Search results for Vitamin E

1757 hits were found for Vitamin E

# Family MCID Name MIFTS Score
1
VTM028 Vitamin E, Familial Isolated Deficiency of 52 9.902
2
ATX019 Ataxia with Vitamin E Deficiency 34 8.761
3
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 22 2.960
4
c HPT021 Hepatitis 74 0.731
5
P HPT007 Hepatitis E 56 0.597
6
c BRS047 Breast Cancer 100 0.340
7
KRT002 Keratomalacia 51 0.338
8
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.336
9
c ALZ034 Alzheimer Disease 88 0.335
10
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.309
11
VTM002 Vitamin B12 Deficiency 48 0.307
12
RCK004 Rickets 66 0.305
13
c LVR013 Liver Disease 77 0.287
14
NTR005 Nutritional Deficiency Disease 60 0.285
15
c DBT009 Diabetes Mellitus 67 0.283
16
c PRS040 Prostate Cancer 93 0.272
17
c KDN018 Kidney Disease 71 0.266
18
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.257
19
c HRT032 Heart Disease 76 0.251
20
P PRS136 Prostate Cancer, Hereditary, 6 40 0.246
21
P PRS130 Prostate Cancer, Hereditary, 8 37 0.246
22
c THL005 Thalassemia 65 0.244
23
AST005 Asthma 81 0.244
24
c CLR023 Colorectal Cancer 99 0.238
25
P HPT016 Hepatitis B 70 0.237
26
DMN002 Dementia 69 0.226
27
c OST002 Osteoporosis 74 0.217
28
c MLT020 Multiple Sclerosis 76 0.216
29
c LNG032 Lung Cancer 99 0.215
30
c LKM002 Leukemia 72 0.215
31
P HPT003 Hepatitis a 66 0.215
32
c CRN018 Coronary Artery Anomaly 74 0.212
33
ART140 Arteries, Anomalies of 67 0.210
34
VTM033 Vitamin K Deficiency Bleeding 47 0.209
35
c ADN016 Adenocarcinoma 71 0.209
36
GST053 Gastric Cancer 78 0.209
37
FTT001 Fatty Liver Disease 66 0.207
38
DRM006 Dermatitis 69 0.204
39
AGN016 Aging 63 0.203
40
c CRN300 Coronary Heart Disease 1 62 0.203
41
c ART022 Arthritis 78 0.202
42
c MYC007 Myocardial Infarction 78 0.200
43
ISC004 Ischemia 67 0.199
44
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.198
45
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.193
46
c CRD246 Cardiovascular System Disease 57 0.192
47
DPR016 Depression 73 0.192
48
P CHR089 Chronic Kidney Failure 73 0.192
49
ACQ007 Acquired Immunodeficiency Syndrome 66 0.192
50
c HPT023 Hepatocellular Carcinoma 97 0.189
51
c HYP069 Hyperparathyroidism 59 0.189
52
GST050 Gastrointestinal System Disease 67 0.187
53
P BTT014 Beta-Thalassemia 73 0.186
54
SQM006 Squamous Cell Carcinoma 59 0.185
55
P HPT001 Hepatitis C 69 0.184
56
P PRC016 Pre-Eclampsia 61 0.184
57
URN009 Urinary System Disease 59 0.182
58
c NRP001 Neuropathy 63 0.181
59
c DRR001 Diarrhea 58 0.180
60
VSC007 Vascular Disease 72 0.177
61
BND020 Bone Disease 65 0.177
62
LNG099 Lung Disease 70 0.175
63
P HMG003 Hemoglobin E Disease 43 0.175
64
ISC006 Ischemic Heart Disease 72 0.174
65
c ATR011 Atrial Fibrillation 69 0.174
66
c OVR042 Ovarian Cancer 83 0.169
67
NNL002 Nonalcoholic Steatohepatitis 55 0.169
68
MLN008 Melanoma 64 0.168
69
c DRM053 Dermatitis, Atopic 73 0.167
70
GLC008 Glucose Metabolism Disease 54 0.166
71
VRL011 Viral Infectious Disease 69 0.165
72
ATM095 Autoimmune Disease 68 0.164
73
c RHM011 Rheumatoid Arthritis 82 0.164
74
c ART021 Arteriosclerosis 61 0.164
75
c INF037 Inflammatory Bowel Disease 56 0.163
77
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.160
78
c ECL001 Eclampsia 59 0.159
79
c LYM118 Lymphoma 69 0.158
80
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.157
81
c PNC035 Pancreatic Cancer 83 0.156
82
ALL026 Allergic Hypersensitivity Disease 68 0.155
83
CRH001 Crohn's Disease 79 0.154
84
c LPS004 Lupus Erythematosus 69 0.153
85
c INT068 Intestinal Disease 62 0.153
86
SKN016 Skin Disease 68 0.153
87
HMN044 Human Immunodeficiency Virus Type 1 75 0.152
88
THR024 Thrombosis 64 0.152
89
PSY004 Psychotic Disorder 74 0.150
90
c PLY011 Polycystic Ovary Syndrome 64 0.148
91
P HPT073 Hepatitis C Virus 73 0.147
92
BNF002 Bone Fracture 50 0.146
93
P VRL010 Viral Hepatitis 60 0.145
94
c PSR002 Psoriasis 67 0.144
95
MNT002 Mental Depression 65 0.144
96
c INF038 Influenza 75 0.144
97
P SML038 Small Cell Cancer of the Lung 69 0.144
98
CRB039 Cerebrovascular Disease 70 0.144
99
CYS001 Cystic Fibrosis 83 0.144
100
SKN027 Skin Conditions 51 0.143
101
DFC004 Deficiency Anemia 65 0.142
102
P SYS001 Systemic Lupus Erythematosus 88 0.140
103
CNG034 Congestive Heart Failure 71 0.139
104
PRN011 Pernicious Anemia 52 0.139
105
c SCH015 Schizophrenia 73 0.138
106
c PRP019 Peripheral Nervous System Disease 66 0.138
107
c PNM007 Pneumonia 72 0.137
108
ANX010 Anxiety 73 0.136
109
CLT003 Colitis 65 0.136
110
RSP006 Respiratory System Disease 64 0.136
111
c ENC004 Encephalitis 66 0.136
112
c RHN004 Rhinitis 63 0.136
113
c LYM031 Lymphocytic Leukemia 61 0.136
114
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.135
115
c HML002 Hemolytic Anemia 65 0.135
116
BRN106 Burns 59 0.135
117
LVR012 Liver Cirrhosis 67 0.134
118
ATH013 Atherosclerosis Susceptibility 61 0.134
119
HYP266 Hypoxia 63 0.134
120
c BLD134 Bladder Cancer 71 0.133
121
c INF032 Infertility 60 0.133
122
IMM136 Immune System Disease 57 0.133
123
NRL016 Neural Tube Defects 79 0.133
124
c ENC018 Encephalopathy 65 0.132
126
c NRV007 Nervous System Disease 72 0.132
127
DST081 Distal Trisomy 11q 20 0.132
128
TRD006 Tardive Dyskinesia 61 0.131
129
ADN018 Adenoma 65 0.131
130
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.131
131
P MCR113 Microvascular Complications of Diabetes 3 58 0.130
132
P MCR120 Microvascular Complications of Diabetes 7 46 0.130
133
P MCR130 Microvascular Complications of Diabetes 6 43 0.130
134
P MCR133 Microvascular Complications of Diabetes 4 43 0.130
135
ALL003 Allergic Rhinitis 69 0.128
136
c VSC018 Visceral Steatosis 38 0.128
137
GST045 Gastroenteritis 65 0.127
138
HYP060 Hyperinsulinism 57 0.127
139
BNR002 Bone Resorption Disease 54 0.127
140
c EPL164 Epilepsy 73 0.127
141
GST033 Gestational Diabetes 63 0.126
142
OST012 Osteoarthritis 81 0.126
143
