Search results for Sodium citrate

1458 hits were found for Sodium citrate

# Family MCID Name MIFTS Score
1
c HYP595 Hypertension, Essential 84 0.391
2
P KDN018 Kidney Disease 70 0.361
3
P INF032 Infertility 57 0.289
4
P PLY011 Polycystic Ovary Syndrome 56 0.288
5
IMP005 Impotence 52 0.287
6
CLT003 Colitis 62 0.286
7
c CHR684 Chronic Kidney Disease 66 0.284
8
HYP005 Hypokalemia 55 0.266
9
48X005 48,xyyy 39 0.260
10
MTB004 Metabolic Acidosis 50 0.259
11
c ACT071 Acute Kidney Failure 59 0.248
12
CNG034 Congestive Heart Failure 70 0.235
13
END030 End Stage Renal Failure 58 0.234
14
NPH091 Nephrolithiasis, Calcium Oxalate 66 0.217
15
P HRT032 Heart Disease 75 0.215
16
ADL002 Adult Syndrome 69 0.212
17
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.212
18
ALL026 Allergic Hypersensitivity Disease 64 0.209
19
c RHB024 Rhabdomyosarcoma 2 65 0.208
20
P BRS047 Breast Cancer 96 0.204
21
LVR012 Liver Cirrhosis 63 0.203
22
P OST002 Osteoporosis 73 0.200
23
P DRR001 Diarrhea 57 0.199
24
P PLM037 Pulmonary Hypertension 68 0.198
25
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.195
26
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.195
27
ULC004 Ulcerative Colitis 73 0.192
28
OST012 Osteoarthritis 78 0.190
29
c PNS012 Paine Syndrome 61 0.188
30
P INF037 Inflammatory Bowel Disease 56 0.187
31
PNG002 Pain Agnosia 51 0.186
32
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.184
33
DWN001 Down Syndrome 70 0.184
34
c EPS039 Episodic Pain Syndrome, Familial, 1 40 0.184
35
IRN002 Iron Metabolism Disease 57 0.182
36
P LVR013 Liver Disease 68 0.180
37
ANV001 Anovulation 47 0.178
38
ISC004 Ischemia 60 0.178
39
P TRN020 Turner Syndrome 65 0.176
40
HYP056 Hypoglycemia 66 0.173
41
DFC004 Deficiency Anemia 75 0.173
42
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.172
43
HYP025 Hyperphosphatemia 47 0.172
44
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.171
45
c MGR028 Migraine with or Without Aura 1 69 0.170
46
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.170
47
P SZR006 Seizure Disorder 58 0.168
48
BNR002 Bone Resorption Disease 48 0.163
49
ATX019 Ataxia with Vitamin E Deficiency 48 0.162
50
P NRB001 Neuroblastoma 71 0.161
51
P CLR023 Colorectal Cancer 98 0.160
52
HYP066 Hyperglycemia 61 0.159
53
P CRD119 Cardiac Arrest 67 0.158
54
c PLY105 Polycystic Ovary Syndrome 1 38 0.157
55
CNS004 Constipation 57 0.157
56
P HYP086 Hypothyroidism 68 0.156
57
CYS001 Cystic Fibrosis 80 0.155
58
DNT012 Dental Caries 51 0.155
59
P ADN016 Adenocarcinoma 64 0.155
60
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.155
61
P HDC001 Headache 57 0.153
62
P PRS040 Prostate Cancer 97 0.152
63
DRM006 Dermatitis 61 0.151
64
THY029 Thyroid Carcinoma 59 0.151
65
P RHN004 Rhinitis 57 0.150
66
HYP266 Hypoxia 56 0.149
67
P GLM045 Glioma 63 0.149
68
GLL048 Glial Tumor 45 0.149
69
VSL002 Visual Epilepsy 58 0.149
70
P ENC018 Encephalopathy 61 0.146
71
P THR014 Thrombocytopenia 68 0.145
72
P DBT009 Diabetes Mellitus 64 0.144
73
P VSC007 Vascular Disease 63 0.144
74
RCK004 Rickets 69 0.144
75
P MYC007 Myocardial Infarction 70 0.143
76
c PRC016 Pre-Eclampsia 63 0.143
77
CRB039 Cerebrovascular Disease 69 0.141
78
P BPL003 Bipolar Disorder 56 0.141
79
AST005 Asthma 77 0.141
80
P CTR002 Cataract 60 0.140
81
c MCR120 Microvascular Complications of Diabetes 7 47 0.140
82
c MJR024 Major Affective Disorder 9 41 0.140
83
c MJR022 Major Affective Disorder 8 38 0.140
84
STR067 Stroke, Ischemic 80 0.140
85
THR024 Thrombosis 56 0.139
86
HRW001 Hair Whorl 36 0.139
87
P CRD246 Cardiovascular System Disease 56 0.139
88
LNG099 Lung Disease 61 0.138
89
c MCR113 Microvascular Complications of Diabetes 3 52 0.138
90
c ACT068 Acute Cystitis 63 0.137
91
c MCR130 Microvascular Complications of Diabetes 6 41 0.137
92
c MCR133 Microvascular Complications of Diabetes 4 41 0.137
93
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.136
94
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.136
95
P NRP001 Neuropathy 56 0.136
96
P DDN001 Duodenal Ulcer 50 0.135
97
HYP060 Hyperinsulinism 54 0.135
98
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.134
99
MYL069 Myeloma, Multiple 85 0.134
100
ADN018 Adenoma 58 0.134
101
P NTR004 Neutropenia 63 0.133
102
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.133
103
ALL003 Allergic Rhinitis 67 0.133
104
c THR092 Thrombophilia Due to Thrombin Defect 73 0.132
105
P RNL007 Renal Tubular Acidosis 50 0.132
106
P BLD124 Bleeding Disorder, Platelet-Type, 11 61 0.132
107
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.132
108
P LYM118 Lymphoma 68 0.131
109
PLM010 Pulmonary Edema 55 0.131
110
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.129
111
P LKM002 Leukemia 66 0.129
112
HLC007 Helicobacter Pylori Infection 59 0.129
113
P CHR345 Chronic Pain 50 0.128
114
HLX001 Helix Syndrome 47 0.127
115
NTR005 Nutritional Deficiency Disease 61 0.127
116
P GST044 Gastritis 55 0.127
117
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.127
118
GLB015 Glioblastoma Multiforme 75 0.127
119
BRN071 Brain Injury 49 0.125
120
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.125
121
c ACT075 Acute Myocardial Infarction 56 0.124
122
HYP064 Hypogonadotropism 40 0.124
123
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.124
124
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.124
125
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.124
126
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.124
127
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.124
128
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.124
129
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.124
130
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.124
131
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.124
132
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.124
133
HYP080 Hypogonadism 50 0.123
134
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.123
135
P EXN002 Exanthem 57 0.122
