease, Late-Onset 76 0.057
533
RCK004 Rickets 66 0.057
534
PTT046 Pituitary Hormone Deficiency, Combined, 2 56 0.057
535
P CMP008 Compartment Syndrome 52 0.057
536
c LBR014 Leber Congenital Amaurosis 4 54 0.057
537
P BRB001 Beriberi 46 0.057
538
CLR030 Clear Cell Renal Cell Carcinoma 49 0.057
539
P SRC025 Sarcoidosis 1 76 0.057
540
P VNS003 Venous Insufficiency 54 0.057
541
CHR073 Choreatic Disease 50 0.057
542
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 38 0.057
543
FRL002 Froelich Syndrome 20 0.057
544
CHL065 Cholangiocarcinoma 64 0.056
545
c PTT056 Pituitary Adenoma 1, Multiple Types 53 0.056
546
BRN041 Bornholm Eye Disease 45 0.056
547
LYM143 Lymphoma, Non-Hodgkin, Familial 73 0.056
548
P MJR007 Major Affective Disorder 1 45 0.056
549
FCL044 Fecal Incontinence 38 0.056
550
P ALP008 Alopecia 56 0.056
551
P HYD006 Hydrocephalus 67 0.056
552
c MTR021 Maturity-Onset Diabetes of the Young, Type 4 41 0.056
553
c BST008 Bestrophinopathy, Autosomal Recessive 33 0.056
554
OVR094 Ovarian Epithelial Cancer 41 0.056
555
END062 Endometrial Hyperplasia 51 0.056
556
P HYP098 Hypereosinophilic Syndrome 67 0.055
557
P END033 Endocarditis 60 0.055
558
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 48 0.055
559
ACR006 Aceruloplasminemia 73 0.055
560
FRZ001 Frozen Shoulder 53 0.055
561
OBS050 Obesity Due to Congenital Leptin Deficiency 18 0.055
562
P CHL066 Cholangitis 51 0.055
563
MTC005 Mitochondrial Metabolism Disease 47 0.055
564
SKN023 Skin Tag 40 0.055
565
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.055
566
P RNL007 Renal Tubular Acidosis 51 0.055
567
P PNS012 Paine Syndrome 60 0.055
568
P MCR010 Microcephaly 55 0.055
569
P FML012 Familial Partial Lipodystrophy 52 0.055
570
EXC002 Exocrine Pancreatic Insufficiency 41 0.055
571
CRV035 Cervical Cancer 76 0.055
572
GST045 Gastroenteritis 65 0.055
573
GYN001 Gynecomastia 47 0.055
574
INF021 Infant Gynecomastia 28 0.055
575
EXP004 Exophthalmos 53 0.054
576
ADR040 Adrenal Gland Pheochromocytoma 49 0.054
577
HYP110 Hyperproinsulinemia 41 0.054
578
CRD223 Cardiac Arrhythmia 55 0.054
579
HMS001 Hemosiderosis 52 0.054
580
SCL022 Scleredema 31 0.054
581
c FCL025 Focal Segmental Glomerulosclerosis 1 51 0.054
582
SLP010 Slipped Capital Femoral Epiphysis 37 0.054
583
P PLY006 Polydactyly 57 0.054
584
ERY003 Erythema Multiforme 62 0.054
585
TRM010 Traumatic Brain Injury 56 0.054
586
ULC004 Ulcerative Colitis 80 0.053
587
c CNT035 Central Nervous System Disease 65 0.053
588
c PRM005 Primary Hyperparathyroidism 60 0.053
589
CRB037 Cerebral Palsy 71 0.053
590
FRN014 Fournier Gangrene 41 0.053
591
INT051 Intussusception 53 0.053
592
HYP784 Hypogonadism, Male 42 0.053
593
c CHR682 Chronic Bilirubin Encephalopathy 33 0.053
594
BLD163 Blood Group, Dombrock System 27 0.053
595
PST053 Postherpetic Neuralgia 45 0.053
596
WLL001 Williams-Beuren Syndrome 63 0.053
597
HDR002 Hidradenitis Suppurativa 57 0.053
598
P HYP724 Hyperlipoproteinemia, Type Iii 63 0.053
599
P PTS002 Ptosis 55 0.053
