Search results for Dexamethasone acetate

1603 hits were found for Dexamethasone acetate

# Family MCID Name MIFTS Score
1
MYL069 Myeloma, Multiple 85 0.601
2
PLS009 Plasma Cell Neoplasm 51 0.456
3
DWN001 Down Syndrome 70 0.390
4
P PRS040 Prostate Cancer 97 0.317
5
MCL006 Macular Retinal Edema 55 0.315
6
P LYM118 Lymphoma 68 0.311
7
LYM019 Lymphosarcoma 46 0.295
8
48X005 48,xyyy 39 0.293
9
PNG002 Pain Agnosia 51 0.290
10
c RHB024 Rhabdomyosarcoma 2 67 0.288
11
c PRS136 Prostate Cancer, Hereditary, 6 33 0.274
12
c PRS130 Prostate Cancer, Hereditary, 8 32 0.274
13
P LKM002 Leukemia 68 0.266
14
P LKM062 Leukemia, Acute Lymphoblastic 69 0.253
15
P NTR004 Neutropenia 63 0.247
16
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.241
17
P CTR002 Cataract 60 0.241
18
DPR016 Depression 63 0.230
19
P BRS047 Breast Cancer 97 0.216
20
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 59 0.216
21
P UVT001 Uveitis 57 0.214
22
P RTN022 Retinal Vein Occlusion 53 0.212
23
P NRP001 Neuropathy 56 0.211
24
c PNS012 Paine Syndrome 61 0.207
25
c EPS039 Episodic Pain Syndrome, Familial, 1 42 0.206
26
P ADN016 Adenocarcinoma 64 0.205
27
P MNN013 Meningitis 66 0.202
28
P TRN020 Turner Syndrome 67 0.201
29
LYM040 Lymphoblastic Lymphoma 54 0.197
30
P THR014 Thrombocytopenia 67 0.194
31
P KDN018 Kidney Disease 72 0.193
32
DBT006 Diabetic Macular Edema 48 0.193
33
LYM133 Lymphoma, Hodgkin, Classic 69 0.192
34
LNG099 Lung Disease 60 0.189
35
MNT002 Mental Depression 58 0.187
36
ADL002 Adult Syndrome 70 0.185
37
RLP002 Relapsing-Remitting Multiple Sclerosis 56 0.184
38
CYT002 Cytokine Deficiency 42 0.184
39
P MLT020 Multiple Sclerosis 72 0.182
40
P AMY004 Amyloidosis 70 0.181
41
ALL026 Allergic Hypersensitivity Disease 62 0.179
42
P PRP019 Peripheral Nervous System Disease 58 0.179
43
c PRM038 Primary Agammaglobulinemia 44 0.179
44
HYP066 Hyperglycemia 61 0.179
45
P BCL017 B-Cell Lymphoma 58 0.177
46
LYM143 Lymphoma, Non-Hodgkin, Familial 72 0.174
47
CNS004 Constipation 58 0.169
48
LMY002 Leiomyoma 52 0.168
49
P MCR115 Microvascular Complications of Diabetes 5 66 0.168
50
ATX019 Ataxia with Vitamin E Deficiency 42 0.167
51
AYM001 Ayme-Gripp Syndrome 57 0.167
52
MCL027 Macular Dystrophy, Dominant Cystoid 50 0.166
53
P END044 Endometriosis 63 0.166
54
c ALM001 Al Amyloidosis 50 0.166
55
PPL061 Papular Epidermal Nevi with Skyline Basal Cell Layers Syndrome 25 0.166
56
ADN018 Adenoma 59 0.164
57
CLT003 Colitis 62 0.164
58
P SZR006 Seizure Disorder 56 0.163
59
P LNG032 Lung Cancer 98 0.161
60
END057 Endometrial Cancer 74 0.160
61
c BCT007 Bacterial Meningitis 55 0.159
62
PLS011 Plasmacytoma 56 0.156
63
ATX031 Ataxia, Combined Cerebellar and Peripheral, with Hearing Loss and Diabetes Mellitus 58 0.154
64
c NRF023 Neurofibromatosis, Type Ii 80 0.154
65
P PLY011 Polycystic Ovary Syndrome 56 0.153
66
MYF001 Myofibroma 45 0.153
67
PRP030 Purpura 54 0.151
68
P INF032 Infertility 57 0.151
69
BRN056 Bronchopulmonary Dysplasia 57 0.150
71
END040 Endogenous Depression 55 0.149
72
OCL006 Ocular Hypertension 53 0.148
73
LPD012 Lipoid Congenital Adrenal Hyperplasia 70 0.147
74
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.147
75
BRN004 Brain Edema 56 0.146
76
P MJR001 Major Depressive Disorder 68 0.146
77
CRV035 Cervical Cancer 76 0.146
78
P LKM071 Leukemia, Chronic Lymphocytic 79 0.145
79
c CNT016 Central Retinal Vein Occlusion 53 0.144
80
VSL002 Visual Epilepsy 59 0.144
81
P DRR001 Diarrhea 55 0.143
82
FCT007 Factor Vii Deficiency 67 0.143
83
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.143
84
AMN001 Amenorrhea 54 0.142
85
GST023 Gastric Ulcer 53 0.142
86
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.142
87
OST012 Osteoarthritis 78 0.141
88
DRM006 Dermatitis 61 0.141
89
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.139
90
P EXN002 Exanthem 57 0.138
91
P HDC001 Headache 57 0.137
92
P MYL006 Myeloid Leukemia 60 0.137
93
P GLM045 Glioma 63 0.136
94
GLL048 Glial Tumor 45 0.136
95
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.136
96
ATM095 Autoimmune Disease 62 0.135
97
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.135
98
AST005 Asthma 76 0.134
99
HYP056 Hypoglycemia 66 0.134
100
P OST002 Osteoporosis 74 0.134
101
P CLR023 Colorectal Cancer 99 0.133
102
P INF037 Inflammatory Bowel Disease 54 0.131
103
47X002 47,xyy 49 0.130
104
P CNJ013 Conjunctivitis 65 0.130
105
ULC004 Ulcerative Colitis 73 0.130
106
c SML038 Small Cell Cancer of the Lung 65 0.129
107
INS024 Insulin-Like Growth Factor I 79 0.129
108
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.129
109
P SNS001 Sensorineural Hearing Loss 60 0.128
110
MNT001 Mantle Cell Lymphoma 69 0.128
111
ALL014 Allergic Encephalomyelitis 38 0.128
112
CHL152 Childhood Acute Lymphocytic Leukemia 44 0.128
113
P OVR042 Ovarian Cancer 88 0.127
114
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.127
115
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.127
116
HYP043 Hyperandrogenism 48 0.126
117
HMN044 Human Immunodeficiency Virus Type 1 71 0.126
118
DFF005 Diffuse Large B-Cell Lymphoma 55 0.126
119
GLB015 Glioblastoma Multiforme 75 0.126
120
P ALP008 Alopecia 54 0.125
121
SHR059 Short Stature, Onychodysplasia, Facial Dysmorphism, and Hypotrichosis 47 0.124
122
P PRC019 Precocious Puberty 46 0.124
123
P ART022 Arthritis 69 0.123
124
ISC004 Ischemia 58 0.123
125
MCR004 Macroglobulinemia 49 0.123
126
P FLL037 Follicular Lymphoma 67 0.121
127
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.120
128
HYP005 Hypokalemia 55 0.120
129
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.119
130
c HYP595 Hypertension, Essential 84 0.118
131
P PNM007 Pneumonia 68 0.118
132
49X006 49, Xxxxy Syndrome 41 0.118
133
P END047 Endophthalmitis 53 0.117
134
CNN003 Conn's Syndrome 79 0.116
135
ACQ007 Acquired Immunodeficiency Syndrome 60 0.116
136
P CHR345 Chronic Pain 44 0.116
137
BNR002 Bone Resorption Disease 48 0.116
138
CHL079 Children's Interstitial Lung Disease 26 0.115