136
GST092 Gastroesophageal Reflux 65 0.121
137
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.121
138
P HYP069 Hyperparathyroidism 62 0.120
139
OVR029 Ovarian Hyperstimulation Syndrome 63 0.120
140
TXC005 Toxic Shock Syndrome 61 0.120
141
P HPT023 Hepatocellular Carcinoma 100 0.120
142
P EPL164 Epilepsy 71 0.119
143
OCL069 Ocular Motor Apraxia 51 0.118
144
P LCT001 Lactic Acidosis 51 0.118
145
c PRS136 Prostate Cancer, Hereditary, 6 33 0.117
146
c PRS130 Prostate Cancer, Hereditary, 8 32 0.117
147
PPT005 Peptic Ulcer Disease 58 0.117
148
CHL014 Cholera 55 0.116
149
ANX010 Anxiety 72 0.116
150
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.115
151
P ART106 Arterial Calcification, Generalized, of Infancy, 1 48 0.114
152
CYT002 Cytokine Deficiency 44 0.114
153
CHL079 Children's Interstitial Lung Disease 27 0.114
154
TRM010 Traumatic Brain Injury 53 0.113
155
PLS009 Plasma Cell Neoplasm 51 0.113
156
IRN001 Iron Deficiency Anemia 58 0.113
157
P NRC002 Narcolepsy 51 0.113
158
P CRN018 Coronary Artery Anomaly 63 0.112
159
c HYP836 Hypercholesterolemia, Familial, 1 72 0.112
160
SPN186 Spinal Cord Injury 60 0.112
161
P ECL001 Eclampsia 51 0.112
162
NPH003 Nephrocalcinosis 51 0.112
163
FTT001 Fatty Liver Disease 61 0.110
164
P BND020 Bone Disease 59 0.110
165
P CYS018 Cystitis 59 0.110
167
P RNL015 Renal Hypertension 48 0.109
168
GST023 Gastric Ulcer 53 0.109
169
P MLN007 Male Infertility 56 0.109
170
LYM019 Lymphosarcoma 47 0.108
171
AMN001 Amenorrhea 54 0.108
172
P LNG032 Lung Cancer 97 0.108
173
HMN044 Human Immunodeficiency Virus Type 1 71 0.107
174
P TRM003 Tremor 53 0.107
175
ATH013 Atherosclerosis Susceptibility 66 0.107
176
DPR016 Depression 63 0.107
177
P CNJ013 Conjunctivitis 65 0.107
178
ACQ007 Acquired Immunodeficiency Syndrome 60 0.107
179
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 56 0.106
180
P DBT005 Diabetes Insipidus 55 0.106
181
P NPH012 Nephrotic Syndrome 63 0.105
182
LPD008 Lipid Metabolism Disorder 62 0.105
183
47X002 47,xyy 49 0.105
184
PLM033 Pulmonary Embolism 59 0.105
185
GLS018 Glass Syndrome 53 0.105
186
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.105
187
ANG054 Angina Pectoris 66 0.105
188
c ACT027 Acute Pancreatitis 59 0.104
189
P ART022 Arthritis 70 0.104
190
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.104
191
HPR003 Heparin-Induced Thrombocytopenia 47 0.104
192
P LYM031 Lymphocytic Leukemia 55 0.104
193
P RHM011 Rheumatoid Arthritis 80 0.103
194
HYP017 Hypophosphatemia 49 0.103
195
ATM095 Autoimmune Disease 61 0.103
196
HYP043 Hyperandrogenism 48 0.103
197
P END044 Endometriosis 62 0.103
198
P ESP024 Esophagitis 62 0.103
199
OST017 Osteomyelitis 64 0.103
200
URM002 Uremia 49 0.102
201
P RSP003 Respiratory Failure 74 0.102
202
ART140 Arteries, Anomalies of 53 0.102
203
P PNM007 Pneumonia 68 0.102
204
P PRP019 Peripheral Nervous System Disease 57 0.101
205
P PNC044 Pancreatitis 61 0.101
206
P GST053 Gastric Cancer 83 0.100
207
NNL005 Non-Alcoholic Fatty Liver Disease 62 0.100
208
CLC001 Calciphylaxis 51 0.100
209
c MLG068 Malignant Glioma 45 0.100
210
GNG013 Gingivitis 59 0.099
211
IMM167 Immune Deficiency Disease 78 0.099
212
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 56 0.099
213
KRT006 Keratoconjunctivitis 53 0.099
214
P OVR042 Ovarian Cancer 89 0.098
215
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.097
216
P HYP076 Hyperthyroidism 55 0.097
217
ALC007 Alcohol Dependence 66 0.097
218
c SYS001 Systemic Lupus Erythematosus 86 0.097
219
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.096
220
MNT002 Mental Depression 57 0.096
221
P MCR115 Microvascular Complications of Diabetes 5 66 0.096
222
P INT143 Interstitial Cystitis 61 0.096
223
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.095
224
P BLD134 Bladder Cancer 78 0.095
225
P DRM053 Dermatitis, Atopic 66 0.095
226
P CRN300 Coronary Heart Disease 1 63 0.095
227
CRD223 Cardiac Arrhythmia 60 0.094
228
P PNC035 Pancreatic Cancer 84 0.094
229
PRS045 Prostatic Hypertrophy 52 0.093
230
P ATR011 Atrial Fibrillation 66 0.093
231
EYD002 Eye Disease 58 0.093
232
DRY001 Dry Eye Syndrome 47 0.093
233
ESP021 Esophageal Cancer 90 0.093
234
OST159 Osteogenic Sarcoma 66 0.093
235
SPS057 Spasticity 41 0.093
236
BRN028 Brain Cancer 73 0.093
237
c PRM038 Primary Agammaglobulinemia 43 0.093
238
ALL009 Allergic Conjunctivitis 50 0.092
239
P NRF023 Neurofibromatosis, Type Ii 76 0.092
240
P MYL006 Myeloid Leukemia 60 0.092
241
HPT004 Hepatic Coma 43 0.092
242
BCT022 Bacterial Infectious Disease 56 0.092
243
PRT036 Peritonitis 65 0.092
244
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.092
245
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.092
246
P URT039 Urticaria 58 0.092
247
P SCK005 Sickle Cell Disease 50 0.092
248
PRS021 Prostatic Adenoma 51 0.092
249
BRN056 Bronchopulmonary Dysplasia 57 0.092
250
P MJR007 Major Affective Disorder 1 43 0.091
251
P LPS004 Lupus Erythematosus 61 0.091
252
RHM027 Rheumatic Disease 56 0.090
253
P MLT020 Multiple Sclerosis 72 0.090
254
KRT001 Keratoconjunctivitis Sicca 50 0.090
255
P SRC025 Sarcoidosis 1 70 0.090
256
SPN035 Spindle Cell Sarcoma 51 0.090
257
P PRD008 Periodontitis 62 0.089
258
HPT019 Hepatic Encephalopathy 60 0.089
259
MST005 Mastitis 53 0.089
260
AGN016 Aging 56 0.089
261
GST045 Gastroenteritis 59 0.089
262
P GLM007 Glomerulonephritis 57 0.089
263
P SJG008 Sjogren Syndrome 56 0.089
264
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.089
265
GLC003 Glucose Intolerance 54 0.088
266
SRC014 Sarcoma 65 0.088
267
c LKM061 Leukemia, Acute Myeloid 83 0.088
268
IRR002 Irritable Bowel Syndrome 63 0.088
269
PRT013 Portal Hypertension 60 0.088
270
HMS001 Hemosiderosis 54 0.088
271
P MYP004 Myopathy 64 0.088
272
P GLM040 Glioma Susceptibility 1 81 0.088
273
ANX004 Anoxia 42 0.088
274
P CNR004 Cone-Rod Dystrophy 2 71 0.087
275
P INS002 in Situ Carcinoma 52 0.087
276
P DST107 Distal Renal Tubular Acidosis 41 0.087
