Search results for Calcium carbonate

1888 hits were found for Calcium carbonate

# Family MCID Name MIFTS Score
1
P HYP069 Hyperparathyroidism 63 0.417
2
P KDN018 Kidney Disease 72 0.372
3
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.357
4
BNR002 Bone Resorption Disease 48 0.348
5
P OST002 Osteoporosis 74 0.331
6
RCK004 Rickets 68 0.319
7
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.312
8
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.312
9
NPH009 Nephrolithiasis 55 0.305
10
c CHR684 Chronic Kidney Disease 70 0.301
11
HYP025 Hyperphosphatemia 48 0.292
12
c SCN007 Secondary Hyperparathyroidism 51 0.279
13
URL001 Urolithiasis 45 0.279
14
PRT037 Pertussis 65 0.269
15
HYP266 Hypoxia 57 0.264
16
c HYP595 Hypertension, Essential 84 0.263
17
P CLR023 Colorectal Cancer 99 0.262
18
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.259
19
P BND020 Bone Disease 59 0.242
20
P NRB001 Neuroblastoma 72 0.234
21
HLX001 Helix Syndrome 47 0.231
22
END086 End Stage Renal Disease 51 0.227
23
ISC004 Ischemia 58 0.226
24
MTB004 Metabolic Acidosis 50 0.222
25
LVR012 Liver Cirrhosis 62 0.222
26
P CRD119 Cardiac Arrest 67 0.221
27
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.216
28
48X005 48,xyyy 39 0.214
29
CNG034 Congestive Heart Failure 69 0.214
30
c PRM005 Primary Hyperparathyroidism 58 0.213
31
HRW001 Hair Whorl 36 0.209
32
P HYP024 Hypoparathyroidism 56 0.208
33
ANX004 Anoxia 40 0.208
34
LPP008 Lipoprotein Quantitative Trait Locus 62 0.206
35
P ADN016 Adenocarcinoma 64 0.203
36
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.203
37
P ENC018 Encephalopathy 61 0.201
38
ANG054 Angina Pectoris 66 0.200
39
ADN018 Adenoma 59 0.195
40
ART140 Arteries, Anomalies of 52 0.193
41
P CRN300 Coronary Heart Disease 1 63 0.192
42
ATH013 Atherosclerosis Susceptibility 65 0.192
43
P VSC007 Vascular Disease 63 0.190
44
P LVR013 Liver Disease 68 0.187
45
P GLM045 Glioma 63 0.186
46
P HRT032 Heart Disease 75 0.186
47
c PRC016 Pre-Eclampsia 63 0.186
48
ALL026 Allergic Hypersensitivity Disease 62 0.184
49
GLL048 Glial Tumor 45 0.184
50
47X002 47,xyy 49 0.182
51
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.179
52
P RCT021 Rectum Cancer 52 0.176
53
LNG099 Lung Disease 60 0.175
54
P RSP003 Respiratory Failure 74 0.175
55
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.174
56
OST159 Osteogenic Sarcoma 66 0.172
57
OCL069 Ocular Motor Apraxia 51 0.170
58
PPL052 Papillomatosis, Confluent and Reticulated 33 0.166
59
DNT012 Dental Caries 53 0.164
60
P ALZ034 Alzheimer Disease 88 0.164
61
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.163
62
P PLM037 Pulmonary Hypertension 67 0.163
63
P MYC007 Myocardial Infarction 70 0.159
64
P PRS040 Prostate Cancer 97 0.159
65
P PNC035 Pancreatic Cancer 84 0.159
66
c ACT071 Acute Kidney Failure 60 0.157
67
CHL014 Cholera 59 0.157
68
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.157
69
GLB015 Glioblastoma Multiforme 75 0.156
70
P BPL003 Bipolar Disorder 56 0.155
71
c AMY091 Amyotrophic Lateral Sclerosis 1 89 0.155
72
P BRS047 Breast Cancer 97 0.155
73
P LTR001 Lateral Sclerosis 54 0.154
74
P MSC005 Muscular Dystrophy 66 0.154
75
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.154
76
c MGR028 Migraine with or Without Aura 1 67 0.152
77
c MJR024 Major Affective Disorder 9 41 0.152
78
c MJR022 Major Affective Disorder 8 38 0.152
79
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.151
80
HYP056 Hypoglycemia 66 0.149
81
P HYP076 Hyperthyroidism 55 0.149
82
P NRP001 Neuropathy 56 0.149
83
P PHC003 Pheochromocytoma 71 0.148
84
P LNG032 Lung Cancer 98 0.148
85
FTT001 Fatty Liver Disease 61 0.148
86
ADR040 Adrenal Gland Pheochromocytoma 46 0.148
87
P HYP086 Hypothyroidism 69 0.148
88
P PRD008 Periodontitis 64 0.147
89
MTH071 Methane Production 26 0.147
90
c GLL024 Gallbladder Disease 1 53 0.147
91
P RNL007 Renal Tubular Acidosis 51 0.146
92
THY029 Thyroid Carcinoma 59 0.146
93
P SZR006 Seizure Disorder 56 0.145
94
AGN016 Aging 56 0.145
95
OST011 Osteomalacia 52 0.143
96
VSL002 Visual Epilepsy 59 0.143
97
CMP034 Complete Androgen Insensitivity Syndrome 46 0.142
98
c ATR087 Atrial Standstill 1 75 0.141
99
CYS001 Cystic Fibrosis 81 0.141
100
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.140
101
P HPT023 Hepatocellular Carcinoma 100 0.140
102
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.139
103
RNL011 Renal Osteodystrophy 50 0.138
104
P DRR001 Diarrhea 55 0.138
105
LPD008 Lipid Metabolism Disorder 62 0.136
106
TXC005 Toxic Shock Syndrome 62 0.136
107
DPR016 Depression 63 0.135
108
CRB039 Cerebrovascular Disease 67 0.134
109
CNS004 Constipation 58 0.134
110
HYP066 Hyperglycemia 61 0.132
111
BRN071 Brain Injury 49 0.132
112
ATM095 Autoimmune Disease 62 0.131
113
TTN003 Tetanus 65 0.130
114
URM002 Uremia 49 0.130
115
P MLG056 Malignant Hyperthermia 67 0.129
116
P LYM118 Lymphoma 68 0.129
117
OST012 Osteoarthritis 78 0.128
118
IRN002 Iron Metabolism Disease 57 0.128
119
CLC006 Calcinosis 48 0.127
120
CYT002 Cytokine Deficiency 42 0.126
121
c RHB024 Rhabdomyosarcoma 2 67 0.126
122
NPH003 Nephrocalcinosis 51 0.126
123
INS001 Insulinoma 60 0.126
124
GT001 Gout 64 0.126
125
P ART021 Arteriosclerosis 54 0.125
126
HYP005 Hypokalemia 55 0.125
127
P SRC025 Sarcoidosis 1 70 0.124
128
P ECL001 Eclampsia 50 0.124
129
P PNC025 Panic Disorder 53 0.124
130
P CRD246 Cardiovascular System Disease 57 0.124
131
c HYP836 Hypercholesterolemia, Familial, 1 73 0.124
132
c ACT027 Acute Pancreatitis 60 0.124
133
P HDC001 Headache 57 0.123
134
IDP073 Idiopathic Hypercalciuria 43 0.123
135
P PNC044 Pancreatitis 61 0.123
136
P TRN020 Turner Syndrome 67 0.122
137
OST017 Osteomyelitis 64 0.122
138
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.121
139
P GST053 Gastric Cancer 83 0.121
140
c MCR120 Microvascular Complications of Diabetes 7 47 0.121
