Search results for Vitamin C

2030 hits were found for Vitamin C

# Family MCID Name MIFTS Score
1
HYP781 Hypoascorbemia 42 4.360
2
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 51 3.564
3
P HPT021 Hepatitis 76 0.606
4
c HPT001 Hepatitis C 71 0.562
5
c HPT073 Hepatitis C Virus 72 0.448
6
P BRS047 Breast Cancer 100 0.376
7
P LVR013 Liver Disease 75 0.318
8
RCK004 Rickets 62 0.300
9
VTM002 Vitamin B12 Deficiency 47 0.274
10
c HPT003 Hepatitis a 61 0.265
11
END072 Endotheliitis 45 0.263
12
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 91 0.262
13
P PRS040 Prostate Cancer 90 0.256
14
VRL011 Viral Infectious Disease 63 0.256
15
PRS047 Prostatitis 60 0.253
16
AGN016 Aging 64 0.240
17
P DBT009 Diabetes Mellitus 64 0.238
18
P KDN018 Kidney Disease 68 0.237
19
P CLR023 Colorectal Cancer 97 0.236
20
P LYN001 Lynch Syndrome 71 0.231
21
P LKM002 Leukemia 72 0.229
22
P HPT023 Hepatocellular Carcinoma 94 0.229
23
P HYP607 Hypercholesterolemia, Familial 79 0.206
24
TYP041 Type I 56 0.205
25
P HRT032 Heart Disease 74 0.205
26
P OST002 Osteoporosis 76 0.205
27
P HYP061 Hypertrophic Cardiomyopathy 64 0.203
28
P LNG032 Lung Cancer 98 0.201
29
ISC004 Ischemia 65 0.197
30
P LYM118 Lymphoma 70 0.195
31
P FNC027 Fanconi Anemia, Complementation Group a 78 0.195
32
THR024 Thrombosis 61 0.190
33
c FML346 Familial Adenomatous Polyposis 1 62 0.189
34
ACQ007 Acquired Immunodeficiency Syndrome 63 0.188
35
INS024 Insulin-Like Growth Factor I 82 0.187
36
c CHR089 Chronic Kidney Failure 72 0.187
37
P ART022 Arthritis 76 0.186
38
ART140 Arteries, Anomalies of 65 0.185
39
P HYP069 Hyperparathyroidism 58 0.185
40
P MYC007 Myocardial Infarction 79 0.184
41
c MCL042 Macular Degeneration, Age-Related, 1 84 0.184
42
P LNG028 Long Qt Syndrome 65 0.184
43
P ATX030 Ataxia-Telangiectasia 79 0.183
44
P CRN018 Coronary Artery Anomaly 68 0.183
45
c HPT016 Hepatitis B 67 0.179
46
P ADN016 Adenocarcinoma 70 0.178
47
BND020 Bone Disease 62 0.176
48
URN009 Urinary System Disease 55 0.176
49
P THY032 Thyroiditis 55 0.174
50
P ZLL001 Zellweger Syndrome 56 0.174
51
P PNC044 Pancreatitis 64 0.173
52
c NRF024 Neurofibromatosis, Type I 66 0.171
53
P LBR001 Leber Congenital Amaurosis 64 0.170
54
MTH078 Methylmalonic Aciduria, Cblb Type 61 0.169
55
MLN008 Melanoma 62 0.161
56
GST050 Gastrointestinal System Disease 64 0.160
57
AST005 Asthma 82 0.160
58
c CRN300 Coronary Heart Disease 1 64 0.159
59
P THR014 Thrombocytopenia 64 0.158
60
OCL033 Oculocerebral Syndrome with Hypopigmentation 45 0.157
61
CYS001 Cystic Fibrosis 84 0.157
62
GST053 Gastric Cancer 77 0.156
63
P ALZ034 Alzheimer Disease 87 0.155
64
GLC008 Glucose Metabolism Disease 52 0.155
65
P PLM037 Pulmonary Hypertension 75 0.154
66
LNG099 Lung Disease 67 0.154
67
P MLT020 Multiple Sclerosis 78 0.154
68
P RHM011 Rheumatoid Arthritis 80 0.154
69
LVR012 Liver Cirrhosis 68 0.153
70
NRL016 Neural Tube Defects 78 0.153
71
GST019 Gastrointestinal Stromal Tumor 73 0.153
72
VSC007 Vascular Disease 68 0.153
73
NRN002 Neuronitis 41 0.153
74
P XRD010 Xeroderma Pigmentosum, Variant Type 68 0.152
75
DPR016 Depression 72 0.151
76
P NRB001 Neuroblastoma 72 0.151
77
P PNC035 Pancreatic Cancer 79 0.151
78
P INF038 Influenza 76 0.151
79
P NRP001 Neuropathy 63 0.151
80
ATM095 Autoimmune Disease 64 0.150
81
c PLM164 Pulmonary Hypertension, Primary, 1 66 0.149
82
P INT068 Intestinal Disease 64 0.148
83
P MTR004 Maturity-Onset Diabetes of the Young 60 0.148
84
PRT011 Protein C Deficiency 49 0.148
85
P INF037 Inflammatory Bowel Disease 53 0.147
86
BNF002 Bone Fracture 55 0.146
87
SQM006 Squamous Cell Carcinoma 59 0.145
88
P LPS004 Lupus Erythematosus 68 0.144
89
MTC097 Mitochondrial Complex Iv Deficiency 54 0.141
90
LGH007 Leigh Syndrome 67 0.139
91
CRH001 Crohn's Disease 78 0.139
92
c SYS001 Systemic Lupus Erythematosus 86 0.137
93
P MYL006 Myeloid Leukemia 68 0.137
94
P PNM007 Pneumonia 69 0.137
95
IMM136 Immune System Disease 56 0.137
96
RTN023 Retinitis 50 0.137
97
c SML038 Small Cell Cancer of the Lung 68 0.136
98
SKN016 Skin Disease 66 0.136
99
c THR092 Thrombophilia Due to Thrombin Defect 67 0.136
100
P MGL001 Megaloblastic Anemia 51 0.136
101
ISC006 Ischemic Heart Disease 72 0.135
102
c LKM061 Leukemia, Acute Myeloid 80 0.133
103
P OVR042 Ovarian Cancer 81 0.132
104
SKN027 Skin Conditions 48 0.132
105
ADN018 Adenoma 63 0.131
106
P PRD008 Periodontitis 66 0.131
107
P PSR002 Psoriasis 65 0.129
108
P NNL004 Nonalcoholic Fatty Liver Disease 51 0.129
109
P ART021 Arteriosclerosis 60 0.129
110
P ATR011 Atrial Fibrillation 68 0.128
111
ALP046 Alport Syndrome, X-Linked 75 0.127
112
HYP060 Hyperinsulinism 56 0.127
113
c TBR025 Tuberous Sclerosis 1 62 0.127
114
P DRR001 Diarrhea 56 0.127
115
c CNG006 Congenital Hypothyroidism 60 0.127
116
DSR002 Disorders of Intracellular Cobalamin Metabolism 19 0.126
117
FTT001 Fatty Liver Disease 60 0.125
118
NRL018 Neural Tube Defects, Folate-Sensitive 44 0.125
119
RSP006 Respiratory System Disease 63 0.124
120
c VRL010 Viral Hepatitis 59 0.123
121
DRM006 Dermatitis 66 0.123
122
HMN044 Human Immunodeficiency Virus Type 1 70 0.122
123
c PRM012 Primary Polycythemia 52 0.121
124
P OST001 Osteopetrosis 61 0.120
125
CNG034 Congestive Heart Failure 72 0.120
126
c GLC092 Glaucoma, Primary Open Angle 57 0.120
127
P CTR002 Cataract 60 0.120
128
P MYP004 Myopathy 68 0.120
129
P INF032 Infertility 59 0.119
130
DMN002 Dementia 68 0.119
131
CRB009 Cerebritis 41 0.119
132
VNH007 Von Hippel-Lindau Syndrome 69 0.118
133
P HRD008 Hereditary Hemorrhagic Telangiectasia 61 0.118
134
WRN001 Werner Syndrome 69 0.118
135
BSL036 Basal Cell Nevus Syndrome 65 0.118
136
ATX019 Ataxia with Vitamin E Deficiency 31 0.117
137
CLN019 Colonic Disease 54 0.117
138
c PRC016 Pre-Eclampsia 59 0.116
139
c ACT075 Acute Myocardial Infarction 58 0.116
140
HYP266 Hypoxia 61 0.116
141
FND002 Fundus Dystrophy 49 0.116
142
SPS003 Spastic Diplegia 54 0.115
143
P THL005 Thalassemia 64 0.115
144
ACR006 Aceruloplasminemia 73 0.114
145
P DYS154 Dystonia 64 0.114
146
P ENC018 Encephalopathy 62 0.114
147
P NRV007 Nervous System Disease 73 0.114
148
PRP019 Peripheral Nervous System Disease 60 0.113
149
P ANR048 Aniridia 1 65 0.113
