Search results for Vitamin C

2455 hits were found for Vitamin C

# Family MCID Name MIFTS Score
1
HYP781 Hypoascorbemia 49 4.417
2
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 51 3.602
3
c HPT021 Hepatitis 74 0.722
4
P HPT001 Hepatitis C 69 0.678
5
P HPT073 Hepatitis C Virus 73 0.525
6
c BRS047 Breast Cancer 100 0.403
7
RCK004 Rickets 66 0.362
8
c LVR013 Liver Disease 77 0.344
9
KRT002 Keratomalacia 51 0.340
10
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 56 0.338
11
ACT236 Acute Motor and Sensory Axonal Neuropathy 23 0.312
12
VTM002 Vitamin B12 Deficiency 48 0.306
13
NTR005 Nutritional Deficiency Disease 60 0.271
14
c DBT026 Diabetes Mellitus, Noninsulin-Dependent 92 0.266
15
c DBT009 Diabetes Mellitus 67 0.266
16
c LYN001 Lynch Syndrome 72 0.260
17
c KDN018 Kidney Disease 71 0.260
18
P HPT003 Hepatitis a 66 0.253
19
c HPT023 Hepatocellular Carcinoma 97 0.252
20
c LKM002 Leukemia 72 0.247
21
c PRS040 Prostate Cancer 93 0.243
22
VRL011 Viral Infectious Disease 69 0.234
23
c OST002 Osteoporosis 74 0.222
24
c HYP069 Hyperparathyroidism 59 0.220
25
c CLR023 Colorectal Cancer 99 0.219
26
P HPT016 Hepatitis B 70 0.218
27
c HYP061 Hypertrophic Cardiomyopathy 59 0.218
28
c HRT032 Heart Disease 76 0.213
29
P PRS136 Prostate Cancer, Hereditary, 6 40 0.207
30
P PRS130 Prostate Cancer, Hereditary, 8 37 0.207
31
c ATX030 Ataxia-Telangiectasia 83 0.203
32
CYS001 Cystic Fibrosis 83 0.203
33
P CHR089 Chronic Kidney Failure 73 0.202
34
c FNC027 Fanconi Anemia, Complementation Group a 81 0.200
35
c ART022 Arthritis 78 0.200
36
c LYM118 Lymphoma 69 0.199
37
VTM033 Vitamin K Deficiency Bleeding 47 0.197
38
c HYP607 Hypercholesterolemia, Familial 82 0.196
39
c LNG032 Lung Cancer 99 0.195
40
LVR012 Liver Cirrhosis 67 0.191
41
ISC004 Ischemia 67 0.191
42
c MYC007 Myocardial Infarction 78 0.191
43
THR024 Thrombosis 64 0.189
44
P FML346 Familial Adenomatous Polyposis 1 67 0.188
45
HMN014 Human Immunodeficiency Virus Infectious Disease 62 0.188
47
NRL016 Neural Tube Defects 79 0.184
48
c ADN016 Adenocarcinoma 71 0.182
49
BND020 Bone Disease 65 0.182
50
ART140 Arteries, Anomalies of 67 0.180
51
c CRN018 Coronary Artery Anomaly 74 0.180
52
ACQ007 Acquired Immunodeficiency Syndrome 66 0.179
53
c LNG028 Long Qt Syndrome 65 0.176
54
c MLT020 Multiple Sclerosis 76 0.175
55
INS024 Insulin-Like Growth Factor I 83 0.174
56
AST005 Asthma 81 0.173
57
c NRP001 Neuropathy 63 0.173
58
P NRF024 Neurofibromatosis, Type I 69 0.170
59
MLN008 Melanoma 64 0.169
60
c ATR011 Atrial Fibrillation 69 0.167
61
c INF037 Inflammatory Bowel Disease 56 0.166
62
c CRN300 Coronary Heart Disease 1 62 0.165
63
c HRD086 Hereditary Hypophosphatemic Rickets 45 0.163
64
c RHM011 Rheumatoid Arthritis 82 0.163
65
c ALZ034 Alzheimer Disease 88 0.163
66
URN009 Urinary System Disease 59 0.163
67
c CRD246 Cardiovascular System Disease 57 0.161
68
FTT001 Fatty Liver Disease 66 0.161
69
c ZLL001 Zellweger Syndrome 57 0.160
70
P TBR025 Tuberous Sclerosis 1 72 0.160
71
c NNL004 Nonalcoholic Fatty Liver Disease 56 0.160
72
P PRC016 Pre-Eclampsia 61 0.159
73
NRL018 Neural Tube Defects, Folate-Sensitive 47 0.159
74
c LBR001 Leber Congenital Amaurosis 64 0.157
75
DPR016 Depression 73 0.157
77
c LPS004 Lupus Erythematosus 69 0.157
78
c THR014 Thrombocytopenia 65 0.157
79
DRM006 Dermatitis 69 0.156
80
P PRX059 Peroxisome Biogenesis Disorder 1a 51 0.156
81
ATM095 Autoimmune Disease 68 0.156
82
AGN016 Aging 63 0.154
83
c OVR042 Ovarian Cancer 83 0.153
84
GST050 Gastrointestinal System Disease 67 0.151
85
VSC007 Vascular Disease 72 0.151
86
LNG099 Lung Disease 70 0.150
87
P SYS001 Systemic Lupus Erythematosus 88 0.149
88
XRD010 Xeroderma Pigmentosum, Variant Type 71 0.149
89
c MTH008 Methylmalonic Acidemia 47 0.148
90
c PNC035 Pancreatic Cancer 83 0.148
91
GST019 Gastrointestinal Stromal Tumor 74 0.147
92
c PLY011 Polycystic Ovary Syndrome 64 0.147
93
GST053 Gastric Cancer 78 0.146
94
c TBR001 Tuberous Sclerosis 69 0.146
95
c INF038 Influenza 75 0.146
96
OCL033 Oculocerebral Syndrome with Hypopigmentation 46 0.146
97
c PSR002 Psoriasis 67 0.146
98
P SCN007 Secondary Hyperparathyroidism 56 0.144
99
c NRB001 Neuroblastoma 73 0.143
100
c INT068 Intestinal Disease 62 0.143
101
c NRF023 Neurofibromatosis, Type Ii 76 0.142
102
PRN011 Pernicious Anemia 52 0.142
103
c DRR001 Diarrhea 58 0.142
104
HMN044 Human Immunodeficiency Virus Type 1 75 0.141
105
PRT011 Protein C Deficiency 49 0.140
106
P VRL010 Viral Hepatitis 60 0.139
107
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.139
108
SQM006 Squamous Cell Carcinoma 59 0.138
109
GLC008 Glucose Metabolism Disease 54 0.138
110
c THL005 Thalassemia 65 0.138
111
c MTR004 Maturity-Onset Diabetes of the Young 61 0.138
112
c LYM033 Lymphoproliferative Syndrome 63 0.138
113
P PLM164 Pulmonary Hypertension, Primary, 1 71 0.138
114
ISC006 Ischemic Heart Disease 72 0.138
115
c MYL006 Myeloid Leukemia 68 0.137
116
P BDY007 Body Mass Index Quantitative Trait Locus 1 48 0.137
117
c CTR002 Cataract 58 0.136
118
CRH001 Crohn's Disease 79 0.136
119
c PRD008 Periodontitis 66 0.136
120
MTC097 Mitochondrial Complex Iv Deficiency 55 0.135
121
BNF002 Bone Fracture 50 0.135
122
P LKM061 Leukemia, Acute Myeloid 83 0.134
123
c PNM007 Pneumonia 72 0.133
124
P THR092 Thrombophilia Due to Thrombin Defect 70 0.133
125
ALL026 Allergic Hypersensitivity Disease 68 0.133
126
PYR016 Pyridoxine Deficiency 39 0.132
127
LGH007 Leigh Syndrome 66 0.131
128
P SML038 Small Cell Cancer of the Lung 69 0.131
129
c ART021 Arteriosclerosis 61 0.130
130
CMM005 Common Cold 62 0.129
131
CNG034 Congestive Heart Failure 71 0.128
132
END030 End Stage Renal Failure 60 0.127
133
c PRP019 Peripheral Nervous System Disease 66 0.127
134
P FTT008 Fatty Liver Disease, Nonalcoholic 1 61 0.125
135
SKN016 Skin Disease 68 0.125
136
c ECL001 Eclampsia 59 0.125
137
P BTT014 Beta-Thalassemia 73 0.124
138
CNN005 Connective Tissue Disease 67 0.124
139
c MGL001 Megaloblastic Anemia 52 0.124
140
c BLD134 Bladder Cancer 71 0.124
141
DMN002 Dementia 69 0.124
142
