Search results for Vitamin C

4751 hits were found for Vitamin C

# Family MCID Name MIFTS Score
1
RCK004 Rickets 68 166.036
2
c HPT001 Hepatitis C 62 126.171
3
c HPT073 Hepatitis C Virus 71 109.627
4
KRT002 Keratomalacia 55 103.419
5
P HPT021 Hepatitis 69 78.294
6
HYP781 Hypoascorbemia 52 72.879
7
VTM002 Vitamin B12 Deficiency 48 63.739
8
VTM033 Vitamin K Deficiency Bleeding 48 60.854
9
P HYP069 Hyperparathyroidism 62 50.955
10
c CHR684 Chronic Kidney Disease 69 50.265
11
c TYP009 Type 2 Diabetes Mellitus 92 49.466
12
P VTM027 Vitamin D-Dependent Rickets, Type 2a 53 49.041
13
P OST002 Osteoporosis 76 49.001
14
PRT011 Protein C Deficiency 47 48.969
15
LVR012 Liver Cirrhosis 63 48.438
16
P LVR013 Liver Disease 69 48.194
17
c HYP836 Hypercholesterolemia, Familial, 1 73 48.079
18
VTM028 Vitamin E, Familial Isolated Deficiency of 53 48.048
19
P DBT009 Diabetes Mellitus 67 47.441
20
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 47.410
21
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 47.358
22
c THR082 Thrombophilia Due to Activated Protein C Resistance 59 45.940
23
P KDN018 Kidney Disease 72 45.369
24
LPD008 Lipid Metabolism Disorder 62 44.547
25
NNL005 Non-Alcoholic Fatty Liver Disease 63 44.481
26
ATX019 Ataxia with Vitamin E Deficiency 44 43.894
27
DFC004 Deficiency Anemia 74 43.254
28
FTT001 Fatty Liver Disease 62 42.402
29
c HPT016 Hepatitis B 62 42.179
30
P BRS047 Breast Cancer 98 42.062
31
ATH013 Atherosclerosis Susceptibility 63 41.229
32
BNR002 Bone Resorption Disease 47 40.534
33
P CRN300 Coronary Heart Disease 1 73 40.322
34
c NMN015 Niemann-Pick Disease, Type C1 68 40.306
35
48X005 48,xyyy 39 40.230
36
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 59 40.126
37
c SCN007 Secondary Hyperparathyroidism 51 39.784
38
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 39.727
39
P HPT023 Hepatocellular Carcinoma 96 39.250
40
P ATR011 Atrial Fibrillation 66 39.087
41
c PRC016 Pre-Eclampsia 65 38.791
42
THR068 Thrombophilia Due to Protein C Deficiency, Autosomal Recessive 38 38.255
43
P CLR023 Colorectal Cancer 100 38.146
44
IRN002 Iron Metabolism Disease 57 38.016
45
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 35 37.919
46
P BND020 Bone Disease 59 37.875
47
LPP008 Lipoprotein Quantitative Trait Locus 65 37.635
48
HMC014 Homocysteinemia 52 37.407
49
END086 End Stage Renal Disease 52 37.384
50
IMM167 Immune Deficiency Disease 78 37.333
51
CRH001 Crohn's Disease 80 37.297
52
ART140 Arteries, Anomalies of 53 37.283
53
PYR009 Pyridoxine Deficiency Anemia 35 36.789
54
INS024 Insulin-Like Growth Factor I 78 36.766
55
CYS001 Cystic Fibrosis 78 36.498
56
P HRT032 Heart Disease 81 36.394
57
c HPT003 Hepatitis a 63 36.329
58
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 65 36.326
59
AGN016 Aging 54 36.131
60
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 56 36.119
61
P VSC007 Vascular Disease 63 35.860
62
RPD005 Rapidly Involuting Congenital Hemangioma 46 35.558
63
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 35.394
64
c ATR087 Atrial Standstill 1 74 35.167
65
P AST005 Asthma 76 35.143
66
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 45 34.942
67
P MLT020 Multiple Sclerosis 79 34.802
68
P NRP001 Neuropathy 60 34.789
69
c THR092 Thrombophilia Due to Thrombin Defect 74 34.587
70
HLX001 Helix Syndrome 48 34.579
71
c VRL010 Viral Hepatitis 53 34.283
72
CSY001 C Syndrome 61 34.221
73
P DRR001 Diarrhea 55 33.574
74
HMN044 Human Immunodeficiency Virus Type 1 78 33.531
75
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 33.495
76
P RHM011 Rheumatoid Arthritis 82 33.457
77
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 33.413
78
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 33.408
79
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 33.371
80
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 33.370
81
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 33.368
82
c LKM061 Leukemia, Acute Myeloid 83 33.359
83
OST011 Osteomalacia 52 33.331
84
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 33.271
85
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 33.269
86
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 33.268
87
P PRS040 Prostate Cancer 95 32.899
88
CHL123 Chlamydia 58 32.824
89
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 80 32.718
90
P INF037 Inflammatory Bowel Disease 53 32.646
91
CYT002 Cytokine Deficiency 43 32.515
92
SCK003 Sickle Cell Anemia 74 32.257
93
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 32.190
94
ISC004 Ischemia 61 32.040
95
P ALZ034 Alzheimer Disease 87 32.033
96
PRT251 Proteinuria, Chronic Benign 57 31.990
97
c TYP008 Type 1 Diabetes Mellitus 70 31.834
98
MGL001 Megaloblastic Anemia 58 31.827
99
P LKM002 Leukemia 67 31.769
100
P NRB001 Neuroblastoma 66 31.591
101
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 31 31.537
102
MTH077 Methylmalonic Aciduria, Cbla Type 43 31.507
103
P PSR002 Psoriasis 63 31.488
104
MTH078 Methylmalonic Aciduria, Cblb Type 42 31.419
105
P ART022 Arthritis 71 31.183
106
HYP066 Hyperglycemia 61 31.151
107
P PRD008 Periodontitis 64 30.872
108
P THL005 Thalassemia 56 30.705
109
ATX038 Ataxia and Polyneuropathy, Adult-Onset 46 30.588
110
PST011 Pustulosis of Palm and Sole 52 30.507
