Search results for Vitamin C

3237 hits were found for Vitamin C

# Family MCID Name MIFTS Score
1
HYP781 Hypoascorbemia 50 4.723
2
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 53 3.589
3
RCK004 Rickets 69 0.982
4
c HPT001 Hepatitis C 63 0.852
5
c HPT073 Hepatitis C Virus 70 0.788
6
P HPT021 Hepatitis 67 0.501
7
KRT002 Keratomalacia 48 0.456
8
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.441
9
P LVR013 Liver Disease 68 0.426
10
LVR012 Liver Cirrhosis 63 0.374
11
VTM002 Vitamin B12 Deficiency 48 0.374
12
P KDN018 Kidney Disease 70 0.373
13
P HYP069 Hyperparathyroidism 62 0.356
14
c CHR684 Chronic Kidney Disease 66 0.339
15
P OST002 Osteoporosis 73 0.330
16
P BRS047 Breast Cancer 96 0.329
17
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.313
18
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.312
19
ATM095 Autoimmune Disease 61 0.308
20
P CLR023 Colorectal Cancer 98 0.298
21
DFC004 Deficiency Anemia 75 0.288
22
P HPT023 Hepatocellular Carcinoma 100 0.287
23
VTM033 Vitamin K Deficiency Bleeding 48 0.286
24
c SCN007 Secondary Hyperparathyroidism 50 0.277
25
BNR002 Bone Resorption Disease 48 0.272
26
c HPT016 Hepatitis B 59 0.256
27
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.250
28
END030 End Stage Renal Failure 58 0.250
29
48X005 48,xyyy 39 0.248
30
c PRC016 Pre-Eclampsia 63 0.246
31
OST011 Osteomalacia 52 0.245
32
c VRL010 Viral Hepatitis 51 0.245
33
c HYP836 Hypercholesterolemia, Familial, 1 72 0.243
34
P CRN300 Coronary Heart Disease 1 63 0.242
35
ATH013 Atherosclerosis Susceptibility 66 0.242
36
P BND020 Bone Disease 59 0.241
37
P PRS040 Prostate Cancer 97 0.241
38
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.240
39
FTT001 Fatty Liver Disease 61 0.238
40
c HPT003 Hepatitis a 63 0.238
41
P VSC007 Vascular Disease 63 0.234
42
P DBT009 Diabetes Mellitus 64 0.233
43
P PSR002 Psoriasis 62 0.227
44
P DRR001 Diarrhea 57 0.226
45
CYS001 Cystic Fibrosis 80 0.225
46
P NRP001 Neuropathy 56 0.224
47
IRN002 Iron Metabolism Disease 57 0.224
48
PST011 Pustulosis of Palm and Sole 52 0.224
49
HMC014 Homocysteinemia 53 0.222
50
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.221
51
P INF037 Inflammatory Bowel Disease 56 0.220
52
P CRN018 Coronary Artery Anomaly 63 0.218
53
P HRT032 Heart Disease 75 0.217
54
P LKM002 Leukemia 66 0.215
55
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.214
56
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.211
57
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.211
58
HLX001 Helix Syndrome 47 0.209
59
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.208
60
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.208
61
LPD008 Lipid Metabolism Disorder 62 0.207
62
HMN044 Human Immunodeficiency Virus Type 1 71 0.207
63
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.206
64
ART140 Arteries, Anomalies of 53 0.205
65
P CRD246 Cardiovascular System Disease 56 0.205
66
ISC004 Ischemia 60 0.204
67
CYT002 Cytokine Deficiency 44 0.204
68
P ATR011 Atrial Fibrillation 66 0.203
69
c THR092 Thrombophilia Due to Thrombin Defect 73 0.202
70
P ALZ034 Alzheimer Disease 88 0.201
71
P LNG032 Lung Cancer 97 0.201
72
P SKN015 Skin Carcinoma 67 0.198
73
P ADN016 Adenocarcinoma 64 0.198
74
PRT037 Pertussis 65 0.195
75
P MLT020 Multiple Sclerosis 72 0.193
76
CRH001 Crohn's Disease 74 0.193
77
DRM006 Dermatitis 61 0.193
78
ADN018 Adenoma 58 0.193
79
CRB039 Cerebrovascular Disease 69 0.193
81
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.192
82
PRN011 Pernicious Anemia 52 0.192
83
c SYS001 Systemic Lupus Erythematosus 86 0.192
84
NRL016 Neural Tube Defects 82 0.191
85
P BLD134 Bladder Cancer 78 0.191
86
P GST053 Gastric Cancer 83 0.190
87
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.190
88
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.189
89
IMM167 Immune Deficiency Disease 78 0.189
90
c LKM061 Leukemia, Acute Myeloid 83 0.189
91
P MYL006 Myeloid Leukemia 60 0.188
92
P PNC035 Pancreatic Cancer 84 0.188
93
P LYM118 Lymphoma 68 0.188
94
STR067 Stroke, Ischemic 80 0.187
95
P OVR042 Ovarian Cancer 89 0.184
96
P MYP004 Myopathy 64 0.184
97
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.183
98
ALL026 Allergic Hypersensitivity Disease 64 0.182
99
c ATR087 Atrial Standstill 1 74 0.182
100
CNG034 Congestive Heart Failure 70 0.182
101
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.181
102
P NRB001 Neuroblastoma 71 0.181
103
OST159 Osteogenic Sarcoma 66 0.180
104
HYP066 Hyperglycemia 61 0.180
105
P THL005 Thalassemia 60 0.180
106
P LPS004 Lupus Erythematosus 61 0.180
107
NTR005 Nutritional Deficiency Disease 61 0.178
108
P LYN001 Lynch Syndrome 77 0.177
109
P PRD008 Periodontitis 62 0.177
110
P PRP019 Peripheral Nervous System Disease 57 0.177
111
P THR014 Thrombocytopenia 68 0.177
112
TXC005 Toxic Shock Syndrome 61 0.176
113
P MYC007 Myocardial Infarction 70 0.176
114
SKN016 Skin Disease 63 0.176
115
P NRF023 Neurofibromatosis, Type Ii 76 0.176
116
P PLY011 Polycystic Ovary Syndrome 56 0.176
117
c MCR120 Microvascular Complications of Diabetes 7 47 0.175
118
MSL001 Measles 61 0.174
119
P HYP086 Hypothyroidism 68 0.174
120
P ALP008 Alopecia 56 0.173
121
c HYP595 Hypertension, Essential 84 0.173
122
P NTR004 Neutropenia 63 0.173
123
c MCR113 Microvascular Complications of Diabetes 3 52 0.173
124
c MCR130 Microvascular Complications of Diabetes 6 41 0.171
125
CHL068 Cholestasis 60 0.171
126
c MCR133 Microvascular Complications of Diabetes 4 41 0.171
127
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.170
128
P CTR002 Cataract 60 0.170
129
PYR009 Pyridoxine Deficiency Anemia 34 0.170
130
P LYM031 Lymphocytic Leukemia 55 0.170
131
GST033 Gestational Diabetes 57 0.170
132
OST012 Osteoarthritis 78 0.168
133
P GST044 Gastritis 55 0.167
134
P HYP061 Hypertrophic Cardiomyopathy 66 0.167
135
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.167
136
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.167
137
