Search results for Amiodarone

497 hits were found for Amiodarone

# Family MCID Name MIFTS Score
1
P ATR011 Atrial Fibrillation 66 0.622
2
c GRV008 Graves Disease 1 56 0.547
3
P HYP086 Hypothyroidism 69 0.535
4
c VNT034 Ventricular Fibrillation, Paroxysmal Familial, 1 67 0.493
5
P HYP076 Hyperthyroidism 55 0.477
6
CNG034 Congestive Heart Failure 69 0.361
7
P CRD119 Cardiac Arrest 67 0.315
8
P PLM036 Pulmonary Fibrosis 65 0.310
9
c FML001 Familial Atrial Fibrillation 65 0.293
10
P NRP001 Neuropathy 56 0.293
11
CRD132 Cardiac Conduction Defect 58 0.292
12
P THY032 Thyroiditis 52 0.266
13
c DLT002 Dilated Cardiomyopathy 79 0.251
14
P HRT032 Heart Disease 75 0.251
15
GTR002 Goiter 53 0.242
16
P OPT006 Optic Nerve Disease 60 0.225
17
CRD223 Cardiac Arrhythmia 60 0.221
18
KRT008 Keratopathy 47 0.221
19
c ATR087 Atrial Standstill 1 75 0.211
20
LNG099 Lung Disease 60 0.211
21
WLF001 Wolff-Parkinson-White Syndrome 66 0.204
22
SYN036 Syncope 45 0.184
23
P MYC007 Myocardial Infarction 70 0.179
24
ATR057 Atrioventricular Block 55 0.179
25
P HYP061 Hypertrophic Cardiomyopathy 70 0.169
26
LPP008 Lipoprotein Quantitative Trait Locus 62 0.169
27
P PRP019 Peripheral Nervous System Disease 58 0.169
28
P HYP724 Hyperlipoproteinemia, Type Iii 73 0.166
29
ANG054 Angina Pectoris 66 0.166
30
P RSP003 Respiratory Failure 74 0.163
31
c ACT075 Acute Myocardial Infarction 57 0.163
32
c FBR046 Fibrosis of Extraocular Muscles, Congenital, 1 57 0.160
33
P GRV001 Graves' Disease 55 0.158
34
ART140 Arteries, Anomalies of 52 0.158
35
CHG001 Chagas Disease 66 0.155
36
P CRN300 Coronary Heart Disease 1 63 0.152
37
P MYP004 Myopathy 70 0.146
38
LVR012 Liver Cirrhosis 62 0.143
39
48X005 48,xyyy 39 0.143
40
P PNM007 Pneumonia 68 0.140
41
VNT035 Ventricular Tachycardia, Catecholaminergic Polymorphic, 1, with or Without Atrial Dysfunction and/or Dilated Cardiomyopathy 63 0.140
42
HYP005 Hypokalemia 55 0.140
43
ALL026 Allergic Hypersensitivity Disease 62 0.137
44
INT066 Interstitial Lung Disease 60 0.137
45
P TRM003 Tremor 54 0.133
46
P HPT021 Hepatitis 67 0.130
47
BRN002 Bronchiolitis 59 0.130
48
c DWL002 Dowling-Degos Disease 1 58 0.130
49
P SCK002 Sick Sinus Syndrome 55 0.130
50
CRB039 Cerebrovascular Disease 67 0.126
51
P KDN018 Kidney Disease 72 0.123
52
BRN012 Bronchiolitis Obliterans 55 0.123
53
STR067 Stroke, Ischemic 81 0.119
54
P LNG028 Long Qt Syndrome 66 0.119
55
ATX038 Ataxia and Polyneuropathy, Adult-Onset 45 0.119
56
P LVR013 Liver Disease 68 0.115
57
P EXN002 Exanthem 57 0.115
58
CRD178 Cardiac Conduction Disease with or Without Dilated Cardiomyopathy 43 0.111
59
P MLT008 Multinodular Goiter 42 0.111
60
HYD038 Hydrops Fetalis, Nonimmune 62 0.107
61
ENC067 Encephalopathy, Progressive, Early-Onset, with Episodic Rhabdomyolysis 55 0.107