111
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 30.472
112
P PRP019 Peripheral Nervous System Disease 58 30.459
113
ATM095 Autoimmune Disease 61 30.253
114
P LNG032 Lung Cancer 98 30.214
115
P MYP004 Myopathy 67 30.094
116
c HMG001 Hemoglobin C Disease 41 30.023
117
P PLY011 Polycystic Ovary Syndrome 57 29.989
118
TXC005 Toxic Shock Syndrome 62 29.981
119
THR067 Thrombophilia Due to Protein C Deficiency, Autosomal Dominant 29 29.874
120
P SKN015 Skin Carcinoma 71 29.850
121
P PNC035 Pancreatic Cancer 86 29.780
122
P BLD134 Bladder Cancer 79 29.757
123
STR067 Stroke, Ischemic 80 29.580
125
P OVR042 Ovarian Cancer 88 29.299
126
P MYC007 Myocardial Infarction 70 29.247
127
CNG034 Congestive Heart Failure 69 29.158
128
PRT037 Pertussis 65 29.115
129
ULC004 Ulcerative Colitis 74 29.059
130
P MYC084 Mycobacterium Tuberculosis 1 68 28.980
131
PLM129 Pulmonary Disease, Chronic Obstructive 74 28.862
132
P MYL006 Myeloid Leukemia 61 28.718
133
P GST053 Gastric Cancer 83 28.614
134
47X002 47,xyy 48 28.541
135
P LYM118 Lymphoma 67 28.496
136
P LPS004 Lupus Erythematosus 61 28.481
137
CLT003 Colitis 63 28.474
138
P HYP086 Hypothyroidism 69 28.439
139
c SYS001 Systemic Lupus Erythematosus 87 28.430
140
P PNM007 Pneumonia 67 28.325
141
P GST044 Gastritis 55 28.291
142
P RTN008 Retinitis Pigmentosa 80 28.256
143
P HRD086 Hereditary Hypophosphatemic Rickets 40 27.921
144
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 27.907
145
P INF032 Infertility 57 27.892
146
P MLN008 Melanoma 76 27.841
147
GST033 Gestational Diabetes 61 27.779
148
P BCL017 B-Cell Lymphoma 59 27.745
149
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 27.727
150
c MCR120 Microvascular Complications of Diabetes 7 47 27.671
151
OST159 Osteogenic Sarcoma 66 27.447
152
OST012 Osteoarthritis 77 27.384
153
c MCR113 Microvascular Complications of Diabetes 3 52 27.338
154
VTM029 Vitamin D Hydroxylation-Deficient Rickets, Type 1b 27 27.299
155
THR024 Thrombosis 56 27.068
156
DRM006 Dermatitis 62 26.890
157
P ENC018 Encephalopathy 62 26.888
158
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 26.825
159
P SZR006 Seizure Disorder 70 26.817
160
ALL029 Allergic Disease 59 26.816
161
ALC007 Alcohol Dependence 66 26.791
162
CHL068 Cholestasis 61 26.771
163
c MCR130 Microvascular Complications of Diabetes 6 41 26.761
164
c MCR133 Microvascular Complications of Diabetes 4 41 26.631
165
P THR014 Thrombocytopenia 66 26.498
166
VTM010 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 2 23 26.406
167
LNG099 Lung Disease 62 26.363
168
NNL006 Non-Alcoholic Steatohepatitis 54 26.358
169
c FML021 Familial Hypercholesterolemia 72 26.259
170
P ADN016 Adenocarcinoma 63 26.235
171
c HYP595 Hypertension, Essential 85 26.156
172
P DRM053 Dermatitis, Atopic 65 26.049
173
NRL016 Neural Tube Defects 81 26.040
174
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 25.949
175
P ALC033 Alcohol Use Disorder 61 25.890
176
P ECL001 Eclampsia 52 25.856
177
P CTR002 Cataract 60 25.796
178
HYP266 Hypoxia 57 25.697
179
c SML038 Small Cell Cancer of the Lung 69 25.563
180
MSL001 Measles 61 25.544
181
SKN016 Skin Disease 63 25.492
182
RNL114 Renal Cell Carcinoma, Nonpapillary 80 25.487
183
ADN018 Adenoma 59 25.222
184
INT323 Intraocular Pressure Quantitative Trait Locus 64 25.216
185
P HYP750 Hypertriglyceridemia, Familial 62 25.098
186
c AMY091 Amyotrophic Lateral Sclerosis 1 88 25.067
187
TTN003 Tetanus 65 25.010
188
GLL048 Glial Tumor 52 24.944
189
P PNC044 Pancreatitis 61 24.903
190
DPR016 Depression 65 24.876
191
BCT022 Bacterial Infectious Disease 56 24.829
192
CRB039 Cerebrovascular Disease 66 24.817
193
P LKM062 Leukemia, Acute Lymphoblastic 69 24.746
194
ESP021 Esophageal Cancer 83 24.687
195
CVD001 Covid-19 57 24.678
196
P NTR004 Neutropenia 63 24.555
197
MYL069 Myeloma, Multiple 77 24.516
198
DSS032 Disease by Infectious Agent 55 24.456
199
PRP027 Peripheral Vascular Disease 71 24.440
200
P ALP008 Alopecia 54 24.302
201
P CND004 Candidiasis 58 24.275
202
P ATS364 Autism 69 24.258
203
SVR001 Severe Acute Respiratory Syndrome 67 24.218
204
SQM006 Squamous Cell Carcinoma 60 24.200
205
MNT002 Mental Depression 57 23.974
206
GLM045 Glioma 63 23.958
207
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 23.899
208
THY029 Thyroid Carcinoma 51 23.898
209
P EPL164 Epilepsy 68 23.748
210
GLB002 Glioblastoma 67 23.736
211
P THY032 Thyroiditis 57 23.597
212
c ATS007 Autism Spectrum Disorder 72 23.442
213
PRP030 Purpura 54 23.252
214
P IMR002 Imerslund-Grasbeck Syndrome 1 42 23.222
215
ATS010 Autosomal Recessive Disease 42 23.222
216
c PRM005 Primary Hyperparathyroidism 59 23.169
217
c DLT002 Dilated Cardiomyopathy 78 23.160
218
P INF038 Influenza 68 23.134
219
MYL009 Myelodysplastic Syndrome 67 23.057
220
c ACT075 Acute Myocardial Infarction 56 23.013
221
STM007 Stomatitis 54 22.832
222
c BTT014 Beta-Thalassemia 72 22.760
223
PRN011 Pernicious Anemia 53 22.757
224
SPN186 Spinal Cord Injury 61 22.739
225
PLM001 Pulmonary Tuberculosis 69 22.738
226
c MCR115 Microvascular Complications of Diabetes 5 65 22.721
227
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 22.704
228
P VSC011 Vasculitis 61 22.663
229
P RTN024 Retinoblastoma 73 22.655
230
