Search results for Vitamin C

3280 hits were found for Vitamin C

# Family MCID Name MIFTS Score
1
HYP781 Hypoascorbemia 51 4.731
2
MTH054 Methylmalonic Aciduria and Homocystinuria, Cblc Type 54 3.602
3
RCK004 Rickets 68 0.962
4
c HPT001 Hepatitis C 62 0.802
5
c HPT073 Hepatitis C Virus 72 0.742
6
P HPT021 Hepatitis 67 0.470
7
KRT002 Keratomalacia 47 0.446
8
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.431
9
P LVR013 Liver Disease 68 0.406
10
VTM002 Vitamin B12 Deficiency 48 0.368
11
P KDN018 Kidney Disease 72 0.362
12
LVR012 Liver Cirrhosis 62 0.356
13
P HYP069 Hyperparathyroidism 63 0.349
14
c CHR684 Chronic Kidney Disease 70 0.328
15
P BRS047 Breast Cancer 97 0.323
16
P OST002 Osteoporosis 74 0.320
17
P CLR023 Colorectal Cancer 99 0.308
18
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.303
19
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.302
20
ATM095 Autoimmune Disease 62 0.301
21
VTM033 Vitamin K Deficiency Bleeding 48 0.281
22
DFC004 Deficiency Anemia 70 0.277
23
P HPT023 Hepatocellular Carcinoma 100 0.272
24
c SCN007 Secondary Hyperparathyroidism 51 0.270
25
BNR002 Bone Resorption Disease 48 0.264
26
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.262
27
P RTN008 Retinitis Pigmentosa 79 0.253
28
c HPT016 Hepatitis B 59 0.242
29
c PRC016 Pre-Eclampsia 63 0.240
30
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.240
31
OST011 Osteomalacia 52 0.239
32
P BND020 Bone Disease 59 0.237
33
48X005 48,xyyy 39 0.235
34
c VRL010 Viral Hepatitis 52 0.234
35
FTT001 Fatty Liver Disease 61 0.232
36
END086 End Stage Renal Disease 51 0.232
37
P PRS040 Prostate Cancer 97 0.231
38
P CRN300 Coronary Heart Disease 1 63 0.231
39
ATH013 Atherosclerosis Susceptibility 65 0.230
40
c HYP836 Hypercholesterolemia, Familial, 1 73 0.229
41
c HPT003 Hepatitis a 62 0.227
42
P VSC007 Vascular Disease 63 0.225
43
P DBT009 Diabetes Mellitus 64 0.224
44
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.223
45
IRN002 Iron Metabolism Disease 57 0.219
46
P DRR001 Diarrhea 55 0.219
47
CYS001 Cystic Fibrosis 81 0.217
48
P NRP001 Neuropathy 56 0.217
49
P PSR002 Psoriasis 62 0.217
50
HMC014 Homocysteinemia 53 0.217
51
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.213
52
PST011 Pustulosis of Palm and Sole 52 0.213
53
LPP008 Lipoprotein Quantitative Trait Locus 62 0.210
54
P INF037 Inflammatory Bowel Disease 54 0.209
55
P LKM002 Leukemia 68 0.206
56
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.204
57
P HRT032 Heart Disease 75 0.204
58
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.203
59
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.203
60
LPD008 Lipid Metabolism Disorder 62 0.203
61
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.202
62
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.201
63
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.200
64
P CRD246 Cardiovascular System Disease 57 0.199
65
ART140 Arteries, Anomalies of 52 0.198
66
P ALZ034 Alzheimer Disease 88 0.197
67
HLX001 Helix Syndrome 47 0.197
68
CYT002 Cytokine Deficiency 42 0.197
69
HMN044 Human Immunodeficiency Virus Type 1 71 0.197
70
c THR092 Thrombophilia Due to Thrombin Defect 73 0.197
71
ISC004 Ischemia 58 0.194
72
P ATR011 Atrial Fibrillation 66 0.193
73
P SKN015 Skin Carcinoma 66 0.193
74
P MYL006 Myeloid Leukemia 60 0.193
75
NRL016 Neural Tube Defects 82 0.191
76
P MLT020 Multiple Sclerosis 72 0.190
77
P LNG032 Lung Cancer 98 0.190
78
PRN011 Pernicious Anemia 53 0.188
79
P ADN016 Adenocarcinoma 64 0.187
80
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.186
81
CRH001 Crohn's Disease 74 0.186
82
PRT037 Pertussis 65 0.185
83
DRM006 Dermatitis 61 0.185
84
c SYS001 Systemic Lupus Erythematosus 86 0.185
85
ADN018 Adenoma 59 0.184
86
c ATR087 Atrial Standstill 1 75 0.183
87
c LKM061 Leukemia, Acute Myeloid 84 0.182
88
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.182
89
STR067 Stroke, Ischemic 81 0.181
90
P BLD134 Bladder Cancer 79 0.181
91
P LYN001 Lynch Syndrome 77 0.181
92
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.180
93
P MYP004 Myopathy 70 0.179
94
c NRF023 Neurofibromatosis, Type Ii 80 0.179
95
P LYM118 Lymphoma 68 0.178
96
P GST053 Gastric Cancer 83 0.178
97
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.178
98
IMM167 Immune Deficiency Disease 78 0.177
99
P OVR042 Ovarian Cancer 88 0.176
100
P PNC035 Pancreatic Cancer 84 0.175
101
NTR005 Nutritional Deficiency Disease 62 0.174
103
P PRD008 Periodontitis 64 0.174
104
OST159 Osteogenic Sarcoma 66 0.174
105
P NRB001 Neuroblastoma 72 0.174
106
P PLY011 Polycystic Ovary Syndrome 56 0.173
107
CNG034 Congestive Heart Failure 69 0.173
108
TXC005 Toxic Shock Syndrome 62 0.173
109
P LPS004 Lupus Erythematosus 61 0.173
110
P THL005 Thalassemia 60 0.173
111
P PRP019 Peripheral Nervous System Disease 58 0.172
112
HYP066 Hyperglycemia 61 0.171
113
SKN016 Skin Disease 63 0.171
114
CRB039 Cerebrovascular Disease 67 0.171
115
MSL001 Measles 62 0.170
116
INS024 Insulin-Like Growth Factor I 79 0.170
117
P MYC007 Myocardial Infarction 70 0.170
118
GST033 Gestational Diabetes 61 0.169
119
c MCR120 Microvascular Complications of Diabetes 7 47 0.169
120
P HYP086 Hypothyroidism 69 0.169
121
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.167
122
P ALP008 Alopecia 54 0.167
123
P THR014 Thrombocytopenia 67 0.167
124
c MCR113 Microvascular Complications of Diabetes 3 52 0.167
125
P NTR004 Neutropenia 63 0.166
126
PYR009 Pyridoxine Deficiency Anemia 34 0.166
127
c MCR130 Microvascular Complications of Diabetes 6 41 0.166
128
c HYP595 Hypertension, Essential 84 0.165
129
c MCR133 Microvascular Complications of Diabetes 4 41 0.165
130
CHL068 Cholestasis 61 0.165
131
P ATX030 Ataxia-Telangiectasia 82 0.165
132
LNG099 Lung Disease 60 0.164
133
P CTR002 Cataract 60 0.164
134
OST012 Osteoarthritis 78 0.163
135
P GST044 Gastritis 56 0.162
136
DPR016 Depression 63 0.161
137
P HYP061 Hypertrophic Cardiomyopathy 70 0.161
138
P RHM011 Rheumatoid Arthritis 80 0.160
139
TTN003 Tetanus 65 0.159
