Search results for Dexamethasone

1907 hits were found for Dexamethasone

# Family MCID Name MIFTS Score
1
c HYP731 Hyperaldosteronism, Familial, Type I 60 6.465
2
MYL069 Myeloma, Multiple 85 0.791
3
PLS009 Plasma Cell Neoplasm 51 0.596
4
DWN001 Down Syndrome 70 0.409
5
MCL006 Macular Retinal Edema 55 0.387
6
P LYM118 Lymphoma 68 0.363
7
PNG002 Pain Agnosia 51 0.362
8
LYM019 Lymphosarcoma 46 0.348
9
P LKM062 Leukemia, Acute Lymphoblastic 69 0.297
10
P LKM002 Leukemia 68 0.293
11
48X005 48,xyyy 39 0.272
12
P RTN022 Retinal Vein Occlusion 53 0.260
13
P NTR004 Neutropenia 63 0.256
14
DPR016 Depression 63 0.255
15
DBT006 Diabetic Macular Edema 48 0.250
16
P MNN013 Meningitis 66 0.243
17
c RHB024 Rhabdomyosarcoma 2 67 0.239
18
LYM040 Lymphoblastic Lymphoma 54 0.236
19
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.229
20
P NRP001 Neuropathy 56 0.228
21
P UVT001 Uveitis 57 0.227
22
P THR014 Thrombocytopenia 67 0.225
23
P AMY004 Amyloidosis 70 0.224
24
P CTR002 Cataract 60 0.223
25
LYM133 Lymphoma, Hodgkin, Classic 69 0.216
26
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.215
27
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.215
28
c PNS012 Paine Syndrome 61 0.215
29
P PRP019 Peripheral Nervous System Disease 58 0.209
30
c ALM001 Al Amyloidosis 50 0.205
31
c PRM038 Primary Agammaglobulinemia 44 0.205
32
LNG099 Lung Disease 60 0.201
33
MNT002 Mental Depression 58 0.199
34
c BCT007 Bacterial Meningitis 55 0.198
35
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.196
36
P BCL017 B-Cell Lymphoma 58 0.191
37
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.189
38
BRN056 Bronchopulmonary Dysplasia 57 0.189
39
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.183
40
PLS011 Plasmacytoma 56 0.180
41
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.179
42
PRP030 Purpura 54 0.179
43
HYP066 Hyperglycemia 61 0.174
44
END040 Endogenous Depression 55 0.174
45
P MJR001 Major Depressive Disorder 68 0.172
46
CNS004 Constipation 58 0.172
47
c CNT016 Central Retinal Vein Occlusion 53 0.170
48
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.168
49
CYT002 Cytokine Deficiency 42 0.168
50
ADL002 Adult Syndrome 70 0.166
51
P MCR115 Microvascular Complications of Diabetes 5 66 0.164
52
P TRN020 Turner Syndrome 67 0.162
53
P SNS001 Sensorineural Hearing Loss 60 0.157
54
P LNG032 Lung Cancer 98 0.150
55
BRN004 Brain Edema 56 0.150
56
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.150
57
AYM001 Ayme-Gripp Syndrome 57 0.150
58
OCL006 Ocular Hypertension 53 0.149
59
FCT007 Factor Vii Deficiency 67 0.148
60
ALL026 Allergic Hypersensitivity Disease 62 0.148
61
DFF005 Diffuse Large B-Cell Lymphoma 55 0.143
62
P END047 Endophthalmitis 53 0.138
63
MNT001 Mantle Cell Lymphoma 69 0.138
64
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.135
65
P LKM071 Leukemia, Chronic Lymphocytic 79 0.134
66
P KDN018 Kidney Disease 72 0.134
67
P HDC001 Headache 57 0.134
68
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.134
69
MCR004 Macroglobulinemia 49 0.134
70
CRP002 Croup 44 0.134
71
ATX019 Ataxia with Vitamin E Deficiency 42 0.134
72
P BRS047 Breast Cancer 97 0.132
73
MLN003 Melancholia 38 0.132
74
SDD008 Sudden Sensorineural Hearing Loss 43 0.131
75
P PRS040 Prostate Cancer 97 0.130
76
P GLM045 Glioma 63 0.128
77
HMT002 Hematologic Cancer 62 0.128
78
P FLL037 Follicular Lymphoma 67 0.127
79
ADN018 Adenoma 59 0.127
80
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.127
81
GLL048 Glial Tumor 45 0.126
82
AST005 Asthma 76 0.125
83
P CNJ013 Conjunctivitis 65 0.124
84
P EXN002 Exanthem 57 0.123
85
c SML038 Small Cell Cancer of the Lung 65 0.122
86
P MYL006 Myeloid Leukemia 60 0.122
87
OST012 Osteoarthritis 78 0.121
88
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.120
89
P PNM007 Pneumonia 68 0.119
90
c PST005 Posterior Uveitis 54 0.119
91
INS024 Insulin-Like Growth Factor I 79 0.118
92
OST003 Osteonecrosis 61 0.118
93
BRN002 Bronchiolitis 59 0.116
94
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.116
95
LYM012 Lymphoplasmacytic Lymphoma 47 0.114
96
GLB015 Glioblastoma Multiforme 75 0.113
97
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.113
98
WLD007 Waldenstroem's Macroglobulinemia 61 0.113
99
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.113
100
c MGR028 Migraine with or Without Aura 1 67 0.112
101
RTN017 Retinal Detachment 61 0.112
102
P RSP003 Respiratory Failure 74 0.111
103
LYM027 Lymphopenia 58 0.111
104
MYL009 Myelodysplastic Syndrome 70 0.110
105
ISC004 Ischemia 58 0.110
106
PLS016 Plasma Cell Leukemia 53 0.110
107
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.110
108
RTC005 Reticulosarcoma 47 0.110
110
c LKM061 Leukemia, Acute Myeloid 84 0.107
111
ATM095 Autoimmune Disease 62 0.107
112
c FLL041 Follicular Lymphoma 1 49 0.107
113
HYP056 Hypoglycemia 66 0.106
114
P PMP001 Pemphigus 54 0.106
115
47X002 47,xyy 49 0.106
116
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.106
117
OTT002 Otitis Media 72 0.105
118
PNM013 Pneumococcal Meningitis 42 0.104
119
CHL079 Children's Interstitial Lung Disease 26 0.104
120
CLF027 Cleft Palate, Isolated 64 0.103
121
EYD002 Eye Disease 58 0.103
122
P DRR001 Diarrhea 55 0.103
123
P CHR345 Chronic Pain 44 0.103
124
c PRS136 Prostate Cancer, Hereditary, 6 33 0.103
125
c PRS130 Prostate Cancer, Hereditary, 8 32 0.103
126
c BRN108 Branchiootic Syndrome 1 62 0.102
127
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.102
128
HYP060 Hyperinsulinism 54 0.102
129
LTH001 Lethal Midline Granuloma 44 0.102
130
P CLR023 Colorectal Cancer 99 0.100
131
DFC004 Deficiency Anemia 70 0.100
132
TXC005 Toxic Shock Syndrome 62 0.100
133
MNR012 Meniere Disease 57 0.100
134
ACT011 Acute Contagious Conjunctivitis 40 0.100
135
CNN003 Conn's Syndrome 79 0.099
136
P OST002 Osteoporosis 74 0.099
137
P ART022 Arthritis 69 0.099
138
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.099
139
TXC002 Toxic Encephalopathy 53 0.099
140