c FNC027 Fanconi Anemia, Complementation Group a 81 22.601
231
P SCK005 Sickle Cell Disease 56 22.505
232
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 35 22.405
233
HLC007 Helicobacter Pylori Infection 67 22.382
234
P CRD246 Cardiovascular System Disease 56 22.352
235
P MSC005 Muscular Dystrophy 67 22.228
236
P RHN004 Rhinitis 57 22.188
237
MLR004 Malaria 80 22.167
238
P BRB001 Beriberi 44 22.157
239
SVR004 Severe Combined Immunodeficiency 72 22.126
240
P SCH015 Schizophrenia 74 22.068
241
GLC003 Glucose Intolerance 54 22.037
242
CRV035 Cervical Cancer 73 22.029
243
CNS004 Constipation 56 22.019
244
c ACT027 Acute Pancreatitis 60 22.016
246
P HML002 Hemolytic Anemia 62 21.947
247
EPL131 Epilepsy, Pyridoxine-Dependent 45 21.941
248
ACQ007 Acquired Immunodeficiency Syndrome 59 21.812
249
PRT036 Peritonitis 65 21.793
250
P GLM007 Glomerulonephritis 60 21.748
251
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 68 21.698
252
P DMN002 Dementia 66 21.664
253
PYR016 Pyridoxine Deficiency 29 21.629
254
HMN014 Human Immunodeficiency Virus Infectious Disease 54 21.621
255
P CLC063 Celiac Disease 1 66 21.521
256
IRR002 Irritable Bowel Syndrome 65 21.472
257
GST045 Gastroenteritis 58 21.375
258
P HYP061 Hypertrophic Cardiomyopathy 69 21.372
259
P ADL010 Adult Respiratory Distress Syndrome 71 21.360
260
P CRD119 Cardiac Arrest 67 21.346
261
MLD018 Mild Cognitive Impairment 48 21.341
262
P ATX030 Ataxia-Telangiectasia 80 21.339
263
P ACN011 Acne 57 21.308
264
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 38 21.162
265
FCT002 Factor Xi Deficiency 62 21.141
266
PLM033 Pulmonary Embolism 58 21.136
267
IRN001 Iron Deficiency Anemia 58 21.132
268
P NGH001 Night Blindness 52 21.129
269
P CHR345 Chronic Pain 50 21.012
270
P EXN002 Exanthem 58 21.001
271
c MGR028 Migraine with or Without Aura 1 64 20.920
272
P MJR001 Major Depressive Disorder 68 20.915
273
HYP056 Hypoglycemia 65 20.898
274
HYP060 Hyperinsulinism 54 20.855
275
c ACT071 Acute Kidney Failure 60 20.682
276
EPL166 Epilepsy, Early-Onset, Vitamin B6-Dependent 23 20.672
277
NPH009 Nephrolithiasis 54 20.664
278
P LTR001 Lateral Sclerosis 58 20.497
279
P RRH023 Rare Hereditary Hemochromatosis 54 20.483
280
HRW001 Hair Whorl 35 20.450
281
P PLY019 Polyneuropathy 52 20.389
282
HYP017 Hypophosphatemia 49 20.367
283
HMS001 Hemosiderosis 48 20.349
284
P SRC025 Sarcoidosis 1 71 20.292
285
NRR001 Neuroretinitis 42 20.283
286
RTN023 Retinitis 46 20.254
287
P LNG064 Lung Cancer Susceptibility 3 70 19.987
288
WRF003 Warfarin Syndrome 29 19.975
289
P RSP003 Respiratory Failure 74 19.927
290
DWN001 Down Syndrome 70 19.882
291
P HYP024 Hypoparathyroidism 55 19.852
292
P HMC002 Homocystinuria 53 19.831
293
URM002 Uremia 47 19.802
294
DPH001 Diphtheria 59 19.789
295
P HRP006 Herpes Simplex 65 19.785
296
P THR015 Thrombophilia 51 19.744
297
LYM133 Lymphoma, Hodgkin, Classic 74 19.698
298
P EYD002 Eye Disease 57 19.635
299
LPT014 Leptin Deficiency or Dysfunction 78 19.635
300
GST019 Gastrointestinal Stromal Tumor 78 19.613
301
CMM005 Common Cold 56 19.611
302
P PRK057 Parkinson Disease, Late-Onset 80 19.575
303
DSS008 Disease of Mental Health 74 19.573
304
MTH021 Methylmalonic Acidemia with Homocystinuria 44 19.561
305
P HYP076 Hyperthyroidism 53 19.515
306
P LYN001 Lynch Syndrome 76 19.504
307
ADN090 Adenosylcobalamin Deficiency 32 19.499
308
P ART021 Arteriosclerosis 54 19.486
309
P OPN001 Open-Angle Glaucoma 55 19.481
310
ALL003 Allergic Rhinitis 67 19.427
311
LSH001 Leishmaniasis 64 19.379
312
LYM143 Lymphoma, Non-Hodgkin, Familial 75 19.343
313
c BRN108 Branchiootic Syndrome 1 62 19.289
314
P KLZ004 Kala-Azar 1 41 19.256
315
ANG054 Angina Pectoris 66 19.241
316
P CNR004 Cone-Rod Dystrophy 2 74 19.195
317
P NPH012 Nephrotic Syndrome 60 19.154
318
P RCT021 Rectum Cancer 54 19.090
319
CHL014 Cholera 62 19.067
320
P URN019 Urinary Tract Infection 49 18.885
321
P SLP006 Sleep Apnea 69 18.757
322
P END044 Endometriosis 62 18.738
323
SKN019 Skin Melanoma 71 18.599
324
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 18.548
325
PRM236 Primary Biliary Cholangitis 60 18.534
326
DBT010 Diabetic Neuropathy 54 18.501
327
c ACT073 Acute Leukemia 58 18.458
328
P PRK039 Parkinsonism 55 18.438
329
P ATT013 Attention Deficit-Hyperactivity Disorder 64 18.341
330
BRN071 Brain Injury 50 18.303
331
INT007 Intermediate Coronary Syndrome 54 18.236
332
c LKM063 Leukemia, Chronic Myeloid 71 18.212
333
PPL052 Papillomatosis, Confluent and Reticulated 34 18.153
334
P MNN013 Meningitis 65 18.122
335
P MLN007 Male Infertility 56 18.052
336
BRK010 Burkitt Lymphoma 66 18.031
337
RBF001 Riboflavin Deficiency 49 17.855
338
HYP025 Hyperphosphatemia 48 17.825
339
CLR108 Colorectal Adenoma 64 17.821
340
PRT013 Portal Hypertension 59 17.795
341
PRT002 Paratyphoid Fever 54 17.742
342
P PLM036 Pulmonary Fibrosis 66 17.739
343
FCT013 Factor V Leiden Thrombophilia 20 17.718
344
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 17.671
345
P GRF003 Graft-Versus-Host Disease 71 17.647
346
ANX010 Anxiety 70 17.629
347
ENT011 Enterocolitis 55 17.569
348
P OVR082 Overgrowth Syndrome 49 17.527
349
VRL011 Viral Infectious Disease 61 17.522
350
OCL069 Ocular Motor Apraxia 57 17.510
351
END057 Endometrial Cancer 72 17.500
352