141
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.121
142
DWN001 Down Syndrome 70 0.121
143
P HYP726 Hypercalcemia, Infantile, 1 58 0.120
144
c MCR113 Microvascular Complications of Diabetes 3 52 0.120
145
c MCR130 Microvascular Complications of Diabetes 6 41 0.120
146
c MCR133 Microvascular Complications of Diabetes 4 41 0.120
147
PNG002 Pain Agnosia 51 0.120
148
c NRF023 Neurofibromatosis, Type Ii 80 0.119
149
ADL002 Adult Syndrome 70 0.119
150
SPN186 Spinal Cord Injury 60 0.119
151
P MYP004 Myopathy 70 0.119
152
P LKM002 Leukemia 68 0.118
153
MSC157 Muscular Dystrophy, Duchenne Type 72 0.118
154
c ACT075 Acute Myocardial Infarction 57 0.118
155
P PLM036 Pulmonary Fibrosis 65 0.118
156
TRM010 Traumatic Brain Injury 51 0.117
157
P MCR115 Microvascular Complications of Diabetes 5 66 0.117
158
HYP017 Hypophosphatemia 50 0.117
159
SQM006 Squamous Cell Carcinoma 60 0.116
160
ALC007 Alcohol Dependence 66 0.116
161
P PRP019 Peripheral Nervous System Disease 58 0.116
162
MNT002 Mental Depression 58 0.116
163
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.116
164
P ART023 Arthropathy 62 0.116
165
P NTR004 Neutropenia 63 0.115
166
STR067 Stroke, Ischemic 81 0.115
167
CLN015 Colon Adenocarcinoma 65 0.114
168
P CTR002 Cataract 60 0.112
169
P OVR042 Ovarian Cancer 88 0.112
170
c SML038 Small Cell Cancer of the Lung 65 0.112
171
HMN044 Human Immunodeficiency Virus Type 1 71 0.112
172
LYM019 Lymphosarcoma 46 0.111
173
P TRM003 Tremor 54 0.111
174
P OST001 Osteopetrosis 70 0.111
175
PLM010 Pulmonary Edema 54 0.110
176
P DBT009 Diabetes Mellitus 64 0.110
177
P BNG032 Benign Mesothelioma 46 0.110
178
P LKM062 Leukemia, Acute Lymphoblastic 69 0.110
179
P PSR002 Psoriasis 62 0.109
180
ESP021 Esophageal Cancer 90 0.109
181
HYP060 Hyperinsulinism 54 0.109
182
P OVR082 Overgrowth Syndrome 50 0.109
183
CRN030 Coronary Stenosis 50 0.109
184
CLR108 Colorectal Adenoma 64 0.108
185
DFC004 Deficiency Anemia 70 0.107
186
ANX010 Anxiety 73 0.107
187
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.107
188
GTR002 Goiter 53 0.107
189
P DDN001 Duodenal Ulcer 52 0.107
190
P HYP061 Hypertrophic Cardiomyopathy 70 0.106
191
PLY150 Polykaryocytosis Inducer 31 0.106
192
ATX019 Ataxia with Vitamin E Deficiency 42 0.106
193
P ATR011 Atrial Fibrillation 66 0.106
194
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.105
195
P SLP006 Sleep Apnea 69 0.105
196
P AST007 Astrocytoma 51 0.105
197
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.105
198
ATR057 Atrioventricular Block 55 0.105
199
c DLT002 Dilated Cardiomyopathy 79 0.105
200
PST011 Pustulosis of Palm and Sole 52 0.104
201
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.104
202
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.104
203
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.104
204
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.104
205
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.104
206
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.104
207
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.104
208
PRT036 Peritonitis 64 0.104
209
c DWL002 Dowling-Degos Disease 1 58 0.104
210
P CHR345 Chronic Pain 44 0.104
211
INT007 Intermediate Coronary Syndrome 55 0.104
212
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.104
213
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.104
214
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.104
215
P RHN004 Rhinitis 57 0.103
216
PLM033 Pulmonary Embolism 59 0.103
217
MCS002 Mucositis 56 0.102
218
CRD223 Cardiac Arrhythmia 60 0.101
219
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.101
220
AST005 Asthma 76 0.100
221
NTR005 Nutritional Deficiency Disease 62 0.100
222
P LNG064 Lung Cancer Susceptibility 3 78 0.100
223
STT001 Status Epilepticus 60 0.099
224
P PNM007 Pneumonia 68 0.099
225
NRL016 Neural Tube Defects 82 0.098
226
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.098
227
P MLN008 Melanoma 69 0.098
228
DRM006 Dermatitis 61 0.098
229
BCT022 Bacterial Infectious Disease 56 0.097
230
P OPN001 Open-Angle Glaucoma 49 0.097
231
P BCL017 B-Cell Lymphoma 58 0.097
232
PPT005 Peptic Ulcer Disease 59 0.097
233
P BLD134 Bladder Cancer 79 0.097
234
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.097
235
MYL069 Myeloma, Multiple 85 0.097
236
CRD132 Cardiac Conduction Defect 58 0.096
237
P DMN002 Dementia 66 0.096
238
BRN024 Bronchitis 68 0.096
239
CRB004 Cerebral Artery Occlusion 45 0.096
240
P ATS308 Autosomal Dominant Cerebellar Ataxia 60 0.095
241
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.095
242
SYN036 Syncope 45 0.095
243
PRP027 Peripheral Vascular Disease 71 0.095
244
MDD011 Mood Disorder 62 0.095
245
P INF037 Inflammatory Bowel Disease 54 0.095
246
P HYP733 Hypercalciuria, Absorptive, 2 45 0.095
247
c GRV008 Graves Disease 1 56 0.095
248
ACQ007 Acquired Immunodeficiency Syndrome 60 0.094
249
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.094
250
SKN016 Skin Disease 63 0.094
251
CHL068 Cholestasis 61 0.094
252
IMM167 Immune Deficiency Disease 78 0.094
253
c SCL052 Scleroderma, Familial Progressive 61 0.093
254
ART016 Aortic Aneurysm 69 0.092
255
INS024 Insulin-Like Growth Factor I 79 0.092
256
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.092
257
LYM133 Lymphoma, Hodgkin, Classic 69 0.091
258
OST003 Osteonecrosis 61 0.091
259
OCL006 Ocular Hypertension 53 0.091
260
PRT013 Portal Hypertension 59 0.091
261
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.091
262
ALL003 Allergic Rhinitis 67 0.091
263
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.090
264
GST092 Gastroesophageal Reflux 67 0.090
265
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.090
266
P EPL164 Epilepsy 71 0.090
267
PRT029 Parathyroid Adenoma 50 0.089
268
RTN023 Retinitis 46 0.089