150
CNG008 Congenital Ichthyosiform Erythroderma 60 0.113
151
P SCH015 Schizophrenia 69 0.113
152
OST012 Osteoarthritis 82 0.113
153
P GLM045 Glioma 54 0.112
154
P HYP818 Hypobetalipoproteinemia, Familial, 1 54 0.112
155
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.112
156
MNT002 Mental Depression 57 0.111
157
GLB002 Glioblastoma 72 0.111
158
P FCL005 Focal Segmental Glomerulosclerosis 59 0.110
159
P TBR001 Tuberous Sclerosis 68 0.110
160
P FRN006 Frontotemporal Dementia 67 0.110
161
MYL069 Myeloma, Multiple 83 0.109
162
CRB039 Cerebrovascular Disease 67 0.109
163
P PLY011 Polycystic Ovary Syndrome 63 0.109
164
P THR015 Thrombophilia 57 0.109
165
P CRV039 Cervicitis 49 0.108
166
P EXN002 Exanthem 61 0.108
167
P ESP024 Esophagitis 63 0.108
168
c 3MT016 3-Methylglutaconic Aciduria, Type Iii 59 0.108
169
PLC008 Placenta Disease 61 0.107
170
P RTN024 Retinoblastoma 70 0.106
171
c BTT014 Beta-Thalassemia 69 0.106
172
SCN001 Secondary Hyperparathyroidism of Renal Origin 50 0.106
173
P SZR006 Seizure Disorder 56 0.106
174
P LNG064 Lung Cancer Susceptibility 3 76 0.105
175
END030 End Stage Renal Failure 56 0.105
176
c FTT008 Fatty Liver Disease, Nonalcoholic 1 39 0.105
177
ESP021 Esophageal Cancer 77 0.105
178
CHL061 Childhood Leukemia 55 0.104
179
c PRM005 Primary Hyperparathyroidism 59 0.104
180
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 62 0.104
181
CMM005 Common Cold 61 0.104
182
c CNT035 Central Nervous System Disease 63 0.103
183
VTM001 Vitamin K Deficiency Hemorrhagic Disease 40 0.103
184
ABT001 Abetalipoproteinemia 63 0.103
185
P BLD134 Bladder Cancer 69 0.103
186
GST045 Gastroenteritis 64 0.103
187
P NPH012 Nephrotic Syndrome 59 0.103
188
PSY004 Psychotic Disorder 71 0.103
189
P ECL001 Eclampsia 57 0.103
190
P RTN016 Retinal Degeneration 54 0.102
191
BRN106 Burns 56 0.102
192
SKN019 Skin Melanoma 69 0.102
193
CLT003 Colitis 62 0.102
194
PRT118 Protoporphyria, Erythropoietic 58 0.102
195
P ALP008 Alopecia 58 0.102
196
RNL065 Renal Cell Carcinoma, Papillary, 1 70 0.102
197
P NGH001 Night Blindness 51 0.102
198
HYP066 Hyperglycemia 63 0.101
199
P DRM053 Dermatitis, Atopic 67 0.101
200
ANR040 Aneurysm 60 0.101
201
LPD008 Lipid Metabolism Disorder 58 0.101
202
P MLT074 Multiple Endocrine Neoplasia 55 0.100
203
NNL002 Nonalcoholic Steatohepatitis 50 0.100
204
MLR004 Malaria 83 0.100
205
P BLD051 Blood Coagulation Disease 50 0.100
206
P MNN013 Meningitis 70 0.100
207
PLM129 Pulmonary Disease, Chronic Obstructive 72 0.099
208
LYM019 Lymphosarcoma 55 0.099
209
P LYM033 Lymphoproliferative Syndrome 55 0.099
210
BRS051 Breast Disease 66 0.099
211
CRY004 Cryoglobulinemia 49 0.099
212
CLR108 Colorectal Adenoma 60 0.099
213
P HMR003 Hemorrhagic Disease 60 0.099
214
RCT017 Rectal Disease 39 0.099
215
PRP030 Purpura 61 0.099
216
RNL114 Renal Cell Carcinoma, Nonpapillary 59 0.098
217
ANX010 Anxiety 72 0.098
218
GLC003 Glucose Intolerance 56 0.098
219
PNC034 Pancreas Disease 57 0.098
220
c ERL006 Early-Onset Familial Alzheimer Disease 38 0.098
221
BRN028 Brain Cancer 72 0.098
222
NRM005 Neuromuscular Disease 60 0.097
223
WVR001 Weaver Syndrome 61 0.097
224
TTN003 Tetanus 64 0.097
225
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 53 0.097
226
RHM027 Rheumatic Disease 62 0.097
227
P HYP086 Hypothyroidism 64 0.097
228
P TRC086 Trichohepatoenteric Syndrome 1 54 0.097
229
c ATM006 Autoimmune Lymphoproliferative Syndrome 70 0.096
230
ERY029 Erythermalgia, Primary 54 0.096
231
P CRN037 Craniosynostosis 67 0.096
232
P CRV035 Cervical Cancer 69 0.096
233
P DLT002 Dilated Cardiomyopathy 76 0.096
234
CNN005 Connective Tissue Disease 64 0.096
235
ENT004 Enthesopathy 46 0.096
236
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.096
237
c MYT021 Myotonic Dystrophy 1 68 0.096
238
PRN011 Pernicious Anemia 50 0.096
239
P MTC003 Metachromatic Leukodystrophy 71 0.096
240
PLM001 Pulmonary Tuberculosis 71 0.095
241
PNC033 Pancreas Adenocarcinoma 64 0.095
242
NRT004 Neuritis 57 0.095
243
P BCL006 B-Cell Lymphomas 65 0.095
244
P ART023 Arthropathy 67 0.095
245
GST040 Gastric Adenocarcinoma 63 0.094
246
PDT001 Pediatric Lymphoma 45 0.094
247
c ADL001 Adult Lymphoma 39 0.094
248
CYS036 Cystinosis, Nephropathic 48 0.094
249
OST015 Osteochondrodysplasia 53 0.094
250
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 59 0.094
251
P RTN008 Retinitis Pigmentosa 81 0.093
252
P HML002 Hemolytic Anemia 62 0.093
253
c TRC078 Trichohepatoenteric Syndrome 2 34 0.093
254
c PRC031 Preeclampsia/eclampsia 1 39 0.093
255
P HMC002 Homocystinuria 50 0.093
256
BRN038 Bronchial Disease 56 0.093
257
MYL009 Myelodysplastic Syndrome 70 0.093
258
P HMP002 Hemophagocytic Lymphohistiocytosis 67 0.093
259
SRC014 Sarcoma 68 0.092
260
P VSC018 Visceral Steatosis 37 0.092
261
LYM024 Lymphatic System Disease 54 0.092
262
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 55 0.092
263
CYS010 Cystinosis 54 0.092
264
P NJM001 Nijmegen Breakage Syndrome 70 0.092
265
c LKM071 Leukemia, Chronic Lymphocytic 75 0.091
266
JNT002 Joint Disorders 59 0.091
267
CLC006 Calcinosis 51 0.090
268
LPD012 Lipoid Congenital Adrenal Hyperplasia 69 0.090
269
EPL131 Epilepsy, Pyridoxine-Dependent 37 0.090
270
P MDL005 Medulloblastoma 75 0.090
271
IRN002 Iron Metabolism Disease 55 0.089
272
ANG054 Angina Pectoris 66 0.089
273
SQM013 Squamous Cell Carcinoma, Head and Neck 76 0.089
274
c ATS307 Autosomal Recessive Cerebellar Ataxia 27 0.089
275
P DBT085 Diabetes Mellitus, Insulin-Dependent 65 0.089
276
CNS004 Constipation 56 0.088
277
P GST044 Gastritis 60 0.088
278
HLC001 Holocarboxylase Synthetase Deficiency 58 0.088
279
c WLM018 Wilms Tumor 5 60 0.088
280
ULC004 Ulcerative Colitis 72 0.088
281
P CLL015 Collagen Disease 52 0.088
282
c ATS007 Autism Spectrum Disorder 61 0.087
283
P LYM026 Lymphoblastic Leukemia 64 0.087
284
PHN003 Phenylketonuria 73 0.087
285
BLD131 Bladder Urothelial Carcinoma 60 0.086
286
P MYP006 Myopia 56 0.086
287
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 36 0.086
288
PLM033 Pulmonary Embolism 62 0.086
289
MSC157 Muscular Dystrophy, Duchenne Type 68 0.086
290
MTH009 Mouth Disease 63 0.086
291
SLP005 Sleep Disorder 59 0.086
292
