Search results for Calcium citrate

1386 hits were found for Calcium citrate

# Family MCID Name MIFTS Score
1
NPH009 Nephrolithiasis 55 0.412
2
P HYP069 Hyperparathyroidism 63 0.379
3
URL001 Urolithiasis 45 0.354
4
P KDN018 Kidney Disease 72 0.340
5
P OST002 Osteoporosis 74 0.338
6
BNR002 Bone Resorption Disease 48 0.325
7
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.323
8
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.323
9
RCK004 Rickets 68 0.315
10
c HYP595 Hypertension, Essential 84 0.313
11
P PLY011 Polycystic Ovary Syndrome 56 0.299
12
P INF032 Infertility 57 0.296
13
IMP005 Impotence 52 0.285
14
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.273
15
c CHR684 Chronic Kidney Disease 70 0.269
16
HYP025 Hyperphosphatemia 48 0.239
17
PRT037 Pertussis 65 0.237
18
c SCN007 Secondary Hyperparathyroidism 51 0.236
19
END086 End Stage Renal Disease 51 0.231
20
c PRM005 Primary Hyperparathyroidism 58 0.222
21
48X005 48,xyyy 39 0.220
22
P CLR023 Colorectal Cancer 99 0.219
23
P BND020 Bone Disease 59 0.213
24
P BRS047 Breast Cancer 97 0.208
25
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.205
26
MTB004 Metabolic Acidosis 50 0.204
27
c ACT071 Acute Kidney Failure 60 0.202
28
c PRC016 Pre-Eclampsia 63 0.196
29
CNG034 Congestive Heart Failure 69 0.195
30
c RHB024 Rhabdomyosarcoma 2 67 0.194
31
P NRB001 Neuroblastoma 72 0.193
32
LPP008 Lipoprotein Quantitative Trait Locus 62 0.190
33
HYP005 Hypokalemia 55 0.188
34
ANG054 Angina Pectoris 66 0.187
35
ISC004 Ischemia 58 0.186
36
P HRT032 Heart Disease 75 0.183
37
P HYP024 Hypoparathyroidism 56 0.183
38
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.182
39
ANV001 Anovulation 47 0.182
40
P PLM037 Pulmonary Hypertension 67 0.182
41
P ADN016 Adenocarcinoma 64 0.176
42
HYP266 Hypoxia 57 0.175
43
ART140 Arteries, Anomalies of 52 0.175
44
IRN002 Iron Metabolism Disease 57 0.174
45
ADN018 Adenoma 59 0.173
46
HLX001 Helix Syndrome 47 0.173
47
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.173
48
c PLY105 Polycystic Ovary Syndrome 1 38 0.171
49
DWN001 Down Syndrome 70 0.165
50
ATH013 Atherosclerosis Susceptibility 65 0.162
51
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.162
52
NPH003 Nephrocalcinosis 51 0.158
53
ALL026 Allergic Hypersensitivity Disease 62 0.157
54
P VSC007 Vascular Disease 63 0.156
55
P GLM045 Glioma 63 0.155
56
GLL048 Glial Tumor 45 0.154
57
P CRN300 Coronary Heart Disease 1 63 0.152
58
P PRS040 Prostate Cancer 97 0.152
59
P LYM118 Lymphoma 68 0.151
60
P CRD119 Cardiac Arrest 67 0.150
61
P DRR001 Diarrhea 55 0.150
62
OST017 Osteomyelitis 64 0.147
63
CHL014 Cholera 59 0.147
64
IDP073 Idiopathic Hypercalciuria 43 0.146
65
DNT012 Dental Caries 53 0.145
66
CNS004 Constipation 58 0.144
67
P MYC007 Myocardial Infarction 70 0.143
68
P SRC025 Sarcoidosis 1 70 0.143
69
c MGR028 Migraine with or Without Aura 1 67 0.141
70
LPD008 Lipid Metabolism Disorder 62 0.140
71
P LVR013 Liver Disease 68 0.140
72
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.140
73
P MSC005 Muscular Dystrophy 66 0.140
74
HYP056 Hypoglycemia 66 0.139
75
HYP080 Hypogonadism 50 0.139
76
P ECL001 Eclampsia 50 0.139
77
PNG002 Pain Agnosia 51 0.138
78
OST159 Osteogenic Sarcoma 66 0.138
79
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.138
80
DFC004 Deficiency Anemia 70 0.137
81
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.137
82
47X002 47,xyy 49 0.136
83
P RNL007 Renal Tubular Acidosis 51 0.136
84
P DDN001 Duodenal Ulcer 52 0.136
85
P ALZ034 Alzheimer Disease 88 0.136
86
HYP060 Hyperinsulinism 54 0.135
87
P MLN007 Male Infertility 55 0.133
88
P LKM002 Leukemia 68 0.133
89
ADL002 Adult Syndrome 70 0.133
90
P TRN020 Turner Syndrome 67 0.132
91
MYL069 Myeloma, Multiple 85 0.132
92
HYP017 Hypophosphatemia 50 0.131
93
ATX019 Ataxia with Vitamin E Deficiency 42 0.131
94
LYM019 Lymphosarcoma 46 0.130
95
OVR029 Ovarian Hyperstimulation Syndrome 64 0.130
96
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.130
97
c HYP836 Hypercholesterolemia, Familial, 1 73 0.129
98
ANX004 Anoxia 40 0.129
99
P HYP086 Hypothyroidism 69 0.128
100
INS001 Insulinoma 60 0.128
101
P RCT021 Rectum Cancer 52 0.128
102
AGN016 Aging 56 0.127
103
P NRP001 Neuropathy 56 0.126
104
OST011 Osteomalacia 52 0.125
105
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.125
106
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.124
107
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.123
108
P CRD246 Cardiovascular System Disease 57 0.123
109
AMN001 Amenorrhea 54 0.123
110
P LTR001 Lateral Sclerosis 54 0.123
111
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.122
112
CRB039 Cerebrovascular Disease 67 0.122
113
c ATR087 Atrial Standstill 1 75 0.121
114
P SZR006 Seizure Disorder 56 0.121
115
URM002 Uremia 49 0.121
116
HRW001 Hair Whorl 36 0.120
117
P MLG056 Malignant Hyperthermia 67 0.120
118
LVR012 Liver Cirrhosis 62 0.120
119
STR067 Stroke, Ischemic 81 0.120
120
P ART023 Arthropathy 62 0.120
121
HMS001 Hemosiderosis 54 0.120
122
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.120
123
TTN003 Tetanus 65 0.120
124
GT001 Gout 64 0.120
125
P PHC003 Pheochromocytoma 71 0.119
126
P HYP076 Hyperthyroidism 55 0.119
127
ADR040 Adrenal Gland Pheochromocytoma 46 0.119
128
P PRD008 Periodontitis 64 0.118
129
P DBT009 Diabetes Mellitus 64 0.118
130
P ENC018 Encephalopathy 61 0.117
131
CYS001 Cystic Fibrosis 81 0.117
132
P RRH023 Rare Hereditary Hemochromatosis 41 0.117
133
DPR016 Depression 63 0.116
134
OST012 Osteoarthritis 78 0.116
135
HYP066 Hyperglycemia 61 0.116
136
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.116
137
c ACT075 Acute Myocardial Infarction 57 0.115
138
PPT005 Peptic Ulcer Disease 59 0.115
139
GLB015 Glioblastoma Multiforme 75 0.115
140
INT007 Intermediate Coronary Syndrome 55 0.114
141
c ACT027 Acute Pancreatitis 60 0.114
142
CLC006 Calcinosis 48 0.114
143
P HYP726 Hypercalcemia, Infantile, 1 58 0.113
144
NTR005 Nutritional Deficiency Disease 62 0.113