HYP060 Hyperinsulinism 57 0.123
143
c MYP004 Myopathy 65 0.123
144
c HML002 Hemolytic Anemia 65 0.123
145
OST012 Osteoarthritis 81 0.123
146
CLT003 Colitis 65 0.123
147
c DRM053 Dermatitis, Atopic 73 0.122
148
c EPL164 Epilepsy 73 0.122
149
IMM136 Immune System Disease 57 0.122
150
BCT022 Bacterial Infectious Disease 63 0.121
151
P ACT075 Acute Myocardial Infarction 57 0.121
152
GST033 Gestational Diabetes 63 0.121
153
ADN018 Adenoma 65 0.121
154
BNR002 Bone Resorption Disease 54 0.121
155
SKN027 Skin Conditions 51 0.120
156
BSL036 Basal Cell Nevus Syndrome 68 0.120
157
GST071 Gastrointestinal Carcinoma 46 0.119
158
c INF032 Infertility 60 0.119
159
GST049 Gastrointestinal System Cancer 62 0.119
160
P CNG006 Congenital Hypothyroidism 64 0.119
161
c RTN024 Retinoblastoma 73 0.119
162
NNL002 Nonalcoholic Steatohepatitis 55 0.119
163
DFC004 Deficiency Anemia 65 0.119
164
WRN001 Werner Syndrome 74 0.119
165
P PRM005 Primary Hyperparathyroidism 60 0.118
166
HYP266 Hypoxia 63 0.118
167
c LYM031 Lymphocytic Leukemia 61 0.118
168
c OST001 Osteopetrosis 63 0.117
169
P MCR130 Microvascular Complications of Diabetes 6 43 0.117
170
TTN003 Tetanus 66 0.117
171
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 52 0.117
172
c RTN008 Retinitis Pigmentosa 79 0.117
173
c SCH015 Schizophrenia 73 0.117
174
P MCR113 Microvascular Complications of Diabetes 3 58 0.116
175
P MCR120 Microvascular Complications of Diabetes 7 46 0.116
176
P MCR133 Microvascular Complications of Diabetes 4 43 0.116
177
DSR002 Disorders of Intracellular Cobalamin Metabolism 17 0.116
178
MYL069 Myeloma, Multiple 85 0.116
179
P GLC092 Glaucoma, Primary Open Angle 58 0.115
180
IRN002 Iron Metabolism Disease 60 0.115
181
c DYS154 Dystonia 66 0.115
182
ACR006 Aceruloplasminemia 72 0.115
183
c ENC018 Encephalopathy 65 0.114
184
c HRD008 Hereditary Hemorrhagic Telangiectasia 61 0.113
185
P ATS007 Autism Spectrum Disorder 68 0.112
186
c TRC086 Trichohepatoenteric Syndrome 1 61 0.112
187
RSP006 Respiratory System Disease 64 0.112
188
ESP021 Esophageal Cancer 84 0.112
189
c DBT085 Diabetes Mellitus, Insulin-Dependent 73 0.112
190
CLN019 Colonic Disease 62 0.111
191
PLM001 Pulmonary Tuberculosis 74 0.111
192
THY028 Thyroid Cancer 72 0.111
193
GLB002 Glioblastoma 75 0.111
194
c ANR048 Aniridia 1 63 0.110
195
c ATS364 Autism 68 0.110
196
MNT002 Mental Depression 65 0.110
197
c ALP008 Alopecia 56 0.110
198
HYP066 Hyperglycemia 65 0.110
199
c DLT002 Dilated Cardiomyopathy 74 0.109
200
c SKN015 Skin Carcinoma 65 0.109
201
VSL002 Visual Epilepsy 33 0.109
202
CRB039 Cerebrovascular Disease 70 0.109
203
SLF012 Sulfite Oxidase Deficiency Due to Molybdenum Cofactor Deficiency 23 0.109
204
LPD008 Lipid Metabolism Disorder 65 0.109
205
MLR004 Malaria 85 0.108
206
P LRG017 Large Intestine Cancer 63 0.108
207
ATX019 Ataxia with Vitamin E Deficiency 34 0.108
208
P NMN015 Niemann-Pick Disease, Type C1 68 0.107
209
PHN003 Phenylketonuria 75 0.107
210
FND002 Fundus Dystrophy 51 0.107
211
c GLM045 Glioma 56 0.107
212
c NPH012 Nephrotic Syndrome 59 0.106
213
c HYP086 Hypothyroidism 66 0.106
214
c NRV007 Nervous System Disease 72 0.106
215
SPS003 Spastic Diplegia 49 0.105
216
GST045 Gastroenteritis 65 0.105
217
PLM129 Pulmonary Disease, Chronic Obstructive 75 0.105
218
CRY004 Cryoglobulinemia 50 0.105
219
c EXN002 Exanthem 62 0.104
220
RHM027 Rheumatic Disease 65 0.104
221
c LNG064 Lung Cancer Susceptibility 3 80 0.104
222
c HYP818 Hypobetalipoproteinemia, Familial, 1 51 0.103
223
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.103
224
c RTN016 Retinal Degeneration 56 0.103
225
c FRN006 Frontotemporal Dementia 69 0.103
226
c MNN013 Meningitis 71 0.103
227
GLC003 Glucose Intolerance 59 0.103
228
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 63 0.103
229
P ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 67 0.102
230
c FCL005 Focal Segmental Glomerulosclerosis 60 0.101
231
PRP030 Purpura 62 0.101
232
NPH009 Nephrolithiasis 58 0.101
233
LYM019 Lymphosarcoma 59 0.100
234
TXC005 Toxic Shock Syndrome 66 0.100
235
MSC157 Muscular Dystrophy, Duchenne Type 66 0.100
236
PLC008 Placenta Disease 59 0.100
237
P INF071 Inflammatory Bowel Disease 1 57 0.100
238
c THY032 Thyroiditis 54 0.100
239
c LCH002 Lichen Planus 59 0.100
240
c GST044 Gastritis 61 0.099
241
SRC014 Sarcoma 70 0.099
242
c NMN002 Niemann-Pick Disease 50 0.099
243
c BCL006 B-Cell Lymphomas 66 0.099
244
c PNC044 Pancreatitis 62 0.099
245
BRN106 Burns 59 0.098
246
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.098
247
WVR001 Weaver Syndrome 61 0.098
248
ULC004 Ulcerative Colitis 80 0.098
249
ANX010 Anxiety 73 0.098
250
c HYP609 Hypophosphatemic Rickets, X-Linked Dominant 60 0.098
251
P ATS013 Autosomal Recessive Congenital Ichthyosis 63 0.098
252
ABT001 Abetalipoproteinemia 67 0.098
253
PRD007 Periodontal Disease 66 0.097
254
BNG081 Benign Childhood Occipital Epilepsy, Panayiotopoulos Type 25 0.097
255
NPH091 Nephrolithiasis, Calcium Oxalate 54 0.097
256
LYM143 Lymphoma, Non-Hodgkin, Familial 74 0.097
257
RNL114 Renal Cell Carcinoma, Nonpapillary 63 0.097
258
c LFR001 Li-Fraumeni Syndrome 71 0.097
259
CLR108 Colorectal Adenoma 64 0.096
260
RNL065 Renal Cell Carcinoma, Papillary, 1 71 0.096
261
INT253 Intestinal Benign Neoplasm 57 0.096
262
PSY004 Psychotic Disorder 74 0.096
263
c NGH001 Night Blindness 50 0.096
264
P BNM022 Bone Mineral Density Quantitative Trait Locus 8 40 0.096
265
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 46 0.096
266
P AMY091 Amyotrophic Lateral Sclerosis 1 90 0.095
267
c FML018 Familial Mediterranean Fever 74 0.095
268
DSS008 Disease of Mental Health 70 0.095
269
c NJM001 Nijmegen Breakage Syndrome 70 0.095
270
BRS051 Breast Disease 68 0.095
271
RCT017 Rectal Disease 42 0.095
272
ANG054 Angina Pectoris 70 0.094
273
PNC033 Pancreas Adenocarcinoma 67 0.094
274
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 35 0.094
275
c HMR003 Hemorrhagic Disease 59 0.094
276
NRT004 Neuritis 58 0.094
277
c BLD051 Blood Coagulation Disease 51 0.093
278
P PRT132 Protoporphyria, Erythropoietic, 1 59 0.093