600
P PTT006 Pituitary Adenoma 54 0.053
601
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 69 0.053
602
ART002 Arts Syndrome 55 0.053
603
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 62 0.052
604
ART008 Arteriosclerosis Obliterans 42 0.052
605
P PNC045 Pancreatic Agenesis 39 0.052
606
c JVN010 Juvenile Rheumatoid Arthritis 70 0.052
607
P ENC004 Encephalitis 66 0.052
608
P FNG006 Feingold Syndrome 1 46 0.052
609
HYP085 Hypothalamic Disease 46 0.052
610
OTT002 Otitis Media 69 0.052
611
VRC005 Varicose Veins 66 0.052
612
DST006 Diastolic Heart Failure 46 0.052
613
FXF002 Fox-Fordyce Disease 40 0.052
614
P VSC011 Vasculitis 66 0.052
615
CLC006 Calcinosis 53 0.052
616
P MYS003 Myasthenia Gravis 73 0.052
617
MYL009 Myelodysplastic Syndrome 70 0.052
618
TND005 Tendinitis 45 0.052
619
c MYT021 Myotonic Dystrophy 1 71 0.052
621
MNS002 Mini Stroke 25 0.052
622
VSC002 Vascular Dementia 57 0.052
623
CRN024 Corneal Disease 45 0.052
624
c INF145 Infantile Liver Failure Syndrome 1 47 0.051
625
P MSC005 Muscular Dystrophy 66 0.051
626
c CNT075 Central Precocious Puberty 52 0.051
627
HYP068 Hyperostosis 51 0.051
628
TND004 Tendinopathy 47 0.051
629
P UTR058 Uterine Anomalies 60 0.051
630
P HYP607 Hypercholesterolemia, Familial 81 0.050
631
c BTT014 Beta-Thalassemia 72 0.050
632
TBC004 Tobacco Addiction 64 0.050
633
c ACT073 Acute Leukemia 62 0.050
634
c SVR005 Severe Pre-Eclampsia 55 0.050
635
HDR003 Hidradenitis 52 0.050
636
PNN001 Panniculitis 49 0.050
637
P THR015 Thrombophilia 56 0.050
638
END038 Endocrine Pancreas Disease 39 0.050
639
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.050
640
c ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.050
641
DCB001 Decubitus Ulcer 47 0.050
642
c PLM164 Pulmonary Hypertension, Primary, 1 70 0.050
643
PRP016 Paraplegia 54 0.050
644
P CHR084 Chromosomal Disease 42 0.050
645
SPN027 Spinal Stenosis 61 0.050
646
P NTR004 Neutropenia 60 0.050
647
CHL068 Cholestasis 60 0.050
648
P HYP614 Hyperlipidemia, Familial Combined 55 0.050
649
CRD137 Cardiogenic Shock 42 0.050
650
DXT002 Dextrocardia with Situs Inversus 39 0.050
651
HYP026 Hypoglycemic Coma 42 0.050
652
c SML038 Small Cell Cancer of the Lung 68 0.049
653
HMR039 Hemorrhage, Intracerebral 62 0.049
654
SQM006 Squamous Cell Carcinoma 58 0.049
655
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.049
656
CLC001 Calciphylaxis 52 0.049
657
STF001 Stiff-Person Syndrome 64 0.049
658
CRY035 Cryptorchidism, Unilateral or Bilateral 61 0.049
659
P ACT105 Acute Mountain Sickness 57 0.049
660
KRT002 Keratomalacia 51 0.049
661
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.049
662
GNG011 Gingival Disease 49 0.049
663
HRT012 Heart Valve Disease 58 0.049
664
P INT070 Intestinal Obstruction 55 0.049
665
FND002 Fundus Dystrophy 51 0.049
666
ALL014 Allergic Encephalomyelitis 43 0.049
667
P ASP006 Aspergillosis 66 0.049
668
c EPS039 Episodic Pain Syndrome, Familial, 1 31 0.049
669
CYT008 Cytomegalovirus Infection 62 0.048
670