269
NRR001 Neuroretinitis 42 0.089
270
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.089
271
P INF032 Infertility 57 0.088
272
P ART022 Arthritis 69 0.088
273
HMS001 Hemosiderosis 54 0.088
274
P PLY014 Polycystic Kidney Disease 62 0.088
275
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.088
276
P MJR007 Major Affective Disorder 1 43 0.088
277
P HNT016 Huntington Disease 72 0.088
278
LYM040 Lymphoblastic Lymphoma 54 0.088
279
P KDN017 Kidney Cancer 60 0.087
280
c ATS007 Autism Spectrum Disorder 67 0.087
281
ANR040 Aneurysm 59 0.087
282
IMP005 Impotence 52 0.087
283
DYS073 Dysphagia 50 0.086
284
P LCT001 Lactic Acidosis 51 0.086
285
MYC005 Myocardial Stunning 46 0.086
286
c BRN108 Branchiootic Syndrome 1 62 0.086
287
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.085
288
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.085
289
P END044 Endometriosis 63 0.085
290
GST023 Gastric Ulcer 53 0.085
291
P PLY019 Polyneuropathy 56 0.085
292
P SCK005 Sickle Cell Disease 50 0.084
293
P RTN008 Retinitis Pigmentosa 79 0.084
294
RYN005 Raynaud Phenomenon 47 0.084
295
P RRH023 Rare Hereditary Hemochromatosis 41 0.083
297
CRV035 Cervical Cancer 76 0.083
298
P ANP001 Anaplastic Large Cell Lymphoma 58 0.083
299
c FNC043 Fanconi Anemia, Complementation Group E 62 0.083
300
AMN003 Amnestic Disorder 54 0.083
301
MLR004 Malaria 81 0.082
302
P MJR001 Major Depressive Disorder 68 0.082
303
SVR004 Severe Combined Immunodeficiency 73 0.082
304
P NPH012 Nephrotic Syndrome 60 0.082
305
P CNR004 Cone-Rod Dystrophy 2 73 0.082
306
c ACT068 Acute Cystitis 63 0.082
307
CLT003 Colitis 62 0.082
308
P ATS364 Autism 70 0.081
309
SYN007 Synovitis 54 0.081
310
PLC002 Plica Syndrome 36 0.081
311
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.081
312
SCK003 Sickle Cell Anemia 74 0.081
313
RTR008 Root Resorption 45 0.081
314
GLC003 Glucose Intolerance 54 0.081
315
HMC014 Homocysteinemia 53 0.081
316
LMB062 Limb Ischemia 55 0.081
317
HYP014 Hyperuricemia 52 0.081
318
c PCH010 Pachyonychia Congenita 3 44 0.081
319
CLR030 Clear Cell Renal Cell Carcinoma 53 0.080
320
c SYS001 Systemic Lupus Erythematosus 86 0.080
321
P MYL006 Myeloid Leukemia 60 0.080
322
PTT037 Pituitary Tumors 44 0.080
323
P ADL010 Adult Respiratory Distress Syndrome 65 0.080
324
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.080
325
END040 Endogenous Depression 55 0.080
326
CHL079 Children's Interstitial Lung Disease 26 0.080
327
P SCH015 Schizophrenia 74 0.080
328
P SKN015 Skin Carcinoma 66 0.080
329
PST092 Posttransplant Acute Limbic Encephalitis 29 0.080
330
P GRV001 Graves' Disease 55 0.080
331
PNC129 Pancreatic Adenocarcinoma 68 0.079
332
P CHN012 Chondrosarcoma 56 0.079
333
TBC004 Tobacco Addiction 64 0.079
334
c LKM061 Leukemia, Acute Myeloid 84 0.079
335
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.079
336
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.079
337
BLR008 Bilirubin Metabolic Disorder 57 0.079
338
SRC014 Sarcoma 65 0.078
339
P RHM011 Rheumatoid Arthritis 80 0.078
340
CHR072 Chordoma 58 0.078
341
PLM001 Pulmonary Tuberculosis 69 0.078
342
NRM005 Neuromuscular Disease 64 0.078
343
P FBR017 Fibrosarcoma 56 0.078
344
c THR092 Thrombophilia Due to Thrombin Defect 73 0.078
345
P GST044 Gastritis 56 0.078
346
c GLC092 Glaucoma, Primary Open Angle 62 0.077
347
SFT003 Soft Tissue Sarcoma 56 0.077
348
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.077
349
CLN045 Colonic Benign Neoplasm 46 0.077
350
INT075 Intracranial Hypertension 53 0.077
351
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.077
352
P PRK057 Parkinson Disease, Late-Onset 78 0.077
353
P SYS005 Systemic Scleroderma 68 0.077
354
P HRP006 Herpes Simplex 65 0.077
355
P THL005 Thalassemia 60 0.077
356
MMM001 Mammary Paget's Disease 53 0.077
357
CRH001 Crohn's Disease 74 0.076
358
P THR014 Thrombocytopenia 67 0.076
359
SPN035 Spindle Cell Sarcoma 53 0.076
360
P PRM002 Primary Hyperoxaluria 62 0.076
361
P MYS003 Myasthenia Gravis 68 0.076
362
P DYS154 Dystonia 65 0.076
363
LSH001 Leishmaniasis 63 0.076
364
P KLZ004 Kala-Azar 1 41 0.076
365
P INS002 in Situ Carcinoma 53 0.076
366
BRN004 Brain Edema 56 0.076
367
P DST107 Distal Renal Tubular Acidosis 42 0.076
368
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.076
369
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.075
370
HPT004 Hepatic Coma 45 0.075
371
PLM031 Poliomyelitis 64 0.075
372
P LCT002 Lactose Intolerance 53 0.075
373
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.075
374
c CHR682 Chronic Bilirubin Encephalopathy 39 0.075
375
PPL022 Papilloma 54 0.075
376
CRB090 Cerebral Hypoxia 44 0.075
377
c ACT134 Acute Liver Failure 56 0.075
378
MSC007 Muscle Hypertrophy 64 0.075
379
CHG001 Chagas Disease 66 0.074
380
PNM008 Pneumothorax 56 0.074
381
P PLY011 Polycystic Ovary Syndrome 56 0.074
382
P LPS004 Lupus Erythematosus 61 0.074
383
ADN011 Adenoid Cystic Carcinoma 70 0.074
384
P PRD021 Periodic Paralysis 45 0.074
385
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 32 0.073
386
c MJR008 Major Affective Disorder 2 35 0.073
387
THY030 Thyroid Gland Disease 52 0.073
388
PTH003 Pathologic Nystagmus 52 0.073
389
P GLM007 Glomerulonephritis 57 0.073
390
ANT018 Anthracosis 48 0.073
391
P BRS044 Breast Adenocarcinoma 59 0.073
392
P HMN010 Hemangioma 61 0.073
393
c MJR023 Major Affective Disorder 7 33 0.073
394
c MJR003 Major Affective Disorder 6 33 0.073
395
c MJR006 Major Affective Disorder 5 33 0.073
396
c MJR004 Major Affective Disorder 4 28 0.073
397
c CRV002 Cervix Uteri Carcinoma in Situ 46 0.072
398
P PNM006 Pneumoconiosis 56 0.072
399
PRM020 Premenstrual Tension 40 0.072
400
ALL006 Allergic Asthma 56 0.072
401
CRD137 Cardiogenic Shock 47 0.072
402
TLN003 Telangiectasis 52 0.072
403
ORL011 Oral Cancer 60 0.072
404
STM007 Stomatitis 50 0.072
