Search results for Hypoglycemic Agents

1326 hits were found for Hypoglycemic Agents

# Family MCID Name MIFTS Score
1
HYP056 Hypoglycemia 66 0.493
2
OCL069 Ocular Motor Apraxia 51 0.298
3
HYP066 Hyperglycemia 61 0.289
4
P DBT009 Diabetes Mellitus 64 0.246
5
HYP026 Hypoglycemic Coma 38 0.240
6
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.225
7
P ENC018 Encephalopathy 61 0.202
8
HYP060 Hyperinsulinism 54 0.165
9
P KDN018 Kidney Disease 70 0.164
10
P CLR023 Colorectal Cancer 98 0.156
11
c CHR684 Chronic Kidney Disease 66 0.154
12
ADN018 Adenoma 58 0.154
13
P LYM031 Lymphocytic Leukemia 55 0.152
14
P LNG032 Lung Cancer 97 0.151
15
P DRR001 Diarrhea 57 0.150
16
P HPT023 Hepatocellular Carcinoma 100 0.148
17
CNG034 Congestive Heart Failure 70 0.147
18
LPD008 Lipid Metabolism Disorder 62 0.145
19
MYL069 Myeloma, Multiple 85 0.144
20
P BRS047 Breast Cancer 96 0.143
21
P OVR042 Ovarian Cancer 89 0.142
22
P SZR006 Seizure Disorder 58 0.140
23
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.140
24
VSL002 Visual Epilepsy 58 0.139
25
P LKM002 Leukemia 66 0.138
26
ALL026 Allergic Hypersensitivity Disease 64 0.138
27
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.137
28
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.134
29
ISC004 Ischemia 60 0.131
30
GLB015 Glioblastoma Multiforme 75 0.131
31
P NRP001 Neuropathy 56 0.130
32
ATM095 Autoimmune Disease 61 0.130
33
c SML038 Small Cell Cancer of the Lung 65 0.130
34
c HYP595 Hypertension, Essential 84 0.129
35
48X005 48,xyyy 39 0.129
36
MYL009 Myelodysplastic Syndrome 70 0.127
37
P PSR002 Psoriasis 62 0.126
38
PST011 Pustulosis of Palm and Sole 52 0.126
39
P LYM118 Lymphoma 68 0.126
40
c HPT073 Hepatitis C Virus 70 0.125
41
INS001 Insulinoma 60 0.125
42
P PNC035 Pancreatic Cancer 84 0.123
43
P HRT032 Heart Disease 75 0.123
44
GLL048 Glial Tumor 45 0.123
45
BRN071 Brain Injury 49 0.122
46
c HPT001 Hepatitis C 63 0.122
47
P PRS040 Prostate Cancer 97 0.122
48
GST033 Gestational Diabetes 57 0.121
49
CRB039 Cerebrovascular Disease 69 0.120
50
BCT022 Bacterial Infectious Disease 56 0.119
51
P GLM045 Glioma 63 0.118
52
P RHM011 Rheumatoid Arthritis 80 0.118
53
P ADN016 Adenocarcinoma 64 0.118
54
P VSC007 Vascular Disease 63 0.117
55
P LVR013 Liver Disease 68 0.117
56
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.117
57
HMN044 Human Immunodeficiency Virus Type 1 71 0.117
58
P ALZ034 Alzheimer Disease 88 0.117
59
CHL123 Chlamydia 59 0.117
60
ANG054 Angina Pectoris 66 0.116
61
P HRP006 Herpes Simplex 65 0.116
62
P PRP019 Peripheral Nervous System Disease 57 0.114
63
P NRB001 Neuroblastoma 71 0.113
64
P INF037 Inflammatory Bowel Disease 56 0.111
65
P BLD134 Bladder Cancer 78 0.111
66
P HPT021 Hepatitis 67 0.111
67
END030 End Stage Renal Failure 58 0.110
68
P MYC007 Myocardial Infarction 70 0.110
69
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.109
70
DFC004 Deficiency Anemia 75 0.109
71
ATH013 Atherosclerosis Susceptibility 66 0.109
72
HYP266 Hypoxia 56 0.108
73
P ART022 Arthritis 70 0.108
74
DRM006 Dermatitis 61 0.108
75
c HYP836 Hypercholesterolemia, Familial, 1 72 0.107
76
c MCR120 Microvascular Complications of Diabetes 7 47 0.107
77
DWN001 Down Syndrome 70 0.106
78
P TRM003 Tremor 53 0.106
79
c MCR113 Microvascular Complications of Diabetes 3 52 0.106
80
c MCR130 Microvascular Complications of Diabetes 6 41 0.106
81
c MCR133 Microvascular Complications of Diabetes 4 41 0.106
82
CRH001 Crohn's Disease 74 0.105
83
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.104
84
P CRN300 Coronary Heart Disease 1 63 0.103
85
SKN016 Skin Disease 63 0.103
86
P CRN018 Coronary Artery Anomaly 63 0.103
87
P CND004 Candidiasis 57 0.102
88
P EXN002 Exanthem 57 0.102
89
PPT005 Peptic Ulcer Disease 58 0.102
90
P OST002 Osteoporosis 73 0.101
91
CNS004 Constipation 57 0.101
92
SRC014 Sarcoma 65 0.101
93
c LKM071 Leukemia, Chronic Lymphocytic 79 0.101
94
SPN035 Spindle Cell Sarcoma 51 0.101
95
DPR016 Depression 63 0.101
96
P NRF023 Neurofibromatosis, Type Ii 76 0.100
97
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.100
98
P MCR115 Microvascular Complications of Diabetes 5 66 0.100
99
P FBR017 Fibrosarcoma 56 0.100
100
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.100
101
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.100
102
LVR012 Liver Cirrhosis 63 0.099
103
STR067 Stroke, Ischemic 80 0.099
104
P BNG032 Benign Mesothelioma 45 0.099
105
SVR004 Severe Combined Immunodeficiency 73 0.098
106
P CRD119 Cardiac Arrest 67 0.097
107
GLC003 Glucose Intolerance 54 0.097
108
P GST053 Gastric Cancer 83 0.097
109
P BCL017 B-Cell Lymphoma 58 0.097
110
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.097
111
P LKM062 Leukemia, Acute Lymphoblastic 68 0.097
112
c HPT016 Hepatitis B 59 0.096
113
P PNM007 Pneumonia 68 0.096
114
HRW001 Hair Whorl 36 0.096
115
P THR014 Thrombocytopenia 68 0.096
116
P CTR002 Cataract 60 0.096
117
P ALP008 Alopecia 56 0.096
118
ACQ007 Acquired Immunodeficiency Syndrome 60 0.095
119
ART140 Arteries, Anomalies of 53 0.094
120
P CRD246 Cardiovascular System Disease 56 0.094
121
c ACT071 Acute Kidney Failure 59 0.094
122
P LCT001 Lactic Acidosis 51 0.094
123
ULC004 Ulcerative Colitis 73 0.094
124
AST005 Asthma 77 0.094
125
ANX010 Anxiety 72 0.093
126
LNG099 Lung Disease 61 0.093
127
RHM027 Rheumatic Disease 56 0.092
128
PRT036 Peritonitis 65 0.092
129
c ACT068 Acute Cystitis 63 0.091
130
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
131
P ENC004 Encephalitis 61 0.091
132
PLM001 Pulmonary Tuberculosis 70 0.091
133
P PRD008 Periodontitis 62 0.091
134
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.091
135
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.090
137
LYM133 Lymphoma, Hodgkin, Classic 69 0.090
138
BNR002 Bone Resorption Disease 48 0.090
139
TXC005 Toxic Shock Syndrome 61 0.090
140
LYM019 Lymphosarcoma 47 0.090
141
P MLT020 Multiple Sclerosis 72 0.090
142
c SVR001 Severe Acute Respiratory Syndrome 55 0.090
143
P HDC001 Headache 57 0.089
144