STM007 Stomatitis 52 0.086
293
MSL001 Measles 64 0.086
294
P ATS364 Autism 70 0.085
295
P GLM007 Glomerulonephritis 61 0.085
296
c OVR114 Ovarian Cancer 1 62 0.085
297
SPP011 Suppression of Tumorigenicity 12 61 0.085
298
P EHL052 Ehlers-Danlos Syndrome, Vascular Type 55 0.085
299
PRT036 Peritonitis 66 0.085
300
PGT001 Paget's Disease of Bone 59 0.085
301
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 52 0.085
302
c BRT028 Brittle Cornea Syndrome 1 28 0.085
303
PRS042 Prostate Disease 44 0.084
304
P EPL164 Epilepsy 69 0.084
305
RTN018 Retinal Disease 56 0.084
306
TNG002 Tangier Disease 64 0.084
307
STR067 Stroke, Ischemic 82 0.084
308
PRP080 Peripheral Artery Disease 53 0.083
309
P PRX010 Paroxysmal Ventricular Fibrillation 28 0.083
310
MSC004 Muscle Tissue Disease 39 0.083
311
HDC001 Headache 59 0.083
312
MDD011 Mood Disorder 63 0.083
313
CHD001 Chediak-Higashi Syndrome 65 0.083
314
DMY004 Demyelinating Disease 57 0.083
315
c INF071 Inflammatory Bowel Disease 1 53 0.083
316
P PRM002 Primary Hyperoxaluria 53 0.082
317
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.082
318
PRT030 Parathyroid Gland Disease 49 0.082
319
P MSC033 Muscle Disorders 52 0.082
320
P TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 50 0.082
321
P GRV001 Graves' Disease 61 0.082
322
FND001 Fundus Albipunctatus 53 0.082
323
VSC008 Vascular Hemostatic Disease 36 0.082
324
P DMN001 Diamond-Blackfan Anemia 69 0.081
325
PLM134 Pulmonary Fibrosis, Idiopathic 73 0.081
326
VSC011 Vasculitis 65 0.081
327
BRC012 Brucellosis 70 0.081
328
P PSD087 Pseudoxanthoma Elasticum 67 0.081
329
P NTR004 Neutropenia 60 0.081
330
c MCP004 Mucopolysaccharidosis Iv 59 0.081
331
c RHB011 Rhabdoid Tumor Predisposition Syndrome 2 26 0.081
332
GST033 Gestational Diabetes 60 0.080
333
c PNS012 Paine Syndrome 62 0.080
334
c VSC019 Vesicoureteral Reflux 1 57 0.080
335
SCK005 Sickle Cell Disease 54 0.080
336
SCK003 Sickle Cell Anemia 72 0.080
337
P CRY007 Cryoglobulinemia, Familial Mixed 54 0.080
338
c LKM062 Leukemia, Acute Lymphoblastic 69 0.080
339
HMS001 Hemosiderosis 51 0.080
340
IRN001 Iron Deficiency Anemia 55 0.080
341
P MRQ003 Morquio Syndrome 31 0.080
342
ALP103 Alpha-1-Antitrypsin Deficiency 61 0.079
343
c HMC039 Hemochromatosis, Type 1 70 0.079
344
MCS002 Mucositis 60 0.079
345
P KRB001 Krabbe Disease 69 0.078
346
KRT019 Keratitis, Hereditary 52 0.078
347
NPH009 Nephrolithiasis 55 0.078
348
P NSP012 Nasopharyngeal Carcinoma 67 0.078
349
P FML018 Familial Mediterranean Fever 73 0.078
350
KND001 Kindler Syndrome 50 0.077
351
HMG005 Hemoglobinopathy 53 0.077
352
PRD007 Periodontal Disease 64 0.077
353
c PRM196 Premature Ovarian Failure 1 71 0.077
354
c MCP024 Mucopolysaccharidosis Type Vi 62 0.077
355
P RHN004 Rhinitis 61 0.077
356
P ORT004 Orthostatic Intolerance 68 0.077
357
FLT009 Folate Malabsorption, Hereditary 35 0.077
358
c ART101 Aortic Valve Disease 2 73 0.077
359
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.077
360
CD4003 Cd40 Ligand Deficiency 44 0.076
361
MTC008 Mitochondrial Complex Iii Deficiency 32 0.076
362
LYM133 Lymphoma, Hodgkin, Classic 71 0.076
363
SPR004 Supravalvular Aortic Stenosis 53 0.076
364
HYP810 Hypereosinophilic Syndrome, Idiopathic 58 0.076
365
MTY001 Mutyh-Associated Polyposis 48 0.076
366
c ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 59 0.076
367
VTM027 Vitamin D-Dependent Rickets, Type 2a 51 0.076
368
c CRD187 Cardiomyopathy, Dilated, 3b 46 0.076
369
P MCR115 Microvascular Complications of Diabetes 5 71 0.076
370
P MSC005 Muscular Dystrophy 66 0.076
371
P GNT009 Giant Axonal Neuropathy 51 0.076
372
c GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 37 0.076
373
WLL001 Williams-Beuren Syndrome 63 0.075
374
PHR003 Pharyngitis 59 0.075
375
DFC004 Deficiency Anemia 61 0.075
376
HMT018 Hematopoietic Stem Cell Transplantation 57 0.075
377
P END044 Endometriosis 64 0.075
378
P MJR001 Major Depressive Disorder 65 0.075
379
OVR063 Overnutrition 53 0.075
380
P HYP802 Hypocalcemia, Autosomal Dominant 1 62 0.075
381
APL001 Aplastic Anemia 73 0.074
382
c LKM004 Leukemia, B-Cell, Chronic 36 0.074
383
GRN017 Granulocytopenia 43 0.074
384
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 40 0.074
385
P PRK057 Parkinson Disease, Late-Onset 76 0.074
386
P AMY004 Amyloidosis 68 0.074
387
ACT118 Acute Non Lymphoblastic Leukemia 32 0.074
388
PRM236 Primary Biliary Cholangitis 55 0.074
389
DFF005 Diffuse Large B-Cell Lymphoma 56 0.074
390
LNG039 Lung Squamous Cell Carcinoma 59 0.074
391
c PRG126 Progressive Familial Heart Block 47 0.074
392
P PRP029 Porphyria 62 0.074
393
c ACT071 Acute Kidney Failure 54 0.074
394
EWN002 Ewing's Family of Tumors 56 0.074
395
GNG013 Gingivitis 63 0.073
396
THY030 Thyroid Gland Disease 51 0.073
397
GND003 Gonadal Disease 46 0.073
398
CHL068 Cholestasis 60 0.073
399
SPN186 Spinal Cord Injury 68 0.073
400
ANX004 Anoxia 49 0.073
401
HYP458 Hyper Ige Syndrome 49 0.072
402
THY028 Thyroid Cancer 66 0.072
403
ILT001 Ileitis 56 0.072
404
P ESS003 Essential Thrombocythemia 70 0.072
405
OPT006 Optic Nerve Disease 57 0.072
406
P CMR001 Camurati-Engelmann Disease 61 0.072
407
c HYP595 Hypertension, Essential 76 0.072
408
GYR004 Gyrate Atrophy of Choroid and Retina 50 0.072
409
P PRM006 Primary Biliary Cirrhosis 53 0.072
410
P PRP003 Porphyria Cutanea Tarda 66 0.071
411
c HYP794 Hyperoxaluria, Primary, Type I 41 0.071
412
HYP348 Hyperglycinuria 33 0.071
413
BTT001 Bietti Crystalline Corneoretinal Dystrophy 36 0.071
414
ADR007 Adrenoleukodystrophy 71 0.071
415
NRN004 Neuroendocrine Tumor 58 0.071
416
P OVR049 Ovarian Disease 59 0.071
417
c THR082 Thrombophilia Due to Activated Protein C Resistance 46 0.071
418
c SVR003 Severe Congenital Neutropenia 58 0.071
419
c MTR002 Mitral Valve Insufficiency 46 0.070
420
c BLR024 Biliary Cirrhosis, Primary, 1 36 0.070
421
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 55 0.070
422
TRN018 Transitional Cell Carcinoma 61 0.070
423
P AST007 Astrocytoma 51 0.070
424
HPD002 Hepadnavirus Infection 25 0.070
425
FBR012 Fabry Disease 71 0.070
426
HLC007 Helicobacter Pylori Infection 63 0.070
427
BTN003 Biotinidase Deficiency 56 0.070
428