P MGL001 Megaloblastic Anemia 51 0.048
671
URN022 Urinary Tract Infections, Recurrent 34 0.048
672
MLR004 Malaria 84 0.048
673
DRG003 Drug Dependence 51 0.048
674
SYN036 Syncope 49 0.048
675
XP2001 Xp22.3 Microdeletion Syndrome 22 0.048
676
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 16 0.048
677
BLL003 Bell's Palsy 53 0.048
678
MCR011 Microinvasive Gastric Cancer 47 0.048
679
KPS004 Kaposi Sarcoma 77 0.048
680
INT079 Intrahepatic Cholangiocarcinoma 55 0.048
681
RDC002 Radiculopathy 55 0.048
682
P ART084 Arteriovenous Fistula 48 0.048
683
ALL006 Allergic Asthma 61 0.047
684
P MYP006 Myopia 59 0.047
685
CHL067 Cholecystitis 58 0.047
686
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 44 0.047
687
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 22 0.047
688
c HNT004 Huntington Disease-Like 2 47 0.047
689
SWL001 Swallowing Disorders 36 0.047
690
EPP010 Epiphysiolysis of the Hip 26 0.047
691
c HYP768 Hyperlipoproteinemia, Type I 47 0.047
692
P RTN024 Retinoblastoma 72 0.047
693
P SKN015 Skin Carcinoma 65 0.047
694
HYP020 Hyperprolactinemia 63 0.047
695
SPN035 Spindle Cell Sarcoma 53 0.047
696
NVS015 Nevus Comedonicus 42 0.047
697
c GLC092 Glaucoma, Primary Open Angle 57 0.047
698
c CNG124 Congenital Rubella 48 0.047
699
PSD088 Pseudobulbar Affect 39 0.047
700
STT004 Steatorrhea 43 0.046
701
ELP001 Elephantiasis 38 0.046
702
CHP002 Chops Syndrome 38 0.046
703
P HMP007 Hemophilia 62 0.046
704
HLX001 Helix Syndrome 40 0.046
705
P HLP001 Holoprosencephaly 65 0.046
706
SNL007 Senile Cataract 40 0.046
707
PSD014 Pseudopseudohypoparathyroidism 55 0.046
708
SPN021 Spinal Meningioma 50 0.046
709
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 32 0.046
710
c HMP029 Hemophilia a 70 0.046
711
P SNS014 Sinusitis 65 0.046
712
TTH006 Tooth Disease 54 0.046
713
c LPD032 Lipodystrophy, Congenital Generalized, Type 1 50 0.046
714
IDP033 Idiopathic Edema 41 0.046
715
c MYS011 Myasthenia Gravis Congenital 33 0.046
716
CNN005 Connective Tissue Disease 67 0.046
717
CHL014 Cholera 60 0.046
718
GLC036 Glucagonoma 50 0.046
719
CLN019 Colonic Disease 62 0.045
720
KRN002 Kearns-Sayre Syndrome 63 0.045
721
NNT012 Neonatal Jaundice 52 0.045
722
c PRM038 Primary Agammaglobulinemia 41 0.045
723
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 25 0.045
724
PRT018 Portal Vein Thrombosis 50 0.045
725
P END044 Endometriosis 65 0.045
726
c CNG006 Congenital Hypothyroidism 59 0.045
727
c CNG216 Congenital Hydrocephalus 57 0.045
728
P DDN001 Duodenal Ulcer 51 0.045
729
P ALP009 Alopecia Areata 66 0.045
730
c ART101 Aortic Valve Disease 2 63 0.045
731
P ANT006 Antiphospholipid Syndrome 60 0.045
732
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 56 0.045
733
P KRT007 Keratoconus 50 0.045
734
P ACQ009 Acquired Metabolic Disease 35 0.045
735
DSR011 Disorganization, Mouse, Homolog of 22 0.045
736
HRP004 Herpes Zoster 63 0.044
737
HYP030 Hypoactive Sexual Desire Disorder 44 0.044
738
END072 Endotheliitis 39 0.044
739
P SCL018 Scoliosis 58 0.044