405
P ENC004 Encephalitis 61 0.072
406
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.072
407
THR024 Thrombosis 57 0.072
408
LPT014 Leptin Deficiency or Dysfunction 74 0.071
409
BRN028 Brain Cancer 74 0.071
410
ILS001 Ileus 51 0.071
411
P SCL018 Scoliosis 60 0.071
412
GST045 Gastroenteritis 59 0.071
413
THY111 Thyroid Carcinoma, Familial Medullary 67 0.071
414
INT066 Interstitial Lung Disease 60 0.071
415
IRR002 Irritable Bowel Syndrome 65 0.070
416
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.070
417
c BNG091 Benign Chronic Pemphigus 58 0.070
418
NPH098 Nephrolithiasis, X-Linked Recessive, with Renal Failure 41 0.070
419
ULC004 Ulcerative Colitis 73 0.070
420
c OST163 Osteopetrosis, Autosomal Recessive 3 55 0.070
421
P PSD015 Pseudohypoparathyroidism 56 0.070
422
CHR073 Choreatic Disease 52 0.070
423
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 47 0.070
424
P DRM053 Dermatitis, Atopic 66 0.070
425
TRN015 Transient Cerebral Ischemia 63 0.070
426
P MSC003 Muscular Atrophy 52 0.070
427
SCN001 Secondary Hyperparathyroidism of Renal Origin 27 0.070
428
c MLG068 Malignant Glioma 46 0.070
429
P ALP008 Alopecia 54 0.069
430
GST050 Gastrointestinal System Disease 56 0.069
431
P MYT002 Myotonic Dystrophy 49 0.069
432
P PRM006 Primary Biliary Cirrhosis 62 0.069
433
ANT024 Anthrax Disease 58 0.069
434
GRN017 Granulocytopenia 44 0.069
435
c PRS136 Prostate Cancer, Hereditary, 6 33 0.069
436
c PRS130 Prostate Cancer, Hereditary, 8 32 0.069
437
CRV045 Cervical Intraepithelial Neoplasia 39 0.069
438
URT049 Urate Oxidase, Pseudogene 25 0.069
439
P DBT005 Diabetes Insipidus 55 0.069
440
P ALC033 Alcohol Use Disorder 58 0.069
441
P EXN002 Exanthem 57 0.068
442
CLR109 Colorectal Adenocarcinoma 51 0.068
443
ENM002 Enamel Erosion 26 0.068
444
c MCR129 Microvascular Complications of Diabetes 1 66 0.068
445
P PLM034 Pulmonary Emphysema 55 0.068
446
P TXP001 Toxoplasmosis 60 0.068
447
P PYL005 Pyelonephritis 56 0.068
448
ENT004 Enthesopathy 49 0.068
449
HPT019 Hepatic Encephalopathy 60 0.068
450
P HML002 Hemolytic Anemia 63 0.068
451
KLD004 Keloid Disorder 40 0.068
452
ALL014 Allergic Encephalomyelitis 38 0.067
453
c MNN043 Meningioma, Familial 74 0.067
454
MNN042 Meningioma, Radiation-Induced 62 0.067
455
SPN021 Spinal Meningioma 50 0.067
456
SCR001 Secretory Meningioma 41 0.067
457
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.067
458
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.067
459
ERY051 Erythroleukemia, Familial 56 0.067
460
HND015 Hand Skill, Relative 33 0.067
461
HDN002 Head Injury 46 0.067
462
ORL015 Oral Squamous Cell Carcinoma 43 0.067
463
P MLN007 Male Infertility 55 0.067
464
P CND004 Candidiasis 58 0.067
465
SBC016 Subacute Delirium 44 0.066
466
P RTN016 Retinal Degeneration 53 0.066
467
BRR014 Barrett Esophagus 65 0.066
468
49X006 49, Xxxxy Syndrome 41 0.066
469
END057 Endometrial Cancer 74 0.066
470
PPL001 Papillary Adenoma 44 0.066
471
MCL006 Macular Retinal Edema 55 0.066
472
GLS018 Glass Syndrome 57 0.066
473
SQM002 Squamous Cell Papilloma 46 0.065
474
c PNS012 Paine Syndrome 61 0.065
475
P MLT020 Multiple Sclerosis 72 0.065
476
c PRM038 Primary Agammaglobulinemia 44 0.065
477
P HYD006 Hydrocephalus 66 0.065
478
SCH014 Schistosomiasis 57 0.065
479
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.065
480
CNT047 Contact Dermatitis 58 0.065
481
P GLM040 Glioma Susceptibility 1 81 0.065
482
WTH001 Withdrawal Disorder 48 0.065
483
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.065
484
CHL004 Cholelithiasis 49 0.065
485
P GRF003 Graft-Versus-Host Disease 72 0.065
486
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.064
487
TXC002 Toxic Encephalopathy 53 0.064
488
P HYP098 Hypereosinophilic Syndrome 67 0.064
489
NTR046 Neutrophil Migration 50 0.064
490
RST023 Resting Heart Rate, Variation in 41 0.064
491
PLP001 Pulpitis 49 0.064
492
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.064
493
P MVM001 Movement Disease 63 0.064
494
RTN020 Retinal Vascular Disease 46 0.064
495
P NSP012 Nasopharyngeal Carcinoma 66 0.064
496
P PLY018 Polycythemia 56 0.064
497
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.064
498
NRT001 Neurotic Disorder 53 0.064
499
P SPP010 Suppressor of Tumorigenicity 3 51 0.064
500
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.064
501
P PMP001 Pemphigus 54 0.064
502
CHL065 Cholangiocarcinoma 68 0.064
503
CNN005 Connective Tissue Disease 68 0.064
504
GNG003 Gingival Recession 44 0.064
505
c PRD040 Periodontitis, Chronic 53 0.063
506
CLC001 Calciphylaxis 51 0.063
507
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.063
508
P SNS001 Sensorineural Hearing Loss 60 0.063
509
c MCR112 Microvascular Complications of Diabetes 2 41 0.063
510
NWB001 Newborn Respiratory Distress Syndrome 58 0.063
511
P SJG008 Sjogren Syndrome 61 0.063
512
PRP080 Peripheral Artery Disease 53 0.063
513
c LKM063 Leukemia, Chronic Myeloid 72 0.063
514
P CRB059 Cerebellar Degeneration 37 0.063
515
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.062
516
HYP457 Hypertrophic Scars 42 0.062
517
BNN003 Bone Inflammation Disease 48 0.062
518
c LKM005 Leukemia, T-Cell, Chronic 34 0.062
519
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.062
520
CRB037 Cerebral Palsy 69 0.062
521
P RTN024 Retinoblastoma 73 0.062
522
c ACT073 Acute Leukemia 58 0.062
523
INT079 Intrahepatic Cholangiocarcinoma 51 0.062
524
THY125 Thyroid Gland Medullary Carcinoma 50 0.062
525
ATS010 Autosomal Recessive Disease 48 0.062
526
c DRR009 Diarrhea 6 46 0.062
527
P MTR003 Mitral Valve Stenosis 50 0.062
528
P ACT105 Acute Mountain Sickness 52 0.061
529
BRK010 Burkitt Lymphoma 67 0.061
530
PRP016 Paraplegia 52 0.061
531
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.061
532
P HYP750 Hypertriglyceridemia, Familial 62 0.061