THR100 Thrombocytopenic Purpura, Autoimmune 62 0.070
429
ATX010 Ataxia Neuropathy Spectrum 35 0.070
430
P ALP009 Alopecia Areata 63 0.070
431
c GLY008 Glycogen Storage Disease Ii 64 0.070
432
c ACT210 Acute Respiratory Distress Syndrome 61 0.070
433
BRN080 Brain Ischemia 44 0.069
434
c HMP029 Hemophilia a 68 0.069
435
c PNC108 Pancreatitis, Hereditary 59 0.069
436
P FML052 Familial Cold Autoinflammatory Syndrome 53 0.069
437
ABD017 Abdominal Obesity-Metabolic Syndrome Quantitative Trait Locus 2 48 0.069
438
PRD004 Prediabetes Syndrome 45 0.069
439
MLN007 Male Infertility 53 0.069
440
P GRF003 Graft-Versus-Host Disease 71 0.069
441
P LTR001 Lateral Sclerosis 58 0.069
442
TRN022 Transcobalamin Ii Deficiency 46 0.068
443
P HYP035 Hypophosphatasia 58 0.068
444
WLS001 Wilson Disease 71 0.068
445
FDL002 Food Allergy 55 0.068
446
P BRN120 Bronchus Cancer 49 0.068
447
P HYP111 Hyperprolinemia 34 0.068
448
c CRP023 Carpenter Syndrome 1 54 0.068
449
NSP002 Nasopharyngitis 46 0.068
450
P SLP006 Sleep Apnea 66 0.068
451
URT039 Urticaria 60 0.068
452
P LCH002 Lichen Planus 57 0.067
453
BRN071 Brain Injury 53 0.067
454
FCT007 Factor Vii Deficiency 61 0.067
455
ATN005 Autonomic Dysfunction 50 0.067
456
ART016 Aortic Aneurysm 69 0.067
457
PRP027 Peripheral Vascular Disease 70 0.067
458
P TYR004 Tyrosinemia 48 0.067
459
IRR002 Irritable Bowel Syndrome 62 0.067
460
P SCK002 Sick Sinus Syndrome 53 0.067
461
P CHR345 Chronic Pain 51 0.067
462
P ATR005 Atrophic Gastritis 48 0.067
463
CHN016 Cohen Syndrome 47 0.066
464
GLC006 Galactosemia 65 0.066
465
TRN015 Transient Cerebral Ischemia 56 0.066
466
PRT014 Protein S Deficiency 47 0.066
467
BLD044 Bladder Disease 55 0.066
468
CHL065 Cholangiocarcinoma 63 0.066
469
LYM067 Lymphoid Leukemia 44 0.066
470
HYP056 Hypoglycemia 62 0.066
471
RLP002 Relapsing-Remitting Multiple Sclerosis 57 0.066
472
c HMP004 Hemophilia B 67 0.066
473
c LKM063 Leukemia, Chronic Myeloid 70 0.066
474
P KDN017 Kidney Cancer 58 0.066
475
P SCL057 Scoliosis, Isolated 1 40 0.066
476
OVR012 Ovarian Serous Cystadenocarcinoma 48 0.066
477
FCT006 Factor V Deficiency 53 0.066
478
URM002 Uremia 52 0.066
479
P MYL005 Myelofibrosis 70 0.065
480
c BSL007 Basal Cell Carcinoma 64 0.065
481
P CRB048 Cerebral Cavernous Malformations 57 0.065
482
DBT010 Diabetic Neuropathy 59 0.065
483
P ALG028 Alagille Syndrome 1 73 0.065
484
P DST101 Distal Hereditary Motor Neuropathies 28 0.065
485
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.065
486
GT001 Gout 57 0.065
487
c ATS347 Autosomal Dominant Polycystic Kidney Disease 60 0.065
488
P ACT074 Acute Lymphocytic Leukemia 59 0.065
489
BCK006 Back Pain 44 0.065
490
P ADL010 Adult Respiratory Distress Syndrome 66 0.065
491
OST097 Osteoporotic Fracture 41 0.065
492
c VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 35 0.065
493
P PLY019 Polyneuropathy 57 0.065
494
PRT037 Pertussis 68 0.064
495
CRD119 Cardiac Arrest 62 0.064
496
P CNG003 Congenital Dyserythropoietic Anemia 41 0.064
497
PNG002 Pain Agnosia 42 0.064
498
P LRY019 Laryngitis 56 0.064
499
ALL003 Allergic Rhinitis 67 0.064
500
NWB001 Newborn Respiratory Distress Syndrome 52 0.064
501
RSP007 Respiratory Distress Syndrome, Infant 34 0.064
502
P CHR084 Chromosomal Disease 40 0.064
503
P HYP599 Hypoparathyroidism, Familial Isolated 37 0.064
504
P HMP007 Hemophilia 60 0.064
505
CYS013 Cystinuria 63 0.063
506
c HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 40 0.063
507
APH001 Aphthous Stomatitis 63 0.063
508
HYP017 Hypophosphatemia 46 0.063
509
P VTL001 Vitelliform Macular Dystrophy 42 0.063
510
APN008 Apnea, Obstructive Sleep 67 0.063
511
HRP008 Herpes Simiae 16 0.063
512
DNN002 Donnai-Barrow Syndrome 43 0.063
513
BRN056 Bronchopulmonary Dysplasia 60 0.063
514
PRT038 Protein-Energy Malnutrition 51 0.063
515
P OPN001 Open-Angle Glaucoma 51 0.063
516
P CHR012 Chronic Granulomatous Disease 69 0.063
517
MTC027 Mitochondrial Trifunctional Protein Deficiency 54 0.063
518
GLN010 Glanzmann Thrombasthenia 65 0.063
519
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 21 0.063
520
FCT002 Factor Xi Deficiency 64 0.062
521
ISL003 Isolated Growth Hormone Deficiency 55 0.062
522
P BPL003 Bipolar Disorder 59 0.062
523
CRD223 Cardiac Arrhythmia 54 0.062
524
P PSD015 Pseudohypoparathyroidism 50 0.062
525
c WLM013 Wilms Tumor 1 64 0.062
526
c MSC121 Muscular Dystrophy, Limb-Girdle, Type 2a 58 0.062
527
OCL006 Ocular Hypertension 53 0.062
528
P CLC063 Celiac Disease 1 71 0.062
529
ACQ031 Acquired Idiopathic Sideroblastic Anemia 36 0.062
530
P NRN021 Neuronal Ceroid Lipofuscinosis 61 0.062
531
c PYR007 Pyridoxine-Refractory Autosomal Recessive Sideroblastic Anemia 30 0.062
532
BRR014 Barrett Esophagus 63 0.062
533
c MGL018 Megaloblastic Anemia 1 42 0.062
534
DRR014 Darier-White Disease 61 0.062
535
UTR024 Uterine Carcinosarcoma 59 0.062
536
P RTN022 Retinal Vein Occlusion 52 0.062
537
GLC022 Glucose/galactose Malabsorption 41 0.062
538
PYR015 Pyridoxal 5'-Phosphate-Dependent Epilepsy 17 0.062
539
ERY003 Erythema Multiforme 60 0.061
540
RFS006 Refsum Disease, Classic 62 0.061
541
P MCL013 Mucolipidosis Iv 67 0.061
542
CLN015 Colon Adenocarcinoma 53 0.061
543
P MSC003 Muscular Atrophy 54 0.061
544
INT007 Intermediate Coronary Syndrome 52 0.061
545
P HYP058 Hypervitaminosis a 47 0.061
546
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 56 0.061
547
c MCR130 Microvascular Complications of Diabetes 6 40 0.061
548
ART001 Arterial Tortuosity Syndrome 53 0.061
549
PRP001 Propionic Acidemia 62 0.061
550
c CHR579 Chiari Malformation Type Ii 45 0.061
551
BLD137 Blood Group--Ahonen 17 0.061
552
P FLL037 Follicular Lymphoma 69 0.061
553
END057 Endometrial Cancer 65 0.061
554
P OVR046 Ovarian Cyst 50 0.061
555
P RTT002 Rett Syndrome 82 0.060
556
c AFB002 Afibrinogenemia, Congenital 60 0.060
557
SPN041 Spinal Cord Disease 51 0.060
558
BRN002 Bronchiolitis 59 0.060
559
c MCR113 Microvascular Complications of Diabetes 3 52 0.060
560
c MCR120 Microvascular Complications of Diabetes 7 37 0.060
561
c MCR133 Microvascular Complications of Diabetes 4 35 0.060
562
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.060
563