P ADN016 Adenocarcinoma 64 0.098
141
DRM006 Dermatitis 61 0.098
142
c ACT027 Acute Pancreatitis 60 0.098
143
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.097
144
P SRC025 Sarcoidosis 1 70 0.097
145
BRK010 Burkitt Lymphoma 67 0.097
146
HYP266 Hypoxia 57 0.097
147
P ACT105 Acute Mountain Sickness 52 0.097
148
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.097
149
49X006 49, Xxxxy Syndrome 41 0.097
150
c ACT073 Acute Leukemia 58 0.095
151
P STR020 Strabismus 55 0.095
152
OCL069 Ocular Motor Apraxia 51 0.095
153
MCH006 Mechanical Strabismus 42 0.095
154
c LKM005 Leukemia, T-Cell, Chronic 34 0.095
155
P CNR004 Cone-Rod Dystrophy 2 73 0.094
156
NWB001 Newborn Respiratory Distress Syndrome 58 0.094
157
GLC003 Glucose Intolerance 54 0.094
158
SBC016 Subacute Delirium 44 0.094
159
ALL003 Allergic Rhinitis 67 0.093
160
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.093
161
P CRN026 Corneal Edema 43 0.093
162
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.093
163
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.091
164
SKN016 Skin Disease 63 0.091
165
BNR002 Bone Resorption Disease 48 0.091
166
HDN002 Head Injury 46 0.091
167
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.091
168
P NRB001 Neuroblastoma 72 0.090
169
OST159 Osteogenic Sarcoma 66 0.090
170
P PRS038 Personality Disorder 65 0.090
171
PMS001 Poems Syndrome 60 0.090
172
P RHN004 Rhinitis 57 0.090
173
PRP036 Peripheral T-Cell Lymphoma 53 0.090
174
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.090
175
P HYP098 Hypereosinophilic Syndrome 67 0.089
176
P MSC003 Muscular Atrophy 52 0.089
177
GLC106 Glucocorticoid Resistance, Generalized 48 0.089
178
BCK006 Back Pain 42 0.089
179
PLM010 Pulmonary Edema 54 0.087
180
TBR011 Tuberculous Meningitis 48 0.087
181
P OVR042 Ovarian Cancer 88 0.086
182
ANX010 Anxiety 73 0.086
183
P HRP006 Herpes Simplex 65 0.086
184
SPN186 Spinal Cord Injury 60 0.086
185
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.086
186
LNG031 Lung Benign Neoplasm 51 0.086
187
BRN071 Brain Injury 49 0.086
188
c PRM226 Primary Central Nervous System Lymphoma 48 0.086
189
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.086
190
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.084
191
P RHM011 Rheumatoid Arthritis 80 0.084
192
P LVR013 Liver Disease 68 0.084
193
P DRM053 Dermatitis, Atopic 66 0.084
194
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.084
195
c FNC043 Fanconi Anemia, Complementation Group E 62 0.084
196
P VSC011 Vasculitis 62 0.084
197
P ENC018 Encephalopathy 61 0.084
198
P ALP008 Alopecia 54 0.084
199
P CNT005 Central Nervous System Lymphoma 53 0.084
200
HYP043 Hyperandrogenism 48 0.084
201
STR067 Stroke, Ischemic 81 0.083
202
P GRF003 Graft-Versus-Host Disease 72 0.083
203
P MYP004 Myopathy 70 0.083
204
P ADL010 Adult Respiratory Distress Syndrome 65 0.083
205
P SZR006 Seizure Disorder 56 0.083
206
P PLY019 Polyneuropathy 56 0.083
207
IRD001 Iridocyclitis 53 0.083
208
P RTN018 Retinal Disease 53 0.083
209
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.083
210
P OPN001 Open-Angle Glaucoma 49 0.083
211
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.083
212
P OTT001 Otitis Externa 39 0.083
213
HDG004 Hodgkin's Granuloma 23 0.083
214
HDG006 Hodgkin's Paragranuloma 22 0.083
215
c THR092 Thrombophilia Due to Thrombin Defect 73 0.081
216
ALC007 Alcohol Dependence 66 0.081
217
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.081
218
THR024 Thrombosis 57 0.081
219
HYP005 Hypokalemia 55 0.081
220
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.081
221
PRS012 Pars Planitis 48 0.081
222
HMP009 Haemophilus Influenzae 43 0.081
223
NRR001 Neuroretinitis 42 0.081
224
P BPL003 Bipolar Disorder 56 0.080
225
P ADL017 Adult T-Cell Leukemia 56 0.080
226
ADR008 Adrenal Adenoma 55 0.080
227
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.080
228
TRP009 Triple X Syndrome 42 0.080
229
c HYP595 Hypertension, Essential 84 0.078
230
P PNC035 Pancreatic Cancer 84 0.078
231
CRB037 Cerebral Palsy 69 0.078
232
P HPT021 Hepatitis 67 0.078
233
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.078
234
ANR007 Anorexia Nervosa 63 0.078
235
ING001 Inguinal Hernia 60 0.078
236
P INF032 Infertility 57 0.078
237
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.078
238
P PLY011 Polycystic Ovary Syndrome 56 0.078
239
MCS002 Mucositis 56 0.078
240
SNS003 Sensory Peripheral Neuropathy 54 0.078
241
KRT006 Keratoconjunctivitis 53 0.078
242
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.078
243
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.078
244
RTN023 Retinitis 46 0.078
245
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.078
246
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.078
247
RSP007 Respiratory Distress Syndrome, Infant 30 0.078
248
SVR004 Severe Combined Immunodeficiency 73 0.077
249
P DMN002 Dementia 66 0.077
250
P PNC044 Pancreatitis 61 0.077
251
P NPH012 Nephrotic Syndrome 60 0.077
252
PHR003 Pharyngitis 57 0.077
253
P INF037 Inflammatory Bowel Disease 54 0.077
254
HLL004 Hellp Syndrome 54 0.077
255
TLN003 Telangiectasis 52 0.077
256
P HPT023 Hepatocellular Carcinoma 100 0.075
257
c SYS001 Systemic Lupus Erythematosus 86 0.075
258
c LKM063 Leukemia, Chronic Myeloid 72 0.075
259
P HYP086 Hypothyroidism 69 0.075
260
P PLM036 Pulmonary Fibrosis 65 0.075
261
VSL002 Visual Epilepsy 59 0.075
262
TRM010 Traumatic Brain Injury 51 0.075
263
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.075
264
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.075
265
c EXD008 Exudative Vitreoretinopathy 1 71 0.074
266
KRT019 Keratitis, Hereditary 65 0.074
267
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.074
268
HRP004 Herpes Zoster 60 0.074
269
P HYP076 Hyperthyroidism 55 0.074
270
MTN003 Motion Sickness 53 0.074
271
BLP005 Blepharitis 50 0.074
272
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.074
273
IMM167 Immune Deficiency Disease 78 0.072
274