140
AST005 Asthma 76 0.159
141
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.158
142
VSL002 Visual Epilepsy 59 0.158
143
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.158
144
P MLN008 Melanoma 69 0.158
145
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.158
146
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.158
147
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.158
148
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.158
149
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.158
150
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.158
151
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.158
152
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.158
153
NNL006 Non-Alcoholic Steatohepatitis 54 0.157
154
PLM001 Pulmonary Tuberculosis 69 0.156
155
ALL026 Allergic Hypersensitivity Disease 62 0.156
156
P DRM053 Dermatitis, Atopic 66 0.156
157
P ECL001 Eclampsia 50 0.155
158
THR024 Thrombosis 57 0.155
159
ULC004 Ulcerative Colitis 73 0.155
160
c PRM005 Primary Hyperparathyroidism 58 0.153
161
AGN016 Aging 56 0.152
162
PRP030 Purpura 54 0.152
163
47X002 47,xyy 49 0.151
164
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.151
165
LGH007 Leigh Syndrome 70 0.151
166
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.149
167
P BCL017 B-Cell Lymphoma 58 0.149
168
THY029 Thyroid Carcinoma 59 0.149
169
ATX019 Ataxia with Vitamin E Deficiency 42 0.148
170
ALC007 Alcohol Dependence 66 0.148
171
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.147
172
P GLM007 Glomerulonephritis 57 0.147
173
P PNM007 Pneumonia 68 0.146
174
P HML002 Hemolytic Anemia 63 0.146
175
MNT002 Mental Depression 58 0.145
176
P NGH001 Night Blindness 48 0.143
177
P GLM045 Glioma 63 0.143
178
SQM006 Squamous Cell Carcinoma 60 0.143
179
P VSC011 Vasculitis 62 0.143
180
PRT011 Protein C Deficiency 44 0.142
181
MGL001 Megaloblastic Anemia 51 0.141
182
CHL079 Children's Interstitial Lung Disease 26 0.141
183
GLL048 Glial Tumor 45 0.141
184
HMS001 Hemosiderosis 54 0.140
185
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.140
186
GLC003 Glucose Intolerance 54 0.139
187
CLT003 Colitis 62 0.139
188
VRL011 Viral Infectious Disease 61 0.139
189
P MSC005 Muscular Dystrophy 66 0.139
190
CMM005 Common Cold 57 0.139
191
ACQ007 Acquired Immunodeficiency Syndrome 60 0.139
192
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.138
193
ESP021 Esophageal Cancer 90 0.138
194
P CNR004 Cone-Rod Dystrophy 2 73 0.138
195
P SZR006 Seizure Disorder 56 0.136
196
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.136
197
c ACT075 Acute Myocardial Infarction 57 0.136
198
BCT022 Bacterial Infectious Disease 56 0.136
199
HYP017 Hypophosphatemia 50 0.136
200
CRY004 Cryoglobulinemia 48 0.135
201
P ART022 Arthritis 69 0.135
202
P THY032 Thyroiditis 52 0.135
203
P ENC018 Encephalopathy 61 0.135
204
P INF032 Infertility 57 0.135
205
c RHB024 Rhabdomyosarcoma 2 67 0.134
206
P RRH023 Rare Hereditary Hemochromatosis 41 0.134
207
P ATS364 Autism 70 0.133
208
P MCR115 Microvascular Complications of Diabetes 5 66 0.133
209
P TRN020 Turner Syndrome 67 0.132
210
P HYP076 Hyperthyroidism 55 0.132
211
KRT001 Keratoconjunctivitis Sicca 49 0.132
212
PRP027 Peripheral Vascular Disease 71 0.132
213
XRP001 Xerophthalmia 41 0.132
214
c ATS007 Autism Spectrum Disorder 67 0.132
215
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.131
216
P SRC025 Sarcoidosis 1 70 0.131
217
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.130
218
P RTN024 Retinoblastoma 73 0.130
219
DWN001 Down Syndrome 70 0.130
220
MYL009 Myelodysplastic Syndrome 70 0.130
221
P ART021 Arteriosclerosis 54 0.130
222
P ALC033 Alcohol Use Disorder 58 0.130
223
c SML038 Small Cell Cancer of the Lung 65 0.129
224
c DLT002 Dilated Cardiomyopathy 79 0.129
225
P EXN002 Exanthem 57 0.128
226
c PRM038 Primary Agammaglobulinemia 44 0.128
227
NPH009 Nephrolithiasis 55 0.128
228
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.128
229
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.127
230
c NRF024 Neurofibromatosis, Type I 77 0.127
231
P MYC084 Mycobacterium Tuberculosis 1 68 0.127
232
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.127
233
P LKM062 Leukemia, Acute Lymphoblastic 69 0.127
234
ATS010 Autosomal Recessive Disease 48 0.127
235
c FML346 Familial Adenomatous Polyposis 1 66 0.127
236
GST019 Gastrointestinal Stromal Tumor 78 0.126
237
P PHC003 Pheochromocytoma 71 0.126
238
HYP266 Hypoxia 57 0.126
239
GLB015 Glioblastoma Multiforme 75 0.126
240
c DBT099 Diabetes Mellitus, Type I 65 0.126
241
c FNC027 Fanconi Anemia, Complementation Group a 81 0.126
242
STM007 Stomatitis 50 0.125
243
c BTT014 Beta-Thalassemia 74 0.125
244
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.125
245
P NPH012 Nephrotic Syndrome 60 0.124
246
P LCH002 Lichen Planus 53 0.123
247
URM002 Uremia 49 0.123
248
P SCK005 Sickle Cell Disease 50 0.122
249
P HYP750 Hypertriglyceridemia, Familial 62 0.122
250
P CHR071 Charcot-Marie-Tooth Disease 65 0.122
251
P INF038 Influenza 68 0.122
252
ANG054 Angina Pectoris 66 0.122
253
P RHN004 Rhinitis 57 0.122
254
PLM033 Pulmonary Embolism 59 0.121
255
P CHR345 Chronic Pain 44 0.121
256
LPT014 Leptin Deficiency or Dysfunction 74 0.120
257
IRN001 Iron Deficiency Anemia 59 0.120
258
LYM133 Lymphoma, Hodgkin, Classic 69 0.120
259
MYL069 Myeloma, Multiple 85 0.120
260
P HYP024 Hypoparathyroidism 56 0.120
261
DPH001 Diphtheria 60 0.120
262
P DMN002 Dementia 66 0.119
263
P PLY019 Polyneuropathy 56 0.119
264
P PRM011 Primary Ciliary Dyskinesia 69 0.119
265
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.119
266
P PRM006 Primary Biliary Cirrhosis 62 0.119
267
DSR002 Disorders of Intracellular Cobalamin Metabolism 31 0.118
268
CLR108 Colorectal Adenoma 64 0.118
269
TQP001 Taqi Polymorphism 32 0.118
270
c ACT071 Acute Kidney Failure 60 0.117
271
c THR082 Thrombophilia Due to Activated Protein C Resistance 61 0.117
272
P LTR001 Lateral Sclerosis 54 0.116
273
