Search results for Vitamin E

1362 hits were found for Vitamin E

# Family MCID Name MIFTS Score
1
VTM028 Vitamin E, Familial Isolated Deficiency of 52 9.847
2
ATX019 Ataxia with Vitamin E Deficiency 31 8.721
3
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 22 2.941
4
P HPT021 Hepatitis 76 0.518
5
c HPT007 Hepatitis E 53 0.363
6
P ALZ034 Alzheimer Disease 87 0.349
7
AGN016 Aging 64 0.342
8
P BRS047 Breast Cancer 100 0.330
9
PRS047 Prostatitis 60 0.309
10
P PRS040 Prostate Cancer 90 0.290
11
END072 Endotheliitis 45 0.284
12
VTM002 Vitamin B12 Deficiency 47 0.278
13
P DBT009 Diabetes Mellitus 64 0.273
14
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.258
15
P LVR013 Liver Disease 75 0.247
16
P CLR023 Colorectal Cancer 97 0.247
17
P HRT032 Heart Disease 74 0.246
18
P KDN018 Kidney Disease 68 0.246
19
RCK004 Rickets 62 0.241
20
DMN002 Dementia 68 0.236
21
GST053 Gastric Cancer 77 0.231
22
AST005 Asthma 82 0.228
23
P LNG032 Lung Cancer 98 0.227
24
P CRN018 Coronary Artery Anomaly 68 0.226
25
ART140 Arteries, Anomalies of 65 0.225
26
P ADN016 Adenocarcinoma 70 0.220
27
c HPT016 Hepatitis B 67 0.217
28
P THL005 Thalassemia 64 0.210
29
P PNC044 Pancreatitis 64 0.208
30
c CRN300 Coronary Heart Disease 1 64 0.208
31
P OST002 Osteoporosis 76 0.208
32
ISC004 Ischemia 65 0.207
33
SQM006 Squamous Cell Carcinoma 59 0.206
34
ACQ007 Acquired Immunodeficiency Syndrome 63 0.204
35
URN009 Urinary System Disease 55 0.199
36
GST050 Gastrointestinal System Disease 64 0.199
37
VRL011 Viral Infectious Disease 63 0.199
38
P MLT020 Multiple Sclerosis 78 0.199
39
P ART022 Arthritis 76 0.198
40
P MYC007 Myocardial Infarction 79 0.195
41
DPR016 Depression 72 0.195
42
TYP041 Type I 56 0.195
43
c HPT003 Hepatitis a 61 0.193
44
GLC008 Glucose Metabolism Disease 52 0.189
45
VSC007 Vascular Disease 68 0.187
46
P LKM002 Leukemia 72 0.186
47
P HPT023 Hepatocellular Carcinoma 94 0.185
48
c CHR089 Chronic Kidney Failure 72 0.183
49
DRM006 Dermatitis 66 0.179
50
c HPT001 Hepatitis C 71 0.177
51
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.176
52
P THY032 Thyroiditis 55 0.175
53
LNG099 Lung Disease 67 0.175
54
BND020 Bone Disease 62 0.174
55
FTT001 Fatty Liver Disease 60 0.170
56
ATM095 Autoimmune Disease 64 0.167
57
ISC006 Ischemic Heart Disease 72 0.167
58
P NRP001 Neuropathy 63 0.166
59
P PNC035 Pancreatic Cancer 79 0.164
60
SKN016 Skin Disease 66 0.163
61
P OVR042 Ovarian Cancer 81 0.163
62
PSY004 Psychotic Disorder 71 0.162
63
BNF002 Bone Fracture 55 0.161
64
P INT068 Intestinal Disease 64 0.160
65
P ART021 Arteriosclerosis 60 0.160
66
P RHM011 Rheumatoid Arthritis 80 0.160
67
c SML038 Small Cell Cancer of the Lung 68 0.159
68
MLN008 Melanoma 62 0.159
69
SKN027 Skin Conditions 48 0.158
70
P LYM118 Lymphoma 70 0.158
71
ADN018 Adenoma 63 0.156
72
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.156
73
IMM136 Immune System Disease 56 0.156
74
c BTT014 Beta-Thalassemia 69 0.155
75
P DRM053 Dermatitis, Atopic 67 0.154
76
KRT002 Keratomalacia 54 0.154
77
P HYP069 Hyperparathyroidism 58 0.154
78
NNL002 Nonalcoholic Steatohepatitis 50 0.153
79
P INF038 Influenza 76 0.153
80
THR024 Thrombosis 61 0.152
81
HMN044 Human Immunodeficiency Virus Type 1 70 0.152
82
CRB039 Cerebrovascular Disease 67 0.152
83
MNT002 Mental Depression 57 0.152
84
CRB009 Cerebritis 41 0.151
85
P DRR001 Diarrhea 56 0.149
86
RSP006 Respiratory System Disease 63 0.148
87
P NRV007 Nervous System Disease 73 0.148
88
c HPT073 Hepatitis C Virus 72 0.148
89
P ESP024 Esophagitis 63 0.144
90
NRN002 Neuronitis 41 0.143
91
P LPS004 Lupus Erythematosus 68 0.141
92
RTN023 Retinitis 50 0.141
93
P ENC018 Encephalopathy 62 0.141
94
P PNM007 Pneumonia 69 0.141
95
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.140
96
ANR040 Aneurysm 60 0.139
97
P VSC018 Visceral Steatosis 37 0.139
98
P SCH015 Schizophrenia 69 0.139
99
ANX010 Anxiety 72 0.137
100
P INF032 Infertility 59 0.137
101
P INF037 Inflammatory Bowel Disease 53 0.137
102
CNG034 Congestive Heart Failure 72 0.135
103
P PSR002 Psoriasis 65 0.134
104
HYP266 Hypoxia 61 0.134
105
HYP060 Hyperinsulinism 56 0.133
106
SPS003 Spastic Diplegia 54 0.132
107
GST045 Gastroenteritis 64 0.131
108
CRH001 Crohn's Disease 78 0.129
109
P ATR011 Atrial Fibrillation 68 0.128
110
c SYS001 Systemic Lupus Erythematosus 86 0.128
111
P RHN004 Rhinitis 61 0.127
112
c PRC016 Pre-Eclampsia 59 0.126
113
c MCL042 Macular Degeneration, Age-Related, 1 84 0.126
114
BRN106 Burns 56 0.125
115
c CNT035 Central Nervous System Disease 63 0.125
116
P PRD008 Periodontitis 66 0.125
117
CLN019 Colonic Disease 54 0.125
118
PLC008 Placenta Disease 61 0.125
119
PRP019 Peripheral Nervous System Disease 60 0.125
120
P ECL001 Eclampsia 57 0.124
121
c VRL010 Viral Hepatitis 59 0.124
122
P CRV039 Cervicitis 49 0.124
123
CYS001 Cystic Fibrosis 84 0.123
124
P BLD134 Bladder Cancer 69 0.122
125
CNN005 Connective Tissue Disease 64 0.122
126
BRS051 Breast Disease 66 0.122
127
CLT003 Colitis 62 0.122
128
RHM027 Rheumatic Disease 62 0.120
129
OST012 Osteoarthritis 82 0.120
130
ENT004 Enthesopathy 46 0.119
131
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.119
132
P MYP004 Myopathy 68 0.118
133
END030 End Stage Renal Failure 56 0.117
134
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.117
135
RTN018 Retinal Disease 56 0.116
136
BRN038 Bronchial Disease 56 0.116
137
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.116
138
P ART023 Arthropathy 67 0.114
139
P CLL015 Collagen Disease 52 0.114
140
LVR012 Liver Cirrhosis 68 0.114
141
JNT002 Joint Disorders 59 0.113
142
CLR108 Colorectal Adenoma 60 0.113
143
SLP005 Sleep Disorder 59 0.112
144
NRM005 Neuromuscular Disease 60 0.112
145
MDD011 Mood Disorder 63 0.112
146
ABT001 Abetalipoproteinemia 63 0.112
147
VTM001 Vitamin K Deficiency Hemorrhagic Disease 40 0.112
148
MLR004 Malaria 83 0.111
149
ALL003 Allergic Rhinitis 67 0.110
150
P NGH001 Night Blindness 51 0.110
151
NRT004 Neuritis 57 0.107
152
DMY004 Demyelinating Disease 57 0.107
153