END030 End Stage Renal Failure 60 0.125
144
BCT022 Bacterial Infectious Disease 63 0.125
145
MLR004 Malaria 85 0.125
146
DSS008 Disease of Mental Health 70 0.125
147
c SKN015 Skin Carcinoma 65 0.124
148
RHM027 Rheumatic Disease 65 0.124
149
P EXD008 Exudative Vitreoretinopathy 1 73 0.123
150
GST049 Gastrointestinal System Cancer 62 0.122
151
GST071 Gastrointestinal Carcinoma 46 0.122
152
IRN002 Iron Metabolism Disease 60 0.121
153
c TRC086 Trichohepatoenteric Syndrome 1 61 0.121
154
SPS003 Spastic Diplegia 49 0.121
155
c RTN008 Retinitis Pigmentosa 79 0.121
156
c CTR002 Cataract 58 0.121
157
PLC008 Placenta Disease 59 0.121
158
c PRD008 Periodontitis 66 0.120
159
BRS051 Breast Disease 68 0.120
160
c MYP004 Myopathy 65 0.119
161
P ACT068 Acute Cystitis 56 0.118
162
CNN005 Connective Tissue Disease 67 0.117
163
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.117
164
FSH001 Fish-Eye Disease 51 0.116
165
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.116
166
P LRG017 Large Intestine Cancer 63 0.116
167
PLM001 Pulmonary Tuberculosis 74 0.116
168
CLN019 Colonic Disease 62 0.115
169
FDL002 Food Allergy 54 0.115
170
BRN056 Bronchopulmonary Dysplasia 61 0.114
171
P PRM005 Primary Hyperparathyroidism 60 0.114
172
HYP066 Hyperglycemia 65 0.114
173
LPD008 Lipid Metabolism Disorder 65 0.113
174
ULC004 Ulcerative Colitis 80 0.112
175
c LKM062 Leukemia, Acute Lymphoblastic 70 0.112
176
HDC001 Headache 63 0.112
177
c ATS364 Autism 68 0.112
178
THY028 Thyroid Cancer 72 0.111
179
BRN071 Brain Injury 54 0.111
180
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.111
181
BRN038 Bronchial Disease 58 0.110
182
P ACT075 Acute Myocardial Infarction 57 0.110
183
RTN018 Retinal Disease 58 0.110
184
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.110
185
c ALP008 Alopecia 56 0.110
186
GLC003 Glucose Intolerance 59 0.110
187
CHL068 Cholestasis 60 0.109
188
LNG031 Lung Benign Neoplasm 56 0.109
189
P CNT035 Central Nervous System Disease 65 0.109
190
PLM017 Pulmonary Alveolar Microlithiasis 52 0.109
191
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.108
192
MDD011 Mood Disorder 65 0.108
193
ART016 Aortic Aneurysm 71 0.107
194
c PNC044 Pancreatitis 62 0.107
195
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.106
196
c PRK057 Parkinson Disease, Late-Onset 77 0.106
197
RTN023 Retinitis 48 0.106
198
ABT001 Abetalipoproteinemia 67 0.105
199
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.104
200
P OVR114 Ovarian Cancer 1 66 0.104
201
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.104
202
NRM005 Neuromuscular Disease 61 0.104
203
c ART023 Arthropathy 68 0.104
204
CMM005 Common Cold 62 0.104
205
IRN001 Iron Deficiency Anemia 54 0.104
206
NPH009 Nephrolithiasis 58 0.103
207
P ACT134 Acute Liver Failure 53 0.103
208
P ACT074 Acute Lymphocytic Leukemia 62 0.103
209
c NGH001 Night Blindness 50 0.103
210
P ACT210 Acute Respiratory Distress Syndrome 66 0.103
211
JNT002 Joint Disorders 64 0.103
212
c CLL015 Collagen Disease 52 0.103
213
c PYL005 Pyelonephritis 57 0.102
214
CLR108 Colorectal Adenoma 64 0.102
215
ANG054 Angina Pectoris 70 0.101
216
c HYP086 Hypothyroidism 66 0.101
217
c MSC033 Muscle Disorders 56 0.101
218
NRT004 Neuritis 58 0.101
219
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.100
220
STR067 Stroke, Ischemic 84 0.100
221
STM007 Stomatitis 53 0.100
222
DRL001 Dural Sinus Malformation 23 0.100
223
c GST044 Gastritis 61 0.100
224
c NPH012 Nephrotic Syndrome 59 0.099
225
HMT018 Hematopoietic Stem Cell Transplantation 59 0.099
226
c RTN016 Retinal Degeneration 56 0.099
227
P HYP595 Hypertension, Essential 77 0.099
228
RCT017 Rectal Disease 42 0.099
229
HYP781 Hypoascorbemia 49 0.099
230
HMP009 Haemophilus Influenzae 51 0.099
231
c CLC063 Celiac Disease 1 72 0.099
232
c RTN024 Retinoblastoma 73 0.098
233
SPN186 Spinal Cord Injury 66 0.098
234
SCK003 Sickle Cell Anemia 75 0.098
235
c MYL006 Myeloid Leukemia 68 0.098
236
INT253 Intestinal Benign Neoplasm 57 0.098
237
URM002 Uremia 53 0.098
238
HMC014 Homocysteinemia 52 0.097
239
c SBS003 Substance Abuse 61 0.097
240
PRM236 Primary Biliary Cholangitis 63 0.097
241
c THR014 Thrombocytopenia 65 0.097
242
SLP005 Sleep Disorder 60 0.096
243
c PRM006 Primary Biliary Cirrhosis 54 0.096
244
c MNN013 Meningitis 71 0.096
245
DMY004 Demyelinating Disease 60 0.096
246
VSC002 Vascular Dementia 58 0.096
247
c DNG005 Dengue Virus 64 0.096
248
INT002 Intermittent Claudication 64 0.096
249
PNC034 Pancreas Disease 60 0.096
250
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.095
251
c END044 Endometriosis 65 0.095
252
PRD007 Periodontal Disease 66 0.095
253
CRH005 Crohn's Colitis 61 0.095
254
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.095
255
c GLM045 Glioma 56 0.095
256
PRS042 Prostate Disease 47 0.095
257
c EXN002 Exanthem 62 0.095
258
HLC007 Helicobacter Pylori Infection 66 0.095
259
ORL015 Oral Squamous Cell Carcinoma 48 0.094
260
MCS002 Mucositis 60 0.094
261
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.094
262
P PNC106 Pancreatic Agenesis 1 52 0.094
263
P SPN225 Spondyloarthropathy 1 76 0.094
264
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.094
265
PLM033 Pulmonary Embolism 64 0.093
266
INS024 Insulin-Like Growth Factor I 83 0.093
267
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.093
268
SCK005 Sickle Cell Disease 57 0.093
269
c NRB001 Neuroblastoma 73 0.093
270
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.092
271
c LYM033 Lymphoproliferative Syndrome 63 0.092
272
P TRC078 Trichohepatoenteric Syndrome 2 35 0.092
273
TRN018 Transitional Cell Carcinoma 63 0.092
274
P INF071 Inflammatory Bowel Disease 1 57 0.092
275
ESP021 Esophageal Cancer 84 0.091
276
TRM010 Traumatic Brain Injury 56 0.091
277
HMG005 Hemoglobinopathy 54 0.091
278
END057 Endometrial Cancer 69 0.091
279
c HMR003 Hemorrhagic Disease 59 0.091