DPR016 Depression 63 0.166
138
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.166
139
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.166
140
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.166
141
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.166
142
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.166
143
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.166
144
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.166
145
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.166
146
THR024 Thrombosis 56 0.166
147
LNG099 Lung Disease 61 0.166
148
TTN003 Tetanus 64 0.166
149
MLN008 Melanoma 69 0.166
150
INS024 Insulin-Like Growth Factor I 79 0.166
151
P RHM011 Rheumatoid Arthritis 80 0.164
152
VSL002 Visual Epilepsy 58 0.164
153
AST005 Asthma 77 0.163
154
PLM001 Pulmonary Tuberculosis 70 0.162
155
P MGL001 Megaloblastic Anemia 55 0.162
156
ATX019 Ataxia with Vitamin E Deficiency 48 0.160
157
P DRM053 Dermatitis, Atopic 66 0.160
158
47X002 47,xyy 49 0.159
159
P ECL001 Eclampsia 51 0.158
160
ULC004 Ulcerative Colitis 73 0.158
161
PRP030 Purpura 55 0.157
162
c PRM005 Primary Hyperparathyroidism 58 0.157
163
AGN016 Aging 56 0.157
164
NNL006 Non-Alcoholic Steatohepatitis 51 0.156
165
P GLM007 Glomerulonephritis 57 0.156
166
P BCL017 B-Cell Lymphoma 58 0.155
167
THY029 Thyroid Carcinoma 59 0.154
168
PRT011 Protein C Deficiency 45 0.154
169
ALC007 Alcohol Dependence 66 0.154
170
P ATX030 Ataxia-Telangiectasia 83 0.154
171
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.154
172
LGH007 Leigh Syndrome 70 0.151
173
P GLM045 Glioma 63 0.151
174
P VSC011 Vasculitis 62 0.150
175
SQM006 Squamous Cell Carcinoma 60 0.150
176
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.149
177
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.149
178
MNT002 Mental Depression 57 0.149
179
GLL048 Glial Tumor 45 0.148
180
HMS001 Hemosiderosis 54 0.147
181
P HML002 Hemolytic Anemia 62 0.147
182
P PNM007 Pneumonia 68 0.147
183
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 61 0.146
184
c RHB024 Rhabdomyosarcoma 2 65 0.145
185
ACQ007 Acquired Immunodeficiency Syndrome 60 0.144
186
P MSC005 Muscular Dystrophy 66 0.144
187
CRY004 Cryoglobulinemia 49 0.144
188
GLC003 Glucose Intolerance 54 0.144
189
VRL011 Viral Infectious Disease 61 0.144
190
CHL079 Children's Interstitial Lung Disease 27 0.143
191
P MTH008 Methylmalonic Acidemia 51 0.143
192
c FNC027 Fanconi Anemia, Complementation Group a 81 0.142
193
CMM005 Common Cold 56 0.142
194
BCT022 Bacterial Infectious Disease 56 0.142
195
c ACT075 Acute Myocardial Infarction 56 0.142
196
ESP021 Esophageal Cancer 90 0.142
197
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.142
198
P ENC018 Encephalopathy 61 0.141
199
c FML001 Familial Atrial Fibrillation 66 0.141
200
CLT003 Colitis 62 0.141
201
P NGH001 Night Blindness 47 0.141
202
P RRH023 Rare Hereditary Hemochromatosis 41 0.140
203
P SZR006 Seizure Disorder 58 0.140
204
P THY032 Thyroiditis 53 0.140
205
HYP017 Hypophosphatemia 49 0.140
206
P ART022 Arthritis 70 0.139
207
P INF032 Infertility 57 0.139
208
P TRN020 Turner Syndrome 65 0.139
209
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.139
210
P HYP076 Hyperthyroidism 55 0.138
211
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.138
212
DWN001 Down Syndrome 70 0.137
213
PRP027 Peripheral Vascular Disease 71 0.137
214
P NPH012 Nephrotic Syndrome 63 0.137
215
MYL009 Myelodysplastic Syndrome 70 0.136
216
KRT001 Keratoconjunctivitis Sicca 50 0.136
217
P ALC033 Alcohol Use Disorder 58 0.136
218
c SML038 Small Cell Cancer of the Lung 65 0.136
219
P SRC025 Sarcoidosis 1 70 0.136
220
XRP001 Xerophthalmia 42 0.136
221
P ART021 Arteriosclerosis 54 0.135
222
GLB015 Glioblastoma Multiforme 75 0.135
223
P ATS364 Autism 65 0.135
224
P MCR115 Microvascular Complications of Diabetes 5 66 0.135
225
P EXN002 Exanthem 57 0.134
226
c PRM038 Primary Agammaglobulinemia 43 0.133
227
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.133
228
c ATS007 Autism Spectrum Disorder 67 0.132
229
ATS010 Autosomal Recessive Disease 48 0.132
230
P LKM062 Leukemia, Acute Lymphoblastic 68 0.132
231
P RTN024 Retinoblastoma 72 0.131
232
P PHC003 Pheochromocytoma 71 0.131
233
P MYC084 Mycobacterium Tuberculosis 1 68 0.131
234
HYP266 Hypoxia 56 0.129
235
c DLT002 Dilated Cardiomyopathy 79 0.129
236
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.129
237
P LCH002 Lichen Planus 54 0.129
238
STM007 Stomatitis 49 0.129
239
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.128
240
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.128
241
c BTT014 Beta-Thalassemia 72 0.128
242
MYL069 Myeloma, Multiple 85 0.127
243
URM002 Uremia 49 0.127
244
c FML346 Familial Adenomatous Polyposis 1 70 0.126
245
P RHN004 Rhinitis 57 0.126
246
P HYP750 Hypertriglyceridemia, Familial 61 0.126
247
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.126
248
PLM033 Pulmonary Embolism 59 0.125
249
P INF038 Influenza 68 0.125
250
LYM133 Lymphoma, Hodgkin, Classic 69 0.125
251
DPH001 Diphtheria 60 0.125
252
P SCK005 Sickle Cell Disease 50 0.125
253
ANG054 Angina Pectoris 66 0.125
254
P CHR345 Chronic Pain 50 0.125
255
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.124
256
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.124
257
P DMN002 Dementia 67 0.124
258
IRN001 Iron Deficiency Anemia 58 0.123
259
P HMC002 Homocystinuria 54 0.123
260
P PRM006 Primary Biliary Cirrhosis 61 0.123
261
P PLY019 Polyneuropathy 56 0.123
262
CLR108 Colorectal Adenoma 64 0.122
263
P HYP024 Hypoparathyroidism 55 0.122
264
P PRM011 Primary Ciliary Dyskinesia 69 0.122
265
c THR082 Thrombophilia Due to Activated Protein C Resistance 60 0.122
266
TQP001 Taqi Polymorphism 32 0.121
267
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.120
268
P RTN008 Retinitis Pigmentosa 77 0.120
269
SVR004 Severe Combined Immunodeficiency 73 0.120
270
P LTR001 Lateral Sclerosis 53 0.120
271