PNC034 Pancreas Disease 57 0.107
154
c OVR114 Ovarian Cancer 1 62 0.107
155
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.107
156
ULC004 Ulcerative Colitis 72 0.106
157
HDC001 Headache 59 0.106
158
P PLY011 Polycystic Ovary Syndrome 63 0.105
159
PRS042 Prostate Disease 44 0.105
160
PLM001 Pulmonary Tuberculosis 71 0.105
161
c ACT075 Acute Myocardial Infarction 58 0.104
162
P TRC086 Trichohepatoenteric Syndrome 1 54 0.103
163
P EPL164 Epilepsy 69 0.103
164
GLC003 Glucose Intolerance 56 0.102
165
P ENC004 Encephalitis 65 0.102
166
RCT017 Rectal Disease 39 0.102
167
P ALP008 Alopecia 58 0.102
168
BRN071 Brain Injury 53 0.101
169
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.101
170
P EXN002 Exanthem 61 0.101
171
c PRM005 Primary Hyperparathyroidism 59 0.100
172
HYP066 Hyperglycemia 63 0.099
173
P NPH012 Nephrotic Syndrome 59 0.099
174
FDL002 Food Allergy 55 0.099
175
MCS002 Mucositis 60 0.099
176
NRL016 Neural Tube Defects 78 0.098
177
P BLD051 Blood Coagulation Disease 50 0.098
178
TRN018 Transitional Cell Carcinoma 61 0.098
179
HMT018 Hematopoietic Stem Cell Transplantation 57 0.098
180
P GST044 Gastritis 60 0.098
181
P HMR003 Hemorrhagic Disease 60 0.098
182
LYM019 Lymphosarcoma 55 0.098
183
c TRC078 Trichohepatoenteric Syndrome 2 34 0.097
184
LPD008 Lipid Metabolism Disorder 58 0.097
185
P RTN016 Retinal Degeneration 54 0.097
186
P GLM045 Glioma 54 0.096
187
P NSP012 Nasopharyngeal Carcinoma 67 0.096
188
P PRK057 Parkinson Disease, Late-Onset 76 0.096
189
ILT001 Ileitis 56 0.096
190
c INF071 Inflammatory Bowel Disease 1 53 0.096
191
STM007 Stomatitis 52 0.096
192
P MSC033 Muscle Disorders 52 0.096
193
MSC004 Muscle Tissue Disease 39 0.096
194
HPD002 Hepadnavirus Infection 25 0.096
195
P LYM026 Lymphoblastic Leukemia 64 0.095
196
ORL015 Oral Squamous Cell Carcinoma 45 0.095
197
NSP002 Nasopharyngitis 46 0.095
198
ANG054 Angina Pectoris 66 0.095
199
PDT001 Pediatric Lymphoma 45 0.094
200
c ADL001 Adult Lymphoma 39 0.094
201
STR067 Stroke, Ischemic 82 0.093
202
CHL061 Childhood Leukemia 55 0.093
203
OVR063 Overnutrition 53 0.093
204
IRN002 Iron Metabolism Disease 55 0.093
205
HMG005 Hemoglobinopathy 53 0.093
206
P MYL006 Myeloid Leukemia 68 0.093
207
VSC002 Vascular Dementia 58 0.092
208
CLC006 Calcinosis 51 0.092
209
PRT036 Peritonitis 66 0.092
210
P ATS364 Autism 70 0.092
211
CHL068 Cholestasis 60 0.091
212
P HYP086 Hypothyroidism 64 0.091
213
P NRB001 Neuroblastoma 72 0.091
214
c LKM062 Leukemia, Acute Lymphoblastic 69 0.091
215
ART016 Aortic Aneurysm 69 0.091
216
CMM005 Common Cold 61 0.090
217
P CTR002 Cataract 60 0.090
218
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.090
219
c GLC092 Glaucoma, Primary Open Angle 57 0.090
220
HYP781 Hypoascorbemia 42 0.090
221
P LRY019 Laryngitis 56 0.089
222
SCK003 Sickle Cell Anemia 72 0.089
223
LYM024 Lymphatic System Disease 54 0.089
224
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.089
225
P RTN008 Retinitis Pigmentosa 81 0.089
226
MTH009 Mouth Disease 63 0.089
227
P END044 Endometriosis 64 0.089
228
SRC014 Sarcoma 68 0.088
229
INS024 Insulin-Like Growth Factor I 82 0.088
230
P MNN013 Meningitis 70 0.088
231
BRN080 Brain Ischemia 44 0.088
232
P MGL001 Megaloblastic Anemia 51 0.088
233
PLM033 Pulmonary Embolism 62 0.088
234
GND003 Gonadal Disease 46 0.088
235
URM002 Uremia 52 0.087
236
TRD006 Tardive Dyskinesia 59 0.087
237
HRP008 Herpes Simiae 16 0.087
238
NPH009 Nephrolithiasis 55 0.087
239
PRP080 Peripheral Artery Disease 53 0.086
240
c PRC031 Preeclampsia/eclampsia 1 39 0.086
241
PRT030 Parathyroid Gland Disease 49 0.086
242
P GRV001 Graves' Disease 61 0.086
243
c ART101 Aortic Valve Disease 2 73 0.086
244
P MJR001 Major Depressive Disorder 65 0.086
245
DWN001 Down Syndrome 69 0.085
246
c ACT071 Acute Kidney Failure 54 0.085
247
GNG013 Gingivitis 63 0.085
248
BRC012 Brucellosis 70 0.085
249
c HYP595 Hypertension, Essential 76 0.085
250
MYL009 Myelodysplastic Syndrome 70 0.085
251
P RTN024 Retinoblastoma 70 0.084
252
P OVR049 Ovarian Disease 59 0.084
253
CNS004 Constipation 56 0.084
254
IRN001 Iron Deficiency Anemia 55 0.084
255
c ACT210 Acute Respiratory Distress Syndrome 61 0.084
256
c LKM061 Leukemia, Acute Myeloid 80 0.083
257
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.083
258
P CRV035 Cervical Cancer 69 0.083
259
P ADL010 Adult Respiratory Distress Syndrome 66 0.083
260
P HML002 Hemolytic Anemia 62 0.083
261
URN022 Urinary Tract Infections, Recurrent 29 0.082
262
PRT038 Protein-Energy Malnutrition 51 0.082
263
P CHR084 Chromosomal Disease 40 0.082
264
MYL069 Myeloma, Multiple 83 0.082
265
ESP021 Esophageal Cancer 77 0.082
266
PRD004 Prediabetes Syndrome 45 0.082
267
SPN186 Spinal Cord Injury 68 0.082
268
ANX004 Anoxia 49 0.082
269
P HMC002 Homocystinuria 50 0.082
270
P OVR046 Ovarian Cyst 50 0.082
271
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.082
272
SCK005 Sickle Cell Disease 54 0.082
273
P OPN001 Open-Angle Glaucoma 51 0.081
274
P CLC063 Celiac Disease 1 71 0.081
275
NRN004 Neuroendocrine Tumor 58 0.081
276
c PNS012 Paine Syndrome 62 0.081
277
DFC004 Deficiency Anemia 61 0.081
278
HLC007 Helicobacter Pylori Infection 63 0.081
279
BRN056 Bronchopulmonary Dysplasia 60 0.080
280
P LTR001 Lateral Sclerosis 58 0.080
281
MVM001 Movement Disease 60 0.080
282
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.079
283
PRP027 Peripheral Vascular Disease 70 0.079
284
VSC008 Vascular Hemostatic Disease 36 0.079
285
LYM067 Lymphoid Leukemia 44 0.079
286
NWB001 Newborn Respiratory Distress Syndrome 52 0.079
287
RSP007 Respiratory Distress Syndrome, Infant 34 0.079
288
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.078
289
P CNJ013 Conjunctivitis 63 0.078
290
CHY002 Chylomicron Retention Disease 52 0.078
291
c PYR010 Peyronie's Disease 53 0.078
292
VSC011 Vasculitis 65 0.077
293
P XRD010 Xeroderma Pigmentosum, Variant Type 68 0.077
294
URT039 Urticaria 60 0.077
295
P SLP006 Sleep Apnea 66 0.077
296
P ACT074 Acute Lymphocytic Leukemia 59 0.077
297
