Search results for obesity diabetes

1451 hits were found for obesity diabetes

# Family MCID Name MIFTS Score
1
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 9.067
2
P ABD013 Abdominal Obesity-Metabolic Syndrome 3 27 4.234
3
c DBT009 Diabetes Mellitus 67 1.632
4
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 1.212
5
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.766
6
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.766
7
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.766
8
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.766
9
GLC008 Glucose Metabolism Disease 54 0.746
10
GST033 Gestational Diabetes 63 0.722
11
MRB003 Morbid Obesity 62 0.711
12
c NRP001 Neuropathy 63 0.651
13
c MCR115 Microvascular Complications of Diabetes 5 71 0.609
14
c KDN018 Kidney Disease 71 0.599
15
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.590
16
NTR005 Nutritional Deficiency Disease 60 0.584
17
P MCR113 Microvascular Complications of Diabetes 3 58 0.577
18
P MCR120 Microvascular Complications of Diabetes 7 46 0.577
19
P MCR130 Microvascular Complications of Diabetes 6 43 0.576
20
P MCR133 Microvascular Complications of Diabetes 4 43 0.576
21
OVR063 Overnutrition 53 0.565
22
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.512
23
GLC003 Glucose Intolerance 59 0.512
24
FTT001 Fatty Liver Disease 66 0.504
25
HYP056 Hypoglycemia 64 0.503
26
HYP066 Hyperglycemia 65 0.494
27
c LVR013 Liver Disease 77 0.493
28
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.451
29
DBT010 Diabetic Neuropathy 60 0.437
30
HYP060 Hyperinsulinism 57 0.434
31
c DBT005 Diabetes Insipidus 55 0.430
32
DBT084 Diabetes Mellitus, Ketosis-Prone 62 0.417
33
c HRT032 Heart Disease 76 0.385
34
LPD008 Lipid Metabolism Disorder 65 0.366
35
c PLY011 Polycystic Ovary Syndrome 64 0.366
36
c PRP019 Peripheral Nervous System Disease 66 0.349
37
c SLP006 Sleep Apnea 70 0.348
38
ATM095 Autoimmune Disease 68 0.345
39
ETN001 Eating Disorder 65 0.342
40
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.339
41
ART140 Arteries, Anomalies of 67 0.336
42
c CRN018 Coronary Artery Anomaly 74 0.327
43
DPR016 Depression 73 0.325
44
c CRD246 Cardiovascular System Disease 57 0.317
45
c CRN300 Coronary Heart Disease 1 62 0.314
46
IMM136 Immune System Disease 57 0.311
47
P CHR089 Chronic Kidney Failure 73 0.300
48
VSC007 Vascular Disease 72 0.300
49
ISC004 Ischemia 67 0.295
50
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.292
51
c MYC007 Myocardial Infarction 78 0.288
53
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.270
54
ATN004 Autonomic Neuropathy 46 0.269
55
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.266
56
c PRD008 Periodontitis 66 0.264
57
AST005 Asthma 81 0.257
58
DBT002 Diabetic Autonomic Neuropathy 46 0.256
59
NNL002 Nonalcoholic Steatohepatitis 55 0.246
60
c PLY019 Polyneuropathy 58 0.244
61
ANX010 Anxiety 73 0.244
62
ISC006 Ischemic Heart Disease 72 0.244
63
c BRS047 Breast Cancer 100 0.244
64
AGN016 Aging 63 0.241
65
IMP005 Impotence 58 0.240
66
PRD007 Periodontal Disease 66 0.236
67
PLC008 Placenta Disease 59 0.230
68
RTN018 Retinal Disease 58 0.229
69
PRD004 Prediabetes Syndrome 51 0.229
70
URN009 Urinary System Disease 59 0.227
71
CNG034 Congestive Heart Failure 71 0.224
72
DBT008 Diabetic Angiopathy 48 0.220
73
DSS008 Disease of Mental Health 70 0.219
74
SPS003 Spastic Diplegia 49 0.215
75
MNT002 Mental Depression 65 0.214
76
c PNC044 Pancreatitis 62 0.213
77
OBS037 Obesity-Hypoventilation Syndrome 50 0.212
78
APN008 Apnea, Obstructive Sleep 68 0.209
79
c ART021 Arteriosclerosis 61 0.208
80
HYP835 Hypothalamic Obesity 44 0.208
81
c ART022 Arthritis 78 0.207
82
c HPT021 Hepatitis 74 0.206
83
c MTR004 Maturity-Onset Diabetes of the Young 61 0.203
84
c CTR002 Cataract 58 0.202
85
c HYP086 Hypothyroidism 66 0.202
86
P PRC016 Pre-Eclampsia 61 0.201
87
HYP080 Hypogonadism 53 0.200
88
c INF032 Infertility 60 0.198
89
OST012 Osteoarthritis 81 0.197
90
INS024 Insulin-Like Growth Factor I 83 0.196
91
c PRD006 Prader-Willi Syndrome 62 0.196
92
ACN002 Acanthosis Nigricans 65 0.195
93
THR024 Thrombosis 64 0.193
94
END030 End Stage Renal Failure 60 0.192
95
GST092 Gastroesophageal Reflux 66 0.192
96
GST037 Gastroparesis 59 0.188
97
c THY032 Thyroiditis 54 0.187
98
END057 Endometrial Cancer 69 0.186
99
HYP266 Hypoxia 63 0.184
100
DBT004 Diabetic Polyneuropathy 50 0.182
101
NRT004 Neuritis 58 0.179
102
c VSC018 Visceral Steatosis 38 0.179
103
FSH001 Fish-Eye Disease 51 0.175
104
P TRC078 Trichohepatoenteric Syndrome 2 35 0.175
106
SLP005 Sleep Disorder 60 0.172
107
c OST002 Osteoporosis 74 0.171
108
P PRD040 Periodontitis, Chronic 60 0.171
109
NRM005 Neuromuscular Disease 61 0.171
110
ATH013 Atherosclerosis Susceptibility 61 0.170
111
c TRC086 Trichohepatoenteric Syndrome 1 61 0.170
112
ANR007 Anorexia Nervosa 68 0.170
113
PRP027 Peripheral Vascular Disease 72 0.168
114
c RTN016 Retinal Degeneration 56 0.167
115
DST081 Distal Trisomy 11q 20 0.165
116
P HYP595 Hypertension, Essential 77 0.164
117
c ALZ034 Alzheimer Disease 88 0.164
118
GST050 Gastrointestinal System Disease 67 0.162
119
FTL021 Fetal Macrosomia 47 0.162
120
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.161
121
P ATR087 Atrial Standstill 1 69 0.160
122
P ACT075 Acute Myocardial Infarction 57 0.160
123
c NRV007 Nervous System Disease 72 0.158
124
c CLR023 Colorectal Cancer 99 0.158
125
c HYP750 Hypertriglyceridemia, Familial 58 0.158
126
c LKM002 Leukemia 72 0.158
127
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.157
128
P HPT001 Hepatitis C 69 0.157
129
c PNC035 Pancreatic Cancer 83 0.155
130
c CLC063 Celiac Disease 1 72 0.155
131
P ACT027 Acute Pancreatitis 59 0.155
132
SXL003 Sexual Disorder 53 0.154
133
c ADN016 Adenocarcinoma 71 0.153
134
DNT012 Dental Caries 52 0.152
135
c SCH015 Schizophrenia 73 0.151
136
HYP064 Hypogonadotropism 42 0.150
137
PRP080 Peripheral Artery Disease 56 0.150
138
