Search results for Fluorides

1082 hits were found for Fluorides

# Family MCID Name MIFTS Score
1
BTY001 Butyrylcholinesterase Deficiency 50 5.769
2
DNT012 Dental Caries 53 0.983
3
DNT001 Dental Fluorosis 43 0.581
4
P OST002 Osteoporosis 74 0.385
5
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.381
6
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.381
7
GNG013 Gingivitis 59 0.325
8
ALL026 Allergic Hypersensitivity Disease 62 0.296
9
RTC003 Root Caries 33 0.258
10
ENM001 Enamel Caries 28 0.228
11
ENM002 Enamel Erosion 26 0.220
12
HRW001 Hair Whorl 36 0.189
13
P BND020 Bone Disease 59 0.177
14
BNR002 Bone Resorption Disease 48 0.172
15
P DNT007 Dentin Sensitivity 36 0.164
16
CHL079 Children's Interstitial Lung Disease 26 0.161
17
OST159 Osteogenic Sarcoma 66 0.155
18
HYP005 Hypokalemia 55 0.151
19
48X005 48,xyyy 39 0.144
20
PRT037 Pertussis 65 0.143
21
P PRD008 Periodontitis 64 0.135
22
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.135
23
GLS018 Glass Syndrome 57 0.128
24
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.128
25
DNT010 Dentin Caries 32 0.128
26
P OTS001 Otosclerosis 49 0.126
27
END081 Endosteal Hyperostosis, Autosomal Dominant 60 0.117
28
P KDN018 Kidney Disease 72 0.109
29
OST011 Osteomalacia 52 0.109
30
GNG003 Gingival Recession 44 0.109
31
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.102
32
RTR008 Root Resorption 45 0.100
33
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.100
34
CHL014 Cholera 59 0.098
35
GNG011 Gingival Disease 45 0.098
36
MYL069 Myeloma, Multiple 85 0.090
37
c RHB024 Rhabdomyosarcoma 2 67 0.090
38
P HYP069 Hyperparathyroidism 63 0.088
39
TTH007 Tooth Erosion 31 0.088
40
c CHR684 Chronic Kidney Disease 70 0.085
41
P HYP086 Hypothyroidism 69 0.085
42
ATH013 Atherosclerosis Susceptibility 65 0.085
43
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.082
44
LPP008 Lipoprotein Quantitative Trait Locus 62 0.082
45
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.082
46
ANK001 Ankylosis 51 0.082
47
47X002 47,xyy 49 0.082
48
ATX019 Ataxia with Vitamin E Deficiency 42 0.082
49
BRT054 Brittle Bone Disorder 72 0.080
50
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.080
51
P NRB001 Neuroblastoma 72 0.077
52
ADL002 Adult Syndrome 70 0.077
53
P CRD119 Cardiac Arrest 67 0.077
54
MMM001 Mammary Paget's Disease 53 0.077
55
GTR002 Goiter 53 0.077
56
ART140 Arteries, Anomalies of 52 0.077
58
P TRN020 Turner Syndrome 67 0.074
59
HYP066 Hyperglycemia 61 0.074
60
OST003 Osteonecrosis 61 0.074
61
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.074
62
P NRP001 Neuropathy 56 0.074
63
P PRS040 Prostate Cancer 97 0.071
64
RCK004 Rickets 68 0.071
65
NTR005 Nutritional Deficiency Disease 62 0.071
66
BCT022 Bacterial Infectious Disease 56 0.071
67
MCS002 Mucositis 56 0.071
68
PRS037 Periostitis 38 0.071
69
c HYP836 Hypercholesterolemia, Familial, 1 73 0.067
70
P CRN300 Coronary Heart Disease 1 63 0.067
71
P ANP001 Anaplastic Large Cell Lymphoma 58 0.067
72
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.067
73
STM007 Stomatitis 50 0.067
74
RNL011 Renal Osteodystrophy 50 0.067
75
c PRS136 Prostate Cancer, Hereditary, 6 33 0.067
76
c PRS130 Prostate Cancer, Hereditary, 8 32 0.067
77
P BLD134 Bladder Cancer 79 0.064
78
INS024 Insulin-Like Growth Factor I 79 0.064
79
P RSP003 Respiratory Failure 74 0.064
80
DWN001 Down Syndrome 70 0.064
81
c ART101 Aortic Valve Disease 2 65 0.064
82
P ART023 Arthropathy 62 0.064
83
DRM006 Dermatitis 61 0.064
84
P BCL017 B-Cell Lymphoma 58 0.064
85
P BNC003 Bone Cancer 58 0.064
86
END086 End Stage Renal Disease 51 0.064
87
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.064
88
PST092 Posttransplant Acute Limbic Encephalitis 29 0.064
89
DNT002 Dentine Erosion 16 0.064
90
AST005 Asthma 76 0.060
91
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.060
92
HMN044 Human Immunodeficiency Virus Type 1 71 0.060
93
DFC004 Deficiency Anemia 70 0.060
94
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.060
95
P ATT013 Attention Deficit-Hyperactivity Disorder 65 0.060
96
P ADN016 Adenocarcinoma 64 0.060
97
ACQ007 Acquired Immunodeficiency Syndrome 60 0.060
98
PNG002 Pain Agnosia 51 0.060
99
c SCN007 Secondary Hyperparathyroidism 51 0.060
100
DFF006 Diffuse Idiopathic Skeletal Hyperostosis 48 0.060
101
HLX001 Helix Syndrome 47 0.060
102
CYT002 Cytokine Deficiency 42 0.060
103
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.060
104
BCK006 Back Pain 42 0.060
105
c PLM127 Pulmonary Hypertension, Primary, 3 34 0.060
106
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.060
107
P BRS047 Breast Cancer 97 0.056
108
P HRT032 Heart Disease 75 0.056
109
P ATS364 Autism 70 0.056
110
P MYC007 Myocardial Infarction 70 0.056
111
P SLP006 Sleep Apnea 69 0.056
112
P VSC007 Vascular Disease 63 0.056
113
ISC004 Ischemia 58 0.056
114
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.056
115
P PLY019 Polyneuropathy 56 0.056
116
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.056
117
P CHR345 Chronic Pain 44 0.056
118
P ALZ034 Alzheimer Disease 88 0.052
119
STR067 Stroke, Ischemic 81 0.052
120
c NRF023 Neurofibromatosis, Type Ii 80 0.052
121
OST012 Osteoarthritis 78 0.052
122
CRH001 Crohn's Disease 74 0.052
123
c SPN225 Spondyloarthropathy 1 73 0.052
124
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.052
125
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.052
126
CRB039 Cerebrovascular Disease 67 0.052
127
c ATS007 Autism Spectrum Disorder 67 0.052
128
ANG054 Angina Pectoris 66 0.052
129
P DBT009 Diabetes Mellitus 64 0.052
130
OST017 Osteomyelitis 64 0.052
131
DPR016 Depression 63 0.052
132
ETN001 Eating Disorder 60 0.052
133
ANR040 Aneurysm 59 0.052
134
MNT002 Mental Depression 58 0.052
135
INT007 Intermediate Coronary Syndrome 55 0.052
136
SPN051 Spondylitis 51 0.052
137
CRT013 Carotid Stenosis 50 0.052
138
PLP001 Pulpitis 49 0.052
139
CLC006 Calcinosis 48 0.052
140
PPL052 Papillomatosis, Confluent and Reticulated 33 0.052
141
INF009 Inflammatory Spondylopathy 31 0.052
142