277
VRC005 Varicose Veins 60 0.087
278
BRN024 Bronchitis 68 0.087
279
P BCL017 B-Cell Lymphoma 58 0.087
280
c MJR008 Major Affective Disorder 2 34 0.087
281
c MJR003 Major Affective Disorder 6 33 0.087
282
c MJR006 Major Affective Disorder 5 33 0.087
283
c MJR023 Major Affective Disorder 7 33 0.087
284
c MJR004 Major Affective Disorder 4 28 0.087
285
c ATR087 Atrial Standstill 1 74 0.086
286
PRP027 Peripheral Vascular Disease 71 0.086
287
c MCR129 Microvascular Complications of Diabetes 1 66 0.086
288
PRS129 Prostatic Hyperplasia, Benign 49 0.086
289
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.086
290
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 57 0.086
291
PRT037 Pertussis 65 0.086
292
P ALZ034 Alzheimer Disease 88 0.086
293
RRS014 Rare Surgical Neurologic Disease 32 0.085
294
P RRH023 Rare Hereditary Hemochromatosis 41 0.085
295
STM007 Stomatitis 49 0.085
296
MLN008 Melanoma 69 0.085
297
HYP020 Hyperprolactinemia 64 0.085
298
CLC006 Calcinosis 48 0.085
299
c SML038 Small Cell Cancer of the Lung 65 0.085
300
P SLP006 Sleep Apnea 69 0.084
301
ENT011 Enterocolitis 50 0.084
302
c LKM071 Leukemia, Chronic Lymphocytic 79 0.084
303
PRT058 Pure Autonomic Failure 59 0.084
304
P PHC003 Pheochromocytoma 71 0.084
305
ENT004 Enthesopathy 48 0.084
306
ADR040 Adrenal Gland Pheochromocytoma 46 0.084
307
INS024 Insulin-Like Growth Factor I 79 0.083
308
P PYL005 Pyelonephritis 56 0.083
309
P PNC025 Panic Disorder 53 0.083
310
P AST007 Astrocytoma 50 0.083
311
P PLY014 Polycystic Kidney Disease 59 0.082
312
DBT010 Diabetic Neuropathy 55 0.082
313
MYL009 Myelodysplastic Syndrome 70 0.082
314
P MSC005 Muscular Dystrophy 66 0.082
315
PSY004 Psychotic Disorder 67 0.082
316
ANR040 Aneurysm 58 0.082
317
INT007 Intermediate Coronary Syndrome 55 0.082
318
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.082
319
CHL068 Cholestasis 60 0.081
320
P ADL010 Adult Respiratory Distress Syndrome 63 0.081
321
c DLT002 Dilated Cardiomyopathy 79 0.081
322
SBC016 Subacute Delirium 44 0.081
323
P ALP008 Alopecia 56 0.081
324
CRB004 Cerebral Artery Occlusion 44 0.081
325
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.081
326
KRT019 Keratitis, Hereditary 67 0.081
327
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.081
328
NRL016 Neural Tube Defects 82 0.080
329
MXD026 Mixed Glioma 45 0.080
330
BCK006 Back Pain 42 0.080
331
P MLG056 Malignant Hyperthermia 67 0.080
332
GT001 Gout 63 0.080
333
SKN016 Skin Disease 63 0.079
334
PPT001 Peptic Esophagitis 51 0.079
335
SYN007 Synovitis 55 0.079
336
ILS001 Ileus 51 0.079
337
END057 Endometrial Cancer 74 0.079
338
NNL006 Non-Alcoholic Steatohepatitis 51 0.079
339
TTN003 Tetanus 64 0.079
340
P SCH015 Schizophrenia 75 0.078
341
SXL003 Sexual Disorder 48 0.078
342
CNN005 Connective Tissue Disease 66 0.078
343
c ACT134 Acute Liver Failure 51 0.078
344
P OVR049 Ovarian Disease 53 0.078
345
c CNT033 Central Nervous System Cancer 46 0.078
346
SFT003 Soft Tissue Sarcoma 56 0.078
347
MCS002 Mucositis 55 0.078
348
c SCL052 Scleroderma, Familial Progressive 62 0.077
349
SCK003 Sickle Cell Anemia 72 0.077
350
c FNC043 Fanconi Anemia, Complementation Group E 62 0.077
351
FBR047 Fibromyalgia 59 0.077
352
P LKM062 Leukemia, Acute Lymphoblastic 68 0.077
353
P MYC008 Myocarditis 59 0.077
354
LNG031 Lung Benign Neoplasm 50 0.077
355
P PLM036 Pulmonary Fibrosis 61 0.077
356
IDP011 Idiopathic Interstitial Pneumonia 63 0.077
357
P NRV006 Nervous System Cancer 48 0.077
358
ARG004 Argyria 28 0.077
359
FLR002 Filariasis 55 0.077
360
P AMY004 Amyloidosis 70 0.077
361
CRD132 Cardiac Conduction Defect 59 0.076
362
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.076
363
P HYP024 Hypoparathyroidism 55 0.076
364
IDP073 Idiopathic Hypercalciuria 43 0.076
365
BRN004 Brain Edema 55 0.076
366
CRH001 Crohn's Disease 74 0.076
367
P HYP098 Hypereosinophilic Syndrome 66 0.075
368
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.075
369
GST050 Gastrointestinal System Disease 56 0.075
370
49X006 49, Xxxxy Syndrome 41 0.075
371
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.075
372
HYP014 Hyperuricemia 51 0.075
373
c PRM005 Primary Hyperparathyroidism 58 0.075
374
P HYP802 Hypocalcemia, Autosomal Dominant 1 68 0.075
375
NWB001 Newborn Respiratory Distress Syndrome 58 0.075
376
MSC007 Muscle Hypertrophy 63 0.074
377
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.074
378
MLR004 Malaria 80 0.074
379
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.074
380
LPD012 Lipoid Congenital Adrenal Hyperplasia 71 0.074
381
MCL006 Macular Retinal Edema 55 0.074
382
MDD011 Mood Disorder 62 0.074
383
PLM001 Pulmonary Tuberculosis 70 0.074
384
LYM133 Lymphoma, Hodgkin, Classic 69 0.074
385
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 36 0.073
386
c XNT010 Xanthinuria, Type I 50 0.073
387
INT075 Intracranial Hypertension 53 0.073
388
P HPT021 Hepatitis 67 0.073
389
P HYP750 Hypertriglyceridemia, Familial 61 0.073
390
P CND004 Candidiasis 57 0.073
391
P MYC033 Myoclonus 46 0.073
392
GST020 Gastric Antral Vascular Ectasia 41 0.073
393
SCH014 Schistosomiasis 56 0.073
394
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.073
395
P BCT020 Bacteremia 2 44 0.072
396
RDN001 Reading Disorder 40 0.072
397
P ART023 Arthropathy 62 0.072
398
c MLG074 Malignant Mesenchymoma 39 0.072
399
P HRP006 Herpes Simplex 65 0.072
400
GTR002 Goiter 52 0.072
401
c MCR112 Microvascular Complications of Diabetes 2 41 0.072
402
KRT009 Keratosis 53 0.071
403
P SYP003 Syphilis 59 0.071
404
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.071
405
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 61 0.071
406
URN010 Urinary Tract Obstruction 57 0.071
407
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.071
408
P LTR001 Lateral Sclerosis 53 0.071
409
P PSR002 Psoriasis 62 0.071
410
PST011 Pustulosis of Palm and Sole 52 0.071
411
BRS099 Breast Ductal Carcinoma 62 0.070
412
c ACT073 Acute Leukemia 58 0.070