P SCH015 Schizophrenia 74 0.072
275
BRN024 Bronchitis 68 0.072
276
P VSC007 Vascular Disease 63 0.072
277
c GLC092 Glaucoma, Primary Open Angle 62 0.072
278
P PTN014 Patent Ductus Arteriosus 1 60 0.072
279
PST028 Post-Traumatic Stress Disorder 58 0.072
280
P GLM007 Glomerulonephritis 57 0.072
281
P PTT006 Pituitary Adenoma 55 0.072
282
P LCH002 Lichen Planus 53 0.072
283
MRG003 Marginal Zone B-Cell Lymphoma 52 0.072
284
RDC002 Radiculopathy 50 0.072
285
DYS073 Dysphagia 50 0.072
286
PLP001 Pulpitis 49 0.072
287
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.072
288
c CHR064 Chronic Monocytic Leukemia 33 0.072
289
CNG034 Congestive Heart Failure 69 0.070
290
MDD011 Mood Disorder 62 0.070
291
SQM006 Squamous Cell Carcinoma 60 0.070
292
P ANP001 Anaplastic Large Cell Lymphoma 58 0.070
293
PMP006 Pemphigus Vulgaris, Familial 57 0.070
294
CMR002 Coumarin Resistance 56 0.070
295
ALL006 Allergic Asthma 56 0.070
296
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.070
297
P AST007 Astrocytoma 51 0.070
298
PLS025 Plasmablastic Lymphoma 47 0.070
299
P VTR007 Vitreoretinopathy 46 0.070
300
LGH004 Light Chain Deposition Disease 40 0.070
301
P GLM040 Glioma Susceptibility 1 81 0.068
302
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.068
303
P PHC003 Pheochromocytoma 71 0.068
304
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.068
305
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.068
306
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.068
307
P RCT021 Rectum Cancer 52 0.068
308
ADR040 Adrenal Gland Pheochromocytoma 46 0.068
309
c DRR009 Diarrhea 6 46 0.068
310
PTT037 Pituitary Tumors 44 0.068
311
CVD001 Covid-19 44 0.068
312
ENT001 Enterocele 39 0.068
313
P ATX030 Ataxia-Telangiectasia 82 0.066
314
MLR004 Malaria 81 0.066
315
P LNG064 Lung Cancer Susceptibility 3 78 0.066
316
HMN044 Human Immunodeficiency Virus Type 1 71 0.066
317
P MYC084 Mycobacterium Tuberculosis 1 68 0.066
318
c MCL013 Mucolipidosis Iv 66 0.066
319
SRC014 Sarcoma 65 0.066
320
P SJG008 Sjogren Syndrome 61 0.066
321
c ACT071 Acute Kidney Failure 60 0.066
322
CHL014 Cholera 59 0.066
323
P HYP726 Hypercalcemia, Infantile, 1 58 0.066
324
GLS018 Glass Syndrome 57 0.066
325
ERY051 Erythroleukemia, Familial 56 0.066
326
c INT064 Intermediate Uveitis 55 0.066
327
ENT011 Enterocolitis 51 0.066
328
ALL009 Allergic Conjunctivitis 50 0.066
329
ORL013 Oral Lichen Planus 45 0.066
330
HRN029 Hearing Loss, Noise-Induced 37 0.066
331
STR019 Steroid-Induced Glaucoma 32 0.066
332
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.066
333
CHL065 Cholangiocarcinoma 68 0.065
334
CRB039 Cerebrovascular Disease 67 0.065
335
P NRV007 Nervous System Disease 66 0.065
336
P ART023 Arthropathy 62 0.065
337
P ENC004 Encephalitis 61 0.065
338
PRN019 Perinatal Necrotizing Enterocolitis 59 0.065
339
MNN032 Meningococcal Meningitis 54 0.065
340
ILS001 Ileus 51 0.065
341
SPL004 Splenic Marginal Zone Lymphoma 51 0.065
342
ALN001 Aland Island Eye Disease 50 0.065
343
P CTN015 Cutaneous T Cell Lymphoma 49 0.065
344
c MLG068 Malignant Glioma 46 0.065
345
c OVR114 Ovarian Cancer 1 38 0.065
346
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.065
347
c ATR087 Atrial Standstill 1 75 0.063
348
BRN028 Brain Cancer 74 0.063
349
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.063
350
PRT037 Pertussis 65 0.063
351
CLT003 Colitis 62 0.063
352
P LPS004 Lupus Erythematosus 61 0.063
353
ACQ007 Acquired Immunodeficiency Syndrome 60 0.063
354
P BND020 Bone Disease 59 0.063
355
c CHR417 Chronic Graft Versus Host Disease 57 0.063
356
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.063
357
SPN035 Spindle Cell Sarcoma 53 0.063
358
NRT004 Neuritis 52 0.063
359
ADT003 Auditory System Disease 48 0.063
360
DRY001 Dry Eye Syndrome 47 0.063
361
KHN001 Kuhnt-Junius Degeneration 47 0.063
362
NSS002 Neisseria Meningitidis Infection 47 0.063
363
EPC002 Epicondylitis 41 0.063
364
PRR004 Preretinal Fibrosis 37 0.063
365
c NRF023 Neurofibromatosis, Type Ii 80 0.061
366
P HRT032 Heart Disease 75 0.061
367
P RTN024 Retinoblastoma 73 0.061
368
P PLM037 Pulmonary Hypertension 67 0.061
369
CLN015 Colon Adenocarcinoma 65 0.061
370
c DPH024 Diaphragmatic Hernia, Congenital 63 0.061
371
LPD008 Lipid Metabolism Disorder 62 0.061
372
c SVR001 Severe Acute Respiratory Syndrome 62 0.061
373
c SCL052 Scleroderma, Familial Progressive 61 0.061
374
P CYS018 Cystitis 59 0.061
375
TNS005 Tonsillitis 57 0.061
376
P FBR017 Fibrosarcoma 56 0.061
377
BCT022 Bacterial Infectious Disease 56 0.061
378
GST023 Gastric Ulcer 53 0.061
379
c FML008 Familial Retinoblastoma 53 0.061
380
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.061
381
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.061
382
P OVR049 Ovarian Disease 52 0.061
383
END086 End Stage Renal Disease 51 0.061
384
KRT001 Keratoconjunctivitis Sicca 49 0.061
385
CRY014 Cryptococcal Meningitis 48 0.061
386
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.061
387
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.061
388
RTN020 Retinal Vascular Disease 46 0.061
389
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.061
390
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.061
391
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.061
392
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.061
393
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.061
394
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.061
395
IDP033 Idiopathic Edema 44 0.061
396
TST015 Testicular Disease 43 0.061
397
P AVS003 Avascular Necrosis 42 0.061
398
ALL014 Allergic Encephalomyelitis 38 0.061
399
HRW001 Hair Whorl 36 0.061
400
P RTN008 Retinitis Pigmentosa 79 0.059
401
P HYP061 Hypertrophic Cardiomyopathy 70 0.059
402
P MLN008 Melanoma 69 0.059
403
ACT119 Acute Promyelocytic Leukemia 63 0.059
404
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.059
405
P PSR002 Psoriasis 62 0.059
406
P TXP001 Toxoplasmosis 60 0.059
407