P RHM011 Rheumatoid Arthritis 80 0.048
143
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.048
144
c MNN043 Meningioma, Familial 74 0.048
145
P AMY004 Amyloidosis 70 0.048
146
P ART022 Arthritis 69 0.048
147
ART016 Aortic Aneurysm 69 0.048
148
P LYM118 Lymphoma 68 0.048
149
P DMN002 Dementia 66 0.048
150
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.048
151
ATM095 Autoimmune Disease 62 0.048
152
MNN042 Meningioma, Radiation-Induced 62 0.048
153
P SNS001 Sensorineural Hearing Loss 60 0.048
154
c ACT071 Acute Kidney Failure 60 0.048
155
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.048
156
P CND004 Candidiasis 58 0.048
157
P CRD246 Cardiovascular System Disease 57 0.048
158
P GST044 Gastritis 56 0.048
159
NPH009 Nephrolithiasis 55 0.048
160
c PRD040 Periodontitis, Chronic 53 0.048
161
SPN021 Spinal Meningioma 50 0.048
162
DYS073 Dysphagia 50 0.048
163
URM002 Uremia 49 0.048
164
P BLP047 Blepharocheilodontic Syndrome 1 48 0.048
165
KRT002 Keratomalacia 47 0.048
166
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.048
167
GST020 Gastric Antral Vascular Ectasia 41 0.048
168
49X006 49, Xxxxy Syndrome 41 0.048
169
SCR001 Secretory Meningioma 41 0.048
170
OST115 Osteonecrosis of the Jaw 40 0.048
171
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.048
172
ARG004 Argyria 27 0.048
173
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.048
174
P HPT023 Hepatocellular Carcinoma 100 0.043
175
P LNG032 Lung Cancer 98 0.043
176
c HYP595 Hypertension, Essential 84 0.043
177
GLB015 Glioblastoma Multiforme 75 0.043
178
ANX010 Anxiety 73 0.043
179
OTT002 Otitis Media 72 0.043
180
LYM133 Lymphoma, Hodgkin, Classic 69 0.043
181
P LKM002 Leukemia 68 0.043
182
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.043
183
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.043
184
c DBT099 Diabetes Mellitus, Type I 65 0.043
185
P GLM045 Glioma 63 0.043
186
SKN016 Skin Disease 63 0.043
187
LPD008 Lipid Metabolism Disorder 62 0.043
188
P HYP750 Hypertriglyceridemia, Familial 62 0.043
189
LVR012 Liver Cirrhosis 62 0.043
190
THY029 Thyroid Carcinoma 59 0.043
191
P PLV020 Pelvic Organ Prolapse 57 0.043
192
IRN002 Iron Metabolism Disease 57 0.043
193
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.043
194
c ACT075 Acute Myocardial Infarction 57 0.043
195
THR024 Thrombosis 57 0.043
196
ORL005 Oral Candidiasis 56 0.043
197
P MYP006 Myopia 55 0.043
198
P SCL048 Sclerosteosis 55 0.043
199
P INF037 Inflammatory Bowel Disease 54 0.043
200
PLM010 Pulmonary Edema 54 0.043
201
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.043
202
NPH003 Nephrocalcinosis 51 0.043
203
P AGG001 Aggressive Periodontitis 50 0.043
204
MTB004 Metabolic Acidosis 50 0.043
205
BNN003 Bone Inflammation Disease 48 0.043
206
HYP025 Hyperphosphatemia 48 0.043
207
TTH006 Tooth Disease 46 0.043
208
KRT013 Keratolytic Winter Erythema 46 0.043
209
GLL048 Glial Tumor 45 0.043
210
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.043
211
URL001 Urolithiasis 45 0.043
212
P BCT020 Bacteremia 2 44 0.043
213
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.043
214
c CHR682 Chronic Bilirubin Encephalopathy 39 0.043
215
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.043
216
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.043
217
c PLM128 Pulmonary Hypertension, Primary, 2 29 0.043
218
PDT043 Pediatric Acute-Onset Neuropsychiatric Syndrome 26 0.043
219
P CLR023 Colorectal Cancer 99 0.037
220
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.037
221
c SYS001 Systemic Lupus Erythematosus 86 0.037
223
P GST053 Gastric Cancer 83 0.037
224
IMM167 Immune Deficiency Disease 78 0.037
225
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.037
226
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.037
227
c ATR087 Atrial Standstill 1 75 0.037
228
c ART115 Aortic Valve Disease 1 75 0.037
229
END057 Endometrial Cancer 74 0.037
230
P NJM001 Nijmegen Breakage Syndrome 74 0.037
231
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.037
232
P HNT016 Huntington Disease 72 0.037
233
P EPL164 Epilepsy 71 0.037
234
P SRC025 Sarcoidosis 1 70 0.037
235
P OST001 Osteopetrosis 70 0.037
236
P OCL013 Oculodentodigital Dysplasia 69 0.037
237
P PNM007 Pneumonia 68 0.037
238
c MCR129 Microvascular Complications of Diabetes 1 66 0.037
239
HYP056 Hypoglycemia 66 0.037
240
P HRP006 Herpes Simplex 65 0.037
241
ANG020 Angiosarcoma 64 0.037
242
P NTR004 Neutropenia 63 0.037
243
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.037
244
PLG002 Plague 63 0.037
245
c OPT053 Optic Atrophy 1 63 0.037
246
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.037
247
c FNC043 Fanconi Anemia, Complementation Group E 62 0.037
248
P PSR002 Psoriasis 62 0.037
249
CHL068 Cholestasis 61 0.037
250
GST033 Gestational Diabetes 61 0.037
251
SPN186 Spinal Cord Injury 60 0.037
252
LNG099 Lung Disease 60 0.037
253
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.037
254
IGR001 Ige Responsiveness, Atopic 59 0.037
255
BRN002 Bronchiolitis 59 0.037
256
P PGT001 Paget's Disease of Bone 58 0.037
257
CRD132 Cardiac Conduction Defect 58 0.037
258
EYD002 Eye Disease 58 0.037
259
CNS004 Constipation 58 0.037
260
P END033 Endocarditis 57 0.037
261
HYP266 Hypoxia 57 0.037
262
SPN041 Spinal Cord Disease 56 0.037
263
P SZR006 Seizure Disorder 56 0.037
264
BRN004 Brain Edema 56 0.037
265
AGN016 Aging 56 0.037
266
c FML035 Familial Hyperlipidemia 55 0.037
267
P DRR001 Diarrhea 55 0.037
268
DFF005 Diffuse Large B-Cell Lymphoma 55 0.037
269
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.037
270
P HYP076 Hyperthyroidism 55 0.037
271
P DBT005 Diabetes Insipidus 55 0.037
272
SYN007 Synovitis 54 0.037
273
P SPN052 Spondyloarthropathy 54 0.037
274
PRT082 Preterm Premature Rupture of the Membranes 54 0.037
275
HRT012 Heart Valve Disease 53 0.037
276
INF034 Infective Endocarditis 53 0.037
277
c PSR017 Psoriasis 2 53 0.037
278
NRT004 Neuritis 52 0.037
279
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.037
280
PST011 Pustulosis of Palm and Sole 52 0.037
281
c PSR023 Psoriasis 1 52 0.037