413
P THL005 Thalassemia 60 0.070
414
P BNG032 Benign Mesothelioma 45 0.070
415
PRN019 Perinatal Necrotizing Enterocolitis 54 0.070
416
ACR041 Acromelic Frontonasal Dysostosis 52 0.070
417
PRS047 Prostatitis 56 0.070
418
PPL001 Papillary Adenoma 45 0.070
419
SQM006 Squamous Cell Carcinoma 60 0.070
420
c INH020 Inherited Metabolic Disorder 46 0.070
421
ACR007 Acromegaly 71 0.070
422
DYS015 Dysentery 50 0.070
423
P OPT006 Optic Nerve Disease 57 0.069
424
c SCN007 Secondary Hyperparathyroidism 50 0.069
425
P ATS364 Autism 65 0.069
426
CNN003 Conn's Syndrome 79 0.069
427
P SYS005 Systemic Scleroderma 70 0.069
428
P MNN013 Meningitis 65 0.069
429
THY122 Thyroid Gland Cancer 58 0.069
430
P SLP005 Sleep Disorder 59 0.069
431
c HPT016 Hepatitis B 59 0.069
432
LYM040 Lymphoblastic Lymphoma 54 0.069
433
P KDN017 Kidney Cancer 61 0.069
434
P THY032 Thyroiditis 53 0.069
435
c PCH010 Pachyonychia Congenita 3 43 0.069
436
PLC008 Placenta Disease 49 0.069
437
SYN036 Syncope 45 0.068
438
PPL052 Papillomatosis, Confluent and Reticulated 34 0.068
439
CRB037 Cerebral Palsy 68 0.068
440
OVR094 Ovarian Epithelial Cancer 38 0.068
441
P OCY003 Oocyte Maturation Defect 1 45 0.068
442
MMM001 Mammary Paget's Disease 53 0.068
443
P DYS154 Dystonia 65 0.068
444
PPL022 Papilloma 54 0.068
445
RTN023 Retinitis 46 0.067
446
NRR001 Neuroretinitis 43 0.067
447
P HYP265 Hypotonia 42 0.067
448
APN008 Apnea, Obstructive Sleep 65 0.067
449
DSS009 Disseminated Intravascular Coagulation 57 0.067
450
P OVR046 Ovarian Cyst 45 0.067
451
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.067
452
MRG003 Marginal Zone B-Cell Lymphoma 53 0.067
453
P OVR082 Overgrowth Syndrome 50 0.067
454
c INF145 Infantile Liver Failure Syndrome 1 50 0.067
455
P UVT001 Uveitis 57 0.066
456
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.066
457
SQM002 Squamous Cell Papilloma 42 0.066
458
BRN002 Bronchiolitis 59 0.066
459
P ALC033 Alcohol Use Disorder 58 0.066
460
HYP781 Hypoascorbemia 50 0.066
461
c DNT047 Dentinogenesis Imperfecta Type 2 33 0.066
462
MCR004 Macroglobulinemia 50 0.066
463
ASP008 Aspiration Pneumonitis 42 0.066
464
MNT001 Mantle Cell Lymphoma 66 0.066
465
GLS001 Gliosarcoma 54 0.066
466
ACT119 Acute Promyelocytic Leukemia 63 0.066
467
THY030 Thyroid Gland Disease 51 0.066
468
ASC001 Ascaridiasis 35 0.065
469
SKN019 Skin Melanoma 67 0.065
470
BRK010 Burkitt Lymphoma 67 0.065
471
INT067 Interstitial Nephritis 46 0.065
472
GRD007 Grade Iii Astrocytoma 59 0.065
473
P END033 Endocarditis 57 0.065
474
END040 Endogenous Depression 54 0.065
475
ENT001 Enterocele 39 0.065
476
AZS001 Azoospermia 50 0.064
477
CMR002 Coumarin Resistance 56 0.064
478
ACT003 Acute Kidney Tubular Necrosis 45 0.064
479
PPL049 Papillon-Lefevre Syndrome 63 0.064
480
NRT001 Neurotic Disorder 52 0.064
481
ASC010 Ascaris Lumbricoides Infection 49 0.064
482
c BRS049 Breast Carcinoma in Situ 50 0.063
483
OLG001 Oligospermia 45 0.063
484
P PRK057 Parkinson Disease, Late-Onset 76 0.063
485
FCT007 Factor Vii Deficiency 66 0.063
486
P PTN014 Patent Ductus Arteriosus 1 60 0.063
487
ONC002 Onchocerciasis 51 0.063
488
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.063
489
DYS073 Dysphagia 50 0.063
490
ECT026 Ectopic Pregnancy 49 0.063
491
c BRN108 Branchiootic Syndrome 1 61 0.063
492
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.063
493
P FNC004 Fanconi Syndrome 50 0.063
494
ATS010 Autosomal Recessive Disease 48 0.063
495
HYP189 Hypoadrenalism 37 0.063
496
DCT002 Ductal Carcinoma in Situ 59 0.063
497
PRP007 Priapism 48 0.063
498
LPT014 Leptin Deficiency or Dysfunction 73 0.063
499
c LRG017 Large Intestine Cancer 47 0.063
500
PRS063 Paresthesia 43 0.063
501
RYN005 Raynaud Phenomenon 46 0.062
502
P DNT007 Dentin Sensitivity 35 0.062
503
CRV035 Cervical Cancer 76 0.062
504
c FML001 Familial Atrial Fibrillation 66 0.062
505
P NRV007 Nervous System Disease 66 0.062
506
IDP033 Idiopathic Edema 43 0.062
507
PST092 Posttransplant Acute Limbic Encephalitis 29 0.062
508
KPS004 Kaposi Sarcoma 75 0.062
509
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.062
510
ATN011 Autoinflammation with Infantile Enterocolitis 43 0.062
511
HRT011 Heart Septal Defect 50 0.062
512
c OVR114 Ovarian Cancer 1 38 0.062
513
P HYP730 Hypogonadotropic Hypogonadism 53 0.062
514
P GRF003 Graft-Versus-Host Disease 71 0.062
515
TXC002 Toxic Encephalopathy 52 0.062
516
CYN002 Cyanosis, Transient Neonatal 45 0.062
517
c HPT001 Hepatitis C 63 0.061
518
c THY109 Thyroid Cancer, Nonmedullary, 1 55 0.061
519
c MST023 Mesothelioma, Malignant 57 0.061
520
KRT002 Keratomalacia 48 0.061
521
MCN017 Meconium Ileus 52 0.061
522
CYT018 Cytochrome P450 2d6 Variant 27 0.061
523
c EXD008 Exudative Vitreoretinopathy 1 69 0.061
524
LYM012 Lymphoplasmacytic Lymphoma 61 0.061
525
PRC013 Pericarditis 54 0.061
526
P HYP733 Hypercalciuria, Absorptive, 2 46 0.061
527
OTT002 Otitis Media 71 0.061
528
CRB086 Cerebral Aneurysms 40 0.061
529
c BTT014 Beta-Thalassemia 72 0.061
530
P OLG002 Oligodendroglioma 67 0.061
531
P DRM010 Dermatomyositis 61 0.060
532
PRP030 Purpura 55 0.060
533
HMP005 Hemiplegia 54 0.060
534
c CHR064 Chronic Monocytic Leukemia 34 0.060
535
P TMP001 Temporal Lobe Epilepsy 50 0.060
536
TRP009 Triple X Syndrome 42 0.060
537
ASP007 Aspiration Pneumonia 48 0.060
538
P BRN035 Brain Stem Glioma 51 0.060
539
CHR074 Choriocarcinoma 46 0.060
540
CYT004 Cytomegalic Inclusion Disease 31 0.060
541
P FLL037 Follicular Lymphoma 66 0.060
542
BLR008 Bilirubin Metabolic Disorder 57 0.060
543
P MDL005 Medulloblastoma 77 0.060
544
c LKM063 Leukemia, Chronic Myeloid 71 0.060
545
DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.060
546
P GLL022 Guillain-Barre Syndrome 59 0.060
547
P INT070 Intestinal Obstruction 58 0.060
548
P PLY019 Polyneuropathy 56 0.060
549
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.059
550
SPS003 Spastic Diplegia 50 0.059
551
MSL001 Measles 61 0.059
552
TND005 Tendinitis 52 0.059
553