P ANG001 Angelman Syndrome 61 0.060
564
FBR047 Fibromyalgia 57 0.060
565
CRT016 Carotid Artery Disease 57 0.060
566
P AST055 Asthma-Related Traits 1 30 0.060
567
SPN051 Spondylitis 55 0.060
568
ATM052 Autoimmune Disease 1 34 0.060
569
P HYP076 Hyperthyroidism 56 0.060
570
P PTY003 Pityriasis Rubra Pilaris 50 0.060
571
c LYN004 Lynch Syndrome I 58 0.060
572
c EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 44 0.060
573
GLB015 Glioblastoma Multiforme 60 0.059
574
MYL031 Myeloproliferative Neoplasm 63 0.059
575
P TYS001 Tay-Sachs Disease 71 0.059
576
c HYP543 Hypoplastic Left Heart Syndrome 1 42 0.059
577
c EXD008 Exudative Vitreoretinopathy 1 69 0.059
578
INC002 Inclusion Body Myositis 63 0.059
579
FXF002 Fox-Fordyce Disease 40 0.059
580
CHR619 Chromosome 2q35 Duplication Syndrome 55 0.059
581
P RSP003 Respiratory Failure 70 0.059
582
P DYS021 Dysautonomia 43 0.059
583
c AMG001 Amegakaryocytic Thrombocytopenia, Congenital 52 0.059
584
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 27 0.059
585
GNG011 Gingival Disease 49 0.058
586
RST001 Restless Legs Syndrome 52 0.058
587
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 46 0.058
588
c ART138 Aortic Aneurysm, Familial Abdominal, 1 64 0.058
589
P CNJ013 Conjunctivitis 63 0.058
590
PHT003 Phototoxic Dermatitis 40 0.058
591
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 46 0.058
592
SMT004 Smith-Lemli-Opitz Syndrome 68 0.058
593
P PRP034 Purpura Fulminans 45 0.058
594
PRP056 Porphyria, Acute Hepatic 42 0.058
595
P ORF002 Orofacial Cleft 41 0.058
596
c ACT027 Acute Pancreatitis 60 0.058
597
P ATT013 Attention Deficit-Hyperactivity Disorder 66 0.058
598
CRN024 Corneal Disease 47 0.058
599
PRS063 Paresthesia 37 0.057
600
PRS129 Prostatic Hyperplasia, Benign 48 0.057
601
HYP080 Hypogonadism 51 0.057
602
ORL011 Oral Cancer 59 0.057
603
KRT009 Keratosis 53 0.057
604
MVM001 Movement Disease 60 0.057
605
CRB011 Cerebrotendinous Xanthomatosis 63 0.057
606
P LCT002 Lactose Intolerance 47 0.057
607
CMP010 Complex Regional Pain Syndrome 57 0.057
608
OVR094 Ovarian Epithelial Cancer 38 0.057
609
DWN001 Down Syndrome 69 0.057
610
ENT011 Enterocolitis 54 0.057
611
DPH001 Diphtheria 62 0.057
612
CRB045 Cerebellar Hypoplasia 48 0.057
613
ALC006 Alcoholic Hepatitis 62 0.056
614
BDY007 Body Mass Index Quantitative Trait Locus 1 26 0.056
615
PLS009 Plasma Cell Neoplasm 51 0.056
616
PNC001 Pancytopenia 51 0.056
617
c ATM011 Autoimmune Hepatitis 62 0.056
618
P SHR001 Short Bowel Syndrome 51 0.056
619
P SNS014 Sinusitis 62 0.056
620
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 44 0.056
621
c PLY105 Polycystic Ovary Syndrome 1 30 0.056
622
HMP009 Haemophilus Influenzae 49 0.056
623
P ENC004 Encephalitis 65 0.056
624
MCK007 Muckle-Wells Syndrome 64 0.056
625
ALC007 Alcohol Dependence 65 0.056
626
c INS002 in Situ Carcinoma 56 0.056
627
DNT012 Dental Caries 51 0.056
628
PLC007 Placental Abruption 50 0.056
629
HML018 Homologous Wasting Disease 18 0.056
630
PNC041 Pancreatic Ductal Adenocarcinoma 52 0.056
631
c LKM056 Leukemia, Chronic Lymphocytic 2 41 0.055
632
CHY002 Chylomicron Retention Disease 52 0.055
633
ARM001 Aromatase Deficiency 52 0.055
634
ATN002 Autonomic Nervous System Disease 51 0.055
635
DGN001 Degenerative Disc Disease 53 0.055
636
HMC014 Homocysteinemia 48 0.055
637
P ALC004 Alcohol Abuse 63 0.055
638
P UVT001 Uveitis 60 0.055
639
MCR017 Macrocytic Anemia 45 0.055
640
CHR074 Choriocarcinoma 47 0.055
641
P GCH001 Gaucher's Disease 62 0.055
642
ATR013 Atrichia with Papular Lesions 35 0.055
643
c MLG068 Malignant Glioma 38 0.055
644
FNC005 Functional Colonic Disease 31 0.054
645
P MYS005 Myositis 63 0.054
646
DYS073 Dysphagia 46 0.054
647
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 21 0.054
648
NSD001 Nose Disease 50 0.054
649
STT009 Sutton Disease 2 29 0.054
650
MNS002 Mini Stroke 23 0.054
651
HRP004 Herpes Zoster 60 0.054
652
P MTC069 Mitochondrial Disorders 49 0.054
653
BRN024 Bronchitis 66 0.054
654
P ACT008 Actinic Keratosis 54 0.054
655
GTR002 Goiter 52 0.054
656
c SCL052 Scleroderma, Familial Progressive 64 0.054
657
c STR084 Stargardt Disease 1 48 0.054
658
TRD006 Tardive Dyskinesia 59 0.054
659
HRT012 Heart Valve Disease 44 0.054
660
SPS057 Spasticity 41 0.054
661
SWL001 Swallowing Disorders 36 0.054
662
ASP002 Aspartylglucosaminuria 56 0.054
663
c SPN225 Spondyloarthropathy 1 71 0.054
664
ACT119 Acute Promyelocytic Leukemia 59 0.054
665
ADR054 Adrenocortical Carcinoma, Hereditary 70 0.053
666
OTT002 Otitis Media 66 0.053
667
THY111 Thyroid Carcinoma, Familial Medullary 69 0.053
668
URN022 Urinary Tract Infections, Recurrent 29 0.053
669
GNR004 Generalized Anxiety Disorder 53 0.053
670
BSL008 Basal Ganglia Disease 46 0.053
671
VGN023 Vaginitis 58 0.053
672
CRV040 Cervix Carcinoma 53 0.053
673
GST092 Gastroesophageal Reflux 64 0.053
674
LMY002 Leiomyoma 57 0.053
675
c ACT073 Acute Leukemia 60 0.053
676
P ANT006 Antiphospholipid Syndrome 59 0.053
677
STM006 Stomach Disease 52 0.053
678
c BCT007 Bacterial Meningitis 58 0.053
679
OPT009 Optic Neuritis 53 0.053
680
HYD046 Hydatidiform Mole, Recurrent, 1 52 0.053
681
MTC061 Mitochondrial Dna Depletion Syndrome 1 44 0.053
682
ORL013 Oral Lichen Planus 51 0.053
683
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.053
684
CHR008 Choroiditis 46 0.053
685
SFT003 Soft Tissue Sarcoma 58 0.053
686
P ANP001 Anaplastic Large Cell Lymphoma 59 0.053
687
P ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 51 0.052
688
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 44 0.052
689
ADN011 Adenoid Cystic Carcinoma 65 0.052
690
MTR014 Motor Neuron Disease 61 0.052
691
INT088 Intrinsic Factor Deficiency 35 0.052
692
AMN002 Amino Acid Metabolic Disorder 47 0.052
693
P PLY014 Polycystic Kidney Disease 60 0.052
694
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.052
695
P TCL004 T-Cell Leukemia 50 0.052
696
CHR005 Chorioamnionitis 51 0.052
697
BRN004 Brain Edema 55 0.052
698
ESP023 Esophageal Disease 56 0.052
699
SPN369 Spinal Disease 42 0.052
700
SCH014 Schistosomiasis 62 0.052
701
OVR029 Ovarian Hyperstimulation Syndrome 64 0.052
702
LSH001 Leishmaniasis 70 0.052
703
TTH006 Tooth Disease 53 0.051