139
DFC004 Deficiency Anemia 70 0.114
140
HMT002 Hematologic Cancer 62 0.114
141
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 90 0.114
142
GLC003 Glucose Intolerance 54 0.112
143
MYL009 Myelodysplastic Syndrome 70 0.112
144
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.112
145
c ACT071 Acute Kidney Failure 60 0.112
146
P RSP003 Respiratory Failure 74 0.112
147
c LKM061 Leukemia, Acute Myeloid 84 0.112
148
ALL003 Allergic Rhinitis 67 0.111
149
SKN016 Skin Disease 63 0.111
150
c MGR028 Migraine with or Without Aura 1 67 0.111
151
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.111
152
LPD008 Lipid Metabolism Disorder 62 0.111
153
OST003 Osteonecrosis 61 0.110
154
P EPL164 Epilepsy 71 0.110
155
P LVR013 Liver Disease 68 0.110
156
CRP002 Croup 44 0.110
157
TCL028 T-Cell Lymphoblastic Leukemia/lymphoma 47 0.109
158
P HPT023 Hepatocellular Carcinoma 100 0.109
159
TCL023 T-Cell Lymphoma, Subcutaneous Panniculitis-Like 50 0.109
160
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.108
161
IMM167 Immune Deficiency Disease 78 0.108
162
WLD007 Waldenstroem's Macroglobulinemia 61 0.108
163
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.108
164
SDD008 Sudden Sensorineural Hearing Loss 43 0.108
165
P RHM011 Rheumatoid Arthritis 80 0.107
166
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.107
167
LYM012 Lymphoplasmacytic Lymphoma 47 0.107
168
c THR092 Thrombophilia Due to Thrombin Defect 73 0.107
169
c FLL041 Follicular Lymphoma 1 49 0.107
170
P RHN004 Rhinitis 57 0.107
171
HYP266 Hypoxia 57 0.106
172
EYD002 Eye Disease 58 0.106
173
c PST005 Posterior Uveitis 54 0.106
174
END086 End Stage Renal Disease 51 0.106
175
RTN017 Retinal Detachment 61 0.106
176
ACT011 Acute Contagious Conjunctivitis 40 0.106
177
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.106
178
P RTN018 Retinal Disease 53 0.105
179
P OPN001 Open-Angle Glaucoma 49 0.105
180
HYP060 Hyperinsulinism 54 0.104
181
OTT002 Otitis Media 72 0.104
182
P NRB001 Neuroblastoma 72 0.104
183
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.104
184
THR024 Thrombosis 57 0.104
185
LYM027 Lymphopenia 58 0.103
186
TXC005 Toxic Shock Syndrome 62 0.103
187
P VSC007 Vascular Disease 63 0.103
188
P CRN026 Corneal Edema 43 0.103
189
BRK010 Burkitt Lymphoma 67 0.102
190
MLN003 Melancholia 38 0.102
191
c ACT027 Acute Pancreatitis 60 0.101
192
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 48 0.101
193
P ADL010 Adult Respiratory Distress Syndrome 65 0.101
194
PLM010 Pulmonary Edema 54 0.101
195
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.100
196
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.100
197
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.100
198
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.100
199
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.100
200
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.100
201
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.100
202
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.100
203
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.100
204
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.100
205
P PMP001 Pemphigus 54 0.100
206
CNG034 Congestive Heart Failure 69 0.100
207
P DRM053 Dermatitis, Atopic 66 0.100
208
BCK006 Back Pain 42 0.100
209
RTC005 Reticulosarcoma 47 0.099
210
MTB004 Metabolic Acidosis 50 0.099
211
P OTT001 Otitis Externa 39 0.099
212
ANX010 Anxiety 73 0.099
213
P HPT021 Hepatitis 67 0.099
214
c ACT073 Acute Leukemia 58 0.098
215
P SRC025 Sarcoidosis 1 70 0.098
216
IRD001 Iridocyclitis 53 0.098
217
MYM001 Myoma 54 0.098
218
c FNC043 Fanconi Anemia, Complementation Group E 62 0.098
219
P ENC018 Encephalopathy 61 0.098
220
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.098
221
P CNR004 Cone-Rod Dystrophy 2 73 0.097
222
BRN002 Bronchiolitis 59 0.097
223
OCL069 Ocular Motor Apraxia 51 0.097
224
P DMN002 Dementia 66 0.097
225
P HRT032 Heart Disease 75 0.097
226
P DBT009 Diabetes Mellitus 64 0.097
227
SBC016 Subacute Delirium 44 0.096
228
CLF027 Cleft Palate, Isolated 64 0.096
229
c LKM005 Leukemia, T-Cell, Chronic 34 0.096
230
c CHR684 Chronic Kidney Disease 70 0.096
231
LNG031 Lung Benign Neoplasm 51 0.095
232
LTH001 Lethal Midline Granuloma 44 0.095
233
PLS016 Plasma Cell Leukemia 53 0.095
234
OST062 Osteoarthritis with Mild Chondrodysplasia 47 0.095
235
P MYP004 Myopathy 70 0.095
236
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.094
237
HDN002 Head Injury 46 0.094
238
P PRS038 Personality Disorder 65 0.093
239
c SYS001 Systemic Lupus Erythematosus 86 0.092
240
P MSC003 Muscular Atrophy 52 0.092
241
P HRP006 Herpes Simplex 65 0.092
242
ACR007 Acromegaly 71 0.091
243
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.091
244
ALC007 Alcohol Dependence 66 0.091
245
STR067 Stroke, Ischemic 81 0.091
246
ATH013 Atherosclerosis Susceptibility 65 0.091
247
c DRR009 Diarrhea 6 46 0.091
248
PRP036 Peripheral T-Cell Lymphoma 53 0.090
249
c LKM056 Leukemia, Chronic Lymphocytic 2 48 0.090
250
TRP009 Triple X Syndrome 42 0.090
251
TXC002 Toxic Encephalopathy 53 0.090
252
c HYP836 Hypercholesterolemia, Familial, 1 73 0.090
253
c PLY105 Polycystic Ovary Syndrome 1 38 0.090
254
KHN001 Kuhnt-Junius Degeneration 47 0.090
255
P VSC011 Vasculitis 62 0.089
256
c BRN108 Branchiootic Syndrome 1 62 0.089
257
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.089
258
P PNC035 Pancreatic Cancer 84 0.089
259
SPN186 Spinal Cord Injury 60 0.089
260
LVR012 Liver Cirrhosis 62 0.089
261
OST159 Osteogenic Sarcoma 66 0.089
262
NWB001 Newborn Respiratory Distress Syndrome 58 0.088
263
P HYP086 Hypothyroidism 69 0.088
264
P ANP001 Anaplastic Large Cell Lymphoma 58 0.088
265
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.088
266
CHL014 Cholera 59 0.087
267
GLS018 Glass Syndrome 57 0.087
268
P GRF003 Graft-Versus-Host Disease 72 0.087
269
RNL114 Renal Cell Carcinoma, Nonpapillary 78 0.086
270
