Search results for Tocopherol

1395 hits were found for Tocopherol

# Family MCID Name MIFTS Score
1
RPD005 Rapidly Involuting Congenital Hemangioma 48 6.309
2
KRT002 Keratomalacia 54 5.944
3
ATX019 Ataxia with Vitamin E Deficiency 44 5.602
4
ATX049 Ataxia with Vitamin 3 Deficiency 52 5.233
5
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 4.497
6
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 4.284
7
ATH013 Atherosclerosis Susceptibility 63 4.145
8
AGN016 Aging 54 4.063
9
c HYP836 Hypercholesterolemia, Familial, 1 73 3.968
10
P AST005 Asthma 76 3.966
11
NNL005 Non-Alcoholic Fatty Liver Disease 63 3.857
12
FTT001 Fatty Liver Disease 61 3.619
13
OST003 Osteonecrosis 61 3.532
14
P MYP004 Myopathy 67 3.513
15
P CRN300 Coronary Heart Disease 1 73 3.422
16
ART140 Arteries, Anomalies of 52 3.364
17
P RHN004 Rhinitis 57 3.345
18
P ALZ034 Alzheimer Disease 87 3.335
19
P BRS047 Breast Cancer 97 3.325
20
P MSC005 Muscular Dystrophy 66 3.323
21
c CHR684 Chronic Kidney Disease 74 3.221
22
P KDN018 Kidney Disease 72 3.219
23
P THL005 Thalassemia 56 3.194
24
ALL006 Allergic Asthma 56 3.163
25
P SKN015 Skin Carcinoma 71 3.089
26
48X005 48,xyyy 39 3.080
27
ALL003 Allergic Rhinitis 66 3.037
28
LPP008 Lipoprotein Quantitative Trait Locus 65 3.035
29
ABT001 Abetalipoproteinemia 68 3.024
30
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 2.985
31
P PRS040 Prostate Cancer 95 2.970
32
c BTT014 Beta-Thalassemia 72 2.889
34
CYS001 Cystic Fibrosis 77 2.775
35
OST115 Osteonecrosis of the Jaw 40 2.774
36
CHL068 Cholestasis 61 2.738
37
ESP021 Esophageal Cancer 84 2.713
38
END086 End Stage Renal Disease 54 2.703
39
HYP066 Hyperglycemia 60 2.671
40
ISC004 Ischemia 61 2.667
41
NNL006 Non-Alcoholic Steatohepatitis 54 2.664
42
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.652
43
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 2.646
44
c PRC016 Pre-Eclampsia 64 2.606
45
LVR012 Liver Cirrhosis 62 2.595
46
P LVR013 Liver Disease 68 2.568
47
c TYP008 Type 1 Diabetes Mellitus 77 2.559
48
MLR004 Malaria 78 2.545
49
DFC004 Deficiency Anemia 74 2.526
50
P CTR002 Cataract 59 2.516
51
CYT002 Cytokine Deficiency 43 2.492
52
HYP781 Hypoascorbemia 52 2.490
53
P PRK039 Parkinsonism 55 2.482
54
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 2.426
55
MCS002 Mucositis 55 2.335
56
c TYP009 Type 2 Diabetes Mellitus 92 2.274
57
c PCH010 Pachyonychia Congenita 3 43 2.266
58
ADN018 Adenoma 58 2.251
59
BTT017 Beta-Thalassemia Major 53 2.240
60
HMS001 Hemosiderosis 48 2.200
61
P RRH023 Rare Hereditary Hemochromatosis 53 2.196
62
P INF032 Infertility 60 2.183
63
P NRP001 Neuropathy 59 2.183
64
P SZR006 Seizure Disorder 69 2.182
65
P NRB001 Neuroblastoma 66 2.179
66
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 2.171
67
PLX004 Plexopathy 29 2.168
68
INT002 Intermittent Claudication 61 2.157
69
LPD008 Lipid Metabolism Disorder 61 2.145
70
P ART021 Arteriosclerosis 53 2.143
71
MST005 Mastitis 52 2.143
72
c AMY091 Amyotrophic Lateral Sclerosis 1 88 2.129
73
P LTR001 Lateral Sclerosis 58 2.129
74
MLD018 Mild Cognitive Impairment 48 2.114
75
c ACT075 Acute Myocardial Infarction 55 2.068
76
ORL011 Oral Cancer 60 2.057
77
P PRD008 Periodontitis 64 2.054
78
P PNC035 Pancreatic Cancer 86 2.038
79
HLC007 Helicobacter Pylori Infection 67 2.032
80
c HRD202 Hereditary Lymphedema I 55 2.013
81
HYP266 Hypoxia 56 2.005
82
c ACT071 Acute Kidney Failure 60 1.974
83
P CRD246 Cardiovascular System Disease 55 1.969
84
P PNC044 Pancreatitis 61 1.967
85
END040 Endogenous Depression 54 1.958
86
P HYP750 Hypertriglyceridemia, Familial 62 1.945
87
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.939
88
SQM006 Squamous Cell Carcinoma 59 1.925
89
ANG054 Angina Pectoris 65 1.925
90
P PRP019 Peripheral Nervous System Disease 57 1.925
91
CLT003 Colitis 63 1.903
92
OST012 Osteoarthritis 77 1.903
93
P MYC007 Myocardial Infarction 69 1.899
94
P MLN007 Male Infertility 56 1.895
95
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.889
96
DWN001 Down Syndrome 70 1.885
97
P ADN016 Adenocarcinoma 63 1.879
98
P HRT032 Heart Disease 84 1.878
99
CRB039 Cerebrovascular Disease 65 1.828
100
DRM006 Dermatitis 62 1.812
101
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 1.805
102
P RTN008 Retinitis Pigmentosa 79 1.775
103
NRR001 Neuroretinitis 42 1.775
104
RTN023 Retinitis 45 1.775
105
PRP027 Peripheral Vascular Disease 71 1.766
106
CRV002 Cervix Uteri Carcinoma in Situ 48 1.756
107
CRV045 Cervical Intraepithelial Neoplasia 38 1.756
108
P ANR048 Aniridia 1 66 1.751
109
P PRS038 Personality Disorder 65 1.727
110
c MCR120 Microvascular Complications of Diabetes 7 47 1.716
111
c ACT073 Acute Leukemia 59 1.709
112
P BLD134 Bladder Cancer 79 1.693
113
P INF038 Influenza 68 1.693
114
RDT004 Radiation Induced Brachial Plexopathy 15 1.684
115
c HPT001 Hepatitis C 61 1.676
116
c HNT011 Huntington Disease-Like 3 33 1.676
117
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 1.671
118
P FRG001 Fragile X Syndrome 70 1.666
119
c HPT003 Hepatitis a 63 1.661
120
c ACT027 Acute Pancreatitis 60 1.660
121
c EXD008 Exudative Vitreoretinopathy 1 71 1.647
122
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 1.639
123
CLR108 Colorectal Adenoma 63 1.622
124
BRS051 Breast Disease 58 1.622