HLC007 Helicobacter Pylori Infection 59 0.120
272
PRT013 Portal Hypertension 60 0.120
273
c ACT071 Acute Kidney Failure 59 0.120
274
c FML008 Familial Retinoblastoma 53 0.119
275
GST019 Gastrointestinal Stromal Tumor 76 0.119
276
P MNN013 Meningitis 65 0.119
277
P THR015 Thrombophilia 50 0.118
278
INT007 Intermediate Coronary Syndrome 55 0.118
279
LPT014 Leptin Deficiency or Dysfunction 73 0.117
280
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.116
281
SPN186 Spinal Cord Injury 60 0.116
282
HYP025 Hyperphosphatemia 47 0.116
283
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.116
284
HYP056 Hypoglycemia 66 0.116
285
VTM027 Vitamin D-Dependent Rickets, Type 2a 55 0.115
286
LSH001 Leishmaniasis 63 0.115
287
P KLZ004 Kala-Azar 1 41 0.115
288
P CLC063 Celiac Disease 1 68 0.115
289
c MGR028 Migraine with or Without Aura 1 69 0.115
290
c NRF024 Neurofibromatosis, Type I 71 0.115
291
P MJR001 Major Depressive Disorder 68 0.115
292
c ATM011 Autoimmune Hepatitis 62 0.114
293
CHL014 Cholera 55 0.114
294
c PCH010 Pachyonychia Congenita 3 43 0.114
295
P EPL164 Epilepsy 71 0.114
296
P LBR001 Leber Congenital Amaurosis 67 0.114
297
P HRP006 Herpes Simplex 65 0.114
298
HYP060 Hyperinsulinism 54 0.114
299
P HMP007 Hemophilia 51 0.114
300
P GRV001 Graves' Disease 55 0.114
301
P END044 Endometriosis 62 0.114
302
P PRK057 Parkinson Disease, Late-Onset 76 0.114
303
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.113
304
CRV035 Cervical Cancer 76 0.113
305
ALL014 Allergic Encephalomyelitis 39 0.113
306
KRT009 Keratosis 53 0.113
307
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.113
308
c GLC092 Glaucoma, Primary Open Angle 62 0.112
309
DSR002 Disorders of Intracellular Cobalamin Metabolism 30 0.112
310
c PRD040 Periodontitis, Chronic 54 0.112
311
ALL003 Allergic Rhinitis 67 0.111
312
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.111
313
c ACT073 Acute Leukemia 58 0.110
314
MLR004 Malaria 80 0.110
315
P RCT021 Rectum Cancer 53 0.110
316
c LKM063 Leukemia, Chronic Myeloid 71 0.110
317
c TBR025 Tuberous Sclerosis 1 76 0.110
318
SPL018 Splenomegaly 48 0.109
319
ANX010 Anxiety 72 0.109
320
P TBR001 Tuberous Sclerosis 70 0.109
321
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.109
322
c DWL002 Dowling-Degos Disease 1 58 0.109
323
P ZLL001 Zellweger Syndrome 64 0.109
324
RTN023 Retinitis 46 0.109
325
NRR001 Neuroretinitis 43 0.109
326
c NMN015 Niemann-Pick Disease, Type C1 68 0.109
327
P RSP003 Respiratory Failure 74 0.109
328
EYD002 Eye Disease 58 0.109
329
ADL002 Adult Syndrome 69 0.109
330
RHM027 Rheumatic Disease 56 0.108
331
P LNG064 Lung Cancer Susceptibility 3 77 0.108
332
P ATR005 Atrophic Gastritis 50 0.108
333
P GRF003 Graft-Versus-Host Disease 71 0.108
334
RNL011 Renal Osteodystrophy 49 0.107
335
PLM031 Poliomyelitis 57 0.107
336
P HYP058 Hypervitaminosis a 49 0.107
337
P NMN002 Niemann-Pick Disease 60 0.107
338
P OPN001 Open-Angle Glaucoma 49 0.106
339
P CNR004 Cone-Rod Dystrophy 2 71 0.106
340
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.106
341
c SPN225 Spondyloarthropathy 1 73 0.106
342
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.105
343
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.105
344
P SCH015 Schizophrenia 75 0.105
345
LYM019 Lymphosarcoma 47 0.105
346
DBT010 Diabetic Neuropathy 55 0.105
347
P PRP029 Porphyria 62 0.105
348
P SYP003 Syphilis 59 0.105
349
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.105
350
MTC097 Mitochondrial Complex Iv Deficiency 56 0.105
351
P SLP006 Sleep Apnea 69 0.104
352
c PRX059 Peroxisome Biogenesis Disorder 1a 57 0.104
353
CNS004 Constipation 57 0.104
354
BRK010 Burkitt Lymphoma 67 0.104
355
PPT005 Peptic Ulcer Disease 58 0.104
356
PLC008 Placenta Disease 49 0.103
357
PNC001 Pancytopenia 54 0.103
358
P MLN007 Male Infertility 56 0.103
359
P HDC001 Headache 57 0.102
360
P CRD119 Cardiac Arrest 67 0.102
361
P BRB001 Beriberi 44 0.102
362
P PNC044 Pancreatitis 61 0.102
363
MRF001 Marfan Syndrome 75 0.101
364
PRT036 Peritonitis 65 0.101
365
MDD011 Mood Disorder 62 0.101
366
P DYS154 Dystonia 65 0.101
367
SCK003 Sickle Cell Anemia 72 0.101
368
KRT019 Keratitis, Hereditary 67 0.101
369
DSS009 Disseminated Intravascular Coagulation 57 0.101
370
ACR006 Aceruloplasminemia 73 0.101
371
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.101
372
P HMR003 Hemorrhagic Disease 52 0.101
373
PNC129 Pancreatic Adenocarcinoma 67 0.100
374
HRW001 Hair Whorl 36 0.100
375
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.100
376
BRN056 Bronchopulmonary Dysplasia 57 0.100
377
DFF005 Diffuse Large B-Cell Lymphoma 56 0.100
378
MCS002 Mucositis 55 0.100
379
c FML021 Familial Hypercholesterolemia 68 0.100
380
P OST001 Osteopetrosis 71 0.099
381
CHL123 Chlamydia 59 0.099
382
P HYP726 Hypercalcemia, Infantile, 1 57 0.099
383
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.099
384
P TRM003 Tremor 53 0.099
385
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.099
386
BRN071 Brain Injury 49 0.099
387
DNT012 Dental Caries 51 0.099
388
P OVR082 Overgrowth Syndrome 50 0.099
389
HYP081 Hypolipoproteinemia 50 0.099
390
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.099
391
SKN019 Skin Melanoma 67 0.099
392
IDP011 Idiopathic Interstitial Pneumonia 63 0.099
393
P HYP098 Hypereosinophilic Syndrome 66 0.099
394
FDL002 Food Allergy 49 0.098
395
TRN015 Transient Cerebral Ischemia 62 0.098
396
P PLM036 Pulmonary Fibrosis 61 0.098
397
GTR002 Goiter 52 0.098
398
ORL011 Oral Cancer 60 0.098
399
OCL069 Ocular Motor Apraxia 51 0.098
400
P INS002 in Situ Carcinoma 52 0.098
401
c HMC039 Hemochromatosis, Type 1 74 0.098
402
GST045 Gastroenteritis 59 0.097
403
GST050 Gastrointestinal System Disease 56 0.097
404
FBR047 Fibromyalgia 59 0.097
405
ACT119 Acute Promyelocytic Leukemia 63 0.097
406
P RTN016 Retinal Degeneration 53 0.097
407
P SBS003 Substance Abuse 54 0.097
408
PPL052 Papillomatosis, Confluent and Reticulated 34 0.097
409