PRS045 Prostatic Hypertrophy 53 0.086
271
P BPL003 Bipolar Disorder 56 0.086
272
P HYP098 Hypereosinophilic Syndrome 67 0.086
273
MNR012 Meniere Disease 57 0.086
274
c PRM226 Primary Central Nervous System Lymphoma 48 0.086
275
P SCH015 Schizophrenia 74 0.086
276
P INT143 Interstitial Cystitis 61 0.085
277
P CNT005 Central Nervous System Lymphoma 53 0.085
278
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.085
279
P BND020 Bone Disease 59 0.085
280
P GLM007 Glomerulonephritis 57 0.084
281
SQM006 Squamous Cell Carcinoma 60 0.084
282
LYM129 Lymphoma, Mucosa-Associated Lymphoid Type 64 0.084
283
P GLM040 Glioma Susceptibility 1 81 0.084
284
BRN071 Brain Injury 49 0.084
285
ALL009 Allergic Conjunctivitis 50 0.084
286
P PSR002 Psoriasis 62 0.084
287
P MYC007 Myocardial Infarction 70 0.084
288
CNT047 Contact Dermatitis 58 0.084
289
P CRD246 Cardiovascular System Disease 57 0.084
290
P DDN001 Duodenal Ulcer 52 0.084
291
MDD011 Mood Disorder 62 0.083
292
P PTT006 Pituitary Adenoma 55 0.083
293
PTT037 Pituitary Tumors 44 0.083
294
KRT019 Keratitis, Hereditary 65 0.083
295
CYS001 Cystic Fibrosis 81 0.083
296
c MCR129 Microvascular Complications of Diabetes 1 66 0.083
297
MNN042 Meningioma, Radiation-Induced 62 0.083
298
NRR001 Neuroretinitis 42 0.083
299
SVR004 Severe Combined Immunodeficiency 73 0.083
300
P PNC044 Pancreatitis 61 0.083
301
P STR020 Strabismus 55 0.083
302
MCH006 Mechanical Strabismus 42 0.083
303
RSP019 Respiratory Distress Syndrome in Premature Infants 58 0.082
304
NTR005 Nutritional Deficiency Disease 62 0.082
305
PST011 Pustulosis of Palm and Sole 52 0.082
306
HDG002 Hodgkin's Lymphoma, Lymphocytic-Histiocytic Predominance 42 0.082
307
HDG004 Hodgkin's Granuloma 23 0.082
308
HDG006 Hodgkin's Paragranuloma 22 0.082
309
HYP081 Hypolipoproteinemia 51 0.082
310
CMR002 Coumarin Resistance 56 0.082
311
SRC014 Sarcoma 65 0.082
312
PNM013 Pneumococcal Meningitis 42 0.082
313
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.082
314
P HYP076 Hyperthyroidism 55 0.082
315
c LKM063 Leukemia, Chronic Myeloid 72 0.082
316
c MNN043 Meningioma, Familial 74 0.081
317
SPN021 Spinal Meningioma 50 0.081
318
SCR001 Secretory Meningioma 41 0.081
319
LYM002 Lymphoplasmacyte-Rich Meningioma 36 0.081
320
P OVR049 Ovarian Disease 52 0.081
321
RTN023 Retinitis 46 0.081
322
BRN024 Bronchitis 68 0.081
323
HRP004 Herpes Zoster 60 0.080
324
P KDN017 Kidney Cancer 60 0.080
325
HRW001 Hair Whorl 36 0.080
326
P ADL017 Adult T-Cell Leukemia 56 0.080
327
TRM010 Traumatic Brain Injury 51 0.080
328
OVR094 Ovarian Epithelial Cancer 38 0.080
329
P CRN300 Coronary Heart Disease 1 63 0.080
330
LPP008 Lipoprotein Quantitative Trait Locus 62 0.080
331
HYP025 Hyperphosphatemia 48 0.080
332
P NPH012 Nephrotic Syndrome 60 0.080
333
TLN003 Telangiectasis 52 0.080
334
ERY051 Erythroleukemia, Familial 56 0.079
335
PPT005 Peptic Ulcer Disease 59 0.079
336
CRB039 Cerebrovascular Disease 67 0.079
337
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.079
338
P LPS004 Lupus Erythematosus 61 0.079
339
SPN035 Spindle Cell Sarcoma 53 0.079
340
BCT022 Bacterial Infectious Disease 56 0.079
341
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.079
342
MCS002 Mucositis 56 0.079
343
PRS021 Prostatic Adenoma 51 0.079
344
END041 Endometrial Adenocarcinoma 63 0.079
345
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.079
346
FCL014 Focal Epilepsy 54 0.079
347
AGN016 Aging 56 0.079
348
c ADL052 Adult Acute Lymphocytic Leukemia 47 0.078
349
FNG017 Fungal Infectious Disease 53 0.078
350
PLS025 Plasmablastic Lymphoma 47 0.078
351
FTT001 Fatty Liver Disease 61 0.078
352
c DBT099 Diabetes Mellitus, Type I 65 0.078
353
PRS012 Pars Planitis 48 0.077
354
GLC086 Glucocorticoid-Induced Osteoporosis 43 0.077
355
RCK004 Rickets 68 0.077
356
KRT006 Keratoconjunctivitis 53 0.077
357
BLY001 B-Lymphoblastic Leukemia/lymphoma 48 0.077
358
RSP007 Respiratory Distress Syndrome, Infant 30 0.077
359
TBR011 Tuberculous Meningitis 48 0.077
360
c MLG068 Malignant Glioma 46 0.077
361
c OVR114 Ovarian Cancer 1 38 0.077
362
BRN028 Brain Cancer 74 0.077
363
P ACT010 Acth-Secreting Pituitary Adenoma 55 0.077
364
P ACT105 Acute Mountain Sickness 52 0.077
366
RTN193 Retinitis Pigmentosa and Erythrocytic Microcytosis 52 0.077
367
P PLY019 Polyneuropathy 56 0.076
368
c MCR112 Microvascular Complications of Diabetes 2 41 0.076
369
RDC002 Radiculopathy 50 0.076
370
c CHR064 Chronic Monocytic Leukemia 33 0.076
371
ENT004 Enthesopathy 49 0.076
372
NRT004 Neuritis 52 0.076
373
LYM048 Lymphoma, Large-Cell, Immunoblastic 29 0.075
374
TCL027 T-Cell Acute Lymphoblastic Leukemia 51 0.075
375
HMP009 Haemophilus Influenzae 43 0.075
376
P RCT021 Rectum Cancer 52 0.075
377
P GST053 Gastric Cancer 83 0.075
378
GLC106 Glucocorticoid Resistance, Generalized 48 0.075
379
ANV001 Anovulation 47 0.075
380
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.075
381
PHR003 Pharyngitis 57 0.074
382
c PCH010 Pachyonychia Congenita 3 44 0.074
383
ART140 Arteries, Anomalies of 52 0.074
384
ADN027 Adenomyosis 56 0.074
385
CHL068 Cholestasis 61 0.074
386
P PHC003 Pheochromocytoma 71 0.074
387
ADR040 Adrenal Gland Pheochromocytoma 46 0.074
388
c FML035 Familial Hyperlipidemia 55 0.073
389
P AST007 Astrocytoma 51 0.073
390
CRB037 Cerebral Palsy 69 0.073
391
ANR007 Anorexia Nervosa 63 0.073
392
P BCL004 B-Cell Non-Hodgkin Lymphoma 44 0.073
393
ADR057 Adrenogenital Syndrome 32 0.073
394
CLN015 Colon Adenocarcinoma 65 0.073
395
c ATR087 Atrial Standstill 1 75 0.073
396
PRT037 Pertussis 65 0.073
397
P LCH002 Lichen Planus 53 0.073
398
DYS073 Dysphagia 50 0.073
399
CHR661 Choreoathetosis and Congenital Hypothyroidism with or Without Pulmonary Dysfunction 48 0.073
400
CHL065 Cholangiocarcinoma 68 0.073
401
P ENC004 Encephalitis 61 0.073
402
TND005 Tendinitis 54 0.073
403
STR019 Steroid-Induced Glaucoma 32 0.072
404
P SLP006 Sleep Apnea 69 0.072
405
ADR054 Adrenocortical Carcinoma, Hereditary 66 0.072
406
