Search results for sodium fluoride

973 hits were found for sodium fluoride

# Family MCID Name MIFTS Score
1
DNT012 Dental Caries 53 0.825
2
DNT001 Dental Fluorosis 43 0.447
3
P OST002 Osteoporosis 74 0.402
4
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.397
5
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.397
6
ALL026 Allergic Hypersensitivity Disease 62 0.340
7
c HYP595 Hypertension, Essential 84 0.309
8
GNG013 Gingivitis 59 0.301
9
P KDN018 Kidney Disease 72 0.300
10
CLT003 Colitis 62 0.266
11
HYP005 Hypokalemia 55 0.260
12
48X005 48,xyyy 39 0.255
13
HRW001 Hair Whorl 36 0.236
14
c CHR684 Chronic Kidney Disease 70 0.229
15
RTC003 Root Caries 33 0.220
16
BNR002 Bone Resorption Disease 48 0.207
17
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.202
18
ENM002 Enamel Erosion 26 0.200
19
CNG034 Congestive Heart Failure 69 0.195
20
P HRT032 Heart Disease 75 0.192
21
ENM001 Enamel Caries 28 0.190
22
OST012 Osteoarthritis 78 0.187
23
P BND020 Bone Disease 59 0.186
24
ADL002 Adult Syndrome 70 0.185
25
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.184
26
P NRB001 Neuroblastoma 72 0.182
27
CHL079 Children's Interstitial Lung Disease 26 0.178
28
MTB004 Metabolic Acidosis 50 0.178
29
PRT037 Pertussis 65 0.176
30
ULC004 Ulcerative Colitis 73 0.175
31
P INF037 Inflammatory Bowel Disease 54 0.175
32
LVR012 Liver Cirrhosis 62 0.172
33
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.170
34
P DNT007 Dentin Sensitivity 36 0.169
35
OST159 Osteogenic Sarcoma 66 0.168
36
P PRD008 Periodontitis 64 0.167
37
HYP066 Hyperglycemia 61 0.167
38
P HYP086 Hypothyroidism 69 0.166
39
END086 End Stage Renal Disease 51 0.161
40
DRM006 Dermatitis 61 0.160
41
c ACT071 Acute Kidney Failure 60 0.158
42
ISC004 Ischemia 58 0.154
43
P DRR001 Diarrhea 55 0.154
44
c RHB024 Rhabdomyosarcoma 2 67 0.154
45
PNG002 Pain Agnosia 51 0.153
46
P SZR006 Seizure Disorder 56 0.152
47
HYP056 Hypoglycemia 66 0.151
48
P TRN020 Turner Syndrome 67 0.149
49
P CRD119 Cardiac Arrest 67 0.149
50
GLS018 Glass Syndrome 57 0.148
51
AST005 Asthma 76 0.145
52
THY029 Thyroid Carcinoma 59 0.145
53
CYS001 Cystic Fibrosis 81 0.144
54
CHL014 Cholera 59 0.144
55
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.141
56
ATX019 Ataxia with Vitamin E Deficiency 42 0.141
57
P NRP001 Neuropathy 56 0.140
58
c MGR028 Migraine with or Without Aura 1 67 0.138
59
P ADN016 Adenocarcinoma 64 0.137
60
VSL002 Visual Epilepsy 59 0.136
61
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.136
62
P MYC007 Myocardial Infarction 70 0.134
63
DWN001 Down Syndrome 70 0.133
64
P EPL164 Epilepsy 71 0.133
65
P DBT009 Diabetes Mellitus 64 0.131
66
P CHR345 Chronic Pain 44 0.131
67
c PNS012 Paine Syndrome 61 0.130
68
P VSC007 Vascular Disease 63 0.130
69
P CLR023 Colorectal Cancer 99 0.129
70
P PRS040 Prostate Cancer 97 0.128
71
ATH013 Atherosclerosis Susceptibility 65 0.128
72
P OTS001 Otosclerosis 49 0.128
73
HLX001 Helix Syndrome 47 0.127
74
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.126
75
P GLM045 Glioma 63 0.126
76
GLL048 Glial Tumor 45 0.126
77
NTR005 Nutritional Deficiency Disease 62 0.124
78
DFC004 Deficiency Anemia 70 0.124
79
LPP008 Lipoprotein Quantitative Trait Locus 62 0.123
80
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.122
81
P LVR013 Liver Disease 68 0.121
82
PLM010 Pulmonary Edema 54 0.121
83
MYL069 Myeloma, Multiple 85 0.121
84
P CTR002 Cataract 60 0.120
85
P CRD246 Cardiovascular System Disease 57 0.120
86
STR067 Stroke, Ischemic 81 0.119
87
c HYP836 Hypercholesterolemia, Familial, 1 73 0.119
88
HYP266 Hypoxia 57 0.119
89
RCK004 Rickets 68 0.118
90
P CRN300 Coronary Heart Disease 1 63 0.118
91
CNT047 Contact Dermatitis 58 0.118
92
THR024 Thrombosis 57 0.117
93
P HYP069 Hyperparathyroidism 63 0.117
94
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.117
95
HMN044 Human Immunodeficiency Virus Type 1 71 0.117
96
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.117
97
47X002 47,xyy 49 0.117
98
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.116
99
CRB039 Cerebrovascular Disease 67 0.116
100
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.116
101
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.116
102
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.115
103
OST011 Osteomalacia 52 0.115
104
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.115
105
ACQ007 Acquired Immunodeficiency Syndrome 60 0.114
106
DNT010 Dentin Caries 32 0.114
107
P NPH012 Nephrotic Syndrome 60 0.114
108
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.114
109
BCT022 Bacterial Infectious Disease 56 0.113
110
c PRS136 Prostate Cancer, Hereditary, 6 33 0.113
111
c PRS130 Prostate Cancer, Hereditary, 8 32 0.113
112
c THR092 Thrombophilia Due to Thrombin Defect 73 0.113
113
CYT002 Cytokine Deficiency 42 0.112
114
ART140 Arteries, Anomalies of 52 0.112
115
CNS004 Constipation 58 0.111
116
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.111
117
P LNG028 Long Qt Syndrome 66 0.111
118
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.111
119
P ENC018 Encephalopathy 61 0.111
120
NPH009 Nephrolithiasis 55 0.110
121
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.110
122
P RHN004 Rhinitis 57 0.110
123
GTR002 Goiter 53 0.110
124
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.110
125
P BRS047 Breast Cancer 97 0.109
126
P RSP003 Respiratory Failure 74 0.109