P HYP726 Hypercalcemia, Infantile, 1 58 0.116
274
P PRK057 Parkinson Disease, Late-Onset 78 0.116
275
P HMC002 Homocystinuria 53 0.116
276
HLC007 Helicobacter Pylori Infection 59 0.115
277
SVR004 Severe Combined Immunodeficiency 73 0.115
278
P MNN013 Meningitis 66 0.115
279
c TBR025 Tuberous Sclerosis 1 77 0.115
280
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.115
281
PRT013 Portal Hypertension 59 0.114
282
P CLC063 Celiac Disease 1 66 0.114
283
MNN028 Mononeuropathy of the Median Nerve, Mild 46 0.114
284
HYP025 Hyperphosphatemia 48 0.114
285
P THR015 Thrombophilia 51 0.113
286
c FML001 Familial Atrial Fibrillation 65 0.113
287
FND002 Fundus Dystrophy 55 0.113
288
INT007 Intermediate Coronary Syndrome 55 0.113
289
SPN186 Spinal Cord Injury 60 0.113
290
c FML008 Familial Retinoblastoma 53 0.113
291
HYP056 Hypoglycemia 66 0.113
292
P MJR001 Major Depressive Disorder 68 0.113
293
LSH001 Leishmaniasis 63 0.113
294
P KLZ004 Kala-Azar 1 41 0.113
295
c MGR028 Migraine with or Without Aura 1 67 0.112
296
P RSP003 Respiratory Failure 74 0.112
297
c EXD008 Exudative Vitreoretinopathy 1 71 0.112
298
P MTH008 Methylmalonic Acidemia 50 0.111
299
HYP060 Hyperinsulinism 54 0.111
300
P END044 Endometriosis 63 0.111
301
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.111
302
VTM028 Vitamin E, Familial Isolated Deficiency of 52 0.111
303
XRD010 Xeroderma Pigmentosum, Variant Type 73 0.111
304
c PCH010 Pachyonychia Congenita 3 44 0.111
305
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.110
306
P CRY007 Cryoglobulinemia, Familial Mixed 50 0.109
307
P GRV001 Graves' Disease 55 0.109
308
c ATM011 Autoimmune Hepatitis 63 0.109
309
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.109
310
ALL014 Allergic Encephalomyelitis 38 0.109
311
P HMP007 Hemophilia 51 0.109
312
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.108
313
c GLC092 Glaucoma, Primary Open Angle 62 0.108
314
CHL014 Cholera 59 0.108
315
P HRP006 Herpes Simplex 65 0.108
316
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.108
317
KRT009 Keratosis 51 0.108
318
P EPL164 Epilepsy 71 0.108
319
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.107
320
c PRD040 Periodontitis, Chronic 53 0.107
321
P RCT021 Rectum Cancer 52 0.107
322
CRV035 Cervical Cancer 76 0.107
323
c INH030 Inherited Retinal Disorder 51 0.107
324
ALL003 Allergic Rhinitis 67 0.107
325
ADL002 Adult Syndrome 70 0.107
326
EYD002 Eye Disease 58 0.106
327
MLR004 Malaria 81 0.106
328
c NMN015 Niemann-Pick Disease, Type C1 68 0.106
329
P GRF003 Graft-Versus-Host Disease 72 0.106
330
c ACT073 Acute Leukemia 58 0.106
331
P LNG064 Lung Cancer Susceptibility 3 78 0.105
332
CVD001 Covid-19 44 0.105
333
c DWL002 Dowling-Degos Disease 1 58 0.105
334
RTN023 Retinitis 46 0.105
335
NRR001 Neuroretinitis 42 0.105
336
P ATR005 Atrophic Gastritis 50 0.105
337
c ACT027 Acute Pancreatitis 60 0.104
338
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.104
339
P HYP058 Hypervitaminosis a 48 0.104
340
P NRP063 Neuropathy, Congenital Hypomyelinating, 1, Autosomal Recessive 57 0.104
341
SPL018 Splenomegaly 48 0.104
342
RNL011 Renal Osteodystrophy 50 0.104
343
ABT001 Abetalipoproteinemia 69 0.104
344
ANX010 Anxiety 73 0.104
345
DBT010 Diabetic Neuropathy 54 0.103
346
PLM031 Poliomyelitis 64 0.103
347
NSS002 Neisseria Meningitidis Infection 47 0.103
348
c BRN108 Branchiootic Syndrome 1 62 0.103
349
P OPN001 Open-Angle Glaucoma 49 0.103
350
c SPN225 Spondyloarthropathy 1 73 0.102
351
LYM019 Lymphosarcoma 46 0.102
352
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.101
353
CNS004 Constipation 58 0.101
354
KRT019 Keratitis, Hereditary 65 0.101
355
MTC097 Mitochondrial Complex Iv Deficiency 59 0.101
356
MRF001 Marfan Syndrome 77 0.101
357
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.101
358
P SLP006 Sleep Apnea 69 0.101
359
c INF071 Inflammatory Bowel Disease 1 67 0.101
360
P NMN002 Niemann-Pick Disease 59 0.100
361
PLC008 Placenta Disease 50 0.100
362
SCK003 Sickle Cell Anemia 74 0.100
363
P SYP003 Syphilis 58 0.100
364
P PRP029 Porphyria 62 0.100
365
P SCH015 Schizophrenia 74 0.100
366
P BRB001 Beriberi 46 0.100
367
P MLN007 Male Infertility 55 0.100
368
PPT005 Peptic Ulcer Disease 59 0.099
369
PNC001 Pancytopenia 54 0.099
370
P PLM036 Pulmonary Fibrosis 65 0.099
371
P HDC001 Headache 57 0.099
372
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.099
373
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.098
374
PNC129 Pancreatic Adenocarcinoma 68 0.098
375
MCS002 Mucositis 56 0.098
376
DSS009 Disseminated Intravascular Coagulation 57 0.098
377
P OVR082 Overgrowth Syndrome 50 0.098
378
BRN056 Bronchopulmonary Dysplasia 57 0.098
379
VTM009 Vitamin K-Dependent Clotting Factors, Combined Deficiency of, 1 31 0.098
380
PHN003 Phenylketonuria 75 0.097
381
DFF005 Diffuse Large B-Cell Lymphoma 55 0.097
382
P HMR003 Hemorrhagic Disease 53 0.097
383
c FML021 Familial Hypercholesterolemia 66 0.097
384
c SVR001 Severe Acute Respiratory Syndrome 62 0.097
385
HRW001 Hair Whorl 36 0.097
386
c CNG411 Congenital Disorder of Glycosylation, Type in 68 0.097
387
P PNC044 Pancreatitis 61 0.097
388
P CRD119 Cardiac Arrest 67 0.096
389
BRK010 Burkitt Lymphoma 67 0.096
390
TRN015 Transient Cerebral Ischemia 63 0.096
391
HYP081 Hypolipoproteinemia 51 0.096
392
SKN019 Skin Melanoma 68 0.096
393
MDD011 Mood Disorder 62 0.096
394
FDL002 Food Allergy 51 0.096
395
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.096
396
P IMR002 Imerslund-Grasbeck Syndrome 1 43 0.096
397
PRT036 Peritonitis 64 0.096
398
DNT012 Dental Caries 53 0.096
399
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.096
400
P TRM003 Tremor 54 0.096
401
BSL036 Basal Cell Nevus Syndrome 73 0.095
402
P TBR001 Tuberous Sclerosis 70 0.095
403
ENT011 Enterocolitis 51 0.095
404
BRN071 Brain Injury 49 0.095
405
GST050 Gastrointestinal System Disease 56 0.094
406
ORL011 Oral Cancer 60 0.094
407
P HYP098 Hypereosinophilic Syndrome 67 0.094
408
P URT039 Urticaria 58 0.094
409
CHL123 Chlamydia 59 0.094