740
c MNN043 Meningioma, Familial 63 0.044
741
P PLV020 Pelvic Organ Prolapse 62 0.044
742
SPN041 Spinal Cord Disease 54 0.044
743
PPT001 Peptic Esophagitis 45 0.044
744
c BRD018 Bardet-Biedl Syndrome 6 44 0.044
745
CRD220 Cardiac Valvular Defect, Developmental 36 0.044
746
PHN003 Phenylketonuria 74 0.044
747
SYN007 Synovitis 59 0.044
748
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 55 0.044
749
PTL001 Patulous Eustachian Tube 31 0.044
750
P TMP003 Temporal Arteritis 69 0.044
751
P CHR071 Charcot-Marie-Tooth Disease 65 0.044
752
SDD008 Sudden Sensorineural Hearing Loss 45 0.044
753
CRB085 Cerebral Hemorrhage 42 0.044
754
BRN024 Bronchitis 70 0.044
755
c LPM012 Lipomatosis, Multiple 65 0.044
756
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 63 0.044
757
CRB009 Cerebritis 39 0.044
758
ACH004 Achondroplasia 68 0.043
759
PPL022 Papilloma 58 0.043
760
P OCY003 Oocyte Maturation Defect 1 42 0.043
761
P RNL015 Renal Hypertension 49 0.043
762
HYP017 Hypophosphatemia 49 0.043
763
SCK003 Sickle Cell Anemia 74 0.043
764
P MYC008 Myocarditis 59 0.043
765
P ACQ022 Acquired Generalized Lipodystrophy 51 0.043
766
P GLM045 Glioma 55 0.043
767
c LPD040 Lipodystrophy, Familial Partial, Type 1 43 0.043
768
SFT003 Soft Tissue Sarcoma 59 0.042
769
INT253 Intestinal Benign Neoplasm 57 0.042
770
CHR005 Chorioamnionitis 53 0.042
771
CRH005 Crohn's Colitis 61 0.042
772
MNC006 Monoclonal Gammopathy of Uncertain Significance 53 0.042
773
c CHR431 Chronic Venous Insufficiency 50 0.042
774
BRC010 Brachial Plexus Lesion 47 0.042
775
PLM005 Pleomorphic Lipoma 40 0.042
776
CRY036 Cryptogenic Cirrhosis 38 0.042
777
P HML002 Hemolytic Anemia 64 0.042
778
CMP010 Complex Regional Pain Syndrome 63 0.042
779
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 42 0.042
780
CDQ001 Cauda Equina Syndrome 40 0.042
781
HPT067 Hepatocellular Adenoma 44 0.042
782
SCR001 Secretory Meningioma 41 0.042
783
PST028 Post-Traumatic Stress Disorder 63 0.042
784
P PRT013 Portal Hypertension 61 0.042
785
BLD044 Bladder Disease 57 0.042
786
BLR008 Bilirubin Metabolic Disorder 54 0.042
787
MSC190 Muscular Disease 53 0.042
788
EMP001 Empty Sella Syndrome 43 0.042
789
MSC004 Muscle Tissue Disease 39 0.042
790
LRN001 Laurence-Moon Syndrome 46 0.042
791
TRC026 Tracheal Disease 36 0.042
792
HYP364 Hyperostosis Frontalis Interna 29 0.042
793
P HRP006 Herpes Simplex 71 0.041
794
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 64 0.041
795
DSS009 Disseminated Intravascular Coagulation 58 0.041
796
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 52 0.041
797
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 46 0.041
798
NPH010 Nephrosclerosis 45 0.041
799
P BNC003 Bone Cancer 62 0.041
800
c PSD108 Pseudohypoparathyroidism, Type Ia 56 0.041
801
AML029 Ameloblastoma 53 0.041
802
c BRD016 Bardet-Biedl Syndrome 4 47 0.041
803
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 53 0.041
804
P ACT010 Acth-Secreting Pituitary Adenoma 52 0.041
805
