Search results for Vitamin E

2449 hits were found for Vitamin E

# Family MCID Name MIFTS Score
1
VTM028 Vitamin E, Familial Isolated Deficiency of 52 10.332
2
ATX019 Ataxia with Vitamin E Deficiency 42 8.320
3
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 32 2.954
4
RCK004 Rickets 68 0.957
5
c HPT007 Hepatitis E 53 0.570
6
KRT002 Keratomalacia 47 0.479
7
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.460
8
P HPT021 Hepatitis 67 0.414
9
VTM002 Vitamin B12 Deficiency 48 0.374
10
ATH013 Atherosclerosis Susceptibility 65 0.373
11
P KDN018 Kidney Disease 72 0.353
12
P LVR013 Liver Disease 68 0.352
13
P ALZ034 Alzheimer Disease 88 0.345
14
P HYP069 Hyperparathyroidism 63 0.335
15
P CLR023 Colorectal Cancer 99 0.322
16
P OST002 Osteoporosis 74 0.317
17
P DRR001 Diarrhea 55 0.311
18
c HPT016 Hepatitis B 59 0.303
19
c CHR684 Chronic Kidney Disease 70 0.301
20
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.300
21
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.300
22
P BRS047 Breast Cancer 97 0.297
23
VTM033 Vitamin K Deficiency Bleeding 48 0.296
24
DFC004 Deficiency Anemia 70 0.295
25
P CRN300 Coronary Heart Disease 1 63 0.286
26
c PRC016 Pre-Eclampsia 63 0.281
27
ATM095 Autoimmune Disease 62 0.281
28
P VSC007 Vascular Disease 63 0.275
29
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.272
30
c VRL010 Viral Hepatitis 52 0.271
31
BNR002 Bone Resorption Disease 48 0.265
32
c HYP836 Hypercholesterolemia, Familial, 1 73 0.264
33
c SCN007 Secondary Hyperparathyroidism 51 0.262
34
P THL005 Thalassemia 60 0.262
35
P PRS040 Prostate Cancer 97 0.261
36
HYP781 Hypoascorbemia 51 0.259
37
FTT001 Fatty Liver Disease 61 0.258
38
DRM006 Dermatitis 61 0.258
39
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.254
40
LVR012 Liver Cirrhosis 62 0.253
41
c HPT003 Hepatitis a 62 0.248
42
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.245
43
OST011 Osteomalacia 52 0.241
44
P DRM053 Dermatitis, Atopic 66 0.240
45
P DBT009 Diabetes Mellitus 64 0.236
46
P CRD246 Cardiovascular System Disease 57 0.236
47
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.234
48
LPD008 Lipid Metabolism Disorder 62 0.234
49
IRN002 Iron Metabolism Disease 57 0.233
50
P GST053 Gastric Cancer 83 0.232
51
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.232
52
P HRT032 Heart Disease 75 0.231
53
48X005 48,xyyy 39 0.230
54
HMC014 Homocysteinemia 53 0.229
55
LPP008 Lipoprotein Quantitative Trait Locus 62 0.229
56
P MLT020 Multiple Sclerosis 72 0.228
57
P INF037 Inflammatory Bowel Disease 54 0.225
58
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.224
59
P NRP001 Neuropathy 56 0.224
60
P ADN016 Adenocarcinoma 64 0.220
61
P BND020 Bone Disease 59 0.220
62
END086 End Stage Renal Disease 51 0.220
63
CYS001 Cystic Fibrosis 81 0.218
64
P SKN015 Skin Carcinoma 66 0.216
65
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.216
66
ART140 Arteries, Anomalies of 52 0.215
67
P PSR002 Psoriasis 62 0.214
68
P LNG032 Lung Cancer 98 0.211
69
CRB039 Cerebrovascular Disease 67 0.211
70
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.210
71
CYT002 Cytokine Deficiency 42 0.209
72
CRH001 Crohn's Disease 74 0.209
73
STR067 Stroke, Ischemic 81 0.208
74
PST011 Pustulosis of Palm and Sole 52 0.208
75
P HPT023 Hepatocellular Carcinoma 100 0.205
76
NTR005 Nutritional Deficiency Disease 62 0.205
77
ADN018 Adenoma 59 0.204
78
P RHN004 Rhinitis 57 0.202
79
HLX001 Helix Syndrome 47 0.201
80
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.200
81
AST005 Asthma 76 0.200
82
CHL068 Cholestasis 61 0.200
83
P MYP004 Myopathy 70 0.199
84
ALL026 Allergic Hypersensitivity Disease 62 0.198
85
c HMG003 Hemoglobin E Disease 45 0.198
86
P OVR042 Ovarian Cancer 88 0.197
87
P DMN002 Dementia 66 0.197
88
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.196
89
SKN016 Skin Disease 63 0.195
90
P PNC035 Pancreatic Cancer 84 0.195
91
HMN044 Human Immunodeficiency Virus Type 1 71 0.194
92
NNL006 Non-Alcoholic Steatohepatitis 54 0.194
93
P MYC007 Myocardial Infarction 70 0.194
94
P BLD134 Bladder Cancer 79 0.192
95
c HYP595 Hypertension, Essential 84 0.191
96
CNG034 Congestive Heart Failure 69 0.190
97
P ECL001 Eclampsia 50 0.189
98
P ATR011 Atrial Fibrillation 66 0.188
99
c BTT014 Beta-Thalassemia 74 0.188
100
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.187
101
ISC004 Ischemia 58 0.187
102
c SYS001 Systemic Lupus Erythematosus 86 0.187
103
SQM006 Squamous Cell Carcinoma 60 0.186
105
AGN016 Aging 56 0.185
106
c MCR120 Microvascular Complications of Diabetes 7 47 0.184
107
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.184
108
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.184
109
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.184
110
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.184
111
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.184
112
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.184
113
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.184
114
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.184
115
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.184
116
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.184
117
PRN011 Pernicious Anemia 53 0.184
118
ALL003 Allergic Rhinitis 67 0.184
119
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.183
120
LNG099 Lung Disease 60 0.183
121
IGR001 Ige Responsiveness, Atopic 59 0.182
122
c MCR113 Microvascular Complications of Diabetes 3 52 0.181
123
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.180
124
c MCR130 Microvascular Complications of Diabetes 6 41 0.180
125
c MCR133 Microvascular Complications of Diabetes 4 41 0.180
126
P PRP019 Peripheral Nervous System Disease 58 0.180
127
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.179
128
P LPS004 Lupus Erythematosus 61 0.179
129
OST012 Osteoarthritis 78 0.178
130