c HPT023 Hepatocellular Carcinoma 97 0.149
139
c INF038 Influenza 75 0.148
140
c PRS040 Prostate Cancer 93 0.148
141
LVR012 Liver Cirrhosis 67 0.148
142
CYT017 Cytophagic Histiocytic Panniculitis 26 0.144
143
BRN106 Burns 59 0.142
144
DMN002 Dementia 69 0.142
145
c RHM011 Rheumatoid Arthritis 82 0.141
146
c ECL001 Eclampsia 59 0.141
147
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.141
148
CRN036 Craniopharyngioma 68 0.141
149
c HYP014 Hyperuricemia 56 0.140
150
P PRS136 Prostate Cancer, Hereditary, 6 40 0.140
151
P PRS130 Prostate Cancer, Hereditary, 8 37 0.140
152
c MSC007 Muscle Hypertrophy 64 0.140
153
c RSP003 Respiratory Failure 72 0.139
154
LMB062 Limb Ischemia 54 0.138
155
c PSR002 Psoriasis 67 0.137
156
c ART023 Arthropathy 68 0.136
157
P TYP024 Type Ii Mixed Cryoglobulinemia 40 0.136
158
c ENC018 Encephalopathy 65 0.135
159
ANG054 Angina Pectoris 70 0.132
160
c ATR011 Atrial Fibrillation 69 0.131
161
IRN002 Iron Metabolism Disease 60 0.130
162
BND020 Bone Disease 65 0.130
163
HYP043 Hyperandrogenism 50 0.128
164
RTN020 Retinal Vascular Disease 54 0.127
165
MDD011 Mood Disorder 65 0.126
166
P PRC031 Preeclampsia/eclampsia 1 41 0.125
167
c OVR049 Ovarian Disease 63 0.124
168
JNT002 Joint Disorders 64 0.124
169
c LYM118 Lymphoma 69 0.124
170
INS001 Insulinoma 66 0.123
171
GND003 Gonadal Disease 49 0.123
172
LNG099 Lung Disease 70 0.122
173
MNG006 Monogenic Diabetes 41 0.121
174
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.121
175
BLM002 Bulimia Nervosa 61 0.118
176
CRB039 Cerebrovascular Disease 70 0.118
177
P PLY105 Polycystic Ovary Syndrome 1 43 0.117
178
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.117
179
CYT002 Cytokine Deficiency 39 0.115
180
CRT049 Critical Limb Ischemia 52 0.115
181
ADN018 Adenoma 65 0.114
182
c MLT020 Multiple Sclerosis 76 0.114
183
ALL026 Allergic Hypersensitivity Disease 68 0.114
184
CLF033 Cleft Mitral Valve 22 0.114
185
HYP730 Hypogonadotropic Hypogonadism 58 0.114
186
THR013 Thoracic Outlet Syndrome 57 0.114
187
c MJR001 Major Depressive Disorder 67 0.113
188
LYM053 Lymphomatous Thyroiditis 27 0.113
189
c HYP083 Hypopituitarism 59 0.113
190
c DRR001 Diarrhea 58 0.113
191
THY030 Thyroid Gland Disease 51 0.113
192
HLC007 Helicobacter Pylori Infection 66 0.112
193
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.112
194
CNN003 Conn's Syndrome 73 0.111
195
c PNM007 Pneumonia 72 0.111
196
P BDY005 Body Mass Index Quantitative Trait Locus 9 29 0.109
197
P BDY006 Body Mass Index Quantitative Trait Locus 8 27 0.109
198
P BDY012 Body Mass Index Quantitative Trait Locus 7 27 0.109
199
c BPL003 Bipolar Disorder 61 0.109
200
DST089 Distal Trisomy 3p 22 0.109
201
P BDY015 Body Mass Index Quantitative Trait Locus 12 28 0.108
202
P BDY010 Body Mass Index Quantitative Trait Locus 4 27 0.108
203
CYS001 Cystic Fibrosis 83 0.108
204
GT001 Gout 62 0.108
205
BRR014 Barrett Esophagus 71 0.108
206
MTH009 Mouth Disease 66 0.106
207
DFC004 Deficiency Anemia 65 0.106
208
c LYM031 Lymphocytic Leukemia 61 0.106
209
P GLL024 Gallbladder Disease 1 45 0.105
210
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.105
211
ACT088 Acute Insulin Response 50 0.105
212
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.105
213
c HYP069 Hyperparathyroidism 59 0.105
214
P ACT068 Acute Cystitis 56 0.105
215
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.104
216
DWN001 Down Syndrome 72 0.104
217
RST023 Resting Heart Rate, Variation in 44 0.104
218
c ATT013 Attention Deficit-Hyperactivity Disorder 67 0.103
219
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.103
220
DBT087 Diabetes Insipidus, Neurohypophyseal 62 0.103
221
c AMY004 Amyloidosis 69 0.103
222
RSP006 Respiratory System Disease 64 0.103
223
GST053 Gastric Cancer 78 0.103
224
ATX010 Ataxia Neuropathy Spectrum 39 0.102
225
c OVR046 Ovarian Cyst 52 0.102
226
c LKM062 Leukemia, Acute Lymphoblastic 70 0.102
227
BNF002 Bone Fracture 50 0.102
228
NRL016 Neural Tube Defects 79 0.102
229
P PNC128 Pain - Chronic 46 0.102
230
PLM033 Pulmonary Embolism 64 0.101
231
c ANR048 Aniridia 1 63 0.101
232
P THR092 Thrombophilia Due to Thrombin Defect 70 0.101
233
DBT007 Diabetic Cataract 38 0.101
234
SPN331 Spondyloocular Syndrome 42 0.101
235
CRP001 Carpal Tunnel Syndrome 72 0.101
236
P BRD013 Bardet-Biedl Syndrome 12 49 0.100
237
DRL001 Dural Sinus Malformation 23 0.100
238
c EPL164 Epilepsy 73 0.100
239
PTT009 Pituitary Gland Disease 59 0.100
240
P MTR002 Mitral Valve Insufficiency 50 0.100
241
HRN028 Horns in Sheep 24 0.100
242
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.100
243
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.100
244
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.099
245
P BRD014 Bardet-Biedl Syndrome 2 61 0.099
246
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.099
247
c ACT232 Acute Necrotizing Encephalopathy 30 0.099
248
BLD137 Blood Group--Ahonen 21 0.099
249
c LCT001 Lactic Acidosis 53 0.099
250
LPT014 Leptin Deficiency or Dysfunction 40 0.099
251
MCR141 Mucormycosis 51 0.099
252
c BRD002 Bardet-Biedl Syndrome 65 0.098
253
HDC001 Headache 63 0.097
254
P BRD012 Bardet-Biedl Syndrome 11 52 0.097
255
P BRD011 Bardet-Biedl Syndrome 10 45 0.097
256
MTB004 Metabolic Acidosis 51 0.097
257
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.097
258
STM006 Stomach Disease 56 0.097
259
c ESP024 Esophagitis 62 0.097
260
SPN186 Spinal Cord Injury 66 0.097
261
c INF037 Inflammatory Bowel Disease 56 0.097
262
P ACT210 Acute Respiratory Distress Syndrome 66 0.097
263
c ATS364 Autism 68 0.096
264
P SPN225 Spondyloarthropathy 1 76 0.096
265
RTN023 Retinitis 48 0.096
266
ACR007 Acromegaly 71 0.095
267
c EXN002 Exanthem 62 0.095
268
NPH009 Nephrolithiasis 58 0.095
269
BWN003 Bowenoid Papulosis 43 0.095
270
P LPD015 Lipodystrophy, Familial Partial, Type 2 61 0.095
271
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.095
272
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.094