62
HYP645 Hyperthyroxinemia, Dystransthyretinemic 31 0.107
63
HYP029 Hyperthyroxinemia 31 0.107
64
c CNG006 Congenital Hypothyroidism 64 0.103
65
c ACT071 Acute Kidney Failure 60 0.103
66
NDL007 Nodular Goiter 47 0.103
67
P ADL010 Adult Respiratory Distress Syndrome 65 0.099
68
ARR042 Arrhythmogenic Right Ventricular Cardiomyopathy 62 0.099
69
TXC005 Toxic Shock Syndrome 62 0.099
70
P MYC008 Myocarditis 59 0.099
71
CRY001 Cryptogenic Organizing Pneumonia 53 0.099
72
MYX004 Myxedema 43 0.099
73
PLM129 Pulmonary Disease, Chronic Obstructive 73 0.094
74
LSH001 Leishmaniasis 63 0.094
75
P ENC018 Encephalopathy 61 0.094
76
P PNC044 Pancreatitis 61 0.094
77
c ACT027 Acute Pancreatitis 60 0.094
78
PLM010 Pulmonary Edema 54 0.094
79
RHM028 Rheumatic Heart Disease 53 0.094
80
HRT012 Heart Valve Disease 53 0.094
81
THR016 Thrombophlebitis 51 0.094
82
P KLZ004 Kala-Azar 1 41 0.094
83
c PRG042 Progressive Familial Heart Block, Type Ia 69 0.089
84
P HYP098 Hypereosinophilic Syndrome 67 0.089
85
ALP042 Alpha/beta T-Cell Lymphopenia with Gamma/delta T-Cell Expansion, Severe Cytomegalovirus Infection, and Autoimmunity 66 0.089
86
CHL068 Cholestasis 61 0.089
87
ISC004 Ischemia 58 0.089
88
NNR004 Nonarteritic Anterior Ischemic Optic Neuropathy 57 0.089
89
INT007 Intermediate Coronary Syndrome 55 0.089
90
c SBC007 Subacute Thyroiditis 45 0.089
91
P LNG032 Lung Cancer 98 0.084
92
PLM134 Pulmonary Fibrosis, Idiopathic 77 0.084
93
HSH003 Hashimoto Thyroiditis 62 0.084
94
THY029 Thyroid Carcinoma 59 0.084
95
c ACT134 Acute Liver Failure 56 0.084
96
THY030 Thyroid Gland Disease 52 0.084
97
OCL069 Ocular Motor Apraxia 51 0.084
98
47X002 47,xyy 49 0.084
99
ATX019 Ataxia with Vitamin E Deficiency 42 0.084
100
ACR008 Acrocallosal Syndrome 69 0.079
101
P THR014 Thrombocytopenia 67 0.079
102
P VSC011 Vasculitis 62 0.079
103
P CRD246 Cardiovascular System Disease 57 0.079
104
P MTR003 Mitral Valve Stenosis 50 0.079
105
SNT005 Sinoatrial Node Disease 49 0.079
106
RST023 Resting Heart Rate, Variation in 41 0.079
107
c THR092 Thrombophilia Due to Thrombin Defect 73 0.073
108
c NRD033 Neurodegeneration with Brain Iron Accumulation 2a 69 0.073
109
P PLY019 Polyneuropathy 56 0.073
110
P ESN008 Eosinophilic Pneumonia 50 0.073
111
HMP001 Hemopericardium 48 0.073
112
SBC016 Subacute Delirium 44 0.073
113
BCK006 Back Pain 42 0.073
114
DFF031 Diffuse Alveolar Hemorrhage 30 0.073
115
FBR012 Fabry Disease 72 0.067
116
P BRG001 Brugada Syndrome 71 0.067
117
HYP056 Hypoglycemia 66 0.067
118
P NTR004 Neutropenia 63 0.067
119
P VSC007 Vascular Disease 63 0.067
120
DPR016 Depression 63 0.067
121
CTN007 Cutaneous Leishmaniasis 62 0.067
122
HYP066 Hyperglycemia 61 0.067
123
P LPS004 Lupus Erythematosus 61 0.067
124
EXT034 Extrinsic Allergic Alveolitis 58 0.067