PRM236 Primary Biliary Cholangitis 55 0.077
298
THY030 Thyroid Gland Disease 51 0.077
299
c PLY105 Polycystic Ovary Syndrome 1 30 0.077
300
MSL001 Measles 64 0.077
301
BSL008 Basal Ganglia Disease 46 0.076
302
TRN015 Transient Cerebral Ischemia 56 0.076
303
P ALP009 Alopecia Areata 63 0.076
304
P PRM006 Primary Biliary Cirrhosis 53 0.076
305
c MTR002 Mitral Valve Insufficiency 46 0.076
306
c BLR024 Biliary Cirrhosis, Primary, 1 36 0.076
307
c THR092 Thrombophilia Due to Thrombin Defect 67 0.076
308
P THR014 Thrombocytopenia 64 0.076
309
PNG002 Pain Agnosia 42 0.076
310
DYS073 Dysphagia 46 0.075
311
BRN028 Brain Cancer 72 0.075
312
SKN019 Skin Melanoma 69 0.075
313
P MSC003 Muscular Atrophy 54 0.075
314
BCK006 Back Pain 44 0.075
315
CHL065 Cholangiocarcinoma 63 0.075
316
HMS001 Hemosiderosis 51 0.075
317
TRM010 Traumatic Brain Injury 55 0.075
318
P BCL006 B-Cell Lymphomas 65 0.074
319
DYS015 Dysentery 43 0.074
320
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.074
321
P AMY004 Amyloidosis 68 0.074
322
HYP056 Hypoglycemia 62 0.074
323
c CHR579 Chiari Malformation Type Ii 45 0.074
324
P SNS014 Sinusitis 62 0.074
325
BLD131 Bladder Urothelial Carcinoma 60 0.073
326
P LNG064 Lung Cancer Susceptibility 3 76 0.073
327
ORL011 Oral Cancer 59 0.073
328
PRD007 Periodontal Disease 64 0.073
329
TTH006 Tooth Disease 53 0.073
330
GST040 Gastric Adenocarcinoma 63 0.073
331
MCR017 Macrocytic Anemia 45 0.073
332
c ALP101 Alpha-Thalassemia 59 0.073
333
c MCR113 Microvascular Complications of Diabetes 3 52 0.073
334
c MCR130 Microvascular Complications of Diabetes 6 40 0.073
335
c MCR120 Microvascular Complications of Diabetes 7 37 0.073
336
c MCR133 Microvascular Complications of Diabetes 4 35 0.073
337
PRP030 Purpura 61 0.073
338
GST033 Gestational Diabetes 60 0.073
339
EWN002 Ewing's Family of Tumors 56 0.073
340
RST001 Restless Legs Syndrome 52 0.073
341
MNS002 Mini Stroke 23 0.073
342
APN008 Apnea, Obstructive Sleep 67 0.073
343
P MYS005 Myositis 63 0.072
344
GT001 Gout 57 0.072
345
PNC041 Pancreatic Ductal Adenocarcinoma 52 0.072
346
P MYP006 Myopia 56 0.072
347
P CHR345 Chronic Pain 51 0.072
348
P ATR005 Atrophic Gastritis 48 0.072
349
P HYP607 Hypercholesterolemia, Familial 79 0.071
350
SPP011 Suppression of Tumorigenicity 12 61 0.071
351
P MCR115 Microvascular Complications of Diabetes 5 71 0.071
352
PRS063 Paresthesia 37 0.071
353
P BPL003 Bipolar Disorder 59 0.071
354
c LKM071 Leukemia, Chronic Lymphocytic 75 0.071
355
c LKM004 Leukemia, B-Cell, Chronic 36 0.071
356
TTN003 Tetanus 64 0.070
357
P SZR006 Seizure Disorder 56 0.070
358
END057 Endometrial Cancer 65 0.070
359
P GRF003 Graft-Versus-Host Disease 71 0.070
360
P ANR048 Aniridia 1 65 0.070
361
MST005 Mastitis 55 0.070
362
INT007 Intermediate Coronary Syndrome 52 0.070
363
P HYP058 Hypervitaminosis a 47 0.070
364
ENT011 Enterocolitis 54 0.070
365
BRN002 Bronchiolitis 59 0.069
366
P BRN120 Bronchus Cancer 49 0.069
367
THY028 Thyroid Cancer 66 0.069
368
c BSL007 Basal Cell Carcinoma 64 0.069
369
KRT009 Keratosis 53 0.069
370
BLD137 Blood Group--Ahonen 17 0.069
371
P GLM007 Glomerulonephritis 61 0.069
372
GLB002 Glioblastoma 72 0.068
373
BRN024 Bronchitis 66 0.068
374
GST092 Gastroesophageal Reflux 64 0.068
375
PLC007 Placental Abruption 50 0.068
376
c ACT134 Acute Liver Failure 52 0.068
377
LRG015 Large Intestine Adenoma 17 0.068
378
P PYL005 Pyelonephritis 56 0.068
379
NSD001 Nose Disease 50 0.067
380
CRT016 Carotid Artery Disease 57 0.067
381
P UVT001 Uveitis 60 0.067
382
c INS002 in Situ Carcinoma 56 0.067
383
OPT006 Optic Nerve Disease 57 0.067
384
SPN041 Spinal Cord Disease 51 0.067
385
P CMR001 Camurati-Engelmann Disease 61 0.067
386
c EXD008 Exudative Vitreoretinopathy 1 69 0.067
387
P HYP076 Hyperthyroidism 56 0.067
388
GNR004 Generalized Anxiety Disorder 53 0.067
389
OVR094 Ovarian Epithelial Cancer 38 0.067
390
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.067
391
SPN050 Spinocerebellar Degeneration 40 0.067
392
c ATS007 Autism Spectrum Disorder 61 0.066
393
P SHR001 Short Bowel Syndrome 51 0.066
394
APH001 Aphthous Stomatitis 63 0.066
395
P PSD015 Pseudohypoparathyroidism 50 0.066
396
OTT002 Otitis Media 66 0.066
397
P NTR004 Neutropenia 60 0.066
398
HDN002 Head Injury 47 0.066
399
P AST007 Astrocytoma 51 0.066
400
P ACT008 Actinic Keratosis 54 0.066
401
SCH012 Schizoaffective Disorder 54 0.066
402
P HYP024 Hypoparathyroidism 54 0.066
403
P SCL057 Scoliosis, Isolated 1 40 0.065
404
SPN051 Spondylitis 55 0.065
405
SWL001 Swallowing Disorders 36 0.065
406
TXC002 Toxic Encephalopathy 55 0.065
407
OST097 Osteoporotic Fracture 41 0.065
408
APL001 Aplastic Anemia 73 0.065
409
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.064
410
PHT003 Phototoxic Dermatitis 40 0.064
411
HMC014 Homocysteinemia 48 0.064
412
FND002 Fundus Dystrophy 49 0.064
413
P ASP006 Aspergillosis 65 0.064
414
KRT006 Keratoconjunctivitis 55 0.064
415
ERY003 Erythema Multiforme 60 0.064
416
P SML001 Small Cell Carcinoma 58 0.064
417
P KDN017 Kidney Cancer 58 0.064
418
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.064
419
P THR015 Thrombophilia 57 0.064
420
ART004 Aortic Atherosclerosis 47 0.063
421
PNC033 Pancreas Adenocarcinoma 64 0.063
422
PST021 Postpartum Depression 53 0.063
423
GRN017 Granulocytopenia 43 0.063
424
ENC005 Encephalomalacia 36 0.063
425
P HML001 Hemolytic-Uremic Syndrome 50 0.063
426
c SCL052 Scleroderma, Familial Progressive 64 0.063
427
ALC006 Alcoholic Hepatitis 62 0.063
428
MTR014 Motor Neuron Disease 61 0.062
429
P PLY019 Polyneuropathy 57 0.062
430
CRD119 Cardiac Arrest 62 0.062
431
MRB003 Morbid Obesity 60 0.062
432
P RSP003 Respiratory Failure 70 0.062
433
MLN007 Male Infertility 53 0.062
434
c ACT027 Acute Pancreatitis 60 0.062
435
P CYS018 Cystitis 56 0.062
436
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.062
437
PHR003 Pharyngitis 59 0.061
438
P ALC004 Alcohol Abuse 63 0.061
439
HRW001 Hair Whorl 32 0.061
440
P ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.061
441