P ALC033 Alcohol Use Disorder 58 0.059
408
PNC001 Pancytopenia 54 0.059
409
CYS005 Cysticercosis 53 0.059
410
BRD004 Borderline Personality Disorder 53 0.059
411
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.059
412
STM007 Stomatitis 50 0.059
413
MNN020 Meningococcal Infection 46 0.059
414
GRN017 Granulocytopenia 44 0.059
415
c MJR024 Major Affective Disorder 9 41 0.059
416
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.059
417
c MJR022 Major Affective Disorder 8 38 0.059
418
SML011 Smoldering Myeloma 33 0.059
419
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.059
420
c INF152 Infectious Posterior Uveitis 19 0.059
421
c NNN032 Non-Infectious Posterior Uveitis 19 0.059
422
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.057
423
KPS004 Kaposi Sarcoma 75 0.057
424
CRH001 Crohn's Disease 74 0.057
425
RCK004 Rickets 68 0.057
426
P HYD006 Hydrocephalus 66 0.057
427
NTR005 Nutritional Deficiency Disease 62 0.057
428
CHL068 Cholestasis 61 0.057
429
SFT003 Soft Tissue Sarcoma 56 0.057
430
P GRV001 Graves' Disease 55 0.057
431
ACT058 Active Peptic Ulcer Disease 55 0.057
432
SYN007 Synovitis 54 0.057
433
TND005 Tendinitis 54 0.057
434
PST011 Pustulosis of Palm and Sole 52 0.057
435
INT079 Intrahepatic Cholangiocarcinoma 51 0.057
436
P PNV001 Panuveitis 50 0.057
437
ACT084 Acute Stress Disorder 47 0.057
438
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.057
439
c PLY105 Polycystic Ovary Syndrome 1 38 0.057
440
PLC002 Plica Syndrome 36 0.057
441
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.057
442
HML018 Homologous Wasting Disease 22 0.057
443
ULC004 Ulcerative Colitis 73 0.054
444
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.054
445
P DBT009 Diabetes Mellitus 64 0.054
446
c ACT068 Acute Cystitis 63 0.054
447
FTT001 Fatty Liver Disease 61 0.054
448
THY029 Thyroid Carcinoma 59 0.054
449
PLM033 Pulmonary Embolism 59 0.054
450
P LYM033 Lymphoproliferative Syndrome 59 0.054
451
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.054
452
BRN038 Bronchial Disease 53 0.054
453
P PNC025 Panic Disorder 53 0.054
454
c CNT035 Central Nervous System Disease 52 0.054
455
P DDN001 Duodenal Ulcer 52 0.054
456
PRV004 Periventricular Leukomalacia 52 0.054
457
CHR078 Chorioretinitis 50 0.054
458
DYS009 Dysthymic Disorder 49 0.054
459
P INN002 Inner Ear Disease 47 0.054
460
P HRT035 Heart Block, Congenital 46 0.054
461
P MYC033 Myoclonus 46 0.054
462
TND004 Tendinopathy 43 0.054
463
BNM001 Bone Marrow Cancer 43 0.054
464
RDC006 Red Cell Aplasia 43 0.054
465
MCL003 Macular Holes 40 0.054
466
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.054
467
OVR094 Ovarian Epithelial Cancer 38 0.054
468
CNT060 Central Serous Chorioretinopathy 38 0.054
469
P GST053 Gastric Cancer 83 0.052
470
CYS001 Cystic Fibrosis 81 0.052
471
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.052
472
P MYC007 Myocardial Infarction 70 0.052
473
c INF071 Inflammatory Bowel Disease 1 67 0.052
474
P NSP012 Nasopharyngeal Carcinoma 66 0.052
475
c MCR129 Microvascular Complications of Diabetes 1 66 0.052
476
PPL049 Papillon-Lefevre Syndrome 65 0.052
477
P THY023 Thymoma 65 0.052
478
PRT036 Peritonitis 64 0.052
479
P PRD008 Periodontitis 64 0.052
480
c PRC016 Pre-Eclampsia 63 0.052
481
P HYP750 Hypertriglyceridemia, Familial 62 0.052
482
MNN042 Meningioma, Radiation-Induced 62 0.052
483
LVR012 Liver Cirrhosis 62 0.052
484
P KDN017 Kidney Cancer 60 0.052
485
CRD223 Cardiac Arrhythmia 60 0.052
486
P CHR285 Chronic Myelomonocytic Leukemia 60 0.052
487
c HPT016 Hepatitis B 59 0.052
488
P MLN069 Melanoma, Uveal 59 0.052
489
CNT047 Contact Dermatitis 58 0.052
490
P PLV020 Pelvic Organ Prolapse 57 0.052
491
GST050 Gastrointestinal System Disease 56 0.052
492
LMB062 Limb Ischemia 55 0.052
493
GLS001 Gliosarcoma 54 0.052
494
FNG017 Fungal Infectious Disease 53 0.052
495
HRP009 Herpes Simplex Encephalitis 52 0.052
496
c THY107 Thymoma, Familial 52 0.052
497
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.052
498
INT054 Intraocular Lymphoma 48 0.052
499
SPL018 Splenomegaly 48 0.052
500
GRM005 Germ Cell Cancer 47 0.052
501
P PRR002 Pure Red-Cell Aplasia 47 0.052
502
EXT010 Extramedullary Plasmacytoma 45 0.052
503
GST020 Gastric Antral Vascular Ectasia 41 0.052
504
LCR013 Lacrimal Duct Defect 41 0.052
505
c MCR112 Microvascular Complications of Diabetes 2 41 0.052
506
P MLG074 Malignant Mesenchymoma 40 0.052
507
ALD013 Aldosterone-Producing Adenoma 39 0.052
508
c BCT006 Bacterial Conjunctivitis 37 0.052
509
VRS002 Virus-Associated Trichodysplasia Spinulosa 32 0.052
510
ADR057 Adrenogenital Syndrome 32 0.052
511
CRV035 Cervical Cancer 76 0.050
512
c MNN043 Meningioma, Familial 74 0.050
513
P SLP006 Sleep Apnea 69 0.050
514
P MYS003 Myasthenia Gravis 68 0.050
515
MYC006 Mycosis Fungoides 66 0.050
516
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.050
517
HYP780 Hypoadrenocorticism, Familial 63 0.050
518
c HPT001 Hepatitis C 62 0.050
519
VRL011 Viral Infectious Disease 61 0.050
520
SZR001 Sezary's Disease 60 0.050
521
P TST021 Testicular Germ Cell Tumor 60 0.050
522
c JVN061 Juvenile Arthritis 60 0.050
523
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.050
524
PPT005 Peptic Ulcer Disease 59 0.050
525
BLR008 Bilirubin Metabolic Disorder 57 0.050
526
AGN016 Aging 56 0.050
527
P MNC007 Monocytic Leukemia 53 0.050
528
MST005 Mastitis 53 0.050
529
PRP080 Peripheral Artery Disease 53 0.050
530
P INT068 Intestinal Disease 53 0.050
531
P SPP010 Suppressor of Tumorigenicity 3 51 0.050
532
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.050
533
AVD001 Avoidant Personality Disorder 51 0.050
534
SPN021 Spinal Meningioma 50 0.050
535
FSC004 Fasciitis 50 0.050
536
P SCL015 Scleritis 48 0.050
537
KRT008 Keratopathy 47 0.050
538
CRN027 Corneal Neovascularization 47 0.050
539
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.050
540
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.050
541
TST014 Testicular Cancer 46 0.050