273
DRM006 Dermatitis 69 0.094
274
THY028 Thyroid Cancer 72 0.093
275
c LYM025 Lymphedema 55 0.093
276
ATM052 Autoimmune Disease 1 41 0.093
277
ART016 Aortic Aneurysm 71 0.093
278
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.093
279
BRS090 Breast Reconstruction 44 0.093
280
PNM001 Pneumocystosis 58 0.093
281
PSY004 Psychotic Disorder 74 0.093
282
INT075 Intracranial Hypertension 58 0.092
283
GRW007 Growth Hormone Deficiency 53 0.092
284
PNG002 Pain Agnosia 54 0.092
285
c CRD119 Cardiac Arrest 66 0.092
286
c CRD132 Cardiac Conduction Defect 64 0.091
287
GNR004 Generalized Anxiety Disorder 55 0.091
288
SMT008 Smith-Magenis Syndrome 58 0.091
289
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.091
290
P HPT016 Hepatitis B 70 0.090
291
PRS129 Prostatic Hyperplasia, Benign 53 0.090
292
RHM027 Rheumatic Disease 65 0.090
293
GNG013 Gingivitis 63 0.090
294
P HPT073 Hepatitis C Virus 73 0.089
295
NTR027 Neutrophil Actin Dysfunction 32 0.089
296
c GLL020 Gallbladder Disease 64 0.089
297
c AXN002 Axenfeld-Rieger Syndrome 62 0.089
298
c ATX030 Ataxia-Telangiectasia 83 0.089
299
FBR047 Fibromyalgia 62 0.088
300
c LPS004 Lupus Erythematosus 69 0.088
301
P CHR579 Chiari Malformation Type Ii 49 0.088
302
c OVR042 Ovarian Cancer 83 0.088
303
c TRM003 Tremor 56 0.087
304
P MYT020 Myotonic Dystrophy 2 59 0.087
305
ALC007 Alcohol Dependence 70 0.087
306
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.087
307
c CLL015 Collagen Disease 52 0.087
308
AND002 Androgen Insensitivity Syndrome 62 0.087
309
LPT006 Leptin Receptor Deficiency 40 0.087
311
P SYS001 Systemic Lupus Erythematosus 88 0.087
312
STR067 Stroke, Ischemic 84 0.086
313
c THR014 Thrombocytopenia 65 0.086
314
ALR002 Al-Raqad Syndrome 41 0.086
315
ACQ007 Acquired Immunodeficiency Syndrome 66 0.086
316
c MSC003 Muscular Atrophy 56 0.086
317
CLT003 Colitis 65 0.086
318
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.085
319
c ANG001 Angelman Syndrome 65 0.085
320
FRN020 Frontal Fibrosing Alopecia 32 0.085
321
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.085
322
INT007 Intermediate Coronary Syndrome 50 0.085
323
URM002 Uremia 53 0.085
324
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.085
325
CLL003 Cellulitis 61 0.085
326
c GLM007 Glomerulonephritis 62 0.084
327
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.084
328
ART001 Arterial Tortuosity Syndrome 59 0.084
329
P ALP106 Alport Syndrome 1, X-Linked 49 0.084
330
PRS021 Prostatic Adenoma 55 0.084
331
MLN008 Melanoma 64 0.084
332
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 63 0.084
333
c PLM037 Pulmonary Hypertension 77 0.083
334
PRT058 Pure Autonomic Failure 66 0.083
335
SKN016 Skin Disease 68 0.083
336
HPT082 Hepatic Adenomas, Familial 49 0.083
337
SVR004 Severe Combined Immunodeficiency 70 0.083
338
IRN001 Iron Deficiency Anemia 54 0.083
339
HNM002 Hinman Syndrome 29 0.083
340
PSR001 Psoriatic Arthritis 68 0.082
341
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.082
342
c PRC019 Precocious Puberty 52 0.082
343
OCL069 Ocular Motor Apraxia 51 0.082
344
ADP007 Adie Pupil 43 0.082
345
APP008 Appendicitis 66 0.082
346
c HST010 Histiocytosis 63 0.081
347
BCT004 Bacteriuria 52 0.081
348
ANV001 Anovulation 49 0.081
349
ALX002 Alexithymia 43 0.080
350
P AMY091 Amyotrophic Lateral Sclerosis 1 90 0.080
351
P ATS007 Autism Spectrum Disorder 68 0.080
352
c INT068 Intestinal Disease 62 0.080
353
c RTN008 Retinitis Pigmentosa 79 0.080
354
BCT022 Bacterial Infectious Disease 63 0.080
355
P MTR018 Maturity-Onset Diabetes of the Young, Type 1 51 0.080
356
c PYL005 Pyelonephritis 57 0.080
357
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 60 0.080
358
CLB026 Colobomatous Microphthalmia 40 0.080
359
BRN038 Bronchial Disease 58 0.080
360
c MYC084 Mycobacterium Tuberculosis 1 68 0.079
361
LNG108 Langerhans Cell Histiocytosis 63 0.079
362
P MGR028 Migraine with or Without Aura 1 69 0.079
363
CRN030 Coronary Stenosis 52 0.079
364
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.079
365
ALS001 Alstrom Syndrome 55 0.079
366
c KDN017 Kidney Cancer 59 0.078
367
BRC012 Brucellosis 71 0.078
368
NRR001 Neuroretinitis 48 0.078
369
PST011 Pustulosis of Palm and Sole 50 0.078
370
c LNG032 Lung Cancer 99 0.078
371
c ACR001 Aicardi-Goutieres Syndrome 63 0.078
372
c HYP076 Hyperthyroidism 56 0.078
373
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.078
374
c PRS038 Personality Disorder 68 0.077
375
c ALC004 Alcohol Abuse 69 0.077
376
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 23 0.077
377
SCH012 Schizoaffective Disorder 54 0.077
378
MYC088 Mycobacterium Avium Complex Infections 34 0.077
379
AND005 Androgen Insensitivity Syndrome, Mild 19 0.077
380
CHL004 Cholelithiasis 52 0.077
381
c HYP050 Hyperinsulinemic Hypoglycemia 55 0.077
382
P ACR116 Aicardi-Goutieres Syndrome 1 48 0.077
383
VTM002 Vitamin B12 Deficiency 48 0.077
384
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 36 0.076
385
END040 Endogenous Depression 59 0.076
386
CNS004 Constipation 58 0.076
387
c NRC002 Narcolepsy 59 0.075
388
SKN027 Skin Conditions 51 0.075
389
CNG376 Congenital Leptin Deficiency 26 0.075
390
DWR001 Dwarfism 48 0.075
391
c MYP004 Myopathy 65 0.075
392
AMN001 Amenorrhea 56 0.075
393
P SCN007 Secondary Hyperparathyroidism 56 0.075
394
c RCT021 Rectum Cancer 58 0.075
395
c LPM005 Lipomatosis 53 0.074
396
P HPT003 Hepatitis a 66 0.074
397
FSC004 Fasciitis 50 0.074
398
c DYS021 Dysautonomia 49 0.074
399
CRH001 Crohn's Disease 79 0.074
400
RFR010 Refractory Anemia 41 0.074
401
c DRM053 Dermatitis, Atopic 73 0.074
402
c TRN020 Turner Syndrome 72 0.074
403
c GST044 Gastritis 61 0.074
404
MTB007 Metabolic Encephalomyopathic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 53 0.074
405
PLY112 Polyarteritis Nodosa, Childhood-Onset 51 0.074
406
IGG001 Iga Glomerulonephritis 58 0.073
407
c HYP265 Hypotonia 43 0.073
408
WRN001 Werner Syndrome 74 0.073