P HYP086 Hypothyroidism 68 0.089
145
MLN008 Melanoma 69 0.089
146
c ACT075 Acute Myocardial Infarction 56 0.089
147
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.089
148
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.089
149
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.089
150
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.089
151
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.089
152
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.089
153
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.089
154
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.089
155
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.089
156
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.089
157
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.089
158
PRP027 Peripheral Vascular Disease 71 0.089
159
c THR092 Thrombophilia Due to Thrombin Defect 73 0.089
160
P ATR011 Atrial Fibrillation 66 0.089
161
c PRM038 Primary Agammaglobulinemia 43 0.089
162
CYT002 Cytokine Deficiency 44 0.089
163
c RHB024 Rhabdomyosarcoma 2 65 0.088
164
P HYP076 Hyperthyroidism 55 0.088
165
P KDN017 Kidney Cancer 61 0.088
166
47X002 47,xyy 49 0.088
167
ALC007 Alcohol Dependence 66 0.088
168
SQM006 Squamous Cell Carcinoma 60 0.088
169
FTT001 Fatty Liver Disease 61 0.087
170
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.087
171
P HYP069 Hyperparathyroidism 62 0.087
172
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.086
173
CLT003 Colitis 62 0.086
174
PSR001 Psoriatic Arthritis 62 0.086
175
THR024 Thrombosis 56 0.086
176
P URT039 Urticaria 58 0.086
177
c SPN225 Spondyloarthropathy 1 73 0.086
178
PLM033 Pulmonary Embolism 59 0.086
179
HYP005 Hypokalemia 55 0.086
180
P MNN013 Meningitis 65 0.086
181
INT007 Intermediate Coronary Syndrome 55 0.086
182
PRT037 Pertussis 65 0.085
183
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.085
184
P RHN004 Rhinitis 57 0.085
185
P HYP750 Hypertriglyceridemia, Familial 61 0.084
186
PNG002 Pain Agnosia 51 0.084
187
SBC016 Subacute Delirium 44 0.084
188
P INF038 Influenza 68 0.084
189
KRT019 Keratitis, Hereditary 67 0.084
190
MNT002 Mental Depression 57 0.084
191
DRM011 Dermatophytosis 52 0.084
192
P PNC044 Pancreatitis 61 0.083
193
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.083
194
P DMN002 Dementia 67 0.083
195
HMP005 Hemiplegia 54 0.083
196
P SKN015 Skin Carcinoma 67 0.083
197
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.083
198
c HPT003 Hepatitis a 63 0.083
199
P SRC025 Sarcoidosis 1 70 0.083
200
IMP005 Impotence 52 0.082
201
c ATR087 Atrial Standstill 1 74 0.082
202
CRV035 Cervical Cancer 76 0.082
203
P MYP004 Myopathy 64 0.082
204
CLN015 Colon Adenocarcinoma 63 0.082
205
ADL002 Adult Syndrome 69 0.082
206
IMM167 Immune Deficiency Disease 78 0.081
207
c MGR028 Migraine with or Without Aura 1 69 0.081
208
LNG031 Lung Benign Neoplasm 50 0.081
209
IRN002 Iron Metabolism Disease 57 0.081
210
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.081
211
SYN036 Syncope 45 0.081
212
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.081
213
LWC001 Low Compliance Bladder 42 0.081
214
P DDN001 Duodenal Ulcer 50 0.081
215
GST023 Gastric Ulcer 53 0.080
216
P UVT001 Uveitis 57 0.080
217
PLM010 Pulmonary Edema 55 0.080
218
CYS001 Cystic Fibrosis 80 0.080
219
P NPH012 Nephrotic Syndrome 63 0.080
220
P VSC011 Vasculitis 62 0.080
221
GRN017 Granulocytopenia 44 0.080
222
CRD223 Cardiac Arrhythmia 60 0.080
223
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.080
224
OST012 Osteoarthritis 78 0.079
225
END057 Endometrial Cancer 74 0.079
226
P RSP003 Respiratory Failure 74 0.079
227
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.079
228
P LTR001 Lateral Sclerosis 53 0.079
229
BRN028 Brain Cancer 73 0.078
230
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.078
231
P ALC033 Alcohol Use Disorder 58 0.078
232
P GLM007 Glomerulonephritis 57 0.078
233
SFT003 Soft Tissue Sarcoma 56 0.078
234
P HYP050 Hyperinsulinemic Hypoglycemia 54 0.078
235
ENT004 Enthesopathy 48 0.078
237
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.077
238
OVR094 Ovarian Epithelial Cancer 38 0.076
239
P LNG064 Lung Cancer Susceptibility 3 77 0.076
240
SPN186 Spinal Cord Injury 60 0.076
241
c VRL010 Viral Hepatitis 51 0.076
242
P MJR001 Major Depressive Disorder 68 0.076
243
P DRM053 Dermatitis, Atopic 66 0.076
244
MSL001 Measles 61 0.076
245
THY029 Thyroid Carcinoma 59 0.075
246
MLR004 Malaria 80 0.075
247
P BND020 Bone Disease 59 0.075
248
P SCH015 Schizophrenia 75 0.075
249
P GRF003 Graft-Versus-Host Disease 71 0.075
250
TRM010 Traumatic Brain Injury 53 0.075
251
c MLG068 Malignant Glioma 45 0.075
252
P HMN010 Hemangioma 61 0.075
253
c SYS001 Systemic Lupus Erythematosus 86 0.075
254
TRN015 Transient Cerebral Ischemia 62 0.075
255
ESP021 Esophageal Cancer 90 0.075
256
DYS015 Dysentery 50 0.075
257
c MCR129 Microvascular Complications of Diabetes 1 66 0.074
258
P PLM037 Pulmonary Hypertension 68 0.074
259
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.074
260
P TRN020 Turner Syndrome 65 0.074
261
GT001 Gout 63 0.074
262
ANT024 Anthrax Disease 58 0.074
263
c PRC016 Pre-Eclampsia 63 0.074
264
AGN016 Aging 56 0.073
265
MCL006 Macular Retinal Edema 55 0.073
266
P BPL003 Bipolar Disorder 56 0.073
267
P RCT021 Rectum Cancer 53 0.073
268
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.073
269
c ACT027 Acute Pancreatitis 59 0.073
270
EYD002 Eye Disease 58 0.072
271
c MJR024 Major Affective Disorder 9 41 0.072
272
c MJR022 Major Affective Disorder 8 38 0.072
273
IDP011 Idiopathic Interstitial Pneumonia 63 0.072
274
c CHR064 Chronic Monocytic Leukemia 34 0.072
275
STT001 Status Epilepticus 59 0.072
276
GST050 Gastrointestinal System Disease 56 0.072
277
DBT010 Diabetic Neuropathy 55 0.072
278
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.072
279
c PRS136 Prostate Cancer, Hereditary, 6 33 0.072
280
c PRS130 Prostate Cancer, Hereditary, 8 32 0.072
281
HYP014 Hyperuricemia 51 0.072
282
SKN019 Skin Melanoma 67 0.072
283