c ACT068 Acute Cystitis 63 0.072
407
PLM033 Pulmonary Embolism 59 0.072
408
PMS001 Poems Syndrome 60 0.072
409
PRT036 Peritonitis 64 0.072
410
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.072
411
ANG046 Angioimmunoblastic T-Cell Lymphoma 52 0.071
412
P PLM037 Pulmonary Hypertension 67 0.071
413
P CYS018 Cystitis 59 0.071
414
P FBR017 Fibrosarcoma 56 0.071
415
STM007 Stomatitis 50 0.071
416
c MJR024 Major Affective Disorder 9 41 0.071
417
c MJR022 Major Affective Disorder 8 38 0.071
418
DRY001 Dry Eye Syndrome 47 0.071
419
P SPP010 Suppressor of Tumorigenicity 3 51 0.071
420
P NRV007 Nervous System Disease 66 0.071
421
P ART023 Arthropathy 62 0.071
422
ILS001 Ileus 51 0.071
423
IRN002 Iron Metabolism Disease 57 0.071
424
P PLM036 Pulmonary Fibrosis 65 0.071
425
c CHL157 Childhood B-Cell Acute Lymphoblastic Leukemia 33 0.071
426
PLR008 Pleurisy 50 0.071
427
P LNG064 Lung Cancer Susceptibility 3 78 0.071
428
c GLC092 Glaucoma, Primary Open Angle 62 0.071
429
PST028 Post-Traumatic Stress Disorder 58 0.071
430
MRG003 Marginal Zone B-Cell Lymphoma 52 0.071
431
PLP001 Pulpitis 49 0.071
432
KRT001 Keratoconjunctivitis Sicca 49 0.070
433
P ASP006 Aspergillosis 69 0.070
434
ANR040 Aneurysm 59 0.070
435
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.070
436
CRH001 Crohn's Disease 74 0.070
437
c MCR120 Microvascular Complications of Diabetes 7 47 0.070
438
PMP006 Pemphigus Vulgaris, Familial 57 0.069
439
ALL006 Allergic Asthma 56 0.069
440
P GST044 Gastritis 56 0.069
441
P HYP750 Hypertriglyceridemia, Familial 62 0.069
442
OVR029 Ovarian Hyperstimulation Syndrome 64 0.069
443
IMP005 Impotence 52 0.069
444
c MCL013 Mucolipidosis Iv 66 0.069
445
c INT064 Intermediate Uveitis 55 0.069
446
HYP780 Hypoadrenocorticism, Familial 63 0.069
447
c SCN036 Secondary Progressive Multiple Sclerosis 51 0.069
448
ADR008 Adrenal Adenoma 55 0.069
449
VSL013 Visual Impairment and Progressive Phthisis Bulbi 41 0.068
451
CVD001 Covid-19 44 0.068
452
ADR056 Adrenal Insufficiency, Congenital, with 46,xy Sex Reversal, Partial or Complete 56 0.068
453
SNS003 Sensory Peripheral Neuropathy 54 0.068
454
CMM005 Common Cold 57 0.068
455
P CND004 Candidiasis 58 0.068
456
HYP080 Hypogonadism 50 0.068
457
PPL001 Papillary Adenoma 44 0.068
458
MTN003 Motion Sickness 53 0.067
459
P MYC084 Mycobacterium Tuberculosis 1 68 0.067
460
P SJG008 Sjogren Syndrome 61 0.067
461
SFT003 Soft Tissue Sarcoma 56 0.067
462
INT079 Intrahepatic Cholangiocarcinoma 51 0.067
463
P CHR012 Chronic Granulomatous Disease 67 0.067
464
P PLY169 Polycystic Liver Disease 1 with or Without Kidney Cysts 60 0.067
465
GST050 Gastrointestinal System Disease 56 0.067
466
P RTN024 Retinoblastoma 73 0.067
467
c SCL052 Scleroderma, Familial Progressive 61 0.067
468
c FML008 Familial Retinoblastoma 53 0.067
469
IDP033 Idiopathic Edema 44 0.067
470
HLL004 Hellp Syndrome 54 0.067
471
P ATR011 Atrial Fibrillation 66 0.066
472
c CHR417 Chronic Graft Versus Host Disease 57 0.066
473
EPC002 Epicondylitis 41 0.066
474
P HMP002 Hemophagocytic Lymphohistiocytosis 54 0.066
475
ENT001 Enterocele 39 0.066
476
P URT039 Urticaria 58 0.066
477
P CTN015 Cutaneous T Cell Lymphoma 49 0.066
478
NDL020 Nodal Marginal Zone B-Cell Lymphoma 34 0.066
479
BNM001 Bone Marrow Cancer 43 0.065
480
KPS004 Kaposi Sarcoma 75 0.065
481
SYN007 Synovitis 54 0.065
482
PLC002 Plica Syndrome 36 0.065
483
P NSP012 Nasopharyngeal Carcinoma 66 0.065
484
P MLN008 Melanoma 69 0.065
485
ACT119 Acute Promyelocytic Leukemia 63 0.065
486
P ALC033 Alcohol Use Disorder 58 0.065
487
c MLN055 Melanoma, Cutaneous Malignant 10 52 0.065
488
P VTR007 Vitreoretinopathy 46 0.065
489
c SVR001 Severe Acute Respiratory Syndrome 62 0.065
490
MLR004 Malaria 81 0.065
491
P HYP726 Hypercalcemia, Infantile, 1 58 0.065
492
ENT011 Enterocolitis 51 0.065
493
ORL013 Oral Lichen Planus 45 0.065
494
WTH001 Withdrawal Disorder 48 0.064
495
PRR004 Preretinal Fibrosis 37 0.064
496
PRS129 Prostatic Hyperplasia, Benign 49 0.064
497
ING001 Inguinal Hernia 60 0.064
498
P THY023 Thymoma 65 0.064
499
c PRC016 Pre-Eclampsia 63 0.064
500
P CHR285 Chronic Myelomonocytic Leukemia 60 0.064
501
c THY107 Thymoma, Familial 52 0.064
502
VTR013 Vitreoretinopathy, Neovascular Inflammatory 62 0.064
503
c HPT001 Hepatitis C 62 0.064
504
PRN019 Perinatal Necrotizing Enterocolitis 59 0.064
505
SPL004 Splenic Marginal Zone Lymphoma 51 0.064
506
ALN001 Aland Island Eye Disease 50 0.064
507
KRT002 Keratomalacia 47 0.063
508
ALL010 Allergic Contact Dermatitis 56 0.063
509
PRP027 Peripheral Vascular Disease 71 0.063
510
P ALP009 Alopecia Areata 60 0.063
511
CYT018 Cytochrome P450 2d6 Variant 27 0.063
512
AZS001 Azoospermia 50 0.063
513
TNS005 Tonsillitis 57 0.063
514
PSY004 Psychotic Disorder 67 0.063
515
P ATX030 Ataxia-Telangiectasia 82 0.062
516
CRD223 Cardiac Arrhythmia 60 0.062
517
GLS001 Gliosarcoma 54 0.062
518
SXL003 Sexual Disorder 47 0.062
519
THY029 Thyroid Carcinoma 59 0.062
520
TND004 Tendinopathy 43 0.062
521
NSS002 Neisseria Meningitidis Infection 47 0.062
522
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.062
523
P BNG032 Benign Mesothelioma 46 0.062
524
P GRV001 Graves' Disease 55 0.062
525
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.062
526
MYL031 Myeloproliferative Neoplasm 66 0.062
527
P HYP061 Hypertrophic Cardiomyopathy 70 0.061
528
RDN001 Reading Disorder 40 0.061
529
P TRM003 Tremor 54 0.061
530
RTN020 Retinal Vascular Disease 46 0.061
531
TST015 Testicular Disease 43 0.061
532
P AVS003 Avascular Necrosis 42 0.061
533
IRR002 Irritable Bowel Syndrome 65 0.061
534
CRC006 Carcinoid Syndrome 55 0.061
535
c EXD008 Exudative Vitreoretinopathy 1 71 0.061
536
BLP005 Blepharitis 50 0.061
537
P PRD008 Periodontitis 64 0.061
538
P MLG074 Malignant Mesenchymoma 40 0.061
539
MYC006 Mycosis Fungoides 66 0.061
540
SZR001 Sezary's Disease 60 0.061
541
FSC004 Fasciitis 50 0.061
542
c PRM340 Primary Adrenal Insufficiency 36 0.061
543