279
BRN028 Brain Cancer 74 0.093
280
MSL001 Measles 66 0.093
281
NRM005 Neuromuscular Disease 61 0.093
282
HMC014 Homocysteinemia 52 0.093
283
c HMC002 Homocystinuria 51 0.093
284
P ACT210 Acute Respiratory Distress Syndrome 66 0.093
285
c CRN037 Craniosynostosis 66 0.092
286
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.092
287
c LKM062 Leukemia, Acute Lymphoblastic 70 0.092
288
CRV035 Cervical Cancer 76 0.092
289
ERY029 Erythermalgia, Primary 58 0.091
290
c MSC033 Muscle Disorders 56 0.091
291
P CNT035 Central Nervous System Disease 65 0.091
292
P THR082 Thrombophilia Due to Activated Protein C Resistance 60 0.091
293
MYL009 Myelodysplastic Syndrome 71 0.091
294
IMM106 Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked 73 0.091
295
IRN001 Iron Deficiency Anemia 54 0.090
296
SCK005 Sickle Cell Disease 57 0.090
297
CLC006 Calcinosis 53 0.090
298
P ATM006 Autoimmune Lymphoproliferative Syndrome 71 0.090
299
c ACR001 Aicardi-Goutieres Syndrome 63 0.090
300
STM007 Stomatitis 53 0.090
301
P PNC106 Pancreatic Agenesis 1 52 0.090
302
c PTY003 Pityriasis Rubra Pilaris 52 0.090
303
c MTC003 Metachromatic Leukodystrophy 71 0.089
304
c NTR004 Neutropenia 61 0.089
305
P TRC078 Trichohepatoenteric Syndrome 2 35 0.089
306
PNC034 Pancreas Disease 60 0.089
307
LPD012 Lipoid Congenital Adrenal Hyperplasia 72 0.089
308
c CHN059 Chondrocalcinosis 47 0.089
309
P HYP595 Hypertension, Essential 77 0.089
310
P PRD040 Periodontitis, Chronic 60 0.089
311
c ART023 Arthropathy 68 0.089
312
c FML011 Familial Adenomatous Polyposis 72 0.088
313
P PRC031 Preeclampsia/eclampsia 1 41 0.088
314
LYM024 Lymphatic System Disease 55 0.088
315
STR067 Stroke, Ischemic 84 0.088
316
CNS004 Constipation 58 0.088
317
c PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 52 0.088
318
LNG031 Lung Benign Neoplasm 56 0.088
319
ATX010 Ataxia Neuropathy Spectrum 39 0.088
320
c HYP073 Hypersensitivity Reaction Type Iv Disease 51 0.088
321
c GRV001 Graves' Disease 61 0.088
322
BRN038 Bronchial Disease 58 0.087
323
HDC001 Headache 63 0.087
324
c GLM007 Glomerulonephritis 62 0.087
325
SQM013 Squamous Cell Carcinoma, Head and Neck 82 0.087
326
MTH009 Mouth Disease 66 0.087
327
c PSD087 Pseudoxanthoma Elasticum 68 0.086
328
CYS010 Cystinosis 55 0.086
329
CYS036 Cystinosis, Nephropathic 51 0.086
330
RTN023 Retinitis 48 0.086
331
JNT002 Joint Disorders 64 0.086
332
HLC007 Helicobacter Pylori Infection 66 0.086
333
c ABD014 Abdominal Obesity-Metabolic Syndrome 1 58 0.086
334
PLM134 Pulmonary Fibrosis, Idiopathic 74 0.086
335
P OVR114 Ovarian Cancer 1 66 0.086
336
c PRK057 Parkinson Disease, Late-Onset 77 0.086
337
c MCR115 Microvascular Complications of Diabetes 5 71 0.086
338
P RHB011 Rhabdoid Tumor Predisposition Syndrome 2 27 0.086
339
CHL068 Cholestasis 60 0.086
340
c VSC018 Visceral Steatosis 38 0.086
341
P MYT021 Myotonic Dystrophy 1 72 0.085
342
c HMP002 Hemophagocytic Lymphohistiocytosis 68 0.085
343
c VSC011 Vasculitis 67 0.085
344
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.085
345
GST040 Gastric Adenocarcinoma 66 0.085
346
P SPN225 Spondyloarthropathy 1 76 0.085
347
P LKM071 Leukemia, Chronic Lymphocytic 78 0.085
348
PRM236 Primary Biliary Cholangitis 63 0.085
349
LYM133 Lymphoma, Hodgkin, Classic 73 0.085
350
SPN186 Spinal Cord Injury 66 0.084
351
BLD131 Bladder Urothelial Carcinoma 62 0.084
352
SZR026 Seizures, Sensorineural Deafness, Ataxia, Mental Retardation, and Electrolyte Imbalance 59 0.084
353
MDD011 Mood Disorder 65 0.084
354
c HML033 Hemolytic Uremic Syndrome, Atypical 1 65 0.084
355
PLM033 Pulmonary Embolism 64 0.084
356
SCK003 Sickle Cell Anemia 75 0.084
357
c MDL005 Medulloblastoma 77 0.083
358
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 63 0.083
359
EPL131 Epilepsy, Pyridoxine-Dependent 38 0.083
360
c END044 Endometriosis 65 0.083
361
HLC001 Holocarboxylase Synthetase Deficiency 53 0.083
362
P ATS307 Autosomal Recessive Cerebellar Ataxia 28 0.083
363
P ALP106 Alport Syndrome 1, X-Linked 49 0.083
364
IRR002 Irritable Bowel Syndrome 64 0.083
365
MSC190 Muscular Disease 55 0.083
366
c RHN004 Rhinitis 63 0.083
367
c PRM006 Primary Biliary Cirrhosis 54 0.082
368
c CLC063 Celiac Disease 1 72 0.082
369
DST089 Distal Trisomy 3p 22 0.082
370
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 37 0.082
371
P BLR024 Biliary Cirrhosis, Primary, 1 39 0.082
372
BRK010 Burkitt Lymphoma 69 0.082
373
c PLY006 Polydactyly 58 0.082
374
CHN016 Cohen Syndrome 54 0.082
375
c HYP802 Hypocalcemia, Autosomal Dominant 1 66 0.081
376
RTN018 Retinal Disease 58 0.081
377
P MCP052 Mucopolysaccharidosis, Type Vi 62 0.081
378
c EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.081
379
DMY004 Demyelinating Disease 60 0.081
380
P EXD008 Exudative Vitreoretinopathy 1 73 0.081
381
BRR014 Barrett Esophagus 71 0.081
382
c SLP006 Sleep Apnea 70 0.081
383
HMT018 Hematopoietic Stem Cell Transplantation 59 0.081
384
SKN019 Skin Melanoma 67 0.081
385
c CLL015 Collagen Disease 52 0.080
386
c PRP029 Porphyria 60 0.080
387
P ATM011 Autoimmune Hepatitis 66 0.080
388
c PGT001 Paget's Disease of Bone 62 0.080
389
PRP080 Peripheral Artery Disease 56 0.080
390
P HMC039 Hemochromatosis, Type 1 74 0.080
391
PRT010 Parathyroid Carcinoma 65 0.080
392
P WLM018 Wilms Tumor 5 64 0.079
393
HMS001 Hemosiderosis 52 0.079
394
c GRF003 Graft-Versus-Host Disease 72 0.079
395
VSC008 Vascular Hemostatic Disease 45 0.079
396
c KRB001 Krabbe Disease 66 0.079
397
c NSP012 Nasopharyngeal Carcinoma 66 0.079
398
c THR015 Thrombophilia 56 0.079
399
CHD001 Chediak-Higashi Syndrome 67 0.079
400
c MSC005 Muscular Dystrophy 66 0.079
401
P LYN004 Lynch Syndrome I 59 0.079
402
URT039 Urticaria 60 0.079
403
BRN056 Bronchopulmonary Dysplasia 61 0.079
404
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 61 0.079
405
KRT019 Keratitis, Hereditary 63 0.079
406
FML063 Familial Glucocorticoid Deficiency 41 0.078
407
c MLN007 Male Infertility 52 0.078
408
c CRY007 Cryoglobulinemia, Familial Mixed 55 0.078
409
c BRT029 Brittle Cornea Syndrome 2 54 0.078
