Search results for Digoxin

941 hits were found for Digoxin

# Family MCID Name MIFTS Score
1
P ATR011 Atrial Fibrillation 66 11.792
2
CNG034 Congestive Heart Failure 69 10.839
3
P HRT032 Heart Disease 84 8.912
4
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 5.890
5
ATR057 Atrioventricular Block 54 5.055
6
c HYP595 Hypertension, Essential 84 4.963
7
c PRC016 Pre-Eclampsia 64 4.856
8
c DLT002 Dilated Cardiomyopathy 79 4.693
9
HYP005 Hypokalemia 55 4.511
10
48X005 48,xyyy 39 4.344
11
c FML001 Familial Atrial Fibrillation 65 4.254
12
ADL002 Adult Syndrome 69 4.234
13
P PRS040 Prostate Cancer 95 3.747
14
c ACT071 Acute Kidney Failure 60 3.699
15
P ECL001 Eclampsia 52 3.688
16
P BRS047 Breast Cancer 97 3.659
17
DGT004 Digitalis Poisoning 13 3.652
18
P PNC044 Pancreatitis 61 3.547
19
SYS003 Systolic Heart Failure 49 3.451
20
c TYP009 Type 2 Diabetes Mellitus 92 3.413
21
c ACT027 Acute Pancreatitis 60 3.401
22
END086 End Stage Renal Disease 54 3.345
23
CYT018 Cytochrome P450 2d6 Variant 26 3.326
24
P CRD119 Cardiac Arrest 68 3.266
25
P LVR013 Liver Disease 68 3.247
26
HYD038 Hydrops Fetalis, Nonimmune 57 3.245
27
c LYM150 Lymphatic Malformation 7 43 3.245
28
P DBT009 Diabetes Mellitus 67 3.214
29
HYP266 Hypoxia 56 3.195
30
P SZR006 Seizure Disorder 69 3.188
31
URM002 Uremia 47 3.147
32
P TRN020 Turner Syndrome 67 3.136
33
c ACT075 Acute Myocardial Infarction 55 3.124
34
c ATR087 Atrial Standstill 1 74 3.107
35
SNG003 Single Ventricular Heart 30 2.986
36
P KDN018 Kidney Disease 72 2.960
37
P ANR048 Aniridia 1 66 2.916
38
P PNC035 Pancreatic Cancer 86 2.896
39
P RHM011 Rheumatoid Arthritis 81 2.862
40
P ART022 Arthritis 70 2.862
41
MNT002 Mental Depression 56 2.838
42
P MLN008 Melanoma 75 2.809
43
DPR016 Depression 65 2.804
44
P HYP076 Hyperthyroidism 53 2.796
45
c SML038 Small Cell Cancer of the Lung 69 2.730
46
c SVR005 Severe Pre-Eclampsia 50 2.724
47
c CHR684 Chronic Kidney Disease 74 2.685
48
P CRN300 Coronary Heart Disease 1 73 2.676
49
CRD137 Cardiogenic Shock 56 2.640
50
c BLD140 Blood Group, I System 47 2.635
51
P ALZ034 Alzheimer Disease 87 2.602
52
RST023 Resting Heart Rate, Variation in 40 2.599
53
DST006 Diastolic Heart Failure 45 2.599
54
HND015 Hand Skill, Relative 29 2.585
55
NNL006 Non-Alcoholic Steatohepatitis 54 2.564
56
ANG054 Angina Pectoris 65 2.562
57
RHM028 Rheumatic Heart Disease 56 2.527
58
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 62 2.523
59
P VSC007 Vascular Disease 62 2.494
60
P PTN014 Patent Ductus Arteriosus 1 59 2.482
61
c HPT003 Hepatitis a 63 2.460
62
P LNG032 Lung Cancer 98 2.447
63
LPP008 Lipoprotein Quantitative Trait Locus 65 2.425
64
c HPT073 Hepatitis C Virus 71 2.410
65
P MJR001 Major Depressive Disorder 68 2.398
66
ART140 Arteries, Anomalies of 52 2.321
67
NNL005 Non-Alcoholic Fatty Liver Disease 63 2.314
68
P FTT008 Fatty Liver Disease, Nonalcoholic 1 48 2.288
69
ALC007 Alcohol Dependence 65 2.260
70
c PRG042 Progressive Familial Heart Block, Type Ia 65 2.246
71
P SCK002 Sick Sinus Syndrome 55 2.218
72
WLF001 Wolff-Parkinson-White Syndrome 63 2.197
73
RHB024 Rhabdomyosarcoma 2 65 2.141
74
HMN014 Human Immunodeficiency Virus Infectious Disease 54 2.141
75
CRD223 Cardiac Arrhythmia 63 2.101
76
CRD132 Cardiac Conduction Defect 59 2.088
77
INT007 Intermediate Coronary Syndrome 53 2.085
78
P HYP086 Hypothyroidism 69 2.061
79
c HPT001 Hepatitis C 61 2.031
80
P HPT021 Hepatitis 68 2.004
81
P FNG006 Feingold Syndrome 1 61 1.980
82
c PRS130 Prostate Cancer, Hereditary, 8 32 1.980
83
c PRS136 Prostate Cancer, Hereditary, 6 33 1.980
84
P EPL164 Epilepsy 70 1.980
85
PRS047 Prostatitis 58 1.980
86
P MTR003 Mitral Valve Stenosis 53 1.974
87
HRT011 Heart Septal Defect 49 1.933
88
47X002 47,xyy 48 1.907
89
P HNT016 Huntington Disease 73 1.905
90
P ANG015 Angioedema 56 1.905
91
P AMY004 Amyloidosis 69 1.900
92
P PLM037 Pulmonary Hypertension 69 1.893
93
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 66 1.893
94
BRN024 Bronchitis 67 1.878
95
P VNT002 Ventricular Septal Defect 58 1.877
96
CHL068 Cholestasis 61 1.863
97
DWN001 Down Syndrome 70 1.845
98
AGN016 Aging 54 1.829
99
AND005 Androgen Insensitivity Syndrome, Mild 21 1.829
100
c PRM038 Primary Agammaglobulinemia 47 1.829
101
PLM010 Pulmonary Edema 54 1.803
102
P ALC033 Alcohol Use Disorder 67 1.772
103
ANT039 Antisynthetase Syndrome 55 1.771
104
CNS004 Constipation 56 1.751
105
BDR001 Bidirectional Tachycardia 14 1.741
106
HRT012 Heart Valve Disease 53 1.718
107
SKN019 Skin Melanoma 70 1.698
108
P RSP003 Respiratory Failure 74 1.685
109
c PRG043 Progressive Familial Heart Block, Type Ib 54 1.678
110
RGH001 Right Bundle Branch Block 47 1.678
111
SNT005 Sinoatrial Node Disease 47 1.675
112
c GRV008 Graves Disease 1 54 1.673
113
KRT009 Keratosis 52 1.649
114
P SCH015 Schizophrenia 74 1.637
115
P PRC031 Preeclampsia/eclampsia 1 43 1.633
116
GYN001 Gynecomastia 48 1.624
117
INF021 Infant Gynecomastia 30 1.624
118
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 44 1.622
119
CMP040 Complement Component 4, Partial Deficiency of 34 1.620
120
TRG019 Trigonocephaly with Short Stature and Developmental Delay 38 1.620
121
C1N001 C1 Inhibitor Deficiency 43 1.620