410
URL001 Urolithiasis 45 0.094
411
FBR047 Fibromyalgia 58 0.094
412
c LKM063 Leukemia, Chronic Myeloid 72 0.094
413
c HMC039 Hemochromatosis, Type 1 74 0.094
414
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.094
415
PPL052 Papillomatosis, Confluent and Reticulated 33 0.094
416
GTR002 Goiter 53 0.094
417
P INS002 in Situ Carcinoma 53 0.094
418
ACT119 Acute Promyelocytic Leukemia 63 0.093
419
OCL069 Ocular Motor Apraxia 51 0.093
420
MSC157 Muscular Dystrophy, Duchenne Type 72 0.093
421
IGR001 Ige Responsiveness, Atopic 59 0.093
422
GST045 Gastroenteritis 59 0.093
423
IRR002 Irritable Bowel Syndrome 65 0.093
424
NPH003 Nephrocalcinosis 51 0.092
425
PRP080 Peripheral Artery Disease 53 0.092
426
SPN051 Spondylitis 51 0.092
427
BRN024 Bronchitis 68 0.092
428
BLR008 Bilirubin Metabolic Disorder 57 0.092
429
INF009 Inflammatory Spondylopathy 31 0.092
430
P HYP265 Hypotonia 43 0.092
431
P RTN016 Retinal Degeneration 53 0.091
432
P SBS003 Substance Abuse 55 0.091
433
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.091
434
c PNS012 Paine Syndrome 61 0.091
435
END057 Endometrial Cancer 74 0.091
436
P LKM071 Leukemia, Chronic Lymphocytic 79 0.091
437
P PLR004 Pleuropulmonary Blastoma 65 0.091
438
ALL006 Allergic Asthma 56 0.091
439
HSH003 Hashimoto Thyroiditis 62 0.090
440
c SCL052 Scleroderma, Familial Progressive 61 0.090
441
PRS045 Prostatic Hypertrophy 53 0.090
442
P FBR017 Fibrosarcoma 56 0.090
443
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.090
444
VRC005 Varicose Veins 60 0.090
445
HNS001 Hansen's Disease 34 0.090
446
ERY051 Erythroleukemia, Familial 56 0.090
447
CRH005 Crohn's Colitis 53 0.089
448
P LPR021 Leprosy 3 69 0.089
449
P BPL003 Bipolar Disorder 56 0.089
450
c FNC043 Fanconi Anemia, Complementation Group E 62 0.089
451
P MSC003 Muscular Atrophy 52 0.089
452
P ANT006 Antiphospholipid Syndrome 55 0.089
453
PPL022 Papilloma 54 0.089
454
VCC001 Vaccinia 49 0.089
455
c ACT068 Acute Cystitis 63 0.089
456
c MJR024 Major Affective Disorder 9 41 0.088
457
c MJR022 Major Affective Disorder 8 38 0.088
458
c DRR009 Diarrhea 6 46 0.088
459
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.088
460
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.088
461
TRN018 Transitional Cell Carcinoma 56 0.088
462
THY030 Thyroid Gland Disease 52 0.088
463
BRT054 Brittle Bone Disorder 72 0.088
464
c NRP053 Neuropathy, Hereditary Sensory and Autonomic, Type Iia 65 0.088
465
PND002 Pendred Syndrome 65 0.088
466
c HYP057 Hypervitaminosis D 42 0.088
467
P ANR048 Aniridia 1 63 0.088
468
ORL015 Oral Squamous Cell Carcinoma 43 0.088
469
MST005 Mastitis 53 0.088
470
GST040 Gastric Adenocarcinoma 70 0.087
471
HMP009 Haemophilus Influenzae 43 0.087
472
P NSP012 Nasopharyngeal Carcinoma 66 0.087
473
DRR016 Diarrhea 2, with Microvillus Atrophy 60 0.087
474
P AMY004 Amyloidosis 70 0.087
475
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.086
476
CNT047 Contact Dermatitis 58 0.086
477
BRN002 Bronchiolitis 59 0.086
478
PRS129 Prostatic Hyperplasia, Benign 49 0.086
479
P SYS005 Systemic Scleroderma 68 0.086
480
PSY004 Psychotic Disorder 67 0.085
481
P MYC008 Myocarditis 59 0.085
482
P PLM037 Pulmonary Hypertension 67 0.085
483
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.085
484
SRC014 Sarcoma 65 0.085
485
SCH014 Schistosomiasis 57 0.085
486
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.085
487
MSC007 Muscle Hypertrophy 64 0.085
488
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.085
489
KHL003 Kohlschutter-Tonz Syndrome 65 0.085
490
PRS021 Prostatic Adenoma 51 0.085
491
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.085
492
P HYD006 Hydrocephalus 66 0.085
493
P MYP006 Myopia 55 0.084
494
ANR007 Anorexia Nervosa 63 0.084
495
EPL131 Epilepsy, Pyridoxine-Dependent 49 0.084
496
MTH078 Methylmalonic Aciduria, Cblb Type 51 0.084
497
MCR017 Macrocytic Anemia 44 0.084
498
TRM010 Traumatic Brain Injury 51 0.084
499
P OST001 Osteopetrosis 70 0.084
500
P VTM026 Vitamin D Hydroxylation-Deficient Rickets, Type 1a 38 0.084
501
BCK006 Back Pain 42 0.084
502
P KDN017 Kidney Cancer 60 0.084
503
c BSL007 Basal Cell Carcinoma 68 0.084
504
CNN005 Connective Tissue Disease 68 0.084
505
P SLP005 Sleep Disorder 59 0.084
506
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.084
507
c MCR129 Microvascular Complications of Diabetes 1 66 0.083
508
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.083
509
P DYS154 Dystonia 65 0.083
510
P LCT001 Lactic Acidosis 51 0.083
511
c PRS136 Prostate Cancer, Hereditary, 6 33 0.083
512
DSS008 Disease of Mental Health 58 0.083
513
c TBR026 Tuberous Sclerosis 2 72 0.083
514
SQM002 Squamous Cell Papilloma 46 0.083
515
LMY002 Leiomyoma 52 0.083
516
c PRS130 Prostate Cancer, Hereditary, 8 32 0.083
517
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.083
518
P PRP003 Porphyria Cutanea Tarda 67 0.083
519
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.082
520
P OPT006 Optic Nerve Disease 60 0.082
521
MTH077 Methylmalonic Aciduria, Cbla Type 42 0.082
522
ENT004 Enthesopathy 49 0.082
523
PRT038 Protein-Energy Malnutrition 54 0.082
524
CLN015 Colon Adenocarcinoma 65 0.082
525
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.082
526
SPN035 Spindle Cell Sarcoma 53 0.081
527
P SCL018 Scoliosis 60 0.081
528
P SPP010 Suppressor of Tumorigenicity 3 51 0.081
529
HPT004 Hepatic Coma 45 0.081
530
PST092 Posttransplant Acute Limbic Encephalitis 29 0.081
531
ORL013 Oral Lichen Planus 45 0.080
532
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.080
533
P ADL010 Adult Respiratory Distress Syndrome 65 0.080
534
HRD160 Hereditary Combined Deficiency of Vitamin K-Dependent Clotting Factors 22 0.080
535
SBC016 Subacute Delirium 44 0.080
536
PNG002 Pain Agnosia 51 0.080
537
OTT002 Otitis Media 72 0.080
538
CLC006 Calcinosis 48 0.080
539
c CWD006 Cowden Syndrome 1 78 0.080
540
DMY004 Demyelinating Disease 52 0.080
541
GNG013 Gingivitis 59 0.080
542
c HMP029 Hemophilia a 67 0.080
543
CMR002 Coumarin Resistance 56 0.080