125
ENC005 Encephalomalacia 43 1.617
126
P LNG032 Lung Cancer 98 1.612
127
P HPT021 Hepatitis 68 1.609
128
MNT002 Mental Depression 56 1.609
129
DPR016 Depression 65 1.609
130
47X002 47,xyy 48 1.603
131
CRV035 Cervical Cancer 72 1.597
132
SCK003 Sickle Cell Anemia 74 1.596
133
P ECL001 Eclampsia 52 1.594
134
BRC011 Brachial Plexus Neuropathy 37 1.590
135
c ALP101 Alpha-Thalassemia 62 1.590
136
RTN020 Retinal Vascular Disease 45 1.578
137
P EYD002 Eye Disease 57 1.578
138
TRD006 Tardive Dyskinesia 53 1.578
139
c MCR115 Microvascular Complications of Diabetes 5 65 1.560
140
SKN016 Skin Disease 62 1.560
141
c HNT004 Huntington Disease-Like 2 51 1.558
142
GST023 Gastric Ulcer 52 1.550
143
GLM045 Glioma 62 1.550
144
GLL048 Glial Tumor 52 1.542
145
ULC004 Ulcerative Colitis 74 1.540
146
P CLR023 Colorectal Cancer 100 1.528
147
P PRK057 Parkinson Disease, Late-Onset 79 1.513
148
P GST044 Gastritis 55 1.512
149
BCT022 Bacterial Infectious Disease 56 1.502
150
P HYP076 Hyperthyroidism 53 1.500
151
P DRM053 Dermatitis, Atopic 65 1.497
152
P ADL010 Adult Respiratory Distress Syndrome 71 1.497
153
PRT036 Peritonitis 65 1.492
154
ALL029 Allergic Disease 61 1.489
155
c SPR086 Spermatogenic Failure 3 47 1.487
156
MYL009 Myelodysplastic Syndrome 67 1.486
157
P ALP008 Alopecia 53 1.486
158
PRT251 Proteinuria, Chronic Benign 58 1.483
159
DBT010 Diabetic Neuropathy 54 1.476
160
P VSC007 Vascular Disease 62 1.475
161
PRP080 Peripheral Artery Disease 54 1.474
162
NRT001 Neurotic Disorder 56 1.474
163
ANX004 Anoxia 40 1.474
164
c FML021 Familial Hypercholesterolemia 71 1.459
165
OST159 Osteogenic Sarcoma 66 1.452
166
P KLZ004 Kala-Azar 1 41 1.451
167
LSH001 Leishmaniasis 63 1.451
168
PST092 Posttransplant Acute Limbic Encephalitis 29 1.445
169
P HML002 Hemolytic Anemia 62 1.440
170
PRS129 Prostatic Hyperplasia, Benign 48 1.435
171
PRS021 Prostatic Adenoma 43 1.435
172
PRS045 Prostatic Hypertrophy 52 1.435
173
P DBT009 Diabetes Mellitus 67 1.427
174
c HPT016 Hepatitis B 62 1.425
175
P PLM036 Pulmonary Fibrosis 65 1.425
176
HRW001 Hair Whorl 35 1.420
177
P BRS044 Breast Adenocarcinoma 58 1.420
178
KHN001 Kuhnt-Junius Degeneration 48 1.414
179
P LKM002 Leukemia 66 1.397
180
ALC007 Alcohol Dependence 65 1.388
181
c MCR133 Microvascular Complications of Diabetes 4 41 1.386
182
c MCR113 Microvascular Complications of Diabetes 3 52 1.386
183
c MCR130 Microvascular Complications of Diabetes 6 41 1.386
184
ACT098 Acute Erythroid Leukemia 55 1.386
185
BRN004 Brain Edema 54 1.386
186
LKP003 Leukoplakia 39 1.386
187
STT001 Status Epilepticus 58 1.382
188
c PNS012 Paine Syndrome 60 1.380
189
c EPS039 Episodic Pain Syndrome, Familial, 1 42 1.380
190
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 1.380
191
NTR005 Nutritional Deficiency Disease 60 1.380
192
AND005 Androgen Insensitivity Syndrome, Mild 21 1.380
193
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 1.378
194
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 1.378
195
SPN186 Spinal Cord Injury 61 1.378
196
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.377
197
BRN071 Brain Injury 50 1.377
198
ACQ007 Acquired Immunodeficiency Syndrome 58 1.372
199
P GST053 Gastric Cancer 82 1.367
200
P ACN011 Acne 55 1.359
201
P OST002 Osteoporosis 77 1.356
202
IGG001 Iga Glomerulonephritis 50 1.340
203
PRT038 Protein-Energy Malnutrition 53 1.340
204
PPT005 Peptic Ulcer Disease 58 1.340
205
P MLN008 Melanoma 75 1.334
206
P FBR017 Fibrosarcoma 55 1.330
207
GLC003 Glucose Intolerance 53 1.322
208
RCK004 Rickets 65 1.322
209
ACT119 Acute Promyelocytic Leukemia 62 1.321
210
P BCL017 B-Cell Lymphoma 57 1.321
211
RTN003 Retinal Ischemia 48 1.310
212
LNG099 Lung Disease 62 1.304
213
P MLT020 Multiple Sclerosis 79 1.297
214
RLP002 Relapsing-Remitting Multiple Sclerosis 56 1.297
215
c SVR005 Severe Pre-Eclampsia 50 1.288
216
IRN002 Iron Metabolism Disease 56 1.287
217
CRB004 Cerebral Artery Occlusion 46 1.277
218
URT010 Ureteral Obstruction 45 1.276
219
BNR002 Bone Resorption Disease 47 1.271
220
P RCT021 Rectum Cancer 54 1.259
221
ENT011 Enterocolitis 55 1.258
222
c HYP595 Hypertension, Essential 84 1.256
223
VSC003 Visceral Leishmaniasis 54 1.256
224
P SCK005 Sickle Cell Disease 56 1.243
225
TRM010 Traumatic Brain Injury 50 1.240
226
PRN019 Perinatal Necrotizing Enterocolitis 60 1.240
227
STM007 Stomatitis 52 1.238
228
P PLM037 Pulmonary Hypertension 69 1.220
229
ADR040 Adrenal Gland Pheochromocytoma 45 1.216
230
P PHC003 Pheochromocytoma 70 1.216
231
P ALC033 Alcohol Use Disorder 67 1.214
232
PLM001 Pulmonary Tuberculosis 69 1.204
233
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 1.202
234
RTN017 Retinal Detachment 60 1.201
235
ORL012 Oral Leukoplakia 35 1.201
236
P OVR042 Ovarian Cancer 88 1.193
237
DBT008 Diabetic Angiopathy 47 1.180
238
VTM033 Vitamin K Deficiency Bleeding 50 1.169
239
P LCH002 Lichen Planus 55 1.169
240
ORL013 Oral Lichen Planus 45 1.169
241
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.169
242
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 1.169
243
TXC005 Toxic Shock Syndrome 62 1.161
244
PRM013 Premature Menopause 57 1.146
245
LMB062 Limb Ischemia 55 1.146
246
P MSC003 Muscular Atrophy 52 1.146
247
KRT009 Keratosis 52 1.137
248