P CTR002 Cataract 60 0.177
131
P LKM002 Leukemia 68 0.175
132
DPR016 Depression 63 0.175
133
ULC004 Ulcerative Colitis 73 0.174
134
PYR009 Pyridoxine Deficiency Anemia 34 0.174
135
P PRD008 Periodontitis 64 0.172
136
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.171
137
47X002 47,xyy 49 0.170
138
P PLY011 Polycystic Ovary Syndrome 56 0.169
139
P MSC005 Muscular Dystrophy 66 0.169
140
TXC005 Toxic Shock Syndrome 62 0.169
141
GST033 Gestational Diabetes 61 0.168
142
NRL016 Neural Tube Defects 82 0.167
143
P RHM011 Rheumatoid Arthritis 80 0.166
144
HYP066 Hyperglycemia 61 0.166
145
c HPT001 Hepatitis C 62 0.166
146
P ALP008 Alopecia 54 0.165
147
MSL001 Measles 62 0.164
148
CHL079 Children's Interstitial Lung Disease 26 0.163
149
P GST044 Gastritis 56 0.162
150
c NRF023 Neurofibromatosis, Type Ii 80 0.161
151
P HML002 Hemolytic Anemia 63 0.161
152
CLT003 Colitis 62 0.160
153
DWN001 Down Syndrome 70 0.159
154
c ACT068 Acute Cystitis 63 0.158
155
P ART021 Arteriosclerosis 54 0.158
156
PLM001 Pulmonary Tuberculosis 69 0.158
157
P LYM118 Lymphoma 68 0.157
158
P MLN008 Melanoma 69 0.157
159
P NGH001 Night Blindness 48 0.155
160
MNT002 Mental Depression 58 0.155
161
P HYP750 Hypertriglyceridemia, Familial 62 0.155
162
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.154
163
FDL002 Food Allergy 51 0.153
164
P INF032 Infertility 57 0.152
165
P HYP086 Hypothyroidism 69 0.152
166
DSS008 Disease of Mental Health 58 0.151
167
BCT022 Bacterial Infectious Disease 56 0.151
168
ACQ007 Acquired Immunodeficiency Syndrome 60 0.150
169
P MYL006 Myeloid Leukemia 60 0.150
170
IMM167 Immune Deficiency Disease 78 0.150
171
OST159 Osteogenic Sarcoma 66 0.148
172
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.147
173
P SZR006 Seizure Disorder 56 0.147
174
P LKM062 Leukemia, Acute Lymphoblastic 69 0.147
175
c RHB024 Rhabdomyosarcoma 2 67 0.146
176
PRP027 Peripheral Vascular Disease 71 0.146
177
P NRB001 Neuroblastoma 72 0.146
178
ALL006 Allergic Asthma 56 0.146
179
THR024 Thrombosis 57 0.146
180
P ENC018 Encephalopathy 61 0.146
181
P ENC004 Encephalitis 61 0.145
182
P TRN020 Turner Syndrome 67 0.145
183
P NTR004 Neutropenia 63 0.145
184
c PRM005 Primary Hyperparathyroidism 58 0.145
185
P HRP006 Herpes Simplex 65 0.145
186
P PNM007 Pneumonia 68 0.145
187
THY029 Thyroid Carcinoma 59 0.144
188
MGL001 Megaloblastic Anemia 51 0.144
189
c HPT073 Hepatitis C Virus 72 0.144
190
P PRK057 Parkinson Disease, Late-Onset 78 0.143
191
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.143
192
P ART022 Arthritis 69 0.143
193
PRT037 Pertussis 65 0.143
194
ESP021 Esophageal Cancer 90 0.142
195
ALC007 Alcohol Dependence 66 0.141
196
URM002 Uremia 49 0.141
197
c ACT134 Acute Liver Failure 56 0.141
198
VSL002 Visual Epilepsy 59 0.141
199
TTN003 Tetanus 65 0.141
200
c DBT099 Diabetes Mellitus, Type I 65 0.139
201
P PYL005 Pyelonephritis 56 0.138
202
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.138
203
HMS001 Hemosiderosis 54 0.138
204
c THR092 Thrombophilia Due to Thrombin Defect 73 0.138
205
P HYP098 Hypereosinophilic Syndrome 67 0.138
206
P ATS364 Autism 70 0.137
207
GLC003 Glucose Intolerance 54 0.137
208
KRT001 Keratoconjunctivitis Sicca 49 0.137
209
HYP266 Hypoxia 57 0.136
210
P RTN024 Retinoblastoma 73 0.136
211
c FML008 Familial Retinoblastoma 53 0.136
212
MST005 Mastitis 53 0.135
213
P CLC063 Celiac Disease 1 66 0.135
214
VSC002 Vascular Dementia 57 0.134
215
P NPH012 Nephrotic Syndrome 60 0.134
216
NPH009 Nephrolithiasis 55 0.134
217
P RRH023 Rare Hereditary Hemochromatosis 41 0.134
218
P HYP076 Hyperthyroidism 55 0.134
219
c SML038 Small Cell Cancer of the Lung 65 0.134
220
c ACT075 Acute Myocardial Infarction 57 0.134
221
P MCR115 Microvascular Complications of Diabetes 5 66 0.134
222
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.134
223
ANX010 Anxiety 73 0.133
224
ANG054 Angina Pectoris 66 0.133
225
CLR108 Colorectal Adenoma 64 0.131
226
IRN001 Iron Deficiency Anemia 59 0.131
227
HYP017 Hypophosphatemia 50 0.130
228
P HYP024 Hypoparathyroidism 56 0.130
229
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.129
230
BRN056 Bronchopulmonary Dysplasia 57 0.129
231
FDB001 Foodborne Botulism 55 0.128
232
c LKM061 Leukemia, Acute Myeloid 84 0.128
233
CVD001 Covid-19 44 0.128
234
c ACT071 Acute Kidney Failure 60 0.127
235
P END044 Endometriosis 63 0.127
236
PRT036 Peritonitis 64 0.127
237
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.127
238
P THR014 Thrombocytopenia 67 0.126
239
XRP001 Xerophthalmia 41 0.126
240
CMM005 Common Cold 57 0.126
241
BRN071 Brain Injury 49 0.126
242
P SCK005 Sickle Cell Disease 50 0.126
243
GLL048 Glial Tumor 45 0.126
244
P CHR345 Chronic Pain 44 0.125
245
MLR004 Malaria 81 0.125
246
P HML001 Hemolytic-Uremic Syndrome 53 0.125
247
P GLM045 Glioma 63 0.125
248
c EXD008 Exudative Vitreoretinopathy 1 71 0.125
249
c PCH010 Pachyonychia Congenita 3 44 0.124
250
GST045 Gastroenteritis 59 0.124
251
P LTR001 Lateral Sclerosis 54 0.124
252
c FNC043 Fanconi Anemia, Complementation Group E 62 0.124
253
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.124
254
P URT039 Urticaria 58 0.124
255
P MYC084 Mycobacterium Tuberculosis 1 68 0.123
256
KRT009 Keratosis 51 0.123
257
P SCH015 Schizophrenia 74 0.123
258
TQP001 Taqi Polymorphism 32 0.123
259
TRD006 Tardive Dyskinesia 54 0.122
260
P MNN013 Meningitis 66 0.122
261
ART016 Aortic Aneurysm 69 0.121
262
EYD002 Eye Disease 58 0.121
263
P PLY019 Polyneuropathy 56 0.121
264
ORL015 Oral Squamous Cell Carcinoma 43 0.121
265
ABT001 Abetalipoproteinemia 69 0.121
266
P HMC002 Homocystinuria 53 0.121
267
P HDC001 Headache 57 0.121
268
c MGR028 Migraine with or Without Aura 1 67 0.121
269
SPN186 Spinal Cord Injury 60 0.121
270
P DNG005 Dengue Virus 59 0.121
271
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.120
272
ENT011 Enterocolitis 51 0.120