127
RTR008 Root Resorption 45 0.109
128
GNG003 Gingival Recession 44 0.109
129
STM007 Stomatitis 50 0.108
130
OCL069 Ocular Motor Apraxia 51 0.108
131
P DBT005 Diabetes Insipidus 55 0.108
132
c ACT075 Acute Myocardial Infarction 57 0.107
133
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.106
134
P LKM002 Leukemia 68 0.105
136
GLB015 Glioblastoma Multiforme 75 0.105
137
IRN002 Iron Metabolism Disease 57 0.104
138
LNG099 Lung Disease 60 0.104
139
ATM095 Autoimmune Disease 62 0.104
140
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.104
141
MCS002 Mucositis 56 0.103
142
P BLD134 Bladder Cancer 79 0.103
143
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.103
144
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.102
145
P HPT023 Hepatocellular Carcinoma 100 0.102
146
HYP025 Hyperphosphatemia 48 0.102
147
ADN018 Adenoma 59 0.102
148
P BCL017 B-Cell Lymphoma 58 0.101
149
P THR014 Thrombocytopenia 67 0.101
150
URM002 Uremia 49 0.100
151
ALL003 Allergic Rhinitis 67 0.100
152
P LNG032 Lung Cancer 98 0.099
153
P NTR004 Neutropenia 63 0.099
154
P ART022 Arthritis 69 0.099
155
ANG054 Angina Pectoris 66 0.098
156
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.098
157
ARG004 Argyria 27 0.098
158
P SLP006 Sleep Apnea 69 0.097
159
P RHM011 Rheumatoid Arthritis 80 0.097
160
P GST044 Gastritis 56 0.097
161
P CYS018 Cystitis 59 0.097
162
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.096
163
P LYM118 Lymphoma 68 0.096
164
MMM001 Mammary Paget's Disease 53 0.096
165
c ACT068 Acute Cystitis 63 0.095
166
CLC006 Calcinosis 48 0.095
167
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.095
168
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.095
169
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.095
170
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.095
171
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.095
172
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.095
173
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.095
174
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.095
175
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.095
176
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.095
177
P GST053 Gastric Cancer 83 0.095
178
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.094
179
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.094
180
IMM167 Immune Deficiency Disease 78 0.093
181
P PNM007 Pneumonia 68 0.093
182
c DBT099 Diabetes Mellitus, Type I 65 0.093
183
P ALZ034 Alzheimer Disease 88 0.093
184
EYD002 Eye Disease 58 0.092
185
P MCR115 Microvascular Complications of Diabetes 5 66 0.092
186
P LCT001 Lactic Acidosis 51 0.092
187
URL001 Urolithiasis 45 0.091
188
PLM033 Pulmonary Embolism 59 0.091
189
CHL068 Cholestasis 61 0.090
190
SPN186 Spinal Cord Injury 60 0.090
191
BRN004 Brain Edema 56 0.090
192
c SYS001 Systemic Lupus Erythematosus 86 0.089
193
CRD132 Cardiac Conduction Defect 58 0.089
194
DPR016 Depression 63 0.089
195
ANX010 Anxiety 73 0.089
196
INS024 Insulin-Like Growth Factor I 79 0.089
197
P TRM003 Tremor 54 0.088
198
BRN071 Brain Injury 49 0.088
199
BCK006 Back Pain 42 0.088
200
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.088
201
TRM010 Traumatic Brain Injury 51 0.088
202
P ATS364 Autism 70 0.087
203
PST092 Posttransplant Acute Limbic Encephalitis 29 0.087
204
P HYP076 Hyperthyroidism 55 0.087
205
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.087
206
INT007 Intermediate Coronary Syndrome 55 0.086
207
c PRC016 Pre-Eclampsia 63 0.086
208
HYP060 Hyperinsulinism 54 0.086
209
FTT001 Fatty Liver Disease 61 0.086
210
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.085
211
BRT054 Brittle Bone Disorder 72 0.085
212
P ART023 Arthropathy 62 0.085
213
P GLM007 Glomerulonephritis 57 0.085
214
ANR040 Aneurysm 59 0.085
215
c ATR087 Atrial Standstill 1 75 0.085
216
SKN016 Skin Disease 63 0.084
217
LPD008 Lipid Metabolism Disorder 62 0.084
218
P LPS004 Lupus Erythematosus 61 0.084
219
P DRM053 Dermatitis, Atopic 66 0.084
220
PPL052 Papillomatosis, Confluent and Reticulated 33 0.084
221
P MYL006 Myeloid Leukemia 60 0.084
222
LYM019 Lymphosarcoma 46 0.082
223
P SJG008 Sjogren Syndrome 61 0.082
224
HYP017 Hypophosphatemia 50 0.082
225
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.082
226
P ANP001 Anaplastic Large Cell Lymphoma 58 0.082
227
P INT143 Interstitial Cystitis 61 0.082
228
TTH007 Tooth Erosion 31 0.082
229
CRH001 Crohn's Disease 74 0.081
230
MNT002 Mental Depression 58 0.081
231
OST003 Osteonecrosis 61 0.081
232
c MCR129 Microvascular Complications of Diabetes 1 66 0.081
233
P MLT020 Multiple Sclerosis 72 0.080
234
ANX004 Anoxia 40 0.080
235
VRC005 Varicose Veins 60 0.080
236
P CND004 Candidiasis 58 0.080
237
P HRP006 Herpes Simplex 65 0.080
238
NPH003 Nephrocalcinosis 51 0.079
239
P PHC003 Pheochromocytoma 71 0.079
240
ADR040 Adrenal Gland Pheochromocytoma 46 0.079
241
c MLG068 Malignant Glioma 46 0.079
242
OST017 Osteomyelitis 64 0.079
243
GNG011 Gingival Disease 45 0.079
244
P ATR011 Atrial Fibrillation 66 0.079
245
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.078
247
P MYP004 Myopathy 70 0.078
248
P ESP024 Esophagitis 62 0.078
249
c FNC043 Fanconi Anemia, Complementation Group E 62 0.078
250
ANK001 Ankylosis 51 0.078
251
PLP001 Pulpitis 49 0.078
252
c LKM061 Leukemia, Acute Myeloid 84 0.078
253