145
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.113
146
LNG099 Lung Disease 60 0.113
147
c MCR120 Microvascular Complications of Diabetes 7 47 0.112
148
VSL002 Visual Epilepsy 59 0.112
149
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.112
150
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.112
151
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.112
152
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.112
153
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.112
154
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.112
155
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.112
156
c MCR113 Microvascular Complications of Diabetes 3 52 0.112
157
P BPL003 Bipolar Disorder 56 0.112
158
c MCR130 Microvascular Complications of Diabetes 6 41 0.111
159
c MCR133 Microvascular Complications of Diabetes 4 41 0.111
160
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.111
161
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.111
162
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.111
163
c MJR024 Major Affective Disorder 9 41 0.111
164
c MJR022 Major Affective Disorder 8 38 0.111
165
MSC157 Muscular Dystrophy, Duchenne Type 72 0.111
166
BRN071 Brain Injury 49 0.111
167
TXC005 Toxic Shock Syndrome 62 0.111
168
c GLL024 Gallbladder Disease 1 53 0.110
169
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.110
170
c DLT002 Dilated Cardiomyopathy 79 0.110
171
P OVR042 Ovarian Cancer 88 0.109
172
SPN186 Spinal Cord Injury 60 0.109
173
c ACT068 Acute Cystitis 63 0.109
174
FTT001 Fatty Liver Disease 61 0.108
175
CYT002 Cytokine Deficiency 42 0.107
176
HLC007 Helicobacter Pylori Infection 59 0.107
177
THY029 Thyroid Carcinoma 59 0.107
178
INS024 Insulin-Like Growth Factor I 79 0.107
179
c PNS012 Paine Syndrome 61 0.106
180
HYP043 Hyperandrogenism 48 0.106
181
P MYP004 Myopathy 70 0.106
182
TRM010 Traumatic Brain Injury 51 0.106
183
HMN044 Human Immunodeficiency Virus Type 1 71 0.106
184
P PNC044 Pancreatitis 61 0.106
185
ATM095 Autoimmune Disease 62 0.105
186
P CHR345 Chronic Pain 44 0.105
187
MNT002 Mental Depression 58 0.105
188
P END044 Endometriosis 63 0.104
189
ALC007 Alcohol Dependence 66 0.104
190
P THR014 Thrombocytopenia 67 0.104
191
P HDC001 Headache 57 0.104
192
P ATR011 Atrial Fibrillation 66 0.104
193
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.104
194
P PLY014 Polycystic Kidney Disease 62 0.103
195
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.103
196
P LKM062 Leukemia, Acute Lymphoblastic 69 0.103
197
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.103
198
P CTR002 Cataract 60 0.102
199
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.102
200
P HYP733 Hypercalciuria, Absorptive, 2 45 0.102
201
CRN030 Coronary Stenosis 50 0.102
202
P PNC035 Pancreatic Cancer 84 0.101
203
PPL052 Papillomatosis, Confluent and Reticulated 33 0.100
204
IRR002 Irritable Bowel Syndrome 65 0.100
205
P LNG032 Lung Cancer 98 0.099
206
HYP020 Hyperprolactinemia 64 0.098
207
CRD223 Cardiac Arrhythmia 60 0.098
208
GLS018 Glass Syndrome 57 0.098
209
GLC003 Glucose Intolerance 54 0.098
210
P NTR004 Neutropenia 63 0.098
211
P OVR082 Overgrowth Syndrome 50 0.097
212
P GST044 Gastritis 56 0.097
213
PLS009 Plasma Cell Neoplasm 51 0.096
214
P MCR115 Microvascular Complications of Diabetes 5 66 0.096
215
ANX010 Anxiety 73 0.096
216
P HPT023 Hepatocellular Carcinoma 100 0.096
217
P DST107 Distal Renal Tubular Acidosis 42 0.096
218
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.096
219
P PRP019 Peripheral Nervous System Disease 58 0.096
220
P GST053 Gastric Cancer 83 0.095
221
IRN001 Iron Deficiency Anemia 59 0.095
222
IMM167 Immune Deficiency Disease 78 0.095
223
ACQ007 Acquired Immunodeficiency Syndrome 60 0.095
224
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.094
225
RNL011 Renal Osteodystrophy 50 0.094
226
P RHM011 Rheumatoid Arthritis 80 0.094
227
P ART022 Arthritis 69 0.093
228
P RHN004 Rhinitis 57 0.093
229
P AST007 Astrocytoma 51 0.093
230
P HYP061 Hypertrophic Cardiomyopathy 70 0.093
231
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.092
232
RYN005 Raynaud Phenomenon 47 0.092
233
CHL079 Children's Interstitial Lung Disease 26 0.092
234
LYM040 Lymphoblastic Lymphoma 54 0.091
235
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.091
236
P ART021 Arteriosclerosis 54 0.091
237
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.090
238
P BCL017 B-Cell Lymphoma 58 0.090
239
c PRM038 Primary Agammaglobulinemia 44 0.090
240
ESP021 Esophageal Cancer 90 0.089
241
THR024 Thrombosis 57 0.089
242
AST005 Asthma 76 0.088
243
P TRM003 Tremor 54 0.088
244
P LCT001 Lactic Acidosis 51 0.088
245
P INF037 Inflammatory Bowel Disease 54 0.088
246
PRS021 Prostatic Adenoma 51 0.088
247
CRD132 Cardiac Conduction Defect 58 0.087
248
PRT029 Parathyroid Adenoma 50 0.087
249
P PSR002 Psoriasis 62 0.087
250
PRS045 Prostatic Hypertrophy 53 0.087
251
c NRF023 Neurofibromatosis, Type Ii 80 0.086
252
PRS129 Prostatic Hyperplasia, Benign 49 0.086
253
P PNM007 Pneumonia 68 0.086
254
ATR057 Atrioventricular Block 55 0.085
255
PRP027 Peripheral Vascular Disease 71 0.085
256
P PRM002 Primary Hyperoxaluria 62 0.085
257
SXL003 Sexual Disorder 47 0.085
258
c ATS347 Autosomal Dominant Polycystic Kidney Disease 65 0.085
259
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.084
260
P EXN002 Exanthem 57 0.084
261
P INS002 in Situ Carcinoma 53 0.084
262
DRM006 Dermatitis 61 0.084
263
c XNT010 Xanthinuria, Type I 53 0.083
264
c PRS136 Prostate Cancer, Hereditary, 6 33 0.083
265
c PRS130 Prostate Cancer, Hereditary, 8 32 0.083
266
GST092 Gastroesophageal Reflux 67 0.083
267
c SYS001 Systemic Lupus Erythematosus 86 0.083
268
MMM001 Mammary Paget's Disease 53 0.083
269
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.082
270
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.082
271
SKN016 Skin Disease 63 0.082
272
PST011 Pustulosis of Palm and Sole 52 0.082
273