273
SVR004 Severe Combined Immunodeficiency 73 0.120
274
P INS002 in Situ Carcinoma 53 0.119
275
TRM010 Traumatic Brain Injury 51 0.119
276
P GLM007 Glomerulonephritis 57 0.119
277
c SVR001 Severe Acute Respiratory Syndrome 62 0.119
278
ADL002 Adult Syndrome 70 0.119
279
ATS010 Autosomal Recessive Disease 48 0.119
280
P HYP058 Hypervitaminosis a 48 0.118
281
RTN023 Retinitis 46 0.118
282
NRR001 Neuroretinitis 42 0.118
283
P THY032 Thyroiditis 52 0.118
284
c FML035 Familial Hyperlipidemia 55 0.118
285
BRN024 Bronchitis 68 0.118
286
c ATS007 Autism Spectrum Disorder 67 0.118
287
MYL009 Myelodysplastic Syndrome 70 0.118
288
ALL014 Allergic Encephalomyelitis 38 0.118
289
c PNS012 Paine Syndrome 61 0.117
290
END057 Endometrial Cancer 74 0.117
291
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.117
292
P EXN002 Exanthem 57 0.117
293
P PRM006 Primary Biliary Cirrhosis 62 0.117
294
CHL014 Cholera 59 0.116
295
ORL011 Oral Cancer 60 0.116
296
P PNC044 Pancreatitis 61 0.115
297
PRS045 Prostatic Hypertrophy 53 0.115
298
P EPL164 Epilepsy 71 0.115
299
P RSP003 Respiratory Failure 74 0.115
300
P SRC025 Sarcoidosis 1 70 0.115
301
HLC007 Helicobacter Pylori Infection 59 0.115
302
P BCL017 B-Cell Lymphoma 58 0.115
303
P RTN008 Retinitis Pigmentosa 79 0.115
304
LPT014 Leptin Deficiency or Dysfunction 74 0.115
305
HYP056 Hypoglycemia 66 0.114
306
SPL018 Splenomegaly 48 0.113
307
HMP009 Haemophilus Influenzae 43 0.113
308
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.113
309
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.113
310
PRP030 Purpura 54 0.112
311
c PRM038 Primary Agammaglobulinemia 44 0.112
312
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.112
313
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.112
314
c ATR087 Atrial Standstill 1 75 0.112
315
P ATR005 Atrophic Gastritis 50 0.112
316
MYL069 Myeloma, Multiple 85 0.112
317
DNT012 Dental Caries 53 0.111
318
CRV035 Cervical Cancer 76 0.111
319
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.111
320
CHC001 Chickenpox 60 0.110
321
CNT047 Contact Dermatitis 58 0.110
322
MCS002 Mucositis 56 0.110
323
P GRF003 Graft-Versus-Host Disease 72 0.110
324
P MJR001 Major Depressive Disorder 68 0.110
325
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.110
326
PRS021 Prostatic Adenoma 51 0.109
327
HMG005 Hemoglobinopathy 56 0.109
328
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.109
329
P RCT021 Rectum Cancer 52 0.108
330
PLM031 Poliomyelitis 64 0.108
331
P GRV001 Graves' Disease 55 0.108
332
INS024 Insulin-Like Growth Factor I 79 0.108
333
URL001 Urolithiasis 45 0.108
334
P LPR021 Leprosy 3 69 0.108
335
HNS001 Hansen's Disease 34 0.108
336
HYP025 Hyperphosphatemia 48 0.107
337
STM007 Stomatitis 50 0.107
338
P CNR004 Cone-Rod Dystrophy 2 73 0.107
339
ANR040 Aneurysm 59 0.107
340
c ACT027 Acute Pancreatitis 60 0.107
341
PLM033 Pulmonary Embolism 59 0.106
342
SCK003 Sickle Cell Anemia 74 0.106
343
DYS015 Dysentery 52 0.106
344
HYP081 Hypolipoproteinemia 51 0.106
345
PRS129 Prostatic Hyperplasia, Benign 49 0.106
346
c DWL002 Dowling-Degos Disease 1 58 0.106
347
P ALC033 Alcohol Use Disorder 58 0.106
348
PPT005 Peptic Ulcer Disease 59 0.106
349
GTR002 Goiter 53 0.106
350
P MLN007 Male Infertility 55 0.105
351
CHR178 Chromosomal Triplication 35 0.105
352
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.105
353
P AMY004 Amyloidosis 70 0.105
354
TBC004 Tobacco Addiction 64 0.104
355
PLC008 Placenta Disease 50 0.104
356
c PRS136 Prostate Cancer, Hereditary, 6 33 0.104
357
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.104
358
c PRS130 Prostate Cancer, Hereditary, 8 32 0.104
359
P VSC011 Vasculitis 62 0.103
360
HRW001 Hair Whorl 36 0.103
361
c SCL052 Scleroderma, Familial Progressive 61 0.103
362
c SPN225 Spondyloarthropathy 1 73 0.103
363
BCK006 Back Pain 42 0.103
364
GST050 Gastrointestinal System Disease 56 0.103
365
BLR008 Bilirubin Metabolic Disorder 57 0.103
366
P VSC018 Visceral Steatosis 33 0.103
367
P TRM003 Tremor 54 0.102
368
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.102
369
OCL069 Ocular Motor Apraxia 51 0.102
370
TRN015 Transient Cerebral Ischemia 63 0.102
371
c DRR009 Diarrhea 6 46 0.102
372
P PLM036 Pulmonary Fibrosis 65 0.101
373
PST092 Posttransplant Acute Limbic Encephalitis 29 0.101
374
RNL011 Renal Osteodystrophy 50 0.101
375
INT007 Intermediate Coronary Syndrome 55 0.101
376
LYM133 Lymphoma, Hodgkin, Classic 69 0.101
377
P CYS018 Cystitis 59 0.101
378
CHL123 Chlamydia 59 0.101
379
DPH001 Diphtheria 60 0.101
380
c INF071 Inflammatory Bowel Disease 1 67 0.101
381
LYM019 Lymphosarcoma 46 0.101
382
SBC016 Subacute Delirium 44 0.100
383
P LNG064 Lung Cancer Susceptibility 3 78 0.100
384
CCC002 Coccidiosis 51 0.100
385
P NSP012 Nasopharyngeal Carcinoma 66 0.100
386
P HMR003 Hemorrhagic Disease 53 0.099
387
DBT010 Diabetic Neuropathy 54 0.099
388
TRN018 Transitional Cell Carcinoma 56 0.099
389
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.099
390
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.099
391
c ALP101 Alpha-Thalassemia 62 0.099
392
PRN019 Perinatal Necrotizing Enterocolitis 59 0.099
393
P SLP006 Sleep Apnea 69 0.099
394
P CRD119 Cardiac Arrest 67 0.098
395
P OVR082 Overgrowth Syndrome 50 0.098
396
OVR094 Ovarian Epithelial Cancer 38 0.098
397
CRB037 Cerebral Palsy 69 0.097
398
CNS004 Constipation 58 0.097
399
P SYS005 Systemic Scleroderma 68 0.097
400
PRT038 Protein-Energy Malnutrition 54 0.097
401
P BRB001 Beriberi 46 0.096
402
SKN019 Skin Melanoma 68 0.096
403
INT002 Intermittent Claudication 61 0.096
404
P INF038 Influenza 68 0.096
405
NPH003 Nephrocalcinosis 51 0.096
406
IMP005 Impotence 52 0.096
407
c HYP057 Hypervitaminosis D 42 0.096
408
CRH005 Crohn's Colitis 53 0.096
409
c BRN108 Branchiootic Syndrome 1 62 0.096
410
GLB015 Glioblastoma Multiforme 75 0.096
411