282
ART074 Aortic Dissection 52 0.037
283
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.037
284
OCL069 Ocular Motor Apraxia 51 0.037
285
PLS009 Plasma Cell Neoplasm 51 0.037
286
BRX001 Bruxism 50 0.037
287
CRN030 Coronary Stenosis 50 0.037
288
PYD002 Pyoderma 50 0.037
289
ART017 Aortic Disease 49 0.037
290
VCC001 Vaccinia 49 0.037
291
LRN003 Learning Disability 49 0.037
292
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.037
293
FBR009 Fibrous Dysplasia 48 0.037
294
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.037
295
c PSR032 Psoriasis 11 47 0.037
296
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.037
297
LYM019 Lymphosarcoma 46 0.037
298
P ART106 Arterial Calcification, Generalized, of Infancy, 1 46 0.037
299
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.037
300
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.037
301
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.037
302
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.037
303
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.037
304
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.037
305
MRG013 Mirage Syndrome 43 0.037
306
ORL015 Oral Squamous Cell Carcinoma 43 0.037
307
TRP009 Triple X Syndrome 42 0.037
308
P AVS003 Avascular Necrosis 42 0.037
309
c PSR028 Psoriasis 7 42 0.037
310
c PSR018 Psoriasis 13 41 0.037
311
LKP003 Leukoplakia 39 0.037
312
OST160 Osteoid Osteoma 37 0.037
313
PLC002 Plica Syndrome 36 0.037
314
c PRM243 Primary Bone Cancer 24 0.037
315
MNS002 Mini Stroke 19 0.037
316
P OVR042 Ovarian Cancer 88 0.030
317
c LKM061 Leukemia, Acute Myeloid 84 0.030
318
P PNC035 Pancreatic Cancer 84 0.030
319
CYS001 Cystic Fibrosis 81 0.030
320
P GLM040 Glioma Susceptibility 1 81 0.030
321
P LKM071 Leukemia, Chronic Lymphocytic 79 0.030
322
P LNG064 Lung Cancer Susceptibility 3 78 0.030
323
P PRK057 Parkinson Disease, Late-Onset 78 0.030
324
MRF001 Marfan Syndrome 77 0.030
325
P SCH015 Schizophrenia 74 0.030
326
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.030
327
P CNR004 Cone-Rod Dystrophy 2 73 0.030
328
P MLT020 Multiple Sclerosis 72 0.030
329
c HPT073 Hepatitis C Virus 72 0.030
330
P GRF003 Graft-Versus-Host Disease 72 0.030
331
c LKM063 Leukemia, Chronic Myeloid 72 0.030
332
P PHC003 Pheochromocytoma 71 0.030
333
PRP027 Peripheral Vascular Disease 71 0.030
334
CNG034 Congestive Heart Failure 69 0.030
335
PLM001 Pulmonary Tuberculosis 69 0.030
336
P MLN008 Melanoma 69 0.030
337
EWN003 Ewing Sarcoma 69 0.030
338
P LKM062 Leukemia, Acute Lymphoblastic 69 0.030
339
P MYC084 Mycobacterium Tuberculosis 1 68 0.030
340
CHL065 Cholangiocarcinoma 68 0.030
341
c BSL007 Basal Cell Carcinoma 68 0.030
342
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.030
343
P THR014 Thrombocytopenia 67 0.030
344
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.030
345
c INF071 Inflammatory Bowel Disease 1 67 0.030
346
FCT007 Factor Vii Deficiency 67 0.030
347
BRK010 Burkitt Lymphoma 67 0.030
348
P CHR012 Chronic Granulomatous Disease 67 0.030
349
FLL027 Fallopian Tube Carcinoma 67 0.030
350
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.030
351
ALC007 Alcohol Dependence 66 0.030
352
P FML364 Familial Thoracic Aortic Aneurysm and Aortic Dissection 66 0.030
353
c FML021 Familial Hypercholesterolemia 66 0.030
354
P NSP012 Nasopharyngeal Carcinoma 66 0.030
355
P MCR115 Microvascular Complications of Diabetes 5 66 0.030
356
KHL003 Kohlschutter-Tonz Syndrome 65 0.030
357
IRR002 Irritable Bowel Syndrome 65 0.030
358
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.030
359
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.030
360
DGR001 Digeorge Syndrome 64 0.030
361
HMT002 Hematologic Cancer 62 0.030
362
CLT003 Colitis 62 0.030
363
c HPT003 Hepatitis a 62 0.030
364
TKY002 Takayasu Arteritis 62 0.030
365
c SVR001 Severe Acute Respiratory Syndrome 62 0.030
366
P VSC011 Vasculitis 62 0.030
367
P PRM006 Primary Biliary Cirrhosis 62 0.030
368
MSL001 Measles 62 0.030
369
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.030
370
FTT001 Fatty Liver Disease 61 0.030
371
c PNS012 Paine Syndrome 61 0.030
372
P ENC018 Encephalopathy 61 0.030
373
P SJG008 Sjogren Syndrome 61 0.030
374
SDD001 Sudden Infant Death Syndrome 61 0.030
375
P LPS004 Lupus Erythematosus 61 0.030
376
P HMN010 Hemangioma 61 0.030
377
P ART067 Aortic Aneurysm, Familial Thoracic 1 61 0.030
378
P MYL006 Myeloid Leukemia 60 0.030
379
NPH091 Nephrolithiasis, Calcium Oxalate 60 0.030
380
P KDN017 Kidney Cancer 60 0.030
381
P NPH012 Nephrotic Syndrome 60 0.030
382
DPH001 Diphtheria 60 0.030
383
CHR288 Chronic Recurrent Multifocal Osteomyelitis 60 0.030
384
P SCL018 Scoliosis 60 0.030
385
P ALP009 Alopecia Areata 60 0.030
386
SQM006 Squamous Cell Carcinoma 60 0.030
387
P ATR010 Atrial Heart Septal Defect 60 0.030
388
ORL011 Oral Cancer 60 0.030
389
P THL005 Thalassemia 60 0.030
390
CHL123 Chlamydia 59 0.030
391
VSL002 Visual Epilepsy 59 0.030
392
P MLN069 Melanoma, Uveal 59 0.030
393
P CYS018 Cystitis 59 0.030
394
ADN018 Adenoma 59 0.030
395
c ACT073 Acute Leukemia 58 0.030
396
P SYP003 Syphilis 58 0.030
397
PST028 Post-Traumatic Stress Disorder 58 0.030
398
SPS150 Spastic Ataxia, Charlevoix-Saguenay Type 58 0.030
399
P ALC033 Alcohol Use Disorder 58 0.030
400
CNT047 Contact Dermatitis 58 0.030
401
P URT039 Urticaria 58 0.030
402
P INF032 Infertility 57 0.030
403
P OPT009 Optic Neuritis 57 0.030
404
BLM002 Bulimia Nervosa 57 0.030
405
MCR013 Microphthalmia 57 0.030
406
CMM005 Common Cold 57 0.030
407
c BSL024 Basal Cell Carcinoma 1 56 0.030
408
P MYS005 Myositis 56 0.030
409
ATR057 Atrioventricular Block 55 0.030
410
ORP003 Oropharynx Cancer 55 0.030
411
c CRD184 Ceroid Lipofuscinosis, Neuronal, 5 55 0.030
412
CHR100 Chronic Ulcer of Skin 55 0.030
413
ACT058 Active Peptic Ulcer Disease 55 0.030
414
P SBS003 Substance Abuse 55 0.030
415
P DRM007 Dermatitis Herpetiformis 55 0.030
416
HMZ003 Homozygous Familial Hypercholesterolemia 55 0.030
417
URN010 Urinary Tract Obstruction 55 0.030
418
END040 Endogenous Depression 55 0.030