125
INT303 Intracranial Hypertension, Idiopathic 57 0.067
126
c PRG043 Progressive Familial Heart Block, Type Ib 54 0.067
127
INT075 Intracranial Hypertension 53 0.067
128
NRT004 Neuritis 52 0.067
129
P PRC012 Pericardial Effusion 51 0.067
130
PPL021 Papilledema 49 0.067
131
SYS003 Systolic Heart Failure 49 0.067
132
EBL001 Ebola Hemorrhagic Fever 49 0.067
133
CRD137 Cardiogenic Shock 47 0.067
134
SPS204 Spastic Paraplegia, Intellectual Disability, Nystagmus, and Obesity 45 0.067
135
c BDY007 Body Mass Index Quantitative Trait Locus 1 42 0.067
136
49X006 49, Xxxxy Syndrome 41 0.067
137
TXC008 Toxic Optic Neuropathy 23 0.067
138
c NRF023 Neurofibromatosis, Type Ii 80 0.060
139
c HPT073 Hepatitis C Virus 72 0.060
140
P TTR001 Tetralogy of Fallot 70 0.060
141
c CHR684 Chronic Kidney Disease 70 0.060
142
P PLM037 Pulmonary Hypertension 67 0.060
143
YMN001 Yemenite Deaf-Blind Hypopigmentation Syndrome 65 0.060
144
ATM095 Autoimmune Disease 62 0.060
145
IDP011 Idiopathic Interstitial Pneumonia 59 0.060
146
NNL006 Non-Alcoholic Steatohepatitis 54 0.060
147
PNC001 Pancytopenia 54 0.060
148
HRT011 Heart Septal Defect 50 0.060
149
HYP006 Hypertensive Heart Disease 49 0.060
150
LFT001 Left Bundle Branch Hemiblock 49 0.060
151
c MTR002 Mitral Valve Insufficiency 48 0.060
152
LPD009 Lipid Storage Disease 46 0.060
153
HPT004 Hepatic Coma 45 0.060
154
GRN017 Granulocytopenia 44 0.060
155
DRG002 Drug-Induced Hepatitis 43 0.060
156
RTN135 Retinal Dystrophy, Iris Coloboma, and Comedogenic Acne Syndrome 40 0.060
157
HYP344 Hyperthyroidism, Familial Gestational 39 0.060
158
MLT131 Multifocal Atrial Tachycardia 18 0.060
159
P HPT023 Hepatocellular Carcinoma 100 0.052
160
MYL069 Myeloma, Multiple 85 0.052
161
MLR004 Malaria 81 0.052
162
CYS001 Cystic Fibrosis 81 0.052
163
P PRT133 Proteasome-Associated Autoinflammatory Syndrome 1 81 0.052
164
AST005 Asthma 76 0.052
165
P APL001 Aplastic Anemia 74 0.052
166
c ATM006 Autoimmune Lymphoproliferative Syndrome 74 0.052
167
c HYP836 Hypercholesterolemia, Familial, 1 73 0.052
168
DFC004 Deficiency Anemia 70 0.052
169
P AMY004 Amyloidosis 70 0.052
170
DWN001 Down Syndrome 70 0.052
171
ADL002 Adult Syndrome 70 0.052
172
c CRD086 Cardiomyopathy, Familial Hypertrophic, 1 68 0.052
173
ANM044 Anemia, X-Linked, with or Without Neutropenia and/or Platelet Abnormalities 67 0.052
174
TRN015 Transient Cerebral Ischemia 63 0.052
175
c HPT001 Hepatitis C 62 0.052
176
FTT001 Fatty Liver Disease 61 0.052
177
ALC006 Alcoholic Hepatitis 61 0.052
178
HPT019 Hepatic Encephalopathy 60 0.052
179
P URT039 Urticaria 58 0.052
180
NWB001 Newborn Respiratory Distress Syndrome 58 0.052
181
EYD002 Eye Disease 58 0.052
182
P GLM007 Glomerulonephritis 57 0.052
183
CRB197 Carbonic Anhydrase Va Deficiency, Hyperammonemia Due to 57 0.052