410
OPT006 Optic Nerve Disease 60 0.078
411
WLS001 Wilson Disease 71 0.078
412
P BRT028 Brittle Cornea Syndrome 1 29 0.078
413
PRX028 Peroxisomal Acyl-Coa Oxidase Deficiency 52 0.078
414
URM002 Uremia 53 0.078
415
ANR007 Anorexia Nervosa 68 0.078
416
c MJR001 Major Depressive Disorder 67 0.077
417
c ANG001 Angelman Syndrome 65 0.077
418
FRY006 Fryns Microphthalmia Syndrome 51 0.077
419
HYP056 Hypoglycemia 64 0.077
420
PFF001 Pfeiffer Syndrome 79 0.077
421
c ALP009 Alopecia Areata 68 0.077
422
HMG005 Hemoglobinopathy 54 0.077
423
P THR001 Thrombocytopenia Due to Platelet Alloimmunization 61 0.077
424
BNG080 Benign Childhood Occipital Epilepsy, Gastaut Type 19 0.077
425
ALP103 Alpha-1-Antitrypsin Deficiency 62 0.077
426
c OPN001 Open-Angle Glaucoma 53 0.077
427
TNG002 Tangier Disease 64 0.077
428
c ART106 Arterial Calcification, Generalized, of Infancy, 1 37 0.077
429
BRN071 Brain Injury 54 0.077
430
ALL014 Allergic Encephalomyelitis 43 0.077
431
APL001 Aplastic Anemia 75 0.076
432
MSC004 Muscle Tissue Disease 39 0.076
433
P ACT074 Acute Lymphocytic Leukemia 62 0.076
434
PRS042 Prostate Disease 47 0.076
435
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.076
436
FND001 Fundus Albipunctatus 56 0.076
437
SPR004 Supravalvular Aortic Stenosis 53 0.076
438
SLP005 Sleep Disorder 60 0.076
439
ATM052 Autoimmune Disease 1 41 0.076
440
DBT010 Diabetic Neuropathy 60 0.076
441
FBR047 Fibromyalgia 62 0.075
442
SPP011 Suppression of Tumorigenicity 12 62 0.075
443
c HMP007 Hemophilia 62 0.075
444
P LKM063 Leukemia, Chronic Myeloid 74 0.075
445
ALL003 Allergic Rhinitis 69 0.075
446
FSH001 Fish-Eye Disease 51 0.075
447
c PRM002 Primary Hyperoxaluria 54 0.075
448
c DMN001 Diamond-Blackfan Anemia 71 0.075
449
HYP017 Hypophosphatemia 48 0.075
450
THR100 Thrombocytopenic Purpura, Autoimmune 68 0.075
451
P MCP004 Mucopolysaccharidosis Iv 60 0.075
452
c MRQ003 Morquio Syndrome 32 0.075
453
PRT030 Parathyroid Gland Disease 51 0.075
454
c LTR001 Lateral Sclerosis 60 0.075
455
SPN051 Spondylitis 55 0.075
456
BRC012 Brucellosis 71 0.075
457
c TMR018 Tumoral Calcinosis, Hyperphosphatemic, Familial, 1 56 0.074
458
END035 Endocrine Gland Cancer 57 0.074
459
WLL001 Williams-Beuren Syndrome 64 0.074
460
TRN018 Transitional Cell Carcinoma 63 0.074
461
P VSC019 Vesicoureteral Reflux 1 58 0.074
462
CRH005 Crohn's Colitis 61 0.074
463
c AMY004 Amyloidosis 69 0.074
464
ENT011 Enterocolitis 55 0.074
465
DFF005 Diffuse Large B-Cell Lymphoma 58 0.073
466
P ACT071 Acute Kidney Failure 54 0.073
467
HMP009 Haemophilus Influenzae 51 0.073
468
P PNC128 Pain - Chronic 46 0.073
469
GLB015 Glioblastoma Multiforme 64 0.073
470
c SCL057 Scoliosis, Isolated 1 46 0.073
471
TRD006 Tardive Dyskinesia 61 0.073
472
MYL005 Myelofibrosis 70 0.073
473
INT002 Intermittent Claudication 64 0.073
474
P LBR014 Leber Congenital Amaurosis 4 55 0.073
475
ART001 Arterial Tortuosity Syndrome 59 0.073
476
MLR006 Male Reproductive Organ Cancer 50 0.073
477
P ERL029 Early-Onset, Autosomal Dominant Alzheimer Disease 60 0.072
478
PRP027 Peripheral Vascular Disease 72 0.072
479
MTC008 Mitochondrial Complex Iii Deficiency 32 0.072
480
ORL013 Oral Lichen Planus 53 0.072
481
c MYP006 Myopia 62 0.072
482
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 67 0.072
483
P CRD187 Cardiomyopathy, Dilated, 3b 48 0.072
484
BTN003 Biotinidase Deficiency 55 0.071
485
ADR007 Adrenoleukodystrophy 72 0.071
486
P PRM196 Premature Ovarian Failure 1 69 0.071
487
ACT118 Acute Non Lymphoblastic Leukemia 33 0.071
488
P ACT068 Acute Cystitis 56 0.071
489
c SBS003 Substance Abuse 61 0.071
490
OST097 Osteoporotic Fracture 36 0.071
491
PRT037 Pertussis 71 0.071
493
ALC007 Alcohol Dependence 70 0.071
494
P LKM004 Leukemia, B-Cell, Chronic 38 0.071
495
CD4003 Cd40 Ligand Deficiency 45 0.071
496
RLP002 Relapsing-Remitting Multiple Sclerosis 59 0.071
497
CHL065 Cholangiocarcinoma 65 0.071
498
c MSC007 Muscle Hypertrophy 64 0.071
499
FDL002 Food Allergy 54 0.071
500
CHL109 Childhood Apraxia of Speech 36 0.071
501
c CMR001 Camurati-Engelmann Disease 62 0.070
502
ART016 Aortic Aneurysm 71 0.070
503
c CRD119 Cardiac Arrest 66 0.070
504
P PSR017 Psoriasis 2 54 0.070
505
END057 Endometrial Cancer 69 0.070
506
P ATR087 Atrial Standstill 1 69 0.070
507
P GLY008 Glycogen Storage Disease Ii 67 0.070
508
c GNT009 Giant Axonal Neuropathy 52 0.070
509
P GNT049 Giant Axonal Neuropathy 1, Autosomal Recessive 43 0.070
510
FLT009 Folate Malabsorption, Hereditary 34 0.070
511
GRN017 Granulocytopenia 52 0.070
512
P MTR002 Mitral Valve Insufficiency 50 0.070
513
c ORT004 Orthostatic Intolerance 69 0.070
514
PHR003 Pharyngitis 58 0.070
515
LSH001 Leishmaniasis 72 0.070
516
c ESS003 Essential Thrombocythemia 70 0.070
517
PLM017 Pulmonary Alveolar Microlithiasis 52 0.070
518
THY030 Thyroid Gland Disease 51 0.070
519
c HYP076 Hyperthyroidism 56 0.070
520
c BDY004 Body Mass Index Quantitative Trait Locus 11 74 0.070
521
c RSP003 Respiratory Failure 72 0.069
522
P HYD046 Hydatidiform Mole, Recurrent, 1 56 0.069
523
PLS011 Plasmacytoma 62 0.069
524
OVR063 Overnutrition 53 0.069
525
GND003 Gonadal Disease 49 0.069
526
BRN080 Brain Ischemia 43 0.069
527
HYP458 Hyper Ige Syndrome 52 0.069
528
P INS002 in Situ Carcinoma 60 0.069
529
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 47 0.069
530
P SCL052 Scleroderma, Familial Progressive 68 0.068
531
GT001 Gout 62 0.068
532
ATH013 Atherosclerosis Susceptibility 61 0.068
533
P ACT027 Acute Pancreatitis 59 0.068
534
GYR004 Gyrate Atrophy of Choroid and Retina 51 0.068
535
MDL020 Midline Interhemispheric Variant of Holoprosencephaly 46 0.068
536
c PRP003 Porphyria Cutanea Tarda 67 0.068
537
ILT001 Ileitis 59 0.068
538
APH001 Aphthous Stomatitis 65 0.068
539
c OVR049 Ovarian Disease 63 0.068
540
P PRG126 Progressive Familial Heart Block 51 0.068
541
CRN239 Carnitine Deficiency, Systemic Primary 54 0.068
542
P HMP029 Hemophilia a 70 0.068
543
c RCT021 Rectum Cancer 58 0.068
544
LNG039 Lung Squamous Cell Carcinoma 62 0.068
545
c PLY019 Polyneuropathy 58 0.068