P LKM062 Leukemia, Acute Lymphoblastic 69 1.134
249
P HYP768 Hyperlipoproteinemia, Type I 67 1.134
250
CNT047 Contact Dermatitis 57 1.125
251
P PNM007 Pneumonia 64 1.125
252
P DMN002 Dementia 65 1.112
253
P MTR014 Motor Neuron Disease 65 1.112
254
HYP056 Hypoglycemia 65 1.112
255
MYC005 Myocardial Stunning 45 1.109
256
ALL014 Allergic Encephalomyelitis 34 1.109
257
ACT228 Acute Radiation Syndrome 30 1.101
258
IMP005 Impotence 52 1.099
259
PRM020 Premenstrual Tension 39 1.096
260
P RTN018 Retinal Disease 53 1.085
261
P HYP086 Hypothyroidism 69 1.085
262
CRB090 Cerebral Hypoxia 42 1.082
263
BRN024 Bronchitis 67 1.079
264
TTN003 Tetanus 64 1.079
265
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 1.069
266
P NPH012 Nephrotic Syndrome 62 1.069
267
ART016 Aortic Aneurysm 69 1.069
268
P DDN001 Duodenal Ulcer 53 1.068
269
CLR109 Colorectal Adenocarcinoma 50 1.059
270
HRN029 Hearing Loss, Noise-Induced 37 1.056
271
P ENC018 Encephalopathy 62 1.056
272
THR024 Thrombosis 56 1.053
273
BLR001 Biliary Atresia 55 1.053
274
GST092 Gastroesophageal Reflux 60 1.049
275
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.046
276
HYP081 Hypolipoproteinemia 49 1.046
277
HNT002 Hantavirus Pulmonary Syndrome 55 1.046
278
INT323 Intraocular Pressure Quantitative Trait Locus 63 1.045
279
P LKM071 Leukemia, Chronic Lymphocytic 74 1.040
280
VSC002 Vascular Dementia 59 1.040
281
INT007 Intermediate Coronary Syndrome 53 1.040
282
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.027
283
c BSL007 Basal Cell Carcinoma 68 1.027
284
P MNC007 Monocytic Leukemia 48 1.027
285
P ATR005 Atrophic Gastritis 50 1.027
286
GLT007 Glutathione Synthetase Deficiency 48 1.027
287
P OPN001 Open-Angle Glaucoma 55 1.023
288
P LYM118 Lymphoma 69 1.023
289
P EPL164 Epilepsy 70 1.023
290
P UVT001 Uveitis 57 1.023
291
GNG013 Gingivitis 59 1.023
292
PNC001 Pancytopenia 52 1.020
293
GST019 Gastrointestinal Stromal Tumor 78 1.020
294
HMN044 Human Immunodeficiency Virus Type 1 76 1.010
295
END072 Endotheliitis 36 1.010
296
P NMN002 Niemann-Pick Disease 60 1.004
297
P OVR082 Overgrowth Syndrome 42 1.004
298
PYR010 Peyronie's Disease 50 1.004
299
P PLY011 Polycystic Ovary Syndrome 57 1.004
300
END057 Endometrial Cancer 71 0.993
301
ARG007 Argininemia 59 0.993
302
c LPD044 Lipodystrophy, Familial Partial, Type 7 25 0.988
303
LPT014 Leptin Deficiency or Dysfunction 77 0.984
304
P OPT006 Optic Nerve Disease 57 0.984
305
P NGH001 Night Blindness 52 0.984
306
P EPD016 Epidermolysis Bullosa 53 0.981
307
PPL052 Papillomatosis, Confluent and Reticulated 34 0.980
308
SDD001 Sudden Infant Death Syndrome 60 0.980
309
SNL007 Senile Cataract 40 0.980
310
P SPP010 Suppressor of Tumorigenicity 3 51 0.968
311
NRM005 Neuromuscular Disease 63 0.968
312
HDN002 Head Injury 44 0.968
313
PRS047 Prostatitis 58 0.967
314
STR067 Stroke, Ischemic 79 0.967
315
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 0.962
316
c LKM061 Leukemia, Acute Myeloid 83 0.962
317
P HRD217 Hereditary Optic Neuropathy 36 0.962
318
HMC014 Homocysteinemia 52 0.958
319
CRT015 Carotid Artery Occlusion 45 0.954
320
P ATX030 Ataxia-Telangiectasia 80 0.941
321
ORL015 Oral Squamous Cell Carcinoma 43 0.941
322
c NMN014 Niemann-Pick Disease, Type C2 49 0.941
323
TLN003 Telangiectasis 51 0.941
324
P CNJ013 Conjunctivitis 66 0.937
325
MCL006 Macular Retinal Edema 56 0.930
326
MTG002 Mutagen Sensitivity 35 0.911
327
AMN003 Amnestic Disorder 54 0.911
328
NRX001 Neuroaxonal Dystrophy 38 0.911
329
P INS002 in Situ Carcinoma 53 0.911
330
SPL018 Splenomegaly 47 0.911
331
BNN003 Bone Inflammation Disease 47 0.907
332
PLC008 Placenta Disease 49 0.907
333
RFR010 Refractory Anemia 49 0.907
334
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.904
336
MTB004 Metabolic Acidosis 48 0.895
337
P RSP003 Respiratory Failure 74 0.895
338
OST017 Osteomyelitis 63 0.895
339
PNC129 Pancreatic Adenocarcinoma 65 0.895
340
PRS063 Paresthesia 39 0.895
341
ORP003 Oropharynx Cancer 54 0.895
342
CHP002 Chops Syndrome 47 0.894
343
P PLY019 Polyneuropathy 53 0.894
344
GST033 Gestational Diabetes 61 0.894
345
P RTN016 Retinal Degeneration 52 0.894
346
c PRG106 Progressive Muscular Dystrophy 31 0.892
347
P SHR001 Short Bowel Syndrome 53 0.884
348
URM002 Uremia 47 0.884
349
P MTH007 Methemoglobinemia 46 0.878
350
YLL001 Yellow Nail Syndrome 41 0.878
351
SVR004 Severe Combined Immunodeficiency 71 0.878
352
P BNG032 Benign Mesothelioma 53 0.878
353
P ORL007 Oral Cavity Cancer 52 0.878
354
c PRS130 Prostate Cancer, Hereditary, 8 32 0.874
355
c PRS136 Prostate Cancer, Hereditary, 6 33 0.874
356
ANG049 Angioedema Induced by Ace Inhibitors 39 0.874
357
P TRN020 Turner Syndrome 67 0.874
358
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.874
359
c BRN108 Branchiootic Syndrome 1 63 0.869
360
P RST001 Restless Legs Syndrome 52 0.869
361
DRY001 Dry Eye Syndrome 49 0.869
362
LMY002 Leiomyoma 51 0.869
363
DBT002 Diabetic Autonomic Neuropathy 40 0.869
364
MYF001 Myofibroma 42 0.869
365
BRN056 Bronchopulmonary Dysplasia 57 0.866
366
c VRL010 Viral Hepatitis 52 0.864
367
c SML038 Small Cell Cancer of the Lung 69 0.863
368
LNG031 Lung Benign Neoplasm 51 0.863
369
BRN028 Brain Cancer 73 0.859
370
P NSP012 Nasopharyngeal Carcinoma 60 0.859
371
P SYS005 Systemic Scleroderma 73 0.859
372