MTC206 Mitochondrial Complex Iv Deficiency, Nuclear Type 5 52 17.457
353
P PLM037 Pulmonary Hypertension 72 17.452
354
P GRV001 Graves' Disease 55 17.402
355
PST092 Posttransplant Acute Limbic Encephalitis 28 17.334
356
NTR005 Nutritional Deficiency Disease 61 17.313
357
P VTM031 Vitamin B12 Plasma Level Quantitative Trait Locus 1 14 17.293
358
c PCH010 Pachyonychia Congenita 3 43 17.228
359
RLP002 Relapsing-Remitting Multiple Sclerosis 56 17.211
360
P MTH008 Methylmalonic Acidemia 52 17.211
361
CND006 Candida Glabrata 30 17.205
362
P LKM071 Leukemia, Chronic Lymphocytic 75 17.192
363
CHL147 Chlamydia Pneumonia 47 17.162
364
P ANR048 Aniridia 1 64 17.116
365
CRY004 Cryoglobulinemia 48 17.032
366
P PHC003 Pheochromocytoma 69 17.030
367
DSS009 Disseminated Intravascular Coagulation 57 16.985
368
PLC008 Placenta Disease 49 16.972
369
MCS002 Mucositis 56 16.950
370
SRC014 Sarcoma 65 16.950
371
P HYP265 Hypotonia 42 16.875
372
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 16.834
373
P SCL018 Scoliosis 57 16.761
374
PNC129 Pancreatic Adenocarcinoma 65 16.753
375
P NMN002 Niemann-Pick Disease 60 16.744
376
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 25 16.718
377
c PRD040 Periodontitis, Chronic 52 16.718
378
P TRM003 Tremor 48 16.701
379
SPL018 Splenomegaly 49 16.689
380
P ATR005 Atrophic Gastritis 50 16.669
381
P NSP012 Nasopharyngeal Carcinoma 61 16.547
382
KRT001 Keratoconjunctivitis Sicca 50 16.538
383
SPN035 Spindle Cell Sarcoma 54 16.537
384
P LCH002 Lichen Planus 54 16.505
385
XRP001 Xerophthalmia 41 16.463
386
P BRN019 Bernard-Soulier Syndrome 61 16.447
387
DFF005 Diffuse Large B-Cell Lymphoma 54 16.438
388
HYP080 Hypogonadism 50 16.436
389
c DWL002 Dowling-Degos Disease 1 58 16.399
390
P HMP007 Hemophilia 52 16.398
391
P HYP098 Hypereosinophilic Syndrome 66 16.324
392
c GLC092 Glaucoma, Primary Open Angle 62 16.292
393
c SCL052 Scleroderma, Familial Progressive 61 16.264
394
KRT009 Keratosis 53 16.221
395
MDD011 Mood Disorder 62 16.186
396
P AMY004 Amyloidosis 70 16.170
397
TRN015 Transient Cerebral Ischemia 63 16.158
398
BRN024 Bronchitis 67 16.114
399
XRD010 Xeroderma Pigmentosum, Variant Type 73 16.106
400
PNG002 Pain Agnosia 51 16.082
401
P HDC001 Headache 57 16.053
402
HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 16.025
403
NPH091 Nephrolithiasis, Calcium Oxalate 61 15.951
404
NSS002 Neisseria Meningitidis Infection 47 15.950
405
TRM010 Traumatic Brain Injury 51 15.946
406
P BPL003 Bipolar Disorder 56 15.938
407
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 53 15.912
408
P FBR017 Fibrosarcoma 56 15.818
409
DYS073 Dysphagia 53 15.800
410
ORL011 Oral Cancer 60 15.791
411
BCK006 Back Pain 47 15.762
412
c TBR025 Tuberous Sclerosis 1 84 15.756
413
PHN003 Phenylketonuria 76 15.729
414
SPN051 Spondylitis 51 15.726
415
BRN056 Bronchopulmonary Dysplasia 56 15.710
416
IGR001 Ige Responsiveness, Atopic 59 15.706
417
c SPN225 Spondyloarthropathy 1 70 15.667
418
P HMR003 Hemorrhagic Disease 59 15.665
419
P MSC003 Muscular Atrophy 52 15.636
420
HMP009 Haemophilus Influenzae 41 15.624
421
P TRN020 Turner Syndrome 67 15.523
422
P MYP006 Myopia 56 15.518
423
PLM134 Pulmonary Fibrosis, Idiopathic 76 15.499
424
RNL011 Renal Osteodystrophy 49 15.444
425
CHL065 Cholangiocarcinoma 58 15.428
426
P CNJ013 Conjunctivitis 66 15.394
427
P URT039 Urticaria 58 15.393
428
P CHR071 Charcot-Marie-Tooth Disease 64 15.354
429
BLR008 Bilirubin Metabolic Disorder 57 15.352
430
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 15.339
431
P PRS038 Personality Disorder 65 15.330
432
ACT119 Acute Promyelocytic Leukemia 62 15.310
433
INF009 Inflammatory Spondylopathy 30 15.304
434
P KDN017 Kidney Cancer 61 15.279
435
c ATM011 Autoimmune Hepatitis 63 15.266
436
c OVR114 Ovarian Cancer 1 59 15.254
437
ALL014 Allergic Encephalomyelitis 34 15.247
438
PRS045 Prostatic Hypertrophy 53 15.240
439
c ACT068 Acute Cystitis 61 15.215
440
PNC001 Pancytopenia 53 15.167
441
VRC005 Varicose Veins 60 15.134
442
ABT001 Abetalipoproteinemia 68 15.111
443
FBR047 Fibromyalgia 58 15.086
444
c MJR022 Major Affective Disorder 8 38 15.083
445
c MJR024 Major Affective Disorder 9 41 15.083
446
PRP080 Peripheral Artery Disease 54 15.080
447
GST040 Gastric Adenocarcinoma 67 15.072
448
c BSL007 Basal Cell Carcinoma 68 15.032
449
ANR040 Aneurysm 61 15.022
450
MST005 Mastitis 53 14.987
451
SQM013 Squamous Cell Carcinoma, Head and Neck 73 14.966
452
BRT054 Brittle Bone Disorder 74 14.938
453
P SYP003 Syphilis 59 14.929
454
P INS002 in Situ Carcinoma 53 14.904
455
INT079 Intrahepatic Cholangiocarcinoma 51 14.880
456
ORL015 Oral Squamous Cell Carcinoma 43 14.801
457
ALL006 Allergic Asthma 56 14.792
458
DNT012 Dental Caries 53 14.784
459
CRH005 Crohn's Colitis 53 14.716
460
P ANT006 Antiphospholipid Syndrome 55 14.700
461
PRS021 Prostatic Adenoma 43 14.694
462
GNG013 Gingivitis 59 14.691
463
P HYP058 Hypervitaminosis a 47 14.686
464
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 14.637
465
THY030 Thyroid Gland Disease 50 14.602
466
P LCT001 Lactic Acidosis 51 14.584
467
GTR002 Goiter 53 14.568
468
P GCH001 Gaucher's Disease 70 14.559
469
P DYS154 Dystonia 64 14.514
470
VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 14.500
471
PRS129 Prostatic Hyperplasia, Benign 49 14.484