184
P ANG015 Angioedema 57 0.052
185
P MYS005 Myositis 56 0.052
186
P DRR001 Diarrhea 55 0.052
187
P ALP008 Alopecia 54 0.052
188
c VRL010 Viral Hepatitis 52 0.052
189
IMP005 Impotence 52 0.052
190
PTH003 Pathologic Nystagmus 52 0.052
192
c ALM001 Al Amyloidosis 50 0.052
193
ACT029 Acute Interstitial Pneumonia 49 0.052
194
CRD001 Cardiac Tamponade 47 0.052
195
CYN002 Cyanosis, Transient Neonatal 45 0.052
196
CVD001 Covid-19 44 0.052
197
CRN322 Coronavirus Infectious Disease 40 0.052
198
c ATM022 Autoimmune Myocarditis 35 0.052
199
TRD008 Triiodothyronine Receptor Auxiliary Protein 34 0.052
200
ART110 Arteritic Anterior Ischemic Optic Neuropathy 33 0.052
201
THY001 Thyroid Crisis 31 0.052
202
ISC001 Ischemic Neuropathy 29 0.052
203
CHL079 Children's Interstitial Lung Disease 26 0.052
204
DFF002 Diffuse Pulmonary Fibrosis 25 0.052
205
P CLR023 Colorectal Cancer 99 0.042
206
c SYS001 Systemic Lupus Erythematosus 86 0.042
208
c PLM164 Pulmonary Hypertension, Primary, 1 75 0.042
209
c HMC039 Hemochromatosis, Type 1 74 0.042
210
P PHC003 Pheochromocytoma 71 0.042
211
P SRC025 Sarcoidosis 1 70 0.042
212
P SLP006 Sleep Apnea 69 0.042
213
ART016 Aortic Aneurysm 69 0.042
214
c BSL007 Basal Cell Carcinoma 68 0.042
215
P 3MT016 3-Methylglutaconic Aciduria, Type Iii 67 0.042
216
P TRN020 Turner Syndrome 67 0.042
217
c RHB024 Rhabdomyosarcoma 2 67 0.042
218
ALC007 Alcohol Dependence 66 0.042
219
P HML002 Hemolytic Anemia 63 0.042
220
c ATM011 Autoimmune Hepatitis 63 0.042
221
LPD008 Lipid Metabolism Disorder 62 0.042
222
c FNC043 Fanconi Anemia, Complementation Group E 62 0.042
223
c SVR001 Severe Acute Respiratory Syndrome 62 0.042
224
P HYP750 Hypertriglyceridemia, Familial 62 0.042
225
P ORT004 Orthostatic Intolerance 62 0.042
226
VRL011 Viral Infectious Disease 61 0.042
227
P VNT002 Ventricular Septal Defect 60 0.042
228
P FTT008 Fatty Liver Disease, Nonalcoholic 1 60 0.042
229
P CTR002 Cataract 60 0.042
230
CHL014 Cholera 59 0.042
231
c ART138 Aortic Aneurysm, Familial Abdominal, 1 59 0.042
232
P SLP005 Sleep Disorder 59 0.042
233
PLM033 Pulmonary Embolism 59 0.042
234
PRT058 Pure Autonomic Failure 59 0.042
235
VSL002 Visual Epilepsy 59 0.042
236
P MTR012 Mitral Valve Disease 58 0.042
237
CNS004 Constipation 58 0.042
238
P OPT009 Optic Neuritis 57 0.042
239
P PLY041 Polymyositis 57 0.042
240
THR024 Thrombosis 57 0.042
241
P END033 Endocarditis 57 0.042
242
BLR008 Bilirubin Metabolic Disorder 57 0.042
243
HYP266 Hypoxia 57 0.042
244
P SZR006 Seizure Disorder 56 0.042
245
P ATR001 Atrioventricular Septal Defect 55 0.042
246
VSC003 Visceral Leishmaniasis 55 0.042
247
BRN014 Bronchopneumonia 54 0.042
248
SNS003 Sensory Peripheral Neuropathy 54 0.042
249
c FML191 Familial Long Qt Syndrome 53 0.042
250