533
P AMY004 Amyloidosis 70 0.061
534
c SVR001 Severe Acute Respiratory Syndrome 62 0.061
535
TRD006 Tardive Dyskinesia 54 0.061
536
c FML008 Familial Retinoblastoma 53 0.061
537
P MYC008 Myocarditis 59 0.061
538
c XNT010 Xanthinuria, Type I 53 0.061
539
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.061
540
APN008 Apnea, Obstructive Sleep 64 0.061
541
ZLL002 Zollinger-Ellison Syndrome 55 0.061
542
NRN004 Neuroendocrine Tumor 55 0.061
543
VSC002 Vascular Dementia 57 0.060
544
CHR100 Chronic Ulcer of Skin 55 0.060
545
P TMP001 Temporal Lobe Epilepsy 50 0.060
546
c SPN225 Spondyloarthropathy 1 73 0.060
547
CHL067 Cholecystitis 57 0.060
548
KHL003 Kohlschutter-Tonz Syndrome 65 0.060
549
c MST023 Mesothelioma, Malignant 57 0.060
550
P LTH003 Lethal Congenital Contracture Syndrome 40 0.060
551
ANR007 Anorexia Nervosa 63 0.059
552
BRT054 Brittle Bone Disorder 72 0.059
553
P MTR014 Motor Neuron Disease 65 0.059
554
TRG002 Trigeminal Neuralgia 60 0.059
555
TND005 Tendinitis 54 0.059
556
PLG002 Plague 63 0.059
557
VRC005 Varicose Veins 60 0.059
558
EYD002 Eye Disease 58 0.059
559
LNG031 Lung Benign Neoplasm 51 0.059
560
P LKM071 Leukemia, Chronic Lymphocytic 79 0.059
561
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.059
562
ACR007 Acromegaly 71 0.059
563
P SLP005 Sleep Disorder 59 0.059
564
NNL006 Non-Alcoholic Steatohepatitis 54 0.059
565
CRB086 Cerebral Aneurysms 40 0.059
566
c BSL007 Basal Cell Carcinoma 68 0.059
567
HMP009 Haemophilus Influenzae 43 0.058
568
CND006 Candida Glabrata 32 0.058
569
SDD001 Sudden Infant Death Syndrome 61 0.058
570
GNG013 Gingivitis 59 0.058
571
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.058
572
ACT003 Acute Kidney Tubular Necrosis 45 0.058
573
P LPR021 Leprosy 3 69 0.058
574
HNS001 Hansen's Disease 34 0.058
575
HYD002 Hydronephrosis 60 0.058
576
ING001 Inguinal Hernia 60 0.058
577
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.058
578
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.058
579
HYP081 Hypolipoproteinemia 51 0.057
580
MTS001 Mutism 46 0.057
582
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.057
583
P HRD086 Hereditary Hypophosphatemic Rickets 40 0.057
584
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.057
585
P OPT006 Optic Nerve Disease 60 0.057
586
CRT015 Carotid Artery Occlusion 45 0.057
587
P VSC011 Vasculitis 62 0.057
588
c PNC108 Pancreatitis, Hereditary 70 0.057
589
P CMP008 Compartment Syndrome 49 0.056
590
HRN029 Hearing Loss, Noise-Induced 37 0.056
591
DBT010 Diabetic Neuropathy 54 0.056
592
P RTN018 Retinal Disease 53 0.056
593
SPN051 Spondylitis 51 0.056
594
c ECT041 Ectodermal Dysplasia-Syndactyly Syndrome 2 35 0.056
595
P THY032 Thyroiditis 52 0.056
596
c BPL002 Bipolar I Disorder 49 0.056
597
ARG004 Argyria 27 0.056
598
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.056
599
P DRM010 Dermatomyositis 61 0.056
600
GSG001 Gas Gangrene 53 0.056
601
MST005 Mastitis 53 0.055
602
IDP070 Idiopathic Scoliosis 42 0.055
603
INT002 Intermittent Claudication 61 0.055
604
DPH001 Diphtheria 60 0.055
605
WLL004 Wallerian Degeneration 39 0.055
606
INF009 Inflammatory Spondylopathy 31 0.055
607
SKN019 Skin Melanoma 68 0.055
608
TRN018 Transitional Cell Carcinoma 56 0.055
609
RSP007 Respiratory Distress Syndrome, Infant 30 0.055
610
CVD001 Covid-19 44 0.055
611
ENT011 Enterocolitis 51 0.055
612
GST040 Gastric Adenocarcinoma 70 0.055
613
c JVN010 Juvenile Rheumatoid Arthritis 64 0.055
614
BCK006 Back Pain 42 0.055
615
EMB004 Embryonal Carcinoma 56 0.055
616
CRT013 Carotid Stenosis 50 0.055
617
c HPT016 Hepatitis B 59 0.054
618
P MYS005 Myositis 56 0.054
619
c ART101 Aortic Valve Disease 2 65 0.054
620
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.054
621
BRN056 Bronchopulmonary Dysplasia 57 0.054
622
DMP001 Dumping Syndrome 44 0.054
623
P RNL015 Renal Hypertension 47 0.054
624
P TBR001 Tuberous Sclerosis 70 0.054
625
P RHB003 Rhabdomyosarcoma 63 0.054
626
P CYS018 Cystitis 59 0.054
627
OVR094 Ovarian Epithelial Cancer 38 0.054
628
c SVR005 Severe Pre-Eclampsia 50 0.053
629
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.053
630
KRT009 Keratosis 51 0.053
631
P CLC063 Celiac Disease 1 66 0.053
632
CRN019 Coronary Artery Vasospasm 46 0.053
633
OST004 Osteitis Fibrosa 41 0.053
634
P CLS010 Cluster Headache 42 0.053
635
ANP008 Anaplastic Oligoastrocytoma 30 0.053
636
P THY023 Thymoma 65 0.053
637
c THY107 Thymoma, Familial 52 0.053
638
PSY004 Psychotic Disorder 67 0.052
639
PST028 Post-Traumatic Stress Disorder 58 0.052
640
P VNS003 Venous Insufficiency 55 0.052
641
c HMC039 Hemochromatosis, Type 1 74 0.052
642
P BRT004 Bartter Disease 52 0.052
643
RSC001 Rosacea 54 0.052
644
c DBT099 Diabetes Mellitus, Type I 65 0.052
645
PRS045 Prostatic Hypertrophy 53 0.052
646
OBS002 Obsessive-Compulsive Disorder 68 0.052
647
c VRL010 Viral Hepatitis 52 0.052
648
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.052
649
RDN001 Reading Disorder 40 0.052
650
LKP003 Leukoplakia 39 0.052
651
OST016 Osteochondrosis 53 0.052
652
P MLG074 Malignant Mesenchymoma 40 0.052
653
c HPT073 Hepatitis C Virus 72 0.052
654
P ESP024 Esophagitis 62 0.052
655
P MYP006 Myopia 55 0.052
656
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.052
657
CNT097 Central Hypoventilation Syndrome, Congenital 71 0.051
658
HRT011 Heart Septal Defect 50 0.051
659
SPL018 Splenomegaly 48 0.051
660
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.051
661
P FBR031 Febrile Seizures 53 0.051
662
P ATX030 Ataxia-Telangiectasia 82 0.051
663
BNG077 Benign Idiopathic Neonatal Seizures 26 0.051
664
P NRV007 Nervous System Disease 66 0.051
665
P SML001 Small Cell Carcinoma 52 0.051
666
PLS009 Plasma Cell Neoplasm 51 0.051
667
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.051
668
PRS021 Prostatic Adenoma 51 0.051