P SCH015 Schizophrenia 74 0.078
254
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.077
255
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.077
256
AGN016 Aging 56 0.077
257
PRP027 Peripheral Vascular Disease 71 0.077
258
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.077
259
GST020 Gastric Antral Vascular Ectasia 41 0.077
260
MCL006 Macular Retinal Edema 55 0.077
261
SPS057 Spasticity 45 0.077
262
P URT039 Urticaria 58 0.076
263
c NRF023 Neurofibromatosis, Type Ii 80 0.076
264
P HYP750 Hypertriglyceridemia, Familial 62 0.075
265
ALC007 Alcohol Dependence 66 0.074
266
THY030 Thyroid Gland Disease 52 0.074
267
P PSR002 Psoriasis 62 0.073
268
PST011 Pustulosis of Palm and Sole 52 0.073
269
ENT004 Enthesopathy 49 0.073
270
P AMY004 Amyloidosis 70 0.073
271
49X006 49, Xxxxy Syndrome 41 0.073
272
c SPN225 Spondyloarthropathy 1 73 0.073
273
c SCN007 Secondary Hyperparathyroidism 51 0.072
274
P MLG056 Malignant Hyperthermia 67 0.072
275
LYM133 Lymphoma, Hodgkin, Classic 69 0.072
276
P SNS001 Sensorineural Hearing Loss 60 0.072
277
P PLY019 Polyneuropathy 56 0.072
278
P LKM071 Leukemia, Chronic Lymphocytic 79 0.072
279
P MLN008 Melanoma 69 0.072
280
c ART101 Aortic Valve Disease 2 65 0.072
281
DYS073 Dysphagia 50 0.071
282
P OVR042 Ovarian Cancer 88 0.071
283
c PRM038 Primary Agammaglobulinemia 44 0.071
284
ESP021 Esophageal Cancer 90 0.071
285
c DLT002 Dilated Cardiomyopathy 79 0.071
286
P PNC035 Pancreatic Cancer 84 0.070
287
SQM006 Squamous Cell Carcinoma 60 0.070
288
P BNC003 Bone Cancer 58 0.070
289
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.070
290
P RTN016 Retinal Degeneration 53 0.070
291
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.069
292
P DMN002 Dementia 66 0.069
293
KRT002 Keratomalacia 47 0.069
294
PLM001 Pulmonary Tuberculosis 69 0.069
295
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.069
296
SDD001 Sudden Infant Death Syndrome 61 0.069
297
PLS009 Plasma Cell Neoplasm 51 0.069
298
c ATS007 Autism Spectrum Disorder 67 0.069
299
SPN051 Spondylitis 51 0.069
300
INF009 Inflammatory Spondylopathy 31 0.069
301
P LKM062 Leukemia, Acute Lymphoblastic 69 0.068
302
P HYP098 Hypereosinophilic Syndrome 67 0.068
303
OTT002 Otitis Media 72 0.068
304
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.068
305
c SML038 Small Cell Cancer of the Lung 65 0.068
306
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.067
307
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.067
308
P GLM040 Glioma Susceptibility 1 81 0.067
309
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.067
310
SYN007 Synovitis 54 0.067
311
PLC002 Plica Syndrome 36 0.067
312
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.066
313
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.066
314
BRN028 Brain Cancer 74 0.066
315
P MSC005 Muscular Dystrophy 66 0.066
316
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.066
317
SPN035 Spindle Cell Sarcoma 53 0.066
318
IGR001 Ige Responsiveness, Atopic 59 0.066
319
SRC014 Sarcoma 65 0.065
320
HYP081 Hypolipoproteinemia 51 0.065
321
CVD001 Covid-19 44 0.065
322
ALL006 Allergic Asthma 56 0.065
323
P AST007 Astrocytoma 51 0.065
324
c MNN043 Meningioma, Familial 74 0.064
325
MNN042 Meningioma, Radiation-Induced 62 0.064
326
SPN021 Spinal Meningioma 50 0.064
327
SCR001 Secretory Meningioma 41 0.064
328
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.064
329
BRN002 Bronchiolitis 59 0.064
330
P HMN010 Hemangioma 61 0.064
331
P THL005 Thalassemia 60 0.064
332
SCK003 Sickle Cell Anemia 74 0.064
333
P ADL010 Adult Respiratory Distress Syndrome 65 0.064
334
KRT013 Keratolytic Winter Erythema 46 0.064
335
c PRD040 Periodontitis, Chronic 53 0.063
336
MYL009 Myelodysplastic Syndrome 70 0.063
337
BRN024 Bronchitis 68 0.063
338
P TMP001 Temporal Lobe Epilepsy 50 0.063
339
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.063
340
LNG031 Lung Benign Neoplasm 51 0.063
341
SBC016 Subacute Delirium 44 0.063
342
P CNR004 Cone-Rod Dystrophy 2 73 0.062
343
MSL001 Measles 62 0.062
344
c FML035 Familial Hyperlipidemia 55 0.062
345
ART016 Aortic Aneurysm 69 0.062
346
NNL006 Non-Alcoholic Steatohepatitis 54 0.062
347
SYN036 Syncope 45 0.062
348
ORL005 Oral Candidiasis 56 0.062
349
P BCT020 Bacteremia 2 44 0.062
350
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.062
351
ETN001 Eating Disorder 60 0.062
352
LYM040 Lymphoblastic Lymphoma 54 0.062
353
MXD026 Mixed Glioma 45 0.062
354
c HYP272 Hypercholesterolemia, Familial, 3 44 0.062
355
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.061
356
P MYC008 Myocarditis 59 0.061
357
P ALC033 Alcohol Use Disorder 58 0.061
358
GLC003 Glucose Intolerance 54 0.061
359
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.061
360
P MYP006 Myopia 55 0.061
361
c CHR682 Chronic Bilirubin Encephalopathy 39 0.061
362
END057 Endometrial Cancer 74 0.061
363
P HNT016 Huntington Disease 72 0.061
364
P HPT021 Hepatitis 67 0.060
365
RNL011 Renal Osteodystrophy 50 0.060
366
P SYP003 Syphilis 58 0.060
367
NWB001 Newborn Respiratory Distress Syndrome 58 0.060
368
PPL022 Papilloma 54 0.060
369
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.060
370
VCC001 Vaccinia 49 0.060
371
PRS037 Periostitis 38 0.059
372
BRK010 Burkitt Lymphoma 67 0.059
373
P NSP012 Nasopharyngeal Carcinoma 66 0.059
374
P VSC011 Vasculitis 62 0.059
375
c ACT073 Acute Leukemia 58 0.059
376