546
c KBK002 Kabuki Syndrome 1 67 0.067
547
PRD004 Prediabetes Syndrome 51 0.067
548
LYM067 Lymphoid Leukemia 47 0.067
549
BRN039 Bronchial Neoplasm 43 0.067
550
P HYP794 Hyperoxaluria, Primary, Type I 43 0.067
551
P SZR007 Seizures, Benign Familial Infantile, 3 46 0.067
552
c ART153 Arthrochalasia Ehlers-Danlos Syndrome 22 0.067
553
CMP010 Complex Regional Pain Syndrome 64 0.067
554
CRD223 Cardiac Arrhythmia 56 0.067
555
c RTT002 Rett Syndrome 83 0.067
556
TRN015 Transient Cerebral Ischemia 59 0.066
557
DNN002 Donnai-Barrow Syndrome 55 0.066
558
DPH001 Diphtheria 63 0.066
559
EWN002 Ewing's Family of Tumors 57 0.066
560
P MGR028 Migraine with or Without Aura 1 69 0.066
561
MCS002 Mucositis 60 0.066
562
c BPL003 Bipolar Disorder 61 0.066
563
OVR094 Ovarian Epithelial Cancer 41 0.066
564
ACY010 Acyl-Coa Dehydrogenase, Very Long-Chain, Deficiency of 60 0.066
565
P CNG027 Congenital Hemolytic Anemia 52 0.066
566
c MSC003 Muscular Atrophy 56 0.066
567
ACN002 Acanthosis Nigricans 65 0.066
568
SPP010 Suppressor of Tumorigenicity 3 60 0.066
569
c AST007 Astrocytoma 51 0.066
570
c ATT013 Attention Deficit-Hyperactivity Disorder 67 0.065
571
HYP810 Hypereosinophilic Syndrome, Idiopathic 60 0.065
572
c ALC004 Alcohol Abuse 69 0.065
573
HYP348 Hyperglycinuria 36 0.065
574
c SZR006 Seizure Disorder 61 0.065
575
PRM050 Primary Orthostatic Tremor 34 0.065
576
HPD002 Hepadnavirus Infection 25 0.065
577
c VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 65 0.065
578
BTT001 Bietti Crystalline Corneoretinal Dystrophy 46 0.065
579
c PRG047 Progressive Familial Intrahepatic Cholestasis 56 0.065
580
P SVR003 Severe Congenital Neutropenia 58 0.065
581
PNG002 Pain Agnosia 54 0.065
582
PRS129 Prostatic Hyperplasia, Benign 53 0.065
583
FBR012 Fabry Disease 72 0.064
584
c ATR005 Atrophic Gastritis 49 0.064
585
TRN022 Transcobalamin Ii Deficiency 48 0.064
586
P ART138 Aortic Aneurysm, Familial Abdominal, 1 66 0.064
587
GLC006 Galactosemia 65 0.064
588
DST081 Distal Trisomy 11q 20 0.064
589
PRP001 Propionic Acidemia 61 0.064
590
NWB001 Newborn Respiratory Distress Syndrome 61 0.064
591
NRN004 Neuroendocrine Tumor 56 0.064
592
c KDN017 Kidney Cancer 59 0.064
593
P MGL018 Megaloblastic Anemia 1 46 0.064
594
DWN001 Down Syndrome 72 0.064
595
c MYC084 Mycobacterium Tuberculosis 1 68 0.064
596
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 45 0.064
597
DNT012 Dental Caries 52 0.064
598
NPH003 Nephrocalcinosis 51 0.064
599
ORL015 Oral Squamous Cell Carcinoma 48 0.064
600
PRN019 Perinatal Necrotizing Enterocolitis 58 0.064
601
c ADL010 Adult Respiratory Distress Syndrome 64 0.063
602
c NRN021 Neuronal Ceroid Lipofuscinosis 62 0.063
603
RGD002 Rigidity and Multifocal Seizure Syndrome, Lethal Neonatal 40 0.063
604
THR013 Thoracic Outlet Syndrome 57 0.063
605
c SLL003 Salla Disease 53 0.063
606
c SCL018 Scoliosis 59 0.063
607
c SYP003 Syphilis 58 0.063
608
BLD044 Bladder Disease 57 0.063
609
OST159 Osteogenic Sarcoma 67 0.063
610
CRB011 Cerebrotendinous Xanthomatosis 65 0.063
611
HSH003 Hashimoto Thyroiditis 67 0.063
612
P CRP023 Carpenter Syndrome 1 59 0.063
613
c PNS012 Paine Syndrome 63 0.063
614
P HYP752 Hypocalciuric Hypercalcemia, Familial, Type I 42 0.063
615
P PNC108 Pancreatitis, Hereditary 61 0.062
616
c HYP035 Hypophosphatasia 58 0.062
617
PRM020 Premenstrual Tension 53 0.062
618
c GLM040 Glioma Susceptibility 1 64 0.062
619
KRT009 Keratosis 55 0.062
620
c HYP111 Hyperprolinemia 35 0.062
621
c RST001 Restless Legs Syndrome 60 0.062
622
c ENC004 Encephalitis 66 0.062
623
P HYP798 Hypophosphatemic Rickets, X-Linked Recessive 63 0.062
624
c VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 37 0.062
625
PRT038 Protein-Energy Malnutrition 53 0.062
626
RSP007 Respiratory Distress Syndrome, Infant 38 0.062
627
c OVR046 Ovarian Cyst 52 0.062
628
ERY003 Erythema Multiforme 63 0.062
629
CYT002 Cytokine Deficiency 39 0.062
630
P HMP004 Hemophilia B 67 0.062
631
FCT002 Factor Xi Deficiency 63 0.062
632
DRR014 Darier-White Disease 62 0.062
633
c FBR017 Fibrosarcoma 61 0.062
634
CRB169 Cerebellar Atrophy, Developmental Delay, and Seizures 46 0.062
635
CRV045 Cervical Intraepithelial Neoplasia 45 0.062
636
c SCK002 Sick Sinus Syndrome 54 0.062
637
c DNT020 Dent Disease 1 60 0.062
638
GLL008 Gilles De La Tourette Syndrome 69 0.061
639
SMT004 Smith-Lemli-Opitz Syndrome 69 0.061
640
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 50 0.061
641
c TYR004 Tyrosinemia 49 0.061
642
DRL001 Dural Sinus Malformation 23 0.061
643
OCL006 Ocular Hypertension 56 0.061
644
c HRP006 Herpes Simplex 71 0.061
645
P ATS347 Autosomal Dominant Polycystic Kidney Disease 61 0.061
646
MVM001 Movement Disease 67 0.061
647
c ALG028 Alagille Syndrome 1 71 0.061
648
BRN002 Bronchiolitis 62 0.061
650
HRN028 Horns in Sheep 24 0.061
651
PRT036 Peritonitis 67 0.061
652
BRT054 Brittle Bone Disorder 71 0.061
653
IMP005 Impotence 58 0.061
654
c CRB048 Cerebral Cavernous Malformations 65 0.061
655
c UVT001 Uveitis 62 0.061
656
END040 Endogenous Depression 59 0.061
657
P WLM013 Wilms Tumor 1 68 0.061
658
c CHR012 Chronic Granulomatous Disease 70 0.061
659
PLC007 Placental Abruption 51 0.061
660
RSS026 Roussy-Levy Hereditary Areflexic Dystasia 48 0.061
661
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 45 0.061
662
CRP001 Carpal Tunnel Syndrome 72 0.061
663
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 65 0.061
664
HML018 Homologous Wasting Disease 25 0.060
665
THY111 Thyroid Carcinoma, Familial Medullary 71 0.060
666
OVR012 Ovarian Serous Cystadenocarcinoma 52 0.060
667
P HYP793 Hypertrophic Osteoarthropathy, Primary, Autosomal Recessive, 1 41 0.060
668
PST011 Pustulosis of Palm and Sole 50 0.060
669
c CHR084 Chromosomal Disease 40 0.060
670
MST005 Mastitis 57 0.060
671
PNC041 Pancreatic Ductal Adenocarcinoma 54 0.060
672
BRN024 Bronchitis 70 0.060
673
BLD054 Blood Protein Disease 43 0.060
674
c ANT006 Antiphospholipid Syndrome 60 0.060
675
P PSR028 Psoriasis 7 43 0.060
676
P PSR032 Psoriasis 11 43 0.060
677
P PSR018 Psoriasis 13 42 0.060