SYN007 Synovitis 54 0.082
274
PLC002 Plica Syndrome 36 0.082
275
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.082
276
c SML038 Small Cell Cancer of the Lung 65 0.082
277
P CNR004 Cone-Rod Dystrophy 2 73 0.082
278
c SCL052 Scleroderma, Familial Progressive 61 0.081
279
c THR092 Thrombophilia Due to Thrombin Defect 73 0.081
280
LYM133 Lymphoma, Hodgkin, Classic 69 0.081
281
P MYL006 Myeloid Leukemia 60 0.081
282
P MLN008 Melanoma 69 0.081
283
CRB004 Cerebral Artery Occlusion 45 0.080
284
ACR007 Acromegaly 71 0.080
285
P ALP008 Alopecia 54 0.080
286
c LKM061 Leukemia, Acute Myeloid 84 0.080
287
GST023 Gastric Ulcer 53 0.079
288
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.079
289
END057 Endometrial Cancer 74 0.079
290
BRN056 Bronchopulmonary Dysplasia 57 0.079
291
MLR004 Malaria 81 0.078
292
PLM010 Pulmonary Edema 54 0.078
293
c ATS007 Autism Spectrum Disorder 67 0.078
294
P RSP003 Respiratory Failure 74 0.078
295
c DRR009 Diarrhea 6 46 0.078
296
P BLD134 Bladder Cancer 79 0.077
297
ALL003 Allergic Rhinitis 67 0.077
298
P THL005 Thalassemia 60 0.077
299
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.077
300
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.077
301
OCL069 Ocular Motor Apraxia 51 0.076
302
P EPL164 Epilepsy 71 0.076
303
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.076
304
SRC014 Sarcoma 65 0.076
305
SPN035 Spindle Cell Sarcoma 53 0.076
306
MSC007 Muscle Hypertrophy 64 0.076
307
P DMN002 Dementia 66 0.076
308
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.075
309
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.075
310
BRN024 Bronchitis 68 0.075
311
PPL001 Papillary Adenoma 44 0.075
312
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.075
313
LPT014 Leptin Deficiency or Dysfunction 74 0.075
314
MDD011 Mood Disorder 62 0.075
315
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.075
316
AZS001 Azoospermia 50 0.075
317
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.075
318
CRH001 Crohn's Disease 74 0.075
319
HYP014 Hyperuricemia 52 0.075
320
P TXP001 Toxoplasmosis 60 0.075
321
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.074
322
GTR002 Goiter 53 0.074
323
P SCK005 Sickle Cell Disease 50 0.074
324
P MJR001 Major Depressive Disorder 68 0.074
325
ANR040 Aneurysm 59 0.074
326
CNN005 Connective Tissue Disease 68 0.074
327
THY111 Thyroid Carcinoma, Familial Medullary 67 0.074
328
BCT022 Bacterial Infectious Disease 56 0.073
329
CLT003 Colitis 62 0.073
330
ECT026 Ectopic Pregnancy 50 0.073
331
APN006 Apnea of Prematurity 24 0.073
332
P RNL015 Renal Hypertension 47 0.073
333
P LPS004 Lupus Erythematosus 61 0.073
334
P GLM040 Glioma Susceptibility 1 81 0.073
335
49X006 49, Xxxxy Syndrome 41 0.072
336
MYC005 Myocardial Stunning 46 0.072
337
PLM001 Pulmonary Tuberculosis 69 0.072
338
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.072
339
PLM033 Pulmonary Embolism 59 0.072
340
c BRN108 Branchiootic Syndrome 1 62 0.072
341
THY125 Thyroid Gland Medullary Carcinoma 50 0.072
342
MCS002 Mucositis 56 0.072
343
c LKM005 Leukemia, T-Cell, Chronic 34 0.072
344
BRS099 Breast Ductal Carcinoma 62 0.071
345
P OCY003 Oocyte Maturation Defect 1 45 0.071
346
ENT011 Enterocolitis 51 0.071
347
CLN045 Colonic Benign Neoplasm 46 0.071
348
P LKM071 Leukemia, Chronic Lymphocytic 79 0.071
349
c MLG068 Malignant Glioma 46 0.071
350
P ATS364 Autism 70 0.071
351
P SYS005 Systemic Scleroderma 68 0.071
352
P SCL018 Scoliosis 60 0.071
353
P OVR049 Ovarian Disease 52 0.070
354
PNC129 Pancreatic Adenocarcinoma 68 0.070
355
TRN015 Transient Cerebral Ischemia 63 0.070
356
P PYL005 Pyelonephritis 56 0.070
357
SCK003 Sickle Cell Anemia 74 0.070
358
c CHR682 Chronic Bilirubin Encephalopathy 39 0.070
359
P CYS039 Cystic Kidney Disease 54 0.070
360
DBT010 Diabetic Neuropathy 54 0.070
361
P GLM007 Glomerulonephritis 57 0.070
362
P AMY004 Amyloidosis 70 0.070
363
FCT007 Factor Vii Deficiency 67 0.070
364
ILS001 Ileus 51 0.070
365
P PRK057 Parkinson Disease, Late-Onset 78 0.069
366
CNT033 Central Nervous System Cancer 47 0.069
367
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.069
368
P NPH012 Nephrotic Syndrome 60 0.069
369
P LCT002 Lactose Intolerance 53 0.069
370
GST050 Gastrointestinal System Disease 56 0.069
371
P PRC031 Preeclampsia/eclampsia 1 38 0.068
372
P HYP750 Hypertriglyceridemia, Familial 62 0.068
373
P PLM036 Pulmonary Fibrosis 65 0.068
374
OVR094 Ovarian Epithelial Cancer 38 0.068
375
P MLT020 Multiple Sclerosis 72 0.068
376
c ACT073 Acute Leukemia 58 0.068
377
c PCH010 Pachyonychia Congenita 3 44 0.068
378
BRN028 Brain Cancer 74 0.068
379
HYD002 Hydronephrosis 60 0.068
380
MST005 Mastitis 53 0.067
381
P HYP265 Hypotonia 43 0.067
382
DNT006 Dental Pulp Necrosis 41 0.067
383
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.067
384
c ACT134 Acute Liver Failure 56 0.067
385
PLC008 Placenta Disease 50 0.067
386
P HYP730 Hypogonadotropic Hypogonadism 52 0.067
387
HPR003 Heparin-Induced Thrombocytopenia 48 0.067
388
SFT003 Soft Tissue Sarcoma 56 0.067
389
PHS001 Phosphorus Metabolism Disease 40 0.067
390
GST033 Gestational Diabetes 61 0.067
391
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.067
392
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.066
393
NRL016 Neural Tube Defects 82 0.066
394
GNG013 Gingivitis 59 0.066
395
HRT015 Heritable Pulmonary Arterial Hypertension 44 0.066
396
CRB037 Cerebral Palsy 69 0.066
397
P MSC003 Muscular Atrophy 52 0.066
398
P OPT006 Optic Nerve Disease 60 0.066
399
c SVR005 Severe Pre-Eclampsia 50 0.066
400
c HMC039 Hemochromatosis, Type 1 74 0.066
401
P DRM053 Dermatitis, Atopic 66 0.066
402
DCT002 Ductal Carcinoma in Situ 59 0.066
403
CHL068 Cholestasis 61 0.066
404
OST003 Osteonecrosis 61 0.066
405
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.065
406
SQM006 Squamous Cell Carcinoma 60 0.065
407
URN010 Urinary Tract Obstruction 55 0.065
408
BCK006 Back Pain 42 0.065
409
ART016 Aortic Aneurysm 69 0.065
410