542
P BNG032 Benign Mesothelioma 46 0.050
543
P CRN024 Corneal Disease 44 0.050
544
ADR041 Adrenal Cortical Adenoma 43 0.050
545
MXD050 Mixed Phenotype Acute Leukemia 43 0.050
546
DRG024 Drug Allergy 42 0.050
547
SCR001 Secretory Meningioma 41 0.050
548
VTR003 Vitreous Detachment 39 0.050
549
HYP344 Hyperthyroidism, Familial Gestational 39 0.050
550
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.050
551
c PRM340 Primary Adrenal Insufficiency 36 0.050
552
ACT012 Acute Hemorrhagic Conjunctivitis 36 0.050
553
GRM010 Germ Cells Tumors 34 0.050
554
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.050
555
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.050
556
END057 Endometrial Cancer 74 0.047
557
ACR007 Acromegaly 71 0.047
558
PRP027 Peripheral Vascular Disease 71 0.047
559
MYL005 Myelofibrosis 70 0.047
560
c CHR684 Chronic Kidney Disease 70 0.047
561
OBS002 Obsessive-Compulsive Disorder 68 0.047
562
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.047
563
MYL031 Myeloproliferative Neoplasm 66 0.047
564
c JVN010 Juvenile Rheumatoid Arthritis 64 0.047
565
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.047
566
P ORT004 Orthostatic Intolerance 62 0.047
567
P ALP009 Alopecia Areata 60 0.047
568
P MYC008 Myocarditis 59 0.047
569
P URT039 Urticaria 58 0.047
570
P FCL005 Focal Segmental Glomerulosclerosis 57 0.047
571
P ANG015 Angioedema 57 0.047
572
PNM008 Pneumothorax 56 0.047
573
P GST044 Gastritis 56 0.047
574
P AGN002 Agnosia 55 0.047
575
P SBS003 Substance Abuse 55 0.047
576
CRH005 Crohn's Colitis 53 0.047
577
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.047
578
ART140 Arteries, Anomalies of 52 0.047
579
P HYP040 Hypospadias 51 0.047
580
c PYR010 Peyronie's Disease 50 0.047
581
NTR046 Neutrophil Migration 50 0.047
582
P MGR001 Migraine Without Aura 49 0.047
583
CHL061 Childhood Leukemia 48 0.047
584
ASP007 Aspiration Pneumonia 48 0.047
585
RTN001 Retinal Vasculitis 47 0.047
586
CHR074 Choriocarcinoma 47 0.047
587
CHR008 Choroiditis 46 0.047
588
P CLS010 Cluster Headache 42 0.047
589
c CHR682 Chronic Bilirubin Encephalopathy 39 0.047
590
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.047
591
CYT018 Cytochrome P450 2d6 Variant 27 0.047
592
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.047
593
P BLD134 Bladder Cancer 79 0.044
594
P MDL005 Medulloblastoma 77 0.044
595
SKN019 Skin Melanoma 68 0.044
596
P CRD119 Cardiac Arrest 67 0.044
597
PSY004 Psychotic Disorder 67 0.044
598
P ATR011 Atrial Fibrillation 66 0.044
599
ATH013 Atherosclerosis Susceptibility 65 0.044
600
c DBT099 Diabetes Mellitus, Type I 65 0.044
601
NRM005 Neuromuscular Disease 64 0.044
602
P HML002 Hemolytic Anemia 63 0.044
603
INT146 Intervertebral Disc Disease 63 0.044
604
STT001 Status Epilepticus 60 0.044
605
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.044
606
CRY005 Cryptococcosis 58 0.044
607
FML063 Familial Glucocorticoid Deficiency 58 0.044
608
c LKM070 Leukemia, Acute Monocytic 57 0.044
609
P HYP024 Hypoparathyroidism 56 0.044
610
ORP003 Oropharynx Cancer 55 0.044
611
ORL004 Oral Submucous Fibrosis 55 0.044
612
P MYP006 Myopia 55 0.044
613
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.044
614
PRC013 Pericarditis 54 0.044
615
AMN001 Amenorrhea 54 0.044
616
P RTN016 Retinal Degeneration 53 0.044
617
CLF001 Cleft Lip 53 0.044
618
NRT001 Neurotic Disorder 53 0.044
619
P PRC012 Pericardial Effusion 51 0.044
620
PLR008 Pleurisy 50 0.044
621
c AMY009 Amyloidosis Aa 50 0.044
622
P KRT007 Keratoconus 50 0.044
623
HST010 Histiocytosis 48 0.044
624
c BCT013 Bacterial Pneumonia 48 0.044
625
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.044
626
HMP001 Hemopericardium 48 0.044
627
P HMN032 Human Herpesvirus 8 47 0.044
628
ANV001 Anovulation 47 0.044
629
KRT013 Keratolytic Winter Erythema 46 0.044
630
LYM051 Lymphomatoid Granulomatosis 45 0.044
631
AGR002 Agoraphobia 45 0.044
632
c PCH010 Pachyonychia Congenita 3 44 0.044
633
TNS014 Tenosynovitis 44 0.044
634
PPL001 Papillary Adenoma 44 0.044
635
P CRN035 Cranial Nerve Palsy 42 0.044
636
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.044
637
DNT006 Dental Pulp Necrosis 41 0.044
638
RDN001 Reading Disorder 40 0.044
639
OST115 Osteonecrosis of the Jaw 40 0.044
640
C1N001 C1 Inhibitor Deficiency 39 0.044
642
PLN007 Plantar Fasciitis 32 0.044
643
BLP006 Blepharoconjunctivitis 31 0.044
644
c ANT023 Anterior Scleritis 29 0.044
645
c ACT047 Acute Endophthalmitis 29 0.044
646
TST003 Testicular Leukemia 27 0.044
647
MLG164 Malignant Epithelial Tumor of Ovary 26 0.044
648
P MLT020 Multiple Sclerosis 72 0.041
649
P ASP006 Aspergillosis 69 0.041
650
SVR097 Severe Cutaneous Adverse Reaction 69 0.041
651
MYX005 Myxoid Liposarcoma 66 0.041
652
P LPS002 Liposarcoma 65 0.041
653
APN008 Apnea, Obstructive Sleep 64 0.041
654
MGK001 Megakaryocytic Leukemia 64 0.041
655
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.041
656
P OPT006 Optic Nerve Disease 60 0.041
657
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.041
658
ANR040 Aneurysm 59 0.041
659
ADR005 Adrenal Carcinoma 58 0.041
660
ERY003 Erythema Multiforme 58 0.041
661
CHL067 Cholecystitis 57 0.041
662
IRN002 Iron Metabolism Disease 57 0.041
663
THY122 Thyroid Gland Cancer 57 0.041
664
P CRD246 Cardiovascular System Disease 57 0.041
665
SPN041 Spinal Cord Disease 56 0.041
666
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.041
667
c GRV008 Graves Disease 1 56 0.041
668
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.041
669
CRT017 Cartilage Disease 54 0.041
670
PLM012 Pulmonary Sarcoidosis 53 0.041
671
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.041
672
INT075 Intracranial Hypertension 53 0.041
673
MCN017 Meconium Ileus 52 0.041
674
THY030 Thyroid Gland Disease 52 0.041
675
ACT200 Acute Monoblastic Leukemia 52 0.041
676
ACT017 Acute Chest Syndrome 51 0.041
677
CHR005 Chorioamnionitis 51 0.041
678
P SCK005 Sickle Cell Disease 50 0.041
679
