Search results for alpha-Tocopherol acetate

830 hits were found for alpha-Tocopherol acetate

# Family MCID Name MIFTS Score
1
P PRS040 Prostate Cancer 95 19.571
2
P MLT020 Multiple Sclerosis 79 15.300
3
RLP002 Relapsing-Remitting Multiple Sclerosis 56 13.550
4
PRS047 Prostatitis 58 11.778
5
LMY002 Leiomyoma 51 11.377
6
P END044 Endometriosis 62 10.719
7
P SZR006 Seizure Disorder 69 10.646
8
MYF001 Myofibroma 42 10.376
9
END057 Endometrial Cancer 71 10.229
10
CLT003 Colitis 63 9.928
11
c HYP836 Hypercholesterolemia, Familial, 1 73 9.896
12
AGN016 Aging 54 9.817
13
ATX019 Ataxia with Vitamin E Deficiency 44 9.692
14
48X005 48,xyyy 39 9.647
15
P KDN018 Kidney Disease 72 9.508
16
P BRS047 Breast Cancer 97 9.101
17
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 9.005
18
P CTR002 Cataract 59 8.885
19
P ADN016 Adenocarcinoma 63 8.756
20
ATH013 Atherosclerosis Susceptibility 63 8.747
21
CRV035 Cervical Cancer 72 8.539
22
P ACN011 Acne 55 8.299
23
KRT002 Keratomalacia 54 8.233
24
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 8.212
25
P EPL164 Epilepsy 70 8.194
26
P PLY011 Polycystic Ovary Syndrome 57 8.055
27
P INF032 Infertility 60 7.978
28
RPD005 Rapidly Involuting Congenital Hemangioma 48 7.968
29
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 7.903
30
END086 End Stage Renal Disease 54 7.840
31
GST023 Gastric Ulcer 52 7.770
32
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 7.671
33
ULC004 Ulcerative Colitis 74 7.649
34
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 7.588
35
c CHR684 Chronic Kidney Disease 74 7.382
37
P MYP004 Myopathy 67 6.899
38
c TYP009 Type 2 Diabetes Mellitus 92 6.851
39
ATX049 Ataxia with Vitamin 3 Deficiency 52 6.781
40
CRV002 Cervix Uteri Carcinoma in Situ 48 6.777
41
CRV045 Cervical Intraepithelial Neoplasia 38 6.777
42
FTT001 Fatty Liver Disease 61 6.756
43
P ALZ034 Alzheimer Disease 87 6.690
44
NNL005 Non-Alcoholic Fatty Liver Disease 63 6.687
45
HYP066 Hyperglycemia 60 6.650
46
PRS045 Prostatic Hypertrophy 52 6.265
47
ADN018 Adenoma 58 6.265
48
P SKN015 Skin Carcinoma 71 6.256
49
CYT002 Cytokine Deficiency 43 6.238
50
c ACT071 Acute Kidney Failure 60 6.203
51
DWN001 Down Syndrome 70 6.172
52
ALL029 Allergic Disease 61 6.123
53
DFC004 Deficiency Anemia 74 6.070
54
LPP008 Lipoprotein Quantitative Trait Locus 65 6.059
55
P CRN300 Coronary Heart Disease 1 73 6.052
56
MTH071 Methane Production 25 6.026
57
P NRB001 Neuroblastoma 66 5.992
58
c TYP008 Type 1 Diabetes Mellitus 77 5.971
59
P LNG032 Lung Cancer 98 5.959
60
LPD008 Lipid Metabolism Disorder 61 5.866
61
PRS021 Prostatic Adenoma 43 5.849
62
DRM006 Dermatitis 62 5.848
63
P LVR013 Liver Disease 68 5.772
64
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 5.768
65
PRT036 Peritonitis 65 5.686
66
HYP025 Hyperphosphatemia 47 5.678
67
c MCR115 Microvascular Complications of Diabetes 5 65 5.577
68
P THL005 Thalassemia 56 5.544
69
MTB004 Metabolic Acidosis 48 5.464
70
P DBT009 Diabetes Mellitus 67 5.444
71
CYS001 Cystic Fibrosis 77 5.442
72
OST012 Osteoarthritis 77 5.401
73
P UVT001 Uveitis 57 5.378
74
ALL014 Allergic Encephalomyelitis 34 5.348
75
CHL068 Cholestasis 61 5.341
76
GLL048 Glial Tumor 52 5.319
77
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 5.307
78
P LKM002 Leukemia 66 5.300
79
SKN016 Skin Disease 62 5.294
80
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 5.277
81
P OST002 Osteoporosis 77 5.276
82
GLM045 Glioma 62 5.271
83
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 5.263
84
P DRM053 Dermatitis, Atopic 65 5.259
85
PRS129 Prostatic Hyperplasia, Benign 48 5.254
86
P NRP001 Neuropathy 59 5.204
87
NRR001 Neuroretinitis 42 5.178
88
RTN023 Retinitis 45 5.170
89
P ALP008 Alopecia 53 5.159
90
c ACT027 Acute Pancreatitis 60 5.115
91
c HYP595 Hypertension, Essential 84 5.098
92
P PNC035 Pancreatic Cancer 86 5.095
93
HRW001 Hair Whorl 35 5.074
94
ACQ007 Acquired Immunodeficiency Syndrome 58 5.030
95
ACT098 Acute Erythroid Leukemia 55 5.005
96
FCL014 Focal Epilepsy 53 4.978
97
ATM095 Autoimmune Disease 61 4.937
98
c ACT073 Acute Leukemia 59 4.870
99
P RHN004 Rhinitis 57 4.861
100
P ART021 Arteriosclerosis 53 4.853
101
c MCR120 Microvascular Complications of Diabetes 7 47 4.849
102
P HRT032 Heart Disease 84 4.840
103
ART140 Arteries, Anomalies of 52 4.813
104
PRT251 Proteinuria, Chronic Benign 58 4.791
105
P HPT023 Hepatocellular Carcinoma 95 4.785
106
CNT047 Contact Dermatitis 57 4.769
107
CNS004 Constipation 56 4.763