PRT010 Parathyroid Carcinoma 67 0.065
412
P MYC008 Myocarditis 59 0.065
413
STM007 Stomatitis 50 0.064
414
ULC004 Ulcerative Colitis 73 0.064
415
SBC016 Subacute Delirium 44 0.064
416
PRT013 Portal Hypertension 59 0.064
417
P ALC033 Alcohol Use Disorder 58 0.064
418
c INF145 Infantile Liver Failure Syndrome 1 50 0.064
419
P LNG028 Long Qt Syndrome 66 0.064
420
P ESP024 Esophagitis 62 0.064
421
P CYS018 Cystitis 59 0.064
422
P MLG074 Malignant Mesenchymoma 40 0.064
423
c MCR129 Microvascular Complications of Diabetes 1 66 0.064
424
c LKM063 Leukemia, Chronic Myeloid 72 0.064
425
PRT036 Peritonitis 64 0.063
426
BRK010 Burkitt Lymphoma 67 0.063
427
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.063
428
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.063
429
P SCH015 Schizophrenia 74 0.063
430
GST045 Gastroenteritis 59 0.063
431
RDN001 Reading Disorder 40 0.063
432
c FML021 Familial Hypercholesterolemia 66 0.062
433
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.062
434
LWC001 Low Compliance Bladder 43 0.062
435
P GRF003 Graft-Versus-Host Disease 72 0.062
436
SYN036 Syncope 45 0.062
437
WTH001 Withdrawal Disorder 48 0.062
438
PRN019 Perinatal Necrotizing Enterocolitis 59 0.062
439
P URT039 Urticaria 58 0.062
440
TRP009 Triple X Syndrome 42 0.062
441
TND005 Tendinitis 54 0.061
442
CMR002 Coumarin Resistance 56 0.061
443
P TMP001 Temporal Lobe Epilepsy 50 0.061
444
P SLP006 Sleep Apnea 69 0.061
445
P MYS005 Myositis 56 0.061
446
OLG001 Oligospermia 45 0.061
447
P BCT020 Bacteremia 2 44 0.061
448
HYP784 Hypogonadism, Male 40 0.061
449
MYL009 Myelodysplastic Syndrome 70 0.061
450
ENT004 Enthesopathy 49 0.061
451
MNT001 Mantle Cell Lymphoma 69 0.061
452
P KDN017 Kidney Cancer 60 0.061
453
HPT004 Hepatic Coma 45 0.061
454
GST020 Gastric Antral Vascular Ectasia 41 0.061
455
ACR041 Acromelic Frontonasal Dysostosis 52 0.061
456
P ADL017 Adult T-Cell Leukemia 56 0.060
457
ANR007 Anorexia Nervosa 63 0.060
458
TXC002 Toxic Encephalopathy 53 0.060
459
GST040 Gastric Adenocarcinoma 70 0.060
460
P BRS044 Breast Adenocarcinoma 59 0.060
461
SPS057 Spasticity 45 0.060
462
P DRM010 Dermatomyositis 61 0.060
463
SCH014 Schistosomiasis 57 0.060
464
ERY051 Erythroleukemia, Familial 56 0.060
465
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.060
466
P SYP003 Syphilis 58 0.060
467
c GRV008 Graves Disease 1 56 0.059
468
c DBT099 Diabetes Mellitus, Type I 65 0.059
469
P ANP001 Anaplastic Large Cell Lymphoma 58 0.059
470
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.059
471
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.059
472
END040 Endogenous Depression 55 0.059
473
LNG031 Lung Benign Neoplasm 51 0.059
474
MDL009 Medullary Sponge Kidney 40 0.059
475
RTN023 Retinitis 46 0.059
476
NRR001 Neuroretinitis 42 0.059
477
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.059
478
BRR014 Barrett Esophagus 65 0.059
479
BRT054 Brittle Bone Disorder 72 0.059
480
P MYS003 Myasthenia Gravis 68 0.059
481
P RTN016 Retinal Degeneration 53 0.059
482
MXD026 Mixed Glioma 45 0.059
483
HPT019 Hepatic Encephalopathy 60 0.058
484
P PLY019 Polyneuropathy 56 0.058
485
PPL049 Papillon-Lefevre Syndrome 65 0.058
486
PRS047 Prostatitis 56 0.058
487
CYT018 Cytochrome P450 2d6 Variant 27 0.058
488
c HPT016 Hepatitis B 59 0.058
489
P FBR017 Fibrosarcoma 56 0.058
490
P HRP006 Herpes Simplex 65 0.058
491
CLC001 Calciphylaxis 51 0.058
492
c BRS049 Breast Carcinoma in Situ 51 0.058
493
c FNC043 Fanconi Anemia, Complementation Group E 62 0.058
494
SPT004 Septic Arthritis 58 0.058
495
c ART101 Aortic Valve Disease 2 65 0.057
496
CHL004 Cholelithiasis 49 0.057
497
OLG003 Oligohydramnios 51 0.057
498
PRT058 Pure Autonomic Failure 59 0.057
499
P THY032 Thyroiditis 52 0.057
500
c FML001 Familial Atrial Fibrillation 65 0.057
501
P DYS154 Dystonia 65 0.057
502
P ADL010 Adult Respiratory Distress Syndrome 65 0.057
503
PLC007 Placental Abruption 48 0.057
504
INT067 Interstitial Nephritis 48 0.057
505
P PTN014 Patent Ductus Arteriosus 1 60 0.057
506
EYD002 Eye Disease 58 0.057
507
DSS009 Disseminated Intravascular Coagulation 57 0.057
508
HRT012 Heart Valve Disease 53 0.057
509
P PNC025 Panic Disorder 53 0.057
510
P LNG064 Lung Cancer Susceptibility 3 78 0.057
511
c FML035 Familial Hyperlipidemia 55 0.056
512
PLS025 Plasmablastic Lymphoma 47 0.056
513
c MCR112 Microvascular Complications of Diabetes 2 41 0.056
514
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.056
515
ASC001 Ascaridiasis 35 0.056
516
P MYT002 Myotonic Dystrophy 49 0.056
517
NNL006 Non-Alcoholic Steatohepatitis 54 0.056
518
P MTR014 Motor Neuron Disease 65 0.056
519
PST092 Posttransplant Acute Limbic Encephalitis 29 0.056
520
APP009 Appendix Adenocarcinoma 44 0.056
521
FBR047 Fibromyalgia 58 0.056
522
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.056
523
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.055
524
SPS003 Spastic Diplegia 51 0.055
525
URN009 Urinary System Disease 48 0.055
526
LWR018 Lower Urinary Tract Obstruction, Congenital 40 0.055
527
DGR001 Digeorge Syndrome 64 0.055
528
DYS015 Dysentery 52 0.055
529
CYS013 Cystinuria 63 0.055
530
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.055
531
BLR008 Bilirubin Metabolic Disorder 57 0.055
532
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.055
533
P RTN018 Retinal Disease 53 0.055
534
ACT003 Acute Kidney Tubular Necrosis 45 0.055
535
ASC010 Ascaris Lumbricoides Infection 50 0.055
536
P OVR046 Ovarian Cyst 47 0.055
537
c PNC108 Pancreatitis, Hereditary 70 0.055
538
P THY023 Thymoma 65 0.055
539
CHL067 Cholecystitis 57 0.055
540
c THY107 Thymoma, Familial 52 0.055
541
VTM033 Vitamin K Deficiency Bleeding 48 0.055
542
c BTT014 Beta-Thalassemia 74 0.055
543
P MNC007 Monocytic Leukemia 53 0.055
544
HMT002 Hematologic Cancer 62 0.055
545
NRM005 Neuromuscular Disease 64 0.054
546
c HYP794 Hyperoxaluria, Primary, Type I 63 0.054
547
GNG003 Gingival Recession 44 0.054
548
ETH012 Ethylene Glycol Poisoning 26 0.054