c INF145 Infantile Liver Failure Syndrome 1 50 0.041
680
STT002 Status Asthmaticus 50 0.041
681
ATY042 Atypical Chronic Myeloid Leukemia 49 0.041
682
ENT004 Enthesopathy 49 0.041
683
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.041
684
WTH001 Withdrawal Disorder 48 0.041
685
ATS010 Autosomal Recessive Disease 48 0.041
686
ACT098 Acute Erythroid Leukemia 48 0.041
687
BNN003 Bone Inflammation Disease 48 0.041
688
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.041
689
CYN002 Cyanosis, Transient Neonatal 45 0.041
690
HMR023 Hemorrhagic Cystitis 45 0.041
691
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.041
692
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.041
693
CHL149 Childhood Acute Myeloid Leukemia 44 0.041
694
SKN005 Skin Atrophy 43 0.041
695
P TST026 Testicular Germ Cell Cancer 43 0.041
696
MST004 Mast Cell Neoplasm 42 0.041
697
ARC002 Arachnoiditis 42 0.041
698
PRS063 Paresthesia 41 0.041
699
DND018 Dendritic Cell Tumor 40 0.041
700
EXT007 Extracutaneous Mastocytoma 38 0.041
701
BLS007 Blastic Plasmacytoid Dendritic Cell 38 0.041
702
SWL001 Swallowing Disorders 38 0.041
703
SPN354 Spinal Arachnoiditis 36 0.041
704
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.041
705
SCL025 Scleromyxedema 32 0.041
706
ERY066 Erythema Multiforme Major 30 0.041
707
PST092 Posttransplant Acute Limbic Encephalitis 29 0.041
708
c INF019 Infectious Anterior Uveitis 28 0.041
709
NCR009 Necrobiotic Xanthogranuloma 26 0.041
710
CHR208 Chromosome 17p Deletion 23 0.041
711
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.041
712
PLS037 Plasma Cell Tumor 22 0.041
713
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.041
714
P NNN030 Non-Infectious Anterior Uveitis 14 0.041
715
P APL001 Aplastic Anemia 74 0.038
716
P EPL164 Epilepsy 71 0.038
717
CNN005 Connective Tissue Disease 68 0.038
718
P OLG002 Oligodendroglioma 67 0.038
719
LPT001 Leptospirosis 66 0.038
720
TTN003 Tetanus 65 0.038
721
P MST009 Mastocytosis 64 0.038
722
OST017 Osteomyelitis 64 0.038
723
TYP007 Typhoid Fever 63 0.038
724
P LMY004 Leiomyosarcoma 63 0.038
725
P ESP024 Esophagitis 62 0.038
726
P INT143 Interstitial Cystitis 61 0.038
727
CHR066 Chronic Fatigue Syndrome 61 0.038
728
APP008 Appendicitis 61 0.038
729
TRG002 Trigeminal Neuralgia 60 0.038
730
INS001 Insulinoma 60 0.038
731
ETN001 Eating Disorder 60 0.038
732
PNM001 Pneumocystosis 59 0.038
733
IGR001 Ige Responsiveness, Atopic 59 0.038
734
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.038
735
P INT070 Intestinal Obstruction 58 0.038
736
SPT004 Septic Arthritis 58 0.038
737
P BNC003 Bone Cancer 58 0.038
738
LNG108 Langerhans Cell Histiocytosis 58 0.038
739
P GLL018 Gallbladder Cancer 57 0.038
740
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.038
741
P OPT009 Optic Neuritis 57 0.038
742
CMM005 Common Cold 57 0.038
743
CYT008 Cytomegalovirus Infection 57 0.038
744
PGM001 Pigmented Villonodular Synovitis 56 0.038
745
P PYL005 Pyelonephritis 56 0.038
746
VGT001 Vogt-Koyanagi-Harada Disease 55 0.038
747
HRY003 Hairy Cell Leukemia 55 0.038
748
SMT008 Smith-Magenis Syndrome 54 0.038
749
PTT009 Pituitary Gland Disease 54 0.038
750
CLL003 Cellulitis 54 0.038
751
OST016 Osteochondrosis 53 0.038
752
NVS001 Neovascular Glaucoma 53 0.038
753
CTS003 Coats Disease 53 0.038
754
c GLL024 Gallbladder Disease 1 53 0.038
755
P LRY019 Laryngitis 52 0.038
756
PRP016 Paraplegia 52 0.038
757
c ACT135 Acute Graft Versus Host Disease 52 0.038
759
NRM004 Neuroma 51 0.038
760
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.038
761
INT071 Intestinal Perforation 51 0.038
762
SCH012 Schizoaffective Disorder 50 0.038
763
CYT005 Cytomegalovirus Retinitis 50 0.038
764
PPL021 Papilledema 49 0.038
765
P END046 Endometritis 49 0.038
766
GST049 Gastrointestinal System Cancer 49 0.038
767
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.038
768
ADR016 Adrenal Cortical Carcinoma 48 0.038
769
RFR010 Refractory Anemia 48 0.038
770
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.038
771
P CLB034 Coloboma, Ocular, Autosomal Dominant 47 0.038
772
c MCR120 Microvascular Complications of Diabetes 7 47 0.038
773
P CLL015 Collagen Disease 47 0.038
774
KRT002 Keratomalacia 47 0.038
775
c CNG216 Congenital Hydrocephalus 47 0.038
776
GST071 Gastrointestinal Carcinoma 47 0.038
777
P BLD051 Blood Coagulation Disease 46 0.038
778
FCL012 Facial Paralysis 46 0.038
779
CLN045 Colonic Benign Neoplasm 46 0.038
780
LKS001 Leukostasis 46 0.038
781
MXD026 Mixed Glioma 45 0.038
782
CRB004 Cerebral Artery Occlusion 45 0.038
783
SPP008 Suppurative Otitis Media 45 0.038
784
TNS007 Taeniasis 45 0.038
785
DBT090 Diabetes and Deafness, Maternally Inherited 44 0.038
786
LRY022 Laryngoonychocutaneous Syndrome 44 0.038
787
P BCT020 Bacteremia 2 44 0.038
788
CRB090 Cerebral Hypoxia 44 0.038
789
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.038
790
RFR003 Refractive Error 43 0.038
791
MRG013 Mirage Syndrome 43 0.038
792
STL007 Steel Syndrome 43 0.038
793
P MJR007 Major Affective Disorder 1 43 0.038
794
CHR286 Chronic Neutrophilic Leukemia 42 0.038
795
SNL007 Senile Cataract 42 0.038
796
BKS003 Beukes Hip Dysplasia 41 0.038
797
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.038
798
NRV004 Nerve Compression Syndrome 40 0.038
799
KLD004 Keloid Disorder 40 0.038
800
FML039 Female Reproductive System Disease 39 0.038
801
INC003 Inclusion Conjunctivitis 37 0.038
802
c CHR097 Chronic Purulent Otitis Media 33 0.038
803
c TST046 Testicular Germ Cell Tumor 1 29 0.038
804
c ACQ016 Acquired Pure Red Cell Aplasia 27 0.038
805
THY006 Thymus Lymphoma 26 0.038
806
ESP021 Esophageal Cancer 90 0.035
807
PFF001 Pfeiffer Syndrome 79 0.035
808
SCK003 Sickle Cell Anemia 74 0.035
809
c HPT073 Hepatitis C Virus 72 0.035
810
P OCL013 Oculodentodigital Dysplasia 69 0.035
811
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.035
812
P INF038 Influenza 68 0.035
813
PNC129 Pancreatic Adenocarcinoma 68 0.035
814
GST092 Gastroesophageal Reflux 67 0.035