c HPT016 Hepatitis B 59 0.059
377
ENT011 Enterocolitis 51 0.059
378
BNN003 Bone Inflammation Disease 48 0.058
379
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.058
380
P ALP008 Alopecia 54 0.058
381
c CHR064 Chronic Monocytic Leukemia 33 0.058
382
P SLP005 Sleep Disorder 59 0.058
383
SQM002 Squamous Cell Papilloma 46 0.058
384
P END033 Endocarditis 57 0.058
385
AYM001 Ayme-Gripp Syndrome 57 0.058
386
SFT003 Soft Tissue Sarcoma 56 0.058
387
AMN003 Amnestic Disorder 54 0.058
388
TND005 Tendinitis 54 0.058
389
P BNG032 Benign Mesothelioma 46 0.058
390
CRB086 Cerebral Aneurysms 40 0.058
391
P LNG064 Lung Cancer Susceptibility 3 78 0.057
392
c SVR001 Severe Acute Respiratory Syndrome 62 0.057
393
ATR057 Atrioventricular Block 55 0.057
394
CNN005 Connective Tissue Disease 68 0.057
395
RTN023 Retinitis 46 0.057
396
NRR001 Neuroretinitis 42 0.057
397
P PRK057 Parkinson Disease, Late-Onset 78 0.057
398
P GRF003 Graft-Versus-Host Disease 72 0.057
399
c LKM063 Leukemia, Chronic Myeloid 72 0.057
400
c INF071 Inflammatory Bowel Disease 1 67 0.057
401
IRR002 Irritable Bowel Syndrome 65 0.057
402
P KDN017 Kidney Cancer 60 0.057
403
P SBS003 Substance Abuse 55 0.057
404
c SYS043 Systemic Lupus Erythematosus 1 38 0.057
405
c PSR017 Psoriasis 2 53 0.057
406
NRT004 Neuritis 52 0.057
407
P UVT001 Uveitis 57 0.056
408
FDL002 Food Allergy 51 0.056
409
ATS010 Autosomal Recessive Disease 48 0.056
410
CHL065 Cholangiocarcinoma 68 0.056
411
CMM005 Common Cold 57 0.056
412
URN010 Urinary Tract Obstruction 55 0.056
413
INT079 Intrahepatic Cholangiocarcinoma 51 0.056
414
HRT012 Heart Valve Disease 53 0.055
415
c PSR023 Psoriasis 1 52 0.055
416
c PSR032 Psoriasis 11 47 0.055
417
c PSR028 Psoriasis 7 42 0.055
418
c PSR018 Psoriasis 13 41 0.055
419
MSC007 Muscle Hypertrophy 64 0.055
420
ACT119 Acute Promyelocytic Leukemia 63 0.055
421
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.055
422
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.055
423
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.055
424
c HPT003 Hepatitis a 62 0.055
425
END040 Endogenous Depression 55 0.055
426
P RTN024 Retinoblastoma 73 0.054
427
RHM001 Rheumatic Fever 60 0.054
428
c FML008 Familial Retinoblastoma 53 0.054
429
P MLG074 Malignant Mesenchymoma 40 0.054
430
DNT002 Dentine Erosion 16 0.054
431
P INF032 Infertility 57 0.054
432
NRT001 Neurotic Disorder 53 0.054
433
MRG003 Marginal Zone B-Cell Lymphoma 52 0.054
434
P FLL037 Follicular Lymphoma 67 0.054
435
APN008 Apnea, Obstructive Sleep 64 0.054
436
c HPT001 Hepatitis C 62 0.054
437
WTH001 Withdrawal Disorder 48 0.054
438
TND004 Tendinopathy 43 0.054
439
P SRC025 Sarcoidosis 1 70 0.053
440
P PGT001 Paget's Disease of Bone 58 0.053
441
ORL015 Oral Squamous Cell Carcinoma 43 0.053
442
TRP009 Triple X Syndrome 42 0.053
443
P SYS005 Systemic Scleroderma 68 0.053
444
SKN019 Skin Melanoma 68 0.053
445
PRS045 Prostatic Hypertrophy 53 0.053
446
HYP781 Hypoascorbemia 51 0.053
447
CYT005 Cytomegalovirus Retinitis 50 0.053
448
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.053
449
ACR041 Acromelic Frontonasal Dysostosis 52 0.053
450
DFF036 Differentiated Thyroid Carcinoma 52 0.053
451
P SPP010 Suppressor of Tumorigenicity 3 51 0.053
452
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.053
453
PLS025 Plasmablastic Lymphoma 47 0.053
454
ATM052 Autoimmune Disease 1 37 0.053
455
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.053
456
OST115 Osteonecrosis of the Jaw 40 0.052
457
BRX001 Bruxism 50 0.052
458
CRN030 Coronary Stenosis 50 0.052
459
P NRV007 Nervous System Disease 66 0.052
460
c FML001 Familial Atrial Fibrillation 65 0.052
461
THY122 Thyroid Gland Cancer 57 0.052
462
c MST023 Mesothelioma, Malignant 57 0.052
463
PRP080 Peripheral Artery Disease 53 0.052
464
DYS015 Dysentery 52 0.052
465
P MSC003 Muscular Atrophy 52 0.052
466
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.052
467
CRT013 Carotid Stenosis 50 0.052
468
DPH001 Diphtheria 60 0.052
469
SPL004 Splenic Marginal Zone Lymphoma 51 0.052
470
ENT001 Enterocele 39 0.052
471
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.052
472
MLR004 Malaria 81 0.051
473
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.051
474
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.051
475
P DRM010 Dermatomyositis 61 0.051
476
P HYP024 Hypoparathyroidism 56 0.051
477
c GRV008 Graves Disease 1 56 0.051
478
CRT017 Cartilage Disease 54 0.051
479
TLN003 Telangiectasis 52 0.051
480
PRS021 Prostatic Adenoma 51 0.051
481
P OCL013 Oculodentodigital Dysplasia 69 0.051
482
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.051
483
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.051
484
HMT002 Hematologic Cancer 62 0.051
485
CHL123 Chlamydia 59 0.051
486
ACT058 Active Peptic Ulcer Disease 55 0.051
487
ASP007 Aspiration Pneumonia 48 0.051
488
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.050
489
P MDL005 Medulloblastoma 77 0.050
490
CRV035 Cervical Cancer 76 0.050
491
P PLM036 Pulmonary Fibrosis 65 0.050
492
P ART005 Arteriovenous Malformation 65 0.050
493
DSS008 Disease of Mental Health 58 0.050
494
P INT068 Intestinal Disease 53 0.050
495
ILS001 Ileus 51 0.050
496
c FLL041 Follicular Lymphoma 1 49 0.050
497
P MYC084 Mycobacterium Tuberculosis 1 68 0.049
498
OCL006 Ocular Hypertension 53 0.049
499
P SHR001 Short Bowel Syndrome 53 0.049
500
ANR004 Anuria 46 0.049