544
HPT019 Hepatic Encephalopathy 60 0.080
545
OVR094 Ovarian Epithelial Cancer 38 0.079
547
WRN001 Werner Syndrome 69 0.079
548
P ART023 Arthropathy 62 0.079
549
CLF027 Cleft Palate, Isolated 64 0.079
550
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.079
551
P ALP009 Alopecia Areata 60 0.079
552
CHL065 Cholangiocarcinoma 68 0.078
553
P OCL013 Oculodentodigital Dysplasia 69 0.078
554
c ACT134 Acute Liver Failure 56 0.078
555
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.078
556
BRC012 Brucellosis 64 0.078
557
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.078
558
MTB004 Metabolic Acidosis 50 0.078
559
CRB037 Cerebral Palsy 69 0.078
560
P FML018 Familial Mediterranean Fever 73 0.078
561
INT079 Intrahepatic Cholangiocarcinoma 51 0.078
562
HYP080 Hypogonadism 50 0.078
563
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.078
564
PRN019 Perinatal Necrotizing Enterocolitis 59 0.077
565
CRD132 Cardiac Conduction Defect 58 0.077
566
LYM027 Lymphopenia 58 0.077
567
NWC001 Newcastle Disease 45 0.077
568
P APL001 Aplastic Anemia 74 0.077
569
P UVT001 Uveitis 57 0.077
570
DYS073 Dysphagia 50 0.077
571
CRB004 Cerebral Artery Occlusion 45 0.077
572
LKP003 Leukoplakia 39 0.077
573
P MPL001 Maple Syrup Urine Disease 69 0.077
574
P MVM001 Movement Disease 63 0.077
575
P ALP004 Alport Syndrome 68 0.077
576
CRP001 Carpal Tunnel Syndrome 67 0.076
577
P CRN037 Craniosynostosis 68 0.076
578
HYP014 Hyperuricemia 52 0.076
579
PRM020 Premenstrual Tension 40 0.076
580
c FML035 Familial Hyperlipidemia 55 0.076
581
P ENC004 Encephalitis 61 0.076
582
c PSR023 Psoriasis 1 52 0.076
583
P GLM040 Glioma Susceptibility 1 81 0.076
584
P AST007 Astrocytoma 51 0.076
585
BRN028 Brain Cancer 74 0.075
586
IMP005 Impotence 52 0.075
587
ERY029 Erythermalgia, Primary 58 0.075
588
ATM052 Autoimmune Disease 1 37 0.075
589
c SVR005 Severe Pre-Eclampsia 50 0.075
590
CHR066 Chronic Fatigue Syndrome 61 0.075
591
MMM001 Mammary Paget's Disease 53 0.075
592
BLD131 Bladder Urothelial Carcinoma 62 0.074
593
ADR040 Adrenal Gland Pheochromocytoma 46 0.074
594
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.074
595
P PLL002 Pellagra 46 0.074
596
ANR040 Aneurysm 59 0.074
597
PPL049 Papillon-Lefevre Syndrome 65 0.074
598
c GRV008 Graves Disease 1 56 0.074
599
HMG005 Hemoglobinopathy 56 0.074
600
c HYP272 Hypercholesterolemia, Familial, 3 44 0.074
601
NRL018 Neural Tube Defects, Folate-Sensitive 48 0.074
602
c MCR112 Microvascular Complications of Diabetes 2 41 0.074
603
c PSR017 Psoriasis 2 53 0.073
604
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.073
605
P CHL066 Cholangitis 51 0.073
606
P HYP818 Hypobetalipoproteinemia, Familial, 1 56 0.073
607
TLN003 Telangiectasis 52 0.073
608
HYP005 Hypokalemia 55 0.072
609
P END033 Endocarditis 57 0.072
610
P PLY170 Polycystic Kidney Disease 4 with or Without Polycystic Liver Disease 64 0.072
611
CRN030 Coronary Stenosis 50 0.072
612
GT001 Gout 64 0.072
613
c ALP101 Alpha-Thalassemia 62 0.072
614
MTC114 Mitochondrial Myopathy, Encephalopathy, Lactic Acidosis, and Stroke-Like Episodes 61 0.072
615
THY111 Thyroid Carcinoma, Familial Medullary 67 0.072
616
MYL005 Myelofibrosis 70 0.072
617
CMP010 Complex Regional Pain Syndrome 58 0.072
618
P BNG032 Benign Mesothelioma 46 0.072
619
VSC003 Visceral Leishmaniasis 55 0.072
620
P DNG005 Dengue Virus 59 0.072
621
NRT004 Neuritis 52 0.072
622
GST023 Gastric Ulcer 53 0.072
623
49X006 49, Xxxxy Syndrome 41 0.072
624
TRD006 Tardive Dyskinesia 54 0.072
625
P INT068 Intestinal Disease 53 0.072
626
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.071
627
FCT007 Factor Vii Deficiency 67 0.071
628
END040 Endogenous Depression 55 0.071
629
APH001 Aphthous Stomatitis 57 0.071
630
ANX004 Anoxia 40 0.071
631
ART016 Aortic Aneurysm 69 0.071
632
P SHR001 Short Bowel Syndrome 53 0.071
633
CHR178 Chromosomal Triplication 35 0.071
634
HYP043 Hyperandrogenism 48 0.071
635
DGN001 Degenerative Disc Disease 48 0.071
636
ACR007 Acromegaly 71 0.071
637
P FRN006 Frontotemporal Dementia 68 0.071
638
PRM329 Premature Aging 35 0.070
639
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.070
640
c GLL024 Gallbladder Disease 1 53 0.070
641
LNG031 Lung Benign Neoplasm 51 0.070
642
P LFR001 Li-Fraumeni Syndrome 72 0.070
643
P PRC031 Preeclampsia/eclampsia 1 38 0.070
644
PSR001 Psoriatic Arthritis 61 0.070
645
P BRS044 Breast Adenocarcinoma 59 0.070
646
MMB001 Membranoproliferative Glomerulonephritis 55 0.070
647
WLS001 Wilson Disease 71 0.070
648
BLR001 Biliary Atresia 50 0.070
649
P MLT074 Multiple Endocrine Neoplasia 56 0.070
650
NRT001 Neurotic Disorder 53 0.070
651
c PNC108 Pancreatitis, Hereditary 70 0.070
652
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.070
653
NWB001 Newborn Respiratory Distress Syndrome 58 0.069
654
c EPL184 Epileptic Encephalopathy, Early Infantile, 6 70 0.069
655
P RTN018 Retinal Disease 53 0.069
656
VSC002 Vascular Dementia 57 0.069
657
P CND004 Candidiasis 58 0.069
659
OST003 Osteonecrosis 61 0.069
660
DYS015 Dysentery 52 0.069
661
SNS003 Sensory Peripheral Neuropathy 54 0.069
662
c WLM013 Wilms Tumor 1 65 0.069
663
P SJG008 Sjogren Syndrome 61 0.069
664
CHG001 Chagas Disease 66 0.069
665
c ACT135 Acute Graft Versus Host Disease 52 0.069
666
BRR014 Barrett Esophagus 65 0.069
667
P MDL005 Medulloblastoma 77 0.069
668
c CNG006 Congenital Hypothyroidism 64 0.069
669
MNN020 Meningococcal Infection 46 0.069
670
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.069
671
P PSD087 Pseudoxanthoma Elasticum 65 0.069
672
CHC001 Chickenpox 60 0.068
673
MTH009 Mouth Disease 56 0.068
674
P MTC069 Mitochondrial Disorders 56 0.068
675
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.068
676
THY125 Thyroid Gland Medullary Carcinoma 50 0.068
677
P DYS007 Dyskeratosis Congenita 67 0.068
678
RBF001 Riboflavin Deficiency 49 0.068
679
P TRC086 Trichohepatoenteric Syndrome 1 62 0.068
680
PLY150 Polykaryocytosis Inducer 31 0.068
681
ALP103 Alpha-1-Antitrypsin Deficiency 64 0.068
682