472
P GLM040 Glioma Susceptibility 1 71 14.470
473
VCC001 Vaccinia 47 14.465
475
HSH003 Hashimoto Thyroiditis 60 14.459
476
CRD223 Cardiac Arrhythmia 63 14.435
477
KRT019 Keratitis, Hereditary 66 14.416
478
HYP014 Hyperuricemia 51 14.357
479
LMY002 Leiomyoma 51 14.334
480
P ENC004 Encephalitis 61 14.329
481
MSC157 Muscular Dystrophy, Duchenne Type 79 14.327
482
PLM031 Poliomyelitis 63 14.322
483
PRS047 Prostatitis 58 14.314
484
FDL002 Food Allergy 47 14.309
485
CNN005 Connective Tissue Disease 67 14.301
486
MTB004 Metabolic Acidosis 48 14.296
487
PPL022 Papilloma 53 14.291
488
P RTN016 Retinal Degeneration 52 14.290
489
PPT005 Peptic Ulcer Disease 58 14.253
490
c HMC039 Hemochromatosis, Type 1 73 14.224
491
URL001 Urolithiasis 46 14.069
492
CRD132 Cardiac Conduction Defect 60 14.045
493
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 14.021
494
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 14.005
495
BRC012 Brucellosis 66 14.000
496
P SYS005 Systemic Scleroderma 74 13.966
497
P ART023 Arthropathy 61 13.962
498
P CHL066 Cholangitis 52 13.941
499
c EXD008 Exudative Vitreoretinopathy 1 71 13.929
500
FND002 Fundus Dystrophy 55 13.928
501
P MCR010 Microcephaly 60 13.925
502
P CRY007 Cryoglobulinemia, Familial Mixed 49 13.924
503
PST028 Post-Traumatic Stress Disorder 59 13.914
504
THY111 Thyroid Carcinoma, Familial Medullary 67 13.914
505
BRN002 Bronchiolitis 57 13.895
506
P MYC008 Myocarditis 59 13.883
507
P SLP005 Sleep Disorder 61 13.828
508
P SNS001 Sensorineural Hearing Loss 59 13.822
509
P SPP010 Suppressor of Tumorigenicity 3 51 13.809
510
P BNG032 Benign Mesothelioma 53 13.785
511
P OPT006 Optic Nerve Disease 58 13.781
512
c HMP029 Hemophilia a 68 13.779
513
PSY004 Psychotic Disorder 66 13.749
514
SCH014 Schistosomiasis 56 13.742
515
TLN003 Telangiectasis 51 13.739
516
HMZ003 Homozygous Familial Hypercholesterolemia 60 13.736
517
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 38 13.733
518
MTH055 Methylmalonic Aciduria and Homocystinuria, Cbld Type 38 13.696
519
c GLL024 Gallbladder Disease 1 52 13.668
520
OTT002 Otitis Media 71 13.659
521
CLF027 Cleft Palate, Isolated 64 13.652
522
MTC116 Mitochondrial Myopathy, Infantile, Transient 42 13.643
523
CLN015 Colon Adenocarcinoma 65 13.640
524
c BLD140 Blood Group, I System 46 13.579
525
CRB037 Cerebral Palsy 67 13.560
526
SQM002 Squamous Cell Papilloma 46 13.552
527
GST050 Gastrointestinal System Disease 55 13.536
528
IMP005 Impotence 52 13.513
529
FCT001 Factor Viii Deficiency 60 13.476
530
P HYD006 Hydrocephalus 61 13.474
531
P END033 Endocarditis 58 13.460
532
P SBS003 Substance Abuse 54 13.442
533
HPT004 Hepatic Coma 43 13.406
534
ART016 Aortic Aneurysm 68 13.402
535
IDP085 Idiopathic Infantile Hypercalcemia 32 13.395
536
LGH007 Leigh Syndrome 70 13.386
537
P PRN023 Prion Disease 60 13.382
538
P ESP024 Esophagitis 60 13.370
539
OST003 Osteonecrosis 61 13.350
540
TRN018 Transitional Cell Carcinoma 56 13.350
541
ENT004 Enthesopathy 51 13.328
542
LYM019 Lymphosarcoma 46 13.311
543
ACT098 Acute Erythroid Leukemia 55 13.290
544
c ACT134 Acute Liver Failure 59 13.280
545
PRN019 Perinatal Necrotizing Enterocolitis 60 13.274
546
P MCR129 Microvascular Complications of Diabetes 1 68 13.272
547
CMP010 Complex Regional Pain Syndrome 60 13.244
548
HMC042 Homocystinuria-Megaloblastic Anemia, Cble Complementation Type 33 13.210
549
c NRF024 Neurofibromatosis, Type I 72 13.206
550
NPH003 Nephrocalcinosis 49 13.192
551
KPS004 Kaposi Sarcoma 77 13.187
552
OST017 Osteomyelitis 63 13.168
553
ANX004 Anoxia 40 13.143
554
P PRP029 Porphyria 60 13.118
555
AGN018 Agenesis of Corpus Callosum, Cardiac, Ocular, and Genital Syndrome 57 13.105
556
P UVT001 Uveitis 57 13.061
557
WST001 West Syndrome 59 13.054
558
P LNG028 Long Qt Syndrome 64 13.026
559
INT066 Interstitial Lung Disease 60 12.997
560
VTM035 Vitamin D-Dependent Rickets, Type 3 16 12.966
561
HMG005 Hemoglobinopathy 56 12.939
562
CRY003 Cryptosporidiosis 56 12.923
563
OVR094 Ovarian Epithelial Cancer 39 12.888
564
P DNG005 Dengue Virus 56 12.884
565
QFV001 Q Fever 62 12.882
566
GT001 Gout 64 12.881
567
c PLM164 Pulmonary Hypertension, Primary, 1 76 12.878
568
P TBR001 Tuberous Sclerosis 69 12.873
569
FRN006 Frontotemporal Dementia 68 12.855
570
NWC001 Newcastle Disease 47 12.850
571
HPT019 Hepatic Encephalopathy 59 12.817
572
P PRM011 Primary Ciliary Dyskinesia 69 12.783
573
CRN030 Coronary Stenosis 50 12.767
574
CHC001 Chickenpox 57 12.761
575
CRB004 Cerebral Artery Occlusion 45 12.758
576
MCR013 Microphthalmia 60 12.747
577
ADR040 Adrenal Gland Pheochromocytoma 46 12.742
578
P INT068 Intestinal Disease 53 12.739
579
PRT038 Protein-Energy Malnutrition 53 12.739
580
c CHL119 Cholangitis, Primary Sclerosing 58 12.701
581
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 12.694
582
SBC016 Subacute Delirium 43 12.669
583
c HNT004 Huntington Disease-Like 2 52 12.665
584
P PLY014 Polycystic Kidney Disease 69 12.654
585
P APL001 Aplastic Anemia 73 12.646
586
PRT014 Protein S Deficiency 41 12.610
587
LYM027 Lymphopenia 56 12.605
588
PSR001 Psoriatic Arthritis 62 12.599
589
P SHR001 Short Bowel Syndrome 53 12.598
590
P FML011 Familial Adenomatous Polyposis 71 12.584
591
P LPR021 Leprosy 3 71 12.577
592