108
P PNC044 Pancreatitis 61 4.719
109
c ACT075 Acute Myocardial Infarction 55 4.656
110
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 4.645
111
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 4.645
112
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 4.645
113
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 4.645
114
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 4.645
115
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 4.645
116
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 4.645
117
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 4.645
118
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 4.645
119
MST005 Mastitis 52 4.622
120
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 4.616
121
P ADL010 Adult Respiratory Distress Syndrome 71 4.612
122
NNL006 Non-Alcoholic Steatohepatitis 54 4.612
123
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 4.596
124
IMM167 Immune Deficiency Disease 77 4.586
125
HYP266 Hypoxia 56 4.581
126
P AST005 Asthma 76 4.560
127
PPT005 Peptic Ulcer Disease 58 4.557
128
P LTR001 Lateral Sclerosis 58 4.548
129
c AMY091 Amyotrophic Lateral Sclerosis 1 88 4.539
130
P MSC005 Muscular Dystrophy 66 4.534
131
PPL022 Papilloma 53 4.522
132
SQM002 Squamous Cell Papilloma 45 4.514
133
INT323 Intraocular Pressure Quantitative Trait Locus 63 4.489
134
P GST053 Gastric Cancer 82 4.459
135
c BTT014 Beta-Thalassemia 72 4.446
136
P INF037 Inflammatory Bowel Disease 53 4.439
137
PRT037 Pertussis 49 4.429
138
P INS002 in Situ Carcinoma 53 4.427
139
LVR012 Liver Cirrhosis 62 4.373
140
c PRC016 Pre-Eclampsia 64 4.371
141
P FBR017 Fibrosarcoma 55 4.351
142
HMS001 Hemosiderosis 48 4.325
143
P CLR023 Colorectal Cancer 100 4.321
144
c PCH010 Pachyonychia Congenita 3 43 4.316
145
PRM020 Premenstrual Tension 39 4.312
146
c THR092 Thrombophilia Due to Thrombin Defect 74 4.308
147
P EYD002 Eye Disease 57 4.297
148
BRN004 Brain Edema 54 4.266
149
HMN014 Human Immunodeficiency Virus Infectious Disease 54 4.244
150
CHL014 Cholera 62 4.240
151
P MYC007 Myocardial Infarction 69 4.239
152
ALC007 Alcohol Dependence 65 4.219
153
ISC004 Ischemia 61 4.195
154
P HYP750 Hypertriglyceridemia, Familial 62 4.187
155
P LYM118 Lymphoma 69 4.169
156
OST159 Osteogenic Sarcoma 66 4.154
157
P RRH023 Rare Hereditary Hemochromatosis 53 4.148
158
P GST044 Gastritis 55 4.130
159
ORL011 Oral Cancer 60 4.099
160
GLB002 Glioblastoma 67 4.097
161
P PHC003 Pheochromocytoma 70 4.090
162
ADR040 Adrenal Gland Pheochromocytoma 45 4.088
163
P DDN001 Duodenal Ulcer 53 4.049
164
MYL009 Myelodysplastic Syndrome 67 4.017
165
c SML038 Small Cell Cancer of the Lung 69 4.015
166
INT002 Intermittent Claudication 61 4.001
167
P GLM040 Glioma Susceptibility 1 70 3.980
168
PLM129 Pulmonary Disease, Chronic Obstructive 74 3.967
169
P ANP001 Anaplastic Large Cell Lymphoma 61 3.961
170
ALL003 Allergic Rhinitis 66 3.952
171
SQM006 Squamous Cell Carcinoma 59 3.947
172
MYL069 Myeloma, Multiple 77 3.935
173
47X002 47,xyy 48 3.934
174
DBT010 Diabetic Neuropathy 54 3.922
175
IMP005 Impotence 52 3.911
176
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 3.895
177
c HNT004 Huntington Disease-Like 2 51 3.891
178
SQM013 Squamous Cell Carcinoma, Head and Neck 75 3.871
179
IRN002 Iron Metabolism Disease 56 3.864
180
CRH001 Crohn's Disease 80 3.861
181
ANX004 Anoxia 40 3.848
182
P CLC063 Celiac Disease 1 66 3.847
183
c HNT011 Huntington Disease-Like 3 33 3.818
184
MNT002 Mental Depression 56 3.808
185
P DMN002 Dementia 65 3.805
186
THR024 Thrombosis 56 3.805
187
P VSC007 Vascular Disease 62 3.731
188
MLD018 Mild Cognitive Impairment 48 3.723
189
P PLM037 Pulmonary Hypertension 69 3.702
190
P ALC033 Alcohol Use Disorder 67 3.697
191
RNL114 Renal Cell Carcinoma, Nonpapillary 79 3.682
192
P OPN001 Open-Angle Glaucoma 55 3.670
193
P BRS044 Breast Adenocarcinoma 58 3.670
194
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 3.664
195
TLN003 Telangiectasis 51 3.650
196
ESP021 Esophageal Cancer 84 3.632
197
ENT004 Enthesopathy 51 3.619
198
CRB004 Cerebral Artery Occlusion 46 3.607
199
P PRP019 Peripheral Nervous System Disease 57 3.578
200
P PRD008 Periodontitis 64 3.575
201
P HYP076 Hyperthyroidism 53 3.557
202
DPR016 Depression 65 3.550
203
P ART022 Arthritis 70 3.550
204
URM002 Uremia 47 3.527
205
c MCR113 Microvascular Complications of Diabetes 3 52 3.506
206
P RTN018 Retinal Disease 53 3.503
207
TTN003 Tetanus 64 3.497
208