KWS001 Kwashiorkor 46 0.041
806
c LKM063 Leukemia, Chronic Myeloid 73 0.041
807
P NSP012 Nasopharyngeal Carcinoma 65 0.041
808
PYD002 Pyoderma 52 0.041
809
SHH001 Sheehan Syndrome 50 0.041
810
GLC022 Glucose/galactose Malabsorption 44 0.041
811
DGR001 Digeorge Syndrome 61 0.041
812
ISL003 Isolated Growth Hormone Deficiency 52 0.041
813
P END046 Endometritis 52 0.041
814
ALB001 Albright's Hereditary Osteodystrophy 51 0.041
815
P HYP263 Hypersomnia 45 0.041
816
SCR011 Scrapie 43 0.041
817
INT146 Intervertebral Disc Disease 64 0.040
818
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.040
819
P BCK002 Beckwith-Wiedemann Syndrome 58 0.040
820
P TXP001 Toxoplasmosis 66 0.040
821
P LTR001 Lateral Sclerosis 60 0.040
822
TBR011 Tuberculous Meningitis 55 0.040
823
c HYP555 Hypertriglyceridemia, Transient Infantile 34 0.040
824
BRN056 Bronchopulmonary Dysplasia 60 0.040
825
RCT017 Rectal Disease 43 0.040
826
END041 Endometrial Adenocarcinoma 60 0.039
827
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.039
828
PRS042 Prostate Disease 47 0.039
829
PRT038 Protein-Energy Malnutrition 53 0.039
830
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.039
831
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.039
832
VSL002 Visual Epilepsy 37 0.039
833
GST007 Gastric Dilatation 32 0.039
834
BLD164 Blood Group, Gerbich System 31 0.039
835
GST019 Gastrointestinal Stromal Tumor 73 0.039
836
ANG020 Angiosarcoma 59 0.039
837
P THR005 Thrombotic Thrombocytopenic Purpura 62 0.039
838
P SLV001 Silver-Russell Syndrome 57 0.039
839
HDN002 Head Injury 52 0.039
840
ISL001 Islet Cell Tumor 51 0.039
841
HYP077 Hypertrichosis 49 0.039
842
P OPT070 Optic Nerve Hypoplasia, Bilateral 48 0.039
843
MTR007 Motor Peripheral Neuropathy 41 0.039
844
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.039
845
c CRT085 Carotid Intimal Medial Thickness 2 26 0.039
846
P GLL022 Guillain-Barre Syndrome 66 0.039
847
PRS047 Prostatitis 56 0.039
848
INF034 Infective Endocarditis 56 0.039
849
MTC097 Mitochondrial Complex Iv Deficiency 56 0.039
850
GST040 Gastric Adenocarcinoma 66 0.038
851
c AMY009 Amyloidosis Aa 55 0.038
852
P BLD051 Blood Coagulation Disease 52 0.038
853
INT052 Intestinal Volvulus 43 0.038
854
c ATM011 Autoimmune Hepatitis 67 0.038
855
ART004 Aortic Atherosclerosis 45 0.038
856
ICH020 Ichthyosis Prematurity Syndrome 45 0.038
857
BRK012 Broken Heart Syndrome 39 0.038
858
MNC002 Munchausen by Proxy 32 0.038
859
NRN002 Neuronitis 32 0.038
860
P GRF003 Graft-Versus-Host Disease 71 0.038
861
c INF071 Inflammatory Bowel Disease 1 60 0.038
862
OST011 Osteomalacia 52 0.038
863
ESN002 Eosinophilia-Myalgia Syndrome 50 0.038
864
PPL021 Papilledema 48 0.038
865
NRT001 Neurotic Disorder 47 0.038
866
P MYS005 Myositis 61 0.038
867
CHK001 Chikungunya 61 0.038
868
MST005 Mastitis 57 0.038
869
ATR057 Atrioventricular Block 54 0.038
870
OCC006 Occipital Horn Syndrome 51 0.038
871
c CRD093 Cardiomyopathy, Dilated, 1a 44 0.038
872
MYX004 Myxedema 43 0.038
873