549
c SVR001 Severe Acute Respiratory Syndrome 62 0.054
550
SYS003 Systolic Heart Failure 49 0.054
551
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.054
552
P MTC069 Mitochondrial Disorders 56 0.054
553
OPT003 Opiate Dependence 50 0.054
554
CVD001 Covid-19 44 0.054
555
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.054
556
P RTN008 Retinitis Pigmentosa 79 0.054
557
RYN001 Raynaud Disease 48 0.054
558
KRT002 Keratomalacia 47 0.054
559
KPS004 Kaposi Sarcoma 75 0.054
560
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.054
561
P END033 Endocarditis 57 0.054
562
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.054
563
P MYC033 Myoclonus 46 0.054
564
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.054
565
RST023 Resting Heart Rate, Variation in 41 0.054
566
GYN001 Gynecomastia 49 0.054
567
INF021 Infant Gynecomastia 31 0.054
568
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.054
569
PTH003 Pathologic Nystagmus 52 0.054
570
c EXD008 Exudative Vitreoretinopathy 1 71 0.054
571
P URF003 Urofacial Syndrome 1 57 0.054
572
MCR004 Macroglobulinemia 49 0.054
573
P CND004 Candidiasis 58 0.053
574
c OVR114 Ovarian Cancer 1 38 0.053
575
P NRV007 Nervous System Disease 66 0.053
576
P HMP007 Hemophilia 51 0.053
577
CNN003 Conn's Syndrome 79 0.053
578
THY122 Thyroid Gland Cancer 57 0.053
579
P MJR007 Major Affective Disorder 1 43 0.053
580
PRS063 Paresthesia 41 0.052
581
P DNT007 Dentin Sensitivity 36 0.052
582
PSY004 Psychotic Disorder 67 0.052
583
KRT019 Keratitis, Hereditary 65 0.052
584
MRG003 Marginal Zone B-Cell Lymphoma 52 0.052
585
P PGT001 Paget's Disease of Bone 58 0.052
586
c HYP272 Hypercholesterolemia, Familial, 3 44 0.052
587
HRT011 Heart Septal Defect 50 0.052
588
BWN001 Bowen-Conradi Syndrome 52 0.052
589
KHL003 Kohlschutter-Tonz Syndrome 65 0.052
590
RTN020 Retinal Vascular Disease 46 0.052
591
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.051
592
c JVN010 Juvenile Rheumatoid Arthritis 64 0.051
593
PST028 Post-Traumatic Stress Disorder 58 0.051
594
NRT001 Neurotic Disorder 53 0.051
595
c INH020 Inherited Metabolic Disorder 47 0.051
596
c MCL013 Mucolipidosis Iv 66 0.051
597
HLL004 Hellp Syndrome 54 0.051
598
P BNG032 Benign Mesothelioma 46 0.051
599
FLL027 Fallopian Tube Carcinoma 67 0.051
600
GLS001 Gliosarcoma 54 0.051
601
BCT004 Bacteriuria 49 0.051
602
BRN004 Brain Edema 56 0.051
603
MLG086 Malignant Hyperthermia Susceptibility 39 0.051
604
CRV035 Cervical Cancer 76 0.051
605
P SLP005 Sleep Disorder 59 0.051
606
PRP030 Purpura 54 0.051
607
RNL077 Renal Fibrosis 47 0.051
608
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.050
609
c MNN043 Meningioma, Familial 74 0.050
610
MNN042 Meningioma, Radiation-Induced 62 0.050
611
VRC005 Varicose Veins 60 0.050
612
P MGR003 Migraine with Aura 52 0.050
613
SPN021 Spinal Meningioma 50 0.050
614
DST006 Diastolic Heart Failure 45 0.050
615
SCR001 Secretory Meningioma 41 0.050
616
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
617
c MLT156 Multiple Endocrine Neoplasia, Type I 72 0.050
618
SKN019 Skin Melanoma 68 0.050
619
P HPT021 Hepatitis 67 0.050
620
P HYD006 Hydrocephalus 66 0.050
621
P SJG008 Sjogren Syndrome 61 0.050
622
HMR039 Hemorrhage, Intracerebral 57 0.050
623
PRT038 Protein-Energy Malnutrition 54 0.050
624
P MNN013 Meningitis 66 0.050
625
P INT143 Interstitial Cystitis 61 0.050
626
P ACT105 Acute Mountain Sickness 52 0.050
627
HYP781 Hypoascorbemia 51 0.050
628
WLD007 Waldenstroem's Macroglobulinemia 61 0.050
629
P HYP535 Hypogonadotropic Hypogonadism 7 with or Without Anosmia 59 0.050
630
P PRG092 Pregnancy Loss, Recurrent 1 40 0.050
631
TYP007 Typhoid Fever 63 0.050
632
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.050
633
MCN017 Meconium Ileus 52 0.050
634
P BRN035 Brain Stem Glioma 52 0.050
635
ASP004 Asphyxia Neonatorum 46 0.049
636
P ASP006 Aspergillosis 69 0.049
637
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.049
638
CYS014 Cystadenocarcinoma 51 0.049
639
P FNC004 Fanconi Syndrome 50 0.049
640
KRT008 Keratopathy 47 0.049
641
P FNC034 Fanconi Renotubular Syndrome 2 40 0.049
642
FRZ001 Frozen Shoulder 53 0.049
643
PRP007 Priapism 47 0.049
644
P VNT002 Ventricular Septal Defect 60 0.049
645
GRD007 Grade Iii Astrocytoma 59 0.049
646
NWB001 Newborn Respiratory Distress Syndrome 58 0.049
647
PLC005 Placental Insufficiency 57 0.049
648
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.049
649
ENT001 Enterocele 39 0.049
650
MLT157 Multiple System Atrophy 1 70 0.049
651
THY030 Thyroid Gland Disease 52 0.048
652
DYS073 Dysphagia 50 0.048
653
c HPT073 Hepatitis C Virus 72 0.048
654
c INF071 Inflammatory Bowel Disease 1 67 0.048
655
c PLY168 Polycystic Kidney Disease 1 with or Without Polycystic Liver Disease 66 0.048
656
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.048
657
P HML002 Hemolytic Anemia 63 0.048
658
P MVM001 Movement Disease 63 0.048
659
DPH001 Diphtheria 60 0.048
660
P INT068 Intestinal Disease 53 0.048
661
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.048
662
P MDL005 Medulloblastoma 77 0.048
663
P PTT006 Pituitary Adenoma 55 0.048
664
ONC002 Onchocerciasis 52 0.048
665
LYM012 Lymphoplasmacytic Lymphoma 47 0.048
666
PLM031 Poliomyelitis 64 0.048
667
CHR074 Choriocarcinoma 47 0.048
668
P ALP009 Alopecia Areata 60 0.047
669
VRC001 Varicocele 49 0.047
670
PRM003 Premature Ejaculation 44 0.047
671
CNT060 Central Serous Chorioretinopathy 38 0.047
672
P FLL037 Follicular Lymphoma 67 0.047
673
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.047
674
VRL011 Viral Infectious Disease 61 0.047
675
CHR100 Chronic Ulcer of Skin 55 0.047
676
c FLL041 Follicular Lymphoma 1 49 0.047
677
PRC013 Pericarditis 54 0.047
678
ASP008 Aspiration Pneumonitis 45 0.047
679
PPT001 Peptic Esophagitis 52 0.047
680
PRV004 Periventricular Leukomalacia 52 0.047
681
ACR008 Acrocallosal Syndrome 69 0.047
682
MYL031 Myeloproliferative Neoplasm 66 0.047
683
CHL123 Chlamydia 59 0.047
684