P HMC002 Homocystinuria 52 0.859
373
LYM133 Lymphoma, Hodgkin, Classic 74 0.853
374
LYM143 Lymphoma, Non-Hodgkin, Familial 79 0.853
375
NPH009 Nephrolithiasis 54 0.853
376
P PRP029 Porphyria 60 0.853
377
P TRM003 Tremor 50 0.853
378
c DWL002 Dowling-Degos Disease 1 58 0.842
379
GLB002 Glioblastoma 67 0.842
381
RHM001 Rheumatic Fever 59 0.840
382
ADL002 Adult Syndrome 69 0.836
383
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 0.836
384
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 58 0.836
385
MNR012 Meniere Disease 55 0.836
386
MCL027 Macular Dystrophy, Dominant Cystoid 51 0.836
387
EHL052 Ehlers-Danlos Syndrome, Vascular Type 63 0.836
388
CNT017 Central Nervous System Origin Vertigo 43 0.836
389
DBT006 Diabetic Macular Edema 48 0.836
390
CHY002 Chylomicron Retention Disease 64 0.831
391
CLF001 Cleft Lip 54 0.831
392
CRD005 Cardia Cancer 38 0.820
393
c LKM063 Leukemia, Chronic Myeloid 71 0.817
394
GTR002 Goiter 52 0.817
395
THY029 Thyroid Carcinoma 54 0.817
396
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.808
397
P ORF002 Orofacial Cleft 42 0.808
398
EXT007 Extracutaneous Mastocytoma 38 0.808
399
MST004 Mast Cell Neoplasm 41 0.808
400
INS001 Insulinoma 59 0.796
401
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 0.792
402
c LKM005 Leukemia, T-Cell, Chronic 33 0.792
403
P HYP098 Hypereosinophilic Syndrome 66 0.792
404
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.787
405
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 0.787
406
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.787
407
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 0.787
408
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 0.787
409
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.787
410
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.787
411
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.787
412
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 0.787
413
P HYP111 Hyperprolinemia 44 0.783
414
EXC002 Exocrine Pancreatic Insufficiency 42 0.783
415
LYS002 Lysosomal Storage Disease 51 0.783
416
ISL109 Isolated Cleft Lip 33 0.783
417
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.770
418
KWS002 Kawasaki Disease 65 0.770
419
DSS032 Disease by Infectious Agent 55 0.770
420
P HNT016 Huntington Disease 73 0.770
421
ALC009 Alcoholic Liver Cirrhosis 54 0.770
422
VRC001 Varicocele 48 0.770
423
OBS082 Obstructive Nephropathy 41 0.770
424
P VTR007 Vitreoretinopathy 45 0.770
425
TNG002 Tangier Disease 64 0.763
426
KRN002 Kearns-Sayre Syndrome 63 0.763
427
PLM129 Pulmonary Disease, Chronic Obstructive 74 0.758
428
INS024 Insulin-Like Growth Factor I 77 0.756
429
KSH001 Keshan Disease 31 0.756
430
LRY022 Laryngoonychocutaneous Syndrome 43 0.756
431
ACT088 Acute Insulin Response 39 0.756
432
TST015 Testicular Disease 42 0.756
433
CHL004 Cholelithiasis 48 0.756
434
ANV001 Anovulation 46 0.756
435
c NMN015 Niemann-Pick Disease, Type C1 68 0.756
436
HRP004 Herpes Zoster 60 0.756
437
HVY002 Heavy Metal Poisoning 22 0.756
438
PRQ002 Paraquat Poisoning 28 0.756
439
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.741
440
CLF027 Cleft Palate, Isolated 64 0.741
441
ANM045 Anemia, Nonspherocytic Hemolytic, Due to G6pd Deficiency 50 0.741
442
KWS001 Kwashiorkor 44 0.741
443
CNS004 Constipation 56 0.741
444
GST040 Gastric Adenocarcinoma 66 0.741
445
P SLP005 Sleep Disorder 62 0.741
446
HPT022 Hepatoblastoma 54 0.741
447
P AMY004 Amyloidosis 69 0.741
448
CHR066 Chronic Fatigue Syndrome 60 0.741
449
CLF004 Cleft Lip/palate 57 0.741
450
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 0.737
451
P PLY014 Polycystic Kidney Disease 71 0.726
452
c SYS001 Systemic Lupus Erythematosus 86 0.726
453
ACT003 Acute Kidney Tubular Necrosis 46 0.726
454
P BND020 Bone Disease 60 0.726
455
MDD011 Mood Disorder 62 0.726
456
c NMN013 Niemann-Pick Disease, Type a 63 0.726
457
P TRC031 Trichorhinophalangeal Syndrome 37 0.726
458
P FRD001 Friedreich Ataxia 62 0.726
459
P VNS003 Venous Insufficiency 54 0.724
460
CHR431 Chronic Venous Insufficiency 48 0.724
461
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.710
462
P HYP058 Hypervitaminosis a 47 0.710
463
CRY035 Cryptorchidism, Unilateral or Bilateral 57 0.710
464
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.710
465
c SCL052 Scleroderma, Familial Progressive 60 0.710
466
ALC006 Alcoholic Hepatitis 61 0.710
467
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.710
468
P VSC018 Visceral Steatosis 32 0.710
469
P LPS004 Lupus Erythematosus 61 0.710
470
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.710
472
ATS010 Autosomal Recessive Disease 42 0.693
473
MDD018 Middle East Respiratory Syndrome 44 0.693
474
OTT002 Otitis Media 71 0.693
475
c ATR087 Atrial Standstill 1 74 0.693
476
HMR023 Hemorrhagic Cystitis 43 0.693
477
c GLC092 Glaucoma, Primary Open Angle 61 0.693
478
OPS001 Opisthorchiasis 41 0.693
479
ACT078 Acute Porphyria 50 0.693
480
P PRN023 Prion Disease 60 0.693
481
HYP014 Hyperuricemia 51 0.693
482
P CYS018 Cystitis 59 0.693
483
c DLT002 Dilated Cardiomyopathy 79 0.693
484
DSS009 Disseminated Intravascular Coagulation 56 0.693
485
MRS001 Marasmus 41 0.693
486
PLM010 Pulmonary Edema 54 0.693
487
CHR074 Choriocarcinoma 46 0.693
488