PLY150 Polykaryocytosis Inducer 29 12.528
593
c ATM006 Autoimmune Lymphoproliferative Syndrome 75 12.525
594
RHB024 Rhabdomyosarcoma 2 67 12.442
595
DMY004 Demyelinating Disease 50 12.432
596
HNS001 Hansen's Disease 32 12.336
597
APH001 Aphthous Stomatitis 58 12.315
598
P MVM001 Movement Disease 61 12.299
599
c BRS111 Breast-Ovarian Cancer, Familial 2 53 12.284
600
ISL116 Isolated Complex Iii Deficiency 23 12.278
601
VSC003 Visceral Leishmaniasis 55 12.262
602
GST092 Gastroesophageal Reflux 61 12.247
603
BTT017 Beta-Thalassemia Major 51 12.241
604
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 46 12.229
605
PNC041 Pancreatic Ductal Adenocarcinoma 51 12.221
606
c HNT011 Huntington Disease-Like 3 34 12.202
607
P ATS308 Autosomal Dominant Cerebellar Ataxia 64 12.181
608
P CRP001 Carpal Tunnel Syndrome 66 12.164
609
VSC002 Vascular Dementia 60 12.147
610
c LKM005 Leukemia, T-Cell, Chronic 34 12.142
611
P BRS044 Breast Adenocarcinoma 58 12.094
612
BRN028 Brain Cancer 74 12.079
613
P RBL001 Rubella 58 12.017
614
BLR001 Biliary Atresia 55 12.010
615
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 68 11.999
616
CRY005 Cryptococcosis 60 11.983
617
c DNT047 Dentinogenesis Imperfecta Type 2 35 11.968
618
TQP001 Taqi Polymorphism 29 11.933
619
ANR007 Anorexia Nervosa 60 11.932
620
c INH020 Inherited Metabolic Disorder 48 11.931
621
P USH001 Usher Syndrome 64 11.900
622
CHG001 Chagas Disease 66 11.898
623
P FML018 Familial Mediterranean Fever 73 11.892
624
MTC008 Mitochondrial Complex Iii Deficiency 35 11.863
625
P RTN018 Retinal Disease 53 11.846
626
MTH009 Mouth Disease 57 11.819
627
BLD131 Bladder Urothelial Carcinoma 60 11.815
628
P ALP009 Alopecia Areata 59 11.807
629
HYP005 Hypokalemia 55 11.804
630
ALC006 Alcoholic Hepatitis 61 11.790
631
P HNT016 Huntington Disease 73 11.784
632
MSC007 Muscle Hypertrophy 64 11.757
633
ADL002 Adult Syndrome 70 11.753
634
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 11.736
635
HYP057 Hypervitaminosis D 37 11.713
636
CMM004 Common Variable Immunodeficiency 72 11.703
637
P HYP818 Hypobetalipoproteinemia, Familial, 1 60 11.697
638
MLG169 Malignant Astrocytoma 57 11.692
639
MCR017 Macrocytic Anemia 44 11.683
640
P HYP726 Hypercalcemia, Infantile, 1 58 11.681
641
P HMN038 Human Coronavirus Sensitivity 30 11.667
642
ISL099 Isolated Methylmalonic Acidemia 36 11.667
643
ANT039 Antisynthetase Syndrome 55 11.660
644
P NRF002 Neurofibromatosis 57 11.648
645
PRP016 Paraplegia 52 11.634
646
c JVN010 Juvenile Rheumatoid Arthritis 66 11.627
647
ORL013 Oral Lichen Planus 46 11.576
648
c ATS239 Autosomal Recessive Hypophosphatemic Rickets 50 11.572
649
CHL067 Cholecystitis 60 11.564
650
THR004 Thrombocytosis 53 11.508
651
CRT013 Carotid Stenosis 51 11.504
652
c ATS347 Autosomal Dominant Polycystic Kidney Disease 66 11.484
653
PTH003 Pathologic Nystagmus 52 11.466
654
P PRP003 Porphyria Cutanea Tarda 66 11.459
655
P ICH004 Ichthyosis 56 11.458
656
CNT047 Contact Dermatitis 57 11.445
657
INS001 Insulinoma 59 11.400
658
LBR036 Leber Plus Disease 66 11.383
659
c MCR112 Microvascular Complications of Diabetes 2 42 11.358
660
c NMN014 Niemann-Pick Disease, Type C2 49 11.354
661
CLC006 Calcinosis 47 11.344
662
NRT004 Neuritis 53 11.328
663
MRF001 Marfan Syndrome 76 11.321
664
CLF001 Cleft Lip 53 11.313
665
P MDL005 Medulloblastoma 75 11.306
666
P ASP006 Aspergillosis 72 11.288
667
P PYL005 Pyelonephritis 57 11.285
668
GST023 Gastric Ulcer 52 11.249
669
HGH043 High Grade Glioma 45 11.238
670
P MTR014 Motor Neuron Disease 65 11.233
671
ETN001 Eating Disorder 59 11.216
672
ACR007 Acromegaly 70 11.212
673
PYR037 Pyruvate Carboxylase Deficiency 45 11.203
674
P MYS005 Myositis 56 11.183
675
P DDN001 Duodenal Ulcer 53 11.172
676
THY125 Thyroid Gland Medullary Carcinoma 48 11.171
677
P CRV039 Cervicitis 52 11.159
678
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 64 11.157
679
P NJM001 Nijmegen Breakage Syndrome 76 11.152
680
P MST009 Mastocytosis 64 11.152
681
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 69 11.146
682
CTN007 Cutaneous Leishmaniasis 62 11.125
683
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 66 11.082
684
PRM329 Premature Aging 36 11.057
685
NNH002 Non-a-E Hepatitis 21 11.046
686
FDB001 Foodborne Botulism 55 11.024
687
ESP002 Esophageal Varix 51 11.013
688
SNS003 Sensory Peripheral Neuropathy 52 11.004
689
P ANP001 Anaplastic Large Cell Lymphoma 61 11.000
690
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 10.972
691
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 63 10.955
692
BCT002 Bacterial Vaginosis 53 10.945
693
CLS016 Clostridium Difficile Colitis 49 10.901
694
P PLY018 Polycythemia 56 10.891
695
c THY109 Thyroid Cancer, Nonmedullary, 1 55 10.876
696
c ART138 Aortic Aneurysm, Familial Abdominal, 1 61 10.857
697
P OST001 Osteopetrosis 71 10.812
698
MTH071 Methane Production 25 10.785
699
MLT157 Multiple System Atrophy 1 69 10.777
700
c ACT135 Acute Graft Versus Host Disease 51 10.773
701
P SCL009 Sclerosing Cholangitis 48 10.769
702
DGN001 Degenerative Disc Disease 49 10.766
703
WRN001 Werner Syndrome 69 10.761
704
PLS011 Plasmacytoma 56 10.751
705
ORL005 Oral Candidiasis 56 10.748
706
HYP043 Hyperandrogenism 48 10.743
707
GLC009 Glucosephosphate Dehydrogenase Deficiency 53 10.737
