Search results for Digoxin

476 hits were found for Digoxin

# Family MCID Name MIFTS Score
1
CNG034 Congestive Heart Failure 70 0.605
2
P ATR011 Atrial Fibrillation 66 0.413
3
P HRT032 Heart Disease 75 0.412
4
P KDN018 Kidney Disease 70 0.267
5
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 66 0.243
6
ATR057 Atrioventricular Block 55 0.196
7
P CRD119 Cardiac Arrest 67 0.187
8
ADL002 Adult Syndrome 69 0.165
9
c FML001 Familial Atrial Fibrillation 66 0.165
10
c PRC016 Pre-Eclampsia 63 0.165
11
c HYP595 Hypertension, Essential 84 0.162
12
HYP005 Hypokalemia 55 0.162
13
DGT004 Digitalis Poisoning 14 0.162
14
c DLT002 Dilated Cardiomyopathy 79 0.153
15
P LVR013 Liver Disease 68 0.153
16
P CRN300 Coronary Heart Disease 1 63 0.147
17
P BRS047 Breast Cancer 96 0.141
18
URM002 Uremia 49 0.141
19
CYT018 Cytochrome P450 2d6 Variant 27 0.141
20
c ATR087 Atrial Standstill 1 74 0.137
21
ANG054 Angina Pectoris 66 0.137
22
END030 End Stage Renal Failure 58 0.137
23
48X005 48,xyyy 39 0.137
24
HYP266 Hypoxia 56 0.134
25
c ACT075 Acute Myocardial Infarction 56 0.134
26
P DBT026 Diabetes Mellitus, Noninsulin-Dependent 89 0.130
27
HYD038 Hydrops Fetalis, Nonimmune 61 0.130
28
SYS003 Systolic Heart Failure 50 0.130
29
P DBT009 Diabetes Mellitus 64 0.126
30
P HYP724 Hyperlipoproteinemia, Type Iii 72 0.123
31
P CRN018 Coronary Artery Anomaly 63 0.123
32
c ACT071 Acute Kidney Failure 59 0.123
33
INT007 Intermediate Coronary Syndrome 55 0.123
34
P HYP076 Hyperthyroidism 55 0.119
35
P MYC007 Myocardial Infarction 70 0.115
36
HND015 Hand Skill, Relative 33 0.115
37
ART140 Arteries, Anomalies of 53 0.111
38
P PRS040 Prostate Cancer 97 0.106
39
ISC004 Ischemia 60 0.106
40
P ECL001 Eclampsia 51 0.106
41
DST006 Diastolic Heart Failure 44 0.102
42
WLF001 Wolff-Parkinson-White Syndrome 65 0.097
43
P TRN020 Turner Syndrome 65 0.097
44
c MTR018 Maturity-Onset Diabetes of the Young, Type 1 60 0.097
45
P PTN014 Patent Ductus Arteriosus 1 60 0.097
46
P SZR006 Seizure Disorder 58 0.097
47
RST023 Resting Heart Rate, Variation in 41 0.097
48
P ART022 Arthritis 70 0.087
49
P HYP086 Hypothyroidism 68 0.087
50
c PRG042 Progressive Familial Heart Block, Type Ia 67 0.087
51
HYD058 Hydrops, Lactic Acidosis, and Sideroblastic Anemia 63 0.087
52
CRD223 Cardiac Arrhythmia 60 0.087
53
RHM028 Rheumatic Heart Disease 53 0.087
54
VTM033 Vitamin K Deficiency Bleeding 48 0.087
55
CRD137 Cardiogenic Shock 48 0.087
56
P ALZ034 Alzheimer Disease 88 0.081
57
P RHM011 Rheumatoid Arthritis 80 0.081
58
DWN001 Down Syndrome 70 0.081
59
MLN008 Melanoma 69 0.081
60
P PLM037 Pulmonary Hypertension 68 0.081
61
DPR016 Depression 63 0.081
62
P ENC018 Encephalopathy 61 0.081
63
c PRG043 Progressive Familial Heart Block, Type Ib 58 0.081
64
MNT002 Mental Depression 57 0.081
65
P MTR003 Mitral Valve Stenosis 50 0.081
66
47X002 47,xyy 49 0.081
67
c SVR005 Severe Pre-Eclampsia 49 0.081
68
SNG003 Single Ventricular Heart 30 0.081
69
BDR001 Bidirectional Tachycardia 19 0.081
70
P CLR023 Colorectal Cancer 98 0.075
71
P PNC035 Pancreatic Cancer 84 0.075