678
NTR027 Neutrophil Actin Dysfunction 32 0.060
679
ORL011 Oral Cancer 60 0.060
680
GTR002 Goiter 54 0.060
681
P HMG001 Hemoglobin C Disease 43 0.060
682
CLN015 Colon Adenocarcinoma 57 0.060
683
c GCH001 Gaucher's Disease 66 0.060
684
c TYS001 Tay-Sachs Disease 70 0.060
685
MTC005 Mitochondrial Metabolism Disease 46 0.060
686
INC002 Inclusion Body Myositis 64 0.060
687
MTC027 Mitochondrial Trifunctional Protein Deficiency 55 0.059
688
MRB003 Morbid Obesity 62 0.059
689
P CHR579 Chiari Malformation Type Ii 49 0.059
690
APN008 Apnea, Obstructive Sleep 68 0.059
691
FCT007 Factor Vii Deficiency 61 0.059
692
CHL123 Chlamydia 66 0.059
693
c VTL001 Vitelliform Macular Dystrophy 43 0.059
694
RFS006 Refsum Disease, Classic 63 0.059
695
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 38 0.059
696
P FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 41 0.059
697
c CNG003 Congenital Dyserythropoietic Anemia 42 0.059
698
c PLY018 Polycythemia 60 0.059
699
CHR066 Chronic Fatigue Syndrome 68 0.059
700
c SHR001 Short Bowel Syndrome 52 0.058
701
c PLM036 Pulmonary Fibrosis 70 0.058
702
c TRM003 Tremor 56 0.058
703
SPN041 Spinal Cord Disease 55 0.058
704
HYP080 Hypogonadism 53 0.058
705
c HYP599 Hypoparathyroidism, Familial Isolated 37 0.058
706
INT007 Intermediate Coronary Syndrome 50 0.058
707
P MCL013 Mucolipidosis Iv 59 0.058
708
c ACT232 Acute Necrotizing Encephalopathy 30 0.058
709
BLD137 Blood Group--Ahonen 21 0.058
710
c RTN022 Retinal Vein Occlusion 54 0.058
711
c HYP058 Hypervitaminosis a 48 0.058
712
P ACT134 Acute Liver Failure 53 0.058
713
LMY014 Leiomyoma, Uterine 57 0.058
714
c AXN002 Axenfeld-Rieger Syndrome 62 0.058
715
P ATS406 Autosomal Recessive Pyridoxine-Refractory Sideroblastic Anemia 2 37 0.058
716
GNG013 Gingivitis 63 0.058
717
LYM040 Lymphoblastic Lymphoma 58 0.058
718
CYS013 Cystinuria 65 0.057
719
c PRT013 Portal Hypertension 61 0.057
720
STT009 Sutton Disease 2 32 0.057
721
P BCT007 Bacterial Meningitis 61 0.057
722
DSS009 Disseminated Intravascular Coagulation 58 0.057
723
PLY001 Polycythemia Vera 76 0.057
724
ACT058 Active Peptic Ulcer Disease 53 0.057
725
OTT002 Otitis Media 68 0.057
726
P BSL007 Basal Cell Carcinoma 65 0.057
727
HRP008 Herpes Simiae 16 0.057
728
CNT047 Contact Dermatitis 64 0.057
729
P ART101 Aortic Valve Disease 2 68 0.057
730
OST003 Osteonecrosis 67 0.057
731
NWC001 Newcastle Disease 53 0.057
732
c CHR071 Charcot-Marie-Tooth Disease 65 0.057
733
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.057
734
ISL003 Isolated Growth Hormone Deficiency 53 0.057
735
c MTC133 Mitochondrial Myopathy 52 0.057
736
PYR015 Pyridoxal 5'-Phosphate-Dependent Epilepsy 17 0.057
737
BLR001 Biliary Atresia 57 0.057
738
LMY002 Leiomyoma 58 0.056
739
PNC001 Pancytopenia 53 0.056
740
c PLM037 Pulmonary Hypertension 77 0.056
741
HMC016 Homocystinuria Due to Cbs Deficiency 24 0.056
742
GLC022 Glucose/galactose Malabsorption 44 0.056
743
RPD005 Rapidly Involuting Congenital Hemangioma 24 0.056
744
PRT014 Protein S Deficiency 46 0.056
745
P LKM056 Leukemia, Chronic Lymphocytic 2 43 0.056
746
DGS002 Degos 'en Cocarde' Erythrokeratoderma 26 0.056
747
BRN139 Brain Small Vessel Disease 1 with or Without Ocular Anomalies 36 0.056
748
DYS073 Dysphagia 53 0.056
749
APP008 Appendicitis 66 0.056
751
CRD220 Cardiac Valvular Defect, Developmental 36 0.056
752
BRB001 Beriberi 43 0.056
753
ALC006 Alcoholic Hepatitis 62 0.056
754
PST021 Postpartum Depression 55 0.056
755
c OPT009 Optic Neuritis 55 0.056
756
STH001 Saethre-Chotzen Syndrome 64 0.056
757
c MYS005 Myositis 62 0.056
759
VRC005 Varicose Veins 67 0.055
760
PRT082 Preterm Premature Rupture of the Membranes 57 0.055
761
P PLY105 Polycystic Ovary Syndrome 1 43 0.055
762
c PSD015 Pseudohypoparathyroidism 51 0.055
763
PHT003 Phototoxic Dermatitis 44 0.055
764
c FLL037 Follicular Lymphoma 71 0.055
765
PSR001 Psoriatic Arthritis 68 0.055
766
PLY112 Polyarteritis Nodosa, Childhood-Onset 51 0.055
767
MYL031 Myeloproliferative Neoplasm 64 0.055
768
TRM010 Traumatic Brain Injury 56 0.055
769
ACT119 Acute Promyelocytic Leukemia 61 0.055
770
c PLY041 Polymyositis 59 0.055
771
PRS063 Paresthesia 45 0.055
772
P EHL078 Ehlers-Danlos Syndrome, Kyphoscoliotic Type, 1 45 0.055
773
CHR074 Choriocarcinoma 50 0.055
774
FNC005 Functional Colonic Disease 29 0.055
775
c PRC017 Precursor Lymphoblastic Lymphoma/leukemia 30 0.055
776
ASP002 Aspartylglucosaminuria 56 0.055
777
P AMG001 Amegakaryocytic Thrombocytopenia, Congenital 49 0.055
778
MCR017 Macrocytic Anemia 46 0.055
779
HYP005 Hypokalemia 56 0.055
780
CRT016 Carotid Artery Disease 58 0.055
781
c CRD132 Cardiac Conduction Defect 64 0.054
782
c FML068 Familial Hypocalciuric Hypercalcemia 50 0.054
783
P SVR005 Severe Pre-Eclampsia 55 0.054
784
P MSC169 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 1 48 0.054
785
c PLY014 Polycystic Kidney Disease 63 0.054
786
SCH014 Schistosomiasis 62 0.054
787
CHR619 Chromosome 2q35 Duplication Syndrome 58 0.054
788
ALP012 Alpha-Methylacyl-Coa Racemase Deficiency 49 0.054
789
c SNS014 Sinusitis 64 0.054
790
c KRT007 Keratoconus 50 0.054
791
PRP056 Porphyria, Acute Hepatic 47 0.054
792
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 29 0.054
793
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.054
794
DHY002 Dihydropyrimidine Dehydrogenase Deficiency 57 0.054
795
P HYP543 Hypoplastic Left Heart Syndrome 1 44 0.054
796
INT079 Intrahepatic Cholangiocarcinoma 55 0.054
797
MTR014 Motor Neuron Disease 60 0.054
798
c DNG005 Dengue Virus 64 0.054
799
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 29 0.053
800
P STR084 Stargardt Disease 1 54 0.053
801
ATR013 Atrichia with Papular Lesions 42 0.053
802
RHM001 Rheumatic Fever 63 0.053
804
c DYS021 Dysautonomia 49 0.053
805
CLF027 Cleft Palate, Isolated 66 0.053
806
HRP004 Herpes Zoster 63 0.053
807
HDN002 Head Injury 52 0.053
808
MTH078 Methylmalonic Aciduria, Cblb Type 40 0.053
809
P ACT073 Acute Leukemia 62 0.053
810
c JVN024 Juvenile Hereditary Hemochromatosis 44 0.053
811