815
FLL027 Fallopian Tube Carcinoma 67 0.035
816
P BLD062 Bile Duct Cancer 67 0.035
817
ANG054 Angina Pectoris 66 0.035
818
P SKN015 Skin Carcinoma 66 0.035
819
PND002 Pendred Syndrome 65 0.035
820
OVR029 Ovarian Hyperstimulation Syndrome 64 0.035
821
MSC007 Muscle Hypertrophy 64 0.035
822
P HMN010 Hemangioma 61 0.035
823
CHC001 Chickenpox 60 0.035
824
ORL011 Oral Cancer 60 0.035
825
PRT058 Pure Autonomic Failure 59 0.035
826
P BRS044 Breast Adenocarcinoma 59 0.035
827
GRD007 Grade Iii Astrocytoma 59 0.035
828
c DWL002 Dowling-Degos Disease 1 58 0.035
829
P GLL020 Gallbladder Disease 57 0.035
830
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.035
831
DSS009 Disseminated Intravascular Coagulation 57 0.035
832
c MST023 Mesothelioma, Malignant 57 0.035
833
APH001 Aphthous Stomatitis 57 0.035
834
P END033 Endocarditis 57 0.035
835
VSC002 Vascular Dementia 57 0.035
836
SCH014 Schistosomiasis 57 0.035
837
TRN018 Transitional Cell Carcinoma 56 0.035
838
ADN027 Adenomyosis 56 0.035
839
ALL010 Allergic Contact Dermatitis 56 0.035
840
P DYS193 Dystonia 11, Myoclonic 55 0.035
841
INT007 Intermediate Coronary Syndrome 55 0.035
842
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.035
843
PRT082 Preterm Premature Rupture of the Membranes 54 0.035
844
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.035
845
P TRM003 Tremor 54 0.035
846
P HMR003 Hemorrhagic Disease 53 0.035
847
GTR002 Goiter 53 0.035
848
c PSR017 Psoriasis 2 53 0.035
849
DMY004 Demyelinating Disease 52 0.035
850
IMP005 Impotence 52 0.035
851
c PSR023 Psoriasis 1 52 0.035
852
PTH003 Pathologic Nystagmus 52 0.035
853
c VRL005 Viral Pneumonia 52 0.035
854
P TRT010 Teratoma 52 0.035
855
LMY002 Leiomyoma 52 0.035
856
OLG003 Oligohydramnios 51 0.035
857
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.035
858
P ECL001 Eclampsia 50 0.035
859
P TMP001 Temporal Lobe Epilepsy 50 0.035
860
OCL022 Ocular Melanoma 50 0.035
861
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.035
862
c CHR418 Chronic Leukemia 49 0.035
863
CHR563 Chronic Eosinophilic Leukemia 48 0.035
864
SXL003 Sexual Disorder 47 0.035
865
VRN004 Vernal Keratoconjunctivitis 47 0.035
866
c PSR032 Psoriasis 11 47 0.035
867
LPD004 Lipoid Nephrosis 46 0.035
868
SPN020 Spondylosis 46 0.035
869
PLL012 Pollen Allergy 46 0.035
870
GST010 Gestational Trophoblastic Neoplasm 46 0.035
871
c ACT042 Acute Pyelonephritis 46 0.035
872
SYN036 Syncope 45 0.035
873
RCH001 Richter's Syndrome 45 0.035
874
ATY001 Atypical Depressive Disorder 45 0.035
876
PRT030 Parathyroid Gland Disease 45 0.035
877
CRT015 Carotid Artery Occlusion 45 0.035
878
MYF001 Myofibroma 45 0.035
879
OVR112 Ovarian Germ Cell Cancer 45 0.035
880
ASP008 Aspiration Pneumonitis 45 0.035
881
APP009 Appendix Adenocarcinoma 44 0.035
882
FCH001 Fuchs' Endothelial Dystrophy 44 0.035
883
SMN007 Seminoma 43 0.035
884
P MLT008 Multinodular Goiter 42 0.035
885
PRS115 Prosthetic Joint Infection 42 0.035
886
c PSR028 Psoriasis 7 42 0.035
887
BP1002 Bap1 Tumor Predisposition Syndrome 42 0.035
888
OCL011 Ocular Motility Disease 42 0.035
889
c MLG079 Malignant Pleural Mesothelioma 42 0.035
890
c PSR018 Psoriasis 13 41 0.035
891
GRM004 Germinoma 40 0.035
892
ADR004 Adrenal Cortical Adenocarcinoma 39 0.035
893
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.035
894
ESN006 Eosinophilic Meningitis 38 0.035
895
OPT010 Optic Papillitis 38 0.035
896
c ACT067 Acute Conjunctivitis 38 0.035
897
TRP005 Trophoblastic Neoplasm 38 0.035
898
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 37 0.035
899
TST043 Testicular Seminoma 35 0.035
900
CHR178 Chromosomal Triplication 35 0.035
901
PDT001 Pediatric Lymphoma 35 0.035
902
c ATM021 Autoimmune Inner Ear Disease 34 0.035
903
CHR034 Chromophobe Adenoma 34 0.035
904
SPP003 Suppurative Periapical Periodontitis 34 0.035
905
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.035
906
BNN005 Bunion 33 0.035
907
RFR002 Refractory Hairy Cell Leukemia 33 0.035
908
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.035
909
c ENC060 Encephalopathy, Acute, Infection-Induced 1 32 0.035
910
CRD220 Cardiac Valvular Defect, Developmental 29 0.035
911
BRW002 Brown's Tendon Sheath Syndrome 28 0.035
912
DQR001 De Quervain Disease 28 0.035
913
TST020 Testis Seminoma 28 0.035
914
OTM001 Otomycosis 27 0.035
915
CLS052 Classic Hairy Cell Leukemia 27 0.035
916
SPC030 Specific Language Disorder 26 0.035
917
PRQ002 Paraquat Poisoning 26 0.035
918
NNT021 Neonatal Meningitis 25 0.035
919
JVN026 Jeavons Syndrome 24 0.035
920
c NNT025 Neonatal Systemic Lupus Erythematosus 20 0.035
921
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.031
922
LPT014 Leptin Deficiency or Dysfunction 74 0.031
923
c HYP836 Hypercholesterolemia, Familial, 1 73 0.031
924
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.031
925
GST040 Gastric Adenocarcinoma 70 0.031
926
PLM001 Pulmonary Tuberculosis 69 0.031
927
ACR008 Acrocallosal Syndrome 69 0.031
928
ART016 Aortic Aneurysm 69 0.031
929
THY111 Thyroid Carcinoma, Familial Medullary 67 0.031
930
P CHR012 Chronic Granulomatous Disease 67 0.031
931
CRP001 Carpal Tunnel Syndrome 67 0.031
932
P MSC005 Muscular Dystrophy 66 0.031
933
KHL003 Kohlschutter-Tonz Syndrome 65 0.031
934
CRN036 Craniopharyngioma 65 0.031
935
ACR006 Aceruloplasminemia 65 0.031
936
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.031
937
MSM014 Mismatch Repair Cancer Syndrome 65 0.031
938
IRR002 Irritable Bowel Syndrome 65 0.031
939
PTT048 Pituitary Adenoma, Prolactin-Secreting 65 0.031
940
GT001 Gout 64 0.031
941
HYP020 Hyperprolactinemia 64 0.031
942
P RHB003 Rhabdomyosarcoma 63 0.031
943
P CRN300 Coronary Heart Disease 1 63 0.031
944
P END044 Endometriosis 63 0.031
945
LPP008 Lipoprotein Quantitative Trait Locus 62 0.031
946
P TRC086 Trichohepatoenteric Syndrome 1 62 0.031
947
c ANM038 Anemia, Autoimmune Hemolytic 62 0.031
948
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.031
949
WST001 West Syndrome 61 0.031