280
ENT011 Enterocolitis 55 0.091
281
MST005 Mastitis 57 0.091
282
LYM019 Lymphosarcoma 59 0.091
283
c NSP012 Nasopharyngeal Carcinoma 66 0.091
284
c BLD051 Blood Coagulation Disease 51 0.091
285
P ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 67 0.090
286
MLR006 Male Reproductive Organ Cancer 50 0.090
287
MYL069 Myeloma, Multiple 85 0.090
288
c THY032 Thyroiditis 54 0.090
289
CLC006 Calcinosis 53 0.090
290
P INS002 in Situ Carcinoma 60 0.090
291
URT039 Urticaria 60 0.090
292
c OPN001 Open-Angle Glaucoma 53 0.089
293
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.089
294
ILT001 Ileitis 59 0.089
295
c HYP024 Hypoparathyroidism 56 0.088
296
PYR009 Pyridoxine Deficiency Anemia 28 0.088
297
SRC014 Sarcoma 70 0.088
298
MSC190 Muscular Disease 55 0.088
299
MSC004 Muscle Tissue Disease 39 0.088
300
P PRC031 Preeclampsia/eclampsia 1 41 0.088
301
DWN001 Down Syndrome 72 0.087
302
P LKM061 Leukemia, Acute Myeloid 83 0.087
303
ANR007 Anorexia Nervosa 68 0.087
304
c HYP073 Hypersensitivity Reaction Type Iv Disease 51 0.087
305
c SLP006 Sleep Apnea 70 0.087
306
P GLC092 Glaucoma, Primary Open Angle 58 0.087
307
CRV035 Cervical Cancer 76 0.086
308
MSL001 Measles 66 0.086
309
P INF145 Infantile Liver Failure Syndrome 1 48 0.086
310
SPN331 Spondyloocular Syndrome 42 0.086
311
PRP027 Peripheral Vascular Disease 72 0.086
312
P ACT071 Acute Kidney Failure 54 0.086
313
c ADL010 Adult Respiratory Distress Syndrome 64 0.086
314
c MCR115 Microvascular Complications of Diabetes 5 71 0.086
315
HPD002 Hepadnavirus Infection 25 0.086
316
c MJR001 Major Depressive Disorder 67 0.085
317
P LBR014 Leber Congenital Amaurosis 4 55 0.085
318
OVR063 Overnutrition 53 0.085
319
LYM024 Lymphatic System Disease 55 0.085
320
P AMY091 Amyotrophic Lateral Sclerosis 1 90 0.085
321
XRD010 Xeroderma Pigmentosum, Variant Type 71 0.085
322
MYL009 Myelodysplastic Syndrome 71 0.085
323
c GRF003 Graft-Versus-Host Disease 72 0.084
324
c GRV001 Graves' Disease 61 0.084
325
c HMC002 Homocystinuria 51 0.084
326
P SCL052 Scleroderma, Familial Progressive 68 0.084
327
c MGL001 Megaloblastic Anemia 52 0.084
328
c ALP009 Alopecia Areata 68 0.084
329
P PRD040 Periodontitis, Chronic 60 0.084
330
GND003 Gonadal Disease 49 0.084
331
BRN080 Brain Ischemia 43 0.084
332
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.083
333
MTH009 Mouth Disease 66 0.083
334
CNS004 Constipation 58 0.083
335
ORL011 Oral Cancer 60 0.082
336
c SZR006 Seizure Disorder 61 0.082
337
c OVR046 Ovarian Cyst 52 0.082
338
P ATS007 Autism Spectrum Disorder 68 0.081
339
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.081
340
c OVR049 Ovarian Disease 63 0.081
341
P PNC128 Pain - Chronic 46 0.081
342
ALL006 Allergic Asthma 61 0.081
343
PRN019 Perinatal Necrotizing Enterocolitis 58 0.081
344
c AMY004 Amyloidosis 69 0.080
345
OVR094 Ovarian Epithelial Cancer 41 0.080
346
HYP056 Hypoglycemia 64 0.080
347
c NRF023 Neurofibromatosis, Type Ii 76 0.080
348
MVM001 Movement Disease 67 0.079
349
c MLN007 Male Infertility 52 0.079
350
PRP030 Purpura 62 0.079
351
PRP080 Peripheral Artery Disease 56 0.079
352
P ALP101 Alpha-Thalassemia 61 0.079
353
P THR092 Thrombophilia Due to Thrombin Defect 70 0.079
354
ALL014 Allergic Encephalomyelitis 43 0.078
355
BRC012 Brucellosis 71 0.078
356
c SCL057 Scoliosis, Isolated 1 46 0.078
357
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.078
358
END035 Endocrine Gland Cancer 57 0.078
359
c SHR001 Short Bowel Syndrome 52 0.078
360
PRT030 Parathyroid Gland Disease 51 0.078
361
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 23 0.078
362
SKN019 Skin Melanoma 67 0.078
363
P ACT027 Acute Pancreatitis 59 0.078
364
PLC007 Placental Abruption 51 0.078
365
BRN024 Bronchitis 70 0.078
366
NWB001 Newborn Respiratory Distress Syndrome 61 0.078
367
RSP007 Respiratory Distress Syndrome, Infant 38 0.078
368
c HML001 Hemolytic-Uremic Syndrome 55 0.077
369
c CYS018 Cystitis 58 0.077
370
TTN003 Tetanus 66 0.077
371
PRT038 Protein-Energy Malnutrition 53 0.077
372
c LTR001 Lateral Sclerosis 60 0.077
373
SPN051 Spondylitis 55 0.077
374
c CHR084 Chromosomal Disease 40 0.077
375
CHL065 Cholangiocarcinoma 65 0.077
376
HRP008 Herpes Simiae 16 0.077
377
c SNS014 Sinusitis 64 0.077
378
P MTR002 Mitral Valve Insufficiency 50 0.077
379
c CRD119 Cardiac Arrest 66 0.077
380
URN022 Urinary Tract Infections, Recurrent 34 0.077
381
APH001 Aphthous Stomatitis 65 0.076
382
LYM067 Lymphoid Leukemia 47 0.076
383
TXC005 Toxic Shock Syndrome 66 0.076
384
P MGR028 Migraine with or Without Aura 1 69 0.076
385
P PLY105 Polycystic Ovary Syndrome 1 43 0.076
386
PRT036 Peritonitis 67 0.075
387
DYS015 Dysentery 45 0.075
388
c RCT021 Rectum Cancer 58 0.075
389
VSC008 Vascular Hemostatic Disease 45 0.075
390
GLB002 Glioblastoma 75 0.075
391
c RSP003 Respiratory Failure 72 0.075
392
TRN015 Transient Cerebral Ischemia 59 0.075
393
OST097 Osteoporotic Fracture 36 0.075
394
MYL005 Myelofibrosis 70 0.075
395
c RST001 Restless Legs Syndrome 60 0.075
396
c LNG064 Lung Cancer Susceptibility 3 80 0.074
397
c BCL006 B-Cell Lymphomas 66 0.074
398
THR013 Thoracic Outlet Syndrome 57 0.074
399
DYS073 Dysphagia 53 0.074
400
CRV045 Cervical Intraepithelial Neoplasia 45 0.074
401
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 0.074
402
c CNJ013 Conjunctivitis 65 0.074
403
CHC001 Chickenpox 50 0.074
404
c MSC003 Muscular Atrophy 56 0.074
405
c HYP607 Hypercholesterolemia, Familial 82 0.074
406
PRS129 Prostatic Hyperplasia, Benign 53 0.074
407
FBR047 Fibromyalgia 62 0.074
408
PRD004 Prediabetes Syndrome 51 0.074
409
ATX010 Ataxia Neuropathy Spectrum 39 0.073
410
KRT009 Keratosis 55 0.073
411
c HYP076 Hyperthyroidism 56 0.073
412
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.073
413
CCC002 Coccidiosis 50 0.073
414
IRR002 Irritable Bowel Syndrome 64 0.073
415
BRN028 Brain Cancer 74 0.073