P GLL022 Guillain-Barre Syndrome 59 0.047
685
P UVT001 Uveitis 57 0.047
686
LRN003 Learning Disability 49 0.047
687
RTC005 Reticulosarcoma 47 0.047
688
ATN004 Autonomic Neuropathy 45 0.047
689
BNM001 Bone Marrow Cancer 43 0.047
690
c CHR064 Chronic Monocytic Leukemia 33 0.047
691
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.047
692
c BNG091 Benign Chronic Pemphigus 58 0.047
693
P VNS003 Venous Insufficiency 55 0.047
694
GST037 Gastroparesis 54 0.047
695
ALP041 Alopecia, Neurologic Defects, and Endocrinopathy Syndrome 51 0.047
696
GNT002 Giant Cell Glioblastoma 50 0.047
697
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.047
698
INT053 Intracranial Vasospasm 24 0.047
699
SLC024 Slc4a1-Associated Distal Renal Tubular Acidosis 19 0.047
700
NRN004 Neuroendocrine Tumor 55 0.047
701
HMC014 Homocysteinemia 53 0.047
702
BRS064 Bursitis 48 0.047
703
CHR178 Chromosomal Triplication 35 0.047
704
MYL005 Myelofibrosis 70 0.046
705
P HYP098 Hypereosinophilic Syndrome 67 0.046
706
PPL022 Papilloma 54 0.046
707
GST049 Gastrointestinal System Cancer 49 0.046
708
GST071 Gastrointestinal Carcinoma 47 0.046
709
SQM002 Squamous Cell Papilloma 46 0.046
711
P RTN024 Retinoblastoma 73 0.046
712
P PMP001 Pemphigus 54 0.046
713
ADR007 Adrenoleukodystrophy 75 0.046
714
APN008 Apnea, Obstructive Sleep 64 0.046
715
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.046
716
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.046
717
PRT035 Peritoneum Cancer 44 0.046
718
c SPR086 Spermatogenic Failure 3 44 0.046
719
P OCL013 Oculodentodigital Dysplasia 69 0.046
720
P PLY018 Polycythemia 56 0.046
721
INT030 Intracranial Aneurysm 56 0.046
722
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.046
723
ANT024 Anthrax Disease 58 0.046
724
P BNC003 Bone Cancer 58 0.046
725
LMB062 Limb Ischemia 55 0.046
726
P SML001 Small Cell Carcinoma 52 0.046
727
CCN002 Cocaine Abuse 49 0.046
728
THR035 Thrombasthenia 40 0.046
729
MGC001 Megacolon 46 0.045
730
OPD001 Opioid Abuse 46 0.045
731
GST010 Gestational Trophoblastic Neoplasm 46 0.045
732
TRD006 Tardive Dyskinesia 54 0.045
733
c FML008 Familial Retinoblastoma 53 0.045
734
c HPT001 Hepatitis C 62 0.045
735
P MTR012 Mitral Valve Disease 58 0.045
736
ATS010 Autosomal Recessive Disease 48 0.045
737
HRN029 Hearing Loss, Noise-Induced 37 0.045
738
PRP001 Propionic Acidemia 65 0.045
739
HMG005 Hemoglobinopathy 56 0.045
740
c PYR010 Peyronie's Disease 50 0.045
741
ASP007 Aspiration Pneumonia 48 0.045
742
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.045
743
CRP001 Carpal Tunnel Syndrome 67 0.045
744
P PRM006 Primary Biliary Cirrhosis 62 0.045
745
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.045
746
P MYP006 Myopia 55 0.045
747
GRW007 Growth Hormone Deficiency 46 0.045
748
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.045
749
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.045
750
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.044
751
P INT070 Intestinal Obstruction 58 0.044
752
HMT008 Hematuria, Benign Familial 56 0.044
753
P DBT005 Diabetes Insipidus 55 0.044
754
HMP005 Hemiplegia 55 0.044
755
LPT006 Leptin Receptor Deficiency 48 0.044
756
OPD006 Opioid Addiction 48 0.044
757
P VSC011 Vasculitis 62 0.044
758
CRT013 Carotid Stenosis 50 0.044
759
GST019 Gastrointestinal Stromal Tumor 78 0.044
760
PNM008 Pneumothorax 56 0.044
761
PLS011 Plasmacytoma 56 0.044
762
CYN002 Cyanosis, Transient Neonatal 45 0.044
763
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.044
764
DFF003 Diffuse Scleroderma 41 0.044
765
MSC152 Muscular Dystrophy, Becker Type 63 0.044
766
c ALP101 Alpha-Thalassemia 62 0.044
767
ING001 Inguinal Hernia 60 0.044
768
ETN001 Eating Disorder 60 0.044
769
INC002 Inclusion Body Myositis 58 0.044
770
P FCL005 Focal Segmental Glomerulosclerosis 57 0.044
771
PRD004 Prediabetes Syndrome 47 0.044
772
URT014 Ureterolithiasis 44 0.044
773
c SRC023 Sarcoidosis 2 43 0.044
774
HML018 Homologous Wasting Disease 22 0.044
775
PSR001 Psoriatic Arthritis 61 0.043
776
c JVN061 Juvenile Arthritis 60 0.043
777
RDC002 Radiculopathy 50 0.043
778
CRB086 Cerebral Aneurysms 40 0.043
779
MTH071 Methane Production 26 0.043
780
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.043
781
MCN001 Mucinous Adenocarcinoma 49 0.043
782
c HYP057 Hypervitaminosis D 42 0.043
783
c RNL046 Renal Tubular Acidosis, Distal, Autosomal Dominant 37 0.043
784
c MJR008 Major Affective Disorder 2 35 0.043
785
c MJR023 Major Affective Disorder 7 33 0.043
786
c MJR003 Major Affective Disorder 6 33 0.043
787
c MJR006 Major Affective Disorder 5 33 0.043
788
c MJR004 Major Affective Disorder 4 28 0.043
789
ORG002 Organic Acidemia 44 0.043
790
TXC001 Toxic Megacolon 38 0.043
791
MLG164 Malignant Epithelial Tumor of Ovary 26 0.043
792
ACT119 Acute Promyelocytic Leukemia 63 0.043
793
P CHR285 Chronic Myelomonocytic Leukemia 60 0.043
794
c MST023 Mesothelioma, Malignant 57 0.043
795
CMM005 Common Cold 57 0.043
796
P PLM034 Pulmonary Emphysema 55 0.043
797
FNG017 Fungal Infectious Disease 53 0.043
798
NPH018 Nephrogenic Systemic Fibrosis 50 0.043
799
DRY001 Dry Eye Syndrome 47 0.043
800
GRM010 Germ Cells Tumors 34 0.043
801
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.043
802
SNG003 Single Ventricular Heart 30 0.043
803
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.043
804
OTT002 Otitis Media 72 0.043
805
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.043
806
c ACT135 Acute Graft Versus Host Disease 52 0.043
807
P SPP010 Suppressor of Tumorigenicity 3 51 0.043
808
CNT017 Central Nervous System Origin Vertigo 45 0.043
809
P DNT020 Dent Disease 1 62 0.042
810
P OLG002 Oligodendroglioma 67 0.042
811
P BNG030 Benign Ependymoma 60 0.042
812
AYM001 Ayme-Gripp Syndrome 57 0.042
813
CLL010 Cellular Ependymoma 54 0.042
814
c TRC022 Tricuspid Valve Insufficiency 45 0.042
815
c HMP004 Hemophilia B 68 0.042
816
MSL001 Measles 62 0.042
817
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.042