669
HYP080 Hypogonadism 50 0.051
670
SYS003 Systolic Heart Failure 49 0.051
671
PRS129 Prostatic Hyperplasia, Benign 49 0.051
672
P HYP265 Hypotonia 43 0.051
673
P HPT021 Hepatitis 67 0.051
674
THY122 Thyroid Gland Cancer 57 0.051
675
DYS015 Dysentery 52 0.051
676
P BRB001 Beriberi 46 0.051
677
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.051
678
PRP030 Purpura 54 0.051
679
DNT001 Dental Fluorosis 43 0.051
680
P PRC031 Preeclampsia/eclampsia 1 38 0.051
681
P BRG001 Brugada Syndrome 71 0.050
682
CHD004 Chudley-Mccullough Syndrome 46 0.050
683
P ADL017 Adult T-Cell Leukemia 56 0.050
684
GST033 Gestational Diabetes 61 0.050
685
AMN001 Amenorrhea 54 0.050
686
PLS025 Plasmablastic Lymphoma 47 0.050
687
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.050
688
P MCH002 Machado-Joseph Disease 62 0.049
689
CTN007 Cutaneous Leishmaniasis 62 0.049
690
DSS009 Disseminated Intravascular Coagulation 57 0.049
691
KRT002 Keratomalacia 47 0.049
692
ATN005 Autonomic Dysfunction 46 0.049
693
TRP009 Triple X Syndrome 42 0.049
694
CHR178 Chromosomal Triplication 35 0.049
695
P APL001 Aplastic Anemia 74 0.049
696
SLC006 Silicosis 56 0.049
697
VCC001 Vaccinia 49 0.049
698
P OBS001 Obstructive Jaundice 50 0.049
699
CYN003 Cyanide Poisoning 24 0.049
700
P DNG005 Dengue Virus 59 0.049
701
HLC007 Helicobacter Pylori Infection 59 0.049
702
P SCK002 Sick Sinus Syndrome 55 0.049
703
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.049
704
PRN032 Paraneoplastic Cerebellar Degeneration 28 0.049
705
VLK001 Volkmann Contracture 25 0.049
706
c FML021 Familial Hypercholesterolemia 66 0.049
707
MYT011 Myotonia 34 0.049
708
P FLL037 Follicular Lymphoma 67 0.048
709
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.048
710
PSR001 Psoriatic Arthritis 61 0.048
711
VRL011 Viral Infectious Disease 61 0.048
712
RNL077 Renal Fibrosis 47 0.048
713
P TRC031 Trichorhinophalangeal Syndrome 40 0.048
714
P BNC003 Bone Cancer 58 0.048
715
BRD001 Brody Myopathy 57 0.048
716
PPL049 Papillon-Lefevre Syndrome 65 0.048
717
BHR001 Behr Syndrome 51 0.048
719
PCD001 Pica Disease 41 0.048
720
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.048
721
ETH012 Ethylene Glycol Poisoning 26 0.048
722
ACH005 Achalasia 51 0.048
723
CHR074 Choriocarcinoma 47 0.048
724
P CHL066 Cholangitis 51 0.048
725
CYN002 Cyanosis, Transient Neonatal 45 0.048
726
DSS008 Disease of Mental Health 58 0.048
727
ACT058 Active Peptic Ulcer Disease 55 0.048
728
PPT001 Peptic Esophagitis 52 0.048
729
FCT007 Factor Vii Deficiency 67 0.048
730
SNS003 Sensory Peripheral Neuropathy 54 0.048
731
P PLY041 Polymyositis 57 0.047
732
c INH020 Inherited Metabolic Disorder 47 0.047
733
ADG002 Audiogenic Seizures 25 0.047
734
RTN017 Retinal Detachment 61 0.047
735
MYL005 Myelofibrosis 70 0.047
736
P NRF002 Neurofibromatosis 56 0.047
737
P TRT010 Teratoma 52 0.047
738
PRS063 Paresthesia 41 0.047
739
P URT039 Urticaria 58 0.047
740
P MNC007 Monocytic Leukemia 53 0.047
741
P INT068 Intestinal Disease 53 0.047
742
DGN001 Degenerative Disc Disease 48 0.047
743
c HYP798 Hypophosphatemic Rickets, X-Linked Recessive 60 0.047
744
GST030 Gastrinoma 45 0.047
745
P UVT001 Uveitis 57 0.047
746
SXL003 Sexual Disorder 47 0.047
747
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.047
748
MYL009 Myelodysplastic Syndrome 70 0.046
749
P FRN006 Frontotemporal Dementia 68 0.046
750
c JVN061 Juvenile Arthritis 60 0.046
751
DMY004 Demyelinating Disease 52 0.046
752
c EXD008 Exudative Vitreoretinopathy 1 71 0.046
753
P VNT002 Ventricular Septal Defect 60 0.046
754
CLF001 Cleft Lip 53 0.046
755
VTM002 Vitamin B12 Deficiency 48 0.046
756
P ART005 Arteriovenous Malformation 65 0.046
757
c HPT001 Hepatitis C 62 0.046
758
P MTC069 Mitochondrial Disorders 56 0.046
759
DFF005 Diffuse Large B-Cell Lymphoma 55 0.046
760
P MNN013 Meningitis 66 0.046
761
TYP007 Typhoid Fever 63 0.046
762
P TCD001 Tic Disorder 53 0.046
763
ACT084 Acute Stress Disorder 47 0.046
764
MNT001 Mantle Cell Lymphoma 69 0.046
765
URN010 Urinary Tract Obstruction 55 0.046
766
P HMP007 Hemophilia 51 0.046
767
P FNC004 Fanconi Syndrome 50 0.046
768
CCN002 Cocaine Abuse 49 0.046
769
KRT008 Keratopathy 47 0.046
770
URT010 Ureteral Obstruction 45 0.046
771
P FNC034 Fanconi Renotubular Syndrome 2 40 0.046
772
MCN001 Mucinous Adenocarcinoma 49 0.046
773
APP009 Appendix Adenocarcinoma 44 0.046
774
c ACT135 Acute Graft Versus Host Disease 52 0.046
775
PLC008 Placenta Disease 50 0.046
776
P CHL002 Childhood Absence Epilepsy 61 0.045
777
P PRN023 Prion Disease 57 0.045
778
NWC001 Newcastle Disease 45 0.045
779
P INF038 Influenza 68 0.045
780
ETN001 Eating Disorder 60 0.045
781
PHS001 Phosphorus Metabolism Disease 40 0.045
782
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.045
783
P SYP003 Syphilis 58 0.045
784
c VSC019 Vesicoureteral Reflux 1 57 0.045
785
OST115 Osteonecrosis of the Jaw 40 0.045
786
SPP011 Suppression of Tumorigenicity 12 59 0.045
787
HYP020 Hyperprolactinemia 64 0.044
788
MLD001 Melioidosis 68 0.044
789
P PRC012 Pericardial Effusion 51 0.044
790
HMP001 Hemopericardium 48 0.044
791
P BRN022 Bronchiectasis 59 0.044
792
AGR002 Agoraphobia 45 0.044
793
c HPT003 Hepatitis a 62 0.044
794
HRY003 Hairy Cell Leukemia 55 0.044
795
LMY002 Leiomyoma 52 0.044
796
KRT013 Keratolytic Winter Erythema 46 0.044
797
MXD026 Mixed Glioma 45 0.044
798
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.044
799
P CHR012 Chronic Granulomatous Disease 67 0.044
800
SCH012 Schizoaffective Disorder 50 0.044
801
BRN002 Bronchiolitis 59 0.044
802
c RNG015 Ring Chromosome 2 26 0.044
803
HRT012 Heart Valve Disease 53 0.044
804
RYN001 Raynaud Disease 48 0.044
805
MDL009 Medullary Sponge Kidney 40 0.044
806
P MYC084 Mycobacterium Tuberculosis 1 68 0.044
807
RDC002 Radiculopathy 50 0.044
808
c FLL041 Follicular Lymphoma 1 49 0.044