P ENC018 Encephalopathy 62 3.496
209
BNR002 Bone Resorption Disease 47 3.491
210
P LKM071 Leukemia, Chronic Lymphocytic 74 3.488
211
P SCK005 Sickle Cell Disease 56 3.486
212
HYP056 Hypoglycemia 65 3.481
213
INS024 Insulin-Like Growth Factor I 77 3.464
214
P LKM062 Leukemia, Acute Lymphoblastic 69 3.462
215
P BLD134 Bladder Cancer 79 3.455
216
MCL006 Macular Retinal Edema 56 3.428
217
c SYS001 Systemic Lupus Erythematosus 86 3.427
218
P TRM003 Tremor 50 3.412
219
P SPP010 Suppressor of Tumorigenicity 3 51 3.406
220
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 3.405
221
TXC005 Toxic Shock Syndrome 62 3.396
222
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 3.387
223
MLR004 Malaria 78 3.387
224
AZS001 Azoospermia 45 3.378
225
SPN186 Spinal Cord Injury 61 3.373
226
ACT119 Acute Promyelocytic Leukemia 62 3.371
227
PLM010 Pulmonary Edema 54 3.366
228
BRS051 Breast Disease 58 3.356
229
ANV001 Anovulation 46 3.343
230
P ESP024 Esophagitis 60 3.333
231
c DNT047 Dentinogenesis Imperfecta Type 2 35 3.332
232
END040 Endogenous Depression 54 3.314
233
HLC007 Helicobacter Pylori Infection 67 3.308
234
NTR005 Nutritional Deficiency Disease 60 3.298
235
P SYS005 Systemic Scleroderma 73 3.296
236
P CRD246 Cardiovascular System Disease 55 3.296
237
P PSR002 Psoriasis 63 3.291
238
PST011 Pustulosis of Palm and Sole 52 3.287
239
P MLN007 Male Infertility 56 3.278
240
P MLN008 Melanoma 75 3.276
241
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 3.270
242
P KDN017 Kidney Cancer 60 3.267
243
P RSP003 Respiratory Failure 74 3.262
244
PST092 Posttransplant Acute Limbic Encephalitis 29 3.246
245
P LPS004 Lupus Erythematosus 61 3.243
246
P ASP006 Aspergillosis 71 3.241
247
RTN017 Retinal Detachment 60 3.225
248
c LKM005 Leukemia, T-Cell, Chronic 33 3.215
249
P MSC003 Muscular Atrophy 52 3.195
250
P CHR012 Chronic Granulomatous Disease 69 3.192
251
P HYP069 Hyperparathyroidism 62 3.190
252
P PLM036 Pulmonary Fibrosis 65 3.185
253
RCK004 Rickets 65 3.184
254
CRB039 Cerebrovascular Disease 65 3.173
255
ART016 Aortic Aneurysm 69 3.163
256
c SCN007 Secondary Hyperparathyroidism 51 3.159
257
c MCR133 Microvascular Complications of Diabetes 4 41 3.153
258
c MCR130 Microvascular Complications of Diabetes 6 41 3.153
259
P OVR042 Ovarian Cancer 88 3.145
260
P HYP086 Hypothyroidism 69 3.145
261
ENC005 Encephalomalacia 43 3.135
262
MCS002 Mucositis 55 3.133
263
c ATR087 Atrial Standstill 1 74 3.125
264
TRD006 Tardive Dyskinesia 53 3.115
265
BRN024 Bronchitis 67 3.112
266
IGG001 Iga Glomerulonephritis 50 3.106
267
ANG054 Angina Pectoris 65 3.098
268
OTT002 Otitis Media 71 3.047
269
P NSP012 Nasopharyngeal Carcinoma 60 3.044
270
GST092 Gastroesophageal Reflux 60 3.039
271
P MTR014 Motor Neuron Disease 65 3.017
272
P KLZ004 Kala-Azar 1 41 3.012
273
LSH001 Leishmaniasis 63 3.012
274
c ALP101 Alpha-Thalassemia 62 2.999
275
CMM005 Common Cold 55 2.998
276
P HRP006 Herpes Simplex 65 2.997
277
P BND020 Bone Disease 60 2.961
278
RTN020 Retinal Vascular Disease 45 2.923
279
HYP781 Hypoascorbemia 52 2.905
280
P CYS018 Cystitis 59 2.895
281
P ATX030 Ataxia-Telangiectasia 80 2.884
282
LNG031 Lung Benign Neoplasm 51 2.867
283
BTT017 Beta-Thalassemia Major 53 2.861
284
KRT009 Keratosis 52 2.858
285
c FML021 Familial Hypercholesterolemia 71 2.833
286
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 2.824
287
P HML002 Hemolytic Anemia 62 2.822
288
FNG017 Fungal Infectious Disease 54 2.817
289
LKP003 Leukoplakia 39 2.816
290
PNC129 Pancreatic Adenocarcinoma 65 2.809
291
MLG169 Malignant Astrocytoma 57 2.803
292
STT001 Status Epilepticus 58 2.790
293
GLC003 Glucose Intolerance 53 2.789
294
ALL006 Allergic Asthma 56 2.779
295
P BCL017 B-Cell Lymphoma 57 2.773
296
P HNT016 Huntington Disease 73 2.756
297
P OPT006 Optic Nerve Disease 57 2.731
298
CNG034 Congestive Heart Failure 69 2.714
299
LNG099 Lung Disease 62 2.714
300
HNT002 Hantavirus Pulmonary Syndrome 55 2.703
301
CHL065 Cholangiocarcinoma 58 2.696
302
INT079 Intrahepatic Cholangiocarcinoma 51 2.696
303
ENT011 Enterocolitis 55 2.693
304
P NPH012 Nephrotic Syndrome 62 2.692
305
SCK003 Sickle Cell Anemia 74 2.677
306
P CHR345 Chronic Pain 50 2.651
307
P HPT021 Hepatitis 68 2.649
308
P BNG032 Benign Mesothelioma 53 2.648
309
P PRK039 Parkinsonism 55 2.634
310
P RTN008 Retinitis Pigmentosa 79 2.630
311
CHL123 Chlamydia 58 2.617
312
BRN071 Brain Injury 50 2.613
313
PRN019 Perinatal Necrotizing Enterocolitis 60 2.610
314