GRM010 Germ Cells Tumors 34 0.061
544
BRN038 Bronchial Disease 53 0.060
545
RDC006 Red Cell Aplasia 43 0.060
546
c CHR682 Chronic Bilirubin Encephalopathy 39 0.060
547
PDG002 Pdgfrb-Associated Chronic Eosinophilic Leukemia 27 0.060
548
DMY004 Demyelinating Disease 52 0.060
549
P HYP069 Hyperparathyroidism 63 0.060
550
KHL003 Kohlschutter-Tonz Syndrome 65 0.060
551
ORL005 Oral Candidiasis 56 0.060
552
URM002 Uremia 49 0.060
553
PPL022 Papilloma 54 0.059
554
SQM002 Squamous Cell Papilloma 46 0.059
555
P OPT006 Optic Nerve Disease 60 0.059
556
P SCK005 Sickle Cell Disease 50 0.059
557
P RTN008 Retinitis Pigmentosa 79 0.059
558
c HMP022 Hemophagocytic Lymphohistiocytosis, Familial, 1 63 0.059
559
PNC001 Pancytopenia 54 0.059
560
MNN020 Meningococcal Infection 46 0.059
561
P CHL156 Childhood T-Cell Acute Lymphoblastic Leukemia 38 0.059
562
P BCL013 B-Cell Adult Acute Lymphocytic Leukemia 32 0.059
563
VRL011 Viral Infectious Disease 61 0.059
564
P MNC007 Monocytic Leukemia 53 0.059
565
MST005 Mastitis 53 0.059
566
c INF071 Inflammatory Bowel Disease 1 67 0.059
567
c HPT016 Hepatitis B 59 0.059
568
P PRR002 Pure Red-Cell Aplasia 47 0.059
569
EXT010 Extramedullary Plasmacytoma 45 0.059
570
ORL011 Oral Cancer 60 0.059
571
HRY003 Hairy Cell Leukemia 55 0.059
572
ADR016 Adrenal Cortical Carcinoma 48 0.059
573
CRB004 Cerebral Artery Occlusion 45 0.059
574
P HMR005 Hemorrhoid 46 0.059
575
P INS002 in Situ Carcinoma 53 0.058
576
P CRD119 Cardiac Arrest 67 0.058
577
P HML002 Hemolytic Anemia 63 0.058
578
NRT001 Neurotic Disorder 53 0.058
579
P MYC033 Myoclonus 46 0.058
580
MCL003 Macular Holes 40 0.058
581
CNT060 Central Serous Chorioretinopathy 38 0.058
582
LGH004 Light Chain Deposition Disease 40 0.058
583
MNN032 Meningococcal Meningitis 54 0.058
584
PST092 Posttransplant Acute Limbic Encephalitis 29 0.058
585
ACT058 Active Peptic Ulcer Disease 55 0.058
586
P ART021 Arteriosclerosis 54 0.057
587
TTN003 Tetanus 65 0.057
588
P HYP040 Hypospadias 51 0.057
589
P INT068 Intestinal Disease 53 0.057
590
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.057
591
LYM051 Lymphomatoid Granulomatosis 45 0.057
592
P TXP001 Toxoplasmosis 60 0.057
593
GRN017 Granulocytopenia 44 0.057
594
SML011 Smoldering Myeloma 33 0.057
595
c INF152 Infectious Posterior Uveitis 19 0.057
596
c NNN032 Non-Infectious Posterior Uveitis 19 0.057
597
PPL049 Papillon-Lefevre Syndrome 65 0.057
598
INT054 Intraocular Lymphoma 48 0.057
599
GST020 Gastric Antral Vascular Ectasia 41 0.057
600
ADR005 Adrenal Carcinoma 58 0.056
601
ERY003 Erythema Multiforme 58 0.056
602
STT002 Status Asthmaticus 50 0.056
603
MYL075 Myelodysplastic/myeloproliferative Neoplasm 49 0.056
604
PRS063 Paresthesia 41 0.056
605
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 0.056
606
GYN001 Gynecomastia 49 0.056
607
INF021 Infant Gynecomastia 31 0.056
608
P LYM033 Lymphoproliferative Syndrome 59 0.056
609
ESP021 Esophageal Cancer 90 0.056
610
P SKN015 Skin Carcinoma 66 0.056
611
P BRS044 Breast Adenocarcinoma 59 0.056
612
c PSR017 Psoriasis 2 53 0.056
613
c PSR023 Psoriasis 1 52 0.056
614
c PSR032 Psoriasis 11 47 0.056
615
c PSR028 Psoriasis 7 42 0.056
616
c PSR018 Psoriasis 13 41 0.056
617
ADR004 Adrenal Cortical Adenocarcinoma 39 0.056
618
ETN001 Eating Disorder 60 0.056
619
HRN029 Hearing Loss, Noise-Induced 37 0.056
620
P HYD006 Hydrocephalus 66 0.055
621
P PNV001 Panuveitis 50 0.055
622
ACT084 Acute Stress Disorder 47 0.055
623
HML018 Homologous Wasting Disease 22 0.055
624
c MCL062 Mucolipidosis Ii Alpha/beta 68 0.055
625
P ORT004 Orthostatic Intolerance 62 0.055
626
P ANG015 Angioedema 57 0.055
627
PNM008 Pneumothorax 56 0.055
628
P SBS003 Substance Abuse 55 0.055
629
PLY118 Polyglucosan Body Myopathy 1 with or Without Immunodeficiency 53 0.055
630
NTR046 Neutrophil Migration 50 0.055
631
CHR074 Choriocarcinoma 47 0.055
632
c TCL024 T-Cell Non-Hodgkin Lymphoma 34 0.055
633
P BLD134 Bladder Cancer 79 0.055
634
ACT193 Acute Myeloid Leukemia with Abnormal Bone Marrow Eosinophils Inv(16)(p13q22) or T(16;16)(p13;q22) 54 0.055
635
KRT013 Keratolytic Winter Erythema 46 0.055
636
PLN007 Plantar Fasciitis 32 0.055
637
MLG164 Malignant Epithelial Tumor of Ovary 26 0.055
638
P MYS003 Myasthenia Gravis 68 0.055
639
P TST021 Testicular Germ Cell Tumor 60 0.055
640
P CRN024 Corneal Disease 44 0.055
641
ADR041 Adrenal Cortical Adenoma 43 0.055
642
ATY042 Atypical Chronic Myeloid Leukemia 49 0.055
643
c HPT073 Hepatitis C Virus 72 0.055
644
HRP009 Herpes Simplex Encephalitis 52 0.055
645
GRM005 Germ Cell Cancer 47 0.055
646
P LMY004 Leiomyosarcoma 63 0.054
647
P INT070 Intestinal Obstruction 58 0.054
648
P OPT009 Optic Neuritis 57 0.054
649
P PYL005 Pyelonephritis 56 0.054
650
c GLL024 Gallbladder Disease 1 53 0.054
651
MXD026 Mixed Glioma 45 0.054
652
CHR078 Chorioretinitis 50 0.054
653
P INN002 Inner Ear Disease 47 0.054
654
GT001 Gout 64 0.054
655
PST021 Postpartum Depression 50 0.054
656
CHC001 Chickenpox 60 0.053
657
PLL012 Pollen Allergy 46 0.053
658
P MDL005 Medulloblastoma 77 0.053
659
NRM005 Neuromuscular Disease 64 0.053
660
c LKM070 Leukemia, Acute Monocytic 57 0.053
661
P HYP024 Hypoparathyroidism 56 0.053
662
P KRT007 Keratoconus 50 0.053
663
MNC006 Monoclonal Gammopathy of Uncertain Significance 48 0.053
664
OBS002 Obsessive-Compulsive Disorder 68 0.053
665
MLT163 Multiple Pterygium Syndrome, Escobar Variant 64 0.053
666
ASP007 Aspiration Pneumonia 48 0.053
667
P DBT005 Diabetes Insipidus 55 0.053
668
APN008 Apnea, Obstructive Sleep 64 0.053
669
INT075 Intracranial Hypertension 53 0.053
670
c INF145 Infantile Liver Failure Syndrome 1 50 0.053
671
ATS010 Autosomal Recessive Disease 48 0.053
672
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.053
673
ADT003 Auditory System Disease 48 0.053
674
P SCL015 Scleritis 48 0.053
675
CRN027 Corneal Neovascularization 47 0.053
676
MXD050 Mixed Phenotype Acute Leukemia 43 0.053
677
HYP344 Hyperthyroidism, Familial Gestational 39 0.053
678