c LKM071 Leukemia, Chronic Lymphocytic 79 0.096
410
IRR002 Irritable Bowel Syndrome 63 0.096
411
c PNS012 Paine Syndrome 61 0.096
412
ENT011 Enterocolitis 50 0.096
413
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.096
414
IGR001 Ige Responsiveness, Atopic 59 0.096
415
BLR008 Bilirubin Metabolic Disorder 57 0.095
416
NPH003 Nephrocalcinosis 51 0.095
417
c INF071 Inflammatory Bowel Disease 1 68 0.095
418
NSS002 Neisseria Meningitidis Infection 46 0.095
419
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 65 0.095
420
P FBR017 Fibrosarcoma 56 0.095
421
BRN024 Bronchitis 68 0.095
422
PRP080 Peripheral Artery Disease 53 0.095
423
SPN051 Spondylitis 52 0.095
424
ERY051 Erythroleukemia, Familial 56 0.095
425
P URT039 Urticaria 58 0.095
426
PHN003 Phenylketonuria 75 0.095
427
c ACT027 Acute Pancreatitis 59 0.095
428
c SCL052 Scleroderma, Familial Progressive 62 0.094
429
END057 Endometrial Cancer 74 0.094
430
VCC001 Vaccinia 49 0.094
431
HSH003 Hashimoto Thyroiditis 62 0.094
432
PPL022 Papilloma 54 0.094
433
INF009 Inflammatory Spondylopathy 32 0.094
434
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.094
435
HNS001 Hansen's Disease 34 0.094
436
c BRN108 Branchiootic Syndrome 1 61 0.094
437
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.093
438
P LPR021 Leprosy 3 67 0.093
439
P MSC003 Muscular Atrophy 52 0.093
440
VRC005 Varicose Veins 60 0.093
441
TRN018 Transitional Cell Carcinoma 56 0.093
442
PRS045 Prostatic Hypertrophy 52 0.093
443
P BPL003 Bipolar Disorder 56 0.093
444
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.093
445
P HYP265 Hypotonia 42 0.092
446
P CHR071 Charcot-Marie-Tooth Disease 64 0.092
447
P ANT006 Antiphospholipid Syndrome 54 0.092
448
HMP009 Haemophilus Influenzae 42 0.092
449
c MJR024 Major Affective Disorder 9 41 0.092
450
c MJR022 Major Affective Disorder 8 38 0.092
451
P AMY004 Amyloidosis 70 0.092
452
P NSP012 Nasopharyngeal Carcinoma 67 0.092
453
THY030 Thyroid Gland Disease 51 0.091
454
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.091
455
ABT001 Abetalipoproteinemia 67 0.091
456
GST040 Gastric Adenocarcinoma 70 0.091
457
P BRD002 Bardet-Biedl Syndrome 66 0.091
458
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.091
459
MST005 Mastitis 53 0.091
460
c ACT068 Acute Cystitis 63 0.091
461
CRH005 Crohn's Colitis 52 0.090
462
ALL006 Allergic Asthma 56 0.090
463
c CNG006 Congenital Hypothyroidism 65 0.089
464
BRN002 Bronchiolitis 59 0.089
465
P ANR048 Aniridia 1 63 0.089
466
P MTR004 Maturity-Onset Diabetes of the Young 66 0.089
467
c HYP057 Hypervitaminosis D 41 0.089
468
P SYS005 Systemic Scleroderma 70 0.089
469
TRM010 Traumatic Brain Injury 53 0.088
470
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.088
471
P PLM037 Pulmonary Hypertension 68 0.088
472
ORL015 Oral Squamous Cell Carcinoma 43 0.088
473
P LYM033 Lymphoproliferative Syndrome 60 0.088
474
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.088
475
P HYD006 Hydrocephalus 65 0.088
476
PSY004 Psychotic Disorder 67 0.088
477
P MYP006 Myopia 55 0.088
478
SRC014 Sarcoma 65 0.088
479
SQM002 Squamous Cell Papilloma 42 0.088
480
CLN015 Colon Adenocarcinoma 63 0.088
481
PRS129 Prostatic Hyperplasia, Benign 49 0.088
482
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 66 0.087
483
P KDN017 Kidney Cancer 61 0.087
484
MSC157 Muscular Dystrophy, Duchenne Type 71 0.087
485
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.087
486
CNT047 Contact Dermatitis 57 0.087
487
BCK006 Back Pain 42 0.087
488
BSL036 Basal Cell Nevus Syndrome 72 0.087
489
P MYC008 Myocarditis 59 0.087
490
ANR007 Anorexia Nervosa 63 0.087
491
c EXD008 Exudative Vitreoretinopathy 1 69 0.086
492
c BSL007 Basal Cell Carcinoma 68 0.086
493
SCH014 Schistosomiasis 56 0.086
494
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.086
495
SPP010 Suppressor of Tumorigenicity 3 51 0.086
496
PRS021 Prostatic Adenoma 51 0.086
497
P PRP003 Porphyria Cutanea Tarda 67 0.086
498
c PRS136 Prostate Cancer, Hereditary, 6 33 0.086
499
CNN005 Connective Tissue Disease 66 0.086
500
P LCT001 Lactic Acidosis 51 0.086
501
c PRS130 Prostate Cancer, Hereditary, 8 32 0.086
502
P FCL005 Focal Segmental Glomerulosclerosis 58 0.086
503
P SLP005 Sleep Disorder 59 0.085
504
MCR017 Macrocytic Anemia 41 0.085
505
HPT004 Hepatic Coma 43 0.085
506
OPT066 Optic Atrophy with or Without Deafness, Ophthalmoplegia, Myopathy, Ataxia, and Neuropathy 57 0.085
507
LMY002 Leiomyoma 50 0.085
508
PST092 Posttransplant Acute Limbic Encephalitis 29 0.085
509
c LRG017 Large Intestine Cancer 47 0.085
510
ENT004 Enthesopathy 48 0.084
511
MSC007 Muscle Hypertrophy 63 0.084
512
c MCR129 Microvascular Complications of Diabetes 1 66 0.084
513
CMR002 Coumarin Resistance 56 0.084
514
SPN035 Spindle Cell Sarcoma 51 0.084
515
OTT002 Otitis Media 71 0.084
516
PRT038 Protein-Energy Malnutrition 54 0.084
517
KHL003 Kohlschutter-Tonz Syndrome 64 0.084
518
ORL013 Oral Lichen Planus 45 0.084
519
HPT019 Hepatic Encephalopathy 60 0.083
520
c FNC043 Fanconi Anemia, Complementation Group E 62 0.083
521
P OPT006 Optic Nerve Disease 57 0.083
522
PNG002 Pain Agnosia 51 0.083
523
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.083
525
DSS008 Disease of Mental Health 57 0.082
526
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.082
527
P ENC004 Encephalitis 61 0.082
528
CLF027 Cleft Palate, Isolated 64 0.082
529
GNG013 Gingivitis 59 0.082
530
CLC006 Calcinosis 48 0.082
531
OVR094 Ovarian Epithelial Cancer 38 0.082
532
P ALP009 Alopecia Areata 60 0.082
533
P GLM040 Glioma Susceptibility 1 81 0.082
534
MTB004 Metabolic Acidosis 50 0.081
535
CHL065 Cholangiocarcinoma 67 0.081
536
DMY004 Demyelinating Disease 52 0.081
537
CRB037 Cerebral Palsy 68 0.081
538
HYP080 Hypogonadism 50 0.081
539
P AST007 Astrocytoma 50 0.081
540
INT079 Intrahepatic Cholangiocarcinoma 50 0.081
541
HYP064 Hypogonadotropism 40 0.080
542
BRN028 Brain Cancer 73 0.080
543
c ACT134 Acute Liver Failure 51 0.080
544