c BSL007 Basal Cell Carcinoma 68 0.095
412
PSY004 Psychotic Disorder 67 0.095
413
c ATM011 Autoimmune Hepatitis 63 0.095
414
P INT068 Intestinal Disease 53 0.095
415
OTT002 Otitis Media 72 0.095
416
PPL052 Papillomatosis, Confluent and Reticulated 33 0.094
417
P SHR001 Short Bowel Syndrome 53 0.094
418
c FML001 Familial Atrial Fibrillation 65 0.094
419
P DFF019 Diffuse Gastric Cancer 45 0.094
420
P OPN001 Open-Angle Glaucoma 49 0.094
421
c FML021 Familial Hypercholesterolemia 66 0.094
422
c GLC092 Glaucoma, Primary Open Angle 62 0.094
423
PLL012 Pollen Allergy 46 0.093
424
c PRD040 Periodontitis, Chronic 53 0.093
425
PNG002 Pain Agnosia 51 0.093
426
ANR007 Anorexia Nervosa 63 0.093
427
PPL022 Papilloma 54 0.092
428
BRN002 Bronchiolitis 59 0.092
429
VRL011 Viral Infectious Disease 61 0.092
430
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.092
431
GST040 Gastric Adenocarcinoma 70 0.092
432
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.092
433
HYP060 Hyperinsulinism 54 0.092
434
PRP080 Peripheral Artery Disease 53 0.092
435
MCR017 Macrocytic Anemia 44 0.091
436
KHL003 Kohlschutter-Tonz Syndrome 65 0.091
437
NWC001 Newcastle Disease 45 0.091
438
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.091
439
BRS099 Breast Ductal Carcinoma 62 0.091
440
P PLM037 Pulmonary Hypertension 67 0.091
441
CLC006 Calcinosis 48 0.090
442
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.090
443
IRR002 Irritable Bowel Syndrome 65 0.090
444
MDD011 Mood Disorder 62 0.090
445
HRP004 Herpes Zoster 60 0.090
446
P HYD006 Hydrocephalus 66 0.090
447
PRT013 Portal Hypertension 59 0.090
448
P BPL003 Bipolar Disorder 56 0.090
449
P MSC003 Muscular Atrophy 52 0.090
450
c ACT073 Acute Leukemia 58 0.089
451
P MVM001 Movement Disease 63 0.089
452
c SVR005 Severe Pre-Eclampsia 50 0.089
453
CRD132 Cardiac Conduction Defect 58 0.089
454
HPT004 Hepatic Coma 45 0.089
455
SPN051 Spondylitis 51 0.088
456
INF009 Inflammatory Spondylopathy 31 0.088
457
BLR001 Biliary Atresia 50 0.088
458
P LKM071 Leukemia, Chronic Lymphocytic 79 0.088
459
P GLL022 Guillain-Barre Syndrome 59 0.088
460
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.088
461
DSS009 Disseminated Intravascular Coagulation 57 0.088
462
HDN002 Head Injury 46 0.088
463
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.087
464
c MJR024 Major Affective Disorder 9 41 0.087
465
c MJR022 Major Affective Disorder 8 38 0.087
466
PRM020 Premenstrual Tension 40 0.087
467
KRT019 Keratitis, Hereditary 65 0.087
468
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.087
469
LKP003 Leukoplakia 39 0.086
470
END040 Endogenous Depression 55 0.086
471
MTB004 Metabolic Acidosis 50 0.086
472
NRT001 Neurotic Disorder 53 0.086
473
HPT019 Hepatic Encephalopathy 60 0.086
474
FBR047 Fibromyalgia 58 0.086
476
P ADL010 Adult Respiratory Distress Syndrome 65 0.085
477
P CNJ013 Conjunctivitis 65 0.085
478
SQM002 Squamous Cell Papilloma 46 0.085
479
P CHL066 Cholangitis 51 0.085
480
P UVT001 Uveitis 57 0.085
481
P ALP009 Alopecia Areata 60 0.084
482
CLF027 Cleft Palate, Isolated 64 0.084
483
PNC129 Pancreatic Adenocarcinoma 68 0.084
484
ETN001 Eating Disorder 60 0.084
485
P SCL018 Scoliosis 60 0.084
486
VCC001 Vaccinia 49 0.084
487
CLN015 Colon Adenocarcinoma 65 0.083
488
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.083
489
CRV045 Cervical Intraepithelial Neoplasia 39 0.083
490
SCH014 Schistosomiasis 57 0.083
491
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.083
492
PNC001 Pancytopenia 54 0.083
493
P FML011 Familial Adenomatous Polyposis 72 0.083
494
P SLP005 Sleep Disorder 59 0.083
495
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.083
496
ART004 Aortic Atherosclerosis 47 0.083
497
LMY002 Leiomyoma 52 0.082
498
BRR014 Barrett Esophagus 65 0.082
499
P MTH008 Methylmalonic Acidemia 50 0.082
500
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.082
501
MMM001 Mammary Paget's Disease 53 0.082
502
P KDN017 Kidney Cancer 60 0.082
503
c GLL024 Gallbladder Disease 1 53 0.082
504
ENT004 Enthesopathy 49 0.082
505
SRC014 Sarcoma 65 0.082
506
P MYC008 Myocarditis 59 0.082
507
CLR109 Colorectal Adenocarcinoma 51 0.082
509
LSH001 Leishmaniasis 63 0.082
510
P KLZ004 Kala-Azar 1 41 0.082
511
P HYP265 Hypotonia 43 0.081
512
P LCH002 Lichen Planus 53 0.081
513
P SPP010 Suppressor of Tumorigenicity 3 51 0.081
514
GNG013 Gingivitis 59 0.081
515
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.081
516
MLK006 Milk Allergy 48 0.081
517
THY030 Thyroid Gland Disease 52 0.081
518
P RTN016 Retinal Degeneration 53 0.080
519
c MCR129 Microvascular Complications of Diabetes 1 66 0.080
520
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.080
521
P PRC031 Preeclampsia/eclampsia 1 38 0.080
522
P FRD001 Friedreich Ataxia 64 0.080
523
P ART023 Arthropathy 62 0.080
524
ACT119 Acute Promyelocytic Leukemia 63 0.080
525
HYP005 Hypokalemia 55 0.080
526
NRT004 Neuritis 52 0.080
527
SPN035 Spindle Cell Sarcoma 53 0.079
528
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.079
529
CHY002 Chylomicron Retention Disease 65 0.079
530
P CND004 Candidiasis 58 0.079
531
LYM027 Lymphopenia 58 0.079
532
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.078
533
OST003 Osteonecrosis 61 0.078
534
STT001 Status Epilepticus 60 0.078
535
c HNT004 Huntington Disease-Like 2 50 0.078
536
DMY004 Demyelinating Disease 52 0.078
537
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.078
538
c DLT002 Dilated Cardiomyopathy 79 0.078
539
c HNT011 Huntington Disease-Like 3 38 0.078
540
CHL065 Cholangiocarcinoma 68 0.078
541
CRN030 Coronary Stenosis 50 0.077
542
GST023 Gastric Ulcer 53 0.077
543
GT001 Gout 64 0.077
544
P PLY018 Polycythemia 56 0.077
545
CMR002 Coumarin Resistance 56 0.077
546
KRT006 Keratoconjunctivitis 53 0.077
547
MSC007 Muscle Hypertrophy 64 0.077
548
49X006 49, Xxxxy Syndrome 41 0.077
549