HDN002 Head Injury 44 2.606
315
ANX010 Anxiety 70 2.606
316
KRT019 Keratitis, Hereditary 66 2.606
317
ART002 Arts Syndrome 66 2.596
318
PPL052 Papillomatosis, Confluent and Reticulated 34 2.594
319
P OVR082 Overgrowth Syndrome 42 2.578
320
P SCH015 Schizophrenia 74 2.570
321
ALL010 Allergic Contact Dermatitis 56 2.562
322
P PRP029 Porphyria 60 2.549
323
NRT001 Neurotic Disorder 56 2.542
324
SXL003 Sexual Disorder 49 2.528
325
CLF027 Cleft Palate, Isolated 64 2.525
326
NRM005 Neuromuscular Disease 63 2.522
327
PLM033 Pulmonary Embolism 58 2.519
328
PLM001 Pulmonary Tuberculosis 69 2.517
329
LPT014 Leptin Deficiency or Dysfunction 77 2.511
330
TRM010 Traumatic Brain Injury 50 2.508
331
BCT022 Bacterial Infectious Disease 56 2.507
332
HYP060 Hyperinsulinism 53 2.499
333
c DLT002 Dilated Cardiomyopathy 79 2.496
334
VSC003 Visceral Leishmaniasis 54 2.495
335
P GLM007 Glomerulonephritis 59 2.494
336
P PRS038 Personality Disorder 65 2.490
337
AMN003 Amnestic Disorder 54 2.484
338
P SRC025 Sarcoidosis 1 70 2.480
339
DSS009 Disseminated Intravascular Coagulation 56 2.475
340
P ATR005 Atrophic Gastritis 50 2.473
341
P AMY004 Amyloidosis 69 2.445
342
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 2.444
343
P RHM011 Rheumatoid Arthritis 81 2.444
344
PRP030 Purpura 54 2.441
345
CLN015 Colon Adenocarcinoma 64 2.439
346
PNN001 Panniculitis 52 2.422
347
STM007 Stomatitis 52 2.416
348
HRP004 Herpes Zoster 60 2.407
349
c LKM063 Leukemia, Chronic Myeloid 71 2.393
350
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 2.387
351
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 2.387
352
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 2.378
353
URT010 Ureteral Obstruction 45 2.377
354
BCK006 Back Pain 43 2.360
355
HGH043 High Grade Glioma 46 2.357
356
BRN028 Brain Cancer 73 2.341
357
ORL015 Oral Squamous Cell Carcinoma 43 2.332
358
HLX001 Helix Syndrome 47 2.331
359
SPS057 Spasticity 43 2.326
360
P SML001 Small Cell Carcinoma 52 2.322
361
CLR109 Colorectal Adenocarcinoma 50 2.321
362
GYN001 Gynecomastia 48 2.312
363
INF021 Infant Gynecomastia 30 2.312
364
P RTN024 Retinoblastoma 72 2.305
365
P MNC007 Monocytic Leukemia 48 2.305
366
THR016 Thrombophlebitis 50 2.302
367
GTR002 Goiter 52 2.301
368
LYM143 Lymphoma, Non-Hodgkin, Familial 79 2.293
369
MYC005 Myocardial Stunning 45 2.292
370
SNL007 Senile Cataract 40 2.281
371
P PRK057 Parkinson Disease, Late-Onset 79 2.275
372
c HPT016 Hepatitis B 62 2.274
373
PNG002 Pain Agnosia 51 2.270
374
TND005 Tendinitis 54 2.268
375
c HPT003 Hepatitis a 63 2.262
376
P LNG064 Lung Cancer Susceptibility 3 70 2.258
377
c ALM001 Al Amyloidosis 54 2.254
378
c GLL024 Gallbladder Disease 1 53 2.248
379
ANR040 Aneurysm 60 2.243
380
c SCL052 Scleroderma, Familial Progressive 60 2.242
381
ABT001 Abetalipoproteinemia 68 2.236
382
GST033 Gestational Diabetes 61 2.233
383
WLS001 Wilson Disease 70 2.226
384
P SLP006 Sleep Apnea 69 2.221
385
P URN019 Urinary Tract Infection 49 2.218
386
P SBR004 Seborrheic Dermatitis 44 2.218
387
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 2.210
388
P VTR007 Vitreoretinopathy 45 2.210
389
BRK010 Burkitt Lymphoma 66 2.209
390
P HYP061 Hypertrophic Cardiomyopathy 69 2.202
391
LYM133 Lymphoma, Hodgkin, Classic 74 2.199
392
EPT021 Epithelial Recurrent Erosion Dystrophy 46 2.197
393
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 2.195
394
SCH014 Schistosomiasis 56 2.195
395
P LCT001 Lactic Acidosis 50 2.187
396
P HYP058 Hypervitaminosis a 47 2.183
397
P ENC004 Encephalitis 61 2.180
398
P ECL001 Eclampsia 52 2.177
399
P PNM007 Pneumonia 64 2.162
400
HPT019 Hepatic Encephalopathy 59 2.162
401
INS001 Insulinoma 59 2.162
402
VSC002 Vascular Dementia 59 2.160
403
HPT004 Hepatic Coma 43 2.154
404
PRT038 Protein-Energy Malnutrition 53 2.137
405
PLY150 Polykaryocytosis Inducer 29 2.115
406
PST053 Postherpetic Neuralgia 40 2.114
407
SVR004 Severe Combined Immunodeficiency 71 2.107
408
P INF038 Influenza 68 2.099
409
STR067 Stroke, Ischemic 79 2.092
410
RFR010 Refractory Anemia 49 2.092
411
CND006 Candida Glabrata 29 2.078
412
PRS063 Paresthesia 39 2.078
413
CLC006 Calcinosis 47 2.050
414
P VSC011 Vasculitis 61 2.045
415
FLR002 Filariasis 55 2.035
416
c HPT001 Hepatitis C 61 2.033
417
CRT015 Carotid Artery Occlusion 45 2.030
418
CHR074 Choriocarcinoma 46 2.029
419
c DWL002 Dowling-Degos Disease 1 58 2.026
420
GST019 Gastrointestinal Stromal Tumor 78 2.022
421
OPS001 Opisthorchiasis 41 2.017