P ART023 Arthropathy 62 0.080
545
NWC001 Newcastle Disease 44 0.080
546
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.080
547
P UVT001 Uveitis 57 0.080
548
CRD132 Cardiac Conduction Defect 59 0.080
549
PRN019 Perinatal Necrotizing Enterocolitis 54 0.080
550
SBC016 Subacute Delirium 44 0.080
551
PRM020 Premenstrual Tension 39 0.080
552
c CWD006 Cowden Syndrome 1 77 0.080
553
P APL001 Aplastic Anemia 74 0.079
554
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.079
555
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.079
556
c HMP029 Hemophilia a 65 0.079
557
LKP003 Leukoplakia 39 0.079
558
DYS073 Dysphagia 50 0.079
559
P SCL018 Scoliosis 60 0.079
560
c SVR005 Severe Pre-Eclampsia 49 0.079
561
c PSR023 Psoriasis 1 49 0.079
562
CRB004 Cerebral Artery Occlusion 44 0.079
563
FND002 Fundus Dystrophy 51 0.078
564
P MVM001 Movement Disease 61 0.078
565
MMM001 Mammary Paget's Disease 53 0.078
566
c FML035 Familial Hyperlipidemia 55 0.078
567
CRP001 Carpal Tunnel Syndrome 67 0.078
568
HYP014 Hyperuricemia 51 0.078
569
IMP005 Impotence 52 0.078
570
CHR066 Chronic Fatigue Syndrome 61 0.078
571
TLN003 Telangiectasis 51 0.077
572
NRL018 Neural Tube Defects, Folate-Sensitive 49 0.077
573
BLD131 Bladder Urothelial Carcinoma 61 0.077
574
P PLR004 Pleuropulmonary Blastoma 65 0.077
575
HMG005 Hemoglobinopathy 55 0.077
576
P EPS003 Episodic Ataxia 60 0.077
577
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 64 0.077
578
P MLT074 Multiple Endocrine Neoplasia 55 0.077
579
c GRV008 Graves Disease 1 55 0.077
580
LYM027 Lymphopenia 57 0.077
581
ADR040 Adrenal Gland Pheochromocytoma 46 0.077
582
PPL049 Papillon-Lefevre Syndrome 63 0.077
583
ANR040 Aneurysm 58 0.077
584
P FRN006 Frontotemporal Dementia 70 0.077
585
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.077
586
P PLL002 Pellagra 45 0.076
587
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.076
588
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.076
589
P BNG032 Benign Mesothelioma 45 0.076
590
P CRN037 Craniosynostosis 68 0.076
591
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 52 0.076
592
P OCL013 Oculodentodigital Dysplasia 69 0.076
593
P END033 Endocarditis 57 0.076
594
MYL005 Myelofibrosis 67 0.076
595
WRN001 Werner Syndrome 69 0.075
596
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.075
597
CRN030 Coronary Stenosis 50 0.075
598
c MCR112 Microvascular Complications of Diabetes 2 41 0.075
599
HYP005 Hypokalemia 55 0.075
600
P FML018 Familial Mediterranean Fever 72 0.075
601
NRT004 Neuritis 53 0.075
602
CMP010 Complex Regional Pain Syndrome 58 0.075
603
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.075
604
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.074
605
ANX004 Anoxia 42 0.074
606
CHR178 Chromosomal Triplication 35 0.074
607
P CHL066 Cholangitis 50 0.074
608
MMB001 Membranoproliferative Glomerulonephritis 53 0.074
609
GT001 Gout 63 0.074
610
PRT014 Protein S Deficiency 50 0.074
611
TRD006 Tardive Dyskinesia 55 0.074
612
P TRC086 Trichohepatoenteric Syndrome 1 59 0.074
613
P HML033 Hemolytic Uremic Syndrome, Atypical 1 69 0.074
614
GST023 Gastric Ulcer 53 0.074
615
LNG031 Lung Benign Neoplasm 50 0.074
616
P SHR001 Short Bowel Syndrome 52 0.074
617
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.074
619
APH001 Aphthous Stomatitis 57 0.074
620
END040 Endogenous Depression 54 0.074
621
c NGH026 Night Blindness, Congenital Stationary, Type 1a 51 0.074
622
c GLL024 Gallbladder Disease 1 52 0.073
623
FCT001 Factor Viii Deficiency 55 0.073
624
VSC003 Visceral Leishmaniasis 55 0.073
625
P BRS044 Breast Adenocarcinoma 59 0.073
626
c ALP101 Alpha-Thalassemia 62 0.073
627
THY111 Thyroid Carcinoma, Familial Medullary 67 0.073
628
DYS015 Dysentery 50 0.073
629
HYP043 Hyperandrogenism 48 0.073
630
P INT068 Intestinal Disease 52 0.072
631
BLR001 Biliary Atresia 50 0.072
632
P PLY014 Polycystic Kidney Disease 59 0.072
633
P NPH005 Nephronophthisis 58 0.072
634
SNS003 Sensory Peripheral Neuropathy 53 0.072
635
c ATS013 Autosomal Recessive Congenital Ichthyosis 66 0.072
636
PSR001 Psoriatic Arthritis 62 0.072
637
c INH030 Inherited Retinal Disorder 47 0.072
638
P CND004 Candidiasis 57 0.072
639
P PSD087 Pseudoxanthoma Elasticum 67 0.072
640
VSC002 Vascular Dementia 57 0.072
641
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 50 0.072
642
DGN001 Degenerative Disc Disease 48 0.072
643
NRT001 Neurotic Disorder 52 0.072
644
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 69 0.072
645
FCT007 Factor Vii Deficiency 66 0.072
646
ERY029 Erythermalgia, Primary 58 0.072
647
CHG001 Chagas Disease 66 0.072
648
ATM052 Autoimmune Disease 1 37 0.072
649
PLY150 Polykaryocytosis Inducer 31 0.072
650
CYS010 Cystinosis 60 0.072
651
P RTN018 Retinal Disease 52 0.072
652
ACR007 Acromegaly 71 0.071
653
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 38 0.071
654
P PRC031 Preeclampsia/eclampsia 1 37 0.071
655
CHC001 Chickenpox 60 0.071
656
P NJM001 Nijmegen Breakage Syndrome 72 0.071
657
c PSR017 Psoriasis 2 52 0.071
658
RRS014 Rare Surgical Neurologic Disease 32 0.071
659
BRR014 Barrett Esophagus 64 0.071
660
P DNG005 Dengue Virus 57 0.071
661
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.071
662
c PNC108 Pancreatitis, Hereditary 69 0.071
663
CHR074 Choriocarcinoma 46 0.071
664
P HML001 Hemolytic-Uremic Syndrome 52 0.071
665
PRM329 Premature Aging 39 0.071
666
OST003 Osteonecrosis 61 0.071
667
KPS004 Kaposi Sarcoma 75 0.071
668
OST017 Osteomyelitis 64 0.071
669
MTH009 Mouth Disease 56 0.071
670
INT066 Interstitial Lung Disease 59 0.070
671
c MGL018 Megaloblastic Anemia 1 48 0.070
672
PLM010 Pulmonary Edema 55 0.070
673
49X006 49, Xxxxy Syndrome 41 0.070
674
ART016 Aortic Aneurysm 68 0.070
675
c TBR026 Tuberous Sclerosis 2 71 0.070
676
P ADL010 Adult Respiratory Distress Syndrome 63 0.070
677
P MPL001 Maple Syrup Urine Disease 69 0.070
678
P CHN059 Chondrocalcinosis 51 0.070
679
ALC006 Alcoholic Hepatitis 61 0.070