P ALP009 Alopecia Areata 60 0.059
554
BCT004 Bacteriuria 48 0.059
555
GST040 Gastric Adenocarcinoma 70 0.059
556
P BRS044 Breast Adenocarcinoma 59 0.059
557
c CHR682 Chronic Bilirubin Encephalopathy 38 0.059
558
c GLL024 Gallbladder Disease 1 52 0.059
559
c FML035 Familial Hyperlipidemia 55 0.059
560
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.058
561
P RTN018 Retinal Disease 52 0.058
562
OLG003 Oligohydramnios 52 0.058
563
P PRC031 Preeclampsia/eclampsia 1 37 0.058
564
MSC157 Muscular Dystrophy, Duchenne Type 71 0.058
565
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.058
566
MYF002 Myofascial Pain Syndrome 42 0.058
567
c HYP272 Hypercholesterolemia, Familial, 3 43 0.057
568
HRT012 Heart Valve Disease 53 0.057
569
c INF071 Inflammatory Bowel Disease 1 68 0.057
570
P MTR014 Motor Neuron Disease 64 0.057
571
P MVM001 Movement Disease 61 0.057
572
P MGR001 Migraine Without Aura 48 0.057
573
c SYS043 Systemic Lupus Erythematosus 1 38 0.057
574
RTN017 Retinal Detachment 60 0.057
575
P DMN002 Dementia 67 0.057
576
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.057
577
ORL005 Oral Candidiasis 56 0.057
578
RNL077 Renal Fibrosis 47 0.057
579
PLS025 Plasmablastic Lymphoma 47 0.057
580
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.057
581
CYS013 Cystinuria 62 0.056
582
GNT002 Giant Cell Glioblastoma 52 0.056
583
FLL027 Fallopian Tube Carcinoma 67 0.056
584
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.056
585
MGC001 Megacolon 46 0.056
586
SPT004 Septic Arthritis 57 0.056
587
PNM008 Pneumothorax 56 0.056
588
c FLL041 Follicular Lymphoma 1 49 0.056
589
P HYP120 Hypoaldosteronism 37 0.056
590
P HMN010 Hemangioma 61 0.056
591
P ART021 Arteriosclerosis 54 0.056
592
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 59 0.056
593
GST033 Gestational Diabetes 57 0.055
594
P CHR285 Chronic Myelomonocytic Leukemia 59 0.055
595
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.055
596
P ATT013 Attention Deficit-Hyperactivity Disorder 64 0.055
597
THY121 Thyroid Gland Anaplastic Carcinoma 63 0.055
598
P MSC003 Muscular Atrophy 52 0.055
599
P CHL066 Cholangitis 50 0.055
600
KRT013 Keratolytic Winter Erythema 46 0.055
601
KRT008 Keratopathy 46 0.055
602
DST006 Diastolic Heart Failure 44 0.055
603
LWC001 Low Compliance Bladder 42 0.055
604
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.055
605
c MCL013 Mucolipidosis Iv 64 0.055
606
ANR007 Anorexia Nervosa 63 0.055
607
P MYS005 Myositis 56 0.055
608
OST011 Osteomalacia 52 0.055
609
TND004 Tendinopathy 44 0.055
610
VRC001 Varicocele 49 0.055
611
TXC001 Toxic Megacolon 39 0.055
612
MLG164 Malignant Epithelial Tumor of Ovary 26 0.055
613
c ATS347 Autosomal Dominant Polycystic Kidney Disease 59 0.054
614
CHL123 Chlamydia 59 0.054
615
GRM010 Germ Cells Tumors 34 0.054
616
c ATS007 Autism Spectrum Disorder 67 0.054
617
CMM005 Common Cold 56 0.054
618
P INT068 Intestinal Disease 52 0.054
619
SYS003 Systolic Heart Failure 50 0.054
620
P LNG064 Lung Cancer Susceptibility 3 77 0.054
621
PLL012 Pollen Allergy 45 0.054
622
RRD056 Rare Disease in Surgical Orthopedic 28 0.054
623
ADR007 Adrenoleukodystrophy 74 0.054
624
P BNG030 Benign Ependymoma 60 0.054
625
PRT038 Protein-Energy Malnutrition 54 0.054
626
CLL010 Cellular Ependymoma 53 0.054
627
HYD002 Hydronephrosis 59 0.054
628
HMG005 Hemoglobinopathy 55 0.054
629
TYP007 Typhoid Fever 63 0.054
630
HYP784 Hypogonadism, Male 39 0.054
631
GYN001 Gynecomastia 49 0.053
632
INF021 Infant Gynecomastia 31 0.053
633
MYL031 Myeloproliferative Neoplasm 65 0.053
634
HMT002 Hematologic Cancer 62 0.053
635
INS001 Insulinoma 60 0.053
636
BNM001 Bone Marrow Cancer 43 0.053
637
SPR126 Superior Semicircular Canal Dehiscence 40 0.053
638
c HMG029 Hemoglobin Se Disease 38 0.053
639
P PRC017 Precursor Lymphoblastic Lymphoma/leukemia 35 0.053
640
RSP007 Respiratory Distress Syndrome, Infant 30 0.053
641
P VNT002 Ventricular Septal Defect 60 0.053
642
ERY051 Erythroleukemia, Familial 56 0.053
643
P VNS003 Venous Insufficiency 55 0.053
644
SPP010 Suppressor of Tumorigenicity 3 51 0.053
645
P TCL004 T-Cell Leukemia 47 0.053
646
CRT017 Cartilage Disease 54 0.053
647
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.053
648
P HYD006 Hydrocephalus 65 0.052
649
P TXP001 Toxoplasmosis 60 0.052
650
PLR007 Pleural Empyema 49 0.052
651
PST028 Post-Traumatic Stress Disorder 58 0.052
652
P MTC069 Mitochondrial Disorders 56 0.052
653
GST037 Gastroparesis 53 0.052
654
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 42 0.052
655
P RTN024 Retinoblastoma 72 0.052
656
c FML008 Familial Retinoblastoma 53 0.052
657
HPT014 Hepatorenal Syndrome 50 0.052
658
LMB062 Limb Ischemia 55 0.052
659
P SBS003 Substance Abuse 54 0.052
660
EPC002 Epicondylitis 41 0.052
661
c MNN043 Meningioma, Familial 74 0.052
662
P MJR001 Major Depressive Disorder 68 0.052
663
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 65 0.052
664
MNN042 Meningioma, Radiation-Induced 62 0.052
665
VRL011 Viral Infectious Disease 61 0.052
666
c THY102 Thyroid Cancer, Nonmedullary, 2 57 0.052
667
SPL004 Splenic Marginal Zone Lymphoma 51 0.052
668
SPN021 Spinal Meningioma 47 0.052
669
SCR001 Secretory Meningioma 37 0.052
670
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.052
671
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.052
672
BRN038 Bronchial Disease 53 0.052
673
P RCT021 Rectum Cancer 53 0.052
674
VTM033 Vitamin K Deficiency Bleeding 48 0.052
675
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.052
676
APP009 Appendix Adenocarcinoma 44 0.052
677
P PRG092 Pregnancy Loss, Recurrent 1 40 0.052
678
P VSC011 Vasculitis 62 0.051
679
WTH001 Withdrawal Disorder 48 0.051
680
GRN017 Granulocytopenia 44 0.051
681
WST001 West Syndrome 60 0.051
682
CHL067 Cholecystitis 58 0.051
683
DNT006 Dental Pulp Necrosis 40 0.051
684
c CHR417 Chronic Graft Versus Host Disease 56 0.051
685
PLS011 Plasmacytoma 56 0.051
686
c SVR005 Severe Pre-Eclampsia 49 0.051