501
ASP008 Aspiration Pneumonitis 45 0.049
502
INF034 Infective Endocarditis 53 0.049
503
PYD002 Pyoderma 50 0.049
504
BRN056 Bronchopulmonary Dysplasia 57 0.049
505
c ACT134 Acute Liver Failure 56 0.049
506
PRS063 Paresthesia 41 0.049
507
P HYP061 Hypertrophic Cardiomyopathy 70 0.048
508
P MJR001 Major Depressive Disorder 68 0.048
509
BRR014 Barrett Esophagus 65 0.048
510
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.048
511
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.048
512
FNG017 Fungal Infectious Disease 53 0.048
513
CRD137 Cardiogenic Shock 47 0.048
514
URT010 Ureteral Obstruction 45 0.048
515
CYN002 Cyanosis, Transient Neonatal 45 0.048
516
DST006 Diastolic Heart Failure 45 0.048
517
c FML021 Familial Hypercholesterolemia 66 0.048
518
ORL011 Oral Cancer 60 0.048
519
FSC004 Fasciitis 50 0.048
520
ART074 Aortic Dissection 52 0.048
521
MSC157 Muscular Dystrophy, Duchenne Type 72 0.047
522
MNT001 Mantle Cell Lymphoma 69 0.047
523
P OLG002 Oligodendroglioma 67 0.047
524
P SKN015 Skin Carcinoma 66 0.047
525
c PRM005 Primary Hyperparathyroidism 58 0.047
526
P OVR082 Overgrowth Syndrome 50 0.047
527
PRS129 Prostatic Hyperplasia, Benign 49 0.047
528
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.047
529
c HPT073 Hepatitis C Virus 72 0.047
530
EWN003 Ewing Sarcoma 69 0.047
531
FCT007 Factor Vii Deficiency 67 0.047
532
FLL027 Fallopian Tube Carcinoma 67 0.047
533
P ALP009 Alopecia Areata 60 0.047
534
P MYS005 Myositis 56 0.047
535
DMP001 Dumping Syndrome 44 0.047
536
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.047
537
P PRS038 Personality Disorder 65 0.046
538
BLL006 Bullous Pemphigoid 62 0.046
539
P CHR285 Chronic Myelomonocytic Leukemia 60 0.046
540
GRD007 Grade Iii Astrocytoma 59 0.046
541
P PLY011 Polycystic Ovary Syndrome 56 0.046
542
ERY051 Erythroleukemia, Familial 56 0.046
543
CNT033 Central Nervous System Cancer 47 0.046
544
c LKM005 Leukemia, T-Cell, Chronic 34 0.046
545
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.046
546
GST033 Gestational Diabetes 61 0.046
547
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.046
548
CHR100 Chronic Ulcer of Skin 55 0.046
549
HRT011 Heart Septal Defect 50 0.046
550
LPT014 Leptin Deficiency or Dysfunction 74 0.045
551
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.045
552
VRL011 Viral Infectious Disease 61 0.045
553
P VNS003 Venous Insufficiency 55 0.045
554
GLS001 Gliosarcoma 54 0.045
555
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.045
556
P PLV020 Pelvic Organ Prolapse 57 0.045
557
c ART115 Aortic Valve Disease 1 75 0.045
558
ANG020 Angiosarcoma 64 0.045
559
PLG002 Plague 63 0.045
560
DFF005 Diffuse Large B-Cell Lymphoma 55 0.045
561
LRN003 Learning Disability 49 0.045
562
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.045
563
FBR009 Fibrous Dysplasia 48 0.045
564
P PRM006 Primary Biliary Cirrhosis 62 0.044
565
GST040 Gastric Adenocarcinoma 70 0.044
566
CRP001 Carpal Tunnel Syndrome 67 0.044
567
P MST009 Mastocytosis 64 0.044
568
INT066 Interstitial Lung Disease 60 0.044
569
P OPT006 Optic Nerve Disease 60 0.044
570
TRN018 Transitional Cell Carcinoma 56 0.044
571
RSP007 Respiratory Distress Syndrome, Infant 30 0.044
572
P BLD062 Bile Duct Cancer 67 0.043
573
MYL031 Myeloproliferative Neoplasm 66 0.043
574
c JVN010 Juvenile Rheumatoid Arthritis 64 0.043
575
PLM031 Poliomyelitis 64 0.043
576
P SPN046 Spinal Muscular Atrophy 62 0.043
577
P BRS044 Breast Adenocarcinoma 59 0.043
578
HMR039 Hemorrhage, Intracerebral 57 0.043
579
P ADL017 Adult T-Cell Leukemia 56 0.043
580
P INS002 in Situ Carcinoma 53 0.043
581
P RCT021 Rectum Cancer 52 0.043
582
c INF145 Infantile Liver Failure Syndrome 1 50 0.043
583
MCR004 Macroglobulinemia 49 0.043
584
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.043
585
BNM001 Bone Marrow Cancer 43 0.043
586
PLY150 Polykaryocytosis Inducer 31 0.043
587
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.043
588
PST028 Post-Traumatic Stress Disorder 58 0.043
589
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.043
590
P MNC007 Monocytic Leukemia 53 0.043
591
CRH005 Crohn's Colitis 53 0.043
592
ILT001 Ileitis 50 0.043
593
P SPN052 Spondyloarthropathy 54 0.043
594
P BLP047 Blepharocheilodontic Syndrome 1 48 0.043
595
TTH006 Tooth Disease 46 0.042
596
c MCL013 Mucolipidosis Iv 66 0.042
597
c ALP101 Alpha-Thalassemia 62 0.042
598
c DWL002 Dowling-Degos Disease 1 58 0.042
599
MTH009 Mouth Disease 56 0.042
600
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.042
601
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.042
602
APP009 Appendix Adenocarcinoma 44 0.042
603
KHL003 Kohlschutter-Tonz Syndrome 65 0.041
604
P OPT009 Optic Neuritis 57 0.041
605
BLM002 Bulimia Nervosa 57 0.041
606
SRS001 Serous Cystadenocarcinoma 52 0.041
607
P HYD006 Hydrocephalus 66 0.041
608
LYM027 Lymphopenia 58 0.041
609
APH001 Aphthous Stomatitis 57 0.041
610
CMR002 Coumarin Resistance 56 0.041
611
PRT038 Protein-Energy Malnutrition 54 0.041
612
c CNT035 Central Nervous System Disease 52 0.041
613
THR004 Thrombocytosis 51 0.041
614
ATY042 Atypical Chronic Myeloid Leukemia 49 0.041
615
c DRM054 Dermatitis, Atopic, 2 44 0.041
616
c OVR114 Ovarian Cancer 1 38 0.041
617
P NJM001 Nijmegen Breakage Syndrome 74 0.041
618
SPN041 Spinal Cord Disease 56 0.041
619
PRT082 Preterm Premature Rupture of the Membranes 54 0.041