P PLY014 Polycystic Kidney Disease 62 0.068
683
ADR007 Adrenoleukodystrophy 75 0.068
684
INT066 Interstitial Lung Disease 60 0.068
685
c LKM005 Leukemia, T-Cell, Chronic 34 0.068
686
c HYP843 Hypoalphalipoproteinemia, Primary, 2 52 0.068
687
c PRT132 Protoporphyria, Erythropoietic, 1 61 0.068
688
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.067
689
c HYP841 Hypoalphalipoproteinemia, Primary, 1 41 0.067
690
PLM010 Pulmonary Edema 54 0.067
691
HMC040 Homocystinuria Due to Cystathionine Beta-Synthase Deficiency 52 0.067
692
P BRL012 Bare Lymphocyte Syndrome, Type Ii 66 0.067
693
OST017 Osteomyelitis 64 0.067
694
P NRV007 Nervous System Disease 66 0.067
695
KPS004 Kaposi Sarcoma 75 0.067
696
P MST009 Mastocytosis 64 0.067
697
PYR016 Pyridoxine Deficiency 30 0.067
698
CHR074 Choriocarcinoma 47 0.067
699
c NMN014 Niemann-Pick Disease, Type C2 51 0.067
700
c LTN004 Late-Onset Retinal Degeneration 59 0.067
701
ALC006 Alcoholic Hepatitis 61 0.067
702
HRP004 Herpes Zoster 60 0.067
703
FML307 Familial Calcium Pyrophosphate Deposition 40 0.067
704
TNG002 Tangier Disease 65 0.067
705
P ANG001 Angelman Syndrome 69 0.067
706
c SPN207 Spinocerebellar Ataxia, Autosomal Recessive 8 49 0.067
707
P DDN001 Duodenal Ulcer 52 0.066
708
CTN007 Cutaneous Leishmaniasis 62 0.066
709
ISL099 Isolated Methylmalonic Acidemia 29 0.066
710
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.066
711
CRV045 Cervical Intraepithelial Neoplasia 39 0.066
712
STT001 Status Epilepticus 60 0.066
713
MTH076 Methylmalonic Aciduria Due to Methylmalonyl-Coa Mutase Deficiency 50 0.066
714
APN008 Apnea, Obstructive Sleep 64 0.066
715
CHN016 Cohen Syndrome 63 0.066
716
P PRS038 Personality Disorder 65 0.066
717
c MYT021 Myotonic Dystrophy 1 69 0.066
718
P VTR007 Vitreoretinopathy 46 0.066
719
BDD001 Budd-Chiari Syndrome 63 0.066
720
P LBR014 Leber Congenital Amaurosis 4 56 0.066
721
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.066
722
P CYS018 Cystitis 59 0.066
723
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.066
724
P VSC018 Visceral Steatosis 33 0.066
725
CLR109 Colorectal Adenocarcinoma 51 0.066
726
HYL004 Hyaline Fibromatosis Syndrome 67 0.066
727
P PLY018 Polycythemia 56 0.066
728
BRS051 Breast Disease 58 0.066
729
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.066
730
P HML001 Hemolytic-Uremic Syndrome 53 0.066
731
P HYP733 Hypercalciuria, Absorptive, 2 45 0.066
732
P HNT016 Huntington Disease 72 0.065
733
INT002 Intermittent Claudication 61 0.065
734
ESP002 Esophageal Varix 51 0.065
735
CYS036 Cystinosis, Nephropathic 51 0.065
736
c XNT010 Xanthinuria, Type I 53 0.065
737
THR004 Thrombocytosis 51 0.065
738
P PRP034 Purpura Fulminans 43 0.065
739
MND021 Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome 65 0.065
740
c INH020 Inherited Metabolic Disorder 47 0.065
741
P ICH004 Ichthyosis 54 0.065
742
P FLL037 Follicular Lymphoma 67 0.065
743
c HYP243 Hyperparathyroidism 1 51 0.065
744
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.065
745
P ESP024 Esophagitis 62 0.065
746
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.065
747
P LYM033 Lymphoproliferative Syndrome 59 0.064
748
P MYS005 Myositis 56 0.064
749
P PTY003 Pityriasis Rubra Pilaris 58 0.064
750
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.064
751
CRT013 Carotid Stenosis 50 0.064
752
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.064
753
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.064
754
c PLY105 Polycystic Ovary Syndrome 1 38 0.064
755
c CHR682 Chronic Bilirubin Encephalopathy 39 0.064
756
c PSR032 Psoriasis 11 47 0.064
757
c PSR028 Psoriasis 7 42 0.064
758
c PSR018 Psoriasis 13 41 0.064
759
P PTT014 Pitt-Hopkins Syndrome 63 0.064
760
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.064
761
LMY014 Leiomyoma, Uterine 56 0.063
762
c PRD013 Periodic Fever, Familial, Autosomal Dominant 67 0.063
763
PRT029 Parathyroid Adenoma 50 0.063
764
c BLC008 Bile Acid Synthesis Defect, Congenital, 2 50 0.063
765
GLS007 Glossitis 47 0.063
766
HYP636 Hypocalcemic Vitamin D-Dependent Rickets 39 0.063
767
ORT008 Orotic Aciduria 55 0.063
768
P MCR010 Microcephaly 59 0.063
769
P NRF002 Neurofibromatosis 56 0.063
770
c ART101 Aortic Valve Disease 2 65 0.063
771
c INF145 Infantile Liver Failure Syndrome 1 50 0.063
772
WGN007 Wagner Vitreoretinopathy 38 0.063
773
WGN003 Wagner Syndrome 36 0.063
774
c PSD066 Pseudohypoparathyroidism, Type Ib 55 0.063
775
P PYL005 Pyelonephritis 56 0.063
776
MYF001 Myofibroma 45 0.063
777
GYR004 Gyrate Atrophy of Choroid and Retina 57 0.063
778
ATN005 Autonomic Dysfunction 46 0.063
779
c JVN010 Juvenile Rheumatoid Arthritis 64 0.063
780
RNL078 Renal Dysplasia 50 0.063
781
RTN020 Retinal Vascular Disease 46 0.063
782
c CHL119 Cholangitis, Primary Sclerosing 57 0.063
783
P BRD002 Bardet-Biedl Syndrome 66 0.063
784
P HYP035 Hypophosphatasia 61 0.063
785
P CRB101 Cerebrooculofacioskeletal Syndrome 1 60 0.062
786
PTZ001 Peutz-Jeghers Syndrome 70 0.062
787
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.062
788
PRS063 Paresthesia 41 0.062
789
PRT014 Protein S Deficiency 44 0.062
790
OMN001 Omenn Syndrome 67 0.062
791
c HMG029 Hemoglobin Se Disease 39 0.062
792
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.062
793
INS001 Insulinoma 60 0.062
794
c GLY060 Glycogen Storage Disease Ia 63 0.062
795
FDB001 Foodborne Botulism 55 0.062
796
HLC001 Holocarboxylase Synthetase Deficiency 48 0.062
797
PGM030 Pigmentation Anomaly of the Skin 26 0.062
798
c CHR064 Chronic Monocytic Leukemia 33 0.062
799
ACN002 Acanthosis Nigricans 60 0.062
800
FLT009 Folate Malabsorption, Hereditary 50 0.062
801
P MTC003 Metachromatic Leukodystrophy 70 0.062
802
BRN004 Brain Edema 56 0.062
803
BTN003 Biotinidase Deficiency 60 0.062
804
BNN003 Bone Inflammation Disease 48 0.062
805
AMN001 Amenorrhea 54 0.061
806
ALL010 Allergic Contact Dermatitis 56 0.061
807
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.061
808
P CNJ013 Conjunctivitis 65 0.061
809