680
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.070
681
BRT054 Brittle Bone Disorder 70 0.070
682
P PRS038 Personality Disorder 65 0.070
683
c CRV002 Cervix Uteri Carcinoma in Situ 44 0.070
684
CRV045 Cervical Intraepithelial Neoplasia 39 0.070
685
CLR109 Colorectal Adenocarcinoma 50 0.070
686
P DDN001 Duodenal Ulcer 50 0.070
687
HRP004 Herpes Zoster 60 0.069
688
P PRP034 Purpura Fulminans 42 0.069
689
c ACT135 Acute Graft Versus Host Disease 51 0.069
690
P LFR001 Li-Fraumeni Syndrome 72 0.069
691
P MDL005 Medulloblastoma 77 0.069
692
THR004 Thrombocytosis 51 0.069
693
PYR016 Pyridoxine Deficiency 30 0.069
694
P HYP818 Hypobetalipoproteinemia, Familial, 1 58 0.069
695
P PGT001 Paget's Disease of Bone 60 0.069
696
P ANG001 Angelman Syndrome 67 0.069
697
THY125 Thyroid Gland Medullary Carcinoma 51 0.069
698
P SJG008 Sjogren Syndrome 56 0.069
699
INT002 Intermittent Claudication 61 0.069
700
P FLL037 Follicular Lymphoma 66 0.069
701
P PLY018 Polycythemia 55 0.068
702
P NRV007 Nervous System Disease 66 0.068
703
P PNT019 Pontocerebellar Hypoplasia 46 0.068
704
RBF001 Riboflavin Deficiency 45 0.068
705
BRS051 Breast Disease 58 0.068
706
P HNT016 Huntington Disease 71 0.068
707
P CYS018 Cystitis 59 0.068
708
P MYS005 Myositis 56 0.068
709
STT001 Status Epilepticus 59 0.068
710
P HYP733 Hypercalciuria, Absorptive, 2 46 0.068
711
APN008 Apnea, Obstructive Sleep 65 0.068
712
c INH020 Inherited Metabolic Disorder 46 0.068
713
P ICH004 Ichthyosis 54 0.067
714
P VSC018 Visceral Steatosis 33 0.067
715
ESP002 Esophageal Varix 51 0.067
716
ISL099 Isolated Methylmalonic Acidemia 30 0.067
717
PLS011 Plasmacytoma 56 0.067
718
c HYP272 Hypercholesterolemia, Familial, 3 43 0.067
719
WLS001 Wilson Disease 70 0.067
720
P TCL004 T-Cell Leukemia 47 0.067
721
ALP103 Alpha-1-Antitrypsin Deficiency 63 0.067
722
CYS036 Cystinosis, Nephropathic 51 0.066
723
P MTC069 Mitochondrial Disorders 56 0.066
724
NRF026 Neurofibromatosis, Type Iv, of Riccardi 63 0.066
725
c CHR682 Chronic Bilirubin Encephalopathy 38 0.066
726
P MST009 Mastocytosis 63 0.066
727
c PSR028 Psoriasis 7 39 0.066
728
c PSR032 Psoriasis 11 38 0.066
729
c PSR018 Psoriasis 13 38 0.066
730
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.066
731
SCN001 Secondary Hyperparathyroidism of Renal Origin 28 0.066
732
BDD001 Budd-Chiari Syndrome 62 0.066
733
c CHR064 Chronic Monocytic Leukemia 34 0.066
734
INS001 Insulinoma 60 0.066
735
c INF145 Infantile Liver Failure Syndrome 1 50 0.066
736
PFF001 Pfeiffer Syndrome 79 0.066
737
CRT013 Carotid Stenosis 50 0.066
738
P ESP024 Esophagitis 62 0.066
739
LMY014 Leiomyoma, Uterine 56 0.066
740
c ATS307 Autosomal Recessive Cerebellar Ataxia 41 0.066
741
GLS007 Glossitis 47 0.065
742
FDB001 Foodborne Botulism 56 0.065
743
c CHL119 Cholangitis, Primary Sclerosing 57 0.065
744
P ALP004 Alport Syndrome 68 0.065
745
IGG001 Iga Glomerulonephritis 48 0.065
746
PRT029 Parathyroid Adenoma 50 0.065
747
WLL001 Williams-Beuren Syndrome 62 0.065
748
P PYL005 Pyelonephritis 56 0.065
749
ATX010 Ataxia Neuropathy Spectrum 38 0.064
750
PRS063 Paresthesia 43 0.064
751
BNN003 Bone Inflammation Disease 48 0.064
752
ACN002 Acanthosis Nigricans 60 0.064
753
P MCR010 Microcephaly 58 0.064
754
c PLY105 Polycystic Ovary Syndrome 1 38 0.064
755
c WLM018 Wilms Tumor 5 62 0.064
756
RTN020 Retinal Vascular Disease 48 0.064
757
P CNJ013 Conjunctivitis 65 0.064
758
AZS001 Azoospermia 50 0.064
759
EMB004 Embryonal Carcinoma 57 0.064
760
PGM030 Pigmentation Anomaly of the Skin 25 0.064
761
MYF001 Myofibroma 42 0.064
762
NWB001 Newborn Respiratory Distress Syndrome 58 0.064
763
c JVN010 Juvenile Rheumatoid Arthritis 67 0.064
764
BRN004 Brain Edema 55 0.064
765
P MTR014 Motor Neuron Disease 64 0.064
766
KRN002 Kearns-Sayre Syndrome 63 0.064
767
ADR007 Adrenoleukodystrophy 74 0.064
768
P MTC133 Mitochondrial Myopathy 49 0.064
769
RFR010 Refractory Anemia 48 0.063
770
c MYT021 Myotonic Dystrophy 1 66 0.063
771
P GCH001 Gaucher's Disease 64 0.063
772
CHL067 Cholecystitis 58 0.063
773
ALL010 Allergic Contact Dermatitis 55 0.063
774
P MTC003 Metachromatic Leukodystrophy 70 0.063
775
c HPT007 Hepatitis E 52 0.063
776
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.063
777
ARB001 Ariboflavinosis 36 0.063
778
ATN005 Autonomic Dysfunction 47 0.063
779
RHM001 Rheumatic Fever 61 0.063
780
BCT002 Bacterial Vaginosis 52 0.063
781
FML307 Familial Calcium Pyrophosphate Deposition 38 0.063
782
WGN007 Wagner Vitreoretinopathy 38 0.063
783
WGN003 Wagner Syndrome 35 0.063
784
BTN003 Biotinidase Deficiency 60 0.063
785
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.063
786
c BCT007 Bacterial Meningitis 55 0.063
787
P RTN022 Retinal Vein Occlusion 52 0.063
788
c PRD013 Periodic Fever, Familial, Autosomal Dominant 65 0.063
789
c MLG068 Malignant Glioma 45 0.063
790
PST021 Postpartum Depression 50 0.063
791
P SNS001 Sensorineural Hearing Loss 61 0.062
792
AMN001 Amenorrhea 54 0.062
793
P LCT002 Lactose Intolerance 53 0.062
794
PND002 Pendred Syndrome 60 0.062
795
CTN007 Cutaneous Leishmaniasis 61 0.062
796
GYR004 Gyrate Atrophy of Choroid and Retina 56 0.062
797
CRD223 Cardiac Arrhythmia 60 0.062
798
c HPT015 Hepatitis D 49 0.062
799
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.062
800
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.062
801
MCC012 Mccune-Albright Syndrome 70 0.062
802
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.062
803
CHY002 Chylomicron Retention Disease 64 0.062
804
NRM005 Neuromuscular Disease 63 0.062
805
MTH021 Methylmalonic Acidemia with Homocystinuria 46 0.061
806
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.061
807
FRY006 Fryns Microphthalmia Syndrome 54 0.061
808
P FML011 Familial Adenomatous Polyposis 72 0.061
809
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 51 0.061
810
P VTR007 Vitreoretinopathy 46 0.061
811
P RST001 Restless Legs Syndrome 54 0.061
812