P LPS004 Lupus Erythematosus 61 0.072
284
P ATX030 Ataxia-Telangiectasia 83 0.072
285
P ART021 Arteriosclerosis 54 0.071
286
ATX019 Ataxia with Vitamin E Deficiency 48 0.071
287
P AMY004 Amyloidosis 70 0.071
288
P PLM036 Pulmonary Fibrosis 61 0.071
289
OST017 Osteomyelitis 64 0.071
290
TLN003 Telangiectasis 51 0.071
291
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.071
292
P GLM040 Glioma Susceptibility 1 81 0.071
293
MNT001 Mantle Cell Lymphoma 66 0.070
294
GNG013 Gingivitis 59 0.070
295
P SYP003 Syphilis 59 0.070
296
c DLT002 Dilated Cardiomyopathy 79 0.070
297
MTB004 Metabolic Acidosis 50 0.070
298
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.070
299
SPP010 Suppressor of Tumorigenicity 3 51 0.070
300
RRS014 Rare Surgical Neurologic Disease 32 0.070
301
ANR007 Anorexia Nervosa 63 0.070
302
VRL011 Viral Infectious Disease 61 0.070
303
P PLY019 Polyneuropathy 56 0.070
304
DSS008 Disease of Mental Health 57 0.069
305
INS024 Insulin-Like Growth Factor I 79 0.069
306
P PRK057 Parkinson Disease, Late-Onset 76 0.069
307
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.069
308
ORL011 Oral Cancer 60 0.069
309
BRN004 Brain Edema 55 0.069
310
BCK006 Back Pain 42 0.069
311
ALL003 Allergic Rhinitis 67 0.069
312
IRR002 Irritable Bowel Syndrome 63 0.069
313
RDN001 Reading Disorder 40 0.069
314
PPL022 Papilloma 54 0.068
315
HNS001 Hansen's Disease 34 0.068
316
GLS018 Glass Syndrome 53 0.068
317
AMN001 Amenorrhea 54 0.068
318
c LKM063 Leukemia, Chronic Myeloid 71 0.068
319
P AST007 Astrocytoma 50 0.068
320
P SCK005 Sickle Cell Disease 50 0.068
321
P LPR021 Leprosy 3 67 0.068
322
P CHR345 Chronic Pain 50 0.068
323
c OVR114 Ovarian Cancer 1 38 0.068
324
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.068
325
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.068
326
CRD132 Cardiac Conduction Defect 59 0.067
327
ANR040 Aneurysm 58 0.067
328
PLS009 Plasma Cell Neoplasm 51 0.067
329
SCK003 Sickle Cell Anemia 72 0.067
330
P SLP006 Sleep Apnea 69 0.067
331
P PHC003 Pheochromocytoma 71 0.067
332
c DWL002 Dowling-Degos Disease 1 58 0.067
333
DFF005 Diffuse Large B-Cell Lymphoma 56 0.067
334
AMN003 Amnestic Disorder 54 0.067
335
HPT004 Hepatic Coma 43 0.067
336
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.067
337
P RTN018 Retinal Disease 52 0.067
338
c CHR682 Chronic Bilirubin Encephalopathy 38 0.067
339
HRP004 Herpes Zoster 60 0.067
340
ADR040 Adrenal Gland Pheochromocytoma 46 0.067
341
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.067
342
c FNC043 Fanconi Anemia, Complementation Group E 62 0.067
343
BRK010 Burkitt Lymphoma 67 0.066
344
c LRG017 Large Intestine Cancer 47 0.066
345
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.066
346
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.066
347
P PLY011 Polycystic Ovary Syndrome 56 0.066
348
c MLG074 Malignant Mesenchymoma 39 0.066
349
P EPL164 Epilepsy 71 0.066
350
P ESP024 Esophagitis 62 0.066
351
SPS057 Spasticity 41 0.066
352
P MDL005 Medulloblastoma 77 0.066
353
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.066
354
HMS001 Hemosiderosis 54 0.066
355
P HMP007 Hemophilia 51 0.066
356
P TCL004 T-Cell Leukemia 47 0.066
357
P HYD006 Hydrocephalus 65 0.066
358
P FLL037 Follicular Lymphoma 66 0.065
359
GST092 Gastroesophageal Reflux 65 0.065
360
SQM002 Squamous Cell Papilloma 42 0.065
361
P THL005 Thalassemia 60 0.065
362
HPT019 Hepatic Encephalopathy 60 0.065
363
P MYC033 Myoclonus 46 0.065
364
ISL001 Islet Cell Tumor 56 0.065
365
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.065
366
PNC129 Pancreatic Adenocarcinoma 67 0.065
367
CHL065 Cholangiocarcinoma 67 0.065
368
LPT014 Leptin Deficiency or Dysfunction 73 0.064
369
INT002 Intermittent Claudication 61 0.064
370
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.064
371
ERY051 Erythroleukemia, Familial 56 0.064
372
SXL003 Sexual Disorder 48 0.064
373
P RRH023 Rare Hereditary Hemochromatosis 41 0.064
374
NRN004 Neuroendocrine Tumor 55 0.064
375
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.064
376
CHL068 Cholestasis 60 0.064
377
SYN007 Synovitis 55 0.064
378
P HYP083 Hypopituitarism 53 0.064
379
P ECL001 Eclampsia 51 0.064
380
NNL006 Non-Alcoholic Steatohepatitis 51 0.064
381
INT079 Intrahepatic Cholangiocarcinoma 50 0.064
382
URM002 Uremia 49 0.063
383
P MYC084 Mycobacterium Tuberculosis 1 68 0.063
384
P CTN015 Cutaneous T Cell Lymphoma 49 0.063
385
APH002 Aphasia 57 0.063
386
OBS002 Obsessive-Compulsive Disorder 68 0.063
387
FCT007 Factor Vii Deficiency 66 0.063
388
P MYC008 Myocarditis 59 0.063
389
PRT058 Pure Autonomic Failure 59 0.063
390
c FML035 Familial Hyperlipidemia 55 0.063
391
P SLP005 Sleep Disorder 59 0.062
392
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.062
393
RCK004 Rickets 69 0.062
394
PRT013 Portal Hypertension 60 0.062
395
KRT009 Keratosis 53 0.062
396
PRP080 Peripheral Artery Disease 53 0.062
397
CRC021 Carcinosarcoma 61 0.062
398
NRT001 Neurotic Disorder 52 0.062
399
c MNN043 Meningioma, Familial 74 0.062
400
MNN042 Meningioma, Radiation-Induced 62 0.062
401
SPN021 Spinal Meningioma 47 0.062
402
SCR001 Secretory Meningioma 37 0.062
403
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.062
404
P RTN024 Retinoblastoma 72 0.062
405
c FML008 Familial Retinoblastoma 53 0.062
406
ILS001 Ileus 51 0.062
407
c HYP272 Hypercholesterolemia, Familial, 3 43 0.061
408
CMM005 Common Cold 56 0.061
409
OCL006 Ocular Hypertension 53 0.061
410
c GLL024 Gallbladder Disease 1 52 0.061
411
TRP009 Triple X Syndrome 42 0.061
412
HMR039 Hemorrhage, Intracerebral 57 0.061
413
ATR057 Atrioventricular Block 55 0.061
414
c MST023 Mesothelioma, Malignant 57 0.061
415
P INT068 Intestinal Disease 52 0.061
416
HDN002 Head Injury 45 0.061
417
PPL001 Papillary Adenoma 45 0.061
418
ANX004 Anoxia 42 0.060
419
c FML001 Familial Atrial Fibrillation 66 0.060
420
CNN005 Connective Tissue Disease 66 0.060
421
P HML002 Hemolytic Anemia 62 0.060
422
NTR005 Nutritional Deficiency Disease 61 0.060
423
END040 Endogenous Depression 54 0.060