422
P RTN016 Retinal Degeneration 52 2.014
423
ORL012 Oral Leukoplakia 35 2.014
424
P END046 Endometritis 46 2.004
425
GST040 Gastric Adenocarcinoma 66 2.003
426
c HPT073 Hepatitis C Virus 71 1.986
427
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 27 1.979
428
c BRN108 Branchiootic Syndrome 1 63 1.972
430
RHM001 Rheumatic Fever 59 1.971
431
DBT008 Diabetic Angiopathy 47 1.968
432
c ACT134 Acute Liver Failure 57 1.953
433
P RCT021 Rectum Cancer 54 1.944
434
CHR066 Chronic Fatigue Syndrome 60 1.938
435
HMR023 Hemorrhagic Cystitis 43 1.934
436
P PLY014 Polycystic Kidney Disease 71 1.929
437
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 1.927
438
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 1.927
439
ECH003 Echinococcosis 52 1.921
440
ANG049 Angioedema Induced by Ace Inhibitors 39 1.917
441
HMG005 Hemoglobinopathy 55 1.916
442
ALC006 Alcoholic Hepatitis 61 1.914
443
LKN025 Leukoencephalopathy, Hereditary Diffuse, with Spheroids 66 1.910
444
ETN001 Eating Disorder 59 1.891
445
CHC001 Chickenpox 56 1.887
446
PRQ002 Paraquat Poisoning 28 1.885
447
SVR001 Severe Acute Respiratory Syndrome 68 1.879
448
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 1.878
449
P EPD016 Epidermolysis Bullosa 53 1.878
450
PNC001 Pancytopenia 52 1.868
451
c PLM127 Pulmonary Hypertension, Primary, 3 34 1.865
452
TRY001 Trypanosomiasis 50 1.859
453
CHP002 Chops Syndrome 47 1.850
454
CRB090 Cerebral Hypoxia 42 1.849
455
P SKN067 Skin/hair/eye Pigmentation, Variation in, 2 30 1.829
456
c PRT132 Protoporphyria, Erythropoietic, 1 61 1.821
457
PLC008 Placenta Disease 49 1.818
458
P NGH001 Night Blindness 52 1.816
459
P HYP098 Hypereosinophilic Syndrome 66 1.816
460
P ALP009 Alopecia Areata 59 1.806
461
TBC004 Tobacco Addiction 63 1.806
462
HPT022 Hepatoblastoma 54 1.782
463
P MCR010 Microcephaly 59 1.779
464
BRN056 Bronchopulmonary Dysplasia 57 1.777
465
CHL152 Childhood Acute Lymphocytic Leukemia 50 1.773
466
VTM002 Vitamin B12 Deficiency 48 1.773
467
MCR011 Microinvasive Gastric Cancer 41 1.767
468
CLR108 Colorectal Adenoma 63 1.763
469
c ATM075 Autoimmune Encephalitis 39 1.761
470
HYP114 Hypertensive Nephropathy 35 1.758
471
c SPR086 Spermatogenic Failure 3 47 1.721
472
c BSL007 Basal Cell Carcinoma 68 1.721
473
c WLM013 Wilms Tumor 1 65 1.710
474
OCL069 Ocular Motor Apraxia 57 1.702
475
ATS010 Autosomal Recessive Disease 42 1.691
476
KRN002 Kearns-Sayre Syndrome 63 1.690
477
RNL077 Renal Fibrosis 46 1.681
478
c FNC027 Fanconi Anemia, Complementation Group a 81 1.679
479
SPL018 Splenomegaly 47 1.677
480
GST045 Gastroenteritis 58 1.675
481
P PYL005 Pyelonephritis 56 1.669
482
P TMP001 Temporal Lobe Epilepsy 49 1.667
483
CLF001 Cleft Lip 54 1.661
484
GLT007 Glutathione Synthetase Deficiency 48 1.659
485
OBS082 Obstructive Nephropathy 41 1.656
486
RTN003 Retinal Ischemia 48 1.641
487
P VNS003 Venous Insufficiency 54 1.632
488
EXC002 Exocrine Pancreatic Insufficiency 42 1.625
489
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 1.615
490
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 1.612
491
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 1.607
492
c SVR005 Severe Pre-Eclampsia 50 1.605
493
c PRG042 Progressive Familial Heart Block, Type Ia 65 1.603
494
c PRM093 Premature Ovarian Failure 7 47 1.602
495
P TRC031 Trichorhinophalangeal Syndrome 37 1.601
496
OST003 Osteonecrosis 61 1.599
497
CHR100 Chronic Ulcer of Skin 57 1.592
498
CRD137 Cardiogenic Shock 56 1.591
499
ACT088 Acute Insulin Response 39 1.585
500
ALC009 Alcoholic Liver Cirrhosis 54 1.576
501
FLR001 Filarial Elephantiasis 59 1.561
502
HYP081 Hypolipoproteinemia 49 1.557
503
LRY022 Laryngoonychocutaneous Syndrome 43 1.541
504
SBC016 Subacute Delirium 42 1.537
505
CHG001 Chagas Disease 65 1.535
506
P LKD001 Leukodystrophy 58 1.531
507
P GRV001 Graves' Disease 54 1.530
508
c INH020 Inherited Metabolic Disorder 47 1.527
509
HVY002 Heavy Metal Poisoning 22 1.522
510
LMB062 Limb Ischemia 55 1.520
511
c VRL010 Viral Hepatitis 52 1.518
512
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 1.517
513
DSS012 Disseminated Infection with Mycobacterium Avium Complex 18 1.508
514
MSN004 Mesenchymal Cell Neoplasm 42 1.491
515
HMC014 Homocysteinemia 52 1.488
516
URL001 Urolithiasis 45 1.484
517
GNG013 Gingivitis 59 1.482
518
P PRP003 Porphyria Cutanea Tarda 66 1.478
519
CRD223 Cardiac Arrhythmia 63 1.474
520
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 57 1.473
521