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.061
813
c ART101 Aortic Valve Disease 2 63 0.061
814
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.061
815
P MMB011 Membranous Nephropathy 50 0.061
816
P ALP106 Alport Syndrome 1, X-Linked 55 0.061
817
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.061
818
TNG002 Tangier Disease 65 0.061
819
HRT012 Heart Valve Disease 53 0.061
820
P RNL007 Renal Tubular Acidosis 50 0.061
821
THR013 Thoracic Outlet Syndrome 53 0.061
822
RRD056 Rare Disease in Surgical Orthopedic 28 0.061
823
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 65 0.061
824
BRS099 Breast Ductal Carcinoma 62 0.061
825
BRC012 Brucellosis 61 0.061
826
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.061
827
DWR001 Dwarfism 44 0.061
828
P PSD015 Pseudohypoparathyroidism 56 0.061
829
LNG039 Lung Squamous Cell Carcinoma 65 0.061
830
LMB062 Limb Ischemia 55 0.060
831
CLF001 Cleft Lip 53 0.060
832
P RBL001 Rubella 58 0.060
833
BLL006 Bullous Pemphigoid 62 0.060
834
MCL006 Macular Retinal Edema 55 0.060
835
RNL077 Renal Fibrosis 47 0.060
836
PRD004 Prediabetes Syndrome 47 0.060
837
HRP008 Herpes Simiae 25 0.060
838
c HMP004 Hemophilia B 67 0.060
839
PLY001 Polycythemia Vera 69 0.060
840
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 51 0.060
841
c PLM127 Pulmonary Hypertension, Primary, 3 33 0.060
842
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.060
843
P MMP001 Mumps 57 0.060
844
P PTY003 Pityriasis Rubra Pilaris 58 0.060
845
APP008 Appendicitis 60 0.060
846
FML063 Familial Glucocorticoid Deficiency 51 0.060
847
SPP011 Suppression of Tumorigenicity 12 59 0.060
848
c GCH015 Gaucher Disease, Type I 70 0.059
849
P HYP035 Hypophosphatasia 60 0.059
850
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.059
851
SYN007 Synovitis 55 0.059
852
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.059
853
P BRL012 Bare Lymphocyte Syndrome, Type Ii 65 0.059
854
GLS018 Glass Syndrome 53 0.059
855
STT009 Sutton Disease 2 30 0.059
856
THY124 Thyroid Gland Papillary Carcinoma 52 0.059
857
P AGG001 Aggressive Periodontitis 50 0.059
858
ORT008 Orotic Aciduria 54 0.059
859
PRS047 Prostatitis 56 0.059
860
P MNC007 Monocytic Leukemia 54 0.059
861
P PMP001 Pemphigus 55 0.059
862
c MLT156 Multiple Endocrine Neoplasia, Type I 71 0.059
863
DBT084 Diabetes Mellitus, Ketosis-Prone 59 0.059
864
TRP009 Triple X Syndrome 42 0.059
865
PHR003 Pharyngitis 56 0.058
866
INT075 Intracranial Hypertension 53 0.058
867
GLY010 Glycine Encephalopathy 60 0.058
868
c SVR001 Severe Acute Respiratory Syndrome 55 0.058
869
P ASP006 Aspergillosis 66 0.058
870
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 58 0.058
871
THR123 Thrombotic Microangiopathy 38 0.058
872
CHD001 Chediak-Higashi Syndrome 66 0.058
873
PRT018 Portal Vein Thrombosis 50 0.058
874
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 67 0.058
875
ORL012 Oral Leukoplakia 39 0.058
876
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.058
877
PLG002 Plague 57 0.058
878
c HMG029 Hemoglobin Se Disease 38 0.058
879
P TXP001 Toxoplasmosis 60 0.058
880
P CHR453 Charcot-Marie-Tooth Hereditary Neuropathy 45 0.058
881
c MLT160 Multiple Endocrine Neoplasia, Type Iia 69 0.058
882
c PRG047 Progressive Familial Intrahepatic Cholestasis 62 0.058
883
MCR013 Microphthalmia 60 0.057
884
c GLY060 Glycogen Storage Disease Ia 61 0.057
885
PRT082 Preterm Premature Rupture of the Membranes 54 0.057
886
P OBS001 Obstructive Jaundice 48 0.057
887
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.057
888
HLC001 Holocarboxylase Synthetase Deficiency 48 0.057
889
P SCL009 Sclerosing Cholangitis 47 0.057
890
TYP007 Typhoid Fever 63 0.057
891
CHR005 Chorioamnionitis 51 0.057
892
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 62 0.057
893
c PRM196 Premature Ovarian Failure 1 68 0.057
894
MYC006 Mycosis Fungoides 66 0.057
895
P FRD001 Friedreich Ataxia 63 0.057
896
MTC005 Mitochondrial Metabolism Disease 48 0.057
897
CHL004 Cholelithiasis 49 0.057
898
GST092 Gastroesophageal Reflux 65 0.057
899
MYL031 Myeloproliferative Neoplasm 65 0.057
900
P PRM002 Primary Hyperoxaluria 62 0.057
901
P KRB001 Krabbe Disease 69 0.057
902
P PTT014 Pitt-Hopkins Syndrome 60 0.057
903
RDN001 Reading Disorder 40 0.057
904
KRT006 Keratoconjunctivitis 53 0.056
905
MTH078 Methylmalonic Aciduria, Cblb Type 50 0.056
906
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.056
907
CRT017 Cartilage Disease 54 0.056
908
GRN017 Granulocytopenia 44 0.056
909
P TCD001 Tic Disorder 54 0.056
910
PRT010 Parathyroid Carcinoma 66 0.056
911
P EXD001 Exudative Vitreoretinopathy 56 0.056
912
ETN001 Eating Disorder 59 0.056
913
GRW007 Growth Hormone Deficiency 43 0.056
914
ART001 Arterial Tortuosity Syndrome 66 0.056
915
SCH012 Schizoaffective Disorder 50 0.056
916
SXL003 Sexual Disorder 48 0.056
917
CLR030 Clear Cell Renal Cell Carcinoma 53 0.056
918
c MYS033 Miyoshi Muscular Dystrophy 1 56 0.056
919
PTZ001 Peutz-Jeghers Syndrome 69 0.056
920
P CHR012 Chronic Granulomatous Disease 67 0.056
921
GLM044 Glomerular Disease 39 0.056
922
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 26 0.056
923
GST020 Gastric Antral Vascular Ectasia 41 0.056
924
P ACR001 Aicardi-Goutieres Syndrome 65 0.056
925
c HYP768 Hyperlipoproteinemia, Type I 52 0.056
926
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.056
927
KWS002 Kawasaki Disease 64 0.056
928
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.056
929
THR016 Thrombophlebitis 51 0.056
930
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 0.056
931
ANV001 Anovulation 47 0.056
932
CYT018 Cytochrome P450 2d6 Variant 27 0.056
933
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 49 0.056
934
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.056
935
P MLG056 Malignant Hyperthermia 67 0.055
936
INT303 Intracranial Hypertension, Idiopathic 56 0.055
937
CMM004 Common Variable Immunodeficiency 67 0.055
938
P TRC031 Trichorhinophalangeal Syndrome 40 0.055
