Search results for obesity AND diabetes

1026 hits were found for obesity AND diabetes

# Family MCID Name MIFTS Score
1
BDY004 Body Mass Index Quantitative Trait Locus 11 68 7.971
2
c ABD013 Abdominal Obesity-Metabolic Syndrome 3 25 4.237
3
P DBT009 Diabetes Mellitus 64 1.520
4
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 1.266
5
GLC008 Glucose Metabolism Disease 52 0.874
6
OVR063 Overnutrition 53 0.614
7
MRB003 Morbid Obesity 60 0.555
8
P NRP001 Neuropathy 63 0.543
9
TYP041 Type I 56 0.520
10
GST033 Gestational Diabetes 60 0.512
11
AGN016 Aging 64 0.502
12
P KDN018 Kidney Disease 68 0.499
13
P MCR115 Microvascular Complications of Diabetes 5 71 0.478
14
HYP066 Hyperglycemia 63 0.442
15
HYP056 Hypoglycemia 62 0.426
16
c MCR113 Microvascular Complications of Diabetes 3 52 0.406
17
c MCR120 Microvascular Complications of Diabetes 7 37 0.405
18
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.405
19
c MCR130 Microvascular Complications of Diabetes 6 40 0.404
20
c MCR133 Microvascular Complications of Diabetes 4 35 0.404
21
END072 Endotheliitis 45 0.403
22
GLC003 Glucose Intolerance 56 0.396
23
HYP060 Hyperinsulinism 56 0.389
24
P PNC044 Pancreatitis 64 0.376
25
FTT001 Fatty Liver Disease 60 0.374
26
P HPT021 Hepatitis 76 0.369
27
ATM095 Autoimmune Disease 64 0.369
28
DBT010 Diabetic Neuropathy 59 0.365
29
IMM136 Immune System Disease 56 0.363
30
P LVR013 Liver Disease 75 0.360
31
P HRT032 Heart Disease 74 0.357
32
P DBT005 Diabetes Insipidus 54 0.347
33
DPR016 Depression 72 0.332
34
ART140 Arteries, Anomalies of 65 0.330
35
P PLY011 Polycystic Ovary Syndrome 63 0.327
36
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.323
37
P CRN018 Coronary Artery Anomaly 68 0.322
38
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.317
39
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.311
40
P SLP006 Sleep Apnea 66 0.303
41
c CRN300 Coronary Heart Disease 1 64 0.301
42
DBT084 Diabetes Mellitus, Ketosis-Prone 52 0.291
43
VSC007 Vascular Disease 68 0.289
44
P MYC007 Myocardial Infarction 79 0.284
45
c CHR089 Chronic Kidney Failure 72 0.278
46
ISC004 Ischemia 65 0.277
47
PRP019 Peripheral Nervous System Disease 60 0.277
48
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.275
49
ATN004 Autonomic Neuropathy 46 0.263
50
ANX010 Anxiety 72 0.259
51
RTN018 Retinal Disease 56 0.258
52
URN009 Urinary System Disease 55 0.258
53
DBT008 Diabetic Angiopathy 47 0.253
54
APN008 Apnea, Obstructive Sleep 67 0.253
55
P PRD008 Periodontitis 66 0.253
56
PLC008 Placenta Disease 61 0.253
57
P THY032 Thyroiditis 55 0.251
58
ETN001 Eating Disorder 61 0.251
59
RTN023 Retinitis 50 0.250
60
PRD004 Prediabetes Syndrome 45 0.250
61
ISC006 Ischemic Heart Disease 72 0.249
62
P PLY019 Polyneuropathy 57 0.244
63
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.242
64
SPS003 Spastic Diplegia 54 0.242
65
AST005 Asthma 82 0.238
66
MNT002 Mental Depression 57 0.228
67
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.226
68
P BRS047 Breast Cancer 100 0.219
69
P ART021 Arteriosclerosis 60 0.219
70
LPD008 Lipid Metabolism Disorder 58 0.215
71
SLP005 Sleep Disorder 59 0.212
72
DBT004 Diabetic Polyneuropathy 51 0.211
73
INS024 Insulin-Like Growth Factor I 82 0.210
74
P MTR004 Maturity-Onset Diabetes of the Young 60 0.210
75
NRT004 Neuritis 57 0.202
76
P INF032 Infertility 59 0.198
77
c TRC078 Trichohepatoenteric Syndrome 2 34 0.195
78
NRM005 Neuromuscular Disease 60 0.194
79
P VSC018 Visceral Steatosis 37 0.192
80
P HYP086 Hypothyroidism 64 0.189
81
PRD007 Periodontal Disease 64 0.189
82
CNG034 Congestive Heart Failure 72 0.188
83
P ART022 Arthritis 76 0.188
84
P RTN016 Retinal Degeneration 54 0.188
85
ACN002 Acanthosis Nigricans 60 0.186
86
HYP080 Hypogonadism 51 0.184
87
THR024 Thrombosis 61 0.182
88
FTL021 Fetal Macrosomia 46 0.180
89
P CTR002 Cataract 60 0.179
90
PRS047 Prostatitis 60 0.179
91
P PRD006 Prader-Willi Syndrome 61 0.179
92
c MCL042 Macular Degeneration, Age-Related, 1 84 0.178
93
GST037 Gastroparesis 56 0.176
94
CRB009 Cerebritis 41 0.174
95
OST012 Osteoarthritis 82 0.173
96
P NRV007 Nervous System Disease 73 0.173
97
GST050 Gastrointestinal System Disease 64 0.171
98
NNL002 Nonalcoholic Steatohepatitis 50 0.170
99
DBT002 Diabetic Autonomic Neuropathy 43 0.166
100
HYP266 Hypoxia 61 0.160
101
c PRC016 Pre-Eclampsia 59 0.159
102
NRN002 Neuronitis 41 0.158
103
PRP027 Peripheral Vascular Disease 70 0.157
104
P OST002 Osteoporosis 76 0.157
105
ATN005 Autonomic Dysfunction 50 0.156
106
HYP043 Hyperandrogenism 50 0.155
107
P PRS040 Prostate Cancer 90 0.154
108
P SCH015 Schizophrenia 69 0.153
109
GST092 Gastroesophageal Reflux 64 0.150
110
OBS037 Obesity-Hypoventilation Syndrome 46 0.150
111
c HYP595 Hypertension, Essential 76 0.149
112
CRN036 Craniopharyngioma 64 0.142
113
P ALZ034 Alzheimer Disease 87 0.141
114
END030 End Stage Renal Failure 56 0.140
115
IMP005 Impotence 55 0.139
116
P CLR023 Colorectal Cancer 97 0.138
117
BRN106 Burns 56 0.137
118
ANG054 Angina Pectoris 66 0.135
119
MNG006 Monogenic Diabetes 37 0.135
120
c ACT075 Acute Myocardial Infarction 58 0.135
121
GND003 Gonadal Disease 46 0.135
122
c HPT001 Hepatitis C 71 0.134
123
P INF038 Influenza 76 0.134
124
c PRC031 Preeclampsia/eclampsia 1 39 0.133
125
P OVR049 Ovarian Disease 59 0.133
126
ANR040 Aneurysm 60 0.133
127
P TRC086 Trichohepatoenteric Syndrome 1 54 0.132
128
P ADN016 Adenocarcinoma 70 0.131
129
LNG099 Lung Disease 67 0.131
130
RSP006 Respiratory System Disease 63 0.130
131
P ART023 Arthropathy 67 0.128
132
P MYP006 Myopia 56 0.128
133
P LKM002 Leukemia 72 0.127
134
LPT014 Leptin Deficiency or Dysfunction 37 0.127
135
P PNC035 Pancreatic Cancer 79 0.126