HMT002 Hematologic Cancer 61 1.472
522
P MTH007 Methemoglobinemia 46 1.461
523
P INT068 Intestinal Disease 53 1.455
524
LNG015 Lingual-Facial-Buccal Dyskinesia 47 1.450
525
HRT012 Heart Valve Disease 53 1.444
527
CHL004 Cholelithiasis 48 1.430
528
P MST009 Mastocytosis 64 1.430
529
P HRD217 Hereditary Optic Neuropathy 36 1.428
530
HRN029 Hearing Loss, Noise-Induced 37 1.420
531
CRB086 Cerebral Aneurysms 40 1.415
532
HMG002 Hemoglobinuria 50 1.414
533
CRC021 Carcinosarcoma 62 1.404
534
VTM033 Vitamin K Deficiency Bleeding 50 1.400
536
P APL001 Aplastic Anemia 73 1.391
537
P MYC033 Myoclonus 46 1.387
538
PRT013 Portal Hypertension 59 1.383
539
THY029 Thyroid Carcinoma 54 1.378
540
c HYP724 Hyperlipoproteinemia, Type Iii 66 1.376
541
c GRV008 Graves Disease 1 54 1.372
542
P LCH002 Lichen Planus 55 1.371
543
ANR007 Anorexia Nervosa 59 1.366
544
INT067 Interstitial Nephritis 47 1.361
545
P SMK004 Smoking As a Quantitative Trait Locus 3 44 1.358
546
P DYS154 Dystonia 64 1.356
547
P RNL015 Renal Hypertension 45 1.353
548
TNG002 Tangier Disease 64 1.348
549
ART004 Aortic Atherosclerosis 46 1.347
550
OLG001 Oligospermia 45 1.345
551
BLR001 Biliary Atresia 55 1.323
552
CRH005 Crohn's Colitis 53 1.321
553
PRM236 Primary Biliary Cholangitis 62 1.321
554
PRC051 Paracetamol Poisoning 29 1.318
555
c GLC092 Glaucoma, Primary Open Angle 61 1.315
556
BRC012 Brucellosis 66 1.305
557
DYS073 Dysphagia 53 1.302
558
FML037 Female Breast Cancer 51 1.301
559
TNS005 Tonsillitis 57 1.292
560
CLF004 Cleft Lip/palate 57 1.283
561
SPN041 Spinal Cord Disease 54 1.281
562
CLL003 Cellulitis 53 1.281
563
STM006 Stomach Disease 47 1.277
564
P HYP111 Hyperprolinemia 44 1.269
565
IRN001 Iron Deficiency Anemia 58 1.268
566
P CTN015 Cutaneous T Cell Lymphoma 48 1.266
567
CHL073 Cholestasis-Lymphedema Syndrome 40 1.262
568
RTR001 Retrograde Amnesia 41 1.260
569
CHR431 Chronic Venous Insufficiency 48 1.259
570
ILS001 Ileus 49 1.254
571
P ORL007 Oral Cavity Cancer 52 1.242
572
MTH009 Mouth Disease 57 1.241
573
ARG007 Argininemia 59 1.235
574
P PTS002 Ptosis 52 1.230
575
PRS036 Parasitic Protozoa Infectious Disease 44 1.212
576
P MRC003 Mercury Poisoning 48 1.211
577
SPP008 Suppurative Otitis Media 42 1.208
578
P END047 Endophthalmitis 53 1.205
579
CHR097 Chronic Purulent Otitis Media 34 1.198
580
PHN003 Phenylketonuria 76 1.196
581
DPH001 Diphtheria 59 1.193
582
EXT034 Extrinsic Allergic Alveolitis 56 1.192
583
P EPD009 Epidermolysis Bullosa Dystrophica 66 1.187
584
PLY100 Polyploidy 36 1.186
586
PRP027 Peripheral Vascular Disease 71 1.169
587
PLC005 Placental Insufficiency 56 1.161
588
INT075 Intracranial Hypertension 52 1.157
589
CHL045 Choline Deficiency Disease 39 1.157
590
MLG079 Malignant Pleural Mesothelioma 42 1.150
591
PPT001 Peptic Esophagitis 51 1.149
592
P AVS003 Avascular Necrosis 41 1.148
593
URT049 Urate Oxidase, Pseudogene 24 1.142
594
EHL052 Ehlers-Danlos Syndrome, Vascular Type 63 1.141
595
PRP016 Paraplegia 52 1.139
596
HYP835 Hypothalamic Obesity 38 1.134
597
SKN019 Skin Melanoma 70 1.129
598
PNC034 Pancreas Disease 49 1.121
599
NRL016 Neural Tube Defects 81 1.120
600
INT007 Intermediate Coronary Syndrome 53 1.120
601
TST015 Testicular Disease 42 1.116
602
CRN019 Coronary Artery Vasospasm 47 1.116
603
P HMC002 Homocystinuria 52 1.112
604
c PNC106 Pancreatic Agenesis 1 51 1.110
605
P SHR001 Short Bowel Syndrome 53 1.106
606
ACT078 Acute Porphyria 50 1.105
607
FBR019 Fibromatosis 44 1.098
608
PLM134 Pulmonary Fibrosis, Idiopathic 76 1.094
609
P SNS001 Sensorineural Hearing Loss 59 1.091
610
P SJG008 Sjogren Syndrome 61 1.091
611
ASC010 Ascaris Lumbricoides Infection 49 1.086
612
CMM004 Common Variable Immunodeficiency 72 1.078
613
c EXD008 Exudative Vitreoretinopathy 1 71 1.077
614
c CHR098 Chronic Pyelonephritis 34 1.061
615
ATR057 Atrioventricular Block 54 1.056
616
BLR008 Bilirubin Metabolic Disorder 57 1.042
617
CHR178 Chromosomal Triplication 34 1.035
618
NRN001 Neuroendocrine Carcinoma 47 1.032
619
SCT002 Scotoma 42 1.028
620
NPH009 Nephrolithiasis 54 1.018
621
ELP001 Elephantiasis 44 1.011
622
MCR191 Microscopic Colitis 46 1.010
623
c ART115 Aortic Valve Disease 1 72 1.010
624
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 1.007
625
NRX001 Neuroaxonal Dystrophy 38 1.006
626
P HYD006 Hydrocephalus 63 1.004
627
PSD088 Pseudobulbar Affect 33 0.994
628
EMB004 Embryonal Carcinoma 55 0.990
629
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.977
630