P HYP614 Hyperlipidemia, Familial Combined 56 0.061
442
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.061
443
DRY001 Dry Eye Syndrome 51 0.061
444
c SPN225 Spondyloarthropathy 1 71 0.061
445
BLD044 Bladder Disease 55 0.061
446
EPD070 Epidermoid Cysts 47 0.061
447
P ATS366 Autism X-Linked 2 43 0.061
448
CLR109 Colorectal Adenocarcinoma 53 0.061
449
P PLM037 Pulmonary Hypertension 75 0.061
450
CRB037 Cerebral Palsy 71 0.061
451
P FRD012 Friedreich Ataxia 1 64 0.061
452
CLN015 Colon Adenocarcinoma 53 0.061
453
HYP080 Hypogonadism 51 0.061
454
STT009 Sutton Disease 2 29 0.061
455
P HRP006 Herpes Simplex 69 0.060
456
CNR004 Cone-Rod Dystrophy 2 67 0.060
457
P TRM003 Tremor 54 0.060
458
SPL018 Splenomegaly 46 0.060
459
BLL006 Bullous Pemphigoid 63 0.060
460
BRS099 Breast Ductal Carcinoma 56 0.060
461
P TRN020 Turner Syndrome 68 0.060
462
P MSC005 Muscular Dystrophy 66 0.060
463
MCL006 Macular Retinal Edema 51 0.060
464
ACR006 Aceruloplasminemia 73 0.060
465
SPP010 Suppressor of Tumorigenicity 3 54 0.060
466
DBT010 Diabetic Neuropathy 59 0.060
467
TRP004 Tropical Sprue 37 0.060
468
PLS007 Plasmodium Falciparum Malaria 57 0.060
469
FXF002 Fox-Fordyce Disease 40 0.059
470
ALL006 Allergic Asthma 59 0.059
471
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.059
472
PRS129 Prostatic Hyperplasia, Benign 48 0.059
473
P AST055 Asthma-Related Traits 1 30 0.059
474
DFF005 Diffuse Large B-Cell Lymphoma 56 0.059
475
PRV006 Pervasive Developmental Disorder 55 0.058
476
LMY002 Leiomyoma 57 0.058
477
MTC005 Mitochondrial Metabolism Disease 44 0.058
478
SPS057 Spasticity 41 0.058
479
BLR001 Biliary Atresia 57 0.058
480
CCC002 Coccidiosis 52 0.058
481
SCH014 Schistosomiasis 62 0.058
482
P LRY044 Larynx Cancer 60 0.058
483
INT002 Intermittent Claudication 61 0.057
484
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.057
485
BRN004 Brain Edema 55 0.057
486
MLK006 Milk Allergy 45 0.057
487
GNG011 Gingival Disease 49 0.057
488
HRT012 Heart Valve Disease 44 0.057
489
ALC007 Alcohol Dependence 65 0.057
490
PRN019 Perinatal Necrotizing Enterocolitis 56 0.057
491
HMP009 Haemophilus Influenzae 49 0.056
492
CLR030 Clear Cell Renal Cell Carcinoma 49 0.056
493
P CHL066 Cholangitis 52 0.056
494
c LBR014 Leber Congenital Amaurosis 4 49 0.056
495
TCD001 Tic Disorder 54 0.056
496
CRT013 Carotid Stenosis 52 0.056
497
LNS003 Lens Disease 39 0.056
498
FBR047 Fibromyalgia 57 0.056
499
EPD016 Epidermolysis Bullosa 56 0.056
500
HYD046 Hydatidiform Mole, Recurrent, 1 52 0.056
501
GST010 Gestational Trophoblastic Neoplasm 44 0.056
502
LYM133 Lymphoma, Hodgkin, Classic 71 0.055
503
BLD053 Blood Platelet Disease 55 0.055
504
c CRP023 Carpenter Syndrome 1 54 0.055
505
EXC002 Exocrine Pancreatic Insufficiency 43 0.055
506
CYT008 Cytomegalovirus Infection 56 0.055
507
ADN011 Adenoid Cystic Carcinoma 65 0.055
508
P MYL005 Myelofibrosis 70 0.055
509
PTT009 Pituitary Gland Disease 56 0.054
510
CHR074 Choriocarcinoma 47 0.054
511
KWS001 Kwashiorkor 42 0.054
512
SPN369 Spinal Disease 42 0.054
513
PNL013 Penile Disease 37 0.054
514
c ATM011 Autoimmune Hepatitis 62 0.054
515
c CHL119 Cholangitis, Primary Sclerosing 59 0.054
516
CRV002 Cervix Uteri Carcinoma in Situ 47 0.054
517
c ACT042 Acute Pyelonephritis 46 0.054
518
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 63 0.054
519
KRT001 Keratoconjunctivitis Sicca 62 0.054
520
P RTN022 Retinal Vein Occlusion 52 0.054
521
CHR008 Choroiditis 46 0.054
522
MYL031 Myeloproliferative Neoplasm 63 0.054
523
HRP004 Herpes Zoster 60 0.054
524
P DBT005 Diabetes Insipidus 54 0.054
525
PLS009 Plasma Cell Neoplasm 51 0.054
526
INT303 Intracranial Hypertension, Idiopathic 50 0.054
527
INC002 Inclusion Body Myositis 63 0.054
528
SQM013 Squamous Cell Carcinoma, Head and Neck 76 0.054
529
P PMP001 Pemphigus 54 0.054
530
AMN002 Amino Acid Metabolic Disorder 47 0.054
531
P FRN006 Frontotemporal Dementia 67 0.053
532
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.053
533
P INT001 Intrahepatic Cholestasis 60 0.053
534
P FRG001 Fragile X Syndrome 69 0.053
535
OST003 Osteonecrosis 63 0.053
536
ACT119 Acute Promyelocytic Leukemia 59 0.053
537
PPL022 Papilloma 58 0.053
538
STM006 Stomach Disease 52 0.053
539
CHR005 Chorioamnionitis 51 0.053
540
RFR010 Refractory Anemia 49 0.053
541
CRN024 Corneal Disease 47 0.053
542
ATM052 Autoimmune Disease 1 34 0.053
543
VSC009 Vascular Skin Disease 20 0.053
544
MYM001 Myoma 55 0.053
545
INT074 Intracranial Arteriosclerosis 15 0.053
546
P DYS154 Dystonia 64 0.053
547
P HMR012 Hemorrhagic Fever 57 0.053
548
AMN001 Amenorrhea 55 0.053
549
ORP003 Oropharynx Cancer 51 0.053
550
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.053
551
CRV045 Cervical Intraepithelial Neoplasia 43 0.053
552
BCT002 Bacterial Vaginosis 54 0.053
553
CRD223 Cardiac Arrhythmia 54 0.053
554
P PTY003 Pityriasis Rubra Pilaris 50 0.053
555
GLS007 Glossitis 45 0.053
556
AMN012 Aminoacidopathies 24 0.053
557
P MMB011 Membranous Nephropathy 57 0.052
558
EPD046 Epididymitis 36 0.052
559
SRC027 Sarcoma, Synovial 56 0.052
560
c CHR417 Chronic Graft Versus Host Disease 64 0.052
561
LMY014 Leiomyoma, Uterine 53 0.052
562
SNS003 Sensory Peripheral Neuropathy 53 0.052
563
P HRD018 Hair Disease 51 0.052
564
SYN036 Syncope 47 0.052
565
CRN031 Cranial Nerve Disease 45 0.052
566
LKP003 Leukoplakia 42 0.052
567
TTH004 Tethered Spinal Cord Syndrome 38 0.052
568
FNT004 Fainting 36 0.052
569
c ACT073 Acute Leukemia 60 0.052
570
P PMP005 Pemphigus Vulgaris 55 0.052
571
YLL001 Yellow Nail Syndrome 52 0.052
572
BCT004 Bacteriuria 47 0.052
573
c LKM056 Leukemia, Chronic Lymphocytic 2 41 0.052
574
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.052
575
GTR002 Goiter 52 0.051
576
HML018 Homologous Wasting Disease 18 0.051
577
INB001 Inborn Amino Acid Metabolism Disorder 16 0.051
578
SFT003 Soft Tissue Sarcoma 58 0.051
579
P HYP014 Hyperuricemia 55 0.051
580
HYP081 Hypolipoproteinemia 48 0.051
581
HYP457 Hypertrophic Scars 47 0.051
582
P HYP724 Hyperlipoproteinemia, Type Iii 58 0.051