136
P RSP003 Respiratory Failure 70 0.126
137
BDY019 Body Mass Index Quantitative Trait Locus 18 27 0.126
138
BDY005 Body Mass Index Quantitative Trait Locus 9 27 0.126
139
BDY006 Body Mass Index Quantitative Trait Locus 8 23 0.126
140
BDY012 Body Mass Index Quantitative Trait Locus 7 23 0.126
141
P ESP024 Esophagitis 63 0.125
142
P HYP014 Hyperuricemia 55 0.125
143
BDY015 Body Mass Index Quantitative Trait Locus 12 25 0.125
144
BDY017 Body Mass Index Quantitative Trait Locus 14 25 0.125
145
BDY010 Body Mass Index Quantitative Trait Locus 4 25 0.125
146
BDY020 Body Mass Index Quantitative Trait Locus 19 25 0.125
147
PRP080 Peripheral Artery Disease 53 0.124
148
DMN002 Dementia 68 0.123
149
c PLY105 Polycystic Ovary Syndrome 1 30 0.123
150
P ENC018 Encephalopathy 62 0.123
151
ANR007 Anorexia Nervosa 62 0.123
152
GNG011 Gingival Disease 49 0.123
153
MTH009 Mouth Disease 63 0.123
154
P ECL001 Eclampsia 57 0.123
155
P PSR002 Psoriasis 65 0.123
156
BDY011 Body Mass Index Quantitative Trait Locus 10 24 0.121
157
P RHM011 Rheumatoid Arthritis 80 0.121
158
DNT012 Dental Caries 51 0.120
159
P DRR001 Diarrhea 56 0.120
160
BND020 Bone Disease 62 0.120
161
END057 Endometrial Cancer 65 0.119
162
LMB062 Limb Ischemia 51 0.119
163
DBT007 Diabetic Cataract 32 0.119
164
MDD011 Mood Disorder 63 0.118
165
BNF002 Bone Fracture 55 0.118
166
THY030 Thyroid Gland Disease 51 0.118
167
P PNM007 Pneumonia 69 0.116
168
c ACT027 Acute Pancreatitis 60 0.115
169
GNG013 Gingivitis 63 0.113
170
INS001 Insulinoma 65 0.113
171
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.112
172
CNN003 Conn's Syndrome 71 0.111
173
CRB039 Cerebrovascular Disease 67 0.110
174
P OVR046 Ovarian Cyst 50 0.110
175
SVR004 Severe Combined Immunodeficiency 69 0.109
176
P CLC063 Celiac Disease 1 71 0.109
177
c LPD015 Lipodystrophy, Familial Partial, Type 2 59 0.109
178
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.109
179
P EXN002 Exanthem 61 0.108
180
CMB081 Combined Immunodeficiency, X-Linked 64 0.108
181
LVR012 Liver Cirrhosis 68 0.107
182
DDN006 Duodenitis 48 0.107
183
P ANR048 Aniridia 1 65 0.106
184
BLD137 Blood Group--Ahonen 17 0.106
185
BLM002 Bulimia Nervosa 58 0.105
186
P AMY004 Amyloidosis 68 0.104
187
c MTR002 Mitral Valve Insufficiency 46 0.104
188
P HYP083 Hypopituitarism 58 0.104
189
P ATR011 Atrial Fibrillation 68 0.104
190
PNM001 Pneumocystosis 55 0.104
191
JNT002 Joint Disorders 59 0.103
192
PRT036 Peritonitis 66 0.103
193
HYP064 Hypogonadotropism 40 0.103
194
RST023 Resting Heart Rate, Variation in 42 0.102
195
HPT082 Hepatic Adenomas, Familial 53 0.102
196
PTT009 Pituitary Gland Disease 56 0.102
197
HYP730 Hypogonadotropic Hypogonadism 56 0.101
198
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.100
199
P LYM118 Lymphoma 70 0.100
200
P EPL164 Epilepsy 69 0.100
201
LPT006 Leptin Receptor Deficiency 38 0.100
202
SKN016 Skin Disease 66 0.100
203
MTB004 Metabolic Acidosis 48 0.099
204
P BRD002 Bardet-Biedl Syndrome 62 0.099
205
STM006 Stomach Disease 52 0.099
206
CYS001 Cystic Fibrosis 84 0.099
207
PSY004 Psychotic Disorder 71 0.098
208
c MYT020 Myotonic Dystrophy 2 56 0.098
209
P BPL003 Bipolar Disorder 59 0.098
210
c BRD013 Bardet-Biedl Syndrome 12 44 0.098
211
P MJR001 Major Depressive Disorder 65 0.098
212
ADN018 Adenoma 63 0.097
213
P HPT023 Hepatocellular Carcinoma 94 0.097
214
IRN002 Iron Metabolism Disease 55 0.096
215
P GLL020 Gallbladder Disease 64 0.096
216
GST053 Gastric Cancer 77 0.096
217
ALP046 Alport Syndrome, X-Linked 75 0.096
218
NRL016 Neural Tube Defects 78 0.095
219
P CLL015 Collagen Disease 52 0.095
220
GNR004 Generalized Anxiety Disorder 53 0.094
221
P TRM003 Tremor 54 0.094
222
GT001 Gout 57 0.094
223
c BRD014 Bardet-Biedl Syndrome 2 58 0.093
224
c BRD012 Bardet-Biedl Syndrome 11 45 0.093
225
c BRD011 Bardet-Biedl Syndrome 10 41 0.093
226
INT007 Intermediate Coronary Syndrome 52 0.093
227
c CHR579 Chiari Malformation Type Ii 45 0.093
228
RHM027 Rheumatic Disease 62 0.093
229
HDC001 Headache 59 0.092
230
ALR002 Al-Raqad Syndrome 31 0.092
231
c ART101 Aortic Valve Disease 2 73 0.092
232
GRW007 Growth Hormone Deficiency 51 0.092
233
ANV001 Anovulation 48 0.092
234
ENT004 Enthesopathy 46 0.091
235
ACT088 Acute Insulin Response 43 0.091
236
SKN027 Skin Conditions 48 0.091
237
P HYP069 Hyperparathyroidism 58 0.090
238
PNG002 Pain Agnosia 42 0.090
239
c PRD040 Periodontitis, Chronic 49 0.089
240
ANX004 Anoxia 49 0.089
241
P MLT020 Multiple Sclerosis 78 0.089
242
P LCT001 Lactic Acidosis 50 0.088
243
HYP085 Hypothalamic Disease 48 0.088
244
DWN001 Down Syndrome 69 0.087
245
BRN038 Bronchial Disease 56 0.087
246
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.087
247
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.086
248
SCH012 Schizoaffective Disorder 54 0.086
249
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.086
250
P DYS021 Dysautonomia 43 0.084
251
c THR092 Thrombophilia Due to Thrombin Defect 67 0.084
252
NPH009 Nephrolithiasis 55 0.084
253
CRD119 Cardiac Arrest 62 0.084
254
P CHR345 Chronic Pain 51 0.084
255
BRC012 Brucellosis 70 0.083
256
c HPT073 Hepatitis C Virus 72 0.083
257
ALS001 Alstrom Syndrome 54 0.083
258
URM002 Uremia 52 0.083
259
P HYP265 Hypotonia 40 0.082
260
IRN001 Iron Deficiency Anemia 55 0.082
261
PNC034 Pancreas Disease 57 0.082
262
NCR002 Necrobiosis Lipoidica 38 0.082
263
ACQ007 Acquired Immunodeficiency Syndrome 63 0.081
264
SPN186 Spinal Cord Injury 68 0.081
265
OBS081 Obesity, Early-Onset, with Adrenal Insufficiency and Red Hair 34 0.081
266
FBR065 Fibrocalculous Pancreatopathy 18 0.081
267
P LYM026 Lymphoblastic Leukemia 64 0.081
268
P MYL005 Myelofibrosis 70 0.081
269