416
CYT002 Cytokine Deficiency 39 0.073
417
P LKM071 Leukemia, Chronic Lymphocytic 78 0.072
418
P PYR010 Peyronie's Disease 55 0.072
419
EPD015 Epidemic Typhus 52 0.072
420
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.072
421
XP2001 Xp22.3 Microdeletion Syndrome 26 0.072
422
BLD131 Bladder Urothelial Carcinoma 62 0.072
423
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.072
424
PLY001 Polycythemia Vera 76 0.072
425
ETN001 Eating Disorder 65 0.072
426
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 46 0.072
427
PNG002 Pain Agnosia 54 0.072
428
HDN002 Head Injury 52 0.072
429
SPP010 Suppressor of Tumorigenicity 3 60 0.072
430
END040 Endogenous Depression 59 0.072
431
PRM020 Premenstrual Tension 53 0.072
432
CRB011 Cerebrotendinous Xanthomatosis 65 0.072
433
LYM133 Lymphoma, Hodgkin, Classic 73 0.072
434
ALC007 Alcohol Dependence 70 0.071
435
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 55 0.071
436
P ATM011 Autoimmune Hepatitis 66 0.071
437
P LKM004 Leukemia, B-Cell, Chronic 38 0.071
438
CHL123 Chlamydia 66 0.071
439
OPT006 Optic Nerve Disease 60 0.070
440
TTH006 Tooth Disease 54 0.070
441
MCR017 Macrocytic Anemia 46 0.070
442
c VSC011 Vasculitis 67 0.070
443
BRN039 Bronchial Neoplasm 43 0.070
444
c SCL018 Scoliosis 59 0.070
445
HMS001 Hemosiderosis 52 0.070
446
c MYC084 Mycobacterium Tuberculosis 1 68 0.070
447
DST089 Distal Trisomy 3p 22 0.070
448
P CNG027 Congenital Hemolytic Anemia 52 0.070
449
c HRP006 Herpes Simplex 71 0.070
450
P CHR579 Chiari Malformation Type Ii 49 0.070
451
PLL012 Pollen Allergy 52 0.069
452
BSL008 Basal Ganglia Disease 49 0.069
453
EPD016 Epidermolysis Bullosa 58 0.069
454
OST003 Osteonecrosis 67 0.069
455
c BPL003 Bipolar Disorder 61 0.069
456
LYM040 Lymphoblastic Lymphoma 58 0.069
457
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 30 0.069
458
GT001 Gout 62 0.069
459
c NTR004 Neutropenia 61 0.069
460
c VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65 0.069
461
c ATT013 Attention Deficit-Hyperactivity Disorder 67 0.069
462
c MSC005 Muscular Dystrophy 66 0.069
463
c ATR005 Atrophic Gastritis 49 0.068
464
NWC001 Newcastle Disease 53 0.068
465
c PLY041 Polymyositis 59 0.068
466
PST021 Postpartum Depression 55 0.068
467
ACN002 Acanthosis Nigricans 65 0.068
468
c UVT001 Uveitis 62 0.068
469
MLK006 Milk Allergy 48 0.068
470
IMP005 Impotence 58 0.068
471
c MYS005 Myositis 62 0.068
472
c TRM003 Tremor 56 0.067
473
c PNS012 Paine Syndrome 63 0.067
474
INT007 Intermediate Coronary Syndrome 50 0.067
475
OTT002 Otitis Media 68 0.067
476
GLB015 Glioblastoma Multiforme 64 0.067
477
BLR001 Biliary Atresia 57 0.067
478
HMR039 Hemorrhage, Intracerebral 62 0.067
479
c PRP029 Porphyria 60 0.067
480
DBT010 Diabetic Neuropathy 60 0.067
481
c ANR048 Aniridia 1 63 0.067
482
BRN002 Bronchiolitis 62 0.067
483
MRB003 Morbid Obesity 62 0.067
484
P SVR001 Severe Acute Respiratory Syndrome 60 0.067
485
c ASP006 Aspergillosis 67 0.067
486
BRR014 Barrett Esophagus 71 0.066
487
c ALC004 Alcohol Abuse 69 0.066
488
MTR014 Motor Neuron Disease 60 0.066
489
GNR004 Generalized Anxiety Disorder 55 0.066
490
CHY002 Chylomicron Retention Disease 53 0.066
491
GST040 Gastric Adenocarcinoma 66 0.066
492
PRS063 Paresthesia 45 0.066
493
c GLM007 Glomerulonephritis 62 0.065
494
IGR001 Ige Responsiveness, Atopic 59 0.065
495
P ART101 Aortic Valve Disease 2 68 0.065
496
c HYP058 Hypervitaminosis a 48 0.065
497
CRB037 Cerebral Palsy 71 0.065
498
ERY003 Erythema Multiforme 63 0.065
499
c PLY018 Polycythemia 60 0.065
500
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.065
501
P BSL007 Basal Cell Carcinoma 65 0.065
502
EWN002 Ewing's Family of Tumors 57 0.065
503
MNS002 Mini Stroke 25 0.065
504
PHK010 Phakomatosis Spilorosea 18 0.065
505
KRT006 Keratoconjunctivitis 55 0.065
506
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.065
507
c PLM037 Pulmonary Hypertension 77 0.065
508
APL001 Aplastic Anemia 75 0.065
510
CNT047 Contact Dermatitis 64 0.064
511
c PLG001 Pelger-Huet Anomaly 54 0.064
512
c ANG001 Angelman Syndrome 65 0.064
513
PHT003 Phototoxic Dermatitis 44 0.064
514
c SJG008 Sjogren Syndrome 60 0.064
515
CHL014 Cholera 61 0.064
516
APN008 Apnea, Obstructive Sleep 68 0.063
517
KWS001 Kwashiorkor 46 0.063
518
NRN004 Neuroendocrine Tumor 56 0.063
519
c OBS001 Obstructive Jaundice 54 0.063
520
LMY002 Leiomyoma 58 0.063
521
GTR002 Goiter 54 0.063
522
P PSR017 Psoriasis 2 54 0.063
523
FND002 Fundus Dystrophy 51 0.063
524
STT009 Sutton Disease 2 32 0.063
525
SPN050 Spinocerebellar Degeneration 45 0.063
526
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.063
527
c ACT232 Acute Necrotizing Encephalopathy 30 0.063
528
BLD137 Blood Group--Ahonen 21 0.063
529
THY030 Thyroid Gland Disease 51 0.063
530
c INT143 Interstitial Cystitis 67 0.063
531
P THY109 Thyroid Cancer, Nonmedullary, 1 60 0.062
532
c ATX030 Ataxia-Telangiectasia 83 0.062
533
GST092 Gastroesophageal Reflux 66 0.062
534
PRT082 Preterm Premature Rupture of the Membranes 57 0.062
535
SPN041 Spinal Cord Disease 55 0.062
536
HYP080 Hypogonadism 53 0.062
537
c PLY019 Polyneuropathy 58 0.062
538
TXC002 Toxic Encephalopathy 57 0.062
539
c TTR001 Tetralogy of Fallot 71 0.062
540
TCK001 Tick-Borne Encephalitis 56 0.062
541
c GLL022 Guillain-Barre Syndrome 64 0.062
542
PNC033 Pancreas Adenocarcinoma 67 0.062
543
ALC006 Alcoholic Hepatitis 62 0.062
544
PLM010 Pulmonary Edema 60 0.062
545
BRN004 Brain Edema 59 0.061
546
c CMR001 Camurati-Engelmann Disease 62 0.061
547
c CHL066 Cholangitis 52 0.061
548
LRG015 Large Intestine Adenoma 17 0.061
549
PLS007 Plasmodium Falciparum Malaria 58 0.061
550
NSD001 Nose Disease 52 0.061
551
c PSD015 Pseudohypoparathyroidism 51 0.060
552
c PLM036 Pulmonary Fibrosis 70 0.060
553
THR016 Thrombophlebitis 54 0.060
554
c KRT007 Keratoconus 50 0.060
555
CRT016 Carotid Artery Disease 58 0.060