409
VRL011 Viral Infectious Disease 69 0.073
410
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.073
411
c TTR001 Tetralogy of Fallot 71 0.073
412
GSG001 Gas Gangrene 48 0.073
413
PNC034 Pancreas Disease 60 0.072
414
c WLF004 Wolfram Syndrome 60 0.072
415
ATN002 Autonomic Nervous System Disease 54 0.072
416
BRN071 Brain Injury 54 0.071
417
CHR100 Chronic Ulcer of Skin 53 0.071
418
P ACT071 Acute Kidney Failure 54 0.071
419
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.071
420
INT002 Intermittent Claudication 64 0.071
421
c NPH012 Nephrotic Syndrome 59 0.071
422
RNL051 Renal Cysts and Diabetes Syndrome 53 0.071
423
P MTR019 Maturity-Onset Diabetes of the Young, Type 2 52 0.071
424
NCR002 Necrobiosis Lipoidica 39 0.070
425
P HMC039 Hemochromatosis, Type 1 74 0.070
426
CLR108 Colorectal Adenoma 64 0.070
427
HPR003 Heparin-Induced Thrombocytopenia 49 0.069
428
PRS063 Paresthesia 45 0.069
429
FBR065 Fibrocalculous Pancreatopathy 18 0.069
430
ADL002 Adult Syndrome 55 0.069
431
SKN023 Skin Tag 43 0.069
432
c CND004 Candidiasis 63 0.068
433
DYS073 Dysphagia 53 0.068
434
c FCL005 Focal Segmental Glomerulosclerosis 60 0.068
435
P BRD010 Bardet-Biedl Syndrome 1 58 0.068
436
GST049 Gastrointestinal System Cancer 62 0.068
437
GST071 Gastrointestinal Carcinoma 46 0.068
438
c BLD134 Bladder Cancer 71 0.068
439
c RST001 Restless Legs Syndrome 60 0.068
440
c SHR029 Short Syndrome 57 0.068
441
ASP030 Aspirin Resistance 46 0.068
442
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.068
443
PHK010 Phakomatosis Spilorosea 18 0.068
444
P ACT074 Acute Lymphocytic Leukemia 62 0.068
445
SYS003 Systolic Heart Failure 46 0.068
446
PNC033 Pancreas Adenocarcinoma 67 0.068
447
LRN002 Laron Syndrome 63 0.067
448
INT303 Intracranial Hypertension, Idiopathic 53 0.067
449
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 27 0.067
450
MYL005 Myelofibrosis 70 0.067
451
BNR002 Bone Resorption Disease 54 0.067
452
c SBS003 Substance Abuse 61 0.067
453
PRT036 Peritonitis 67 0.067
454
MYL069 Myeloma, Multiple 85 0.066
455
PLM010 Pulmonary Edema 60 0.066
456
c MYL006 Myeloid Leukemia 68 0.066
457
c MLN007 Male Infertility 52 0.066
458
BRS051 Breast Disease 68 0.066
459
c SZR006 Seizure Disorder 61 0.066
460
HRN026 Hernia, Hiatus 49 0.066
461
c PHC003 Pheochromocytoma 73 0.066
462
CRT013 Carotid Stenosis 52 0.066
463
c PSD015 Pseudohypoparathyroidism 51 0.066
464
OST097 Osteoporotic Fracture 36 0.065
465
CYS009 Cystadenoma 41 0.065
466
PRP098 Proprotein Convertase 1/3 Deficiency 31 0.065
467
DYS014 Dyspepsia 56 0.065
468
c ADL010 Adult Respiratory Distress Syndrome 64 0.065
469
OBS082 Obstructive Nephropathy 52 0.065
470
GTR002 Goiter 54 0.065
471
OBS015 Obesity, Hyperphagia, and Developmental Delay 26 0.065
472
HMT018 Hematopoietic Stem Cell Transplantation 59 0.065
473
PPT005 Peptic Ulcer Disease 64 0.065
474
TRN015 Transient Cerebral Ischemia 59 0.064
475
CHL123 Chlamydia 66 0.064
476
c SLL003 Salla Disease 53 0.064
477
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.064
478
STS002 Situs Inversus 50 0.064
479
c MMP001 Mumps 61 0.064
480
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.064
481
SRC014 Sarcoma 70 0.064
482
c SJG008 Sjogren Syndrome 60 0.064
483
PST021 Postpartum Depression 55 0.064
484
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 43 0.064
485
c OPN001 Open-Angle Glaucoma 53 0.063
486
WLS003 Wilson-Turner X-Linked Mental Retardation Syndrome 44 0.063
487
c GLY013 Glycogen Storage Disease 62 0.063
488
PLM017 Pulmonary Alveolar Microlithiasis 52 0.063
489
c RHN004 Rhinitis 63 0.063
490
c CMR001 Camurati-Engelmann Disease 62 0.063
491
LYM027 Lymphopenia 57 0.063
492
CRT016 Carotid Artery Disease 58 0.062
493
P VRL010 Viral Hepatitis 60 0.062
494
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.062
495
MRB006 Morbid Obesity and Spermatogenic Failure 19 0.062
496
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.062
497
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 73 0.062
498
PRP030 Purpura 62 0.062
499
c SCL057 Scoliosis, Isolated 1 46 0.062
500
LYM133 Lymphoma, Hodgkin, Classic 73 0.062
501
c SNS001 Sensorineural Hearing Loss 60 0.062
502
IRR002 Irritable Bowel Syndrome 64 0.061
503
RCK004 Rickets 66 0.061
504
P LKM060 Leukemia, Acute Lymphoblastic 3 52 0.061
505
CHN016 Cohen Syndrome 54 0.061
506
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 55 0.061
507
P LRG017 Large Intestine Cancer 63 0.061
508
c PLY018 Polycythemia 60 0.061
509
c DLT002 Dilated Cardiomyopathy 74 0.061
510
HMC014 Homocysteinemia 52 0.061
511
P CRP023 Carpenter Syndrome 1 59 0.061
512
DMP001 Dumping Syndrome 46 0.061
513
P BLD140 Blood Group, I System 26 0.061
514
NCR007 Necrotizing Fasciitis 51 0.060
515
PMP004 Pemphigus Foliaceus 47 0.060
516
c NRF023 Neurofibromatosis, Type Ii 76 0.060
517
P PTT057 Pituitary Adenoma 4, Acth-Secreting 55 0.060
518
HYP081 Hypolipoproteinemia 49 0.060
519
BRB001 Beriberi 43 0.060
520
ERY029 Erythermalgia, Primary 58 0.060
521
P LKM061 Leukemia, Acute Myeloid 83 0.060
522
HMN044 Human Immunodeficiency Virus Type 1 75 0.060
523
OPT006 Optic Nerve Disease 60 0.060
524
LRN003 Learning Disability 53 0.060
525
ACH005 Achalasia 54 0.060
526
DVR002 Diverticulitis 46 0.060
527
DYS011 Dyskinesia of Esophagus 42 0.060
528
MHM001 Mehmo Syndrome 33 0.060
529
ESP021 Esophageal Cancer 84 0.060
530
P PRM005 Primary Hyperparathyroidism 60 0.060
531
P PNC106 Pancreatic Agenesis 1 52 0.059
532
SLD003 Sialadenitis 49 0.059
533
c PRK057 Parkinson Disease, Late-Onset 77 0.059
534
c HYP061 Hypertrophic Cardiomyopathy 59 0.059
535
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 0.059
536
LPD012 Lipoid Congenital Adrenal Hyperplasia 72 0.059
537
SPN051 Spondylitis 55 0.059
538
c RNL007 Renal Tubular Acidosis 51 0.059
539
UND005 Undifferentiated Pleomorphic Sarcoma 51 0.059
540
EPD070 Epidermoid Cysts 50 0.058
541
WRN003 Wernicke Encephalopathy 49 0.058
542