MDS022 Mediastinitis 41 0.038
874
c HNT011 Huntington Disease-Like 3 40 0.038
875
P SPN046 Spinal Muscular Atrophy 66 0.037
876
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 56 0.037
877
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 53 0.037
878
HNT002 Hantavirus Pulmonary Syndrome 52 0.037
879
BRN080 Brain Ischemia 43 0.037
880
HNS001 Hansen's Disease 36 0.037
881
INS034 Insulinomatosis and Diabetes Mellitus 24 0.037
882
BRN028 Brain Cancer 72 0.037
883
CHR178 Chromosomal Triplication 41 0.037
884
URT039 Urticaria 60 0.037
885
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 58 0.037
886
URN010 Urinary Tract Obstruction 58 0.037
887
P MYT002 Myotonic Dystrophy 52 0.037
888
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 49 0.037
889
GLC096 Galactorrhea 47 0.037
890
NTR007 Neutral Lipid Storage Disease with Myopathy 37 0.037
891
DFN039 Deafness-Infertility Syndrome 34 0.037
892
c BPL002 Bipolar I Disorder 49 0.037
893
c BRD015 Bardet-Biedl Syndrome 3 43 0.037
894
DDN027 Duodenum Disease 43 0.037
895
TQP001 Taqi Polymorphism 35 0.037
896
APL001 Aplastic Anemia 74 0.036
897
CHR066 Chronic Fatigue Syndrome 68 0.036
898
c THY109 Thyroid Cancer, Nonmedullary, 1 59 0.036
899
P ICH004 Ichthyosis 57 0.036
900
FCT001 Factor Viii Deficiency 56 0.036
901
PLC007 Placental Abruption 51 0.036
902
ART031 Aortic Coarctation 49 0.036
903
SXD002 Sex Development Disorder 49 0.036
905
c CRN243 Carney Complex, Type 1 45 0.036
906
c HYP602 Hyperoxaluria, Primary, Type Ii 38 0.036
907
CRN167 Caronte 19 0.036
908
ING001 Inguinal Hernia 61 0.036
909
P PLM034 Pulmonary Emphysema 59 0.036
910
PHR003 Pharyngitis 58 0.036
911
BKR002 Baker-Gordon Syndrome 40 0.036
912
IMM167 Immune Deficiency Disease 63 0.036
913
GST023 Gastric Ulcer 58 0.036
914
HLL004 Hellp Syndrome 57 0.036
915
ACT049 Acute Disseminated Encephalomyelitis 56 0.036
916
TLN003 Telangiectasis 56 0.036
917
c ALZ056 Alzheimer Disease 3 53 0.036
918
QDR001 Quadriplegia 51 0.036
919
P RTN014 Retinal Artery Occlusion 50 0.036
920
c MLG069 Malignant Hypertension 50 0.036
921
PTT037 Pituitary Tumors 48 0.036
922
PNC120 Pancreas, Dorsal, Agenesis of 25 0.036
923
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 14 0.036
924
SKN019 Skin Melanoma 67 0.035
925
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.035
926
PLL001 Pallister-Hall Syndrome 61 0.035
927
P MLT074 Multiple Endocrine Neoplasia 56 0.035
928
NRN004 Neuroendocrine Tumor 56 0.035
929
P TRT010 Teratoma 52 0.035
930
HPT009 Hepatopulmonary Syndrome 52 0.035
931
c HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 45 0.035
932
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 40 0.035
933
NRV004 Nerve Compression Syndrome 39 0.035
934
HNC001 Henoch-Schoenlein Purpura 61 0.035
935
END035 Endocrine Gland Cancer 57 0.035
936
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 56 0.035
937
KRT006 Keratoconjunctivitis 55 0.035
938
P SCL009 Sclerosing Cholangitis 51 0.035
939
CLD007 Cold Agglutinin Disease 50 0.035