556
PLM031 Poliomyelitis 61 0.060
557
MCL006 Macular Retinal Edema 55 0.060
558
NTR027 Neutrophil Actin Dysfunction 32 0.060
559
YLL002 Yellow Fever 65 0.060
560
c LCH002 Lichen Planus 59 0.060
561
c THR015 Thrombophilia 56 0.060
562
c ACT008 Actinic Keratosis 55 0.060
563
SCH012 Schizoaffective Disorder 54 0.060
564
ATM052 Autoimmune Disease 1 41 0.060
565
c SYS005 Systemic Scleroderma 70 0.060
566
c KDN017 Kidney Cancer 59 0.060
567
CLR109 Colorectal Adenocarcinoma 54 0.059
568
HRN028 Horns in Sheep 24 0.059
569
SWL001 Swallowing Disorders 36 0.059
570
P JVN010 Juvenile Rheumatoid Arthritis 72 0.059
571
OST159 Osteogenic Sarcoma 67 0.059
572
c SML001 Small Cell Carcinoma 61 0.059
573
OBS082 Obstructive Nephropathy 52 0.059
574
ACR006 Aceruloplasminemia 72 0.059
575
LKP003 Leukoplakia 43 0.059
576
DRY001 Dry Eye Syndrome 53 0.059
577
c PTY003 Pityriasis Rubra Pilaris 52 0.059
578
DNT012 Dental Caries 52 0.058
579
c DYS154 Dystonia 66 0.058
580
PRS021 Prostatic Adenoma 55 0.058
581
ALL010 Allergic Contact Dermatitis 61 0.058
582
SXL003 Sexual Disorder 53 0.058
583
IDP070 Idiopathic Scoliosis 38 0.058
584
CYT008 Cytomegalovirus Infection 61 0.058
585
c ALL008 Allergic Bronchopulmonary Aspergillosis 57 0.058
586
INT303 Intracranial Hypertension, Idiopathic 53 0.058
587
GRN017 Granulocytopenia 52 0.058
589
c MMB011 Membranous Nephropathy 59 0.058
590
c FRD012 Friedreich Ataxia 1 67 0.057
591
HML018 Homologous Wasting Disease 25 0.057
592
HRW001 Hair Whorl 33 0.057
593
c AST007 Astrocytoma 51 0.057
594
P MJR004 Major Affective Disorder 4 40 0.057
595
CRP001 Carpal Tunnel Syndrome 72 0.057
596
PRV006 Pervasive Developmental Disorder 56 0.057
597
CRD223 Cardiac Arrhythmia 56 0.057
598
c OPT009 Optic Neuritis 55 0.057
599
c ESP024 Esophagitis 62 0.057
600
IGG001 Iga Glomerulonephritis 58 0.057
601
BLR008 Bilirubin Metabolic Disorder 53 0.057
602
HRP004 Herpes Zoster 63 0.057
603
BLL006 Bullous Pemphigoid 65 0.057
604
c SLL003 Salla Disease 53 0.057
605
ART004 Aortic Atherosclerosis 45 0.057
606
P LKM056 Leukemia, Chronic Lymphocytic 2 43 0.057
607
ENC005 Encephalomalacia 42 0.056
608
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.056
609
LMY014 Leiomyoma, Uterine 57 0.056
610
CLR030 Clear Cell Renal Cell Carcinoma 49 0.056
611
SDD001 Sudden Infant Death Syndrome 63 0.056
612
P CRP023 Carpenter Syndrome 1 59 0.056
613
c TRN020 Turner Syndrome 72 0.056
614
SPP011 Suppression of Tumorigenicity 12 62 0.056
615
BLD044 Bladder Disease 57 0.056
616
GNG013 Gingivitis 63 0.056
617
NRR001 Neuroretinitis 48 0.056
618
P LKM063 Leukemia, Chronic Myeloid 74 0.056
619
LSH001 Leishmaniasis 72 0.055
620
c MSC007 Muscle Hypertrophy 64 0.055
621
EPD070 Epidermoid Cysts 50 0.055
622
INT075 Intracranial Hypertension 58 0.055
623
HSH003 Hashimoto Thyroiditis 67 0.055
624
BCT004 Bacteriuria 52 0.055
625
DCB001 Decubitus Ulcer 47 0.055
626
MYM001 Myoma 57 0.055
627
BLD054 Blood Protein Disease 43 0.055
628
PRT037 Pertussis 71 0.055
629
DFF005 Diffuse Large B-Cell Lymphoma 58 0.055
630
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.055
631
CRT013 Carotid Stenosis 52 0.055
632
c END033 Endocarditis 60 0.055
633
SQM013 Squamous Cell Carcinoma, Head and Neck 82 0.055
634
c HYP614 Hyperlipidemia, Familial Combined 56 0.055
635
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.055
636
BLD053 Blood Platelet Disease 56 0.055
637
c ATS366 Autism X-Linked 2 45 0.055
638
BRB001 Beriberi 43 0.055
639
ACT119 Acute Promyelocytic Leukemia 61 0.054
640
P ACT042 Acute Pyelonephritis 47 0.054
641
CLF027 Cleft Palate, Isolated 66 0.054
642
SYN036 Syncope 49 0.054
643
c DLT002 Dilated Cardiomyopathy 74 0.054
644
c SNS001 Sensorineural Hearing Loss 60 0.054
645
BRN022 Bronchiectasis 58 0.054
646
ORL013 Oral Lichen Planus 53 0.054
647
c HYP818 Hypobetalipoproteinemia, Familial, 1 51 0.054
648
PHN003 Phenylketonuria 75 0.054
649
HRT012 Heart Valve Disease 57 0.054
650
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.054
651
TRP004 Tropical Sprue 36 0.054
652
CRD220 Cardiac Valvular Defect, Developmental 36 0.054
653
CHR066 Chronic Fatigue Syndrome 68 0.054
654
c ANT006 Antiphospholipid Syndrome 60 0.054
655
MTC005 Mitochondrial Metabolism Disease 46 0.054
656
P PSR028 Psoriasis 7 43 0.054
657
P PSR032 Psoriasis 11 43 0.054
658
P PSR018 Psoriasis 13 42 0.054
659
CLL003 Cellulitis 61 0.053
660
c TCD001 Tic Disorder 60 0.053
661
c FRN006 Frontotemporal Dementia 69 0.053
662
ALL009 Allergic Conjunctivitis 53 0.053
663
c HYP098 Hypereosinophilic Syndrome 67 0.053
664
SPL018 Splenomegaly 48 0.053
665
VCC001 Vaccinia 52 0.053
666
P ATR087 Atrial Standstill 1 69 0.053
667
c PMP001 Pemphigus 56 0.053
668
P DPH024 Diaphragmatic Hernia, Congenital 66 0.053
669
KRT001 Keratoconjunctivitis Sicca 63 0.053
670
c DBT005 Diabetes Insipidus 55 0.053
671
c MYP006 Myopia 62 0.053
672
PLM134 Pulmonary Fibrosis, Idiopathic 74 0.053
673
ACT088 Acute Insulin Response 50 0.053
674
PRS034 Parasitic Helminthiasis Infectious Disease 51 0.053
675
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 73 0.053
676
P CHL119 Cholangitis, Primary Sclerosing 63 0.053
677
PPL022 Papilloma 58 0.053
678
CRV040 Cervix Carcinoma 53 0.053
679
CHR074 Choriocarcinoma 50 0.053
680
SPS057 Spasticity 44 0.053
681
c HYP014 Hyperuricemia 56 0.052
682
AMN001 Amenorrhea 56 0.052
683
OCL006 Ocular Hypertension 56 0.052
684
c CND004 Candidiasis 63 0.052
685
INT079 Intrahepatic Cholangiocarcinoma 55 0.052
686
OBS002 Obsessive-Compulsive Disorder 69 0.052
687
c GLM040 Glioma Susceptibility 1 64 0.052
688
CNN004 Connective Tissue Cancer 46 0.052
689
MYF001 Myofibroma 38 0.052
690
c LRY044 Larynx Cancer 60 0.052
691
c FNC027 Fanconi Anemia, Complementation Group a 81 0.052
692
c HYP061 Hypertrophic Cardiomyopathy 59 0.052
693
c RTN022 Retinal Vein Occlusion 54 0.051
694