72
STR067 Stroke, Ischemic 80 0.075
73
P EPL164 Epilepsy 71 0.075
74
CRB039 Cerebrovascular Disease 69 0.075
75
BRN024 Bronchitis 68 0.075
76
P THR014 Thrombocytopenia 68 0.075
77
SKN019 Skin Melanoma 67 0.075
78
P HPT021 Hepatitis 67 0.075
79
P VSC007 Vascular Disease 63 0.075
80
LNG099 Lung Disease 61 0.075
81
P PNC044 Pancreatitis 61 0.075
82
CHL068 Cholestasis 60 0.075
83
c ACT027 Acute Pancreatitis 59 0.075
84
ATX019 Ataxia with Vitamin E Deficiency 48 0.075
85
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.075
86
GST020 Gastric Antral Vascular Ectasia 41 0.075
87
P LNG032 Lung Cancer 97 0.069
88
P BDY004 Body Mass Index Quantitative Trait Locus 11 76 0.069
89
HMN044 Human Immunodeficiency Virus Type 1 71 0.069
90
P AMY004 Amyloidosis 70 0.069
91
c HPT073 Hepatitis C Virus 70 0.069
92
P MJR001 Major Depressive Disorder 68 0.069
93
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 66 0.069
94
c SML038 Small Cell Cancer of the Lung 65 0.069
95
c HPT001 Hepatitis C 63 0.069
96
HYP066 Hyperglycemia 61 0.069
97
P VNT002 Ventricular Septal Defect 60 0.069
98
GST050 Gastrointestinal System Disease 56 0.069
99
HMN014 Human Immunodeficiency Virus Infectious Disease 55 0.069
100
P SCK002 Sick Sinus Syndrome 55 0.069
101
PLM010 Pulmonary Edema 55 0.069
102
c BDY021 Body Mass Index Quantitative Trait Locus 20 52 0.069
103
c BDY020 Body Mass Index Quantitative Trait Locus 19 52 0.069
104
HRT011 Heart Septal Defect 50 0.069
105
GYN001 Gynecomastia 49 0.069
106
c BDY005 Body Mass Index Quantitative Trait Locus 9 48 0.069
107
RGH001 Right Bundle Branch Block 47 0.069
108
c BDY019 Body Mass Index Quantitative Trait Locus 18 47 0.069
109
c BDY010 Body Mass Index Quantitative Trait Locus 4 46 0.069
110
c BDY015 Body Mass Index Quantitative Trait Locus 12 46 0.069
111
c BDY017 Body Mass Index Quantitative Trait Locus 14 45 0.069
112
c BDY011 Body Mass Index Quantitative Trait Locus 10 45 0.069
113
c BDY006 Body Mass Index Quantitative Trait Locus 8 44 0.069
114
c BDY012 Body Mass Index Quantitative Trait Locus 7 44 0.069
115
c PRS136 Prostate Cancer, Hereditary, 6 33 0.069
116
c PRS130 Prostate Cancer, Hereditary, 8 32 0.069
117
INF021 Infant Gynecomastia 31 0.069
118
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.069
119
c LKM061 Leukemia, Acute Myeloid 83 0.061
120
IMM167 Immune Deficiency Disease 78 0.061
121
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.061
122
P HNT016 Huntington Disease 71 0.061
123
ACR007 Acromegaly 71 0.061
124
P SLP006 Sleep Apnea 69 0.061
125
P DBT085 Diabetes Mellitus, Insulin-Dependent 67 0.061
126
P LKM002 Leukemia 66 0.061
127
c CHR684 Chronic Kidney Disease 66 0.061
128
HYP056 Hypoglycemia 66 0.061
129
P ABD014 Abdominal Obesity-Metabolic Syndrome 1 64 0.061
130
ALL026 Allergic Hypersensitivity Disease 64 0.061
131
P ADN016 Adenocarcinoma 64 0.061
132
LVR012 Liver Cirrhosis 63 0.061
133
c HRD002 Hereditary Angioedema 61 0.061
134
ATM095 Autoimmune Disease 61 0.061
135
P MYL006 Myeloid Leukemia 60 0.061
136
CRD132 Cardiac Conduction Defect 59 0.061