704
PPL022 Papilloma 58 0.051
705
PLS011 Plasmacytoma 60 0.051
706
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 31 0.051
707
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.051
708
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 55 0.051
709
CYS019 Cystathioninuria 30 0.051
710
ORL015 Oral Squamous Cell Carcinoma 45 0.051
711
GLC098 Glaucoma-Related Pigment Dispersion Syndrome 47 0.051
712
BRK010 Burkitt Lymphoma 68 0.051
713
c CNT016 Central Retinal Vein Occlusion 49 0.051
714
HDN002 Head Injury 47 0.051
715
MRB003 Morbid Obesity 60 0.051
716
HPT070 Hepatosplenic T-Cell Lymphoma 43 0.051
717
PRT018 Portal Vein Thrombosis 50 0.051
718
NRV006 Nervous System Cancer 60 0.051
719
RFR010 Refractory Anemia 49 0.051
720
RFL001 Reflex Sympathetic Dystrophy 51 0.051
721
c LBR014 Leber Congenital Amaurosis 4 49 0.051
722
RFR003 Refractive Error 44 0.050
723
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 63 0.050
724
P CHR071 Charcot-Marie-Tooth Disease 65 0.050
725
P FBR017 Fibrosarcoma 61 0.050
726
PST021 Postpartum Depression 53 0.050
727
HYP025 Hyperphosphatemia 48 0.050
728
PYR016 Pyridoxine Deficiency 36 0.050
729
P DYS007 Dyskeratosis Congenita 67 0.050
730
LKC009 Leukocyte Adhesion Deficiency, Type I 57 0.050
731
SNS003 Sensory Peripheral Neuropathy 53 0.050
732
P PRT013 Portal Hypertension 59 0.050
733
HMC016 Homocystinuria Due to Cbs Deficiency 20 0.050
734
CNC002 Cinca Syndrome 62 0.050
735
P FML068 Familial Hypocalciuric Hypercalcemia 48 0.050
736
P TRM003 Tremor 54 0.050
737
SCH012 Schizoaffective Disorder 54 0.050
738
P DBT005 Diabetes Insipidus 54 0.050
739
AZS001 Azoospermia 45 0.050
740
P SCL018 Scoliosis 55 0.050
741
SPC010 Speech and Communication Disorders 52 0.050
742
ALG001 Algoneurodystrophy 39 0.050
743
BCT002 Bacterial Vaginosis 54 0.050
744
AMN012 Aminoacidopathies 24 0.050
745
FLL027 Fallopian Tube Carcinoma 62 0.050
746
HYP005 Hypokalemia 53 0.050
747
HMT002 Hematologic Cancer 63 0.050
748
P SML001 Small Cell Carcinoma 58 0.049
749
BLD053 Blood Platelet Disease 55 0.049
750
MTC005 Mitochondrial Metabolism Disease 44 0.049
751
LKP003 Leukoplakia 42 0.049
752
BRT054 Brittle Bone Disorder 69 0.049
753
SPH010 Sphingolipidosis 47 0.049
754
NPH003 Nephrocalcinosis 48 0.049
755
PRV006 Pervasive Developmental Disorder 55 0.049
756
LRG015 Large Intestine Adenoma 17 0.049
757
PSR001 Psoriatic Arthritis 65 0.049
758
P AGG001 Aggressive Periodontitis 54 0.049
759
c MCL066 Macular Dystrophy, Vitelliform, 2 42 0.049
760
GLT007 Glutathione Synthetase Deficiency 46 0.049
761
CMP028 Complement Component 2 Deficiency 45 0.049
762
P CNN004 Connective Tissue Cancer 45 0.049
763
CLR030 Clear Cell Renal Cell Carcinoma 49 0.049
764
PRN019 Perinatal Necrotizing Enterocolitis 56 0.049
765
CNR004 Cone-Rod Dystrophy 2 67 0.049
766
INB001 Inborn Amino Acid Metabolism Disorder 16 0.049
767
P HRP006 Herpes Simplex 69 0.049
768
VNW001 Von Willebrand's Disease 60 0.049
769
LMY014 Leiomyoma, Uterine 53 0.048
770
HYP043 Hyperandrogenism 50 0.048
771
SYN036 Syncope 47 0.048
772
c CRD089 Cardiomyopathy, Familial Hypertrophic, 14 22 0.048
773
SPP010 Suppressor of Tumorigenicity 3 54 0.048
774
LPD009 Lipid Storage Disease 51 0.048
775
MTB004 Metabolic Acidosis 48 0.048
776
P PLM036 Pulmonary Fibrosis 69 0.048
777
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 45 0.048
778
PRT029 Parathyroid Adenoma 49 0.048
779
P ATS366 Autism X-Linked 2 43 0.048
780
PRP036 Peripheral T-Cell Lymphoma 56 0.048
781
c ART115 Aortic Valve Disease 1 61 0.048
782
PLM031 Poliomyelitis 58 0.048
783
TXC002 Toxic Encephalopathy 55 0.048
784
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 41 0.048
785
c CHR417 Chronic Graft Versus Host Disease 64 0.047
786
P HRD018 Hair Disease 51 0.047
787
P THR005 Thrombotic Thrombocytopenic Purpura 63 0.047
788
KLD001 Keloids 49 0.047
789
c MNN047 Mannosidosis, Alpha B, Lysosomal 56 0.047
790
LYS002 Lysosomal Storage Disease 56 0.047
791
P MSC007 Muscle Hypertrophy 58 0.047
792
c AMY087 Amyloidosis, Hereditary, Transthyretin-Related 57 0.047
793
HYP776 Hyperparathyroidism, Neonatal Severe 40 0.047
794
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.047
795
P ASP006 Aspergillosis 65 0.047
796
BLR006 Biliary Tract Disease 54 0.047
797
P PMP001 Pemphigus 54 0.047
798
PRT035 Peritoneum Cancer 42 0.047
799
P LRY044 Larynx Cancer 60 0.047
800
MTH077 Methylmalonic Aciduria, Cbla Type 26 0.047
801
NRR001 Neuroretinitis 46 0.046
802
CRN031 Cranial Nerve Disease 45 0.046
803
P SPN046 Spinal Muscular Atrophy 63 0.046
804
P MTC133 Mitochondrial Myopathy 54 0.046
805
P FRG001 Fragile X Syndrome 69 0.046
806
CRB085 Cerebral Hemorrhage 47 0.046
807
SYS003 Systolic Heart Failure 46 0.046
808
DYS014 Dyspepsia 54 0.046
809
c SVR005 Severe Pre-Eclampsia 53 0.046
810
SBC017 Sebaceous Gland Disease 38 0.046
811
MNK001 Menkes Disease 63 0.046
812
MYF002 Myofascial Pain Syndrome 43 0.046
813
BRS099 Breast Ductal Carcinoma 56 0.046
814
P CYS018 Cystitis 56 0.046
815
DCT002 Ductal Carcinoma in Situ 55 0.046
816
HMR039 Hemorrhage, Intracerebral 57 0.046
817
P CTN003 Cutaneous Lupus Erythematosus 52 0.046
818
CHC001 Chickenpox 49 0.046
819
c PSR017 Psoriasis 2 39 0.046
820
DBF001 D-Bifunctional Protein Deficiency 57 0.046
821
c BNG091 Benign Chronic Pemphigus 52 0.046
822
P AGM019 Agammaglobulinemia, X-Linked 68 0.046
823
OST003 Osteonecrosis 63 0.046
824
P ORL007 Oral Cavity Cancer 61 0.045
825
CRV002 Cervix Uteri Carcinoma in Situ 47 0.045
826
HYP457 Hypertrophic Scars 47 0.045
827
c MLG079 Malignant Pleural Mesothelioma 46 0.045
828
DSS009 Disseminated Intravascular Coagulation 55 0.045
829
P BRN035 Brain Stem Glioma 50 0.045
830
P PLY018 Polycythemia 58 0.045
831
P CHR285 Chronic Myelomonocytic Leukemia 62 0.045
832
MST005 Mastitis 55 0.045
833
FNT004 Fainting 36 0.045
834
P MCR010 Microcephaly 57 0.045
835
P CTN015 Cutaneous T Cell Lymphoma 55 0.045
836
CLC001 Calciphylaxis 52 0.045
837
DBT008 Diabetic Angiopathy 47 0.045
838
BRB001 Beriberi 41 0.045
839
PCK003 Pick Disease of Brain 65 0.045
840
VCC001 Vaccinia 50 0.045
841
P UTR058 Uterine Anomalies 59 0.045
842
ORL012 Oral Leukoplakia 47 0.045