939
KRT013 Keratolytic Winter Erythema 46 0.055
940
LYM040 Lymphoblastic Lymphoma 54 0.055
941
IDP070 Idiopathic Scoliosis 37 0.055
942
OBS002 Obsessive-Compulsive Disorder 68 0.055
943
c WLM013 Wilms Tumor 1 65 0.055
944
RSC001 Rosacea 55 0.055
945
c HNT011 Huntington Disease-Like 3 38 0.055
946
FND001 Fundus Albipunctatus 61 0.055
947
DRY001 Dry Eye Syndrome 47 0.055
948
LWC001 Low Compliance Bladder 42 0.055
949
ADN011 Adenoid Cystic Carcinoma 70 0.055
950
c MST023 Mesothelioma, Malignant 57 0.055
951
P PLY041 Polymyositis 57 0.055
952
P LRY044 Larynx Cancer 54 0.055
953
PST028 Post-Traumatic Stress Disorder 58 0.055
954
HDN002 Head Injury 45 0.055
955
DNN002 Donnai-Barrow Syndrome 56 0.055
956
MNN020 Meningococcal Infection 45 0.055
957
P MYS003 Myasthenia Gravis 68 0.054
958
P SML001 Small Cell Carcinoma 52 0.054
959
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 39 0.054
960
MNN032 Meningococcal Meningitis 46 0.054
961
RNL078 Renal Dysplasia 49 0.054
962
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.054
963
TRN022 Transcobalamin Ii Deficiency 45 0.054
964
P ALG028 Alagille Syndrome 1 73 0.054
965
P KRT007 Keratoconus 49 0.054
966
P RTT002 Rett Syndrome 80 0.054
967
c ACT004 Acute Diarrhea 39 0.054
968
c HNT004 Huntington Disease-Like 2 49 0.054
969
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.054
970
c SYS043 Systemic Lupus Erythematosus 1 38 0.054
971
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.054
972
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.054
973
ACT064 Acute Necrotizing Encephalitis 32 0.054
974
BLD137 Blood Group--Ahonen 19 0.054
975
ATN004 Autonomic Neuropathy 44 0.054
976
OMN001 Omenn Syndrome 66 0.054
977
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.054
978
P PRG092 Pregnancy Loss, Recurrent 1 40 0.054
979
YLL002 Yellow Fever 60 0.054
980
P TYR004 Tyrosinemia 58 0.054
981
GLL008 Gilles De La Tourette Syndrome 66 0.054
982
P THY023 Thymoma 65 0.054
983
c THY107 Thymoma, Familial 54 0.054
984
TNS005 Tonsillitis 57 0.054
985
CYT008 Cytomegalovirus Infection 56 0.054
986
URT010 Ureteral Obstruction 46 0.053
987
HPT022 Hepatoblastoma 56 0.053
988
c DPH024 Diaphragmatic Hernia, Congenital 64 0.053
989
P BRN022 Bronchiectasis 59 0.053
990
EXC002 Exocrine Pancreatic Insufficiency 41 0.053
991
CHL152 Childhood Acute Lymphocytic Leukemia 43 0.053
992
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.053
993
c VSC019 Vesicoureteral Reflux 1 59 0.053
994
c GLY008 Glycogen Storage Disease Ii 70 0.053
995
FCT029 Factor V and Factor Viii, Combined Deficiency of, 1 30 0.053
996
TRT001 Teratocarcinoma 46 0.053
997
FLT009 Folate Malabsorption, Hereditary 39 0.053
998
PTH003 Pathologic Nystagmus 51 0.053
999
PRP001 Propionic Acidemia 66 0.053
1000
RFR003 Refractive Error 44 0.053
1001
P OPT009 Optic Neuritis 56 0.053
1002
FBR012 Fabry Disease 71 0.053
1003
SFT003 Soft Tissue Sarcoma 56 0.053
1004
ACT084 Acute Stress Disorder 48 0.053
1005
LPT006 Leptin Receptor Deficiency 47 0.053
1006
HMR039 Hemorrhage, Intracerebral 57 0.053
1007
CLL003 Cellulitis 54 0.053
1008
P MYC033 Myoclonus 46 0.053
1009
NRN004 Neuroendocrine Tumor 55 0.053
1010
P DRM010 Dermatomyositis 61 0.053
1011
LYS012 Lysosomal Acid Lipase Deficiency 64 0.053
1012
P DMN001 Diamond-Blackfan Anemia 69 0.053
1013
P PRN023 Prion Disease 57 0.053
1014
SPS019 Spastic Paraparesis 40 0.053
1015
P ACT008 Actinic Keratosis 52 0.053
1016
PLC007 Placental Abruption 48 0.053
1017
WST001 West Syndrome 60 0.052
1019
GRG001 Greig Cephalopolysyndactyly Syndrome 67 0.052
1020
HMT002 Hematologic Cancer 62 0.052
1021
CHL109 Childhood Apraxia of Speech 44 0.052
1022
INT088 Intrinsic Factor Deficiency 34 0.052
1023
GLL018 Gallbladder Cancer 56 0.052
1024
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 60 0.052
1025
RFL001 Reflex Sympathetic Dystrophy 53 0.052
1026
c MNN043 Meningioma, Familial 74 0.052
1027
PLL001 Pallister-Hall Syndrome 64 0.052
1028
SMT004 Smith-Lemli-Opitz Syndrome 69 0.052
1029
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.052
1030
KLD004 Keloid Disorder 40 0.052
1031
PRP036 Peripheral T-Cell Lymphoma 53 0.052
1032
SPR004 Supravalvular Aortic Stenosis 58 0.052
1033
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 58 0.052
1034
THY122 Thyroid Gland Cancer 58 0.052
1035
P VNW001 Von Willebrand's Disease 64 0.052
1036
ARG004 Argyria 28 0.052
1037
NNT012 Neonatal Jaundice 53 0.052
1038
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.052
1039
P LYM025 Lymphedema 53 0.051
1040
OVR029 Ovarian Hyperstimulation Syndrome 63 0.051
1041
P ANG015 Angioedema 54 0.051
1042
MLT157 Multiple System Atrophy 1 70 0.051
1043
CYS013 Cystinuria 62 0.051
1044
PRT058 Pure Autonomic Failure 59 0.051
1045
CRT016 Carotid Artery Disease 52 0.051
1046
c DSB006 Desbuquois Dysplasia 1 48 0.051
1047
SPT004 Septic Arthritis 57 0.051
1048
GRD001 Giardiasis 45 0.051
1049
SPS057 Spasticity 41 0.051
1050
INC002 Inclusion Body Myositis 64 0.051
1051
DRR014 Darier-White Disease 61 0.051
1052
ILS001 Ileus 51 0.051
1053
GLC006 Galactosemia 65 0.051
1054
c CNT016 Central Retinal Vein Occlusion 49 0.051
1055
P NRN021 Neuronal Ceroid Lipofuscinosis 63 0.051
1056
GSG001 Gas Gangrene 50 0.051
1057
c HYP794 Hyperoxaluria, Primary, Type I 48 0.051
1058
P END047 Endophthalmitis 52 0.051
1059
CHR103 Charge Syndrome 66 0.051
1060
P TRT010 Teratoma 51 0.051
1061
GLC106 Glucocorticoid Resistance, Generalized 48 0.051
1062
DCT002 Ductal Carcinoma in Situ 59 0.051
1063
CLN045 Colonic Benign Neoplasm 49 0.051
1064
P SCL057 Scoliosis, Isolated 1 41 0.051
1065
SYS071 Systemic Autoimmune Disease 37 0.051
1066
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.051
1067
PRS034 Parasitic Helminthiasis Infectious Disease 49 0.050
1068
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 60 0.050
1069
P STR020 Strabismus 56 0.050
1070
c LTN004 Late-Onset Retinal Degeneration 52 0.050
1071
c MCL013 Mucolipidosis Iv 64