424
P INS002 in Situ Carcinoma 52 0.060
425
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 48 0.060
426
RTC005 Reticulosarcoma 49 0.060
427
P SBS003 Substance Abuse 54 0.060
428
SPL018 Splenomegaly 48 0.060
429
c ATM011 Autoimmune Hepatitis 62 0.060
430
P PNC025 Panic Disorder 53 0.060
431
HMT002 Hematologic Cancer 62 0.060
432
P PYL005 Pyelonephritis 56 0.060
433
P MYP006 Myopia 55 0.060
434
WTH001 Withdrawal Disorder 48 0.060
435
CYT018 Cytochrome P450 2d6 Variant 27 0.060
436
P GRV001 Graves' Disease 55 0.059
437
PLC008 Placenta Disease 49 0.059
438
c FNC027 Fanconi Anemia, Complementation Group a 81 0.059
439
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.059
440
FLL027 Fallopian Tube Carcinoma 67 0.059
441
P OPT006 Optic Nerve Disease 57 0.059
442
GLS001 Gliosarcoma 54 0.059
443
P OPN001 Open-Angle Glaucoma 49 0.059
444
MXD026 Mixed Glioma 45 0.059
445
HYP781 Hypoascorbemia 50 0.059
446
IMM064 Immunodeficiency, Common Variable, 10 44 0.059
447
ATN004 Autonomic Neuropathy 44 0.059
448
EWN003 Ewing Sarcoma 68 0.059
449
DBT006 Diabetic Macular Edema 48 0.059
450
ATS010 Autosomal Recessive Disease 48 0.059
451
ART016 Aortic Aneurysm 68 0.059
452
P MSC005 Muscular Dystrophy 66 0.059
453
P ADL010 Adult Respiratory Distress Syndrome 63 0.059
454
TRD006 Tardive Dyskinesia 55 0.059
455
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.059
456
CHR100 Chronic Ulcer of Skin 53 0.059
457
CRN030 Coronary Stenosis 50 0.059
458
CRD137 Cardiogenic Shock 48 0.059
459
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.058
460
P INT143 Interstitial Cystitis 61 0.058
461
LYM027 Lymphopenia 57 0.058
462
CMR002 Coumarin Resistance 56 0.058
463
CRH005 Crohn's Colitis 52 0.058
464
TXC002 Toxic Encephalopathy 52 0.058
465
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.058
466
PPL049 Papillon-Lefevre Syndrome 63 0.058
467
c ACT134 Acute Liver Failure 51 0.058
468
GST019 Gastrointestinal Stromal Tumor 76 0.058
469
HYP081 Hypolipoproteinemia 50 0.058
470
c MCR112 Microvascular Complications of Diabetes 2 41 0.058
471
BLR008 Bilirubin Metabolic Disorder 57 0.058
472
ASP007 Aspiration Pneumonia 48 0.058
473
P ANG015 Angioedema 54 0.057
474
c FLL041 Follicular Lymphoma 1 49 0.057
475
GST020 Gastric Antral Vascular Ectasia 41 0.057
476
49X006 49, Xxxxy Syndrome 41 0.057
477
c BSL007 Basal Cell Carcinoma 68 0.057
478
P ALP009 Alopecia Areata 60 0.057
479
THY122 Thyroid Gland Cancer 58 0.057
480
c ADL017 Adult T-Cell Leukemia 57 0.057
481
c PRD040 Periodontitis, Chronic 54 0.057
482
P MSC003 Muscular Atrophy 52 0.057
483
DYS073 Dysphagia 50 0.057
484
MCR004 Macroglobulinemia 50 0.057
485
PST092 Posttransplant Acute Limbic Encephalitis 29 0.057
486
P GLY013 Glycogen Storage Disease 59 0.057
487
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.057
488
HRP008 Herpes Simiae 25 0.057
489
P ATS364 Autism 65 0.057
490
MSC007 Muscle Hypertrophy 63 0.057
491
P MVM001 Movement Disease 61 0.057
492
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.057
494
c CNT033 Central Nervous System Cancer 46 0.057
495
ANG049 Angioedema Induced by Ace Inhibitors 40 0.057
496
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.057
497
P DBT005 Diabetes Insipidus 55 0.056
498
P PRS038 Personality Disorder 65 0.056
499
IGR001 Ige Responsiveness, Atopic 59 0.056
500
CLL003 Cellulitis 54 0.056
501
P TCD001 Tic Disorder 54 0.056
502
P PTT006 Pituitary Adenoma 54 0.056
503
HYP080 Hypogonadism 50 0.056
504
HYP064 Hypogonadotropism 40 0.056
505
MYL031 Myeloproliferative Neoplasm 65 0.056
506
KRT013 Keratolytic Winter Erythema 46 0.056
507
DRG024 Drug Allergy 43 0.056
508
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.056
509
c INF071 Inflammatory Bowel Disease 1 68 0.056
510
MYC006 Mycosis Fungoides 66 0.056
511
KHL003 Kohlschutter-Tonz Syndrome 64 0.056
512
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.056
513
P BNC003 Bone Cancer 57 0.056
514
CLR109 Colorectal Adenocarcinoma 50 0.056
515
P NRV006 Nervous System Cancer 48 0.056
516
PST021 Postpartum Depression 50 0.056
517
ACR007 Acromegaly 71 0.056
518
P OCL013 Oculodentodigital Dysplasia 69 0.055
519
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.055
520
P MTR014 Motor Neuron Disease 64 0.055
521
HRT012 Heart Valve Disease 53 0.055
522
c ACT135 Acute Graft Versus Host Disease 51 0.055
523
c INF145 Infantile Liver Failure Syndrome 1 50 0.055
524
ATM052 Autoimmune Disease 1 37 0.055
525
ADR016 Adrenal Cortical Carcinoma 48 0.055
526
RST023 Resting Heart Rate, Variation in 41 0.055
527
FNT004 Fainting 31 0.055
528
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.055
529
APN008 Apnea, Obstructive Sleep 65 0.055
530
c GLC092 Glaucoma, Primary Open Angle 62 0.055
531
SPP011 Suppression of Tumorigenicity 12 59 0.055
532
PST028 Post-Traumatic Stress Disorder 58 0.055
533
ORL005 Oral Candidiasis 56 0.055
534
ACR041 Acromelic Frontonasal Dysostosis 52 0.055
535
NRR001 Neuroretinitis 43 0.055
536
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.055
537
NRM005 Neuromuscular Disease 63 0.055
538
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.055
539
KRT002 Keratomalacia 48 0.055
540
P MLT074 Multiple Endocrine Neoplasia 55 0.055
541
P TRC086 Trichohepatoenteric Syndrome 1 59 0.054
542
TBC004 Tobacco Addiction 64 0.054
543
P PRM006 Primary Biliary Cirrhosis 61 0.054
544
THY030 Thyroid Gland Disease 51 0.054
545
TNP001 Tinea Pedis 47 0.054
546
RTN023 Retinitis 46 0.054
547
P MJR007 Major Affective Disorder 1 43 0.054
548
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.054
549
CRB037 Cerebral Palsy 68 0.054
550
c BRN108 Branchiootic Syndrome 1 61 0.054
551
c PNS012 Paine Syndrome 61 0.054
552
P INT070 Intestinal Obstruction 58 0.054
553
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.054
554
P HMR005 Hemorrhoid 46 0.054
555
P EPN001 Ependymoblastoma 45 0.054
556
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.054
557
c PRM005 Primary Hyperparathyroidism 58 0.054
558