818
VTM027 Vitamin D-Dependent Rickets, Type 2a 56 0.042
819
P CLS010 Cluster Headache 42 0.042
820
CRN288 Corneal Dystrophy, Band-Shaped 38 0.042
821
PLG002 Plague 63 0.041
822
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.041
823
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.041
824
c MTR002 Mitral Valve Insufficiency 48 0.041
825
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.041
826
MYC006 Mycosis Fungoides 66 0.041
827
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.041
828
ART002 Arts Syndrome 64 0.041
829
SZR001 Sezary's Disease 60 0.041
830
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.041
831
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.041
832
P THR015 Thrombophilia 51 0.041
833
RFR010 Refractory Anemia 48 0.041
834
VTM002 Vitamin B12 Deficiency 48 0.041
835
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.041
836
GLN010 Glanzmann Thrombasthenia 66 0.041
837
INT066 Interstitial Lung Disease 60 0.041
838
DFF005 Diffuse Large B-Cell Lymphoma 55 0.041
839
INT075 Intracranial Hypertension 53 0.041
840
BHR001 Behr Syndrome 51 0.041
841
PRP017 Periapical Periodontitis 46 0.041
842
P CNJ013 Conjunctivitis 65 0.041
843
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.041
844
MNR012 Meniere Disease 57 0.041
845
GNR004 Generalized Anxiety Disorder 56 0.041
846
HRY003 Hairy Cell Leukemia 55 0.041
847
c CNT035 Central Nervous System Disease 52 0.041
848
LMY002 Leiomyoma 52 0.041
849
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.041
850
SPL004 Splenic Marginal Zone Lymphoma 51 0.041
851
P MGR001 Migraine Without Aura 49 0.041
852
HST010 Histiocytosis 48 0.041
853
SPL018 Splenomegaly 48 0.041
854
ANT018 Anthracosis 48 0.041
855
KRT013 Keratolytic Winter Erythema 46 0.041
856
MYF001 Myofibroma 45 0.041
857
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.041
858
P VNW001 Von Willebrand's Disease 65 0.041
859
c DPH024 Diaphragmatic Hernia, Congenital 63 0.041
860
P END084 Endocrine System Disease 45 0.041
861
P PRG002 Progesterone-Receptor Positive Breast Cancer 35 0.041
862
BRS051 Breast Disease 58 0.040
863
EMB004 Embryonal Carcinoma 56 0.040
864
SPN051 Spondylitis 51 0.040
865
URT010 Ureteral Obstruction 45 0.040
866
GRN017 Granulocytopenia 44 0.040
867
c LCL006 Localized Scleroderma 62 0.040
868
BRN002 Bronchiolitis 59 0.040
869
JVN009 Juvenile Pilocytic Astrocytoma 55 0.040
870
DFF035 Diffuse Cutaneous Systemic Sclerosis 49 0.040
871
LMT001 Limited Scleroderma 47 0.040
872
SMN007 Seminoma 43 0.040
873
P INF038 Influenza 68 0.040
874
P RHB003 Rhabdomyosarcoma 63 0.040
875
P GLY013 Glycogen Storage Disease 60 0.040
876
P SBS003 Substance Abuse 55 0.040
877
P SLM003 Salmonellosis 55 0.040
878
CRT017 Cartilage Disease 54 0.040
879
LYS002 Lysosomal Storage Disease 52 0.040
880
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.040
881
P HYP040 Hypospadias 51 0.040
882
P TTR001 Tetralogy of Fallot 70 0.040
883
P ESS003 Essential Thrombocythemia 68 0.040
884
CNT061 Conotruncal Heart Malformations 63 0.040
885
P MLN069 Melanoma, Uveal 59 0.040
886
CMP010 Complex Regional Pain Syndrome 58 0.040
887
NTR018 Neutrophilia, Hereditary 52 0.040
888
LNG015 Lingual-Facial-Buccal Dyskinesia 50 0.040
889
BLD053 Blood Platelet Disease 49 0.040
890
CRY008 Cryopyrin-Associated Periodic Syndrome 47 0.040
891
SRT004 Serotonin Syndrome 47 0.040
892
IDP033 Idiopathic Edema 44 0.040
893
CTS005 Catastrophic Antiphospholipid Syndrome 42 0.040
894
NPH078 Nephrolithiasis, Uric Acid 41 0.040
895
PST053 Postherpetic Neuralgia 40 0.040
896
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.040
897
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.040
898
PNM010 Pneumothorax, Primary Spontaneous 60 0.040
899
c LKM070 Leukemia, Acute Monocytic 57 0.040
900
VLC001 Velocardiofacial Syndrome 54 0.040
901
P HMR003 Hemorrhagic Disease 53 0.040
902
ABN011 Abnormal Hair, Joint Laxity, and Developmental Delay 50 0.040
903
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.040
904
PRL017 Prolymphocytic Leukemia 47 0.040
905
c OPT050 Opitz Gbbb Syndrome, Type Ii 47 0.040
906
ANP006 Anaplastic Ependymoma 46 0.040
907
c MLG064 Malignant Ependymoma 41 0.040
908
DBT002 Diabetic Autonomic Neuropathy 41 0.040
909
RSP007 Respiratory Distress Syndrome, Infant 30 0.040
910
INF009 Inflammatory Spondylopathy 31 0.039
911
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.039
912
MTH009 Mouth Disease 56 0.039
913
THR004 Thrombocytosis 51 0.039
914
PST021 Postpartum Depression 50 0.039
915
DMP001 Dumping Syndrome 44 0.039
916
URM005 Uremic Pruritus 42 0.039
917
P MYC084 Mycobacterium Tuberculosis 1 68 0.038
918
DRG003 Drug Dependence 47 0.038
919
DNT001 Dental Fluorosis 43 0.038
920
ARG004 Argyria 27 0.038
921
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.038
922
PLY001 Polycythemia Vera 69 0.038
923
MST024 Mastocytosis, Cutaneous 69 0.038
924
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.038
925
c HMP029 Hemophilia a 67 0.038
926
MGK001 Megakaryocytic Leukemia 64 0.038
927
P DST002 Distal Arthrogryposis 63 0.038
928
P PTT014 Pitt-Hopkins Syndrome 63 0.038
929
c ART144 Arthrogryposis, Distal, Type 1a 61 0.038
930
PTN001 Patent Foramen Ovale 60 0.038
931
MXD005 Mixed Connective Tissue Disease 58 0.038
932
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.038
933
LBL001 Lobular Neoplasia 56 0.038
934
RFL001 Reflex Sympathetic Dystrophy 54 0.038
935
PLM012 Pulmonary Sarcoidosis 53 0.038
936
ALK024 Alkuraya-Kucinskas Syndrome 51 0.038
937
P CHL066 Cholangitis 51 0.038
938
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.038
939
MNC019 Monocarboxylate Transporter 1 Deficiency 47 0.038
940
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.038
941
MCC013 Mucocutaneous Ulceration, Chronic 39 0.038
942
c SYS043 Systemic Lupus Erythematosus 1 38 0.038
943
P HYP120 Hypoaldosteronism 36 0.038
944
MSC012 Muscular Dystrophy, Duchenne and Becker Type 34 0.038
945