P ANT006 Antiphospholipid Syndrome 55 0.077
550
SNS003 Sensory Peripheral Neuropathy 54 0.077
551
HSH003 Hashimoto Thyroiditis 62 0.077
552
c PLY105 Polycystic Ovary Syndrome 1 38 0.076
553
INT079 Intrahepatic Cholangiocarcinoma 51 0.076
554
P OPT006 Optic Nerve Disease 60 0.076
555
P BNG032 Benign Mesothelioma 46 0.076
556
CRB004 Cerebral Artery Occlusion 45 0.076
557
DYS073 Dysphagia 50 0.076
558
P ESP024 Esophagitis 62 0.076
559
P ASP006 Aspergillosis 69 0.076
560
P PRP029 Porphyria 62 0.075
561
DFF005 Diffuse Large B-Cell Lymphoma 55 0.075
562
P SYP003 Syphilis 58 0.075
563
CHP002 Chops Syndrome 44 0.075
564
PLM010 Pulmonary Edema 54 0.075
565
P END033 Endocarditis 57 0.075
566
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.075
567
BRS051 Breast Disease 58 0.075
568
CRP001 Carpal Tunnel Syndrome 67 0.074
569
AMN001 Amenorrhea 54 0.074
570
P PLL002 Pellagra 46 0.074
571
c PSR023 Psoriasis 1 52 0.074
572
c CHR682 Chronic Bilirubin Encephalopathy 39 0.074
573
P RTN018 Retinal Disease 53 0.074
574
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.074
575
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.074
577
P ATX030 Ataxia-Telangiectasia 82 0.073
578
TCK001 Tick-Borne Encephalitis 56 0.073
579
TRP009 Triple X Syndrome 42 0.073
580
MYL005 Myelofibrosis 70 0.073
581
c PSR017 Psoriasis 2 53 0.073
582
c ACT135 Acute Graft Versus Host Disease 52 0.073
583
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.073
584
BLL006 Bullous Pemphigoid 62 0.073
585
P APL001 Aplastic Anemia 74 0.073
586
PNC034 Pancreas Disease 48 0.073
587
SPN050 Spinocerebellar Degeneration 42 0.073
588
P SBS003 Substance Abuse 55 0.072
589
P MCR010 Microcephaly 59 0.072
590
c PSR032 Psoriasis 11 47 0.072
591
c PSR028 Psoriasis 7 42 0.072
592
c PSR018 Psoriasis 13 41 0.072
593
PST021 Postpartum Depression 50 0.072
594
P MTR014 Motor Neuron Disease 65 0.072
595
HYP080 Hypogonadism 50 0.072
596
RBF001 Riboflavin Deficiency 49 0.072
597
PHN003 Phenylketonuria 75 0.072
598
LNG031 Lung Benign Neoplasm 51 0.072
599
CNN005 Connective Tissue Disease 68 0.072
600
P NRV007 Nervous System Disease 66 0.072
601
ALL010 Allergic Contact Dermatitis 56 0.072
602
P MYP006 Myopia 55 0.072
603
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.072
604
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.072
605
ATM052 Autoimmune Disease 1 37 0.072
606
c LKM063 Leukemia, Chronic Myeloid 72 0.072
607
P MYS005 Myositis 56 0.072
608
P EPD016 Epidermolysis Bullosa 53 0.072
609
ENC005 Encephalomalacia 43 0.072
610
P AST007 Astrocytoma 51 0.072
611
BLD131 Bladder Urothelial Carcinoma 62 0.071
612
c JVN010 Juvenile Rheumatoid Arthritis 64 0.071
613
TYP007 Typhoid Fever 63 0.071
614
c PYR010 Peyronie's Disease 50 0.071
615
P THR015 Thrombophilia 51 0.071
616
c HMC039 Hemochromatosis, Type 1 74 0.071
617
APH001 Aphthous Stomatitis 57 0.071
618
CHR074 Choriocarcinoma 47 0.071
619
c PNC106 Pancreatic Agenesis 1 51 0.071
620
c DNG003 Dengue Disease 59 0.071
621
c ACT042 Acute Pyelonephritis 46 0.071
622
CHG001 Chagas Disease 66 0.071
623
ERY051 Erythroleukemia, Familial 56 0.070
624
PRS047 Prostatitis 56 0.070
625
KWS001 Kwashiorkor 44 0.070
626
P DDN001 Duodenal Ulcer 52 0.070
627
P SJG008 Sjogren Syndrome 61 0.070
628
CHL067 Cholecystitis 57 0.070
629
CHR066 Chronic Fatigue Syndrome 61 0.070
630
MYF001 Myofibroma 45 0.070
631
c CHL119 Cholangitis, Primary Sclerosing 57 0.070
632
P HYP733 Hypercalciuria, Absorptive, 2 45 0.069
633
P RST001 Restless Legs Syndrome 54 0.069
634
LYM040 Lymphoblastic Lymphoma 54 0.069
635
BNN003 Bone Inflammation Disease 48 0.069
636
P TRC086 Trichohepatoenteric Syndrome 1 62 0.069
637
CRD223 Cardiac Arrhythmia 60 0.069
638
GLS018 Glass Syndrome 57 0.069
639
OST017 Osteomyelitis 64 0.069
640
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.069
641
CLF001 Cleft Lip 53 0.068
642
c GRV008 Graves Disease 1 56 0.068
643
CHL004 Cholelithiasis 49 0.068
644
P OBS001 Obstructive Jaundice 50 0.068
645
ORL012 Oral Leukoplakia 39 0.068
646
YLL002 Yellow Fever 61 0.068
647
WST005 West Nile Virus 54 0.068
648
NWB001 Newborn Respiratory Distress Syndrome 58 0.068
649
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.068
650
P BRS044 Breast Adenocarcinoma 59 0.068
651
CRT013 Carotid Stenosis 50 0.068
652
c MCR112 Microvascular Complications of Diabetes 2 41 0.068
653
APN008 Apnea, Obstructive Sleep 64 0.068
654
P BRN022 Bronchiectasis 59 0.068
655
P FBR017 Fibrosarcoma 56 0.068
656
EPD015 Epidemic Typhus 45 0.068
657
BRC012 Brucellosis 64 0.068
658
ORL013 Oral Lichen Planus 45 0.068
659
RDN001 Reading Disorder 40 0.068
660
TLN003 Telangiectasis 52 0.067
661
CLR030 Clear Cell Renal Cell Carcinoma 53 0.067
662
RNL077 Renal Fibrosis 47 0.067
663
c JVN061 Juvenile Arthritis 60 0.067
664
BCT002 Bacterial Vaginosis 53 0.067
665
BRN004 Brain Edema 56 0.067
666
c ACT004 Acute Diarrhea 39 0.067
667
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.067
668
HYP014 Hyperuricemia 52 0.067
669
GST092 Gastroesophageal Reflux 67 0.067
670
ALC006 Alcoholic Hepatitis 61 0.067
671
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.067
672
EXC002 Exocrine Pancreatic Insufficiency 42 0.066
673
PRS063 Paresthesia 41 0.066
674
IGG001 Iga Glomerulonephritis 48 0.066
675
ANX004 Anoxia 40 0.066
676
ACN002 Acanthosis Nigricans 60 0.066
677
HMR039 Hemorrhage, Intracerebral 57 0.066
678
P PMP001 Pemphigus 54 0.066
679
P PSD015 Pseudohypoparathyroidism 56 0.066
680
THR004 Thrombocytosis 51 0.066
681
P LRY044 Larynx Cancer 55 0.066
682
PSR001 Psoriatic Arthritis 61 0.066
683
DCT002 Ductal Carcinoma in Situ 59 0.066
684
PLY001 Polycythemia Vera 69 0.066
685
PGM030 Pigmentation Anomaly of the Skin 26 0.065
686
ARG004 Argyria 27 0.065
687
P DYS154 Dystonia 65 0.065
688
DRY001 Dry Eye Syndrome 47 0.065
689
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.065