CNN003 Conn's Syndrome 79 0.054
559
c SRC023 Sarcoidosis 2 43 0.054
560
P MLN007 Male Infertility 56 0.053
561
MTN003 Motion Sickness 52 0.053
562
CCN002 Cocaine Abuse 48 0.053
563
P APL001 Aplastic Anemia 74 0.053
564
GST040 Gastric Adenocarcinoma 70 0.053
565
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.053
566
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.053
567
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.053
568
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.053
569
c SYS043 Systemic Lupus Erythematosus 1 38 0.053
570
HMG005 Hemoglobinopathy 55 0.053
571
NRT004 Neuritis 53 0.053
572
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.053
573
c ATS007 Autism Spectrum Disorder 67 0.053
574
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.053
575
NWB001 Newborn Respiratory Distress Syndrome 58 0.053
576
MRG003 Marginal Zone B-Cell Lymphoma 53 0.053
577
SNS003 Sensory Peripheral Neuropathy 53 0.053
578
OPT003 Opiate Dependence 50 0.053
579
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.053
580
HYP043 Hyperandrogenism 48 0.053
581
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.053
582
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 33 0.053
583
GNR004 Generalized Anxiety Disorder 56 0.053
584
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.053
585
c MCL013 Mucolipidosis Iv 64 0.052
586
LYM040 Lymphoblastic Lymphoma 54 0.052
587
P CRN028 Corneal Ulcer 47 0.052
588
HRT040 Hirata Disease 37 0.052
589
NRL016 Neural Tube Defects 82 0.052
590
CRN036 Craniopharyngioma 65 0.052
591
c ALP101 Alpha-Thalassemia 62 0.052
592
FCL014 Focal Epilepsy 54 0.052
593
PRN014 Paronychia 49 0.052
594
HYP020 Hyperprolactinemia 64 0.052
595
FBR047 Fibromyalgia 59 0.052
596
P MYS005 Myositis 56 0.052
597
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.052
598
IGG001 Iga Glomerulonephritis 48 0.052
599
PRM127 Primary Cutaneous Diffuse Large B-Cell Lymphoma, Leg Type 38 0.052
600
c MJR008 Major Affective Disorder 2 34 0.052
601
c MJR003 Major Affective Disorder 6 33 0.052
602
c MJR006 Major Affective Disorder 5 33 0.052
603
c MJR023 Major Affective Disorder 7 33 0.052
604
c MJR004 Major Affective Disorder 4 28 0.052
605
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.052
606
DMP001 Dumping Syndrome 44 0.052
607
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.052
608
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.052
609
LMB062 Limb Ischemia 55 0.052
610
c CNT035 Central Nervous System Disease 54 0.052
611
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.052
612
CLN045 Colonic Benign Neoplasm 49 0.052
613
VTM033 Vitamin K Deficiency Bleeding 48 0.052
614
CCN001 Cocaine Dependence 48 0.052
615
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.052
616
c PNC108 Pancreatitis, Hereditary 69 0.051
617
CRP001 Carpal Tunnel Syndrome 67 0.051
618
ETN001 Eating Disorder 59 0.051
619
c SCN036 Secondary Progressive Multiple Sclerosis 55 0.051
620
GSG001 Gas Gangrene 50 0.051
621
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.051
622
SPR126 Superior Semicircular Canal Dehiscence 40 0.051
623
c HMG029 Hemoglobin Se Disease 38 0.051
624
P DYS193 Dystonia 11, Myoclonic 56 0.051
625
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.051
626
SPS003 Spastic Diplegia 50 0.051
627
SCL003 Social Phobia 48 0.051
628
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.051
629
PTT037 Pituitary Tumors 44 0.051
630
ADR007 Adrenoleukodystrophy 74 0.051
631
P THY023 Thymoma 65 0.051
632
BRS099 Breast Ductal Carcinoma 62 0.051
633
P ANP001 Anaplastic Large Cell Lymphoma 61 0.051
634
P TST021 Testicular Germ Cell Tumor 61 0.051
635
P SNS001 Sensorineural Hearing Loss 61 0.051
636
P SCL018 Scoliosis 60 0.051
637
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.051
638
c THY107 Thymoma, Familial 54 0.051
639
PRP016 Paraplegia 53 0.051
640
c LKM070 Leukemia, Acute Monocytic 53 0.051
641
BHR001 Behr Syndrome 49 0.051
642
OPD006 Opioid Addiction 48 0.051
643
ATN005 Autonomic Dysfunction 47 0.051
644
FML063 Familial Glucocorticoid Deficiency 51 0.050
645
P SML001 Small Cell Carcinoma 52 0.050
646
GRM005 Germ Cell Cancer 47 0.050
647
OPD001 Opioid Abuse 45 0.050
648
APP009 Appendix Adenocarcinoma 44 0.050
649
P ANR048 Aniridia 1 63 0.050
650
ACR006 Aceruloplasminemia 73 0.050
651
c BTT014 Beta-Thalassemia 72 0.050
652
BRR014 Barrett Esophagus 64 0.050
653
LYM012 Lymphoplasmacytic Lymphoma 61 0.050
654
ERY003 Erythema Multiforme 57 0.050
655
VSC002 Vascular Dementia 57 0.050
656
CYS014 Cystadenocarcinoma 51 0.050
657
PLS016 Plasma Cell Leukemia 46 0.050
658
BNM001 Bone Marrow Cancer 43 0.050
659
HML018 Homologous Wasting Disease 22 0.050
660
MSC157 Muscular Dystrophy, Duchenne Type 71 0.050
661
c ART101 Aortic Valve Disease 2 63 0.050
662
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.050
663
ORP003 Oropharynx Cancer 54 0.050
664
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.050
665
DMY004 Demyelinating Disease 52 0.050
666
KRT001 Keratoconjunctivitis Sicca 50 0.050
667
GST049 Gastrointestinal System Cancer 49 0.050
668
SMT001 Somatization Disorder 48 0.050
669
PRD004 Prediabetes Syndrome 47 0.050
670
LPT006 Leptin Receptor Deficiency 47 0.050
671
AYM001 Ayme-Gripp Syndrome 46 0.050
672
IMM136 Immune System Disease 45 0.050
673
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.050
674
PLY068 Polysubstance Abuse 43 0.050
675
C1N001 C1 Inhibitor Deficiency 40 0.050
676
c HMC039 Hemochromatosis, Type 1 74 0.049
677
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.049
678
YLL002 Yellow Fever 60 0.049
679
P PLY014 Polycystic Kidney Disease 59 0.049
680
BRS051 Breast Disease 58 0.049
681
P GLL020 Gallbladder Disease 58 0.049
682
P PRV006 Pervasive Developmental Disorder 57 0.049
683
PGM001 Pigmented Villonodular Synovitis 56 0.049
684
CRT017 Cartilage Disease 54 0.049
685
HMT008 Hematuria, Benign Familial 53 0.049
686
DRG003 Drug Dependence 47 0.049
687
RFR003 Refractive Error 44 0.049
688
ADR004 Adrenal Cortical Adenocarcinoma 38 0.049