c PLY014 Polycystic Kidney Disease 63 0.058
543
ERY003 Erythema Multiforme 63 0.058
544
HYD002 Hydronephrosis 52 0.058
545
ALL003 Allergic Rhinitis 69 0.058
546
HSH003 Hashimoto Thyroiditis 67 0.058
547
NWB001 Newborn Respiratory Distress Syndrome 61 0.058
548
c CMP008 Compartment Syndrome 52 0.058
549
P LBR014 Leber Congenital Amaurosis 4 55 0.058
550
c FML012 Familial Partial Lipodystrophy 52 0.058
551
c VNS003 Venous Insufficiency 54 0.058
552
FRL002 Froelich Syndrome 20 0.057
553
CRV035 Cervical Cancer 76 0.057
554
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.057
555
FCL044 Fecal Incontinence 38 0.057
556
CHL065 Cholangiocarcinoma 65 0.057
557
c MSC033 Muscle Disorders 56 0.057
558
P PTT056 Pituitary Adenoma 1, Multiple Types 51 0.057
559
c HYD006 Hydrocephalus 66 0.057
560
BLD163 Blood Group, Dombrock System 23 0.057
561
ULC004 Ulcerative Colitis 80 0.057
562
c PLY006 Polydactyly 58 0.056
563
c VSC011 Vasculitis 67 0.056
564
END062 Endometrial Hyperplasia 51 0.056
565
c ALP008 Alopecia 56 0.056
566
P CRD065 Cardiomyopathy, Familial Hypertrophic, 2 45 0.056
567
INT051 Intussusception 51 0.056
568
CRB037 Cerebral Palsy 71 0.056
569
OBS050 Obesity Due to Congenital Leptin Deficiency 23 0.056
570
MTC005 Mitochondrial Metabolism Disease 46 0.056
571
RSP007 Respiratory Distress Syndrome, Infant 38 0.056
572
c END033 Endocarditis 60 0.055
573
P GRV008 Graves Disease 1 57 0.055
574
c MCR010 Microcephaly 59 0.055
575
GST045 Gastroenteritis 65 0.055
576
GYN001 Gynecomastia 47 0.055
577
P MJR004 Major Affective Disorder 4 40 0.055
578
EXC002 Exocrine Pancreatic Insufficiency 42 0.055
579
c PNS012 Paine Syndrome 63 0.055
580
P CHR682 Chronic Bilirubin Encephalopathy 22 0.055
581
P FCL025 Focal Segmental Glomerulosclerosis 1 52 0.055
582
SLP010 Slipped Capital Femoral Epiphysis 38 0.055
583
SCL022 Scleredema 31 0.055
584
P CNT075 Central Precocious Puberty 52 0.054
585
c BCL006 B-Cell Lymphomas 66 0.054
586
TRM010 Traumatic Brain Injury 56 0.054
587
END038 Endocrine Pancreas Disease 36 0.054
588
ACR006 Aceruloplasminemia 72 0.054
589
FRZ001 Frozen Shoulder 53 0.054
590
CRD223 Cardiac Arrhythmia 56 0.054
591
HMS001 Hemosiderosis 52 0.054
592
WLL001 Williams-Beuren Syndrome 64 0.053
593
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.053
594
MYL009 Myelodysplastic Syndrome 71 0.053
595
c PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 70 0.053
596
ART002 Arts Syndrome 56 0.053
597
CHL147 Chlamydia Pneumonia 42 0.053
598
c SRC025 Sarcoidosis 1 76 0.053
599
P CNT035 Central Nervous System Disease 65 0.053
600
c THR015 Thrombophilia 56 0.053
601
PST053 Postherpetic Neuralgia 45 0.053
602
ART008 Arteriosclerosis Obliterans 42 0.053
603
c PNC045 Pancreatic Agenesis 40 0.053
604
c ENC004 Encephalitis 66 0.053
605
c FNG006 Feingold Syndrome 1 47 0.053
606
HYP085 Hypothalamic Disease 46 0.053
607
OTT002 Otitis Media 68 0.053
608
PRP016 Paraplegia 55 0.053
609
VRC005 Varicose Veins 67 0.053
610
HYP068 Hyperostosis 52 0.053
611
DST006 Diastolic Heart Failure 46 0.053
612
FXF002 Fox-Fordyce Disease 41 0.053
613
c MGL001 Megaloblastic Anemia 52 0.052
614
DXT002 Dextrocardia with Situs Inversus 39 0.052
615
STF001 Stiff-Person Syndrome 64 0.052
616
P HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 62 0.052
617
P MTR026 Maturity-Onset Diabetes of the Young, Type 9 31 0.052
618
KRT002 Keratomalacia 51 0.052
619
P INF145 Infantile Liver Failure Syndrome 1 48 0.052
620
VSC002 Vascular Dementia 58 0.052
621
c MSC005 Muscular Dystrophy 66 0.052
622
TBC004 Tobacco Addiction 64 0.052
623
HYP784 Hypogonadism, Male 43 0.052
624
MNS002 Mini Stroke 25 0.052
625
CLC006 Calcinosis 53 0.052
626
c CHL066 Cholangitis 52 0.052
627
c ALP009 Alopecia Areata 68 0.051
628
TND004 Tendinopathy 47 0.051
629
DCB001 Decubitus Ulcer 47 0.051
630
HYP110 Hyperproinsulinemia 41 0.051
631
c UTR058 Uterine Anomalies 60 0.051
632
P MTR044 Maturity-Onset Diabetes of the Young, Type 10 39 0.051
633
HDR002 Hidradenitis Suppurativa 57 0.051
634
HDR003 Hidradenitis 49 0.051
635
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.051
636
P SML038 Small Cell Cancer of the Lung 69 0.051
637
P ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.051
638
CRN024 Corneal Disease 45 0.051
639
SPN027 Spinal Stenosis 62 0.051
640
c NTR004 Neutropenia 61 0.051
641
CHL068 Cholestasis 60 0.051
642
c HYP614 Hyperlipidemia, Familial Combined 56 0.050
643
EXP004 Exophthalmos 52 0.050
644
P MYT021 Myotonic Dystrophy 1 72 0.050
646
P JVN010 Juvenile Rheumatoid Arthritis 72 0.050
647
END072 Endotheliitis 39 0.050
648
c PTS002 Ptosis 55 0.050
649
CLC001 Calciphylaxis 53 0.050
650
c HYP607 Hypercholesterolemia, Familial 82 0.050
651
HYP026 Hypoglycemic Coma 44 0.050
652
c ACT105 Acute Mountain Sickness 58 0.050
653
PNN001 Panniculitis 52 0.050
654
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.050
655
c ACQ022 Acquired Generalized Lipodystrophy 54 0.050
656
P LPD032 Lipodystrophy, Congenital Generalized, Type 1 48 0.050
657
IDP033 Idiopathic Edema 42 0.050
658
c INT070 Intestinal Obstruction 55 0.049
659
FND002 Fundus Dystrophy 51 0.049
660
ALL014 Allergic Encephalomyelitis 43 0.049
661
c ASP006 Aspergillosis 67 0.049
662
c MYS003 Myasthenia Gravis 74 0.049
663
CYT008 Cytomegalovirus Infection 61 0.049
664
SQM006 Squamous Cell Carcinoma 59 0.049
665
c PTT006 Pituitary Adenoma 54 0.049
666
URN022 Urinary Tract Infections, Recurrent 34 0.049
667
c CHR084 Chromosomal Disease 40 0.049
668
ELP001 Elephantiasis 38 0.049
669
P HMP029 Hemophilia a 70 0.049
670
P ART101 Aortic Valve Disease 2 68 0.049
671
DRG003 Drug Dependence 51 0.049
672
GNG011 Gingival Disease 49 0.049
673
c ACQ009 Acquired Metabolic Disease 32 0.049
674
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 13 0.049
675
c FML035 Familial Hyperlipidemia 50 0.048
676
P EPS039 Episodic Pain Syndrome, Familial, 1 27 0.048
677
MCR011 Microinvasive Gastric Cancer 47 0.048
678