687
DFF003 Diffuse Scleroderma 42 0.051
688
CHR066 Chronic Fatigue Syndrome 61 0.051
689
ING001 Inguinal Hernia 60 0.051
690
P CNT110 Contractures, Pterygia, and Variable Skeletal Fusions Syndrome 1a 60 0.051
692
RFR010 Refractory Anemia 48 0.051
693
DBT002 Diabetic Autonomic Neuropathy 41 0.051
694
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.051
695
P ACT105 Acute Mountain Sickness 52 0.051
696
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.051
697
P NSP012 Nasopharyngeal Carcinoma 67 0.051
698
P END047 Endophthalmitis 52 0.051
699
P RTN022 Retinal Vein Occlusion 52 0.050
700
PTH003 Pathologic Nystagmus 51 0.050
701
ATM052 Autoimmune Disease 1 37 0.050
702
MTH071 Methane Production 26 0.050
703
ART016 Aortic Aneurysm 68 0.050
704
c JVN010 Juvenile Rheumatoid Arthritis 67 0.050
705
TRN015 Transient Cerebral Ischemia 62 0.050
706
c ADL017 Adult T-Cell Leukemia 57 0.050
707
HMP009 Haemophilus Influenzae 42 0.050
708
P HML002 Hemolytic Anemia 62 0.050
709
ATR057 Atrioventricular Block 55 0.050
710
JVN009 Juvenile Pilocytic Astrocytoma 55 0.050
711
DGR001 Digeorge Syndrome 63 0.050
712
P ACT010 Acth-Secreting Pituitary Adenoma 57 0.050
713
P HYP040 Hypospadias 51 0.050
714
P OCL013 Oculodentodigital Dysplasia 69 0.049
715
MYC006 Mycosis Fungoides 66 0.049
716
IRD001 Iridocyclitis 50 0.049
717
ANP009 Anaplastic Oligodendroglioma 43 0.049
718
FLR001 Filarial Elephantiasis 50 0.049
719
c INF023 Inflammatory Breast Carcinoma 49 0.049
720
CTR172 Citrullinemia, Classic 64 0.049
721
FRZ001 Frozen Shoulder 53 0.049
722
NRT004 Neuritis 53 0.049
723
P SBR004 Seborrheic Dermatitis 45 0.049
724
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 59 0.049
725
DSS008 Disease of Mental Health 57 0.049
726
c GRV008 Graves Disease 1 55 0.049
727
P MYT002 Myotonic Dystrophy 49 0.049
728
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.049
729
c FML021 Familial Hypercholesterolemia 68 0.049
730
c ALP101 Alpha-Thalassemia 62 0.049
731
MNR012 Meniere Disease 57 0.049
732
HMR039 Hemorrhage, Intracerebral 57 0.049
733
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.049
734
CHL004 Cholelithiasis 49 0.049
735
OBS168 Obsolete: Atypical Teratoid/rhabdoid Tumor 22 0.049
736
P APL001 Aplastic Anemia 74 0.048
737
ACR008 Acrocallosal Syndrome 68 0.048
738
PNC129 Pancreatic Adenocarcinoma 67 0.048
739
P FBR017 Fibrosarcoma 56 0.048
740
INT030 Intracranial Aneurysm 56 0.048
741
P PLY018 Polycythemia 55 0.048
742
P PTT006 Pituitary Adenoma 54 0.048
743
CRN030 Coronary Stenosis 50 0.048
744
CHR178 Chromosomal Triplication 35 0.048
745
ARG002 Argininosuccinic Aciduria 60 0.048
746
P OBS001 Obstructive Jaundice 48 0.048
747
BRS064 Bursitis 47 0.048
748
MYC005 Myocardial Stunning 46 0.048
749
P CLS010 Cluster Headache 43 0.048
750
BWN001 Bowen-Conradi Syndrome 51 0.048
751
P ATX030 Ataxia-Telangiectasia 83 0.047
752
c HPT073 Hepatitis C Virus 70 0.047
753
c ART101 Aortic Valve Disease 2 63 0.047
754
c CNT035 Central Nervous System Disease 54 0.047
755
ATY042 Atypical Chronic Myeloid Leukemia 49 0.047
756
SPL018 Splenomegaly 48 0.047
757
c PRM093 Premature Ovarian Failure 7 47 0.047
758
P HMN032 Human Herpesvirus 8 46 0.047
759
PLC007 Placental Abruption 48 0.047
760
GST010 Gestational Trophoblastic Neoplasm 46 0.047
761
P VNW001 Von Willebrand's Disease 64 0.047
762
P SCL018 Scoliosis 60 0.047
763
OPT003 Opiate Dependence 50 0.047
764
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.047
765
CRP001 Carpal Tunnel Syndrome 67 0.047
766
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 64 0.047
767
c PSR017 Psoriasis 2 52 0.047
768
URT010 Ureteral Obstruction 46 0.047
769
SCR003 Secretory Diarrhea 36 0.047
770
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.047
771
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.047
772
P MNC007 Monocytic Leukemia 54 0.047
773
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.047
774
OVR112 Ovarian Germ Cell Cancer 43 0.047
775
P CYS039 Cystic Kidney Disease 54 0.046
776
ETN001 Eating Disorder 59 0.046
777
LYM022 Lymphangioma 53 0.046
778
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.046
779
HML018 Homologous Wasting Disease 22 0.046
780
P HYP061 Hypertrophic Cardiomyopathy 66 0.046
781
c HPT003 Hepatitis a 63 0.046
782
VCC001 Vaccinia 49 0.046
783
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 58 0.046
784
P URF003 Urofacial Syndrome 1 57 0.046
785
URN009 Urinary System Disease 48 0.046
786
PHS001 Phosphorus Metabolism Disease 40 0.046
787
BRT054 Brittle Bone Disorder 70 0.046
788
P RHB003 Rhabdomyosarcoma 62 0.046
789
PLM031 Poliomyelitis 57 0.046
790
c PSR023 Psoriasis 1 49 0.046
791
ANR004 Anuria 46 0.046
792
c PSR028 Psoriasis 7 39 0.046
793
c PSR032 Psoriasis 11 38 0.046
794
c PSR018 Psoriasis 13 38 0.046
795
KHL003 Kohlschutter-Tonz Syndrome 64 0.045
796
NPH018 Nephrogenic Systemic Fibrosis 50 0.045
797
GST049 Gastrointestinal System Cancer 49 0.045
798
GST071 Gastrointestinal Carcinoma 45 0.045
799
HRP004 Herpes Zoster 60 0.045
800
PRP001 Propionic Acidemia 66 0.045
801
P PRM002 Primary Hyperoxaluria 62 0.045
802
DYS009 Dysthymic Disorder 48 0.045
803
P END084 Endocrine System Disease 44 0.045
804
OPD001 Opioid Abuse 45 0.045
805
PRM003 Premature Ejaculation 44 0.045
806
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.045
807
INC002 Inclusion Body Myositis 64 0.045
808
LMY002 Leiomyoma 50 0.045
809
MYF001 Myofibroma 42 0.045
810
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.045
811
YLL002 Yellow Fever 60 0.045
812
P LYM025 Lymphedema 53 0.045
813
FSC004 Fasciitis 50 0.045
814
GNG003 Gingival Recession 44 0.045
815
GST019 Gastrointestinal Stromal Tumor 76 0.044
816
c LCL006 Localized Scleroderma 62 0.044
817
P ATR010 Atrial Heart Septal Defect 60 0.044
818
PRV004 Periventricular Leukomalacia 51 0.044
819
P SPR086 Spermatogenic Failure 3 44 0.044
820
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.044
821