CRB008 Cerebral Atherosclerosis 44 0.051
695
c HYD006 Hydrocephalus 66 0.051
696
c THR005 Thrombotic Thrombocytopenic Purpura 65 0.051
697
c UTR058 Uterine Anomalies 60 0.051
698
CLN015 Colon Adenocarcinoma 57 0.051
699
PRS047 Prostatitis 57 0.051
700
ADT003 Auditory System Disease 52 0.051
701
BCT002 Bacterial Vaginosis 56 0.051
702
P MGL018 Megaloblastic Anemia 1 46 0.051
703
RHM001 Rheumatic Fever 63 0.051
704
CLF001 Cleft Lip 56 0.051
706
EXC002 Exocrine Pancreatic Insufficiency 42 0.051
707
STM006 Stomach Disease 56 0.051
708
c PSD087 Pseudoxanthoma Elasticum 68 0.051
709
MYL031 Myeloproliferative Neoplasm 64 0.051
711
ADN011 Adenoid Cystic Carcinoma 67 0.050
712
PHR003 Pharyngitis 58 0.050
713
HYP005 Hypokalemia 56 0.050
714
AMN012 Aminoacidopathies 25 0.050
715
CMM004 Common Variable Immunodeficiency 71 0.050
716
DPH001 Diphtheria 63 0.050
717
HLL004 Hellp Syndrome 52 0.050
718
SPN369 Spinal Disease 47 0.050
719
c FRG001 Fragile X Syndrome 70 0.050
720
CHR005 Chorioamnionitis 53 0.050
721
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 48 0.050
722
P MLG068 Malignant Glioma 47 0.050
723
LNS003 Lens Disease 40 0.050
724
P ACT004 Acute Diarrhea 39 0.050
725
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.050
726
P ACT073 Acute Leukemia 62 0.050
727
c PMP005 Pemphigus Vulgaris 58 0.050
728
VRC001 Varicocele 53 0.050
729
P PMP006 Pemphigus Vulgaris, Familial 41 0.050
730
c CHR071 Charcot-Marie-Tooth Disease 65 0.050
731
P ACT135 Acute Graft Versus Host Disease 58 0.050
732
MMM001 Mammary Paget's Disease 56 0.050
733
SNS003 Sensory Peripheral Neuropathy 56 0.050
734
DYS014 Dyspepsia 56 0.050
735
PST011 Pustulosis of Palm and Sole 50 0.050
736
CRN031 Cranial Nerve Disease 43 0.050
737
PRM050 Primary Orthostatic Tremor 34 0.050
738
PRS036 Parasitic Protozoa Infectious Disease 53 0.050
739
HYP064 Hypogonadotropism 42 0.050
740
FXF002 Fox-Fordyce Disease 41 0.050
741
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.050
742
P SVR005 Severe Pre-Eclampsia 55 0.049
743
MTB004 Metabolic Acidosis 51 0.049
744
AMN002 Amino Acid Metabolic Disorder 49 0.049
745
INB001 Inborn Amino Acid Metabolism Disorder 16 0.049
746
c FML011 Familial Adenomatous Polyposis 72 0.049
747
c PRT013 Portal Hypertension 61 0.049
748
c CRB088 Cerebral Atrophy 42 0.049
749
c HYP724 Hyperlipoproteinemia, Type Iii 61 0.049
750
c TMP001 Temporal Lobe Epilepsy 57 0.049
751
MYC006 Mycosis Fungoides 74 0.049
752
PSR001 Psoriatic Arthritis 68 0.049
753
PPT005 Peptic Ulcer Disease 64 0.049
754
CHL004 Cholelithiasis 52 0.049
755
HYP457 Hypertrophic Scars 48 0.049
756
c OCY003 Oocyte Maturation Defect 1 42 0.049
757
PNL013 Penile Disease 39 0.049
758
c CYT020 Cytomegalic Congenital Adrenal Hypoplasia 25 0.049
759
DBT008 Diabetic Angiopathy 48 0.049
760
FNT004 Fainting 36 0.049
761
ACT118 Acute Non Lymphoblastic Leukemia 33 0.049
762
c MYS003 Myasthenia Gravis 74 0.049
763
c HMR012 Hemorrhagic Fever 60 0.049
764
DSS009 Disseminated Intravascular Coagulation 58 0.049
765
PNM001 Pneumocystosis 58 0.049
766
c HMG032 Hemoglobin H Disease 55 0.049
767
KLD001 Keloids 51 0.049
768
c HYP087 Hypotrichosis 50 0.049
769
CRB085 Cerebral Hemorrhage 46 0.049
770
DBT002 Diabetic Autonomic Neuropathy 46 0.048
771
INC002 Inclusion Body Myositis 64 0.048
772
ANG005 Anogenital Venereal Wart 54 0.048
773
c MYT002 Myotonic Dystrophy 52 0.048
774
MYT026 Myotonia Atrophica 29 0.048
775
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.048
776
KWS002 Kawasaki Disease 72 0.048
777
SCH014 Schistosomiasis 62 0.048
778
GST023 Gastric Ulcer 58 0.048
779
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 0.048
780
c HRD018 Hair Disease 50 0.048
781
CLN045 Colonic Benign Neoplasm 48 0.048
782
CRN024 Corneal Disease 45 0.048
783
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.048
784
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.048
785
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.048
786
TTH004 Tethered Spinal Cord Syndrome 41 0.048
787
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.048
788
END014 Endemic Typhus 36 0.048
789
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 36 0.048
790
FST001 Foster-Kennedy Syndrome 33 0.048
791
VSC009 Vascular Skin Disease 20 0.048
792
c PTN014 Patent Ductus Arteriosus 1 62 0.048
793
c PLM034 Pulmonary Emphysema 59 0.048
794
HVY002 Heavy Metal Poisoning 24 0.048
795
WRN001 Werner Syndrome 74 0.047
796
GLS007 Glossitis 47 0.047
797
WRN005 Wrinkles 42 0.047
798
SCR035 Sacral Agenesis with Vertebral Anomalies 40 0.047
799
CYT017 Cytophagic Histiocytic Panniculitis 26 0.047
800
INT074 Intracranial Arteriosclerosis 16 0.047
801
TYP007 Typhoid Fever 68 0.047
802
BRK010 Burkitt Lymphoma 69 0.047
803
c FBR017 Fibrosarcoma 61 0.047
804
ORP003 Oropharynx Cancer 60 0.047
805
c CTN015 Cutaneous T Cell Lymphoma 56 0.047
806
CNN001 Cannabis Dependence 44 0.047
807
CNN002 Cannabis Abuse 42 0.047
808
c CRD132 Cardiac Conduction Defect 64 0.046
809
P MCR129 Microvascular Complications of Diabetes 1 66 0.046
810
SHG001 Shigellosis 59 0.046
811
GNG011 Gingival Disease 49 0.046
812
ORL012 Oral Leukoplakia 48 0.046
813
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.046
814
c TXP001 Toxoplasmosis 65 0.046
815
RNL077 Renal Fibrosis 51 0.046
816
PLY112 Polyarteritis Nodosa, Childhood-Onset 51 0.046
817
c WSK001 Wiskott-Aldrich Syndrome 76 0.046
818
c AXN002 Axenfeld-Rieger Syndrome 62 0.046
819
HYP081 Hypolipoproteinemia 49 0.046
820
CRV069 Cervix Disease 47 0.046
821
MSC157 Muscular Dystrophy, Duchenne Type 66 0.046
822
c OST001 Osteopetrosis 63 0.046
823
c HMP007 Hemophilia 62 0.046
824
PTT009 Pituitary Gland Disease 59 0.046
825
THR004 Thrombocytosis 55 0.046
826
DBT006 Diabetic Macular Edema 49 0.046
827
BLN006 Blind Loop Syndrome 43 0.046
828
ART001 Arterial Tortuosity Syndrome 59 0.046
829