OST011 Osteomalacia 52 0.970
631
MSL001 Measles 61 0.968
632
SNS003 Sensory Peripheral Neuropathy 51 0.959
633
PRP001 Propionic Acidemia 65 0.955
634
CRB037 Cerebral Palsy 67 0.949
635
OST017 Osteomyelitis 63 0.941
636
NWC001 Newcastle Disease 48 0.939
637
P OBS001 Obstructive Jaundice 49 0.936
638
P ALG028 Alagille Syndrome 1 73 0.932
639
P FRG001 Fragile X Syndrome 70 0.932
640
P SPN046 Spinal Muscular Atrophy 62 0.932
641
ACT003 Acute Kidney Tubular Necrosis 46 0.924
642
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.921
643
KWS001 Kwashiorkor 44 0.921
644
ALC010 Alcoholic Cardiomyopathy 42 0.906
645
P ACT008 Actinic Keratosis 54 0.904
646
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 0.898
647
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 0.894
648
MSC157 Muscular Dystrophy, Duchenne Type 79 0.875
649
P BRN022 Bronchiectasis 59 0.870
650
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.862
651
P PRX003 Paroxysmal Nocturnal Hemoglobinuria 64 0.862
652
P SCL018 Scoliosis 57 0.858
653
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.858
654
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.857
655
P FRD001 Friedreich Ataxia 62 0.855
656
FDL002 Food Allergy 47 0.854
657
P BLD062 Bile Duct Cancer 68 0.847
658
P CRD119 Cardiac Arrest 68 0.846
659
P SDR002 Siderosis 42 0.843
660
P LPS002 Liposarcoma 64 0.840
661
ADN075 Adenomyoma 32 0.837
662
MTN003 Motion Sickness 50 0.831
663
GGN002 Gigantism 33 0.820
664
XRD010 Xeroderma Pigmentosum, Variant Type 72 0.818
665
P MYG005 Myoglobinuria 40 0.818
666
SCB001 Scabies 49 0.816
667
c PRG106 Progressive Muscular Dystrophy 31 0.813
668
EXN003 Exencephaly 30 0.811
669
PYR009 Pyridoxine Deficiency Anemia 35 0.806
670
CRT013 Carotid Stenosis 51 0.804
671
P FTL001 Fetal Alcohol Syndrome 55 0.800
672
P SLP005 Sleep Disorder 62 0.797
673
SBC001 Subacute Sclerosing Panencephalitis 53 0.790
674
P HYP265 Hypotonia 42 0.789
675
CLL014 Cll/sll 45 0.787
677
FDB001 Foodborne Botulism 55 0.780
678
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.780
679
P PTN014 Patent Ductus Arteriosus 1 59 0.779
680
P ICH004 Ichthyosis 56 0.760
681
ORL013 Oral Lichen Planus 45 0.759
682
P HML001 Hemolytic-Uremic Syndrome 52 0.759
683
P PLY019 Polyneuropathy 53 0.754
684
P MTC133 Mitochondrial Myopathy 51 0.752
685
P CHL066 Cholangitis 51 0.740
686
DNG003 Dengue Disease 65 0.738
687
P MMP001 Mumps 56 0.732
688
VRG001 Variegate Porphyria 55 0.732
689
PPL002 Papillary Carcinoma 46 0.732
690
KWS002 Kawasaki Disease 65 0.722
691
THY006 Thymus Lymphoma 27 0.721
692
NRD001 Neurodermatitis 39 0.712
693
P RBL001 Rubella 58 0.712
694
ACT228 Acute Radiation Syndrome 30 0.712
695
SPS019 Spastic Paraparesis 38 0.712
696
BLM002 Bulimia Nervosa 57 0.711
697
ONC007 Oncocytoma 49 0.707
698
P TTR001 Tetralogy of Fallot 69 0.707
699
IDP091 Idiopathic Nephrotic Syndrome 49 0.703
700
HMR039 Hemorrhage, Intracerebral 57 0.702
701
c RTN047 Retinitis Pigmentosa 18 45 0.701
702
PTH003 Pathologic Nystagmus 52 0.701
703
VLV047 Volvulus of Midgut 55 0.689
704
ASP007 Aspiration Pneumonia 49 0.689
705
CHL147 Chlamydia Pneumonia 47 0.684
706
CRN030 Coronary Stenosis 50 0.679
707
IGR001 Ige Responsiveness, Atopic 59 0.674
708
PLM031 Poliomyelitis 62 0.673
709
ADR007 Adrenoleukodystrophy 74 0.669
710
ADR022 Adrenomyeloneuropathy 39 0.669
711
RST023 Resting Heart Rate, Variation in 40 0.649
712
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.637
713
P TXP001 Toxoplasmosis 60 0.636
714
MNK001 Menkes Disease 64 0.633
715
P MMB011 Membranous Nephropathy 50 0.626
716
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.626
717
SDD008 Sudden Sensorineural Hearing Loss 41 0.617
718
PGM003 Pigmentation Disease 45 0.614
719
ANR004 Anuria 44 0.614
720
TXC020 Toxic Oil Syndrome 32 0.614
721
PRT082 Preterm Premature Rupture of the Membranes 56 0.602
722
BHC003 Behcet Syndrome 71 0.596
723
MTC005 Mitochondrial Metabolism Disease 45 0.593
724
P HYP838 Hyperlipidemia, Familial Combined, 3 61 0.583
725
RYN005 Raynaud Phenomenon 45 0.570
726
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 0.564
727
RSC001 Rosacea 55 0.563
728
DSS008 Disease of Mental Health 74 0.555
729
P ACT105 Acute Mountain Sickness 52 0.552
730
P GLC113 Galactosemia I 65 0.536
731
PLS007 Plasmodium Falciparum Malaria 52 0.536
732
SND001 Sandhoff Disease 66 0.530
733
P GLY013 Glycogen Storage Disease 59 0.526
734
DDN006 Duodenitis 50 0.517
735
WST005 West Nile Virus 55 0.516