950
PNM010 Pneumothorax, Primary Spontaneous 60 0.031
951
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.031
952
P SCL018 Scoliosis 60 0.031
953
HPT019 Hepatic Encephalopathy 60 0.031
954
PRT013 Portal Hypertension 59 0.031
955
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.031
956
P SLP005 Sleep Disorder 59 0.031
957
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.031
958
P SYP003 Syphilis 58 0.031
959
P CND004 Candidiasis 58 0.031
960
CST005 Castleman Disease 57 0.031
961
PRL032 Perlman Syndrome 57 0.031
962
APH002 Aphasia 57 0.031
963
c SML009 Small Intestine Adenocarcinoma 57 0.031
964
P CHN012 Chondrosarcoma 56 0.031
965
EMB004 Embryonal Carcinoma 56 0.031
966
ORL005 Oral Candidiasis 56 0.031
967
NRN004 Neuroendocrine Tumor 55 0.031
968
P ANT006 Antiphospholipid Syndrome 55 0.031
969
CRC006 Carcinoid Syndrome 55 0.031
970
RSC001 Rosacea 54 0.031
971
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.031
972
MYM001 Myoma 54 0.031
973
FRZ001 Frozen Shoulder 53 0.031
974
P AMY084 Amyloidosis, Finnish Type 53 0.031
975
BCT002 Bacterial Vaginosis 53 0.031
976
P HML001 Hemolytic-Uremic Syndrome 53 0.031
977
EXP004 Exophthalmos 52 0.031
978
DRM011 Dermatophytosis 52 0.031
979
P SML001 Small Cell Carcinoma 52 0.031
980
P CRN276 Corneal Endothelial Dystrophy 52 0.031
981
FML037 Female Breast Cancer 52 0.031
982
PPT001 Peptic Esophagitis 52 0.031
983
P MGR003 Migraine with Aura 52 0.031
984
SRS001 Serous Cystadenocarcinoma 52 0.031
985
P LCT001 Lactic Acidosis 51 0.031
986
CYS014 Cystadenocarcinoma 51 0.031
987
BLL003 Bell's Palsy 51 0.031
988
HYP781 Hypoascorbemia 51 0.031
989
BRX001 Bruxism 50 0.031
990
PST021 Postpartum Depression 50 0.031
991
RSP006 Respiratory System Disease 50 0.031
992
P SML016 Small Intestine Cancer 50 0.031
993
c SVR005 Severe Pre-Eclampsia 50 0.031
994
THY125 Thyroid Gland Medullary Carcinoma 50 0.031
995
MTB004 Metabolic Acidosis 50 0.031
996
HYP080 Hypogonadism 50 0.031
997
HYP017 Hypophosphatemia 50 0.031
998
INP001 Inappropriate Adh Syndrome 49 0.031
999
MNN009 Meningoencephalitis 49 0.031
1000
MYL003 Myeloid Sarcoma 49 0.031
1001
URM002 Uremia 49 0.031
1002
c DSB006 Desbuquois Dysplasia 1 48 0.031
1003
BRS064 Bursitis 48 0.031
1004
CRC014 Carcinoid Tumors, Intestinal 47 0.031
1005
PRD004 Prediabetes Syndrome 47 0.031
1006
AST006 Astigmatism 47 0.031
1007
MLT113 Multicentric Castleman Disease 47 0.031
1008
P CRC039 Coarctation of Aorta 47 0.031
1009
CNT033 Central Nervous System Cancer 47 0.031
1010
P HMR005 Hemorrhoid 46 0.031
1011
P HRN001 Horner's Syndrome 45 0.031
1012
RSP021 Respiratory Allergy 45 0.031
1013
HPT004 Hepatic Coma 45 0.031
1014
PRL008 Paralytic Ileus 45 0.031
1015
P OCY003 Oocyte Maturation Defect 1 45 0.031
1016
CLL014 Cll/sll 45 0.031
1017
END035 Endocrine Gland Cancer 45 0.031
1018
c ATM099 Autoimmune Uveitis 45 0.031
1019
c DRM054 Dermatitis, Atopic, 2 44 0.031
1020
APP010 Appendix Cancer 44 0.031
1021
IRT001 Iritis 44 0.031
1022
P PRL003 Proliferative Glomerulonephritis 44 0.031
1023
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.031
1024
PRT035 Peritoneum Cancer 44 0.031
1025
P HYP073 Hypersensitivity Reaction Type Iv Disease 44 0.031
1026
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 0.031
1027
URT014 Ureterolithiasis 44 0.031
1028
ANP009 Anaplastic Oligodendroglioma 43 0.031
1029
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.031
1030
MCR011 Microinvasive Gastric Cancer 43 0.031
1031
c SRC023 Sarcoidosis 2 43 0.031
1032
PMP004 Pemphigus Foliaceus 43 0.031
1033
BNS003 Binswanger's Disease 42 0.031
1034
P ACT244 Acth-Independent Cushing Syndrome 42 0.031
1035
c PST022 Posterior Uveal Melanoma 42 0.031
1036
FTL021 Fetal Macrosomia 42 0.031
1037
c ATS383 Autosomal Dominant Non-Syndromic Intellectual Disability 1 41 0.031
1038
LRG008 Large Granular Lymphocyte Leukemia 41 0.031
1039
CRN322 Coronavirus Infectious Disease 40 0.031
1040
c ADL096 Adult Hepatocellular Carcinoma 40 0.031
1041
SPR126 Superior Semicircular Canal Dehiscence 40 0.031
1042
ANG049 Angioedema Induced by Ace Inhibitors 40 0.031
1043
ADJ001 Adjustment Disorder 40 0.031
1044
PLC009 Placenta Praevia 39 0.031
1045
PTT003 Pituitary-Dependent Cushing's Disease 39 0.031
1046
OCL025 Ocular Toxoplasmosis 39 0.031
1047
c HMG029 Hemoglobin Se Disease 39 0.031
1048
DSS010 Dissociative Disorder 39 0.031
1049
c ATM075 Autoimmune Encephalitis 38 0.031
1050
c SYS043 Systemic Lupus Erythematosus 1 38 0.031
1051
BLD054 Blood Protein Disease 38 0.031
1052
ATM052 Autoimmune Disease 1 37 0.031
1053
c DFN360 Deafness, Autosomal Dominant 69 37 0.031
1054
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.031
1055
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.031
1056
PSD088 Pseudobulbar Affect 36 0.031
1057
INT003 Intracranial Hypotension 35 0.031
1058
c PRM301 Primary Cutaneous T-Cell Lymphoma 35 0.031
1059
c HYP438 Hyperaldosteronism, Familial, Type Iii 35 0.031
1060
CNT018 Central Nervous System Leukemia 34 0.031
1061
SML014 Small Intestine Leiomyosarcoma 34 0.031
1062
VST001 Vestibular Neuronitis 34 0.031
1063
LTT002 Letterer-Siwe Disease 33 0.031
1064
SML008 Small Intestine Lymphoma 33 0.031
1065
SHL001 Shoulder Impingement Syndrome 32 0.031
1066
DFF029 Diffuse Large B-Cell Lymphoma of the Central Nervous System 30 0.031
1067
SCT001 Sciatic Neuropathy 29 0.031
1068
TMP019 Temporomandibular Joint Anomaly 28 0.031
1069
c DRR018 Diarrhea 9 28 0.031
1070
P CRB210 Cerebrofacial Arteriovenous Metameric Syndrome 28 0.031
1071
PRR019 Perioral Myoclonia with Absences 27 0.031
1072
PGM030 Pigmentation Anomaly of the Skin 26 0.031
1073
c ATS386 Autosomal Dominant Non-Syndromic Intellectual Disability 4 25 0.031
1074
OCC008 Occipital Neuralgia 25 0.031
1075
c PRS134 Prostate Cancer, Hereditary, 3 24 0.031
1076
TRG006 Trigger Thumb 23 0.031
1077
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.031
1078
c ADL093 Adult Acute Monocytic Leukemia 20 0.031
1079