HPT082 Hepatic Adenomas, Familial 49 0.046
830
ADP007 Adie Pupil 43 0.046
831
HNM002 Hinman Syndrome 29 0.046
832
MTR003 Mitral Valve Stenosis 51 0.046
833
HPR003 Heparin-Induced Thrombocytopenia 49 0.046
834
LRY018 Laryngeal Squamous Cell Carcinoma 48 0.046
835
PLS011 Plasmacytoma 62 0.046
836
HPT019 Hepatic Encephalopathy 60 0.046
837
BRS099 Breast Ductal Carcinoma 57 0.046
838
c MTH007 Methemoglobinemia 47 0.046
839
HPT004 Hepatic Coma 45 0.046
840
GRN007 Granuloma Annulare 45 0.046
841
c NRV006 Nervous System Cancer 60 0.045
842
SPR004 Supravalvular Aortic Stenosis 53 0.045
843
GRW007 Growth Hormone Deficiency 53 0.045
844
MYF002 Myofascial Pain Syndrome 43 0.045
845
GRD001 Giardiasis 42 0.045
846
P CHR417 Chronic Graft Versus Host Disease 67 0.045
847
INT146 Intervertebral Disc Disease 65 0.045
848
WLL001 Williams-Beuren Syndrome 64 0.045
849
c AGG001 Aggressive Periodontitis 56 0.045
850
CRN030 Coronary Stenosis 52 0.045
851
HYP189 Hypoadrenalism 43 0.045
852
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 62 0.045
853
c MCR010 Microcephaly 59 0.045
854
c ANG015 Angioedema 58 0.045
855
BLR006 Biliary Tract Disease 53 0.045
856
PNN001 Panniculitis 52 0.045
857
c MTC133 Mitochondrial Myopathy 52 0.045
858
EXC003 Excessive Tearing 39 0.045
859
P MST023 Mesothelioma, Malignant 63 0.045
860
LRY017 Laryngeal Disease 51 0.045
861
c PYR039 Peyronie Disease 47 0.045
862
BRT054 Brittle Bone Disorder 71 0.044
863
P JVN004 Juvenile Myelomonocytic Leukemia 70 0.044
864
c CHR285 Chronic Myelomonocytic Leukemia 65 0.044
865
c HYP750 Hypertriglyceridemia, Familial 58 0.044
866
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.044
867
c HYP040 Hypospadias 59 0.044
868
P ALP106 Alport Syndrome 1, X-Linked 49 0.044
869
c CHN044 Chondrodysplasia Punctata Syndrome 45 0.044
870
ADR007 Adrenoleukodystrophy 72 0.044
871
c GCH001 Gaucher's Disease 66 0.044
872
DBT062 Diabetic Foot Ulcers 59 0.044
873
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 59 0.044
874
ESP023 Esophageal Disease 59 0.044
875
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.044
876
c INT070 Intestinal Obstruction 55 0.044
877
ADR012 Adrenal Gland Disease 52 0.044
878
SPC010 Speech and Communication Disorders 51 0.044
879
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.044
880
ADR022 Adrenomyeloneuropathy 42 0.044
881
c CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 39 0.044
882
HNS001 Hansen's Disease 36 0.044
883
GST019 Gastrointestinal Stromal Tumor 74 0.044
884
c PRS038 Personality Disorder 68 0.044
885
AND002 Androgen Insensitivity Syndrome 62 0.044
886
PLG002 Plague 59 0.044
887
c PNC025 Panic Disorder 57 0.044
888
CRZ002 Crouzon Syndrome with Acanthosis Nigricans 44 0.044
889
ALR002 Al-Raqad Syndrome 41 0.044
890
SVR004 Severe Combined Immunodeficiency 70 0.044
891
CMB003 Combined T Cell and B Cell Immunodeficiency 55 0.044
892
ALP103 Alpha-1-Antitrypsin Deficiency 62 0.043
893
DCT002 Ductal Carcinoma in Situ 58 0.043
894
c CMP008 Compartment Syndrome 52 0.043
895
ASP004 Asphyxia Neonatorum 45 0.043
896
SCH003 Schizophreniform Disorder 43 0.043
897
LCR008 Lacrimal Apparatus Disease 43 0.043
899
WVR001 Weaver Syndrome 61 0.043
900
PRP036 Peripheral T-Cell Lymphoma 57 0.043
901
SBC017 Sebaceous Gland Disease 45 0.043
902
ART005 Arteriovenous Malformation 66 0.043
903
c FCL005 Focal Segmental Glomerulosclerosis 60 0.043
904
CHL067 Cholecystitis 59 0.043
905
P BSL024 Basal Cell Carcinoma 1 41 0.043
906
P MYS011 Myasthenia Gravis Congenital 33 0.043
907
ORP004 Oropharyngeal Cancer, Adult 23 0.043
908
HMT002 Hematologic Cancer 64 0.043
909
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.043
910
c PRM002 Primary Hyperoxaluria 54 0.043
911
EXP004 Exophthalmos 52 0.043
912
P RTN162 Retinitis Pigmentosa 2 52 0.043
913
PRX001 Peroxisomal Disease 46 0.043
914
RFR003 Refractive Error 46 0.043
915
SYS003 Systolic Heart Failure 46 0.043
916
ADR010 Adrenal Cortical Hypofunction 43 0.043
917
PRX034 Peroxisome Disorders 30 0.043
918
CRC034 Carcinoma Showing Thymus-Like Differentiation 29 0.043
919
P RTN181 Retinitis Pigmentosa 2, X-Linked 20 0.043
920
LNG039 Lung Squamous Cell Carcinoma 62 0.042
921
SBC016 Subacute Delirium 34 0.042
922
c CTN003 Cutaneous Lupus Erythematosus 55 0.042
923
P INH020 Inherited Metabolic Disorder 54 0.042
924
RBF001 Riboflavin Deficiency 45 0.042
925
c DRM010 Dermatomyositis 66 0.042
926
c ACR001 Aicardi-Goutieres Syndrome 63 0.042
927
c ESP035 Esophagitis, Eosinophilic, 1 60 0.042
928
YLL001 Yellow Nail Syndrome 51 0.042
929
P ACR116 Aicardi-Goutieres Syndrome 1 48 0.042
930
MYC088 Mycobacterium Avium Complex Infections 34 0.042
931
AND005 Androgen Insensitivity Syndrome, Mild 19 0.042
932
VRN004 Vernal Keratoconjunctivitis 56 0.042
933
GLL018 Gallbladder Cancer 55 0.042
934
c GLL020 Gallbladder Disease 64 0.042
935
P HYD046 Hydatidiform Mole, Recurrent, 1 56 0.042
936
GST010 Gestational Trophoblastic Neoplasm 47 0.042
937
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 45 0.042
938
ATR076 Atrophic Muscular Disease 34 0.042
939
SFT003 Soft Tissue Sarcoma 60 0.041
940
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 57 0.041
941
c ICH004 Ichthyosis 57 0.041
942
ALC009 Alcoholic Liver Cirrhosis 52 0.041
943
PRT129 Prothrombin Deficiency, Congenital 50 0.041
944
IDP073 Idiopathic Hypercalciuria 48 0.041
945
P MLG079 Malignant Pleural Mesothelioma 45 0.041
946
c SBR004 Seborrheic Dermatitis 42 0.041
947
PRX005 Peroxisomal Biogenesis Disorder 41 0.041
948
SPS019 Spastic Paraparesis 35 0.041
949
SDN002 Sudanophilic Cerebral Sclerosis 29 0.041
950
SYN007 Synovitis 61 0.041
951
APH002 Aphasia 60 0.041
952
SXD002 Sex Development Disorder 49 0.041
953
DRR003 Diarrhea 5, with Tufting Enteropathy, Congenital 48 0.041
954
HYP082 Hypopharynx Cancer 43 0.041
955
ATX038 Ataxia and Polyneuropathy, Adult-Onset 41 0.041