P ESP024 Esophagitis 62 0.053
679
APP008 Appendicitis 61 0.053
680
CYT008 Cytomegalovirus Infection 57 0.053
681
LPT014 Leptin Deficiency or Dysfunction 74 0.052
682
BCT002 Bacterial Vaginosis 53 0.052
683
P LCT001 Lactic Acidosis 51 0.052
684
P MLN069 Melanoma, Uveal 59 0.052
685
c PTT057 Pituitary Adenoma 4, Acth-Secreting 51 0.052
686
SPL018 Splenomegaly 48 0.052
687
GST092 Gastroesophageal Reflux 67 0.052
688
DSS009 Disseminated Intravascular Coagulation 57 0.052
689
HYP276 Hypercarotenemia and Vitamin a Deficiency, Autosomal Dominant 54 0.052
690
RFR002 Refractory Hairy Cell Leukemia 33 0.052
691
CLS052 Classic Hairy Cell Leukemia 27 0.052
692
P ALZ034 Alzheimer Disease 88 0.052
693
CRY014 Cryptococcal Meningitis 48 0.052
694
SKN019 Skin Melanoma 68 0.051
695
P VTL004 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 1 60 0.051
696
TNS014 Tenosynovitis 44 0.051
697
c VTL009 Vitiligo-Associated Multiple Autoimmune Disease Susceptibility 6 42 0.051
698
SVR097 Severe Cutaneous Adverse Reaction 69 0.051
699
SPN041 Spinal Cord Disease 56 0.051
700
MCN017 Meconium Ileus 52 0.051
701
BNN003 Bone Inflammation Disease 48 0.051
702
CHL149 Childhood Acute Myeloid Leukemia 44 0.051
703
ARC002 Arachnoiditis 42 0.051
704
SPN354 Spinal Arachnoiditis 36 0.051
705
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 32 0.051
706
ERY066 Erythema Multiforme Major 30 0.051
707
c INF019 Infectious Anterior Uveitis 28 0.051
708
P NNN030 Non-Infectious Anterior Uveitis 14 0.051
709
MYL005 Myelofibrosis 70 0.051
710
CRH005 Crohn's Colitis 53 0.051
711
CHL061 Childhood Leukemia 48 0.051
712
P OLG002 Oligodendroglioma 67 0.051
713
INS001 Insulinoma 60 0.051
714
PTT009 Pituitary Gland Disease 54 0.051
715
c ACT135 Acute Graft Versus Host Disease 52 0.051
716
P CLL015 Collagen Disease 47 0.051
717
NRV004 Nerve Compression Syndrome 40 0.051
718
P PNC025 Panic Disorder 53 0.051
719
c CNT035 Central Nervous System Disease 52 0.051
720
P MSC005 Muscular Dystrophy 66 0.051
721
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.051
722
NRN004 Neuroendocrine Tumor 55 0.051
723
FRZ001 Frozen Shoulder 53 0.051
724
CNT033 Central Nervous System Cancer 47 0.051
725
c DRM054 Dermatitis, Atopic, 2 44 0.051
726
MCR011 Microinvasive Gastric Cancer 43 0.051
727
c SCN007 Secondary Hyperparathyroidism 51 0.051
728
PRP080 Peripheral Artery Disease 53 0.051
729
TST014 Testicular Cancer 46 0.051
730
RLP008 Relapsed/refractory Diffuse Large B-Cell Lymphoma 31 0.051
731
P OCL013 Oculodentodigital Dysplasia 69 0.050
732
MSC007 Muscle Hypertrophy 64 0.050
733
ASP008 Aspiration Pneumonitis 45 0.050
734
CYS005 Cysticercosis 53 0.050
735
BRD004 Borderline Personality Disorder 53 0.050
736
MGK001 Megakaryocytic Leukemia 64 0.049
737
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.049
738
CRT017 Cartilage Disease 54 0.049
739
ACT098 Acute Erythroid Leukemia 48 0.049
740
SKN005 Skin Atrophy 43 0.049
741
P TST026 Testicular Germ Cell Cancer 43 0.049
742
ART016 Aortic Aneurysm 69 0.049
743
CRP001 Carpal Tunnel Syndrome 67 0.049
744
HYP020 Hyperprolactinemia 64 0.049
745
P RHB003 Rhabdomyosarcoma 63 0.049
746
HPT019 Hepatic Encephalopathy 60 0.049
747
DRM011 Dermatophytosis 52 0.049
748
BRS064 Bursitis 48 0.049
749
CRC014 Carcinoid Tumors, Intestinal 47 0.049
750
HPT004 Hepatic Coma 45 0.049
751
c ATM075 Autoimmune Encephalitis 38 0.049
752
BCK003 Background Diabetic Retinopathy 46 0.049
753
P SBR004 Seborrheic Dermatitis 45 0.049
754
c SCN052 Secondary Adrenal Insufficiency 36 0.049
755
INT146 Intervertebral Disc Disease 63 0.049
756
STT001 Status Epilepticus 60 0.049
757
PRC013 Pericarditis 54 0.049
758
HST010 Histiocytosis 48 0.049
759
P CRN035 Cranial Nerve Palsy 42 0.049
760
C1N001 C1 Inhibitor Deficiency 39 0.049
761
TST003 Testicular Leukemia 27 0.049
762
OST017 Osteomyelitis 64 0.049
763
TRG002 Trigeminal Neuralgia 60 0.049
764
IGR001 Ige Responsiveness, Atopic 59 0.049
765
P BCT020 Bacteremia 2 44 0.049
766
P MYC008 Myocarditis 59 0.049
767
P FCL005 Focal Segmental Glomerulosclerosis 57 0.049
768
RTN001 Retinal Vasculitis 47 0.049
769
P CLS010 Cluster Headache 42 0.049
770
P HYP802 Hypocalcemia, Autosomal Dominant 1 69 0.049
771
PNC129 Pancreatic Adenocarcinoma 68 0.049
772
ANG054 Angina Pectoris 66 0.049
773
P ECL001 Eclampsia 50 0.049
774
P OVR046 Ovarian Cyst 47 0.048
775
P ECT045 Ectodermal Dysplasia-Syndactyly Syndrome 1 39 0.048
776
c ACT134 Acute Liver Failure 56 0.048
777
THR016 Thrombophlebitis 51 0.048
778
PNN001 Panniculitis 51 0.048
779
CRT064 Corticosterone Methyloxidase Deficiency 20 0.048
780
P OCY003 Oocyte Maturation Defect 1 45 0.048
781
c SYS043 Systemic Lupus Erythematosus 1 38 0.048
782
ATM052 Autoimmune Disease 1 37 0.048
783
BLR008 Bilirubin Metabolic Disorder 57 0.048
784
AVD001 Avoidant Personality Disorder 51 0.048
785
OPS006 Opsoclonus-Myoclonus Syndrome 47 0.048
786
DRG024 Drug Allergy 42 0.048
787
ARG004 Argyria 27 0.048
788
CNN005 Connective Tissue Disease 68 0.047
789
P MST009 Mastocytosis 64 0.047
790
P BNC003 Bone Cancer 58 0.047
791
PGM001 Pigmented Villonodular Synovitis 56 0.047
792
RFR010 Refractory Anemia 48 0.047
793
c HYP864 Hypoparathyroidism, Familial Isolated, 1 48 0.047
794
FCL012 Facial Paralysis 46 0.047
795
c TST046 Testicular Germ Cell Tumor 1 29 0.047
796
HYP257 Hypoparathyroidism, Sensorineural Deafness, and Renal Disease 59 0.047
797
THY122 Thyroid Gland Cancer 57 0.047
798
CHR005 Chorioamnionitis 51 0.047
799
HMR023 Hemorrhagic Cystitis 45 0.047
800
SWL001 Swallowing Disorders 38 0.047
801
c PRM108 Primary Progressive Multiple Sclerosis 51 0.047
802
PRV004 Periventricular Leukomalacia 52 0.047
803
DYS009 Dysthymic Disorder 49 0.047
804
P HRT035 Heart Block, Congenital 46 0.047
805
c DWL002 Dowling-Degos Disease 1 58 0.047
806
c MST023 Mesothelioma, Malignant 57 0.047
807
TCL002 T-Cell Large Granular Lymphocyte Leukemia 49 0.047
808
c CHR418 Chronic Leukemia 49 0.047
809