LNG073 Long-Chain 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 60 0.053
812
c LCT001 Lactic Acidosis 53 0.053
813
CYS019 Cystathioninuria 42 0.053
814
TXC002 Toxic Encephalopathy 57 0.053
815
c SRC025 Sarcoidosis 1 76 0.053
816
ALL010 Allergic Contact Dermatitis 61 0.053
817
SXL003 Sexual Disorder 53 0.053
818
HRT012 Heart Valve Disease 57 0.053
819
CYT017 Cytophagic Histiocytic Panniculitis 26 0.053
820
P JVN010 Juvenile Rheumatoid Arthritis 72 0.053
821
GST092 Gastroesophageal Reflux 66 0.052
822
CRN024 Corneal Disease 45 0.052
823
c SPN046 Spinal Muscular Atrophy 65 0.052
824
IDP070 Idiopathic Scoliosis 38 0.052
825
RST011 Restrictive Dermopathy, Lethal 45 0.052
826
c PRS038 Personality Disorder 68 0.052
827
BSL008 Basal Ganglia Disease 49 0.052
828
CRB045 Cerebellar Hypoplasia 50 0.052
829
MTB004 Metabolic Acidosis 51 0.052
830
c LCT002 Lactose Intolerance 47 0.052
831
VSC002 Vascular Dementia 58 0.052
832
AND002 Androgen Insensitivity Syndrome 62 0.052
833
ALC009 Alcoholic Liver Cirrhosis 52 0.052
834
BRN004 Brain Edema 59 0.052
835
SWL001 Swallowing Disorders 36 0.052
836
WST001 West Syndrome 60 0.052
837
OBS002 Obsessive-Compulsive Disorder 69 0.052
838
INT146 Intervertebral Disc Disease 65 0.052
839
PRD013 Periodic Fever, Familial, Autosomal Dominant 64 0.052
840
MCK007 Muckle-Wells Syndrome 64 0.051
841
c ERY053 Erythrokeratodermia Variabilis Et Progressiva 1 52 0.051
842
TTH006 Tooth Disease 54 0.051
843
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 55 0.051
844
CHC001 Chickenpox 50 0.051
845
ATN002 Autonomic Nervous System Disease 54 0.051
846
INT075 Intracranial Hypertension 58 0.051
847
URN022 Urinary Tract Infections, Recurrent 34 0.051
848
SNS003 Sensory Peripheral Neuropathy 56 0.051
849
c ORF002 Orofacial Cleft 40 0.051
850
LKP003 Leukoplakia 43 0.051
851
c NRV006 Nervous System Cancer 60 0.051
852
CNN004 Connective Tissue Cancer 46 0.051
853
P MTC061 Mitochondrial Dna Depletion Syndrome 1 46 0.051
854
ALL006 Allergic Asthma 61 0.051
855
IGG001 Iga Glomerulonephritis 58 0.051
856
DGN001 Degenerative Disc Disease 51 0.051
858
RBR001 Roberts Syndrome 56 0.051
859
c SML001 Small Cell Carcinoma 61 0.051
860
P JVN004 Juvenile Myelomonocytic Leukemia 70 0.051
861
ARM001 Aromatase Deficiency 52 0.051
862
KPS004 Kaposi Sarcoma 77 0.051
863
KWS002 Kawasaki Disease 72 0.051
864
PRV006 Pervasive Developmental Disorder 56 0.050
865
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 21 0.050
866
P ART115 Aortic Valve Disease 1 70 0.050
867
NSD001 Nose Disease 52 0.050
868
P DPH024 Diaphragmatic Hernia, Congenital 66 0.050
869
GRW007 Growth Hormone Deficiency 53 0.050
870
c PRP034 Purpura Fulminans 46 0.050
871
NRR001 Neuroretinitis 48 0.050
872
ADN011 Adenoid Cystic Carcinoma 67 0.050
873
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 32 0.050
874
P ACT135 Acute Graft Versus Host Disease 58 0.050
875
c MCR010 Microcephaly 59 0.050
876
c CNJ013 Conjunctivitis 65 0.050
877
P CRD089 Cardiomyopathy, Familial Hypertrophic, 14 23 0.050
878
c AGG001 Aggressive Periodontitis 56 0.050
879
P HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 56 0.050
880
c SJG008 Sjogren Syndrome 60 0.050
881
CRV040 Cervix Carcinoma 53 0.050
882
EMB004 Embryonal Carcinoma 60 0.050
883
CHR005 Chorioamnionitis 53 0.050
884
FXF002 Fox-Fordyce Disease 41 0.050
885
c THR005 Thrombotic Thrombocytopenic Purpura 65 0.050
886
P USH036 Usher Syndrome, Type I 60 0.050
887
ACT088 Acute Insulin Response 50 0.050
888
c PYL005 Pyelonephritis 57 0.050
889
VCC001 Vaccinia 52 0.050
890
OVR029 Ovarian Hyperstimulation Syndrome 65 0.050
891
DBT002 Diabetic Autonomic Neuropathy 46 0.049
892
PPL022 Papilloma 58 0.049
893
SPH010 Sphingolipidosis 50 0.049
894
INT066 Interstitial Lung Disease 65 0.049
895
c ACT008 Actinic Keratosis 55 0.049
896
GNR004 Generalized Anxiety Disorder 55 0.049
897
MNS002 Mini Stroke 25 0.049
898
P MLG068 Malignant Glioma 47 0.049
899
SYN036 Syncope 49 0.049
900
c OCL013 Oculodentodigital Dysplasia 59 0.049
901
P MYT029 Myotonia Congenita, Autosomal Recessive 38 0.049
902
BCT002 Bacterial Vaginosis 56 0.049
903
P MCR129 Microvascular Complications of Diabetes 1 66 0.049
904
c HYP014 Hyperuricemia 56 0.049
905
c SNS001 Sensorineural Hearing Loss 60 0.049
906
c DBT005 Diabetes Insipidus 55 0.049
907
BWN003 Bowenoid Papulosis 43 0.049
908
INT088 Intrinsic Factor Deficiency 36 0.049
909
c TCL004 T-Cell Leukemia 53 0.049
910
HMT002 Hematologic Cancer 64 0.049
911
THR004 Thrombocytosis 55 0.049
912
c CYT020 Cytomegalic Congenital Adrenal Hypoplasia 25 0.049
913
c CHR285 Chronic Myelomonocytic Leukemia 65 0.049
914
LWC002 Lowe Oculocerebrorenal Syndrome 67 0.049
915
DYS014 Dyspepsia 56 0.048
916
AMN002 Amino Acid Metabolic Disorder 49 0.048
918
BLR008 Bilirubin Metabolic Disorder 53 0.048
919
SPN369 Spinal Disease 47 0.048
920
SCR035 Sacral Agenesis with Vertebral Anomalies 40 0.048
921
CYT008 Cytomegalovirus Infection 61 0.048
922
STM006 Stomach Disease 56 0.048
923
PLM031 Poliomyelitis 61 0.048
924
P BDY020 Body Mass Index Quantitative Trait Locus 19 43 0.048
925
P BDY019 Body Mass Index Quantitative Trait Locus 18 43 0.048
926
P BDY017 Body Mass Index Quantitative Trait Locus 14 41 0.048
927
P BDY011 Body Mass Index Quantitative Trait Locus 10 41 0.048
928
P THY109 Thyroid Cancer, Nonmedullary, 1 60 0.048
929
c DYS007 Dyskeratosis Congenita 67 0.048
930
c PMP001 Pemphigus 56 0.048
931
AMN012 Aminoacidopathies 25 0.048
932
c TTR001 Tetralogy of Fallot 71 0.048
933
P BNG091 Benign Chronic Pemphigus 54 0.048
934
c CYS018 Cystitis 58 0.048
935
CRB085 Cerebral Hemorrhage 46 0.048
936
SFT003 Soft Tissue Sarcoma 60 0.048
937
CMM004 Common Variable Immunodeficiency 71 0.048
938
c ASP006 Aspergillosis 67 0.048
939
c ESP024 Esophagitis 62 0.048
940
SPC010 Speech and Communication Disorders 51 0.048
941
MTH021 Methylmalonic Acidemia with Homocystinuria 39 0.048
942
CLR030 Clear Cell Renal Cell Carcinoma 49 0.048
943
RDN004 Radin Blood Group Antigen 29 0.048
944
HYP025 Hyperphosphatemia 49 0.048
945