620
ART017 Aortic Disease 49 0.041
621
LKP003 Leukoplakia 39 0.041
622
P DRM007 Dermatitis Herpetiformis 55 0.040
623
PYD001 Pyoderma Gangrenosum 54 0.040
624
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.040
625
P HMP007 Hemophilia 51 0.040
626
c DRM040 Dermatitis Herpetiformis, Familial 35 0.040
627
P INF038 Influenza 68 0.039
628
P TXP001 Toxoplasmosis 60 0.039
629
P BNG030 Benign Ependymoma 60 0.039
630
c CHR417 Chronic Graft Versus Host Disease 57 0.039
631
PLS011 Plasmacytoma 56 0.039
632
CLL010 Cellular Ependymoma 54 0.039
633
BRN038 Bronchial Disease 53 0.039
634
P BRN035 Brain Stem Glioma 52 0.039
635
GNT002 Giant Cell Glioblastoma 50 0.039
636
PRP017 Periapical Periodontitis 46 0.039
637
LWC001 Low Compliance Bladder 43 0.039
638
c MLG079 Malignant Pleural Mesothelioma 42 0.039
639
OSM001 Osmotic Diarrhea 32 0.039
640
HML018 Homologous Wasting Disease 22 0.039
641
P SCL048 Sclerosteosis 55 0.039
642
P AGG001 Aggressive Periodontitis 50 0.039
643
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.039
644
c OPT053 Optic Atrophy 1 63 0.038
645
MRG013 Mirage Syndrome 43 0.038
646
MNS002 Mini Stroke 19 0.038
647
P FML011 Familial Adenomatous Polyposis 72 0.038
648
MYC006 Mycosis Fungoides 66 0.038
649
WLD007 Waldenstroem's Macroglobulinemia 61 0.038
650
P HRD011 Hereditary Spherocytosis 60 0.038
651
P PLY018 Polycythemia 56 0.038
652
P FBR017 Fibrosarcoma 56 0.038
653
HMG005 Hemoglobinopathy 56 0.038
654
INT030 Intracranial Aneurysm 56 0.038
655
HMS001 Hemosiderosis 54 0.038
656
P CNT005 Central Nervous System Lymphoma 53 0.038
657
LYM012 Lymphoplasmacytic Lymphoma 47 0.038
658
CLN045 Colonic Benign Neoplasm 46 0.038
659
ANP009 Anaplastic Oligodendroglioma 43 0.038
660
c BSL007 Basal Cell Carcinoma 68 0.038
661
P SCL018 Scoliosis 60 0.038
662
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.038
663
ORP003 Oropharynx Cancer 55 0.038
664
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.038
665
CHL056 Cheilitis 48 0.038
666
RTC005 Reticulosarcoma 47 0.038
667
LTH001 Lethal Midline Granuloma 44 0.038
668
ACR008 Acrocallosal Syndrome 69 0.037
669
PNC129 Pancreatic Adenocarcinoma 68 0.037
670
CRN036 Craniopharyngioma 65 0.037
671
c WLM018 Wilms Tumor 5 61 0.037
672
SZR001 Sezary's Disease 60 0.037
673
SPP011 Suppression of Tumorigenicity 12 59 0.037
674
INC002 Inclusion Body Myositis 58 0.037
675
BRN012 Bronchiolitis Obliterans 55 0.037
676
P MLN007 Male Infertility 55 0.037
677
VGN023 Vaginitis 54 0.037
678
GST037 Gastroparesis 54 0.037
679
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.037
680
PLS007 Plasmodium Falciparum Malaria 52 0.037
681
P TRT010 Teratoma 52 0.037
682
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.037
683
CYS014 Cystadenocarcinoma 51 0.037
684
HMR023 Hemorrhagic Cystitis 45 0.037
685
CNT017 Central Nervous System Origin Vertigo 45 0.037
686
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.037
687
P RRH023 Rare Hereditary Hemochromatosis 41 0.037
688
WLL004 Wallerian Degeneration 39 0.037
689
DGR001 Digeorge Syndrome 64 0.036
690
P ATR010 Atrial Heart Septal Defect 60 0.036
691
P MLN069 Melanoma, Uveal 59 0.036
692
c BSL024 Basal Cell Carcinoma 1 56 0.036
693
AMN001 Amenorrhea 54 0.036
694
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.036
695
P CLR019 Color Blindness 48 0.036
696
ORB013 Orbital Disease 42 0.036
697
BRN034 Brain Meningioma 33 0.036
698
BNG077 Benign Idiopathic Neonatal Seizures 26 0.036
699
OVR029 Ovarian Hyperstimulation Syndrome 64 0.035
700
P VNT002 Ventricular Septal Defect 60 0.035
701
P PRV006 Pervasive Developmental Disorder 57 0.035
702
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.035
703
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.035
704
CRT016 Carotid Artery Disease 52 0.035
705
PLM017 Pulmonary Alveolar Microlithiasis 50 0.035
706
PLC008 Placenta Disease 50 0.035
707
CCN002 Cocaine Abuse 49 0.035
708
GST049 Gastrointestinal System Cancer 49 0.035
709
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.035
710
c PRM226 Primary Central Nervous System Lymphoma 48 0.035
711
MLK006 Milk Allergy 48 0.035
712
PPL002 Papillary Carcinoma 47 0.035
713
GST071 Gastrointestinal Carcinoma 47 0.035
714
P CRC039 Coarctation of Aorta 47 0.035
715
DNT008 Denture Stomatitis 35 0.035
716
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.035
717
P OVR096 Overlap Myositis 27 0.035
718
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.035
719
P AVS003 Avascular Necrosis 42 0.035
720
OST160 Osteoid Osteoma 37 0.035
721
P FRG001 Fragile X Syndrome 70 0.033
722
PLY001 Polycythemia Vera 69 0.033
723
END041 Endometrial Adenocarcinoma 63 0.033
724
P LYM033 Lymphoproliferative Syndrome 59 0.033
725
c LKM070 Leukemia, Acute Monocytic 57 0.033
726
LNN001 Lennox-Gastaut Syndrome 57 0.033
727
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.033
728
FBR008 Fibrillary Astrocytoma 51 0.033
729
SKN013 Skin Benign Neoplasm 51 0.033
730
ASC010 Ascaris Lumbricoides Infection 50 0.033
731
P PNB001 Pineoblastoma 50 0.033
732
CLR003 Clear Cell Adenocarcinoma 50 0.033
733
P ATR005 Atrophic Gastritis 50 0.033
734
HYP043 Hyperandrogenism 48 0.033
735
CLS016 Clostridium Difficile Colitis 48 0.033
736
c MTR002 Mitral Valve Insufficiency 48 0.033
737
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.033
738
P EPN001 Ependymoblastoma 44 0.033
739