809
BNG018 Benign Paroxysmal Positional Nystagmus 37 0.044
810
OTT002 Otitis Media 72 0.043
811
P OCL013 Oculodentodigital Dysplasia 69 0.043
812
P END033 Endocarditis 57 0.043
813
P ASP006 Aspergillosis 69 0.043
814
P PSD087 Pseudoxanthoma Elasticum 65 0.043
815
FDL002 Food Allergy 51 0.043
816
CYS014 Cystadenocarcinoma 51 0.043
817
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.043
818
c ATM011 Autoimmune Hepatitis 63 0.043
819
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.043
820
HYP815 Hyperuricemia, Pulmonary Hypertension, Renal Failure, and Alkalosis Syndrome 53 0.043
821
c FML035 Familial Hyperlipidemia 55 0.043
822
FRZ001 Frozen Shoulder 53 0.043
823
LWC001 Low Compliance Bladder 43 0.043
824
SNG003 Single Ventricular Heart 30 0.043
825
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.043
826
P GLY013 Glycogen Storage Disease 60 0.043
827
CHL123 Chlamydia 59 0.043
828
LYM027 Lymphopenia 58 0.043
829
QDR001 Quadriplegia 48 0.043
830
PYR009 Pyridoxine Deficiency Anemia 34 0.043
831
c CHR064 Chronic Monocytic Leukemia 33 0.043
832
MST020 Mast Cell Activation Syndrome 26 0.043
833
P FML011 Familial Adenomatous Polyposis 72 0.042
834
c PLY162 Polyposis Syndrome, Hereditary Mixed, 1 63 0.042
835
CYS013 Cystinuria 63 0.042
836
IRN001 Iron Deficiency Anemia 59 0.042
837
CNT033 Central Nervous System Cancer 47 0.042
838
TRT001 Teratocarcinoma 45 0.042
839
MNR003 Mineral Metabolism Disease 39 0.042
840
P DNT007 Dentin Sensitivity 36 0.042
841
P AGN002 Agnosia 55 0.042
842
APR001 Apraxia 52 0.042
843
KRT019 Keratitis, Hereditary 65 0.042
844
ERY003 Erythema Multiforme 58 0.042
845
c BCT007 Bacterial Meningitis 55 0.042
846
HMP005 Hemiplegia 55 0.042
847
NRT004 Neuritis 52 0.042
848
RTN003 Retinal Ischemia 50 0.042
849
ECT026 Ectopic Pregnancy 50 0.042
850
HYP006 Hypertensive Heart Disease 49 0.042
851
c BTT014 Beta-Thalassemia 74 0.042
852
P GCH001 Gaucher's Disease 63 0.042
853
BLL006 Bullous Pemphigoid 62 0.042
854
PRN019 Perinatal Necrotizing Enterocolitis 59 0.042
855
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.042
856
ANR004 Anuria 46 0.041
857
P SYR003 Syringoma 37 0.041
858
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.041
859
LFT001 Left Bundle Branch Hemiblock 49 0.041
860
HVY002 Heavy Metal Poisoning 22 0.041
861
KPS004 Kaposi Sarcoma 75 0.041
862
MLT157 Multiple System Atrophy 1 70 0.041
863
c SPN301 Spinocerebellar Ataxia 2 58 0.041
864
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.041
865
SPN020 Spondylosis 46 0.041
866
EXS001 Exostosis 46 0.041
867
P MYC033 Myoclonus 46 0.041
868
CHL056 Cheilitis 48 0.041
869
ORL012 Oral Leukoplakia 39 0.041
870
P PRS038 Personality Disorder 65 0.041
871
ALL010 Allergic Contact Dermatitis 56 0.041
872
MDD018 Middle East Respiratory Syndrome 43 0.041
873
FNT004 Fainting 30 0.041
874
MYC006 Mycosis Fungoides 66 0.041
875
GST037 Gastroparesis 54 0.041
876
c MLG079 Malignant Pleural Mesothelioma 42 0.041
877
P DNT020 Dent Disease 1 62 0.041
878
SPT004 Septic Arthritis 58 0.041
879
SPS057 Spasticity 45 0.041
880
P SCL057 Scoliosis, Isolated 1 41 0.041
881
ENM001 Enamel Caries 28 0.041
882
NRF007 Neurofibroma 64 0.041
883
ANG005 Anogenital Venereal Wart 55 0.041
884
STT002 Status Asthmaticus 50 0.041
885
VRR004 Verrucous Carcinoma 49 0.041
886
c GCH015 Gaucher Disease, Type I 70 0.041
887
AZS001 Azoospermia 50 0.041
888
c PLY105 Polycystic Ovary Syndrome 1 38 0.041
889
SVR097 Severe Cutaneous Adverse Reaction 69 0.041
890
DCT002 Ductal Carcinoma in Situ 59 0.041
891
AVN001 Avian Influenza 59 0.041
892
SRC027 Sarcoma, Synovial 58 0.041
893
SPS003 Spastic Diplegia 51 0.041
894
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.041
895
PLY100 Polyploidy 40 0.041
896
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.041
897
ERY066 Erythema Multiforme Major 30 0.041
898
P RTT002 Rett Syndrome 80 0.040
899
MYL031 Myeloproliferative Neoplasm 66 0.040
900
c ALP101 Alpha-Thalassemia 62 0.040
901
P NMN002 Niemann-Pick Disease 59 0.040
902
P FCL005 Focal Segmental Glomerulosclerosis 57 0.040
903
P PTS002 Ptosis 53 0.040
904
SPN019 Spondylolisthesis 51 0.040
905
RTC005 Reticulosarcoma 47 0.040
906
BNM001 Bone Marrow Cancer 43 0.040
907
AMN006 Aminoaciduria 38 0.040
908
HML018 Homologous Wasting Disease 22 0.040
909
GNR004 Generalized Anxiety Disorder 56 0.040
910
MRG003 Marginal Zone B-Cell Lymphoma 52 0.040
911
HYP781 Hypoascorbemia 51 0.040
912
P OTS001 Otosclerosis 49 0.040
913
TTH007 Tooth Erosion 31 0.040
914
P EPL140 Epilepsy, Idiopathic Generalized 62 0.040
915
WLL001 Williams-Beuren Syndrome 60 0.040
916
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.040
917
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.040
918
P MGR003 Migraine with Aura 52 0.040
919
BRS064 Bursitis 48 0.040
920
DST006 Diastolic Heart Failure 45 0.040
921
APH002 Aphasia 57 0.040
922
AKN002 Akinetic Mutism 37 0.040
923
c HYP260 Hypophosphatemic Rickets, Autosomal Dominant 60 0.039
924
P OLG002 Oligodendroglioma 67 0.039
925
SPN050 Spinocerebellar Degeneration 42 0.039
926
ACN002 Acanthosis Nigricans 60 0.039
927
P LCH002 Lichen Planus 53 0.039
928
P THR015 Thrombophilia 51 0.039
929
CHP002 Chops Syndrome 44 0.039
930
MCR011 Microinvasive Gastric Cancer 43 0.039
931
FBR047 Fibromyalgia 58 0.039
932
P SHR001 Short Bowel Syndrome 53 0.039
933
GST020 Gastric Antral Vascular Ectasia 41 0.039
934
HYP540 Hypertension, Diastolic 40 0.039
935
c NMN015 Niemann-Pick Disease, Type C1 68 0.039
936
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.039
937
MYM001 Myoma 54 0.039
938
CNT017 Central Nervous System Origin Vertigo 45 0.039
939
c ACT004 Acute Diarrhea 39 0.039
940
HYP264 Hypertonia 38 0.039
941
P CHR285 Chronic Myelomonocytic Leukemia 60 0.038
942
INT051 Intussusception 53 0.038
943