P MSC003 Muscular Atrophy 52 0.042
251
PNG002 Pain Agnosia 51 0.042
252
END086 End Stage Renal Disease 51 0.042
253
CHR515 Chronic Atrial and Intestinal Dysrhythmia 50 0.042
254
STM007 Stomatitis 50 0.042
255
LRN003 Learning Disability 49 0.042
256
RGH001 Right Bundle Branch Block 48 0.042
257
DRG013 Drug-Induced Lupus Erythematosus 48 0.042
258
HYP025 Hyperphosphatemia 48 0.042
259
SXL003 Sexual Disorder 47 0.042
260
STV007 Stevens-Johnson Syndrome/toxic Epidermal Necrolysis 47 0.042
261
c SHR030 Short Qt Syndrome 46 0.042
262
ANT039 Antisynthetase Syndrome 46 0.042
263
ADR040 Adrenal Gland Pheochromocytoma 46 0.042
264
CRN019 Coronary Artery Vasospasm 46 0.042
265
c DRR009 Diarrhea 6 46 0.042
266
TSY002 Toe Syndactyly, Telecanthus, and Anogenital and Renal Malformations 45 0.042
267
P PRD021 Periodic Paralysis 45 0.042
268
PTT037 Pituitary Tumors 44 0.042
269
TST015 Testicular Disease 43 0.042
270
P HYP265 Hypotonia 43 0.042
271
CYT002 Cytokine Deficiency 42 0.042
272
c FML294 Familial Short Qt Syndrome 41 0.042
273
PLM068 Pulmonary Vein Stenosis 39 0.042
274
END028 Endemic Goiter 37 0.042
275
PLM011 Plummer's Disease 35 0.042
276
SBV001 Subvalvular Aortic Stenosis 33 0.042
277
IMM039 Immune Hydrops Fetalis 30 0.042
278
c ACT053 Acute Thyroiditis 27 0.042
279
CHT001 Chaotic Atrial Tachycardia 10 0.042
280
P PRS040 Prostate Cancer 97 0.030
281
P BRS047 Breast Cancer 97 0.030
282
P ALZ034 Alzheimer Disease 88 0.030
283
c LKM061 Leukemia, Acute Myeloid 84 0.030
284
c HYP595 Hypertension, Essential 84 0.030
285
P BLD134 Bladder Cancer 79 0.030
286
CNN003 Conn's Syndrome 79 0.030
287
c ART115 Aortic Valve Disease 1 75 0.030
288
P OST002 Osteoporosis 74 0.030
289
c BTT014 Beta-Thalassemia 74 0.030
290
PRP027 Peripheral Vascular Disease 71 0.030
291
MYL005 Myelofibrosis 70 0.030
292
P SPR120 Supranuclear Palsy, Progressive, 1 68 0.030
293
P LYM118 Lymphoma 68 0.030
294
P TMP003 Temporal Arteritis 68 0.030
295
c NMN015 Niemann-Pick Disease, Type C1 68 0.030
296
P FRN006 Frontotemporal Dementia 68 0.030
297
GST092 Gastroesophageal Reflux 67 0.030
298
P MLG056 Malignant Hyperthermia 67 0.030
299
THY121 Thyroid Gland Anaplastic Carcinoma 66 0.030
300
P DMN002 Dementia 66 0.030
301
P SKN015 Skin Carcinoma 66 0.030
302
c LNG044 Long Qt Syndrome 1 66 0.030
303
c SML038 Small Cell Cancer of the Lung 65 0.030
304
CRN036 Craniopharyngioma 65 0.030
305
P CNJ013 Conjunctivitis 65 0.030
306
KRT019 Keratitis, Hereditary 65 0.030
307
P MTR004 Maturity-Onset Diabetes of the Young 65 0.030
308
c ART101 Aortic Valve Disease 2 65 0.030
309
ACH022 Achalasia-Addisonianism-Alacrima Syndrome 65 0.030
310
PRT037 Pertussis 65 0.030
311
GRN037 Granulomatosis with Polyangiitis 65 0.030
312
ATH013 Atherosclerosis Susceptibility 65 0.030
313