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.033
740
ASC001 Ascaridiasis 35 0.033
741
MRF001 Marfan Syndrome 77 0.033
742
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.033
743
NTR018 Neutrophilia, Hereditary 52 0.033
744
P CTN015 Cutaneous T Cell Lymphoma 49 0.033
745
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.033
746
SPN040 Spinal Cancer 44 0.033
747
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.033
748
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.033
749
END028 Endemic Goiter 37 0.033
750
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 0.033
751
ALV001 Alveolar Periostitis 30 0.033
752
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.031
753
SCH036 Scheie Syndrome 72 0.031
754
MYL005 Myelofibrosis 70 0.031
755
P TTR001 Tetralogy of Fallot 70 0.031
756
c HMP029 Hemophilia a 67 0.031
757
c ATM011 Autoimmune Hepatitis 63 0.031
758
BLD131 Bladder Urothelial Carcinoma 62 0.031
759
PSR001 Psoriatic Arthritis 61 0.031
760
PNM001 Pneumocystosis 59 0.031
761
DCT002 Ductal Carcinoma in Situ 59 0.031
762
LYM021 Lymphadenitis 57 0.031
763
GNR004 Generalized Anxiety Disorder 56 0.031
764
ISL001 Islet Cell Tumor 56 0.031
765
P NRF002 Neurofibromatosis 56 0.031
766
NRN004 Neuroendocrine Tumor 55 0.031
767
FLR002 Filariasis 55 0.031
768
P AML002 Amelogenesis Imperfecta 55 0.031
769
P LRY044 Larynx Cancer 55 0.031
770
P TCD001 Tic Disorder 53 0.031
771
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.031
772
P OVR049 Ovarian Disease 52 0.031
773
c ACT135 Acute Graft Versus Host Disease 52 0.031
774
P PRC012 Pericardial Effusion 51 0.031
775
OPT003 Opiate Dependence 50 0.031
776
c CHR431 Chronic Venous Insufficiency 49 0.031
777
HMP001 Hemopericardium 48 0.031
778
LPT006 Leptin Receptor Deficiency 48 0.031
779
CRN027 Corneal Neovascularization 47 0.031
780
ACT084 Acute Stress Disorder 47 0.031
781
ANP006 Anaplastic Ependymoma 46 0.031
782
PNC056 Pineocytoma 45 0.031
783
LYM051 Lymphomatoid Granulomatosis 45 0.031
784
CHL149 Childhood Acute Myeloid Leukemia 44 0.031
785
PRT035 Peritoneum Cancer 44 0.031
786
TST015 Testicular Disease 43 0.031
787
PLY068 Polysubstance Abuse 43 0.031
788
CHR286 Chronic Neutrophilic Leukemia 42 0.031
789
c MLG064 Malignant Ependymoma 41 0.031
790
PNL014 Pineal Gland Cancer 41 0.031
791
HYP001 Hypochromic Microcytic Anemia 38 0.031
792
SWL001 Swallowing Disorders 38 0.031
793
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.031
794
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.031
795
c ADL008 Adult Oligodendroglioma 34 0.031
796
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.031
797
PLN007 Plantar Fasciitis 32 0.031
798
c MLG023 Malignant Adult Ependymoma 15 0.031
799
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 0.030
800
TKY002 Takayasu Arteritis 62 0.030
801
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.030
802
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.030
803
MCR013 Microphthalmia 57 0.030
804
CLR030 Clear Cell Renal Cell Carcinoma 53 0.030
805
PRP036 Peripheral T-Cell Lymphoma 53 0.030
806
P SML001 Small Cell Carcinoma 52 0.030
807
c ACH020 Achromatopsia 2 50 0.030
808
TRT020 Tritanopia 49 0.030
809
EXS001 Exostosis 46 0.030
810
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.030
811
INT276 Interatrial Communication 42 0.030
812
CLR033 Color Vision Deficiency 41 0.030
813
SLT009 Solitary Bone Cyst 39 0.030
814
SML011 Smoldering Myeloma 33 0.030
815
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.030
816
HYP823 Hypotonia, Ataxia, Developmental Delay, and Tooth Enamel Defect Syndrome 28 0.030
817
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.030
818
HDG004 Hodgkin's Granuloma 23 0.030
819
HDG006 Hodgkin's Paragranuloma 22 0.030
820
c NRF024 Neurofibromatosis, Type I 77 0.029
821
P TMP003 Temporal Arteritis 68 0.029
822
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.029
823
NRF007 Neurofibroma 64 0.029
824
MGK001 Megakaryocytic Leukemia 64 0.029
825
MSS001 Masa Syndrome 62 0.029
826
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.029
827
BRS051 Breast Disease 58 0.029
828
MXD005 Mixed Connective Tissue Disease 58 0.029
829
ECH003 Echinococcosis 53 0.029
830
CLF001 Cleft Lip 53 0.029
831
INT051 Intussusception 53 0.029
832
ACT200 Acute Monoblastic Leukemia 52 0.029
833
AZS001 Azoospermia 50 0.029
834
SLD003 Sialadenitis 49 0.029
835
ADT003 Auditory System Disease 48 0.029
836
CCN001 Cocaine Dependence 48 0.029
837
PRS012 Pars Planitis 48 0.029
838
OPD006 Opioid Addiction 48 0.029
839
SXL003 Sexual Disorder 47 0.029
840
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.029
841
c CNG216 Congenital Hydrocephalus 47 0.029
842
HYP082 Hypopharynx Cancer 47 0.029
843
ASP004 Asphyxia Neonatorum 46 0.029
844
FLL008 Folliculitis 46 0.029
845
HMR002 Hemarthrosis 45 0.029
846
CYS009 Cystadenoma 44 0.029
847
HPT067 Hepatocellular Adenoma 44 0.029
848
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.029
849
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.029
850
MDD018 Middle East Respiratory Syndrome 43 0.029
851
c HYP057 Hypervitaminosis D 42 0.029
852
ABD010 Abdominal Wall Defect 36 0.029
853
c ADL093 Adult Acute Monocytic Leukemia 20 0.029
854
P FRN006 Frontotemporal Dementia 68 0.027
855
HYL004 Hyaline Fibromatosis Syndrome 67 0.027
856
P CLC063 Celiac Disease 1 66 0.027
857