690
P LCT001 Lactic Acidosis 51 0.065
691
BRN028 Brain Cancer 74 0.065
692
GRD001 Giardiasis 45 0.065
693
PRD004 Prediabetes Syndrome 47 0.065
694
THR013 Thoracic Outlet Syndrome 54 0.065
695
P KRT007 Keratoconus 50 0.065
696
PRM329 Premature Aging 35 0.065
697
NRM005 Neuromuscular Disease 64 0.064
698
BCT004 Bacteriuria 49 0.064
699
HYP043 Hyperandrogenism 48 0.064
700
c HMG029 Hemoglobin Se Disease 39 0.064
701
P RBL001 Rubella 59 0.064
702
P ICH004 Ichthyosis 54 0.064
703
P HNT016 Huntington Disease 72 0.064
704
PRT029 Parathyroid Adenoma 50 0.064
705
MCR011 Microinvasive Gastric Cancer 43 0.064
706
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.064
707
c INF145 Infantile Liver Failure Syndrome 1 50 0.064
708
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.063
709
RTN020 Retinal Vascular Disease 46 0.063
710
HRT012 Heart Valve Disease 53 0.063
711
STT009 Sutton Disease 2 30 0.063
712
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.063
713
P SNS001 Sensorineural Hearing Loss 60 0.063
714
SYN007 Synovitis 54 0.063
715
PLC002 Plica Syndrome 36 0.063
716
VSC003 Visceral Leishmaniasis 55 0.063
717
IDP070 Idiopathic Scoliosis 42 0.063
718
PLY150 Polykaryocytosis Inducer 31 0.063
719
GLS007 Glossitis 47 0.063
720
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.062
721
HRP008 Herpes Simiae 25 0.062
722
P ACT008 Actinic Keratosis 53 0.062
723
c MST023 Mesothelioma, Malignant 57 0.062
724
CMP010 Complex Regional Pain Syndrome 58 0.062
725
PLC007 Placental Abruption 48 0.062
726
MSC157 Muscular Dystrophy, Duchenne Type 72 0.061
727
P ANR048 Aniridia 1 63 0.061
728
P SCL009 Sclerosing Cholangitis 48 0.061
729
c ART101 Aortic Valve Disease 2 65 0.061
730
P HMP007 Hemophilia 51 0.061
731
P ALL008 Allergic Bronchopulmonary Aspergillosis 53 0.061
732
MCR013 Microphthalmia 57 0.061
733
P HYP061 Hypertrophic Cardiomyopathy 70 0.061
734
P PTN014 Patent Ductus Arteriosus 1 60 0.061
735
P OCL013 Oculodentodigital Dysplasia 69 0.061
736
ASC010 Ascaris Lumbricoides Infection 50 0.061
737
P FRN006 Frontotemporal Dementia 68 0.061
738
P MTR003 Mitral Valve Stenosis 50 0.061
739
c HPT015 Hepatitis D 49 0.061
740
P ANG001 Angelman Syndrome 69 0.060
741
P FTL001 Fetal Alcohol Syndrome 57 0.060
742
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.060
743
PST028 Post-Traumatic Stress Disorder 58 0.060
744
c DPH024 Diaphragmatic Hernia, Congenital 63 0.060
745
MYC006 Mycosis Fungoides 66 0.060
746
P PRS038 Personality Disorder 65 0.060
747
PPL049 Papillon-Lefevre Syndrome 65 0.060
748
PPL001 Papillary Adenoma 44 0.060
749
IMM162 Immunoglobulin E Concentration, Serum 28 0.060
750
SCH003 Schizophreniform Disorder 56 0.059
751
ATN005 Autonomic Dysfunction 46 0.059
752
CYT018 Cytochrome P450 2d6 Variant 27 0.059
753
MCL006 Macular Retinal Edema 55 0.059
754
PMP006 Pemphigus Vulgaris, Familial 57 0.059
755
ACT084 Acute Stress Disorder 47 0.059
756
c LTN004 Late-Onset Retinal Degeneration 59 0.059
757
P NRF002 Neurofibromatosis 56 0.059
758
ASC001 Ascaridiasis 35 0.059
759
DGN001 Degenerative Disc Disease 48 0.059
760
INT303 Intracranial Hypertension, Idiopathic 57 0.059
761
VRC005 Varicose Veins 60 0.058
762
HRN029 Hearing Loss, Noise-Induced 37 0.058
763
VRC001 Varicocele 49 0.058
764
P SCL057 Scoliosis, Isolated 1 41 0.058
765
c ANM038 Anemia, Autoimmune Hemolytic 62 0.058
766
P MMB011 Membranous Nephropathy 50 0.058
767
P MYS003 Myasthenia Gravis 68 0.058
768
P PLY014 Polycystic Kidney Disease 62 0.058
769
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.058
770
ATX010 Ataxia Neuropathy Spectrum 34 0.058
771
ACT064 Acute Necrotizing Encephalitis 33 0.058
772
BLD137 Blood Group--Ahonen 16 0.058
773
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.058
774
INF034 Infective Endocarditis 53 0.057
775
c PNC108 Pancreatitis, Hereditary 70 0.057
776
SCH012 Schizoaffective Disorder 50 0.057
777
LRY018 Laryngeal Squamous Cell Carcinoma 44 0.057
778
LMY014 Leiomyoma, Uterine 56 0.057
779
P GLL018 Gallbladder Cancer 57 0.057
780
ALL009 Allergic Conjunctivitis 50 0.057
781
c SPR086 Spermatogenic Failure 3 44 0.057
782
PLS007 Plasmodium Falciparum Malaria 52 0.057
783
SDD001 Sudden Infant Death Syndrome 61 0.057
784
LWC001 Low Compliance Bladder 43 0.057
785
KRT013 Keratolytic Winter Erythema 46 0.057
786
c DRM054 Dermatitis, Atopic, 2 44 0.057
787
P DRM010 Dermatomyositis 61 0.056
788
P PTY003 Pityriasis Rubra Pilaris 58 0.056
789
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.056
790
PRT082 Preterm Premature Rupture of the Membranes 54 0.056
791
HYP068 Hyperostosis 48 0.056
792
P STR020 Strabismus 55 0.056
793
MCH006 Mechanical Strabismus 42 0.056
794
AYM001 Ayme-Gripp Syndrome 57 0.056
795
SPP011 Suppression of Tumorigenicity 12 59 0.056
796
P HYP838 Hyperlipidemia, Familial Combined, 3 56 0.056
797
THR016 Thrombophlebitis 51 0.056
798
P CTN015 Cutaneous T Cell Lymphoma 49 0.056
799
ACR007 Acromegaly 71 0.055
800
P TMP001 Temporal Lobe Epilepsy 50 0.055
801
P INT143 Interstitial Cystitis 61 0.055
802
NRN004 Neuroendocrine Tumor 55 0.055
803
c MLG068 Malignant Glioma 46 0.055
804
SPS057 Spasticity 45 0.055
805
c CHR417 Chronic Graft Versus Host Disease 57 0.055
806
LMB062 Limb Ischemia 55 0.055
807
LBL001 Lobular Neoplasia 56 0.055
808
SPR126 Superior Semicircular Canal Dehiscence 40 0.055
809
c INH020 Inherited Metabolic Disorder 47 0.055
810
PLS009 Plasma Cell Neoplasm 51 0.055
811
c XLN227 X-Linked Chondrodysplasia Punctata 1 36 0.055
812
P PRG092 Pregnancy Loss, Recurrent 1 40 0.055
813
RFR010 Refractory Anemia 48 0.055
814
c MNN043 Meningioma, Familial 74 0.055
815
LYM021 Lymphadenitis 57 0.055
816
P TXP001 Toxoplasmosis 60 0.055
817
PLG002 Plague 63 0.054
818
DCB001 Decubitus Ulcer 61 0.054
819
MTH009 Mouth Disease 56 0.054
820
PRP016 Paraplegia 52 0.054
821
P MMP001 Mumps 58 0.054
822