137
VSL002 Visual Epilepsy 58 0.061
138
CNS004 Constipation 57 0.061
139
P HDC001 Headache 57 0.061
140
c ANG068 Angioedema, Hereditary, Type I 56 0.061
141
THR024 Thrombosis 56 0.061
142
c GRV008 Graves Disease 1 55 0.061
143
HYP060 Hyperinsulinism 54 0.061
144
P ANG015 Angioedema 54 0.061
145
P RNL015 Renal Hypertension 48 0.061
146
ACT113 Acute Myeloblastic Leukemia with Maturation 46 0.061
147
ANR004 Anuria 46 0.061
148
SBC016 Subacute Delirium 44 0.061
149
C1N001 C1 Inhibitor Deficiency 40 0.061
150
ANG049 Angioedema Induced by Ace Inhibitors 40 0.061
151
P PRC031 Preeclampsia/eclampsia 1 37 0.061
152
CMP040 Complement Component 4, Partial Deficiency of 33 0.061
153
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.053
154
CYS001 Cystic Fibrosis 80 0.053
155
SQM013 Squamous Cell Carcinoma, Head and Neck 80 0.053
156
KPS004 Kaposi Sarcoma 75 0.053
157
P SCH015 Schizophrenia 75 0.053
158
P RSP003 Respiratory Failure 74 0.053
159
VNH007 Von Hippel-Lindau Syndrome 73 0.053
160
PRP027 Peripheral Vascular Disease 71 0.053
161
P SRC025 Sarcoidosis 1 70 0.053
162
MYL009 Myelodysplastic Syndrome 70 0.053
163
OBS002 Obsessive-Compulsive Disorder 68 0.053
164
P DMN002 Dementia 67 0.053
165
c MCL062 Mucolipidosis Ii Alpha/beta 66 0.053
166
ATH013 Atherosclerosis Susceptibility 66 0.053
167
SRC014 Sarcoma 65 0.053
168
P HRP006 Herpes Simplex 65 0.053
169
APN008 Apnea, Obstructive Sleep 65 0.053
170
c FNC043 Fanconi Anemia, Complementation Group E 62 0.053
171
TXC005 Toxic Shock Syndrome 61 0.053
172
P ERY058 Erythrocytosis, Familial, 1 61 0.053
173
ACQ007 Acquired Immunodeficiency Syndrome 60 0.053
174
PPT005 Peptic Ulcer Disease 58 0.053
175
TMR010 Tumor Predisposition Syndrome 58 0.053
176
BLM002 Bulimia Nervosa 57 0.053
177
OBS525 Obsolete: Squamous Cell Carcinoma of Head and Neck 57 0.053
178
P EXN002 Exanthem 57 0.053
179
P DRR001 Diarrhea 57 0.053
180
SFT003 Soft Tissue Sarcoma 56 0.053
181
AGN016 Aging 56 0.053
182
CMR002 Coumarin Resistance 56 0.053
183
P PLY018 Polycythemia 55 0.053
184
END040 Endogenous Depression 54 0.053
185
GLC003 Glucose Intolerance 54 0.053
186
HMS001 Hemosiderosis 54 0.053
187
c ERY048 Erythrocytosis, Familial, 2 53 0.053
188
P ART018 Aortic Valve Insufficiency 53 0.053
189
KRT009 Keratosis 53 0.053
190
NRT001 Neurotic Disorder 52 0.053
191
P ACT105 Acute Mountain Sickness 52 0.053
192
CHR073 Choreatic Disease 52 0.053
193
P ACT008 Actinic Keratosis 52 0.053
194
P PRC012 Pericardial Effusion 51 0.053
195
SPN035 Spindle Cell Sarcoma 51 0.053
196
LNG031 Lung Benign Neoplasm 50 0.053
197
SNT005 Sinoatrial Node Disease 49 0.053
198
HMP001 Hemopericardium 46 0.053
199
P HMN032 Human Herpesvirus 8 46 0.053
200
CHR607 Chorea, Childhood-Onset, with Psychomotor Retardation 46 0.053
201
SYN036 Syncope 45 0.053
202
c TRC022 Tricuspid Valve Insufficiency 45 0.053
203
c PRM038 Primary Agammaglobulinemia 43 0.053
204
c CHR546 Chronic Mountain Sickness 42 0.053
205
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.053
206
BP1002 Bap1 Tumor Predisposition Syndrome 41 0.053