122
c ANG068 Angioedema, Hereditary, Type I 57 1.620
123
ANG049 Angioedema Induced by Ace Inhibitors 39 1.620
124
c HRD002 Hereditary Angioedema 61 1.620
125
ATX019 Ataxia with Vitamin E Deficiency 44 1.620
126
P EXN002 Exanthem 58 1.605
127
P MYC007 Myocardial Infarction 69 1.604
128
P LKM002 Leukemia 66 1.598
129
TRC022 Tricuspid Valve Insufficiency 47 1.580
130
MYL009 Myelodysplastic Syndrome 67 1.566
131
HYP060 Hyperinsulinism 53 1.554
132
BCT022 Bacterial Infectious Disease 56 1.548
133
KRT002 Keratomalacia 54 1.524
134
END040 Endogenous Depression 54 1.524
135
c LKM061 Leukemia, Acute Myeloid 83 1.524
136
P MYL006 Myeloid Leukemia 60 1.524
137
P PLY018 Polycythemia 56 1.524
138
P VSC018 Visceral Steatosis 32 1.524
139
ISC004 Ischemia 61 1.523
140
HYP066 Hyperglycemia 60 1.508
141
CRT084 Creatinine Clearance Quantitative Trait Locus 25 1.506
142
P THR014 Thrombocytopenia 66 1.506
143
GST050 Gastrointestinal System Disease 55 1.494
144
MTR002 Mitral Valve Insufficiency 51 1.483
145
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 62 1.479
146
ANR040 Aneurysm 60 1.467
147
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 65 1.459
148
P RNL015 Renal Hypertension 45 1.426
149
HMS001 Hemosiderosis 48 1.423
150
P RRH023 Rare Hereditary Hemochromatosis 53 1.423
151
c MCL062 Mucolipidosis Ii Alpha/beta 69 1.423
152
c PRM012 Primary Polycythemia 58 1.423
153
AMD002 Amed Syndrome, Digenic 37 1.423
154
SRC014 Sarcoma 64 1.423
155
VTM033 Vitamin K Deficiency Bleeding 50 1.423
156
LNG031 Lung Benign Neoplasm 51 1.423
157
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 79 1.423
158
SQM013 Squamous Cell Carcinoma, Head and Neck 75 1.423
159
SPN035 Spindle Cell Sarcoma 51 1.423
160
SFT003 Soft Tissue Sarcoma 57 1.423
161
NRT001 Neurotic Disorder 56 1.423
162
P MLG074 Malignant Mesenchymoma 40 1.423
163
FTT001 Fatty Liver Disease 61 1.423
164
P ACT008 Actinic Keratosis 54 1.423
165
ACT113 Acute Myeloblastic Leukemia with Maturation 46 1.423
166
CRB039 Cerebrovascular Disease 65 1.414
167
ANR004 Anuria 44 1.403
168
ACR007 Acromegaly 70 1.403
169
HYP056 Hypoglycemia 65 1.395
170
c TYP008 Type 1 Diabetes Mellitus 77 1.391
171
P HYP061 Hypertrophic Cardiomyopathy 69 1.388
172
P MYC008 Myocarditis 59 1.380
173
PRP027 Peripheral Vascular Disease 71 1.368
174
LPD008 Lipid Metabolism Disorder 61 1.358
175
PLM129 Pulmonary Disease, Chronic Obstructive 74 1.358
176
P ART018 Aortic Valve Insufficiency 52 1.338
177
ATH013 Atherosclerosis Susceptibility 63 1.334
178
SYN036 Syncope 44 1.330
179
HMP001 Hemopericardium 47 1.328
180
P PRC012 Pericardial Effusion 50 1.328
181
SBC016 Subacute Delirium 42 1.324
182
ACQ007 Acquired Immunodeficiency Syndrome 58 1.272
183
P ORT004 Orthostatic Intolerance 62 1.267
184
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 40 1.260
185
CHR073 Choreatic Disease 53 1.260
186
PPT005 Peptic Ulcer Disease 58 1.235
187
PRC013 Pericarditis 53 1.223
188
P ENC018 Encephalopathy 62 1.194
189
SCN049 Second-Degree Atrioventricular Block 34 1.183
190
P SRC025 Sarcoidosis 1 70 1.179
191
LNG099 Lung Disease 62 1.162
192
P ART021 Arteriosclerosis 53 1.156
193
CYS001 Cystic Fibrosis 77 1.147
194
PLM033 Pulmonary Embolism 58 1.140
195
BLM002 Bulimia Nervosa 57 1.130
196
TXC005 Toxic Shock Syndrome 62 1.129
197
HPT014 Hepatorenal Syndrome 49 1.129
198
CHR005 Chorioamnionitis 50 1.117
199
P RTN016 Retinal Degeneration 52 1.117
200
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 60 1.115
201
P CRV039 Cervicitis 52 1.115
202
HPT004 Hepatic Coma 43 1.105
203
HPT019 Hepatic Encephalopathy 59 1.105
204
PST011 Pustulosis of Palm and Sole 52 1.105
205
ATN005 Autonomic Dysfunction 45 1.105
206
ALL014 Allergic Encephalomyelitis 34 1.105
207
P PSR002 Psoriasis 63 1.105
208
SXL003 Sexual Disorder 49 1.093
209
P INT068 Intestinal Disease 53 1.093
210
SBC001 Subacute Sclerosing Panencephalitis 53 1.093
211
P RTN024 Retinoblastoma 72 1.080
212
c BDY007 Body Mass Index Quantitative Trait Locus 1 40 1.080
213
EXT006 Extrahepatic Cholestasis 41 1.080
214
P VSC011 Vasculitis 61 1.080
215
ATR089 Atrioventricular Dissociation 21 1.067
216
P OVR042 Ovarian Cancer 88 1.067
217
P URN019 Urinary Tract Infection 49 1.067
218
P SBS003 Substance Abuse 54 1.061
219
P MJR007 Major Affective Disorder 1 42 1.049
220
c PLM164 Pulmonary Hypertension, Primary, 1 80 1.049
221
ATM095 Autoimmune Disease 61 1.039
222
LWC001 Low Compliance Bladder 44 1.039
223
P BCL017 B-Cell Lymphoma 57 1.039
224
P DBT005 Diabetes Insipidus 54 1.039
225
P BDY004 Body Mass Index Quantitative Trait Locus 11 83 1.032
226
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 1.032
227
c BDY012 Body Mass Index Quantitative Trait Locus 7 43 1.032
228
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 1.032
229
c BDY005 Body Mass Index Quantitative Trait Locus 9 47 1.032
230
c BDY006 Body Mass Index Quantitative Trait Locus 8 43 1.032
231
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 1.032
232
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 1.032
233
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 1.032
234
c BDY020 Body Mass Index Quantitative Trait Locus 19 51 1.032
235