MSN004 Mesenchymal Cell Neoplasm 42 0.693
489
P TMP001 Temporal Lobe Epilepsy 49 0.693
490
P NRC002 Narcolepsy 55 0.693
491
P INT070 Intestinal Obstruction 57 0.693
492
HYP835 Hypothalamic Obesity 38 0.693
493
VTM002 Vitamin B12 Deficiency 48 0.675
494
P ANP001 Anaplastic Large Cell Lymphoma 61 0.675
495
P GLM040 Glioma Susceptibility 1 70 0.675
496
MLG169 Malignant Astrocytoma 57 0.675
497
PRC003 Proctitis 49 0.675
498
AMN001 Amenorrhea 53 0.675
499
PLR008 Pleurisy 49 0.675
500
PLC005 Placental Insufficiency 56 0.675
501
PST011 Pustulosis of Palm and Sole 52 0.675
502
P THY023 Thymoma 64 0.675
503
c THY107 Thymoma, Familial 42 0.675
504
CHL045 Choline Deficiency Disease 39 0.675
505
P PSR002 Psoriasis 63 0.675
506
RDT013 Radiation Proctitis 47 0.675
507
MYL069 Myeloma, Multiple 77 0.655
508
ANX010 Anxiety 70 0.655
509
GLT039 Glutathione Peroxidase Deficiency 33 0.655
510
MTH071 Methane Production 25 0.655
511
c THR092 Thrombophilia Due to Thrombin Defect 74 0.655
512
HRY003 Hairy Cell Leukemia 61 0.655
513
PNC034 Pancreas Disease 49 0.655
514
PPL002 Papillary Carcinoma 46 0.655
515
c PNC106 Pancreatic Agenesis 1 51 0.655
516
LYS012 Lysosomal Acid Lipase Deficiency 64 0.655
517
PNN001 Panniculitis 52 0.655
518
P HRP006 Herpes Simplex 65 0.655
519
MSL001 Measles 61 0.655
520
P MYC084 Mycobacterium Tuberculosis 1 68 0.653
521
HYP060 Hyperinsulinism 53 0.653
522
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.633
523
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.633
524
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.633
525
ATM095 Autoimmune Disease 61 0.633
526
SMT004 Smith-Lemli-Opitz Syndrome 69 0.633
527
CHL065 Cholangiocarcinoma 58 0.633
528
P UTR058 Uterine Anomalies 47 0.633
529
c LKM070 Leukemia, Acute Monocytic 56 0.633
530
CHR100 Chronic Ulcer of Skin 57 0.633
531
DYS015 Dysentery 50 0.633
532
INT079 Intrahepatic Cholangiocarcinoma 51 0.633
533
CHL056 Cheilitis 46 0.633
534
P HYP061 Hypertrophic Cardiomyopathy 69 0.633
535
BLR008 Bilirubin Metabolic Disorder 57 0.633
536
P MRC003 Mercury Poisoning 48 0.633
537
P MYL006 Myeloid Leukemia 60 0.633
538
LNG015 Lingual-Facial-Buccal Dyskinesia 47 0.633
539
ORL006 Oral Mucosa Leukoplakia 22 0.633
540
ACT200 Acute Monoblastic Leukemia 40 0.633
541
P TYR004 Tyrosinemia 49 0.633
542
OST173 Osteoradionecrosis of the Mandible 13 0.633
543
P DRM010 Dermatomyositis 61 0.631
544
FTL004 Fetal Erythroblastosis 33 0.631
545
THR016 Thrombophlebitis 50 0.631
546
P INF037 Inflammatory Bowel Disease 53 0.610
547
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 0.608
548
c MCP044 Mucopolysaccharidosis, Type Iiib 59 0.608
549
c CRD183 Ceroid Lipofuscinosis, Neuronal, 2 56 0.608
550
DFF005 Diffuse Large B-Cell Lymphoma 55 0.608
551
P SML001 Small Cell Carcinoma 52 0.608
552
P END046 Endometritis 46 0.608
553
TRY001 Trypanosomiasis 50 0.608
554
c HYP597 Hyperprolinemia, Type Ii 43 0.608
555
c MST023 Mesothelioma, Malignant 56 0.608
556
SRC014 Sarcoma 64 0.608
557
c CNG027 Congenital Hemolytic Anemia 49 0.608
558
PRT037 Pertussis 49 0.608
559
SCH014 Schistosomiasis 56 0.608
560
AZS001 Azoospermia 45 0.608
561
BLD041 Bladder Calculus 28 0.608
562
SPP011 Suppression of Tumorigenicity 12 61 0.608
563
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.608
564
SPN035 Spindle Cell Sarcoma 51 0.608
565
CRC021 Carcinosarcoma 62 0.608
566
MLG079 Malignant Pleural Mesothelioma 42 0.608
567
KRT063 Keratocystic Odontogenic Tumor 39 0.608
568
c GRV008 Graves Disease 1 54 0.578
569
c TYR012 Tyrosinemia, Type I 61 0.578
570
c PRM196 Premature Ovarian Failure 1 58 0.578
571
P DNG005 Dengue Virus 55 0.578
572
c TYP058 Type 2 Diabetes 5 25 0.578
573
P MYF003 Myofibrillar Myopathy 50 0.578
574
PLY150 Polykaryocytosis Inducer 29 0.578
575
c FNC027 Fanconi Anemia, Complementation Group a 81 0.578
576
HYP114 Hypertensive Nephropathy 35 0.578
577
ASC010 Ascaris Lumbricoides Infection 49 0.578
578
AML013 Amelogenesis Imperfecta, Hypomaturation Type, Iia1 24 0.578
579
BRC012 Brucellosis 66 0.578
580
PRS036 Parasitic Protozoa Infectious Disease 44 0.578
581
LYM027 Lymphopenia 56 0.578
582
ELP001 Elephantiasis 44 0.578
583
HYP080 Hypogonadism 49 0.578
584
FLR001 Filarial Elephantiasis 59 0.578
585
FLR002 Filariasis 55 0.578
586
ANT018 Anthracosis 51 0.578
587
P MST009 Mastocytosis 64 0.578
588
CLL003 Cellulitis 53 0.578
589
c RTN047 Retinitis Pigmentosa 18 45 0.578
590
RDC002 Radiculopathy 51 0.578
591
P HMP007 Hemophilia 52 0.578
592
ASH001 Asherman's Syndrome 34 0.578
593
c ALM001 Al Amyloidosis 54 0.578
594
PLM033 Pulmonary Embolism 58 0.578
595
LRN003 Learning Disability 49 0.578
596
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 0.578
597
PRC051 Paracetamol Poisoning 29 0.578
598
P SCH015 Schizophrenia 74 0.577
599
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.577
600
NRL016 Neural Tube Defects 81 0.577
601
IRN001 Iron Deficiency Anemia 58 0.577
602
CRH001 Crohn's Disease 80 0.577
603
P ACT008 Actinic Keratosis 54 0.577
604
CRT013 Carotid Stenosis 51 0.558
605
P DRR001 Diarrhea 55 0.558
606
PRX001 Peroxisomal Disease 46 0.558
607
ANT039 Antisynthetase Syndrome 55 0.544
608
P PSD087 Pseudoxanthoma Elasticum 66 0.539
610
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.539