207
P RRH023 Rare Hereditary Hemochromatosis 41 0.053
208
c MLG074 Malignant Mesenchymoma 39 0.053
209
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.053
210
CMP080 Complement Hyperactivation, Angiopathic Thrombosis, and Protein-Losing Enteropathy 38 0.053
211
PLM134 Pulmonary Fibrosis, Idiopathic 75 0.043
212
GLB015 Glioblastoma Multiforme 75 0.043
213
ULC004 Ulcerative Colitis 73 0.043
214
P RTN024 Retinoblastoma 72 0.043
215
PLM001 Pulmonary Tuberculosis 70 0.043
216
P INF038 Influenza 68 0.043
217
P PNM007 Pneumonia 68 0.043
218
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.043
219
P HYD006 Hydrocephalus 65 0.043
220
P ART005 Arteriovenous Malformation 65 0.043
221
c RHB024 Rhabdomyosarcoma 2 65 0.043
222
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.043
223
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.043
224
CLN015 Colon Adenocarcinoma 63 0.043
225
IRR002 Irritable Bowel Syndrome 63 0.043
226
IDP011 Idiopathic Interstitial Pneumonia 63 0.043
227
P ORT004 Orthostatic Intolerance 63 0.043
228
P NTR004 Neutropenia 63 0.043
229
P NPH012 Nephrotic Syndrome 63 0.043
230
LPD008 Lipid Metabolism Disorder 62 0.043
231
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 62 0.043
232
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 62 0.043
233
TRN015 Transient Cerebral Ischemia 62 0.043
234
P VSC011 Vasculitis 62 0.043
235
P PLM036 Pulmonary Fibrosis 61 0.043
236
SDD001 Sudden Infant Death Syndrome 61 0.043
237
ART141 Arteriovenous Malformations of the Brain 61 0.043
238
HPT019 Hepatic Encephalopathy 60 0.043
239
RTN017 Retinal Detachment 60 0.043
240
P MYC008 Myocarditis 59 0.043
241
ANR040 Aneurysm 58 0.043
242
P BCL017 B-Cell Lymphoma 58 0.043
243
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.043
244
P BPL003 Bipolar Disorder 56 0.043
245
BCT022 Bacterial Infectious Disease 56 0.043
246
P CRD246 Cardiovascular System Disease 56 0.043
247
ANG005 Anogenital Venereal Wart 56 0.043
248
P INF037 Inflammatory Bowel Disease 56 0.043
249
PRP030 Purpura 55 0.043
250
P DBT005 Diabetes Insipidus 55 0.043
251
P SBS003 Substance Abuse 54 0.043
252
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.043
253
P ART021 Arteriosclerosis 54 0.043
254
P TCD001 Tic Disorder 54 0.043
255
PRC013 Pericarditis 54 0.043
256
P RTN016 Retinal Degeneration 53 0.043
257
INT075 Intracranial Hypertension 53 0.043
258
HRT012 Heart Valve Disease 53 0.043
259
c FML008 Familial Retinoblastoma 53 0.043
260
SBC001 Subacute Sclerosing Panencephalitis 52 0.043
261
P SHR001 Short Bowel Syndrome 52 0.043
262
P INT068 Intestinal Disease 52 0.043
263
CHR005 Chorioamnionitis 51 0.043
264
NNL006 Non-Alcoholic Steatohepatitis 51 0.043
265
SCH012 Schizoaffective Disorder 50 0.043
266
HPT014 Hepatorenal Syndrome 50 0.043
267
DYS073 Dysphagia 50 0.043
268
CRV040 Cervix Carcinoma 50 0.043
269
P OVR082 Overgrowth Syndrome 50 0.043
270
SXL003 Sexual Disorder 48 0.043
271
HYP025 Hyperphosphatemia 47 0.043
272
ATN005 Autonomic Dysfunction 47 0.043
273