PLM001 Pulmonary Tuberculosis 69 1.032
236
ALL029 Allergic Disease 61 1.032
237
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 46 1.024
238
P SHR001 Short Bowel Syndrome 53 1.024
239
P NPH012 Nephrotic Syndrome 62 1.024
240
SDD001 Sudden Infant Death Syndrome 60 1.024
241
PLY100 Polyploidy 36 1.024
242
OBS002 Obsessive-Compulsive Disorder 68 1.019
243
P CRD246 Cardiovascular System Disease 55 1.019
244
CLN015 Colon Adenocarcinoma 64 1.008
245
P HYD006 Hydrocephalus 63 0.992
246
IRR002 Irritable Bowel Syndrome 65 0.992
247
P OVR082 Overgrowth Syndrome 42 0.992
248
LFT001 Left Bundle Branch Hemiblock 47 0.991
249
HYP006 Hypertensive Heart Disease 48 0.991
250
GLC003 Glucose Intolerance 53 0.987
251
P MTR012 Mitral Valve Disease 57 0.981
252
P DXT004 Dextro-Looped Transposition of the Great Arteries 58 0.975
253
P PLM036 Pulmonary Fibrosis 65 0.975
254
GLB002 Glioblastoma 67 0.971
255
P LPM005 Lipomatosis 47 0.956
256
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.956
257
DYS073 Dysphagia 53 0.956
258
c MJR008 Major Affective Disorder 2 34 0.948
259
c MJR006 Major Affective Disorder 5 32 0.948
260
c MJR003 Major Affective Disorder 6 32 0.948
261
c MJR004 Major Affective Disorder 4 28 0.948
262
c MJR023 Major Affective Disorder 7 33 0.948
263
c MJR024 Major Affective Disorder 9 40 0.948
264
c MJR022 Major Affective Disorder 8 37 0.948
265
SCH012 Schizoaffective Disorder 49 0.948
266
P BPL003 Bipolar Disorder 56 0.948
267
CVD001 Covid-19 58 0.936
268
PLM134 Pulmonary Fibrosis, Idiopathic 76 0.936
269
PRP030 Purpura 54 0.936
270
P NRB001 Neuroblastoma 66 0.936
271
P HYP055 Hypoplastic Left Heart Syndrome 65 0.927
272
PST048 Postural Orthostatic Tachycardia Syndrome 46 0.918
273
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.918
274
P INF038 Influenza 68 0.918
276
HYP025 Hyperphosphatemia 47 0.915
277
CHR096 Chronic Pulmonary Heart Disease 41 0.891
278
P DYS005 Dyslexia 40 0.891
279
PRS129 Prostatic Hyperplasia, Benign 48 0.891
280
PRS021 Prostatic Adenoma 43 0.891
281
PRS045 Prostatic Hypertrophy 52 0.891
282
c MCR115 Microvascular Complications of Diabetes 5 65 0.878
283
P BLY001 B-Lymphoblastic Leukemia/lymphoma 52 0.878
284
c SCL052 Scleroderma, Familial Progressive 60 0.865
285
SVR004 Severe Combined Immunodeficiency 71 0.865
286
P THL005 Thalassemia 56 0.865
287
PRP007 Priapism 46 0.865
288
P MSC005 Muscular Dystrophy 66 0.865
289
RPD005 Rapidly Involuting Congenital Hemangioma 48 0.864
290
RTN017 Retinal Detachment 60 0.864
291
P ART005 Arteriovenous Malformation 65 0.864
292
INT075 Intracranial Hypertension 52 0.864
293
END020 Endocardial Fibroelastosis 54 0.851
294
CLT003 Colitis 63 0.851
295
P UVT001 Uveitis 57 0.851
296
P DRR001 Diarrhea 55 0.851
297
LVR012 Liver Cirrhosis 62 0.851
298
CHR178 Chromosomal Triplication 34 0.851
299
THY029 Thyroid Carcinoma 54 0.851
300
PLM070 Pulmonic Stenosis 49 0.837
301
c ATM099 Autoimmune Uveitis 44 0.837
302
TRD008 Triiodothyronine Receptor Auxiliary Protein 33 0.837
303
c HYP836 Hypercholesterolemia, Familial, 1 73 0.837
304
P OPT006 Optic Nerve Disease 57 0.837
305
RYS001 Reye Syndrome 49 0.837
306
MSC157 Muscular Dystrophy, Duchenne Type 79 0.837
307
ART141 Arteriovenous Malformations of the Brain 58 0.832
308
P TCD001 Tic Disorder 50 0.832
309
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.822
310
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.822
311
BRK010 Burkitt Lymphoma 66 0.822
312
DFC004 Deficiency Anemia 74 0.822
313
SVR001 Severe Acute Respiratory Syndrome 68 0.822
314
END021 Endomyocardial Fibrosis 56 0.822
315
P CLR019 Color Blindness 47 0.822
316
ART016 Aortic Aneurysm 69 0.822
317
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.806
318
CRV035 Cervical Cancer 72 0.806
319
PRT251 Proteinuria, Chronic Benign 58 0.806
320
OTT002 Otitis Media 71 0.806
321
IMM167 Immune Deficiency Disease 77 0.806
322
P LYM118 Lymphoma 69 0.806
323
SCR003 Secretory Diarrhea 35 0.806
324
c VRL010 Viral Hepatitis 52 0.806
325
P CND004 Candidiasis 57 0.806
326
ESP018 Esophageal Candidiasis 47 0.806
327
INT066 Interstitial Lung Disease 60 0.806
328
PHR003 Pharyngitis 57 0.806
329
BRS050 Breast Cyst 38 0.806
330
CMB007 Combined Immunodeficiency 56 0.790
331
LYM157 Lymph Node Carcinoma 33 0.790
332
P CLR023 Colorectal Cancer 100 0.790
333
P DMN002 Dementia 65 0.790
334
BLR008 Bilirubin Metabolic Disorder 57 0.790
335
CYT002 Cytokine Deficiency 43 0.790
336
OVR094 Ovarian Epithelial Cancer 39 0.790
337
c ACT134 Acute Liver Failure 57 0.790
340
OST017 Osteomyelitis 63 0.773
341
BRN002 Bronchiolitis 57 0.773
342
ANG011 Angiodysplasia 42 0.773
343
RHM001 Rheumatic Fever 59 0.773
344
c ALM001 Al Amyloidosis 54 0.773
345
P INF037 Inflammatory Bowel Disease 53 0.754
346
P CRC039 Coarctation of Aorta 46 0.754
347
P LNG064 Lung Cancer Susceptibility 3 70 0.754
348
CRV040 Cervix Carcinoma 50 0.754
349
P ADN016 Adenocarcinoma 63 0.754
350
PLR008 Pleurisy 49 0.754
351
P URT039 Urticaria 57 0.754
352
RTN003 Retinal Ischemia 48 0.754
353
ANR007 Anorexia Nervosa 59 0.754
354
c RNG011 Ring Chromosome 16 16 0.754
355
P MTR014 Motor Neuron Disease 65 0.754
356
c JVN010 Juvenile Rheumatoid Arthritis 66 0.754