P PRC019 Precocious Puberty 52 0.081
270
c HPT003 Hepatitis a 61 0.080
271
PRS063 Paresthesia 37 0.079
272
P INT068 Intestinal Disease 64 0.079
273
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.079
274
THY028 Thyroid Cancer 66 0.079
275
P MSC003 Muscular Atrophy 54 0.078
276
P THR014 Thrombocytopenia 64 0.077
277
VRL011 Viral Infectious Disease 63 0.077
278
ATN002 Autonomic Nervous System Disease 51 0.077
279
INT075 Intracranial Hypertension 52 0.077
280
ACR007 Acromegaly 69 0.076
281
RNL051 Renal Cysts and Diabetes Syndrome 44 0.076
282
P CRV039 Cervicitis 49 0.076
283
P GLM007 Glomerulonephritis 61 0.076
284
BCK006 Back Pain 44 0.076
285
P TRN020 Turner Syndrome 68 0.076
286
SXL003 Sexual Disorder 44 0.076
287
P LYM025 Lymphedema 63 0.076
288
VTM002 Vitamin B12 Deficiency 47 0.075
289
JJN008 Jejunoileitis 41 0.075
290
SYS003 Systolic Heart Failure 46 0.075
291
P OVR042 Ovarian Cancer 81 0.074
292
P LNG032 Lung Cancer 98 0.074
293
c LKM062 Leukemia, Acute Lymphoblastic 69 0.074
294
P PSD015 Pseudohypoparathyroidism 50 0.074
295
c SYS001 Systemic Lupus Erythematosus 86 0.073
296
P MYP004 Myopathy 68 0.073
297
STR067 Stroke, Ischemic 82 0.072
298
c MTR019 Maturity-Onset Diabetes of the Young, Type 2 43 0.072
299
BRS051 Breast Disease 66 0.072
300
PLM033 Pulmonary Embolism 62 0.072
301
CHL004 Cholelithiasis 50 0.072
302
CNS004 Constipation 56 0.072
303
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.072
304
PSR001 Psoriatic Arthritis 65 0.071
305
AMN001 Amenorrhea 55 0.071
306
RPD006 Rapid-Onset Childhood Obesity-Hypothalamic Dysfunction-Hypoventilation-Autonomic Dysregulation Syndrome 26 0.071
307
P NRC002 Narcolepsy 63 0.070
308
FBR047 Fibromyalgia 57 0.070
309
LRN002 Laron Syndrome 62 0.070
310
ALX002 Alexithymia 42 0.070
311
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.070
312
CHR008 Choroiditis 46 0.070
313
P LPS004 Lupus Erythematosus 68 0.070
314
P HYP076 Hyperthyroidism 56 0.070
315
P RTN008 Retinitis Pigmentosa 81 0.070
316
c BLD140 Blood Group, I System 23 0.069
317
VGN023 Vaginitis 58 0.069
318
P CND004 Candidiasis 60 0.069
319
MHM001 Mehmo Syndrome 28 0.069
320
P CMR001 Camurati-Engelmann Disease 61 0.068
321
LYM027 Lymphopenia 55 0.068
322
CHN016 Cohen Syndrome 47 0.068
323
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.068
324
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.068
325
CLT003 Colitis 62 0.068
326
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.068
327
DFC004 Deficiency Anemia 61 0.068
328
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 42 0.068
329
P HST010 Histiocytosis 59 0.068
330
P LPM005 Lipomatosis 50 0.067
331
MRB006 Morbid Obesity and Spermatogenic Failure 20 0.067
332
INT303 Intracranial Hypertension, Idiopathic 50 0.067
333
OBS015 Obesity, Hyperphagia, and Developmental Delay 24 0.067
334
MNN017 Mononeuropathy 43 0.067
335
P FCL005 Focal Segmental Glomerulosclerosis 59 0.067
336
P ATS364 Autism 70 0.067
337
PRP098 Proprotein Convertase 1/3 Deficiency 29 0.067
338
c ACT071 Acute Kidney Failure 54 0.067
339
P KDN017 Kidney Cancer 58 0.067
340
P ADL010 Adult Respiratory Distress Syndrome 66 0.066
341
ART016 Aortic Aneurysm 69 0.066
342
EPD070 Epidermoid Cysts 47 0.066
343
P MYL006 Myeloid Leukemia 68 0.066
344
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.065
345
c CRP023 Carpenter Syndrome 1 54 0.064
346
PST021 Postpartum Depression 53 0.064
347
DWR001 Dwarfism 45 0.064
348
PST055 Postural Hypotension 40 0.064
349
SCL022 Scleredema 28 0.064
350
CRN030 Coronary Stenosis 51 0.064
351
c ACT210 Acute Respiratory Distress Syndrome 61 0.064
352
ALC007 Alcohol Dependence 65 0.064
353
EXC002 Exocrine Pancreatic Insufficiency 43 0.064
354
ERY029 Erythermalgia, Primary 54 0.063
355
P VNS003 Venous Insufficiency 54 0.063
356
BRN071 Brain Injury 53 0.063
357
LNG108 Langerhans Cell Histiocytosis 63 0.063
358
PST053 Postherpetic Neuralgia 44 0.063
359
MLN008 Melanoma 62 0.063
360
c FML012 Familial Partial Lipodystrophy 52 0.063
361
ART008 Arteriosclerosis Obliterans 42 0.062
362
P MCR010 Microcephaly 57 0.062
363
DRM006 Dermatitis 66 0.062
364
OBS050 Obesity Due to Congenital Leptin Deficiency 23 0.062
365
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 47 0.061
366
c HPT016 Hepatitis B 67 0.061
367
P AST055 Asthma-Related Traits 1 30 0.061
368
P PRT078 Partial Lipodystrophy 46 0.061
369
CRP001 Carpal Tunnel Syndrome 66 0.061
370
P NPH012 Nephrotic Syndrome 59 0.061
371
P PLM037 Pulmonary Hypertension 75 0.061
372
APP008 Appendicitis 64 0.060
373
INT002 Intermittent Claudication 61 0.060
374
c VRL010 Viral Hepatitis 59 0.060
375
CLL003 Cellulitis 53 0.060
376
NWB001 Newborn Respiratory Distress Syndrome 52 0.060
377
MTC005 Mitochondrial Metabolism Disease 44 0.060
378
RSP007 Respiratory Distress Syndrome, Infant 34 0.060
379
P SCL057 Scoliosis, Isolated 1 40 0.060
380
P PLY006 Polydactyly 57 0.060
381
PSD088 Pseudobulbar Affect 37 0.060
382
BLD163 Blood Group, Dombrock System 22 0.059
383
P INF037 Inflammatory Bowel Disease 53 0.059
384
DMP001 Dumping Syndrome 44 0.059
385
P THR015 Thrombophilia 57 0.059
386
c CNT075 Central Precocious Puberty 51 0.059
387
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.059
388
WLL001 Williams-Beuren Syndrome 63 0.059
389
P HYP614 Hyperlipidemia, Familial Combined 56 0.059
390
CRT016 Carotid Artery Disease 57 0.059
391
c CRD065 Cardiomyopathy, Familial Hypertrophic, 2 41 0.058
392
c PTT057 Pituitary Adenoma 4, Acth-Secreting 45 0.058
393
PHR003 Pharyngitis 59 0.058
394
c HMC039 Hemochromatosis, Type 1 70 0.058
395
DYS073 Dysphagia 46 0.058
396
MNN028 Mononeuropathy of the Median Nerve, Mild 37 0.058
397