BRR014 Barrett Esophagus 64 0.044
822
TRD006 Tardive Dyskinesia 55 0.044
823
SPN051 Spondylitis 52 0.044
824
INF009 Inflammatory Spondylopathy 32 0.044
825
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.044
826
P INF038 Influenza 68 0.043
827
P BNC003 Bone Cancer 57 0.043
828
MTH009 Mouth Disease 56 0.043
829
c PRM092 Primary Lateral Sclerosis, Adult, 1 52 0.043
830
THR004 Thrombocytosis 51 0.043
831
P THR015 Thrombophilia 50 0.043
832
APL002 Aplasia of Lacrimal and Salivary Glands 50 0.043
833
c DRM054 Dermatitis, Atopic, 2 45 0.043
834
DMP001 Dumping Syndrome 44 0.043
835
EXN003 Exencephaly 31 0.043
836
P RTN008 Retinitis Pigmentosa 77 0.043
837
c LKM070 Leukemia, Acute Monocytic 53 0.043
838
P HMR003 Hemorrhagic Disease 52 0.043
839
P HMP007 Hemophilia 51 0.043
840
FBR008 Fibrillary Astrocytoma 50 0.043
841
c MLG054 Malignant Histiocytosis 50 0.043
842
RYN001 Raynaud Disease 49 0.043
843
RTC005 Reticulosarcoma 49 0.043
844
ANP006 Anaplastic Ependymoma 46 0.043
845
SBP004 Subependymoma 46 0.043
846
PRT035 Peritoneum Cancer 44 0.043
847
c MLG064 Malignant Ependymoma 41 0.043
848
PSD088 Pseudobulbar Affect 36 0.043
849
CHL057 Childhood Brain Stem Glioma 29 0.043
850
c MLG023 Malignant Adult Ependymoma 15 0.043
851
P ASP006 Aspergillosis 66 0.043
852
SZR001 Sezary's Disease 60 0.043
853
P PRV006 Pervasive Developmental Disorder 57 0.043
854
HRY003 Hairy Cell Leukemia 55 0.043
855
CHR100 Chronic Ulcer of Skin 53 0.043
856
CYS014 Cystadenocarcinoma 51 0.043
857
c CHR418 Chronic Leukemia 50 0.043
858
P MGR003 Migraine with Aura 50 0.043
859
INT054 Intraocular Lymphoma 48 0.043
860
CNT017 Central Nervous System Origin Vertigo 44 0.043
861
PST053 Postherpetic Neuralgia 42 0.043
862
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.043
863
BLR002 Bile Reflux 39 0.043
864
P OVR096 Overlap Myositis 27 0.043
865
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.043
866
P MYC084 Mycobacterium Tuberculosis 1 68 0.043
867
HPT022 Hepatoblastoma 56 0.043
868
c DPH024 Diaphragmatic Hernia, Congenital 64 0.042
869
c PYR010 Peyronie's Disease 50 0.042
870
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 34 0.042
871
c TRC022 Tricuspid Valve Insufficiency 45 0.042
872
P SLM003 Salmonellosis 54 0.042
873
HMC014 Homocysteinemia 53 0.042
874
CND002 Conduct Disorder 51 0.042
875
MNN028 Mononeuropathy of the Median Nerve, Mild 42 0.042
876
NSP002 Nasopharyngitis 41 0.042
877
P HYP263 Hypersomnia 41 0.042
878
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.042
879
P MST009 Mastocytosis 63 0.042
880
DPH001 Diphtheria 60 0.042
881
INT066 Interstitial Lung Disease 59 0.042
882
RLP002 Relapsing-Remitting Multiple Sclerosis 55 0.042
883
THY111 Thyroid Carcinoma, Familial Medullary 67 0.042
884
MSC152 Muscular Dystrophy, Becker Type 63 0.042
885
HYP780 Hypoadrenocorticism, Familial 62 0.042
886
P ANP001 Anaplastic Large Cell Lymphoma 61 0.042
887
CMP010 Complex Regional Pain Syndrome 58 0.042
888
P FCL005 Focal Segmental Glomerulosclerosis 58 0.042
889
P MTR012 Mitral Valve Disease 57 0.042
890
P HYP726 Hypercalcemia, Infantile, 1 57 0.042
891
c INT064 Intermediate Uveitis 55 0.042
892
EPT010 Epithelial-Myoepithelial Carcinoma 53 0.042
893
SRS001 Serous Cystadenocarcinoma 52 0.042
894
MSC190 Muscular Disease 51 0.042
895
THY125 Thyroid Gland Medullary Carcinoma 51 0.042
896
CHL018 Childhood Medulloblastoma 49 0.042
897
END021 Endomyocardial Fibrosis 48 0.042
898
HRN029 Hearing Loss, Noise-Induced 37 0.042
899
PLC005 Placental Insufficiency 57 0.041
900
HYP030 Hypoactive Sexual Desire Disorder 39 0.041
901
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.041
902
P HYP055 Hypoplastic Left Heart Syndrome 62 0.041
903
SLC006 Silicosis 56 0.041
904
HMT008 Hematuria, Benign Familial 53 0.041
905
c ACT135 Acute Graft Versus Host Disease 51 0.041
906
c ALM001 Al Amyloidosis 50 0.041
907
LRN003 Learning Disability 49 0.041
908
VTM002 Vitamin B12 Deficiency 48 0.041
909
LPT006 Leptin Receptor Deficiency 47 0.041
910
MYX001 Myxopapillary Ependymoma 45 0.041
911
c ADL008 Adult Oligodendroglioma 35 0.041
912
c ADL054 Adult Brain Stem Glioma 30 0.041
913
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.041
914
P PRM006 Primary Biliary Cirrhosis 61 0.041
915
THR013 Thoracic Outlet Syndrome 53 0.041
916
MTN003 Motion Sickness 52 0.041
917
PRP017 Periapical Periodontitis 46 0.041
918
ACT011 Acute Contagious Conjunctivitis 40 0.041
919
P VSC018 Visceral Steatosis 33 0.041
920
OST003 Osteonecrosis 61 0.041
921
ACT058 Active Peptic Ulcer Disease 55 0.041
922
c VRL010 Viral Hepatitis 51 0.041
923
c BCT013 Bacterial Pneumonia 47 0.041
924
ATN004 Autonomic Neuropathy 44 0.041
925
CNT097 Central Hypoventilation Syndrome, Congenital 70 0.040
926
PLY001 Polycythemia Vera 69 0.040
927
PTT048 Pituitary Adenoma, Prolactin-Secreting 64 0.040
928
P LYM033 Lymphoproliferative Syndrome 60 0.040
929
CYS010 Cystinosis 60 0.040
930
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 56 0.040
931
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 55 0.040
932
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 53 0.040
933
SBP001 Subependymal Giant Cell Astrocytoma 48 0.040
934
ADR016 Adrenal Cortical Carcinoma 48 0.040
935
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 47 0.040
936
INT017 Intestinal Schistosomiasis 47 0.040
937
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.040
938
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.040
939
CRB026 Cerebellar Astrocytoma 35 0.040
940
CHL006 Childhood Oligodendroglioma 35 0.040
941
HND015 Hand Skill, Relative 33 0.040
942
RFR002 Refractory Hairy Cell Leukemia 32 0.040
943
P RRL003 Rare Lymphatic Malformation 31 0.040
944
CLS052 Classic Hairy Cell Leukemia 27 0.040
945
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 26 0.040
946
CHL009 Childhood Cerebral Astrocytoma 14 0.040
947
MLT157 Multiple System Atrophy 1 70 0.040
948
DFF035 Diffuse Cutaneous Systemic Sclerosis 48 0.040