708
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 50 10.732
709
P HYP035 Hypophosphatasia 62 10.728
710
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 63 10.713
711
APN008 Apnea, Obstructive Sleep 67 10.698
712
KWS002 Kawasaki Disease 65 10.691
713
P MTC069 Mitochondrial Disorders 57 10.690
714
P RST001 Restless Legs Syndrome 52 10.685
715
STT001 Status Epilepticus 59 10.679
716
P PSD015 Pseudohypoparathyroidism 55 10.659
717
c INF071 Inflammatory Bowel Disease 1 65 10.655
718
LKP003 Leukoplakia 39 10.642
719
BRR014 Barrett Esophagus 66 10.626
720
CHR074 Choriocarcinoma 46 10.605
721
c GRV008 Graves Disease 1 54 10.601
722
HRP004 Herpes Zoster 61 10.597
723
P MTR004 Maturity-Onset Diabetes of the Young 68 10.578
724
CHY002 Chylomicron Retention Disease 64 10.558
725
SYN007 Synovitis 55 10.556
726
c SVR005 Severe Pre-Eclampsia 50 10.554
727
CMB007 Combined Immunodeficiency 57 10.551
728
P NRN021 Neuronal Ceroid Lipofuscinosis 65 10.534
729
P BRG001 Brugada Syndrome 69 10.525
730
CHR066 Chronic Fatigue Syndrome 60 10.519
731
PRS063 Paresthesia 39 10.502
732
HDN002 Head Injury 44 10.493
733
NRM005 Neuromuscular Disease 63 10.490
734
PLC002 Plica Syndrome 35 10.470
735
CHL004 Cholelithiasis 49 10.470
736
c ALP101 Alpha-Thalassemia 62 10.467
737
DYS015 Dysentery 50 10.443
739
P GLL022 Guillain-Barre Syndrome 60 10.438
740
MYL005 Myelofibrosis 71 10.416
741
PLM010 Pulmonary Edema 55 10.408
742
IGG001 Iga Glomerulonephritis 50 10.402
743
CHR178 Chromosomal Triplication 34 10.399
744
P CYS018 Cystitis 59 10.362
745
CRV002 Cervix Uteri Carcinoma in Situ 47 10.359
746
CRV045 Cervical Intraepithelial Neoplasia 39 10.359
747
SCR011 Scrapie 39 10.323
748
MMM001 Mammary Paget's Disease 53 10.302
749
c PLM127 Pulmonary Hypertension, Primary, 3 34 10.280
750
c PSR023 Psoriasis 1 52 10.256
751
BSL036 Basal Cell Nevus Syndrome 73 10.243
752
P BRN022 Bronchiectasis 60 10.221
753
CMR002 Coumarin Resistance 59 10.215
754
P THR005 Thrombotic Thrombocytopenic Purpura 64 10.212
755
CLR109 Colorectal Adenocarcinoma 50 10.194
756
c HPT007 Hepatitis E 51 10.164
757
c HYP788 Hypophosphatemic Rickets, Autosomal Recessive, 1 28 10.161
758
SPS057 Spasticity 42 10.160
759
MYF001 Myofibroma 42 10.156
760
c PNC108 Pancreatitis, Hereditary 69 10.150
761
BNN003 Bone Inflammation Disease 48 10.117
762
MNN043 Meningioma, Familial 79 10.114
763
CMP002 Campylobacteriosis 50 10.107
764
BTN003 Biotinidase Deficiency 62 10.080
765
c HPT015 Hepatitis D 49 10.054
766
c HMP004 Hemophilia B 68 10.026
767
HMN047 Human Cytomegalovirus Infection 57 10.019
768
P CHR012 Chronic Granulomatous Disease 69 10.019
769
P ERL057 Early Infantile Epileptic Encephalopathy 60 10.017
770
P MYS003 Myasthenia Gravis 68 10.015
771
P MLT074 Multiple Endocrine Neoplasia 59 10.012
772
AMN001 Amenorrhea 54 10.008
773
BRS051 Breast Disease 58 9.990
774
ART002 Arts Syndrome 66 9.989
775
INT002 Intermittent Claudication 61 9.989
776
PRM020 Premenstrual Tension 39 9.972
777
P KRT007 Keratoconus 50 9.972
778
c USH036 Usher Syndrome, Type I 61 9.963
779
PPL049 Papillon-Lefevre Syndrome 66 9.962
780
P FLL037 Follicular Lymphoma 74 9.955
781
P TXP001 Toxoplasmosis 60 9.953
782
LMY014 Leiomyoma, Uterine 56 9.946
783
AVN001 Avian Influenza 61 9.936
784
P STR022 Stargardt Disease 61 9.930
785
FML035 Familial Hyperlipidemia 55 9.883
786
KRN002 Kearns-Sayre Syndrome 63 9.878
787
OBS002 Obsessive-Compulsive Disorder 68 9.845
788
DSR002 Disorders of Intracellular Cobalamin Metabolism 29 9.838
789
BRN004 Brain Edema 54 9.836
790
LMB062 Limb Ischemia 55 9.834
791
ADR007 Adrenoleukodystrophy 73 9.799
792
P NRV007 Nervous System Disease 67 9.797
793
ATN005 Autonomic Dysfunction 46 9.794
794
P PSD087 Pseudoxanthoma Elasticum 67 9.791
795
P PRP034 Purpura Fulminans 41 9.790
796
P CNG001 Congenital Myasthenic Syndrome 68 9.781
797
P HML001 Hemolytic-Uremic Syndrome 52 9.780
798
END040 Endogenous Depression 55 9.757
799
APP008 Appendicitis 62 9.750
800
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 34 9.746
801
RNL065 Renal Cell Carcinoma, Papillary, 1 79 9.742
802
P VTR007 Vitreoretinopathy 46 9.721
803
CRT084 Creatinine Clearance Quantitative Trait Locus 25 9.720
804
RTN020 Retinal Vascular Disease 46 9.710
805
STT009 Sutton Disease 2 29 9.710
806
c PRM038 Primary Agammaglobulinemia 47 9.700
807
P NNN008 Noonan Syndrome 1 77 9.699
808
c FML346 Familial Adenomatous Polyposis 1 65 9.689
809
P SJG008 Sjogren Syndrome 61 9.676
810
c GLY008 Glycogen Storage Disease Ii 72 9.664
811
MCL006 Macular Retinal Edema 57 9.661
812
ATN004 Autonomic Neuropathy 42 9.653
813
P PLL002 Pellagra 46 9.645
814
GRW007 Growth Hormone Deficiency 46 9.643
815
P MYC033 Myoclonus 47 9.642
816
CHP002 Chops Syndrome 47 9.637
817
TTH006 Tooth Disease 51 9.628
818
GSG001 Gas Gangrene 52 9.623
819
P VNW001 Von Willebrand's Disease 65 9.587
820
P HYP838 Hyperlipidemia, Familial Combined, 3 61 9.573
821
c WLM013 Wilms Tumor 1 66 9.564
822
P FCL005 Focal Segmental Glomerulosclerosis 57 9.555
823
TRD006 Tardive Dyskinesia 53 9.545
824
P THY023 Thymoma 64 9.542
825
INT075 Intracranial Hypertension 53 9.540
826
PRT018 Portal Vein Thrombosis 50 9.539
827
P JBR020 Joubert Syndrome 1 74 9.537
828
P BRD002 Bardet-Biedl Syndrome 66 9.525