956
P GRV008 Graves Disease 1 57 0.041
957
ACT011 Acute Contagious Conjunctivitis 51 0.041
958
P PLM022 Pulmonary Valve Insufficiency 44 0.041
960
OST017 Osteomyelitis 65 0.040
961
c PLY014 Polycystic Kidney Disease 63 0.040
962
PST028 Post-Traumatic Stress Disorder 63 0.040
963
MNR012 Meniere Disease 57 0.040
964
CHR073 Choreatic Disease 50 0.040
965
UVL010 Uveal Disease 45 0.040
966
HYP030 Hypoactive Sexual Desire Disorder 44 0.040
967
P HYP602 Hyperoxaluria, Primary, Type Ii 38 0.040
968
c ORT004 Orthostatic Intolerance 69 0.040
969
c BNC003 Bone Cancer 61 0.040
970
P BCT007 Bacterial Meningitis 61 0.040
971
c MNC007 Monocytic Leukemia 57 0.040
972
LPD009 Lipid Storage Disease 53 0.040
973
IDP024 Idiopathic Inflammatory Myopathy 52 0.040
974
c MTC069 Mitochondrial Disorders 51 0.040
975
CHL061 Childhood Leukemia 51 0.040
976
P CNT016 Central Retinal Vein Occlusion 50 0.040
977
CHR178 Chromosomal Triplication 41 0.040
978
OLG001 Oligospermia 41 0.040
979
LYM017 Lyme Disease 71 0.040
980
PCK003 Pick Disease of Brain 66 0.040
981
FLR002 Filariasis 59 0.040
982
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.040
983
c SPN046 Spinal Muscular Atrophy 65 0.040
984
c EPD009 Epidermolysis Bullosa Dystrophica 58 0.040
985
c SCL009 Sclerosing Cholangitis 51 0.040
986
HMG002 Hemoglobinuria 51 0.040
987
BWN003 Bowenoid Papulosis 43 0.040
988
P HYP555 Hypertriglyceridemia, Transient Infantile 43 0.040
989
WRN002 Wernicke-Korsakoff Syndrome 53 0.040
991
P MCR112 Microvascular Complications of Diabetes 2 42 0.040
992
NRV004 Nerve Compression Syndrome 39 0.040
993
PSD088 Pseudobulbar Affect 39 0.040
994
FNC005 Functional Colonic Disease 29 0.040
995
c CHR012 Chronic Granulomatous Disease 70 0.040
996
P WLM018 Wilms Tumor 5 64 0.040
997
c SPN052 Spondyloarthropathy 58 0.040
998
ESP020 Esophageal Atresia 55 0.040
999
c LPC002 Lip Cancer 55 0.040
1000
c END046 Endometritis 53 0.040
1001
c PRR002 Pure Red-Cell Aplasia 52 0.040
1002
DRG003 Drug Dependence 51 0.040
1003
URT010 Ureteral Obstruction 49 0.040
1004
TRC109 Tracheoesophageal Fistula with or Without Esophageal Atresia 46 0.040
1005
LCH009 Lichen Sclerosus 46 0.040
1006
SDD008 Sudden Sensorineural Hearing Loss 46 0.040
1007
GLT007 Glutathione Synthetase Deficiency 46 0.040
1008
DSC009 Discoid Lupus Erythematosus 44 0.040
1009
NSP002 Nasopharyngitis 39 0.040
1010
END041 Endometrial Adenocarcinoma 60 0.039
1011
c MYC008 Myocarditis 59 0.039
1012
HYD002 Hydronephrosis 52 0.039
1013
LCH016 Lichen Sclerosus Et Atrophicus 39 0.039
1014
CHG001 Chagas Disease 73 0.039
1015
ACR007 Acromegaly 71 0.039
1016
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 63 0.039
1017
RFS006 Refsum Disease, Classic 63 0.039
1018
VSC003 Visceral Leishmaniasis 61 0.039
1019
c INT099 Intrahepatic Cholestasis of Pregnancy 59 0.039
1020
ONC002 Onchocerciasis 54 0.039
1021
SLV003 Salivary Gland Disease 51 0.039
1022
SKN023 Skin Tag 43 0.039
1023
NRX001 Neuroaxonal Dystrophy 35 0.039
1024
P BLD140 Blood Group, I System 26 0.039
1025
P CHR682 Chronic Bilirubin Encephalopathy 22 0.039
1026
KPS004 Kaposi Sarcoma 77 0.039
1027
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.039
1028
P LCL006 Localized Scleroderma 65 0.039
1029
TNS005 Tonsillitis 61 0.039
1030
LYS002 Lysosomal Storage Disease 56 0.039
1031
RTN020 Retinal Vascular Disease 54 0.039
1032
NNT012 Neonatal Jaundice 52 0.039
1033
SPH010 Sphingolipidosis 50 0.039
1034
INT071 Intestinal Perforation 45 0.039
1035
RST023 Resting Heart Rate, Variation in 44 0.039
1036
P HYP794 Hyperoxaluria, Primary, Type I 43 0.039
1037
P CNG031 Congenital Nervous System Abnormality 40 0.039
1038
P VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.039
1039
c LCT001 Lactic Acidosis 53 0.039
1040
LKC003 Leukocyte Disease 52 0.039
1041
PRT029 Parathyroid Adenoma 52 0.039
1042
PRN021 Paranasal Sinus Disease 51 0.039
1043
CNJ012 Conjunctival Disease 50 0.039
1044
ACR002 Acrocapitofemoral Dysplasia 40 0.039
1045
BCK003 Background Diabetic Retinopathy 38 0.039
1046
ATR073 Atrophic Glossitis 33 0.039
1047
c PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.038
1048
CHK001 Chikungunya 61 0.038
1049
c MLG056 Malignant Hyperthermia 60 0.038
1050
P INF023 Inflammatory Breast Carcinoma 57 0.038
1051
TRC008 Trachoma 54 0.038
1052
CRY004 Cryoglobulinemia 50 0.038
1053
SHW001 Shwartzman Phenomenon 37 0.038
1054
SKN020 Skin Papilloma 35 0.038
1055
WLS001 Wilson Disease 71 0.038
1056
HYP458 Hyper Ige Syndrome 52 0.038
1057
c RTT002 Rett Syndrome 83 0.038
1058
c HNT016 Huntington Disease 74 0.038
1059
c SPR120 Supranuclear Palsy, Progressive, 1 71 0.038
1060
MCR013 Microphthalmia 61 0.038
1061
c PRC012 Pericardial Effusion 54 0.038
1062
NRN001 Neuroendocrine Carcinoma 53 0.038
1063
HMP001 Hemopericardium 45 0.038
1064
KSH001 Keshan Disease 35 0.038
1065
c HST010 Histiocytosis 63 0.037
1066
c TCL004 T-Cell Leukemia 53 0.037
1067
P HMC039 Hemochromatosis, Type 1 74 0.037
1068
NRF007 Neurofibroma 67 0.037
1069
c ANP001 Anaplastic Large Cell Lymphoma 60 0.037
1070
HMP005 Hemiplegia 56 0.037
1071
DFF036 Differentiated Thyroid Carcinoma 55 0.037
1072
P BLC007 Bile Acid Synthesis Defect, Congenital, 1 44 0.037
1073
RFR010 Refractory Anemia 41 0.037
1074
VTM003 Vitamin Metabolic Disorder 20 0.037
1075
c FTL001 Fetal Alcohol Syndrome 64 0.037
1076
TRG002 Trigeminal Neuralgia 60 0.037
1077
c ATS308 Autosomal Dominant Cerebellar Ataxia 58 0.037
1078
c LKD001 Leukodystrophy 57 0.037
1079
CLF004 Cleft Lip/palate 56 0.037
1080
P ANT034 Anterior Uveitis 54 0.037
1081
c ARC016 Auriculocondylar Syndrome 1 48 0.037
1082
HRT015 Heritable Pulmonary Arterial Hypertension 48 0.037
1083
KHN001 Kuhnt-Junius Degeneration 48 0.037
1084
P ADL052 Adult Acute Lymphocytic Leukemia 46 0.037
1085
SLT001 Solitary Osseous Plasmacytoma 40 0.037
1086
ACL001 Acalculous Cholecystitis 39 0.037