611
VSC053 Visceral Steatosis, Congenital 35 0.539
612
DCT002 Ductal Carcinoma in Situ 58 0.539
613
HYP025 Hyperphosphatemia 47 0.539
614
MTN003 Motion Sickness 50 0.539
615
P ALG028 Alagille Syndrome 1 73 0.539
616
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.539
617
P CRP001 Carpal Tunnel Syndrome 66 0.539
618
TBC004 Tobacco Addiction 63 0.539
619
c WLM013 Wilms Tumor 1 65 0.539
620
P SPN046 Spinal Muscular Atrophy 62 0.539
621
ASP008 Aspiration Pneumonitis 43 0.539
622
PRP016 Paraplegia 52 0.539
623
P ICH004 Ichthyosis 56 0.539
624
ECH003 Echinococcosis 52 0.539
625
CDQ001 Cauda Equina Syndrome 37 0.539
626
SKN022 Skin Squamous Cell Carcinoma 54 0.539
627
SKN005 Skin Atrophy 41 0.539
628
ICH054 Ichthyosis, X-Linked 51 0.539
629
MNK001 Menkes Disease 64 0.539
630
PLY021 Polyradiculopathy 32 0.539
631
PRP030 Purpura 54 0.539
632
NNT008 Neonatal Abstinence Syndrome 40 0.539
633
SCT002 Scotoma 42 0.539
634
RTR001 Retrograde Amnesia 41 0.539
635
ORL004 Oral Submucous Fibrosis 56 0.539
636
P CRB059 Cerebellar Degeneration 36 0.539
637
c BCT013 Bacterial Pneumonia 47 0.539
638
CRT011 Carotenemia 23 0.539
639
DSC009 Discoid Lupus Erythematosus 43 0.539
640
RDT016 Radiation-Induced Plexopathy 8 0.539
641
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.539
642
c INH020 Inherited Metabolic Disorder 47 0.538
643
ADR007 Adrenoleukodystrophy 74 0.538
644
ADR022 Adrenomyeloneuropathy 39 0.538
645
RFS006 Refsum Disease, Classic 63 0.516
646
P RHM011 Rheumatoid Arthritis 81 0.516
647
HPT004 Hepatic Coma 43 0.516
648
HPT019 Hepatic Encephalopathy 59 0.516
649
TRN015 Transient Cerebral Ischemia 62 0.516
650
P CHR345 Chronic Pain 50 0.516
651
MTC005 Mitochondrial Metabolism Disease 45 0.516
652
P KRT007 Keratoconus 50 0.491
653
P SLP006 Sleep Apnea 69 0.491
654
PRT082 Preterm Premature Rupture of the Membranes 56 0.491
655
P FCS012 Facioscapulohumeral Muscular Dystrophy 1 68 0.491
656
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.491
657
CRB008 Cerebral Atherosclerosis 46 0.491
658
P ART022 Arthritis 70 0.491
659
SKN019 Skin Melanoma 70 0.491
660
P MTC069 Mitochondrial Disorders 57 0.491
661
P ACT105 Acute Mountain Sickness 52 0.491
662
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.462
663
P MYS005 Myositis 56 0.462
664
CNG034 Congestive Heart Failure 69 0.462
665
CLL014 Cll/sll 45 0.462
666
P INT068 Intestinal Disease 53 0.462
667
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.462
668
DYS073 Dysphagia 53 0.462
669
P ZLL001 Zellweger Syndrome 65 0.462
670
PRN071 Parenteral Nutrition-Associated Cholestasis 23 0.462
671
PHN003 Phenylketonuria 76 0.448
672
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.446
673
PRT025 Protein-Deficiency Anemia 27 0.446
674
c ACT068 Acute Cystitis 61 0.446
675
PRR001 Periarthritis 33 0.446
676
ATR003 Atrophic Rhinitis 39 0.446
677
NNT012 Neonatal Jaundice 53 0.446
678
P URT039 Urticaria 57 0.446
679
PTT037 Pituitary Tumors 44 0.446
680
HMG002 Hemoglobinuria 50 0.446
681
STM006 Stomach Disease 47 0.446
682
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.423
683
P LKD001 Leukodystrophy 58 0.423
684
CVD001 Covid-19 58 0.423
685
APN008 Apnea, Obstructive Sleep 66 0.423
686
P NJM001 Nijmegen Breakage Syndrome 75 0.423
687
CRH005 Crohn's Colitis 53 0.423
688
P HMN038 Human Coronavirus Sensitivity 30 0.423
689
c PRX045 Peroxisome Biogenesis Disorder 1b 61 0.423
690
P SJG008 Sjogren Syndrome 61 0.423
691
P ATS364 Autism 72 0.423
692
DSS008 Disease of Mental Health 74 0.423
693
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 58 0.423
694
P END044 Endometriosis 62 0.423
695
SCH003 Schizophreniform Disorder 54 0.423
696
P THR014 Thrombocytopenia 66 0.423
697
FML035 Familial Hyperlipidemia 55 0.423
698
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.423
699
PHT003 Phototoxic Dermatitis 27 0.423
700
AVN001 Avian Influenza 61 0.423
701
HMN014 Human Immunodeficiency Virus Infectious Disease 54 0.423
702
MCP033 Mucopolysaccharidoses 44 0.423
703
SBC016 Subacute Delirium 42 0.423
704
P ALP009 Alopecia Areata 59 0.423
705
P LNG064 Lung Cancer Susceptibility 3 70 0.407
706
P CLC063 Celiac Disease 1 66 0.396
707
ALL010 Allergic Contact Dermatitis 56 0.374
708
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.362
709
ANR040 Aneurysm 60 0.350
710
CHR005 Chorioamnionitis 50 0.337
711
CRN017 Coronary Thrombosis 46 0.337
712
CLN015 Colon Adenocarcinoma 64 0.337
713
MSC157 Muscular Dystrophy, Duchenne Type 79 0.337
714
ANR007 Anorexia Nervosa 59 0.337
715
SPN050 Spinocerebellar Degeneration 39 0.337
716
c CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 70 0.329
717
P MJR007 Major Affective Disorder 1 42 0.329
718
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.329
719
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.329
720
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 37 0.329
721
FCS002 Fucosidosis 62 0.329
722
P MTC003 Metachromatic Leukodystrophy 71 0.329
723
c DSB006 Desbuquois Dysplasia 1 48 0.329
724
c MJR008 Major Affective Disorder 2 34 0.329
725
MNT252 Mental Retardation, Skeletal Dysplasia, and Abducens Palsy 36 0.329
726
c NGH026 Night Blindness, Congenital Stationary, Type 1a 47 0.329
727
THR017 Thoracoabdominal Syndrome 40 0.329
728