AND019 Andersen Cardiodysrhythmic Periodic Paralysis 65 0.030
314
P ART062 Arthrogryposis, Renal Dysfunction, and Cholestasis 1 65 0.030
315
P DBT009 Diabetes Mellitus 64 0.030
316
APN008 Apnea, Obstructive Sleep 64 0.030
317
GT001 Gout 64 0.030
318
GST106 Gastrointestinal Ulceration, Recurrent, with Dysfunctional Platelets 64 0.030
319
MSC007 Muscle Hypertrophy 64 0.030
320
P ADN016 Adenocarcinoma 64 0.030
321
P HYP370 Hypokalemic Periodic Paralysis, Type 1 64 0.030
322
P GLM045 Glioma 63 0.030
323
P GCH001 Gaucher's Disease 63 0.030
324
c PRC016 Pre-Eclampsia 63 0.030
325
P BLD124 Bleeding Disorder, Platelet-Type, 11 63 0.030
326
SKN016 Skin Disease 63 0.030
327
P HYP055 Hypoplastic Left Heart Syndrome 63 0.030
328
c ACT068 Acute Cystitis 63 0.030
329
P PSR002 Psoriasis 62 0.030
330
c HPT003 Hepatitis a 62 0.030
331
NNL005 Non-Alcoholic Fatty Liver Disease 61 0.030
332
DRM006 Dermatitis 61 0.030
333
P MYL006 Myeloid Leukemia 60 0.030
334
P NPH012 Nephrotic Syndrome 60 0.030
335
DPH001 Diphtheria 60 0.030
336
CNG410 Congenital Heart Defects, Hamartomas of Tongue, and Polysyndactyly 60 0.030
337
ACQ007 Acquired Immunodeficiency Syndrome 60 0.030
338
VRC005 Varicose Veins 60 0.030
339
P GLY013 Glycogen Storage Disease 60 0.030
340
P THL005 Thalassemia 60 0.030
341
PRT013 Portal Hypertension 59 0.030
342
P BRN022 Bronchiectasis 59 0.030
343
P LYM033 Lymphoproliferative Syndrome 59 0.030
344
P NMN002 Niemann-Pick Disease 59 0.030
345
P GLL022 Guillain-Barre Syndrome 59 0.030
346
ADN018 Adenoma 59 0.030
347
ANR040 Aneurysm 59 0.030
348
ANT024 Anthrax Disease 58 0.030
349
P ALC033 Alcohol Use Disorder 58 0.030
350
P CND004 Candidiasis 58 0.030
351
BRN056 Bronchopulmonary Dysplasia 57 0.030
352
MNR012 Meniere Disease 57 0.030
353
MLT161 Multinucleated Neurons, Anhydramnios, Renal Dysplasia, Cerebellar Hypoplasia, and Hydranencephaly 57 0.030
354
FRC011 Fructose Intolerance, Hereditary 57 0.030
355
P PYL005 Pyelonephritis 56 0.030
356
PSD063 Pseudohyperkalemia, Familial, 2, Due to Red Cell Leak 56 0.030
357
P HYP024 Hypoparathyroidism 56 0.030
358
BRN004 Brain Edema 56 0.030
359
AGN016 Aging 56 0.030
360
c THY109 Thyroid Cancer, Nonmedullary, 1 56 0.030
361
c FML035 Familial Hyperlipidemia 55 0.030
362
MCL006 Macular Retinal Edema 55 0.030
363
P DBT005 Diabetes Insipidus 55 0.030
364
HMP005 Hemiplegia 55 0.030
365
RSC001 Rosacea 54 0.030
366
GLC003 Glucose Intolerance 54 0.030
367
P DXT004 Dextro-Looped Transposition of the Great Arteries 54 0.030
368
P ART021 Arteriosclerosis 54 0.030
369
CLL003 Cellulitis 54 0.030
370
PRS045 Prostatic Hypertrophy 53 0.030
371
P PLM006 Pulmonary Alveolar Proteinosis 53 0.030
372
INF034 Infective Endocarditis 53 0.030
373
P PTS002 Ptosis 53 0.030
374
LYS002 Lysosomal Storage Disease 52 0.030
375