ARB001 Ariboflavinosis 40 0.048
946
ACT103 Acute Lymphoblastic Leukemia, Childhood 55 0.048
947
P CNT016 Central Retinal Vein Occlusion 50 0.047
948
P MCL066 Macular Dystrophy, Vitelliform, 2 44 0.047
949
PYG003 Pyogenic Sterile Arthritis, Pyoderma Gangrenosum, and Acne 38 0.047
950
P MNN047 Mannosidosis, Alpha B, Lysosomal 58 0.047
951
P MLG079 Malignant Pleural Mesothelioma 45 0.047
952
ACR007 Acromegaly 71 0.047
953
PLM010 Pulmonary Edema 60 0.047
954
INB001 Inborn Amino Acid Metabolism Disorder 16 0.047
955
BLD053 Blood Platelet Disease 56 0.047
956
c OBS001 Obstructive Jaundice 54 0.047
957
GLM004 Gliomatosis Cerebri 58 0.047
958
RFR003 Refractive Error 46 0.047
959
P PTT056 Pituitary Adenoma 1, Multiple Types 51 0.047
960
LKC009 Leukocyte Adhesion Deficiency, Type I 61 0.047
961
FCT001 Factor Viii Deficiency 56 0.047
962
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.047
963
LPD009 Lipid Storage Disease 53 0.047
964
c CHL066 Cholangitis 52 0.047
965
SNS008 Sensory Ataxic Neuropathy, Dysarthria, and Ophthalmoparesis 51 0.047
966
MNT001 Mantle Cell Lymphoma 75 0.047
967
SDD001 Sudden Infant Death Syndrome 63 0.047
968
HMR039 Hemorrhage, Intracerebral 62 0.047
969
DBF001 D-Bifunctional Protein Deficiency 56 0.047
970
P ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 23 0.047
971
INT303 Intracranial Hypertension, Idiopathic 53 0.047
972
P CHL119 Cholangitis, Primary Sclerosing 63 0.047
973
ESP023 Esophageal Disease 59 0.047
974
P MCR112 Microvascular Complications of Diabetes 2 42 0.047
975
DBT084 Diabetes Mellitus, Ketosis-Prone 62 0.047
976
P VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 65 0.047
977
SCH012 Schizoaffective Disorder 54 0.046
978
CHY002 Chylomicron Retention Disease 53 0.046
979
EPD015 Epidemic Typhus 52 0.046
980
HYP064 Hypogonadotropism 42 0.046
981
KLD001 Keloids 51 0.046
982
c DYS193 Dystonia 11, Myoclonic 56 0.046
983
P GCH015 Gaucher Disease, Type I 65 0.046
984
CNC002 Cinca Syndrome 65 0.046
985
PRS034 Parasitic Helminthiasis Infectious Disease 51 0.046
986
VSC003 Visceral Leishmaniasis 61 0.046
987
c RHB008 Rhabdoid Tumor Predisposition Syndrome 1 57 0.046
988
MCL006 Macular Retinal Edema 55 0.046
989
CLN045 Colonic Benign Neoplasm 48 0.046
990
RFL001 Reflex Sympathetic Dystrophy 55 0.046
991
P CRD086 Cardiomyopathy, Familial Hypertrophic, 1 59 0.046
992
MYC006 Mycosis Fungoides 74 0.046
993
PRS047 Prostatitis 57 0.046
994
P HPT007 Hepatitis E 56 0.046
995
c ANP001 Anaplastic Large Cell Lymphoma 60 0.046
996
DRY001 Dry Eye Syndrome 53 0.046
997
c BRS044 Breast Adenocarcinoma 60 0.046
998
CLR109 Colorectal Adenocarcinoma 54 0.046
999
c AGM019 Agammaglobulinemia, X-Linked 73 0.046
1000
c CTN003 Cutaneous Lupus Erythematosus 55 0.046
1001
AZS001 Azoospermia 47 0.046
1002
CRB037 Cerebral Palsy 71 0.045
1003
MTH077 Methylmalonic Aciduria, Cbla Type 30 0.045
1004
LYS002 Lysosomal Storage Disease 56 0.045
1005
c EPD009 Epidermolysis Bullosa Dystrophica 58 0.045
1006
GLY022 Glyceraldehyde-3-Phosphate Dehydrogenase Deficiency 30 0.045
1007
KRT006 Keratoconjunctivitis 55 0.045
1008
DBT008 Diabetic Angiopathy 48 0.045
1009
c ATS366 Autism X-Linked 2 45 0.045
1010
ALG001 Algoneurodystrophy 40 0.045
1011
c HYD006 Hydrocephalus 66 0.045
1012
EPD002 Epidermolytic Hyperkeratosis 56 0.045
1013
MYM001 Myoma 57 0.045
1014
P ALP101 Alpha-Thalassemia 61 0.045
1015
c MYC008 Myocarditis 59 0.045
1016
c HML001 Hemolytic-Uremic Syndrome 55 0.045
1017
c ATS411 Autosomal Dominant Epidermolytic Ichthyosis 35 0.045
1018
SND001 Sandhoff Disease 66 0.045
1019
MMM001 Mammary Paget's Disease 56 0.045
1020
MLT157 Multiple System Atrophy 1 73 0.045
1021
MMM006 Mammographic Density 47 0.045
1022
DYS015 Dysentery 45 0.045
1023
LRG015 Large Intestine Adenoma 17 0.045
1024
PPT005 Peptic Ulcer Disease 64 0.045
1025
SYS003 Systolic Heart Failure 46 0.045
1026
GLT007 Glutathione Synthetase Deficiency 46 0.045
1027
THM002 Thiamine-Responsive Megaloblastic Anemia Syndrome 47 0.045
1028
P MSC171 Muscular Dystrophy, Limb-Girdle, Autosomal Recessive 5 39 0.045
1029
c ICH004 Ichthyosis 57 0.045
1030
NSS002 Neisseria Meningitidis Infection 51 0.045
1031
BRN022 Bronchiectasis 58 0.045
1032
P PYR010 Peyronie's Disease 55 0.044
1033
c MYS003 Myasthenia Gravis 74 0.044
1034
DCT002 Ductal Carcinoma in Situ 58 0.044
1035
OST017 Osteomyelitis 65 0.044
1036
PRP036 Peripheral T-Cell Lymphoma 57 0.044
1037
CLF001 Cleft Lip 56 0.044
1038
c HRD018 Hair Disease 50 0.044
1039
SBC017 Sebaceous Gland Disease 45 0.044
1040
TRD008 Triiodothyronine Receptor Auxiliary Protein 27 0.044
1041
PCK003 Pick Disease of Brain 66 0.044
1042
P RTN162 Retinitis Pigmentosa 2 52 0.044
1043
PRT035 Peritoneum Cancer 47 0.044
1044
FLL027 Fallopian Tube Carcinoma 64 0.044
1045
P MJR004 Major Affective Disorder 4 40 0.044
1046
P CRB175 Cerebral Arteriopathy, Autosomal Dominant, with Subcortical Infarcts and Leukoencephalopathy, Type 1 69 0.044
1047
INT323 Intraocular Pressure Quantitative Trait Locus 38 0.044
1048
SPN404 Spinal and Bulbar Muscular Atrophy, X-Linked 1 62 0.044
1049
PLS007 Plasmodium Falciparum Malaria 58 0.044
1050
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 49 0.044
1051
c CND004 Candidiasis 63 0.044
1052
HPT082 Hepatic Adenomas, Familial 49 0.044
1053
ADP007 Adie Pupil 43 0.044
1054
HNM002 Hinman Syndrome 29 0.044
1055
c INT070 Intestinal Obstruction 55 0.044
1056
THR016 Thrombophlebitis 54 0.044
1057
CRT013 Carotid Stenosis 52 0.044
1058
HNS001 Hansen's Disease 36 0.044
1059
CHL014 Cholera 61 0.044
1060
c TMP003 Temporal Arteritis 68 0.044
1061
CHL067 Cholecystitis 59 0.044
1062
MYF001 Myofibroma 38 0.044
1063
c MNC007 Monocytic Leukemia 57 0.044
1064
CRN030 Coronary Stenosis 52 0.044
1065
IRN004 Iron-Refractory Iron Deficiency Anemia 42 0.044
1066
c BRN035 Brain Stem Glioma 52 0.043
1067
c UTR058 Uterine Anomalies 60 0.043
1068
NRF026 Neurofibromatosis, Type Iv, of Riccardi 76 0.043
1069
c FRG001 Fragile X Syndrome 70 0.043
1070
c ANG015 Angioedema 58 0.043
1071
DFF036 Differentiated Thyroid Carcinoma 55 0.043