357
OCL006 Ocular Hypertension 53 0.754
358
IDP033 Idiopathic Edema 41 0.745
359
c MCR133 Microvascular Complications of Diabetes 4 41 0.734
360
P OST002 Osteoporosis 77 0.734
361
c SPN225 Spondyloarthropathy 1 70 0.734
362
PSR001 Psoriatic Arthritis 61 0.734
363
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 45 0.734
364
c MCR113 Microvascular Complications of Diabetes 3 52 0.734
365
c MCR130 Microvascular Complications of Diabetes 6 41 0.734
366
c MCR120 Microvascular Complications of Diabetes 7 47 0.734
367
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.734
368
P ATS364 Autism 72 0.734
369
c HRD202 Hereditary Lymphedema I 55 0.734
370
P BRB001 Beriberi 44 0.734
371
SPN051 Spondylitis 51 0.734
372
NRN004 Neuroendocrine Tumor 55 0.734
373
IRN002 Iron Metabolism Disease 56 0.734
374
INF009 Inflammatory Spondylopathy 30 0.734
375
IRN001 Iron Deficiency Anemia 58 0.734
376
CHR074 Choriocarcinoma 46 0.734
377
OST012 Osteoarthritis 77 0.734
378
CHR066 Chronic Fatigue Syndrome 60 0.734
379
ETN001 Eating Disorder 59 0.734
380
BNG077 Benign Idiopathic Neonatal Seizures 22 0.734
381
MYX004 Myxedema 43 0.713
382
MYL069 Myeloma, Multiple 77 0.713
383
WTH001 Withdrawal Disorder 47 0.713
384
MTB004 Metabolic Acidosis 48 0.713
385
ILT001 Ileitis 49 0.713
386
CRT072 Creutzfeldt-Jakob Disease 67 0.713
387
PLC006 Placental Choriocarcinoma 38 0.713
388
PPL022 Papilloma 53 0.713
389
ACQ001 Acquired Color Blindness 31 0.713
390
P ART023 Arthropathy 60 0.713
391
SPN020 Spondylosis 46 0.713
392
P INT099 Intrahepatic Cholestasis of Pregnancy 61 0.713
393
P MLG056 Malignant Hyperthermia 65 0.713
394
CRT015 Carotid Artery Occlusion 45 0.713
395
STR067 Stroke, Ischemic 79 0.690
396
c GLL024 Gallbladder Disease 1 53 0.689
397
P RTN008 Retinitis Pigmentosa 79 0.689
398
NRR001 Neuroretinitis 42 0.689
399
EBS001 Ebstein Anomaly 54 0.689
400
APH002 Aphasia 55 0.689
401
FRS012 First-Degree Atrioventricular Block 39 0.689
402
P ATR001 Atrioventricular Septal Defect 55 0.689
403
SQM002 Squamous Cell Papilloma 45 0.689
404
CRB033 Cerebral Degeneration 36 0.689
405
P CYS018 Cystitis 59 0.689
406
PRM236 Primary Biliary Cholangitis 62 0.689
407
RTN023 Retinitis 45 0.689
408
ANX004 Anoxia 40 0.689
409
SPC005 Speech Disorder 46 0.689
410
UNL002 Unilateral Retinoblastoma 37 0.689
411
P CHL066 Cholangitis 51 0.689
412
IMM039 Immune Hydrops Fetalis 33 0.689
413
HLC007 Helicobacter Pylori Infection 67 0.662
414
HMR023 Hemorrhagic Cystitis 43 0.662
415
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 33 0.662
416
MBT001 Mobitz Type Ii Atrioventricular Block 34 0.662
417
STT001 Status Epilepticus 58 0.662
418
CNT025 Central Pontine Myelinolysis 42 0.662
419
P GCH001 Gaucher's Disease 69 0.662
420
ATN004 Autonomic Neuropathy 42 0.662
421
P ADL010 Adult Respiratory Distress Syndrome 71 0.662
422
CRT028 Cor Triatriatum 25 0.662
423
P FML187 Familial Hypertension 34 0.662
424
P EPL140 Epilepsy, Idiopathic Generalized 60 0.630
425
KWS002 Kawasaki Disease 65 0.630
426
c MGR028 Migraine with or Without Aura 1 64 0.630
427
BSL009 Basal Ganglia Calcification 45 0.630
428
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 65 0.630
429
P DYS154 Dystonia 64 0.630
430
KWS001 Kwashiorkor 44 0.630
431
SKN016 Skin Disease 62 0.630
432
GNG012 Gingival Overgrowth 49 0.630
433
c HPT007 Hepatitis E 50 0.630
434
P EYD002 Eye Disease 57 0.630
435
CRY036 Cryptogenic Cirrhosis 36 0.630
436
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 39 0.630
437
P MNN013 Meningitis 65 0.630
438
c BRN108 Branchiootic Syndrome 1 63 0.588
439
P MDL005 Medulloblastoma 75 0.588
440
INT303 Intracranial Hypertension, Idiopathic 56 0.588
441
INT323 Intraocular Pressure Quantitative Trait Locus 63 0.588
442
ART017 Aortic Disease 49 0.588
443
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 60 0.588
444
PPL021 Papilledema 49 0.588
445
ABD002 Abducens Nerve Disease 38 0.588
446
GST033 Gestational Diabetes 61 0.588
447
PNC129 Pancreatic Adenocarcinoma 65 0.588
448
P RBL001 Rubella 58 0.588
449
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 58 0.586
450
P MYC084 Mycobacterium Tuberculosis 1 68 0.544
451
PRP009 Peripartum Cardiomyopathy 54 0.523
452
RSP019 Respiratory Distress Syndrome in Premature Infants 52 0.488
453
TRG002 Trigeminal Neuralgia 61 0.488
454
FBR032 Fibromuscular Dysplasia 47 0.488
455
c ACT249 Acute Asthma 40 0.488
456
P PLY019 Polyneuropathy 53 0.488
457
NWB001 Newborn Respiratory Distress Syndrome 56 0.488
458
ANR010 Aneurysm of Sinus of Valsalva 29 0.488
459
P PRD008 Periodontitis 64 0.488
460
FXD003 Fixed Drug Eruption 34 0.488
461
MTB008 Metabolic Crises, Recurrent, with Rhabdomyolysis, Cardiac Arrhythmias, and Neurodegeneration 42 0.483
462
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 52 0.483
463
MLT131 Multifocal Atrial Tachycardia 17 0.450
464
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 58 0.443
465
c HYP724 Hyperlipoproteinemia, Type Iii 66 0.443
466
c BDY021 Body Mass Index Quantitative Trait Locus 20 49 0.443
467
NRN005 Neuronal Ceroid-Lipofuscinoses 61 0.443
468
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 52 0.443
469