843
P VTM029 Vitamin D Hydroxylation-Deficient Rickets, Type 1b 24 0.045
844
c ALP101 Alpha-Thalassemia 59 0.045
845
ALR002 Al-Raqad Syndrome 31 0.045
846
c ACT135 Acute Graft Versus Host Disease 56 0.045
847
BLR001 Biliary Atresia 57 0.045
848
LNS003 Lens Disease 39 0.045
849
RCT018 Rectal Neoplasm 54 0.045
850
c MSC120 Muscular Dystrophy, Limb-Girdle, Type 2c 51 0.045
851
c SPN327 Spinocerebellar Ataxia, Autosomal Recessive 1 60 0.045
852
IRN004 Iron-Refractory Iron Deficiency Anemia 42 0.045
853
P TMP003 Temporal Arteritis 66 0.045
854
c RTN162 Retinitis Pigmentosa 2 50 0.045
855
CRV045 Cervical Intraepithelial Neoplasia 43 0.045
856
PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 62 0.045
857
P MLN069 Melanoma, Uveal 58 0.045
858
GRW007 Growth Hormone Deficiency 51 0.044
859
c ANM036 Anemia, Sideroblastic, 1 55 0.044
860
P FML011 Familial Adenomatous Polyposis 71 0.044
861
P LCT001 Lactic Acidosis 50 0.044
862
HYP189 Hypoadrenalism 43 0.044
863
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 69 0.044
864
P GLL020 Gallbladder Disease 64 0.044
865
P GST049 Gastrointestinal System Cancer 59 0.044
866
c CHL119 Cholangitis, Primary Sclerosing 59 0.044
867
MRG003 Marginal Zone B-Cell Lymphoma 56 0.044
868
EXC002 Exocrine Pancreatic Insufficiency 43 0.044
869
ICH054 Ichthyosis, X-Linked 58 0.044
870
VSC002 Vascular Dementia 58 0.044
871
SPS019 Spastic Paraparesis 35 0.044
872
CYT008 Cytomegalovirus Infection 56 0.044
873
SKL017 Skeletal Dysplasias 48 0.044
874
c ALZ056 Alzheimer Disease 3 47 0.044
875
P HYP087 Hypotrichosis 48 0.044
876
IDP070 Idiopathic Scoliosis 41 0.044
877
NTH001 Netherton Syndrome 60 0.044
878
THR004 Thrombocytosis 54 0.044
879
MNT001 Mantle Cell Lymphoma 73 0.043
880
P GRM010 Germ Cells Tumors 36 0.043
881
RTC005 Reticulosarcoma 49 0.043
882
BDY004 Body Mass Index Quantitative Trait Locus 11 68 0.043
883
CHR177 Chromophobe Renal Cell Carcinoma 55 0.043
884
PPT005 Peptic Ulcer Disease 61 0.043
885
NRF026 Neurofibromatosis, Type Iv, of Riccardi 73 0.043
886
PLM010 Pulmonary Edema 56 0.043
887
CRV069 Cervix Disease 35 0.043
888
MNN020 Meningococcal Infection 47 0.043
889
c GCH015 Gaucher Disease, Type I 57 0.043
890
CLS016 Clostridium Difficile Colitis 47 0.043
891
HTC003 Hutchinson-Gilford Progeria Syndrome 62 0.043
892
P EPD009 Epidermolysis Bullosa Dystrophica 58 0.043
893
HST017 Histiocytosis-Lymphadenopathy Plus Syndrome 40 0.043
894
P MYS003 Myasthenia Gravis 72 0.043
895
BLL006 Bullous Pemphigoid 63 0.043
896
P MNC007 Monocytic Leukemia 57 0.043
897
CHL067 Cholecystitis 57 0.043
898
MCR004 Macroglobulinemia 53 0.043
899
c PYR010 Peyronie's Disease 53 0.043
900
INT303 Intracranial Hypertension, Idiopathic 50 0.043
901
DYS015 Dysentery 43 0.043
902
P BRN009 Burning Mouth Syndrome 53 0.043
903
FCL044 Fecal Incontinence 38 0.043
904
MSC152 Muscular Dystrophy, Becker Type 60 0.043
905
INT002 Intermittent Claudication 61 0.042
906
P PYL005 Pyelonephritis 56 0.042
907
KRT006 Keratoconjunctivitis 55 0.042
908
MCL006 Macular Retinal Edema 51 0.042
909
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.042
910
CNJ012 Conjunctival Disease 48 0.042
911
TTH004 Tethered Spinal Cord Syndrome 38 0.042
912
c MLG074 Malignant Mesenchymoma 54 0.042
913
NRF007 Neurofibroma 65 0.042
914
P HYP614 Hyperlipidemia, Familial Combined 56 0.042
915
c ADL017 Adult T-Cell Leukemia 62 0.042
916
P ATS308 Autosomal Dominant Cerebellar Ataxia 54 0.042
917
c DNR003 Duane Retraction Syndrome 1 34 0.042
918
NST002 Nestor-Guillermo Progeria Syndrome 25 0.042
919
P INT001 Intrahepatic Cholestasis 60 0.042
920
c FCL025 Focal Segmental Glomerulosclerosis 1 59 0.042
921
PRT082 Preterm Premature Rupture of the Membranes 52 0.042
922
c INH004 Inherited Blood Coagulation Disease 41 0.042
923
SND001 Sandhoff Disease 64 0.042
924
RHB001 Rhabdoid Cancer 62 0.042
925
P MMB011 Membranous Nephropathy 57 0.042
926
c CRD147 Cardiomyopathy, Familial Hypertrophic, 20 36 0.042
927
P INT070 Intestinal Obstruction 56 0.042
928
BRN022 Bronchiectasis 55 0.042
929
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.042
930
CRT013 Carotid Stenosis 52 0.042
931
CHL123 Chlamydia 64 0.042
932
PRP032 Porphyria Variegata 55 0.042
933
P SYP003 Syphilis 51 0.042
934
HPT019 Hepatic Encephalopathy 58 0.042
935
P BRS044 Breast Adenocarcinoma 58 0.042
936
DDN006 Duodenitis 48 0.042
937
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.042
938
P KRT007 Keratoconus 48 0.042
939
MLT157 Multiple System Atrophy 1 73 0.042
940
P SBS003 Substance Abuse 57 0.042
941
GLC009 Glucosephosphate Dehydrogenase Deficiency 48 0.042
942
P CRD132 Cardiac Conduction Defect 59 0.041
943
P HYP014 Hyperuricemia 55 0.041
944
P HMG032 Hemoglobin H Disease 52 0.041
945
KRT008 Keratopathy 43 0.041
946
GRY002 Gray Platelet Syndrome 55 0.041
947
P DYS193 Dystonia 11, Myoclonic 51 0.041
948
MGK001 Megakaryocytic Leukemia 63 0.041
949
CRP001 Carpal Tunnel Syndrome 66 0.041
950
MYM001 Myoma 55 0.041
951
PGM003 Pigmentation Disease 45 0.041
952
HYP064 Hypogonadotropism 40 0.041
953
FLL029 Fallopian Tube Disease 35 0.041
954
INT074 Intracranial Arteriosclerosis 15 0.041
955
NSS002 Neisseria Meningitidis Infection 49 0.041
956
P TRN020 Turner Syndrome 68 0.041
957
RTC009 Reticulum Cell Sarcoma 52 0.041
958
INT038 Interdigitating Dendritic Cell Sarcoma 44 0.041
959
P ENC011 Encephalomyopathy 40 0.041
960
APP008 Appendicitis 64 0.041
961
GLL018 Gallbladder Cancer 51 0.041
962
P FRD012 Friedreich Ataxia 1 64 0.041
963
CLF027 Cleft Palate, Isolated 63 0.041
964
P PLM034 Pulmonary Emphysema 58 0.041
965
INT075 Intracranial Hypertension 52 0.041
966
PRX077 Peroxisomal Biogenesis Disorders 40 0.041
967
TST014 Testicular Cancer 53 0.041
968
SPL018 Splenomegaly 46 0.041
969
VRC005 Varicose Veins 64 0.041
970
PST028 Post-Traumatic Stress Disorder 58 0.041
971
PLS007 Plasmodium Falciparum Malaria 57 0.041
972
INT066 Interstitial Lung Disease 62 0.041
973
INT079 Intrahepatic Cholangiocarcinoma 52 0.041
974
HMC041 Homocystinuria Due to Deficiency of N -Methylenetetrahydrofolate Reductase Activity 41 0.041
975
P ANG015 Angioedema 57 0.040
976
HLL004 Hellp Syndrome 52 0.040