419
PYD001 Pyoderma Gangrenosum 54 0.030
420
GLC003 Glucose Intolerance 54 0.030
421
P ALP008 Alopecia 54 0.030
422
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.030
423
AMN001 Amenorrhea 54 0.030
424
LYM040 Lymphoblastic Lymphoma 54 0.030
425
CLR030 Clear Cell Renal Cell Carcinoma 53 0.030
426
P MNC007 Monocytic Leukemia 53 0.030
427
PRP036 Peripheral T-Cell Lymphoma 53 0.030
428
CRH005 Crohn's Colitis 53 0.030
429
P RTN016 Retinal Degeneration 53 0.030
430
OCL006 Ocular Hypertension 53 0.030
431
P SHR001 Short Bowel Syndrome 53 0.030
432
NRT001 Neurotic Disorder 53 0.030
433
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.030
434
ACR041 Acromelic Frontonasal Dysostosis 52 0.030
435
P SML001 Small Cell Carcinoma 52 0.030
436
MRG003 Marginal Zone B-Cell Lymphoma 52 0.030
437
THY030 Thyroid Gland Disease 52 0.030
438
DFF036 Differentiated Thyroid Carcinoma 52 0.030
439
NTR018 Neutrophilia, Hereditary 52 0.030
440
SRS001 Serous Cystadenocarcinoma 52 0.030
441
P HMP007 Hemophilia 51 0.030
442
P SPP010 Suppressor of Tumorigenicity 3 51 0.030
443
P LCT001 Lactic Acidosis 51 0.030
444
INT079 Intrahepatic Cholangiocarcinoma 51 0.030
445
SPL004 Splenic Marginal Zone Lymphoma 51 0.030
446
HYP081 Hypolipoproteinemia 51 0.030
447
FSC004 Fasciitis 50 0.030
448
c ACH020 Achromatopsia 2 50 0.030
449
ILT001 Ileitis 50 0.030
450
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.030
451
HRT011 Heart Septal Defect 50 0.030
452
HYP017 Hypophosphatemia 50 0.030
453
CRN048 Craniofacial-Deafness-Hand Syndrome 49 0.030
454
TRT020 Tritanopia 49 0.030
455
P CTN015 Cutaneous T Cell Lymphoma 49 0.030
456
HST010 Histiocytosis 48 0.030
457
ASP007 Aspiration Pneumonia 48 0.030
458
P CLR019 Color Blindness 48 0.030
459
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.030
460
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.030
461
CHL056 Cheilitis 48 0.030
462
RTC005 Reticulosarcoma 47 0.030
463
PLS025 Plasmablastic Lymphoma 47 0.030
464
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.030
465
EXS001 Exostosis 46 0.030
466
ADR040 Adrenal Gland Pheochromocytoma 46 0.030
467
ANR004 Anuria 46 0.030
468
c MLG068 Malignant Glioma 46 0.030
469
MXD026 Mixed Glioma 45 0.030
470
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.030
471
ASP008 Aspiration Pneumonitis 45 0.030
472
LTH001 Lethal Midline Granuloma 44 0.030
473
SPN040 Spinal Cancer 44 0.030
474
c HYP272 Hypercholesterolemia, Familial, 3 44 0.030
475
DMP001 Dumping Syndrome 44 0.030
476
c PRM038 Primary Agammaglobulinemia 44 0.030
477
CVD001 Covid-19 44 0.030
478
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.030
479
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.030
480
ORB013 Orbital Disease 42 0.030
481
INT276 Interatrial Communication 42 0.030
482
CLR033 Color Vision Deficiency 41 0.030
483
TTT001 Tatton-Brown-Rahman Syndrome 41 0.030
484
SLT009 Solitary Bone Cyst 39 0.030
485
ENT001 Enterocele 39 0.030
486
NTR042 Neutrophilic Dermatosis, Acute Febrile 38 0.030
487
c SYS043 Systemic Lupus Erythematosus 1 38 0.030
488
GLB021 Global Developmental Delay, Absent or Hypoplastic Corpus Callosum, and Dysmorphic Facies 38 0.030
489
ATM052 Autoimmune Disease 1 37 0.030
490
CHR079 Choroid Disease 37 0.030
491
END028 Endemic Goiter 37 0.030
492
DNT046 Dental Abscess 35 0.030
493
c DRM040 Dermatitis Herpetiformis, Familial 35 0.030
494
ANT066 Anterior Cutaneous Nerve Entrapment Syndrome 34 0.030
495
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.030
496
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.030
497
SML011 Smoldering Myeloma 33 0.030
498
c CHR064 Chronic Monocytic Leukemia 33 0.030
499
BRN034 Brain Meningioma 33 0.030
500
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.030
501
EXT064 Extraoral Halitosis Due to Methanethiol Oxidase Deficiency 30 0.030
502
ALV001 Alveolar Periostitis 30 0.030
503
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.030
504
HYP823 Hypotonia, Ataxia, Developmental Delay, and Tooth Enamel Defect Syndrome 28 0.030
505
BNG077 Benign Idiopathic Neonatal Seizures 26 0.030
506
EPL050 Epilepsy, Partial, with Pericentral Spikes 25 0.030
507
PRN071 Parenteral Nutrition-Associated Cholestasis 25 0.030
508
HDG004 Hodgkin's Granuloma 23 0.030
509
HDG006 Hodgkin's Paragranuloma 22 0.030
510
CMB039 Combined Pulmonary Fibrosis-Emphysema Syndrome 20 0.030
511
ESP021 Esophageal Cancer 90 0.021
512
MLR004 Malaria 81 0.021
513
c DLT002 Dilated Cardiomyopathy 79 0.021
514
P MDL005 Medulloblastoma 77 0.021
515
c TBR025 Tuberous Sclerosis 1 77 0.021
516
c NRF024 Neurofibromatosis, Type I 77 0.021
517
CRV035 Cervical Cancer 76 0.021
518
P NNN008 Noonan Syndrome 1 76 0.021
519
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.021
520
BRN028 Brain Cancer 74 0.021
521
SCK003 Sickle Cell Anemia 74 0.021
522
LPT014 Leptin Deficiency or Dysfunction 74 0.021
523
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.021
524
ULC004 Ulcerative Colitis 73 0.021
525
c THR092 Thrombophilia Due to Thrombin Defect 73 0.021
526
P RTN024 Retinoblastoma 73 0.021
527
MSC157 Muscular Dystrophy, Duchenne Type 72 0.021
528
SCH036 Scheie Syndrome 72 0.021
529
c TBR026 Tuberous Sclerosis 2 72 0.021
530
P FML011 Familial Adenomatous Polyposis 72 0.021
531
P WSK001 Wiskott-Aldrich Syndrome 72 0.021
532
GST040 Gastric Adenocarcinoma 70 0.021
533
MYL009 Myelodysplastic Syndrome 70 0.021
534
MYL005 Myelofibrosis 70 0.021
535
ADN011 Adenoid Cystic Carcinoma 70 0.021
536
P HYP061 Hypertrophic Cardiomyopathy 70 0.021
537
P FRG001 Fragile X Syndrome 70 0.021
538
P TTR001 Tetralogy of Fallot 70 0.021
539
P MYP004 Myopathy 70 0.021
540
P TBR001 Tuberous Sclerosis 70 0.021
541
P DMN001 Diamond-Blackfan Anemia 69 0.021
542
PLY001 Polycythemia Vera 69 0.021
543
ACR008 Acrocallosal Syndrome 69 0.021
544
MNT001 Mantle Cell Lymphoma 69 0.021
545
P TMP003 Temporal Arteritis 68 0.021
546
P LVR013 Liver Disease 68 0.021
547
P SYS005 Systemic Scleroderma 68 0.021
548
SKN019 Skin Melanoma 68 0.021
549
P INF038 Influenza 68 0.021
550