c MTR002 Mitral Valve Insufficiency 47 0.043
274
MCR209 Microcephaly, Epilepsy, and Diabetes Syndrome 47 0.043
275
PST048 Postural Orthostatic Tachycardia Syndrome 45 0.043
276
P LPM005 Lipomatosis 45 0.043
277
VLV044 Vulvar Intraepithelial Neoplasia 44 0.043
278
HPT004 Hepatic Coma 43 0.043
279
P MJR007 Major Affective Disorder 1 43 0.043
280
c CHR096 Chronic Pulmonary Heart Disease 43 0.043
281
LWC001 Low Compliance Bladder 42 0.043
282
c MJR024 Major Affective Disorder 9 41 0.043
283
P DYS005 Dyslexia 40 0.043
284
EXT006 Extrahepatic Cholestasis 40 0.043
285
PLY100 Polyploidy 40 0.043
286
ALL014 Allergic Encephalomyelitis 39 0.043
287
c MJR022 Major Affective Disorder 8 38 0.043
288
SCN049 Second-Degree Atrioventricular Block 36 0.043
289
c MJR008 Major Affective Disorder 2 34 0.043
290
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.043
291
c CHR064 Chronic Monocytic Leukemia 34 0.043
292
c MJR003 Major Affective Disorder 6 33 0.043
293
c MJR006 Major Affective Disorder 5 33 0.043
294
c MJR023 Major Affective Disorder 7 33 0.043
295
c MJR004 Major Affective Disorder 4 28 0.043
296
CHL079 Children's Interstitial Lung Disease 27 0.043
297
ATR089 Atrioventricular Dissociation 20 0.043
298
P OVR042 Ovarian Cancer 89 0.031
300
MYL069 Myeloma, Multiple 85 0.031
301
OST012 Osteoarthritis 78 0.031
302
P LNG064 Lung Cancer Susceptibility 3 77 0.031
303
P RTN008 Retinitis Pigmentosa 77 0.031
304
P MDL005 Medulloblastoma 77 0.031
305
AST005 Asthma 77 0.031
306
CRV035 Cervical Cancer 76 0.031
307
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.031
308
DFC004 Deficiency Anemia 75 0.031
309
CRH001 Crohn's Disease 74 0.031
310
SVR004 Severe Combined Immunodeficiency 73 0.031
311
c SPN225 Spondyloarthropathy 1 73 0.031
312
P OST002 Osteoporosis 73 0.031
313
c THR092 Thrombophilia Due to Thrombin Defect 73 0.031
314
P MLT020 Multiple Sclerosis 72 0.031
315
c HYP836 Hypercholesterolemia, Familial, 1 72 0.031
316
MSC157 Muscular Dystrophy, Duchenne Type 71 0.031
317
P NRB001 Neuroblastoma 71 0.031
318
OTT002 Otitis Media 71 0.031
319
c GCH015 Gaucher Disease, Type I 70 0.031
320
c MGR028 Migraine with or Without Aura 1 69 0.031
321
CRT072 Creutzfeldt-Jakob Disease 69 0.031
322
ART016 Aortic Aneurysm 68 0.031
323
P MYC084 Mycobacterium Tuberculosis 1 68 0.031
324
P MLG056 Malignant Hyperthermia 67 0.031
325
BRK010 Burkitt Lymphoma 67 0.031
326
c JVN010 Juvenile Rheumatoid Arthritis 67 0.031
327
P HYP061 Hypertrophic Cardiomyopathy 66 0.031
328
ALC007 Alcohol Dependence 66 0.031
329
P MCR115 Microvascular Complications of Diabetes 5 66 0.031
330
P MSC005 Muscular Dystrophy 66 0.031
331
P MNN013 Meningitis 65 0.031
332
P ATS364 Autism 65 0.031
333
P DYS154 Dystonia 65 0.031
334
KWS002 Kawasaki Disease 64 0.031
335
P MTR014 Motor Neuron Disease 64 0.031
336
OST017 Osteomyelitis 64 0.031
337
KHL003 Kohlschutter-Tonz Syndrome 64 0.031
338
P GCH001 Gaucher's Disease 64 0.031
339
c CRD177 Ceroid Lipofuscinosis, Neuronal, 1 63 0.031
340
MSC007 Muscle Hypertrophy 63 0.031
341
P ADL010 Adult Respiratory Distress Syndrome 63 0.031