P FCL005 Focal Segmental Glomerulosclerosis 57 0.061
810
P RST001 Restless Legs Syndrome 54 0.061
811
c BCT007 Bacterial Meningitis 55 0.061
812
c MLG068 Malignant Glioma 46 0.061
813
PFF001 Pfeiffer Syndrome 79 0.061
814
P RBL001 Rubella 59 0.061
815
P SNS001 Sensorineural Hearing Loss 60 0.061
816
BCT002 Bacterial Vaginosis 53 0.061
817
EMB004 Embryonal Carcinoma 56 0.061
818
P MTC133 Mitochondrial Myopathy 49 0.061
819
CHL067 Cholecystitis 57 0.061
820
KRN002 Kearns-Sayre Syndrome 63 0.061
821
P MTR014 Motor Neuron Disease 65 0.061
822
CHD001 Chediak-Higashi Syndrome 66 0.061
823
GLY010 Glycine Encephalopathy 62 0.061
824
c MLT160 Multiple Endocrine Neoplasia, Type Iia 70 0.061
825
GLC106 Glucocorticoid Resistance, Generalized 48 0.061
826
c HPT007 Hepatitis E 53 0.061
827
ART001 Arterial Tortuosity Syndrome 66 0.060
828
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.060
829
IGG001 Iga Glomerulonephritis 48 0.060
830
PST021 Postpartum Depression 50 0.060
831
CRD223 Cardiac Arrhythmia 60 0.060
832
c HYP768 Hyperlipoproteinemia, Type I 67 0.060
833
PRD004 Prediabetes Syndrome 47 0.060
834
RHM001 Rheumatic Fever 60 0.060
835
P GCH001 Gaucher's Disease 63 0.060
836
PRT010 Parathyroid Carcinoma 67 0.060
837
c MCP052 Mucopolysaccharidosis, Type Vi 67 0.060
838
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.060
839
IDP070 Idiopathic Scoliosis 42 0.060
840
CHY002 Chylomicron Retention Disease 65 0.060
841
c HMP004 Hemophilia B 68 0.060
842
RFR010 Refractory Anemia 48 0.060
843
GRW007 Growth Hormone Deficiency 46 0.060
844
NRM005 Neuromuscular Disease 64 0.059
845
P RNL007 Renal Tubular Acidosis 51 0.059
846
CYT018 Cytochrome P450 2d6 Variant 27 0.059
847
c BLD140 Blood Group, I System 32 0.059
848
ALP077 Alpha-Methylacetoacetic Aciduria 55 0.059
849
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.059
850
GLS018 Glass Syndrome 57 0.059
851
c JVN061 Juvenile Arthritis 60 0.059
852
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.059
853
P RTN022 Retinal Vein Occlusion 53 0.059
854
MTH021 Methylmalonic Acidemia with Homocystinuria 46 0.059
855
MNN032 Meningococcal Meningitis 54 0.059
856
c HYP369 Hypophosphatemic Rickets, Autosomal Recessive, 2 29 0.059
857
P MMP001 Mumps 58 0.059
858
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.059
859
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.059
860
LMB062 Limb Ischemia 55 0.059
861
P MNC007 Monocytic Leukemia 53 0.059
862
P THR005 Thrombotic Thrombocytopenic Purpura 61 0.059
863
MCC012 Mccune-Albright Syndrome 70 0.059
864
P FML011 Familial Adenomatous Polyposis 72 0.059
865
P PNT019 Pontocerebellar Hypoplasia 46 0.059
866
P LCT002 Lactose Intolerance 53 0.059
867
BLL006 Bullous Pemphigoid 62 0.059
868
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 62 0.059
869
RNL077 Renal Fibrosis 47 0.059
870
DNN002 Donnai-Barrow Syndrome 56 0.058
871
c HPT015 Hepatitis D 49 0.058
872
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.058
873
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.058
874
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.058
875
LNG039 Lung Squamous Cell Carcinoma 66 0.058
876
CLF001 Cleft Lip 53 0.058
877
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.058
878
P PSD015 Pseudohypoparathyroidism 56 0.058
879
DWR001 Dwarfism 44 0.058
880
P ALP106 Alport Syndrome 1, X-Linked 55 0.058
881
TRP009 Triple X Syndrome 42 0.058
882
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.058
883
PYR022 Pyruvate Dehydrogenase E1-Alpha Deficiency 60 0.058
884
AZS001 Azoospermia 50 0.058
885
PYR021 Pyridoxamine 5-Prime-Phosphate Oxidase Deficiency 47 0.058
886
BRS099 Breast Ductal Carcinoma 62 0.058
887
MCL006 Macular Retinal Edema 55 0.058
888
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.058
889
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.058
890
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.058
891
PLY001 Polycythemia Vera 69 0.058
892
HYP741 Hyperparathyroidism 2 with Jaw Tumors 53 0.058
893
THR123 Thrombotic Microangiopathy 36 0.058
894
THR013 Thoracic Outlet Syndrome 54 0.057
895
P PMP001 Pemphigus 54 0.057
896
PRS047 Prostatitis 56 0.057
897
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.057
898
c ALZ056 Alzheimer Disease 3 57 0.057
899
STT009 Sutton Disease 2 30 0.057
900
PRP001 Propionic Acidemia 65 0.057
901
TRN022 Transcobalamin Ii Deficiency 45 0.057
902
HRP008 Herpes Simiae 25 0.057
903
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.057
904
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.057
905
SPP011 Suppression of Tumorigenicity 12 59 0.057
906
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.057
907
ACR006 Aceruloplasminemia 65 0.057
908
FND001 Fundus Albipunctatus 60 0.057
909
MCR013 Microphthalmia 57 0.057
910
P NPH005 Nephronophthisis 59 0.057
911
P MMB011 Membranous Nephropathy 50 0.057
912
c PRX059 Peroxisome Biogenesis Disorder 1a 56 0.057
913
P AGG001 Aggressive Periodontitis 50 0.056
914
APP008 Appendicitis 61 0.056
915
MTC005 Mitochondrial Metabolism Disease 49 0.056
916
c GCH015 Gaucher Disease, Type I 70 0.056
917
c GLY008 Glycogen Storage Disease Ii 70 0.056
918
PRT082 Preterm Premature Rupture of the Membranes 54 0.056
919
EHL052 Ehlers-Danlos Syndrome, Vascular Type 56 0.056
920
PHR003 Pharyngitis 57 0.056
921
KRT006 Keratoconjunctivitis 53 0.056
922
PRL032 Perlman Syndrome 57 0.056
923
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.056
924
SYN007 Synovitis 54 0.056
925
PLC002 Plica Syndrome 36 0.056
926
PRT018 Portal Vein Thrombosis 50 0.056
927
ORL012 Oral Leukoplakia 39 0.056
928
WST001 West Syndrome 61 0.056
929
MTH056 Methylmalonic Aciduria and Homocystinuria, Cblf Type 38 0.056
930
ANV001 Anovulation 47 0.056
931
CHR005 Chorioamnionitis 51 0.056
932
P SCL057 Scoliosis, Isolated 1 41 0.055
933
LBR036 Leber Plus Disease 66 0.055
934
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.055
935
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.055
936
c USH036 Usher Syndrome, Type I 60 0.055