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.021
551
BRN024 Bronchitis 68 0.021
552
CNN005 Connective Tissue Disease 68 0.021
553
P MJR001 Major Depressive Disorder 68 0.021
554
P FRN006 Frontotemporal Dementia 68 0.021
555
PNC129 Pancreatic Adenocarcinoma 68 0.021
556
HYL004 Hyaline Fibromatosis Syndrome 67 0.021
557
P HPT021 Hepatitis 67 0.021
558
P OLG002 Oligodendroglioma 67 0.021
559
P FLL037 Follicular Lymphoma 67 0.021
560
ALL003 Allergic Rhinitis 67 0.021
561
c HMP029 Hemophilia a 67 0.021
562
P HYP098 Hypereosinophilic Syndrome 67 0.021
563
P BLD062 Bile Duct Cancer 67 0.021
564
CRP001 Carpal Tunnel Syndrome 67 0.021
565
P MLG056 Malignant Hyperthermia 67 0.021
566
c MGR028 Migraine with or Without Aura 1 67 0.021
567
MYC006 Mycosis Fungoides 66 0.021
568
P CLC063 Celiac Disease 1 66 0.021
569
P LNG028 Long Qt Syndrome 66 0.021
570
P MSC005 Muscular Dystrophy 66 0.021
571
P SKN015 Skin Carcinoma 66 0.021
572
c FML346 Familial Adenomatous Polyposis 1 66 0.021
573
c DBT091 Diabetes Insipidus, Nephrogenic, Autosomal 66 0.021
574
P ATR011 Atrial Fibrillation 66 0.021
575
P HYD006 Hydrocephalus 66 0.021
576
P DRM053 Dermatitis, Atopic 66 0.021
577
MYL031 Myeloproliferative Neoplasm 66 0.021
578
P NRV007 Nervous System Disease 66 0.021
579
c MCL013 Mucolipidosis Iv 66 0.021
580
c SML038 Small Cell Cancer of the Lung 65 0.021
581
c HYP604 Hyperinsulinemic Hypoglycemia, Familial, 2 65 0.021
582
CRN036 Craniopharyngioma 65 0.021
583
P PLM036 Pulmonary Fibrosis 65 0.021
584
c FML001 Familial Atrial Fibrillation 65 0.021
585
P ART005 Arteriovenous Malformation 65 0.021
586
DMN031 Dementia, Lewy Body 65 0.021
587
SRC014 Sarcoma 65 0.021
588
P MTR004 Maturity-Onset Diabetes of the Young 65 0.021
589
P PSD087 Pseudoxanthoma Elasticum 65 0.021
590
ATM096 Autoimmune Polyendocrine Syndrome, Type I, with or Without Reversible Metaphyseal Dysplasia 65 0.021
591
BRR014 Barrett Esophagus 65 0.021
592
ATX029 Ataxia, Early-Onset, with Oculomotor Apraxia and Hypoalbuminemia 65 0.021
593
GRN037 Granulomatosis with Polyangiitis 65 0.021
594
P PRS038 Personality Disorder 65 0.021
595
P ADL010 Adult Respiratory Distress Syndrome 65 0.021
596
APN008 Apnea, Obstructive Sleep 64 0.021
597
ALC028 Alacrima, Achalasia, and Mental Retardation Syndrome 64 0.021
598
P NRN021 Neuronal Ceroid Lipofuscinosis 64 0.021
599
NRF007 Neurofibroma 64 0.021
600
OVR029 Ovarian Hyperstimulation Syndrome 64 0.021
601
c MSC036 Muscular Dystrophy-Dystroglycanopathy , Type C, 5 64 0.021
602
P MST009 Mastocytosis 64 0.021
603
TBC004 Tobacco Addiction 64 0.021
604
c JVN010 Juvenile Rheumatoid Arthritis 64 0.021
605
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.021
606
MSC007 Muscle Hypertrophy 64 0.021
607
PLM031 Poliomyelitis 64 0.021
608
P CRN015 Cornelia De Lange Syndrome 64 0.021
609
DSM004 Desmoid Tumor 64 0.021
610
MGK001 Megakaryocytic Leukemia 64 0.021
611
c PRC016 Pre-Eclampsia 63 0.021
612
ACT119 Acute Promyelocytic Leukemia 63 0.021
613
END041 Endometrial Adenocarcinoma 63 0.021
614
CHR063 Chronic Mucocutaneous Candidiasis 63 0.021
615
P HRD008 Hereditary Hemorrhagic Telangiectasia 63 0.021
616
c ACT068 Acute Cystitis 63 0.021
617
c ATM011 Autoimmune Hepatitis 63 0.021
618
c ALP101 Alpha-Thalassemia 62 0.021
619
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.021
620
c HPT001 Hepatitis C 62 0.021
621
3HY005 3-Hydroxyacyl-Coa Dehydrogenase Deficiency 62 0.021
622
P SPN046 Spinal Muscular Atrophy 62 0.021
623
P ESP024 Esophagitis 62 0.021
624
BLL006 Bullous Pemphigoid 62 0.021
625
CHR619 Chromosome 2q35 Duplication Syndrome 62 0.021
626
P FRN044 Frontotemporal Dementia and/or Amyotrophic Lateral Sclerosis 1 62 0.021
627
CRC021 Carcinosarcoma 62 0.021
628
MSS001 Masa Syndrome 62 0.021
629
BLD131 Bladder Urothelial Carcinoma 62 0.021
630
P DRM010 Dermatomyositis 61 0.021
631
PSR001 Psoriatic Arthritis 61 0.021
632
P INT143 Interstitial Cystitis 61 0.021
633
P LYM113 Lymphoproliferative Syndrome, X-Linked, 1 61 0.021
634
WLD007 Waldenstroem's Macroglobulinemia 61 0.021
635
c WLM018 Wilms Tumor 5 61 0.021
636
VRL011 Viral Infectious Disease 61 0.021
637
c HYP304 Hyperinsulinemic Hypoglycemia, Familial, 1 61 0.021
638
SZR001 Sezary's Disease 60 0.021
639
c JVN061 Juvenile Arthritis 60 0.021
640
P TXP001 Toxoplasmosis 60 0.021
641
P BNG030 Benign Ependymoma 60 0.021
642
INT066 Interstitial Lung Disease 60 0.021
643
P VNT002 Ventricular Septal Defect 60 0.021
644
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.021
645
RHM001 Rheumatic Fever 60 0.021
646
PMS001 Poems Syndrome 60 0.021
647
VRC005 Varicose Veins 60 0.021
648
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.021
649
P CTR002 Cataract 60 0.021
650
P CHR285 Chronic Myelomonocytic Leukemia 60 0.021
651
P HRD011 Hereditary Spherocytosis 60 0.021
652
P OPT006 Optic Nerve Disease 60 0.021
653
SPP011 Suppression of Tumorigenicity 12 59 0.021
654
P MYC008 Myocarditis 59 0.021
655
PRC038 Precocious Puberty, Male-Limited 59 0.021
656
PNM001 Pneumocystosis 59 0.021
657
c HPT016 Hepatitis B 59 0.021
658
P SLP005 Sleep Disorder 59 0.021
659
PLM033 Pulmonary Embolism 59 0.021
660
P LYM033 Lymphoproliferative Syndrome 59 0.021
661
DCT002 Ductal Carcinoma in Situ 59 0.021
662
P BRS044 Breast Adenocarcinoma 59 0.021
663
GRD007 Grade Iii Astrocytoma 59 0.021
664
P HMN036 Hemangiopericytoma, Malignant 59 0.021
665
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.021
666
P PLY006 Polydactyly 59 0.021
667
INC002 Inclusion Body Myositis 58 0.021
668
MCS006 Macs Syndrome 58 0.021
669
DST005 Diastrophic Dysplasia 58 0.021
670
c PRM005 Primary Hyperparathyroidism 58 0.021
671
CCC001 Coccidioidomycosis 58 0.021
672
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.021
673
BRS051 Breast Disease 58 0.021
674
NWB001 Newborn Respiratory Distress Syndrome 58 0.021
675
DSS008 Disease of Mental Health 58 0.021
676
c DWL002 Dowling-Degos Disease 1 58 0.021
677
LYM027 Lymphopenia 58 0.021
678
LNG108 Langerhans Cell Histiocytosis 58 0.021
679
MXD005 Mixed Connective Tissue Disease 58 0.021
680