940
P ANX007 Anauxetic Dysplasia 1 41 0.035
941
BRN026 Branch Retinal Artery Occlusion 38 0.035
942
PLG002 Plague 59 0.035
943
P PLY041 Polymyositis 58 0.035
944
PRV006 Pervasive Developmental Disorder 56 0.035
945
CLR109 Colorectal Adenocarcinoma 54 0.035
946
ATS010 Autosomal Recessive Disease 48 0.035
947
SCH003 Schizophreniform Disorder 44 0.035
948
DDN009 Duodenal Obstruction 31 0.035
949
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 26 0.035
950
P WSK001 Wiskott-Aldrich Syndrome 76 0.034
951
P KBK002 Kabuki Syndrome 1 66 0.034
952
DFF005 Diffuse Large B-Cell Lymphoma 58 0.034
953
P PTT014 Pitt-Hopkins Syndrome 54 0.034
954
LYM019 Lymphosarcoma 53 0.034
955
HYP458 Hyper Ige Syndrome 52 0.034
956
c OVR114 Ovarian Cancer 1 51 0.034
957
DNG001 Dengue Shock Syndrome 48 0.034
958
P DCR003 Dacryoadenitis 36 0.034
959
MYL020 Myelomeningocele 53 0.034
960
CHR222 Chromosome 1p36 Deletion Syndrome 49 0.034
961
PST095 Post-Thrombotic Syndrome 51 0.034
962
ARM001 Aromatase Deficiency 51 0.034
963
LPM010 Lipomatosis, Multiple Symmetric 43 0.034
964
P FNC027 Fanconi Anemia, Complementation Group a 81 0.034
965
P PLM036 Pulmonary Fibrosis 70 0.034
966
LSH001 Leishmaniasis 69 0.034
967
OST003 Osteonecrosis 67 0.034
968
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.034
969
CCC001 Coccidioidomycosis 61 0.034
970
ART017 Aortic Disease 56 0.034
971
PYD001 Pyoderma Gangrenosum 55 0.034
972
RGH009 Right Atrial Isomerism 52 0.034
973
CHL109 Childhood Apraxia of Speech 37 0.034
974
PPL001 Papillary Adenoma 35 0.034
975
CNT097 Central Hypoventilation Syndrome, Congenital 65 0.033
976
DGN001 Degenerative Disc Disease 51 0.033
977
TCL003 T Cell Deficiency 46 0.033
978
CLP006 Clopidogrel Resistance 45 0.033
979
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 35 0.033
980
TMP012 Temple Syndrome 34 0.033
981
48X003 48,xxyy Syndrome 33 0.033
982
P FTL001 Fetal Alcohol Syndrome 63 0.033
983
P HYP818 Hypobetalipoproteinemia, Familial, 1 53 0.033
984
ALC009 Alcoholic Liver Cirrhosis 52 0.033
985
NRL004 Neuroleptic Malignant Syndrome 52 0.033
986
CRB004 Cerebral Artery Occlusion 47 0.033
987
ACT055 Actinomycosis 46 0.033
988
PLR007 Pleural Empyema 46 0.033
989
ENT004 Enthesopathy 44 0.033
990
OVR093 Overhydrated Hereditary Stomatocytosis 39 0.033
991
IMM001 Immune-Complex Glomerulonephritis 38 0.033
992
MYS004 Myiasis 37 0.033
993
SBC016 Subacute Delirium 34 0.033
994
RDN004 Radin Blood Group Antigen 28 0.033
995
CHG001 Chagas Disease 72 0.033
996
MVM001 Movement Disease 67 0.033
997
MSC157 Muscular Dystrophy, Duchenne Type 65 0.033
998
c WLM018 Wilms Tumor 5 64 0.033
999
ADT003 Auditory System Disease 52 0.033
1000
P NRB010 Neuroblastoma 1 51 0.033
1001
P CRB101 Cerebrooculofacioskeletal Syndrome 1 50 0.033
1002
HYP006 Hypertensive Heart Disease 49 0.033
1003
MMM006 Mammographic Density 47 0.033
1004
c HYP057 Hypervitaminosis D 43 0.033
1005
c WLM011 Wilms Tumor 6 40 0.033
1006
CMP096 Complete Generalized Lipodystrophy 25 0.033