END038 Endocrine Pancreas Disease 36 0.058
398
WRN001 Werner Syndrome 69 0.058
399
LRN003 Learning Disability 50 0.057
400
CLC006 Calcinosis 51 0.057
401
HLC007 Helicobacter Pylori Infection 63 0.057
402
DRG003 Drug Dependence 51 0.057
403
P ACQ009 Acquired Metabolic Disease 32 0.057
404
P UTR058 Uterine Anomalies 59 0.057
405
ACR006 Aceruloplasminemia 73 0.056
406
P RNL007 Renal Tubular Acidosis 52 0.056
407
c BRD010 Bardet-Biedl Syndrome 1 54 0.056
408
SCN001 Secondary Hyperparathyroidism of Renal Origin 50 0.056
409
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 43 0.056
410
ELP001 Elephantiasis 38 0.056
411
P HYP061 Hypertrophic Cardiomyopathy 64 0.056
412
IRR002 Irritable Bowel Syndrome 62 0.056
413
HYD002 Hydronephrosis 48 0.056
414
CRN024 Corneal Disease 47 0.056
415
P PNC045 Pancreatic Agenesis 40 0.055
416
c LKM061 Leukemia, Acute Myeloid 80 0.055
417
P HYD006 Hydrocephalus 69 0.055
418
CLR108 Colorectal Adenoma 60 0.055
419
P ALP008 Alopecia 58 0.055
420
MDS022 Mediastinitis 40 0.055
421
P GST044 Gastritis 60 0.055
422
P MGL001 Megaloblastic Anemia 51 0.055
423
GLC036 Glucagonoma 51 0.055
424
RCK004 Rickets 62 0.055
425
P DLT002 Dilated Cardiomyopathy 76 0.055
426
c PRM005 Primary Hyperparathyroidism 59 0.055
427
SLD003 Sialadenitis 49 0.055
428
SKN023 Skin Tag 42 0.055
429
SNS003 Sensory Peripheral Neuropathy 53 0.054
430
CNG376 Congenital Leptin Deficiency 20 0.054
431
c CNG012 Congenital Generalized Lipodystrophy 50 0.054
432
URN022 Urinary Tract Infections, Recurrent 29 0.054
433
P CRD132 Cardiac Conduction Defect 59 0.054
434
TRM010 Traumatic Brain Injury 55 0.054
435
c MTR039 Maturity-Onset Diabetes of the Young, Type 11 21 0.054
436
SLP010 Slipped Capital Femoral Epiphysis 37 0.054
437
GSG001 Gas Gangrene 51 0.054
438
FSC004 Fasciitis 47 0.054
439
INT273 Intellectual Disability, Epileptic Seizures, Hypogonadism and Hypogenitalism, Microcephaly, and Obesity 10 0.053
440
PSD014 Pseudopseudohypoparathyroidism 55 0.053
441
CRH001 Crohn's Disease 78 0.053
442
HYP020 Hyperprolactinemia 63 0.053
443
CRD223 Cardiac Arrhythmia 54 0.053
444
STT004 Steatorrhea 41 0.053
445
CLC001 Calciphylaxis 52 0.053
446
FXF002 Fox-Fordyce Disease 40 0.053
447
c MYT021 Myotonic Dystrophy 1 68 0.053
448
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.053
449
FCL044 Fecal Incontinence 38 0.052
450
CRT013 Carotid Stenosis 52 0.052
451
HMS001 Hemosiderosis 51 0.052
452
c HYP795 Hypothyroidism, Congenital, Nongoitrous, 4 54 0.052
453
DST006 Diastolic Heart Failure 46 0.052
454
P MSC005 Muscular Dystrophy 66 0.051
455
P SZR006 Seizure Disorder 56 0.051
456
c SVR005 Severe Pre-Eclampsia 53 0.051
457
GYN001 Gynecomastia 46 0.051
458
P CHR084 Chromosomal Disease 40 0.051
459
ESP021 Esophageal Cancer 77 0.051
460
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.051
461
P CHL066 Cholangitis 52 0.050
462
P HLP001 Holoprosencephaly 66 0.050
463
NRR001 Neuroretinitis 46 0.050
464
c CNT035 Central Nervous System Disease 63 0.050
465
CLN019 Colonic Disease 54 0.050
466
P MSC033 Muscle Disorders 52 0.050
467
c LBR014 Leber Congenital Amaurosis 4 49 0.050
468
MSC004 Muscle Tissue Disease 39 0.050
469
GST007 Gastric Dilatation 33 0.050
470
P INT070 Intestinal Obstruction 56 0.050
471
MLN007 Male Infertility 53 0.050
472
RST001 Restless Legs Syndrome 52 0.050
473
P BLD134 Bladder Cancer 69 0.049
474
P ENC004 Encephalitis 65 0.049
475
VSC002 Vascular Dementia 58 0.049
476
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 22 0.049
477
P ALP009 Alopecia Areata 63 0.049
478
P ACQ022 Acquired Generalized Lipodystrophy 44 0.049
479
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 53 0.049
480
P RHN004 Rhinitis 61 0.048
481
PRP016 Paraplegia 53 0.048
482
FND002 Fundus Dystrophy 49 0.048
483
HRT012 Heart Valve Disease 44 0.048
484
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 59 0.048
485
P ACT092 Acth-Independent Macronodular Adrenal Hyperplasia 53 0.048
486
P PHC003 Pheochromocytoma 73 0.048
487
P OPN001 Open-Angle Glaucoma 51 0.048
488
P SBS003 Substance Abuse 57 0.048
489
HPR003 Heparin-Induced Thrombocytopenia 48 0.048
490
HYP784 Hypogonadism, Male 41 0.048
491
EPD046 Epididymitis 36 0.048
492
ANG020 Angiosarcoma 56 0.048
493
HRN026 Hernia, Hiatus 43 0.048
494
DYS011 Dyskinesia of Esophagus 39 0.048
495
CHP002 Chops Syndrome 31 0.048
496
P HMP007 Hemophilia 60 0.048
497
BRB001 Beriberi 41 0.048
498
OST097 Osteoporotic Fracture 41 0.048
499
P PLY014 Polycystic Kidney Disease 60 0.047
500
HYP068 Hyperostosis 53 0.047
501
SPN051 Spondylitis 55 0.047
502
DYS014 Dyspepsia 54 0.047
503
NPH010 Nephrosclerosis 47 0.047
504
SNL007 Senile Cataract 40 0.047
505
HYP110 Hyperproinsulinemia 39 0.047
506
BRN024 Bronchitis 66 0.046
507
SYN007 Synovitis 60 0.046
508
P PLY018 Polycythemia 58 0.046
509
P ACT105 Acute Mountain Sickness 57 0.046
510
P BLD051 Blood Coagulation Disease 50 0.046
511
INT051 Intussusception 49 0.046
512
IDP033 Idiopathic Edema 42 0.046
513
GST045 Gastroenteritis 64 0.046
514
P SNS014 Sinusitis 62 0.046
515
c CNG006 Congenital Hypothyroidism 60 0.046
516
P PRT013 Portal Hypertension 59 0.046
517
P BCK002 Beckwith-Wiedemann Syndrome 57 0.046
518
PLM010 Pulmonary Edema 56 0.046
519
TTH006 Tooth Disease 53 0.046
520
PRP030 Purpura 61 0.046
521
DCB001 Decubitus Ulcer 45 0.046
522
BLD165 Blood Group, Colton System 23 0.046
523
P GLY013 Glycogen Storage Disease 61 0.046
524
CYT008 Cytomegalovirus Infection 56 0.046
525
SHH001 Sheehan Syndrome 50 0.046
526
P OPT070 Optic Nerve Hypoplasia, Bilateral 43 0.046
527
ADP007 Adie Pupil 41 0.046
528
GLC022 Glucose/galactose Malabsorption 41 0.046
529