P UVT001 Uveitis 57 0.021
681
P GLM007 Glomerulonephritis 57 0.021
682
c CHR417 Chronic Graft Versus Host Disease 57 0.021
683
GRN051 Granulomatous Disease, Chronic, X-Linked 57 0.021
684
BRN056 Bronchopulmonary Dysplasia 57 0.021
685
PLM070 Pulmonic Stenosis 57 0.021
686
P PLY041 Polymyositis 57 0.021
687
P RHN004 Rhinitis 57 0.021
688
P SLV026 Salivary Gland Carcinoma 57 0.021
689
c CRN139 Cornelia De Lange Syndrome 1 57 0.021
690
THY122 Thyroid Gland Cancer 57 0.021
691
LYM021 Lymphadenitis 57 0.021
692
c MST023 Mesothelioma, Malignant 57 0.021
693
APH001 Aphthous Stomatitis 57 0.021
694
P PRV006 Pervasive Developmental Disorder 57 0.021
695
c LKM070 Leukemia, Acute Monocytic 57 0.021
696
HMR039 Hemorrhage, Intracerebral 57 0.021
697
LNN001 Lennox-Gastaut Syndrome 57 0.021
698
P LKD017 Leukodystrophy, Hypomyelinating, 7, with or Without Oligodontia and/or Hypogonadotropic Hypogonadism 57 0.021
699
SKN022 Skin Squamous Cell Carcinoma 57 0.021
700
AYM001 Ayme-Gripp Syndrome 57 0.021
701
P PLY018 Polycythemia 56 0.021
702
P ADL017 Adult T-Cell Leukemia 56 0.021
703
CMR002 Coumarin Resistance 56 0.021
704
P FBR017 Fibrosarcoma 56 0.021
705
P PLY011 Polycystic Ovary Syndrome 56 0.021
706
TRN018 Transitional Cell Carcinoma 56 0.021
707
ALL006 Allergic Asthma 56 0.021
708
PLS011 Plasmacytoma 56 0.021
709
c ACT134 Acute Liver Failure 56 0.021
710
ERY051 Erythroleukemia, Familial 56 0.021
711
SFT003 Soft Tissue Sarcoma 56 0.021
712
GNR004 Generalized Anxiety Disorder 56 0.021
713
ISL001 Islet Cell Tumor 56 0.021
714
MTH009 Mouth Disease 56 0.021
715
HMG005 Hemoglobinopathy 56 0.021
716
P NRF002 Neurofibromatosis 56 0.021
717
INT030 Intracranial Aneurysm 56 0.021
718
P HYP024 Hypoparathyroidism 56 0.021
719
P PNM006 Pneumoconiosis 56 0.021
720
c GRV008 Graves Disease 1 56 0.021
721
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.021
722
BRN012 Bronchiolitis Obliterans 55 0.021
723
FLR001 Filarial Elephantiasis 55 0.021
724
NRN004 Neuroendocrine Tumor 55 0.021
725
MCL006 Macular Retinal Edema 55 0.021
726
P MLN007 Male Infertility 55 0.021
727
DFN344 Deafness, Onychodystrophy, Osteodystrophy, Mental Retardation, and Seizures Syndrome 55 0.021
728
CRC006 Carcinoid Syndrome 55 0.021
729
FLR002 Filariasis 55 0.021
730
EPT010 Epithelial-Myoepithelial Carcinoma 55 0.021
731
P VNS003 Venous Insufficiency 55 0.021
732
P HYP050 Hyperinsulinemic Hypoglycemia 55 0.021
733
P AML002 Amelogenesis Imperfecta 55 0.021
734
P LRY044 Larynx Cancer 55 0.021
735
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.021
736
HYP060 Hyperinsulinism 54 0.021
737
GLS001 Gliosarcoma 54 0.021
738
AMN003 Amnestic Disorder 54 0.021
739
CRT017 Cartilage Disease 54 0.021
740
VGN023 Vaginitis 54 0.021
741
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.021
742
GST037 Gastroparesis 54 0.021
743
AMY027 Amyotrophic Lateral Sclerosis-Parkinsonism/dementia Complex 1 54 0.021
744
PRT038 Protein-Energy Malnutrition 54 0.021
745
TND005 Tendinitis 54 0.021
746
CLL010 Cellular Ependymoma 54 0.021
747
HMS001 Hemosiderosis 54 0.021
748
PPL022 Papilloma 54 0.021
749
P TRM003 Tremor 54 0.021
750
NNL006 Non-Alcoholic Steatohepatitis 54 0.021
751
PRS045 Prostatic Hypertrophy 53 0.021
752
PLM012 Pulmonary Sarcoidosis 53 0.021
753
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.021
754
GST009 Gastroschisis 53 0.021
755
P LCT002 Lactose Intolerance 53 0.021
756
P TCD001 Tic Disorder 53 0.021
757
CRY001 Cryptogenic Organizing Pneumonia 53 0.021
758
c EXS019 Exostoses, Multiple, Type I 53 0.021
759
c DMN023 Diamond-Blackfan Anemia 1 53 0.021
760
P INS002 in Situ Carcinoma 53 0.021
761
PLS016 Plasma Cell Leukemia 53 0.021
762
BRN038 Bronchial Disease 53 0.021
763
ECH003 Echinococcosis 53 0.021
764
P CNT005 Central Nervous System Lymphoma 53 0.021
765
P ORL007 Oral Cavity Cancer 53 0.021
766
FNG017 Fungal Infectious Disease 53 0.021
767
CLF001 Cleft Lip 53 0.021
768
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.021
769
SPN035 Spindle Cell Sarcoma 53 0.021
770
INT051 Intussusception 53 0.021
771
P LMB006 Limb-Girdle Muscular Dystrophy 53 0.021
772
PRP080 Peripheral Artery Disease 53 0.021
773
c FML008 Familial Retinoblastoma 53 0.021
774
P INT068 Intestinal Disease 53 0.021
775
c HYP326 Hyperinsulinemic Hypoglycemia, Familial, 5 53 0.021
776
c CNT035 Central Nervous System Disease 52 0.021
777
FRY006 Fryns Microphthalmia Syndrome 52 0.021
778
P SPN429 Spinocerebellar Ataxia, Autosomal Recessive, with Axonal Neuropathy 2 52 0.021
779
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.021
780
c HYP601 Hyperinsulinemic Hypoglycemia, Familial, 3 52 0.021
781
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.021
782
GLM004 Gliomatosis Cerebri 52 0.021
783
PLS007 Plasmodium Falciparum Malaria 52 0.021
784
P RCT021 Rectum Cancer 52 0.021
785
CRT016 Carotid Artery Disease 52 0.021
786
DYS015 Dysentery 52 0.021
787
P MSC003 Muscular Atrophy 52 0.021
788
ACT200 Acute Monoblastic Leukemia 52 0.021
789
TLN003 Telangiectasis 52 0.021
790
P OVR049 Ovarian Disease 52 0.021
791
INV006 Inverted Papilloma 52 0.021
792
c ACT135 Acute Graft Versus Host Disease 52 0.021
793
P BRN035 Brain Stem Glioma 52 0.021
794
P TRT010 Teratoma 52 0.021
795
THR004 Thrombocytosis 51 0.021
796
MCR088 Microscopic Polyangiitis 51 0.021
797
TRC010 Trichotillomania 51 0.021
798
FCT001 Factor Viii Deficiency 51 0.021
799
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.021
800
PRS021 Prostatic Adenoma 51 0.021
801
FDL002 Food Allergy 51 0.021
802
ILS001 Ileus 51 0.021
803
ENT011 Enterocolitis 51 0.021
804
CYS014 Cystadenocarcinoma 51 0.021
805
LNG031 Lung Benign Neoplasm 51 0.021
806
TRM010 Traumatic Brain Injury 51 0.021
807
P PRC012 Pericardial Effusion 51 0.021
808
ACH005 Achalasia 51 0.021
809
FBR008 Fibrillary Astrocytoma 51 0.021
810
TNG007 Tongue Carcinoma 51 0.021
811
P AST007 Astrocytoma 51 0.021
812
CRV040 Cervix Carcinoma 51 0.021
813
SKN013 Skin Benign Neoplasm 51 0.021
814
HYP781 Hypoascorbemia 51 0.021
815
GNT002 Giant Cell Glioblastoma 50 0.021
816