949
LMT001 Limited Scleroderma 47 0.040
950
NDL024 Nodal Marginal Zone Lymphoma 39 0.040
951
CYS021 Cystic Adenomatoid Malformation of Lung 33 0.040
952
NRM005 Neuromuscular Disease 63 0.039
953
ORL011 Oral Cancer 60 0.039
954
P PGT001 Paget's Disease of Bone 60 0.039
955
P PMP001 Pemphigus 55 0.039
956
DRG024 Drug Allergy 43 0.039
957
ORL015 Oral Squamous Cell Carcinoma 43 0.039
958
HYP264 Hypertonia 38 0.039
959
P NJM001 Nijmegen Breakage Syndrome 72 0.039
960
PNM010 Pneumothorax, Primary Spontaneous 60 0.039
961
ACT200 Acute Monoblastic Leukemia 55 0.039
962
FCT001 Factor Viii Deficiency 55 0.039
963
VLC001 Velocardiofacial Syndrome 54 0.039
964
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 53 0.039
965
FML037 Female Breast Cancer 52 0.039
966
SLD003 Sialadenitis 50 0.039
967
OPD006 Opioid Addiction 48 0.039
968
ASP004 Asphyxia Neonatorum 45 0.039
969
CLL014 Cll/sll 45 0.039
970
c EST002 Estrogen-Receptor Negative Breast Cancer 44 0.039
971
DFF037 Diffuse Intrinsic Pontine Glioma 42 0.039
972
SNG003 Single Ventricular Heart 30 0.039
973
SPP011 Suppression of Tumorigenicity 12 59 0.039
974
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 59 0.039
975
LMY014 Leiomyoma, Uterine 56 0.039
976
BHR001 Behr Syndrome 49 0.039
977
RDC002 Radiculopathy 48 0.039
978
RTN020 Retinal Vascular Disease 48 0.039
979
THY128 Thyroid Tumor 47 0.039
980
ACT029 Acute Interstitial Pneumonia 44 0.039
981
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.039
982
P PRG002 Progesterone-Receptor Positive Breast Cancer 34 0.039
983
INT053 Intracranial Vasospasm 24 0.039
984
GLC025 Galactorrhoea-Hyperprolactinaemia 21 0.039
985
SLC024 Slc4a1-Associated Distal Renal Tubular Acidosis 19 0.039
986
EWN003 Ewing Sarcoma 68 0.038
987
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.038
988
CLL003 Cellulitis 54 0.038
989
P MYG005 Myoglobinuria 43 0.038
990
DNT001 Dental Fluorosis 43 0.038
991
MNG007 Manganese Poisoning 29 0.038
992
P TTR001 Tetralogy of Fallot 69 0.038
993
MST024 Mastocytosis, Cutaneous 67 0.038
994
MYL005 Myelofibrosis 67 0.038
995
c HMP029 Hemophilia a 65 0.038
996
ADR005 Adrenal Carcinoma 58 0.038
997
GNR004 Generalized Anxiety Disorder 56 0.038
998
c BCT007 Bacterial Meningitis 55 0.038
999
OCL022 Ocular Melanoma 53 0.038
1000
PST046 Post-Transplant Lymphoproliferative Disease 53 0.038
1001
AMB001 Amebiasis 49 0.038
1002
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.038
1003
ACT084 Acute Stress Disorder 48 0.038
1004
PRD004 Prediabetes Syndrome 47 0.038
1005
PRL017 Prolymphocytic Leukemia 47 0.038
1006
MNC019 Monocarboxylate Transporter 1 Deficiency 46 0.038
1007
LYM051 Lymphomatoid Granulomatosis 45 0.038
1008
PLR022 Pleural Disease 44 0.038
1009
LTH001 Lethal Midline Granuloma 43 0.038
1010
CHR286 Chronic Neutrophilic Leukemia 41 0.038
1011
MCC013 Mucocutaneous Ulceration, Chronic 39 0.038
1012
ADR004 Adrenal Cortical Adenocarcinoma 38 0.038
1013
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 35 0.038
1014
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.038
1015
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.038
1016
ACT216 Acute Leukemia of Ambiguous Lineage 32 0.038
1017
PDT014 Pediatric Ependymoma 32 0.038
1018
BRN049 Brain Tumor, Childhood 29 0.038
1019
KLB004 Klebsiella Infection 27 0.038
1020
PNL001 Pineal Gland Astrocytoma 15 0.038
1021
P MYS003 Myasthenia Gravis 68 0.038
1022
P GLY013 Glycogen Storage Disease 59 0.038
1023
ANT024 Anthrax Disease 58 0.038
1024
c CNT016 Central Retinal Vein Occlusion 49 0.038
1025
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 49 0.038
1026
CLN045 Colonic Benign Neoplasm 49 0.038
1027
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.038
1028
HRN026 Hernia, Hiatus 45 0.038
1029
GLC024 Glucose Transporter Type 1 Deficiency Syndrome 40 0.038
1030
c RCR002 Recurrent Hypersomnia 32 0.038
1031
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.037
1032
APH002 Aphasia 57 0.037
1033
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 53 0.037
1034
P END046 Endometritis 47 0.037
1035
c MLG079 Malignant Pleural Mesothelioma 42 0.037
1036
c PNC108 Pancreatitis, Hereditary 69 0.037
1037
ART002 Arts Syndrome 63 0.037
1038
PRM126 Primary Peritoneal Carcinoma 62 0.037
1039
HYD038 Hydrops Fetalis, Nonimmune 61 0.037
1040
P PLM034 Pulmonary Emphysema 56 0.037
1041
c CNG216 Congenital Hydrocephalus 50 0.037
1042
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.037
1043
PLS016 Plasma Cell Leukemia 46 0.037
1044
AYM001 Ayme-Gripp Syndrome 46 0.037
1045
c PLM022 Pulmonary Valve Insufficiency 40 0.037
1046
CNT060 Central Serous Chorioretinopathy 38 0.037
1047
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 37 0.037
1048
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.036
1049
HLL004 Hellp Syndrome 53 0.036
1050
EMP011 Emphysema, Congenital Lobar 34 0.036
1051
DFF005 Diffuse Large B-Cell Lymphoma 56 0.036
1052
PLS007 Plasmodium Falciparum Malaria 52 0.036
1053
VLV047 Volvulus of Midgut 50 0.036
1054
c CHR431 Chronic Venous Insufficiency 49 0.036
1055
PYL006 Pyloric Stenosis 48 0.036
1056
GRM005 Germ Cell Cancer 47 0.036
1057
SCH038 Schopf-Schulz-Passarge Syndrome 47 0.036
1058
CLS016 Clostridium Difficile Colitis 46 0.036
1059
URN003 Urinary Schistosomiasis 44 0.036
1060
P CRN024 Corneal Disease 43 0.036
1061
DNT014 Dental Pulp Disease 43 0.036
1062
MCR011 Microinvasive Gastric Cancer 43 0.036
1063
URM005 Uremic Pruritus 39 0.036
1064
CRN288 Corneal Dystrophy, Band-Shaped 38 0.036
1065
SWL001 Swallowing Disorders 38 0.036
1066
BNN005 Bunion 33 0.036
1067
IDP031 Idiopathic Hypersomnia 32 0.036
1068
FNT004 Fainting 31 0.036
1069
c PRM196 Premature Ovarian Failure 1 68 0.036
1070
P ESS003 Essential Thrombocythemia 67 0.036
1071
MGK001 Megakaryocytic Leukemia 64 0.036
1072
MXD005 Mixed Connective Tissue Disease 59 0.036
1073
P PLV020 Pelvic Organ Prolapse 59 0.036
1074
P PRD006 Prader-Willi Syndrome 59 0.036
1075