LPD012 Lipoid Congenital Adrenal Hyperplasia 69 0.046
530
c ATS007 Autism Spectrum Disorder 61 0.046
531
PRT018 Portal Vein Thrombosis 50 0.046
532
CRB037 Cerebral Palsy 71 0.045
533
OTT002 Otitis Media 66 0.045
534
ADR013 Adrenal Gland Hyperfunction 54 0.045
535
GTR002 Goiter 52 0.045
536
WRN003 Wernicke Encephalopathy 45 0.045
537
CNN005 Connective Tissue Disease 64 0.045
538
CYS039 Cystic Kidney Disease 51 0.045
539
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 41 0.045
540
c TYP038 Type 1 Diabetes Mellitus 15 22 0.045
541
c SML038 Small Cell Cancer of the Lung 68 0.045
542
VSC011 Vasculitis 65 0.045
543
CHL123 Chlamydia 64 0.045
544
BLD044 Bladder Disease 55 0.045
545
HYP077 Hypertrichosis 50 0.045
546
TBC004 Tobacco Addiction 60 0.044
547
CHR005 Chorioamnionitis 51 0.044
548
ULC004 Ulcerative Colitis 72 0.044
549
P ALC004 Alcohol Abuse 63 0.044
550
PRT038 Protein-Energy Malnutrition 51 0.044
551
EMP001 Empty Sella Syndrome 42 0.044
552
SPS057 Spasticity 41 0.044
553
IGG001 Iga Glomerulonephritis 55 0.044
554
ART004 Aortic Atherosclerosis 47 0.044
555
P FNG006 Feingold Syndrome 1 45 0.044
556
MYL069 Myeloma, Multiple 83 0.043
557
P MMP001 Mumps 61 0.043
558
CHL068 Cholestasis 60 0.043
559
MCS002 Mucositis 60 0.043
560
P PTS002 Ptosis 53 0.043
561
IMM001 Immune-Complex Glomerulonephritis 38 0.043
562
BRR014 Barrett Esophagus 63 0.043
563
ALL006 Allergic Asthma 59 0.043
564
PST028 Post-Traumatic Stress Disorder 58 0.043
565
PRS042 Prostate Disease 44 0.043
566
LRN001 Laurence-Moon Syndrome 44 0.043
567
TRC026 Tracheal Disease 35 0.043
568
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.043
569
PPL021 Papilledema 49 0.043
570
TND004 Tendinopathy 46 0.043
571
RCT017 Rectal Disease 39 0.043
572
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.043
573
P HYP607 Hypercholesterolemia, Familial 79 0.043
574
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.043
575
BLL003 Bell's Palsy 49 0.043
576
BNC003 Bone Cancer 59 0.042
577
c BPL002 Bipolar I Disorder 49 0.042
578
PST095 Post-Thrombotic Syndrome 52 0.042
579
P END046 Endometritis 50 0.042
580
KWS001 Kwashiorkor 42 0.042
581
c BRD018 Bardet-Biedl Syndrome 6 39 0.042
582
TQP001 Taqi Polymorphism 33 0.042
583
HYP364 Hyperostosis Frontalis Interna 28 0.042
584
P MRL001 Meralgia Paresthetica 27 0.042
585
MYL009 Myelodysplastic Syndrome 70 0.042
586
SNS001 Sensorineural Hearing Loss 56 0.042
587
c CHR431 Chronic Venous Insufficiency 47 0.042
588
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 44 0.042
589
MYX004 Myxedema 43 0.042
590
SPR007 Superior Mesenteric Artery Syndrome 42 0.042
591
PLS029 Plasminogen Activator Inhibitor-1 Deficiency 40 0.042
592
MLR004 Malaria 83 0.041
593
c HMP029 Hemophilia a 68 0.041
594
P DRM053 Dermatitis, Atopic 67 0.041
595
PRV006 Pervasive Developmental Disorder 55 0.041
596
CLR109 Colorectal Adenocarcinoma 53 0.041
597
OST011 Osteomalacia 52 0.041
598
P CNJ013 Conjunctivitis 63 0.040
599
PRT058 Pure Autonomic Failure 59 0.040
600
KRT006 Keratoconjunctivitis 55 0.040
601
c DBT086 Diabetes Mellitus, Noninsulin-Dependent, 5 13 0.040
602
P BCL006 B-Cell Lymphomas 65 0.040
603
PPT005 Peptic Ulcer Disease 61 0.040
604
P NTR004 Neutropenia 60 0.040
605
P HMN010 Hemangioma 60 0.040
606
P MLT074 Multiple Endocrine Neoplasia 55 0.040
607
EXP004 Exophthalmos 51 0.040
608
PLC007 Placental Abruption 50 0.040
609
c MLG042 Malignant Otitis Externa 27 0.040
610
P CRV035 Cervical Cancer 69 0.040
611
END041 Endometrial Adenocarcinoma 60 0.040
612
ARM001 Aromatase Deficiency 52 0.040
613
ACH004 Achondroplasia 66 0.039
614
ISL003 Isolated Growth Hormone Deficiency 55 0.039
615
DSS008 Disease of Mental Health 52 0.039
616
ACH005 Achalasia 51 0.039
617
P NGH001 Night Blindness 51 0.039
618
CLR030 Clear Cell Renal Cell Carcinoma 49 0.039
619
HPT067 Hepatocellular Adenoma 43 0.039
620
c BRD015 Bardet-Biedl Syndrome 3 40 0.039
621
P NRB001 Neuroblastoma 72 0.039
622
SCK003 Sickle Cell Anemia 72 0.039
623
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.039
624
c MLG069 Malignant Hypertension 48 0.039
625
c PTT056 Pituitary Adenoma 1, Multiple Types 44 0.039
626
SMT008 Smith-Magenis Syndrome 53 0.038
627
HYP081 Hypolipoproteinemia 48 0.038
628
PRS129 Prostatic Hyperplasia, Benign 48 0.038
629
ART031 Aortic Coarctation 47 0.038
630
MCR011 Microinvasive Gastric Cancer 46 0.038
631
NNT019 Neonatal Hypothyroidism 39 0.038
632
48X003 48,xxyy Syndrome 34 0.038
633
IDP041 Idiopathic Recurrent Pericarditis 31 0.038
634
CHG001 Chagas Disease 71 0.038
635
P MYS005 Myositis 63 0.038
636
P SLV001 Silver-Russell Syndrome 56 0.038
637
LYM019 Lymphosarcoma 55 0.038
638
PNN001 Panniculitis 49 0.038
639
P CMP008 Compartment Syndrome 47 0.038
640
c HYP057 Hypervitaminosis D 41 0.038
641
P TMP003 Temporal Arteritis 66 0.037
642
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 52 0.037
643
SYN036 Syncope 47 0.037
644
P RTN014 Retinal Artery Occlusion 46 0.037
645
P CRB088 Cerebral Atrophy 39 0.037
646
ATX010 Ataxia Neuropathy Spectrum 35 0.037
647
GGN002 Gigantism 35 0.037
648
P ANT006 Antiphospholipid Syndrome 59 0.036
649
P HYP724 Hyperlipoproteinemia, Type Iii 58 0.036
650
HDR002 Hidradenitis Suppurativa 54 0.036
651
RDC002 Radiculopathy 53 0.036
652
P DDN001 Duodenal Ulcer 52 0.036
653
HYP006 Hypertensive Heart Disease 50 0.036
654
CRB025 Carbohydrate Metabolic Disorder 50 0.036
655
P MTC069 Mitochondrial Disorders 49 0.036
656
HDR003 Hidradenitis 46 0.036
657
c ADL001 Adult Lymphoma 39 0.036
658
SHR082 Short Stature, Microcephaly, and Endocrine Dysfunction 22 0.036
659
ALL003 Allergic Rhinitis 67 0.036
660
ALB001 Albright's Hereditary Osteodystrophy 52 0.036
661