P ACT073 Acute Leukemia 62 0.048
679
P SVR005 Severe Pre-Eclampsia 55 0.048
680
c DDN001 Duodenal Ulcer 52 0.048
681
GLC036 Glucagonoma 51 0.048
682
c ART084 Arteriovenous Fistula 50 0.048
683
CLS049 Classic Phenylketonuria 38 0.048
684
c MYP006 Myopia 62 0.048
685
CHL067 Cholecystitis 59 0.048
686
BLL003 Bell's Palsy 53 0.048
687
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 43 0.048
688
BLD165 Blood Group, Colton System 23 0.048
689
SWL001 Swallowing Disorders 36 0.048
690
BRN024 Bronchitis 70 0.047
691
HYP020 Hyperprolactinemia 64 0.047
692
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 46 0.047
693
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.047
694
PSD088 Pseudobulbar Affect 39 0.047
695
P GLC092 Glaucoma, Primary Open Angle 58 0.047
696
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 43 0.047
697
STT004 Steatorrhea 43 0.047
698
P MTR039 Maturity-Onset Diabetes of the Young, Type 11 21 0.047
699
CHP002 Chops Syndrome 32 0.047
700
MLR004 Malaria 85 0.047
701
P LPD040 Lipodystrophy, Familial Partial, Type 1 43 0.047
702
HRT012 Heart Valve Disease 57 0.046
703
PSD014 Pseudopseudohypoparathyroidism 56 0.046
704
PRT018 Portal Vein Thrombosis 51 0.046
705
SPN021 Spinal Meningioma 50 0.046
706
CLR030 Clear Cell Renal Cell Carcinoma 49 0.046
707
INT079 Intrahepatic Cholangiocarcinoma 55 0.046
708
TTH006 Tooth Disease 54 0.046
709
P MYS011 Myasthenia Gravis Congenital 33 0.046
710
CHL014 Cholera 61 0.046
711
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.046
712
c SKN015 Skin Carcinoma 65 0.046
713
CLN019 Colonic Disease 62 0.046
714
c HLP001 Holoprosencephaly 65 0.046
715
NNT012 Neonatal Jaundice 52 0.046
716
SNL007 Senile Cataract 40 0.046
717
ALL006 Allergic Asthma 61 0.046
718
SFT003 Soft Tissue Sarcoma 60 0.046
719
c END044 Endometriosis 65 0.045
720
P CNG006 Congenital Hypothyroidism 64 0.045
721
PST028 Post-Traumatic Stress Disorder 63 0.045
722
c HMP007 Hemophilia 62 0.045
723
P HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 57 0.045
724
CNN005 Connective Tissue Disease 67 0.045
725
RDC002 Radiculopathy 54 0.045
726
DSR011 Disorganization, Mouse, Homolog of 23 0.045
727
GLN010 Glanzmann Thrombasthenia 69 0.045
728
GLL008 Gilles De La Tourette Syndrome 69 0.045
729
HYP030 Hypoactive Sexual Desire Disorder 44 0.045
730
P PRM038 Primary Agammaglobulinemia 39 0.045
731
c SCL018 Scoliosis 59 0.045
732
c PLV020 Pelvic Organ Prolapse 64 0.045
733
SPN041 Spinal Cord Disease 55 0.045
734
c ANL018 Analbuminemia 48 0.045
735
LRN001 Laurence-Moon Syndrome 46 0.045
736
OVR094 Ovarian Epithelial Cancer 41 0.045
737
CRD220 Cardiac Valvular Defect, Developmental 36 0.045
738
SYN007 Synovitis 61 0.044
739
CRH005 Crohn's Colitis 61 0.044
740
SPN035 Spindle Cell Sarcoma 52 0.044
741
P HNT004 Huntington Disease-Like 2 48 0.044
742
c CHR071 Charcot-Marie-Tooth Disease 65 0.044
743
HMR039 Hemorrhage, Intracerebral 62 0.044
744
HRP004 Herpes Zoster 63 0.044
745
CRB009 Cerebritis 39 0.044
746
ACH004 Achondroplasia 69 0.044
747
ALB001 Albright's Hereditary Osteodystrophy 55 0.044
748
P PSD108 Pseudohypoparathyroidism, Type Ia 57 0.044
749
c OCY003 Oocyte Maturation Defect 1 42 0.044
750
HYP017 Hypophosphatemia 48 0.043
751
FRN014 Fournier Gangrene 42 0.043
752
c MYC008 Myocarditis 59 0.043
753
CRB085 Cerebral Hemorrhage 46 0.043
754
SDD008 Sudden Sensorineural Hearing Loss 46 0.043
755
c NRB001 Neuroblastoma 73 0.043
756
IGR001 Ige Responsiveness, Atopic 59 0.043
757
c GLM045 Glioma 56 0.043
758
c KRT007 Keratoconus 50 0.043
759
SYN036 Syncope 49 0.043
760
PTL001 Patulous Eustachian Tube 31 0.043
761
INT253 Intestinal Benign Neoplasm 57 0.043
762
CHR005 Chorioamnionitis 53 0.043
763
c RTN024 Retinoblastoma 73 0.043
764
MNC006 Monoclonal Gammopathy of Uncertain Significance 54 0.043
765
P CHR431 Chronic Venous Insufficiency 50 0.043
766
BRC010 Brachial Plexus Lesion 46 0.043
767
CRY036 Cryptogenic Cirrhosis 38 0.043
768
GST007 Gastric Dilatation 32 0.043
769
CMP010 Complex Regional Pain Syndrome 64 0.043
770
CHR073 Choreatic Disease 50 0.043
771
NDL021 Nodular Lymphocyte Predominant Hodgkin Lymphoma 49 0.043
772
P FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.043
773
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.043
774
P DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 24 0.043
775
SCK003 Sickle Cell Anemia 75 0.042
776
c SNS014 Sinusitis 64 0.042
777
TND005 Tendinitis 45 0.042
778
BRK012 Broken Heart Syndrome 39 0.042
779
c PRT013 Portal Hypertension 61 0.042
780
LYM019 Lymphosarcoma 59 0.042
781
BLD044 Bladder Disease 57 0.042
782
MSC190 Muscular Disease 55 0.042
783
BLR008 Bilirubin Metabolic Disorder 53 0.042
784
ADR040 Adrenal Gland Pheochromocytoma 48 0.042
785
EMP001 Empty Sella Syndrome 43 0.042
786
MSC004 Muscle Tissue Disease 39 0.042
787
P MNN043 Meningioma, Familial 63 0.042
788
TRC026 Tracheal Disease 37 0.042
789
HYP364 Hyperostosis Frontalis Interna 30 0.042
790
c HRP006 Herpes Simplex 71 0.042
791
c HML002 Hemolytic Anemia 65 0.042
792
DSS009 Disseminated Intravascular Coagulation 58 0.042
793
c ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 53 0.042
794
NPH010 Nephrosclerosis 46 0.042
795
P TYP038 Type 1 Diabetes Mellitus 15 23 0.042
796
c BNC003 Bone Cancer 61 0.042
797
ANG020 Angiosarcoma 59 0.042
798
AML029 Ameloblastoma 53 0.042
799
P LPM012 Lipomatosis, Multiple 66 0.042
800
c ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 54 0.042
801
KWS001 Kwashiorkor 46 0.042
802
P LKM063 Leukemia, Chronic Myeloid 74 0.041
803
c ANT006 Antiphospholipid Syndrome 60 0.041
804
SHH001 Sheehan Syndrome 51 0.041
805
DGR001 Digeorge Syndrome 62 0.041
806
P AMY009 Amyloidosis Aa 56 0.041
807
ISL003 Isolated Growth Hormone Deficiency 53 0.041
808
c END046 Endometritis 53 0.041
809
c HYP263 Hypersomnia 45 0.041
810
SCR011 Scrapie 42 0.041
811
CHR008 Choroiditis 44 0.041
812
APL001 Aplastic Anemia 75 0.041
813