736
PRX001 Peroxisomal Disease 46 0.516
737
P FML011 Familial Adenomatous Polyposis 71 0.506
738
LYS012 Lysosomal Acid Lipase Deficiency 64 0.502
739
HYP561 Hypertelorism, Preauricular Sinus, Punctal Pits, and Deafness 26 0.496
740
c HMC039 Hemochromatosis, Type 1 73 0.489
741
FND002 Fundus Dystrophy 55 0.484
742
P HYP768 Hyperlipoproteinemia, Type I 67 0.480
743
ORP003 Oropharynx Cancer 54 0.474
744
c HMG003 Hemoglobin E Disease 41 0.473
745
BCT021 Bacterial Sepsis 43 0.468
746
RBF001 Riboflavin Deficiency 49 0.465
747
GRD001 Giardiasis 46 0.459
748
GSG001 Gas Gangrene 52 0.459
749
TRN015 Transient Cerebral Ischemia 62 0.458
750
P MLG056 Malignant Hyperthermia 65 0.458
751
MRS001 Marasmus 41 0.447
752
BLR013 Biliary Tract Cancer 43 0.444
753
PRX085 Preaxial Hallucal Polydactyly 28 0.439
754
P JBR020 Joubert Syndrome 1 74 0.434
755
LKS001 Leukostasis 40 0.424
756
P BRB001 Beriberi 44 0.421
757
CCC002 Coccidiosis 50 0.404
758
P MPL001 Maple Syrup Urine Disease 69 0.379
759
RFS006 Refsum Disease, Classic 63 0.377
760
MNG007 Manganese Poisoning 28 0.365
761
PRM329 Premature Aging 36 0.365
762
SLC006 Silicosis 55 0.355
763
SCR011 Scrapie 39 0.355
764
MCN017 Meconium Ileus 52 0.348
765
P HMN038 Human Coronavirus Sensitivity 30 0.348
766
P GLL018 Gallbladder Cancer 53 0.348
767
PHT003 Phototoxic Dermatitis 27 0.348
768
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.344
769
RTC012 Reticuloendotheliosis, X-Linked 35 0.339
770
CRB008 Cerebral Atherosclerosis 46 0.339
771
P SCL009 Sclerosing Cholangitis 46 0.339
772
SPN050 Spinocerebellar Degeneration 39 0.339
773
P FML018 Familial Mediterranean Fever 73 0.334
774
CRT072 Creutzfeldt-Jakob Disease 67 0.334
775
ACY011 Acyl-Coa Dehydrogenase Deficiency 31 0.334
776
HMP001 Hemopericardium 47 0.333
777
P PRC012 Pericardial Effusion 50 0.333
778
P PLM034 Pulmonary Emphysema 58 0.333
779
P ZLL001 Zellweger Syndrome 65 0.333
780
P TCD001 Tic Disorder 50 0.316
781
P HMR003 Hemorrhagic Disease 59 0.316
782
PYR010 Peyronie's Disease 50 0.311
783
c CHL119 Cholangitis, Primary Sclerosing 57 0.311
784
CLS049 Classic Phenylketonuria 42 0.311
785
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.307
786
P CRB088 Cerebral Atrophy 33 0.307
787
CRC034 Carcinoma Showing Thymus-Like Differentiation 22 0.307
788
GLT035 Glutaric Acidemia I 57 0.295
789
HYP774 Hyperornithinemia-Hyperammonemia-Homocitrullinuria Syndrome 54 0.295
790
P MTC069 Mitochondrial Disorders 57 0.295
791
ORN004 Ornithinemia 13 0.295
792
P FML355 Familial Intrahepatic Cholestasis 42 0.295
793
SMT004 Smith-Lemli-Opitz Syndrome 69 0.292
794
WRN003 Wernicke Encephalopathy 45 0.292
795
c OPT051 Opitz Gbbb Syndrome, Type I 45 0.292
796
THY128 Thyroid Tumor 33 0.292
797
c DMN005 Diamond-Blackfan Anemia 2 28 0.276
798
PRP083 Porphyria, Acute Intermittent 64 0.276
799
RYS001 Reye Syndrome 49 0.276
800
SGT001 Sagittal Sinus Thrombosis 36 0.276
801
MTC004 Mitochondrial Encephalomyopathy 43 0.276
802
c INH030 Inherited Retinal Disorder 28 0.276
803
OPP004 Oppositional Defiant Disorder 48 0.267
804
ISV001 Isovaleric Acidemia 54 0.258
805
GLL008 Gilles De La Tourette Syndrome 64 0.258
806
ICH054 Ichthyosis, X-Linked 51 0.258
807
PRP082 Porphyria, Congenital Erythropoietic 56 0.237
808
P STN012 Sting-Associated Vasculopathy, Infantile-Onset 42 0.237
809
HLT002 Halothane Hepatitis 31 0.237
810
c HYD064 Hydrocephalus, Congenital, 1 51 0.237
811
MVL001 Mevalonic Aciduria 65 0.237
812
DSC013 Discrimination, Two-Point, Reduction in 21 0.237
813
TTT001 Tatton-Brown-Rahman Syndrome 45 0.237
814
ACY009 Acyl-Coa Dehydrogenase, Medium-Chain, Deficiency of 58 0.237
815
STN011 Sting-Associated Vasculopathy with Onset in Infancy 44 0.237
816
ART008 Arteriosclerosis Obliterans 40 0.237
817
MDM001 Medium-Chain Acyl-Coenzyme a Dehydrogenase Deficiency 33 0.237
818
P MCH002 Machado-Joseph Disease 63 0.208
819
PRX005 Peroxisomal Biogenesis Disorder 35 0.208
820
c GLC112 Galactosemia Iii 51 0.208
821
c PRP091 Porphyria Cutanea Tarda, Type I 30 0.208
822
HNZ004 Heinz Body Anemias 40 0.208
823
NPH003 Nephrocalcinosis 49 0.208
824
HYP003 Hypermethioninemia 51 0.208
825
CMP006 Complex Partial Epilepsy 36 0.208
826
CRB081 Cerebellar Ataxia, Cayman Type 39 0.208
827
ACT162 Acute Sensory Ataxic Neuropathy 24 0.208
828
CRL001 Cerulean Cataract 26 0.208
829
P CMP008 Compartment Syndrome 50 0.208
830
HRD016 Hereditary Retinal Dystrophy 34 0.208
Content
Loading form....