937
P OBS001 Obstructive Jaundice 50 0.055
938
P ASP006 Aspergillosis 69 0.055
939
GRG001 Greig Cephalopolysyndactyly Syndrome 66 0.055
940
CRT017 Cartilage Disease 54 0.055
941
RDN001 Reading Disorder 40 0.055
942
P ANP001 Anaplastic Large Cell Lymphoma 58 0.055
943
P KRB001 Krabbe Disease 69 0.055
944
HRT012 Heart Valve Disease 53 0.055
945
P TXP001 Toxoplasmosis 60 0.055
946
GST092 Gastroesophageal Reflux 67 0.055
947
P SCL009 Sclerosing Cholangitis 48 0.055
948
CMM004 Common Variable Immunodeficiency 68 0.055
949
LPT006 Leptin Receptor Deficiency 48 0.055
950
LYS012 Lysosomal Acid Lipase Deficiency 65 0.055
951
CHL004 Cholelithiasis 49 0.055
952
MLT092 Multicentric Carpotarsal Osteolysis Syndrome 65 0.055
953
KRT013 Keratolytic Winter Erythema 46 0.055
954
HDN002 Head Injury 46 0.055
955
SXL003 Sexual Disorder 47 0.055
956
GST020 Gastric Antral Vascular Ectasia 41 0.055
957
DRY001 Dry Eye Syndrome 47 0.054
958
TYP007 Typhoid Fever 63 0.054
959
P MTR004 Maturity-Onset Diabetes of the Young 65 0.054
960
ETN001 Eating Disorder 60 0.054
961
DRR014 Darier-White Disease 60 0.054
962
c DSB006 Desbuquois Dysplasia 1 48 0.054
963
KWS002 Kawasaki Disease 65 0.054
964
GLL008 Gilles De La Tourette Syndrome 66 0.054
965
FCT034 Factor V and Factor Viii, Combined Deficiency of, 2 41 0.054
966
CYS013 Cystinuria 63 0.054
967
MLT118 Multiple Acyl-Coa Dehydrogenase Deficiency 68 0.054
968
CLR030 Clear Cell Renal Cell Carcinoma 53 0.054
969
PLG002 Plague 63 0.054
970
GRN017 Granulocytopenia 44 0.054
971
ATX010 Ataxia Neuropathy Spectrum 34 0.054
972
SCH012 Schizoaffective Disorder 50 0.054
973
c PSD114 Pseudohypoaldosteronism, Type I, Autosomal Recessive 59 0.054
974
MYC006 Mycosis Fungoides 66 0.054
975
CHL109 Childhood Apraxia of Speech 44 0.054
976
INT075 Intracranial Hypertension 53 0.053
977
THR016 Thrombophlebitis 51 0.053
978
c SZR007 Seizures, Benign Familial Infantile, 3 42 0.053
979
SMT004 Smith-Lemli-Opitz Syndrome 70 0.053
980
ATN004 Autonomic Neuropathy 45 0.053
981
PST028 Post-Traumatic Stress Disorder 58 0.053
982
P RTT002 Rett Syndrome 80 0.053
983
OBS002 Obsessive-Compulsive Disorder 68 0.053
984
INT303 Intracranial Hypertension, Idiopathic 57 0.053
985
P PGT001 Paget's Disease of Bone 58 0.053
986
LYM040 Lymphoblastic Lymphoma 54 0.053
987
INT088 Intrinsic Factor Deficiency 34 0.053
988
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.053
989
P ALG028 Alagille Syndrome 1 73 0.053
990
SFT003 Soft Tissue Sarcoma 56 0.053
991
NRP051 Neuropathy, Hereditary, with Liability to Pressure Palsies 59 0.053
992
HPT022 Hepatoblastoma 56 0.053
993
c MYS033 Miyoshi Muscular Dystrophy 1 56 0.053
994
LWC001 Low Compliance Bladder 43 0.053
995
RSC001 Rosacea 54 0.053
996
c MNN043 Meningioma, Familial 74 0.053
997
c ACT004 Acute Diarrhea 39 0.052
998
c HNT011 Huntington Disease-Like 3 38 0.052
999
BTT001 Bietti Crystalline Corneoretinal Dystrophy 52 0.052
1000
c CHL132 Cholestasis, Progressive Familial Intrahepatic, 1 57 0.052
1001
P PLY041 Polymyositis 57 0.052
1002
P LRY044 Larynx Cancer 55 0.052
1003
c MST023 Mesothelioma, Malignant 57 0.052
1004
c DPH024 Diaphragmatic Hernia, Congenital 63 0.052
1005
CHR103 Charge Syndrome 67 0.052
1006
SPR004 Supravalvular Aortic Stenosis 58 0.052
1007
GLM044 Glomerular Disease 37 0.052
1008
c OPT053 Optic Atrophy 1 63 0.052
1009
P BRN022 Bronchiectasis 59 0.052
1010
c SYS043 Systemic Lupus Erythematosus 1 38 0.052
1011
AYM001 Ayme-Gripp Syndrome 57 0.052
1012
P KRT007 Keratoconus 50 0.052
1013
P TRC031 Trichorhinophalangeal Syndrome 40 0.052
1014
GLC042 Glucocorticoid Deficiency 1 53 0.052
1015
ADN011 Adenoid Cystic Carcinoma 70 0.052
1016
MYL031 Myeloproliferative Neoplasm 66 0.052
1017
HMT002 Hematologic Cancer 62 0.052
1018
ACT064 Acute Necrotizing Encephalitis 33 0.052
1019
BLD137 Blood Group--Ahonen 16 0.052
1020
P MYS003 Myasthenia Gravis 68 0.052
1021
P SML001 Small Cell Carcinoma 52 0.052
1022
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.052
1023
c HYP794 Hyperoxaluria, Primary, Type I 63 0.052
1024
EXC002 Exocrine Pancreatic Insufficiency 42 0.052
1025
FML026 Familial Lipoprotein Lipase Deficiency 51 0.052
1026
c WLM018 Wilms Tumor 5 61 0.052
1027
CHN055 Chanarin-Dorfman Syndrome 61 0.052
1028
c HNT004 Huntington Disease-Like 2 50 0.052
1029
INF034 Infective Endocarditis 53 0.052
1030
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.052
1031
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.052
1032
ACT084 Acute Stress Disorder 47 0.052
1033
HMR039 Hemorrhage, Intracerebral 57 0.051
1034
MLT157 Multiple System Atrophy 1 70 0.051
1035
AST006 Astigmatism 47 0.051
1036
P DRM010 Dermatomyositis 61 0.051
1037
PTH003 Pathologic Nystagmus 52 0.051
1038
P TCD001 Tic Disorder 53 0.051
1039
YLL002 Yellow Fever 61 0.051
1040
FBR012 Fabry Disease 72 0.051
1041
OVR029 Ovarian Hyperstimulation Syndrome 64 0.051
1042
URT010 Ureteral Obstruction 45 0.051
1043
P PRN023 Prion Disease 57 0.051
1044
PRS034 Parasitic Helminthiasis Infectious Disease 50 0.051
1045
MTC027 Mitochondrial Trifunctional Protein Deficiency 58 0.051
1046
TNS005 Tonsillitis 57 0.051
1047
P THY023 Thymoma 65 0.051
1048
c THY107 Thymoma, Familial 52 0.051
1049
MCR018 Microcytic Anemia 47 0.051
1050
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.051
1051
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.051
1052
P PRG092 Pregnancy Loss, Recurrent 1 40 0.051
1053
SPT004 Septic Arthritis 58 0.051
1054
HYP348 Hyperglycinuria 41 0.051
1055
CYT008 Cytomegalovirus Infection 57 0.051
1056
c MCL013 Mucolipidosis Iv 66 0.051
1057
P MYC033 Myoclonus 46 0.051
1058
RFR003 Refractive Error 43 0.051
1059
P DNT020 Dent Disease 1 62 0.051
1060
ARG004 Argyria 27 0.051
1061
NRN004 Neuroendocrine Tumor 55 0.051
1062
P STR020 Strabismus 55 0.051
1064
PLL001 Pallister-Hall Syndrome 64 0.050
1065
P GLC113 Galactosemia I 64 0.050
1066
ALP097 Alopecia Universalis Congenita 59 0.050
1067
TRT001 Teratocarcinoma 45 0.050
1068
SPS019 Spastic Paraparesis 38 0.050