ENH001 Enhanced S-Cone Syndrome 58 0.443
470
CMP010 Complex Regional Pain Syndrome 59 0.443
471
ENT004 Enthesopathy 51 0.443
472
CRH001 Crohn's Disease 80 0.443
473
c CHR064 Chronic Monocytic Leukemia 36 0.443
474
P LNG028 Long Qt Syndrome 63 0.427
475
P ATR010 Atrial Heart Septal Defect 58 0.427
476
P MYP004 Myopathy 67 0.427
477
OCL069 Ocular Motor Apraxia 57 0.349
478
MDD011 Mood Disorder 62 0.349
479
c CNG006 Congenital Hypothyroidism 63 0.334
480
CYN002 Cyanosis, Transient Neonatal 43 0.334
481
CHG001 Chagas Disease 65 0.334
482
CLC053 Colchicine Poisoning 23 0.334
483
TTN003 Tetanus 64 0.319
484
GST092 Gastroesophageal Reflux 60 0.302
485
CHK001 Chikungunya 60 0.302
486
P HRT035 Heart Block, Congenital 42 0.302
487
P TTR001 Tetralogy of Fallot 69 0.302
488
TRN015 Transient Cerebral Ischemia 62 0.302
489
P DYS021 Dysautonomia 38 0.302
490
PLY012 Polyhydramnios 46 0.302
491
STM007 Stomatitis 52 0.302
492
HMN047 Human Cytomegalovirus Infection 59 0.285
493
c NRP054 Neuropathy, Hereditary Sensory and Autonomic, Type Iii 66 0.285
494
INF034 Infective Endocarditis 53 0.285
495
IMP005 Impotence 52 0.285
496
P TRM003 Tremor 50 0.285
497
BRN056 Bronchopulmonary Dysplasia 57 0.285
498
PRT058 Pure Autonomic Failure 58 0.285
499
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.266
500
ADR040 Adrenal Gland Pheochromocytoma 45 0.266
501
P PHC003 Pheochromocytoma 70 0.266
502
c ACT073 Acute Leukemia 59 0.266
503
P RST002 Restrictive Cardiomyopathy 54 0.266
504
P TRT010 Teratoma 50 0.266
505
CHT001 Chaotic Atrial Tachycardia 10 0.266
506
SRT004 Serotonin Syndrome 54 0.266
507
P MYS005 Myositis 56 0.247
508
ENT011 Enterocolitis 55 0.247
509
c THR092 Thrombophilia Due to Thrombin Defect 74 0.247
510
GT001 Gout 63 0.247
511
DBL002 Double Outlet Right Ventricle 57 0.247
512
P CNJ013 Conjunctivitis 66 0.247
513
PNM008 Pneumothorax 54 0.247
514
CHL123 Chlamydia 58 0.247
515
P GRV001 Graves' Disease 54 0.247
516
c ACT076 Acute Myocarditis 47 0.247
517
P SYS005 Systemic Scleroderma 73 0.247
518
PRN019 Perinatal Necrotizing Enterocolitis 60 0.247
519
TRC062 Tricuspid Atresia 54 0.225
520
PRT019 Protein-Losing Enteropathy 44 0.225
521
P SLP006 Sleep Apnea 69 0.225
522
PNC085 Penicillin Allergy 43 0.225
523
RNL114 Renal Cell Carcinoma, Nonpapillary 79 0.225
524
P HPT023 Hepatocellular Carcinoma 95 0.225
525
c ATM022 Autoimmune Myocarditis 36 0.225
526
PTN001 Patent Foramen Ovale 62 0.225
527
P END044 Endometriosis 62 0.225
528
c FML191 Familial Long Qt Syndrome 54 0.225
529
P PNM007 Pneumonia 64 0.225
530
STN005 St Anthony's Fire 18 0.225
531
SPL018 Splenomegaly 47 0.225
532
P NRV007 Nervous System Disease 66 0.225
533
P ENC004 Encephalitis 61 0.225
534
DSS032 Disease by Infectious Agent 55 0.201
535
PRT013 Portal Hypertension 59 0.201
536
c AMY091 Amyotrophic Lateral Sclerosis 1 88 0.201
537
LMB062 Limb Ischemia 55 0.201
538
DBT084 Diabetes Mellitus, Ketosis-Prone 60 0.201
539
EPD002 Epidermolytic Hyperkeratosis 55 0.201
540
SPR004 Supravalvular Aortic Stenosis 57 0.201
541
NRT004 Neuritis 53 0.201
542
P LTR001 Lateral Sclerosis 58 0.201
543
P PRP029 Porphyria 60 0.201
544
BRN028 Brain Cancer 73 0.201
545
P HYP024 Hypoparathyroidism 55 0.201
546
P NTR004 Neutropenia 62 0.201
547
P LCT001 Lactic Acidosis 50 0.201
548
RYN005 Raynaud Phenomenon 45 0.201
549
SBV001 Subvalvular Aortic Stenosis 31 0.201
550
P ATS411 Autosomal Dominant Epidermolytic Ichthyosis 36 0.201
551
c HMC039 Hemochromatosis, Type 1 73 0.174
552
P MYS003 Myasthenia Gravis 68 0.174
553
c CRN214 Coronary Heart Disease 5 31 0.174
554
INT067 Interstitial Nephritis 47 0.174
555
ATR048 Atrial Tachyarrhythmia with Short Pr Interval 25 0.174
556
PNG002 Pain Agnosia 51 0.174
557
ORL015 Oral Squamous Cell Carcinoma 43 0.174
558
GRN004 Granulomatous Amebic Encephalitis 30 0.174
559
ASP007 Aspiration Pneumonia 49 0.174
560
IFP003 Ifap Syndrome 2 42 0.174
561
PRL045 Proline-Negative Auxotroph of Hamster, Complementation of 16 0.174
562
P TBR001 Tuberous Sclerosis 69 0.174
563
P INF032 Infertility 60 0.174
564
P RTN018 Retinal Disease 53 0.174
565
RTN020 Retinal Vascular Disease 45 0.174
566
HYP014 Hyperuricemia 51 0.174
567
ALC010 Alcoholic Cardiomyopathy 42 0.174
568
ACT038 Acute Retrobulbar Neuritis 24 0.174
569
P ESP024 Esophagitis 60 0.174
570
GTR002 Goiter 52 0.174
571
P MLN007 Male Infertility 56 0.174
572
OLG003 Oligohydramnios 51 0.174
573
GST023 Gastric Ulcer 52 0.174
574
CRD001 Cardiac Tamponade 44 0.174
575
TNS001 Tenosynovial Giant Cell Tumor 41 0.174
576
INT002 Intermittent Claudication 61 0.174
577
THR016 Thrombophlebitis 50 0.174
578
c CNT035 Central Nervous System Disease 53 0.174
579
P THY032 Thyroiditis 56 0.174
580
P HYP265 Hypotonia 42 0.174
581
P BRN022 Bronchiectasis 59 0.174
582
VSC002 Vascular Dementia 59 0.174
583
CRC006 Carcinoid Syndrome 55 0.174
584
ILS001 Ileus 49 0.174
585
KLD004 Keloid Disorder 39 0.174
586
GRW007 Growth Hormone Deficiency 47 0.174
587
MTR027 Mitral Atresia 19 0.174
588
ESN011 Eisenmenger Syndrome 46 0.174
589
P TXP001 Toxoplasmosis 60 0.174
590
P HYP098 Hypereosinophilic Syndrome 66 0.174
591
UNV002 Univentricular Heart 26 0.174
592
URM005 Uremic Pruritus 45 0.174
593