SPN041 Spinal Cord Disease 51 0.036
662
c BRD044 Bardet-Biedl Syndrome 17 45 0.036
663
c BRD016 Bardet-Biedl Syndrome 4 42 0.036
664
c BRD048 Bardet-Biedl Syndrome 18 42 0.036
665
c BRD033 Bardet-Biedl Syndrome 13 41 0.036
666
c BRD020 Bardet-Biedl Syndrome 8 40 0.036
667
c BRD032 Bardet-Biedl Syndrome 14 40 0.036
668
LPM010 Lipomatosis, Multiple Symmetric 39 0.036
669
c BRD017 Bardet-Biedl Syndrome 5 37 0.036
670
c BRD045 Bardet-Biedl Syndrome 19 34 0.036
671
c BRD047 Bardet-Biedl Syndrome 16 33 0.036
672
c BRD019 Bardet-Biedl Syndrome 7 28 0.036
673
c BRD050 Bardet-Biedl Syndrome 21 25 0.036
674
c BRD021 Bardet-Biedl Syndrome 9 23 0.036
675
c BRD051 Bardet-Biedl Syndrome 20 22 0.036
676
CRB089 Cerebral Beriberi 20 0.036
677
P MYS003 Myasthenia Gravis 72 0.036
678
P CHR071 Charcot-Marie-Tooth Disease 65 0.036
679
VRC005 Varicose Veins 64 0.036
680
c ATM011 Autoimmune Hepatitis 62 0.036
681
HRP004 Herpes Zoster 60 0.036
682
SPN027 Spinal Stenosis 59 0.036
683
MST005 Mastitis 55 0.036
684
P PRC012 Pericardial Effusion 53 0.036
685
ISL001 Islet Cell Tumor 53 0.036
686
PTT037 Pituitary Tumors 48 0.036
687
HMC014 Homocysteinemia 48 0.036
688
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.036
689
PHN003 Phenylketonuria 73 0.036
690
TNG002 Tangier Disease 64 0.036
691
DGN001 Degenerative Disc Disease 53 0.036
692
CLN015 Colon Adenocarcinoma 53 0.036
693
NPH091 Nephrolithiasis, Calcium Oxalate 51 0.036
694
P CRN074 Coronary Artery Aneurysm 46 0.036
695
c MCR258 Microcephalic Osteodysplastic Primordial Dwarfism, Type Ii 46 0.036
696
SCH003 Schizophreniform Disorder 43 0.036
697
TCL003 T Cell Deficiency 42 0.036
698
P ADP010 Adiponectin, Serum Level of, Quantitative Trait Locus 1 26 0.036
699
P WSK001 Wiskott-Aldrich Syndrome 77 0.034
700
P SRC025 Sarcoidosis 1 66 0.034
701
P INT001 Intrahepatic Cholestasis 60 0.034
702
STT001 Status Epilepticus 60 0.034
703
P MSC007 Muscle Hypertrophy 58 0.034
704
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.034
705
P GLM045 Glioma 54 0.034
706
OCL006 Ocular Hypertension 53 0.034
707
QDR001 Quadriplegia 52 0.034
708
P THR117 Three M Syndrome 1 51 0.034
709
PRS045 Prostatic Hypertrophy 49 0.034
710
OCC006 Occipital Horn Syndrome 49 0.034
711
HDN002 Head Injury 47 0.034
712
GLC096 Galactorrhea 45 0.034
713
BRN080 Brain Ischemia 44 0.034
714
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 41 0.034
715
c CNT028 Central Retinal Artery Occlusion 40 0.034
716
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.034
717
OVR093 Overhydrated Hereditary Stomatocytosis 34 0.034
718
PRN007 Perinephritis 34 0.034
719
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 32 0.034
720
ART010 Arteriolosclerosis 28 0.034
721
c CRT085 Carotid Intimal Medial Thickness 2 22 0.034
722
MTH081 Mthfr Gene Variant 15 0.034
723
P PRK057 Parkinson Disease, Late-Onset 76 0.034
724
APL001 Aplastic Anemia 73 0.034
725
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.034
726
SKN019 Skin Melanoma 69 0.034
727
CHR066 Chronic Fatigue Syndrome 66 0.034
728
MVM001 Movement Disease 60 0.034
729
P LRY019 Laryngitis 56 0.034
730
P SHR001 Short Bowel Syndrome 51 0.034
731
ECT093 Ectopic Cushing Syndrome 50 0.034
732
ALP093 Alpha-Thalassemia/mental Retardation Syndrome, Chromosome 16-Related 46 0.034
733
ANL022 Anal Fistula 44 0.034
734
ACD008 Acid-Labile Subunit Deficiency 43 0.034
735
ACT055 Actinomycosis 43 0.034
736
CDQ001 Cauda Equina Syndrome 40 0.034
737
ALC005 Alcoholic Pancreatitis 38 0.034
738
TMP012 Temple Syndrome 34 0.034
739
CGN007 Cognitive Function 1, Social 30 0.034
740
c PGM022 Pigmented Nodular Adrenocortical Disease, Primary, 4 23 0.034
741
P GRF003 Graft-Versus-Host Disease 71 0.032
742
P ASP006 Aspergillosis 65 0.032
743
CHL065 Cholangiocarcinoma 63 0.032
744
P MLG056 Malignant Hyperthermia 59 0.032
745
TXC002 Toxic Encephalopathy 55 0.032
746
HPT009 Hepatopulmonary Syndrome 53 0.032
747
P SCL009 Sclerosing Cholangitis 53 0.032
748
DST005 Diastrophic Dysplasia 52 0.032
749
P TRT010 Teratoma 52 0.032
750
TLN003 Telangiectasis 51 0.032
751
P BRT004 Bartter Disease 51 0.032
752
LYM009 Lymphocytic Choriomeningitis 50 0.032
753
PRT029 Parathyroid Adenoma 49 0.032
754
PRM003 Premature Ejaculation 47 0.032
755
CRB004 Cerebral Artery Occlusion 46 0.032
756
SDD008 Sudden Sensorineural Hearing Loss 45 0.032
757
PHC013 Phaeochromocytoma 43 0.032
758
MTR007 Motor Peripheral Neuropathy 40 0.032
759
NTR007 Neutral Lipid Storage Disease with Myopathy 36 0.032
760
P DCR003 Dacryoadenitis 33 0.032
761
SVN002 Sveinsson Chorioretinal Atrophy 29 0.032
762
c LPD040 Lipodystrophy, Familial Partial, Type 1 27 0.032
763
P ANG001 Angelman Syndrome 61 0.032
764
ISL014 Isolated Growth Hormone Deficiency, Type Ia 57 0.032
765
ILT001 Ileitis 56 0.032
766
MYL020 Myelomeningocele 53 0.032
767
GNT050 Genitourinary Tract Anomalies 40 0.032
768
PDT040 Pediatric Hypertension 29 0.032
769
c ACT202 Acth-Independent Macronodular Adrenal Hyperplasia 2 28 0.032
770
NRG005 Neurogenic Hypertension 28 0.032
771
c PGM021 Pigmented Nodular Adrenocortical Disease, Primary, 1 26 0.032
772
c PGM011 Pigmented Nodular Adrenocortical Disease, Primary, 2 25 0.032
773
LYM133 Lymphoma, Hodgkin, Classic 71 0.031
774
P SPN052 Spondyloarthropathy 60 0.031
775
P PRG013 Paraganglioma 56 0.031
776
CHL061 Childhood Leukemia 55 0.031
777
BLR006 Biliary Tract Disease 54 0.031
778
P THY054 Thyrotoxic Periodic Paralysis 53 0.031
779
GLL018 Gallbladder Cancer 51 0.031
780
P CRB185 Cerebellar Ataxia, Mental Retardation, and Dysequilibrium Syndrome 1 49 0.031
781
P KRT007 Keratoconus 48 0.031
782
FML026 Familial Lipoprotein Lipase Deficiency 46 0.031
783