c BCK002 Beckwith-Wiedemann Syndrome 59 0.041
814
VSL002 Visual Epilepsy 33 0.041
815
PYD002 Pyoderma 53 0.040
816
GLC022 Glucose/galactose Malabsorption 44 0.040
817
c TXP001 Toxoplasmosis 65 0.040
818
P CNR004 Cone-Rod Dystrophy 2 63 0.040
819
PHN003 Phenylketonuria 75 0.040
820
NNT019 Neonatal Hypothyroidism 42 0.040
821
RCT017 Rectal Disease 42 0.040
822
PLM005 Pleomorphic Lipoma 39 0.040
823
END041 Endometrial Adenocarcinoma 60 0.040
824
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 52 0.040
825
PRS042 Prostate Disease 47 0.040
826
SCR001 Secretory Meningioma 40 0.040
827
INT146 Intervertebral Disc Disease 65 0.040
828
PRT038 Protein-Energy Malnutrition 53 0.040
829
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.040
830
GST019 Gastrointestinal Stromal Tumor 74 0.039
831
GST040 Gastric Adenocarcinoma 66 0.039
832
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.039
833
PPT001 Peptic Esophagitis 45 0.039
834
KPS004 Kaposi Sarcoma 77 0.039
835
c THR005 Thrombotic Thrombocytopenic Purpura 65 0.039
836
c SLV001 Silver-Russell Syndrome 58 0.039
837
HDN002 Head Injury 52 0.039
838
ISL001 Islet Cell Tumor 51 0.039
839
OCC006 Occipital Horn Syndrome 50 0.039
840
HYP077 Hypertrichosis 49 0.039
841
c OPT070 Optic Nerve Hypoplasia, Bilateral 49 0.039
842
MTR007 Motor Peripheral Neuropathy 41 0.039
843
P CRT085 Carotid Intimal Medial Thickness 2 25 0.039
844
c LTR001 Lateral Sclerosis 60 0.039
845
INF034 Infective Endocarditis 57 0.039
846
PRS047 Prostatitis 57 0.039
847
ICH020 Ichthyosis Prematurity Syndrome 45 0.039
848
AYM001 Ayme-Gripp Syndrome 39 0.039
849
CLR109 Colorectal Adenocarcinoma 54 0.038
850
c BLD051 Blood Coagulation Disease 51 0.038
851
INT052 Intestinal Volvulus 43 0.038
852
c TMP003 Temporal Arteritis 68 0.038
853
c HYP098 Hypereosinophilic Syndrome 67 0.038
854
P ATM011 Autoimmune Hepatitis 66 0.038
855
ART004 Aortic Atherosclerosis 45 0.038
856
MNC002 Munchausen by Proxy 32 0.038
857
c GRF003 Graft-Versus-Host Disease 72 0.038
858
c KBK002 Kabuki Syndrome 1 67 0.038
859
c ICH004 Ichthyosis 57 0.038
860
c ACT010 Acth-Secreting Pituitary Adenoma 52 0.038
861
OST011 Osteomalacia 52 0.038
862
PPL021 Papilledema 49 0.038
863
NRT001 Neurotic Disorder 48 0.038
864
c MYS005 Myositis 62 0.038
865
CHK001 Chikungunya 61 0.038
866
ACT055 Actinomycosis 45 0.038
867
MYX004 Myxedema 44 0.038
868
P CRD093 Cardiomyopathy, Dilated, 1a 41 0.038
869
MDS022 Mediastinitis 41 0.038
870
IMM001 Immune-Complex Glomerulonephritis 38 0.038
871
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 35 0.037
872
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.037
873
INS034 Insulinomatosis and Diabetes Mellitus 25 0.037
874
BRN028 Brain Cancer 74 0.037
875
P VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.037
876
PLL001 Pallister-Hall Syndrome 63 0.037
877
URT039 Urticaria 60 0.037
878
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.037
879
P CNG216 Congenital Hydrocephalus 56 0.037
880
CHN055 Chanarin-Dorfman Syndrome 56 0.037
881
c MYT002 Myotonic Dystrophy 52 0.037
882
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.037
883
GLC096 Galactorrhea 47 0.037
884
P HYP768 Hyperlipoproteinemia, Type I 42 0.037
885
P HNT011 Huntington Disease-Like 3 40 0.037
886
NTR007 Neutral Lipid Storage Disease with Myopathy 38 0.037
887
P BPL002 Bipolar I Disorder 50 0.037
888
P BRD016 Bardet-Biedl Syndrome 4 46 0.037
889
HPT067 Hepatocellular Adenoma 45 0.037
890
DDN027 Duodenum Disease 43 0.037
891
P BRD015 Bardet-Biedl Syndrome 3 41 0.037
892
BRN056 Bronchopulmonary Dysplasia 61 0.037
893
P THY109 Thyroid Cancer, Nonmedullary, 1 60 0.037
894
P HYP602 Hyperoxaluria, Primary, Type Ii 38 0.037
895
XP2001 Xp22.3 Microdeletion Syndrome 26 0.037
896
CMP096 Complete Generalized Lipodystrophy 23 0.037
897
CRN167 Caronte 19 0.037
898
CNT097 Central Hypoventilation Syndrome, Congenital 67 0.037
899
ING001 Inguinal Hernia 61 0.037
900
c PLM034 Pulmonary Emphysema 59 0.037
901
PHR003 Pharyngitis 58 0.037
902
P BRD018 Bardet-Biedl Syndrome 6 40 0.037
903
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.037
904
c NSP012 Nasopharyngeal Carcinoma 66 0.036
905
c VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65 0.036
906
c SPN046 Spinal Muscular Atrophy 65 0.036
907
GST023 Gastric Ulcer 58 0.036
908
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 55 0.036
909
c RTN014 Retinal Artery Occlusion 50 0.036
910
PTT037 Pituitary Tumors 48 0.036
911
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.036
912
c MLT074 Multiple Endocrine Neoplasia 56 0.036
913
NRN004 Neuroendocrine Tumor 56 0.036
914
c LRY019 Laryngitis 54 0.036
915
c PTT014 Pitt-Hopkins Syndrome 54 0.036
916
c TRT010 Teratoma 53 0.036
917
HPT009 Hepatopulmonary Syndrome 52 0.036
918
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.036
919
P HYD019 Hydrocephalus Due to Congenital Stenosis of Aqueduct of Sylvius 47 0.036
920
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 41 0.036
921
SPR007 Superior Mesenteric Artery Syndrome 39 0.036
922
NRV004 Nerve Compression Syndrome 39 0.036
923
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.036
924
c PLM036 Pulmonary Fibrosis 70 0.035
925
TLN003 Telangiectasis 55 0.035
926
KRT006 Keratoconjunctivitis 55 0.035
927
c FNC043 Fanconi Anemia, Complementation Group E 54 0.035
928
QDR001 Quadriplegia 53 0.035
929
c SCL009 Sclerosing Cholangitis 51 0.035
930
BRN080 Brain Ischemia 43 0.035
931
DDN006 Duodenitis 43 0.035
932
P DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.035
933
c PLY041 Polymyositis 59 0.035
934
PLG002 Plague 59 0.035
935
PRV006 Pervasive Developmental Disorder 56 0.035
936
SXD002 Sex Development Disorder 49 0.035
937
c CRN074 Coronary Artery Aneurysm 48 0.035
938
SCH003 Schizophreniform Disorder 43 0.035
939
IDP041 Idiopathic Recurrent Pericarditis 31 0.035
940
DDN009 Duodenal Obstruction 31 0.035
941
c MRL001 Meralgia Paresthetica 27 0.035
942