P SML001 Small Cell Carcinoma 52 0.030
376
PST011 Pustulosis of Palm and Sole 52 0.030
377
P DDN001 Duodenal Ulcer 52 0.030
378
HYP014 Hyperuricemia 52 0.030
379
LYM004 Lymphoid Interstitial Pneumonia 51 0.030
380
c NMN014 Niemann-Pick Disease, Type C2 51 0.030
381
RYS001 Reye Syndrome 51 0.030
382
PRS021 Prostatic Adenoma 51 0.030
383
TRM010 Traumatic Brain Injury 51 0.030
384
P CHL066 Cholangitis 51 0.030
385
PRT029 Parathyroid Adenoma 50 0.030
386
P MMB011 Membranous Nephropathy 50 0.030
387
BLP005 Blepharitis 50 0.030
388
CRN030 Coronary Stenosis 50 0.030
389
c SVR005 Severe Pre-Eclampsia 50 0.030
390
c THY112 Thyroid Hormone Resistance, Generalized, Autosomal Dominant 50 0.030
391
TRY001 Trypanosomiasis 50 0.030
392
P OBS001 Obstructive Jaundice 50 0.030
393
MTB004 Metabolic Acidosis 50 0.030
394
HYP748 Hypertelorism 50 0.030
395
DYS073 Dysphagia 50 0.030
396
HYP080 Hypogonadism 50 0.030
397
INP001 Inappropriate Adh Syndrome 49 0.030
398
P ART018 Aortic Valve Insufficiency 49 0.030
399
GYN001 Gynecomastia 49 0.030
400
PRS129 Prostatic Hyperplasia, Benign 49 0.030
401
BRN071 Brain Injury 49 0.030
402
P CMP008 Compartment Syndrome 49 0.030
403
HST010 Histiocytosis 48 0.030
404
WTH001 Withdrawal Disorder 48 0.030
405
P CLR019 Color Blindness 48 0.030
406
RFR010 Refractory Anemia 48 0.030
407
VTM033 Vitamin K Deficiency Bleeding 48 0.030
408
CLS016 Clostridium Difficile Colitis 48 0.030
409
INT067 Interstitial Nephritis 48 0.030
410
P BNM029 Bone Mineral Density Quantitative Trait Locus 15 48 0.030
411
PLM035 Pulmonary Eosinophilia 48 0.030
412
ASB001 Asbestosis 47 0.030
413
PPL002 Papillary Carcinoma 47 0.030
414
MCC002 Mucocutaneous Leishmaniasis 47 0.030
415
P CRN028 Corneal Ulcer 47 0.030
416
P RNL015 Renal Hypertension 47 0.030
417
CRN017 Coronary Thrombosis 47 0.030
418
c INH020 Inherited Metabolic Disorder 47 0.030
419
SRT004 Serotonin Syndrome 47 0.030
420
ATN005 Autonomic Dysfunction 46 0.030
421
c ACT076 Acute Myocarditis 46 0.030
422
ORC001 Orchitis 46 0.030
423
c CHR037 Chronic Eosinophilic Pneumonia 46 0.030
424
P BNG032 Benign Mesothelioma 46 0.030
425
P MYC033 Myoclonus 46 0.030
426
c ACT042 Acute Pyelonephritis 46 0.030
427
GLL048 Glial Tumor 45 0.030
428
P HRN001 Horner's Syndrome 45 0.030
429
CRD231 Cardiomyopathy, Infantile Histiocytoid 45 0.030
430
c TRC022 Tricuspid Valve Insufficiency 45 0.030
431
PLR022 Pleural Disease 45 0.030
432
CRB004 Cerebral Artery Occlusion 45 0.030
433
INT304 Interstitial Pneumonitis, Desquamative, Familial 45 0.030
434
TWN001 Twin-to-Twin Transfusion Syndrome 45 0.030
435
NNS002 Nonspecific Interstitial Pneumonia 45 0.030
436
THR099 Third-Degree Atrioventricular Block 45 0.030
437
ATN004 Autonomic Neuropathy 45 0.030
438
CRD003 Cardiac Sarcoidosis 44 0.030
439