P BLD134 Bladder Cancer 79 0.142
594
CHR072 Chordoma 57 0.142
595
INS023 Insensitivity to Pain, Congenital, with Anhidrosis 57 0.142
596
c PLM170 Pulmonary Venoocclusive Disease 1, Autosomal Dominant 43 0.142
597
LPD012 Lipoid Congenital Adrenal Hyperplasia 68 0.142
598
ANX010 Anxiety 70 0.142
599
P LKM062 Leukemia, Acute Lymphoblastic 69 0.142
600
P GRF003 Graft-Versus-Host Disease 71 0.142
601
MLD018 Mild Cognitive Impairment 48 0.142
602
MCR013 Microphthalmia 60 0.142
603
P OPN001 Open-Angle Glaucoma 55 0.142
604
P PRK039 Parkinsonism 55 0.142
605
CRB004 Cerebral Artery Occlusion 46 0.142
606
HPT046 Hepatic Veno-Occlusive Disease 55 0.142
607
LGN002 Legionellosis 61 0.142
608
THY111 Thyroid Carcinoma, Familial Medullary 67 0.142
609
c ART115 Aortic Valve Disease 1 72 0.142
610
ISC015 Ischemic Colitis 43 0.142
611
STT041 Stuttering 52 0.142
612
DRG024 Drug Allergy 40 0.142
613
PRP080 Peripheral Artery Disease 54 0.142
614
CHL147 Chlamydia Pneumonia 47 0.142
615
FDB001 Foodborne Botulism 55 0.142
616
P SCL047 Sclerocornea 32 0.142
617
P CTC001 Catecholaminergic Polymorphic Ventricular Tachycardia 63 0.142
618
MTC212 Mitchell Syndrome 26 0.142
619
END057 Endometrial Cancer 71 0.142
620
P KLZ004 Kala-Azar 1 41 0.142
621
c SYS001 Systemic Lupus Erythematosus 86 0.142
622
P NNN008 Noonan Syndrome 1 76 0.142
623
NRL016 Neural Tube Defects 81 0.142
624
c BTT014 Beta-Thalassemia 72 0.142
625
P HML001 Hemolytic-Uremic Syndrome 52 0.142
626
ACT003 Acute Kidney Tubular Necrosis 46 0.142
627
HSH003 Hashimoto Thyroiditis 60 0.142
628
ADR042 Adrenal Hyperplasia, Congenital, Due to 21-Hydroxylase Deficiency 50 0.142
629
c TBR025 Tuberous Sclerosis 1 84 0.142
630
BTT017 Beta-Thalassemia Major 53 0.142
631
MNN009 Meningoencephalitis 48 0.142
632
LMY002 Leiomyoma 51 0.142
633
P ANT001 Anterolateral Myocardial Infarction 34 0.142
634
P ACN011 Acne 55 0.142
635
CNN005 Connective Tissue Disease 66 0.142
636
P MCR010 Microcephaly 59 0.142
637
PRT037 Pertussis 49 0.142
638
DNT012 Dental Caries 53 0.142
639
QDR001 Quadriplegia 49 0.142
640
OLG001 Oligospermia 45 0.142
641
DSS009 Disseminated Intravascular Coagulation 56 0.142
642
CHL004 Cholelithiasis 48 0.142
643
DRF001 Dirofilariasis 32 0.142
644
JPN002 Japanese Encephalitis 61 0.142
645
c MLG069 Malignant Hypertension 46 0.142
646
CNS002 Constrictive Pericarditis 39 0.142
647
PLC005 Placental Insufficiency 56 0.142
648
P MLT074 Multiple Endocrine Neoplasia 58 0.142
649
CLL003 Cellulitis 53 0.142
650
P RHN004 Rhinitis 57 0.142
651
MYF001 Myofibroma 42 0.142
652
THY125 Thyroid Gland Medullary Carcinoma 48 0.142
653
P LNR013 Linear Skin Defects with Multiple Congenital Anomalies 1 52 0.142
654
SPP011 Suppression of Tumorigenicity 12 61 0.142
655
OST159 Osteogenic Sarcoma 66 0.142
656
c INF078 Inflammatory Bowel Disease 2 28 0.142
657
MDS022 Mediastinitis 47 0.142
658
P GST044 Gastritis 55 0.142
659
GST045 Gastroenteritis 58 0.142
660
GLM045 Glioma 62 0.142
661
MST020 Mast Cell Activation Syndrome 27 0.142
662
HRP004 Herpes Zoster 60 0.142
663
GLL048 Glial Tumor 52 0.142
664
NNS035 Nonsyndromic 46,xx Testicular Disorders of Sex Development 10 0.142
665
P PLM025 Pulmonary Venoocclusive Disease 44 0.142
666
LSH001 Leishmaniasis 63 0.142
667
CHC001 Chickenpox 56 0.142
668
P HMR005 Hemorrhoid 49 0.142
669
CMP035 Complete Atrioventricular Canal 24 0.142
670
GNT019 Giant Cell Myocarditis 29 0.142
671
c DNT047 Dentinogenesis Imperfecta Type 2 35 0.142
672
HMP009 Haemophilus Influenzae 41 0.142
673
PRT048 Partial Atrioventricular Canal 36 0.142
674
DXR001 Doxorubicin Induced Cardiomyopathy 32 0.142
675
PRQ002 Paraquat Poisoning 28 0.142
676
c PSD047 Pseudo-Turner Syndrome 52 0.142
677
PST092 Posttransplant Acute Limbic Encephalitis 29 0.142
678
LWF001 Low-Flow Priapism 16 0.142
679
SCR039 Scorpion Envenomation 41 0.142
680
c PRG106 Progressive Muscular Dystrophy 31 0.142
681
IDP056 Idiopathic Neonatal Atrial Flutter 9 0.142
682
CRN270 Coronary Artery Dissection, Spontaneous 32 0.101
683
ESP021 Esophageal Cancer 84 0.101
684
c FNC042 Fanconi Anemia, Complementation Group D2 54 0.101
685
PLL004 Pallister W Syndrome 27 0.101
686
MYP091 Myopathy, Congenital, with Fiber-Type Disproportion 43 0.101
687
BRT005 Barth Syndrome 55 0.101
688
P AST005 Asthma 76 0.101
689
P SPP010 Suppressor of Tumorigenicity 3 51 0.101
690
TKY002 Takayasu Arteritis 61 0.101
691
RGH009 Right Atrial Isomerism 57 0.101
692
HMC014 Homocysteinemia 52 0.101
693
c LKM063 Leukemia, Chronic Myeloid 71 0.101
694
c LNG047 Long Qt Syndrome 2 58 0.101
695
P RTN209 Retinoschisis 1, X-Linked, Juvenile 59 0.101
696
FRN006 Frontotemporal Dementia 68 0.101
697
TWN001 Twin-to-Twin Transfusion Syndrome 46 0.101
698
c BRS111 Breast-Ovarian Cancer, Familial 2 54 0.101
699
P STR092 Striatal Degeneration, Autosomal Dominant 2 44 0.101
700
TND004 Tendinopathy 45 0.101
701
TND005 Tendinitis 54 0.101
702
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 61 0.101
703
ART035 Arterial Calcification of Infancy 58 0.101
704
MNT001 Mantle Cell Lymphoma 65 0.101
706
PLR001 Pleural Tuberculosis 49 0.101
707
P PNM006 Pneumoconiosis 55 0.101
708
MCR011 Microinvasive Gastric Cancer 41 0.101
709