583
BLR006 Biliary Tract Disease 54 0.051
584
TNS005 Tonsillitis 60 0.051
585
THR016 Thrombophlebitis 52 0.051
586
GLB015 Glioblastoma Multiforme 60 0.050
587
OPT009 Optic Neuritis 53 0.050
588
MYF002 Myofascial Pain Syndrome 43 0.050
589
CRV040 Cervix Carcinoma 53 0.050
590
OCL006 Ocular Hypertension 53 0.050
591
DBT008 Diabetic Angiopathy 47 0.050
592
P CNN004 Connective Tissue Cancer 45 0.050
593
HYP189 Hypoadrenalism 43 0.050
594
CHL123 Chlamydia 64 0.050
595
P DNG005 Dengue Virus 55 0.050
596
PRT037 Pertussis 68 0.050
597
P PLM034 Pulmonary Emphysema 58 0.050
598
CHL004 Cholelithiasis 50 0.050
599
DFF036 Differentiated Thyroid Carcinoma 49 0.050
600
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.050
601
c ACT004 Acute Diarrhea 40 0.050
602
c MLG068 Malignant Glioma 38 0.050
603
CNT047 Contact Dermatitis 63 0.050
604
P CTN015 Cutaneous T Cell Lymphoma 55 0.050
605
IGG001 Iga Glomerulonephritis 55 0.050
606
P PYR039 Peyronie Disease 43 0.050
607
LRY017 Laryngeal Disease 38 0.050
608
P PTT006 Pituitary Adenoma 52 0.050
609
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.050
610
P CHN044 Chondrodysplasia Punctata Syndrome 44 0.050
611
PRT029 Parathyroid Adenoma 49 0.049
612
P PNC025 Panic Disorder 55 0.049
613
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.049
614
P UTR058 Uterine Anomalies 59 0.049
615
PLM031 Poliomyelitis 58 0.049
616
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 55 0.049
617
SPC010 Speech and Communication Disorders 52 0.049
618
ADR012 Adrenal Gland Disease 51 0.049
619
P HYP087 Hypotrichosis 48 0.049
620
ORL012 Oral Leukoplakia 47 0.049
621
HYP064 Hypogonadotropism 40 0.049
622
MYF001 Myofibroma 39 0.049
623
LSH001 Leishmaniasis 70 0.048
624
c JVN010 Juvenile Rheumatoid Arthritis 69 0.048
625
P GLL020 Gallbladder Disease 64 0.048
626
P ANG015 Angioedema 57 0.048
627
PNM001 Pneumocystosis 55 0.048
628
HLL004 Hellp Syndrome 52 0.048
629
P HMG032 Hemoglobin H Disease 52 0.048
630
KLD001 Keloids 49 0.048
631
DBT006 Diabetic Macular Edema 48 0.048
632
ASP004 Asphyxia Neonatorum 43 0.048
633
WRN005 Wrinkles 40 0.048
634
P PLY018 Polycythemia 58 0.048
635
CLL003 Cellulitis 53 0.048
636
PRT082 Preterm Premature Rupture of the Membranes 52 0.048
637
P GRM010 Germ Cells Tumors 36 0.048
638
HVY002 Heavy Metal Poisoning 21 0.048
639
NRV006 Nervous System Cancer 60 0.048
640
PRP036 Peripheral T-Cell Lymphoma 56 0.048
641
BRR014 Barrett Esophagus 63 0.048
642
P AGG001 Aggressive Periodontitis 54 0.048
643
P PRM002 Primary Hyperoxaluria 53 0.048
644
RFR003 Refractive Error 44 0.048
645
PRX001 Peroxisomal Disease 44 0.048
646
ADR010 Adrenal Cortical Hypofunction 40 0.048
647
PRX034 Peroxisome Disorders 27 0.048
648
ALP046 Alport Syndrome, X-Linked 75 0.047
649
P CRB088 Cerebral Atrophy 39 0.047
650
c PMP006 Pemphigus Vulgaris, Familial 28 0.047
651
AST054 Australia Antigen 27 0.047
652
P END033 Endocarditis 58 0.047
653
HPT082 Hepatic Adenomas, Familial 53 0.047
654
NRR001 Neuroretinitis 46 0.047
655
MN1001 Mn1 35 0.047
656
PLS011 Plasmacytoma 60 0.047
657
PST028 Post-Traumatic Stress Disorder 58 0.047
658
P LCH002 Lichen Planus 57 0.047
659
SCH003 Schizophreniform Disorder 43 0.047
660
UVL003 Uveal Diseases 22 0.047
661
P FML011 Familial Adenomatous Polyposis 71 0.046
662
P PRP029 Porphyria 62 0.046
663
c WLM018 Wilms Tumor 5 60 0.046
664
P LPC002 Lip Cancer 53 0.046
665
PLL012 Pollen Allergy 48 0.046
666
HYP082 Hypopharynx Cancer 41 0.046
667
ADR007 Adrenoleukodystrophy 71 0.046
668
c LKM063 Leukemia, Chronic Myeloid 70 0.046
669
CLF027 Cleft Palate, Isolated 63 0.046
670
P ANT006 Antiphospholipid Syndrome 59 0.046
671
PLM010 Pulmonary Edema 56 0.046
672
P INT070 Intestinal Obstruction 56 0.046
673
BRN022 Bronchiectasis 55 0.046
674
INT075 Intracranial Hypertension 52 0.046
675
CRN030 Coronary Stenosis 51 0.046
676
EXP004 Exophthalmos 51 0.046
677
PNN001 Panniculitis 49 0.046
678
CRB085 Cerebral Hemorrhage 47 0.046
679
SYS003 Systolic Heart Failure 46 0.046
680
PRX077 Peroxisomal Biogenesis Disorders 40 0.046
681
ADR022 Adrenomyeloneuropathy 39 0.046
682
SPS019 Spastic Paraparesis 35 0.046
683
BLN006 Blind Loop Syndrome 29 0.046
684
SDN002 Sudanophilic Cerebral Sclerosis 27 0.046
685
IRR002 Irritable Bowel Syndrome 62 0.045
686
DYS014 Dyspepsia 54 0.045
687
c SVR005 Severe Pre-Eclampsia 53 0.045
688
SBC017 Sebaceous Gland Disease 38 0.045
689
ACT118 Acute Non Lymphoblastic Leukemia 32 0.045
690
PSR001 Psoriatic Arthritis 65 0.045
691
P PLY014 Polycystic Kidney Disease 60 0.045
692
P FCL005 Focal Segmental Glomerulosclerosis 59 0.045
693
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.045
694
ALL010 Allergic Contact Dermatitis 59 0.045
695
CHL067 Cholecystitis 57 0.045
696
LCR008 Lacrimal Apparatus Disease 44 0.045
697
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.045
698
P TXP001 Toxoplasmosis 64 0.045
699
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.045
700
P FNC027 Fanconi Anemia, Complementation Group a 78 0.045
701
P GLL022 Guillain-Barre Syndrome 60 0.045
702
WLL001 Williams-Beuren Syndrome 63 0.045
703
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.045
704
DBT062 Diabetic Foot Ulcers 59 0.045
705
RHM001 Rheumatic Fever 58 0.045
706
LPD009 Lipid Storage Disease 51 0.045
707
PRT129 Prothrombin Deficiency, Congenital 49 0.045
708
c CNT016 Central Retinal Vein Occlusion 49 0.045
709
ACT103 Acute Lymphoblastic Leukemia, Childhood 48 0.045
710
c MLG079 Malignant Pleural Mesothelioma 46 0.045
711
PRT012 Prothrombin Deficiency 45 0.045
712
RHM035 Rheumatic Fever-Related Antigen 39 0.045
713
END014 Endemic Typhus 37 0.045
714
P DLT002 Dilated Cardiomyopathy 76 0.044
715
PLY001 Polycythemia Vera 74 0.044
716
P DRM010 Dermatomyositis 64 0.044
717
LNG039 Lung Squamous Cell Carcinoma 59 0.044
718
P END046 Endometritis 50 0.044
719
GLT007 Glutathione Synthetase Deficiency 46 0.044
720
P FLL037 Follicular Lymphoma 69 0.044
721
CRP001 Carpal Tunnel Syndrome 66 0.044
722
HMR039 Hemorrhage, Intracerebral 57 0.044