977
P EST001 Estrogen-Receptor Positive Breast Cancer 51 0.040
978
P RFR008 Refractory Anemia with Excess Blasts 33 0.040
979
P EPN002 Ependymoma 55 0.040
980
CLR109 Colorectal Adenocarcinoma 53 0.040
981
P PTT006 Pituitary Adenoma 52 0.040
982
c ACT134 Acute Liver Failure 52 0.040
983
FCT003 Factor X Deficiency 57 0.040
984
MN1001 Mn1 35 0.040
985
HRW001 Hair Whorl 32 0.040
986
APH002 Aphasia 58 0.040
987
c CRD093 Cardiomyopathy, Dilated, 1a 57 0.040
988
ATN007 Autoinflammation, Lipodystrophy, and Dermatosis Syndrome 69 0.040
989
P CHL066 Cholangitis 52 0.040
990
c PSR028 Psoriasis 7 38 0.040
991
c PSR032 Psoriasis 11 38 0.040
992
c PSR018 Psoriasis 13 37 0.040
993
c CHR020 Chronic Interstitial Cystitis 43 0.040
994
MCR018 Microcytic Anemia 43 0.040
995
c PRM126 Primary Peritoneal Carcinoma 60 0.040
996
P FCS002 Fucosidosis 60 0.040
997
P MYC008 Myocarditis 58 0.040
998
CMB081 Combined Immunodeficiency, X-Linked 64 0.040
999
PRP083 Porphyria, Acute Intermittent 61 0.040
1000
P BRN019 Bernard-Soulier Syndrome 59 0.040
1001
CMM004 Common Variable Immunodeficiency 70 0.040
1002
P LKD001 Leukodystrophy 57 0.040
1003
ACL001 Acalculous Cholecystitis 38 0.040
1004
CNT047 Contact Dermatitis 63 0.040
1005
P HMR012 Hemorrhagic Fever 57 0.040
1006
IGG001 Iga Glomerulonephritis 55 0.040
1007
CRN030 Coronary Stenosis 51 0.040
1008
DFF036 Differentiated Thyroid Carcinoma 49 0.040
1009
c PRD040 Periodontitis, Chronic 49 0.040
1010
ANG046 Angioimmunoblastic T-Cell Lymphoma 47 0.040
1011
PSD088 Pseudobulbar Affect 37 0.040
1012
NSP003 Nasopharyngeal Disease 32 0.040
1013
PRN021 Paranasal Sinus Disease 50 0.040
1014
MYF001 Myofibroma 39 0.040
1015
KPS004 Kaposi Sarcoma 73 0.040
1016
NKJ001 Nakajo Syndrome 26 0.040
1017
PLG002 Plague 56 0.040
1018
FRN030 Frontotemporal Dementia with Parkinsonism-17 31 0.040
1019
GLB001 Gilbert Syndrome 56 0.039
1020
RHM001 Rheumatic Fever 58 0.039
1021
GLS001 Gliosarcoma 58 0.039
1022
IMP005 Impotence 55 0.039
1023
PRT129 Prothrombin Deficiency, Congenital 49 0.039
1024
MRG013 Mirage Syndrome 43 0.039
1025
CLN044 Colon Adenoma 42 0.039
1026
RHM035 Rheumatic Fever-Related Antigen 39 0.039
1027
PRM155 Primary Cutaneous Anaplastic Large Cell Lymphoma 39 0.039
1028
MMM006 Mammographic Density 43 0.039
1029
c MCP049 Mucopolysaccharidosis, Type Vii 63 0.039
1030
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 52 0.039
1031
LYM040 Lymphoblastic Lymphoma 57 0.039
1032
PLS025 Plasmablastic Lymphoma 53 0.039
1033
THR016 Thrombophlebitis 52 0.039
1034
HPT082 Hepatic Adenomas, Familial 53 0.039
1035
PLY001 Polycythemia Vera 74 0.039
1036
P RHB003 Rhabdomyosarcoma 56 0.039
1037
c LKM060 Leukemia, Acute Lymphoblastic 3 53 0.039
1038
LRY017 Laryngeal Disease 38 0.039
1039
ACT094 Acute Articular Rheumatism 26 0.039
1040
P RBL001 Rubella 62 0.039
1041
P ATX024 Ataxia-Oculomotor Apraxia 3 40 0.039
1042
LBR002 Leber Hereditary Optic Neuropathy 57 0.039
1043
OCC006 Occipital Horn Syndrome 49 0.039
1044
CRB037 Cerebral Palsy 71 0.038
1045
EXP004 Exophthalmos 51 0.038
1046
CHL004 Cholelithiasis 50 0.038
1047
PNN001 Panniculitis 49 0.038
1048
c WSK002 Wiskott-Aldrich Syndrome 2 27 0.038
1049
PTT009 Pituitary Gland Disease 56 0.038
1050
EPL166 Epilepsy, Early-Onset, Vitamin B6-Dependent 18 0.038
1051
BNC003 Bone Cancer 59 0.038
1052
DBT062 Diabetic Foot Ulcers 59 0.038
1053
P FNC004 Fanconi Syndrome 52 0.038
1054
DBT006 Diabetic Macular Edema 48 0.038
1055
ASP004 Asphyxia Neonatorum 43 0.038
1056
NDL024 Nodal Marginal Zone Lymphoma 41 0.038
1057
RFR001 Refractory Plasma Cell Neoplasm 19 0.038
1058
P PRS038 Personality Disorder 64 0.038
1059
OST017 Osteomyelitis 63 0.038
1060
c HMN021 Human T-Cell Leukemia Virus Type 1 52 0.038
1061
SPL004 Splenic Marginal Zone Lymphoma 51 0.038
1062
c ANT034 Anterior Uveitis 50 0.038
1063
c MCP050 Mucopolysaccharidosis, Type Ii 63 0.038
1064
ALL006 Allergic Asthma 59 0.038
1065
FRN051 Frontotemporal Lobar Degeneration with Tdp43 Inclusions, Grn-Related 52 0.038
1066
TNG003 Tongue Cancer 58 0.038
1067
SNS001 Sensorineural Hearing Loss 56 0.038
1068
c ADL096 Adult Hepatocellular Carcinoma 48 0.038
1069
P MTC004 Mitochondrial Encephalomyopathy 43 0.038
1070
MYC006 Mycosis Fungoides 72 0.038
1071
P CMP008 Compartment Syndrome 47 0.038
1072
HDG004 Hodgkin's Granuloma 28 0.038
1073
HDG006 Hodgkin's Paragranuloma 21 0.038
1074
ADR012 Adrenal Gland Disease 51 0.038
1075
EPD070 Epidermoid Cysts 47 0.038
1076
ULC007 Ulcerative Stomatitis 46 0.038
1077
END041 Endometrial Adenocarcinoma 60 0.038
1078
INS001 Insulinoma 65 0.038
1079
FCT001 Factor Viii Deficiency 51 0.038
1080
PRR002 Pure Red-Cell Aplasia 51 0.038
1081
P TXP001 Toxoplasmosis 64 0.037
1082
P LMY004 Leiomyosarcoma 58 0.037
1083
TRM010 Traumatic Brain Injury 55 0.037
1084
ALC009 Alcoholic Liver Cirrhosis 52 0.037
1085
DRG003 Drug Dependence 51 0.037
1086
PLM175 Pulmonary Fibrosis and/or Bone Marrow Failure, Telomere-Related, 2 38 0.037
1087
PHS023 Phosphoserine Aminotransferase Deficiency 30 0.037
1088
GLT005 Glutamate Formiminotransferase Deficiency 28 0.037
1089
P WSK001 Wiskott-Aldrich Syndrome 77 0.037
1090
P ICH004 Ichthyosis 54 0.037
1091
SWN001 Swine Influenza 42 0.037
1092
P HYP265 Hypotonia 40 0.037
1093
c BSL024 Basal Cell Carcinoma 1 35 0.037
1094
TNS005 Tonsillitis 60 0.037
1095
P ART084 Arteriovenous Fistula 45 0.037
1096
AND014 Androgenic Alopecia 39 0.037
1097
c HYP602 Hyperoxaluria, Primary, Type Ii 37 0.037
1098
RFR007 Refractory Anemia with Excess Blasts in Transformation 24 0.037
1099
c JVN010 Juvenile Rheumatoid Arthritis 69 0.037
1100
ACT103 Acute Lymphoblastic Leukemia, Childhood 48 0.037
1101
P CRN028 Corneal Ulcer 47 0.037
1102
c ACT042 Acute Pyelonephritis 46 0.037
1103
PRT012 Prothrombin Deficiency 45 0.037
1104
CHL013 Cholecystolithiasis 40 0.037
1105
ARG006 Aregenerative Anemia 25 0.037
1106
OBS002 Obsessive-Compulsive Disorder 66 0.037
1107
MYL004 Myelodysplastic Myeloproliferative Cancer 53 0.037
1108
LKC003 Leukocyte Disease 46 0.037
1109
RNL021 Renal Tubular Transport Disease 38 0.037
1110
TRT001 Teratocarcinoma 40 0.037
1111
c OST163 Osteopetrosis, Autosomal Recessive 3 33 0.037
1112
P