1007
P MDL005 Medulloblastoma 76 0.032
1008
HYP190 Hypoalphalipoproteinemia, Primary 60 0.032
1009
EXT034 Extrinsic Allergic Alveolitis 58 0.032
1010
P ANG015 Angioedema 57 0.032
1011
c GLY005 Glycogen Storage Disease Vi 57 0.032
1012
RSP019 Respiratory Distress Syndrome in Premature Infants 56 0.032
1013
PLV003 Pelvic Inflammatory Disease 56 0.032
1014
GLC011 Galactose Epimerase Deficiency 49 0.032
1015
MLK003 Melkersson-Rosenthal Syndrome 44 0.032
1016
GGN002 Gigantism 36 0.032
1017
RHY001 Rhyns Syndrome 35 0.032
1018
FST001 Foster-Kennedy Syndrome 33 0.032
1019
c ORT012 Orthostatic Hypotension 2 33 0.032
1020
P NGH001 Night Blindness 50 0.031
1021
c NRC009 Narcolepsy 1 49 0.031
1022
c BRD044 Bardet-Biedl Syndrome 17 48 0.031
1023
c BRD032 Bardet-Biedl Syndrome 14 47 0.031
1024
c BRD020 Bardet-Biedl Syndrome 8 45 0.031
1025
c BRD033 Bardet-Biedl Syndrome 13 45 0.031
1026
c BRD048 Bardet-Biedl Syndrome 18 42 0.031
1027
c BRD017 Bardet-Biedl Syndrome 5 39 0.031
1028
PLN026 Pilonidal Sinus 39 0.031
1029
c BRD045 Bardet-Biedl Syndrome 19 36 0.031
1030
c BRD047 Bardet-Biedl Syndrome 16 35 0.031
1031
c BRD019 Bardet-Biedl Syndrome 7 33 0.031
1032
BRN049 Brain Tumor, Childhood 32 0.031
1033
c BRD021 Bardet-Biedl Syndrome 9 28 0.031
1034
c BRD050 Bardet-Biedl Syndrome 21 27 0.031
1035
c BRD051 Bardet-Biedl Syndrome 20 24 0.031
1036
CRB089 Cerebral Beriberi 22 0.031
1037
c CWD006 Cowden Syndrome 1 73 0.031
1038
OVR029 Ovarian Hyperstimulation Syndrome 64 0.031
1039
CMM005 Common Cold 62 0.031
1040
BRN002 Bronchiolitis 61 0.031
1041
MCS002 Mucositis 60 0.031
1042
CFF002 Coffin-Lowry Syndrome 59 0.031
1043
c ACT135 Acute Graft Versus Host Disease 58 0.031
1044
LYM040 Lymphoblastic Lymphoma 57 0.031
1045
CYS039 Cystic Kidney Disease 55 0.031
1046
CLB010 Coloboma of Macula 54 0.031
1047
MCK005 Mckusick-Kaufman Syndrome 53 0.031
1048
BLR006 Biliary Tract Disease 52 0.031
1049
PRP009 Peripartum Cardiomyopathy 51 0.031
1050
FML026 Familial Lipoprotein Lipase Deficiency 49 0.031
1051
P CRN074 Coronary Artery Aneurysm 49 0.031
1052
ACD008 Acid-Labile Subunit Deficiency 44 0.031
1053
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.031
1054
IDP041 Idiopathic Recurrent Pericarditis 33 0.031
1055
MYT026 Myotonia Atrophica 28 0.031
1056
SPT019 Septo-Optic Dysplasia Spectrum 27 0.031
1057
P MRL001 Meralgia Paresthetica 27 0.031
1058
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 25 0.031
1059
CHR189 Chromosome 12p Deletion 23 0.031
1060
c FTL070 Fetal Akinesia Deformation Sequence 2 21 0.031
1061
TNG002 Tangier Disease 63 0.031
1062
ILT001 Ileitis 59 0.031
1063
P LPS002 Liposarcoma 56 0.031
1064
ECT026 Ectopic Pregnancy 53 0.031
1065
P THY054 Thyrotoxic Periodic Paralysis 52 0.031
1066
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 45 0.031
1067
c CNG031 Congenital Nervous System Abnormality 40 0.031
1068
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 30 0.031
1069
MLT157 Multiple System Atrophy 1 72 0.030
1070