342
SKN016 Skin Disease 63 0.031
343
c ACT068 Acute Cystitis 63 0.031
344
ANR007 Anorexia Nervosa 63 0.031
345
c HPT003 Hepatitis a 63 0.031
346
c SCL052 Scleroderma, Familial Progressive 62 0.031
347
P PRD008 Periodontitis 62 0.031
348
P ART023 Arthropathy 62 0.031
349
INT323 Intraocular Pressure Quantitative Trait Locus 62 0.031
350
CLT003 Colitis 62 0.031
351
P PSR002 Psoriasis 62 0.031
352
PSR001 Psoriatic Arthritis 62 0.031
353
P EPL140 Epilepsy, Idiopathic Generalized 61 0.031
354
P PRM006 Primary Biliary Cirrhosis 61 0.031
355
CHR066 Chronic Fatigue Syndrome 61 0.031
356
c BRN108 Branchiootic Syndrome 1 61 0.031
357
RHM001 Rheumatic Fever 61 0.031
358
TRG002 Trigeminal Neuralgia 60 0.031
359
P THL005 Thalassemia 60 0.031
360
c ART138 Aortic Aneurysm, Familial Abdominal, 1 60 0.031
361
ETN001 Eating Disorder 59 0.031
362
P SLP005 Sleep Disorder 59 0.031
363
INT066 Interstitial Lung Disease 59 0.031
364
THY029 Thyroid Carcinoma 59 0.031
365
STT001 Status Epilepticus 59 0.031
366
P CYS018 Cystitis 59 0.031
367
BRN002 Bronchiolitis 59 0.031
368
HLC007 Helicobacter Pylori Infection 59 0.031
369
P RBL001 Rubella 58 0.031
370
IRN001 Iron Deficiency Anemia 58 0.031
371
INT324 Intrauterine Growth Retardation, Metaphyseal Dysplasia, Adrenal Hypoplasia Congenita, and Genital Anomalies 58 0.031
372
EYD002 Eye Disease 58 0.031
373
P URT039 Urticaria 58 0.031
374
NWB001 Newborn Respiratory Distress Syndrome 58 0.031
375
P MTR012 Mitral Valve Disease 57 0.031
376
PLM070 Pulmonic Stenosis 57 0.031
377
P OPT006 Optic Nerve Disease 57 0.031
378
P CND004 Candidiasis 57 0.031
379
IRN002 Iron Metabolism Disease 57 0.031
380
BLR008 Bilirubin Metabolic Disorder 57 0.031
381
GST033 Gestational Diabetes 57 0.031
382
P FTT008 Fatty Liver Disease, Nonalcoholic 1 57 0.031
383
P UVT001 Uveitis 57 0.031
384
RSP019 Respiratory Distress Syndrome in Premature Infants 57 0.031
385
APH002 Aphasia 57 0.031
386
c LKM060 Leukemia, Acute Lymphoblastic 3 56 0.031
387
PHR003 Pharyngitis 56 0.031
388
INT303 Intracranial Hypertension, Idiopathic 56 0.031
389
P PLY019 Polyneuropathy 56 0.031
390
RHM027 Rheumatic Disease 56 0.031
391
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 55 0.031
392
P ATR001 Atrioventricular Septal Defect 55 0.031
393
NRN004 Neuroendocrine Tumor 55 0.031
394
EBS001 Ebstein Anomaly 55 0.031
395
P LYM031 Lymphocytic Leukemia 55 0.031
396
c THR001 Thrombocytopenia Due to Platelet Alloimmunization 53 0.031
397
OCL006 Ocular Hypertension 53 0.031
398
P LYM025 Lymphedema 53 0.031
399
SPN051 Spondylitis 52 0.031
400
c MCR113 Microvascular Complications of Diabetes 3 52 0.031
401
CMB003 Combined T Cell and B Cell Immunodeficiency 52 0.031
402
c HPT007 Hepatitis E 52 0.031
403
PST011 Pustulosis of Palm and Sole 52 0.031
404
c GLL024 Gallbladder Disease 1 52 0.031
405
RYS001 Reye Syndrome 51 0.031
406
c VRL010 Viral Hepatitis 51 0.031
407
GNG012 Gingival Overgrowth 51 0.031
408
PLR008 Pleurisy 51 0.031
409
c ACT134 Acute Liver Failure 51 0.031
410
PNC041 Pancreatic Ductal Adenocarcinoma 51 0.031