P OVR082 Overgrowth Syndrome 50 0.021
817
c HYP271 Hyperinsulinemic Hypoglycemia, Familial, 4 50 0.021
818
AZS001 Azoospermia 50 0.021
819
ASC010 Ascaris Lumbricoides Infection 50 0.021
820
c INF145 Infantile Liver Failure Syndrome 1 50 0.021
821
MCP006 Mucoepidermoid Carcinoma 50 0.021
822
CYT005 Cytomegalovirus Retinitis 50 0.021
823
PLM017 Pulmonary Alveolar Microlithiasis 50 0.021
824
P TMP001 Temporal Lobe Epilepsy 50 0.021
825
PLC008 Placenta Disease 50 0.021
826
P PNB001 Pineoblastoma 50 0.021
827
CLR003 Clear Cell Adenocarcinoma 50 0.021
828
OPT003 Opiate Dependence 50 0.021
829
P ATR005 Atrophic Gastritis 50 0.021
830
ATY042 Atypical Chronic Myeloid Leukemia 49 0.021
831
ENT004 Enthesopathy 49 0.021
832
P EST001 Estrogen-Receptor Positive Breast Cancer 49 0.021
833
c CHR431 Chronic Venous Insufficiency 49 0.021
834
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.021
835
PRN014 Paronychia 49 0.021
836
PRS129 Prostatic Hyperplasia, Benign 49 0.021
837
CCN002 Cocaine Abuse 49 0.021
838
SLD003 Sialadenitis 49 0.021
839
MCR004 Macroglobulinemia 49 0.021
840
PLM041 Pulmonary Valve Stenosis 49 0.021
841
GST049 Gastrointestinal System Cancer 49 0.021
842
c FLL041 Follicular Lymphoma 1 49 0.021
843
BKR002 Baker-Gordon Syndrome 49 0.021
844
P CRV031 Cervical Adenocarcinoma 49 0.021
845
BRN071 Brain Injury 49 0.021
846
PTH002 Pathological Gambling 49 0.021
847
HYP043 Hyperandrogenism 48 0.021
848
THY123 Thyroid Gland Follicular Carcinoma 48 0.021
849
WTH001 Withdrawal Disorder 48 0.021
850
ATS010 Autosomal Recessive Disease 48 0.021
851
ADT003 Auditory System Disease 48 0.021
852
CCN001 Cocaine Dependence 48 0.021
853
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.021
854
OLF005 Olfactory Neuroblastoma 48 0.021
855
P NGH001 Night Blindness 48 0.021
856
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.021
857
ACT098 Acute Erythroid Leukemia 48 0.021
858
BLT006 Bilateral Breast Cancer 48 0.021
859
CLS016 Clostridium Difficile Colitis 48 0.021
860
P ASP001 Asperger Syndrome 48 0.021
861
HYP068 Hyperostosis 48 0.021
862
PRS012 Pars Planitis 48 0.021
863
HMP001 Hemopericardium 48 0.021
864
c MTR002 Mitral Valve Insufficiency 48 0.021
865
DSM003 Desmoid Disease, Hereditary 48 0.021
866
LPT006 Leptin Receptor Deficiency 48 0.021
867
c PRM226 Primary Central Nervous System Lymphoma 48 0.021
868
MLK006 Milk Allergy 48 0.021
869
RCT020 Rectum Adenocarcinoma 48 0.021
870
OPD006 Opioid Addiction 48 0.021
871
c HYD064 Hydrocephalus, Congenital, 1 48 0.021
872
ANT018 Anthracosis 48 0.021
873
SXL003 Sexual Disorder 47 0.021
874
ADN009 Adenosquamous Carcinoma 47 0.021
875
DRG003 Drug Dependence 47 0.021
876
ASB001 Asbestosis 47 0.021
877
CRC014 Carcinoid Tumors, Intestinal 47 0.021
878
PPL002 Papillary Carcinoma 47 0.021
880
CRN027 Corneal Neovascularization 47 0.021
881
NRN001 Neuroendocrine Carcinoma 47 0.021
882
ACT084 Acute Stress Disorder 47 0.021
883
SPC010 Speech and Communication Disorders 47 0.021
884
LYM012 Lymphoplasmacytic Lymphoma 47 0.021
885
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.021
886
c CNG216 Congenital Hydrocephalus 47 0.021
887
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.021
888
HYP082 Hypopharynx Cancer 47 0.021
889
GST071 Gastrointestinal Carcinoma 47 0.021
890
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.021
891
ANV001 Anovulation 47 0.021
892
P CRC039 Coarctation of Aorta 47 0.021
893
CNT033 Central Nervous System Cancer 47 0.021
894
CRD137 Cardiogenic Shock 47 0.021
895
P PRC019 Precocious Puberty 46 0.021
896
RTN023 Retinitis 46 0.021
897
c CNT075 Central Precocious Puberty 46 0.021
898
ASP004 Asphyxia Neonatorum 46 0.021
899
P ATM019 Autoimmune Polyendocrine Syndrome 46 0.021
900
ORC001 Orchitis 46 0.021
901
PRP017 Periapical Periodontitis 46 0.021
902
c SPL067 Split-Hand/foot Malformation 1 46 0.021
903
CLN045 Colonic Benign Neoplasm 46 0.021
904
UMB002 Umbilical Hernia 46 0.021
905
P PLL002 Pellagra 46 0.021
906
P LPC002 Lip Cancer 46 0.021
907
P CHR573 Choroid Plexus Cancer 46 0.021
908
FLL008 Folliculitis 46 0.021
909
P BNG032 Benign Mesothelioma 46 0.021
910
ANP006 Anaplastic Ependymoma 46 0.021
911
CHR008 Choroiditis 46 0.021
912
SQM002 Squamous Cell Papilloma 46 0.021
913
P HRD001 Hereditary Multiple Exostoses 46 0.021
914
SVN002 Sveinsson Chorioretinal Atrophy 46 0.021
915
EPD015 Epidemic Typhus 45 0.021
916
SYN036 Syncope 45 0.021
917
CNV002 Conversion Disorder 45 0.021
918
PPL018 Papillary Adenocarcinoma 45 0.021
919
URT010 Ureteral Obstruction 45 0.021
920
CYN002 Cyanosis, Transient Neonatal 45 0.021
921
HMR023 Hemorrhagic Cystitis 45 0.021
922
DST006 Diastolic Heart Failure 45 0.021
923
P OCY003 Oocyte Maturation Defect 1 45 0.021
924
HMR002 Hemarthrosis 45 0.021
925
ESP027 Esophagus Squamous Cell Carcinoma 45 0.021
926
PNC056 Pineocytoma 45 0.021
927
THR099 Third-Degree Atrioventricular Block 45 0.021
928
LYM051 Lymphomatoid Granulomatosis 45 0.021
929
IMP006 Impulse Control Disorder 45 0.021
930
MLN073 Melanosis, Neurocutaneous 45 0.021
931
GRD001 Giardiasis 45 0.021
932
CNT017 Central Nervous System Origin Vertigo 45 0.021
933
ISL121 Isolated Split Hand-Split Foot Malformation 45 0.021
934
SPS057 Spasticity 45 0.021
935
MLC004 Mulchandani-Bhoj-Conlin Syndrome 44 0.021
936
MXD023 Mixed Cell Type Cancer 44 0.021
937
ASP026 Asplenia, Isolated Congenital 44 0.021
938
c DRM054 Dermatitis, Atopic, 2 44 0.021
939
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.021
940
SBC016 Subacute Delirium 44 0.021
941
CYS009 Cystadenoma 44 0.021
942
APP009 Appendix Adenocarcinoma 44 0.021
943
CRD003 Cardiac Sarcoidosis 44 0.021
944
CHL149 Childhood Acute Myeloid Leukemia 44 0.021
945
P SMK004 Smoking As a Quantitative Trait Locus 3 44 0.021
946
APP010 Appendix Cancer 44 0.021
947
ACH015 Achalasia, Familial Esophageal 44 0.021
948
HPT067 Hepatocellular Adenoma 44 0.021
949
HRN003 Heroin Dependence 44 0.021
950
c GZP005 Gaze Palsy, Familial Horizontal, with Progressive Scoliosis 1 44 0.021
951
PRT035 Peritoneum Cancer 44 0.021
952
THR012 Thoracic Cancer 44 0.021