723
ESP023 Esophageal Disease 56 0.044
724
P SCL018 Scoliosis 55 0.044
725
SPR004 Supravalvular Aortic Stenosis 53 0.044
726
P CTN003 Cutaneous Lupus Erythematosus 52 0.044
727
PRN021 Paranasal Sinus Disease 50 0.044
728
VRN004 Vernal Keratoconjunctivitis 55 0.044
729
GST019 Gastrointestinal Stromal Tumor 73 0.043
730
P PLM036 Pulmonary Fibrosis 69 0.043
731
ANR007 Anorexia Nervosa 62 0.043
732
BLD034 Bile Duct Carcinoma 62 0.043
733
P PRT013 Portal Hypertension 59 0.043
734
HPT019 Hepatic Encephalopathy 58 0.043
735
APH002 Aphasia 58 0.043
736
PLG002 Plague 56 0.043
737
c BRS049 Breast Carcinoma in Situ 55 0.043
738
P MTH007 Methemoglobinemia 47 0.043
739
P ATX024 Ataxia-Oculomotor Apraxia 3 40 0.043
740
c BSL024 Basal Cell Carcinoma 1 35 0.043
741
MYC006 Mycosis Fungoides 72 0.043
742
P PSD087 Pseudoxanthoma Elasticum 67 0.043
743
P CHR071 Charcot-Marie-Tooth Disease 65 0.043
744
P GCH001 Gaucher's Disease 62 0.043
745
P FBR017 Fibrosarcoma 61 0.043
746
LYS002 Lysosomal Storage Disease 56 0.043
747
DCT002 Ductal Carcinoma in Situ 55 0.043
748
P MTC069 Mitochondrial Disorders 49 0.043
749
SKL017 Skeletal Dysplasias 48 0.043
750
P CMP008 Compartment Syndrome 47 0.043
751
SPH010 Sphingolipidosis 47 0.043
752
INT071 Intestinal Perforation 45 0.043
753
SKN023 Skin Tag 42 0.043
754
c HYP794 Hyperoxaluria, Primary, Type I 41 0.043
755
OLG001 Oligospermia 40 0.043
756
ATR076 Atrophic Muscular Disease 18 0.043
757
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.043
758
P CHR285 Chronic Myelomonocytic Leukemia 62 0.043
759
WRN002 Wernicke-Korsakoff Syndrome 52 0.043
760
GRW007 Growth Hormone Deficiency 51 0.043
761
CNJ012 Conjunctival Disease 48 0.043
762
BCK003 Background Diabetic Retinopathy 36 0.043
763
ATR073 Atrophic Glossitis 30 0.043
764
SKN020 Skin Papilloma 33 0.042
765
PCK003 Pick Disease of Brain 65 0.042
766
PLM014 Pleomorphic Adenoma 55 0.042
767
GLL018 Gallbladder Cancer 51 0.042
768
VCC001 Vaccinia 50 0.042
769
ANG005 Anogenital Venereal Wart 49 0.042
770
HYP063 Hypersplenism 49 0.042
771
URT010 Ureteral Obstruction 48 0.042
772
FSC004 Fasciitis 47 0.042
773
ALL014 Allergic Encephalomyelitis 36 0.042
774
END041 Endometrial Adenocarcinoma 60 0.042
775
OBS002 Obsessive-Compulsive Disorder 66 0.041
776
c NRF024 Neurofibromatosis, Type I 66 0.041
777
LKC003 Leukocyte Disease 46 0.041
778
c PLM022 Pulmonary Valve Insufficiency 37 0.041
779
PSD088 Pseudobulbar Affect 37 0.041
780
CRV069 Cervix Disease 35 0.041
781
BLC007 Bile Acid Synthesis Defect, Congenital, 1 31 0.041
782
P SYS005 Systemic Scleroderma 66 0.041
783
ART005 Arteriovenous Malformation 63 0.041
784
ETN001 Eating Disorder 61 0.041
785
P MNC007 Monocytic Leukemia 57 0.041
786
P LKD001 Leukodystrophy 57 0.041
787
c ANT034 Anterior Uveitis 50 0.041
788
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.041
789
ACL001 Acalculous Cholecystitis 38 0.041
790
CTN024 Cutaneous Mycosis 33 0.041
791
ALR002 Al-Raqad Syndrome 31 0.041
792
CHR178 Chromosomal Triplication 15 0.041
793
RFS006 Refsum Disease, Classic 62 0.041
794
P SPN052 Spondyloarthropathy 60 0.041
795
VSC003 Visceral Leishmaniasis 58 0.041
796
P PLY041 Polymyositis 56 0.041
797
PRR002 Pure Red-Cell Aplasia 51 0.041
798
ORL013 Oral Lichen Planus 51 0.041
799
c BLD140 Blood Group, I System 23 0.041
800
ALL009 Allergic Conjunctivitis 53 0.040
801
HYP458 Hyper Ige Syndrome 49 0.040
802
NRF007 Neurofibroma 65 0.040
803
DPH001 Diphtheria 62 0.040
804
P ORL007 Oral Cavity Cancer 61 0.040
805
BNC003 Bone Cancer 59 0.040
806
P GST049 Gastrointestinal System Cancer 59 0.040
807
GLS001 Gliosarcoma 58 0.040
808
c ACT135 Acute Graft Versus Host Disease 56 0.040
809
IMP005 Impotence 55 0.040
810
INN002 Inner Ear Disease 54 0.040
811
ATN004 Autonomic Neuropathy 46 0.040
812
VST004 Vestibular Disease 45 0.040
813
MRG013 Mirage Syndrome 43 0.040
814
CLN044 Colon Adenoma 42 0.040
815
P LBY004 Labyrinthitis 41 0.040
816
CHL013 Cholecystolithiasis 40 0.040
817
ATX010 Ataxia Neuropathy Spectrum 35 0.040
818
P RFR008 Refractory Anemia with Excess Blasts 33 0.040
819
FNC005 Functional Colonic Disease 31 0.040
820
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 30 0.040
821
ARG006 Aregenerative Anemia 25 0.040
822
CRC034 Carcinoma Showing Thymus-Like Differentiation 23 0.040
823
P HYP040 Hypospadias 59 0.040
824
MRK001 Merkel Cell Carcinoma 58 0.040
825
MCP006 Mucoepidermoid Carcinoma 51 0.040
826
VRC001 Varicocele 51 0.040
827
PLY020 Polyradiculoneuropathy 46 0.040
828
MCR225 Macrophage Activation Syndrome 44 0.040
829
CMM003 Common Wart 41 0.040
830
P OST001 Osteopetrosis 61 0.039
831
CRC006 Carcinoid Syndrome 60 0.039
832
c PNC108 Pancreatitis, Hereditary 59 0.039
833
TNG003 Tongue Cancer 58 0.039
834
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.039
835
P MTC133 Mitochondrial Myopathy 54 0.039
836
P OBS001 Obstructive Jaundice 52 0.039
837
BLD036 Bile Duct Disease 51 0.039
838
CRB027 Cerebellar Disease 49 0.039
839
DDN006 Duodenitis 48 0.039
840
c ADL052 Adult Acute Lymphocytic Leukemia 46 0.039
841
SLV003 Salivary Gland Disease 45 0.039
842
EPL131 Epilepsy, Pyridoxine-Dependent 37 0.039
843
P MTR062 Maternal Uniparental Disomy of Chromosome 4 15 0.039
844
P MYC008 Myocarditis 58 0.039
845
HMG002 Hemoglobinuria 52 0.039
846
HYD002 Hydronephrosis 48 0.039
847
P SPR120 Supranuclear Palsy, Progressive, 1 70 0.039
848
DMN031 Dementia, Lewy Body 66 0.039
849
ANP031 Anaplastic Thyroid Cancer 63 0.039
850
P LYM025 Lymphedema 63 0.039
851
P GLY013 Glycogen Storage Disease 61 0.039
852
SYN007 Synovitis 60 0.039
853
P SBS003 Substance Abuse 57 0.039
854
P SJG008 Sjogren Syndrome 54 0.039
855
HST009 Histiocytoma 50 0.039
856
P TCL004 T-Cell Leukemia 50 0.039
857
PTT037 Pituitary Tumors 48 0.039
858
NWC001 Newcastle Disease 48 0.039
859
VSC012 Vesiculobullous Skin Disease 41 0.039
860
MDS022 Mediastinitis 40 0.039
861
HYP548 Hypogonadotropic Hypogonadism 2 with or Without Anosmia 32 0.039
862
GST059 Gestational Trophoblastic Tumor 31 0.039