411
c ALM001 Al Amyloidosis 50 0.031
412
RTN003 Retinal Ischemia 50 0.031
413
P CHL066 Cholangitis 50 0.031
414
END020 Endocardial Fibroelastosis 50 0.031
415
ILT001 Ileitis 50 0.031
416
MTB004 Metabolic Acidosis 50 0.031
417
P INT099 Intrahepatic Cholestasis of Pregnancy 49 0.031
418
HYP006 Hypertensive Heart Disease 49 0.031
419
ART017 Aortic Disease 49 0.031
420
LFT001 Left Bundle Branch Hemiblock 49 0.031
421
END021 Endomyocardial Fibrosis 48 0.031
422
PPL021 Papilledema 48 0.031
423
WTH001 Withdrawal Disorder 48 0.031
424
P CLR019 Color Blindness 48 0.031
425
FBR032 Fibromuscular Dysplasia 48 0.031
426
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.031
427
PRP007 Priapism 48 0.031
428
c MCR120 Microvascular Complications of Diabetes 7 47 0.031
429
P CRC039 Coarctation of Aorta 47 0.031
430
CHR074 Choriocarcinoma 46 0.031
431
RTN023 Retinitis 46 0.031
432
SPN020 Spondylosis 46 0.031
433
CNT025 Central Pontine Myelinolysis 45 0.031
434
ESP018 Esophageal Candidiasis 45 0.031
435
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.031
436
KWS001 Kwashiorkor 45 0.031
437
MYX004 Myxedema 44 0.031
438
P BRB001 Beriberi 44 0.031
439
ATN004 Autonomic Neuropathy 44 0.031
440
c ATM099 Autoimmune Uveitis 44 0.031
441
CRT015 Carotid Artery Occlusion 44 0.031
442
CYT002 Cytokine Deficiency 44 0.031
443
ATX038 Ataxia and Polyneuropathy, Adult-Onset 44 0.031
444
IDP033 Idiopathic Edema 43 0.031
445
NRR001 Neuroretinitis 43 0.031
446
ANG011 Angiodysplasia 43 0.031
447
CRB033 Cerebral Degeneration 42 0.031
448
ANX004 Anoxia 42 0.031
449
SPC005 Speech Disorder 42 0.031
450
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 41 0.031
451
NRN005 Neuronal Ceroid-Lipofuscinoses 41 0.031
452
BSL009 Basal Ganglia Calcification 41 0.031
453
c MCR130 Microvascular Complications of Diabetes 6 41 0.031
454
c MCR133 Microvascular Complications of Diabetes 4 41 0.031
455
FRS012 First-Degree Atrioventricular Block 41 0.031
456
EPL001 Epilepsy with Generalized Tonic-Clonic Seizures 39 0.031
457
BRS050 Breast Cyst 38 0.031
458
HMR023 Hemorrhagic Cystitis 38 0.031
459
OVR094 Ovarian Epithelial Cancer 38 0.031
460
ABD002 Abducens Nerve Disease 38 0.031
461
PLT015 Platelet Aggregation, Spontaneous 37 0.031
462
UNL002 Unilateral Retinoblastoma 37 0.031
463
P FML187 Familial Hypertension 37 0.031
464
PLC006 Placental Choriocarcinoma 36 0.031
465
SCR003 Secretory Diarrhea 36 0.031
466
CRY036 Cryptogenic Cirrhosis 36 0.031
467
FXD003 Fixed Drug Eruption 35 0.031
468
CHR178 Chromosomal Triplication 35 0.031
469
HYP806 Hypertension, Early-Onset, Autosomal Dominant, with Severe Exacerbation in Pregnancy 34 0.031
470
INF009 Inflammatory Spondylopathy 32 0.031
471
MBT001 Mobitz Type Ii Atrioventricular Block 31 0.031
472
ANR010 Aneurysm of Sinus of Valsalva 31 0.031
473
IMM039 Immune Hydrops Fetalis 28 0.031
474
CRT028 Cor Triatriatum 27 0.031
475
BNG077 Benign Idiopathic Neonatal Seizures 26 0.031
476
c RNG011 Ring Chromosome 16 17 0.031
Content
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