P ENC008 Encephalocele 46 0.031
784
NNT049 Nontuberculous Mycobacterial Lung Disease 45 0.031
785
TTH032 Tooth Size 44 0.031
786
NTR005 Nutritional Deficiency Disease 43 0.031
787
SPN369 Spinal Disease 42 0.031
788
CHL013 Cholecystolithiasis 40 0.031
789
PRM056 Primrose Syndrome 34 0.031
790
c GLL024 Gallbladder Disease 1 30 0.031
791
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 26 0.031
792
ACR079 Acrodysostosis with Multiple Hormone Resistance 24 0.031
793
CHR189 Chromosome 12p Deletion 24 0.031
794
ACR119 Acrodysostosis 2 with or Without Hormone Resistance 23 0.031
795
HYP531 Hypogonadotropic Hypogonadism 4 with or Without Anosmia 23 0.031
796
c CSH006 Cushing Syndrome Due to Macronodular Adrenal Hyperplasia 23 0.031
797
48X002 48,xxxy Syndrome 21 0.031
798
MSC089 Mosaic Monosomy X 21 0.031
799
c TRN055 Turner Syndrome Due to Structural X Chromosome Anomalies 21 0.031
800
SBR011 Subaortic Stenosis--Short Stature Syndrome 20 0.031
801
HYP686 Hypogonadism, Male, with Mental Retardation and Skeletal Anomalies 19 0.031
802
P END044 Endometriosis 64 0.030
803
OVR029 Ovarian Hyperstimulation Syndrome 64 0.030
804
P SPN046 Spinal Muscular Atrophy 63 0.030
805
LCT022 Lecithin:cholesterol Acyltransferase Deficiency 60 0.030
806
P MYC008 Myocarditis 58 0.030
807
FLR002 Filariasis 57 0.030
808
TRG002 Trigeminal Neuralgia 57 0.030
809
c ACT135 Acute Graft Versus Host Disease 56 0.030
810
PYD001 Pyoderma Gangrenosum 55 0.030
811
KRT009 Keratosis 53 0.030
812
PYD002 Pyoderma 51 0.030
813
P FML035 Familial Hyperlipidemia 47 0.030
814
CRN031 Cranial Nerve Disease 45 0.030
815
PDT001 Pediatric Lymphoma 45 0.030
816
PND004 Pandas 42 0.030
817
SCT001 Sciatic Neuropathy 42 0.030
818
TND005 Tendinitis 41 0.030
819
HMP001 Hemopericardium 41 0.030
820
RNL021 Renal Tubular Transport Disease 38 0.030
821
c MYS011 Myasthenia Gravis Congenital 30 0.030
822
c LPD036 Lipodystrophy, Familial Partial, Type 6 25 0.030
823
c ATM089 Autoimmune Neuropathy 22 0.030
824
RTN071 Retinitis Pigmentosa, Deafness, Mental Retardation, and Hypogonadism 21 0.030
825
PNC065 Pinched Nerve 16 0.030
826
P RTT002 Rett Syndrome 82 0.028
827
P FRG001 Fragile X Syndrome 69 0.028
828
PNC033 Pancreas Adenocarcinoma 64 0.028
829
c PNS012 Paine Syndrome 62 0.028
830
URT039 Urticaria 60 0.028
831
P HYP040 Hypospadias 59 0.028
832
PLC005 Placental Insufficiency 58 0.028
833
TRP002 Tropical Spastic Paraparesis 57 0.028
834
DMY004 Demyelinating Disease 57 0.028
835
P EPL140 Epilepsy, Idiopathic Generalized 57 0.028
836
APP015 Apparent Mineralocorticoid Excess 54 0.028
837
P PTT006 Pituitary Adenoma 52 0.028
838
MGR028 Migraine with or Without Aura 1 49 0.028
839
MNN009 Meningoencephalitis 49 0.028
840
RNL011 Renal Osteodystrophy 49 0.028
841
c CHR037 Chronic Eosinophilic Pneumonia 48 0.028
842
c HYP740 Hyperlipoproteinemia, Type V 48 0.028
843
ASP007 Aspiration Pneumonia 47 0.028
844
HYP457 Hypertrophic Scars 47 0.028
845
NSP002 Nasopharyngitis 46 0.028
846
P HYP750 Hypertriglyceridemia, Familial 44 0.028
847
LCH009 Lichen Sclerosus 44 0.028
848
IDP064 Idiopathic Neutropenia 44 0.028
849
LPD014 Lipodermatosclerosis 42 0.028
850
DYS009 Dysthymic Disorder 41 0.028
851
c WLM011 Wilms Tumor 6 38 0.028
852
47X003 47, Xxy 37 0.028
853
VSC008 Vascular Hemostatic Disease 36 0.028
854
ALL014 Allergic Encephalomyelitis 36 0.028
855
NRV004 Nerve Compression Syndrome 35 0.028
856
c HNT011 Huntington Disease-Like 3 30 0.028
857
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.028
858
P TTR001 Tetralogy of Fallot 69 0.028
859
c HMP004 Hemophilia B 67 0.028
860
P CRN015 Cornelia De Lange Syndrome 64 0.028
861
P KBK002 Kabuki Syndrome 1 63 0.028
862
P KLL001 Kallmann Syndrome 63 0.028
863
LYM021 Lymphadenitis 61 0.028
864
c ACT073 Acute Leukemia 60 0.028
865
P HMR003 Hemorrhagic Disease 60 0.028
866
CHK001 Chikungunya 59 0.028
867
P STS008 Sotos Syndrome 1 56 0.028
868
P SCL018 Scoliosis 55 0.028
869
P ICH004 Ichthyosis 54 0.028
870
c INF071 Inflammatory Bowel Disease 1 53 0.028
871
c CNT015 Central Sleep Apnea 49 0.028
872
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.028
873
CLN044 Colon Adenoma 42 0.028
874
RMN001 Rumination Disorder 41 0.028
875
PST035 Postgastrectomy Syndrome 36 0.028
876
ALG027 Al-Gazali-Bakalinova Syndrome 30 0.028
877
LPD026 Lipedema 29 0.028
878
c NRC017 Narcolepsy 7 18 0.028
879
c LKM063 Leukemia, Chronic Myeloid 70 0.026
880
MSC157 Muscular Dystrophy, Duchenne Type 68 0.026
881
P MCL013 Mucolipidosis Iv 67 0.026
882
P LNG028 Long Qt Syndrome 65 0.026
883
SCH014 Schistosomiasis 62 0.026
884
CRC006 Carcinoid Syndrome 60 0.026
885
TNS005 Tonsillitis 60 0.026
886
P LPS002 Liposarcoma 59 0.026
887
P MNC007 Monocytic Leukemia 57 0.026
888
CMP010 Complex Regional Pain Syndrome 57 0.026
889
c FML116 Familial Cold Autoinflammatory Syndrome 1 57 0.026
890
c VSC019 Vesicoureteral Reflux 1 57 0.026
891
LYM040 Lymphoblastic Lymphoma 57 0.026
892
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.026
893
DFF005 Diffuse Large B-Cell Lymphoma 56 0.026
894
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 56 0.026
895
EXT034 Extrinsic Allergic Alveolitis 56 0.026
896
P PNC025 Panic Disorder 55 0.026
897
FCL014 Focal Epilepsy 55 0.026
898
c CWD006 Cowden Syndrome 1 55 0.026
899
TCD001 Tic Disorder 54 0.026
900
ABL002 Ablepharon-Macrostomia Syndrome 54 0.026
901
LYM024 Lymphatic System Disease 54 0.026
902
OST016 Osteochondrosis 54 0.026
903
P FML052 Familial Cold Autoinflammatory Syndrome 53 0.026
904
c AMY009 Amyloidosis Aa 53 0.026
905
P CPL006 Capillary Hemangioma 53 0.026
906
WLF002 Wolf-Hirschhorn Syndrome 52 0.026
907
SPC010 Speech and Communication Disorders 52 0.026