953
P EPN001 Ependymoblastoma 44 0.021
954
FBR054 Fibroma 44 0.021
955
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 0.021
956
ANP009 Anaplastic Oligodendroglioma 43 0.021
957
TND004 Tendinopathy 43 0.021
958
TST015 Testicular Disease 43 0.021
959
BNM001 Bone Marrow Cancer 43 0.021
960
LWC001 Low Compliance Bladder 43 0.021
961
MGS001 Megaesophagus 43 0.021
962
c SRC023 Sarcoidosis 2 43 0.021
963
SPR008 Supratentorial Primitive Neuroectodermal Tumor 43 0.021
964
PLY068 Polysubstance Abuse 43 0.021
965
MDD018 Middle East Respiratory Syndrome 43 0.021
966
NNT033 Neonatal Hypoxic and Ischemic Brain Injury 43 0.021
967
BLR013 Biliary Tract Cancer 42 0.021
968
CHR286 Chronic Neutrophilic Leukemia 42 0.021
969
c MLG079 Malignant Pleural Mesothelioma 42 0.021
970
c HYP057 Hypervitaminosis D 42 0.021
971
IDP070 Idiopathic Scoliosis 42 0.021
972
NRR001 Neuroretinitis 42 0.021
973
OPT007 Optic Nerve Glioma 42 0.021
974
c ATS307 Autosomal Recessive Cerebellar Ataxia 42 0.021
975
ANC002 Anca-Associated Vasculitis 41 0.021
976
FBR019 Fibromatosis 41 0.021
977
c MLG064 Malignant Ependymoma 41 0.021
978
P NSL008 Nasal Cavity Cancer 41 0.021
979
OST004 Osteitis Fibrosa 41 0.021
980
MYS001 Myositis Ossificans 41 0.021
981
ELP001 Elephantiasis 41 0.021
982
MTL005 Metal Allergy 41 0.021
983
LYM010 Lymph Node Tuberculosis 41 0.021
984
PNL014 Pineal Gland Cancer 41 0.021
985
PRS063 Paresthesia 41 0.021
986
P RRH023 Rare Hereditary Hemochromatosis 41 0.021
987
P SCL057 Scoliosis, Isolated 1 41 0.021
988
KLB003 Klebsiella Pneumonia 41 0.021
989
P SPS008 Spastic Ataxia 41 0.021
990
MRP001 Morphine Dependence 41 0.021
991
P MLG074 Malignant Mesenchymoma 40 0.021
992
c ADL096 Adult Hepatocellular Carcinoma 40 0.021
993
ANX004 Anoxia 40 0.021
994
PPL007 Papillary Serous Adenocarcinoma 40 0.021
995
P DYS005 Dyslexia 40 0.021
996
P ALK015 Alk-Positive Anaplastic Large Cell Lymphoma 40 0.021
997
PRM024 Primary Angle-Closure Glaucoma 40 0.021
998
SBP002 Subependymal Glioma 40 0.021
999
MLT001 Multiple Chemical Sensitivity 40 0.021
1000
CRB086 Cerebral Aneurysms 40 0.021
1001
OCL010 Ocular Hypotension 39 0.021
1002
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.021
1003
ALX001 Alexia 39 0.021
1004
P INT260 Intracranial Berry Aneurysm 39 0.021
1005
WLL004 Wallerian Degeneration 39 0.021
1006
c PGT007 Paget Disease of Bone 3 39 0.021
1007
c ATM002 Autoimmune Polyendocrine Syndrome Type 1 39 0.021
1008
RTC012 Reticuloendotheliosis, X-Linked 39 0.021
1009
c HRD104 Hereditary Multiple Osteochondromas 39 0.021
1010
NRD004 Neurodegeneration Due to Cerebral Folate Transport Deficiency 39 0.021
1011
DSS010 Dissociative Disorder 39 0.021
1012
SLP010 Slipped Capital Femoral Epiphysis 39 0.021
1013
c PLY105 Polycystic Ovary Syndrome 1 38 0.021
1014
c OVR114 Ovarian Cancer 1 38 0.021
1015
HYP001 Hypochromic Microcytic Anemia 38 0.021
1016
THY124 Thyroid Gland Papillary Carcinoma 38 0.021
1017
SWL001 Swallowing Disorders 38 0.021
1018
c ANM035 Anemia, Hypochromic Microcytic, with Iron Overload 1 38 0.021
1019
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.021
1020
TRC020 Tracheitis 36 0.021
1021
ACT040 Acute Poststreptococcal Glomerulonephritis 36 0.021
1022
TTH032 Tooth Size 36 0.021
1023
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.021
1024
ABD010 Abdominal Wall Defect 36 0.021
1025
ENT008 Enteropathy-Associated T-Cell Lymphoma 36 0.021
1026
DNT008 Denture Stomatitis 35 0.021
1027
ASC001 Ascaridiasis 35 0.021
1028
PRM329 Premature Aging 35 0.021
1029
TNN002 Tinea Unguium 35 0.021
1030
NRD001 Neurodermatitis 35 0.021
1031
c MLN043 Melanoma, Cutaneous Malignant 8 34 0.021
1032
c LKM005 Leukemia, T-Cell, Chronic 34 0.021
1033
P BNL002 Bone Lymphoma 34 0.021
1034
DVL001 Developmental Coordination Disorder 34 0.021
1035
P EXT032 Extraosseous Osteosarcoma 34 0.021
1036
HMP018 Hemophilic Arthropathy 34 0.021
1037
ATY022 Atypical Coarctation of Aorta 34 0.021
1038
APP003 Appendiceal Neoplasm 34 0.021
1039
c ADL008 Adult Oligodendroglioma 34 0.021
1040
BRN005 Brain Glioblastoma Multiforme 34 0.021
1041
PLM028 Pulmonary Coin Lesion 33 0.021
1042
PDT021 Pediatric Osteosarcoma 33 0.021
1043
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.021
1044
c BNM018 Bone Mineral Density Quantitative Trait Locus 3 33 0.021
1045
P CRN133 Coronary Artery Disease, Autosomal Dominant, 1 32 0.021
1046
P PLY188 Polyendocrinopathy 32 0.021
1047
OSM001 Osmotic Diarrhea 32 0.021
1048
PLN007 Plantar Fasciitis 32 0.021
1049
PLY150 Polykaryocytosis Inducer 31 0.021
1050
RFR004 Refractory Hematologic Cancer 30 0.021
1051
CRT069 Cortical Malformations, Occipital 30 0.021
1052
RSP007 Respiratory Distress Syndrome, Infant 30 0.021
1053
MYC088 Mycobacterium Avium Complex Infections 29 0.021
1054
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.021
1055
PHT002 Photokeratitis 28 0.021
1056
c PLM121 Pulmonary Hypertension, Primary, 4 28 0.021
1057
PHS025 Phosphatase, Acid, of Tissues 28 0.021
1058
P OVR096 Overlap Myositis 27 0.021
1059
BRN101 Bronchiolitis Obliterans with Obstructive Pulmonary Disease 27 0.021
1060
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.021
1061
NRF026 Neurofibromatosis, Type Iv, of Riccardi 26 0.021
1062
SPN026 Spinal Cord Lymphoma 26 0.021
1063
TTH001 Tooth Ankylosis 26 0.021
1064
STR093 Striatonigral Degeneration, Childhood-Onset 26 0.021
1065
ASB003 Asbestos Intoxication 26 0.021
1066
LBR035 Liberfarb Syndrome 24 0.021
1067
SDD009 Sudden Cardiac Failure, Infantile 24 0.021
1068
INT053 Intracranial Vasospasm 24 0.021
1069
APN006 Apnea of Prematurity 24 0.021
1070
DVL005 Developmental Dyspraxia 23 0.021
1071
c CHR464 Chronic Intestinal Failure 22 0.021
1072
HML018 Homologous Wasting Disease 22 0.021
1073
c PSD047 Pseudo-Turner Syndrome 21 0.021
1075
c ADL093 Adult Acute Monocytic Leukemia 20 0.021
1076
LPN002 Lip and Oral Cavity Cancer 19 0.021
1077
BLN008 Blind Hypotensive Eye 18 0.021
1078
P ANT080 Antigen Defined by Monoclonal Antibody Aj9 18 0.021
1079
PLT016 Platelet Adenylate Cyclase Activity 16 0.021
1080