c INF145 Infantile Liver Failure Syndrome 1 50 0.038
944
NRN001 Neuroendocrine Carcinoma 47 0.038
945
TST014 Testicular Cancer 46 0.038
946
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.038
947
GRM010 Germ Cells Tumors 34 0.038
948
HDG004 Hodgkin's Granuloma 23 0.038
949
HDG006 Hodgkin's Paragranuloma 22 0.038
950
P MDL005 Medulloblastoma 77 0.038
951
ERL001 Early Myoclonic Encephalopathy 62 0.038
952
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.038
953
P MTR012 Mitral Valve Disease 58 0.038
954
PRS047 Prostatitis 56 0.038
955
FCL014 Focal Epilepsy 54 0.038
956
SNT005 Sinoatrial Node Disease 49 0.038
957
ASP026 Asplenia, Isolated Congenital 44 0.038
958
CYT018 Cytochrome P450 2d6 Variant 27 0.038
959
SPR126 Superior Semicircular Canal Dehiscence 40 0.038
960
c INF071 Inflammatory Bowel Disease 1 67 0.038
961
CRP001 Carpal Tunnel Syndrome 67 0.038
962
P GLL018 Gallbladder Cancer 57 0.038
963
INT067 Interstitial Nephritis 48 0.038
964
GRW007 Growth Hormone Deficiency 46 0.038
965
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.037
966
P CNJ013 Conjunctivitis 65 0.037
967
P PRP029 Porphyria 62 0.037
968
P PTN014 Patent Ductus Arteriosus 1 60 0.037
969
P ART153 Arthrochalasia Ehlers-Danlos Syndrome 55 0.037
970
BNG036 Bone Giant Cell Tumor 49 0.037
971
P EPN001 Ependymoblastoma 44 0.037
972
c PRG020 Paragangliomas 3 39 0.037
973
WLS001 Wilson Disease 71 0.037
974
P SPN046 Spinal Muscular Atrophy 62 0.037
975
PNM010 Pneumothorax, Primary Spontaneous 60 0.037
976
P ALP009 Alopecia Areata 60 0.037
977
P HMR003 Hemorrhagic Disease 53 0.037
978
MCN017 Meconium Ileus 52 0.037
979
ASP007 Aspiration Pneumonia 48 0.037
980
DBT006 Diabetic Macular Edema 48 0.037
981
RTR001 Retrograde Amnesia 44 0.037
982
MYX004 Myxedema 43 0.037
983
PCK003 Pick Disease of Brain 68 0.037
984
ACR006 Aceruloplasminemia 65 0.037
985
CLF027 Cleft Palate, Isolated 64 0.037
986
c PRM092 Primary Lateral Sclerosis, Adult, 1 53 0.037
987
AVD001 Avoidant Personality Disorder 51 0.037
988
PLR007 Pleural Empyema 50 0.037
989
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.037
990
CNN003 Conn's Syndrome 79 0.037
991
ACR008 Acrocallosal Syndrome 69 0.037
992
P MCR010 Microcephaly 59 0.037
993
P GLL022 Guillain-Barre Syndrome 59 0.037
994
INC002 Inclusion Body Myositis 58 0.037
995
P GLL020 Gallbladder Disease 57 0.037
996
CMR002 Coumarin Resistance 56 0.037
997
P SBS003 Substance Abuse 55 0.037
998
P SLM003 Salmonellosis 55 0.037
999
CRH005 Crohn's Colitis 53 0.037
1000
LYS002 Lysosomal Storage Disease 52 0.037
1001
HYP043 Hyperandrogenism 48 0.037
1002
PRD004 Prediabetes Syndrome 47 0.037
1003
NDL007 Nodular Goiter 47 0.037
1004
ATN004 Autonomic Neuropathy 45 0.037
1005
P AVS003 Avascular Necrosis 42 0.037
1006
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.037
1007
c CHR098 Chronic Pyelonephritis 38 0.037
1008
PMP006 Pemphigus Vulgaris, Familial 57 0.037
1009
PRN039 Paraneoplastic Syndromes 38 0.037
1010
GST019 Gastrointestinal Stromal Tumor 78 0.037
1011
PLY001 Polycythemia Vera 69 0.037
1012
APP008 Appendicitis 61 0.037
1013
P LRY044 Larynx Cancer 55 0.037
1014
VGN023 Vaginitis 54 0.037
1015
c BCT013 Bacterial Pneumonia 48 0.037
1016
ENT001 Enterocele 39 0.037
1017
VSM001 Vasomotor Rhinitis 38 0.037
1018
TRC005 Tracheal Stenosis 38 0.037
1019
STN013 Stenotrophomonas Maltophilia Infection 25 0.037
1020
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.037
1021
P CNT116 Contractures, Pterygia, and Spondylocarpotarsal Fusion Syndrome 1a 54 0.036
1022
RHM028 Rheumatic Heart Disease 53 0.036
1023
FNG017 Fungal Infectious Disease 53 0.036
1024
P RTN022 Retinal Vein Occlusion 53 0.036
1025
CRT016 Carotid Artery Disease 52 0.036
1026
ESP002 Esophageal Varix 51 0.036
1027
NRM004 Neuroma 51 0.036
1028
HMG002 Hemoglobinuria 50 0.036
1029
IRR003 Irritant Dermatitis 49 0.036
1030
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.036
1031
DRR014 Darier-White Disease 60 0.036
1032
MTH009 Mouth Disease 56 0.036
1033
INT030 Intracranial Aneurysm 56 0.036
1034
VSC003 Visceral Leishmaniasis 55 0.036
1035
RYS001 Reye Syndrome 51 0.036
1036
PST021 Postpartum Depression 50 0.036
1037
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.036
1038
CNC014 Cancer-Associated Retinopathy 34 0.036
1039
CBP002 Cebpe-Associated Autoinflammation-Immunodeficiency-Neutrophil Dysfunction Syndrome 20 0.036
1040
c HMP004 Hemophilia B 68 0.035
1041
P BLD062 Bile Duct Cancer 67 0.035
1042
RHM001 Rheumatic Fever 60 0.035
1043
PRT058 Pure Autonomic Failure 59 0.035
1044
NNT012 Neonatal Jaundice 53 0.035
1045
PLM017 Pulmonary Alveolar Microlithiasis 50 0.035
1046
GST049 Gastrointestinal System Cancer 49 0.035
1047
MLK006 Milk Allergy 48 0.035
1048
GST071 Gastrointestinal Carcinoma 47 0.035
1049
ASP004 Asphyxia Neonatorum 46 0.035
1051
GLM044 Glomerular Disease 37 0.035
1052
P LPS002 Liposarcoma 65 0.035
1053
DFF036 Differentiated Thyroid Carcinoma 52 0.035
1054
PSD088 Pseudobulbar Affect 36 0.035
1055
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.035
1056
P ATR010 Atrial Heart Septal Defect 60 0.035
1057
P FBR003 Fibrous Histiocytoma 44 0.035
1058
c HMG029 Hemoglobin Se Disease 39 0.035
1059
ERY023 Erythroplakia 24 0.035
1060
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.035
1061
c LKM070 Leukemia, Acute Monocytic 57 0.035
1062
AYM001 Ayme-Gripp Syndrome 57 0.035
1063
HMG005 Hemoglobinopathy 56 0.035
1064
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.035
1065
P CRB088 Cerebral Atrophy 37 0.035
1066
INF118 Inflammatory Myopathy with Abundant Macrophages 28 0.035
1067
BRC012 Brucellosis 64 0.035
1068
c MLG084 Malignant Fibrous Histiocytoma 63 0.035
1069
P HMC002 Homocystinuria 53 0.035
1070
BRN032 Brain Glioma 45 0.035
1071
P ECT005 Ectropion 42 0.035
1072
P RRT020 Rare Tumor 41 0.035
1073