P PSD087 Pseudoxanthoma Elasticum 65 0.027
858
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.027
859
CRC021 Carcinosarcoma 62 0.027
860
c JVN061 Juvenile Arthritis 60 0.027
861
PLM070 Pulmonic Stenosis 57 0.027
862
P PNM006 Pneumoconiosis 56 0.027
863
FLR001 Filarial Elephantiasis 55 0.027
864
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.027
865
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.027
866
CRY001 Cryptogenic Organizing Pneumonia 53 0.027
867
PLS016 Plasma Cell Leukemia 53 0.027
868
P ORL007 Oral Cavity Cancer 53 0.027
869
FCT001 Factor Viii Deficiency 51 0.027
870
TNG007 Tongue Carcinoma 51 0.027
871
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.027
872
PLM041 Pulmonary Valve Stenosis 49 0.027
873
BKR002 Baker-Gordon Syndrome 49 0.027
874
P CRV031 Cervical Adenocarcinoma 49 0.027
875
RCT020 Rectum Adenocarcinoma 48 0.027
876
ANT018 Anthracosis 48 0.027
878
NRN001 Neuroendocrine Carcinoma 47 0.027
879
ANV001 Anovulation 47 0.027
880
P PRC019 Precocious Puberty 46 0.027
881
UMB002 Umbilical Hernia 46 0.027
882
CNV002 Conversion Disorder 45 0.027
883
P OCY003 Oocyte Maturation Defect 1 45 0.027
884
MLN073 Melanosis, Neurocutaneous 45 0.027
885
GRD001 Giardiasis 45 0.027
886
c SRC023 Sarcoidosis 2 43 0.027
887
BLR013 Biliary Tract Cancer 42 0.027
888
IDP070 Idiopathic Scoliosis 42 0.027
889
OPT007 Optic Nerve Glioma 42 0.027
890
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.027
891
ELP001 Elephantiasis 41 0.027
892
MTL005 Metal Allergy 41 0.027
893
KLB003 Klebsiella Pneumonia 41 0.027
894
c ADL096 Adult Hepatocellular Carcinoma 40 0.027
895
MLT001 Multiple Chemical Sensitivity 40 0.027
896
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.027
897
c PGT007 Paget Disease of Bone 3 39 0.027
898
c PLY105 Polycystic Ovary Syndrome 1 38 0.027
899
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.027
900
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.027
901
LPN002 Lip and Oral Cavity Cancer 19 0.027
902
P NNN008 Noonan Syndrome 1 76 0.023
903
ADN011 Adenoid Cystic Carcinoma 70 0.023
904
P TBR001 Tuberous Sclerosis 70 0.023
905
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.023
906
P MTR004 Maturity-Onset Diabetes of the Young 65 0.023
907
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.023
908
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.023
909
GRN037 Granulomatosis with Polyangiitis 65 0.023
910
DSM004 Desmoid Tumor 64 0.023
911
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.023
912
PMS001 Poems Syndrome 60 0.023
913
PRC038 Precocious Puberty, Male-Limited 59 0.023
914
P HMN036 Hemangiopericytoma, Malignant 59 0.023
915
DST005 Diastrophic Dysplasia 58 0.023
916
CCC001 Coccidioidomycosis 58 0.023
917
P SLV026 Salivary Gland Carcinoma 57 0.023
918
PLM012 Pulmonary Sarcoidosis 53 0.023
919
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.023
920
GST009 Gastroschisis 53 0.023
921
P LCT002 Lactose Intolerance 53 0.023
922
c EXS019 Exostoses, Multiple, Type I 53 0.023
923
c DMN023 Diamond-Blackfan Anemia 1 53 0.023
924
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.023
925
FRY006 Fryns Microphthalmia Syndrome 52 0.023
926
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.023
927
GLM004 Gliomatosis Cerebri 52 0.023
928
MCP006 Mucoepidermoid Carcinoma 50 0.023
929
P NGH001 Night Blindness 48 0.023
930
ACT098 Acute Erythroid Leukemia 48 0.023
931
P ASP001 Asperger Syndrome 48 0.023
932
HYP068 Hyperostosis 48 0.023
933
DSM003 Desmoid Disease, Hereditary 48 0.023
934
DRG003 Drug Dependence 47 0.023
935
SPC010 Speech and Communication Disorders 47 0.023
936
P PLL002 Pellagra 46 0.023
937
P CHR573 Choroid Plexus Cancer 46 0.023
938
P HRD001 Hereditary Multiple Exostoses 46 0.023
939
SVN002 Sveinsson Chorioretinal Atrophy 46 0.023
940
EPD015 Epidemic Typhus 45 0.023
941
PPL018 Papillary Adenocarcinoma 45 0.023
942
THR099 Third-Degree Atrioventricular Block 45 0.023
943
ASP026 Asplenia, Isolated Congenital 44 0.023
944
CRD003 Cardiac Sarcoidosis 44 0.023
945
THR012 Thoracic Cancer 44 0.023
946
FBR019 Fibromatosis 41 0.023
947
OST004 Osteitis Fibrosa 41 0.023
948
MYS001 Myositis Ossificans 41 0.023
949
P SCL057 Scoliosis, Isolated 1 41 0.023
950
MRP001 Morphine Dependence 41 0.023
951
PPL007 Papillary Serous Adenocarcinoma 40 0.023
952
P DYS005 Dyslexia 40 0.023
953
PRM024 Primary Angle-Closure Glaucoma 40 0.023
954
OCL010 Ocular Hypotension 39 0.023
955
RTC012 Reticuloendotheliosis, X-Linked 39 0.023
956
c HRD104 Hereditary Multiple Osteochondromas 39 0.023
957
DSS010 Dissociative Disorder 39 0.023
958
SLP010 Slipped Capital Femoral Epiphysis 39 0.023
959
THY124 Thyroid Gland Papillary Carcinoma 38 0.023
960
ACT040 Acute Poststreptococcal Glomerulonephritis 36 0.023
961
TTH032 Tooth Size 36 0.023
962
PRM329 Premature Aging 35 0.023
963
NRD001 Neurodermatitis 35 0.023
964
P EXT032 Extraosseous Osteosarcoma 34 0.023
965
BRN005 Brain Glioblastoma Multiforme 34 0.023
966
PLM028 Pulmonary Coin Lesion 33 0.023
967
P PLY188 Polyendocrinopathy 32 0.023
968
CRT069 Cortical Malformations, Occipital 30 0.023
969
PHT002 Photokeratitis 28 0.023
970
PHS025 Phosphatase, Acid, of Tissues 28 0.023
971
INT053 Intracranial Vasospasm 24 0.023
972
c PSD047 Pseudo-Turner Syndrome 21 0.023
973
PLT016 Platelet Adenylate Cyclase Activity 16 0.023
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