829
GLC086 Glucocorticoid-Induced Osteoporosis 43 9.505
830
IDP070 Idiopathic Scoliosis 42 9.497
831
P SCL057 Scoliosis, Isolated 1 40 9.489
832
P MTC133 Mitochondrial Myopathy 50 9.482
833
P ANG015 Angioedema 56 9.471
834
SYN036 Syncope 45 9.459
835
P GLC113 Galactosemia I 66 9.444
836
P RHB003 Rhabdomyosarcoma 66 9.438
837
c BCT007 Bacterial Meningitis 55 9.428
838
P AGM001 Agammaglobulinemia 68 9.423
839
P MMP001 Mumps 57 9.419
840
EMB004 Embryonal Carcinoma 56 9.418
841
PRT029 Parathyroid Adenoma 51 9.405
842
c HYP724 Hyperlipoproteinemia, Type Iii 67 9.392
843
CHL152 Childhood Acute Lymphocytic Leukemia 50 9.391
844
PRM013 Premature Menopause 58 9.387
845
TRC008 Trachoma 53 9.385
846
RNL077 Renal Fibrosis 46 9.361
847
P RTT002 Rett Syndrome 79 9.343
848
VGN023 Vaginitis 56 9.343
849
HRD143 Hereditary Hypercarotenemia and Vitamin a Deficiency 6 9.340
850
P PRM002 Primary Hyperoxaluria 65 9.335
851
ARG004 Argyria 26 9.310
852
SXL003 Sexual Disorder 49 9.310
853
P ZLL001 Zellweger Syndrome 65 9.298
854
PLG002 Plague 58 9.288
855
PLY001 Polycythemia Vera 69 9.276
856
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 26 9.264
857
LNG031 Lung Benign Neoplasm 51 9.263
858
P MCP040 Mucopolysaccharidosis-Plus Syndrome 70 9.261
859
INF034 Infective Endocarditis 54 9.247
860
WRN003 Wernicke Encephalopathy 46 9.243
861
P CRN037 Craniosynostosis 68 9.226
862
DBT084 Diabetes Mellitus, Ketosis-Prone 60 9.219
863
SPP011 Suppression of Tumorigenicity 12 61 9.214
864
P LCT002 Lactose Intolerance 52 9.190
865
RFR003 Refractive Error 41 9.190
866
MDD018 Middle East Respiratory Syndrome 44 9.189
867
P RTN022 Retinal Vein Occlusion 54 9.179
868
P MLG056 Malignant Hyperthermia 66 9.171
869
c ART101 Aortic Valve Disease 2 66 9.169
870
HRT012 Heart Valve Disease 53 9.145
871
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 50 9.141
872
PHR003 Pharyngitis 58 9.133
873
ACT084 Acute Stress Disorder 54 9.125
874
FBR012 Fabry Disease 70 9.113
875
c PNS012 Paine Syndrome 60 9.111
876
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 9.097
877
BRS099 Breast Ductal Carcinoma 61 9.077
878
MNN020 Meningococcal Infection 45 9.077
879
c THY107 Thymoma, Familial 42 9.049
880
HPT022 Hepatoblastoma 54 9.018
881
PRT058 Pure Autonomic Failure 58 9.016
882
DWR001 Dwarfism 44 9.013
883
P AGG001 Aggressive Periodontitis 55 9.005
884
RTN017 Retinal Detachment 60 9.001
885
AZS001 Azoospermia 45 8.985
886
c MST023 Mesothelioma, Malignant 56 8.969
887
c PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 63 8.953
888
P ESS003 Essential Thrombocythemia 69 8.953
889
EXC002 Exocrine Pancreatic Insufficiency 42 8.950
890
ALP103 Alpha-1-Antitrypsin Deficiency 68 8.944
891
P ALP004 Alport Syndrome 69 8.937
892
AVD001 Avoidant Personality Disorder 49 8.936
893
c TBR026 Tuberous Sclerosis 2 71 8.935
894
BDD001 Budd-Chiari Syndrome 62 8.893
895
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 8.893
896
DNG003 Dengue Disease 65 8.881
897
PSD059 Pseudoxanthoma Elasticum-Like Disorder with Multiple Coagulation Factor Deficiency 29 8.878
898
PST021 Postpartum Depression 50 8.875
899
RYN005 Raynaud Phenomenon 45 8.869
900
MMB001 Membranoproliferative Glomerulonephritis 56 8.847
901
P LYM033 Lymphoproliferative Syndrome 59 8.844
902
WLS001 Wilson Disease 70 8.834
903
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 8.831
904
MNN009 Meningoencephalitis 48 8.831
905
CLR030 Clear Cell Renal Cell Carcinoma 54 8.811
906
ILS001 Ileus 50 8.804
907
c FML191 Familial Long Qt Syndrome 55 8.795
908
LYS002 Lysosomal Storage Disease 51 8.768
909
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 8.751
910
P LRY044 Larynx Cancer 54 8.734
911
c OPT053 Optic Atrophy 1 62 8.701
912
P STR020 Strabismus 56 8.693
913
P RNL007 Renal Tubular Acidosis 50 8.666
914
c PSR017 Psoriasis 2 53 8.647
915
P NPH005 Nephronophthisis 56 8.563
916
WST005 West Nile Virus 57 8.553
917
HTC003 Hutchinson-Gilford Progeria Syndrome 65 8.551
918
THR123 Thrombotic Microangiopathy 40 8.549
919
P MNC007 Monocytic Leukemia 47 8.540
920
P OBS001 Obstructive Jaundice 48 8.537
921
NRN004 Neuroendocrine Tumor 59 8.530
922
GLM044 Glomerular Disease 35 8.528
923
RFR010 Refractory Anemia 49 8.525
924
CLL003 Cellulitis 53 8.512
925
P DVL113 Developmental and Epileptic Encephalopathy 43 8.511
926
P GLL018 Gallbladder Cancer 53 8.506
927
THR100 Thrombocytopenic Purpura, Autoimmune 61 8.494
928
c MLT160 Multiple Endocrine Neoplasia, Type Iia 67 8.481
929
NRT001 Neurotic Disorder 56 8.473
930
P PMP001 Pemphigus 55 8.463
931
c USH035 Usher Syndrome Type 2 52 8.447
932
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 8.420
933
c CHR708 Chronic Urticaria 42 8.381
934
ALL010 Allergic Contact Dermatitis 56 8.375
935
NRN005 Neuronal Ceroid-Lipofuscinoses 61 8.370
936
SFT003 Soft Tissue Sarcoma 57 8.362
937
PLY100 Polyploidy 36 8.359
938
MYL031 Myeloproliferative Neoplasm 66 8.340
939
GLS007 Glossitis 47 8.338
940
c MCP001 Mucopolysaccharidosis Iii 69 8.336
941
PRT082 Preterm Premature Rupture of the Membranes 57 8.323
942
P MMB011 Membranous Nephropathy 50 8.316
943
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 70 8.315
944
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 8.313
945
P MTR003