P CHR012 Chronic Granulomatous Disease 67 0.054
823
HYD002 Hydronephrosis 60 0.054
824
P FCL005 Focal Segmental Glomerulosclerosis 57 0.054
825
BRK010 Burkitt Lymphoma 67 0.054
826
SGN002 Signet Ring Cell Adenocarcinoma 45 0.054
827
AMN003 Amnestic Disorder 54 0.054
828
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.054
829
c RST012 Restless Legs Syndrome 1 34 0.054
830
ANV001 Anovulation 47 0.054
831
TRP004 Tropical Sprue 41 0.054
832
OST004 Osteitis Fibrosa 41 0.054
833
RHM001 Rheumatic Fever 60 0.054
834
HLL004 Hellp Syndrome 54 0.054
835
AMB002 Amblyopia 49 0.054
836
SPP007 Suppression Amblyopia 39 0.054
837
c BCT007 Bacterial Meningitis 55 0.054
838
c SYS043 Systemic Lupus Erythematosus 1 38 0.054
839
ADN011 Adenoid Cystic Carcinoma 70 0.053
840
c LKM005 Leukemia, T-Cell, Chronic 34 0.053
841
CLL003 Cellulitis 54 0.053
842
P RNL007 Renal Tubular Acidosis 51 0.053
843
P AGG001 Aggressive Periodontitis 50 0.053
844
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.053
845
P MJR007 Major Affective Disorder 1 43 0.053
846
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.053
847
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.053
848
P TCD001 Tic Disorder 53 0.053
849
SXL003 Sexual Disorder 47 0.053
850
GST020 Gastric Antral Vascular Ectasia 41 0.053
851
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.053
852
KPS004 Kaposi Sarcoma 75 0.053
853
SFT003 Soft Tissue Sarcoma 56 0.053
854
MCR018 Microcytic Anemia 47 0.053
855
P GND004 Gonadal Dysgenesis 48 0.053
856
PPL002 Papillary Carcinoma 47 0.053
857
PLY100 Polyploidy 40 0.053
858
P ANG015 Angioedema 57 0.052
859
ORL004 Oral Submucous Fibrosis 55 0.052
861
P CRB088 Cerebral Atrophy 37 0.052
863
CHR073 Choreatic Disease 52 0.052
864
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.052
865
P OCY003 Oocyte Maturation Defect 1 45 0.052
866
CRT017 Cartilage Disease 54 0.052
867
ATN004 Autonomic Neuropathy 45 0.052
868
FCL012 Facial Paralysis 46 0.052
869
IDP091 Idiopathic Nephrotic Syndrome 42 0.052
870
END041 Endometrial Adenocarcinoma 63 0.052
871
DNG002 Dengue Hemorrhagic Fever 60 0.052
872
ONC002 Onchocerciasis 52 0.052
873
CHR005 Chorioamnionitis 51 0.052
874
P MTH007 Methemoglobinemia 46 0.052
875
SPS003 Spastic Diplegia 51 0.052
876
ACT017 Acute Chest Syndrome 51 0.052
877
P TRT010 Teratoma 52 0.052
878
HMG002 Hemoglobinuria 50 0.052
879
CMM004 Common Variable Immunodeficiency 68 0.052
880
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.052
881
CRT016 Carotid Artery Disease 52 0.052
882
PRM003 Premature Ejaculation 44 0.052
883
IDP073 Idiopathic Hypercalciuria 43 0.052
884
SYN036 Syncope 45 0.052
885
RFR003 Refractive Error 43 0.052
886
c FNC027 Fanconi Anemia, Complementation Group a 81 0.052
887
DMP001 Dumping Syndrome 44 0.052
888
P OST001 Osteopetrosis 70 0.051
889
P PSD087 Pseudoxanthoma Elasticum 65 0.051
890
P OPT009 Optic Neuritis 57 0.051
891
BCK003 Background Diabetic Retinopathy 46 0.051
892
DMN031 Dementia, Lewy Body 65 0.051
893
NTR046 Neutrophil Migration 50 0.051
894
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.051
895
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.051
896
MNN042 Meningioma, Radiation-Induced 62 0.051
897
CLF004 Cleft Lip/palate 54 0.051
898
APP008 Appendicitis 61 0.051
899
HPT022 Hepatoblastoma 56 0.051
900
INC002 Inclusion Body Myositis 58 0.051
901
WLL004 Wallerian Degeneration 39 0.051
902
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 28 0.051
903
ANG005 Anogenital Venereal Wart 55 0.051
904
XNT003 Xanthomatosis 49 0.051
905
AVN001 Avian Influenza 59 0.051
906
GRW007 Growth Hormone Deficiency 46 0.050
907
RSC001 Rosacea 54 0.050
908
P PLY041 Polymyositis 57 0.050
909
P MNC007 Monocytic Leukemia 53 0.050
910
URT010 Ureteral Obstruction 45 0.050
911
TNS005 Tonsillitis 57 0.050
912
RST023 Resting Heart Rate, Variation in 41 0.050
913
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.050
914
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.050
915
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.050
916
CYT008 Cytomegalovirus Infection 57 0.050
917
SPN021 Spinal Meningioma 50 0.050
918
SCR001 Secretory Meningioma 41 0.050
919
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
920
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.050
921
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.050
922
MMM006 Mammographic Density 41 0.050
923
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.050
924
GLM044 Glomerular Disease 37 0.049
925
P SBR004 Seborrheic Dermatitis 45 0.049
927
FCT007 Factor Vii Deficiency 67 0.049
928
P PHC003 Pheochromocytoma 71 0.049
929
MYL031 Myeloproliferative Neoplasm 66 0.049
930
KRN002 Kearns-Sayre Syndrome 63 0.049
931
SKN013 Skin Benign Neoplasm 51 0.049
932
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.049
933
GRN017 Granulocytopenia 44 0.049
934
KWS002 Kawasaki Disease 65 0.049
935
EMB004 Embryonal Carcinoma 56 0.049
936
ART002 Arts Syndrome 64 0.049
937
PNT038 Peanut Allergy 45 0.049
938
FNG017 Fungal Infectious Disease 53 0.049
939
SYS003 Systolic Heart Failure 49 0.049
940
CYN002 Cyanosis, Transient Neonatal 45 0.049
941
RBS001 Rabies 58 0.048
942
NRN001 Neuroendocrine Carcinoma 47 0.048
943
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.048
944
HYP457 Hypertrophic Scars 42 0.048
945
c ART115 Aortic Valve Disease 1 75 0.048
946
ACT058 Active Peptic Ulcer Disease 55 0.048
947
BHR001 Behr Syndrome 51 0.048
948
c MJR008 Major Affective Disorder 2 35 0.048
949
c MJR023 Major Affective Disorder 7 33 0.048
950
c MJR003 Major Affective Disorder 6 33 0.048
951
c MJR006 Major Affective Disorder 5 33 0.048
952
c MJR004 Major Affective Disorder 4 28 0.048
953
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.048
954
BRT054 Brittle Bone Disorder 72 0.048
955
PRT058 Pure Autonomic Failure 59 0.048
956