863
CHR066 Chronic Fatigue Syndrome 66 0.038
864
c MST023 Mesothelioma, Malignant 59 0.038
865
c MCP004 Mucopolysaccharidosis Iv 59 0.038
866
c MLG074 Malignant Mesenchymoma 54 0.038
867
CLF001 Cleft Lip 54 0.038
868
OST015 Osteochondrodysplasia 53 0.038
869
PRP021 Peripheral Nervous System Neoplasm 53 0.038
870
c RTN162 Retinitis Pigmentosa 2 50 0.038
871
CRB025 Carbohydrate Metabolic Disorder 50 0.038
872
P KRT007 Keratoconus 48 0.038
873
SXL003 Sexual Disorder 44 0.038
874
STT004 Steatorrhea 41 0.038
875
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
876
ACQ031 Acquired Idiopathic Sideroblastic Anemia 36 0.038
877
P MRQ003 Morquio Syndrome 31 0.038
878
VTM003 Vitamin Metabolic Disorder 20 0.038
879
TMP001 Temporal Lobe Epilepsy 52 0.038
880
MSC157 Muscular Dystrophy, Duchenne Type 68 0.037
881
YLL002 Yellow Fever 61 0.037
882
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 59 0.037
883
P RHB003 Rhabdomyosarcoma 56 0.037
884
P ZLL001 Zellweger Syndrome 56 0.037
885
ISL001 Islet Cell Tumor 53 0.037
886
APR001 Apraxia 53 0.037
887
SPN119 Spondylarthropathy 45 0.037
888
DCB001 Decubitus Ulcer 45 0.037
889
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 44 0.037
890
CRN019 Coronary Artery Vasospasm 41 0.037
891
LRY004 Laryngotracheitis 34 0.037
892
HRN029 Hearing Loss, Noise-Induced 33 0.037
893
INF009 Inflammatory Spondylopathy 22 0.037
894
KWS002 Kawasaki Disease 70 0.037
895
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 63 0.037
896
CHK001 Chikungunya 59 0.037
897
c INF023 Inflammatory Breast Carcinoma 53 0.037
898
TRC008 Trachoma 51 0.037
899
URT001 Urethritis 43 0.037
900
c WLM011 Wilms Tumor 6 38 0.037
901
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 36 0.037
902
MNT001 Mantle Cell Lymphoma 73 0.036
903
P MYS003 Myasthenia Gravis 72 0.036
904
ALP103 Alpha-1-Antitrypsin Deficiency 61 0.036
905
ZLL002 Zollinger-Ellison Syndrome 58 0.036
906
LYM040 Lymphoblastic Lymphoma 57 0.036
907
HYP730 Hypogonadotropic Hypogonadism 56 0.036
908
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.036
909
GNT002 Giant Cell Glioblastoma 55 0.036
910
c LKM070 Leukemia, Acute Monocytic 55 0.036
911
ISL003 Isolated Growth Hormone Deficiency 55 0.036
912
ERY029 Erythermalgia, Primary 54 0.036
913
OLG003 Oligohydramnios 53 0.036
914
PST095 Post-Thrombotic Syndrome 52 0.036
915
PRT018 Portal Vein Thrombosis 50 0.036
916
P GND004 Gonadal Dysgenesis 50 0.036
917
ACT017 Acute Chest Syndrome 49 0.036
918
P KRT005 Keratoacanthoma 49 0.036
919
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.036
920
P ART084 Arteriovenous Fistula 45 0.036
921
CNT060 Central Serous Chorioretinopathy 44 0.036
922
HYP141 Hyperphenylalaninemia 42 0.036
923
OST115 Osteonecrosis of the Jaw 42 0.036
924
LCH004 Lichen Disease 41 0.036
925
KHN001 Kuhnt-Junius Degeneration 40 0.036
926
DRM009 Dermatomycosis 37 0.036
927
HRD054 Hereditary Neuropathy with Liability to Pressure Palsy 36 0.036
928
NRV004 Nerve Compression Syndrome 35 0.036
929
BLC008 Bile Acid Synthesis Defect, Congenital, 2 29 0.036
930
CHR189 Chromosome 12p Deletion 24 0.036
931
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 23 0.036
932
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.036
933
MCR013 Microphthalmia 60 0.036
934
P CND004 Candidiasis 60 0.036
935
GST027 Gastric Lymphoma 53 0.036
936
PTN001 Patent Foramen Ovale 53 0.036
937
INT079 Intrahepatic Cholangiocarcinoma 52 0.036
938
SKN022 Skin Squamous Cell Carcinoma 50 0.036
939
DSC009 Discoid Lupus Erythematosus 47 0.036
940
P RTN014 Retinal Artery Occlusion 46 0.036
941
ADP007 Adie Pupil 41 0.036
942
NRX001 Neuroaxonal Dystrophy 40 0.036
943
GRN007 Granuloma Annulare 40 0.036
944
KSH001 Keshan Disease 33 0.036
945
WLS001 Wilson Disease 71 0.035
946
CRY004 Cryoglobulinemia 49 0.035
947
P MDL005 Medulloblastoma 75 0.035
948
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.035
949
FBR012 Fabry Disease 71 0.035
950
P ESS003 Essential Thrombocythemia 70 0.035
951
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.035
952
CMB081 Combined Immunodeficiency, X-Linked 64 0.035
953
NRL005 Neurilemmoma 63 0.035
954
P TST021 Testicular Germ Cell Tumor 61 0.035
955
UTR024 Uterine Carcinosarcoma 59 0.035
956
SPN027 Spinal Stenosis 59 0.035
957
P LMY004 Leiomyosarcoma 58 0.035
958
P INT030 Intracranial Aneurysm 57 0.035
959
CHL028 Childhood Type Dermatomyositis 56 0.035
960
PRP016 Paraplegia 53 0.035
961
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.035
962
P TRT010 Teratoma 52 0.035
963
PLR008 Pleurisy 51 0.035
964
P PRN020 Paranasal Sinus Cancer 43 0.035
965
HMC016 Homocystinuria Due to Cbs Deficiency 20 0.035
966
HYP485 Hypercholesterolemia Due to Cholesterol 7alpha-Hydroxylase Deficiency 12 0.035
967
P WSK001 Wiskott-Aldrich Syndrome 77 0.035
968
c LCL006 Localized Scleroderma 64 0.035
969
c ADL017 Adult T-Cell Leukemia 62 0.035
970
P RBL001 Rubella 62 0.035
971
P FTL001 Fetal Alcohol Syndrome 59 0.035
972
P BRS044 Breast Adenocarcinoma 58 0.035
973
HYP190 Hypoalphalipoproteinemia, Primary 58 0.035
974
PRT118 Protoporphyria, Erythropoietic 58 0.035
975
P MCR010 Microcephaly 57 0.035
976
P ACT105 Acute Mountain Sickness 57 0.035
977
SNS001 Sensorineural Hearing Loss 56 0.035
978
P ICH004 Ichthyosis 54 0.035
979
THR004 Thrombocytosis 54 0.035
980
PPL021 Papilledema 49 0.035
981
c ADL096 Adult Hepatocellular Carcinoma 48 0.035
982
c INH020 Inherited Metabolic Disorder 48 0.035
983
UTR043 Uterine Sarcoma 48 0.035
984
ACT088 Acute Insulin Response 43 0.035
985
CWM001 Cow Milk Allergy 42 0.035
986
SWN001 Swine Influenza 42 0.035
987
GNT050 Genitourinary Tract Anomalies 40 0.035
988
MTR007 Motor Peripheral Neuropathy 40 0.035
989
EXC003 Excessive Tearing 36 0.035
990
MCN011 Mucinoses 36 0.035
991
UTR037 Uterine Corpus Sarcoma 25 0.035
992
PDT020 Pediatric Germ Cell Cancer 25 0.035
993
SPN187 Spinocerebellar Atrophy 23 0.035
994
ULC005 Ulcer of Lower Limbs 22 0.035
995
P THY023 Thymoma 65 0.033
996