SCT002 Scotoma 44 0.030
440
FBR054 Fibroma 44 0.030
441
P MYG005 Myoglobinuria 44 0.030
442
CLL021 Collagenous Colitis 42 0.030
443
ALC010 Alcoholic Cardiomyopathy 42 0.030
444
c BNM022 Bone Mineral Density Quantitative Trait Locus 8 42 0.030
445
TTT001 Tatton-Brown-Rahman Syndrome 41 0.030
446
DBT002 Diabetic Autonomic Neuropathy 41 0.030
447
LNR006 Linear Iga Disease 40 0.030
448
c CRD081 Cardiomyopathy, Familial Hypertrophic, 12 39 0.030
449
WLL004 Wallerian Degeneration 39 0.030
450
FLL031 Follicular Adenoma 39 0.030
451
RPD005 Rapidly Involuting Congenital Hemangioma 38 0.030
452
FRS012 First-Degree Atrioventricular Block 38 0.030
453
OPT010 Optic Papillitis 38 0.030
454
SCR039 Scorpion Envenomation 38 0.030
455
ACT167 Acute Generalized Exanthematous Pustulosis 37 0.030
456
FCL041 Focal Myositis 37 0.030
457
c FTL070 Fetal Akinesia Deformation Sequence 2 36 0.030
458
IND003 Indolent Myeloma 36 0.030
459
P CNG024 Congenital Nystagmus 36 0.030
460
P AXN001 Axonal Neuropathy 36 0.030
461
HRW001 Hair Whorl 36 0.030
462
BRK012 Broken Heart Syndrome 35 0.030
463
SRF006 Surfactant Dysfunction 35 0.030
464
c ART068 Aortic Aneurysm, Familial Thoracic 2 34 0.030
465
c ARR048 Arrhythmogenic Right Ventricular Dysplasia, Familial, 4 34 0.030
466
c SHR032 Short Qt Syndrome 2 32 0.030
467
NNT010 Nontoxic Goiter 32 0.030
468
EPD018 Epididymo-Orchitis 32 0.030
469
CRT009 Critical Illness Polyneuropathy 32 0.030
470
c DNT047 Dentinogenesis Imperfecta Type 2 31 0.030
471
INF021 Infant Gynecomastia 31 0.030
472
SNG003 Single Ventricular Heart 30 0.030
473
PLX004 Plexopathy 30 0.030
474
c SHR033 Short Qt Syndrome 3 29 0.030
475
CRD220 Cardiac Valvular Defect, Developmental 29 0.030
476
c ATR092 Atrial Fibrillation, Familial, 15 28 0.030
477
P ATR081 Atrial Standstill 28 0.030
478
ANS021 Anisocoria 27 0.030
479
EXF003 Exfoliative Dermatitis 27 0.030
480
ACT038 Acute Retrobulbar Neuritis 27 0.030
481
IDN001 Iodine Hypothyroidism 26 0.030
482
ASB003 Asbestos Intoxication 26 0.030
483
VLK001 Volkmann Contracture 25 0.030
484
CRT084 Creatinine Clearance Quantitative Trait Locus 25 0.030
485
c TRN047 Transient Congenital Hypothyroidism 23 0.030
486
P PLM064 Pulmonary Sequestration 22 0.030
487
ATR024 Atrial Fibrillation and Stroke 22 0.030
488
PLR025 Pleuroparenchymal Fibroelastosis 22 0.030
489
CRN023 Corneal Deposit 22 0.030
490
CD4008 Cd4/cd8 T-Cell Ratio 20 0.030
491
ATR089 Atrioventricular Dissociation 20 0.030
492
BDR001 Bidirectional Tachycardia 19 0.030
493
ATM054 Autoimmune Disease 3 18 0.030
494
MYP026 Myopathy - Thyrotoxic 17 0.030
495
GRN059 Grn Frontotemporal Dementia 14 0.030
496
ETH013 Euthyroid Graves Orbitopathy 14 0.030
497
TXC006 Toxic Labyrinthitis 11 0.030
Content
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