INT075 Intracranial Hypertension 53 0.048
957
P GLM040 Glioma Susceptibility 1 81 0.048
958
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.048
959
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.048
960
ILS001 Ileus 51 0.048
961
PRR019 Perioral Myoclonia with Absences 27 0.048
962
GST019 Gastrointestinal Stromal Tumor 78 0.048
963
NNT012 Neonatal Jaundice 53 0.048
964
P CRN024 Corneal Disease 44 0.048
965
SPS019 Spastic Paraparesis 38 0.048
966
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.048
967
ORL005 Oral Candidiasis 56 0.048
968
VLV047 Volvulus of Midgut 49 0.048
969
OBS002 Obsessive-Compulsive Disorder 68 0.048
970
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.048
971
GLC008 Glucose Metabolism Disease 40 0.048
972
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.048
973
WLS001 Wilson Disease 71 0.048
974
ING001 Inguinal Hernia 60 0.048
975
ADR040 Adrenal Gland Pheochromocytoma 46 0.048
976
CRY004 Cryoglobulinemia 48 0.048
977
P LYM033 Lymphoproliferative Syndrome 59 0.048
978
ERY003 Erythema Multiforme 58 0.048
979
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.047
980
P MTC069 Mitochondrial Disorders 56 0.047
981
AZS001 Azoospermia 50 0.047
982
THR123 Thrombotic Microangiopathy 36 0.047
983
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.047
984
PNM008 Pneumothorax 56 0.047
985
P FML018 Familial Mediterranean Fever 73 0.047
986
WST001 West Syndrome 61 0.047
987
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.047
988
AND002 Androgen Insensitivity Syndrome 66 0.047
989
P AGM001 Agammaglobulinemia 65 0.047
990
P CLL015 Collagen Disease 47 0.047
991
P THY023 Thymoma 65 0.047
992
P ANP001 Anaplastic Large Cell Lymphoma 58 0.047
993
c THY107 Thymoma, Familial 52 0.047
994
c BCT013 Bacterial Pneumonia 48 0.047
995
AMN006 Aminoaciduria 38 0.047
996
ACT003 Acute Kidney Tubular Necrosis 45 0.047
997
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.046
998
CHL056 Cheilitis 48 0.046
999
P END046 Endometritis 49 0.046
1000
GST010 Gestational Trophoblastic Neoplasm 46 0.046
1001
P CHN044 Chondrodysplasia Punctata Syndrome 43 0.046
1002
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.046
1003
HML018 Homologous Wasting Disease 22 0.046
1004
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.046
1005
CHR100 Chronic Ulcer of Skin 55 0.046
1006
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.046
1007
P SDR003 Sideroblastic Anemia 49 0.046
1008
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.046
1009
SNL007 Senile Cataract 42 0.046
1010
KLD004 Keloid Disorder 40 0.046
1011
c MTR002 Mitral Valve Insufficiency 48 0.046
1012
OST016 Osteochondrosis 53 0.046
1013
TXC002 Toxic Encephalopathy 53 0.046
1014
P BLD051 Blood Coagulation Disease 46 0.046
1015
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.046
1016
PRG080 Progressive Non-Infectious Anterior Vertebral Fusion 35 0.046
1017
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.046
1018
FND002 Fundus Dystrophy 55 0.046
1019
P RTN022 Retinal Vein Occlusion 53 0.046
1020
CLN045 Colonic Benign Neoplasm 46 0.046
1021
c OVR114 Ovarian Cancer 1 38 0.046
1022
APH002 Aphasia 57 0.046
1023
DSR002 Disorders of Intracellular Cobalamin Metabolism 31 0.046
1024
INT066 Interstitial Lung Disease 60 0.046
1025
RHM028 Rheumatic Heart Disease 53 0.046
1026
LRN003 Learning Disability 49 0.046
1027
c INF023 Inflammatory Breast Carcinoma 50 0.046
1028
PFF001 Pfeiffer Syndrome 79 0.045
1029
HMT002 Hematologic Cancer 62 0.045
1030
EXF001 Exfoliation Syndrome 56 0.045
1031
HMP005 Hemiplegia 55 0.045
1032
TST044 Testicular Torsion 47 0.045
1033
IRR003 Irritant Dermatitis 49 0.045
1034
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 60 0.045
1035
GSG001 Gas Gangrene 53 0.045
1036
P MRC003 Mercury Poisoning 48 0.045
1037
KSH001 Keshan Disease 34 0.045
1038
MNN009 Meningoencephalitis 49 0.045
1039
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.045
1040
ALC009 Alcoholic Liver Cirrhosis 53 0.045
1041
P SML001 Small Cell Carcinoma 52 0.045
1042
APR001 Apraxia 52 0.045
1043
NSS002 Neisseria Meningitidis Infection 47 0.045
1044
MLN073 Melanosis, Neurocutaneous 45 0.045
1045
RFL001 Reflex Sympathetic Dystrophy 54 0.045
1046
ART001 Arterial Tortuosity Syndrome 66 0.045
1047
ADR007 Adrenoleukodystrophy 75 0.045
1048
P LBR014 Leber Congenital Amaurosis 4 56 0.045
1049
ACR041 Acromelic Frontonasal Dysostosis 52 0.045
1050
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.045
1051
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.045
1052
P PLM034 Pulmonary Emphysema 55 0.045
1053
CRT072 Creutzfeldt-Jakob Disease 70 0.045
1054
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.045
1055
MCP006 Mucoepidermoid Carcinoma 50 0.045
1056
INS001 Insulinoma 60 0.045
1057
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.045
1058
RSP021 Respiratory Allergy 45 0.045
1059
P GCH001 Gaucher's Disease 63 0.044
1060
DBT006 Diabetic Macular Edema 48 0.044
1061
KHN001 Kuhnt-Junius Degeneration 47 0.044
1062
P LCT002 Lactose Intolerance 53 0.044
1063
DBT002 Diabetic Autonomic Neuropathy 41 0.044
1064
FLR002 Filariasis 55 0.044
1065
PTT037 Pituitary Tumors 44 0.044
1066
MDD018 Middle East Respiratory Syndrome 43 0.044
1067
LPT006 Leptin Receptor Deficiency 48 0.044
1068
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.044
1069
ADR022 Adrenomyeloneuropathy 38 0.044
1070
CYS010 Cystinosis 59 0.044
1071
PRD002 Periodic Limb Movement Disorder 33 0.044
1072
c HNT010 Huntington Disease-Like 1 53 0.044
1073
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.044
1074
P HYP040 Hypospadias 51 0.044
1075
P MYT002 Myotonic Dystrophy 49 0.044
1076
HMP001 Hemopericardium 48 0.044
1077
CRB086 Cerebral Aneurysms 40 0.044
1078
c WLM018 Wilms Tumor 5 61 0.044
1079
P PRC012 Pericardial Effusion 51 0.044
1080
TST014 Testicular Cancer 46 0.044