689
P PRC031 Preeclampsia/eclampsia 1 37 0.049
690
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.049
691
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.049
692
P TBR001 Tuberous Sclerosis 70 0.049
693
MLT157 Multiple System Atrophy 1 70 0.049
694
MGK001 Megakaryocytic Leukemia 64 0.049
695
APP008 Appendicitis 60 0.049
696
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.049
697
MYP139 Myopathy, Proximal, and Ophthalmoplegia 53 0.049
698
SRS001 Serous Cystadenocarcinoma 52 0.049
699
P OCY003 Oocyte Maturation Defect 1 45 0.049
700
CMP090 Complement Component 3 Deficiency, Autosomal Recessive 45 0.049
701
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.049
702
ENT001 Enterocele 39 0.049
703
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 52 0.049
704
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.048
705
DCB001 Decubitus Ulcer 60 0.048
706
URN010 Urinary Tract Obstruction 57 0.048
707
NTR018 Neutrophilia, Hereditary 52 0.048
708
CYS009 Cystadenoma 43 0.048
709
DBT002 Diabetic Autonomic Neuropathy 41 0.048
710
PSD088 Pseudobulbar Affect 36 0.048
711
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.048
712
MSN004 Mesenchymal Cell Neoplasm 41 0.048
713
P FCL005 Focal Segmental Glomerulosclerosis 58 0.048
714
P VNS003 Venous Insufficiency 55 0.048
715
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.048
716
DRY001 Dry Eye Syndrome 47 0.048
717
PLS025 Plasmablastic Lymphoma 47 0.048
718
GST071 Gastrointestinal Carcinoma 45 0.048
720
OBS003 Obsessive-Compulsive Personality Disorder 44 0.048
721
ASP008 Aspiration Pneumonitis 42 0.048
722
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.048
723
PPL052 Papillomatosis, Confluent and Reticulated 34 0.048
724
CHR073 Choreatic Disease 52 0.048
725
MYC005 Myocardial Stunning 46 0.048
726
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.048
727
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.048
728
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 49 0.048
729
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.047
730
P LPS002 Liposarcoma 65 0.047
731
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.047
732
P RST001 Restless Legs Syndrome 54 0.047
733
CLR030 Clear Cell Renal Cell Carcinoma 53 0.047
734
MSC190 Muscular Disease 51 0.047
735
AZS001 Azoospermia 50 0.047
736
GYN001 Gynecomastia 49 0.047
737
RDC002 Radiculopathy 48 0.047
738
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 46 0.047
739
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 42 0.047
740
LKP003 Leukoplakia 39 0.047
741
INF021 Infant Gynecomastia 31 0.047
742
RSP007 Respiratory Distress Syndrome, Infant 30 0.047
743
P CLC063 Celiac Disease 1 68 0.047
744
THY111 Thyroid Carcinoma, Familial Medullary 67 0.047
745
SVR097 Severe Cutaneous Adverse Reaction 67 0.047
746
GLL008 Gilles De La Tourette Syndrome 66 0.047
747
EMB004 Embryonal Carcinoma 57 0.047
748
P LCH002 Lichen Planus 54 0.047
749
PRC013 Pericarditis 54 0.047
750
P RTN016 Retinal Degeneration 53 0.047
751
P RNL015 Renal Hypertension 48 0.047
752
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 46 0.047
753
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.047
754
P UTR058 Uterine Anomalies 48 0.047
755
c FML021 Familial Hypercholesterolemia 68 0.047
756
ALC006 Alcoholic Hepatitis 61 0.047
757
IRN001 Iron Deficiency Anemia 58 0.047
758
P HYP726 Hypercalcemia, Infantile, 1 57 0.047
759
PTT009 Pituitary Gland Disease 54 0.047
760
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.047
761
PTH003 Pathologic Nystagmus 51 0.047
762
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.047
763
LRN003 Learning Disability 49 0.047
764
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 49 0.047
765
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.047
766
RTN020 Retinal Vascular Disease 48 0.047
767
CYN002 Cyanosis, Transient Neonatal 45 0.047
768
P END084 Endocrine System Disease 44 0.047
769
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.047
770
P TMP001 Temporal Lobe Epilepsy 50 0.046
771
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.046
772
BLL006 Bullous Pemphigoid 62 0.046
773
SZR001 Sezary's Disease 60 0.046
774
DCT002 Ductal Carcinoma in Situ 59 0.046
775
MCN017 Meconium Ileus 52 0.046
776
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.046
777
HYP025 Hyperphosphatemia 47 0.046
778
c BSL024 Basal Cell Carcinoma 1 47 0.046
779
P OVR046 Ovarian Cyst 45 0.046
780
MYF002 Myofascial Pain Syndrome 42 0.046
781
URG005 Uruguay Faciocardiomusculoskeletal Syndrome 39 0.046
782
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.046
783
P PRD006 Prader-Willi Syndrome 59 0.046
784
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.046
785
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.046
786
P HMN036 Hemangiopericytoma, Malignant 58 0.046
787
P ATN002 Autonomic Nervous System Disease 52 0.046
788
BCK003 Background Diabetic Retinopathy 44 0.046
789
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.046
790
TRG002 Trigeminal Neuralgia 60 0.046
791
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.046
792
P LYM025 Lymphedema 53 0.046
793
TND005 Tendinitis 52 0.046
794
SPL004 Splenic Marginal Zone Lymphoma 51 0.046
795
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.046
796
c DYS119 Dystonia 9 49 0.046
797
STP011 Stapes Ankylosis with Broad Thumbs and Toes 48 0.046
798
SBS004 Substance Dependence 48 0.046
799
PRT035 Peritoneum Cancer 44 0.046
800
P HYP265 Hypotonia 42 0.046
801
P INT260 Intracranial Berry Aneurysm 40 0.046
802
HND015 Hand Skill, Relative 33 0.046
803
ACN019 Acanthamoeba Keratitis 31 0.046
804
ERY066 Erythema Multiforme Major 28 0.046
805
JVN026 Jeavons Syndrome 24 0.046
806
P FML011 Familial Adenomatous Polyposis 72 0.045
807
c GCH015 Gaucher Disease, Type I 70 0.045
808
P GCH001 Gaucher's Disease 64 0.045
809
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.045
810
ADR005 Adrenal Carcinoma 58 0.045
811
c CHR417 Chronic Graft Versus Host Disease 56 0.045