TRP005 Trophoblastic Neoplasm 38 0.047
810
P CRN233 Corneal Dystrophy, Fuchs Endothelial, 1 37 0.047
811
P PRC012 Pericardial Effusion 51 0.047
812
c BCT013 Bacterial Pneumonia 48 0.047
813
HMP001 Hemopericardium 48 0.047
814
P HMN032 Human Herpesvirus 8 47 0.047
815
DNT006 Dental Pulp Necrosis 41 0.047
816
DSS008 Disease of Mental Health 58 0.046
817
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.046
818
c NGH026 Night Blindness, Congenital Stationary, Type 1a 52 0.046
819
P THY032 Thyroiditis 52 0.046
820
P NGH001 Night Blindness 48 0.046
821
PRL017 Prolymphocytic Leukemia 47 0.046
822
PRM020 Premenstrual Tension 40 0.046
823
PRT013 Portal Hypertension 59 0.046
824
EXP004 Exophthalmos 52 0.046
825
DSS012 Disseminated Infection with Mycobacterium Avium Complex 20 0.046
826
c ACT075 Acute Myocardial Infarction 57 0.046
827
OPT003 Opiate Dependence 50 0.046
828
P PLV020 Pelvic Organ Prolapse 57 0.046
829
LMB062 Limb Ischemia 55 0.046
830
LCR013 Lacrimal Duct Defect 41 0.046
831
ALD013 Aldosterone-Producing Adenoma 39 0.046
832
c BCT006 Bacterial Conjunctivitis 37 0.046
833
P APL001 Aplastic Anemia 74 0.045
834
CHR066 Chronic Fatigue Syndrome 61 0.045
835
PNM001 Pneumocystosis 59 0.045
837
P END046 Endometritis 49 0.045
838
GST049 Gastrointestinal System Cancer 49 0.045
839
GST071 Gastrointestinal Carcinoma 47 0.045
840
c TCL001 T-Cell Adult Acute Lymphocytic Leukemia 43 0.045
841
P MJR007 Major Affective Disorder 1 43 0.045
842
KLD004 Keloid Disorder 40 0.045
843
SCK003 Sickle Cell Anemia 74 0.045
844
P INF038 Influenza 68 0.045
845
FLL027 Fallopian Tube Carcinoma 67 0.045
846
VSC002 Vascular Dementia 57 0.045
847
GST010 Gestational Trophoblastic Neoplasm 46 0.045
848
SYN036 Syncope 45 0.045
849
OVR112 Ovarian Germ Cell Cancer 45 0.045
850
FCH001 Fuchs' Endothelial Dystrophy 44 0.045
851
c FML001 Familial Atrial Fibrillation 65 0.045
852
HSH003 Hashimoto Thyroiditis 62 0.045
853
BRS099 Breast Ductal Carcinoma 62 0.045
854
FBR047 Fibromyalgia 58 0.045
855
SCH003 Schizophreniform Disorder 56 0.045
856
P HYP730 Hypogonadotropic Hypogonadism 52 0.045
858
SPS226 Spastic Paraplegia, Ataxia, and Mental Retardation 37 0.045
859
PLM012 Pulmonary Sarcoidosis 53 0.045
860
THY030 Thyroid Gland Disease 52 0.045
861
ACT200 Acute Monoblastic Leukemia 52 0.045
862
ACT017 Acute Chest Syndrome 51 0.045
863
c FCL025 Focal Segmental Glomerulosclerosis 1 46 0.045
864
CYN002 Cyanosis, Transient Neonatal 45 0.045
865
DND018 Dendritic Cell Tumor 40 0.045
866
BLS007 Blastic Plasmacytoid Dendritic Cell 38 0.045
867
CHR208 Chromosome 17p Deletion 23 0.045
868
AGG011 Aggressive B-Cell Non-Hodgkin Lymphoma 23 0.045
869
INT002 Intermittent Claudication 61 0.044
870
GST040 Gastric Adenocarcinoma 70 0.044
871
APH002 Aphasia 57 0.044
872
P SML001 Small Cell Carcinoma 52 0.044
873
RSP006 Respiratory System Disease 50 0.044
874
PRD004 Prediabetes Syndrome 47 0.044
875
LRG008 Large Granular Lymphocyte Leukemia 41 0.044
876
c ADL096 Adult Hepatocellular Carcinoma 40 0.044
877
ANG049 Angioedema Induced by Ace Inhibitors 40 0.044
878
PSD088 Pseudobulbar Affect 36 0.044
879
SHL001 Shoulder Impingement Syndrome 32 0.044
880
FML063 Familial Glucocorticoid Deficiency 58 0.044
881
ORL004 Oral Submucous Fibrosis 55 0.044
882
P RTN016 Retinal Degeneration 53 0.044
883
KRT008 Keratopathy 47 0.044
884
VTR003 Vitreous Detachment 39 0.044
885
ACT012 Acute Hemorrhagic Conjunctivitis 36 0.044
886
TMR016 Tumor Suppressor Gene on Chromosome 11 28 0.044
887
c JVN004 Juvenile Myelomonocytic Leukemia 67 0.043
888
ANX004 Anoxia 40 0.043
889
PRP075 Peripheral Neuropathy, Myopathy, Hoarseness, and Hearing Loss 37 0.043
890
P LPR021 Leprosy 3 69 0.043
891
GST033 Gestational Diabetes 61 0.043
892
END031 Endometrial Stromal Sarcoma 46 0.043
893
HNS001 Hansen's Disease 34 0.043
894
P GLL020 Gallbladder Disease 57 0.043
895
P END033 Endocarditis 57 0.043
896
SCH014 Schistosomiasis 57 0.043
897
TRN018 Transitional Cell Carcinoma 56 0.043
898
P DYS193 Dystonia 11, Myoclonic 55 0.043
899
INT007 Intermediate Coronary Syndrome 55 0.043
900
c VRL005 Viral Pneumonia 52 0.043
901
P TRT010 Teratoma 52 0.043
902
LPD004 Lipoid Nephrosis 46 0.043
903
SCH060 Schistosoma Mansoni Infection, Susceptibility/ 39 0.043
904
CHR178 Chromosomal Triplication 35 0.043
905
PDT001 Pediatric Lymphoma 35 0.043
906
CRY035 Cryptorchidism, Unilateral or Bilateral 58 0.043
907
SPT004 Septic Arthritis 58 0.043
908
LNG108 Langerhans Cell Histiocytosis 58 0.043
909
APL002 Aplasia of Lacrimal and Salivary Glands 57 0.043
910
VGT001 Vogt-Koyanagi-Harada Disease 55 0.043
911
CLL003 Cellulitis 54 0.043
912
P LRY019 Laryngitis 52 0.043
913
NRM004 Neuroma 51 0.043
914
CYT005 Cytomegalovirus Retinitis 50 0.043
915
LYM138 Lymphoblastic Leukemia, Acute, with Lymphomatous Features 49 0.043
916
P BLD051 Blood Coagulation Disease 46 0.043
917
SPP008 Suppurative Otitis Media 45 0.043
918
RFR003 Refractive Error 43 0.043
919
MRG013 Mirage Syndrome 43 0.043
920
CHR286 Chronic Neutrophilic Leukemia 42 0.043
921
SNL007 Senile Cataract 42 0.043
922
c CHR097 Chronic Purulent Otitis Media 33 0.043
923
P THL005 Thalassemia 60 0.043
924
HLX001 Helix Syndrome 47 0.043
925
CRN036 Craniopharyngioma 65 0.042
926
MSM014 Mismatch Repair Cancer Syndrome 65 0.042
927
P TRC086 Trichohepatoenteric Syndrome 1 62 0.042
928
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.042
929
c ATM082 Autoimmune Lymphoproliferative Syndrome, Type V 54 0.042
930
P CRN276 Corneal Endothelial Dystrophy 52 0.042
931
BLL003 Bell's Palsy 51 0.042
932
HYP781 Hypoascorbemia 51 0.042
933
AST006 Astigmatism 47 0.042
934
CLL014 Cll/sll 45 0.042
935
P PRL003 Proliferative Glomerulonephritis 44 0.042
936
MYL067 Myeloproliferative Disorder, Chronic, with Eosinophilia 37 0.042
937
SML008 Small Intestine Lymphoma 33 0.042
938
c JVN010 Juvenile Rheumatoid Arthritis 64 0.042
939
P AGN002 Agnosia 55 0.042
940
P MGR001 Migraine Without Aura 49 0.042
941