RCK004 Rickets 65 0.101
710
P PLY014 Polycystic Kidney Disease 71 0.101
711
RSP023 Rasopathy 54 0.101
712
CHL152 Childhood Acute Lymphocytic Leukemia 50 0.101
713
MDD018 Middle East Respiratory Syndrome 44 0.101
714
CHR710 Chronic Spontaneous Urticaria 45 0.101
715
ART004 Aortic Atherosclerosis 46 0.101
716
P END033 Endocarditis 58 0.101
717
TNS005 Tonsillitis 57 0.101
718
MRF001 Marfan Syndrome 76 0.101
719
P PRK057 Parkinson Disease, Late-Onset 79 0.101
720
ISL114 Isolated Growth Hormone Deficiency, Type Ii 40 0.101
721
P MLN069 Melanoma, Uveal 59 0.101
722
NPH091 Nephrolithiasis, Calcium Oxalate 61 0.101
723
ANT078 Antipyrine Metabolism 23 0.101
724
c ATR062 Atrial Septal Defect 1 39 0.101
725
ACN002 Acanthosis Nigricans 56 0.101
726
TTL012 Total Anomalous Pulmonary Venous Return 1 57 0.101
727
c ARR045 Arrhythmogenic Right Ventricular Dysplasia, Familial, 1 44 0.101
728
CRN239 Carnitine Deficiency, Systemic Primary 62 0.101
729
CST001 Costello Syndrome 68 0.101
730
c FNC027 Fanconi Anemia, Complementation Group a 81 0.101
731
P LPR021 Leprosy 3 71 0.101
732
c GLY008 Glycogen Storage Disease Ii 72 0.101
733
c DWL002 Dowling-Degos Disease 1 58 0.101
734
KRT071 Keratosis, Seborrheic 56 0.101
735
P OVR106 Ovarian Clear Cell Carcinoma 43 0.101
736
c ATS307 Autosomal Recessive Cerebellar Ataxia 38 0.101
737
RNL077 Renal Fibrosis 46 0.101
738
P ANP001 Anaplastic Large Cell Lymphoma 61 0.101
739
P SCL018 Scoliosis 57 0.101
740
ZKF001 Zika Fever 51 0.101
741
ISL003 Isolated Growth Hormone Deficiency 57 0.101
742
CLS016 Clostridium Difficile Colitis 49 0.101
743
HYP017 Hypophosphatemia 49 0.101
744
TCK001 Tick-Borne Encephalitis 59 0.101
745
c SHR030 Short Qt Syndrome 44 0.101
746
ERY003 Erythema Multiforme 56 0.101
747
IDP070 Idiopathic Scoliosis 41 0.101
748
c 3MT007 3-Methylglutaconic Aciduria 36 0.101
749
LGN006 Legionnaire Disease 52 0.101
750
c MYC058 Myocardial Infarction 2 24 0.101
751
SVR097 Severe Cutaneous Adverse Reaction 68 0.101
752
c FNC029 Fanconi Anemia, Complementation Group I 55 0.101
753
P APL001 Aplastic Anemia 73 0.101
754
LNG108 Langerhans Cell Histiocytosis 57 0.101
755
HMN044 Human Immunodeficiency Virus Type 1 76 0.101
756
BRT054 Brittle Bone Disorder 74 0.101
757
c LNG048 Long Qt Syndrome 3 53 0.101
758
MLR004 Malaria 78 0.101
759
ALL003 Allergic Rhinitis 66 0.101
760
HYP810 Hypereosinophilic Syndrome, Idiopathic 61 0.101
761
HLT001 Holt-Oram Syndrome 66 0.101
762
LNT004 Lentigines 45 0.101
763
GLB001 Gilbert Syndrome 53 0.101
764
P HYP750 Hypertriglyceridemia, Familial 62 0.101
765
MCC012 Mccune-Albright Syndrome 69 0.101
766
ENC010 Encephalocraniocutaneous Lipomatosis 46 0.101
767
ALP103 Alpha-1-Antitrypsin Deficiency 67 0.101
768
P MMB011 Membranous Nephropathy 50 0.101
769
c ART101 Aortic Valve Disease 2 65 0.101
770
c CNG404 Congenital Heart Defects, Multiple Types, 4 39 0.101
771
c PRG020 Paragangliomas 3 39 0.101
772
RTN072 Retinohepatoendocrinologic Syndrome 21 0.101
773
c INF068 Inflammatory Bowel Disease 13 22 0.101
774
LPT014 Leptin Deficiency or Dysfunction 77 0.101
775
P GLM040 Glioma Susceptibility 1 70 0.101
776
PLY131 Polyposis, Skin Pigmentation, Alopecia, and Fingernail Changes 44 0.101
777
IGR001 Ige Responsiveness, Atopic 59 0.101
778
KRT019 Keratitis, Hereditary 66 0.101
779
P STR020 Strabismus 56 0.101
780
THR100 Thrombocytopenic Purpura, Autoimmune 60 0.101
781
P LKM071 Leukemia, Chronic Lymphocytic 74 0.101
782
PHY002 Physical Disorder 41 0.101
783
CNG046 Congenital Fiber-Type Disproportion 52 0.101
784
P INF049 Infantile Myofibromatosis 55 0.101
785
P CHR285 Chronic Myelomonocytic Leukemia 59 0.101
786
ANM031 Anomalous Left Coronary Artery from the Pulmonary Artery 25 0.101
787
BRN014 Bronchopneumonia 52 0.101
788
CRN019 Coronary Artery Vasospasm 47 0.101
789
CMM005 Common Cold 55 0.101
790
THY001 Thyroid Crisis 30 0.101
791
PLS006 Plasmodium Vivax Malaria 51 0.101
792
MLG169 Malignant Astrocytoma 57 0.101
793
GLC009 Glucosephosphate Dehydrogenase Deficiency 52 0.101
794
BRN012 Bronchiolitis Obliterans 56 0.101
795
P ANT006 Antiphospholipid Syndrome 55 0.101
796
NPH009 Nephrolithiasis 54 0.101
797
c INH020 Inherited Metabolic Disorder 47 0.101
798
P PNC025 Panic Disorder 52 0.101
799
INF013 Inferior Myocardial Infarction 33 0.101
800
ANT005 Anteroseptal Myocardial Infarction 25 0.101
801
P BNG030 Benign Ependymoma 51 0.101
802
OVR017 Ovarian Cystic Teratoma 29 0.101
803
P PLC011 Pilocytic Astrocytoma 55 0.101
804
ART012 Aortitis 42 0.101
805
ANT019 Anterograde Amnesia 38 0.101
806
P PRP019 Peripheral Nervous System Disease 57 0.101
807
AMN003 Amnestic Disorder 54 0.101
808
NNT011 Neonatal Anemia 34 0.101
809
c HPT016 Hepatitis B 62 0.101
810
DRG002 Drug-Induced Hepatitis 42 0.101
811
MYL031 Myeloproliferative Neoplasm 66 0.101
812
c BSL007 Basal Cell Carcinoma 68 0.101
813
P CYS017 Cystic Teratoma 41 0.101
814
P CRN037 Craniosynostosis 67 0.101
815
TST015 Testicular Disease 42 0.101
816
PRS030 Persistent Fetal Circulation Syndrome 50 0.101
817
P HYP069 Hyperparathyroidism 62 0.101
818
AMN001 Amenorrhea 53 0.101
819
P RNL007 Renal Tubular Acidosis 52 0.101
820
PLM022 Pulmonary Valve Insufficiency 45 0.101
821