812
ANL018 Analbuminemia 54 0.045
813
CRT016 Carotid Artery Disease 52 0.045
814
NTR046 Neutrophil Migration 50 0.045
815
c BPL002 Bipolar I Disorder 49 0.045
816
IDP033 Idiopathic Edema 43 0.045
817
P CLS010 Cluster Headache 43 0.045
818
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.045
819
BRN049 Brain Tumor, Childhood 29 0.045
820
CRB196 Cerebellar Ataxia, Neuropathy, and Vestibular Areflexia Syndrome 43 0.045
821
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.045
822
GRN037 Granulomatosis with Polyangiitis 64 0.045
823
ART002 Arts Syndrome 63 0.045
824
P CHN012 Chondrosarcoma 56 0.045
825
P ANT006 Antiphospholipid Syndrome 54 0.045
826
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.045
827
ANM046 Anemia, Sideroblastic, and Spinocerebellar Ataxia 53 0.045
828
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.045
829
PLS007 Plasmodium Falciparum Malaria 52 0.045
830
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 51 0.045
831
BRN014 Bronchopneumonia 50 0.045
832
CRT013 Carotid Stenosis 50 0.045
833
RNL077 Renal Fibrosis 47 0.045
834
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.045
835
CNN001 Cannabis Dependence 38 0.045
836
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.045
837
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.045
838
P PRG013 Paraganglioma 52 0.045
839
P CHR012 Chronic Granulomatous Disease 67 0.044
840
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.044
841
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.044
842
TNG003 Tongue Cancer 55 0.044
843
GTR002 Goiter 52 0.044
844
CYS036 Cystinosis, Nephropathic 51 0.044
845
P MGR003 Migraine with Aura 50 0.044
846
P IGN003 Iga Nephropathy 1 49 0.044
847
QDR001 Quadriplegia 48 0.044
848
P MGR001 Migraine Without Aura 48 0.044
849
TND004 Tendinopathy 44 0.044
850
c ORT011 Orthostatic Hypotension 1 43 0.044
851
PRM020 Premenstrual Tension 39 0.044
852
c CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.044
853
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 64 0.044
854
CRN239 Carnitine Deficiency, Systemic Primary 61 0.044
855
GRW007 Growth Hormone Deficiency 43 0.044
856
NSP002 Nasopharyngitis 41 0.044
857
P TMP003 Temporal Arteritis 67 0.044
858
INC002 Inclusion Body Myositis 64 0.044
859
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.044
860
HMC014 Homocysteinemia 53 0.044
861
c BRS049 Breast Carcinoma in Situ 50 0.044
862
CRC014 Carcinoid Tumors, Intestinal 48 0.044
863
NRN001 Neuroendocrine Carcinoma 47 0.044
864
CNG028 Congenital Hypoplastic Anemia 46 0.044
865
c INH020 Inherited Metabolic Disorder 46 0.044
866
CNN002 Cannabis Abuse 44 0.044
867
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.044
868
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.044
869
LRY047 Laryngeal Abductor Paralysis 29 0.044
870
P PRD037 Periodontal Ehlers-Danlos Syndrome 46 0.043
871
ACT088 Acute Insulin Response 41 0.043
872
P CRB088 Cerebral Atrophy 38 0.043
873
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.043
874
P PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 65 0.043
875
c LPM012 Lipomatosis, Multiple 59 0.043
876
P CYS039 Cystic Kidney Disease 54 0.043
877
BRD004 Borderline Personality Disorder 53 0.043
878
P FNC004 Fanconi Syndrome 50 0.043
879
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 50 0.043
880
CLS016 Clostridium Difficile Colitis 46 0.043
881
TNN002 Tinea Unguium 36 0.043
882
c GLC078 Glaucoma 1, Open Angle, F 35 0.043
883
c RST012 Restless Legs Syndrome 1 34 0.043
884
CGN007 Cognitive Function 1, Social 28 0.043
885
FTL073 Fetal Anticonvulsant Syndrome 26 0.043
886
PRS064 Persistent Vegetative State 33 0.043
887
c TBR025 Tuberous Sclerosis 1 76 0.043
888
PRL032 Perlman Syndrome 58 0.043
889
P MTC069 Mitochondrial Disorders 56 0.043
890
THY125 Thyroid Gland Medullary Carcinoma 51 0.043
891
SMT006 Somatoform Disorder 51 0.043
892
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.043
893
ORL013 Oral Lichen Planus 45 0.043
894
c BLR024 Biliary Cirrhosis, Primary, 1 30 0.043
895
P OVR096 Overlap Myositis 27 0.043
896
OVR029 Ovarian Hyperstimulation Syndrome 63 0.042
897
P HYP024 Hypoparathyroidism 55 0.042
898
GRN034 Grange Syndrome 55 0.042
899
CLR003 Clear Cell Adenocarcinoma 50 0.042
900
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.042
901
ORL012 Oral Leukoplakia 39 0.042
902
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.042
903
FTL021 Fetal Macrosomia 42 0.042
904
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.042
905
c PRM196 Premature Ovarian Failure 1 68 0.042
906
MYX005 Myxoid Liposarcoma 66 0.042
907
MSM014 Mismatch Repair Cancer Syndrome 65 0.042
908
P FRD001 Friedreich Ataxia 63 0.042
909
PRM126 Primary Peritoneal Carcinoma 62 0.042
910
c ESS001 Essential Tremor 56 0.042
911
P OPT009 Optic Neuritis 56 0.042
912
P AGN002 Agnosia 54 0.042
913
c LTN004 Late-Onset Retinal Degeneration 52 0.042
914
VLV011 Vulvovaginal Candidiasis 51 0.042
915
LTH001 Lethal Midline Granuloma 43 0.042
916
c ORT012 Orthostatic Hypotension 2 27 0.042
917
P NJM001 Nijmegen Breakage Syndrome 72 0.041
918
c GLY008 Glycogen Storage Disease Ii 70 0.041
919
CLR108 Colorectal Adenoma 64 0.041
920
END041 Endometrial Adenocarcinoma 63 0.041
921
P OVR049 Ovarian Disease 53 0.041
922
P CPL006 Capillary Hemangioma 51 0.041
923
c PRM093 Premature Ovarian Failure 7 47 0.041
924
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 46 0.041
925
CRN020 Coronary Restenosis 39 0.041
926
CHN040 Choanal Atresia and Lymphedema 36 0.041
927
P PRG002 Progesterone-Receptor Positive Breast Cancer 34 0.041
928
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.041
929
BRT037 Brittle Diabetes 25 0.041
930
c HNT004 Huntington Disease-Like 2 49 0.041
931
P FRN006 Frontotemporal Dementia 70 0.041
932
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 61 0.041
933
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.041
934
ACH005 Achalasia 50 0.041
935
P MTR003 Mitral Valve Stenosis 50 0.041