908
MNC006 Monoclonal Gammopathy of Uncertain Significance 51 0.026
909
PRN021 Paranasal Sinus Disease 50 0.026
910
P BRC006 Brachydactyly 50 0.026
911
CYC008 Cyclic Vomiting Syndrome 49 0.026
912
ALL001 Allan-Herndon-Dudley Syndrome 49 0.026
913
KLD001 Keloids 49 0.026
914
SKL017 Skeletal Dysplasias 48 0.026
915
P SDR002 Siderosis 47 0.026
916
AMN002 Amino Acid Metabolic Disorder 47 0.026
917
GLC106 Glucocorticoid Resistance, Generalized 46 0.026
918
IMP006 Impulse Control Disorder 43 0.026
919
TRN007 Transsexualism 43 0.026
920
ASP004 Asphyxia Neonatorum 43 0.026
921
PTT003 Pituitary-Dependent Cushing's Disease 42 0.026
922
SWN001 Swine Influenza 42 0.026
923
CRB008 Cerebral Atherosclerosis 41 0.026
924
HRT008 Heart Conduction Disease 41 0.026
925
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 39 0.026
926
c HNT004 Huntington Disease-Like 2 39 0.026
927
AMR003 Amaurosis Fugax 38 0.026
928
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.026
929
OBS004 Obstructive Hydrocephalus 38 0.026
930
PLN007 Plantar Fasciitis 33 0.026
931
FRN013 Frontotemporal Dementia, Chromosome 3-Linked 32 0.026
932
HNS001 Hansen's Disease 30 0.026
933
BLN006 Blind Loop Syndrome 29 0.026
934
SPT019 Septo-Optic Dysplasia Spectrum 28 0.026
935
LRY026 Laryngeal Cleft 26 0.026
936
CLC017 Calcification of Joints and Arteries 25 0.026
937
AMN012 Aminoacidopathies 24 0.026
938
SKT001 Sakati Syndrome 23 0.026
939
TRN069 Transsexuality 23 0.026
940
c CHM002 Chmp2b-Related Frontotemporal Dementia 18 0.026
941
RTN215 Retinitis Pigmentosa-Intellectual Disability-Deafness-Hypogonadism Syndrome 17 0.026
942
INB001 Inborn Amino Acid Metabolism Disorder 16 0.026
943
P FNC027 Fanconi Anemia, Complementation Group a 78 0.022
944
MLT157 Multiple System Atrophy 1 73 0.022
945
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.022
946
P RTN024 Retinoblastoma 70 0.022
947
RNL065 Renal Cell Carcinoma, Papillary, 1 70 0.022
948
HMN044 Human Immunodeficiency Virus Type 1 70 0.022
949
c NMN015 Niemann-Pick Disease, Type C1 68 0.022
950
CNR004 Cone-Rod Dystrophy 2 67 0.022
951
OBS002 Obsessive-Compulsive Disorder 66 0.022
952
MCK007 Muckle-Wells Syndrome 64 0.022
953
c OVR114 Ovarian Cancer 1 62 0.022
954
INT066 Interstitial Lung Disease 62 0.022
955
CMM005 Common Cold 61 0.022
956
BRN056 Bronchopulmonary Dysplasia 60 0.022
957
c MNN043 Meningioma, Familial 60 0.022
958
MCR013 Microphthalmia 60 0.022
959
P NMN002 Niemann-Pick Disease 60 0.022
960
ING001 Inguinal Hernia 59 0.022
961
BRN002 Bronchiolitis 59 0.022
962
SQM006 Squamous Cell Carcinoma 59 0.022
963
HYP190 Hypoalphalipoproteinemia, Primary 58 0.022
964
CFF002 Coffin-Lowry Syndrome 57 0.022
965
PLS007 Plasmodium Falciparum Malaria 57 0.022
966
SMT006 Somatoform Disorder 55 0.022
967
c BRS049 Breast Carcinoma in Situ 55 0.022
968
PLV003 Pelvic Inflammatory Disease 55 0.022
969
P ACT008 Actinic Keratosis 54 0.022
970
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.022
971
MCN007 Meconium Aspiration Syndrome 54 0.022
972
P LPR002 Leopard Syndrome 54 0.022
973
P SJG008 Sjogren Syndrome 54 0.022
974
KRT002 Keratomalacia 54 0.022
975
ESP020 Esophageal Atresia 53 0.022
976
PRP009 Peripartum Cardiomyopathy 53 0.022
977
c VRL007 Viral Encephalitis 52 0.022
978
c ACT020 Acute T Cell Leukemia 52 0.022
979
WHM001 Whim Syndrome 51 0.022
980
VRC001 Varicocele 51 0.022
981
MTC056 Mitochondrial Dna Depletion Syndrome 4a 51 0.022
982
P AST007 Astrocytoma 51 0.022
983
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 50 0.022
984
PRT030 Parathyroid Gland Disease 49 0.022
985
c CNG216 Congenital Hydrocephalus 49 0.022
986
SPS007 Spastic Cerebral Palsy 47 0.022
987
P HRN001 Horner's Syndrome 46 0.022
988
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.022
989
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.022
990
CND005 Cone Dystrophy 43 0.022
991
MMM006 Mammographic Density 43 0.022
992
MYF002 Myofascial Pain Syndrome 43 0.022
993
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 42 0.022
994
PRM024 Primary Angle-Closure Glaucoma 42 0.022
995
PHY002 Physical Disorder 41 0.022
996
BRR012 Berardinelli-Seip Congenital Lipodystrophy 40 0.022
997
MCR103 Microtia 40 0.022
998
ACL001 Acalculous Cholecystitis 38 0.022
999
c BRD035 Bardet-Biedl Syndrome 15 38 0.022
1000
GRN009 Granulomatous Hepatitis 38 0.022
1001
AYM001 Ayme-Gripp Syndrome 37 0.022
1002
END014 Endemic Typhus 37 0.022
1003
ANS012 Anus Disease 36 0.022
1004
c HYP768 Hyperlipoproteinemia, Type I 36 0.022
1005
MNN042 Meningioma, Radiation-Induced 36 0.022
1006
CGH001 Cough Variant Asthma 35 0.022
1007
ENT005 Entropion 34 0.022
1008
HRS011 Horseshoe Kidney 34 0.022
1009
c CHR057 Chronic Laryngitis 34 0.022
1010
HRT038 Heart, Malformation of 32 0.022
1011
CLB026 Colobomatous Microphthalmia 30 0.022
1012
VRT003 Vertebrobasilar Insufficiency 30 0.022
1013
CHR247 Chromosome 4p Deletion 30 0.022
1014
CRN264 Craniosynostosis with Fibular Aplasia 30 0.022
1015
PRM008 Parametritis 30 0.022
1016
CRT011 Carotenemia 26 0.022
1017
MCL079 Macular Telangiectasia Type 2 26 0.022
1018
CRT020 Cortisone Reductase Deficiency 25 0.022
1019
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 22 0.022
1020
STT003 Steatitis 22 0.022
1021
c PRC047 Precocious Puberty, Central, 1 20 0.022
1022
c LKM055 Leukemia, Acute Lymphoblastic 2 20 0.022
1023
c PRC046 Precocious Puberty, Central, 2 19 0.022
1024
c CHR115 Charcot-Marie-Tooth Neuropathy Type 2a 19 0.022
1025
c PGM012 Pigmented Nodular Adrenocortical Disease, Primary, 3 17 0.022
1026
LPT013 Leptin, Serum Level of, Quantitative Trait Locus 1 12 0.022
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