NNN026 Noonan Syndrome with Multiple Lentigines 65 0.101
822
P RNV001 Renovascular Hypertension 49 0.101
823
IRT001 Iritis 45 0.101
824
P GND004 Gonadal Dysgenesis 46 0.101
825
P BRS053 Breast Fibroadenoma 48 0.101
826
P RTN022 Retinal Vein Occlusion 54 0.101
827
QFV001 Q Fever 61 0.101
828
c PRM005 Primary Hyperparathyroidism 59 0.101
829
P OPT009 Optic Neuritis 57 0.101
830
LYM009 Lymphocytic Choriomeningitis 46 0.101
831
MNC001 Monocular Esotropia 30 0.101
832
ANT018 Anthracosis 51 0.101
833
P PYL005 Pyelonephritis 56 0.101
834
DPH001 Diphtheria 59 0.101
835
P SYP003 Syphilis 59 0.101
836
INS001 Insulinoma 59 0.101
837
P GLM007 Glomerulonephritis 59 0.101
838
HGH043 High Grade Glioma 46 0.101
839
P RHB003 Rhabdomyosarcoma 66 0.101
840
P GLY013 Glycogen Storage Disease 59 0.101
841
P EPD016 Epidermolysis Bullosa 53 0.101
842
HST010 Histiocytosis 49 0.101
843
MCL006 Macular Retinal Edema 56 0.101
844
P BLD062 Bile Duct Cancer 68 0.101
845
INT010 Intracranial Embolism 48 0.101
846
c ACT059 Acute Maxillary Sinusitis 35 0.101
847
PSY004 Psychotic Disorder 66 0.101
848
GRN006 Granulomatous Angiitis 34 0.101
849
P MXL015 Maxillary Sinusitis 37 0.101
850
GST040 Gastric Adenocarcinoma 66 0.101
851
THY123 Thyroid Gland Follicular Carcinoma 53 0.101
852
CHR001 Churg-Strauss Syndrome 61 0.101
853
P GLL018 Gallbladder Cancer 53 0.101
854
PLM058 Pulmonary Atresia with Intact Ventricular Septum 28 0.101
855
P NSP012 Nasopharyngeal Carcinoma 60 0.101
856
c RTN047 Retinitis Pigmentosa 18 45 0.101
857
INT062 Interstitial Myocarditis 22 0.101
858
P THY054 Thyrotoxic Periodic Paralysis 51 0.101
859
CRN030 Coronary Stenosis 50 0.101
860
TRC021 Tricuspid Valve Stenosis 30 0.101
861
MXD005 Mixed Connective Tissue Disease 57 0.101
862
DFF003 Diffuse Scleroderma 41 0.101
863
P NRM002 Normal Pressure Hydrocephalus 49 0.101
864
PNN001 Panniculitis 52 0.101
865
CHR466 Chronic Thromboembolic Pulmonary Hypertension 47 0.101
866
CRT061 Cor Triatriatum Dexter 20 0.101
867
P JVN042 Juvenile Retinoschisis 39 0.101
868
FNT004 Fainting 29 0.101
869
P HRP006 Herpes Simplex 65 0.101
870
ACT058 Active Peptic Ulcer Disease 55 0.101
871
P MSC003 Muscular Atrophy 52 0.101
872
BRN071 Brain Injury 50 0.101
873
P NNT042 Neonatal Lupus Erythematosus 37 0.101
874
PTT037 Pituitary Tumors 44 0.101
875
VSC003 Visceral Leishmaniasis 54 0.101
876
PYR009 Pyridoxine Deficiency Anemia 35 0.101
877
MYC005 Myocardial Stunning 45 0.101
878
DXT001 Dextrocardia 55 0.101
879
CLL010 Cellular Ependymoma 58 0.101
880
P EPD009 Epidermolysis Bullosa Dystrophica 66 0.101
881
HDN002 Head Injury 44 0.101
882
P HDC001 Headache 56 0.101
883
MCH006 Mechanical Strabismus 40 0.101
884
SPN186 Spinal Cord Injury 61 0.101
885
AMR003 Amaurosis Fugax 33 0.101
886
ATR017 Atrial Septal Defect Coronary Sinus 25 0.101
887
ATM076 Autoimmune Retinopathy 26 0.101
888
ALL012 Allergic Angiitis 24 0.101
889
BRK012 Broken Heart Syndrome 42 0.101
890
INV005 Inverted Follicular Keratosis 32 0.101
891
ACH005 Achalasia 54 0.101
892
PRT036 Peritonitis 65 0.101
893
P INT070 Intestinal Obstruction 57 0.101
894
P LPS004 Lupus Erythematosus 61 0.101
895
HPT009 Hepatopulmonary Syndrome 48 0.101
896
GSG001 Gas Gangrene 52 0.101
897
FND002 Fundus Dystrophy 55 0.101
898
PRL008 Paralytic Ileus 44 0.101
899
PTT001 Pituitary Hypoplasia 34 0.101
900
c BCT013 Bacterial Pneumonia 47 0.101
901
P ALP008 Alopecia 53 0.101
902
EXP004 Exophthalmos 50 0.101
903
HYP034 Hypertensive Encephalopathy 43 0.101
904
SHH001 Sheehan Syndrome 44 0.101
905
P CLL015 Collagen Disease 47 0.101
906
P NRP001 Neuropathy 59 0.101
907
CNG117 Congenital Nonhemolytic Jaundice 8 0.101
908
P ENC008 Encephalocele 46 0.101
909
GRN017 Granulocytopenia 42 0.101
910
OGL001 Ogilvie Syndrome 23 0.101
911
P HYP083 Hypopituitarism 52 0.101
912
HNS001 Hansen's Disease 32 0.101
913
LYM035 Lymphangiectasis 30 0.101
914
LYM019 Lymphosarcoma 46 0.101
915
ORL011 Oral Cancer 60 0.101
916
EST005 Esotropia 42 0.101
917
HYP048 Hypotropia 26 0.101
918
CHR078 Chorioretinitis 50 0.101
919
MCR004 Macroglobulinemia 48 0.101
920
CTN007 Cutaneous Leishmaniasis 61 0.101
921
P HMC002 Homocystinuria 52 0.101
922
HYD004 Hydrops of Gallbladder 22 0.101
923
ACR022 Acardia 13 0.101
924
P RRC004 Rare Cardiomyopathy 16 0.101
925
DFF036 Differentiated Thyroid Carcinoma 51 0.101
926
FCL090 Facial Cleft 30 0.101
927
P PRD021 Periodic Paralysis 42 0.101
928
SPC030 Specific Language Disorder 25 0.101
929
PRC051 Paracetamol Poisoning 29 0.101
930
CYN003 Cyanide Poisoning 21 0.101
931
c HRD173 Hereditary Late-Onset Parkinson Disease 50 0.101
932
ERY066 Erythema Multiforme Major 29 0.101
933
ACT174 Acute Peripheral Arterial Occlusion 21 0.101
934
MTB016 Metabolic Myopathy 30 0.101
935
c INH030 Inherited Retinal Disorder 28 0.101
936
JXT004 Juxtaposition of the Atrial Appendages 13 0.101
937
c FML294 Familial Short Qt Syndrome 44 0.101
938
XLN206 X-Linked Intellectual Disability-Macrocephaly-Macroorchidism Syndrome 31 0.101
939
PLM116 Pulmonary Artery Hypoplasia 20 0.101
940
ATR055 Atrial Septal Aneurysm 22 0.101
941
PRC049 Precursor T-Cell Acute Lymphoblastic Leukemia 45 0.101
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