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 0.329
729
c FNC043 Fanconi Anemia, Complementation Group E 62 0.329
730
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 58 0.329
731
PLY161 Polymicrogyria, Bilateral Perisylvian, X-Linked 42 0.329
732
VLC001 Velocardiofacial Syndrome 57 0.329
733
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.329
734
RHB024 Rhabdomyosarcoma 2 65 0.329
735
PLY001 Polycythemia Vera 69 0.329
736
c INF071 Inflammatory Bowel Disease 1 65 0.329
737
c MCP049 Mucopolysaccharidosis, Type Vii 62 0.329
738
MYL005 Myelofibrosis 70 0.329
739
BHR001 Behr Syndrome 50 0.329
740
P TST021 Testicular Germ Cell Tumor 61 0.329
741
SHR109 Short Stature, Auditory Canal Atresia, Mandibular Hypoplasia, and Skeletal Abnormalities 34 0.329
742
ACR041 Acromelic Frontonasal Dysostosis 53 0.329
743
MTC027 Mitochondrial Trifunctional Protein Deficiency 57 0.329
744
LBR038 Leber Hereditary Optic Neuropathy, Modifier of 62 0.329
745
PRS127 Pearson Marrow-Pancreas Syndrome 51 0.329
746
BRD001 Brody Myopathy 54 0.329
747
AYM001 Ayme-Gripp Syndrome 57 0.329
748
c MJR006 Major Affective Disorder 5 32 0.329
749
P BLD124 Bleeding Disorder, Platelet-Type, 11 68 0.329
750
c MCR112 Microvascular Complications of Diabetes 2 42 0.329
751
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 0.329
752
MSC007 Muscle Hypertrophy 64 0.329
753
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 39 0.329
754
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.329
755
VSL013 Visual Impairment and Progressive Phthisis Bulbi 36 0.329
756
ATN013 Autoinflammation, Panniculitis, and Dermatosis Syndrome 48 0.329
757
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.329
758
RSP027 Respiratory Papillomatosis, Juvenile Recurrent, Congenital 47 0.329
759
MNT001 Mantle Cell Lymphoma 65 0.329
760
P PRG092 Pregnancy Loss, Recurrent 1 42 0.329
761
c DRR009 Diarrhea 6 46 0.329
762
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.329
763
c NRP036 Neuropathy, Hereditary Sensory, Type if 33 0.329
764
c PRM108 Primary Progressive Multiple Sclerosis 51 0.329
765
LBR036 Leber Plus Disease 67 0.329
766
c PRM012 Primary Polycythemia 58 0.329
767
SPR126 Superior Semicircular Canal Dehiscence 41 0.329
768
HYP458 Hyper Ige Syndrome 60 0.329
769
c VRL005 Viral Pneumonia 52 0.329
770
c MGR028 Migraine with or Without Aura 1 64 0.329
771
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 64 0.329
772
c OST131 Osteopetrosis, Autosomal Dominant 2 52 0.329
773
c RST012 Restless Legs Syndrome 1 33 0.329
774
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 57 0.329
775
c LKM056 Leukemia, Chronic Lymphocytic 2 47 0.329
776
P CNR004 Cone-Rod Dystrophy 2 75 0.329
777
EHL079 Ehlers-Danlos Syndrome, Dermatosparaxis Type 52 0.329
778
P KHL003 Kohlschutter-Tonz Syndrome 57 0.329
779
P KRB001 Krabbe Disease 69 0.329
780
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.329
781
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.329
782
MNN047 Mannosidosis, Alpha B, Lysosomal 67 0.329
783
P PRC031 Preeclampsia/eclampsia 1 43 0.329
784
GST071 Gastrointestinal Carcinoma 46 0.329
785
P PRV006 Pervasive Developmental Disorder 52 0.329
786
c ATS007 Autism Spectrum Disorder 72 0.329
787
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 44 0.329
788
P EXN002 Exanthem 58 0.329
789
c FML001 Familial Atrial Fibrillation 65 0.329
790
P ATR011 Atrial Fibrillation 66 0.329
791
c OVR114 Ovarian Cancer 1 60 0.329
792
c HYP272 Hypercholesterolemia, Familial, 3 46 0.329
793
P MCR129 Microvascular Complications of Diabetes 1 68 0.329
794
P LBR014 Leber Congenital Amaurosis 4 56 0.329
795
c MJR003 Major Affective Disorder 6 32 0.329
796
c PRM092 Primary Lateral Sclerosis, Adult, 1 38 0.329
797
ACR006 Aceruloplasminemia 63 0.329
798
c HYP575 Hypotrichosis 7 43 0.329
799
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.329
800
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.329
801
c MJR004 Major Affective Disorder 4 28 0.329
802
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 44 0.329
803
LGG001 Legg-Calve-Perthes Disease 60 0.329
804
INC002 Inclusion Body Myositis 57 0.329
805
LMY014 Leiomyoma, Uterine 55 0.329
806
P PHT010 Photoparoxysmal Response 1 45 0.329
807
c BLD140 Blood Group, I System 47 0.329
808
P CMP005 Campomelic Dysplasia 65 0.329
809
c PNC108 Pancreatitis, Hereditary 68 0.329
810
APL002 Aplasia of Lacrimal and Salivary Glands 56 0.329
811
P PYR039 Peyronie Disease 39 0.329
812
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.329
813
c MJR023 Major Affective Disorder 7 33 0.329
814
c MJR024 Major Affective Disorder 9 40 0.329
815
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.329
816
P ATX024 Ataxia-Oculomotor Apraxia 3 46 0.329
817
P OCY003 Oocyte Maturation Defect 1 46 0.329
818
c CNG193 Congenital Disorder of Glycosylation, Type Ip 44 0.329
819
MYP159 Myopathy, Proximal, with Ophthalmoplegia 55 0.329
820
LTN004 Late-Onset Retinal Degeneration 60 0.329
821
PHL006 Phelan-Mcdermid Syndrome 62 0.329
822
NRL018 Neural Tube Defects, Folate-Sensitive 45 0.329
823
BWN001 Bowen-Conradi Syndrome 54 0.329
824
ASP002 Aspartylglucosaminuria 57 0.329
825
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 54 0.329
826