936
c CHR431 Chronic Venous Insufficiency 49 0.041
937
c FCL025 Focal Segmental Glomerulosclerosis 1 47 0.041
938
P GNT008 Giant Cell Tumor 44 0.041
939
GRM004 Germinoma 40 0.041
940
P PRG092 Pregnancy Loss, Recurrent 1 40 0.041
941
ASP030 Aspirin Resistance 40 0.041
942
APR001 Apraxia 51 0.041
943
ADR041 Adrenal Cortical Adenoma 43 0.040
944
P RTT002 Rett Syndrome 80 0.040
945
UND005 Undifferentiated Pleomorphic Sarcoma 66 0.040
946
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.040
947
P NMN002 Niemann-Pick Disease 60 0.040
948
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 57 0.040
949
LYS002 Lysosomal Storage Disease 52 0.040
950
BWN001 Bowen-Conradi Syndrome 51 0.040
951
RTN003 Retinal Ischemia 50 0.040
952
LFT001 Left Bundle Branch Hemiblock 49 0.040
953
ADN009 Adenosquamous Carcinoma 49 0.040
954
MTC005 Mitochondrial Metabolism Disease 48 0.040
955
FCL012 Facial Paralysis 48 0.040
956
c MLG069 Malignant Hypertension 47 0.040
957
OLG001 Oligospermia 45 0.040
958
PHB001 Phobic Disorder 41 0.040
959
ADS004 Aids Dementia Complex 40 0.040
960
ALX002 Alexithymia 39 0.040
961
FRS019 Farsightedness 38 0.040
962
PTT046 Pituitary Hormone Deficiency, Combined, 2 63 0.040
963
c TBR026 Tuberous Sclerosis 2 71 0.040
964
WLS001 Wilson Disease 70 0.040
965
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.040
966
P MCR010 Microcephaly 58 0.040
968
DSM007 Desmoplastic Small Round Cell Tumor 52 0.040
969
VTM002 Vitamin B12 Deficiency 48 0.040
970
CMB081 Combined Immunodeficiency, X-Linked 48 0.040
971
PRP007 Priapism 48 0.040
972
P BRB001 Beriberi 44 0.040
973
THR012 Thoracic Cancer 44 0.040
974
DST006 Diastolic Heart Failure 44 0.040
976
HMN016 Hemangioendothelioma 34 0.040
977
c JVN024 Juvenile Hereditary Hemochromatosis 26 0.040
978
FRN030 Frontotemporal Dementia with Parkinsonism-17 24 0.040
979
c HNT011 Huntington Disease-Like 3 38 0.039
980
c NMN015 Niemann-Pick Disease, Type C1 68 0.039
981
PCK003 Pick Disease of Brain 68 0.039
982
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.039
983
END062 Endometrial Hyperplasia 48 0.039
984
CRN027 Corneal Neovascularization 47 0.039
985
ACN001 Acinar Cell Carcinoma 45 0.039
986
ASP004 Asphyxia Neonatorum 45 0.039
987
MLN073 Melanosis, Neurocutaneous 45 0.039
988
LYM051 Lymphomatoid Granulomatosis 45 0.039
989
HRN003 Heroin Dependence 44 0.039
990
c HRD173 Hereditary Late-Onset Parkinson Disease 43 0.039
991
c PLM150 Pulmonary Alveolar Proteinosis, Acquired 40 0.039
992
P OVR010 Ovarian Brenner Tumor 35 0.039
993
OBS015 Obesity, Hyperphagia, and Developmental Delay 35 0.039
994
HPT085 Hepatitis, Fulminant Viral 32 0.039
995
PGM030 Pigmentation Anomaly of the Skin 25 0.039
996
P MTR004 Maturity-Onset Diabetes of the Young 66 0.039
997
c ACT150 Acute Adrenal Insufficiency 48 0.039
998
PLY012 Polyhydramnios 46 0.039
999
SCH036 Scheie Syndrome 71 0.038
1000
P FRG001 Fragile X Syndrome 68 0.038
1001
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.038
1002
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.038
1003
P ACT105 Acute Mountain Sickness 52 0.038
1004
AMB002 Amblyopia 50 0.038
1005
RCT020 Rectum Adenocarcinoma 46 0.038
1006
AGR002 Agoraphobia 44 0.038
1007
PHY002 Physical Disorder 42 0.038
1008
SPP007 Suppression Amblyopia 39 0.038
1009
P ANG001 Angelman Syndrome 67 0.038
1010
VNH007 Von Hippel-Lindau Syndrome 73 0.038
1011
KND001 Kindler Syndrome 63 0.038
1012
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.038
1013
HYP780 Hypoadrenocorticism, Familial 62 0.038
1014
c PRG126 Progressive Familial Heart Block 58 0.038
1015
PLM102 Palmoplantar Keratoderma, Epidermolytic 56 0.038
1016
SKN022 Skin Squamous Cell Carcinoma 56 0.038
1017
P HYP730 Hypogonadotropic Hypogonadism 53 0.038
1018
FML037 Female Breast Cancer 52 0.038
1019
c MLG054 Malignant Histiocytosis 50 0.038
1020
INP001 Inappropriate Adh Syndrome 49 0.038
1021
PLM136 Palmoplantar Keratoderma, Nonepidermolytic 48 0.038
1022
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.038
1023
LNG111 Lung Non-Squamous Non-Small Cell Carcinoma 34 0.038
1024
LNG039 Lung Squamous Cell Carcinoma 65 0.037
1025
ADR008 Adrenal Adenoma 56 0.037
1026
c HYP768 Hyperlipoproteinemia, Type I 52 0.037
1027
c VRL007 Viral Encephalitis 51 0.037
1028
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 51 0.037
1029
DBT004 Diabetic Polyneuropathy 50 0.037
1030
P PRC019 Precocious Puberty 47 0.037
1031
MMM006 Mammographic Density 41 0.037
1032
ALD013 Aldosterone-Producing Adenoma 38 0.037
1033
ADR022 Adrenomyeloneuropathy 38 0.037
1034
DRG016 Drug Induced Dyskinesia 24 0.037
1035
MDS022 Mediastinitis 47 0.037
1036
P MCP040 Mucopolysaccharidosis-Plus Syndrome 64 0.037
1037
P MCR256 Microphthalmia, Syndromic 9 61 0.037
1038
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.037
1039
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.037
1040
END021 Endomyocardial Fibrosis 48 0.037
1041
DWR001 Dwarfism 44 0.037
1042
MCP033 Mucopolysaccharidoses 38 0.037
1043
RNL001 Renal Artery Obstruction 33 0.037
1044
SPC030 Specific Language Disorder 26 0.037
1045
c DBT093 Diabetes Mellitus, Noninsulin-Dependent, 1 26 0.037
1046
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 67 0.036
1047
BRK012 Broken Heart Syndrome 35 0.036
1048
CHY002 Chylomicron Retention Disease 64 0.036
1049
HYD038 Hydrops Fetalis, Nonimmune 61 0.036
1050
BCL010 B-Cell Expansion with Nfkb and T-Cell Anergy 56 0.036
1051
PRS030 Persistent Fetal Circulation Syndrome 52 0.036
1052
P PST095 Post-Thrombotic Syndrome 50 0.036
1053
INT010 Intracranial Embolism 46 0.036
1054
PRS042 Prostate Disease 44 0.036
1055
XRP001 Xerophthalmia 42 0.036
1056
VLV010 Vulvovaginitis 41 0.036
1057
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.036
1058
CYC005 Cyclothymic Disorder 40 0.036
1059
PNC015 Pancreatic Acinar Cell Adenocarcinoma 40 0.036
1060
PRM024 Primary Angle-Closure Glaucoma 38 0.036
1061
ADR057 Adrenogenital Syndrome 32 0.036
1062
MYC088 Mycobacterium Avium Complex Infections 29 0.036