PLT015 Platelet Aggregation, Spontaneous 40 0.033
997
KLB004 Klebsiella Infection 25 0.033
998
P RTT002 Rett Syndrome 82 0.033
999
P MTC003 Metachromatic Leukodystrophy 71 0.033
1000
CHG001 Chagas Disease 71 0.033
1001
P CHR012 Chronic Granulomatous Disease 69 0.033
1002
P PRP003 Porphyria Cutanea Tarda 66 0.033
1003
DNG002 Dengue Hemorrhagic Fever 66 0.033
1004
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.033
1005
P ESP035 Esophagitis, Eosinophilic, 1 58 0.033
1006
c INT072 Intestinal Pseudo-Obstruction 57 0.033
1007
c CNG021 Congenital Toxoplasmosis 57 0.033
1008
CRV038 Cervical Squamous Cell Carcinoma 57 0.033
1009
CLR003 Clear Cell Adenocarcinoma 56 0.033
1010
ORL004 Oral Submucous Fibrosis 55 0.033
1011
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 0.033
1012
ANK001 Ankylosis 55 0.033
1013
MTC027 Mitochondrial Trifunctional Protein Deficiency 54 0.033
1014
LMB062 Limb Ischemia 51 0.033
1015
NNT012 Neonatal Jaundice 51 0.033
1016
CNG028 Congenital Hypoplastic Anemia 48 0.033
1017
OVR112 Ovarian Germ Cell Cancer 44 0.033
1018
ANM001 Anemia of Prematurity 42 0.033
1019
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 40 0.033
1020
PLM039 Pulmonary Neuroendocrine Tumor 36 0.033
1021
AGR019 Age-Related Hearing Loss 33 0.033
1022
c SPN295 Spinocerebellar Ataxia, Autosomal Recessive 3 30 0.033
1023
ATX038 Ataxia and Polyneuropathy, Adult-Onset 28 0.033
1024
URG001 Urogenital Tuberculosis 27 0.033
1025
PRQ002 Paraquat Poisoning 26 0.033
1026
c MLT093 Multiple Sclerosis 2 20 0.033
1027
CHN075 Chondrodysplasia Punctata, Brachytelephalangic, Autosomal 20 0.033
1028
TYP007 Typhoid Fever 66 0.033
1029
P EPD009 Epidermolysis Bullosa Dystrophica 58 0.033
1030
P RNV001 Renovascular Hypertension 49 0.033
1031
ESN002 Eosinophilia-Myalgia Syndrome 45 0.033
1032
P ATX030 Ataxia-Telangiectasia 79 0.033
1033
OVR029 Ovarian Hyperstimulation Syndrome 64 0.033
1034
PRP001 Propionic Acidemia 62 0.033
1035
P SLV002 Salivary Gland Cancer 61 0.033
1036
RTN017 Retinal Detachment 58 0.033
1037
P HYP083 Hypopituitarism 58 0.033
1038
P DRM007 Dermatitis Herpetiformis 56 0.033
1039
PSD014 Pseudopseudohypoparathyroidism 55 0.033
1040
FND001 Fundus Albipunctatus 53 0.033
1041
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.033
1042
c PRM012 Primary Polycythemia 52 0.033
1043
FCT001 Factor Viii Deficiency 51 0.033
1044
P PNB001 Pineoblastoma 51 0.033
1045
HYP006 Hypertensive Heart Disease 50 0.033
1046
ACN001 Acinar Cell Carcinoma 49 0.033
1047
MNR012 Meniere Disease 49 0.033
1048
GLL017 Gallbladder Adenocarcinoma 46 0.033
1049
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.033
1050
CHL010 Childhood Kidney Cell Carcinoma 43 0.033
1051
c PSR017 Psoriasis 2 39 0.033
1052
c PSR028 Psoriasis 7 38 0.033
1053
c PSR032 Psoriasis 11 38 0.033
1054
CPL005 Capillary Disease 38 0.033
1055
c PSR018 Psoriasis 13 37 0.033
1056
c DRM040 Dermatitis Herpetiformis, Familial 36 0.033
1057
c ACT072 Acute Laryngitis 34 0.033
1058
HNS001 Hansen's Disease 30 0.033
1059
c MYS011 Myasthenia Gravis Congenital 30 0.033
1060
c PRS080 Prostate Cancer, Hereditary, 7 25 0.033
1061
DRG016 Drug Induced Dyskinesia 24 0.033
1062
ACR007 Acromegaly 69 0.030
1063
SVR097 Severe Cutaneous Adverse Reaction 68 0.030
1064
P HYP098 Hypereosinophilic Syndrome 65 0.030
1065
c WLM013 Wilms Tumor 1 64 0.030
1066
ADL030 Adult-Onset Still's Disease 64 0.030
1067
P LPS002 Liposarcoma 59 0.030
1068
DSS009 Disseminated Intravascular Coagulation 55 0.030
1069
c INT064 Intermediate Uveitis 55 0.030
1070
P INF016 Infantile Epileptic Encephalopathy 54 0.030
1071
SMN008 Semantic Dementia 54 0.030
1072
PLR022 Pleural Disease 53 0.030
1073
P HMN036 Hemangiopericytoma, Malignant 53 0.030
1074
ALC009 Alcoholic Liver Cirrhosis 52 0.030
1075
NNT017 Neonatal Adrenoleukodystrophy 52 0.030
1076
NRM004 Neuroma 51 0.030
1077
DRG003 Drug Dependence 51 0.030
1078
FLL008 Folliculitis 50 0.030
1079
CLL014 Cll/sll 45 0.030
1080
NRF003 Neurofibrosarcoma 44 0.030
1081
P CRN026 Corneal Edema 43 0.030
1082
SRC002 Sarcomatoid Renal Cell Carcinoma 43 0.030
1083
PHB001 Phobic Disorder 42 0.030
1084
PLS016 Plasma Cell Leukemia 42 0.030
1085
SCL017 Sclerosing Hemangioma 40 0.030
1086
TRP005 Trophoblastic Neoplasm 40 0.030
1087
SNL007 Senile Cataract 40 0.030
1088
MLN013 Melanoma Metastasis 38 0.030
1089
c VRL017 Viral Hemorrhagic Fever 38 0.030
1090
MNN028 Mononeuropathy of the Median Nerve, Mild 37 0.030
1091
c GRN014 Grn-Related Frontotemporal Dementia 37 0.030
1092
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 36 0.030
1093
GST012 Gastroesophageal Junction Adenocarcinoma 36 0.030
1094
ADN013 Adenoid Squamous Cell Carcinoma 36 0.030
1095
TRC026 Tracheal Disease 35 0.030
1096
LRY011 Larynx Verrucous Carcinoma 31 0.030
1097
PRM153 Primary Progressive Apraxia of Speech 21 0.030
1098
P HNT016 Huntington Disease 70 0.030
1099
SVR004 Severe Combined Immunodeficiency 69 0.030
1100
SMT004 Smith-Lemli-Opitz Syndrome 68 0.030
1101
TKY002 Takayasu Arteritis 66 0.030
1102
IMM174 Immunodeficiency with Hyper-Igm, Type 1 63 0.030
1103
P MMP001 Mumps 61 0.030
1104
VTR013 Vitreoretinopathy, Neovascular Inflammatory 61 0.030
1105
P HST010 Histiocytosis 59 0.030
1106
c PRX045 Peroxisome Biogenesis Disorder 1b 56 0.030
1107
PRP032 Porphyria Variegata 55 0.030
1108
PLS006 Plasmodium Vivax Malaria 55 0.030
1109
P MYT002 Myotonic Dystrophy 50 0.030
1110
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.030
1111
EPD006 Epidermolysis Bullosa Acquisita 49 0.030
1112
ESP002 Esophageal Varix 48 0.030
1113
c OPT051 Opitz Gbbb Syndrome, Type I 47 0.030
1114
GYN001 Gynecomastia 46 0.030
1115
LYM127 Lymphatic Malformations 45 0.030
1116
PRC003 Proctitis 44 0.030
1117
P HRD012 Hereditary Elliptocytosis 42 0.030
1118
CRV043 Cervical Dystonia 41 0.030
1119
CRB086 Cerebral Aneurysms 41 0.030
1120
P AXN001 Axonal Neuropathy 38 0.030
1121
MYT026 Myotonia Atrophica 27 0.030
1122
STT003 Steatitis 22 0.030
1123
P HYD006 Hydrocephalus 69 0.030
1124
P HMN010 Hemangioma 60 0.030