GLS018 Glass Syndrome 60 0.329
827
c MJR022 Major Affective Disorder 8 37 0.329
828
LPT006 Leptin Receptor Deficiency 50 0.329
829
ACD008 Acid-Labile Subunit Deficiency 52 0.329
830
ACT011 Acute Contagious Conjunctivitis 42 0.329
831
BRN139 Brain Small Vessel Disease 1 with or Without Ocular Anomalies 54 0.329
832
PLY105 Polycystic Ovary Syndrome 1 39 0.329
833
SPH010 Sphingolipidosis 47 0.329
834
CHL159 Childhood-Onset Asthma 30 0.329
835
P CHR285 Chronic Myelomonocytic Leukemia 59 0.329
836
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 30 0.329
837
HYP457 Hypertrophic Scars 42 0.329
838
P MYP006 Myopia 55 0.329
839
KRT001 Keratoconjunctivitis Sicca 49 0.329
840
ALV001 Alveolar Periostitis 34 0.329
841
ANS012 Anus Disease 47 0.329
842
MCR019 Microglandular Adenosis 43 0.329
843
THY030 Thyroid Gland Disease 50 0.329
844
MYL031 Myeloproliferative Neoplasm 66 0.329
845
NRN004 Neuroendocrine Tumor 55 0.329
846
BCK003 Background Diabetic Retinopathy 46 0.329
847
P OST001 Osteopetrosis 70 0.329
848
FST001 Foster-Kennedy Syndrome 39 0.329
849
INT074 Intracranial Arteriosclerosis 22 0.329
850
HLL004 Hellp Syndrome 53 0.329
851
MGL001 Megaloblastic Anemia 59 0.329
852
ASP004 Asphyxia Neonatorum 50 0.329
853
OLG003 Oligohydramnios 51 0.329
854
CRT017 Cartilage Disease 52 0.329
855
PRD004 Prediabetes Syndrome 52 0.329
856
BLD131 Bladder Urothelial Carcinoma 59 0.329
857
CRT016 Carotid Artery Disease 52 0.329
858
CRB009 Cerebritis 43 0.329
859
BLD051 Blood Coagulation Disease 53 0.329
860
BRN009 Burning Mouth Syndrome 51 0.329
861
TXC002 Toxic Encephalopathy 51 0.329
862
P ART023 Arthropathy 60 0.329
863
P BPL003 Bipolar Disorder 56 0.329
864
VGN023 Vaginitis 56 0.329
865
CLN045 Colonic Benign Neoplasm 48 0.329
866
PSY004 Psychotic Disorder 66 0.329
867
SKN013 Skin Benign Neoplasm 49 0.329
868
PPL001 Papillary Adenoma 44 0.329
869
GST049 Gastrointestinal System Cancer 49 0.329
870
c MCP050 Mucopolysaccharidosis, Type Ii 73 0.329
871
ABC001 Abcd Syndrome 44 0.329
873
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.329
874
c MSC109 Mosaic Variegated Aneuploidy Syndrome 1 57 0.329
875
SCH036 Scheie Syndrome 73 0.329
876
HRL003 Hurler Syndrome 66 0.329
877
HRL004 Hurler-Scheie Syndrome 58 0.329
878
c HYP807 Hyperinsulinemic Hypoglycemia, Familial, 6 51 0.329
879
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 40 0.329
880
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.329
881
P THY032 Thyroiditis 56 0.329
882
P PLY018 Polycythemia 56 0.329
883
GLC008 Glucose Metabolism Disease 40 0.329
884
PRS011 Persian Gulf Syndrome 35 0.329
885
HYP005 Hypokalemia 55 0.329
886
BNM001 Bone Marrow Cancer 45 0.329
887
P HYP087 Hypotrichosis 41 0.329
888
P HDC001 Headache 56 0.329
889
CNT060 Central Serous Chorioretinopathy 39 0.329
890
CTS005 Catastrophic Antiphospholipid Syndrome 43 0.329
891
BNS003 Binswanger's Disease 41 0.329
892
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.329
893
P NRV007 Nervous System Disease 66 0.329
894
P HMR005 Hemorrhoid 49 0.329
895
RFR003 Refractive Error 41 0.329
897
ZLL011 Zellweger Spectrum Disorder 45 0.329
898
KLD004 Keloid Disorder 39 0.329
899
c HMG029 Hemoglobin Se Disease 41 0.329
900
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.329
901
CRY008 Cryopyrin-Associated Periodic Syndrome 48 0.329
902
LYM019 Lymphosarcoma 46 0.329
903
NNN007 Non-Involuting Congenital Hemangioma 40 0.329
904
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.329
905
P OVR096 Overlap Myositis 27 0.329
907
DSR072 Disorder of Energy Metabolism 10 0.329
908
URM005 Uremic Pruritus 45 0.329
909
P GLL022 Guillain-Barre Syndrome 59 0.324
910
CHL123 Chlamydia 58 0.324
911
CRN030 Coronary Stenosis 50 0.324
912
FML037 Female Breast Cancer 51 0.310
913
CHL147 Chlamydia Pneumonia 47 0.310
914
c HPT073 Hepatitis C Virus 71 0.310
915
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.310
916
P KDN017 Kidney Cancer 60 0.310
917
PLS007 Plasmodium Falciparum Malaria 52 0.310
918
P GLM007 Glomerulonephritis 59 0.310
919
ART004 Aortic Atherosclerosis 46 0.296
920
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.296
921
GST029 Gastric Cardia Adenocarcinoma 29 0.296
922
SNS003 Sensory Peripheral Neuropathy 51 0.296
923
RBF001 Riboflavin Deficiency 49 0.280
924
P DYS154 Dystonia 64 0.280
925
DDN006 Duodenitis 50 0.280
926
c HMC039 Hemochromatosis, Type 1 73 0.264
927
URL001 Urolithiasis 45 0.264
928
P FML011 Familial Adenomatous Polyposis 71 0.264
929
P PRP003 Porphyria Cutanea Tarda 66 0.264
930
CRN019 Coronary Artery Vasospasm 47 0.264
931
ALC011 Alcoholic Neuropathy 35 0.264
932
P LCT001 Lactic Acidosis 50 0.264
933
HYP141 Hyperphenylalaninemia 42 0.264
934
PRX085 Preaxial Hallucal Polydactyly 28 0.247
935
P GLC113 Galactosemia I 65 0.247
936
BCT021 Bacterial Sepsis 43 0.247
937
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.247
938
P ESP024 Esophagitis 60 0.247
939
IDP091 Idiopathic Nephrotic Syndrome 49 0.247
940
c LNG109 Lung Cancer Susceptibility 1 26 0.229
941
RNL077 Renal Fibrosis 46 0.229
942
P MJR001 Major Depressive Disorder 68 0.229
943
P HPT023 Hepatocellular Carcinoma 95 0.229
944
IGR001 Ige Responsiveness, Atopic 59 0.229
945
P MYG005 Myoglobinuria 40 0.229
946
P OBS001 Obstructive Jaundice 49