CHL067 Cholecystitis 57 0.042
942
c GRV008 Graves Disease 1 56 0.042
943
ATN011 Autoinflammation with Infantile Enterocolitis 44 0.042
944
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.041
945
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.041
946
RNL077 Renal Fibrosis 47 0.041
947
GST045 Gastroenteritis 59 0.041
948
BRS051 Breast Disease 58 0.041
949
AMN003 Amnestic Disorder 54 0.041
950
P HMP007 Hemophilia 51 0.041
951
P VNW001 Von Willebrand's Disease 65 0.041
952
c ATM011 Autoimmune Hepatitis 63 0.041
953
VGN019 Vaginal Discharge 46 0.041
954
CND006 Candida Glabrata 32 0.041
955
PFF001 Pfeiffer Syndrome 79 0.040
956
P BLD062 Bile Duct Cancer 67 0.040
957
P HMN010 Hemangioma 61 0.040
958
PRT058 Pure Autonomic Failure 59 0.040
959
APH001 Aphthous Stomatitis 57 0.040
960
GTR002 Goiter 53 0.040
961
CHR563 Chronic Eosinophilic Leukemia 48 0.040
962
SPN020 Spondylosis 46 0.040
963
c ACT042 Acute Pyelonephritis 46 0.040
964
RCH001 Richter's Syndrome 45 0.040
965
c MLG079 Malignant Pleural Mesothelioma 42 0.040
966
c ATM021 Autoimmune Inner Ear Disease 34 0.040
967
BNN005 Bunion 33 0.040
968
ACT114 Acute Myeloblastic Leukemia Without Maturation 33 0.040
969
c ENC060 Encephalopathy, Acute, Infection-Induced 1 32 0.040
970
CRD220 Cardiac Valvular Defect, Developmental 29 0.040
971
SPC030 Specific Language Disorder 26 0.040
972
PRQ002 Paraquat Poisoning 26 0.040
973
ACR006 Aceruloplasminemia 65 0.040
974
P SCL018 Scoliosis 60 0.040
975
P SLP005 Sleep Disorder 59 0.040
976
P SYP003 Syphilis 58 0.040
977
P HML001 Hemolytic-Uremic Syndrome 53 0.040
978
FML037 Female Breast Cancer 52 0.040
979
PPT001 Peptic Esophagitis 52 0.040
980
PRT035 Peritoneum Cancer 44 0.040
981
c SRC023 Sarcoidosis 2 43 0.040
982
CRN322 Coronavirus Infectious Disease 40 0.040
983
PTT003 Pituitary-Dependent Cushing's Disease 39 0.040
984
CRY005 Cryptococcosis 58 0.040
985
ORP003 Oropharynx Cancer 55 0.040
986
P MYP006 Myopia 55 0.040
987
CLF001 Cleft Lip 53 0.040
988
c AMY009 Amyloidosis Aa 50 0.040
989
OST115 Osteonecrosis of the Jaw 40 0.040
990
BLP006 Blepharoconjunctivitis 31 0.040
991
c ANT023 Anterior Scleritis 29 0.040
992
c INV001 Invasive Aspergillosis 49 0.040
993
c PRM093 Premature Ovarian Failure 7 47 0.040
994
P GLL018 Gallbladder Cancer 57 0.040
995
SMT008 Smith-Magenis Syndrome 54 0.040
996
CTS003 Coats Disease 53 0.040
997
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.040
998
PPL021 Papilledema 49 0.040
999
CLN045 Colonic Benign Neoplasm 46 0.040
1000
LRY022 Laryngoonychocutaneous Syndrome 44 0.040
1001
FML039 Female Reproductive System Disease 39 0.040
1002
NRM001 Neuromyelitis Optica 61 0.040
1003
P MYS005 Myositis 56 0.040
1004
HRT012 Heart Valve Disease 53 0.040
1005
GNT002 Giant Cell Glioblastoma 50 0.040
1006
P OVR082 Overgrowth Syndrome 50 0.040
1007
c ACT150 Acute Adrenal Insufficiency 48 0.040
1008
INT253 Intestinal Benign Neoplasm 45 0.040
1009
MLR006 Male Reproductive Organ Cancer 40 0.040
1010
c BSL007 Basal Cell Carcinoma 68 0.039
1011
BLL006 Bullous Pemphigoid 62 0.039
1012
PLR007 Pleural Empyema 50 0.039
1013
CYS009 Cystadenoma 44 0.039
1014
MYL074 Myelodysplastic Syndrome with Excess Blasts 38 0.039
1015
P DNT007 Dentin Sensitivity 36 0.039
1016
CLC004 Calcific Tendinitis 30 0.039
1017
CTR027 Cataract-Glaucoma 27 0.039
1018
RFR007 Refractory Anemia with Excess Blasts in Transformation 27 0.039
1019
P SYS005 Systemic Scleroderma 68 0.038
1020
AND014 Androgenic Alopecia 46 0.038
1021
MYX005 Myxoid Liposarcoma 66 0.038
1022
P LPS002 Liposarcoma 65 0.038
1023
P PRM051 Primary Pigmented Nodular Adrenocortical Disease 53 0.038
1024
JNT004 Joint Laxity, Short Stature, and Myopia 45 0.038
1025
MST004 Mast Cell Neoplasm 42 0.038
1026
EXT007 Extracutaneous Mastocytoma 38 0.038
1027
PLS037 Plasma Cell Tumor 22 0.038
1028
THY020 Thyroid Hyalinizing Trabecular Adenoma 21 0.038
1029
P PRK057 Parkinson Disease, Late-Onset 78 0.038
1030
RNL065 Renal Cell Carcinoma, Papillary, 1 73 0.038
1031
EWN003 Ewing Sarcoma 69 0.038
1032
c VRL010 Viral Hepatitis 52 0.038
1033
OPD006 Opioid Addiction 48 0.038
1034
P RNL015 Renal Hypertension 47 0.038
1035
CRD137 Cardiogenic Shock 47 0.038
1036
PLM001 Pulmonary Tuberculosis 69 0.038
1037
EPL118 Epilepsy, Focal, with Speech Disorder and with or Without Mental Retardation 65 0.038
1038
c ANM038 Anemia, Autoimmune Hemolytic 62 0.038
1039
PNM010 Pneumothorax, Primary Spontaneous 60 0.038
1040
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.038
1041
c HYD046 Hydatidiform Mole, Recurrent, 1 59 0.038
1042
P ANT006 Antiphospholipid Syndrome 55 0.038
1043
SRS001 Serous Cystadenocarcinoma 52 0.038
1044
CYS014 Cystadenocarcinoma 51 0.038
1045
HYP017 Hypophosphatemia 50 0.038
1046
IRT001 Iritis 44 0.038
1047
P ATX024 Ataxia-Oculomotor Apraxia 3 44 0.038
1048
c ALK016 Alk-Negative Anaplastic Large Cell Lymphoma 44 0.038
1049
P ATX039 Ataxia-Pancytopenia Syndrome 43 0.038
1050
SPR126 Superior Semicircular Canal Dehiscence 40 0.038
1051
c HMG029 Hemoglobin Se Disease 39 0.038
1052
c DFN360 Deafness, Autosomal Dominant 69 37 0.038
1053
SYS070 Systemic Epstein-Barr Virus-Positive T-Cell Lymphoma of Childhood 36 0.038
1054
VST001 Vestibular Neuronitis 34 0.038
1055
LTT002 Letterer-Siwe Disease 33 0.038
1056
c ATS386 Autosomal Dominant Non-Syndromic Intellectual Disability 4 25 0.038
1057
OCC008 Occipital Neuralgia 25 0.038
1058
c PRS134 Prostate Cancer, Hereditary, 3 24 0.038
1059
GRD007 Grade Iii Astrocytoma 59 0.037
1060
CHR070 Chronic Inflammatory Demyelinating Polyradiculoneuropathy 57 0.037
1061
PRT082 Preterm Premature Rupture of the Membranes 54 0.037
1062
PTH003 Pathologic Nystagmus 52 0.037
1063
IFP001 Ifap Syndrome with or Without Bresheck Syndrome 51 0.037
1064
APP009 Appendix Adenocarcinoma 44 0.037
1065
SMN007 Seminoma 43 0.037
1066
OCL011 Ocular Motility Disease 42 0.037
1067
TST043 Testicular Seminoma 35 0.037
1068
c SCN069 Secondary Hemophagocytic Lymphohistiocytosis 33 0.037