CNG506 Congenital Amyoplasia 27 0.038
946
P APL001 Aplastic Anemia 74 0.038
947
PRM126 Primary Peritoneal Carcinoma 62 0.038
948
HYD038 Hydrops Fetalis, Nonimmune 62 0.038
949
ORL005 Oral Candidiasis 56 0.038
950
SLC006 Silicosis 56 0.038
951
KRT006 Keratoconjunctivitis 53 0.038
952
IRD001 Iridocyclitis 53 0.038
953
FBR008 Fibrillary Astrocytoma 51 0.038
954
KRT001 Keratoconjunctivitis Sicca 49 0.038
955
SBP004 Subependymoma 46 0.038
956
MYX001 Myxopapillary Ependymoma 46 0.038
957
c EST002 Estrogen-Receptor Negative Breast Cancer 45 0.038
958
ANP009 Anaplastic Oligodendroglioma 43 0.038
959
HYP344 Hyperthyroidism, Familial Gestational 39 0.038
960
c PLM022 Pulmonary Valve Insufficiency 39 0.038
961
PSD088 Pseudobulbar Affect 36 0.038
962
c ADL008 Adult Oligodendroglioma 34 0.038
963
CHL057 Childhood Brain Stem Glioma 32 0.038
964
c ADL054 Adult Brain Stem Glioma 30 0.038
965
c MLG023 Malignant Adult Ependymoma 15 0.038
966
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.037
967
EWN003 Ewing Sarcoma 69 0.037
968
ORL011 Oral Cancer 60 0.037
969
P TRT010 Teratoma 52 0.037
970
VCC001 Vaccinia 49 0.037
971
MNG007 Manganese Poisoning 29 0.037
972
P PNM006 Pneumoconiosis 56 0.037
973
P ANT006 Antiphospholipid Syndrome 55 0.037
974
c PSR017 Psoriasis 2 53 0.037
975
c PSR023 Psoriasis 1 52 0.037
976
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.037
977
c PSR032 Psoriasis 11 47 0.037
978
PRT019 Protein-Losing Enteropathy 45 0.037
979
TND004 Tendinopathy 43 0.037
980
c PSR028 Psoriasis 7 42 0.037
981
c PSR018 Psoriasis 13 41 0.037
982
c HYP555 Hypertriglyceridemia, Transient Infantile 39 0.037
983
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.037
984
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.036
985
PLM070 Pulmonic Stenosis 57 0.036
986
c PLY172 Polycystic Kidney Disease 2 with or Without Polycystic Liver Disease 57 0.036
987
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.036
988
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.036
989
P CRB194 Cerebroretinal Microangiopathy with Calcifications and Cysts 1 53 0.036
990
PRS030 Persistent Fetal Circulation Syndrome 52 0.036
991
FCT001 Factor Viii Deficiency 51 0.036
992
c PRM012 Primary Polycythemia 50 0.036
993
c THR090 Thrombocythemia 1 49 0.036
994
END021 Endomyocardial Fibrosis 49 0.036
995
P MST002 Mast-Cell Leukemia 49 0.036
996
PLM041 Pulmonary Valve Stenosis 49 0.036
997
ADR016 Adrenal Cortical Carcinoma 48 0.036
998
P CPL014 Capillary Malformation-Arteriovenous Malformation 1 48 0.036
999
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.036
1000
ACT084 Acute Stress Disorder 47 0.036
1001
c PRM093 Premature Ovarian Failure 7 47 0.036
1002
HMP009 Haemophilus Influenzae 43 0.036
1003
CLP006 Clopidogrel Resistance 40 0.036
1004
ADR004 Adrenal Cortical Adenocarcinoma 39 0.036
1005
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.036
1006
P VSC018 Visceral Steatosis 33 0.036
1007
P OVR096 Overlap Myositis 27 0.036
1008
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.036
1009
SCR003 Secretory Diarrhea 37 0.036
1010
HVY002 Heavy Metal Poisoning 22 0.036
1011
P HYP609 Hypophosphatemic Rickets, X-Linked Dominant 64 0.036
1012
WST001 West Syndrome 61 0.036
1013
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.036
1014
INT051 Intussusception 53 0.036
1015
P RTN022 Retinal Vein Occlusion 53 0.036
1016
P PRC012 Pericardial Effusion 51 0.036
1017
HMP001 Hemopericardium 48 0.036
1018
TST014 Testicular Cancer 46 0.036
1019
c CHR417 Chronic Graft Versus Host Disease 57 0.035
1020
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.035
1021
ACT200 Acute Monoblastic Leukemia 52 0.035
1022
c ALM001 Al Amyloidosis 50 0.035
1023
SLD003 Sialadenitis 49 0.035
1024
MCR018 Microcytic Anemia 47 0.035
1025
IRN004 Iron-Refractory Iron Deficiency Anemia 47 0.035
1026
SPR126 Superior Semicircular Canal Dehiscence 40 0.035
1027
DFF039 Diffuse Midline Glioma, H3 K27m-Mutant 36 0.035
1028
P GLL020 Gallbladder Disease 57 0.035
1029
CLL003 Cellulitis 54 0.035
1030
P PTS002 Ptosis 53 0.035
1031
c VRL010 Viral Hepatitis 52 0.035
1032
FBR009 Fibrous Dysplasia 48 0.035
1033
P AVS003 Avascular Necrosis 42 0.035
1034
AMN006 Aminoaciduria 38 0.035
1035
P NJM001 Nijmegen Breakage Syndrome 74 0.035
1036
NDL024 Nodal Marginal Zone Lymphoma 38 0.035
1037
P LPS002 Liposarcoma 65 0.034
1038
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.034
1039
KND001 Kindler Syndrome 64 0.034
1040
P LYM033 Lymphoproliferative Syndrome 59 0.034
1041
ADR005 Adrenal Carcinoma 58 0.034
1042
P PRV006 Pervasive Developmental Disorder 57 0.034
1043
FND002 Fundus Dystrophy 55 0.034
1044
P DYS193 Dystonia 11, Myoclonic 55 0.034
1045
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.034
1046
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.034
1047
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.034
1048
P NRC002 Narcolepsy 52 0.034
1049
ACT017 Acute Chest Syndrome 51 0.034
1050
PLR007 Pleural Empyema 50 0.034
1051
OCL022 Ocular Melanoma 50 0.034
1052
CHL018 Childhood Medulloblastoma 49 0.034
1053
INT017 Intestinal Schistosomiasis 48 0.034
1054
ALV007 Alveolar Capillary Dysplasia with Misalignment of Pulmonary Veins 48 0.034
1055
P BLR006 Biliary Tract Disease 47 0.034
1056
c ADL023 Adult Medulloblastoma 44 0.034
1057
MND023 Mend Syndrome 43 0.034
1058
P VTL001 Vitelliform Macular Dystrophy 42 0.034
1059
FBR019 Fibromatosis 41 0.034
1060
c MYT029 Myotonia Congenita, Autosomal Recessive 41 0.034
1061
c ADL096 Adult Hepatocellular Carcinoma 40 0.034
1062
CGN005 Cognitive Impairment with or Without Cerebellar Ataxia 39 0.034
1063
CRB026 Cerebellar Astrocytoma 37 0.034
1064
HND015 Hand Skill, Relative 33 0.034
1065
PDT014 Pediatric Ependymoma 32 0.034
1066
UNV002 Univentricular Heart 28 0.034
1067
CRT064 Corticosterone Methyloxidase Deficiency 20 0.034
1068
PNL001 Pineal Gland Astrocytoma 14 0.034
1069
CHL009 Childhood Cerebral Astrocytoma 14 0.034
1070
P 3MT016