c WSK001 Wiskott-Aldrich Syndrome 76 0.034
943
SKN019 Skin Melanoma 67 0.034
944
P OVR114 Ovarian Cancer 1 66 0.034
945
CRD137 Cardiogenic Shock 41 0.034
946
CDQ001 Cauda Equina Syndrome 40 0.034
947
c STR035 Streptococcal Group a Invasive Disease 30 0.034
948
MYL020 Myelomeningocele 54 0.034
949
c NGH001 Night Blindness 50 0.034
950
TQP001 Taqi Polymorphism 35 0.034
951
ECT026 Ectopic Pregnancy 53 0.034
952
ARM001 Aromatase Deficiency 52 0.034
953
PST095 Post-Thrombotic Syndrome 51 0.034
954
LPM010 Lipomatosis, Multiple Symmetric 43 0.034
955
c FNC027 Fanconi Anemia, Complementation Group a 81 0.034
956
LSH001 Leishmaniasis 72 0.034
957
OST003 Osteonecrosis 67 0.034
958
CCC001 Coccidioidomycosis 61 0.034
959
END035 Endocrine Gland Cancer 57 0.034
960
ART017 Aortic Disease 56 0.034
961
P BLD124 Bleeding Disorder, Platelet-Type, 11 55 0.034
962
MYS004 Myiasis 36 0.034
963
OVR093 Overhydrated Hereditary Stomatocytosis 36 0.034
964
HNS001 Hansen's Disease 36 0.034
965
MTH081 Mthfr Gene Variant 19 0.034
966
P INF071 Inflammatory Bowel Disease 1 57 0.033
967
c SHR001 Short Bowel Syndrome 52 0.033
968
DGN001 Degenerative Disc Disease 51 0.033
969
CLP006 Clopidogrel Resistance 45 0.033
970
P ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 35 0.033
971
TMP012 Temple Syndrome 35 0.033
972
48X003 48,xxyy Syndrome 34 0.033
973
XLN133 X-Linked Intellectual Disability, Shashi Type 26 0.033
974
c ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 26 0.033
975
c FTL001 Fetal Alcohol Syndrome 64 0.033
976
ACR008 Acrocallosal Syndrome 60 0.033
977
VGN023 Vaginitis 58 0.033
978
PYD001 Pyoderma Gangrenosum 58 0.033
979
MST005 Mastitis 57 0.033
980
P GLY005 Glycogen Storage Disease Vi 57 0.033
981
P HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 56 0.033
982
ATR057 Atrioventricular Block 54 0.033
983
RGH009 Right Atrial Isomerism 53 0.033
984
ALC009 Alcoholic Liver Cirrhosis 52 0.033
985
NRL004 Neuroleptic Malignant Syndrome 51 0.033
986
c ARC016 Auriculocondylar Syndrome 1 48 0.033
987
CRB004 Cerebral Artery Occlusion 46 0.033
988
PLR007 Pleural Empyema 46 0.033
989
MLK003 Melkersson-Rosenthal Syndrome 45 0.033
990
ENT004 Enthesopathy 44 0.033
991
BRN026 Branch Retinal Artery Occlusion 36 0.033
992
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 32 0.033
993
CHG001 Chagas Disease 73 0.033
994
c ORT004 Orthostatic Intolerance 69 0.033
995
CHR066 Chronic Fatigue Syndrome 68 0.033
996
MVM001 Movement Disease 67 0.033
997
MSC157 Muscular Dystrophy, Duchenne Type 66 0.033
998
P WLM018 Wilms Tumor 5 64 0.033
999
URN010 Urinary Tract Obstruction 58 0.033
1000
DFF005 Diffuse Large B-Cell Lymphoma 58 0.033
1001
ADT003 Auditory System Disease 52 0.033
1002
PLC007 Placental Abruption 51 0.033
1003
ART031 Aortic Coarctation 50 0.033
1004
HYP006 Hypertensive Heart Disease 50 0.033
1006
MMM006 Mammographic Density 47 0.033
1007
P HYP057 Hypervitaminosis D 43 0.033
1008
P WLM011 Wilms Tumor 6 40 0.033
1009
INF021 Infant Gynecomastia 27 0.033
1010
c MDL005 Medulloblastoma 77 0.032
1011
P CRD086 Cardiomyopathy, Familial Hypertrophic, 1 59 0.032
1012
EXT034 Extrinsic Allergic Alveolitis 58 0.032
1013
c ANG015 Angioedema 58 0.032
1014
HST011 Histoplasmosis 57 0.032
1015
PLV003 Pelvic Inflammatory Disease 55 0.032
1016
GLC011 Galactose Epimerase Deficiency 48 0.032
1017
VSC008 Vascular Hemostatic Disease 45 0.032
1018
GGN002 Gigantism 37 0.032
1019
PPL001 Papillary Adenoma 35 0.032
1020
SBC016 Subacute Delirium 34 0.032
1021
FST001 Foster-Kennedy Syndrome 33 0.032
1022
P ORT012 Orthostatic Hypotension 2 32 0.032
1023
P NRC009 Narcolepsy 1 51 0.031
1024
P BRD044 Bardet-Biedl Syndrome 17 47 0.031
1025
P BRD032 Bardet-Biedl Syndrome 14 45 0.031
1026
P BRD020 Bardet-Biedl Syndrome 8 43 0.031
1027
P BRD033 Bardet-Biedl Syndrome 13 42 0.031
1028
P BRD048 Bardet-Biedl Syndrome 18 42 0.031
1029
PLN026 Pilonidal Sinus 40 0.031
1030
P BRD017 Bardet-Biedl Syndrome 5 39 0.031
1031
P BRD045 Bardet-Biedl Syndrome 19 36 0.031
1032
P BRD047 Bardet-Biedl Syndrome 16 34 0.031
1033
BRN049 Brain Tumor, Childhood 33 0.031
1034
P BRD019 Bardet-Biedl Syndrome 7 30 0.031
1035
P BRD021 Bardet-Biedl Syndrome 9 26 0.031
1036
P BRD050 Bardet-Biedl Syndrome 21 26 0.031
1037
c CYT020 Cytomegalic Congenital Adrenal Hypoplasia 25 0.031
1038
P BRD051 Bardet-Biedl Syndrome 20 23 0.031
1039
CRB089 Cerebral Beriberi 22 0.031
1040
OVR029 Ovarian Hyperstimulation Syndrome 65 0.031
1041
MCS002 Mucositis 60 0.031
1042
P ACT135 Acute Graft Versus Host Disease 58 0.031
1043
LYM040 Lymphoblastic Lymphoma 58 0.031
1044
CYS039 Cystic Kidney Disease 55 0.031
1045
FML026 Familial Lipoprotein Lipase Deficiency 53 0.031
1046
BLR006 Biliary Tract Disease 53 0.031
1047
PRP009 Peripartum Cardiomyopathy 51 0.031
1048
ATS010 Autosomal Recessive Disease 47 0.031
1049
ACD008 Acid-Labile Subunit Deficiency 43 0.031
1050
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.031
1051
SPT019 Septo-Optic Dysplasia Spectrum 32 0.031
1052
MYT026 Myotonia Atrophica 29 0.031
1053
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 23 0.031
1054
TNG002 Tangier Disease 64 0.031
1055
c LPS002 Liposarcoma 60 0.031
1056
ILT001 Ileitis 59 0.031
1057
CLN015 Colon Adenocarcinoma 57 0.031
1058
P MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 46 0.031
1059
TCL003 T Cell Deficiency 43 0.031
1060
P CNG031 Congenital Nervous System Abnormality 40 0.031
1061
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 28 0.031
1062
MLT157 Multiple System Atrophy 1 73 0.031
1063
P ART115 Aortic Valve Disease 1 70 0.031
1064
P WLM013 Wilms Tumor 1 68 0.031
1065
P ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 67 0.031
1066
c HYP802 Hypocalcemia, Autosomal Dominant 1 66 0.031
1067
APH002 Aphasia 60 0.031
1068
c OCL013 Oculodentodigital Dysplasia 59 0.031
1069
HYP190 Hypoalphalipoproteinemia, Primary 59 0.031
1070
WHM001 Whim Syndrome 55 0.031
1071
c PRC012 Pericardial Effusion 54 0.031